From 5b26d9154d521984b62c74a8177daa6c60943058 Mon Sep 17 00:00:00 2001
From: eduardo-proteinms <eduardo@proteinms.net>
Date: Wed, 9 Oct 2024 15:43:58 -0700
Subject: [PATCH] Restructure Tutorial Image naming (#3181)

* Move small images to shared folder and name images that dont come from Skyline
* Update tutorial script to support alt text for s- images
* Fix javascript that numbers figure
* Add figure anchor
* Update javascript so anchor is followed on page load
* tweak skyline.js to remove colons from Chinese and Japanese translations
---
 .../Tutorials/AbsoluteQuant/en/index.html     |  34 +--
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 ...mage-0.png => s-experimental-overview.png} | Bin
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 .../Tutorials/AbsoluteQuant/zh-CHS/index.html |  34 +--
 .../AbsoluteQuant/zh-CHS/invariant.html       |  34 +--
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/en/index.html b/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/en/index.html
index 85fd252a9b..00e522462c 100644
--- a/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/en/index.html
+++ b/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/en/index.html
@@ -60,7 +60,7 @@ <h1>Experimental Overview</h1>
         different calibrants.
     </p>
     <p>
-        <img src="image-0.png" />
+        <img src="s-experimental-overview.png" />
     </p>
     <p>
         <b>Tutorial Figure 1. Experimental Overview</b>
@@ -144,7 +144,7 @@ <h2>Configuring transition settings:</h2>
         The form should now look like this:
     </p>
     <p>
-        <img src="image-1.png" />
+        <img src="s-1.png" />
     </p>
     <ul>
         <li>Click the <b>Filter</b> tab. </li>
@@ -165,7 +165,7 @@ <h2>Configuring transition settings:</h2>
         The <b>Transition Settings</b> form should look like this: 
     </p>
     <p>
-         <img src="image-2.png" />
+         <img src="s-2.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -182,7 +182,7 @@ <h2>Configuring peptide settings:</h2>
         The <b>Edit Isotope Modification</b> form should now look like this:
     </p>
     <p>
-        <img src="image-3.png" />
+        <img src="s-3.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -192,7 +192,7 @@ <h2>Configuring peptide settings:</h2>
         The <b>Peptide Settings</b> form should now look like this:
     </p>
     <p>
-        <img src="image-4.png" />
+        <img src="s-4.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button. </li>
@@ -207,7 +207,7 @@ <h2>Inserting a peptide sequence:</h2>
         <li>Paste “IEAIPQIDK” into the <b>Peptide Sequence</b> cell and “GST-tag” into the <b>Protein Name</b> cell.</li>
     </ul>
     <p>
-        <img src="image-5.png" />
+        <img src="s-5.png" />
     </p>
     <ul>
         <li>Click the <b>Insert</b> button.</li>
@@ -216,7 +216,7 @@ <h2>Inserting a peptide sequence:</h2>
         After performing the above steps, the main Skyline should now look like this:
     </p>
     <p>
-        <img src="image-6.png" />
+        <img src="s-6.png" />
     </p>
     <p>
         Before exporting your first transition list, first save your document to the AbsoluteQuant folder by doing the following:
@@ -242,7 +242,7 @@ <h2>Exporting a transition list:</h2>
         <b>Transition Settings</b> – <b>Prediction</b> tab.
     </p>
     <p>
-        <img src="image-7.png" />
+        <img src="s-7.png" />
     </p>
     <p>
         You can also see that all of the other settings are appropriate for this very simple target list.
@@ -290,7 +290,7 @@ <h2>Importing RAW files into Skyline:</h2>
         The <b>Import Results</b> form should look like this:
     </p>
     <p>
-        <img src="image-8.png" />
+        <img src="s-8.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -299,7 +299,7 @@ <h2>Importing RAW files into Skyline:</h2>
         <li>In the <b>Import Results Files</b> form, find and select all eight “Standard” RAW files as shown below.</li>
     </ul>
     <p>
-        <img src="image-9.png" />
+        <img src="s-9.png" />
     </p>
     <ul>
         <li>Click <b>Open</b> to import the files.</li>
@@ -322,7 +322,7 @@ <h2>Importing RAW files into Skyline:</h2>
         You will see the heavy (Blue) and light (Red) total chromatograms displayed together in a graph for each standard as shown below:
     </p>
     <p>
-        <img src="image-10.png" />
+        <img src="s-10.png" />
     </p>
     <p>
         What to inspect when looking at the chromatographic traces for the standards:
@@ -368,13 +368,13 @@ <h1>Analyzing SRM Data from FOXN1-GST Sample</h1>
         You can then select either the light precursor:
     </p>
     <p>
-        <img src="image-11.png" />
+        <img src="s-11.png" />
     </p>
     <p class="keep-next">
         Or the heavy precursor:
     </p>
     <p>
-        <img src="image-12.png" />
+        <img src="s-12.png" />
     </p>
     <p>
          Verify the following:
@@ -402,7 +402,7 @@ <h1>Analyzing SRM Data from FOXN1-GST Sample</h1>
         points. This is ideal, as this portion of the calibration curve is best for quantification purposes. 
     </p>
     <p>
-        <img src="image-13.png" />
+        <img src="s-13.png" />
     </p>
     <h1>Generating a Calibration Curve</h1>
     <p>
@@ -420,7 +420,7 @@ <h2>Configuring quantification settings:</h2>
         The <b>Peptide Settings</b> form should look like this:
     </p>
     <p>
-        <img src="image-14.png" />
+        <img src="s-14.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -476,7 +476,7 @@ <h2>Specify the analyte concentrations of the external standards:</h2>
         The <b>Document Grid: Replicates</b> form should look like this:
     </p>
     <p>
-        <img src="image-15.png" />
+        <img src="s-15.png" />
     </p>
     <h2>View the calibration curve</h2>
     <ul>
@@ -487,7 +487,7 @@ <h2>View the calibration curve</h2>
         You should see a graph that looks like this:
     </p>
     <p>
-        <img src="image-16.png" />
+        <img src="s-16.png" />
     </p>
     <p>
         The slope and intercept are displayed on the calibration curve. They can be used to convert between peak area ratio and concentration with a
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/en/image-1.png b/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/en/s-1.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/en/image-1.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/en/s-1.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/en/image-10.png b/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/en/s-10.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/en/image-10.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/en/s-10.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/en/image-11.png b/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/en/s-11.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/en/image-11.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/en/s-11.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/en/image-12.png b/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/en/s-12.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/en/image-12.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/en/s-12.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/en/image-13.png b/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/en/s-13.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/en/image-13.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/en/s-13.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/en/image-14.png b/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/en/s-14.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/en/image-14.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/en/s-14.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/en/image-15.png b/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/en/s-15.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/en/image-15.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/en/s-15.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/en/image-16.png b/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/en/s-16.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/en/image-16.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/en/s-16.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/en/image-2.png b/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/en/s-2.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/en/image-2.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/en/s-2.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/en/image-3.png b/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/en/s-3.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/en/image-3.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/en/s-3.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/en/image-4.png b/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/en/s-4.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/en/image-4.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/en/s-4.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/en/image-5.png b/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/en/s-5.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/en/image-5.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/en/s-5.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/en/image-6.png b/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/en/s-6.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/en/image-6.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/en/s-6.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/en/image-7.png b/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/en/s-7.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/en/image-7.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/en/s-7.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/en/image-8.png b/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/en/s-8.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/en/image-8.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/en/s-8.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/en/image-9.png b/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/en/s-9.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/en/image-9.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/en/s-9.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/en/image-0.png b/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/en/s-experimental-overview.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/en/image-0.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/en/s-experimental-overview.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/ja/index.html b/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/ja/index.html
index 8a918a46ab..6268ef75cc 100644
--- a/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/ja/index.html
+++ b/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/ja/index.html
@@ -32,7 +32,7 @@ <h1>実験概要</h1>
         Vantage（四重極質量分析計）を用いて選択イオンモニタリング（SRM）で分析しました。97%以上の純度でに精製され、アミノ酸分析で濃度確認済みのさまざまな量の未標識IEAIPQIDKペプチドを使用して外部標準法による校正曲線が作成できます。安定同位体標識のIEAIPQIDKペプチドも、FOXN1-GNT試料と同じ濃度でこれらのキャリブラントに添加しています（<b>チュートリアル図1C</b>）。各試料内の安定同位体標識ペプチドの濃度が同じであれば値（濃度）はいくらであってもかまいませんが、試料内の安定同位体標識ペプチド量はFOXN1-GSTから生じる未標識のペプチドと量的に近いのが望ましいです。またFOXN1-GSTの未標識ペプチドの濃度はキャリブラントを使用して検定した濃度範囲の中央値に近いのが理想です。
     </p>
     <p>
-        <img src="image-0.png" />
+        <img src="s-experimental-overview.png" />
     </p>
     <p>
         <b>チュートリアル図1. 実験概要</b>
@@ -112,7 +112,7 @@ <h2>トランジション設定を行う</h2>
         フォームは以下のようになります。
     </p>
     <p>
-        <img src="image-1.png" />
+        <img src="s-1.png" />
     </p>
     <ul>
         <li>[ <b>フィルタ</b> ] タブをクリックします。 </li>
@@ -132,7 +132,7 @@ <h2>トランジション設定を行う</h2>
         [ <b>トランジションの設定</b> ] フォームは以下のようになります。 
     </p>
     <p>
-         <img src="image-2.png" />
+         <img src="s-2.png" />
     </p>
     <ul>
         <li>[ <b>OK</b> ] ボタンをクリックします。</li>
@@ -149,7 +149,7 @@ <h2>ペプチド設定を行う</h2>
         [ <b>同位体修飾を編集</b> ] フォームは以下のようになります。
     </p>
     <p>
-        <img src="image-3.png" />
+        <img src="s-3.png" />
     </p>
     <ul>
         <li>[ <b>OK</b> ] ボタンをクリックします。</li>
@@ -159,7 +159,7 @@ <h2>ペプチド設定を行う</h2>
         [ <b>ペプチド設定</b> ] フォームは以下のようになります。
     </p>
     <p>
-        <img src="image-4.png" />
+        <img src="s-4.png" />
     </p>
     <ul>
         <li>[ <b>OK</b> ] ボタンをクリックします。 </li>
@@ -173,7 +173,7 @@ <h2>ペプチドシークエンスを挿入</h2>
         <li>「IEAIPQIDK」を [ <b>ペプチドシークエンス</b> ] セルに貼り付け、「GST-tag」を [ <b>タンパク質名</b> ] セルへ貼り付けます。</li>
     </ul>
     <p>
-        <img src="image-5.png" />
+        <img src="s-5.png" />
     </p>
     <ul>
         <li>[ <b>挿入</b> ] ボタンをクリックします。</li>
@@ -182,7 +182,7 @@ <h2>ペプチドシークエンスを挿入</h2>
         上記手順を実施すると、Skylineの画面は以下のようになります。
     </p>
     <p>
-        <img src="image-6.png" />
+        <img src="s-6.png" />
     </p>
     <p>
         最初のトランジションリストをエクスポートする前に、まず次の手順でドキュメントをAbsoluteQuantフォルダに保存します。
@@ -205,7 +205,7 @@ <h2>トランジションリストのエクスポート</h2>
         <b>衝突エネルギー</b> ] で「Thermo TSQ Vantage」を選択しているので、[ <b>装置タイプ</b> ] リストには自動的に「Thermo」が選択されています。
     </p>
     <p>
-        <img src="image-7.png" />
+        <img src="s-7.png" />
     </p>
     <p>
         また、他の設定もすべてこのターゲットリストに適切であることがわかります。
@@ -250,7 +250,7 @@ <h2>SkylineへのRAWファイルインポート</h2>
         [ <b>結果をインポート</b> ] フォームは以下のようになります。
     </p>
     <p>
-        <img src="image-8.png" />
+        <img src="s-8.png" />
     </p>
     <ul>
         <li>[ <b>OK</b> ] ボタンをクリックします。</li>
@@ -259,7 +259,7 @@ <h2>SkylineへのRAWファイルインポート</h2>
         <li>[ <b>結果ファイルをインポート</b> ] フォームで、以下の8個の「Standard」RAWファイルを選択します。</li>
     </ul>
     <p>
-        <img src="image-9.png" />
+        <img src="s-9.png" />
     </p>
     <ul>
         <li>[ <b>開く</b> ] をクリックしてファイルをインポートします。</li>
@@ -280,7 +280,7 @@ <h2>SkylineへのRAWファイルインポート</h2>
         以下のように各標準の安定同位体標識（青）と未標識（赤）のクロマトグラムが同時にグラフに表示されるのがわかります。
     </p>
     <p>
-        <img src="image-10.png" />
+        <img src="s-10.png" />
     </p>
     <p>
         標準のクロマトグラフトレースを見るときに注目すべきは以下の項目です。
@@ -320,13 +320,13 @@ <h1>FOXN1-GST試料のSRMデータ分析</h1>
         これで未標識ペプチドのプリカーサーイオン
     </p>
     <p>
-        <img src="image-11.png" />
+        <img src="s-11.png" />
     </p>
     <p class="keep-next">
         または安定同位体標識ペプチドのプリカーサーイオンを選択できます。
     </p>
     <p>
-        <img src="image-12.png" />
+        <img src="s-12.png" />
     </p>
     <p>
         以下を確認します。
@@ -351,7 +351,7 @@ <h1>FOXN1-GST試料のSRMデータ分析</h1>
         <b>ピーク領域</b>グラフに表示される値は校正曲線に使用する値となります。このグラフから、FOXN1-GST試料の未標識と安定同位体標識比率は校正点のおよそ中央にあることが簡単にわかります。この濃度範囲は定量化に最適で理想的です。 
     </p>
     <p>
-        <img src="image-13.png" />
+        <img src="s-13.png" />
     </p>
     <h1>校正曲線の作成</h1>
     <p>
@@ -369,7 +369,7 @@ <h2>定量化設定</h2>
         [ <b>ペプチド設定</b> ] フォームは以下のようになります。
     </p>
     <p>
-        <img src="image-14.png" />
+        <img src="s-14.png" />
     </p>
     <ul>
         <li>[ <b>OK</b> ] ボタンをクリックします。</li>
@@ -424,7 +424,7 @@ <h2>外部標準のアナライト濃度指定</h2>
         [<b>ドキュメントグリッド: 繰り返し測定</b> ] フォームは以下のようになります。
     </p>
     <p>
-        <img src="image-15.png" />
+        <img src="s-15.png" />
     </p>
     <h2>校正曲線表示</h2>
     <ul>
@@ -435,7 +435,7 @@ <h2>校正曲線表示</h2>
         以下のようなグラフが表示されます。
     </p>
     <p>
-        <img src="image-16.png" />
+        <img src="s-16.png" />
     </p>
     <p>
         校正曲線線に勾配と切片が表示されています。これを標準の<b>y = m * x + b</b>式と共に使用してピーク領域比と濃度を変換できます。 
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/ja/invariant.html b/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/ja/invariant.html
index e1cb11687a..c63cf91cd3 100644
--- a/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/ja/invariant.html
+++ b/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/ja/invariant.html
@@ -60,7 +60,7 @@ <h1>Experimental Overview</h1>
         different calibrants.
     </p>
     <p>
-        <img src="image-0.png" />
+        <img src="s-experimental-overview.png" />
     </p>
     <p>
         <b>Tutorial Figure 1. Experimental Overview</b>
@@ -144,7 +144,7 @@ <h2>Configuring transition settings:</h2>
         The form should now look like this:
     </p>
     <p>
-        <img src="image-1.png" />
+        <img src="s-1.png" />
     </p>
     <ul>
         <li>Click the <b>Filter</b> tab. </li>
@@ -165,7 +165,7 @@ <h2>Configuring transition settings:</h2>
         The <b>Transition Settings</b> form should look like this: 
     </p>
     <p>
-         <img src="image-2.png" />
+         <img src="s-2.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -182,7 +182,7 @@ <h2>Configuring peptide settings:</h2>
         The <b>Edit Isotope Modification</b> form should now look like this:
     </p>
     <p>
-        <img src="image-3.png" />
+        <img src="s-3.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -192,7 +192,7 @@ <h2>Configuring peptide settings:</h2>
         The <b>Peptide Settings</b> form should now look like this:
     </p>
     <p>
-        <img src="image-4.png" />
+        <img src="s-4.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button. </li>
@@ -207,7 +207,7 @@ <h2>Inserting a peptide sequence:</h2>
         <li>Paste “IEAIPQIDK” into the <b>Peptide Sequence</b> cell and “GST-tag” into the <b>Protein Name</b> cell.</li>
     </ul>
     <p>
-        <img src="image-5.png" />
+        <img src="s-5.png" />
     </p>
     <ul>
         <li>Click the <b>Insert</b> button.</li>
@@ -216,7 +216,7 @@ <h2>Inserting a peptide sequence:</h2>
         After performing the above steps, the main Skyline should now look like this:
     </p>
     <p>
-        <img src="image-6.png" />
+        <img src="s-6.png" />
     </p>
     <p>
         Before exporting your first transition list, first save your document to the AbsoluteQuant folder by doing the following:
@@ -242,7 +242,7 @@ <h2>Exporting a transition list:</h2>
         <b>Transition Settings</b> – <b>Prediction</b> tab.
     </p>
     <p>
-        <img src="image-7.png" />
+        <img src="s-7.png" />
     </p>
     <p>
         You can also see that all of the other settings are appropriate for this very simple target list.
@@ -290,7 +290,7 @@ <h2>Importing RAW files into Skyline:</h2>
         The <b>Import Results</b> form should look like this:
     </p>
     <p>
-        <img src="image-8.png" />
+        <img src="s-8.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -299,7 +299,7 @@ <h2>Importing RAW files into Skyline:</h2>
         <li>In the <b>Import Results Files</b> form, find and select all eight “Standard” RAW files as shown below.</li>
     </ul>
     <p>
-        <img src="image-9.png" />
+        <img src="s-9.png" />
     </p>
     <ul>
         <li>Click <b>Open</b> to import the files.</li>
@@ -322,7 +322,7 @@ <h2>Importing RAW files into Skyline:</h2>
         You will see the heavy (Blue) and light (Red) total chromatograms displayed together in a graph for each standard as shown below:
     </p>
     <p>
-        <img src="image-10.png" />
+        <img src="s-10.png" />
     </p>
     <p>
         What to inspect when looking at the chromatographic traces for the standards:
@@ -368,13 +368,13 @@ <h1>Analyzing SRM Data from FOXN1-GST Sample</h1>
         You can then select either the light precursor:
     </p>
     <p>
-        <img src="image-11.png" />
+        <img src="s-11.png" />
     </p>
     <p class="keep-next">
         Or the heavy precursor:
     </p>
     <p>
-        <img src="image-12.png" />
+        <img src="s-12.png" />
     </p>
     <p>
          Verify the following:
@@ -402,7 +402,7 @@ <h1>Analyzing SRM Data from FOXN1-GST Sample</h1>
         points. This is ideal, as this portion of the calibration curve is best for quantification purposes. 
     </p>
     <p>
-        <img src="image-13.png" />
+        <img src="s-13.png" />
     </p>
     <h1>Generating a Calibration Curve</h1>
     <p>
@@ -420,7 +420,7 @@ <h2>Configuring quantification settings:</h2>
         The <b>Peptide Settings</b> form should look like this:
     </p>
     <p>
-        <img src="image-14.png" />
+        <img src="s-14.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -476,7 +476,7 @@ <h2>Specify the analyte concentrations of the external standards:</h2>
         The <b>Document Grid: Replicates</b> form should look like this:
     </p>
     <p>
-        <img src="image-15.png" />
+        <img src="s-15.png" />
     </p>
     <h2>View the calibration curve</h2>
     <ul>
@@ -487,7 +487,7 @@ <h2>View the calibration curve</h2>
         You should see a graph that looks like this:
     </p>
     <p>
-        <img src="image-16.png" />
+        <img src="s-16.png" />
     </p>
     <p>
         The slope and intercept are displayed on the calibration curve. They can be used to convert between peak area ratio and concentration with a
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/ja/image-1.png b/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/ja/s-1.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/ja/image-1.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/ja/s-1.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/ja/image-10.png b/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/ja/s-10.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/ja/image-10.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/ja/s-10.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/ja/image-11.png b/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/ja/s-11.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/ja/image-11.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/ja/s-11.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/ja/image-12.png b/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/ja/s-12.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/ja/image-12.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/ja/s-12.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/ja/image-13.png b/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/ja/s-13.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/ja/image-13.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/ja/s-13.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/ja/image-14.png b/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/ja/s-14.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/ja/image-14.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/ja/s-14.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/ja/image-15.png b/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/ja/s-15.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/ja/image-15.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/ja/s-15.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/ja/image-16.png b/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/ja/s-16.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/ja/image-16.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/ja/s-16.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/ja/image-2.png b/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/ja/s-2.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/ja/image-2.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/ja/s-2.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/ja/image-3.png b/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/ja/s-3.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/ja/image-3.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/ja/s-3.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/ja/image-4.png b/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/ja/s-4.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/ja/image-4.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/ja/s-4.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/ja/image-5.png b/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/ja/s-5.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/ja/image-5.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/ja/s-5.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/ja/image-6.png b/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/ja/s-6.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/ja/image-6.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/ja/s-6.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/ja/image-7.png b/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/ja/s-7.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/ja/image-7.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/ja/s-7.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/ja/image-8.png b/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/ja/s-8.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/ja/image-8.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/ja/s-8.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/ja/image-9.png b/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/ja/s-9.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/ja/image-9.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/ja/s-9.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/ja/image-0.png b/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/ja/s-experimental-overview.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/ja/image-0.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/ja/s-experimental-overview.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/zh-CHS/index.html b/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/zh-CHS/index.html
index e81670bc23..6a3b356ff1 100644
--- a/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/zh-CHS/index.html
+++ b/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/zh-CHS/index.html
@@ -35,7 +35,7 @@ <h1>实验概述</h1>
         的轻肽浓度处于使用不同校准物测试的浓度范围中间时最佳。
     </p>
     <p>
-        <img src="image-0.png" />
+        <img src="s-experimental-overview.png" />
     </p>
     <p>
         <b>教程图 1. 实验概述</b>
@@ -115,7 +115,7 @@ <h2>配置离子对设置：</h2>
         该表单现在应显示如下：
     </p>
     <p>
-        <img src="image-1.png" />
+        <img src="s-1.png" />
     </p>
     <ul>
         <li>单击<b>过滤器</b>选项卡。 </li>
@@ -135,7 +135,7 @@ <h2>配置离子对设置：</h2>
         <b>离子对设置</b>表单现在应显示如下： 
     </p>
     <p>
-         <img src="image-2.png" />
+         <img src="s-2.png" />
     </p>
     <ul>
         <li>单击<b>确定</b>按钮。</li>
@@ -152,7 +152,7 @@ <h2>配置肽段设置：</h2>
         此时<b>编辑同位素修饰</b>表单应显示如下：
     </p>
     <p>
-        <img src="image-3.png" />
+        <img src="s-3.png" />
     </p>
     <ul>
         <li>单击<b>确定</b>按钮。</li>
@@ -162,7 +162,7 @@ <h2>配置肽段设置：</h2>
         <b>肽段设置</b>表单现在应显示如下：
     </p>
     <p>
-        <img src="image-4.png" />
+        <img src="s-4.png" />
     </p>
     <ul>
         <li>单击<b>确定</b>按钮。 </li>
@@ -176,7 +176,7 @@ <h2>插入肽段序列：</h2>
         <li>将 "IEAIPQIDK" 粘贴到<b>肽段序列</b>单元，将 "GST-tag" 粘贴到<b>蛋白质名称</b>单元。</li>
     </ul>
     <p>
-        <img src="image-5.png" />
+        <img src="s-5.png" />
     </p>
     <ul>
         <li>单击<b>插入</b>按钮。</li>
@@ -185,7 +185,7 @@ <h2>插入肽段序列：</h2>
         完成上述步骤后，Skyline 主页面现在应显示如下：
     </p>
     <p>
-        <img src="image-6.png" />
+        <img src="s-6.png" />
     </p>
     <p>
         在导出您的第一个离子对列表前，先将您的文档保存至 AbsoluteQuant 文件夹，操作如下:
@@ -208,7 +208,7 @@ <h2>导出离子对列表</h2>
         值，<b>仪器类型</b>列表中自动选择了 "Thermo"。
     </p>
     <p>
-        <img src="image-7.png" />
+        <img src="s-7.png" />
     </p>
     <p>
         您还可看到其他所有设置都适合于这个非常简单的目标列表。
@@ -254,7 +254,7 @@ <h2>将 RAW 文件导入 Skyline：</h2>
         <b>导入结果</b>表单应显示如下：
     </p>
     <p>
-        <img src="image-8.png" />
+        <img src="s-8.png" />
     </p>
     <ul>
         <li>单击<b>确定</b>按钮。</li>
@@ -263,7 +263,7 @@ <h2>将 RAW 文件导入 Skyline：</h2>
         <li>在<b>导入结果文件</b>表单中，找到这八个“Standard” RAW 文件并全部选中，如下所示。</li>
     </ul>
     <p>
-        <img src="image-9.png" />
+        <img src="s-9.png" />
     </p>
     <ul>
         <li>单击<b>打开</b>以导入文件。</li>
@@ -284,7 +284,7 @@ <h2>将 RAW 文件导入 Skyline：</h2>
         对于每个标准，您会在界面中同时看到轻（红色）重（蓝色）总色谱图，如下所示：
     </p>
     <p>
-        <img src="image-10.png" />
+        <img src="s-10.png" />
     </p>
     <p>
         查看标准的色谱痕量时所要检查的内容：
@@ -324,13 +324,13 @@ <h1>分析来自于 FOXN1-GST 样品的 SRM 数据</h1>
         然后，您可以选择任何一种轻母离子：
     </p>
     <p>
-        <img src="image-11.png" />
+        <img src="s-11.png" />
     </p>
     <p class="keep-next">
         或是选择重母离子：
     </p>
     <p>
-        <img src="image-12.png" />
+        <img src="s-12.png" />
     </p>
     <p>
         验证以下项：
@@ -354,7 +354,7 @@ <h1>分析来自于 FOXN1-GST 样品的 SRM 数据</h1>
         <b>峰面积</b>图中显示的值就是稍后在校准曲线中使用的值。从该图很容易看出，FOXN1-GST 样品的轻重比居于校准点比率的中间位置。这是理想的状态，因为校准曲线中的这一部分最适合定量的用途。 
     </p>
     <p>
-        <img src="image-13.png" />
+        <img src="s-13.png" />
     </p>
     <h1>生成校准曲线</h1>
     <p>
@@ -372,7 +372,7 @@ <h2>配置定量设置：</h2>
         <b>肽段设置</b>表单应显示如下：
     </p>
     <p>
-        <img src="image-14.png" />
+        <img src="s-14.png" />
     </p>
     <ul>
         <li>单击<b>确定</b>按钮。</li>
@@ -426,7 +426,7 @@ <h2>指定外部标准的分析物浓度：</h2>
         <b>文档网格：重复测定</b>表单应显示如下：
     </p>
     <p>
-        <img src="image-15.png" />
+        <img src="s-15.png" />
     </p>
     <h2>查看校准曲线</h2>
     <ul>
@@ -437,7 +437,7 @@ <h2>查看校准曲线</h2>
         您应当看到如下所示的图：
     </p>
     <p>
-        <img src="image-16.png" />
+        <img src="s-16.png" />
     </p>
     <p>
         斜率和截距显示在校准曲线上。使用标准的 <b>y = m * x + b</b> 方程式可以在峰面积比和浓度之间进行转换 
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/zh-CHS/invariant.html b/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/zh-CHS/invariant.html
index dbd479ec9b..5b06d8c431 100644
--- a/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/zh-CHS/invariant.html
+++ b/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/zh-CHS/invariant.html
@@ -60,7 +60,7 @@ <h1>Experimental Overview</h1>
         different calibrants.
     </p>
     <p>
-        <img src="image-0.png" />
+        <img src="s-experimental-overview.png" />
     </p>
     <p>
         <b>Tutorial Figure 1. Experimental Overview</b>
@@ -144,7 +144,7 @@ <h2>Configuring transition settings:</h2>
         The form should now look like this:
     </p>
     <p>
-        <img src="image-1.png" />
+        <img src="s-1.png" />
     </p>
     <ul>
         <li>Click the <b>Filter</b> tab. </li>
@@ -165,7 +165,7 @@ <h2>Configuring transition settings:</h2>
         The <b>Transition Settings</b> form should look like this: 
     </p>
     <p>
-         <img src="image-2.png" />
+         <img src="s-2.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -182,7 +182,7 @@ <h2>Configuring peptide settings:</h2>
         The <b>Edit Isotope Modification</b> form should now look like this:
     </p>
     <p>
-        <img src="image-3.png" />
+        <img src="s-3.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -192,7 +192,7 @@ <h2>Configuring peptide settings:</h2>
         The <b>Peptide Settings</b> form should now look like this:
     </p>
     <p>
-        <img src="image-4.png" />
+        <img src="s-4.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button. </li>
@@ -207,7 +207,7 @@ <h2>Inserting a peptide sequence:</h2>
         <li>Paste “IEAIPQIDK” into the <b>Peptide Sequence</b> cell and “GST-tag” into the <b>Protein Name</b> cell.</li>
     </ul>
     <p>
-        <img src="image-5.png" />
+        <img src="s-5.png" />
     </p>
     <ul>
         <li>Click the <b>Insert</b> button.</li>
@@ -216,7 +216,7 @@ <h2>Inserting a peptide sequence:</h2>
         After performing the above steps, the main Skyline should now look like this:
     </p>
     <p>
-        <img src="image-6.png" />
+        <img src="s-6.png" />
     </p>
     <p>
         Before exporting your first transition list, first save your document to the AbsoluteQuant folder by doing the following:
@@ -242,7 +242,7 @@ <h2>Exporting a transition list:</h2>
         <b>Transition Settings</b> – <b>Prediction</b> tab.
     </p>
     <p>
-        <img src="image-7.png" />
+        <img src="s-7.png" />
     </p>
     <p>
         You can also see that all of the other settings are appropriate for this very simple target list.
@@ -290,7 +290,7 @@ <h2>Importing RAW files into Skyline:</h2>
         The <b>Import Results</b> form should look like this:
     </p>
     <p>
-        <img src="image-8.png" />
+        <img src="s-8.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -299,7 +299,7 @@ <h2>Importing RAW files into Skyline:</h2>
         <li>In the <b>Import Results Files</b> form, find and select all eight “Standard” RAW files as shown below.</li>
     </ul>
     <p>
-        <img src="image-9.png" />
+        <img src="s-9.png" />
     </p>
     <ul>
         <li>Click <b>Open</b> to import the files.</li>
@@ -322,7 +322,7 @@ <h2>Importing RAW files into Skyline:</h2>
         You will see the heavy (Blue) and light (Red) total chromatograms displayed together in a graph for each standard as shown below:
     </p>
     <p>
-        <img src="image-10.png" />
+        <img src="s-10.png" />
     </p>
     <p>
         What to inspect when looking at the chromatographic traces for the standards:
@@ -368,13 +368,13 @@ <h1>Analyzing SRM Data from FOXN1-GST Sample</h1>
         You can then select either the light precursor:
     </p>
     <p>
-        <img src="image-11.png" />
+        <img src="s-11.png" />
     </p>
     <p class="keep-next">
         Or the heavy precursor:
     </p>
     <p>
-        <img src="image-12.png" />
+        <img src="s-12.png" />
     </p>
     <p>
          Verify the following:
@@ -402,7 +402,7 @@ <h1>Analyzing SRM Data from FOXN1-GST Sample</h1>
         points. This is ideal, as this portion of the calibration curve is best for quantification purposes. 
     </p>
     <p>
-        <img src="image-13.png" />
+        <img src="s-13.png" />
     </p>
     <h1>Generating a Calibration Curve</h1>
     <p>
@@ -420,7 +420,7 @@ <h2>Configuring quantification settings:</h2>
         The <b>Peptide Settings</b> form should look like this:
     </p>
     <p>
-        <img src="image-14.png" />
+        <img src="s-14.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -476,7 +476,7 @@ <h2>Specify the analyte concentrations of the external standards:</h2>
         The <b>Document Grid: Replicates</b> form should look like this:
     </p>
     <p>
-        <img src="image-15.png" />
+        <img src="s-15.png" />
     </p>
     <h2>View the calibration curve</h2>
     <ul>
@@ -487,7 +487,7 @@ <h2>View the calibration curve</h2>
         You should see a graph that looks like this:
     </p>
     <p>
-        <img src="image-16.png" />
+        <img src="s-16.png" />
     </p>
     <p>
         The slope and intercept are displayed on the calibration curve. They can be used to convert between peak area ratio and concentration with a
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/zh-CHS/image-1.png b/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/zh-CHS/s-1.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/zh-CHS/image-1.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/zh-CHS/s-1.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/zh-CHS/image-10.png b/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/zh-CHS/s-10.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/zh-CHS/image-10.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/zh-CHS/s-10.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/zh-CHS/image-11.png b/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/zh-CHS/s-11.png
similarity index 100%
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/zh-CHS/image-12.png b/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/zh-CHS/s-12.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/zh-CHS/image-13.png b/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/zh-CHS/s-13.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/zh-CHS/image-14.png b/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/zh-CHS/s-14.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/zh-CHS/image-15.png b/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/zh-CHS/s-15.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/zh-CHS/image-16.png b/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/zh-CHS/s-16.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/zh-CHS/image-2.png b/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/zh-CHS/s-2.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/zh-CHS/image-3.png b/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/zh-CHS/s-3.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/zh-CHS/image-4.png b/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/zh-CHS/s-4.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/zh-CHS/image-5.png b/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/zh-CHS/s-5.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/zh-CHS/image-6.png b/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/zh-CHS/s-6.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/zh-CHS/image-7.png b/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/zh-CHS/s-7.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/zh-CHS/image-8.png b/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/zh-CHS/s-8.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/zh-CHS/image-9.png b/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/zh-CHS/s-9.png
similarity index 100%
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/zh-CHS/image-0.png b/pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/zh-CHS/s-experimental-overview.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/AbsoluteQuant/zh-CHS/image-0.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/AuditLog/en/index.html b/pwiz_tools/Skyline/Documentation/Tutorials/AuditLog/en/index.html
index e3142f9d7a..d84626b8f7 100644
--- a/pwiz_tools/Skyline/Documentation/Tutorials/AuditLog/en/index.html
+++ b/pwiz_tools/Skyline/Documentation/Tutorials/AuditLog/en/index.html
@@ -81,7 +81,7 @@ <h2>Opening the audit log</h2>
         This should bring up the <b>Audit Log</b> view in its default configuration as shown below:
     </p>
     <p>
-        <img src="image-0.png" />
+        <img src="s-1.png" />
     </p>
     <p>
         In the top right corner, you can see that audit logging is currently enabled, which is the default. By unchecking the box, audit logging can be
@@ -120,7 +120,7 @@ <h1>Reading the Audit Log</h1>
         Now the <b>Audit Log</b> view should look like this:
     </p>
     <p>
-        <img src="image-1.png" />
+        <img src="s-2.png" />
     </p>
     <p>
         Each dark gray message and all messages below it until the next dark gray message or the end of the audit log represent a single undoable
@@ -137,7 +137,7 @@ <h1>Reading the Audit Log</h1>
         You will see a list of the changes you have made to the Skyline document like this:
     </p>
     <p>
-        <img src="image-2.png" />
+        <img src="s-3.png" />
     </p>
     <p>
         Before audit logging was introduced into Skyline, both messages here would have only said <b>Changed settings</b>. Therefore, even if
@@ -177,7 +177,7 @@ <h1>Undoing Changes Using the Audit Log View</h1>
         You will see the list shown below.
     </p>
     <p>
-        <img src="image-3.png" />
+        <img src="s-4.png" />
     </p>
     <p>
         You can see the change you just undid through the <b>Audit Log</b> grid.
@@ -207,7 +207,7 @@ <h1>Inserting a Peptide Sequence</h1>
         The form should now look like this:
     </p>
     <p>
-        <img src="image-4.png" />
+        <img src="s-5.png" />
     </p>
     <ul>
         <li>Click the <b>Insert</b> button.</li>
@@ -216,7 +216,7 @@ <h1>Inserting a Peptide Sequence</h1>
         The <b>Targets</b> view should show the newly added peptide with a light and a heavy labeled precursor:
     </p>
     <p>
-        <img src="image-5.png" />
+        <img src="s-6.png" />
     </p>
     <p>
         If you do not see all of the elements shown above, do the following:
@@ -229,7 +229,7 @@ <h1>Inserting a Peptide Sequence</h1>
         IEAIPQIDK. There are no other detailed messages about this change. The audit log entry consists of a single audit log messages as shown below:
     </p>
     <p>
-        <img src="image-6.png" />
+        <img src="s-7.png" />
     </p>
     <p>
         Note that there is a magnifying glass icon next to the new audit log entry. This appears whenever there is extra information associated with an
@@ -242,7 +242,7 @@ <h1>Inserting a Peptide Sequence</h1>
         This will bring the <b>Audit Log Extra Information</b> form as shown below:
     </p>
     <p>
-        <img src="image-7.png" />
+        <img src="s-8.png" />
     </p>
     <p>
         The extra information window shows all the information that was pasted into the grid when inserting the peptide, including the column header
@@ -284,7 +284,7 @@ <h1>Importing Data Files into Skyline</h1>
         After the import completes, Skyline should have created 9 new replicates. The <b>Audit Log</b> view should now look like this:
     </p>
     <p>
-        <img src="image-8.png" />
+        <img src="s-9.png" />
     </p>
     <p>
         The audit log did not create copies of the files that were imported, but rather just stored the paths of files (here shortened to just the file
@@ -300,7 +300,7 @@ <h1>Importing Data Files into Skyline</h1>
         <li>Click on the magnifying glass to view the extra information.</li>
     </ul>
     <p>
-        <img src="image-9.png" />
+        <img src="s-10.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button to close the form.</li>
@@ -325,7 +325,7 @@ <h1>Calibration Curve Settings</h1>
         This adds the audit log entry shown below:
     </p>
     <p>
-        <img src="image-10.png" />
+        <img src="s-11.png" />
     </p>
     <p>
         The changes made are listed under the heading <b>Peptide Settings – Quantification changed</b> and each step is captured in a
@@ -383,13 +383,13 @@ <h2>Specify the analyte concentrations of the external standards:</h2>
         The <b>Document Grid: Replicates</b> form should look like this:
     </p>
     <p>
-        <img src="image-11.png" />
+        <img src="s-12.png" />
     </p>
     <p>
         Review the <b>Audit Log</b> grid to see that it shows the following:
     </p>
     <p>
-        <img src="image-12.png" />
+        <img src="s-13.png" />
     </p>
     <p>
         The Undo-Redo messages indicates that 16 values were pasted into the <b>Document Grid</b>. There are a total of 17 detailed messages.
@@ -402,7 +402,7 @@ <h2>Specify the analyte concentrations of the external standards:</h2>
         <li>Open the extra information window by clicking on the magnifying glass icon.</li>
     </ul>
     <p>
-        <img src="image-13.png" />
+        <img src="s-14.png" />
     </p>
     <p>
         This displays a much more concise view of the data that was pasted into the document and again the data can be easily copied and pasted to
@@ -436,7 +436,7 @@ <h1>Adjusting Integration Boundaries</h1>
         You should see something like the following:
     </p>
     <p>
-        <img src="image-14.png" />
+        <img src="s-15.png" />
     </p>
     <p>
         The integration boundaries look acceptable and changing them may simply add variance to the peak area calculations. However, you might feel the
@@ -450,7 +450,7 @@ <h1>Adjusting Integration Boundaries</h1>
         Three new rows should appear in the <b>Audit Log</b> view, as shown below:
     </p>
     <p>
-        <img src="image-15.png" />
+        <img src="s-16.png" />
     </p>
     <p>
         Note that the new log entry describes a change related to an item in the <b>Targets</b> window, it uses a format similar to the one
@@ -468,7 +468,7 @@ <h1>Adjusting Integration Boundaries</h1>
         The audit log should look like this:
     </p>
     <p>
-        <img src="image-16.png" />
+        <img src="s-17.png" />
     </p>
     <p>
         Note that the reason entered in the dark gray row is shown in all three new rows. This is the overall reason for the change. To give a
@@ -486,7 +486,7 @@ <h1>Calibration Curve Review</h1>
         The curve fits the first four points, but not as well for the points closer to zero. Use the scroll wheel to zoom in on the lower four points.
     </p>
     <p>
-        <img src="image-17.png" />
+        <img src="s-18.png" />
     </p>
     <p>
         You can see that the last three points fall off the line, which indicates that they are below the limit of detection for this peptide. These
@@ -505,7 +505,7 @@ <h1>Calibration Curve Review</h1>
         Review the <b>Audit Log</b> grid and, you should see four new entries, one for each point you excluded from the calibration:
     </p>
     <p>
-        <img src="image-18.png" />
+        <img src="s-19.png" />
     </p>
     <p>
         You should again add a reason to explain why the replicates were excluded by doing the following:
@@ -527,14 +527,14 @@ <h1>Customizing the Audit Log Display</h1>
         There are three default reports you can choose from (<b>Undo Redo</b>, <b>Summary</b>, and <b>All Info</b>):
     </p>
     <p>
-        <img src="image-19.png" />
+        <img src="s-20.png" />
     </p>
     <ul>
         <li>Click on the <b>Undo Redo</b> menu item.</li>
         <li>Adjust the column widths so you can see their full contents.</li>
     </ul>
     <p>
-        <img src="image-20.png" />
+        <img src="s-21.png" />
     </p>
     <p>
         Now the <b>Audit Log</b> view only displays the <b>Undo Redo</b> messages and not the detail messages, presenting a concise
@@ -562,7 +562,7 @@ <h1>Customizing the Audit Log Display</h1>
         The filled-out form should look like the following:
     </p>
     <p>
-        <img src="image-21.png" />
+        <img src="s-22.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -572,7 +572,7 @@ <h1>Customizing the Audit Log Display</h1>
         be using a different <b>Skyline Version</b>.
     </p>
     <p>
-        <img src="image-22.png" />
+        <img src="s-23.png" />
     </p>
     <p>
         Below is a list of all of the columns you can display and their meaning:
@@ -604,7 +604,7 @@ <h1>Panorama Upload</h1>
         If you have not used Panorama before the following message should appear:
     </p>
     <p>
-        <img src="image-23.png" />
+        <img src="s-24.png" />
     </p>
     <ul>
         <li>Click the <b>Continue</b> button.</li>
@@ -613,7 +613,7 @@ <h1>Panorama Upload</h1>
         The next form should ask you for the URL of the Panorama server you want to use and your credentials. 
     </p>
     <p>
-        <img src="image-24.png" />
+        <img src="s-25.png" />
     </p>
     <ul>
         <li>Enter the URL if you are using your own Panorama server, or leave it as PanoramaWeb.org.</li>
@@ -624,7 +624,7 @@ <h1>Panorama Upload</h1>
         If the connection was successful, the next form should show you the Panorama server URL and the folders on the server available for upload.
     </p>
     <p>
-        <img src="image-25.png" />
+        <img src="s-26.png" />
     </p>
     <ul>
         <li>Click the <b>+</b> next to the URL to expand the list of folders you have access to if necessary.</li>
@@ -638,7 +638,7 @@ <h1>Panorama Upload</h1>
         should look like this:
     </p>
     <p>
-        <img src="image-26.png" />
+        <img src="s-panorama-zip-view.png" />
     </p>
     <table>
         <tr>
@@ -658,7 +658,7 @@ <h1>Panorama Upload</h1>
         Now you should see the following page:
     </p>
     <p>
-        <img src="image-27.png" />
+        <img src="s-panorama-audit-log.png" />
     </p>
     <p>
     </p>
@@ -673,13 +673,13 @@ <h1>Panorama Upload</h1>
         <li>Select <b>AllMessagesView</b> from the dropdown menu. </li>
     </ul>
     <p>
-        <img src="image-28.png" />
+        <img src="s-create-view.png" />
     </p>
     <p>
         Now your page should look like this:
     </p>
     <p>
-        <img src="image-29.png" />
+        <img src="s-customized-view.png" />
     </p>
     <p>
         All the messages and message types in the audit log are now displayed.
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/AuditLog/en/image-0.png b/pwiz_tools/Skyline/Documentation/Tutorials/AuditLog/en/s-1.png
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rename from pwiz_tools/Skyline/Documentation/Tutorials/AuditLog/en/image-0.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/AuditLog/en/s-1.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/AuditLog/en/image-9.png b/pwiz_tools/Skyline/Documentation/Tutorials/AuditLog/en/s-10.png
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rename to pwiz_tools/Skyline/Documentation/Tutorials/AuditLog/en/s-10.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/AuditLog/en/image-10.png b/pwiz_tools/Skyline/Documentation/Tutorials/AuditLog/en/s-11.png
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rename to pwiz_tools/Skyline/Documentation/Tutorials/AuditLog/en/s-24.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/AuditLog/en/image-24.png b/pwiz_tools/Skyline/Documentation/Tutorials/AuditLog/en/s-25.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/AuditLog/en/image-24.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/AuditLog/en/s-25.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/AuditLog/en/image-25.png b/pwiz_tools/Skyline/Documentation/Tutorials/AuditLog/en/s-26.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/AuditLog/en/image-25.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/AuditLog/en/image-2.png b/pwiz_tools/Skyline/Documentation/Tutorials/AuditLog/en/s-3.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/AuditLog/en/image-2.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/AuditLog/en/image-3.png b/pwiz_tools/Skyline/Documentation/Tutorials/AuditLog/en/s-4.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/AuditLog/en/image-3.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/AuditLog/en/image-4.png b/pwiz_tools/Skyline/Documentation/Tutorials/AuditLog/en/s-5.png
similarity index 100%
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/AuditLog/en/image-5.png b/pwiz_tools/Skyline/Documentation/Tutorials/AuditLog/en/s-6.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/AuditLog/en/image-5.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/AuditLog/en/image-6.png b/pwiz_tools/Skyline/Documentation/Tutorials/AuditLog/en/s-7.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/AuditLog/en/image-6.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/AuditLog/en/s-7.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/AuditLog/en/image-7.png b/pwiz_tools/Skyline/Documentation/Tutorials/AuditLog/en/s-8.png
similarity index 100%
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/AuditLog/en/image-8.png b/pwiz_tools/Skyline/Documentation/Tutorials/AuditLog/en/s-9.png
similarity index 100%
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/AuditLog/en/image-28.png b/pwiz_tools/Skyline/Documentation/Tutorials/AuditLog/en/s-create-view.png
similarity index 100%
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/AuditLog/en/image-29.png b/pwiz_tools/Skyline/Documentation/Tutorials/AuditLog/en/s-customized-view.png
similarity index 100%
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/AuditLog/en/image-27.png b/pwiz_tools/Skyline/Documentation/Tutorials/AuditLog/en/s-panorama-audit-log.png
similarity index 100%
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rename to pwiz_tools/Skyline/Documentation/Tutorials/AuditLog/en/s-panorama-audit-log.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/AuditLog/en/image-26.png b/pwiz_tools/Skyline/Documentation/Tutorials/AuditLog/en/s-panorama-zip-view.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/AuditLog/en/image-26.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/en/index.html b/pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/en/index.html
index 7a553b44e3..9e9b8925a8 100644
--- a/pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/en/index.html
+++ b/pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/en/index.html
@@ -113,7 +113,7 @@ <h1>Creating a Simple Custom Report</h1>
         shown below:
     </p>
     <p>
-        <img src="image-0.png" />
+        <img src="s-1.png" />
     </p>
     <p>
         Continue creating a new Skyline custom report template by performing the following steps:
@@ -127,7 +127,7 @@ <h1>Creating a Simple Custom Report</h1>
         The form should now look like this:
     </p>
     <p>
-        <img src="image-1.png" />
+        <img src="s-2.png" />
     </p>
     <ul>
         <li>Expand the field groups <b>Peptides</b> and <b>Replicates</b> by clicking on the <b>‘+’</b> button to see
@@ -138,7 +138,7 @@ <h1>Creating a Simple Custom Report</h1>
         The form should now look like this: 
     </p>
     <p>
-        <img src="image-2.png" />
+        <img src="s-3.png" />
     </p>
     <p>
         Note that the fields in the <b>Edit Report</b> form, shown above, have a distinct hierarchical structure. At the highest level are
@@ -177,7 +177,7 @@ <h1>Creating a Simple Custom Report</h1>
         This should leave the <b>Edit Report</b> form looking like:
     </p>
     <p>
-        <img src="image-3.png" />
+        <img src="s-4.png" />
     </p>
     <ul>
         <li>Click the <b>Preview</b> button in the upper right corner of the <b>Edit Report</b> form.</li>
@@ -186,11 +186,11 @@ <h1>Creating a Simple Custom Report</h1>
         The <b>Preview</b> form should appear looking like this:
     </p>
     <p>
-        <img src="image-4.png" />
+        <img src="s-5.png" />
     </p>
     <p>
         The <b>Preview</b> function is quite helpful when designing report templates. At times it may even serve as a quick substitute for
-        exporting a report to a file. The copy button (<img src="image-5.png" />) on the toolbar will copy all of the data including the column
+        exporting a report to a file. The copy button (<img src="../../shared/copy-button.png" />) on the toolbar will copy all of the data including the column
         headers. You can also select all of the values in the <b>Preview</b> form by clicking the upper-left rectangle to the left of the
         column headers. Pressing Ctrl-C, then copies the full report, excluding the column headers. After copying the data using either method, it can
         be pasted into another tool, such as Excel.
@@ -215,7 +215,7 @@ <h1>Creating a Simple Custom Report</h1>
         below:
     </p>
     <p class="keep-next">
-        <img src="image-6.png" />
+        <img src="s-6.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button again to return to the <b>Export Report</b> form.</li>
@@ -225,7 +225,7 @@ <h1>Creating a Simple Custom Report</h1>
             Report</b> form should now look like:
     </p>
     <p>
-        <img src="image-7.png" />
+        <img src="s-7.png" />
     </p>
     <p>
         From the <b>Export Report</b> form you could now export your new report by selecting ‘Overview’ in the <b>Report</b> list
@@ -274,7 +274,7 @@ <h1>Sharing Report Templates</h1>
         Skyline will present the <b>Manage Reports</b> form, as shown below:
     </p>
     <p>
-        <img src="image-8.png" />
+        <img src="s-8.png" />
     </p>
     <ul>
         <li>Click on ‘Overview’ in the list to select it.</li>
@@ -304,7 +304,7 @@ <h1>Managing Report Templates in Skyline</h1>
         The <b>Manage Reports</b> form should now look like this: 
     </p>
     <p>
-        <img src="image-9.png" />
+        <img src="s-9.png" />
     </p>
     <p>
         To remove the ‘Overview’ item from the list, do the following: 
@@ -317,7 +317,7 @@ <h1>Managing Report Templates in Skyline</h1>
         The <b>Export Report</b> form should now look like this: 
     </p>
     <p>
-        <img src="image-10.png" />
+        <img src="s-10.png" />
     </p>
     <p>
         Just as when you first brought it up in this tutorial. 
@@ -360,7 +360,7 @@ <h1>Modifying Existing Report Templates</h1>
         as shown below: 
     </p>
     <p>
-        <img src="image-11.png" />
+        <img src="s-11.png" />
     </p>
     <p>
         The report name for this new report template has not yet been assigned. To assign it now: 
@@ -433,7 +433,7 @@ <h1>Modifying Existing Report Templates</h1>
             Report</b> form should look like this: 
     </p>
     <p>
-        <img src="image-12.png" />
+        <img src="s-12.png" />
     </p>
     <p>
         To reorder some fields in this new report template, do the following: 
@@ -474,7 +474,7 @@ <h1>Modifying Existing Report Templates</h1>
         The <b>Preview</b> form is shown below, scrolled to show both ‘light’ and ‘heavy’ column names:
     </p>
     <p>
-        <img src="image-13.png" /> 
+        <img src="s-13.png" /> 
     </p>
     <p>
         You might notice that the column ‘heavy Isotope Label Type’ shows ‘heavy’ on every row, and that there is also a column ‘light Isotope Label
@@ -497,7 +497,7 @@ <h1>Modifying Existing Report Templates</h1>
         This will return you to the <b>Export Report</b> form, which should now look like this:
     </p>
     <p>
-        <img src="image-14.png" />
+        <img src="s-14.png" />
     </p>
     <p>
         From here, you could now continue to export the new ‘Study 7’ report to a CSV file by selecting it and clicking the <b>Export</b>
@@ -548,7 +548,7 @@ <h1>Quality Control Summary Reports</h1>
             Reports</b> form should now look like this:
     </p>
     <p>
-        <img src="image-15.png" />
+        <img src="s-15.png" />
     </p>
     <ul>
         <li>Click <b>OK</b> to dismiss the <b>Manage Reports</b> form.</li>
@@ -556,14 +556,14 @@ <h1>Quality Control Summary Reports</h1>
                     Statistics</i></b>.</li>
     </ul>
     <p>
-        <img src="image-16.png" />
+        <img src="s-16.png" />
     </p>
     <p class="keep-next">
         After you choose <b><i>Summary Statistics</i></b>, the <b>Document Grid</b> should look like the
         following:
     </p>
     <p>
-        <img src="image-17.png" />
+        <img src="s-17.png" />
     </p>
     <p>
         This report shows that the data in Study9pilot.sky, taken from 5 replicate injections of the same sample, produce peptide CV values for
@@ -589,7 +589,7 @@ <h1>Quality Control Summary Reports</h1>
         The <b>Customize Report</b> form should look like this:
     </p>
     <p>
-        <img src="image-18.png" />
+        <img src="s-18.png" />
     </p>
     <p>
         To define a new filter on this report:
@@ -604,7 +604,7 @@ <h1>Quality Control Summary Reports</h1>
         The <b>Customize Report</b> form should look like this:
     </p>
     <p>
-        <img src="image-19.png" />
+        <img src="s-19.png" />
     </p>
     <p>
         Note that even though the <b>Cv Total Area</b> column is displayed as a percentage in the <b>Document Grid</b>, on the
@@ -614,7 +614,7 @@ <h1>Quality Control Summary Reports</h1>
         <li>Click the <b>OK</b> button on the <b>Customize Report</b> form to see the rows matching this filter.</li>
     </ul>
     <p>
-        <img src="image-20.png" />
+        <img src="s-20.png" />
     </p>
     <p>
         To inspect the INDISHTQSVSAK peptide more closely, do the following: 
@@ -631,7 +631,7 @@ <h1>Quality Control Summary Reports</h1>
             Area</b> values in the summary report preview, where the majority of the peptides had CV values &lt; 10%.
     </p>
     <p>
-        <img src="image-21.png" />
+        <img src="s-21.png" />
     </p>
     <p>
         Skyline summary reports can be used with quality control data to flag issues early, while Skyline itself provides powerful visual displays to
@@ -655,7 +655,7 @@ <h1>Results Grid View</h1>
         Skyline should now look something like this:
     </p>
     <p>
-        <img src="image-22.png" />
+        <img src="s-22.png" />
     </p>
     <p>
         Now rearrange the windows for better viewing, by doing the following:
@@ -672,7 +672,7 @@ <h1>Results Grid View</h1>
         This should leave Skyline looking something like:
     </p>
     <p>
-        <img src="image-23.png" /> 
+        <img src="s-23.png" /> 
     </p>
     <p>
         Skyline keeps its charts and the <b>Results Grid</b> in synch as you navigate the data. If you click on one of the other rows in the
@@ -699,7 +699,7 @@ <h1>Results Grid View</h1>
         The <b>Results Grid</b> should now look like this:
     </p>
     <p>
-        <img src="image-24.png" />
+        <img src="s-24.png" />
     </p>
     <p>
         All of the other columns in the current <b>Results Grid</b> display are calculated by Skyline and cannot be edited, but you can
@@ -756,7 +756,7 @@ <h1>Custom Annotations</h1>
         The <b>Define Annotation</b> from should now look like this:
     </p>
     <p>
-        <img src="image-25.png" />
+        <img src="s-25.png" />
     </p>
     <p>
         Now save the annotation and add it to your document by doing the following:
@@ -770,7 +770,7 @@ <h1>Custom Annotations</h1>
         The <b>Document Settings</b> form should now look like this:
     </p>
     <p>
-        <img src="image-26.png" />
+        <img src="s-26.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -789,7 +789,7 @@ <h1>Custom Annotations</h1>
         The <b>Customize Report</b> form should now look like the following:
     </p>
     <p>
-        <img src="image-27.png" />
+        <img src="s-27.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -802,7 +802,7 @@ <h1>Custom Annotations</h1>
         The Skyline window should now look something like this:
     </p>
     <p>
-        <img src="image-28.png" />
+        <img src="s-28.png" />
     </p>
     <p>
         The peaks in this document do not have a lot of issues, but this one does have some peak tailing. Check the checkbox in the new
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/en/image-0.png b/pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/en/s-1.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/en/image-0.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/en/s-1.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/en/image-10.png b/pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/en/s-10.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/en/image-10.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/en/s-10.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/en/image-11.png b/pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/en/s-11.png
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rename from pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/en/image-11.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/en/image-12.png b/pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/en/s-12.png
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rename from pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/en/image-27.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/en/s-27.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/en/image-28.png b/pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/en/s-28.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/en/image-28.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/en/s-28.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/en/image-2.png b/pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/en/s-3.png
similarity index 100%
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rename to pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/en/s-3.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/en/image-3.png b/pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/en/s-4.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/en/image-3.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/en/s-4.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/en/image-4.png b/pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/en/s-5.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/en/image-4.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/en/s-5.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/en/image-6.png b/pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/en/s-6.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/en/image-6.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/en/s-6.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/en/image-7.png b/pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/en/s-7.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/en/image-7.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/en/s-7.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/en/image-8.png b/pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/en/s-8.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/en/image-8.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/en/s-8.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/en/image-9.png b/pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/en/s-9.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/en/image-9.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/en/s-9.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/ja/image-5.png b/pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/ja/image-5.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/ja/index.html b/pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/ja/index.html
index 9441e581b2..74cc4bd0b4 100644
--- a/pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/ja/index.html
+++ b/pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/ja/index.html
@@ -91,7 +91,7 @@ <h1>簡単なカスタムレポートの作成</h1>
         [ <b>レポートをエクスポート</b> ] フォームが表示されます。ここには、デフォルトのSkylineレポートテンプレートが表示されていると思います。
     </p>
     <p>
-        <img src="image-0.png" />
+        <img src="s-1.png" />
     </p>
     <p>
         以下の手順を実施して、新しいSkylineカスタムレポートテンプレートの作成を続けます。
@@ -105,7 +105,7 @@ <h1>簡単なカスタムレポートの作成</h1>
         フォームは以下のようになります。
     </p>
     <p>
-        <img src="image-1.png" />
+        <img src="s-2.png" />
     </p>
     <ul>
         <li>[ <b>+</b> ] ボタンをクリックしてフィールドグループである [ <b>ペプチド</b> ] と [ <b>繰り返し測定</b> ] を展開し、エクスポート可能な多数のフィールドを表示させます。</li>
@@ -115,7 +115,7 @@ <h1>簡単なカスタムレポートの作成</h1>
         フォームは以下のようになります。 
     </p>
     <p>
-        <img src="image-2.png" /> 
+        <img src="s-3.png" /> 
     </p>
     <p>
         上記に示す [ <b>レポートを編集</b> ]
@@ -147,7 +147,7 @@ <h1>簡単なカスタムレポートの作成</h1>
         以上の操作で[ <b>レポートを編集</b> ] フォームは以下のようになります。
     </p>
     <p>
-        <img src="image-3.png" />
+        <img src="s-4.png" />
     </p>
     <ul>
         <li>[ <b>レポートを編集</b> ] フォームの最上部右側にある [ <b>プレビュー</b> ] ボタンをクリックします。</li>
@@ -156,11 +156,11 @@ <h1>簡単なカスタムレポートの作成</h1>
         [ <b>プレビュー</b> ] フォームは以下のようになります。
     </p>
     <p>
-        <img src="image-4.png" />
+        <img src="s-5.png" />
     </p>
     <p>
         <b>プレビュー</b>は、レポートテンプレートを設計する場合にかなり便利な機能です。レポートをファイルにエクスポートする代わりにこの機能を使うこともできます。ツールバー上のコピーボタン( <img
-            src="image-5.png" />)は、ヘッダー列を含むすべてのデータをコピーします。また、列ヘッダーの左にある長方形の枠をクリックして [ <b>プレビュー</b> ]
+            src="../../shared/copy-button.png" />)は、ヘッダー列を含むすべてのデータをコピーします。また、列ヘッダーの左にある長方形の枠をクリックして [ <b>プレビュー</b> ]
         フォームのすべての値を選択することもできます。Ctrl+Cキーを押すと、列ヘッダーを除くレポートのすべてがコピーされます。どちらかの方法でデータをコピーしたら、そのデータをExcelなどの別のツールに貼り付けることもできます。
     </p>
     <p>
@@ -179,7 +179,7 @@ <h1>簡単なカスタムレポートの作成</h1>
         以下に示すように、<b>レポート</b>テンプレートリストに新しい <b>Overview</b>レポートテンプレートが表示されます。 
     </p>
     <p class="keep-next">
-        <img src="image-6.png" />
+        <img src="s-6.png" />
     </p>
     <ul>
         <li>再度 [ <b>OK</b> ] ボタンをクリックして [ <b>レポートをエクスポート</b> ] フォームに戻ります。</li>
@@ -188,7 +188,7 @@ <h1>簡単なカスタムレポートの作成</h1>
         今度はSkylineレポートテンプレートリストに新しい<b>Overview</b>レポートテンプレートが追加されています。[ <b>レポートをエクスポート</b> ] フォームは以下のようになります。
     </p>
     <p>
-        <img src="image-7.png" />
+        <img src="s-7.png" />
     </p>
     <p>
         <b>レポート</b>リストで「Overview」を選択し、[ <b>エクスポート</b> ] ボタンをクリックして、[ <b>レポートをエクスポート</b> ]
@@ -230,7 +230,7 @@ <h1>レポートテンプレートの共有</h1>
         Skylineは、以下に示す [ <b>レポートを管理</b> ] フォームを表示します。
     </p>
     <p>
-        <img src="image-8.png" />
+        <img src="s-8.png" />
     </p>
     <ul>
         <li>リストの「Overview」をクリックして選択します。</li>
@@ -257,7 +257,7 @@ <h1>Skylineでのレポートテンプレートの管理</h1>
         [ <b>レポートを管理</b> ] フォームは以下のようになります。 
     </p>
     <p>
-        <img src="image-9.png" />
+        <img src="s-9.png" />
     </p>
     <p>
         リストから「Overview」項目を削除するには、以下の操作を行います。 
@@ -270,7 +270,7 @@ <h1>Skylineでのレポートテンプレートの管理</h1>
         [ <b>レポートをエクスポート</b> ] フォームは以下のようになります。 
     </p>
     <p>
-        <img src="image-10.png" />
+        <img src="s-10.png" />
     </p>
     <p>
         本チュートリアルで最初に開いたときとちょうど同じです。 
@@ -308,7 +308,7 @@ <h1>既存のレポートテンプレートの変更</h1>
         Skylineは、以下のように、「Overview」レポートテンプレートですでに追加したフィールドをもつ [ <b>レポートを編集</b> ] フォームを表示します。 
     </p>
     <p>
-        <img src="image-11.png" />
+        <img src="s-11.png" />
     </p>
     <p>
         この新規レポートテンプレートのレポート名は、まだ指定されていません。レポート名をここで指定するには、以下の操作を行います。 
@@ -373,7 +373,7 @@ <h1>既存のレポートテンプレートの変更</h1>
         これでレポートテンプレートには、元の「Overview」レポートテンプレートよりも多くの詳細が含まれるようになり、[ <b>レポートを編集</b> ] フォームは以下のようになります。 
     </p>
     <p>
-        <img src="image-12.png" />
+        <img src="s-12.png" />
     </p>
     <p>
         この新規レポートテンプレートのフィールドを並べ替えるには、以下の操作を行います。 
@@ -409,7 +409,7 @@ <h1>既存のレポートテンプレートの変更</h1>
         [ <b>プレビュー</b> ] フォームが下記に表示されています。ここでは、「light」列名と「heavy」列名を両方示すために下にスクロールされています。
     </p>
     <p>
-        <img src="image-13.png" /> 
+        <img src="s-13.png" /> 
     </p>
     <p>
         「heavy同位体標識タイプ」列にはすべての行に「heavy」が表示されており、「light同位体標識タイプ」列にはすべての行に「light」が表示されていることに気づかれるかもしれません。列を軸にすると、列リストに含むように追加することはありません。[
@@ -430,7 +430,7 @@ <h1>既存のレポートテンプレートの変更</h1>
         これで [ <b>レポートをエクスポート</b> ] フォームに戻ります。フォームは以下のようになります。
     </p>
     <p>
-        <img src="image-14.png" />
+        <img src="s-14.png" />
     </p>
     <p>
         ここで、つぎに「Study 7」レポートをCSVファイルへエクスポートします。このレポートを選択し、[ <b>エクスポート</b> ] ボタンをクリックするか、[ <b>共有</b> ]
@@ -474,7 +474,7 @@ <h1>品質管理要約レポート</h1>
         「Summary Statistics」という名前の新しいレポートがレポートのリストに追加されており、<br />[ <b>レポートを管理</b> ] フォームは以下のようになります。
     </p>
     <p>
-        <img src="image-15.png" />
+        <img src="s-15.png" />
     </p>
     <ul>
         <li>[ <b>OK</b> ] ボタンをクリックして [ <b>レポートを管理</b> ] フォームを閉じます。</li>
@@ -482,13 +482,13 @@ <h1>品質管理要約レポート</h1>
         </li>
     </ul>
     <p>
-        <img src="image-16.png" />
+        <img src="s-16.png" />
     </p>
     <p class="keep-next">
         [ <b><i>Summary Statistics</i></b> ] を選択すると、[ <b>ドキュメントグリッド</b> ] は以下のようになります。
     </p>
     <p>
-        <img src="image-17.png" />
+        <img src="s-17.png" />
     </p>
     <p>
         このレポートは、Study9pilot.skyファイル内にある5回の同じ試料の繰り返し測定インジェクションで取得されたデータが、<b>FWHMが</b>ほぼ5%未満のCV値、また、ペプチドの<b>総面積が</b>10%未満のCV値をもつことを示しており、それらは赤いボックスでかこまれて示されています。さらに、[
@@ -508,7 +508,7 @@ <h1>品質管理要約レポート</h1>
         [ <b>レポートをカスタマイズ</b> ] フォームは以下のようになります。
     </p>
     <p>
-        <img src="image-18.png" />
+        <img src="s-18.png" />
     </p>
     <p>
         このレポートに新しいフィルタを定義するには、以下の操作を行います。
@@ -523,7 +523,7 @@ <h1>品質管理要約レポート</h1>
         [ <b>レポートをカスタマイズ</b> ] フォームは以下のようになります。
     </p>
     <p>
-        <img src="image-19.png" />
+        <img src="s-19.png" />
     </p>
     <p>
         [ <b>Cv総面積</b> ] 列が [ <b>ドキュメントグリッド</b> ] でパーセンテージとして表示されても、[ フィルタ ] タブでは、数字「20%」は「0.2」と表示されます。
@@ -532,7 +532,7 @@ <h1>品質管理要約レポート</h1>
         <li>[ <b>レポートをカスタマイズ</b> ] フォームで [ <b>OK</b> ] ボタンをクリックし、このフィルタに一致する行を確認します。</li>
     </ul>
     <p>
-        <img src="image-20.png" />
+        <img src="s-20.png" />
     </p>
     <p>
         INDISHTQSVSAKペプチドをもう少し詳しく調べるには、以下の操作を行います。 
@@ -548,7 +548,7 @@ <h1>品質管理要約レポート</h1>
         値がかなり低かったことからもわかるように、[ <b>ピーク面積</b> ] 表示でピーク面積の再現性がより明確に示されることがわかります。これらのペプチドの大部分のCV値が10%未満でした。
     </p>
     <p>
-        <img src="image-21.png" />
+        <img src="s-21.png" />
     </p>
     <p>
         Skyline自体も強力な視覚的表示で問題の原因を探すことができますが、Skyline要約レポートを品質管理データと共に使用すると、問題を早期に知ることができます。
@@ -569,7 +569,7 @@ <h1>[ 結果グリッド ] 表示</h1>
         Skylineは、以下のようになります。
     </p>
     <p>
-        <img src="image-22.png" />
+        <img src="s-22.png" />
     </p>
     <p>
         今度は以下の操作を行ってウィンドウを見やすく並べ替えます。
@@ -585,7 +585,7 @@ <h1>[ 結果グリッド ] 表示</h1>
         これにより以下のようなSkylineの画面が表示されます。
     </p>
     <p>
-        <img src="image-23.png" /> 
+        <img src="s-23.png" /> 
     </p>
     <p>
         Skylineは、データのナビゲーション時にチャートと [ <b>結果グリッド</b> ] の同期を維持します。[ <b>結果グリッド</b> ]
@@ -609,7 +609,7 @@ <h1>[ 結果グリッド ] 表示</h1>
         [ <b>結果グリッド</b> ] は以下のようになります。
     </p>
     <p>
-        <img src="image-24.png" />
+        <img src="s-24.png" />
     </p>
     <p>
         現在の [ <b>結果グリッド</b> ]
@@ -661,7 +661,7 @@ <h1>カスタム注釈</h1>
         [ <b>注釈を定義</b> ] フォームは以下のようになります。
     </p>
     <p>
-        <img src="image-25.png" />
+        <img src="s-25.png" />
     </p>
     <p>
         ここで注釈を保存し、以下の操作を行ってドキュメントに注釈を追加します。
@@ -675,7 +675,7 @@ <h1>カスタム注釈</h1>
         [ <b>ドキュメント設定</b> ] フォームは以下のようになります。
     </p>
     <p>
-        <img src="image-26.png" />
+        <img src="s-26.png" />
     </p>
     <ul>
         <li>[ <b>OK</b> ] ボタンをクリックします。</li>
@@ -693,7 +693,7 @@ <h1>カスタム注釈</h1>
         [ <b>レポートをカスタマイズ</b> ] フォームは以下のようになります。
     </p>
     <p>
-        <img src="image-27.png" />
+        <img src="s-27.png" />
     </p>
     <ul>
         <li>[ <b>OK</b> ] ボタンをクリックします。</li>
@@ -706,7 +706,7 @@ <h1>カスタム注釈</h1>
         これでSkylineウィンドウは以下のようになります。
     </p>
     <p>
-        <img src="image-28.png" /> 
+        <img src="s-28.png" /> 
     </p>
     <p>
         このドキュメントにあるピークは多くの問題があるとはいえませんが、ここで見えているピークは少し尾を引いています。「Rep1」行の新しい [ <b>Tailing</b> ]
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/ja/invariant.html b/pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/ja/invariant.html
index 3e5a2b3c95..a59c6ae41b 100644
--- a/pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/ja/invariant.html
+++ b/pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/ja/invariant.html
@@ -113,7 +113,7 @@ <h1>Creating a Simple Custom Report</h1>
         shown below:
     </p>
     <p>
-        <img src="image-0.png" />
+        <img src="s-1.png" />
     </p>
     <p>
         Continue creating a new Skyline custom report template by performing the following steps:
@@ -127,7 +127,7 @@ <h1>Creating a Simple Custom Report</h1>
         The form should now look like this:
     </p>
     <p>
-        <img src="image-1.png" />
+        <img src="s-2.png" />
     </p>
     <ul>
         <li>Expand the field groups <b>Peptides</b> and <b>Replicates</b> by clicking on the <b>‘+’</b> button to see
@@ -138,7 +138,7 @@ <h1>Creating a Simple Custom Report</h1>
         The form should now look like this: 
     </p>
     <p>
-        <img src="image-2.png" />
+        <img src="s-3.png" />
     </p>
     <p>
         Note that the fields in the <b>Edit Report</b> form, shown above, have a distinct hierarchical structure. At the highest level are
@@ -177,7 +177,7 @@ <h1>Creating a Simple Custom Report</h1>
         This should leave the <b>Edit Report</b> form looking like:
     </p>
     <p>
-        <img src="image-3.png" />
+        <img src="s-4.png" />
     </p>
     <ul>
         <li>Click the <b>Preview</b> button in the upper right corner of the <b>Edit Report</b> form.</li>
@@ -186,11 +186,11 @@ <h1>Creating a Simple Custom Report</h1>
         The <b>Preview</b> form should appear looking like this:
     </p>
     <p>
-        <img src="image-4.png" />
+        <img src="s-5.png" />
     </p>
     <p>
         The <b>Preview</b> function is quite helpful when designing report templates. At times it may even serve as a quick substitute for
-        exporting a report to a file. The copy button (<img src="image-5.png" />) on the toolbar will copy all of the data including the column
+        exporting a report to a file. The copy button (<img src="../../shared/copy-button.png" />) on the toolbar will copy all of the data including the column
         headers. You can also select all of the values in the <b>Preview</b> form by clicking the upper-left rectangle to the left of the
         column headers. Pressing Ctrl-C, then copies the full report, excluding the column headers. After copying the data using either method, it can
         be pasted into another tool, such as Excel.
@@ -215,7 +215,7 @@ <h1>Creating a Simple Custom Report</h1>
         below:
     </p>
     <p class="keep-next">
-        <img src="image-6.png" />
+        <img src="s-6.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button again to return to the <b>Export Report</b> form.</li>
@@ -225,7 +225,7 @@ <h1>Creating a Simple Custom Report</h1>
             Report</b> form should now look like:
     </p>
     <p>
-        <img src="image-7.png" />
+        <img src="s-7.png" />
     </p>
     <p>
         From the <b>Export Report</b> form you could now export your new report by selecting ‘Overview’ in the <b>Report</b> list
@@ -274,7 +274,7 @@ <h1>Sharing Report Templates</h1>
         Skyline will present the <b>Manage Reports</b> form, as shown below:
     </p>
     <p>
-        <img src="image-8.png" />
+        <img src="s-8.png" />
     </p>
     <ul>
         <li>Click on ‘Overview’ in the list to select it.</li>
@@ -304,7 +304,7 @@ <h1>Managing Report Templates in Skyline</h1>
         The <b>Manage Reports</b> form should now look like this: 
     </p>
     <p>
-        <img src="image-9.png" />
+        <img src="s-9.png" />
     </p>
     <p>
         To remove the ‘Overview’ item from the list, do the following: 
@@ -317,7 +317,7 @@ <h1>Managing Report Templates in Skyline</h1>
         The <b>Export Report</b> form should now look like this: 
     </p>
     <p>
-        <img src="image-10.png" />
+        <img src="s-10.png" />
     </p>
     <p>
         Just as when you first brought it up in this tutorial. 
@@ -360,7 +360,7 @@ <h1>Modifying Existing Report Templates</h1>
         as shown below: 
     </p>
     <p>
-        <img src="image-11.png" />
+        <img src="s-11.png" />
     </p>
     <p>
         The report name for this new report template has not yet been assigned. To assign it now: 
@@ -433,7 +433,7 @@ <h1>Modifying Existing Report Templates</h1>
             Report</b> form should look like this: 
     </p>
     <p>
-        <img src="image-12.png" />
+        <img src="s-12.png" />
     </p>
     <p>
         To reorder some fields in this new report template, do the following: 
@@ -474,7 +474,7 @@ <h1>Modifying Existing Report Templates</h1>
         The <b>Preview</b> form is shown below, scrolled to show both ‘light’ and ‘heavy’ column names:
     </p>
     <p>
-        <img src="image-13.png" /> 
+        <img src="s-13.png" /> 
     </p>
     <p>
         You might notice that the column ‘heavy Isotope Label Type’ shows ‘heavy’ on every row, and that there is also a column ‘light Isotope Label
@@ -497,7 +497,7 @@ <h1>Modifying Existing Report Templates</h1>
         This will return you to the <b>Export Report</b> form, which should now look like this:
     </p>
     <p>
-        <img src="image-14.png" />
+        <img src="s-14.png" />
     </p>
     <p>
         From here, you could now continue to export the new ‘Study 7’ report to a CSV file by selecting it and clicking the <b>Export</b>
@@ -548,7 +548,7 @@ <h1>Quality Control Summary Reports</h1>
             Reports</b> form should now look like this:
     </p>
     <p>
-        <img src="image-15.png" />
+        <img src="s-15.png" />
     </p>
     <ul>
         <li>Click <b>OK</b> to dismiss the <b>Manage Reports</b> form.</li>
@@ -556,14 +556,14 @@ <h1>Quality Control Summary Reports</h1>
                     Statistics</i></b>.</li>
     </ul>
     <p>
-        <img src="image-16.png" />
+        <img src="s-16.png" />
     </p>
     <p class="keep-next">
         After you choose <b><i>Summary Statistics</i></b>, the <b>Document Grid</b> should look like the
         following:
     </p>
     <p class="keep-next">
-        <img src="image-17.png" />
+        <img src="s-17.png" />
     </p>
     <p>
         This report shows that the data in Study9pilot.sky, taken from 5 replicate injections of the same sample, produce peptide CV values for
@@ -589,7 +589,7 @@ <h1>Quality Control Summary Reports</h1>
         The <b>Customize Report</b> form should look like this:
     </p>
     <p>
-        <img src="image-18.png" />
+        <img src="s-18.png" />
     </p>
     <p>
         To define a new filter on this report:
@@ -604,7 +604,7 @@ <h1>Quality Control Summary Reports</h1>
         The <b>Customize Report</b> form should look like this:
     </p>
     <p>
-        <img src="image-19.png" />
+        <img src="s-19.png" />
     </p>
     <p>
         Note that even though the <b>Cv Total Area</b> column is displayed as a percentage in the <b>Document Grid</b>, on the
@@ -614,7 +614,7 @@ <h1>Quality Control Summary Reports</h1>
         <li>Click the <b>OK</b> button on the <b>Customize Report</b> form to see the rows matching this filter.</li>
     </ul>
     <p>
-        <img src="image-20.png" />
+        <img src="s-20.png" />
     </p>
     <p>
         To inspect the INDISHTQSVSAK peptide more closely, do the following: 
@@ -631,7 +631,7 @@ <h1>Quality Control Summary Reports</h1>
             Area</b> values in the summary report preview, where the majority of the peptides had CV values &lt; 10%.
     </p>
     <p>
-        <img src="image-21.png" />
+        <img src="s-21.png" />
     </p>
     <p>
         Skyline summary reports can be used with quality control data to flag issues early, while Skyline itself provides powerful visual displays to
@@ -655,7 +655,7 @@ <h1>Results Grid View</h1>
         Skyline should now look something like this:
     </p>
     <p>
-        <img src="image-22.png" />
+        <img src="s-22.png" />
     </p>
     <p>
         Now rearrange the windows for better viewing, by doing the following:
@@ -672,7 +672,7 @@ <h1>Results Grid View</h1>
         This should leave Skyline looking something like:
     </p>
     <p>
-        <img src="image-23.png" /> 
+        <img src="s-23.png" /> 
     </p>
     <p>
         Skyline keeps its charts and the <b>Results Grid</b> in synch as you navigate the data. If you click on one of the other rows in the
@@ -699,7 +699,7 @@ <h1>Results Grid View</h1>
         The <b>Results Grid</b> should now look like this:
     </p>
     <p>
-        <img src="image-24.png" />
+        <img src="s-24.png" />
     </p>
     <p>
         All of the other columns in the current <b>Results Grid</b> display are calculated by Skyline and cannot be edited, but you can
@@ -755,7 +755,7 @@ <h1>Custom Annotations</h1>
         The <b>Define Annotation</b> from should now look like this:
     </p>
     <p>
-        <img src="image-25.png" />
+        <img src="s-25.png" />
     </p>
     <p>
         Now save the annotation and add it to your document by doing the following:
@@ -769,7 +769,7 @@ <h1>Custom Annotations</h1>
         The <b>Document Settings</b> form should now look like this:
     </p>
     <p>
-        <img src="image-26.png" />
+        <img src="s-26.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -788,7 +788,7 @@ <h1>Custom Annotations</h1>
         The <b>Customize Report</b> form should now look like the following:
     </p>
     <p>
-        <img src="image-27.png" />
+        <img src="s-27.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -801,7 +801,7 @@ <h1>Custom Annotations</h1>
         The Skyline window should now look something like this:
     </p>
     <p>
-        <img src="image-28.png" />
+        <img src="s-28.png" />
     </p>
     <p>
         The peaks in this document do not have a lot of issues, but this one does have some peak tailing. Check the checkbox in the new
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/ja/image-0.png b/pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/ja/s-1.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/zh-CHS/index.html b/pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/zh-CHS/index.html
index 4c89e53646..61c1619183 100644
--- a/pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/zh-CHS/index.html
+++ b/pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/zh-CHS/index.html
@@ -91,7 +91,7 @@ <h1>创建简单的自定义报告</h1>
         随即出现<b>导出报告</b>表单，其中可能至少列出 Skyline 默认报告模板，如下所示：
     </p>
     <p>
-        <img src="image-0.png" />
+        <img src="s-1.png" />
     </p>
     <p>
         执行以下步骤，继续创建新的 Skyline 自定义报告模板：
@@ -105,7 +105,7 @@ <h1>创建简单的自定义报告</h1>
         此时，表单将显示如下：
     </p>
     <p>
-        <img src="image-1.png" />
+        <img src="s-2.png" />
     </p>
     <ul>
         <li>单击<b>“+”</b>按钮展开<b>肽段</b>和<b>重复测定</b>字段组，以查看更多可以导出的字段。</li>
@@ -115,7 +115,7 @@ <h1>创建简单的自定义报告</h1>
         此时，表单将显示如下：
     </p>
     <p>
-        <img src="image-2.png" />
+        <img src="s-3.png" />
     </p>
     <p>
         请注意，上面显示的<b>编辑报告</b>表单中的字段有不同的层次结构。位于最高层级的是显示在左侧框底部的<i>蛋白质专用</i>字段（<b>蛋白质名称</b>、<b>蛋白质描述</b>、<b>蛋白质序列</b>、<b>蛋白质注释</b>），在这些字段下面的是展开的<b>重复测定</b>组，其中包含一般的<b>重复测定名称</b>字段和其他字段。Skyline
@@ -139,7 +139,7 @@ <h1>创建简单的自定义报告</h1>
         执行此操作后，<b>编辑报告</b>表单应显示如下：
     </p>
     <p>
-        <img src="image-3.png" />
+        <img src="s-4.png" />
     </p>
     <ul>
         <li>单击<b>编辑报告</b>表单右上角的<b>预览</b>按钮。</li>
@@ -148,11 +148,11 @@ <h1>创建简单的自定义报告</h1>
         此时<b>预览</b>表单将显示如下：
     </p>
     <p>
-        <img src="image-4.png" />
+        <img src="s-5.png" />
     </p>
     <p>
         在设计报告模板时，<b>预览</b>功能相当有用。有时甚至可以使用预览功能来快捷地将报告导出到文件。工具栏上的复制按钮（<img
-            src="image-5.png" />）将复制包括列标题在内的所有数据。您还可以单击列标题左侧左上角的矩形来选择<b>预览</b>表单中的所有值。按 Ctrl-C 复制完整报告（不包括列标题）。使用其中一种方法复制数据后，即可将数据粘贴到 Excel
+            src="../../shared/copy-button.png" />）将复制包括列标题在内的所有数据。您还可以单击列标题左侧左上角的矩形来选择<b>预览</b>表单中的所有值。按 Ctrl-C 复制完整报告（不包括列标题）。使用其中一种方法复制数据后，即可将数据粘贴到 Excel
         等其他工具中。
     </p>
     <p>
@@ -170,7 +170,7 @@ <h1>创建简单的自定义报告</h1>
         您会看到新的 <b>Overview</b> 报告模板出现在<b>报告</b>模板列表中，如下所示：
     </p>
     <p class="keep-next">
-        <img src="image-6.png" />
+        <img src="s-6.png" />
     </p>
     <ul>
         <li>再次单击<b>确定</b>按钮返回<b>导出报告</b>表单。</li>
@@ -179,7 +179,7 @@ <h1>创建简单的自定义报告</h1>
         现在，新的 <b>Overview</b> 报告模板已添加到 Skyline 报告模板列表中。此时<b>导出报告</b>表单将显示如下：
     </p>
     <p>
-        <img src="image-7.png" />
+        <img src="s-7.png" />
     </p>
     <p>
         在<b>导出报告</b>表单中，可以在<b>报告</b>列表中选择“Overview”后单击<b>导出</b>按钮来导出新报告。现在关闭表单，以便从原始的 Skyline 文档视图开始处理。
@@ -221,7 +221,7 @@ <h1>共享报告模板</h1>
         Skyline 将显示<b>管理报告</b>表单，如下所示：
     </p>
     <p>
-        <img src="image-8.png" />
+        <img src="s-8.png" />
     </p>
     <ul>
         <li>单击列表中的 Overview 以将其选定。</li>
@@ -247,7 +247,7 @@ <h1>管理 Skyline 中的报告模板</h1>
         此时，<b>管理报告</b>表单将显示如下：
     </p>
     <p>
-        <img src="image-9.png" />
+        <img src="s-9.png" />
     </p>
     <p>
         要从列表中删除“Overview”项目，请执行以下操作：
@@ -260,7 +260,7 @@ <h1>管理 Skyline 中的报告模板</h1>
         此时<b>导出报告</b>表单将显示如下：
     </p>
     <p>
-        <img src="image-10.png" />
+        <img src="s-10.png" />
     </p>
     <p>
         看起来和您第一次在本教程中打开时一样。
@@ -298,7 +298,7 @@ <h1>修改现有报告模板</h1>
         Skyline 将显示<b>编辑报告</b>表单，其中包含已添加的“Overview”报告模板，如下所示：
     </p>
     <p>
-        <img src="image-11.png" />
+        <img src="s-11.png" />
     </p>
     <p>
         这个新报告模板的报告名称尚未指定。要立即指定名称，请执行以下操作：
@@ -363,7 +363,7 @@ <h1>修改现有报告模板</h1>
         报告模板现在应包含比初始“Overview”报告模板更多的细节，<b>编辑报告</b>表单应如下所示：
     </p>
     <p>
-        <img src="image-12.png" />
+        <img src="s-12.png" />
     </p>
     <p>
         要对这个新报告模板中的某些字段重新排序，请执行以下操作：
@@ -399,7 +399,7 @@ <h1>修改现有报告模板</h1>
         <b>预览</b>表单如下所示，滚动显示“Light”和“Heavy”列名：
     </p>
     <p>
-        <img src="image-13.png" /> 
+        <img src="s-13.png" /> 
     </p>
     <p>
         您可能会注意到，“heavy 同位素标记类型”在每行显示“heavy”，“light 同位素标记类型”在每行显示“light”。当您在一个列上转动时，不会添加多少内容来将它包含在您的列列表中。
@@ -420,7 +420,7 @@ <h1>修改现有报告模板</h1>
         您将返回到<b>导出报告</b>表单，该表单现在显示如下：
     </p>
     <p>
-        <img src="image-14.png" />
+        <img src="s-14.png" />
     </p>
     <p>
         从这里可以选择“Study 7”报告并单击<b>导出</b>按钮，将它导出为 CSV 文件，或者单击<b>共享</b>按钮创建用于共享这份新报告的文件。但在本教程中将执行以下操作：
@@ -464,20 +464,20 @@ <h1>质量控制汇总报告</h1>
         名称为“Summary Statistics”的新报告应已添加到报告列表中，<b>管理报告</b>表单现在应如下所示：
     </p>
     <p>
-        <img src="image-15.png" />
+        <img src="s-15.png" />
     </p>
     <ul>
         <li>单击<b>确定</b>按钮关闭<b>管理报告</b>表单。</li>
         <li>在<b>文档网格</b>表单上单击<b>报告</b>按钮，然后选择 <b><i>Summary Statistics</i></b>。</li>
     </ul>
     <p>
-        <img src="image-16.png" />
+        <img src="s-16.png" />
     </p>
     <p class="keep-next">
         选择 <b><i>Summary Statistics</i></b> 后，<b>文档网格</b>应显示如下：
     </p>
     <p>
-        <img src="image-17.png" />
+        <img src="s-17.png" />
     </p>
     <p>
         本报告表明，Study9pilot.sky 中的数据采集自同一样品的 5 次重复测定进样，所产生的<b>半峰宽</b>的肽段 CV 值大部分低于 5%，大多数情况下的<b>总面积</b>低于
@@ -498,7 +498,7 @@ <h1>质量控制汇总报告</h1>
         <b>自定义报告</b>表单将显示如下：
     </p>
     <p>
-        <img src="image-18.png" />
+        <img src="s-18.png" />
     </p>
     <p>
         要在此报告上定义新过滤器，请执行以下操作：
@@ -513,7 +513,7 @@ <h1>质量控制汇总报告</h1>
         <b>自定义报告</b>表单将显示如下：
     </p>
     <p>
-        <img src="image-19.png" />
+        <img src="s-19.png" />
     </p>
     <p>
         请注意，即使<b>总面积的变异系数</b>列在<b>文档网格</b>中显示为百分比，但在过滤器选项卡上，数字“20%”仍表示为 0.2。
@@ -522,7 +522,7 @@ <h1>质量控制汇总报告</h1>
         <li>单击<b>自定义报告</b>表单上的<b>确定</b>按钮，查看与此过滤器匹配的行。</li>
     </ul>
     <p>
-        <img src="image-20.png" />
+        <img src="s-20.png" />
     </p>
     <p>
         要更仔细地检查 INDISHTQSVSAK 肽段，请执行以下操作：
@@ -538,7 +538,7 @@ <h1>质量控制汇总报告</h1>
         10%。
     </p>
     <p>
-        <img src="image-21.png" />
+        <img src="s-21.png" />
     </p>
     <p>
         Skyline 汇总报告可以与质量控制数据结合使用，以便及早标出问题，同时 Skyline 本身也提供强大的可视化显示，有助于快速发现问题的根源。
@@ -558,7 +558,7 @@ <h1>结果网格视图</h1>
         此时，Skyline 将显示如下：
     </p>
     <p>
-        <img src="image-22.png" />
+        <img src="s-22.png" />
     </p>
     <p>
         为便于查看，现在可以按如下方式重新排列窗口：
@@ -574,7 +574,7 @@ <h1>结果网格视图</h1>
         执行此操作后，Skyline 应显示如下：
     </p>
     <p>
-        <img src="image-23.png" /> 
+        <img src="s-23.png" /> 
     </p>
     <p>
         在您浏览数据时，Skyline 将保持图表与<b>结果网格</b>同步。如果单击<b>结果网格</b>中的另一行，Skyline
@@ -596,7 +596,7 @@ <h1>结果网格视图</h1>
         <b>结果网格</b>现在应显示如下：
     </p>
     <p>
-        <img src="image-24.png" />
+        <img src="s-24.png" />
     </p>
     <p>
         当前<b>结果网格</b>显示中的其他所有列均由 Skyline 进行计算，无法编辑，但可以更改显示的列和显示顺序。在上图中，有几个列被滚动到视图之外。要减少显示的母离子结果列数，请执行以下操作：
@@ -644,7 +644,7 @@ <h1>自定义注释</h1>
         <b>定义注释</b>表单现在将显示如下：
     </p>
     <p>
-        <img src="image-25.png" />
+        <img src="s-25.png" />
     </p>
     <p>
         现在保存注释，并执行以下操作将其添加到您的文档中：
@@ -658,7 +658,7 @@ <h1>自定义注释</h1>
         <b>文档设置</b>表单现在应显示如下：
     </p>
     <p>
-        <img src="image-26.png" />
+        <img src="s-26.png" />
     </p>
     <ul>
         <li>单击<b>确定</b>按钮。</li>
@@ -676,7 +676,7 @@ <h1>自定义注释</h1>
         <b>自定义报告</b>表单现在将显示如下：
     </p>
     <p>
-        <img src="image-27.png" />
+        <img src="s-27.png" />
     </p>
     <ul>
         <li>单击<b>确定</b>按钮。</li>
@@ -688,7 +688,7 @@ <h1>自定义注释</h1>
         Skyline 窗口现在将显示如下：
     </p>
     <p>
-        <img src="image-28.png" /> 
+        <img src="s-28.png" /> 
     </p>
     <p>
         本文档中的峰问题不大，但这一个确实有一些峰拖尾。选中“Rep1”行的新 <b>Tailing</b> 列对应的复选框。将所选选项依次更改为其他 5
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/zh-CHS/invariant.html b/pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/zh-CHS/invariant.html
index a6d3b0379e..ac4935fc85 100644
--- a/pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/zh-CHS/invariant.html
+++ b/pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/zh-CHS/invariant.html
@@ -113,7 +113,7 @@ <h1>Creating a Simple Custom Report</h1>
         shown below:
     </p>
     <p>
-        <img src="image-0.png" />
+        <img src="s-1.png" />
     </p>
     <p>
         Continue creating a new Skyline custom report template by performing the following steps:
@@ -127,7 +127,7 @@ <h1>Creating a Simple Custom Report</h1>
         The form should now look like this:
     </p>
     <p>
-        <img src="image-1.png" />
+        <img src="s-2.png" />
     </p>
     <ul>
         <li>Expand the field groups <b>Peptides</b> and <b>Replicates</b> by clicking on the <b>‘+’</b> button to see
@@ -138,7 +138,7 @@ <h1>Creating a Simple Custom Report</h1>
         The form should now look like this: 
     </p>
     <p>
-        <img src="image-2.png" />
+        <img src="s-3.png" />
     </p>
     <p>
         Note that the fields in the <b>Edit Report</b> form, shown above, have a distinct hierarchical structure. At the highest level are
@@ -177,7 +177,7 @@ <h1>Creating a Simple Custom Report</h1>
         This should leave the <b>Edit Report</b> form looking like:
     </p>
     <p>
-        <img src="image-3.png" />
+        <img src="s-4.png" />
     </p>
     <ul>
         <li>Click the <b>Preview</b> button in the upper right corner of the <b>Edit Report</b> form.</li>
@@ -186,11 +186,11 @@ <h1>Creating a Simple Custom Report</h1>
         The <b>Preview</b> form should appear looking like this:
     </p>
     <p>
-        <img src="image-4.png" />
+        <img src="s-5.png" />
     </p>
     <p>
         The <b>Preview</b> function is quite helpful when designing report templates. At times it may even serve as a quick substitute for
-        exporting a report to a file. The copy button (<img src="image-5.png" />) on the toolbar will copy all of the data including the column
+        exporting a report to a file. The copy button (<img src="../../shared/copy-button.png" />) on the toolbar will copy all of the data including the column
         headers. You can also select all of the values in the <b>Preview</b> form by clicking the upper-left rectangle to the left of the
         column headers. Pressing Ctrl-C, then copies the full report, excluding the column headers. After copying the data using either method, it can
         be pasted into another tool, such as Excel.
@@ -215,7 +215,7 @@ <h1>Creating a Simple Custom Report</h1>
         below:
     </p>
     <p class="keep-next">
-        <img src="image-6.png" />
+        <img src="s-6.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button again to return to the <b>Export Report</b> form.</li>
@@ -225,7 +225,7 @@ <h1>Creating a Simple Custom Report</h1>
             Report</b> form should now look like:
     </p>
     <p>
-        <img src="image-7.png" />
+        <img src="s-7.png" />
     </p>
     <p>
         From the <b>Export Report</b> form you could now export your new report by selecting ‘Overview’ in the <b>Report</b> list
@@ -274,7 +274,7 @@ <h1>Sharing Report Templates</h1>
         Skyline will present the <b>Manage Reports</b> form, as shown below:
     </p>
     <p>
-        <img src="image-8.png" />
+        <img src="s-8.png" />
     </p>
     <ul>
         <li>Click on ‘Overview’ in the list to select it.</li>
@@ -304,7 +304,7 @@ <h1>Managing Report Templates in Skyline</h1>
         The <b>Manage Reports</b> form should now look like this: 
     </p>
     <p>
-        <img src="image-9.png" />
+        <img src="s-9.png" />
     </p>
     <p>
         To remove the ‘Overview’ item from the list, do the following: 
@@ -317,7 +317,7 @@ <h1>Managing Report Templates in Skyline</h1>
         The <b>Export Report</b> form should now look like this: 
     </p>
     <p>
-        <img src="image-10.png" />
+        <img src="s-10.png" />
     </p>
     <p>
         Just as when you first brought it up in this tutorial. 
@@ -360,7 +360,7 @@ <h1>Modifying Existing Report Templates</h1>
         as shown below: 
     </p>
     <p>
-        <img src="image-11.png" />
+        <img src="s-11.png" />
     </p>
     <p>
         The report name for this new report template has not yet been assigned. To assign it now: 
@@ -433,7 +433,7 @@ <h1>Modifying Existing Report Templates</h1>
             Report</b> form should look like this: 
     </p>
     <p>
-        <img src="image-12.png" />
+        <img src="s-12.png" />
     </p>
     <p>
         To reorder some fields in this new report template, do the following: 
@@ -474,7 +474,7 @@ <h1>Modifying Existing Report Templates</h1>
         The <b>Preview</b> form is shown below, scrolled to show both ‘light’ and ‘heavy’ column names:
     </p>
     <p>
-        <img src="image-13.png" /> 
+        <img src="s-13.png" /> 
     </p>
     <p>
         You might notice that the column ‘heavy Isotope Label Type’ shows ‘heavy’ on every row, and that there is also a column ‘light Isotope Label
@@ -497,7 +497,7 @@ <h1>Modifying Existing Report Templates</h1>
         This will return you to the <b>Export Report</b> form, which should now look like this:
     </p>
     <p>
-        <img src="image-14.png" />
+        <img src="s-14.png" />
     </p>
     <p>
         From here, you could now continue to export the new ‘Study 7’ report to a CSV file by selecting it and clicking the <b>Export</b>
@@ -548,7 +548,7 @@ <h1>Quality Control Summary Reports</h1>
             Reports</b> form should now look like this:
     </p>
     <p>
-        <img src="image-15.png" />
+        <img src="s-15.png" />
     </p>
     <ul>
         <li>Click <b>OK</b> to dismiss the <b>Manage Reports</b> form.</li>
@@ -556,14 +556,14 @@ <h1>Quality Control Summary Reports</h1>
                     Statistics</i></b>.</li>
     </ul>
     <p>
-        <img src="image-16.png" />
+        <img src="s-16.png" />
     </p>
     <p class="keep-next">
         After you choose <b><i>Summary Statistics</i></b>, the <b>Document Grid</b> should look like the
         following:
     </p>
     <p class="keep-next">
-        <img src="image-17.png" />
+        <img src="s-17.png" />
     </p>
     <p>
         This report shows that the data in Study9pilot.sky, taken from 5 replicate injections of the same sample, produce peptide CV values for
@@ -589,7 +589,7 @@ <h1>Quality Control Summary Reports</h1>
         The <b>Customize Report</b> form should look like this:
     </p>
     <p>
-        <img src="image-18.png" />
+        <img src="s-18.png" />
     </p>
     <p>
         To define a new filter on this report:
@@ -604,7 +604,7 @@ <h1>Quality Control Summary Reports</h1>
         The <b>Customize Report</b> form should look like this:
     </p>
     <p>
-        <img src="image-19.png" />
+        <img src="s-19.png" />
     </p>
     <p>
         Note that even though the <b>Cv Total Area</b> column is displayed as a percentage in the <b>Document Grid</b>, on the
@@ -614,7 +614,7 @@ <h1>Quality Control Summary Reports</h1>
         <li>Click the <b>OK</b> button on the <b>Customize Report</b> form to see the rows matching this filter.</li>
     </ul>
     <p>
-        <img src="image-20.png" />
+        <img src="s-20.png" />
     </p>
     <p>
         To inspect the INDISHTQSVSAK peptide more closely, do the following: 
@@ -631,7 +631,7 @@ <h1>Quality Control Summary Reports</h1>
             Area</b> values in the summary report preview, where the majority of the peptides had CV values &lt; 10%.
     </p>
     <p>
-        <img src="image-21.png" />
+        <img src="s-21.png" />
     </p>
     <p>
         Skyline summary reports can be used with quality control data to flag issues early, while Skyline itself provides powerful visual displays to
@@ -655,7 +655,7 @@ <h1>Results Grid View</h1>
         Skyline should now look something like this:
     </p>
     <p>
-        <img src="image-22.png" />
+        <img src="s-22.png" />
     </p>
     <p>
         Now rearrange the windows for better viewing, by doing the following:
@@ -672,7 +672,7 @@ <h1>Results Grid View</h1>
         This should leave Skyline looking something like:
     </p>
     <p>
-        <img src="image-23.png" /> 
+        <img src="s-23.png" /> 
     </p>
     <p>
         Skyline keeps its charts and the <b>Results Grid</b> in synch as you navigate the data. If you click on one of the other rows in the
@@ -699,7 +699,7 @@ <h1>Results Grid View</h1>
         The <b>Results Grid</b> should now look like this:
     </p>
     <p>
-        <img src="image-24.png" />
+        <img src="s-24.png" />
     </p>
     <p>
         All of the other columns in the current <b>Results Grid</b> display are calculated by Skyline and cannot be edited, but you can
@@ -754,7 +754,7 @@ <h1>Custom Annotations</h1>
         The <b>Define Annotation</b> from should now look like this:
     </p>
     <p>
-        <img src="image-25.png" />
+        <img src="s-25.png" />
     </p>
     <p>
         Now save the annotation and add it to your document by doing the following:
@@ -768,7 +768,7 @@ <h1>Custom Annotations</h1>
         The <b>Document Settings</b> form should now look like this:
     </p>
     <p>
-        <img src="image-26.png" />
+        <img src="s-26.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -787,7 +787,7 @@ <h1>Custom Annotations</h1>
         The <b>Customize Report</b> form should now look like the following:
     </p>
     <p>
-        <img src="image-27.png" />
+        <img src="s-27.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -800,7 +800,7 @@ <h1>Custom Annotations</h1>
         The Skyline window should now look something like this:
     </p>
     <p>
-        <img src="image-28.png" />
+        <img src="s-28.png" />
     </p>
     <p>
         The peaks in this document do not have a lot of issues, but this one does have some peak tailing. Check the checkbox in the new
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/zh-CHS/image-0.png b/pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/zh-CHS/s-1.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/zh-CHS/image-0.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/zh-CHS/s-1.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/zh-CHS/image-10.png b/pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/zh-CHS/s-10.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/zh-CHS/image-10.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/zh-CHS/s-10.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/zh-CHS/image-11.png b/pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/zh-CHS/s-11.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/zh-CHS/image-11.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/zh-CHS/s-11.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/zh-CHS/image-12.png b/pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/zh-CHS/s-12.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/zh-CHS/image-12.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/zh-CHS/s-12.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/zh-CHS/image-13.png b/pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/zh-CHS/s-13.png
similarity index 100%
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rename to pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/zh-CHS/s-13.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/zh-CHS/image-14.png b/pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/zh-CHS/s-14.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/zh-CHS/image-14.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/zh-CHS/s-14.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/zh-CHS/image-15.png b/pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/zh-CHS/s-15.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/zh-CHS/image-15.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/zh-CHS/s-15.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/zh-CHS/image-16.png b/pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/zh-CHS/s-16.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/zh-CHS/image-16.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/zh-CHS/s-16.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/zh-CHS/image-17.png b/pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/zh-CHS/s-17.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/zh-CHS/image-17.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/zh-CHS/s-17.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/zh-CHS/image-18.png b/pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/zh-CHS/s-18.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/zh-CHS/image-18.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/zh-CHS/s-18.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/zh-CHS/image-19.png b/pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/zh-CHS/s-19.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/zh-CHS/image-19.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/zh-CHS/image-1.png b/pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/zh-CHS/s-2.png
similarity index 100%
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/zh-CHS/image-20.png b/pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/zh-CHS/s-20.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/zh-CHS/image-20.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/zh-CHS/image-21.png b/pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/zh-CHS/s-21.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/zh-CHS/image-21.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/zh-CHS/image-22.png b/pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/zh-CHS/s-22.png
similarity index 100%
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/zh-CHS/image-23.png b/pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/zh-CHS/s-23.png
similarity index 100%
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/zh-CHS/image-24.png b/pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/zh-CHS/s-24.png
similarity index 100%
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/zh-CHS/image-25.png b/pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/zh-CHS/s-25.png
similarity index 100%
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/zh-CHS/image-26.png b/pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/zh-CHS/s-26.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/zh-CHS/image-26.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/zh-CHS/image-27.png b/pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/zh-CHS/s-27.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/zh-CHS/image-27.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/zh-CHS/image-28.png b/pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/zh-CHS/s-28.png
similarity index 100%
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/zh-CHS/image-2.png b/pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/zh-CHS/s-3.png
similarity index 100%
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/zh-CHS/image-3.png b/pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/zh-CHS/s-4.png
similarity index 100%
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/zh-CHS/image-4.png b/pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/zh-CHS/s-5.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/zh-CHS/image-4.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/zh-CHS/image-6.png b/pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/zh-CHS/s-6.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/zh-CHS/image-6.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/zh-CHS/s-6.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/zh-CHS/image-7.png b/pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/zh-CHS/s-7.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/zh-CHS/image-7.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/zh-CHS/s-7.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/zh-CHS/image-8.png b/pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/zh-CHS/s-8.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/zh-CHS/image-8.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/zh-CHS/s-8.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/zh-CHS/image-9.png b/pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/zh-CHS/s-9.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/zh-CHS/image-9.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/zh-CHS/s-9.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/en/index.html b/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/en/index.html
index a9ea7532a4..3ba5ff7b82 100644
--- a/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/en/index.html
+++ b/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/en/index.html
@@ -102,7 +102,7 @@ <h1>Getting Started</h1>
         The Peptide Settings form should now look like:
     </p>
     <p>
-        <img src="image-0.png" />
+        <img src="s-1.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button in the <b>Peptide Settings</b> form.</li>
@@ -130,7 +130,7 @@ <h1>Searching DDA Files to Load Peptides into a Skyline Document</h1>
         Skyline should present a form that looks like this:
     </p>
     <p>
-        <img src="image-1.png" />
+        <img src="s-2.png" />
     </p>
     <p>
         This form can be used to search for peptides in raw data (e.g. RAW, WIFF, *.d, mzML, mz5, mzXML). The mz5 files for this tutorial are
@@ -148,7 +148,7 @@ <h1>Searching DDA Files to Load Peptides into a Skyline Document</h1>
         The wizard form should now look like this:
     </p>
     <p>
-        <img src="image-2.png" />
+        <img src="s-3.png" />
     </p>
     <ul>
         <li>Click the <b>Next</b> button.</li>
@@ -157,7 +157,7 @@ <h1>Searching DDA Files to Load Peptides into a Skyline Document</h1>
         A form should appear asking you how to handle the prefix shared by the three mz5 files: 
     </p>
     <p>
-        <img src="image-3.png" />
+        <img src="s-4.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -175,7 +175,7 @@ <h1>Searching DDA Files to Load Peptides into a Skyline Document</h1>
         only Carbamidomethyl (C):
     </p>
     <p>
-        <img src="image-4.png" />
+        <img src="s-5.png" />
     </p>
     <p>
         These data are SILAC labelled, so you will need to add heavy label modifications here. To add them, do the following:
@@ -192,7 +192,7 @@ <h1>Searching DDA Files to Load Peptides into a Skyline Document</h1>
         The <b>Edit Isotope Modification</b> form should now look like this:
     </p>
     <p>
-        <img src="image-5.png" />
+        <img src="s-6.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button</li>
@@ -214,7 +214,7 @@ <h1>Searching DDA Files to Load Peptides into a Skyline Document</h1>
         The <b>Edit Isotope Modification</b> form should now look like this:
     </p>
     <p>
-        <img src="image-6.png" />
+        <img src="s-7.png" />
     </p>
     <p>
         Skyline automatically calculates both the monoisotopic and average masses, approximately 8 Daltons for Lysine (K) and 10 Daltons for Arginine
@@ -245,7 +245,7 @@ <h1>Searching DDA Files to Load Peptides into a Skyline Document</h1>
         At this point the <b>Add Modifications</b> page should look like:
     </p>
     <p>
-        <img src="image-7.png" />
+        <img src="s-8.png" />
     </p>
     <ul>
         <li>Click the <b>Next</b> button.</li>
@@ -260,7 +260,7 @@ <h1>Searching DDA Files to Load Peptides into a Skyline Document</h1>
         The other fields on this page should default to values you can use for this tutorial, and the wizard should look like this:
     </p>
     <p>
-        <img src="image-8.png" />
+        <img src="s-9.png" />
     </p>
     <ul>
         <li>See the <a href="https://skyline.ms/_webdav/home/software/Skyline/@files/tutorials/MS1Filtering-20_1.pdf#page=9">MS1 Full Scan Filtering
@@ -281,7 +281,7 @@ <h1>Searching DDA Files to Load Peptides into a Skyline Document</h1>
         The wizard should now look like this:
     </p>
     <p>
-        <img src="image-9.png" />
+        <img src="s-10.png" />
     </p>
     <ul>
         <li>Click the <b>Next</b> button.</li>
@@ -299,7 +299,7 @@ <h1>Searching DDA Files to Load Peptides into a Skyline Document</h1>
         The form should now look like this:
     </p>
     <p>
-        <img src="image-10.png" />
+        <img src="s-11.png" />
     </p>
     <p>
         The <b>Max q-value</b> field sets a false discovery rate (FDR) limit allowed for the peptide matches in the search results. In this
@@ -313,7 +313,7 @@ <h1>Searching DDA Files to Load Peptides into a Skyline Document</h1>
         <b>Cancel Search</b> button on this page.
     </p>
     <p>
-        <img src="image-11.png" />
+        <img src="s-12.png" />
     </p>
     <p>
         After the search is finished:
@@ -327,7 +327,7 @@ <h1>Searching DDA Files to Load Peptides into a Skyline Document</h1>
         those peptides will be ignored:
     </p>
     <p>
-        <img src="image-12.png" />
+        <img src="s-13.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button to dismiss the message.</li>
@@ -337,7 +337,7 @@ <h1>Searching DDA Files to Load Peptides into a Skyline Document</h1>
         including proteins in the document:
     </p>
     <p>
-        <img src="image-13.png" />
+        <img src="s-14.png" />
     </p>
     <p>
         Skyline can merge proteins that match the same set of peptides into protein groups and find a minimal list of proteins that explain all the
@@ -373,7 +373,7 @@ <h1>Configuring Skyline to View the Imported Data</h1>
         Your Skyline window should look something like this:
     </p>
     <p>
-        <img src="image-14.png" />
+        <img src="s-15.png" />
     </p>
     <p>
         The document is now fully configured for MS1 Filtering with three DDA runs imported. You will see that the chromatogram in this view is
@@ -400,7 +400,7 @@ <h1>Configuring Skyline to View the Imported Data</h1>
         A window with a graph like this should appear:
     </p>
     <p>
-        <img src="image-15.png" />
+        <img src="s-16.png" />
     </p>
     <p>
         You can dock the <b>Peak Areas</b> window to your desired location by doing the following:
@@ -418,7 +418,7 @@ <h1>Configuring Skyline to View the Imported Data</h1>
         Now your Skyline window should look something like this:
     </p>
     <p>
-        <img src="image-16.png" />
+        <img src="s-17.png" />
     </p>
     <p>
         From this point you can learn more about working with DDA data by consulting the <a
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/en/image-0.png b/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/en/s-1.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/en/image-0.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/en/s-1.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/en/image-9.png b/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/en/s-10.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/en/image-9.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/en/s-10.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/en/image-10.png b/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/en/s-11.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/en/image-10.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/en/image-11.png b/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/en/s-12.png
similarity index 100%
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/en/image-12.png b/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/en/s-13.png
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rename from pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/en/image-12.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/en/s-13.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/en/image-13.png b/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/en/s-14.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/en/image-13.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/en/s-14.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/en/image-14.png b/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/en/s-15.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/en/image-14.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/en/image-15.png b/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/en/s-16.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/en/image-15.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/en/image-16.png b/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/en/s-17.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/en/image-16.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/en/image-1.png b/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/en/s-2.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/en/image-1.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/en/s-2.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/en/image-2.png b/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/en/s-3.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/en/image-2.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/en/s-3.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/en/image-3.png b/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/en/s-4.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/en/image-3.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/en/s-4.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/en/image-4.png b/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/en/s-5.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/en/image-4.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/en/s-5.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/en/image-5.png b/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/en/s-6.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/en/image-5.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/en/s-6.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/en/image-6.png b/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/en/s-7.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/en/image-6.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/en/s-7.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/en/image-7.png b/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/en/s-8.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/en/image-7.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/en/s-8.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/en/image-8.png b/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/en/s-9.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/en/image-8.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/en/s-9.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/ja/index.html b/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/ja/index.html
index 912c85ec2b..c18e3baac2 100644
--- a/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/ja/index.html
+++ b/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/ja/index.html
@@ -92,7 +92,7 @@ <h1>はじめに</h1>
         [ ペプチド設定 ] フォームは以下のようになります。
     </p>
     <p>
-        <img src="image-0.png" />
+        <img src="s-1.png" />
     </p>
     <ul>
         <li>[ <b>ペプチド設定</b> ] フォームの [ <b>OK</b> ] ボタンをクリックします。</li>
@@ -120,7 +120,7 @@ <h1>Skylineドキュメントにペプチドを読み込むDDAファイルの検
         以下のようなフォームが表示されます。
     </p>
     <p>
-        <img src="image-1.png" />
+        <img src="s-2.png" />
     </p>
     <p>
         [ <b>構築</b> ] オプションは、DDA検索エンジンからの出力（CometからのpepXMLファイル、Mascotからの.datなど）に、また [ <b>DDA検索を実行</b> ]
@@ -139,7 +139,7 @@ <h1>Skylineドキュメントにペプチドを読み込むDDAファイルの検
         ウィザードフォームは以下のようになります。
     </p>
     <p>
-        <img src="image-2.png" />
+        <img src="s-3.png" />
     </p>
     <ul>
         <li>[ <b>次へ</b> ] ボタンをクリックします。</li>
@@ -148,7 +148,7 @@ <h1>Skylineドキュメントにペプチドを読み込むDDAファイルの検
         3つのmz5ファイルに共通のプリフィックスをどう取り扱うかを尋ねるフォームが表示されます。 
     </p>
     <p>
-        <img src="image-3.png" />
+        <img src="s-4.png" />
     </p>
     <ul>
         <li>[ <b>OK</b> ] ボタンをクリックします。</li>
@@ -163,7 +163,7 @@ <h1>Skylineドキュメントにペプチドを読み込むDDAファイルの検
         また、このページからドキュメントに修飾を追加することもできます。ドキュメントがデフォルトにリセットされているため、リストはCarbamidomethyl (C)のみで開始となります。
     </p>
     <p>
-        <img src="image-4.png" />
+        <img src="s-5.png" />
     </p>
     <p>
         これらのデータはSILAC標識であるため、ここでヘビー標識の修飾を追加する必要があります。これらを追加するには、以下の操作を行います。
@@ -180,7 +180,7 @@ <h1>Skylineドキュメントにペプチドを読み込むDDAファイルの検
         [ <b>同位体修飾を編集</b> ] フォームは以下のように表示されます。
     </p>
     <p>
-        <img src="image-5.png" />
+        <img src="s-6.png" />
     </p>
     <ul>
         <li>[ <b>OK</b> ] ボタンをクリックします。</li>
@@ -200,7 +200,7 @@ <h1>Skylineドキュメントにペプチドを読み込むDDAファイルの検
         [ <b>同位体修飾を編集</b> ] フォームは以下のように表示されます。
     </p>
     <p>
-        <img src="image-6.png" />
+        <img src="s-7.png" />
     </p>
     <p>
         Skylineは13Cおよび15Nを用いて、モノアイソトピック質量と平均質量のの計算を自動的に行います（リジン（K）については約8ダルトン、アルギニン（R）については約10ダルトンとなります）。ヘビー修飾の追加を終了するには、以下の操作を行います。
@@ -230,7 +230,7 @@ <h1>Skylineドキュメントにペプチドを読み込むDDAファイルの検
         この時点で、[ <b>修飾を追加</b> ] ページは以下のようになります。
     </p>
     <p>
-        <img src="image-7.png" />
+        <img src="s-8.png" />
     </p>
     <ul>
         <li>[ <b>次へ</b> ] ボタンをクリックします。</li>
@@ -245,7 +245,7 @@ <h1>Skylineドキュメントにペプチドを読み込むDDAファイルの検
         このページの他のフィールドは、本チュートリアルで使用可能なデフォルト設定のままにしておいてください。ウィザードは以下のようになります。
     </p>
     <p>
-        <img src="image-8.png" />
+        <img src="s-9.png" />
     </p>
     <ul>
         <li>この設定の詳細については、<a
@@ -266,7 +266,7 @@ <h1>Skylineドキュメントにペプチドを読み込むDDAファイルの検
         ウィザードは以下のようになります。
     </p>
     <p>
-        <img src="image-9.png" />
+        <img src="s-10.png" />
     </p>
     <ul>
         <li>[ <b>次へ</b> ] ボタンをクリックします。</li>
@@ -282,7 +282,7 @@ <h1>Skylineドキュメントにペプチドを読み込むDDAファイルの検
         フォームは以下のようになります。
     </p>
     <p>
-        <img src="image-10.png" />
+        <img src="s-11.png" />
     </p>
     <ul>
         <li>[ <b>次へ</b> ] ボタンをクリックして検索を開始します。</li>
@@ -291,7 +291,7 @@ <h1>Skylineドキュメントにペプチドを読み込むDDAファイルの検
         [ <b>DDA検索</b> ] ページが検索の進捗状況を示します。このページの [ <b>検索をキャンセル</b> ] ボタンをクリックして検索をキャンセルすることもできます。
     </p>
     <p>
-        <img src="image-11.png" />
+        <img src="s-12.png" />
     </p>
     <p>
         検索が完了したら、以下の操作を行います。
@@ -304,7 +304,7 @@ <h1>Skylineドキュメントにペプチドを読み込むDDAファイルの検
         Skylineが検索結果からスペクトルライブラリの構築を開始します。ライブラリの構築が完了するとメッセージボックスが表示され、信頼性が等しい複数の異なるペプチドと解釈することのできるスペクトルがあり、これらのペプチドは無視されるという警告が表示されます。
     </p>
     <p>
-        <img src="image-12.png" />
+        <img src="s-13.png" />
     </p>
     <ul>
         <li>[ <b>OK</b> ] ボタンをクリックしてメッセージを閉じます。</li>
@@ -313,7 +313,7 @@ <h1>Skylineドキュメントにペプチドを読み込むDDAファイルの検
         Skylineはその後、ライブラリのドキュメントへのインポートを開始します。インポートが終了すると、ドキュメントにタンパク質を含む基準を設定するようにプロンプトされます。
     </p>
     <p>
-        <img src="image-13.png" />
+        <img src="s-14.png" />
     </p>
     <ul>
         <li>[ <b>反復ペプチドを削除</b> ] チェックボックスをオンにします（一意ではないペプチドに対して最初に発生するペプチドを維持）。</li>
@@ -340,7 +340,7 @@ <h1>インポートされたデータを表示するSkylineの設定</h1>
         Skylineウィンドウは以下のようになります。
     </p>
     <p>
-        <img src="image-14.png" />
+        <img src="s-15.png" />
     </p>
     <p>
         このドキュメントは、DDAモードでの測定結果3件のインポートを含み、MS1フィルタ向けにフル設定されています。インポートウィザードで [ <b>MS/MSのIDの時間（5分）のスキャンのみを使用します</b> ]
@@ -363,7 +363,7 @@ <h1>インポートされたデータを表示するSkylineの設定</h1>
         グラフを含む次のようなウィンドウが表示されます。
     </p>
     <p>
-        <img src="image-15.png" />
+        <img src="s-16.png" />
     </p>
     <p>
         以下の操作を行うと、[ <b>ピーク領域</b> ] ウィンドウを好きな場所にドッキングできます。
@@ -381,7 +381,7 @@ <h1>インポートされたデータを表示するSkylineの設定</h1>
         Skylineウィンドウは以下のようになります。
     </p>
     <p>
-        <img src="image-16.png" />
+        <img src="s-17.png" />
     </p>
     <p>
         ここからは、<a
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/ja/invariant.html b/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/ja/invariant.html
index e21af11996..159e897133 100644
--- a/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/ja/invariant.html
+++ b/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/ja/invariant.html
@@ -102,7 +102,7 @@ <h1>Getting Started</h1>
         The Peptide Settings form should now look like:
     </p>
     <p>
-        <img src="image-0.png" />
+        <img src="s-1.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button in the <b>Peptide Settings</b> form.</li>
@@ -130,7 +130,7 @@ <h1>Searching DDA Files to Load Peptides into a Skyline Document</h1>
         Skyline should present a form that looks like this:
     </p>
     <p>
-        <img src="image-1.png" />
+        <img src="s-2.png" />
     </p>
     <p>
         The <b>Build</b> options works on the output from DDA search engines (e.g. pepXML files from Comet, .dat from Mascot) and the
@@ -150,7 +150,7 @@ <h1>Searching DDA Files to Load Peptides into a Skyline Document</h1>
         The wizard form should now look like this:
     </p>
     <p>
-        <img src="image-2.png" />
+        <img src="s-3.png" />
     </p>
     <ul>
         <li>Click the <b>Next</b> button.</li>
@@ -159,7 +159,7 @@ <h1>Searching DDA Files to Load Peptides into a Skyline Document</h1>
         A form should appear asking you how to handle the prefix shared by the three mz5 files: 
     </p>
     <p>
-        <img src="image-3.png" />
+        <img src="s-4.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -177,7 +177,7 @@ <h1>Searching DDA Files to Load Peptides into a Skyline Document</h1>
         only Carbamidomethyl (C):
     </p>
     <p>
-        <img src="image-4.png" />
+        <img src="s-5.png" />
     </p>
     <p>
         These data are SILAC labelled, so you will need to add heavy label modifications here. To add them, do the following:
@@ -195,7 +195,7 @@ <h1>Searching DDA Files to Load Peptides into a Skyline Document</h1>
         The <b>Edit Isotope Modification</b> form should now look like this:
     </p>
     <p>
-        <img src="image-5.png" />
+        <img src="s-6.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button</li>
@@ -217,7 +217,7 @@ <h1>Searching DDA Files to Load Peptides into a Skyline Document</h1>
         The <b>Edit Isotope Modification</b> form should now look like this:
     </p>
     <p>
-        <img src="image-6.png" />
+        <img src="s-7.png" />
     </p>
     <p>
         Skyline automatically calculates both the monoisotopic and average masses, approximately 8 Daltons for Lysine (K) and 10 Daltons for Arginine
@@ -249,7 +249,7 @@ <h1>Searching DDA Files to Load Peptides into a Skyline Document</h1>
         At this point the <b>Add Modifications</b> page should look like:
     </p>
     <p>
-        <img src="image-7.png" />
+        <img src="s-8.png" />
     </p>
     <ul>
         <li>Click the <b>Next</b> button.</li>
@@ -264,7 +264,7 @@ <h1>Searching DDA Files to Load Peptides into a Skyline Document</h1>
         The other fields on this page should default to values you can use for this tutorial, and the wizard should look like this:
     </p>
     <p>
-        <img src="image-8.png" />
+        <img src="s-9.png" />
     </p>
     <ul>
         <li>See the <a href="https://skyline.ms/_webdav/home/software/Skyline/@files/tutorials/MS1Filtering-20_1.pdf#page=9">MS1 Full Scan Filtering
@@ -285,7 +285,7 @@ <h1>Searching DDA Files to Load Peptides into a Skyline Document</h1>
         The wizard should now look like this:
     </p>
     <p>
-        <img src="image-9.png" />
+        <img src="s-10.png" />
     </p>
     <ul>
         <li>Click the <b>Next</b> button.</li>
@@ -303,7 +303,7 @@ <h1>Searching DDA Files to Load Peptides into a Skyline Document</h1>
         The form should now look like this:
     </p>
     <p>
-        <img src="image-10.png" />
+        <img src="s-11.png" />
     </p>
     <ul>
         <li>Click the <b>Next</b> button to start the search.</li>
@@ -313,7 +313,7 @@ <h1>Searching DDA Files to Load Peptides into a Skyline Document</h1>
         <b>Cancel Search</b> button on this page.
     </p>
     <p>
-        <img src="image-11.png" />
+        <img src="s-12.png" />
     </p>
     <p>
         After the search is finished:
@@ -327,7 +327,7 @@ <h1>Searching DDA Files to Load Peptides into a Skyline Document</h1>
         those peptides will be ignored:
     </p>
     <p>
-        <img src="image-12.png" />
+        <img src="s-13.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button to dismiss the message.</li>
@@ -337,7 +337,7 @@ <h1>Searching DDA Files to Load Peptides into a Skyline Document</h1>
         including proteins in the document:
     </p>
     <p>
-        <img src="image-13.png" />
+        <img src="s-14.png" />
     </p>
     <ul>
         <li>Check the <b>Remove repeated peptides</b> checkbox (i.e. keep first the occurrence for non-unique peptides).</li>
@@ -367,7 +367,7 @@ <h1>Configuring Skyline to View the Imported Data</h1>
         Your Skyline window should look something like this:
     </p>
     <p>
-        <img src="image-14.png" />
+        <img src="s-15.png" />
     </p>
     <p>
         The document is now fully configured for MS1 Filtering with three DDA runs imported. You will see that the chromatogram in this view is
@@ -394,7 +394,7 @@ <h1>Configuring Skyline to View the Imported Data</h1>
         A window with a graph like this should appear:
     </p>
     <p>
-        <img src="image-15.png" />
+        <img src="s-16.png" />
     </p>
     <p>
         You can dock the <b>Peak Areas</b> window to your desired location by doing the following:
@@ -412,7 +412,7 @@ <h1>Configuring Skyline to View the Imported Data</h1>
         Now your Skyline window should look something like this:
     </p>
     <p>
-        <img src="image-16.png" />
+        <img src="s-17.png" />
     </p>
     <p>
         From this point you can learn more about working with DDA data by consulting the <a
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/ja/image-0.png b/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/ja/s-1.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/ja/image-0.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/ja/s-1.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/ja/image-9.png b/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/ja/s-10.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/ja/image-9.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/ja/s-10.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/ja/image-10.png b/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/ja/s-11.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/ja/image-10.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/ja/s-11.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/ja/image-11.png b/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/ja/s-12.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/ja/image-11.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/ja/s-12.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/ja/image-12.png b/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/ja/s-13.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/ja/image-12.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/ja/s-13.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/ja/image-13.png b/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/ja/s-14.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/ja/image-13.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/ja/s-14.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/ja/image-14.png b/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/ja/s-15.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/ja/image-14.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/ja/s-15.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/ja/image-15.png b/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/ja/s-16.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/ja/image-15.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/ja/s-16.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/ja/image-16.png b/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/ja/s-17.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/ja/image-16.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/ja/s-17.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/ja/image-1.png b/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/ja/s-2.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/ja/image-1.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/ja/s-2.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/ja/image-2.png b/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/ja/s-3.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/ja/image-2.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/ja/s-3.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/ja/image-3.png b/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/ja/s-4.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/ja/image-3.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/ja/s-4.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/ja/image-4.png b/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/ja/s-5.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/ja/image-4.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/ja/s-5.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/ja/image-5.png b/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/ja/s-6.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/ja/image-5.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/ja/s-6.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/ja/image-6.png b/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/ja/s-7.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/ja/image-6.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/ja/s-7.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/ja/image-7.png b/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/ja/s-8.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/ja/image-7.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/ja/s-8.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/ja/image-8.png b/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/ja/s-9.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/ja/image-8.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/ja/s-9.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/zh-CHS/index.html b/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/zh-CHS/index.html
index 6d2e14ba6a..cd85788e8d 100644
--- a/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/zh-CHS/index.html
+++ b/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/zh-CHS/index.html
@@ -92,7 +92,7 @@ <h1>入门指南</h1>
         “肽段设置”表单现在应如下所示：
     </p>
     <p>
-        <img src="image-0.png" />
+        <img src="s-1.png" />
     </p>
     <ul>
         <li>单击<b>肽段设置</b>表单中的<b>确定</b>按钮。</li>
@@ -120,7 +120,7 @@ <h1>搜索 DDA 文件，将肽段载入 Skyline 文档</h1>
         Skyline 将呈现如下所示的表单：
     </p>
     <p>
-        <img src="image-1.png" />
+        <img src="s-2.png" />
     </p>
     <p>
         <b>构建</b>选项适用于 DDA 搜索引擎的输出（如 Comet 的 pepXML 文件，Mascot 的 .dat 文件），<b>执行 DDA 搜索</b>选项适用于原始数据（如 RAW、WIFF、*.d、mzML、mzXML）。本教程中的
@@ -139,7 +139,7 @@ <h1>搜索 DDA 文件，将肽段载入 Skyline 文档</h1>
         此时向导表单将显示如下：
     </p>
     <p>
-        <img src="image-2.png" />
+        <img src="s-3.png" />
     </p>
     <ul>
         <li>单击<b>下一步</b>按钮。</li>
@@ -148,7 +148,7 @@ <h1>搜索 DDA 文件，将肽段载入 Skyline 文档</h1>
         此时将显示一个表单，询问您如何处理这三个 mz5 文件的共有前缀： 
     </p>
     <p>
-        <img src="image-3.png" />
+        <img src="s-4.png" />
     </p>
     <ul>
         <li>单击<b>确定</b>按钮。</li>
@@ -162,7 +162,7 @@ <h1>搜索 DDA 文件，将肽段载入 Skyline 文档</h1>
         您也可以从本页面向文档中添加修饰。由于此文档被重置为默认值，所以列表中只以 Carbamidomethyl (C) 开始：
     </p>
     <p>
-        <img src="image-4.png" />
+        <img src="s-5.png" />
     </p>
     <p>
         这些数据有 SILAC 标签，这里需要添加重标签修饰。添加步骤如下：
@@ -179,7 +179,7 @@ <h1>搜索 DDA 文件，将肽段载入 Skyline 文档</h1>
         此时<b>编辑同位素修饰</b>表单应显示如下：
     </p>
     <p>
-        <img src="image-5.png" />
+        <img src="s-6.png" />
     </p>
     <ul>
         <li>单击<b>确定</b>按钮</li>
@@ -199,7 +199,7 @@ <h1>搜索 DDA 文件，将肽段载入 Skyline 文档</h1>
         此时<b>编辑同位素修饰</b>表单应显示如下：
     </p>
     <p>
-        <img src="image-6.png" />
+        <img src="s-7.png" />
     </p>
     <p>
         Skyline 自动计算单一同位素质量和平均质量偏移，如图，赖氨酸 (K) 质量偏移约为 8 Da，精氨酸 (R) 约为 10 Da，这是由于在这些氨基酸残基中使用了 13 C 和 15 N。要完成添加重修饰：
@@ -229,7 +229,7 @@ <h1>搜索 DDA 文件，将肽段载入 Skyline 文档</h1>
         这时的<b>添加修饰</b>页面应如下所示：
     </p>
     <p>
-        <img src="image-7.png" />
+        <img src="s-8.png" />
     </p>
     <ul>
         <li>单击<b>下一步</b>按钮。</li>
@@ -244,7 +244,7 @@ <h1>搜索 DDA 文件，将肽段载入 Skyline 文档</h1>
         本页面中的其它字段应默认为可用于本教程的值，向导显示如下：
     </p>
     <p>
-        <img src="image-8.png" />
+        <img src="s-9.png" />
     </p>
     <ul>
         <li>参见 <a href="https://skyline.ms/_webdav/home/software/Skyline/@files/tutorials/MS1Filtering-20_1.pdf#page=9">MS1 全扫描筛选教程</a>（第 9
@@ -264,7 +264,7 @@ <h1>搜索 DDA 文件，将肽段载入 Skyline 文档</h1>
         此时向导将显示如下：
     </p>
     <p>
-        <img src="image-9.png" />
+        <img src="s-10.png" />
     </p>
     <ul>
         <li>单击<b>下一步</b>按钮。</li>
@@ -280,7 +280,7 @@ <h1>搜索 DDA 文件，将肽段载入 Skyline 文档</h1>
         该表单现在应显示如下：
     </p>
     <p>
-        <img src="image-10.png" />
+        <img src="s-11.png" />
     </p>
     <ul>
         <li>单击<b>下一步</b>按钮开始搜索。</li>
@@ -289,7 +289,7 @@ <h1>搜索 DDA 文件，将肽段载入 Skyline 文档</h1>
         <b>DDA 搜索</b>页面将显示搜索进度。您也可以单击该页面的<b>取消搜索</b>按钮来取消搜索。
     </p>
     <p>
-        <img src="image-11.png" />
+        <img src="s-12.png" />
     </p>
     <p>
         搜索结束后：
@@ -301,7 +301,7 @@ <h1>搜索 DDA 文件，将肽段载入 Skyline 文档</h1>
         Skyline 将开始根据搜索结果构建谱图库。完成谱图库构建后，将弹出一个消息框，提醒您有些谱图可能被解读为多个置信水平相同的不同肽段，并且这些肽段将被忽略：
     </p>
     <p>
-        <img src="image-12.png" />
+        <img src="s-13.png" />
     </p>
     <ul>
         <li>单击<b>确定</b>按钮关闭此消息。</li>
@@ -310,7 +310,7 @@ <h1>搜索 DDA 文件，将肽段载入 Skyline 文档</h1>
         然后 Skyline 开始将该库导入您的文档。导入完成后，会提示您设置此文档中包含蛋白质的条件：
     </p>
     <p>
-        <img src="image-13.png" />
+        <img src="s-14.png" />
     </p>
     <ul>
         <li>选中<b>删除重复的肽段</b>复选框（即保留第一次出现的非唯一肽段）。</li>
@@ -335,7 +335,7 @@ <h1>配置 Skyline 以查看导入的数据</h1>
         Skyline 窗口应显示如下：
     </p>
     <p>
-        <img src="image-14.png" />
+        <img src="s-15.png" />
     </p>
     <p>
         现在文档已通过所导入的三项 DDA 运行完成了 MS1 筛选的全部配置。由于在导入向导中选择了<b>仅使用 MS/MS ID 5 分钟之内的扫描</b>设置，本视图中的色谱图长度约为 10 分钟（133 至 143 分钟）。请注意，在为 MS1 筛选进行
@@ -358,7 +358,7 @@ <h1>配置 Skyline 以查看导入的数据</h1>
         此时应当会出现一个包含下图的窗口：
     </p>
     <p>
-        <img src="image-15.png" />
+        <img src="s-16.png" />
     </p>
     <p>
         您可以通过下列操作将<b>峰面积</b>窗口停靠在您需要的位置：
@@ -375,7 +375,7 @@ <h1>配置 Skyline 以查看导入的数据</h1>
         现在 Skyline 窗口应显示如下：
     </p>
     <p>
-        <img src="image-16.png" />
+        <img src="s-17.png" />
     </p>
     <p>
         此后您可以查阅 <a href="https://skyline.ms/_webdav/home/software/Skyline/@files/tutorials/MS1Filtering-20_1.pdf">MS1 全扫描筛选教程</a>，来了解有关 DDA 数据处理的更多信息。
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/zh-CHS/invariant.html b/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/zh-CHS/invariant.html
index e21af11996..159e897133 100644
--- a/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/zh-CHS/invariant.html
+++ b/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/zh-CHS/invariant.html
@@ -102,7 +102,7 @@ <h1>Getting Started</h1>
         The Peptide Settings form should now look like:
     </p>
     <p>
-        <img src="image-0.png" />
+        <img src="s-1.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button in the <b>Peptide Settings</b> form.</li>
@@ -130,7 +130,7 @@ <h1>Searching DDA Files to Load Peptides into a Skyline Document</h1>
         Skyline should present a form that looks like this:
     </p>
     <p>
-        <img src="image-1.png" />
+        <img src="s-2.png" />
     </p>
     <p>
         The <b>Build</b> options works on the output from DDA search engines (e.g. pepXML files from Comet, .dat from Mascot) and the
@@ -150,7 +150,7 @@ <h1>Searching DDA Files to Load Peptides into a Skyline Document</h1>
         The wizard form should now look like this:
     </p>
     <p>
-        <img src="image-2.png" />
+        <img src="s-3.png" />
     </p>
     <ul>
         <li>Click the <b>Next</b> button.</li>
@@ -159,7 +159,7 @@ <h1>Searching DDA Files to Load Peptides into a Skyline Document</h1>
         A form should appear asking you how to handle the prefix shared by the three mz5 files: 
     </p>
     <p>
-        <img src="image-3.png" />
+        <img src="s-4.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -177,7 +177,7 @@ <h1>Searching DDA Files to Load Peptides into a Skyline Document</h1>
         only Carbamidomethyl (C):
     </p>
     <p>
-        <img src="image-4.png" />
+        <img src="s-5.png" />
     </p>
     <p>
         These data are SILAC labelled, so you will need to add heavy label modifications here. To add them, do the following:
@@ -195,7 +195,7 @@ <h1>Searching DDA Files to Load Peptides into a Skyline Document</h1>
         The <b>Edit Isotope Modification</b> form should now look like this:
     </p>
     <p>
-        <img src="image-5.png" />
+        <img src="s-6.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button</li>
@@ -217,7 +217,7 @@ <h1>Searching DDA Files to Load Peptides into a Skyline Document</h1>
         The <b>Edit Isotope Modification</b> form should now look like this:
     </p>
     <p>
-        <img src="image-6.png" />
+        <img src="s-7.png" />
     </p>
     <p>
         Skyline automatically calculates both the monoisotopic and average masses, approximately 8 Daltons for Lysine (K) and 10 Daltons for Arginine
@@ -249,7 +249,7 @@ <h1>Searching DDA Files to Load Peptides into a Skyline Document</h1>
         At this point the <b>Add Modifications</b> page should look like:
     </p>
     <p>
-        <img src="image-7.png" />
+        <img src="s-8.png" />
     </p>
     <ul>
         <li>Click the <b>Next</b> button.</li>
@@ -264,7 +264,7 @@ <h1>Searching DDA Files to Load Peptides into a Skyline Document</h1>
         The other fields on this page should default to values you can use for this tutorial, and the wizard should look like this:
     </p>
     <p>
-        <img src="image-8.png" />
+        <img src="s-9.png" />
     </p>
     <ul>
         <li>See the <a href="https://skyline.ms/_webdav/home/software/Skyline/@files/tutorials/MS1Filtering-20_1.pdf#page=9">MS1 Full Scan Filtering
@@ -285,7 +285,7 @@ <h1>Searching DDA Files to Load Peptides into a Skyline Document</h1>
         The wizard should now look like this:
     </p>
     <p>
-        <img src="image-9.png" />
+        <img src="s-10.png" />
     </p>
     <ul>
         <li>Click the <b>Next</b> button.</li>
@@ -303,7 +303,7 @@ <h1>Searching DDA Files to Load Peptides into a Skyline Document</h1>
         The form should now look like this:
     </p>
     <p>
-        <img src="image-10.png" />
+        <img src="s-11.png" />
     </p>
     <ul>
         <li>Click the <b>Next</b> button to start the search.</li>
@@ -313,7 +313,7 @@ <h1>Searching DDA Files to Load Peptides into a Skyline Document</h1>
         <b>Cancel Search</b> button on this page.
     </p>
     <p>
-        <img src="image-11.png" />
+        <img src="s-12.png" />
     </p>
     <p>
         After the search is finished:
@@ -327,7 +327,7 @@ <h1>Searching DDA Files to Load Peptides into a Skyline Document</h1>
         those peptides will be ignored:
     </p>
     <p>
-        <img src="image-12.png" />
+        <img src="s-13.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button to dismiss the message.</li>
@@ -337,7 +337,7 @@ <h1>Searching DDA Files to Load Peptides into a Skyline Document</h1>
         including proteins in the document:
     </p>
     <p>
-        <img src="image-13.png" />
+        <img src="s-14.png" />
     </p>
     <ul>
         <li>Check the <b>Remove repeated peptides</b> checkbox (i.e. keep first the occurrence for non-unique peptides).</li>
@@ -367,7 +367,7 @@ <h1>Configuring Skyline to View the Imported Data</h1>
         Your Skyline window should look something like this:
     </p>
     <p>
-        <img src="image-14.png" />
+        <img src="s-15.png" />
     </p>
     <p>
         The document is now fully configured for MS1 Filtering with three DDA runs imported. You will see that the chromatogram in this view is
@@ -394,7 +394,7 @@ <h1>Configuring Skyline to View the Imported Data</h1>
         A window with a graph like this should appear:
     </p>
     <p>
-        <img src="image-15.png" />
+        <img src="s-16.png" />
     </p>
     <p>
         You can dock the <b>Peak Areas</b> window to your desired location by doing the following:
@@ -412,7 +412,7 @@ <h1>Configuring Skyline to View the Imported Data</h1>
         Now your Skyline window should look something like this:
     </p>
     <p>
-        <img src="image-16.png" />
+        <img src="s-17.png" />
     </p>
     <p>
         From this point you can learn more about working with DDA data by consulting the <a
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/zh-CHS/image-0.png b/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/zh-CHS/s-1.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/zh-CHS/image-0.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/zh-CHS/s-1.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/zh-CHS/image-9.png b/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/zh-CHS/s-10.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/zh-CHS/image-9.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/zh-CHS/s-10.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/zh-CHS/image-10.png b/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/zh-CHS/s-11.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/zh-CHS/image-10.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/zh-CHS/s-11.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/zh-CHS/image-11.png b/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/zh-CHS/s-12.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/zh-CHS/image-11.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/zh-CHS/s-12.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/zh-CHS/image-12.png b/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/zh-CHS/s-13.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/zh-CHS/image-12.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/zh-CHS/s-13.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/zh-CHS/image-13.png b/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/zh-CHS/s-14.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/zh-CHS/image-13.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/zh-CHS/s-14.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/zh-CHS/image-14.png b/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/zh-CHS/s-15.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/zh-CHS/image-14.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/zh-CHS/s-15.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/zh-CHS/image-15.png b/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/zh-CHS/s-16.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/zh-CHS/image-15.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/zh-CHS/s-16.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/zh-CHS/image-16.png b/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/zh-CHS/s-17.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/zh-CHS/image-16.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/zh-CHS/s-17.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/zh-CHS/image-1.png b/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/zh-CHS/s-2.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/zh-CHS/image-1.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/zh-CHS/s-2.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/zh-CHS/image-2.png b/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/zh-CHS/s-3.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/zh-CHS/image-2.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/zh-CHS/s-3.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/zh-CHS/image-3.png b/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/zh-CHS/s-4.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/zh-CHS/image-3.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/zh-CHS/s-4.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/zh-CHS/image-4.png b/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/zh-CHS/s-5.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/zh-CHS/image-4.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/zh-CHS/s-5.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/zh-CHS/image-5.png b/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/zh-CHS/s-6.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/zh-CHS/image-5.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/zh-CHS/s-6.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/zh-CHS/image-6.png b/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/zh-CHS/s-7.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/zh-CHS/image-6.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/zh-CHS/s-7.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/zh-CHS/image-7.png b/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/zh-CHS/s-8.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/zh-CHS/image-7.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/zh-CHS/s-8.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/zh-CHS/image-8.png b/pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/zh-CHS/s-9.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/zh-CHS/image-8.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DDASearch/zh-CHS/s-9.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-PASEF/en/index.html b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-PASEF/en/index.html
index da3791e124..73470e8117 100644
--- a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-PASEF/en/index.html
+++ b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-PASEF/en/index.html
@@ -29,7 +29,7 @@ <h1 class="document-title">Analysis of diaPASEF data in Skyline</h1>
         generate peptide query parameters to analyze the DIA data.
     </p>
     <p>
-        <img src="image-0.png" />
+        <img src="s-pasef-label-free-proteome-quantification.png" />
     </p>
     <p>
         [figure adapted from Navarro, P. et al. A multicenter study benchmarks software tools for label-free proteome quantification. <i>Nature
@@ -130,7 +130,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         The <b>Import Peptide Search</b> wizard should appear looking like this:
     </p>
     <p>
-        <img src="image-1.png" />
+        <img src="s-1.png" />
     </p>
     <ul>
         <li>Click the <b>Add Files</b> button.</li>
@@ -143,7 +143,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         The <b>Spectral Library</b> page of the wizard should now look like this:
     </p>
     <p>
-        <img src="image-2.png" />
+        <img src="s-2.png" />
     </p>
     <p>
         Note: 0.95 is the threshold applied to the PeptideProphet probability computed for every peptide spectrum match in the DDA database search – in
@@ -159,7 +159,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         asking how many of these peptides to use for adjusting RTs for other peptides:
     </p>
     <p>
-        <img src="image-3.png" />
+        <img src="s-3.png" />
     </p>
     <ul>
         <li>In the <b>Peptide count</b> box, enter “15”.</li>
@@ -169,13 +169,13 @@ <h1>Using the Import Peptide Search wizard</h1>
         Skyline will then present a summary form like the one below:
     </p>
     <p>
-        <img src="image-4.png" />
+        <img src="s-4.png" />
     </p>
     <ul>
         <li>Click the <b>Success</b> link (highlighted in blue) to see the linear regression.</li>
     </ul>
     <p>
-        <img src="image-5.png" />
+        <img src="s-5.png" />
     </p>
     <ul>
         <li>Click the <b>Close</b> button.</li>
@@ -207,7 +207,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         The <b>Browse for Results Files</b> should look like this:
     </p>
     <p>
-        <img src="image-6.png" />
+        <img src="s-6.png" />
     </p>
     <ul>
         <li>Click the <b>Open</b> button.</li>
@@ -216,7 +216,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         The <b>Import Peptide Search</b> form should look like this:
     </p>
     <p>
-        <img src="image-7.png" />
+        <img src="s-7.png" />
     </p>
     <ul>
         <li>Click the <b>Next</b> button.</li>
@@ -249,7 +249,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         The <b>Import Peptide Search</b> form should look like:
     </p>
     <p>
-        <img src="image-8.png" /> 
+        <img src="s-8.png" /> 
     </p>
     <ul>
         <li>Click the <b>Next</b> button.</li>
@@ -291,7 +291,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         The <b>Edit Isolation Scheme</b> form should now look like this:
     </p>
     <p>
-        <img src="image-9.png" />
+        <img src="s-9.png" />
     </p>
     <p>
         Skyline has worked out the <b>Start</b> and <b>End</b> <i>m/z</i> values for the DIA isolation ranges measured on the
@@ -307,7 +307,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         You will see a form like the one below:
     </p>
     <p>
-        <img src="image-10.png" />
+        <img src="s-10.png" />
     </p>
     <p>
         You can click-and-drag a rectangle to zoom in or use the mouse scroll-wheel. There is no red for <b>Show gaps</b> or yellow for
@@ -321,7 +321,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         The <b>Import Peptide Search</b> wizard should now look like this:
     </p>
     <p>
-        <img src="image-11.png" />
+        <img src="s-11.png" />
     </p>
     <ul>
         <li>Click the <b>Next</b> button.</li>
@@ -350,7 +350,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         The <b>Import Peptide Search</b> wizard should now look like this:
     </p>
     <p>
-        <img src="image-12.png" />
+        <img src="s-12.png" />
     </p>
     <ul>
         <li>Click the <b>Finish</b> button.</li>
@@ -360,7 +360,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         provided that looks like this:
     </p>
     <p>
-        <img src="image-13.png" />
+        <img src="s-13.png" />
     </p>
     <p>
         Notice that with a <b>Min peptides per protein</b> filter of “1” the 12 proteins found in the FASTA file produce 10 “Mapped”
@@ -380,7 +380,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         Skyline begins extracting chromatograms which should look like this on a standard i7 4-core processor:
     </p>
     <p>
-        <img src="image-14.png" />
+        <img src="s-14.png" />
     </p>
     <p>
         With 6-cores and above all files will be processed in parallel, and on most laptops with 2-cores the import will process 2 files at a time.
@@ -390,7 +390,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         page of the <b>Import Peptide Search</b> wizard. It should look like this:
     </p>
     <p>
-        <img src="image-15.png" />
+        <img src="s-15.png" />
     </p>
     <p>
         It has already been used to re-score the 10 best peaks Skyline found in each set of chromatograms, using its default score, and re-choose the
@@ -418,7 +418,7 @@ <h1>Sample Annotation</h1>
         The <b>Define Annotation</b> window should like this:
     </p>
     <p>
-        <img src="image-16.png" />
+        <img src="s-16.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button. </li>
@@ -453,7 +453,7 @@ <h1>Sample Annotation</h1>
         navigate:
     </p>
     <p>
-        <img src="image-17.png" />
+        <img src="s-17.png" />
     </p>
     <ul>
         <li>Close the <b>Document Grid: Replicates</b> window by clicking on the red X in the upper right hand corner of the form. </li>
@@ -503,10 +503,10 @@ <h1>Inspect the data manually</h1>
     <table class="comp-fig">
         <tr>
             <td class="comp-fig" style="padding: 10px;">
-              <img src="image-18.png" />
+              <img src="s-18.png" />
             </td>
             <td class="comp-fig" style="padding: 10px;">
-              <img src="image-19.png" /> 
+              <img src="s-19.png" /> 
             </td>
         </tr>
     </table>
@@ -515,7 +515,7 @@ <h1>Inspect the data manually</h1>
             easily viewable, as below: </li>
     </ul>
     <p>
-        <img src="image-20.png" />
+        <img src="s-20.png" />
     </p>
     <ul>
         <li>Click on the first E. coli protein: “sp|P63284|CLPB_ECOLI”.</li>
@@ -536,7 +536,7 @@ <h1>Inspect the data manually</h1>
         You get specific information for this peptide in all of the views, as shown below:
     </p>
     <p>
-        <img src="image-21.png" />
+        <img src="s-21.png" />
     </p>
     <p>
         Examine the peak area patterns for the rest of the peptides belonging to this protein. Is the quantitative pattern for the peptides from this
@@ -561,7 +561,7 @@ <h1>Inspect the data manually</h1>
         Notice that if you hover the cursor over a chromatogram curve a circle appears on the curve with the same color as the curve.
     </p>
     <p>
-        <img src="image-22.png" />
+        <img src="s-22.png" />
     </p>
     <ul>
         <li>Click the circle on a chromatogram point.</li>
@@ -571,7 +571,7 @@ <h1>Inspect the data manually</h1>
         on the ion that you selected.
     </p>
     <p>
-        <img src="image-23.png" />
+        <img src="s-23.png" />
     </p>
     <ul>
         <li>Click the black spectrum button in the <b>Full-Scan</b> toolbar to view the mobility dimension.</li>
@@ -580,13 +580,13 @@ <h1>Inspect the data manually</h1>
         Skyline will show the zoomed MS/MS spectrum with the mobility dimension on the y-axis:
     </p>
     <p>
-        <img src="image-24.png" />
+        <img src="s-24.png" />
     </p>
     <ul>
         <li>Click the magnifying glass button in the <b>Full-Scan</b> toolbar to view the full spectrum.</li>
     </ul>
     <p>
-        <img src="image-25.png" />
+        <img src="s-25.png" />
     </p>
     <p>
         Explore the data further manually (including some decoys).
@@ -606,7 +606,7 @@ <h1>Mass error and retention time deviation </h1>
         may want to widen your extraction windows. 
     </p>
     <p>
-        <img src="image-26.png" />
+        <img src="s-26.png" />
     </p>
     <p>
         Note that the distribution appears to have two peaks, one around 3 and one around 6. To understand this better, it helps to know that these are
@@ -639,7 +639,7 @@ <h1>Mass error and retention time deviation </h1>
                 Run</b>. </li>
     </ul>
     <p>
-        <img src="image-27.png" />
+        <img src="s-27.png" />
     </p>
     <ul>
         <li>Right-click the graph, choose <b>Plot</b>, and click <b>Residuals</b>.</li>
@@ -649,7 +649,7 @@ <h1>Mass error and retention time deviation </h1>
         optimized for this analysis? Check the decoys as well.
     </p>
     <p>
-        <img src="image-28.png" />
+        <img src="s-28.png" />
     </p>
     <p>
         <b>Note</b>: As the spectral library for this analysis was constructed from a side-by-side analysis of the same samples. As such, the
@@ -685,7 +685,7 @@ <h1>Quantitative comparison </h1>
         The <b>Edit Group Comparison</b> form should look like this.
     </p>
     <p>
-        <img src="image-29.png" />
+        <img src="s-29.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -711,13 +711,13 @@ <h1>Quantitative comparison </h1>
         (human 1:1, yeast 1:2, E. coli 4:1). Consider the adjusted p values and what you might expect of them.
     </p>
     <p>
-        <img src="image-30.png" />
+        <img src="s-30.png" />
     </p>
     <ul>
         <li>Click the <b>Volcano Plot</b> button in the top left corner of the grid window.</li>
     </ul>
     <p>
-        <img src="image-31.png" />
+        <img src="s-31.png" />
     </p>
     <p>
         You can already see clusters of points around the expected ratios and above the 5% FDR horizontal line for most of the changing peptides. To
@@ -733,7 +733,7 @@ <h1>Quantitative comparison </h1>
         The form should show you the list of peptides with matching protein names like this:
     </p>
     <p>
-        <img src="image-32.png" />
+        <img src="s-32.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -746,7 +746,7 @@ <h1>Quantitative comparison </h1>
         Which should leave the <b>Volcano Plot Formatting</b> form looking like this:
     </p>
     <p>
-        <img src="image-33.png" />
+        <img src="s-33.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -755,7 +755,7 @@ <h1>Quantitative comparison </h1>
         Which should leave the volcano plot looking like this:
     </p>
     <p>
-        <img src="image-34.png" />
+        <img src="s-34.png" />
     </p>
     <p>
         Notice that there are still some gray dots. You can click on any of the dots to cause them to be selected in the <b>Targets</b> view
@@ -794,7 +794,7 @@ <h1>Quantitative comparison </h1>
         The graph should now look like this:
     </p>
     <p>
-        <img src="image-35.png" />
+        <img src="s-35.png" />
     </p>
     <p>
         As with the volcano plot, you can click on the individual bars to select them in the <b>Targets</b> view (so that you can confirm
@@ -821,7 +821,7 @@ <h1>Quantitative comparison </h1>
         The <b>Bar Graph</b> should now show fold-change estimates for all 10 proteins that looks like this:
     </p>
     <p>
-        <img src="image-36.png" />
+        <img src="s-36.png" />
     </p>
     <ul>
         <li>Close the <b>Edit Group Comparison</b> by clicking the X square in the upper-right corner.</li>
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-PASEF/en/image-1.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-PASEF/en/s-1.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-PASEF/en/image-1.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA-PASEF/en/s-1.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-PASEF/en/image-10.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-PASEF/en/s-10.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-PASEF/en/image-10.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA-PASEF/en/s-10.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-PASEF/en/image-11.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-PASEF/en/s-11.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-PASEF/en/image-11.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA-PASEF/en/s-11.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-PASEF/en/image-12.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-PASEF/en/s-12.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-PASEF/en/image-12.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA-PASEF/en/s-12.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-PASEF/en/image-13.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-PASEF/en/s-13.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-PASEF/en/image-13.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA-PASEF/en/s-13.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-PASEF/en/image-14.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-PASEF/en/s-14.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-PASEF/en/image-14.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA-PASEF/en/s-14.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-PASEF/en/image-15.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-PASEF/en/s-15.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-PASEF/en/image-15.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-PASEF/en/image-16.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-PASEF/en/s-16.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-PASEF/en/image-16.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-PASEF/en/image-17.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-PASEF/en/s-17.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-PASEF/en/image-17.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-PASEF/en/image-18.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-PASEF/en/s-18.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-PASEF/en/image-18.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-PASEF/en/image-19.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-PASEF/en/s-19.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-PASEF/en/image-19.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-PASEF/en/image-2.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-PASEF/en/s-2.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-PASEF/en/image-2.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-PASEF/en/image-20.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-PASEF/en/s-20.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-PASEF/en/image-20.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-PASEF/en/image-21.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-PASEF/en/s-21.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-PASEF/en/image-21.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-PASEF/en/image-22.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-PASEF/en/s-22.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-PASEF/en/image-22.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-PASEF/en/image-23.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-PASEF/en/s-23.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-PASEF/en/image-23.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-PASEF/en/image-24.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-PASEF/en/s-24.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-PASEF/en/image-24.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-PASEF/en/image-25.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-PASEF/en/s-25.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-PASEF/en/image-25.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-PASEF/en/image-26.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-PASEF/en/s-26.png
similarity index 100%
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-PASEF/en/image-28.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-PASEF/en/s-28.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-PASEF/en/image-29.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-PASEF/en/s-29.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-PASEF/en/image-3.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-PASEF/en/s-3.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-PASEF/en/image-30.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-PASEF/en/s-30.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-PASEF/en/image-31.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-PASEF/en/s-31.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-PASEF/en/image-32.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-PASEF/en/s-32.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-PASEF/en/image-36.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-PASEF/en/s-36.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-PASEF/en/image-4.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-PASEF/en/s-4.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-PASEF/en/image-5.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-PASEF/en/s-5.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-PASEF/en/image-6.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-PASEF/en/s-6.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-PASEF/en/image-7.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-PASEF/en/s-7.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-PASEF/en/image-8.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-PASEF/en/s-8.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-PASEF/en/image-9.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-PASEF/en/s-9.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-PASEF/en/image-0.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-PASEF/en/s-pasef-label-free-proteome-quantification.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-PASEF/en/image-0.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/en/index.html b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/en/index.html
index 2262a7a642..040686fe01 100644
--- a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/en/index.html
+++ b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/en/index.html
@@ -29,7 +29,7 @@ <h1 class="document-title">Analysis of DIA/SWATH data in Skyline</h1>
         generate peptide query parameters to analyze the DIA data.
     </p>
     <p>
-        <img src="image-0.png" />
+        <img src="s-qe-label-free-proteome-quantification.png" />
     </p>
     <p class="fig-text">
         [figure adapted from Navarro, P. et al. A multicenter study benchmarks software tools for label-free proteome quantification. <i>Nature
@@ -126,7 +126,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         The <b>Import Peptide Search</b> wizard should appear looking like this:
     </p>
     <p>
-        <img src="image-1.png" />
+        <img src="s-1.png" />
     </p>
     <ul>
         <li>Click the <b>Add Files</b> button.</li>
@@ -139,7 +139,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         The <b>Spectral Library</b> page of the wizard should now look like this:
     </p>
     <p>
-        <img src="image-2.png" />
+        <img src="s-2.png" />
     </p>
     <p>
         Note: 0.95 is the threshold applied to the PeptideProphet probability computed for every peptide spectrum match in the DDA database search – in
@@ -155,13 +155,13 @@ <h1>Using the Import Peptide Search wizard</h1>
         into these samples. This should succeed and present a summary form like the one below:
     </p>
     <p>
-         <img src="image-3.png" />
+         <img src="s-3.png" />
     </p>
     <ul>
         <li>Click the <b>Success</b> link (highlighted in blue) to see the linear regression.</li>
     </ul>
     <p>
-        <img src="image-4.png" />
+        <img src="s-4.png" />
     </p>
     <ul>
         <li>Click the <b>Close</b> button.</li>
@@ -193,7 +193,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         The <b>Browse for Results Files</b> should look like this:
     </p>
     <p>
-        <img src="image-5.png" />
+        <img src="s-5.png" />
     </p>
     <ul>
         <li>Click the <b>Open</b> button.</li>
@@ -202,7 +202,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         The <b>Import Peptide Search</b> form should look like this:
     </p>
     <p>
-        <img src="image-6.png" />
+        <img src="s-6.png" />
     </p>
     <ul>
         <li>Click the <b>Next</b> button.</li>
@@ -241,7 +241,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         The <b>Import Peptide Search</b> form should look like:
     </p>
     <p>
-        <img src="image-7.png" /> 
+        <img src="s-7.png" /> 
     </p>
     <ul>
         <li>Click the <b>Next</b> button.</li>
@@ -285,7 +285,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         The <b>Edit Isolation Scheme</b> form should now look like this:
     </p>
     <p>
-        <img src="image-8.png" />
+        <img src="s-8.png" />
     </p>
     <p>
         Skyline has worked out the <b>Start</b> and <b>End</b> <i>m/z</i> values for the DIA isolation ranges measured on the
@@ -310,7 +310,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         You will see a form like the one below:
     </p>
     <p>
-        <img src="image-9.png" />
+        <img src="s-9.png" />
     </p>
     <p>
         You can click-and-drag a rectangle to zoom in or use the mouse scroll-wheel, and see the margins. If you uncheck and re-check <b>Show
@@ -326,7 +326,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         The <b>Import Peptide Search</b> wizard should now look like this:
     </p>
     <p>
-        <img src="image-10.png" />
+        <img src="s-10.png" />
     </p>
     <ul>
         <li>Click the <b>Next</b> button.</li>
@@ -355,7 +355,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         The <b>Import Peptide Search</b> wizard should now look like this:
     </p>
     <p>
-        <img src="image-11.png" />
+        <img src="s-11.png" />
     </p>
     <ul>
         <li>Click the <b>Finish</b> button.</li>
@@ -365,7 +365,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         provided that looks like this:
     </p>
     <p>
-        <img src="image-12.png" />
+        <img src="s-12.png" />
     </p>
     <p>
         Notice that with a <b>Min peptides per protein</b> filter of “1” the 12 proteins found in the FASTA file produce 11 “Mapped”
@@ -385,7 +385,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         Skyline begins extracting chromatograms which should look like this on a standard i7 4-core processor:
     </p>
     <p>
-        <img src="image-13.png" />
+        <img src="s-13.png" />
     </p>
     <p>
         With 6-cores and above all files will be processed in parallel, and on most laptops with 2-cores the import will process 2 files at a time.
@@ -395,7 +395,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         page of the <b>Import Peptide Search</b> wizard. It should look like this:
     </p>
     <p>
-        <img src="image-14.png" />
+        <img src="s-14.png" />
     </p>
     <p>
         It has already been used to re-score the 10 best peaks Skyline found in each set of chromatograms, using its default score, and re-choose the
@@ -423,7 +423,7 @@ <h1>Sample Annotation</h1>
         The <b>Define Annotation</b> window should like this:
     </p>
     <p>
-        <img src="image-15.png" />
+        <img src="s-15.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button. </li>
@@ -458,7 +458,7 @@ <h1>Sample Annotation</h1>
         navigate:
     </p>
     <p>
-        <img src="image-16.png" />
+        <img src="s-16.png" />
     </p>
     <ul>
         <li>Close the <b>Document Grid: Replicates</b> window by clicking on the red X in the upper right hand corner of the form. </li>
@@ -508,10 +508,10 @@ <h1>Inspect the data manually</h1>
     <table class="comp-fig">
         <tr>
             <td class="comp-fig" style="padding: 10px;">
-              <img src="image-17.png" />
+              <img src="s-17.png" />
             </td>
             <td class="comp-fig" style="padding: 10px;">
-              <img src="image-18.png" /> 
+              <img src="s-18.png" /> 
             </td>
         </tr>
     </table>
@@ -521,7 +521,7 @@ <h1>Inspect the data manually</h1>
             easily viewable, as below: </li>
     </ul>
     <p>
-        <img src="image-19.png" />
+        <img src="s-19.png" />
     </p>
     <ul>
         <li>Click on the first E. coli protein: “sp|P63284|CLPB_ECOLI”.</li>
@@ -542,7 +542,7 @@ <h1>Inspect the data manually</h1>
         You get specific information for this peptide in all of the views, as shown below:
     </p>
     <p>
-        <img src="image-20.png" />
+        <img src="s-20.png" />
     </p>
     <p>
         Examine the peak area patterns for the rest of the peptides belonging to this protein. Is the quantitative pattern for the peptides from this
@@ -567,7 +567,7 @@ <h1>Inspect the data manually</h1>
         Notice that if you hover the cursor over a chromatogram curve a circle appears on the curve with the same color as the curve.
     </p>
     <p>
-        <img src="image-21.png" />
+        <img src="s-21.png" />
     </p>
     <ul>
         <li>Click the circle on a chromatogram point.</li>
@@ -577,13 +577,13 @@ <h1>Inspect the data manually</h1>
         you selected.
     </p>
     <p>
-        <img src="image-22.png" />
+        <img src="s-22.png" />
     </p>
     <ul>
         <li>Click the magnifying glass button in the <b>Full-Scan</b> toolbar to view the full spectrum.</li>
     </ul>
     <p>
-        <img src="image-23.png" />
+        <img src="s-23.png" />
     </p>
     <p>
         Explore the data further manually (including some decoys).
@@ -602,7 +602,7 @@ <h1>Mass error and retention time deviation </h1>
         may want to widen your extraction windows. 
     </p>
     <p>
-        <img src="image-24.png" />
+        <img src="s-24.png" />
     </p>
     <p>
         Note that this distribution covers all 6 runs. To understand better how representative it is of each individual run do the following:
@@ -634,7 +634,7 @@ <h1>Mass error and retention time deviation </h1>
                 Run</b>. </li>
     </ul>
     <p>
-        <img src="image-25.png" />
+        <img src="s-25.png" />
     </p>
     <ul>
         <li>Right-click the graph, choose <b>Plot</b>, and click <b>Residuals</b>.</li>
@@ -644,7 +644,7 @@ <h1>Mass error and retention time deviation </h1>
         optimized for this analysis? Check the decoys as well.
     </p>
     <p>
-        <img src="image-26.png" />
+        <img src="s-26.png" />
     </p>
     <p>
         <b>Note</b>: As the spectral library for this analysis was constructed from a side-by-side analysis of the same samples. As such, the
@@ -680,7 +680,7 @@ <h1>Quantitative comparison </h1>
         The <b>Edit Group Comparison</b> form should look like this.
     </p>
     <p>
-        <img src="image-27.png" />
+        <img src="s-27.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -706,13 +706,13 @@ <h1>Quantitative comparison </h1>
         (human 1:1, yeast 1:2, E. coli 4:1). Consider the adjusted p values and what you might expect of them.
     </p>
     <p>
-        <img src="image-28.png" />
+        <img src="s-28.png" />
     </p>
     <ul>
         <li>Click the <b>Volcano Plot</b> button in the top left corner of the grid window.</li>
     </ul>
     <p>
-        <img src="image-29.png" />
+        <img src="s-29.png" />
     </p>
     <p>
         You can already see clusters of points around the expected ratios and above the 5% FDR horizontal line for most of the changing peptides. To
@@ -728,7 +728,7 @@ <h1>Quantitative comparison </h1>
         The form should show you the list of peptides with matching protein names like this:
     </p>
     <p>
-        <img src="image-30.png" />
+        <img src="s-30.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -741,7 +741,7 @@ <h1>Quantitative comparison </h1>
         Which should leave the <b>Volcano Plot Formatting</b> form looking like this:
     </p>
     <p>
-        <img src="image-31.png" />
+        <img src="s-31.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -750,7 +750,7 @@ <h1>Quantitative comparison </h1>
         Which should leave the volcano plot looking like this:
     </p>
     <p>
-        <img src="image-32.png" />
+        <img src="s-32.png" />
     </p>
     <p>
         Notice that there are still some gray dots. You can click on any of the dots to cause them to be selected in the <b>Targets</b> view
@@ -789,7 +789,7 @@ <h1>Quantitative comparison </h1>
         The graph should now look like this:
     </p>
     <p>
-        <img src="image-33.png" />
+        <img src="s-33.png" />
     </p>
     <p>
         As with the volcano plot, you can click on the individual bars to select them in the <b>Targets</b> view (so that you can confirm
@@ -816,7 +816,7 @@ <h1>Quantitative comparison </h1>
         The <b>Bar Graph</b> should now show fold-change estimates for all 11 proteins that looks like this:
     </p>
     <p>
-        <img src="image-34.png" />
+        <img src="s-34.png" />
     </p>
     <ul>
         <li>Close the <b>Edit Group Comparison</b> by clicking the X square in the upper-right corner.</li>
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/en/image-1.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/en/s-1.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/en/image-1.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/en/s-1.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/en/image-10.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/en/s-10.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/en/image-10.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/en/s-10.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/en/image-11.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/en/s-11.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/en/image-11.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/en/s-11.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/en/image-12.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/en/s-12.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/en/image-12.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/en/s-12.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/en/image-13.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/en/s-13.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/en/image-13.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/en/s-13.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/en/image-14.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/en/s-14.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/en/image-14.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/en/s-14.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/en/image-15.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/en/s-15.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/en/image-15.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/en/s-15.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/en/image-16.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/en/s-16.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/en/image-16.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/en/image-17.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/en/s-17.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/en/image-8.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/en/s-8.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/en/image-9.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/en/s-9.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/en/image-9.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/en/image-0.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/en/s-qe-label-free-proteome-quantification.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/en/image-0.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/en/s-qe-label-free-proteome-quantification.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/ja/index.html b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/ja/index.html
index 0f38dafcc2..5f6e91f942 100644
--- a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/ja/index.html
+++ b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/ja/index.html
@@ -24,7 +24,7 @@ <h1 class="document-title">SkylineでのDIA/SWATHデータ分析</h1>
         最初に、データ非依存性測定（DIA）のデータを解析するため、Skylineのパラメータを設定し、次に、生データファイルから定量化情報を抽出します。また、データ依存性解析（DDA）の結果をインポートしてスペクトルライブラリを作成し、DIAのデータを解析するための設定を行います。
     </p>
     <p>
-        <img src="image-0.png" />
+        <img src="s-qe-label-free-proteome-quantification.png" />
     </p>
     <p class="fig-text">
         ［図の出典： Navarro, P. et al. A multicenter study benchmarks software tools for label-free proteome quantification.<i>Nature Biotech</i> 34,
@@ -112,7 +112,7 @@ <h1>ペプチド検索のインポートウィザードの使用</h1>
         すると、<b>ペプチド検索のインポート</b>ウィザードが表示されます。
     </p>
     <p>
-        <img src="image-1.png" />
+        <img src="s-1.png" />
     </p>
     <p>
         注：0.95は、DDAデータベース検索において、すべてのペプチド・スペクトル・マッチ（PSM）に対してPeptideProphetで設定した確率の閾値です。このチュートリアルで用いるデータセットでは、偽陽性率（false discovery rate,
@@ -129,7 +129,7 @@ <h1>ペプチド検索のインポートウィザードの使用</h1>
         ウィザードの [ <b>スペクトルライブラリ</b> ] ページは以下のようになります。
     </p>
     <p>
-        <img src="image-2.png" />
+        <img src="s-2.png" />
     </p>
     <ul>
         <li>[ <b>次へ</b> ] ボタンをクリックします。</li>
@@ -139,13 +139,13 @@ <h1>ペプチド検索のインポートウィザードの使用</h1>
         iRT標準ペプチドに基づいて、ペプチド検索結果のiRT値が校正されます。校正が成功すると、以下のようなライブラリ構築の要約が表示されます。
     </p>
     <p>
-         <img src="image-3.png" />
+         <img src="s-3.png" />
     </p>
     <ul class="keep-next">
         <li><b>成功</b> (青でハイライト) をクリックすると線形回帰の結果が表示されます。</li>
     </ul>
     <p>
-        <img src="image-4.png" />
+        <img src="s-4.png" />
     </p>
     <ul>
         <li>[ <b>閉じる</b> ] ボタンをクリックします。</li>
@@ -175,7 +175,7 @@ <h1>ペプチド検索のインポートウィザードの使用</h1>
         [ <b>結果ファイルを参照</b> ] ページは以下のようになります。
     </p>
     <p>
-        <img src="image-5.png" />
+        <img src="s-5.png" />
     </p>
     <ul>
         <li>[ <b>開く</b> ] ボタンをクリックします。</li>
@@ -184,7 +184,7 @@ <h1>ペプチド検索のインポートウィザードの使用</h1>
         <b>ペプチド検索のインポート</b>フォームは以下のようになります。
     </p>
     <p>
-        <img src="image-6.png" />
+        <img src="s-6.png" />
     </p>
     <ul>
         <li>[ <b>次へ</b> ] ボタンをクリックします。</li>
@@ -221,7 +221,7 @@ <h1>ペプチド検索のインポートウィザードの使用</h1>
         [ <b>ペプチド検索のインポート</b> ] フォームは以下のようになります。
     </p>
     <p>
-        <img src="image-7.png" /> 
+        <img src="s-7.png" /> 
     </p>
     <ul>
         <li>[ <b>次へ</b> ] ボタンをクリックします。</li>
@@ -261,7 +261,7 @@ <h1>ペプチド検索のインポートウィザードの使用</h1>
         [ <b>単離スキームを編集</b> ] フォームは以下のようになります。
     </p>
     <p>
-        <img src="image-8.png" />
+        <img src="s-8.png" />
     </p>
     <p>
         Skylineは、質量分析計で測定されたDIA単離範囲の [ <b>開始</b> ] および [ <b>終了</b> ]
@@ -284,7 +284,7 @@ <h1>ペプチド検索のインポートウィザードの使用</h1>
         以下のようなフォームが表示されます。
     </p>
     <p>
-        <img src="image-9.png" />
+        <img src="s-9.png" />
     </p>
     <p>
         クリック・アンド・ドラッグして囲んだ長方形を使い部分拡大するか、マウスのスクロールホイールを使用して拡大すると、マージンの位置の詳細を見ることができます。[ <b>マージンを表示</b> ] チェックボックスをオフにし、再びオンにすると、グラフのタイトルが
@@ -299,7 +299,7 @@ <h1>ペプチド検索のインポートウィザードの使用</h1>
         <b>ペプチド検索のインポート</b>ウィザードは以下のようになります。
     </p>
     <p>
-        <img src="image-10.png" />
+        <img src="s-10.png" />
     </p>
     <ul>
         <li>[ <b>次へ</b> ] ボタンをクリックします。</li>
@@ -326,7 +326,7 @@ <h1>ペプチド検索のインポートウィザードの使用</h1>
         <b>ペプチド検索のインポート</b>ウィザードは以下のようになります。
     </p>
     <p>
-        <img src="image-11.png" />
+        <img src="s-11.png" />
     </p>
     <ul>
         <li>[ <b>完了</b> ] ボタンをクリックします。</li>
@@ -335,7 +335,7 @@ <h1>ペプチド検索のインポートウィザードの使用</h1>
         設定条件と使用したFASTAシークエンステキストを基に計算されたターゲットを記述したフォームが、以下のように表示されます。
     </p>
     <p>
-        <img src="image-12.png" />
+        <img src="s-12.png" />
     </p>
     <p>
         [<b>タンパク質毎の最小ペプチド数</b> ]
@@ -349,7 +349,7 @@ <h1>ペプチド検索のインポートウィザードの使用</h1>
         Skylineはクロマトグラムの抽出を開始します。標準のi7 4コアプロセッサでは以下のようになります。
     </p>
     <p>
-        <img src="image-13.png" />
+        <img src="s-13.png" />
     </p>
     <p>
         6コア以上ではすべてのファイルが並列処理され、2コアのほとんどのラップトップでは、インポートは2ファイルずつ処理されます。
@@ -359,7 +359,7 @@ <h1>ペプチド検索のインポートウィザードの使用</h1>
         ページで選択したmProhetモデルを表示します。これは以下のようになります。
     </p>
     <p>
-        <img src="image-14.png" />
+        <img src="s-14.png" />
     </p>
     <p>
         mProphetモデルでは、それぞれのクロマトグラムセットの中から、Skylineがデフォルトとして使用するスコアに基づき選んだ10個のベストピークを見直し、最も高いmProphetスコアを与える10個のピークを選びます。これらのピークのmProphetスコア（Skylineでは<b>Detection
@@ -386,7 +386,7 @@ <h1>試料の注釈</h1>
         [ <b>注釈を定義</b> ] ウィンドウは以下のようになります。
     </p>
     <p>
-        <img src="image-15.png" />
+        <img src="s-15.png" />
     </p>
     <ul>
         <li>[ <b>OK</b> ] ボタンをクリックします。 </li>
@@ -418,7 +418,7 @@ <h1>試料の注釈</h1>
         キーボードのEnter、矢印キーを使って移動し、A、B、1、2、3キーを使って以下のスクリーンショットで示すように試料に注釈を付けます。
     </p>
     <p>
-        <img src="image-16.png" />
+        <img src="s-16.png" />
     </p>
     <ul>
         <li>フォームの右上隅にある赤いXをクリックして [ <b>ドキュメントグリッド: 繰り返し測定</b> ] ウィンドウを閉じます。 </li>
@@ -463,10 +463,10 @@ <h1>データのマニュアル検証</h1>
     <table class="comp-fig">
         <tr>
             <td class="comp-fig" style="padding: 10px;">
-              <img src="image-17.png" />
+              <img src="s-17.png" />
             </td>
             <td class="comp-fig" style="padding: 10px;">
-              <img src="image-18.png" /> 
+              <img src="s-18.png" /> 
             </td>
         </tr>
     </table>
@@ -474,7 +474,7 @@ <h1>データのマニュアル検証</h1>
         <li>同様に、[ <b>ピーク領域: 繰り返し測定比較</b> ] ウィンドウと [ <b>ライブラリの一致</b> ] ウィンドウをドッキングし、以下のようにすべての情報が見やすくなるようにします。 </li>
     </ul>
     <p>
-        <img src="image-19.png" />
+        <img src="s-19.png" />
     </p>
     <ul>
         <li>最初のE. coliタンパク質である「sp|P63284|CLPB_ECOLI」をクリックします。</li>
@@ -493,7 +493,7 @@ <h1>データのマニュアル検証</h1>
         下に示すように、すべての表示でこのペプチドに関する情報が表示されます。
     </p>
     <p>
-        <img src="image-20.png" />
+        <img src="s-20.png" />
     </p>
     <p>
         このタンパク質に属する残りのペプチドのピーク領域パターンを調べて下さい。このタンパク質のペプチドの定量パターンは、予想される差異発現パターン（4:1）と一致していますか？
@@ -516,7 +516,7 @@ <h1>データのマニュアル検証</h1>
         クロマトグラム曲線上にカーソルを合わせると、曲線上に曲線と同じ色の丸が表示されます。
     </p>
     <p>
-        <img src="image-21.png" />
+        <img src="s-21.png" />
     </p>
     <ul>
         <li>クロマトグラムポイントにある丸をクリックします。</li>
@@ -525,13 +525,13 @@ <h1>データのマニュアル検証</h1>
         Skylineは選択したクロマトグラムポイントが抽出されたスペクトルを、選択したイオンを拡大して [ <b>フルスキャン</b> ] 表示を開きます。
     </p>
     <p>
-        <img src="image-22.png" />
+        <img src="s-22.png" />
     </p>
     <ul class="keep-next">
         <li>[ <b>フルスキャン</b> ] ツールバーの虫眼鏡ボタンをクリックしてフルスペクトルを表示します。</li>
     </ul>
     <p>
-        <img src="image-23.png" />
+        <img src="s-23.png" />
     </p>
     <p>
         手作業でさらにデータを調べます（デコイを含む）。
@@ -547,7 +547,7 @@ <h1>質量誤差と保持時間偏差 </h1>
         この操作によってデータセットの質量誤差分布が表示されます。抽出ウィンドウ（±20 ppm）はさらに最適化できるでしょうか？一般的には、平均値 ± 3の標準偏差で十分です。ただし、両端の数字が高く、ヒストグラムが途切れているような場合は、抽出ウィンドウを広げた方がいいかもしれません。
     </p>
     <p>
-        <img src="image-24.png" />
+        <img src="s-24.png" />
     </p>
     <p>
         この分布図は6回のランすべてを網羅していることにご注意ください。この分布図が各ランをどの程度よく表しているかを理解するには、以下の操作を行います。
@@ -575,7 +575,7 @@ <h1>質量誤差と保持時間偏差 </h1>
         </li>
     </ul>
     <p>
-        <img src="image-25.png" />
+        <img src="s-25.png" />
     </p>
     <ul>
         <li>グラフを右クリックし、[ <b>プロット</b> ] を選択して [ <b>残余</b> ] をクリックします。</li>
@@ -584,7 +584,7 @@ <h1>質量誤差と保持時間偏差 </h1>
         これにより、このデータセットでの予測保持時間からのずれが表示されます。この分析に対し、抽出ウィンドウ（±5分）はさらに最適化できるでしょうか？デコイも確認してみましょう。
     </p>
     <p>
-        <img src="image-26.png" />
+        <img src="s-26.png" />
     </p>
     <p>
         <b>注：</b>このチュートリアルのスペクトルライブラリは同じ試料を同時に測定した結果を用いて構築しました。そのため、保持時間予測の精度は非常に高くなっています。異なる装置、異なる時間、あるいは試料が異なる場合は、構築したスペクトルライブラリの保持時間の誤差はもっと大きくなると考えられます。
@@ -612,7 +612,7 @@ <h1>定量比較 </h1>
         [ <b>グループ比較を編集</b> ] フォームは以下のようになります。
     </p>
     <p>
-        <img src="image-27.png" />
+        <img src="s-27.png" />
     </p>
     <ul>
         <li>[ <b>OK</b> ] ボタンをクリックします。</li>
@@ -635,13 +635,13 @@ <h1>定量比較 </h1>
         どの生物種からのものか、またその予想比率（ヒト1:1、酵母1:2、E. coli 4:1）を念頭に、表内の複数のペプチドについて推定されている倍率変化を調べます。調整されたP値を調べ、予想される結果について考えてみましょう。
     </p>
     <p>
-        <img src="image-28.png" />
+        <img src="s-28.png" />
     </p>
     <ul class="keep-next">
         <li>グリッドウィンドウの左上隅にある [ <b>ボルケーノプロット</b> ] ボタンをクリックします。</li>
     </ul>
     <p>
-        <img src="image-29.png" />
+        <img src="s-29.png" />
     </p>
     <p>
         表示されたボルケーノプロットでは、変化している点の多くが、予想される倍率変化の周辺に集まっており、また、5% FDRを示す水平線の上にあることがわかります。どの点がどの生物種に属するのかを明確にするため次の操作を行って下さい。
@@ -656,7 +656,7 @@ <h1>定量比較 </h1>
         フォームには、以下のように一致するタンパク質名とともにペプチドの一覧が表示されます。
     </p>
     <p>
-        <img src="image-30.png" />
+        <img src="s-30.png" />
     </p>
     <ul>
         <li>[ <b>OK</b> ] ボタンをクリックします。</li>
@@ -669,7 +669,7 @@ <h1>定量比較 </h1>
         これで [ <b>ボルケーノプロット形式</b> ] フォームは以下のようになります。
     </p>
     <p>
-        <img src="image-31.png" />
+        <img src="s-31.png" />
     </p>
     <ul>
         <li>[ <b>OK</b> ] ボタンをクリックします。</li>
@@ -678,7 +678,7 @@ <h1>定量比較 </h1>
         これでボルケーノプロットは以下のようになります。
     </p>
     <p>
-        <img src="image-32.png" />
+        <img src="s-32.png" />
     </p>
     <p>
         まだグレーのドットがいくつか残っていることに注意してください。これらのドットのどれかをクリックすると、 [ <b>ターゲット</b> ]
@@ -711,7 +711,7 @@ <h1>定量比較 </h1>
         グラフは以下のように表示されます。
     </p>
     <p>
-        <img src="image-33.png" />
+        <img src="s-33.png" />
     </p>
     <p>
         ボルケーノプロット同様、個々の棒をクリックすると [ <b>ターゲット</b> ] 表示で選択されます（グラフ内のさまざまなペプチドがどの生物種からのものかを確認できます）。
@@ -733,7 +733,7 @@ <h1>定量比較 </h1>
         これで<b>棒グラフ</b>は11のタンパク質すべての倍率変化推定値を、以下のように表示するようになります。
     </p>
     <p>
-        <img src="image-34.png" />
+        <img src="s-34.png" />
     </p>
     <ul>
         <li>右上隅にあるXをクリックして [ <b>グループ比較を編集</b> ] を閉じます。</li>
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/ja/invariant.html b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/ja/invariant.html
index ab65da57c5..48ec085ec5 100644
--- a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/ja/invariant.html
+++ b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/ja/invariant.html
@@ -27,7 +27,7 @@ <h1 class="document-title">Analysis of DIA/SWATH data in Skyline</h1>
         generate peptide query parameters to analyze the DIA data.
     </p>
     <p>
-        <img src="image-0.png" />
+        <img src="s-qe-label-free-proteome-quantification.png" />
     </p>
     <p class="fig-text">
         [figure adapted from Navarro, P. et al. A multicenter study benchmarks software tools for label-free proteome quantification. <i>Nature
@@ -124,7 +124,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         The <b>Import Peptide Search</b> wizard should appear looking like this:
     </p>
     <p>
-        <img src="image-1.png" />
+        <img src="s-1.png" />
     </p>
     <p>
         Note: 0.95 is the threshold applied to the PeptideProphet probability computed for every peptide spectrum match in the DDA database search – in
@@ -142,7 +142,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         The <b>Spectral Library</b> page of the wizard should now look like this:
     </p>
     <p>
-        <img src="image-2.png" />
+        <img src="s-2.png" />
     </p>
     <ul>
         <li>Click the <b>Next</b> button.</li>
@@ -153,13 +153,13 @@ <h1>Using the Import Peptide Search wizard</h1>
         into these samples. This should succeed and present a summary form like the one below:
     </p>
     <p>
-         <img src="image-3.png" />
+         <img src="s-3.png" />
     </p>
     <ul>
         <li>Click the <b>Success</b> link (highlighted in blue) to see the linear regression.</li>
     </ul>
     <p>
-        <img src="image-4.png" />
+        <img src="s-4.png" />
     </p>
     <ul>
         <li>Click the <b>Close</b> button.</li>
@@ -191,7 +191,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         The <b>Browse for Results Files</b> should look like this:
     </p>
     <p>
-        <img src="image-5.png" />
+        <img src="s-5.png" />
     </p>
     <ul>
         <li>Click the <b>Open</b> button.</li>
@@ -200,7 +200,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         The <b>Import Peptide Search</b> form should look like this:
     </p>
     <p>
-        <img src="image-6.png" />
+        <img src="s-6.png" />
     </p>
     <ul>
         <li>Click the <b>Next</b> button.</li>
@@ -239,7 +239,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         The <b>Import Peptide Search</b> form should look like:
     </p>
     <p>
-        <img src="image-7.png" /> 
+        <img src="s-7.png" /> 
     </p>
     <ul>
         <li>Click the <b>Next</b> button.</li>
@@ -283,7 +283,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         The <b>Edit Isolation Scheme</b> form should now look like this:
     </p>
     <p>
-        <img src="image-8.png" />
+        <img src="s-8.png" />
     </p>
     <p>
         Skyline has worked out the <b>Start</b> and <b>End</b> <i>m/z</i> values for the DIA isolation ranges measured on the
@@ -308,7 +308,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         You will see a form like the one below:
     </p>
     <p>
-        <img src="image-9.png" />
+        <img src="s-9.png" />
     </p>
     <p>
         You can click-and-drag a rectangle to zoom in or use the mouse scroll-wheel, and see the margins. If you uncheck and re-check <b>Show
@@ -324,7 +324,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         The <b>Import Peptide Search</b> wizard should now look like this:
     </p>
     <p>
-        <img src="image-10.png" />
+        <img src="s-10.png" />
     </p>
     <ul>
         <li>Click the <b>Next</b> button.</li>
@@ -353,7 +353,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         The <b>Import Peptide Search</b> wizard should now look like this:
     </p>
     <p>
-        <img src="image-11.png" />
+        <img src="s-11.png" />
     </p>
     <ul>
         <li>Click the <b>Finish</b> button.</li>
@@ -363,7 +363,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         provided that looks like this:
     </p>
     <p>
-        <img src="image-12.png" />
+        <img src="s-12.png" />
     </p>
     <p>
         Notice that with a <b>Min peptides per protein</b> filter of “1” the 13 proteins found in the FASTA file produce 12
@@ -378,7 +378,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         Skyline begins extracting chromatograms which should look like this on a standard i7 4-core processor:
     </p>
     <p>
-        <img src="image-13.png" />
+        <img src="s-13.png" />
     </p>
     <p>
         With 6-cores and above all files will be processed in parallel, and on most laptops with 2-cores the import will process 2 files at a time.
@@ -388,7 +388,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         page of the <b>Import Peptide Search</b> wizard. It should look like this:
     </p>
     <p>
-        <img src="image-14.png" />
+        <img src="s-14.png" />
     </p>
     <p>
         It has already been used to re-score the 10 best peaks Skyline found in each set of chromatograms, using its default score, and re-choose the
@@ -416,7 +416,7 @@ <h1>Sample Annotation</h1>
         The <b>Define Annotation</b> window should like this:
     </p>
     <p>
-        <img src="image-15.png" />
+        <img src="s-15.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button. </li>
@@ -451,7 +451,7 @@ <h1>Sample Annotation</h1>
         navigate:
     </p>
     <p>
-        <img src="image-16.png" />
+        <img src="s-16.png" />
     </p>
     <ul>
         <li>Close the <b>Document Grid: Replicates</b> window by clicking on the red X in the upper right hand corner of the form. </li>
@@ -501,10 +501,10 @@ <h1>Inspect the data manually</h1>
     <table class="comp-fig">
         <tr>
             <td class="comp-fig" style="padding: 10px;">
-              <img src="image-17.png" />
+              <img src="s-17.png" />
             </td>
             <td class="comp-fig" style="padding: 10px;">
-              <img src="image-18.png" /> 
+              <img src="s-18.png" /> 
             </td>
         </tr>
     </table>
@@ -513,7 +513,7 @@ <h1>Inspect the data manually</h1>
             easily viewable, as below: </li>
     </ul>
     <p>
-        <img src="image-19.png" />
+        <img src="s-19.png" />
     </p>
     <ul>
         <li>Click on the first E. coli protein: “sp|P63284|CLPB_ECOLI”.</li>
@@ -534,7 +534,7 @@ <h1>Inspect the data manually</h1>
         You get specific information for this peptide in all of the views, as shown below:
     </p>
     <p>
-        <img src="image-20.png" />
+        <img src="s-20.png" />
     </p>
     <p>
         Examine the peak area patterns for the rest of the peptides belonging to this protein. Is the quantitative pattern for the peptides from this
@@ -559,7 +559,7 @@ <h1>Inspect the data manually</h1>
         Notice that if you hover the cursor over a chromatogram curve a circle appears on the curve with the same color as the curve.
     </p>
     <p>
-        <img src="image-21.png" />
+        <img src="s-21.png" />
     </p>
     <ul>
         <li>Click the circle on a chromatogram point.</li>
@@ -569,13 +569,13 @@ <h1>Inspect the data manually</h1>
         you selected.
     </p>
     <p>
-        <img src="image-22.png" />
+        <img src="s-22.png" />
     </p>
     <ul>
         <li>Click the magnifying glass button in the <b>Full-Scan</b> toolbar to view the full spectrum.</li>
     </ul>
     <p>
-        <img src="image-23.png" />
+        <img src="s-23.png" />
     </p>
     <p>
         Explore the data further manually (including some decoys).
@@ -594,7 +594,7 @@ <h1>Mass error and retention time deviation </h1>
         may want to widen your extraction windows. 
     </p>
     <p>
-        <img src="image-24.png" />
+        <img src="s-24.png" />
     </p>
     <p>
         Note that this distribution covers all 6 runs. To understand better how representative it is of each individual run do the following:
@@ -626,7 +626,7 @@ <h1>Mass error and retention time deviation </h1>
                 Run</b>. </li>
     </ul>
     <p>
-        <img src="image-25.png" />
+        <img src="s-25.png" />
     </p>
     <ul>
         <li>Right-click the graph, choose <b>Plot</b>, and click <b>Residuals</b>.</li>
@@ -636,7 +636,7 @@ <h1>Mass error and retention time deviation </h1>
         optimized for this analysis? Check the decoys as well.
     </p>
     <p>
-        <img src="image-26.png" />
+        <img src="s-26.png" />
     </p>
     <p>
         <b>Note</b>: As the spectral library for this analysis was constructed from a side-by-side analysis of the same samples. As such, the
@@ -672,7 +672,7 @@ <h1>Quantitative comparison </h1>
         The <b>Edit Group Comparison</b> form should look like this.
     </p>
     <p>
-        <img src="image-27.png" />
+        <img src="s-27.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -698,13 +698,13 @@ <h1>Quantitative comparison </h1>
         (human 1:1, yeast 1:2, E. coli 4:1). Consider the adjusted p values and what you might expect of them.
     </p>
     <p>
-        <img src="image-28.png" />
+        <img src="s-28.png" />
     </p>
     <ul>
         <li>Click the <b>Volcano Plot</b> button in the top left corner of the grid window.</li>
     </ul>
     <p>
-        <img src="image-29.png" />
+        <img src="s-29.png" />
     </p>
     <p>
         You can already see clusters of points around the expected ratios and above the 5% FDR horizontal line for most of the changing peptides. To
@@ -720,7 +720,7 @@ <h1>Quantitative comparison </h1>
         The form should show you the list of peptides with matching protein names like this:
     </p>
     <p>
-        <img src="image-30.png" />
+        <img src="s-30.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -733,7 +733,7 @@ <h1>Quantitative comparison </h1>
         Which should leave the <b>Volcano Plot Formatting</b> form looking like this:
     </p>
     <p>
-        <img src="image-31.png" />
+        <img src="s-31.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -742,7 +742,7 @@ <h1>Quantitative comparison </h1>
         Which should leave the volcano plot looking like this:
     </p>
     <p>
-        <img src="image-32.png" />
+        <img src="s-32.png" />
     </p>
     <p>
         Notice that there are still some gray dots. You can click on any of the dots to cause them to be selected in the <b>Targets</b> view
@@ -781,7 +781,7 @@ <h1>Quantitative comparison </h1>
         The graph should now look like this:
     </p>
     <p>
-        <img src="image-33.png" />
+        <img src="s-33.png" />
     </p>
     <p>
         As with the volcano plot, you can click on the individual bars to select them in the <b>Targets</b> view (so that you can confirm
@@ -808,7 +808,7 @@ <h1>Quantitative comparison </h1>
         The <b>Bar Graph</b> should now show fold-change estimates for all 11 proteins that looks like this:
     </p>
     <p>
-        <img src="image-34.png" />
+        <img src="s-34.png" />
     </p>
     <ul>
         <li>Close the <b>Edit Group Comparison</b> by clicking the X square in the upper-right corner.</li>
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/ja/image-1.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/ja/s-1.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/ja/image-1.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/ja/s-1.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/ja/image-10.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/ja/s-10.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/ja/image-10.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/ja/s-10.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/ja/image-11.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/ja/s-11.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/ja/image-11.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/ja/s-11.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/ja/image-12.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/ja/s-12.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/ja/image-12.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/ja/s-12.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/ja/image-13.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/ja/s-13.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/ja/image-13.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/ja/s-13.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/ja/image-14.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/ja/s-14.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/ja/image-14.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/ja/s-14.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/ja/image-15.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/ja/s-15.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/ja/image-15.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/ja/s-15.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/ja/image-16.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/ja/s-16.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/ja/image-16.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/ja/s-16.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/ja/image-17.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/ja/s-17.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/ja/image-17.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/ja/s-17.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/ja/image-18.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/ja/s-18.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/ja/image-18.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/ja/s-18.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/ja/image-19.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/ja/s-19.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/ja/image-2.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/ja/s-2.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/ja/image-20.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/ja/s-20.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/ja/image-21.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/ja/s-21.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/ja/image-22.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/ja/s-22.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/ja/image-23.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/ja/s-23.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/ja/image-24.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/ja/s-24.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/ja/image-25.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/ja/s-25.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/ja/image-26.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/ja/s-26.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/ja/image-27.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/ja/s-27.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/ja/image-28.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/ja/s-28.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/ja/image-29.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/ja/s-29.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/ja/image-3.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/ja/s-3.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/ja/image-30.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/ja/s-30.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/ja/image-31.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/ja/s-31.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/ja/image-32.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/ja/s-32.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/ja/image-33.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/ja/s-33.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/ja/image-34.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/ja/s-34.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/ja/image-4.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/ja/s-4.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/ja/image-5.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/ja/s-5.png
similarity index 100%
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/ja/image-6.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/ja/s-6.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/ja/image-7.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/ja/s-7.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/ja/image-8.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/ja/s-8.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/ja/image-9.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/ja/s-9.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/ja/image-9.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/ja/s-9.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/ja/image-0.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/ja/s-qe-label-free-proteome-quantification.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/ja/image-0.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/ja/s-qe-label-free-proteome-quantification.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/zh-CHS/index.html b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/zh-CHS/index.html
index 551f85e7dd..3dd6623766 100644
--- a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/zh-CHS/index.html
+++ b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/zh-CHS/index.html
@@ -22,7 +22,7 @@ <h1 class="document-title">Skyline 中的 DIA/SWATH 数据分析</h1>
         为了处理DIA数据集，您首先要在Skyline中设置所有相关参数；然后，您需要从原始数据文件提取定量的信息；最后，您要通过导入DDA数据的搜索结果创建一个质谱图库，从而产生肽段的查询参数。
     </p>
     <p>
-        <img src="image-0.png" />
+        <img src="s-qe-label-free-proteome-quantification.png" />
     </p>
     <p class="fig-text">
         [图片取自 Navarro, P. et al. A multicenter study benchmarks software tools for label-free proteome quantification. <i>Nature Biotech</i> 34,
@@ -112,7 +112,7 @@ <h1>使用“导入肽段搜索”向导</h1>
         <b>导入肽段搜索</b>向导应显示如下：
     </p>
     <p>
-        <img src="image-1.png" />
+        <img src="s-1.png" />
     </p>
     <p>
         注意：0.95 是DDA 数据库搜索中每个肽段谱图匹配度计算的 PeptideProphet 概率阈值 - 在这个特定的数据集中，这相当于 0.2% 的 PSM 错误发现率，但此值在不同数据集中会有所不同，因此应在此处输入您要使用的错误发现率的概率阈值。
@@ -128,7 +128,7 @@ <h1>使用“导入肽段搜索”向导</h1>
         向导中的<b>谱图库</b>页面现在应显示如下：
     </p>
     <p>
-        <img src="image-2.png" />
+        <img src="s-2.png" />
     </p>
     <ul>
         <li>单击<b>下一步</b>按钮。</li>
@@ -137,13 +137,13 @@ <h1>使用“导入肽段搜索”向导</h1>
         Skyline开始创建谱图库，并在<b>构建肽段搜索库</b>表单中显示进度。创建的谱图库将通过加入样品中的Biognosys iRT 标准肽段搜索结果校准 iRT 值。操作成功后，呈现如下所示的表单：
     </p>
     <p>
-         <img src="image-3.png" />
+         <img src="s-3.png" />
     </p>
     <ul>
         <li>单击<b>成功</b>链接（突出显示蓝色）查看线性回归。</li>
     </ul>
     <p>
-        <img src="image-4.png" />
+        <img src="s-4.png" />
     </p>
     <ul>
         <li>单击<b>关闭</b>按钮。</li>
@@ -173,7 +173,7 @@ <h1>使用“导入肽段搜索”向导</h1>
         <b>浏览结果文件</b>应显示如下：
     </p>
     <p>
-        <img src="image-5.png" />
+        <img src="s-5.png" />
     </p>
     <ul>
         <li>单击<b>打开</b>按钮。</li>
@@ -182,7 +182,7 @@ <h1>使用“导入肽段搜索”向导</h1>
         <b>导入肽段搜索</b>表单应显示如下：
     </p>
     <p>
-        <img src="image-6.png" />
+        <img src="s-6.png" />
     </p>
     <ul>
         <li>单击<b>下一步</b>按钮。</li>
@@ -218,7 +218,7 @@ <h1>使用“导入肽段搜索”向导</h1>
         <b>导入肽段搜索</b>表单应显示如下：
     </p>
     <p>
-        <img src="image-7.png" /> 
+        <img src="s-7.png" /> 
     </p>
     <ul>
         <li>单击<b>下一步</b>按钮。</li>
@@ -258,7 +258,7 @@ <h1>使用“导入肽段搜索”向导</h1>
         此时<b>编辑分离方案</b>表单应显示如下：
     </p>
     <p>
-        <img src="image-8.png" />
+        <img src="s-8.png" />
     </p>
     <p>
         Skyline 已解出在质谱仪上测得的 DIA 分离范围的<b>开始</b>和<b>结束</b>质荷比值。可以看出它们重叠了 2 质荷比，为补偿重叠，Skyline 在分离窗口的每侧增加了 1
@@ -280,7 +280,7 @@ <h1>使用“导入肽段搜索”向导</h1>
         随即显示下面这样的表单：
     </p>
     <p>
-        <img src="image-9.png" />
+        <img src="s-9.png" />
     </p>
     <p>
         您可以单击并拖动矩形进行放大，或是使用鼠标滚轮查看边距。如果取消选中<b>显示边距</b>后又重新选中，图形名称将在<b>测量窗口</b>和<b>提取窗口</b>之间切换，并且粉红色的边距条消失后又会重新出现。图中没有红色的<b>显示间距</b>或黄色的<b>显示单循环重叠</b>，二者均为
@@ -294,7 +294,7 @@ <h1>使用“导入肽段搜索”向导</h1>
         <b>导入肽段搜索</b>向导现在显示如下：
     </p>
     <p>
-        <img src="image-10.png" />
+        <img src="s-10.png" />
     </p>
     <ul>
         <li>单击<b>下一步</b>按钮。</li>
@@ -321,7 +321,7 @@ <h1>使用“导入肽段搜索”向导</h1>
         <b>导入肽段搜索</b>向导现在显示如下：
     </p>
     <p>
-        <img src="image-11.png" />
+        <img src="s-11.png" />
     </p>
     <ul>
         <li>单击<b>完成</b>按钮。</li>
@@ -330,7 +330,7 @@ <h1>使用“导入肽段搜索”向导</h1>
         此时应当显示一张表单，其中描述了根据您的设置和所提供的 FASTA 序列文本计算得出的目标，如下所示：
     </p>
     <p>
-        <img src="image-12.png" />
+        <img src="s-12.png" />
     </p>
     <p>
         可以发现，<b>每个蛋白质的最少肽段数</b>过滤器设置为 "1" 时，FASTA 文件中的 13 个蛋白质产生的<b>剩余</b>蛋白质为 12 个。这是因为有 1
@@ -343,7 +343,7 @@ <h1>使用“导入肽段搜索”向导</h1>
         Skyline 开始提取色谱图，在标准的 i7 4 核处理器上显示如下：
     </p>
     <p>
-        <img src="image-13.png" />
+        <img src="s-13.png" />
     </p>
     <p>
         在 6 核及以上的处理器中，所有文件将并行处理；在大多数配备双核处理器的笔记本电脑上，导入过程中一次处理 2 个文件。
@@ -352,7 +352,7 @@ <h1>使用“导入肽段搜索”向导</h1>
         导入完成后，Skyline 将显示您在<b>导入肽段搜索</b>向导中的<b>导入 FASTA</b> 页面上请求的 mProphet 模型。其显示如下：
     </p>
     <p>
-        <img src="image-14.png" />
+        <img src="s-14.png" />
     </p>
     <p>
         系统采用默认的分数对 Skyline 在每组色谱图中找到的 10 个最优峰重新评分，并将这些峰重新选择为 mProphet 得分最高的峰。这些 mProphet 分数（在 Skyline 中叫做<b>检测 Z 得分</b>）进行扩展后，以使 1.0 表示与平均
@@ -377,7 +377,7 @@ <h1>样品注释</h1>
         <b>定义注释</b>窗口应如下所示：
     </p>
     <p>
-        <img src="image-15.png" />
+        <img src="s-15.png" />
     </p>
     <ul>
         <li>单击<b>确定</b>按钮。 </li>
@@ -409,7 +409,7 @@ <h1>样品注释</h1>
         如下面的截屏中所示，使用键盘上的 A，B，1、2、3、Enter 和方向键对样品进行注释：
     </p>
     <p>
-        <img src="image-16.png" />
+        <img src="s-16.png" />
     </p>
     <ul>
         <li>单击表单右上角的红 X，即可关闭<b>文档网格：重复测定</b>窗口。 </li>
@@ -454,10 +454,10 @@ <h1>手动检查数据</h1>
     <table class="comp-fig">
         <tr>
             <td class="comp-fig" style="padding: 10px;">
-              <img src="image-17.png" />
+              <img src="s-17.png" />
             </td>
             <td class="comp-fig" style="padding: 10px;">
-              <img src="image-18.png" /> 
+              <img src="s-18.png" /> 
             </td>
         </tr>
     </table>
@@ -465,7 +465,7 @@ <h1>手动检查数据</h1>
         <li>以同样的方式停靠<b>峰面积：重复测定比较</b>和<b>库匹配</b>窗口，以便轻松查看所有信息，如下所示： </li>
     </ul>
     <p>
-        <img src="image-19.png" />
+        <img src="s-19.png" />
     </p>
     <ul>
         <li>单击第一个大肠杆菌蛋白质："sp|P63284|CLPB_ECOLI"。</li>
@@ -483,7 +483,7 @@ <h1>手动检查数据</h1>
         您将在所有这些视图中获得该肽段的特定信息，如下所示：
     </p>
     <p>
-        <img src="image-20.png" />
+        <img src="s-20.png" />
     </p>
     <p>
         检查属于该蛋白质的其余肽段的峰面积模式。蛋白质肽段的定量模式是否与预期的差异化调控模式 (4:1) 一致？
@@ -505,7 +505,7 @@ <h1>手动检查数据</h1>
         请注意，如果将光标悬停在色谱图曲线上，曲线上就会出现与该曲线同色的圆圈。
     </p>
     <p>
-        <img src="image-21.png" />
+        <img src="s-21.png" />
     </p>
     <ul>
         <li>单击色谱图点上的圆圈。</li>
@@ -514,13 +514,13 @@ <h1>手动检查数据</h1>
         Skyline 将在从中提取该色谱图点的谱图上打开<b>全扫描</b>视图，并放大您选择的离子。
     </p>
     <p>
-        <img src="image-22.png" />
+        <img src="s-22.png" />
     </p>
     <ul>
         <li>单击<b>全扫描</b>工具栏中的放大镜按钮可以查看整个谱图。</li>
     </ul>
     <p>
-        <img src="image-23.png" />
+        <img src="s-23.png" />
     </p>
     <p>
         进一步手动探索数据（包括一些诱饵）。
@@ -536,7 +536,7 @@ <h1>质量误差和保留时间偏差 </h1>
         这将显示质量误差在数据集中的分布。提取窗口 (±20 ppm) 能否进一步优化？一般情况下，平均误差 +/- 3 个标准偏差便足以应对。但是，如果显示的直方图被截止，并且在极端情况下计数很高，则可能需要增宽提取窗口。 
     </p>
     <p>
-        <img src="image-24.png" />
+        <img src="s-24.png" />
     </p>
     <p>
         请注意，此分布涵盖全部 6 次运行。为进一步理解每次运行的代表性，请执行以下操作：
@@ -563,7 +563,7 @@ <h1>质量误差和保留时间偏差 </h1>
         <li>在<b>视图</b>菜单中选择<b>保留时间</b>，然后单击<b>回归</b>，最后单击<b>运行分数</b>。 </li>
     </ul>
     <p>
-        <img src="image-25.png" />
+        <img src="s-25.png" />
     </p>
     <ul>
         <li>右键单击此图，选择<b>绘图</b>，然后单击<b>残差</b>。</li>
@@ -572,7 +572,7 @@ <h1>质量误差和保留时间偏差 </h1>
         随即显示该数据集中与预计保留时间的偏差。能否针对此分析进一步优化提取窗口（±5 分钟）？这时请进一步检查诱饵。
     </p>
     <p>
-        <img src="image-26.png" />
+        <img src="s-26.png" />
     </p>
     <p>
         <b>注意：</b>因为这项分析的谱图库是通过对相同样品进行并排分析构建而成，所以保留时间预测的准确性非常好。在对不同仪器不同时间不同样品分析创建的外部谱图库中，保留时间将导致这些预测中的误差较大。
@@ -602,7 +602,7 @@ <h1>定量比较 </h1>
         <b>编辑群组比较</b>表单应如下显示。
     </p>
     <p>
-        <img src="image-27.png" />
+        <img src="s-27.png" />
     </p>
     <ul>
         <li>单击<b>确定</b>按钮。</li>
@@ -624,13 +624,13 @@ <h1>定量比较 </h1>
         检查表中某些肽段的倍数变化估计值，同时要记住它们来自哪个物种以及预期的比率（人类蛋白质 1:1，酵母 1:2，大肠杆菌 4:1）。考虑已调整的 p 值以及您可能期望的值。
     </p>
     <p>
-        <img src="image-28.png" />
+        <img src="s-28.png" />
     </p>
     <ul>
         <li>单击网格窗口左上角的<b>火山图</b>按钮。</li>
     </ul>
     <p>
-        <img src="image-29.png" />
+        <img src="s-29.png" />
     </p>
     <p>
         对于大多数变化的肽段，已可以看到出现在预期比率附近和 5％ FDR 水平线以上的点簇。为了更好地了解哪些点属于哪种生物体，请执行以下操作：
@@ -645,7 +645,7 @@ <h1>定量比较 </h1>
         表单应显示具有匹配蛋白质名称的肽段列表，如下所示：
     </p>
     <p>
-        <img src="image-30.png" />
+        <img src="s-30.png" />
     </p>
     <ul>
         <li>单击<b>确定</b>按钮。</li>
@@ -658,7 +658,7 @@ <h1>定量比较 </h1>
         <b>火山图格式</b>表单应显示如下：
     </p>
     <p>
-        <img src="image-31.png" />
+        <img src="s-31.png" />
     </p>
     <ul>
         <li>单击<b>确定</b>按钮。</li>
@@ -667,7 +667,7 @@ <h1>定量比较 </h1>
         火山图应显示如下：
     </p>
     <p>
-        <img src="image-32.png" />
+        <img src="s-32.png" />
     </p>
     <p>
         请注意，图中仍有一些灰点。您可以单击其中任意的点，这样它们在<b>目标</b>视图中将处于选中状态，并且将在图中以红色显示测试。您也可以将鼠标光标悬停在任何点上以获取更多信息。通过这种方式，可以看到灰点属于 iRT
@@ -700,7 +700,7 @@ <h1>定量比较 </h1>
         该图现在应显示如下：
     </p>
     <p>
-        <img src="image-33.png" />
+        <img src="s-33.png" />
     </p>
     <p>
         与火山图一样，您可以单击<b>目标</b>视图中的单个条形以将其选定（这样便可确认图中的不同肽段来自哪个物种）。
@@ -723,7 +723,7 @@ <h1>定量比较 </h1>
         现在，<b>条状图</b>应显示所有 11 种蛋白质的倍数变化估算值，如下所示：
     </p>
     <p>
-        <img src="image-34.png" />
+        <img src="s-34.png" />
     </p>
     <ul>
         <li>单击右上角的 X 方格，关闭<b>编辑群组比较</b>。</li>
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/zh-CHS/invariant.html b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/zh-CHS/invariant.html
index eccdfb2f61..555195c302 100644
--- a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/zh-CHS/invariant.html
+++ b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/zh-CHS/invariant.html
@@ -27,7 +27,7 @@ <h1 class="document-title">Analysis of DIA/SWATH data in Skyline</h1>
         generate peptide query parameters to analyze the DIA data.
     </p>
     <p>
-        <img src="image-0.png" />
+        <img src="s-qe-label-free-proteome-quantification.png" />
     </p>
     <p class="fig-text">
         [figure adapted from Navarro, P. et al. A multicenter study benchmarks software tools for label-free proteome quantification. <i>Nature
@@ -124,7 +124,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         The <b>Import Peptide Search</b> wizard should appear looking like this:
     </p>
     <p>
-        <img src="image-1.png" />
+        <img src="s-1.png" />
     </p>
     <p>
         Note: 0.95 is the threshold applied to the PeptideProphet probability computed for every peptide spectrum match in the DDA database search – in
@@ -142,7 +142,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         The <b>Spectral Library</b> page of the wizard should now look like this:
     </p>
     <p>
-        <img src="image-2.png" />
+        <img src="s-2.png" />
     </p>
     <ul>
         <li>Click the <b>Next</b> button.</li>
@@ -153,13 +153,13 @@ <h1>Using the Import Peptide Search wizard</h1>
         into these samples. This should succeed and present a summary form like the one below:
     </p>
     <p>
-         <img src="image-3.png" />
+         <img src="s-3.png" />
     </p>
     <ul>
         <li>Click the <b>Success</b> link (highlighted in blue) to see the linear regression.</li>
     </ul>
     <p>
-        <img src="image-4.png" />
+        <img src="s-4.png" />
     </p>
     <ul>
         <li>Click the <b>Close</b> button.</li>
@@ -191,7 +191,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         The <b>Browse for Results Files</b> should look like this:
     </p>
     <p>
-        <img src="image-5.png" />
+        <img src="s-5.png" />
     </p>
     <ul>
         <li>Click the <b>Open</b> button.</li>
@@ -200,7 +200,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         The <b>Import Peptide Search</b> form should look like this:
     </p>
     <p>
-        <img src="image-6.png" />
+        <img src="s-6.png" />
     </p>
     <ul>
         <li>Click the <b>Next</b> button.</li>
@@ -239,7 +239,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         The <b>Import Peptide Search</b> form should look like:
     </p>
     <p>
-        <img src="image-7.png" /> 
+        <img src="s-7.png" /> 
     </p>
     <ul>
         <li>Click the <b>Next</b> button.</li>
@@ -283,7 +283,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         The <b>Edit Isolation Scheme</b> form should now look like this:
     </p>
     <p>
-        <img src="image-8.png" />
+        <img src="s-8.png" />
     </p>
     <p>
         Skyline has worked out the <b>Start</b> and <b>End</b> <i>m/z</i> values for the DIA isolation ranges measured on the
@@ -308,7 +308,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         You will see a form like the one below:
     </p>
     <p>
-        <img src="image-9.png" />
+        <img src="s-9.png" />
     </p>
     <p>
         You can click-and-drag a rectangle to zoom in or use the mouse scroll-wheel, and see the margins. If you uncheck and re-check <b>Show
@@ -324,7 +324,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         The <b>Import Peptide Search</b> wizard should now look like this:
     </p>
     <p>
-        <img src="image-10.png" />
+        <img src="s-10.png" />
     </p>
     <ul>
         <li>Click the <b>Next</b> button.</li>
@@ -353,7 +353,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         The <b>Import Peptide Search</b> wizard should now look like this:
     </p>
     <p>
-        <img src="image-11.png" />
+        <img src="s-11.png" />
     </p>
     <ul>
         <li>Click the <b>Finish</b> button.</li>
@@ -363,7 +363,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         provided that looks like this:
     </p>
     <p>
-        <img src="image-12.png" />
+        <img src="s-12.png" />
     </p>
     <p>
         Notice that with a <b>Min peptides per protein</b> filter of “1” the 13 proteins found in the FASTA file produce 12
@@ -378,7 +378,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         Skyline begins extracting chromatograms which should look like this on a standard i7 4-core processor:
     </p>
     <p>
-        <img src="image-13.png" />
+        <img src="s-13.png" />
     </p>
     <p>
         With 6-cores and above all files will be processed in parallel, and on most laptops with 2-cores the import will process 2 files at a time.
@@ -388,7 +388,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         page of the <b>Import Peptide Search</b> wizard. It should look like this:
     </p>
     <p>
-        <img src="image-14.png" />
+        <img src="s-14.png" />
     </p>
     <p>
         It has already been used to re-score the 10 best peaks Skyline found in each set of chromatograms, using its default score, and re-choose the
@@ -416,7 +416,7 @@ <h1>Sample Annotation</h1>
         The <b>Define Annotation</b> window should like this:
     </p>
     <p>
-        <img src="image-15.png" />
+        <img src="s-15.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button. </li>
@@ -451,7 +451,7 @@ <h1>Sample Annotation</h1>
         navigate:
     </p>
     <p>
-        <img src="image-16.png" />
+        <img src="s-16.png" />
     </p>
     <ul>
         <li>Close the <b>Document Grid: Replicates</b> window by clicking on the red X in the upper right hand corner of the form. </li>
@@ -501,10 +501,10 @@ <h1>Inspect the data manually</h1>
     <table class="comp-fig">
         <tr>
             <td class="comp-fig" style="padding: 10px;">
-              <img src="image-17.png" />
+              <img src="s-17.png" />
             </td>
             <td class="comp-fig" style="padding: 10px;">
-              <img src="image-18.png" /> 
+              <img src="s-18.png" /> 
             </td>
         </tr>
     </table>
@@ -513,7 +513,7 @@ <h1>Inspect the data manually</h1>
             easily viewable, as below: </li>
     </ul>
     <p>
-        <img src="image-19.png" />
+        <img src="s-19.png" />
     </p>
     <ul>
         <li>Click on the first E. coli protein: “sp|P63284|CLPB_ECOLI”.</li>
@@ -534,7 +534,7 @@ <h1>Inspect the data manually</h1>
         You get specific information for this peptide in all of the views, as shown below:
     </p>
     <p>
-        <img src="image-20.png" />
+        <img src="s-20.png" />
     </p>
     <p>
         Examine the peak area patterns for the rest of the peptides belonging to this protein. Is the quantitative pattern for the peptides from this
@@ -559,7 +559,7 @@ <h1>Inspect the data manually</h1>
         Notice that if you hover the cursor over a chromatogram curve a circle appears on the curve with the same color as the curve.
     </p>
     <p>
-        <img src="image-21.png" />
+        <img src="s-21.png" />
     </p>
     <ul>
         <li>Click the circle on a chromatogram point.</li>
@@ -569,13 +569,13 @@ <h1>Inspect the data manually</h1>
         you selected.
     </p>
     <p>
-        <img src="image-22.png" />
+        <img src="s-22.png" />
     </p>
     <ul>
         <li>Click the magnifying glass button in the <b>Full-Scan</b> toolbar to view the full spectrum.</li>
     </ul>
     <p>
-        <img src="image-23.png" />
+        <img src="s-23.png" />
     </p>
     <p>
         Explore the data further manually (including some decoys).
@@ -594,7 +594,7 @@ <h1>Mass error and retention time deviation </h1>
         may want to widen your extraction windows. 
     </p>
     <p>
-        <img src="image-24.png" />
+        <img src="s-24.png" />
     </p>
     <p>
         Note that this distribution covers all 6 runs. To understand better how representative it is of each individual run do the following:
@@ -626,7 +626,7 @@ <h1>Mass error and retention time deviation </h1>
                 Run</b>. </li>
     </ul>
     <p>
-        <img src="image-25.png" />
+        <img src="s-25.png" />
     </p>
     <ul>
         <li>Right-click the graph, choose <b>Plot</b>, and click <b>Residuals</b>.</li>
@@ -636,7 +636,7 @@ <h1>Mass error and retention time deviation </h1>
         optimized for this analysis? Check the decoys as well.
     </p>
     <p>
-        <img src="image-26.png" />
+        <img src="s-26.png" />
     </p>
     <p>
         <b>Note</b>: As the spectral library for this analysis was constructed from a side-by-side analysis of the same samples. As such, the
@@ -672,7 +672,7 @@ <h1>Quantitative comparison </h1>
         The <b>Edit Group Comparison</b> form should look like this.
     </p>
     <p>
-        <img src="image-27.png" />
+        <img src="s-27.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -698,13 +698,13 @@ <h1>Quantitative comparison </h1>
         (human 1:1, yeast 1:2, E. coli 4:1). Consider the adjusted p values and what you might expect of them.
     </p>
     <p>
-        <img src="image-28.png" />
+        <img src="s-28.png" />
     </p>
     <ul>
         <li>Click the <b>Volcano Plot</b> button in the top left corner of the grid window.</li>
     </ul>
     <p>
-        <img src="image-29.png" />
+        <img src="s-29.png" />
     </p>
     <p>
         You can already see clusters of points around the expected ratios and above the 5% FDR horizontal line for most of the changing peptides. To
@@ -720,7 +720,7 @@ <h1>Quantitative comparison </h1>
         The form should show you the list of peptides with matching protein names like this:
     </p>
     <p>
-        <img src="image-30.png" />
+        <img src="s-30.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -733,7 +733,7 @@ <h1>Quantitative comparison </h1>
         Which should leave the <b>Volcano Plot Formatting</b> form looking like this:
     </p>
     <p>
-        <img src="image-31.png" />
+        <img src="s-31.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -742,7 +742,7 @@ <h1>Quantitative comparison </h1>
         Which should leave the volcano plot looking like this:
     </p>
     <p>
-        <img src="image-32.png" />
+        <img src="s-32.png" />
     </p>
     <p>
         Notice that there are still some gray dots. You can click on any of the dots to cause them to be selected in the <b>Targets</b> view
@@ -781,7 +781,7 @@ <h1>Quantitative comparison </h1>
         The graph should now look like this:
     </p>
     <p>
-        <img src="image-33.png" />
+        <img src="s-33.png" />
     </p>
     <p>
         As with the volcano plot, you can click on the individual bars to select them in the <b>Targets</b> view (so that you can confirm
@@ -808,7 +808,7 @@ <h1>Quantitative comparison </h1>
         The <b>Bar Graph</b> should now show fold-change estimates for all 11 proteins that looks like this:
     </p>
     <p>
-        <img src="image-34.png" />
+        <img src="s-34.png" />
     </p>
     <ul>
         <li>Close the <b>Edit Group Comparison</b> by clicking the X square in the upper-right corner.</li>
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/zh-CHS/image-1.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/zh-CHS/s-1.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/zh-CHS/image-1.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/zh-CHS/s-1.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/zh-CHS/image-10.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/zh-CHS/s-10.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/zh-CHS/image-10.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/zh-CHS/s-10.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/zh-CHS/image-11.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/zh-CHS/s-11.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/zh-CHS/image-11.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/zh-CHS/s-11.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/zh-CHS/image-12.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/zh-CHS/s-12.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/zh-CHS/image-12.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/zh-CHS/s-12.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/zh-CHS/image-13.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/zh-CHS/s-13.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/zh-CHS/image-13.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/zh-CHS/s-13.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/zh-CHS/image-14.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/zh-CHS/s-14.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/zh-CHS/image-14.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/zh-CHS/s-14.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/zh-CHS/image-15.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/zh-CHS/s-15.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/zh-CHS/image-15.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/zh-CHS/s-15.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/zh-CHS/image-16.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/zh-CHS/s-16.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/zh-CHS/image-16.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/zh-CHS/s-16.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/zh-CHS/image-17.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/zh-CHS/s-17.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/zh-CHS/image-17.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/zh-CHS/s-17.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/zh-CHS/image-18.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/zh-CHS/s-18.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/zh-CHS/image-18.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/zh-CHS/s-18.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/zh-CHS/image-19.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/zh-CHS/s-19.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/zh-CHS/image-19.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/zh-CHS/s-19.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/zh-CHS/image-2.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/zh-CHS/s-2.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/zh-CHS/image-2.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/zh-CHS/s-2.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/zh-CHS/image-20.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/zh-CHS/s-20.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/zh-CHS/image-22.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/zh-CHS/s-22.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/zh-CHS/image-25.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/zh-CHS/s-25.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/zh-CHS/image-26.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/zh-CHS/s-26.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/zh-CHS/image-27.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/zh-CHS/s-27.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/zh-CHS/image-28.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/zh-CHS/s-28.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/zh-CHS/image-29.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/zh-CHS/s-29.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/zh-CHS/image-3.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/zh-CHS/s-3.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/zh-CHS/image-30.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/zh-CHS/s-30.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/zh-CHS/image-31.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/zh-CHS/s-31.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/zh-CHS/image-32.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/zh-CHS/s-32.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/zh-CHS/image-0.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/zh-CHS/s-qe-label-free-proteome-quantification.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-QE/zh-CHS/image-0.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/en/index.html b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/en/index.html
index 377476ac08..a8b43eb1ea 100644
--- a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/en/index.html
+++ b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/en/index.html
@@ -29,7 +29,7 @@ <h1 class="document-title">Analysis of DIA/SWATH data in Skyline</h1>
         generate peptide query parameters to analyze the DIA data.
     </p>
     <p>
-        <img src="image-0.png" />
+        <img src="s-ttof-label-free-proteome-quantification.png" />
     </p>
     <p class="fig-text">
         [figure adapted from Navarro, P. et al. A multicenter study benchmarks software tools for label-free proteome quantification. <i>Nature
@@ -124,7 +124,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         The <b>Import Peptide Search</b> wizard should appear looking like this:
     </p>
     <p>
-        <img src="image-1.png" />
+        <img src="s-1.png" />
     </p>
     <ul>
         <li>Click the <b>Add Files</b> button.</li>
@@ -137,7 +137,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         The <b>Spectral Library</b> page of the wizard should now look like this:
     </p>
     <p>
-        <img src="image-2.png" />
+        <img src="s-2.png" />
     </p>
     <p>
         Note: 0.95 is the threshold applied to the PeptideProphet probability computed for every peptide spectrum match in the DDA database search – in
@@ -153,13 +153,13 @@ <h1>Using the Import Peptide Search wizard</h1>
         into these samples. This should succeed and present a summary form like the one below:
     </p>
     <p>
-        <img src="image-3.png" />
+        <img src="s-3.png" />
     </p>
     <ul>
         <li>Click the <b>Success</b> link (highlighted in blue) to see the linear regression.</li>
     </ul>
     <p>
-        <img src="image-4.png" />
+        <img src="s-4.png" />
     </p>
     <ul>
         <li>Click the <b>Close</b> button.</li>
@@ -191,7 +191,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         The <b>Browse for Results Files</b> should look like this:
     </p>
     <p>
-        <img src="image-5.png" />
+        <img src="s-5.png" />
     </p>
     <ul>
         <li>Click the <b>Open</b> button.</li>
@@ -200,7 +200,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         The <b>Import Peptide Search</b> form should look like this:
     </p>
     <p>
-        <img src="image-6.png" />
+        <img src="s-6.png" />
     </p>
     <ul>
         <li>Click the <b>Next</b> button.</li>
@@ -239,7 +239,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         The <b>Import Peptide Search</b> form should look like:
     </p>
     <p>
-        <img src="image-7.png" /> 
+        <img src="s-7.png" /> 
     </p>
     <ul>
         <li>Click the <b>Next</b> button.</li>
@@ -283,7 +283,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         The <b>Edit Isolation Scheme</b> form should now look like this:
     </p>
     <p>
-        <img src="image-8.png" />
+        <img src="s-8.png" />
     </p>
     <p>
         Skyline has worked out the <b>Start</b> and <b>End</b> <i>m/z</i> values for the DIA isolation ranges measured on the
@@ -308,7 +308,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         You will see a form like the one below:
     </p>
     <p>
-        <img src="image-9.png" />
+        <img src="s-9.png" />
     </p>
     <p>
         You can click-and-drag a rectangle to zoom in or use the mouse scroll-wheel, and see the margins. If you uncheck and re-check <b>Show
@@ -324,7 +324,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         The <b>Import Peptide Search</b> wizard should now look like this:
     </p>
     <p>
-        <img src="image-10.png" />
+        <img src="s-10.png" />
     </p>
     <ul>
         <li>Click the <b>Next</b> button.</li>
@@ -353,7 +353,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         The <b>Import Peptide Search</b> wizard should now look like this:
     </p>
     <p>
-        <img src="image-11.png" />
+        <img src="s-11.png" />
     </p>
     <ul>
         <li>Click the <b>Finish</b> button.</li>
@@ -363,7 +363,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         provided that looks like this:
     </p>
     <p>
-        <img src="image-12.png" />
+        <img src="s-12.png" />
     </p>
     <p>
         Notice that with a <b>Min peptides per protein</b> filter of “1” the 12 proteins found in the FASTA file produce 11 “Mapped”
@@ -383,7 +383,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         Skyline begins extracting chromatograms which should look like this on a standard i7 4-core processor:
     </p>
     <p>
-        <img src="image-13.png" />
+        <img src="s-13.png" />
     </p>
     <p>
         With 6-cores and above all files will be processed in parallel, and on most laptops with 2-cores the import will process 2 files at a time.
@@ -393,7 +393,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         page of the <b>Import Peptide Search</b> wizard. It should look like this:
     </p>
     <p>
-        <img src="image-14.png" />
+        <img src="s-14.png" />
     </p>
     <p>
         It has already been used to re-score the 10 best peaks Skyline found in each set of chromatograms, using its default score, and re-choose the
@@ -421,7 +421,7 @@ <h1>Sample Annotation</h1>
         The <b>Define Annotation</b> window should like this:
     </p>
     <p>
-        <img src="image-15.png" />
+        <img src="s-15.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button. </li>
@@ -456,7 +456,7 @@ <h1>Sample Annotation</h1>
         navigate:
     </p>
     <p>
-        <img src="image-16.png" />
+        <img src="s-16.png" />
     </p>
     <ul>
         <li>Close the <b>Document Grid: Replicates</b> window by clicking on the red X in the upper right hand corner of the form. </li>
@@ -506,10 +506,10 @@ <h1>Inspect the data manually</h1>
     <table class="comp-fig">
         <tr>
             <td class="comp-fig" style="padding: 10px;">
-              <img src="image-17.png" />
+              <img src="s-17.png" />
             </td>
             <td class="comp-fig" style="padding: 10px;">
-              <img src="image-18.png" /> 
+              <img src="s-18.png" /> 
             </td>
         </tr>
     </table>
@@ -518,7 +518,7 @@ <h1>Inspect the data manually</h1>
             easily viewable, as below: </li>
     </ul>
     <p>
-        <img src="image-19.png" />
+        <img src="s-19.png" />
     </p>
     <ul>
         <li>Click on the first E. coli protein: “sp|P63284|CLPB_ECOLI”.</li>
@@ -539,7 +539,7 @@ <h1>Inspect the data manually</h1>
         You get specific information for this peptide in all of the views, as shown below:
     </p>
     <p>
-        <img src="image-20.png" />
+        <img src="s-20.png" />
     </p>
     <p>
         Examine the peak area patterns for the rest of the peptides belonging to this protein. Is the quantitative pattern for the peptides from this
@@ -564,7 +564,7 @@ <h1>Inspect the data manually</h1>
         Notice that if you hover the cursor over a chromatogram curve a circle appears on the curve with the same color as the curve.
     </p>
     <p>
-        <img src="image-21.png" />
+        <img src="s-21.png" />
     </p>
     <ul>
         <li>Click the circle on a chromatogram point.</li>
@@ -574,13 +574,13 @@ <h1>Inspect the data manually</h1>
         you selected.
     </p>
     <p>
-        <img src="image-22.png" />
+        <img src="s-22.png" />
     </p>
     <ul>
         <li>Click the magnifying glass button in the <b>Full-Scan</b> toolbar to view the full spectrum.</li>
     </ul>
     <p>
-        <img src="image-23.png" />
+        <img src="s-23.png" />
     </p>
     <p>
         Explore the data further manually (including some decoys).
@@ -599,7 +599,7 @@ <h1>Mass error and retention time deviation </h1>
         may want to widen your extraction windows. 
     </p>
     <p>
-        <img src="image-24.png" />
+        <img src="s-24.png" />
     </p>
     <p>
         Note that the distribution appears to have two peaks, one around 0 and one around 5. To understand this better, it helps to know that these are
@@ -632,7 +632,7 @@ <h1>Mass error and retention time deviation </h1>
                 Run</b>. </li>
     </ul>
     <p>
-        <img src="image-25.png" />
+        <img src="s-25.png" />
     </p>
     <ul>
         <li>Right-click the graph, choose <b>Plot</b>, and click <b>Residuals</b>.</li>
@@ -642,7 +642,7 @@ <h1>Mass error and retention time deviation </h1>
         optimized for this analysis? Check the decoys as well.
     </p>
     <p>
-        <img src="image-26.png" />
+        <img src="s-26.png" />
     </p>
     <p>
         <b>Note</b>: As the spectral library for this analysis was constructed from a side-by-side analysis of the same samples. As such, the
@@ -678,7 +678,7 @@ <h1>Quantitative comparison </h1>
         The <b>Edit Group Comparison</b> form should look like this.
     </p>
     <p>
-        <img src="image-27.png" />
+        <img src="s-27.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -704,13 +704,13 @@ <h1>Quantitative comparison </h1>
         (human 1:1, yeast 1:2, E. coli 4:1). Consider the adjusted p values and what you might expect of them.
     </p>
     <p>
-        <img src="image-28.png" />
+        <img src="s-28.png" />
     </p>
     <ul>
         <li>Click the <b>Volcano Plot</b> button in the top left corner of the grid window.</li>
     </ul>
     <p>
-        <img src="image-29.png" />
+        <img src="s-29.png" />
     </p>
     <p>
         You can already see clusters of points around the expected ratios and above the 5% FDR horizontal line for most of the changing peptides. To
@@ -726,7 +726,7 @@ <h1>Quantitative comparison </h1>
         The form should show you the list of peptides with matching protein names like this:
     </p>
     <p>
-        <img src="image-30.png" />
+        <img src="s-30.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -739,7 +739,7 @@ <h1>Quantitative comparison </h1>
         Which should leave the <b>Volcano Plot Formatting</b> form looking like this:
     </p>
     <p>
-        <img src="image-31.png" />
+        <img src="s-31.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -748,7 +748,7 @@ <h1>Quantitative comparison </h1>
         Which should leave the volcano plot looking like this:
     </p>
     <p>
-        <img src="image-32.png" />
+        <img src="s-32.png" />
     </p>
     <p>
         Notice that there are still some gray dots. You can click on any of the dots to cause them to be selected in the <b>Targets</b> view
@@ -787,7 +787,7 @@ <h1>Quantitative comparison </h1>
         The graph should now look like this:
     </p>
     <p>
-        <img src="image-33.png" />
+        <img src="s-33.png" />
     </p>
     <p>
         As with the volcano plot, you can click on the individual bars to select them in the <b>Targets</b> view (so that you can confirm
@@ -814,7 +814,7 @@ <h1>Quantitative comparison </h1>
         The <b>Bar Graph</b> should now show fold-change estimates for all 11 proteins that looks like this:
     </p>
     <p>
-        <img src="image-34.png" />
+        <img src="s-34.png" />
     </p>
     <ul>
         <li>Close the <b>Edit Group Comparison</b> by clicking the X square in the upper-right corner.</li>
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/en/image-1.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/en/s-1.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/en/image-1.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/en/s-1.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/en/image-10.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/en/s-10.png
similarity index 100%
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/en/image-11.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/en/s-11.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/en/image-14.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/en/s-14.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/en/image-15.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/en/s-15.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/en/image-16.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/en/s-16.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/en/image-17.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/en/s-17.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/en/image-18.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/en/s-18.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/en/image-19.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/en/s-19.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/en/image-2.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/en/s-2.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/en/image-23.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/en/s-23.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/en/image-24.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/en/s-24.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/en/image-27.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/en/s-27.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/en/image-28.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/en/s-28.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/en/image-32.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/en/s-32.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/en/image-33.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/en/s-33.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/en/image-34.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/en/s-34.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/en/image-4.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/en/s-4.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/en/image-5.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/en/s-5.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/en/image-6.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/en/s-6.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/en/image-7.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/en/s-7.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/en/image-8.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/en/s-8.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/en/image-9.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/en/s-9.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/en/image-9.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/en/image-0.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/en/s-ttof-label-free-proteome-quantification.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/en/image-0.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/en/s-ttof-label-free-proteome-quantification.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/index.html b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/index.html
index 8ccf25b6a8..62734d1bb1 100644
--- a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/index.html
+++ b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/index.html
@@ -26,7 +26,7 @@ <h1 class="document-title">SkylineでのDIA/SWATHデータ分析</h1>
         最初は、データ非依存性測定（DIA）のデータを解析するため、Skylineのパラメータを設定し、次に、生データファイルから定量化情報を抽出します。また、データ依存性解析（DDA）の結果をインポートしてスペクトルライブラリを作成し、DIAのデータを解析するための設定を行います。
     </p>
     <p>
-        <img src="image-0.png" />
+        <img src="s-ttof-label-free-proteome-quantification.png" />
     </p>
     <p class="fig-text">
         ［図の出典：Navarro, P. et al. A multicenter study benchmarks software tools for label-free proteome quantification.<i>Nature Biotech</i> 34,
@@ -113,7 +113,7 @@ <h1>ペプチド検索のインポートウィザードの使用</h1>
         すると、<b>ペプチド検索のインポート</b>ウィザードが表示されます。
     </p>
     <p>
-        <img src="image-1.png" />
+        <img src="s-1.png" />
     </p>
     <p>
         注：0.95は、DDAデータベース検索において、すべてのペプチド・スペクトル・マッチ（PSM）に対してPeptideProphetで設定した確率の閾値です。このチュートリアルで用いるデータセットでは、偽陽性率（false discovery rate,
@@ -130,7 +130,7 @@ <h1>ペプチド検索のインポートウィザードの使用</h1>
         ウィザードの [ <b>スペクトルライブラリ</b> ] ページは以下のようになります。
     </p>
     <p>
-        <img src="image-2.png" />
+        <img src="s-2.png" />
     </p>
     <ul>
         <li>[ <b>次へ</b> ] ボタンをクリックします。</li>
@@ -140,13 +140,13 @@ <h1>ペプチド検索のインポートウィザードの使用</h1>
         iRT標準ペプチドに基づいて、ペプチド検索結果のiRT値が校正されます。校正が成功すると、以下のようなライブラリ構築の要約が表示されます。
     </p>
     <p>
-        <img src="image-3.png" />
+        <img src="s-3.png" />
     </p>
     <ul class="keep-next">
         <li><b>成功</b>(青でハイライト) をクリックすると線形回帰の結果が表示されます。</li>
     </ul>
     <p>
-        <img src="image-4.png" />
+        <img src="s-4.png" />
     </p>
     <ul>
         <li>[ <b>閉じる</b> ] ボタンをクリックします。</li>
@@ -176,7 +176,7 @@ <h1>ペプチド検索のインポートウィザードの使用</h1>
         [ <b>結果ファイルを参照</b> ] は以下のようになります。
     </p>
     <p>
-        <img src="image-5.png" />
+        <img src="s-5.png" />
     </p>
     <ul>
         <li>[ <b>開く</b> ] ボタンをクリックします。</li>
@@ -185,7 +185,7 @@ <h1>ペプチド検索のインポートウィザードの使用</h1>
         <b>ペプチド検索のインポート</b>フォームは以下のようになります。
     </p>
     <p>
-        <img src="image-6.png" />
+        <img src="s-6.png" />
     </p>
     <ul>
         <li>[ <b>次へ</b> ] ボタンをクリックします。</li>
@@ -222,7 +222,7 @@ <h1>ペプチド検索のインポートウィザードの使用</h1>
         [ <b>ペプチド検索のインポート</b> ] フォームは以下のようになります。
     </p>
     <p>
-        <img src="image-7.png" /> 
+        <img src="s-7.png" /> 
     </p>
     <ul>
         <li>[ <b>次へ</b> ] ボタンをクリックします。</li>
@@ -262,7 +262,7 @@ <h1>ペプチド検索のインポートウィザードの使用</h1>
         [ <b>単離スキームを編集</b> ] フォームは以下のようになります。
     </p>
     <p>
-        <img src="image-8.png" />
+        <img src="s-8.png" />
     </p>
     <p>
         Skylineは、質量分析計で測定されたDIA単離範囲の [ <b>開始</b> ] および [ <b>終了</b> ]
@@ -285,7 +285,7 @@ <h1>ペプチド検索のインポートウィザードの使用</h1>
         以下のようなフォームが表示されます。
     </p>
     <p>
-        <img src="image-9.png" />
+        <img src="s-9.png" />
     </p>
     <p>
         クリック・アンド・ドラッグして囲んだ長方形を使い部分拡大するか、マウスのスクロールホイールを使用して拡大すると、マージンの位置の詳細を見ることができます。[ <b>マージンを表示</b> ] チェックボックスをオフにし、再びオンにすると、グラフのタイトルが
@@ -300,7 +300,7 @@ <h1>ペプチド検索のインポートウィザードの使用</h1>
         <b>ペプチド検索のインポート</b>ウィザードは以下のようになります。
     </p>
     <p>
-        <img src="image-10.png" />
+        <img src="s-10.png" />
     </p>
     <ul>
         <li>[ <b>次へ</b> ] ボタンをクリックします。</li>
@@ -327,7 +327,7 @@ <h1>ペプチド検索のインポートウィザードの使用</h1>
         <b>ペプチド検索のインポート</b>ウィザードは以下のようになります。
     </p>
     <p>
-        <img src="image-11.png" />
+        <img src="s-11.png" />
     </p>
     <ul>
         <li>[ <b>完了</b> ] ボタンをクリックします。</li>
@@ -336,7 +336,7 @@ <h1>ペプチド検索のインポートウィザードの使用</h1>
         設定条件と使用したFASTAシークエンステキストを基に計算されたターゲットを記述したフォームが、以下のように表示されます。
     </p>
     <p>
-        <img src="image-12.png" />
+        <img src="s-12.png" />
     </p>
     <p>
         [ <b>タンパク質毎の最小ペプチド数</b> ]
@@ -350,7 +350,7 @@ <h1>ペプチド検索のインポートウィザードの使用</h1>
         Skylineはクロマトグラムの抽出を開始します。標準のi7 4コアプロセッサでは以下のようになります。
     </p>
     <p>
-        <img src="image-13.png" />
+        <img src="s-13.png" />
     </p>
     <p>
         6コア以上ではすべてのファイルが並列処理され、2コアのほとんどのラップトップでは、インポートは2ファイルずつ処理されます。
@@ -360,7 +360,7 @@ <h1>ペプチド検索のインポートウィザードの使用</h1>
         ページで選択したmProhetモデルを表示します。これは以下のようになります。
     </p>
     <p>
-        <img src="image-14.png" />
+        <img src="s-14.png" />
     </p>
     <p>
         mProphetモデルでは、それぞれのクロマトグラムセットの中から、Skylineがデフォルトとして使用するスコアに基づき選んだ10個のベストピークを見直し、最も高いmProphetスコアを与える10個のピークを選びます。これらのピークのmProphetスコア（Skylineでは<b>Detection
@@ -387,7 +387,7 @@ <h1>試料の注釈</h1>
         [ <b>注釈を定義</b> ] ウィンドウは以下のようになります。
     </p>
     <p>
-        <img src="image-15.png" />
+        <img src="s-15.png" />
     </p>
     <ul>
         <li>[ <b>OK</b> ] ボタンをクリックします。 </li>
@@ -419,7 +419,7 @@ <h1>試料の注釈</h1>
         キーボードのEnter、矢印キーを使って移動し、A、B、1、2、3キーを使って以下のスクリーンショットで示すように試料に注釈を付けます。
     </p>
     <p>
-        <img src="image-16.png" />
+        <img src="s-16.png" />
     </p>
     <ul>
         <li>フォームの右上隅にある赤いXをクリックして [ <b>ドキュメントグリッド: 繰り返し測定</b> ] ウィンドウを閉じます。 </li>
@@ -464,10 +464,10 @@ <h1>データのマニュアル検証</h1>
     <table class="comp-fig">
         <tr>
             <td class="comp-fig" style="padding: 10px;">
-              <img src="image-17.png" />
+              <img src="s-17.png" />
             </td>
             <td class="comp-fig" style="padding: 10px;">
-              <img src="image-18.png" /> 
+              <img src="s-18.png" /> 
             </td>
         </tr>
     </table>
@@ -475,7 +475,7 @@ <h1>データのマニュアル検証</h1>
         <li>同様に、[ <b>ピーク領域: 繰り返し測定比較</b> ] ウィンドウと [ <b>ライブラリの一致</b> ] ウィンドウをドッキングし、以下のようにすべての情報が見やすくなるようにします。 </li>
     </ul>
     <p>
-        <img src="image-19.png" />
+        <img src="s-19.png" />
     </p>
     <ul>
         <li>最初のE. coliタンパク質である「sp|P63284|CLPB_ECOLI」をクリックします。</li>
@@ -494,7 +494,7 @@ <h1>データのマニュアル検証</h1>
         下に示すように、すべての表示でこのペプチドに関する情報が表示されます。
     </p>
     <p>
-        <img src="image-20.png" />
+        <img src="s-20.png" />
     </p>
     <p>
         このタンパク質に属する残りのペプチドのピーク領域パターンを調べて下さい。このタンパク質のペプチドの定量パターンは、予想される差異発現パターン（4:1）と一致していますか？
@@ -517,7 +517,7 @@ <h1>データのマニュアル検証</h1>
         クロマトグラム曲線上にカーソルを合わせると、曲線上に曲線と同じ色の丸が表示されます。
     </p>
     <p>
-        <img src="image-21.png" />
+        <img src="s-21.png" />
     </p>
     <ul>
         <li>クロマトグラムポイントにある丸をクリックします。</li>
@@ -526,13 +526,13 @@ <h1>データのマニュアル検証</h1>
         Skylineは選択したクロマトグラムポイントが抽出されたスペクトルを、選択したイオンを拡大して [ <b>フルスキャン</b> ] 表示を開きます。
     </p>
     <p>
-        <img src="image-22.png" />
+        <img src="s-22.png" />
     </p>
     <ul class="keep-next">
         <li>[ <b>フルスキャン</b> ] ツールバーの虫眼鏡ボタンをクリックしてフルスペクトルを表示します。</li>
     </ul>
     <p>
-        <img src="image-23.png" />
+        <img src="s-23.png" />
     </p>
     <p>
         手作業でさらにデータを調べます（デコイを含む）。
@@ -548,7 +548,7 @@ <h1>質量誤差と保持時間偏差 </h1>
         この操作によってデータセットの質量誤差分布が表示されます。抽出ウィンドウ（±20 ppm）はさらに最適化できるでしょうか？一般的には、平均差±3の標準偏差で十分です。ただし、両端の数字が高く、ヒストグラムが途切れているような場合は、抽出ウィンドウを広げた方がいいかもしれません。
     </p>
     <p>
-        <img src="image-24.png" />
+        <img src="s-24.png" />
     </p>
     <p>
         分布には、0周辺と5周辺とピークが2つあるように見えることに注意してください。これをよりよく理解するには、これが6回のランすべてでの質量誤差値であることを知っていると有用です。
@@ -577,7 +577,7 @@ <h1>質量誤差と保持時間偏差 </h1>
         </li>
     </ul>
     <p>
-        <img src="image-25.png" />
+        <img src="s-25.png" />
     </p>
     <ul>
         <li>グラフを右クリックし、[ <b>プロット</b> ] を選択して [ <b>残余</b> ] をクリックします。</li>
@@ -586,7 +586,7 @@ <h1>質量誤差と保持時間偏差 </h1>
         これにより、このデータセットでの予測保持時間からのずれが表示されます。この分析に対し、抽出ウィンドウ（±5分）はさらに最適化できるでしょうか？デコイも確認してみましょう。
     </p>
     <p>
-        <img src="image-26.png" />
+        <img src="s-26.png" />
     </p>
     <p>
         <b>注：</b>このチュートリアルのスペクトルライブラリは同じ試料を同時に測定した結果を用いて構築しました。そのため、保持時間予測の精度は非常に高くなっています。異なる装置、異なる時間、あるいは試料が異なる場合は、構築したスペクトルライブラリの保持時間の誤差はもっと大きくなると考えられます。
@@ -614,7 +614,7 @@ <h1>定量比較 </h1>
         [ <b>グループ比較を編集</b> ] フォームは以下のようになります。
     </p>
     <p>
-        <img src="image-27.png" />
+        <img src="s-27.png" />
     </p>
     <ul>
         <li>[ <b>OK</b> ] ボタンをクリックします。</li>
@@ -637,13 +637,13 @@ <h1>定量比較 </h1>
         どの生物種からのものか、またその予想比率（ヒト1:1、酵母1:2、E. coli 4:1）を念頭に、表内の複数のペプチドについて推定されている倍率変化を調べます。調整されたP値を調べ、予想される結果について考えてみましょう。
     </p>
     <p>
-        <img src="image-28.png" />
+        <img src="s-28.png" />
     </p>
     <ul class="keep-next">
         <li>グリッドウィンドウの左上隅にある [ <b>ボルケーノプロット</b> ] ボタンをクリックします。</li>
     </ul>
     <p>
-        <img src="image-29.png" />
+        <img src="s-29.png" />
     </p>
     <p>
         表示されたボルケーノプロットでは、変化している点の多くが、予想される倍率変化の周辺に集まっており、また、5% FDRを示す水平線の上にあることがわかります。どの点がどの生物種に属するのかを明確にするため次の操作を行って下さい。
@@ -658,7 +658,7 @@ <h1>定量比較 </h1>
         フォームには、以下のように一致するタンパク質名とともにペプチドの一覧が表示されます。
     </p>
     <p>
-        <img src="image-30.png" />
+        <img src="s-30.png" />
     </p>
     <ul>
         <li>[ <b>OK</b> ] ボタンをクリックします。</li>
@@ -671,7 +671,7 @@ <h1>定量比較 </h1>
         これで [ <b>ボルケーノプロット形式</b> ] フォームは以下のようになります。
     </p>
     <p>
-        <img src="image-31.png" />
+        <img src="s-31.png" />
     </p>
     <ul>
         <li>[ <b>OK</b> ] ボタンをクリックします。</li>
@@ -680,7 +680,7 @@ <h1>定量比較 </h1>
         これでボルケーノプロットは以下のようになります。
     </p>
     <p>
-        <img src="image-32.png" />
+        <img src="s-32.png" />
     </p>
     <p>
         まだグレーのドットがいくつか残っていることに注意してください。これらのドットのどれかをクリックすると、 [ <b>ターゲット</b> ]
@@ -713,7 +713,7 @@ <h1>定量比較 </h1>
         グラフは以下のように表示されます。
     </p>
     <p>
-        <img src="image-33.png" />
+        <img src="s-33.png" />
     </p>
     <p>
         ボルケーノプロット同様、個々の棒をクリックすると [ <b>ターゲット</b> ] 表示で選択されます（グラフ内のさまざまなペプチドがどの生物種からのものかを確認できます）。
@@ -736,7 +736,7 @@ <h1>定量比較 </h1>
         これで<b>棒グラフ</b>が11のタンパク質すべての倍率変化推定値を、以下のように表示するようになります。
     </p>
     <p>
-        <img src="image-34.png" />
+        <img src="s-34.png" />
     </p>
     <ul>
         <li>右上隅にあるXをクリックして [ <b>グループ比較を編集</b> ] を閉じます。</li>
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/invariant.html b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/invariant.html
index 0a4a6ee01e..d50c47d988 100644
--- a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/invariant.html
+++ b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/invariant.html
@@ -29,7 +29,7 @@ <h1 class="document-title">Analysis of DIA/SWATH data in Skyline</h1>
         generate peptide query parameters to analyze the DIA data.
     </p>
     <p>
-        <img src="image-0.png" />
+        <img src="s-ttof-label-free-proteome-quantification.png" />
     </p>
     <p class="fig-text">
         [figure adapted from Navarro, P. et al. A multicenter study benchmarks software tools for label-free proteome quantification. <i>Nature
@@ -124,7 +124,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         The <b>Import Peptide Search</b> wizard should appear looking like this:
     </p>
     <p>
-        <img src="image-1.png" />
+        <img src="s-1.png" />
     </p>
     <p>
         Note: 0.95 is the threshold applied to the PeptideProphet probability computed for every peptide spectrum match in the DDA database search – in
@@ -142,7 +142,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         The <b>Spectral Library</b> page of the wizard should now look like this:
     </p>
     <p>
-        <img src="image-2.png" />
+        <img src="s-2.png" />
     </p>
     <ul>
         <li>Click the <b>Next</b> button.</li>
@@ -153,13 +153,13 @@ <h1>Using the Import Peptide Search wizard</h1>
         into these samples. This should succeed and present a summary form like the one below:
     </p>
     <p>
-        <img src="image-3.png" />
+        <img src="s-3.png" />
     </p>
     <ul>
         <li>Click the <b>Success</b> link (highlighted in blue) to see the linear regression.</li>
     </ul>
     <p>
-        <img src="image-4.png" />
+        <img src="s-4.png" />
     </p>
     <ul>
         <li>Click the <b>Close</b> button.</li>
@@ -191,7 +191,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         The <b>Browse for Results Files</b> should look like this:
     </p>
     <p>
-        <img src="image-5.png" />
+        <img src="s-5.png" />
     </p>
     <ul>
         <li>Click the <b>Open</b> button.</li>
@@ -200,7 +200,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         The <b>Import Peptide Search</b> form should look like this:
     </p>
     <p>
-        <img src="image-6.png" />
+        <img src="s-6.png" />
     </p>
     <ul>
         <li>Click the <b>Next</b> button.</li>
@@ -239,7 +239,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         The <b>Import Peptide Search</b> form should look like:
     </p>
     <p>
-        <img src="image-7.png" /> 
+        <img src="s-7.png" /> 
     </p>
     <ul>
         <li>Click the <b>Next</b> button.</li>
@@ -283,7 +283,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         The <b>Edit Isolation Scheme</b> form should now look like this:
     </p>
     <p>
-        <img src="image-8.png" />
+        <img src="s-8.png" />
     </p>
     <p>
         Skyline has worked out the <b>Start</b> and <b>End</b> <i>m/z</i> values for the DIA isolation ranges measured on the
@@ -308,7 +308,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         You will see a form like the one below:
     </p>
     <p>
-        <img src="image-9.png" />
+        <img src="s-9.png" />
     </p>
     <p>
         You can click-and-drag a rectangle to zoom in or use the mouse scroll-wheel, and see the margins. If you uncheck and re-check <b>Show
@@ -324,7 +324,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         The <b>Import Peptide Search</b> wizard should now look like this:
     </p>
     <p>
-        <img src="image-10.png" />
+        <img src="s-10.png" />
     </p>
     <ul>
         <li>Click the <b>Next</b> button.</li>
@@ -353,7 +353,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         The <b>Import Peptide Search</b> wizard should now look like this:
     </p>
     <p>
-        <img src="image-11.png" />
+        <img src="s-11.png" />
     </p>
     <ul>
         <li>Click the <b>Finish</b> button.</li>
@@ -363,7 +363,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         provided that looks like this:
     </p>
     <p>
-        <img src="image-12.png" />
+        <img src="s-12.png" />
     </p>
     <p>
         Notice that with a <b>Min peptides per protein</b> filter of “1” the 13 proteins found in the FASTA file produce 12
@@ -378,7 +378,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         Skyline begins extracting chromatograms which should look like this on a standard i7 4-core processor:
     </p>
     <p>
-        <img src="image-13.png" />
+        <img src="s-13.png" />
     </p>
     <p>
         With 6-cores and above all files will be processed in parallel, and on most laptops with 2-cores the import will process 2 files at a time.
@@ -388,7 +388,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         page of the <b>Import Peptide Search</b> wizard. It should look like this:
     </p>
     <p>
-        <img src="image-14.png" />
+        <img src="s-14.png" />
     </p>
     <p>
         It has already been used to re-score the 10 best peaks Skyline found in each set of chromatograms, using its default score, and re-choose the
@@ -416,7 +416,7 @@ <h1>Sample Annotation</h1>
         The <b>Define Annotation</b> window should like this:
     </p>
     <p>
-        <img src="image-15.png" />
+        <img src="s-15.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button. </li>
@@ -451,7 +451,7 @@ <h1>Sample Annotation</h1>
         navigate:
     </p>
     <p>
-        <img src="image-16.png" />
+        <img src="s-16.png" />
     </p>
     <ul>
         <li>Close the <b>Document Grid: Replicates</b> window by clicking on the red X in the upper right hand corner of the form. </li>
@@ -501,10 +501,10 @@ <h1>Inspect the data manually</h1>
     <table class="comp-fig">
         <tr>
             <td class="comp-fig" style="padding: 10px;">
-              <img src="image-17.png" />
+              <img src="s-17.png" />
             </td>
             <td class="comp-fig" style="padding: 10px;">
-              <img src="image-18.png" /> 
+              <img src="s-18.png" /> 
             </td>
         </tr>
     </table>
@@ -513,7 +513,7 @@ <h1>Inspect the data manually</h1>
             easily viewable, as below: </li>
     </ul>
     <p>
-        <img src="image-19.png" />
+        <img src="s-19.png" />
     </p>
     <ul>
         <li>Click on the first E. coli protein: “sp|P63284|CLPB_ECOLI”.</li>
@@ -534,7 +534,7 @@ <h1>Inspect the data manually</h1>
         You get specific information for this peptide in all of the views, as shown below:
     </p>
     <p>
-        <img src="image-20.png" />
+        <img src="s-20.png" />
     </p>
     <p>
         Examine the peak area patterns for the rest of the peptides belonging to this protein. Is the quantitative pattern for the peptides from this
@@ -559,7 +559,7 @@ <h1>Inspect the data manually</h1>
         Notice that if you hover the cursor over a chromatogram curve a circle appears on the curve with the same color as the curve.
     </p>
     <p>
-        <img src="image-21.png" />
+        <img src="s-21.png" />
     </p>
     <ul>
         <li>Click the circle on a chromatogram point.</li>
@@ -569,13 +569,13 @@ <h1>Inspect the data manually</h1>
         you selected.
     </p>
     <p>
-        <img src="image-22.png" />
+        <img src="s-22.png" />
     </p>
     <ul>
         <li>Click the magnifying glass button in the <b>Full-Scan</b> toolbar to view the full spectrum.</li>
     </ul>
     <p>
-        <img src="image-23.png" />
+        <img src="s-23.png" />
     </p>
     <p>
         Explore the data further manually (including some decoys).
@@ -594,7 +594,7 @@ <h1>Mass error and retention time deviation </h1>
         may want to widen your extraction windows. 
     </p>
     <p>
-        <img src="image-24.png" />
+        <img src="s-24.png" />
     </p>
     <p>
         Note that the distribution appears to have two peaks, one around 0 and one around 5. To understand this better, it helps to know that these are
@@ -627,7 +627,7 @@ <h1>Mass error and retention time deviation </h1>
                 Run</b>. </li>
     </ul>
     <p>
-        <img src="image-25.png" />
+        <img src="s-25.png" />
     </p>
     <ul>
         <li>Right-click the graph, choose <b>Plot</b>, and click <b>Residuals</b>.</li>
@@ -637,7 +637,7 @@ <h1>Mass error and retention time deviation </h1>
         optimized for this analysis? Check the decoys as well.
     </p>
     <p>
-        <img src="image-26.png" />
+        <img src="s-26.png" />
     </p>
     <p>
         <b>Note</b>: As the spectral library for this analysis was constructed from a side-by-side analysis of the same samples. As such, the
@@ -673,7 +673,7 @@ <h1>Quantitative comparison </h1>
         The <b>Edit Group Comparison</b> form should look like this.
     </p>
     <p>
-        <img src="image-27.png" />
+        <img src="s-27.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -699,13 +699,13 @@ <h1>Quantitative comparison </h1>
         (human 1:1, yeast 1:2, E. coli 4:1). Consider the adjusted p values and what you might expect of them.
     </p>
     <p>
-        <img src="image-28.png" />
+        <img src="s-28.png" />
     </p>
     <ul>
         <li>Click the <b>Volcano Plot</b> button in the top left corner of the grid window.</li>
     </ul>
     <p>
-        <img src="image-29.png" />
+        <img src="s-29.png" />
     </p>
     <p>
         You can already see clusters of points around the expected ratios and above the 5% FDR horizontal line for most of the changing peptides. To
@@ -721,7 +721,7 @@ <h1>Quantitative comparison </h1>
         The form should show you the list of peptides with matching protein names like this:
     </p>
     <p>
-        <img src="image-30.png" />
+        <img src="s-30.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -734,7 +734,7 @@ <h1>Quantitative comparison </h1>
         Which should leave the <b>Volcano Plot Formatting</b> form looking like this:
     </p>
     <p>
-        <img src="image-31.png" />
+        <img src="s-31.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -743,7 +743,7 @@ <h1>Quantitative comparison </h1>
         Which should leave the volcano plot looking like this:
     </p>
     <p>
-        <img src="image-32.png" />
+        <img src="s-32.png" />
     </p>
     <p>
         Notice that there are still some gray dots. You can click on any of the dots to cause them to be selected in the <b>Targets</b> view
@@ -782,7 +782,7 @@ <h1>Quantitative comparison </h1>
         The graph should now look like this:
     </p>
     <p>
-        <img src="image-33.png" />
+        <img src="s-33.png" />
     </p>
     <p>
         As with the volcano plot, you can click on the individual bars to select them in the <b>Targets</b> view (so that you can confirm
@@ -809,7 +809,7 @@ <h1>Quantitative comparison </h1>
         The <b>Bar Graph</b> should now show fold-change estimates for all 11 proteins that looks like this:
     </p>
     <p>
-        <img src="image-34.png" />
+        <img src="s-34.png" />
     </p>
     <ul>
         <li>Close the <b>Edit Group Comparison</b> by clicking the X square in the upper-right corner.</li>
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/image-1.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/s-1.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/image-1.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/s-1.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/image-10.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/s-10.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/image-10.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/s-10.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/image-11.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/s-11.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/image-11.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/s-11.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/image-12.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/s-12.png
similarity index 100%
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/image-13.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/s-13.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/image-13.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/s-13.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/image-14.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/s-14.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/image-14.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/s-14.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/image-15.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/s-15.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/image-15.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/s-15.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/image-16.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/s-16.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/image-16.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/s-16.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/image-17.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/s-17.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/image-17.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/s-17.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/image-18.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/s-18.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/image-18.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/s-18.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/image-19.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/s-19.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/image-19.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/s-19.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/image-2.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/s-2.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/image-2.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/s-2.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/image-20.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/s-20.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/image-20.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/image-21.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/s-21.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/image-21.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/image-22.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/s-22.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/image-22.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/image-23.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/s-23.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/image-23.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/s-23.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/image-24.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/s-24.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/image-24.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/s-24.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/image-25.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/s-25.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/image-25.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/image-26.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/s-26.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/image-26.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/s-26.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/image-27.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/s-27.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/image-27.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/image-28.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/s-28.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/image-28.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/image-29.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/s-29.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/image-29.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/s-29.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/image-3.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/s-3.png
similarity index 100%
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/image-30.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/s-30.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/image-30.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/image-31.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/s-31.png
similarity index 100%
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/image-32.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/s-32.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/image-32.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/s-32.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/image-33.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/s-33.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/image-33.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/image-34.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/s-34.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/image-34.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/s-34.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/image-4.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/s-4.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/image-4.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/s-4.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/image-5.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/s-5.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/image-5.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/s-5.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/image-6.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/s-6.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/image-6.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/s-6.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/image-7.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/s-7.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/image-7.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/s-7.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/image-8.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/s-8.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/image-8.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/s-8.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/image-9.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/s-9.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/image-9.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/s-9.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/image-0.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/s-ttof-label-free-proteome-quantification.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/image-0.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/ja/s-ttof-label-free-proteome-quantification.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/zh-CHS/index.html b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/zh-CHS/index.html
index 9f90d362b3..20aaedca26 100644
--- a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/zh-CHS/index.html
+++ b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/zh-CHS/index.html
@@ -21,7 +21,7 @@ <h1 class="document-title">Skyline 中的 DIA/SWATH 数据分析</h1>
         为了处理DIA数据集，您首先要在Skyline中设置所有相关参数；然后，您需要从原始数据文件提取定量的信息；最后，您要通过导入DDA数据的搜索结果创建一个质谱图库，从而产生肽段的查询参数。
     </p>
     <p>
-        <img src="image-0.png" />
+        <img src="s-ttof-label-free-proteome-quantification.png" />
     </p>
     <p class="fig-text">
         [图片取自 Navarro, P. et al. A multicenter study benchmarks software tools for label-free proteome quantification. <i>Nature Biotech</i> 34,
@@ -110,7 +110,7 @@ <h1>使用“导入肽段搜索”向导</h1>
         <b>导入肽段搜索</b>向导应显示如下：
     </p>
     <p>
-        <img src="image-1.png" />
+        <img src="s-1.png" />
     </p>
     <p>
         注意：0.95 是 DDA 数据库搜索中每个肽段谱图匹配度计算的 PeptideProphet 概率阈值 - 在这个特定的数据集中，这相当于 0.2% 的 PSM 错误发现率，但此值在不同数据集中会有所不同，因此应在此处输入您要使用的错误发现率的概率阈值。
@@ -126,7 +126,7 @@ <h1>使用“导入肽段搜索”向导</h1>
         向导中的<b>谱图库</b>页面现在应显示如下： 
     </p>
     <p>
-        <img src="image-2.png" />
+        <img src="s-2.png" />
     </p>
     <ul>
         <li>单击<b>下一步</b>按钮。</li>
@@ -135,13 +135,13 @@ <h1>使用“导入肽段搜索”向导</h1>
         Skyline 开始创建谱图库，并在<b>构建肽段搜索库</b>表单中显示进度。创建的谱图库将通过加入样品中的Biognosys iRT 标准肽段搜索结果校准 iRT 值。操作成功后，呈现如下所示的表单：
     </p>
     <p>
-        <img src="image-3.png" />
+        <img src="s-3.png" />
     </p>
     <ul>
         <li>单击<b>成功</b>链接（蓝色突出显示）以查看线性回归。 </li>
     </ul>
     <p>
-        <img src="image-4.png" />
+        <img src="s-4.png" />
     </p>
     <ul>
         <li>单击<b>关闭</b>按钮。</li>
@@ -171,7 +171,7 @@ <h1>使用“导入肽段搜索”向导</h1>
         <b>浏览结果文件</b>应显示如下：
     </p>
     <p>
-        <img src="image-5.png" />
+        <img src="s-5.png" />
     </p>
     <ul>
         <li>单击<b>打开</b>按钮。</li>
@@ -180,7 +180,7 @@ <h1>使用“导入肽段搜索”向导</h1>
         <b>导入肽段搜索</b>表单应显示如下：
     </p>
     <p>
-        <img src="image-6.png" />
+        <img src="s-6.png" />
     </p>
     <ul>
         <li>单击<b>下一步</b>按钮。</li>
@@ -217,7 +217,7 @@ <h1>使用“导入肽段搜索”向导</h1>
         <b>导入肽段搜索</b>表单应显示如下：
     </p>
     <p>
-        <img src="image-7.png" /> 
+        <img src="s-7.png" /> 
     </p>
     <ul>
         <li>单击<b>下一步</b>按钮。</li>
@@ -257,7 +257,7 @@ <h1>使用“导入肽段搜索”向导</h1>
         此时<b>编辑分离方案</b>表单应显示如下：
     </p>
     <p>
-        <img src="image-8.png" />
+        <img src="s-8.png" />
     </p>
     <p>
         Skyline 已解出在质谱仪上测得的 DIA 分离范围的<b>开始</b>和<b>结束</b>质荷比值。可以看出它们重叠了 1.0 质荷比，为补偿重叠，Skyline 在分离窗口的每侧增加了 0.5
@@ -279,7 +279,7 @@ <h1>使用“导入肽段搜索”向导</h1>
         随即显示下面这样的表单：
     </p>
     <p>
-        <img src="image-9.png" />
+        <img src="s-9.png" />
     </p>
     <p>
         您可以单击并拖动矩形进行放大，或是使用鼠标滚轮查看边距。如果取消选中<b>显示边距</b>后又重新选中，图形名称将在<b>测量窗口</b>和<b>提取窗口</b>之间切换，并且粉红色的边距条消失后又会重新出现。图中没有红色的<b>显示间距</b>或黄色的<b>显示单循环重叠</b>，二者均为
@@ -293,7 +293,7 @@ <h1>使用“导入肽段搜索”向导</h1>
         <b>导入肽段搜索</b>向导现在显示如下：
     </p>
     <p>
-        <img src="image-10.png" />
+        <img src="s-10.png" />
     </p>
     <ul>
         <li>单击<b>下一步</b>按钮。</li>
@@ -320,7 +320,7 @@ <h1>使用“导入肽段搜索”向导</h1>
         <b>导入肽段搜索</b>向导现在显示如下：
     </p>
     <p>
-        <img src="image-11.png" />
+        <img src="s-11.png" />
     </p>
     <ul>
         <li>单击<b>完成</b>按钮。</li>
@@ -329,7 +329,7 @@ <h1>使用“导入肽段搜索”向导</h1>
         此时应当显示一张表单，其中描述了根据您的设置和所提供的 FASTA 序列文本计算得出的目标，如下所示：
     </p>
     <p>
-        <img src="image-12.png" />
+        <img src="s-12.png" />
     </p>
     <p>
         可以发现，<b>每个蛋白质的最少肽段数</b>过滤器设置为 "1" 时，FASTA 文件中的 13 个蛋白质产生的<b>剩余</b>蛋白质为 12 个。这是因为有 1
@@ -342,7 +342,7 @@ <h1>使用“导入肽段搜索”向导</h1>
         Skyline 开始提取色谱图，在标准的 i7 4 核处理器上显示如下：
     </p>
     <p>
-        <img src="image-13.png" />
+        <img src="s-13.png" />
     </p>
     <p>
         在 6 核及以上的处理器中，所有文件将并行处理；在大多数配备双核处理器的笔记本电脑上，导入过程中一次处理 2 个文件。
@@ -351,7 +351,7 @@ <h1>使用“导入肽段搜索”向导</h1>
         导入完成后，Skyline 将显示您在<b>导入肽段搜索</b>向导中的<b>导入 FASTA</b> 页面上请求的 mProphet 模型。其显示如下：
     </p>
     <p>
-        <img src="image-14.png" />
+        <img src="s-14.png" />
     </p>
     <p>
         系统采用默认的分数对 Skyline 在每组色谱图中找到的 10 个最优峰重新评分，并将这些峰重新选择为 mProphet 得分最高的峰。这些 mProphet 分数（在 Skyline 中叫做<b>检测 Z 得分</b>）进行扩展后，以使 1.0表示与平均
@@ -376,7 +376,7 @@ <h1>样品注释</h1>
         <b>定义注释</b>窗口应如下所示：
     </p>
     <p>
-        <img src="image-15.png" />
+        <img src="s-15.png" />
     </p>
     <ul>
         <li>单击<b>确定</b>按钮。 </li>
@@ -408,7 +408,7 @@ <h1>样品注释</h1>
         如下面的截屏中所示，使用键盘上的 A，B，1、2、3、Enter 和方向键对样品进行注释：
     </p>
     <p>
-        <img src="image-16.png" />
+        <img src="s-16.png" />
     </p>
     <ul>
         <li>单击表单右上角的红 X，即可关闭<b>文档网格：重复测定</b>窗口。 </li>
@@ -453,10 +453,10 @@ <h1>手动检查数据</h1>
     <table class="comp-fig">
         <tr>
             <td class="comp-fig" style="padding: 10px;">
-              <img src="image-17.png" />
+              <img src="s-17.png" />
             </td>
             <td class="comp-fig" style="padding: 10px;">
-              <img src="image-18.png" /> 
+              <img src="s-18.png" /> 
             </td>
         </tr>
     </table>
@@ -464,7 +464,7 @@ <h1>手动检查数据</h1>
         <li>以同样的方式停靠<b>峰面积：重复测定比较</b>和<b>库匹配</b>窗口，以便轻松查看所有信息，如下所示： </li>
     </ul>
     <p>
-        <img src="image-19.png" />
+        <img src="s-19.png" />
     </p>
     <ul>
         <li>单击第一个大肠杆菌蛋白质："sp|P63284|CLPB_ECOLI"。</li>
@@ -482,7 +482,7 @@ <h1>手动检查数据</h1>
         您将在所有这些视图中获得该肽段的特定信息，如下所示：
     </p>
     <p>
-        <img src="image-20.png" />
+        <img src="s-20.png" />
     </p>
     <p>
         检查属于该蛋白质的其余肽段的峰面积模式。该蛋白质的肽段的定量模式是否与预期的差异化调控模式 (4:1) 一致？ 
@@ -504,7 +504,7 @@ <h1>手动检查数据</h1>
         请注意，如果将光标悬停在色谱图曲线上，曲线上就会出现与该曲线同色的圆圈。
     </p>
     <p>
-        <img src="image-21.png" />
+        <img src="s-21.png" />
     </p>
     <ul>
         <li>单击色谱图点上的圆圈。</li>
@@ -513,13 +513,13 @@ <h1>手动检查数据</h1>
         Skyline 将在从中提取该色谱图点的谱图上打开<b>全扫描</b>视图，并放大您选择的离子。
     </p>
     <p>
-        <img src="image-22.png" />
+        <img src="s-22.png" />
     </p>
     <ul>
         <li>单击<b>全扫描</b>工具栏中的放大镜按钮可以查看整个谱图。</li>
     </ul>
     <p>
-        <img src="image-23.png" />
+        <img src="s-23.png" />
     </p>
     <p>
         进一步手动探索数据（包括一些诱饵）。
@@ -535,7 +535,7 @@ <h1>质量误差和保留时间偏差 </h1>
         这将显示质量误差在数据集中的分布。提取窗口 (±20 ppm) 能否进一步优化？一般情况下，平均误差 +/- 3 个标准偏差便足以应对。但是，如果显示的直方图被截止，并且在极端情况下计数很高，则可能需要增宽提取窗口。 
     </p>
     <p>
-        <img src="image-24.png" />
+        <img src="s-24.png" />
     </p>
     <p>
         请注意，该分布似乎有两个峰，一个在 0 附近，另一个在 5 附近。为更好地理解这一点，应当明白这些是所有 6 次运行的质量误差值。
@@ -562,7 +562,7 @@ <h1>质量误差和保留时间偏差 </h1>
         <li>在<b>视图</b>菜单中选择<b>保留时间</b>，然后单击<b>回归</b>，最后单击<b>运行分数</b>。 </li>
     </ul>
     <p>
-        <img src="image-25.png" />
+        <img src="s-25.png" />
     </p>
     <ul>
         <li>右键单击此图，选择<b>绘图</b>，然后单击<b>残差</b>。 </li>
@@ -571,7 +571,7 @@ <h1>质量误差和保留时间偏差 </h1>
         随即显示该数据集中与预计保留时间的偏差。能否针对此分析进一步优化提取窗口（±5 分钟）？这时请进一步检查诱饵。
     </p>
     <p>
-        <img src="image-26.png" />
+        <img src="s-26.png" />
     </p>
     <p>
         <b>注意：</b>因为这项分析的谱图库是通过对相同样品进行并排分析构建而成，所以保留时间预测的准确性非常好。在对不同仪器不同时间不同样品分析创建的外部谱图库中，保留时间将导致这些预测中的误差较大。
@@ -601,7 +601,7 @@ <h1>定量比较 </h1>
         <b>编辑群组比较</b>表单应如下显示。
     </p>
     <p>
-        <img src="image-27.png" />
+        <img src="s-27.png" />
     </p>
     <ul>
         <li>单击<b>确定</b>按钮。</li>
@@ -623,13 +623,13 @@ <h1>定量比较 </h1>
         检查表中某些肽段的倍数变化估计值，同时要记住它们来自哪个物种以及预期的比率（人类蛋白质 1:1，酵母 1:2，大肠杆菌 4:1）。考虑已调整的 p 值以及您可能期望的值。
     </p>
     <p>
-        <img src="image-28.png" />
+        <img src="s-28.png" />
     </p>
     <ul>
         <li>单击网格窗口左上角的<b>火山图</b>按钮。</li>
     </ul>
     <p>
-        <img src="image-29.png" />
+        <img src="s-29.png" />
     </p>
     <p>
         对于大多数变化的肽段，已可以看到出现在预期比率附近和 5％ FDR 水平线以上的点簇。为了更好地了解哪些点属于哪种生物体，请执行以下操作：
@@ -644,7 +644,7 @@ <h1>定量比较 </h1>
         表单应显示具有匹配蛋白质名称的肽段列表，如下所示：
     </p>
     <p>
-        <img src="image-30.png" />
+        <img src="s-30.png" />
     </p>
     <ul>
         <li>单击<b>确定</b>按钮。</li>
@@ -657,7 +657,7 @@ <h1>定量比较 </h1>
         <b>火山图格式</b>表单应显示如下：
     </p>
     <p>
-        <img src="image-31.png" />
+        <img src="s-31.png" />
     </p>
     <ul>
         <li>单击<b>确定</b>按钮。</li>
@@ -666,7 +666,7 @@ <h1>定量比较 </h1>
         火山图应显示如下：
     </p>
     <p>
-        <img src="image-32.png" />
+        <img src="s-32.png" />
     </p>
     <p>
         请注意，图中仍有一些灰点。您可以单击其中任意的点，这样它们在<b>目标</b>视图中将处于选中状态，并且将在图中以红色显示测试。您也可以将鼠标光标悬停在任何点上以获取更多信息。通过这种方式，可以看到灰点属于 iRT
@@ -699,7 +699,7 @@ <h1>定量比较 </h1>
         该图现在应显示如下：
     </p>
     <p>
-        <img src="image-33.png" />
+        <img src="s-33.png" />
     </p>
     <p>
         与火山图一样，您可以单击<b>目标</b>视图中的单个条形以将其选定（这样便可确认图中的不同肽段来自哪个物种）。
@@ -722,7 +722,7 @@ <h1>定量比较 </h1>
         现在，<b>条状图</b>应显示所有 11 种蛋白质的倍数变化估算值，如下所示：
     </p>
     <p>
-        <img src="image-34.png" />
+        <img src="s-34.png" />
     </p>
     <ul>
         <li>单击右上角的 X 方格，关闭<b>编辑群组比较</b>。</li>
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/zh-CHS/invariant.html b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/zh-CHS/invariant.html
index 4453edf124..1029263db0 100644
--- a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/zh-CHS/invariant.html
+++ b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/zh-CHS/invariant.html
@@ -27,7 +27,7 @@ <h1 class="document-title">Analysis of DIA/SWATH data in Skyline</h1>
         generate peptide query parameters to analyze the DIA data.
     </p>
     <p>
-        <img src="image-0.png" />
+        <img src="s-ttof-label-free-proteome-quantification.png" />
     </p>
     <p class="fig-text">
         [figure adapted from Navarro, P. et al. A multicenter study benchmarks software tools for label-free proteome quantification. <i>Nature
@@ -122,7 +122,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         The <b>Import Peptide Search</b> wizard should appear looking like this:
     </p>
     <p>
-        <img src="image-1.png" />
+        <img src="s-1.png" />
     </p>
     <p>
         Note: 0.95 is the threshold applied to the PeptideProphet probability computed for every peptide spectrum match in the DDA database search – in
@@ -140,7 +140,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         The <b>Spectral Library</b> page of the wizard should now look like this:
     </p>
     <p>
-        <img src="image-2.png" />
+        <img src="s-2.png" />
     </p>
     <ul>
         <li>Click the <b>Next</b> button.</li>
@@ -151,13 +151,13 @@ <h1>Using the Import Peptide Search wizard</h1>
         into these samples. This should succeed and present a summary form like the one below:
     </p>
     <p>
-        <img src="image-3.png" />
+        <img src="s-3.png" />
     </p>
     <ul>
         <li>Click the <b>Success</b> link (highlighted in blue) to see the linear regression.</li>
     </ul>
     <p>
-        <img src="image-4.png" />
+        <img src="s-4.png" />
     </p>
     <ul>
         <li>Click the <b>Close</b> button.</li>
@@ -189,7 +189,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         The <b>Browse for Results Files</b> should look like this:
     </p>
     <p>
-        <img src="image-5.png" />
+        <img src="s-5.png" />
     </p>
     <ul>
         <li>Click the <b>Open</b> button.</li>
@@ -198,7 +198,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         The <b>Import Peptide Search</b> form should look like this:
     </p>
     <p>
-        <img src="image-6.png" />
+        <img src="s-6.png" />
     </p>
     <ul>
         <li>Click the <b>Next</b> button.</li>
@@ -237,7 +237,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         The <b>Import Peptide Search</b> form should look like:
     </p>
     <p>
-        <img src="image-7.png" /> 
+        <img src="s-7.png" /> 
     </p>
     <ul>
         <li>Click the <b>Next</b> button.</li>
@@ -281,7 +281,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         The <b>Edit Isolation Scheme</b> form should now look like this:
     </p>
     <p>
-        <img src="image-8.png" />
+        <img src="s-8.png" />
     </p>
     <p>
         Skyline has worked out the <b>Start</b> and <b>End</b> <i>m/z</i> values for the DIA isolation ranges measured on the
@@ -306,7 +306,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         You will see a form like the one below:
     </p>
     <p>
-        <img src="image-9.png" />
+        <img src="s-9.png" />
     </p>
     <p>
         You can click-and-drag a rectangle to zoom in or use the mouse scroll-wheel, and see the margins. If you uncheck and re-check <b>Show
@@ -322,7 +322,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         The <b>Import Peptide Search</b> wizard should now look like this:
     </p>
     <p>
-        <img src="image-10.png" />
+        <img src="s-10.png" />
     </p>
     <ul>
         <li>Click the <b>Next</b> button.</li>
@@ -351,7 +351,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         The <b>Import Peptide Search</b> wizard should now look like this:
     </p>
     <p>
-        <img src="image-11.png" />
+        <img src="s-11.png" />
     </p>
     <ul>
         <li>Click the <b>Finish</b> button.</li>
@@ -361,7 +361,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         provided that looks like this:
     </p>
     <p>
-        <img src="image-12.png" />
+        <img src="s-12.png" />
     </p>
     <p>
         Notice that with a <b>Min peptides per protein</b> filter of “1” the 13 proteins found in the FASTA file produce 12
@@ -376,7 +376,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         Skyline begins extracting chromatograms which should look like this on a standard i7 4-core processor:
     </p>
     <p>
-        <img src="image-13.png" />
+        <img src="s-13.png" />
     </p>
     <p>
         With 6-cores and above all files will be processed in parallel, and on most laptops with 2-cores the import will process 2 files at a time.
@@ -386,7 +386,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         page of the <b>Import Peptide Search</b> wizard. It should look like this:
     </p>
     <p>
-        <img src="image-14.png" />
+        <img src="s-14.png" />
     </p>
     <p>
         It has already been used to re-score the 10 best peaks Skyline found in each set of chromatograms, using its default score, and re-choose the
@@ -414,7 +414,7 @@ <h1>Sample Annotation</h1>
         The <b>Define Annotation</b> window should like this:
     </p>
     <p>
-        <img src="image-15.png" />
+        <img src="s-15.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button. </li>
@@ -449,7 +449,7 @@ <h1>Sample Annotation</h1>
         navigate:
     </p>
     <p>
-        <img src="image-16.png" />
+        <img src="s-16.png" />
     </p>
     <ul>
         <li>Close the <b>Document Grid: Replicates</b> window by clicking on the red X in the upper right hand corner of the form. </li>
@@ -499,10 +499,10 @@ <h1>Inspect the data manually</h1>
     <table class="comp-fig">
         <tr>
             <td class="comp-fig" style="padding: 10px;">
-              <img src="image-17.png" />
+              <img src="s-17.png" />
             </td>
             <td class="comp-fig" style="padding: 10px;">
-              <img src="image-18.png" /> 
+              <img src="s-18.png" /> 
             </td>
         </tr>
     </table>
@@ -511,7 +511,7 @@ <h1>Inspect the data manually</h1>
             easily viewable, as below: </li>
     </ul>
     <p>
-        <img src="image-19.png" />
+        <img src="s-19.png" />
     </p>
     <ul>
         <li>Click on the first E. coli protein: “sp|P63284|CLPB_ECOLI”.</li>
@@ -532,7 +532,7 @@ <h1>Inspect the data manually</h1>
         You get specific information for this peptide in all of the views, as shown below:
     </p>
     <p>
-        <img src="image-20.png" />
+        <img src="s-20.png" />
     </p>
     <p>
         Examine the peak area patterns for the rest of the peptides belonging to this protein. Is the quantitative pattern for the peptides from this
@@ -557,7 +557,7 @@ <h1>Inspect the data manually</h1>
         Notice that if you hover the cursor over a chromatogram curve a circle appears on the curve with the same color as the curve.
     </p>
     <p>
-        <img src="image-21.png" />
+        <img src="s-21.png" />
     </p>
     <ul>
         <li>Click the circle on a chromatogram point.</li>
@@ -567,13 +567,13 @@ <h1>Inspect the data manually</h1>
         you selected.
     </p>
     <p>
-        <img src="image-22.png" />
+        <img src="s-22.png" />
     </p>
     <ul>
         <li>Click the magnifying glass button in the <b>Full-Scan</b> toolbar to view the full spectrum.</li>
     </ul>
     <p>
-        <img src="image-23.png" />
+        <img src="s-23.png" />
     </p>
     <p>
         Explore the data further manually (including some decoys).
@@ -592,7 +592,7 @@ <h1>Mass error and retention time deviation </h1>
         may want to widen your extraction windows. 
     </p>
     <p>
-        <img src="image-24.png" />
+        <img src="s-24.png" />
     </p>
     <p>
         Note that the distribution appears to have two peaks, one around 0 and one around 5. To understand this better, it helps to know that these are
@@ -625,7 +625,7 @@ <h1>Mass error and retention time deviation </h1>
                 Run</b>. </li>
     </ul>
     <p>
-        <img src="image-25.png" />
+        <img src="s-25.png" />
     </p>
     <ul>
         <li>Right-click the graph, choose <b>Plot</b>, and click <b>Residuals</b>.</li>
@@ -635,7 +635,7 @@ <h1>Mass error and retention time deviation </h1>
         optimized for this analysis? Check the decoys as well.
     </p>
     <p>
-        <img src="image-26.png" />
+        <img src="s-26.png" />
     </p>
     <p>
         <b>Note</b>: As the spectral library for this analysis was constructed from a side-by-side analysis of the same samples. As such, the
@@ -671,7 +671,7 @@ <h1>Quantitative comparison </h1>
         The <b>Edit Group Comparison</b> form should look like this.
     </p>
     <p>
-        <img src="image-27.png" />
+        <img src="s-27.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -697,13 +697,13 @@ <h1>Quantitative comparison </h1>
         (human 1:1, yeast 1:2, E. coli 4:1). Consider the adjusted p values and what you might expect of them.
     </p>
     <p>
-        <img src="image-28.png" />
+        <img src="s-28.png" />
     </p>
     <ul>
         <li>Click the <b>Volcano Plot</b> button in the top left corner of the grid window.</li>
     </ul>
     <p>
-        <img src="image-29.png" />
+        <img src="s-29.png" />
     </p>
     <p>
         You can already see clusters of points around the expected ratios and above the 5% FDR horizontal line for most of the changing peptides. To
@@ -719,7 +719,7 @@ <h1>Quantitative comparison </h1>
         The form should show you the list of peptides with matching protein names like this:
     </p>
     <p>
-        <img src="image-30.png" />
+        <img src="s-30.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -732,7 +732,7 @@ <h1>Quantitative comparison </h1>
         Which should leave the <b>Volcano Plot Formatting</b> form looking like this:
     </p>
     <p>
-        <img src="image-31.png" />
+        <img src="s-31.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -741,7 +741,7 @@ <h1>Quantitative comparison </h1>
         Which should leave the volcano plot looking like this:
     </p>
     <p>
-        <img src="image-32.png" />
+        <img src="s-32.png" />
     </p>
     <p>
         Notice that there are still some gray dots. You can click on any of the dots to cause them to be selected in the <b>Targets</b> view
@@ -780,7 +780,7 @@ <h1>Quantitative comparison </h1>
         The graph should now look like this:
     </p>
     <p>
-        <img src="image-33.png" />
+        <img src="s-33.png" />
     </p>
     <p>
         As with the volcano plot, you can click on the individual bars to select them in the <b>Targets</b> view (so that you can confirm
@@ -807,7 +807,7 @@ <h1>Quantitative comparison </h1>
         The <b>Bar Graph</b> should now show fold-change estimates for all 11 proteins that looks like this:
     </p>
     <p>
-        <img src="image-34.png" />
+        <img src="s-34.png" />
     </p>
     <ul>
         <li>Close the <b>Edit Group Comparison</b> by clicking the X square in the upper-right corner.</li>
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/zh-CHS/image-1.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/zh-CHS/s-1.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/zh-CHS/image-1.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/zh-CHS/s-1.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/zh-CHS/image-10.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/zh-CHS/s-10.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/zh-CHS/image-10.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/zh-CHS/s-10.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/zh-CHS/image-11.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/zh-CHS/s-11.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/zh-CHS/image-11.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/zh-CHS/s-11.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/zh-CHS/image-12.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/zh-CHS/s-12.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/zh-CHS/image-12.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/zh-CHS/s-12.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/zh-CHS/image-13.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/zh-CHS/s-13.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/zh-CHS/image-13.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/zh-CHS/s-13.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/zh-CHS/image-18.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/zh-CHS/s-18.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/zh-CHS/image-19.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/zh-CHS/s-19.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/zh-CHS/image-2.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/zh-CHS/s-2.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/zh-CHS/image-20.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/zh-CHS/s-20.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/zh-CHS/image-27.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/zh-CHS/s-27.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/zh-CHS/image-28.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/zh-CHS/s-28.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/zh-CHS/image-0.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-TTOF/zh-CHS/s-ttof-label-free-proteome-quantification.png
similarity index 100%
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-Umpire-TTOF/en/index.html b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-Umpire-TTOF/en/index.html
index 2ba2cbc9c1..c91cd3d089 100644
--- a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-Umpire-TTOF/en/index.html
+++ b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-Umpire-TTOF/en/index.html
@@ -30,7 +30,7 @@ <h1 class="document-title">Library-Free DIA/SWATH with Skyline</h1>
         parameters to analyze the DIA data. No pre-existing spectral library is required for this data analysis method.
     </p>
     <p>
-        <img src="image-0.png" />
+        <img src="s-ttof-label-free-proteome-quantification.png" />
     </p>
     <p>
         [figure adapted from Navarro, P. et al. A multicenter study benchmarks software tools for label-free proteome quantification. <i>Nature
@@ -119,7 +119,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         The <b>Run Peptide Search</b> wizard should appear looking like this:
     </p>
     <p>
-        <img src="image-1.png" />
+        <img src="s-1.png" />
     </p>
     <ul>
         <li>Click the <b>Add Files</b> button.</li>
@@ -132,7 +132,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         The <b>Spectral Library</b> page of the wizard should now look like this:
     </p>
     <p>
-        <img src="image-2.png" />
+        <img src="s-2.png" />
     </p>
     <ul>
         <li>Click the <b>Next</b> button.</li>
@@ -142,7 +142,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         files: 
     </p>
     <p>
-        <img src="image-3.png" />
+        <img src="s-3.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -160,7 +160,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         Carbamidomethyl (C) and Oxidation (M):
     </p>
     <p>
-        <img src="image-4.png" />
+        <img src="s-4.png" />
     </p>
     <ul>
         <li>Make sure the checkboxes for both modifications are checked.</li>
@@ -184,7 +184,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         The <b>Import Peptide Search</b> form should look like:
     </p>
     <p>
-        <img src="image-5.png" />
+        <img src="s-5.png" />
     </p>
     <ul>
         <li>Click the <b>Next</b> button.</li>
@@ -228,7 +228,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         The <b>Edit Isolation Scheme</b> form should now look like this:
     </p>
     <p>
-        <img src="image-6.png" />
+        <img src="s-6.png" />
     </p>
     <p>
         Skyline has worked out the <b>Start</b> and <b>End</b> <i>m/z</i> values for the DIA isolation ranges measured on the
@@ -253,7 +253,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         You will see a form like the one below:
     </p>
     <p>
-        <img src="image-7.png" />
+        <img src="s-7.png" />
     </p>
     <p>
         You can click-and-drag a rectangle to zoom in or use the mouse scroll-wheel, and see the margins. If you uncheck and re-check <b>Show
@@ -269,7 +269,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         The <b>Import Peptide Search</b> wizard should now look like this:
     </p>
     <p>
-        <img src="image-8.png" />
+        <img src="s-8.png" />
     </p>
     <ul>
         <li>Click the <b>Next</b> button.</li>
@@ -278,7 +278,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         You will see the <b>Import FASTA</b> page, which should look like:
     </p>
     <p>
-        <img src="image-9.png" />
+        <img src="s-9.png" />
     </p>
     <ul>
         <li>Click the <b>Browse</b> button.</li>
@@ -308,7 +308,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         After setting these options, the page should look like:
     </p>
     <p>
-        <img src="image-10.png" />
+        <img src="s-10.png" />
     </p>
     <ul>
         <li>Click the <b>Next</b> button.</li>
@@ -318,7 +318,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         DIA-Umpire settings:
     </p>
     <p>
-        <img src="image-11.png" />
+        <img src="s-11.png" />
     </p>
     <p>
         The main setting here is “Instrument preset” which sets some established defaults for DIA-Umpire parameters according to what kind of
@@ -342,7 +342,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         The form should now look like this:
     </p>
     <p>
-        <img src="image-12.png" />
+        <img src="s-12.png" />
     </p>
     <p>
         The <b>Max q-value</b> field sets a false discovery rate (FDR) limit allowed for the peptide matches in the search results. In this
@@ -360,7 +360,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         also cancel the process here.
     </p>
     <p>
-        <img src="image-13.png" />
+        <img src="s-13.png" />
     </p>
     <p>
         After the search is finished:
@@ -374,13 +374,13 @@ <h1>Using the Import Peptide Search wizard</h1>
         into these samples. This should succeed and present a summary form like the one below:
     </p>
     <p>
-        <img src="image-14.png" />
+        <img src="s-14.png" />
     </p>
     <ul>
         <li>Click the <b>Success</b> link (highlighted in blue) to see the linear regression.</li>
     </ul>
     <p>
-        <img src="image-15.png" />
+        <img src="s-15.png" />
     </p>
     <ul>
         <li>Click the <b>Close</b> button.</li>
@@ -404,7 +404,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         provided that looks like this:
     </p>
     <p>
-        <img src="image-16.png" />
+        <img src="s-16.png" />
     </p>
     <p>
         Notice that with a <b>Min peptides per protein</b> filter of “1” the 13 proteins found in the FASTA file produce 9
@@ -419,14 +419,14 @@ <h1>Using the Import Peptide Search wizard</h1>
         Skyline begins extracting chromatograms:
     </p>
     <p>
-        <img src="image-17.png" />
+        <img src="s-17.png" />
     </p>
     <p class="keep-next">
         After the import is completed, Skyline will show you the mProphet model you requested on the <b>Import FASTA</b>
         page of the <b>Import Peptide Search</b> wizard. It should look like this:
     </p>
     <p>
-        <img src="image-18.png" />
+        <img src="s-18.png" />
     </p>
     <p>
         It has already been used to re-score the 10 best peaks Skyline found in each set of chromatograms, using its default score, and re-choose the
@@ -462,10 +462,10 @@ <h1>Inspect the data manually</h1>
     <table class="comp-fig">
         <tr>
             <td class="comp-fig" style="padding: 10px;">
-              <img src="image-19.png" />
+              <img src="s-19.png" />
             </td>
             <td class="comp-fig" style="padding: 10px;">
-              <img src="image-20.png" /> 
+              <img src="s-20.png" /> 
             </td>
         </tr>
     </table>
@@ -474,7 +474,7 @@ <h1>Inspect the data manually</h1>
             easily viewable, as below: </li>
     </ul>
     <p>
-        <img src="image-21.png" />
+        <img src="s-21.png" />
     </p>
     <ul>
         <li>Click on the first E. coli protein: “sp|P63284|CLPB_ECOLI”.</li>
@@ -495,7 +495,7 @@ <h1>Inspect the data manually</h1>
         You get specific information for this peptide in all of the views, as shown below:
     </p>
     <p>
-        <img src="image-22.png" />
+        <img src="s-22.png" />
     </p>
     <p>
         Examine the peak area patterns for the rest of the peptides belonging to this protein. Is the quantitative pattern for the peptides from this
@@ -520,7 +520,7 @@ <h1>Inspect the data manually</h1>
         Notice that if you hover the cursor over a chromatogram curve a circle appears on the curve with the same color as the curve.
     </p>
     <p>
-        <img src="image-23.png" />
+        <img src="s-23.png" />
     </p>
     <ul>
         <li>Click the circle on a chromatogram point.</li>
@@ -530,13 +530,13 @@ <h1>Inspect the data manually</h1>
         you selected.
     </p>
     <p>
-        <img src="image-24.png" />
+        <img src="s-24.png" />
     </p>
     <ul>
         <li>Click the magnifying glass button in the <b>Full-Scan</b> toolbar to view the full spectrum.</li>
     </ul>
     <p>
-        <img src="image-25.png" />
+        <img src="s-25.png" />
     </p>
     <p>
         Explore the data further manually (including some decoys).
@@ -555,7 +555,7 @@ <h1>Mass error and retention time deviation </h1>
         may want to widen your extraction windows. 
     </p>
     <p>
-        <img src="image-26.png" />
+        <img src="s-26.png" />
     </p>
     <p>
         Note that the distribution appears to have two peaks, one around 0 and one around 5. To understand this better, it helps to know that these are
@@ -588,7 +588,7 @@ <h1>Mass error and retention time deviation </h1>
                 Run</b>. </li>
     </ul>
     <p>
-        <img src="image-27.png" />
+        <img src="s-27.png" />
     </p>
     <ul>
         <li>Right-click the graph, choose <b>Plot</b>, and click <b>Residuals</b>.</li>
@@ -598,7 +598,7 @@ <h1>Mass error and retention time deviation </h1>
         optimized for this analysis? Check the decoys as well.
     </p>
     <p>
-        <img src="image-28.png" />
+        <img src="s-28.png" />
     </p>
     <p>
         <b>Note</b>: The spectral library for this analysis was constructed from the DIA-Umpire pseudo-DDA spectra. As such, the accuracy of
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-Umpire-TTOF/en/image-1.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-Umpire-TTOF/en/s-1.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-Umpire-TTOF/en/image-1.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA-Umpire-TTOF/en/s-1.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-Umpire-TTOF/en/image-10.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-Umpire-TTOF/en/s-10.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-Umpire-TTOF/en/image-10.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA-Umpire-TTOF/en/s-10.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-Umpire-TTOF/en/image-11.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-Umpire-TTOF/en/s-11.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-Umpire-TTOF/en/image-11.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA-Umpire-TTOF/en/s-11.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-Umpire-TTOF/en/image-12.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-Umpire-TTOF/en/s-12.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-Umpire-TTOF/en/image-12.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA-Umpire-TTOF/en/s-12.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-Umpire-TTOF/en/image-13.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-Umpire-TTOF/en/s-13.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-Umpire-TTOF/en/image-13.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA-Umpire-TTOF/en/s-13.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-Umpire-TTOF/en/image-14.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-Umpire-TTOF/en/s-14.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-Umpire-TTOF/en/image-14.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA-Umpire-TTOF/en/s-14.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-Umpire-TTOF/en/image-15.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-Umpire-TTOF/en/s-15.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-Umpire-TTOF/en/image-15.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA-Umpire-TTOF/en/s-15.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-Umpire-TTOF/en/image-16.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-Umpire-TTOF/en/s-16.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-Umpire-TTOF/en/image-16.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-Umpire-TTOF/en/image-17.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-Umpire-TTOF/en/s-17.png
similarity index 100%
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-Umpire-TTOF/en/image-18.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-Umpire-TTOF/en/s-18.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-Umpire-TTOF/en/image-18.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-Umpire-TTOF/en/image-19.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-Umpire-TTOF/en/s-19.png
similarity index 100%
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-Umpire-TTOF/en/image-2.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-Umpire-TTOF/en/s-2.png
similarity index 100%
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-Umpire-TTOF/en/image-20.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-Umpire-TTOF/en/s-20.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-Umpire-TTOF/en/image-20.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA-Umpire-TTOF/en/s-20.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-Umpire-TTOF/en/image-21.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-Umpire-TTOF/en/s-21.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-Umpire-TTOF/en/image-21.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-Umpire-TTOF/en/image-22.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-Umpire-TTOF/en/s-22.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-Umpire-TTOF/en/image-22.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-Umpire-TTOF/en/image-23.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-Umpire-TTOF/en/s-23.png
similarity index 100%
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-Umpire-TTOF/en/image-24.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-Umpire-TTOF/en/s-24.png
similarity index 100%
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-Umpire-TTOF/en/image-25.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-Umpire-TTOF/en/s-25.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-Umpire-TTOF/en/image-25.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-Umpire-TTOF/en/image-26.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-Umpire-TTOF/en/s-26.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-Umpire-TTOF/en/image-26.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-Umpire-TTOF/en/image-27.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-Umpire-TTOF/en/s-27.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-Umpire-TTOF/en/image-27.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-Umpire-TTOF/en/image-28.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-Umpire-TTOF/en/s-28.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-Umpire-TTOF/en/image-28.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-Umpire-TTOF/en/image-3.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-Umpire-TTOF/en/s-3.png
similarity index 100%
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-Umpire-TTOF/en/image-4.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-Umpire-TTOF/en/s-4.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-Umpire-TTOF/en/image-4.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-Umpire-TTOF/en/image-5.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-Umpire-TTOF/en/s-5.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-Umpire-TTOF/en/image-5.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA-Umpire-TTOF/en/s-5.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-Umpire-TTOF/en/image-6.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-Umpire-TTOF/en/s-6.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-Umpire-TTOF/en/image-6.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-Umpire-TTOF/en/image-7.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-Umpire-TTOF/en/s-7.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-Umpire-TTOF/en/image-7.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA-Umpire-TTOF/en/s-7.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-Umpire-TTOF/en/image-8.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-Umpire-TTOF/en/s-8.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-Umpire-TTOF/en/image-8.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA-Umpire-TTOF/en/s-8.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-Umpire-TTOF/en/image-9.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-Umpire-TTOF/en/s-9.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-Umpire-TTOF/en/image-9.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA-Umpire-TTOF/en/s-9.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA-Umpire-TTOF/en/image-0.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA-Umpire-TTOF/en/s-ttof-label-free-proteome-quantification.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA-Umpire-TTOF/en/image-0.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA-Umpire-TTOF/en/s-ttof-label-free-proteome-quantification.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA/en/index.html b/pwiz_tools/Skyline/Documentation/Tutorials/DIA/en/index.html
index 29dc5a7a03..f6fc8c8f64 100644
--- a/pwiz_tools/Skyline/Documentation/Tutorials/DIA/en/index.html
+++ b/pwiz_tools/Skyline/Documentation/Tutorials/DIA/en/index.html
@@ -154,7 +154,7 @@ <h1>Setting Up an Isolation Scheme for DIA</h1>
         The <b>Transition Settings</b> form should look something like this:
     </p>
     <p>
-        <img src="image-0.png" />
+        <img src="s-1.png" />
     </p>
     <table>
         <tr>
@@ -186,7 +186,7 @@ <h1>Setting Up an Isolation Scheme for DIA</h1>
         The <b>Edit Isolation Scheme</b> form should appear as follows:
     </p>
     <p>
-        <img src="image-1.png" />
+        <img src="s-2.png" />
     </p>
     <ul>
         <li>Choose <b>Prespecified isolation windows</b>.</li>
@@ -210,7 +210,7 @@ <h1>Setting Up an Isolation Scheme for DIA</h1>
         efficient at the borders<sup>3</sup>.
     </p>
     <p>
-        <img src="image-2.png" />
+        <img src="s-precursor-frequency-graph.png" />
     </p>
     <p class="fig-text">
         <b>Figure</b>: Histograms calculated from peptide precursors with charges 1-4 found in common libraries of observed peptides. The
@@ -219,7 +219,7 @@ <h1>Setting Up an Isolation Scheme for DIA</h1>
         “Optimal” Boundary indicate the optimize window placement boundaries in this range. (Courtesy of Brian Searle)
     </p>
     <p>
-        <img src="image-3.png" />
+        <img src="s-isolation-window-graphs.png" />
     </p>
     <p class="fig-text">
         Supplemental Figure S1 from Gillet, et al. MCP 2012: c) shows perfect rectangular isolation of the defined range, d) shows less ideal signal
@@ -237,7 +237,7 @@ <h1>Setting Up an Isolation Scheme for DIA</h1>
         The <b>Calculate Isolation Scheme</b> form should look like this:
     </p>
     <p>
-        <img src="image-4.png" />
+        <img src="s-3.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -249,7 +249,7 @@ <h1>Setting Up an Isolation Scheme for DIA</h1>
         The <b>Edit Isolation Scheme</b> form should look like this:
     </p>
     <p>
-        <img src="image-5.png" />
+        <img src="s-4.png" />
     </p>
     <p>
         Skyline also allows you to visualize the precursor <i>m/z</i> range isolations over time, to check that what you have entered is correct:
@@ -262,7 +262,7 @@ <h1>Setting Up an Isolation Scheme for DIA</h1>
         <i>m/z</i> on the x-axis:
     </p>
     <p>
-        <img src="image-6.png" />
+        <img src="s-5.png" />
     </p>
     <ul>
         <li>Click the <b>Close</b> button.</li>
@@ -288,7 +288,7 @@ <h1>Setting Up an Isolation Scheme for DIA</h1>
         The form should look like this:
     </p>
     <p>
-        <img src="image-7.png" />
+        <img src="s-6.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -300,7 +300,7 @@ <h1>Setting Up an Isolation Scheme for DIA</h1>
         Open the file you saved. It should look like this:
     </p>
     <p>
-        <img src="image-8.png" />
+        <img src="s-isolation-list-csv.png" />
     </p>
     <p>
         This isolation scheme is formatted for a Thermo Q Exactive (on which the data in this tutorial were acquired), but Skyline can also export to
@@ -338,7 +338,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         The <b>Import Peptide Search</b> wizard should appear looking like this:
     </p>
     <p>
-        <img src="image-9.png" />
+        <img src="s-7.png" />
     </p>
     <ul>
         <li>Click the <b>Add Files</b> button.</li>
@@ -370,7 +370,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         The <b>Spectral Library</b> page of the wizard should now look like this:
     </p>
     <p>
-        <img src="image-10.png" />
+        <img src="s-8.png" />
     </p>
     <ul>
         <li>Click <b>Next</b> to build a spectral library from these search results.</li>
@@ -389,7 +389,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         The <b>Browse for Results Files</b> form should look like this:
     </p>
     <p>
-        <img src="image-11.png" />
+        <img src="s-9.png" />
     </p>
     <ul>
         <li>Click the <b>Open</b> button.</li>
@@ -398,7 +398,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         The <b>Import Peptide Search</b> form should look like this:
     </p>
     <p>
-        <img src="image-12.png" />
+        <img src="s-10.png" />
     </p>
     <ul>
         <li>Click the <b>Next</b> button.</li>
@@ -414,7 +414,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         The <b>Import Results</b> form should now look like this:
     </p>
     <p>
-        <img src="image-13.png" />
+        <img src="s-11.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -431,7 +431,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         This brings you to the <b>Configure Transition Settings</b> page as shown below:
     </p>
     <p>
-        <img src="image-14.png" />
+        <img src="s-12.png" />
     </p>
     <p>
         You can use these default settings for this tutorial, but you could consider alternatives for your own data in the future.
@@ -462,7 +462,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         configured earlier, but make sure it looks like this:
     </p>
     <p>
-        <img src="image-15.png" />
+        <img src="s-13.png" />
     </p>
     <ul>
         <li>Click the <b>Next</b> button.</li>
@@ -480,7 +480,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         The form should now look like this:
     </p>
     <p>
-        <img src="image-16.png" />
+        <img src="s-14.png" />
     </p>
     <p>
         In this simple introduction with only 6 targeted proteins in the FASTA text you have just included, you will not use decoys or a dynamic peak
@@ -495,7 +495,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         transitions. For every protein, only the peptides that were present in the spectral library are included in this list.
     </p>
     <p>
-        <img src="image-17.png" />
+        <img src="s-15.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -517,7 +517,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         The <b>Targets</b> view should look like this:
     </p>
     <p>
-        <img src="image-18.png" />
+        <img src="s-16.png" />
     </p>
     <p>
         In DIA, it is possible to extract any set of product ions, because the instrument covers every possible precursor-product combination in the
@@ -555,7 +555,7 @@ <h1>Exploring DIA Results</h1>
         The Skyline window should look something like this:
     </p>
     <p>
-        <img src="image-19.png" />
+        <img src="s-17.png" />
     </p>
     <p>
         This is not a great example to start with. It makes things look much worse than they really are. You, as a human observer, can easily tell that
@@ -577,7 +577,7 @@ <h1>Exploring DIA Results</h1>
         this:
     </p>
     <p>
-        <img src="image-20.png" />
+        <img src="s-18.png" />
     </p>
     <p>
         As rules of thumb, you should be looking to see that:
@@ -617,7 +617,7 @@ <h1>Exploring DIA Results</h1>
         The Skyline window should now look something like this:
     </p>
     <p>
-        <img src="image-21.png" />
+        <img src="s-19.png" />
     </p>
     <p>
         Here are a few things to take note of:
@@ -644,7 +644,7 @@ <h1>Exploring DIA Results</h1>
         precursor ion intensities extracted from MS1 scans typically dwarf the product ion intensities extracted from MS/MS scans:
     </p>
     <p>
-        <img src="image-22.png" />
+        <img src="s-20.png" />
     </p>
     <table>
         <tr>
@@ -659,7 +659,7 @@ <h1>Exploring DIA Results</h1>
         The doubly charged precursor of the second peptide should now be selected, and the Skyline Window should look like this:
     </p>
     <p>
-        <img src="image-23.png" />
+        <img src="s-21.png" />
     </p>
     <p>
         All the metrics you were introduced to on the last peptide, mass error, idotp, and dotp, look even better for this precursor. You may feel you
@@ -684,10 +684,10 @@ <h1>Exploring DIA Results</h1>
     <table class="comp-fig">
         <tr>
             <td class="comp-fig">
-                <img src="image-24.png" />
+                <img src="s-22.png" />
             </td>
             <td class="comp-fig">
-                <img src="image-25.png" />
+                <img src="s-23.png" />
             </td>
         </tr>
     </table>
@@ -739,14 +739,14 @@ <h1>Exploring DIA Results</h1>
     </p>
     <ul>
         <li>Hover the mouse cursor over any of the black dashed lines indicating the right integration boundary until the cursor changes to a splitter
-            cursor (<img src="image-26.png" />) with arrows pointing left and right.</li>
+            cursor (<img src="../../shared/vertical-split-cursor-icon.png" />) with arrows pointing left and right.</li>
         <li>Click and drag the boundary to the desired location capturing the full peak.</li>
     </ul>
     <p class="keep-next">
         The plots for this peptide should now look like this:
     </p>
     <p>
-        <img src="image-27.png" />
+        <img src="s-24.png" />
     </p>
     <p>
         The combination of the cyan ID lines, the idotp of 0.99, and the dotp of 096 should give you high confidence in this peak assignment.
@@ -773,7 +773,7 @@ <h1>Understanding Extracted Chromatograms</h1>
         in the MS1 chromatograms.
     </p>
     <p>
-        <img src="image-28.png" />
+        <img src="s-25.png" />
     </p>
     <p>
         You can get a sense of scale in intensity (ions per second) by looking at the <b>Peak Areas</b> plots where the precurors (MS1) total
@@ -796,7 +796,7 @@ <h1>Understanding Extracted Chromatograms</h1>
     </ul>
     <p>
         Skyline will show the <b>Full Scan</b> view displaying a range of the MS1 scan from which the precursor chromatogram points were
-        extracted. You could see the entire MS1 scan by clicking on the button with the magnifying glass and a plus (<img src="image-29.png" />) in
+        extracted. You could see the entire MS1 scan by clicking on the button with the magnifying glass and a plus (<img src="../../shared/magnifying-glass-icon.png" />) in
         the upper right corner of the view. Instead, do the following:
     </p>
     <ul>
@@ -807,7 +807,7 @@ <h1>Understanding Extracted Chromatograms</h1>
         The <b>Full Scan</b> graph should now look something like this:
     </p>
     <p>
-        <img src="image-30.png" />
+        <img src="s-26.png" />
     </p>
     <p>
         The intensities in the centroid-mode peaks are shown as sticks. Intensities that were used to create the points on the chromatograms are
@@ -817,7 +817,7 @@ <h1>Understanding Extracted Chromatograms</h1>
         targeted peptide. Its monoisotopic peak is very close to the M+1 of target.
     </p>
     <ul>
-        <li>Now use the arrow buttons (<img src="image-31.png" />) in the <b>Full Scan</b> view toolbar to review scans between this one and
+        <li>Now use the arrow buttons (<img src="../../shared/arrow-buttons.png" />) in the <b>Full Scan</b> view toolbar to review scans between this one and
             the one that produced the apex of the integrated peak.</li>
     </ul>
     <p>
@@ -836,7 +836,7 @@ <h1>Understanding Extracted Chromatograms</h1>
         You should see a graph in the <b>Full Scan</b> view that looks like this:
     </p>
     <p>
-        <img src="image-32.png" />
+        <img src="s-27.png" />
     </p>
     <p>
         You can see the MS/MS peak that contributed the point to the chromatogram you just clicked on highlighted in aqua and annotated y10. The fact
@@ -849,7 +849,7 @@ <h1>Understanding Extracted Chromatograms</h1>
         You should see a spectrum like plot like this one:
     </p>
     <p>
-        <img src="image-33.png" />
+        <img src="s-28.png" />
     </p>
     <p>
         Again, you can see the tallest peak in a series highlighted and annotated, with the following peaks in the series 0.5 <i>m/z</i> apart,
@@ -871,7 +871,7 @@ <h2>Understanding how interference produces signal dropout</h2>
         <li>Hover the mouse cursor over the apex of the “precursor” peak in the “Pit02” replicate until you see a blue circle appear, and the mouse
             cursor change to a pointing hand.</li>
         <li>Click in the circle.</li>
-        <li>Use the right arrow button (<img src="image-34.png" />) in the <b>Full Scan</b> view toolbar to review the MS1 spectra until you
+        <li>Use the right arrow button (<img src="../../shared/right-arrow-button.png" />) in the <b>Full Scan</b> view toolbar to review the MS1 spectra until you
             reach 41.7 minutes.</li>
     </ul>
     <p>
@@ -881,19 +881,19 @@ <h2>Understanding how interference produces signal dropout</h2>
         By 41.67 minutes it is the largest peak:
     </p>
     <p>
-        <img src="image-35.png" />
+        <img src="s-29.png" />
     </p>
     <p>
         At 41.68 minutes, you can see the extracted peaks shift left in m/z:
     </p>
     <p>
-        <img src="image-36.png" />
+        <img src="s-30.png" />
     </p>
     <p>
         And at 41.70 minutes, they have shifted out of the +/- 20 ppm extraction ranges:
     </p>
     <p>
-        <img src="image-37.png" />
+        <img src="s-31.png" />
     </p>
     <p>
         Extraction from centroided MS/MS spectra for DIA, especially on Thermo Orbitrap instruments, has proven more reliable in broad statistical
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA/ja/index.html b/pwiz_tools/Skyline/Documentation/Tutorials/DIA/ja/index.html
index 9aa58a29d9..630f102d8e 100644
--- a/pwiz_tools/Skyline/Documentation/Tutorials/DIA/ja/index.html
+++ b/pwiz_tools/Skyline/Documentation/Tutorials/DIA/ja/index.html
@@ -126,7 +126,7 @@ <h1>DIAの単離スキームの設定</h1>
         [ <b>トランジションの設定</b> ] フォームは以下のようになります。
     </p>
     <p>
-        <img src="image-0.png" />
+        <img src="s-1.png" />
     </p>
     <table>
         <tr>
@@ -152,7 +152,7 @@ <h1>DIAの単離スキームの設定</h1>
         次のような [ <b>単離スキームを編集</b> ] フォームが表示されます。
     </p>
     <p>
-        <img src="image-1.png" />
+        <img src="s-2.png" />
     </p>
     <ul>
         <li>[ <b>事前に指定した単離ウィンドウ</b> ] を選択します。</li>
@@ -174,14 +174,14 @@ <h1>DIAの単離スキームの設定</h1>
         m/z）必要が少なくなります<sup>3</sup>。
     </p>
     <p>
-        <img src="image-2.png" />
+        <img src="s-precursor-frequency-graph.png" />
     </p>
     <p class="fig-text">
         <b>図：</b>観測されるペプチドの共通ライブラリで見られる1価から4価のペプチドプリカーサーから計算したヒストグラム。一番高いピークは1価から4価のプリカーサーを表し、2番目に高いピークは2価と4価のプリカーサー、そしてさらに小さなピークが3価のみのプリカーサーを表し、4価のみのプリカーサーは3価のみのピークの小さな肩程度にしか現れません。「最適」境界と記されている縦の線は、この範囲での最適化ウィンドウ配置境界を示しています。（Brian
         Searleのご厚意により提供）
     </p>
     <p>
-        <img src="image-3.png" />
+        <img src="s-isolation-window-graphs.png" />
     </p>
     <p class="fig-text">
         Gillet, et al. MCP 2012よりの補足図S1：c) は定義された範囲の完璧な長方形単離を示し、d) は定義された四重極単離範囲のエッジでの0.5 m/zにわたるあまり理想的ではない信号ドロップオフを示し、e) とf)
@@ -195,7 +195,7 @@ <h1>DIAの単離スキームの設定</h1>
         [ <b>単離スキームを計算</b> ] フォームは以下のようになります。
     </p>
     <p>
-        <img src="image-4.png" />
+        <img src="s-3.png" />
     </p>
     <ul>
         <li>[ <b>OK</b> ] ボタンをクリックします。</li>
@@ -207,7 +207,7 @@ <h1>DIAの単離スキームの設定</h1>
         [ <b>単離スキームを編集</b> ] フォームは以下のようになります。
     </p>
     <p>
-        <img src="image-5.png" />
+        <img src="s-4.png" />
     </p>
     <p>
         また、Skylineでは、入力した内容が正しいか確認するために、プリカーサー<i>m/z</i>範囲の単離を経時的に視覚化できます。
@@ -219,7 +219,7 @@ <h1>DIAの単離スキームの設定</h1>
         Y軸をサイクル/時間、X軸を<i>m/z</i>にした、経時的な単離ウィンドウのサイクルのグラフが表示されるはずです。
     </p>
     <p>
-        <img src="image-6.png" />
+        <img src="s-5.png" />
     </p>
     <ul>
         <li>[ <b>閉じる</b> ] ボタンをクリックします。</li>
@@ -244,7 +244,7 @@ <h1>DIAの単離スキームの設定</h1>
         フォームは以下のようになります。
     </p>
     <p>
-        <img src="image-7.png" />
+        <img src="s-6.png" />
     </p>
     <ul>
         <li>[ <b>OK</b> ] ボタンをクリックします。</li>
@@ -256,7 +256,7 @@ <h1>DIAの単離スキームの設定</h1>
         保存したファイルを開きます。これは以下のようになります。
     </p>
     <p>
-        <img src="image-8.png" />
+        <img src="s-isolation-list-csv.png" />
     </p>
     <p>
         この単離スキームは、（このチュートリアルのデータが取得された）Thermo Q Exactive用にフォーマットされていますが、Skylineでは他の複数の装置タイプにエクスポートすることも可能です。
@@ -288,7 +288,7 @@ <h1>ペプチド検索のインポートウィザードの使用</h1>
         以下のような<b>ペプチド検索のインポート</b>ウィザードが表示されます。
     </p>
     <p>
-        <img src="image-9.png" />
+        <img src="s-7.png" />
     </p>
     <p>
         このデータセットでは、[ <b>カットオフスコア</b> ]
@@ -315,7 +315,7 @@ <h1>ペプチド検索のインポートウィザードの使用</h1>
         ウィザードの [ <b>スペクトルライブラリ</b> ] ページは以下のようになります。
     </p>
     <p>
-        <img src="image-10.png" />
+        <img src="s-8.png" />
     </p>
     <ul>
         <li>[ <b>次へ</b> ] をクリックしてこれらの検索結果からスペクトルライブラリを構築します。</li>
@@ -332,7 +332,7 @@ <h1>ペプチド検索のインポートウィザードの使用</h1>
         [ <b>結果ファイルを参照</b> ] フォームは以下のようになります。
     </p>
     <p>
-        <img src="image-11.png" />
+        <img src="s-9.png" />
     </p>
     <ul>
         <li>[ <b>開く</b> ] ボタンをクリックします。</li>
@@ -341,7 +341,7 @@ <h1>ペプチド検索のインポートウィザードの使用</h1>
         <b>ペプチド検索のインポート</b>フォームは以下のようになります。
     </p>
     <p>
-        <img src="image-12.png" />
+        <img src="s-10.png" />
     </p>
     <ul>
         <li>[ <b>次へ</b> ] ボタンをクリックします。</li>
@@ -356,7 +356,7 @@ <h1>ペプチド検索のインポートウィザードの使用</h1>
         [ <b>結果をインポート</b> ] フォームは以下のようになります。
     </p>
     <p>
-        <img src="image-13.png" />
+        <img src="s-11.png" />
     </p>
     <ul>
         <li>[ <b>OK</b> ] ボタンをクリックします。</li>
@@ -372,7 +372,7 @@ <h1>ペプチド検索のインポートウィザードの使用</h1>
         以下のような [ <b>トランジション設定を行う</b> ] ページに移動します。
     </p>
     <p>
-        <img src="image-14.png" />
+        <img src="s-12.png" />
     </p>
     <p>
         このチュートリアルのデフォルト設定を使用することもできますが、今後の自分のデータに合った選択肢を考えるのもいいでしょう。
@@ -399,7 +399,7 @@ <h1>ペプチド検索のインポートウィザードの使用</h1>
         [ <b>フルスキャン設定を行う</b> ] ページに移動します。このページには、先ほど行った設定と同じものが表示されますが、以下のようになっていることを確認してください。
     </p>
     <p>
-        <img src="image-15.png" />
+        <img src="s-13.png" />
     </p>
     <ul>
         <li>[ <b>次へ</b> ] ボタンをクリックします。</li>
@@ -416,7 +416,7 @@ <h1>ペプチド検索のインポートウィザードの使用</h1>
         フォームは以下のようになります。
     </p>
     <p>
-        <img src="image-16.png" />
+        <img src="s-14.png" />
     </p>
     <p>
         今FASTAテキストに6個のターゲットタンパク質だけを含めたこの簡単な導入では、デコイやmProphetアルゴリズムで生成された動的ピーク選択モデルは使用しません。これらのオプションについての詳細は、<a
@@ -430,7 +430,7 @@ <h1>ペプチド検索のインポートウィザードの使用</h1>
         Skylineがタンパク質を6個、ペプチドを21個追加するというフォームを表示します。これによって25個のプリカーサーと225個のトランジションが対象となります。どのタンパク質でも、スペクトルライブラリに存在していたペプチドのみがこのリストに含まれます。
     </p>
     <p>
-        <img src="image-17.png" />
+        <img src="s-15.png" />
     </p>
     <ul>
         <li>[ <b>OK</b> ] ボタンをクリックします。</li>
@@ -449,7 +449,7 @@ <h1>ペプチド検索のインポートウィザードの使用</h1>
         [ <b>ターゲット</b> ] ビューは以下のようになります。
     </p>
     <p>
-        <img src="image-18.png" />
+        <img src="s-16.png" />
     </p>
     <p>
         DIAでは、装置が500-900
@@ -478,7 +478,7 @@ <h1>DIA結果の調査</h1>
         Skylineウィンドウは以下のようになります。
     </p>
     <p>
-        <img src="image-19.png" />
+        <img src="s-17.png" />
     </p>
     <p>
         これはここから始めるのに適した例ではありません。実際よりもずっと悪いように見えてしまいます。人間の観察者として、ユーザーはピーク積分境界に調整が必要なことがすぐにわかります。これはおそらくSkylineがフラグメントのクロマトグラムに基づいて積分境界を選択するためだと思われます。よく見てみると、信号がX軸まで落ちているところがあるのがわかります。セントロイド化されたデータでは、これは通常、先ほど+/-
@@ -495,7 +495,7 @@ <h1>DIA結果の調査</h1>
         もっと多くのターゲットがあるドキュメントでは、各ペプチドプリカーサーに対して強度が最も高いトランジションのみを使用して質量誤差分布を把握します。この2番目のステップは不要かも知れませんが、この場合は分布がわかりやすくなり、以下のようになります。
     </p>
     <p>
-        <img src="image-20.png" />
+        <img src="s-18.png" />
     </p>
     <p>
         経験則として、以下を確認します。
@@ -530,7 +530,7 @@ <h1>DIA結果の調査</h1>
         これでSkylineウィンドウは以下のようになります。
     </p>
     <p>
-        <img src="image-21.png" />
+        <img src="s-19.png" />
     </p>
     <p>
         ここでは以下に注意します。
@@ -553,7 +553,7 @@ <h1>DIA結果の調査</h1>
         荷電状態が複数ある場合には、トランジション分割表示が電荷状態で分割され、イオンタイプでは分割されないことがわかります。また、MS1スキャンから抽出されたプリカーサーイオン強度は、通常MS/MSスキャンから抽出されたプロダクトイオン強度を小さく見せることもわかります。
     </p>
     <p>
-        <img src="image-22.png" />
+        <img src="s-20.png" />
     </p>
     <table>
         <tr>
@@ -568,7 +568,7 @@ <h1>DIA結果の調査</h1>
         これで2つ目のペプチドの2価のプリカーサーが選択され、Skylineウィンドウは以下のようになります。
     </p>
     <p>
-        <img src="image-23.png" />
+        <img src="s-21.png" />
     </p>
     <p>
         最後のペプチド、質量誤差、idotp、dotpに関して導入されたすべての測定は、このプリカーサーでは向上しているように見えます。特に「Pit02」内のピークに対しては、別の積分境界を選択したいと思うかも知れません。別の積分境界を選択し、その後Skylineの [ 元に戻す/やり直し]
@@ -590,10 +590,10 @@ <h1>DIA結果の調査</h1>
     <table class="comp-fig">
         <tr>
             <td class="comp-fig">
-                <img src="image-24.png" />
+                <img src="s-22.png" />
             </td>
             <td class="comp-fig">
-                <img src="image-25.png" />
+                <img src="s-23.png" />
             </td>
         </tr>
     </table>
@@ -633,14 +633,14 @@ <h1>DIA結果の調査</h1>
         192]までは優れたものに見えます。このペプチドのピークは、幅が1分にわたり、あまりガウス形状とは言えません。Skylineは、両ピークに誤って正しい積分境界を与えているため、ピークが2/3しかカバーされていません。これを修正するには、以下の操作を行います。
     </p>
     <ul>
-        <li>正しい積分境界を示す黒の点線の上にマウスカーソルを合わせると、カーソルが左右の矢印のあるスプリッターカーソル (<img src="image-26.png" />) に変わります。</li>
+        <li>正しい積分境界を示す黒の点線の上にマウスカーソルを合わせると、カーソルが左右の矢印のあるスプリッターカーソル (<img src="../../shared/vertical-split-cursor-icon.png" />) に変わります。</li>
         <li>ピーク全体がカバーされるように境界を好きな場所にクリックアンドドラッグします。</li>
     </ul>
     <p class="keep-next">
         このペプチドのプロットは、以下のようになります。
     </p>
     <p>
-        <img src="image-27.png" />
+        <img src="s-24.png" />
     </p>
     <p>
         青緑色のIDライン、idotp 0.99、そしてdotp 096の組み合わせにより、このピークの割り当てにはかなりの信頼性があります。
@@ -662,7 +662,7 @@ <h1>抽出されたクロマトグラムの理解</h1>
         どちらのプリカーサーにも、うまく共溶出しているフラグメントイオンのクロマトグラムがあり、明白な干渉はありません。また、どちらもMS1クロマトグラムの左側で明白な干渉を示しています。
     </p>
     <p>
-        <img src="image-28.png" />
+        <img src="s-25.png" />
     </p>
     <p>
         <b>ピーク面積</b>プロットを見ると、強度の規模（イオン個数/秒）が把握できます。ここでプリカーサー (MS1) は総数100万近く、プロダクト (MS/MS)
@@ -682,7 +682,7 @@ <h1>抽出されたクロマトグラムの理解</h1>
         <li>丸の中をクリックします。</li>
     </ul>
     <p>
-        Skylineは、プリカーサークロマトグラムの点が抽出された幅広いMS1スキャンを表示する<b>フルスキャン</b>ビューを表示します。虫眼鏡のボタンをクリックし、ビューの右上角にあるプラス (<img src="image-29.png" />)
+        Skylineは、プリカーサークロマトグラムの点が抽出された幅広いMS1スキャンを表示する<b>フルスキャン</b>ビューを表示します。虫眼鏡のボタンをクリックし、ビューの右上角にあるプラス (<img src="../../shared/magnifying-glass-icon.png" />)
         をクリックするとMS1スキャン全体が見えるようになります。代わりに、以下の操作を行います。
     </p>
     <ul>
@@ -692,13 +692,13 @@ <h1>抽出されたクロマトグラムの理解</h1>
         <b>フルスキャン</b>グラフは以下のようになります。
     </p>
     <p>
-        <img src="image-30.png" />
+        <img src="s-26.png" />
     </p>
     <p>
         セントロイドモードピークの強度は棒のようになります。クロマトグラフで点を形成していた強度は、クロマトグラムの色で強調表示され、抽出範囲は影付き領域として表示されます。抽出されていなかったM+3およびM+4ピークが影付きピークの右側にあるのが見えます。また、干渉しているピークの頂点を形成していたスペクトルが、このプリカーサーの積分されたピークの左側に表示されています。ターゲットペプチドよりも1ダルトン重い2価のプリカーサーの同位体分布全体が見られます。モノアイソトピックピークは、ターゲットのM+1に非常に近くなっています。
     </p>
     <ul>
-        <li>今度は矢印ボタン（<img src="image-31.png" />、<b>フルスキャン</b>ビューのツールバー内）を使って、これと積分されたピークの頂点を形成していたものとの間にあるスキャンを確認します。</li>
+        <li>今度は矢印ボタン（<img src="../../shared/arrow-buttons.png" />、<b>フルスキャン</b>ビューのツールバー内）を使って、これと積分されたピークの頂点を形成していたものとの間にあるスキャンを確認します。</li>
     </ul>
     <p>
         70.56分には、ターゲットモノアイソトピックフィルタ範囲にあるピークを含む最初のMS1スペクトルが青色で強調表示されます。70.67分までは、モノアイソトピックピークが最も高い最初のMS1スペクトルは見えません。
@@ -714,7 +714,7 @@ <h1>抽出されたクロマトグラムの理解</h1>
         <b>フルスキャン</b>ビュー内のグラフが以下のように表示されます。
     </p>
     <p>
-        <img src="image-32.png" />
+        <img src="s-27.png" />
     </p>
     <p>
         今クリックしたクロマトグラムの点となったMS/MSピークが水色で強調表示され、y10と注釈が付くことがわかります。同位体ピークは1 m/zずつ離れていることからも、これらが1価のイオンからによるものであるという確信が持てます。
@@ -726,7 +726,7 @@ <h1>抽出されたクロマトグラムの理解</h1>
         以下のようなスペクトルプロットが表示されます。
     </p>
     <p>
-        <img src="image-33.png" />
+        <img src="s-28.png" />
     </p>
     <p>
         ここでも、一連の中で一番高いピークが強調表示されて注釈が付きます。そのうち、以下のピークは0.5
@@ -744,7 +744,7 @@ <h2>干渉がどのように信号ドロップアウトを生成するかの理
         <li>K.ELVYETVR.V ペプチドをクリックします。（[ <b>ターゲット</b> ] ビューの3番目）</li>
         <li>「Pit02」繰り返し測定の「プリカーサー」ピークの頂点にマウスを合わせます。青い丸が表示され、マウスカーソルが指差ししている手に変わります。</li>
         <li>丸の中をクリックします。</li>
-        <li>右矢印ボタン（<img src="image-34.png" />、<b>フルスキャン</b>ビューのツールバー内）を使って、41.7分のところまでMS1スペクトルを確認します。</li>
+        <li>右矢印ボタン（<img src="../../shared/right-arrow-button.png" />、<b>フルスキャン</b>ビューのツールバー内）を使って、41.7分のところまでMS1スペクトルを確認します。</li>
     </ul>
     <p>
         時間が経つほど、M-1（モノアイソトピックプリカーサーの左）にあるピークが強くなっていくのがわかります。
@@ -753,19 +753,19 @@ <h2>干渉がどのように信号ドロップアウトを生成するかの理
         41.67分には、最大のピークとなります。
     </p>
     <p>
-        <img src="image-35.png" />
+        <img src="s-29.png" />
     </p>
     <p class="keep-next">
         41.68分で、抽出されたピークのm/zが左にシフトするのがわかります。
     </p>
     <p class="keep-next">
-        <img src="image-36.png" />
+        <img src="s-30.png" />
     </p>
     <p>
         そして41.70分では、+/- 20 ppmの抽出範囲を超えてシフトしています。
     </p>
     <p>
-        <img src="image-37.png" />
+        <img src="s-31.png" />
     </p>
     <p>
         DIAのセントロイド化されたMS/MSスペクトルからの抽出は、特にThermo
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA/ja/invariant.html b/pwiz_tools/Skyline/Documentation/Tutorials/DIA/ja/invariant.html
index 78cae0b16c..fcca7b0594 100644
--- a/pwiz_tools/Skyline/Documentation/Tutorials/DIA/ja/invariant.html
+++ b/pwiz_tools/Skyline/Documentation/Tutorials/DIA/ja/invariant.html
@@ -154,7 +154,7 @@ <h1>Setting Up an Isolation Scheme for DIA</h1>
         The <b>Transition Settings</b> form should look something like this:
     </p>
     <p>
-        <img src="image-0.png" />
+        <img src="s-1.png" />
     </p>
     <table>
         <tr>
@@ -186,7 +186,7 @@ <h1>Setting Up an Isolation Scheme for DIA</h1>
         The <b>Edit Isolation Scheme</b> form should appear as follows:
     </p>
     <p>
-        <img src="image-1.png" />
+        <img src="s-2.png" />
     </p>
     <ul>
         <li>Choose <b>Prespecified isolation windows</b>.</li>
@@ -210,7 +210,7 @@ <h1>Setting Up an Isolation Scheme for DIA</h1>
         efficient at the borders<sup>3</sup>.
     </p>
     <p>
-        <img src="image-2.png" />
+        <img src="s-precursor-frequency-graph.png" />
     </p>
     <p class="fig-text">
         <b>Figure</b>: Histograms calculated from peptide precursors with charges 1-4 found in common libraries of observed peptides. The
@@ -219,7 +219,7 @@ <h1>Setting Up an Isolation Scheme for DIA</h1>
         “Optimal” Boundary indicate the optimize window placement boundaries in this range. (Courtesy of Brian Searle)
     </p>
     <p>
-        <img src="image-3.png" />
+        <img src="s-isolation-window-graphs.png" />
     </p>
     <p class="fig-text">
         Supplemental Figure S1 from Gillet, et al. MCP 2012: c) shows perfect rectangular isolation of the defined range, d) shows less ideal signal
@@ -237,7 +237,7 @@ <h1>Setting Up an Isolation Scheme for DIA</h1>
         The <b>Calculate Isolation Scheme</b> form should look like this:
     </p>
     <p>
-        <img src="image-4.png" />
+        <img src="s-3.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -249,7 +249,7 @@ <h1>Setting Up an Isolation Scheme for DIA</h1>
         The <b>Edit Isolation Scheme</b> form should look like this:
     </p>
     <p>
-        <img src="image-5.png" />
+        <img src="s-4.png" />
     </p>
     <p>
         Skyline also allows you to visualize the precursor <i>m/z</i> range isolations over time, to check that what you have entered is correct:
@@ -262,7 +262,7 @@ <h1>Setting Up an Isolation Scheme for DIA</h1>
         <i>m/z</i> on the x-axis:
     </p>
     <p>
-        <img src="image-6.png" />
+        <img src="s-5.png" />
     </p>
     <ul>
         <li>Click the <b>Close</b> button.</li>
@@ -288,7 +288,7 @@ <h1>Setting Up an Isolation Scheme for DIA</h1>
         The form should look like this:
     </p>
     <p>
-        <img src="image-7.png" />
+        <img src="s-6.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -300,7 +300,7 @@ <h1>Setting Up an Isolation Scheme for DIA</h1>
         Open the file you saved. It should look like this:
     </p>
     <p>
-        <img src="image-8.png" />
+        <img src="s-isolation-list-csv.png" />
     </p>
     <p>
         This isolation scheme is formatted for a Thermo Q Exactive (on which the data in this tutorial were acquired), but Skyline can also export to
@@ -338,7 +338,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         The <b>Import Peptide Search</b> wizard should appear looking like this:
     </p>
     <p>
-        <img src="image-9.png" />
+        <img src="s-7.png" />
     </p>
     <p>
         For this data set a <b>Cut-off score</b> field set to “0.95” means peptide spectrum matches with a PeptideProphet score of 0.95 or
@@ -372,7 +372,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         The <b>Spectral Library</b> page of the wizard should now look like this:
     </p>
     <p>
-        <img src="image-10.png" />
+        <img src="s-8.png" />
     </p>
     <ul>
         <li>Click <b>Next</b> to build a spectral library from these search results.</li>
@@ -391,7 +391,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         The <b>Browse for Results Files</b> form should look like this:
     </p>
     <p>
-        <img src="image-11.png" />
+        <img src="s-9.png" />
     </p>
     <ul>
         <li>Click the <b>Open</b> button.</li>
@@ -400,7 +400,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         The <b>Import Peptide Search</b> form should look like this:
     </p>
     <p>
-        <img src="image-12.png" />
+        <img src="s-10.png" />
     </p>
     <ul>
         <li>Click the <b>Next</b> button.</li>
@@ -416,7 +416,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         The <b>Import Results</b> form should now look like this:
     </p>
     <p>
-        <img src="image-13.png" />
+        <img src="s-11.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -433,7 +433,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         This brings you to the <b>Configure Transition Settings</b> page as shown below:
     </p>
     <p>
-        <img src="image-14.png" />
+        <img src="s-12.png" />
     </p>
     <p>
         You can use these default settings for this tutorial, but you could consider alternatives for your own data in the future.
@@ -464,7 +464,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         configured earlier, but make sure it looks like this:
     </p>
     <p>
-        <img src="image-15.png" />
+        <img src="s-13.png" />
     </p>
     <ul>
         <li>Click the <b>Next</b> button.</li>
@@ -482,7 +482,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         The form should now look like this:
     </p>
     <p>
-        <img src="image-16.png" />
+        <img src="s-14.png" />
     </p>
     <p>
         In this simple introduction with only 6 targeted proteins in the FASTA text you have just included, you will not use decoys or a dynamic peak
@@ -497,7 +497,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         transitions. For every protein, only the peptides that were present in the spectral library are included in this list.
     </p>
     <p>
-        <img src="image-17.png" />
+        <img src="s-15.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -519,7 +519,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         The <b>Targets</b> view should look like this:
     </p>
     <p>
-        <img src="image-18.png" />
+        <img src="s-16.png" />
     </p>
     <p>
         In DIA, it is possible to extract any set of product ions, because the instrument covers every possible precursor-product combination in the
@@ -557,7 +557,7 @@ <h1>Exploring DIA Results</h1>
         The Skyline window should look something like this:
     </p>
     <p>
-        <img src="image-19.png" />
+        <img src="s-17.png" />
     </p>
     <p>
         This is not a great example to start with. It makes things look much worse than they really are. You, as a human observer, can easily tell that
@@ -579,7 +579,7 @@ <h1>Exploring DIA Results</h1>
         this:
     </p>
     <p>
-        <img src="image-20.png" />
+        <img src="s-18.png" />
     </p>
     <p>
         As rules of thumb, you should be looking to see that:
@@ -619,7 +619,7 @@ <h1>Exploring DIA Results</h1>
         The Skyline window should now look something like this:
     </p>
     <p>
-        <img src="image-21.png" />
+        <img src="s-19.png" />
     </p>
     <p>
         Here are a few things to take note of:
@@ -646,7 +646,7 @@ <h1>Exploring DIA Results</h1>
         precursor ion intensities extracted from MS1 scans typically dwarf the product ion intensities extracted from MS/MS scans:
     </p>
     <p>
-        <img src="image-22.png" />
+        <img src="s-20.png" />
     </p>
     <table>
         <tr>
@@ -661,7 +661,7 @@ <h1>Exploring DIA Results</h1>
         The doubly charged precursor of the second peptide should now be selected, and the Skyline Window should look like this:
     </p>
     <p>
-        <img src="image-23.png" />
+        <img src="s-21.png" />
     </p>
     <p>
         All the metrics you were introduced to on the last peptide, mass error, idotp, and dotp, look even better for this precursor. You may feel you
@@ -686,10 +686,10 @@ <h1>Exploring DIA Results</h1>
     <table class="comp-fig">
         <tr>
             <td class="comp-fig">
-                <img src="image-24.png" />
+                <img src="s-22.png" />
             </td>
             <td class="comp-fig">
-                <img src="image-25.png" />
+                <img src="s-23.png" />
             </td>
         </tr>
     </table>
@@ -741,14 +741,14 @@ <h1>Exploring DIA Results</h1>
     </p>
     <ul>
         <li>Hover the mouse cursor over any of the black dashed lines indicating the right integration boundary until the cursor changes to a splitter
-            cursor (<img src="image-26.png" />) with arrows pointing left and right.</li>
+            cursor (<img src="../../shared/vertical-split-cursor-icon.png" />) with arrows pointing left and right.</li>
         <li>Click and drag the boundary to the desired location capturing the full peak.</li>
     </ul>
     <p class="keep-next">
         The plots for this peptide should now look like this:
     </p>
     <p>
-        <img src="image-27.png" />
+        <img src="s-24.png" />
     </p>
     <p>
         The combination of the cyan ID lines, the idotp of 0.99, and the dotp of 096 should give you high confidence in this peak assignment.
@@ -775,7 +775,7 @@ <h1>Understanding Extracted Chromatograms</h1>
         in the MS1 chromatograms.
     </p>
     <p>
-        <img src="image-28.png" />
+        <img src="s-25.png" />
     </p>
     <p>
         You can get a sense of scale in intensity (ions per second) by looking at the <b>Peak Areas</b> plots where the precurors (MS1) total
@@ -798,7 +798,7 @@ <h1>Understanding Extracted Chromatograms</h1>
     </ul>
     <p>
         Skyline will show the <b>Full Scan</b> view displaying a range of the MS1 scan from which the precursor chromatogram points were
-        extracted. You could see the entire MS1 scan by clicking on the button with the magnifying glass and a plus (<img src="image-29.png" />) in
+        extracted. You could see the entire MS1 scan by clicking on the button with the magnifying glass and a plus (<img src="../../shared/magnifying-glass-icon.png" />) in
         the upper right corner of the view. Instead, do the following:
     </p>
     <ul>
@@ -809,7 +809,7 @@ <h1>Understanding Extracted Chromatograms</h1>
         The <b>Full Scan</b> graph should now look something like this:
     </p>
     <p>
-        <img src="image-30.png" />
+        <img src="s-26.png" />
     </p>
     <p>
         The intensities in the centroid-mode peaks are shown as sticks. Intensities that were used to create the points on the chromatograms are
@@ -819,7 +819,7 @@ <h1>Understanding Extracted Chromatograms</h1>
         targeted peptide. Its monoisotopic peak is very close to the M+1 of target.
     </p>
     <ul>
-        <li>Now use the arrow buttons (<img src="image-31.png" />) in the <b>Full Scan</b> view toolbar to review scans between this one and
+        <li>Now use the arrow buttons (<img src="../../shared/arrow-buttons.png" />) in the <b>Full Scan</b> view toolbar to review scans between this one and
             the one that produced the apex of the integrated peak.</li>
     </ul>
     <p>
@@ -838,7 +838,7 @@ <h1>Understanding Extracted Chromatograms</h1>
         You should see a graph in the <b>Full Scan</b> view that looks like this:
     </p>
     <p>
-        <img src="image-32.png" />
+        <img src="s-27.png" />
     </p>
     <p>
         You can see the MS/MS peak that contributed the point to the chromatogram you just clicked on highlighted in aqua and annotated y10. The fact
@@ -851,7 +851,7 @@ <h1>Understanding Extracted Chromatograms</h1>
         You should see a spectrum like plot like this one:
     </p>
     <p>
-        <img src="image-33.png" />
+        <img src="s-28.png" />
     </p>
     <p>
         Again, you can see the tallest peak in a series highlighted and annotated, with the following peaks in the series 0.5 <i>m/z</i> apart,
@@ -873,7 +873,7 @@ <h2>Understanding how interference produces signal dropout</h2>
         <li>Hover the mouse cursor over the apex of the “precursor” peak in the “Pit02” replicate until you see a blue circle appear, and the mouse
             cursor change to a pointing hand.</li>
         <li>Click in the circle.</li>
-        <li>Use the right arrow button (<img src="image-34.png" />) in the <b>Full Scan</b> view toolbar to review the MS1 spectra until you
+        <li>Use the right arrow button (<img src="../../shared/right-arrow-button.png" />) in the <b>Full Scan</b> view toolbar to review the MS1 spectra until you
             reach 41.7 minutes.</li>
     </ul>
     <p>
@@ -883,19 +883,19 @@ <h2>Understanding how interference produces signal dropout</h2>
         By 41.67 minutes it is the largest peak:
     </p>
     <p>
-        <img src="image-35.png" />
+        <img src="s-29.png" />
     </p>
     <p>
         At 41.68 minutes, you can see the extracted peaks shift left in m/z:
     </p>
     <p>
-        <img src="image-36.png" />
+        <img src="s-30.png" />
     </p>
     <p>
         And at 41.70 minutes, they have shifted out of the +/- 20 ppm extraction ranges:
     </p>
     <p>
-        <img src="image-37.png" />
+        <img src="s-31.png" />
     </p>
     <p>
         Extraction from centroided MS/MS spectra for DIA, especially on Thermo Orbitrap instruments, has proven more reliable in broad statistical
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similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA/ja/image-10.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA/ja/s-8.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA/ja/image-11.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA/ja/s-9.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA/ja/image-11.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA/ja/s-9.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA/ja/image-8.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA/ja/s-isolation-list-csv.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA/ja/image-8.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA/ja/s-isolation-list-csv.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA/ja/image-3.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA/ja/s-isolation-window-graphs.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA/ja/image-3.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA/ja/s-isolation-window-graphs.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA/ja/image-2.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA/ja/s-precursor-frequency-graph.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA/ja/image-2.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA/ja/s-precursor-frequency-graph.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/index.html b/pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/index.html
index 98c9c4c983..a147685977 100644
--- a/pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/index.html
+++ b/pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/index.html
@@ -126,7 +126,7 @@ <h1>为 DIA 设置分离方案</h1>
         <b>“离子对设置”</b>表单将显示如下：
     </p>
     <p>
-        <img src="image-0.png" />
+        <img src="s-1.png" />
     </p>
     <table>
         <tr>
@@ -151,7 +151,7 @@ <h1>为 DIA 设置分离方案</h1>
         <b>编辑分离方案</b>表单应显示如下：
     </p>
     <p>
-        <img src="image-1.png" />
+        <img src="s-2.png" />
     </p>
     <ul>
         <li>选择<b>预指定分离窗口</b>。</li>
@@ -171,14 +171,14 @@ <h1>为 DIA 设置分离方案</h1>
         SWATH<sup>2</sup> 原始论文中提出的窗口重叠边缘的需要。
     </p>
     <p>
-        <img src="image-2.png" />
+        <img src="s-precursor-frequency-graph.png" />
     </p>
     <p class="fig-text">
         <b>图：</b>从观察到的肽段常见库中发现的带 1-4 个电荷的肽段母离子计算得出的直方图。最高的峰代表电荷 1-4 的母离子，第二高的峰代表电荷 2 和 4 的母离子，较小的峰只代表电荷 3 的母离子，电荷 4 的母离子作为小肩部仅在电荷 3
         的峰上可见。标有“Optimal” Boundary的垂直线表示此范围内的优化窗口布局边界。（由 Brian Searle 提供）
     </p>
     <p>
-        <img src="image-3.png" />
+        <img src="s-isolation-window-graphs.png" />
     </p>
     <p class="fig-text">
         来自 Gillet 等人的补充图 S1。MCP 2012：c) 显示所定义范围的完美矩形分离，d) 显示在定义的四极分离范围边缘超过 0.5 质荷比的信号衰减不太理想，e 和 f)
@@ -191,7 +191,7 @@ <h1>为 DIA 设置分离方案</h1>
         <b>计算分离方案</b>表单应显示如下：
     </p>
     <p>
-        <img src="image-4.png" />
+        <img src="s-3.png" />
     </p>
     <ul>
         <li>单击<b>确定</b>按钮。</li>
@@ -203,7 +203,7 @@ <h1>为 DIA 设置分离方案</h1>
         <b>编辑分离方案</b>表单应显示如下：
     </p>
     <p>
-        <img src="image-5.png" />
+        <img src="s-4.png" />
     </p>
     <p>
         在 Skyline 中还可以直观地看到母离子<i>质荷比</i>范围内随时间变化的分离情况，用于检查您所输入的信息是否正确。
@@ -215,7 +215,7 @@ <h1>为 DIA 设置分离方案</h1>
         您应当看到分离窗口的周期随时间推移而变化的图形，其中 Y 轴表示周期/时间，X 轴表示<i>质荷比</i>：
     </p>
     <p>
-        <img src="image-6.png" />
+        <img src="s-5.png" />
     </p>
     <ul>
         <li>单击<b>关闭</b>按钮。</li>
@@ -239,7 +239,7 @@ <h1>为 DIA 设置分离方案</h1>
         该表单应显示如下：
     </p>
     <p>
-        <img src="image-7.png" />
+        <img src="s-6.png" />
     </p>
     <ul>
         <li>单击<b>确定</b>按钮。</li>
@@ -251,7 +251,7 @@ <h1>为 DIA 设置分离方案</h1>
         打开您保存的文件。该文件显示如下：
     </p>
     <p>
-        <img src="image-8.png" />
+        <img src="s-isolation-list-csv.png" />
     </p>
     <p>
         这个分离方案的格式针对的是 Thermo Q Exactive（本教程中的数据采集自该仪器），但 Skyline 也可以将其导出到其它几种仪器。
@@ -281,7 +281,7 @@ <h1>使用“导入肽段搜索”向导</h1>
         <b>导入肽段搜索</b>向导应显示如下：
     </p>
     <p>
-        <img src="image-9.png" />
+        <img src="s-7.png" />
     </p>
     <p>
         对于该数据集，<b>截止得分</b>字段设置为“0.95”表明 PeptideProphet 得分为 0.95 或更高的肽段谱图匹配项将包括在内，因为 DDA 数据采用 TPP 处理（在使用 SEQUEST 进行肽段谱图匹配之后）。对于使用 q
@@ -308,7 +308,7 @@ <h1>使用“导入肽段搜索”向导</h1>
         向导中的<b>谱图库</b>页面现在应显示如下：
     </p>
     <p>
-        <img src="image-10.png" />
+        <img src="s-8.png" />
     </p>
     <ul>
         <li>单击<b>下一步</b>，根据搜索结果建立谱图库。</li>
@@ -325,7 +325,7 @@ <h1>使用“导入肽段搜索”向导</h1>
         <b>浏览结果文件</b>表单应显示如下：
     </p>
     <p>
-        <img src="image-11.png" />
+        <img src="s-9.png" />
     </p>
     <ul>
         <li>单击<b>打开</b>按钮。</li>
@@ -334,7 +334,7 @@ <h1>使用“导入肽段搜索”向导</h1>
         <b>导入肽段搜索</b>表单应显示如下：
     </p>
     <p>
-        <img src="image-12.png" />
+        <img src="s-10.png" />
     </p>
     <ul>
         <li>单击<b>下一步</b>按钮。</li>
@@ -349,7 +349,7 @@ <h1>使用“导入肽段搜索”向导</h1>
         <b>导入结果</b>表单现在应显示如下：
     </p>
     <p>
-        <img src="image-13.png" />
+        <img src="s-11.png" />
     </p>
     <ul>
         <li>单击<b>确定</b>按钮。</li>
@@ -364,7 +364,7 @@ <h1>使用“导入肽段搜索”向导</h1>
         随即将前往<b>配置离子对设置</b>页面，如下所示：
     </p>
     <p>
-        <img src="image-14.png" />
+        <img src="s-12.png" />
     </p>
     <p>
         虽然在本教程中可以使用这些默认设置，但日后也可以为自己的数据进行其它设置。
@@ -389,7 +389,7 @@ <h1>使用“导入肽段搜索”向导</h1>
         此时将前往<b>配置全扫描设置</b>页面，其中应显示您早先配置的相同设置，但务必要显示如下：
     </p>
     <p>
-        <img src="image-15.png" />
+        <img src="s-13.png" />
     </p>
     <ul>
         <li>单击<b>下一步</b>按钮。</li>
@@ -405,7 +405,7 @@ <h1>使用“导入肽段搜索”向导</h1>
         该表单现在应显示如下：
     </p>
     <p>
-        <img src="image-16.png" />
+        <img src="s-14.png" />
     </p>
     <p>
         在这个简单的介绍中，您刚刚提供的 FASTA 文本中只有 6 个目标蛋白质，您将不使用诱饵或通过 mProphet 算法生成的动态峰选择模型。有关这些选项的详细信息，请查阅 <a
@@ -418,7 +418,7 @@ <h1>使用“导入肽段搜索”向导</h1>
         Skyline 将显示一个表单，告知您它将添加 6 个蛋白质和 21 个肽段，涵盖 25 个母离子和 225 个离子对。对于每个蛋白质，此列表仅包含谱图库中存在的肽段。
     </p>
     <p>
-        <img src="image-17.png" />
+        <img src="s-15.png" />
     </p>
     <ul>
         <li>单击<b>确定</b>按钮。</li>
@@ -437,7 +437,7 @@ <h1>使用“导入肽段搜索”向导</h1>
         <b>目标</b>视图应显示如下：
     </p>
     <p>
-        <img src="image-18.png" />
+        <img src="s-16.png" />
     </p>
     <p>
         在 DIA 中可以提取任意一组子离子，因为该仪器涵盖 500-900
@@ -468,7 +468,7 @@ <h1>探索 DIA 结果</h1>
         Skyline 窗口应显示如下：
     </p>
     <p>
-        <img src="image-19.png" />
+        <img src="s-17.png" />
     </p>
     <p>
         这并非是适合开始的出色示例，因为它看起来比实际情况更糟。我们一眼就能看出峰积分边界需要调整。这可能是因为 Skyline 根据片段色谱图选择积分边界，如果仔细观察，会发现有些地方的信号衰落至 x 轴。在质心数据中，这通常是由于一个峰移到了提取窗口（您之前设定的提取窗口是 +/-20
@@ -485,7 +485,7 @@ <h1>探索 DIA 结果</h1>
         在包含更多目标的文档中，可能不必执行第二步来了解质量误差分布，仅使用每个肽段母离子的最强离子对。但在本例中，为了让您更准确地判断分布，现在应当显示如下：
     </p>
     <p>
-        <img src="image-20.png" />
+        <img src="s-18.png" />
     </p>
     <p>
         依照经验法则，您应当查看：
@@ -518,7 +518,7 @@ <h1>探索 DIA 结果</h1>
         Skyline 窗口将显示如下：
     </p>
     <p>
-        <img src="image-21.png" />
+        <img src="s-19.png" />
     </p>
     <p>
         这里有几点需要注意：
@@ -540,7 +540,7 @@ <h1>探索 DIA 结果</h1>
         您会看到，在有多个价态时，离子对分割视图会根据价态而不是离子类型进行分割，并且从 MS1 扫描中提取的母离子强度通常会使得从串联质谱扫描中提取的子离子强度相形见绌：
     </p>
     <p>
-        <img src="image-22.png" />
+        <img src="s-20.png" />
     </p>
     <table>
         <tr>
@@ -555,7 +555,7 @@ <h1>探索 DIA 结果</h1>
         现在应选择第二个肽段的双电荷母离子，Skyline 窗口应如下所示：
     </p>
     <p>
-        <img src="image-23.png" />
+        <img src="s-21.png" />
     </p>
     <p>
         对于此母离子而言，您在最后一个肽段上引入的所有指标，即质量误差、同位素点积和点积，看起来更好。您可能会觉得应选择不同的积分边界，尤其是在“Pit02”中的峰上。您可以试一下，然后使用 Skyline
@@ -577,10 +577,10 @@ <h1>探索 DIA 结果</h1>
     <table class="comp-fig">
         <tr>
             <td class="comp-fig">
-                <img src="image-24.png" />
+                <img src="s-22.png" />
             </td>
             <td class="comp-fig">
-                <img src="image-25.png" />
+                <img src="s-23.png" />
             </td>
         </tr>
     </table>
@@ -621,14 +621,14 @@ <h1>探索 DIA 结果</h1>
         的峰。要纠正这一问题，请执行以下操作：
     </p>
     <ul>
-        <li>将鼠标光标悬停在任何指示右侧积分边界的黑色虚线上，直到光标变为带有左右箭头的拆分器光标 (<img src="image-26.png" />) 为止。</li>
+        <li>将鼠标光标悬停在任何指示右侧积分边界的黑色虚线上，直到光标变为带有左右箭头的拆分器光标 (<img src="../../shared/vertical-split-cursor-icon.png" />) 为止。</li>
         <li>单击并拖动边界至捕获完整峰的目标位置。</li>
     </ul>
     <p class="keep-next">
         这个肽段图现在应如下所示：
     </p>
     <p>
-        <img src="image-27.png" />
+        <img src="s-24.png" />
     </p>
     <p>
         在青色 ID 线、0.99 同位素点积和 096 点积的组合之下，您应当对这个峰分配信心十足。
@@ -651,7 +651,7 @@ <h1>了解提取的色谱图</h1>
         这两个母离子都有良好的共洗脱碎片离子色谱图，并且无明显干扰。它们在 MS1 色谱图左侧也表现出明显干扰。
     </p>
     <p>
-        <img src="image-28.png" />
+        <img src="s-25.png" />
     </p>
     <p>
         您可以查看<b>峰面积</b>图来了解强度大小（每秒的离子数），其中母离子 (MS1) 总数接近 100 万，子离子（串联质谱）总数为 20 到 25,000 或 40 到 50 倍的差异。前面看到过，MS1
@@ -670,7 +670,7 @@ <h1>了解提取的色谱图</h1>
         <li>在圆圈中单击。</li>
     </ul>
     <p>
-        Skyline 将显示<b>全扫描</b>视图，其中显示从中提取母离子色谱图点的 MS1 扫描范围。您可以单击带有放大镜的按钮和视图右上角的加号 (<img src="image-29.png" />) 来查看整个 MS1 扫描。执行以下操作：
+        Skyline 将显示<b>全扫描</b>视图，其中显示从中提取母离子色谱图点的 MS1 扫描范围。您可以单击带有放大镜的按钮和视图右上角的加号 (<img src="../../shared/magnifying-glass-icon.png" />) 来查看整个 MS1 扫描。执行以下操作：
     </p>
     <ul>
         <li>确保您查看的是在 70.19 分钟（如标题所示）处采集的谱图，否则使用右上角的箭头按钮导航到此谱图。</li>
@@ -679,14 +679,14 @@ <h1>了解提取的色谱图</h1>
         <b>全扫描</b>图现在应如下所示：
     </p>
     <p>
-        <img src="image-30.png" />
+        <img src="s-26.png" />
     </p>
     <p>
         质心模式峰的强度显示为棒状。用于在色谱图上创建点的强度以色谱图颜色突出显示，提取范围显示为阴影区域。您可以看到未提取到阴影峰右侧的 M+3 和 M+4 峰。您所查看的产生干扰峰顶点的谱图在这个母离子积分峰的左边。您可以看到比目标肽段重 1
         道尔顿的双电荷母离子的完整同位素分布。它的单同位素峰非常接近目标的 M+1。
     </p>
     <ul>
-        <li>现在使用<b>“全扫描”</b>视图工具栏中的箭头按钮 (<img src="image-31.png" />) 来查看这个扫描和产生积分峰顶点的扫描之间的其它扫描。</li>
+        <li>现在使用<b>“全扫描”</b>视图工具栏中的箭头按钮 (<img src="../../shared/arrow-buttons.png" />) 来查看这个扫描和产生积分峰顶点的扫描之间的其它扫描。</li>
     </ul>
     <p>
         在 70.56 分钟处，应看到第一个包含目标单同位素过滤范围内峰的 MS1 谱图，该谱图突出显示为蓝色。直到 70.67 分钟处，您才会看到第一个包含最强单同位素峰的 MS1 谱图。
@@ -702,7 +702,7 @@ <h1>了解提取的色谱图</h1>
         在<b>全扫描</b>视图中应当看到类似这样的图。
     </p>
     <p>
-        <img src="image-32.png" />
+        <img src="s-27.png" />
     </p>
     <p>
         可以看到，对您刚刚在色谱图上单击的点做出贡献的串联质谱峰突出显示为浅绿色，并标注有 y10。从同位素峰相距 1 质荷比这一点，可以更加确信它们是由单电荷离子产生的。
@@ -714,7 +714,7 @@ <h1>了解提取的色谱图</h1>
         您应当看到类似这样的谱图：
     </p>
     <p>
-        <img src="image-33.png" />
+        <img src="s-28.png" />
     </p>
     <p>
         同样，可以看到对一系列峰中最高的峰进行了突出显示和注释，该系列峰中的后续峰相距 0.5 <i>质荷比</i>，表明是双电荷离子的同位素分布。您应当可以更加确信在子离子色谱图中提取的信号与您的目标相匹配。
@@ -732,7 +732,7 @@ <h2>了解干扰如何产生信号衰落</h2>
         <li>单击 K.ELVYETVR.V 肽段（<b>目标</b>视图中的第 3 个）。</li>
         <li>将鼠标光标悬停在“Pit02”重复测定中“母离子”峰的顶点上，直到出现浅绿色的圆圈，并且鼠标光标变为指向的手形标记。</li>
         <li>在圆圈中单击。</li>
-        <li>使用<b>“全扫描”</b>视图工具栏中的右箭头按钮 (<img src="image-34.png" />) 查看 MS1 谱图，直至到达 41.7 分钟处。</li>
+        <li>使用<b>“全扫描”</b>视图工具栏中的右箭头按钮 (<img src="../../shared/right-arrow-button.png" />) 查看 MS1 谱图，直至到达 41.7 分钟处。</li>
     </ul>
     <p>
         您会看到 M-1（单同位素母离子的左侧）处的峰随时间推移而增长。
@@ -741,19 +741,19 @@ <h2>了解干扰如何产生信号衰落</h2>
         它到 41.67 分钟处达到最高峰：
     </p>
     <p>
-        <img src="image-35.png" />
+        <img src="s-29.png" />
     </p>
     <p class="keep-next">
         在 41.68 分钟处，可以看到所提取峰的质荷比左移：
     </p>
     <p class="keep-next">
-        <img src="image-36.png" />
+        <img src="s-30.png" />
     </p>
     <p>
         在 41.70 分钟处，它们已移出 +/- 20 ppm 的提取范围：
     </p>
     <p>
-        <img src="image-37.png" />
+        <img src="s-31.png" />
     </p>
     <p>
         从 DIA 的质心串联质谱谱图中提取，尤其是在 Thermo Orbitrap 仪器上进行，已被证明在广泛的统计测试中更可靠，但在考虑数据时，这仍然是一个有用的概念。当您通常预期它会导致信号增加时，此设置中的干扰会降低总信号。
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/invariant.html b/pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/invariant.html
index f602bcdd79..e80c115869 100644
--- a/pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/invariant.html
+++ b/pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/invariant.html
@@ -154,7 +154,7 @@ <h1>Setting Up an Isolation Scheme for DIA</h1>
         The <b>Transition Settings</b> form should look something like this:
     </p>
     <p>
-        <img src="image-0.png" />
+        <img src="s-1.png" />
     </p>
     <table>
         <tr>
@@ -186,7 +186,7 @@ <h1>Setting Up an Isolation Scheme for DIA</h1>
         The <b>Edit Isolation Scheme</b> form should appear as follows:
     </p>
     <p>
-        <img src="image-1.png" />
+        <img src="s-2.png" />
     </p>
     <ul>
         <li>Choose <b>Prespecified isolation windows</b>.</li>
@@ -210,7 +210,7 @@ <h1>Setting Up an Isolation Scheme for DIA</h1>
         efficient at the borders<sup>3</sup>.
     </p>
     <p>
-        <img src="image-2.png" />
+        <img src="s-precursor-frequency-graph.png" />
     </p>
     <p class="fig-text">
         <b>Figure</b>: Histograms calculated from peptide precursors with charges 1-4 found in common libraries of observed peptides. The
@@ -219,7 +219,7 @@ <h1>Setting Up an Isolation Scheme for DIA</h1>
         “Optimal” Boundary indicate the optimize window placement boundaries in this range. (Courtesy of Brian Searle)
     </p>
     <p>
-        <img src="image-3.png" />
+        <img src="s-isolation-window-graphs.png" />
     </p>
     <p class="fig-text">
         Supplemental Figure S1 from Gillet, et al. MCP 2012: c) shows perfect rectangular isolation of the defined range, d) shows less ideal signal
@@ -237,7 +237,7 @@ <h1>Setting Up an Isolation Scheme for DIA</h1>
         The <b>Calculate Isolation Scheme</b> form should look like this:
     </p>
     <p>
-        <img src="image-4.png" />
+        <img src="s-3.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -249,7 +249,7 @@ <h1>Setting Up an Isolation Scheme for DIA</h1>
         The <b>Edit Isolation Scheme</b> form should look like this:
     </p>
     <p>
-        <img src="image-5.png" />
+        <img src="s-4.png" />
     </p>
     <p>
         Skyline also allows you to visualize the precursor <i>m/z</i> range isolations over time, to check that what you have entered is correct:
@@ -262,7 +262,7 @@ <h1>Setting Up an Isolation Scheme for DIA</h1>
         <i>m/z</i> on the x-axis:
     </p>
     <p>
-        <img src="image-6.png" />
+        <img src="s-5.png" />
     </p>
     <ul>
         <li>Click the <b>Close</b> button.</li>
@@ -288,7 +288,7 @@ <h1>Setting Up an Isolation Scheme for DIA</h1>
         The form should look like this:
     </p>
     <p>
-        <img src="image-7.png" />
+        <img src="s-6.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -300,7 +300,7 @@ <h1>Setting Up an Isolation Scheme for DIA</h1>
         Open the file you saved. It should look like this:
     </p>
     <p>
-        <img src="image-8.png" />
+        <img src="s-isolation-list-csv.png" />
     </p>
     <p>
         This isolation scheme is formatted for a Thermo Q Exactive (on which the data in this tutorial were acquired), but Skyline can also export to
@@ -338,7 +338,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         The <b>Import Peptide Search</b> wizard should appear looking like this:
     </p>
     <p>
-        <img src="image-9.png" />
+        <img src="s-7.png" />
     </p>
     <p>
         For this data set a <b>Cut-off score</b> field set to “0.95” means peptide spectrum matches with a PeptideProphet score of 0.95 or
@@ -372,7 +372,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         The <b>Spectral Library</b> page of the wizard should now look like this:
     </p>
     <p>
-        <img src="image-10.png" />
+        <img src="s-8.png" />
     </p>
     <ul>
         <li>Click <b>Next</b> to build a spectral library from these search results.</li>
@@ -391,7 +391,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         The <b>Browse for Results Files</b> form should look like this:
     </p>
     <p>
-        <img src="image-11.png" />
+        <img src="s-9.png" />
     </p>
     <ul>
         <li>Click the <b>Open</b> button.</li>
@@ -400,7 +400,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         The <b>Import Peptide Search</b> form should look like this:
     </p>
     <p>
-        <img src="image-12.png" />
+        <img src="s-10.png" />
     </p>
     <ul>
         <li>Click the <b>Next</b> button.</li>
@@ -416,7 +416,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         The <b>Import Results</b> form should now look like this:
     </p>
     <p>
-        <img src="image-13.png" />
+        <img src="s-11.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -433,7 +433,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         This brings you to the <b>Configure Transition Settings</b> page as shown below:
     </p>
     <p>
-        <img src="image-14.png" />
+        <img src="s-12.png" />
     </p>
     <p>
         You can use these default settings for this tutorial, but you could consider alternatives for your own data in the future.
@@ -464,7 +464,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         configured earlier, but make sure it looks like this:
     </p>
     <p>
-        <img src="image-15.png" />
+        <img src="s-13.png" />
     </p>
     <ul>
         <li>Click the <b>Next</b> button.</li>
@@ -482,7 +482,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         The form should now look like this:
     </p>
     <p>
-        <img src="image-16.png" />
+        <img src="s-14.png" />
     </p>
     <p>
         In this simple introduction with only 6 targeted proteins in the FASTA text you have just included, you will not use decoys or a dynamic peak
@@ -497,7 +497,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         transitions. For every protein, only the peptides that were present in the spectral library are included in this list.
     </p>
     <p>
-        <img src="image-17.png" />
+        <img src="s-15.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -519,7 +519,7 @@ <h1>Using the Import Peptide Search wizard</h1>
         The <b>Targets</b> view should look like this:
     </p>
     <p>
-        <img src="image-18.png" />
+        <img src="s-16.png" />
     </p>
     <p>
         In DIA, it is possible to extract any set of product ions, because the instrument covers every possible precursor-product combination in the
@@ -557,7 +557,7 @@ <h1>Exploring DIA Results</h1>
         The Skyline window should look something like this:
     </p>
     <p>
-        <img src="image-19.png" />
+        <img src="s-17.png" />
     </p>
     <p>
         This is not a great example to start with. It makes things look much worse than they really are. You, as a human observer, can easily tell that
@@ -579,7 +579,7 @@ <h1>Exploring DIA Results</h1>
         this:
     </p>
     <p>
-        <img src="image-20.png" />
+        <img src="s-18.png" />
     </p>
     <p>
         As rules of thumb, you should be looking to see that:
@@ -619,7 +619,7 @@ <h1>Exploring DIA Results</h1>
         The Skyline window should now look something like this:
     </p>
     <p>
-        <img src="image-21.png" />
+        <img src="s-19.png" />
     </p>
     <p>
         Here are a few things to take note of:
@@ -646,7 +646,7 @@ <h1>Exploring DIA Results</h1>
         precursor ion intensities extracted from MS1 scans typically dwarf the product ion intensities extracted from MS/MS scans:
     </p>
     <p>
-        <img src="image-22.png" />
+        <img src="s-20.png" />
     </p>
     <table>
         <tr>
@@ -661,7 +661,7 @@ <h1>Exploring DIA Results</h1>
         The doubly charged precursor of the second peptide should now be selected, and the Skyline Window should look like this:
     </p>
     <p>
-        <img src="image-23.png" />
+        <img src="s-21.png" />
     </p>
     <p>
         All the metrics you were introduced to on the last peptide, mass error, idotp, and dotp, look even better for this precursor. You may feel you
@@ -686,10 +686,10 @@ <h1>Exploring DIA Results</h1>
     <table class="comp-fig">
         <tr>
             <td class="comp-fig">
-                <img src="image-24.png" />
+                <img src="s-22.png" />
             </td>
             <td class="comp-fig">
-                <img src="image-25.png" />
+                <img src="s-23.png" />
             </td>
         </tr>
     </table>
@@ -741,14 +741,14 @@ <h1>Exploring DIA Results</h1>
     </p>
     <ul>
         <li>Hover the mouse cursor over any of the black dashed lines indicating the right integration boundary until the cursor changes to a splitter
-            cursor (<img src="image-26.png" />) with arrows pointing left and right.</li>
+            cursor (<img src="../../shared/vertical-split-cursor-icon.png" />) with arrows pointing left and right.</li>
         <li>Click and drag the boundary to the desired location capturing the full peak.</li>
     </ul>
     <p class="keep-next">
         The plots for this peptide should now look like this:
     </p>
     <p>
-        <img src="image-27.png" />
+        <img src="s-24.png" />
     </p>
     <p>
         The combination of the cyan ID lines, the idotp of 0.99, and the dotp of 096 should give you high confidence in this peak assignment.
@@ -775,7 +775,7 @@ <h1>Understanding Extracted Chromatograms</h1>
         in the MS1 chromatograms.
     </p>
     <p>
-        <img src="image-28.png" />
+        <img src="s-25.png" />
     </p>
     <p>
         You can get a sense of scale in intensity (ions per second) by looking at the <b>Peak Areas</b> plots where the precurors (MS1) total
@@ -798,7 +798,7 @@ <h1>Understanding Extracted Chromatograms</h1>
     </ul>
     <p>
         Skyline will show the <b>Full Scan</b> view displaying a range of the MS1 scan from which the precursor chromatogram points were
-        extracted. You could see the entire MS1 scan by clicking on the button with the magnifying glass and a plus (<img src="image-29.png" />) in
+        extracted. You could see the entire MS1 scan by clicking on the button with the magnifying glass and a plus (<img src="../../shared/magnifying-glass-icon.png" />) in
         the upper right corner of the view. Instead, do the following:
     </p>
     <ul>
@@ -809,7 +809,7 @@ <h1>Understanding Extracted Chromatograms</h1>
         The <b>Full Scan</b> graph should now look something like this:
     </p>
     <p>
-        <img src="image-30.png" />
+        <img src="s-26.png" />
     </p>
     <p>
         The intensities in the centroid-mode peaks are shown as sticks. Intensities that were used to create the points on the chromatograms are
@@ -819,7 +819,7 @@ <h1>Understanding Extracted Chromatograms</h1>
         targeted peptide. Its monoisotopic peak is very close to the M+1 of target.
     </p>
     <ul>
-        <li>Now use the arrow buttons (<img src="image-31.png" />) in the <b>Full Scan</b> view toolbar to review scans between this one and
+        <li>Now use the arrow buttons (<img src="../../shared/arrow-buttons.png" />) in the <b>Full Scan</b> view toolbar to review scans between this one and
             the one that produced the apex of the integrated peak.</li>
     </ul>
     <p>
@@ -838,7 +838,7 @@ <h1>Understanding Extracted Chromatograms</h1>
         You should see a graph in the <b>Full Scan</b> view that looks like this:
     </p>
     <p>
-        <img src="image-32.png" />
+        <img src="s-27.png" />
     </p>
     <p>
         You can see the MS/MS peak that contributed the point to the chromatogram you just clicked on highlighted in aqua and annotated y10. The fact
@@ -851,7 +851,7 @@ <h1>Understanding Extracted Chromatograms</h1>
         You should see a spectrum like plot like this one:
     </p>
     <p>
-        <img src="image-33.png" />
+        <img src="s-28.png" />
     </p>
     <p>
         Again, you can see the tallest peak in a series highlighted and annotated, with the following peaks in the series 0.5 <i>m/z</i> apart,
@@ -873,7 +873,7 @@ <h2>Understanding how interference produces signal dropout</h2>
         <li>Hover the mouse cursor over the apex of the “precursor” peak in the “Pit02” replicate until you see a blue circle appear, and the mouse
             cursor change to a pointing hand.</li>
         <li>Click in the circle.</li>
-        <li>Use the right arrow button (<img src="image-34.png" />) in the <b>Full Scan</b> view toolbar to review the MS1 spectra until you
+        <li>Use the right arrow button (<img src="../../shared/right-arrow-button.png" />) in the <b>Full Scan</b> view toolbar to review the MS1 spectra until you
             reach 41.7 minutes.</li>
     </ul>
     <p>
@@ -883,19 +883,19 @@ <h2>Understanding how interference produces signal dropout</h2>
         By 41.67 minutes it is the largest peak:
     </p>
     <p>
-        <img src="image-35.png" />
+        <img src="s-29.png" />
     </p>
     <p>
         At 41.68 minutes, you can see the extracted peaks shift left in m/z:
     </p>
     <p>
-        <img src="image-36.png" />
+        <img src="s-30.png" />
     </p>
     <p>
         And at 41.70 minutes, they have shifted out of the +/- 20 ppm extraction ranges:
     </p>
     <p>
-        <img src="image-37.png" />
+        <img src="s-31.png" />
     </p>
     <p>
         Extraction from centroided MS/MS spectra for DIA, especially on Thermo Orbitrap instruments, has proven more reliable in broad statistical
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/image-0.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/s-1.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/image-0.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/s-1.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/image-12.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/s-10.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/image-12.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/s-10.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/image-13.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/s-11.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/image-13.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/s-11.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/image-14.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/s-12.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/image-14.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/s-12.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/image-15.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/s-13.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/image-15.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/s-13.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/image-16.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/s-14.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/image-16.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/s-14.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/image-17.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/s-15.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/image-17.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/s-15.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/image-18.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/s-16.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/image-18.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/s-16.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/image-19.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/s-17.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/image-19.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/s-17.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/image-20.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/s-18.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/image-20.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/s-18.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/image-21.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/s-19.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/image-21.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/s-19.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/image-1.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/s-2.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/image-1.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/s-2.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/image-22.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/s-20.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/image-22.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/s-20.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/image-23.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/s-21.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/image-23.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/s-21.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/image-24.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/s-22.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/image-24.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/s-22.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/image-25.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/s-23.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/image-25.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/s-23.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/image-27.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/s-24.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/image-27.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/s-24.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/image-28.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/s-25.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/image-28.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/s-25.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/image-30.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/s-26.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/image-30.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/s-26.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/image-32.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/s-27.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/image-32.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/s-27.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/image-33.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/s-28.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/image-33.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/s-28.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/image-35.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/s-29.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/image-35.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/s-29.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/image-4.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/s-3.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/image-4.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/s-3.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/image-36.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/s-30.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/image-36.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/s-30.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/image-37.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/s-31.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/image-37.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/s-31.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/image-5.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/s-4.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/image-5.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/s-4.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/image-6.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/s-5.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/image-6.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/s-5.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/image-7.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/s-6.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/image-7.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/s-6.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/image-9.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/s-7.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/image-9.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/s-7.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/image-10.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/s-8.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/image-10.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/s-8.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/image-11.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/s-9.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/image-11.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/s-9.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/image-8.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/s-isolation-list-csv.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/image-8.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/s-isolation-list-csv.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/image-3.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/s-isolation-window-graphs.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/image-3.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/s-isolation-window-graphs.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/image-2.png b/pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/s-precursor-frequency-graph.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/image-2.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/DIA/zh-CHS/s-precursor-frequency-graph.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/en/index.html b/pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/en/index.html
index 3830ffbdb3..0df09e6bfd 100644
--- a/pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/en/index.html
+++ b/pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/en/index.html
@@ -115,7 +115,7 @@ <h1>Preparing a Document to Accept a Transition List</h1>
         The <b>Peptide Settings</b> form should now look something like:
     </p>
     <p>
-        <img src="image-0.png" />
+        <img src="s-1.png" />
     </p>
     <p>
         To set up the background proteome for the MRMer document now, perform the following steps:
@@ -134,7 +134,7 @@ <h1>Preparing a Document to Accept a Transition List</h1>
         The <b>Peptide Settings</b> form should now look something like this:
     </p>
     <p>
-        <img src="image-1.png" />
+        <img src="s-2.png" />
     </p>
     <p>
         Finally, before you can insert the transition list from the MRMer experiment into the current document, you will need to define the isotope
@@ -161,7 +161,7 @@ <h1>Preparing a Document to Accept a Transition List</h1>
         The <b>Edit Isotope Modification</b> form should now look like this:
     </p>
     <p>
-        <img src="image-2.png" />
+        <img src="s-3.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button</li>
@@ -183,7 +183,7 @@ <h1>Preparing a Document to Accept a Transition List</h1>
         The <b>Edit Isotope Modification</b> form should now look like this:
     </p>
     <p>
-        <img src="image-3.png" />
+        <img src="s-4.png" />
     </p>
     <p>
         Skyline automatically calculates both the monoisotopic and average masses, approximately 8 Daltons for Lysine (K) and 10 Daltons for Arginine
@@ -238,7 +238,7 @@ <h1>Inserting a Transition List with Associated Proteins</h1>
         The <b>Insert Transition List</b> form appears:
     </p>
     <p>
-        <img src="image-4.png" />
+        <img src="s-5.png" />
     </p>
     <ul>
         <li>Press Ctrl-V to paste the copied cells into the <b>Insert Transition List</b> form.</li>
@@ -247,7 +247,7 @@ <h1>Inserting a Transition List with Associated Proteins</h1>
         This will bring up the <b>Import Transition List: Identify Columns</b> form, which should look like this:
     </p>
     <p>
-        <img src="image-5.png" />
+        <img src="s-6.png" />
     </p>
     <ul>
         <li>Make sure the <b>Associate Proteins</b> checkbox is ticked.</li>
@@ -269,12 +269,12 @@ <h1>Inserting a Transition List with Associated Proteins</h1>
     </ul>
     <p>
         The main Skyline window should show a number of peptides grouped within their proteins. The peptide icons should contain 3 vertical lines and a
-        baseline (<img src="image-6.png" />), like a very small MS/MS spectrum, in the lower right corner (<img src="image-7.png" />). The presence of
+        baseline (<img src="../../shared/peptide-icon.png" />), like a very small MS/MS spectrum, in the lower right corner (<img src="../../shared/peptide-with-spectrum-lines-icon.png" />). The presence of
         this image indicates the peptide has an associated MS/MS library spectrum. The peptide label should highlight in blue the C-terminal Lysine or
         Arginine, indicating the stable isotope labeled amino acid in the heavy, labeled form:
     </p>
     <p>
-        <img src="image-8.png" />
+        <img src="s-7.png" />
     </p>
     <p>
         You can also see at the bottom right corner of the window, in the status bar, the indicator “1/296 tran”, confirming that all 296 transitions
@@ -299,7 +299,7 @@ <h1>Inserting a Transition List with Associated Proteins</h1>
         show the spectrum that matches the current peptide, and the peak matching the selected transition will be highlighted in red:
     </p>
     <p>
-        <img src="image-9.png" />
+        <img src="s-8.png" />
     </p>
     <p>
         You will notice that not all of the peptides have the most abundant product ions chosen for transitions, like the one shown in the image above,
@@ -367,7 +367,7 @@ <h1>Importing Data</h1>
         This should leave Skyline looking something like:
     </p>
     <p>
-        <img src="image-10.png" />
+        <img src="s-9.png" />
     </p>
     <p>
         You can also change the proportions allocated to the various panes by clicking and dragging the light gray splitter bars between them.
@@ -388,7 +388,7 @@ <h1>Importing Data</h1>
         This should change Skyline to look like:
     </p>
     <p>
-        <img src="image-11.png" />
+        <img src="s-10.png" />
     </p>
     <p>
         If you do not see chromatograms for all three transitions, as shown above, do the following:
@@ -415,7 +415,7 @@ <h1>Importing Data</h1>
         the following before starting the next section:
     </p>
     <ul>
-        <li>Click the pushpin <img src="image-12.png" /> to the left of the X in the upper right corner of the <b>Library Match</b> title
+        <li>Click the pushpin <img src="../../shared/pushpin-icon.png" /> to the left of the X in the upper right corner of the <b>Library Match</b> title
             bar.</li>
     </ul>
     <h2>Removing a Transition Peak with Interference</h2>
@@ -438,7 +438,7 @@ <h2>Removing a Transition Peak with Interference</h2>
         The precursor total area ratio is a weighted mean, using the internal standard peak area as the weights, which simplifies algebraically to:
     </p>
     <p>
-        <img src="image-13.png" />
+        <img src="s-precursor-total-area-ratio-formula.png" />
     </p>
     <p>
         Removing either a light or heavy peak removes the peak for its matching transition. Hence, when only one pair of transitions remain, as with y7
@@ -459,7 +459,7 @@ <h2>Adjusting Peak Boundaries to Exclude Interference</h2>
         This should leave Skyline showing something like:
     </p>
     <p>
-        <img src="image-14.png" />
+        <img src="s-11.png" />
     </p>
     <p>
         In this case, y4 and y3 show ratios of 0.31 and 0.35 respectively and y7 shows 0.23, yielding a weighted mean, precursor total ratio of 0.27.
@@ -505,7 +505,7 @@ <h1>Preparing a Document to Accept the Study 7 Transition List</h1>
         You should be presented with a spreadsheet that looks something like this:
     </p>
     <p>
-        <img src="image-15.png" />
+        <img src="s-transition-list-spreadsheet.png" />
     </p>
     <p>
         You can tell that this is a spreadsheet created manually by someone who put significant effort, using borders, merged cells and highlighting,
@@ -548,7 +548,7 @@ <h1>Preparing a Document to Accept the Study 7 Transition List</h1>
         The <b>Edit Isotope Modification</b> form should now look like this:
     </p>
     <p>
-        <img src="image-16.png" />
+        <img src="s-12.png" />
     </p>
     <p>
         To finish preparing the document for the Study 7 transition list, do the following:
@@ -598,7 +598,7 @@ <h2>Pasting a Transition List into the Document </h2>
         This will bring up the <b>Import Transition List: Identify Columns</b> form, which should look like this:
     </p>
     <p>
-        <img src="image-17.png" />
+        <img src="s-13.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -607,7 +607,7 @@ <h2>Pasting a Transition List into the Document </h2>
         Skyline should present the following error message:
     </p>
     <p>
-        <img src="image-18.png" /> 
+        <img src="s-14.png" /> 
     </p>
     <p>
         Messages like this are not uncommon when working with transition lists created outside Skyline. Others are presented in the Skyline
@@ -640,7 +640,7 @@ <h2>Pasting a Transition List into the Document </h2>
         This should leave the Skyline peptide view looking like:
     </p>
     <p>
-        <img src="image-19.png" />
+        <img src="s-15.png" />
     </p>
     <h2>Adjusting Modifications Manually</h2>
     <p>
@@ -664,7 +664,7 @@ <h2>Adjusting Modifications Manually</h2>
         The <b>Edit Isotope Modification</b> form should look like:
     </p>
     <p>
-        <img src="image-20.png" />
+        <img src="s-16.png" />
     </p>
     <p>
         This modification will apply a varying mass shift to any amino acid, depending on how many Carbon atoms it contains.
@@ -673,7 +673,7 @@ <h2>Adjusting Modifications Manually</h2>
         <li>Click the <b>OK</b> button to return to the <b>Edit Modifications</b> form, which should now look like:</li>
     </ul>
     <p>
-        <img src="image-21.png" />
+        <img src="s-17.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button on the <b>Edit Modifications</b> form to return to the document.</li>
@@ -691,7 +691,7 @@ <h2>Adjusting Modifications Manually</h2>
         The peptide view should now look like this:
     </p>
     <p>
-        <img src="image-22.png" />
+        <img src="s-18.png" />
     </p>
     <p>
         Now expand both the “744.8398++” precursor and the <b>“</b>747.3481++ (heavy)” precursor: 
@@ -744,7 +744,7 @@ <h2>Importing Data from a Multiple Sample WIFF File</h2>
         present you with a form that looks like this:
     </p>
     <p>
-        <img src="image-23.png" />
+        <img src="s-19.png" />
     </p>
     <p>
         For this tutorial, to reduce the time that will be required to complete the import:
@@ -759,7 +759,7 @@ <h2>Importing Data from a Multiple Sample WIFF File</h2>
         use to display information about these replicates:
     </p>
     <p>
-        <img src="image-24.png" />
+        <img src="s-20.png" />
     </p>
     <ul>
         <li>Click the <b>Remove</b> button to accept this operation.</li>
@@ -785,7 +785,7 @@ <h2>Inspecting and Adjusting Peak Integration</h2>
         <li>Adjust the view proportions to look something like the image below.</li>
     </ul>
     <p>
-        <img src="image-25.png" />
+        <img src="s-21.png" />
     </p>
     <p>
         The currently selected peptide “YEVQGEVFTKPQ<b><span class="blue">L</span></b>WP”, which was the peptide at the C-terminal end of CRP
@@ -845,7 +845,7 @@ <h2>Inspecting and Adjusting Peak Integration</h2>
         Skyline should now look something like:
     </p>
     <p>
-        <img src="image-26.png" />
+        <img src="s-22.png" />
     </p>
     <h2>Data Inspection with Peak Areas View</h2>
     <p>
@@ -889,7 +889,7 @@ <h2>Data Inspection with Peak Areas View</h2>
                 class="blue">K</span></b> selected:
     </p>
     <p>
-        <img src="image-27.png" />
+        <img src="s-23.png" />
     </p>
     <p>
         You will see that, indeed, precision among the replicates for each concentration appears to have improved.
@@ -910,7 +910,7 @@ <h2>Data Inspection with Peak Areas View</h2>
                 class="blue">K</span></b> peptide light precursor 564.7746++ selected:
     </p>
     <p>
-        <img src="image-28.png" />
+        <img src="s-24.png" />
     </p>
     <p>
         As expected, the ratios are quite similar. The second and third peptides (INDISHTQSVSA<b><span class="blue">K</span></b> and
@@ -923,7 +923,7 @@ <h2>Data Inspection with Peak Areas View</h2>
         This should cause the peak area graph to look like:
     </p>
     <p>
-        <img src="image-29.png" />
+        <img src="s-25.png" />
     </p>
     <p>
         This seems to indicate some interference in the transition for y3, since its ratio, at low concentrations, is so different from the others for
@@ -940,7 +940,7 @@ <h2>Data Inspection with Peak Areas View</h2>
         The chart should change to something like:
     </p>
     <p>
-        <img src="image-30.png" />
+        <img src="s-26.png" />
     </p>
     <p>
         Again, this chart clearly indicates interference on the transition for y3 (brown) that becomes less of a factor as the concentration of the
@@ -948,7 +948,7 @@ <h2>Data Inspection with Peak Areas View</h2>
         charts, you can click on the individual bars to see the interfering peak, which, in this case, is pretty clear, as in replicate E_03 below:
     </p>
     <p>
-        <img src="image-31.png" />
+        <img src="s-27.png" />
     </p>
     <p>
         As with the case in the MRMer document, you might attempt to adjust the integration boundaries to exclude the interfering peak, but it is
@@ -964,7 +964,7 @@ <h2>Data Inspection with Peak Areas View</h2>
         The <b>Peak Areas</b> chart should have changed to look something like:
     </p>
     <p>
-        <img src="image-32.png" />
+        <img src="s-28.png" />
     </p>
     <p>
         If the peptides do not appear in this order, do the following:
@@ -1052,7 +1052,7 @@ <h2>Settings Concentration Values</h2>
         When you are done entering these values, the <b>Document Grid</b> should look like this:
     </p>
     <p>
-        <img src="image-33.png" />
+        <img src="s-29.png" />
     </p>
     <p>
         You can now use the newly entered concentrations in the <b>Peak Areas: Replicate Comparison</b> graph by doing the following:
@@ -1068,7 +1068,7 @@ <h2>Settings Concentration Values</h2>
         The <b>Peak Areas</b> graph should now look like:
     </p>
     <p>
-        <img src="image-34.png" />
+        <img src="s-30.png" />
     </p>
     <p>
         This graph shows that the CVs are quite low until the very lowest concentrations. You can easily switch to a graph showing the mean ratios with
@@ -1081,7 +1081,7 @@ <h2>Settings Concentration Values</h2>
         This should change the graph to look like:
     </p>
     <p>
-        <img src="image-35.png" />
+        <img src="s-31.png" />
     </p>
     <ul>
         <li>On the <b>File</b> menu, click <b>Save</b>, to end this section. </li>
@@ -1106,7 +1106,7 @@ <h2>Further Exploration</h2>
         appearing as in the chart below:
     </p>
     <p>
-        <img src="image-36.png" />
+        <img src="s-32.png" />
     </p>
     <p>
         The peptide INDISHTQSVSA<b><span class="blue">K</span></b> is the only one of the 4 from the first data set that still has a CV
@@ -1120,7 +1120,7 @@ <h2>Further Exploration</h2>
         for 3 of the “Blank” replicates (though this issue was fixed a long time ago – but after the document data was imported and saved):
     </p>
     <p>
-        <img src="image-37.png" />
+        <img src="s-33.png" />
     </p>
     <p>
         If you correct these by clicking and dragging beneath the x-axis, the CV for the heavy precursor of LSEPAELTDAV<b><span
@@ -1140,7 +1140,7 @@ <h2>Further Exploration</h2>
         <li>Click the “INDISHTQSVSA<b><span class="blue">K</span></b>” peptide.</li>
     </ul>
     <p>
-        <img src="image-38.png" />
+        <img src="s-34.png" />
     </p>
     <p>
         This seems to indicate that the internal standard is doing its job of compensating for variance in measurements of this peptide. To review the
@@ -1153,7 +1153,7 @@ <h2>Further Exploration</h2>
         It would be hard to guess from this chart that the normalization would be so effective:
     </p>
     <p>
-        <img src="image-39.png" />
+        <img src="s-35.png" />
     </p>
     <p>
         Finally, returning to the peptide in which we detected interference in the first data set:
@@ -1167,7 +1167,7 @@ <h2>Further Exploration</h2>
         Here also, you will see clear evidence of interference on the y3 transition:
     </p>
     <p>
-        <img src="image-40.png" />
+        <img src="s-36.png" />
     </p>
     <p>
         Unlike the first data set, however, it is much harder to see the interference by inspecting the individual chromatograms. In this case, due to
@@ -1175,7 +1175,7 @@ <h2>Further Exploration</h2>
         replicate E_03 shown below:
     </p>
     <p>
-        <img src="image-41.png" />
+        <img src="s-37.png" />
     </p>
     <p>
         The NCI CPTAC Study 7 provided quite a lot more data, all of which is now public. Skyline can help you learn a lot about this data quickly,
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/ja/index.html b/pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/ja/index.html
index d84d905423..7ae6099422 100644
--- a/pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/ja/index.html
+++ b/pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/ja/index.html
@@ -97,7 +97,7 @@ <h1>トランジションリストを取り込むためのドキュメントを
         [ <b>ペプチド設定</b> ] は以下のように表示されます。
     </p>
     <p>
-        <img src="image-0.png" />
+        <img src="s-1.png" />
     </p>
     <p>
         ここでMRMerドキュメントのバックグラウンドプロテオームを設定するには、以下の手順を行います。
@@ -116,7 +116,7 @@ <h1>トランジションリストを取り込むためのドキュメントを
         [ <b>ペプチド設定</b> ] は以下のように表示されます。
     </p>
     <p>
-        <img src="image-1.png" />
+        <img src="s-2.png" />
     </p>
     <p>
         最後に、MRMerの実験で用いたトランジションリストを現在作業中のドキュメントに挿入する前に、含まれる同位体修飾を指定する必要があります。MRMerの実験では、ライトペプチド（未標識）と、リジンとアルギニンにアミノ酸残基安定同位体標識(SILAC)を施したヘビーペプチドが使用されていました。最初に適切な同位体修飾を指定せずにMRMerのトランジションリストを挿入すると、トランジションリスト内のヘビーペプチドの<i>m/z</i>値がSkylineにより認識されない場合があります。
@@ -138,7 +138,7 @@ <h1>トランジションリストを取り込むためのドキュメントを
         [ <b>同位体修飾を編集</b> ] フォームは以下のように表示されます。
     </p>
     <p>
-        <img src="image-2.png" />
+        <img src="s-3.png" />
     </p>
     <ul>
         <li>[ <b>OK</b> ] ボタンをクリックします。</li>
@@ -158,7 +158,7 @@ <h1>トランジションリストを取り込むためのドキュメントを
         [ <b>同位体修飾を編集</b> ] フォームは以下のように表示されます。
     </p>
     <p>
-        <img src="image-3.png" />
+        <img src="s-4.png" />
     </p>
     <p>
         Skylineはモノアイソトピック質量と平均質量の両方について13Cおよび15Nを用いて自動的に計算を行います（リジン（K）については約8ダルトン、アルギニン（R）については約10ダルトンとなります）。
@@ -205,7 +205,7 @@ <h1>関連タンパク質とともにトランジションリストを挿入す
         [ <b>トランジションリストの挿入</b> ] フォームが表示されます。
     </p>
     <p>
-        <img src="image-4.png" />
+        <img src="s-5.png" />
     </p>
     <ul>
         <li>Ctrl+Vを押してコピーしたセルを [ <b>トランジションリストの挿入</b> ] フォームに貼り付けます。</li>
@@ -214,7 +214,7 @@ <h1>関連タンパク質とともにトランジションリストを挿入す
         これによって以下のような [<b>トランジションリストのインポート：列の識別</b> ] フォームが表示されます。
     </p>
     <p>
-        <img src="image-5.png" />
+        <img src="s-6.png" />
     </p>
     <ul>
         <li>[ <b>タンパク質の関連付け</b> ] チェックボックスがオンになっていることを確認します。</li>
@@ -233,11 +233,11 @@ <h1>関連タンパク質とともにトランジションリストを挿入す
         <li>Homeキーを押して新たなターゲットリストの一番上までスクロールします。</li>
     </ul>
     <p>
-        ペプチドがそれぞれのタンパク質内にグループ化されて、Skylineのメインウィンドウに表示されます。非常に小さいMS/MSスペクトルのような3本の垂直ラインとベースライン（<img src="image-6.png" />）が、ペプチドのアイコンの右下隅（<img
-            src="image-7.png" />）に描かれています。このアイコンが表示されているペプチドは、MS/MSライブラリスペクトルと関連付けられているものです。C末端リジンまたはアルギニンが青でハイライト表示されており、ヘビーペプチド中の安定同位体で標識されたアミノ酸であることが示されています。
+        ペプチドがそれぞれのタンパク質内にグループ化されて、Skylineのメインウィンドウに表示されます。非常に小さいMS/MSスペクトルのような3本の垂直ラインとベースライン（<img src="../../shared/peptide-icon.png" />）が、ペプチドのアイコンの右下隅（<img
+            src="../../shared/peptide-with-spectrum-lines-icon.png" />）に描かれています。このアイコンが表示されているペプチドは、MS/MSライブラリスペクトルと関連付けられているものです。C末端リジンまたはアルギニンが青でハイライト表示されており、ヘビーペプチド中の安定同位体で標識されたアミノ酸であることが示されています。
     </p>
     <p>
-        <img src="image-8.png" />
+        <img src="s-7.png" />
     </p>
     <p>
         またウィンドウの右下隅にあるステータスバーに、インジケーター「1/296
@@ -259,7 +259,7 @@ <h1>関連タンパク質とともにトランジションリストを挿入す
         ペプチドビュー内で、いくつかのペプチドとトランジションを選んでみましょう。トランジションを確認し、またプロダクトイオンのピークがMS/MSライブラリスペクトルの強度順にランク付けされていることも確認しましょう。ツリービューでペプチドの選択を変更すると、MS/MSスペクトルチャートが更新され、選択したペプチドに対応するスペクトルが表示されます。また、選択したトランジションに一致するピークが赤でハイライト表示されます。
     </p>
     <p>
-        <img src="image-9.png" />
+        <img src="s-8.png" />
     </p>
     <p>
         上記の画面のように、必ずしもすべてのペプチドにおいてトランジション用に選択されたプロダクトイオンがピーク強度の高いものから順に該当するわけではなく、また、該当するすべてのスペクトルが表示されない場合もあります。
@@ -315,7 +315,7 @@ <h1>データをインポートする</h1>
         これにより以下のような画面が表示されます。
     </p>
     <p>
-        <img src="image-10.png" />
+        <img src="s-9.png" />
     </p>
     <p>
         また、間にある薄いグレーのスプリッターバーをクリックしてドラッグすることで、様々な画面の大きさを調整できます。
@@ -336,7 +336,7 @@ <h1>データをインポートする</h1>
         この操作により、以下のような画面が表示されます。
     </p>
     <p>
-        <img src="image-11.png" />
+        <img src="s-10.png" />
     </p>
     <p>
         上記のように、3つすべてのトランジションのクロマトグラムが表示されない場合、以下の操作を行います。
@@ -359,7 +359,7 @@ <h1>データをインポートする</h1>
         labでは、1つ目のオプションを推奨しています。2つ目のオプションでは、干渉領域の境界を決める際に、人の判断に起因する誤差が生じるからです。しかし、このチュートリアルでは両方のオプションを試します。クロマトグラムプロットの場所を広げるため、次のセクションを始める前に以下の操作を行います。
     </p>
     <ul>
-        <li>プッシュピン <img src="image-12.png" />をクリックします。これは [ <b>ライブラリの一致</b> ] タイトルバーの右上隅にあるXの左にあります。</li>
+        <li>プッシュピン <img src="../../shared/pushpin-icon.png" />をクリックします。これは [ <b>ライブラリの一致</b> ] タイトルバーの右上隅にあるXの左にあります。</li>
     </ul>
     <h2>干渉のあるトランジションピークを削除する</h2>
     <p>
@@ -379,7 +379,7 @@ <h2>干渉のあるトランジションピークを削除する</h2>
         プリカーサー総面積比は加重平均であり、 内部標準ピーク面積を重みとして、以下のように簡単な式で表すことができます。
     </p>
     <p>
-        <img src="image-13.png" />
+        <img src="s-precursor-total-area-ratio-formula.png" />
     </p>
     <p>
         ライトまたはヘビーピークのいずれかを削除すると、対応するトランジションのピークも削除されます。したがって一対のトランジションのみが残れば（このケースではy7）、そのトランジションのライトピークとヘビーピークの比率（ここでは0.24）が、プリカーサーの総面積比となります。
@@ -397,7 +397,7 @@ <h2>干渉を除外するためピーク境界を調整する</h2>
         これにより以下のような画面が表示されます。
     </p>
     <p>
-        <img src="image-14.png" />
+        <img src="s-11.png" />
     </p>
     <p>
         この場合、y4およびy3はそれぞれ比率0.31および比率0.35、y7は0.23となり、加重平均の式から、プリカーサー総比率は0.27となります。
@@ -429,7 +429,7 @@ <h1>Study 7のトランジションリストを取り込むためのドキュメ
         以下のようなスプレッドシートが表示されます。
     </p>
     <p>
-        <img src="image-15.png" />
+        <img src="s-transition-list-spreadsheet.png" />
     </p>
     <p>
         これは誰かが相当な労力をかけて手動で作成したスプレッドシートなのでしょう。境界線、統合セル、ハイライト表示を利用して、この一連のトランジションを他人にわかりやすく表示しています。この作業をSkylineは自動で行います。
@@ -466,7 +466,7 @@ <h1>Study 7のトランジションリストを取り込むためのドキュメ
         [ <b>同位体修飾を編集</b> ] は以下のように表示されます。
     </p>
     <p>
-        <img src="image-16.png" />
+        <img src="s-12.png" />
     </p>
     <p>
         以下の手順を行って、Study 7のトランジションリストのドキュメント作成を完了します。
@@ -512,7 +512,7 @@ <h2>トランジションリストをドキュメントに貼り付ける </h2>
         これによって、以下のような [<b>トランジションリストのインポート：列の識別</b> ] フォームが表示されます。
     </p>
     <p>
-        <img src="image-17.png" />
+        <img src="s-13.png" />
     </p>
     <ul>
         <li>[ <b>OK</b> ] ボタンをクリックします。</li>
@@ -521,7 +521,7 @@ <h2>トランジションリストをドキュメントに貼り付ける </h2>
         Skylineに以下のようなエラーメッセージが表示されます。
     </p>
     <p>
-        <img src="image-18.png" /> 
+        <img src="s-14.png" /> 
     </p>
     <p>
         Skyline以外で作成されたトランジションリストを用いて作業する場合、このメッセージがしばしば表示されます。その他のエラーメッセージについては、この項目のSkyline取扱説明ビデオで説明されています（<a
@@ -552,7 +552,7 @@ <h2>トランジションリストをドキュメントに貼り付ける </h2>
         この操作により、Skylineのペプチドビューは以下のように表示されます。
     </p>
     <p>
-        <img src="image-19.png" />
+        <img src="s-15.png" />
     </p>
     <h2>修飾を手動で設定する</h2>
     <p>
@@ -573,7 +573,7 @@ <h2>修飾を手動で設定する</h2>
         [ <b>同位体修飾を編集</b> ] は以下のように表示されます。
     </p>
     <p>
-        <img src="image-20.png" />
+        <img src="s-16.png" />
     </p>
     <p>
         この修飾は、含まれる炭素原子の数に応じて、アミノ酸ごとに異なる質量シフトを適用します。 
@@ -582,7 +582,7 @@ <h2>修飾を手動で設定する</h2>
         <li>[ <b>OK</b> ] ボタンをクリックして [ <b>修飾を編集</b> ] に戻ると、以下のような画面が表示されます。</li>
     </ul>
     <p>
-        <img src="image-21.png" />
+        <img src="s-17.png" />
     </p>
     <ul>
         <li>[ <b>修飾を編集</b> ] の [ <b>OK</b> ] ボタンをクリックして、ドキュメントに戻ります。</li>
@@ -599,7 +599,7 @@ <h2>修飾を手動で設定する</h2>
         ペプチドビューは以下のように表示されます。
     </p>
     <p>
-        <img src="image-22.png" />
+        <img src="s-18.png" />
     </p>
     <p>
         今度は「744.8398++」プリカーサーと「747.3481++ (heavy)」プリカーサーの両方を展開します。 
@@ -649,7 +649,7 @@ <h2>複数サンプルを含むWIFFファイルからデータをインポート
         複数サンプルを含んだWIFFファイル内のサンプル名のリストを読み取るのに1～2秒かかるかもしれませんが、その後以下のようなフォームが表示されます。
     </p>
     <p>
-        <img src="image-23.png" />
+        <img src="s-19.png" />
     </p>
     <p>
         このチュートリアルでは、インポートに必要な時間を短縮するため以下の手順を実行します。
@@ -663,7 +663,7 @@ <h2>複数サンプルを含むWIFFファイルからデータをインポート
         以下のメッセージがSkylineに表示され、ここで、これらすべての繰り返し測定ファイルの名前から、共通のプリフィックスである「7_3_」を削除することができます。
     </p>
     <p>
-        <img src="image-24.png" />
+        <img src="s-20.png" />
     </p>
     <ul>
         <li>[ <b>削除</b> ] ボタンをクリックしこの操作を許可します。</li>
@@ -685,7 +685,7 @@ <h2>ピーク積分を詳しく調べ、調整する</h2>
         <li>以下の画像のようにビュー比率を調整します。</li>
     </ul>
     <p>
-        <img src="image-25.png" />
+        <img src="s-21.png" />
     </p>
     <p>
         現在選択されているペプチド「YEVQGEVFTKPQ<b><span class="blue">L</span></b>WP」はCRPタンパク質のC末端ペプチドですが、Study
@@ -731,7 +731,7 @@ <h2>ピーク積分を詳しく調べ、調整する</h2>
         以下のような画面が表示されます。
     </p>
     <p>
-        <img src="image-26.png" />
+        <img src="s-22.png" />
     </p>
     <h2>ピーク面積ビューによるデータ解析</h2>
     <p>
@@ -768,7 +768,7 @@ <h2>ピーク面積ビューによるデータ解析</h2>
         ペプチドSSDLVALSGGHTFG<b><span class="blue">K</span></b>が選択された状態で、標準化チャートが以下のように表示されます。
     </p>
     <p>
-        <img src="image-27.png" />
+        <img src="s-23.png" />
     </p>
     <p>
         実際に各濃度の繰り返し測定の精度が向上したことがわかります。
@@ -787,7 +787,7 @@ <h2>ピーク面積ビューによるデータ解析</h2>
         6つの定量精度の高いペプチドのうちの一つ、ESDTSYVSL<b><span class="blue">K</span></b>ペプチドライトプリカーサー564.7746++については、以下のようなチャートが得られます。
     </p>
     <p>
-        <img src="image-28.png" />
+        <img src="s-24.png" />
     </p>
     <p>
         予想通り、トランジション間の定量比はかなり近い値になっています。2つ目および3つ目のペプチド（INDISHTQSVSA<b><span class="blue">K</span></b>およびLFTGHPETLE<b><span
@@ -800,7 +800,7 @@ <h2>ピーク面積ビューによるデータ解析</h2>
         ピーク面積グラフは以下のように表示されます。
     </p>
     <p>
-        <img src="image-29.png" />
+        <img src="s-25.png" />
     </p>
     <p>
         このグラフはy3のトランジションで干渉があったことを示しています。なぜなら、低濃度における定量比がこのペプチドのその他のトランジションとあまりに異なっているからです。
@@ -816,13 +816,13 @@ <h2>ピーク面積ビューによるデータ解析</h2>
         チャートは以下のように変更されます。
     </p>
     <p>
-        <img src="image-30.png" />
+        <img src="s-26.png" />
     </p>
     <p>
         ここでも、このチャートは明らかにy3のトランジション（茶色）で干渉があったことが示されており、E以降の繰り返し測定では、内在性ペプチドの濃度が増加するにつれてその干渉が少なくなっています。クロマトグラムチャートと同時に閲覧できるような位置にピークエリアビューを移動させると、個別のバーをクリックしていくことで干渉ピークを見ることができるようになります。この場合では以下の繰り返し測定E_03で見られるように、干渉ピークはかなりはっきりしています。
     </p>
     <p>
-        <img src="image-31.png" />
+        <img src="s-27.png" />
     </p>
     <p>
         MRMerドキュメントと同じように、積分境界を調整して干渉ピークを除外してみることは可能ですが、ペプチドの総ピーク面積に対してy3トランジションのピーク面積は大きくないため、y3トランジションを完全に消去するか、非定量にするほうが良いでしょう。これらの測定精度を評価したい場合は、以下の手順を行います。
@@ -836,7 +836,7 @@ <h2>ピーク面積ビューによるデータ解析</h2>
         [ <b>ピーク面積</b> ] チャートは以下のように変更されます。
     </p>
     <p>
-        <img src="image-32.png" />
+        <img src="s-28.png" />
     </p>
     <p>
         ペプチドがこの順序で並んでいない場合、以下の操作を行います。
@@ -912,7 +912,7 @@ <h2>濃度値を設定する</h2>
         これらの値の入力が終わると、[ <b>ドキュメントグリッド</b> ] は以下のようになります。
     </p>
     <p>
-        <img src="image-33.png" />
+        <img src="s-29.png" />
     </p>
     <p>
         今度は以下の操作を行って、新しく入力された濃度を [ <b>ピーク面積：繰り返し測定比較</b> ] グラフで使用できます。
@@ -928,7 +928,7 @@ <h2>濃度値を設定する</h2>
         [ <b>ピーク面積</b> ] グラフは以下のように表示されます。
     </p>
     <p>
-        <img src="image-34.png" />
+        <img src="s-30.png" />
     </p>
     <p>
         このグラフでは、かなり低い濃度でもCV値は極めて低いことが示されています。以下の操作を行って、平均のピーク面積比とともに標準偏差をエラーバーで示すグラフに切り替えることができます。
@@ -940,7 +940,7 @@ <h2>濃度値を設定する</h2>
         これによりグラフは以下のように変更されます。
     </p>
     <p>
-        <img src="image-35.png" />
+        <img src="s-31.png" />
     </p>
     <ul>
         <li>[ <b>ファイル</b> ] メニューで、[ <b>保存</b> ] をクリックしてこのセクションを終了します。 </li>
@@ -963,7 +963,7 @@ <h2>さらなる解析</h2>
         ファイルはすぐに開かれ、注入された同位体標識標準のCV値がペプチド間で異なっていることが示されます。以下のチャートのように表示されます。
     </p>
     <p>
-        <img src="image-36.png" />
+        <img src="s-32.png" />
     </p>
     <p>
         最初の4つのデータセットのうち、CV値が40%を超えているペプチドはINDISHTQSVSA<b><span class="blue">K</span></b>だけですが、ペプチドLSEPAELTDAV<b><span
@@ -976,7 +976,7 @@ <h2>さらなる解析</h2>
         [ <b>保持時間：繰り返し測定比較</b> ] グラフを見てみると、「空白」繰り返し測定のうち3つについてSkylineは誤ったピークを選択しています（これはすでにかなり前に修正されていますが、ドキュメントデータがインポートされ、保存された後です）。
     </p>
     <p>
-        <img src="image-37.png" />
+        <img src="s-33.png" />
     </p>
     <p>
         X-軸の下をクリック・ドラッグしてこれらのピークを修正すると、LSEPAELTDAV<b><span class="blue">K</span></b>のヘビープリカーサーのCV値は約10%まで低下し、その他のペプチドと同程度になります。
@@ -995,7 +995,7 @@ <h2>さらなる解析</h2>
         <li>「INDISHTQSVSA<b><span class="blue">K</span></b>」ペプチドをクリックします。</li>
     </ul>
     <p>
-        <img src="image-38.png" />
+        <img src="s-34.png" />
     </p>
     <p>
         内部標準によりこのペプチドの定量におけるばらつきが補正されたことがわかります。非標準化データを再確認するには以下の操作を行います。
@@ -1007,7 +1007,7 @@ <h2>さらなる解析</h2>
         このチャートを見て、標準化することによって結果がこんなに劇的に改善されるであろうことを推測するのは難しかったことでしょう。
     </p>
     <p>
-        <img src="image-39.png" />
+        <img src="s-35.png" />
     </p>
     <p>
         最後に、最初のデータセットで干渉が検出されたペプチドを取り上げます。
@@ -1021,13 +1021,13 @@ <h2>さらなる解析</h2>
         ここでも、y3トランジションで干渉があったことがはっきりとわかります。
     </p>
     <p>
-        <img src="image-40.png" />
+        <img src="s-36.png" />
     </p>
     <p>
         しかし最初のデータセットのときとは違い、個々のクロマトグラムを確認しても、干渉は見つけづらくなっています。ここでは、クロマトグラフィーの条件が最初のデータセットとは少し異なるために、y3の積分区域内に2つのピークが混在していると気付くのはほぼ不可能です。以下に繰り返し測定E_03のクロマトグラムを示します。
     </p>
     <p>
-        <img src="image-41.png" />
+        <img src="s-37.png" />
     </p>
     <p>
         NCI CPTAC Study 7は、非常に多くのデータを提供しており、現在そのデータのすべてが公開されています。この研究はSkylineの存在を知っている研究者がいない状態で行われたのですが、それでもSkylineを利用してこのデータから短時間で多くを学ぶことができます。
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/ja/invariant.html b/pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/ja/invariant.html
index c10676b3fe..4a3add8898 100644
--- a/pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/ja/invariant.html
+++ b/pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/ja/invariant.html
@@ -113,7 +113,7 @@ <h1>Preparing a Document to Accept a Transition List</h1>
         The <b>Peptide Settings</b> form should now look something like:
     </p>
     <p>
-        <img src="image-0.png" />
+        <img src="s-1.png" />
     </p>
     <p>
         To set up the background proteome for the MRMer document now, perform the following steps:
@@ -132,7 +132,7 @@ <h1>Preparing a Document to Accept a Transition List</h1>
         The <b>Peptide Settings</b> form should now look something like this:
     </p>
     <p>
-        <img src="image-1.png" />
+        <img src="s-2.png" />
     </p>
     <p>
         Finally, before you can insert the transition list from the MRMer experiment into the current document, you will need to define the isotope
@@ -159,7 +159,7 @@ <h1>Preparing a Document to Accept a Transition List</h1>
         The <b>Edit Isotope Modification</b> form should now look like this:
     </p>
     <p>
-        <img src="image-2.png" />
+        <img src="s-3.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button</li>
@@ -181,7 +181,7 @@ <h1>Preparing a Document to Accept a Transition List</h1>
         The <b>Edit Isotope Modification</b> form should now look like this:
     </p>
     <p>
-        <img src="image-3.png" />
+        <img src="s-4.png" />
     </p>
     <p>
         Skyline automatically calculates both the monoisotopic and average masses, approximately 8 Daltons for Lysine (K) and 10 Daltons for Arginine
@@ -236,7 +236,7 @@ <h1>Inserting a Transition List with Associated Proteins</h1>
         The <b>Insert Transition List</b> form appears:
     </p>
     <p>
-        <img src="image-4.png" />
+        <img src="s-5.png" />
     </p>
     <ul>
         <li>Press Ctrl-V to paste the copied cells into the <b>Insert Transition List</b> form.</li>
@@ -245,7 +245,7 @@ <h1>Inserting a Transition List with Associated Proteins</h1>
         This will bring up the <b>Import Transition List: Identify Columns</b> form, which should look like this:
     </p>
     <p>
-        <img src="image-5.png" />
+        <img src="s-6.png" />
     </p>
     <ul>
         <li>Make sure the <b>Associate Proteins</b> checkbox is ticked.</li>
@@ -267,12 +267,12 @@ <h1>Inserting a Transition List with Associated Proteins</h1>
     </ul>
     <p>
         The main Skyline window should show a number of peptides grouped within their proteins. The peptide icons should contain 3 vertical lines and a
-        baseline (<img src="image-6.png" />), like a very small MS/MS spectrum, in the lower right corner (<img src="image-7.png" />). The presence of
+        baseline (<img src="../../shared/peptide-icon.png" />), like a very small MS/MS spectrum, in the lower right corner (<img src="../../shared/peptide-with-spectrum-lines-icon.png" />). The presence of
         this image indicates the peptide has an associated MS/MS library spectrum. The peptide label should highlight in blue the C-terminal Lysine or
         Arginine, indicating the stable isotope labeled amino acid in the heavy, labeled form:
     </p>
     <p>
-        <img src="image-8.png" />
+        <img src="s-7.png" />
     </p>
     <p>
         You can also see at the bottom right corner of the window, in the status bar, the indicator “1/296 tran”, confirming that all 296 transitions
@@ -297,7 +297,7 @@ <h1>Inserting a Transition List with Associated Proteins</h1>
         show the spectrum that matches the current peptide, and the peak matching the selected transition will be highlighted in red:
     </p>
     <p>
-        <img src="image-9.png" />
+        <img src="s-8.png" />
     </p>
     <p>
         You will notice that not all of the peptides have the most abundant product ions chosen for transitions, like the one shown in the image above,
@@ -365,7 +365,7 @@ <h1>Importing Data</h1>
         This should leave Skyline looking something like:
     </p>
     <p>
-        <img src="image-10.png" />
+        <img src="s-9.png" />
     </p>
     <p>
         You can also change the proportions allocated to the various panes by clicking and dragging the light gray splitter bars between them.
@@ -386,7 +386,7 @@ <h1>Importing Data</h1>
         This should change Skyline to look like:
     </p>
     <p>
-        <img src="image-11.png" />
+        <img src="s-10.png" />
     </p>
     <p>
         If you do not see chromatograms for all three transitions, as shown above, do the following:
@@ -413,7 +413,7 @@ <h1>Importing Data</h1>
         the following before starting the next section:
     </p>
     <ul>
-        <li>Click the pushpin <img src="image-12.png" /> to the left of the X in the upper right corner of the <b>Library Match</b> title
+        <li>Click the pushpin <img src="../../shared/pushpin-icon.png" /> to the left of the X in the upper right corner of the <b>Library Match</b> title
             bar.</li>
     </ul>
     <h2>Removing a Transition Peak with Interference</h2>
@@ -436,7 +436,7 @@ <h2>Removing a Transition Peak with Interference</h2>
         The precursor total area ratio is a weighted mean, using the internal standard peak area as the weights, which simplifies algebraically to:
     </p>
     <p>
-        <img src="image-13.png" />
+        <img src="s-precursor-total-area-ratio-formula.png" />
     </p>
     <p>
         Removing either a light or heavy peak removes the peak for its matching transition. Hence, when only one pair of transitions remain, as with y7
@@ -457,7 +457,7 @@ <h2>Adjusting Peak Boundaries to Exclude Interference</h2>
         This should leave Skyline showing something like:
     </p>
     <p>
-        <img src="image-14.png" />
+        <img src="s-11.png" />
     </p>
     <p>
         In this case, y4 and y3 show ratios of 0.31 and 0.35 respectively and y7 shows 0.23, yielding a weighted mean, precursor total ratio of 0.27.
@@ -502,7 +502,7 @@ <h1>Preparing a Document to Accept the Study 7 Transition List</h1>
         You should be presented with a spreadsheet that looks something like this:
     </p>
     <p>
-        <img src="image-15.png" />
+        <img src="s-transition-list-spreadsheet.png" />
     </p>
     <p>
         You can tell that this is a spreadsheet created manually by someone who put significant effort, using borders, merged cells and highlighting,
@@ -545,7 +545,7 @@ <h1>Preparing a Document to Accept the Study 7 Transition List</h1>
         The <b>Edit Isotope Modification</b> form should now look like this:
     </p>
     <p>
-        <img src="image-16.png" />
+        <img src="s-12.png" />
     </p>
     <p>
         To finish preparing the document for the Study 7 transition list, do the following:
@@ -595,7 +595,7 @@ <h2>Pasting a Transition List into the Document </h2>
         This will bring up the <b>Import Transition List: Identify Columns</b> form, which should look like this:
     </p>
     <p>
-        <img src="image-17.png" />
+        <img src="s-13.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -604,7 +604,7 @@ <h2>Pasting a Transition List into the Document </h2>
         Skyline should present the following error message:
     </p>
     <p>
-        <img src="image-18.png" /> 
+        <img src="s-14.png" /> 
     </p>
     <p>
         Messages like this are not uncommon when working with transition lists created outside Skyline. Others are presented in the Skyline
@@ -637,7 +637,7 @@ <h2>Pasting a Transition List into the Document </h2>
         This should leave the Skyline peptide view looking like:
     </p>
     <p>
-        <img src="image-19.png" />
+        <img src="s-15.png" />
     </p>
     <h2>Adjusting Modifications Manually</h2>
     <p>
@@ -661,7 +661,7 @@ <h2>Adjusting Modifications Manually</h2>
         The <b>Edit Isotope Modification</b> form should look like:
     </p>
     <p>
-        <img src="image-20.png" />
+        <img src="s-16.png" />
     </p>
     <p>
         This modification will apply a varying mass shift to any amino acid, depending on how many Carbon atoms it contains.
@@ -670,7 +670,7 @@ <h2>Adjusting Modifications Manually</h2>
         <li>Click the <b>OK</b> button to return to the <b>Edit Modifications</b> form, which should now look like:</li>
     </ul>
     <p>
-        <img src="image-21.png" />
+        <img src="s-17.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button on the <b>Edit Modifications</b> form to return to the document.</li>
@@ -688,7 +688,7 @@ <h2>Adjusting Modifications Manually</h2>
         The peptide view should now look like this:
     </p>
     <p>
-        <img src="image-22.png" />
+        <img src="s-18.png" />
     </p>
     <p>
         Now expand both the “744.8398++” precursor and the <b>“</b>747.3481++ (heavy)” precursor: 
@@ -741,7 +741,7 @@ <h2>Importing Data from a Multiple Sample WIFF File</h2>
         present you with a form that looks like this:
     </p>
     <p>
-        <img src="image-23.png" />
+        <img src="s-19.png" />
     </p>
     <p>
         For this tutorial, to reduce the time that will be required to complete the import:
@@ -756,7 +756,7 @@ <h2>Importing Data from a Multiple Sample WIFF File</h2>
         use to display information about these replicates:
     </p>
     <p>
-        <img src="image-24.png" />
+        <img src="s-20.png" />
     </p>
     <ul>
         <li>Click the <b>Remove</b> button to accept this operation.</li>
@@ -780,7 +780,7 @@ <h2>Inspecting and Adjusting Peak Integration</h2>
         <li>Adjust the view proportions to look something like the image below.</li>
     </ul>
     <p>
-        <img src="image-25.png" />
+        <img src="s-21.png" />
     </p>
     <p>
         The currently selected peptide “YEVQGEVFTKPQ<b><span class="blue">L</span></b>WP”, which was the peptide at the C-terminal end of CRP
@@ -840,7 +840,7 @@ <h2>Inspecting and Adjusting Peak Integration</h2>
         Skyline should now look something like:
     </p>
     <p>
-        <img src="image-26.png" />
+        <img src="s-22.png" />
     </p>
     <h2>Data Inspection with Peak Areas View</h2>
     <p>
@@ -884,7 +884,7 @@ <h2>Data Inspection with Peak Areas View</h2>
                 class="blue">K</span></b> selected:
     </p>
     <p>
-        <img src="image-27.png" />
+        <img src="s-23.png" />
     </p>
     <p>
         You will see that, indeed, precision among the replicates for each concentration appears to have improved.
@@ -904,7 +904,7 @@ <h2>Data Inspection with Peak Areas View</h2>
         For the 6 well behaved peptides, you should see a chart like the one below, with the ESDTSYVSL<b><span class="blue">K</span></b> peptide light precursor 564.7746++ selected:
     </p>
     <p>
-        <img src="image-28.png" />
+        <img src="s-24.png" />
     </p>
     <p>
         As expected, the ratios are quite similar. The second and third peptides (INDISHTQSVSA<b><span class="blue">K</span></b> and
@@ -917,7 +917,7 @@ <h2>Data Inspection with Peak Areas View</h2>
         This should cause the peak area graph to look like:
     </p>
     <p>
-        <img src="image-29.png" />
+        <img src="s-25.png" />
     </p>
     <p>
         This seems to indicate some interference in the transition for y3, since its ratio, at low concentrations, is so different from the others for
@@ -934,7 +934,7 @@ <h2>Data Inspection with Peak Areas View</h2>
         The chart should change to something like:
     </p>
     <p>
-        <img src="image-30.png" />
+        <img src="s-26.png" />
     </p>
     <p>
         Again, this chart clearly indicates interference on the transition for y3 (brown) that becomes less of a factor as the concentration of the
@@ -942,7 +942,7 @@ <h2>Data Inspection with Peak Areas View</h2>
         charts, you can click on the individual bars to see the interfering peak, which, in this case, is pretty clear, as in replicate E_03 below:
     </p>
     <p>
-        <img src="image-31.png" />
+        <img src="s-27.png" />
     </p>
     <p>
         As with the case in the MRMer document, you might attempt to adjust the integration boundaries to exclude the interfering peak, but it is
@@ -958,7 +958,7 @@ <h2>Data Inspection with Peak Areas View</h2>
         The <b>Peak Areas</b> chart should have changed to look something like:
     </p>
     <p>
-        <img src="image-32.png" />
+        <img src="s-28.png" />
     </p>
     <p>
         If the peptides do not appear in this order, do the following:
@@ -1046,7 +1046,7 @@ <h2>Settings Concentration Values</h2>
         When you are done entering these values, the <b>Document Grid</b> should look like this:
     </p>
     <p>
-        <img src="image-33.png" />
+        <img src="s-29.png" />
     </p>
     <p>
         You can now use the newly entered concentrations in the <b>Peak Areas: Replicate Comparison</b> graph by doing the following:
@@ -1062,7 +1062,7 @@ <h2>Settings Concentration Values</h2>
         The <b>Peak Areas</b> graph should now look like:
     </p>
     <p>
-        <img src="image-34.png" />
+        <img src="s-30.png" />
     </p>
     <p>
         This graph shows that the CVs are quite low until the very lowest concentrations. You can easily switch to a graph showing the mean ratios with
@@ -1075,7 +1075,7 @@ <h2>Settings Concentration Values</h2>
         This should change the graph to look like:
     </p>
     <p>
-        <img src="image-35.png" />
+        <img src="s-31.png" />
     </p>
     <ul>
         <li>On the <b>File</b> menu, click <b>Save</b>, to end this section. </li>
@@ -1100,7 +1100,7 @@ <h2>Further Exploration</h2>
         appearing as in the chart below:
     </p>
     <p>
-        <img src="image-36.png" />
+        <img src="s-32.png" />
     </p>
     <p>
         The peptide INDISHTQSVSA<b><span class="blue">K</span></b> is the only one of the 4 from the first data set that still has a CV
@@ -1114,7 +1114,7 @@ <h2>Further Exploration</h2>
         for 3 of the “Blank” replicates (though this issue was fixed a long time ago – but after the document data was imported and saved):
     </p>
     <p>
-        <img src="image-37.png" />
+        <img src="s-33.png" />
     </p>
     <p>
         If you correct these by clicking and dragging beneath the x-axis, the CV for the heavy precursor of LSEPAELTDAV<b><span
@@ -1135,7 +1135,7 @@ <h2>Further Exploration</h2>
         <li>Click the “INDISHTQSVSA<b><span class="blue">K</span></b>” peptide.</li>
     </ul>
     <p>
-        <img src="image-38.png" />
+        <img src="s-34.png" />
     </p>
     <p>
         This seems to indicate that the internal standard is doing its job of compensating for variance in measurements of this peptide. To review the
@@ -1148,7 +1148,7 @@ <h2>Further Exploration</h2>
         It would be hard to guess from this chart that the normalization would be so effective:
     </p>
     <p>
-        <img src="image-39.png" />
+        <img src="s-35.png" />
     </p>
     <p>
         Finally, returning to the peptide in which we detected interference in the first data set:
@@ -1162,7 +1162,7 @@ <h2>Further Exploration</h2>
         Here also, you will see clear evidence of interference on the y3 transition:
     </p>
     <p>
-        <img src="image-40.png" />
+        <img src="s-36.png" />
     </p>
     <p>
         Unlike the first data set, however, it is much harder to see the interference by inspecting the individual chromatograms. In this case, due to
@@ -1170,7 +1170,7 @@ <h2>Further Exploration</h2>
         replicate E_03 shown below:
     </p>
     <p>
-        <img src="image-41.png" />
+        <img src="s-37.png" />
     </p>
     <p>
         The NCI CPTAC Study 7 provided quite a lot more data, all of which is now public. Skyline can help you learn a lot about this data quickly,
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/ja/image-0.png b/pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/ja/s-1.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/ja/image-0.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/ja/s-1.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/ja/image-11.png b/pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/ja/s-10.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/ja/image-11.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/ja/s-10.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/ja/image-14.png b/pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/ja/s-11.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/ja/image-14.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/ja/s-11.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/ja/image-16.png b/pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/ja/s-12.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/ja/image-16.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/ja/s-12.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/ja/image-17.png b/pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/ja/s-13.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/ja/image-17.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/ja/s-13.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/ja/image-18.png b/pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/ja/s-14.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/ja/image-18.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/ja/s-14.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/ja/image-19.png b/pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/ja/s-15.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/ja/image-19.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/ja/s-15.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/ja/image-20.png b/pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/ja/s-16.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/ja/image-20.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/ja/s-16.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/ja/image-21.png b/pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/ja/s-17.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/ja/image-21.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/ja/s-17.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/ja/image-22.png b/pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/ja/s-18.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/ja/image-22.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/ja/s-18.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/ja/image-23.png b/pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/ja/s-19.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/ja/image-23.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/ja/s-19.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/ja/image-1.png b/pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/ja/s-2.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/ja/image-1.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/ja/image-24.png b/pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/ja/s-20.png
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rename from pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/ja/image-24.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/ja/image-25.png b/pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/ja/s-21.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/ja/image-25.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/ja/image-26.png b/pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/ja/s-22.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/ja/image-28.png b/pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/ja/s-24.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/ja/image-40.png b/pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/ja/s-36.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/ja/image-41.png b/pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/ja/s-37.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/ja/image-3.png b/pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/ja/s-4.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/ja/image-4.png b/pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/ja/s-5.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/ja/image-5.png b/pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/ja/s-6.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/ja/image-8.png b/pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/ja/s-7.png
similarity index 100%
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rename to pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/ja/s-7.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/ja/image-9.png b/pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/ja/s-8.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/ja/image-9.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/ja/s-8.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/ja/image-10.png b/pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/ja/s-9.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/ja/image-10.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/ja/s-9.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/ja/image-13.png b/pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/ja/s-precursor-total-area-ratio-formula.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/ja/image-13.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/ja/s-precursor-total-area-ratio-formula.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/ja/image-15.png b/pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/ja/s-transition-list-spreadsheet.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/ja/image-15.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/ja/s-transition-list-spreadsheet.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/zh-CHS/image-12.png b/pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/zh-CHS/image-12.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/zh-CHS/index.html b/pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/zh-CHS/index.html
index 5eefab2af3..b5abf02b4a 100644
--- a/pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/zh-CHS/index.html
+++ b/pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/zh-CHS/index.html
@@ -97,7 +97,7 @@ <h1>准备接受离子对列表的文档</h1>
         <b>肽段设置</b>表单将显示如下：
     </p>
     <p>
-        <img src="image-0.png" />
+        <img src="s-1.png" />
     </p>
     <p>
         要设置 MRMer 文档的背景蛋白质组，请执行以下步骤：
@@ -116,7 +116,7 @@ <h1>准备接受离子对列表的文档</h1>
         <b>肽段设置</b>表单现在应显示如下：
     </p>
     <p>
-        <img src="image-1.png" />
+        <img src="s-2.png" />
     </p>
     <p>
         最后，在将来自 MRMer 实验的离子对列表导入当前文档之前，您还需要定义所包含肽段的同位素修饰。MRMer 实验包括未标记的轻肽段和对应的重肽段，后者使用细胞培养的稳定同位素氨基酸标记 (SILAC)
@@ -139,7 +139,7 @@ <h1>准备接受离子对列表的文档</h1>
         此时<b>编辑同位素修饰</b>窗口应显示如下：
     </p>
     <p>
-        <img src="image-2.png" />
+        <img src="s-3.png" />
     </p>
     <ul>
         <li>单击<b>确定</b>按钮</li>
@@ -159,7 +159,7 @@ <h1>准备接受离子对列表的文档</h1>
         此时<b>编辑同位素修饰</b>窗口应显示如下：
     </p>
     <p>
-        <img src="image-3.png" />
+        <img src="s-4.png" />
     </p>
     <p>
         Skyline 自动计算单一同位素质量和平均质量偏移，如图，赖氨酸 (K) 质量偏移约为 8 Da，精氨酸 (R) 约为 10 Da，这是由于在这些氨基酸残基中使用了 13 C 和 15 N。
@@ -206,7 +206,7 @@ <h1>插入具有相关蛋白质的离子对列表</h1>
         随即会显示<b>插入离子对列表</b>表单：
     </p>
     <p>
-        <img src="image-4.png" />
+        <img src="s-5.png" />
     </p>
     <ul>
         <li>按 Ctrl-V 将复制的单元格粘贴到<b>插入离子对列表</b>表单。</li>
@@ -215,7 +215,7 @@ <h1>插入具有相关蛋白质的离子对列表</h1>
         此操作将打开<b>导入离子对列表：标识列</b>表单，如下所示：
     </p>
     <p>
-        <img src="image-5.png" />
+        <img src="s-6.png" />
     </p>
     <ul>
         <li>确保选中<b>关联蛋白质</b>复选框。</li>
@@ -234,11 +234,11 @@ <h1>插入具有相关蛋白质的离子对列表</h1>
         <li>按 Home 键滚动到新目标列表顶部。</li>
     </ul>
     <p>
-        Skyline 主窗口将显示若干按照从属蛋白质分组的肽段。肽段图标的右下角应包含 3 条垂直线和一条基线 (<img src="image-6.png" />)，类似于非常小的 MS/MS 谱图 (<img src="image-7.png" />)。出现此图标表明肽段具有对应的
+        Skyline 主窗口将显示若干按照从属蛋白质分组的肽段。肽段图标的右下角应包含 3 条垂直线和一条基线 (<img src="../../shared/peptide-icon.png" />)，类似于非常小的 MS/MS 谱图 (<img src="../../shared/peptide-with-spectrum-lines-icon.png" />)。出现此图标表明肽段具有对应的
         MS/MS 库谱图。标记肽段 C-末端赖氨酸或精氨酸以蓝色突出显示，标明稳定同位素标记的重链形式的氨基酸：
     </p>
     <p>
-        <img src="image-8.png" />
+        <img src="s-7.png" />
     </p>
     <p>
         您还可以在窗口右下角的状态栏中看到指示符 “1/296 tran”，表明 MRMer 离子对列表中的所有 296 个离子对已添加到此文档中。在状态栏的左侧，您可以看到此文档包含 24 个蛋白质、44 个肽段和 88 个母离子，其中每个肽段对应 2 个母离子。
@@ -259,7 +259,7 @@ <h1>插入具有相关蛋白质的离子对列表</h1>
         花点时间在肽段视图中选择单个肽段和离子对。检查这些离子对以及它们的子离子峰在 MS/MS 库谱图中是如何按照强度大小排名。在肽段树形视图选择不同的肽段，则 MS/MS 谱图也会同步更新，显示出与当前肽段匹配的谱图。同时，与已选离子对相匹配的谱峰还会以红色突出显示：
     </p>
     <p>
-        <img src="image-9.png" />
+        <img src="s-8.png" />
     </p>
     <p>
         您会注意到，并非所有的肽段都选择了丰度最高的子离子作为离子对，正如上图显示的那样。同时，并非所有的谱图都有良好的碎片离子匹配。
@@ -315,7 +315,7 @@ <h1>导入数据</h1>
         执行此操作后，Skyline 应显示如下：
     </p>
     <p>
-        <img src="image-10.png" />
+        <img src="s-9.png" />
     </p>
     <p>
         您还可以单击并拖动窗格之间的浅灰色分割控制条，改变分配给各窗格的比例。
@@ -336,7 +336,7 @@ <h1>导入数据</h1>
         Skyline 将发生如下变化：
     </p>
     <p>
-        <img src="image-11.png" />
+        <img src="s-10.png" />
     </p>
     <p>
         如果未看到上图所示的三个离子对的色谱图，请执行以下步骤：
@@ -358,7 +358,7 @@ <h1>导入数据</h1>
         在 MacCoss实验室，我们倾向于第一种选择，是因为第二种选择需要人为确定未知干扰的信号界限，这种不确定因素会引入未知的误差。在本教程中，您可以尝试这两种选择。要给色谱图留出更多的空间，请在开始下一部分之前执行以下操作：
     </p>
     <ul>
-        <li>单击<b>库匹配</b>标题栏右上角 X 左侧的图钉<img src="image-12.png" />。</li>
+        <li>单击<b>库匹配</b>标题栏右上角 X 左侧的图钉<img src="../../shared/pushpin-icon.png" />。</li>
     </ul>
     <h2>移除存在干扰的离子对峰</h2>
     <p>
@@ -378,7 +378,7 @@ <h2>移除存在干扰的离子对峰</h2>
         母离子总面积比值是加权平均值，以内标峰面积作为权重，数学公式表示为：
     </p>
     <p>
-        <img src="image-13.png" />
+        <img src="s-precursor-total-area-ratio-formula.png" />
     </p>
     <p>
         移除轻峰或重峰将移除与其相匹配的离子对的色谱峰。因此，仅有一对离子对保留时，正如本研究中的 y7 所示，离子对轻峰和重峰之间的比值（此处为 0.24）将成为母离子的总面积比值。
@@ -396,7 +396,7 @@ <h2>调整峰边界以排除干扰</h2>
         执行此操作后，Skyline 应显示如下：
     </p>
     <p>
-        <img src="image-14.png" />
+        <img src="s-11.png" />
     </p>
     <p>
         此时，y4 和 y3 的比值分别显示为 0.31 和 0.35，y7 的比值显示为 0.23，加权平均产生的母离子总比值为 0.27。
@@ -429,7 +429,7 @@ <h1>准备接受Study 7 离子对列表的文档</h1>
         您将看到如下所示的电子表格：
     </p>
     <p>
-        <img src="image-15.png" />
+        <img src="s-transition-list-spreadsheet.png" />
     </p>
     <p>
         可以看出，这是由某个人手动创建的电子表格。创建时此人尽了很大努力，使用表格边界、合并单元格和突出显示，让其他人也能够清晰明了地查看这些离子对，而现在 Skyline 可以自动处理这项工作。
@@ -466,7 +466,7 @@ <h1>准备接受Study 7 离子对列表的文档</h1>
         此时<b>编辑同位素修饰</b>窗口应显示如下：
     </p>
     <p>
-        <img src="image-16.png" />
+        <img src="s-12.png" />
     </p>
     <p>
         如要完成 Study 7 离子对列表文档准备，请执行以下步骤：
@@ -511,7 +511,7 @@ <h2>将离子对列表粘贴到文档 </h2>
         这将打开<b>导入离子对列表：标识列</b>表单，如下所示：
     </p>
     <p>
-        <img src="image-17.png" />
+        <img src="s-13.png" />
     </p>
     <ul>
         <li>单击<b>确定</b>按钮。</li>
@@ -520,7 +520,7 @@ <h2>将离子对列表粘贴到文档 </h2>
         Skyline 将呈现以下错误消息：
     </p>
     <p>
-        <img src="image-18.png" /> 
+        <img src="s-14.png" /> 
     </p>
     <p>
         在处理 Skyline 之外创建的离子对列表时，此类消息并不少见。在本主题的 Skyline 教学视频中也可看到（ <a
@@ -550,7 +550,7 @@ <h2>将离子对列表粘贴到文档 </h2>
         执行此操作后，Skyline 肽段视图显示如下：
     </p>
     <p>
-        <img src="image-19.png" />
+        <img src="s-15.png" />
     </p>
     <h2>手动调整修饰</h2>
     <p>
@@ -570,7 +570,7 @@ <h2>手动调整修饰</h2>
         <b>编辑同位素修饰</b>表单如下：
     </p>
     <p>
-        <img src="image-20.png" />
+        <img src="s-16.png" />
     </p>
     <p>
         根据氨基酸所含碳原子数量，这种修饰将能够在任意氨基酸上引入相应的质量偏移。 
@@ -579,7 +579,7 @@ <h2>手动调整修饰</h2>
         <li>单击<b>确定</b>按钮返回<b>编辑修饰</b>表单，表单现在显示如下：</li>
     </ul>
     <p>
-        <img src="image-21.png" />
+        <img src="s-17.png" />
     </p>
     <ul>
         <li>单击<b>编辑修饰</b>表单中的<b>确定</b>按钮，返回文档。</li>
@@ -596,7 +596,7 @@ <h2>手动调整修饰</h2>
         肽段视图现在将如下所示：
     </p>
     <p>
-        <img src="image-22.png" />
+        <img src="s-18.png" />
     </p>
     <p>
         现在展开 “744.8398++” 母离子和<b>“</b>747.3481++（重）”： 
@@ -646,7 +646,7 @@ <h2>从多样品 WIFF 文件导入数据</h2>
         Skyline 可能会花一两秒的时间读取多样品 WIFF 文件中的样品名称列表，然后它将呈现如下表单：
     </p>
     <p>
-        <img src="image-23.png" />
+        <img src="s-19.png" />
     </p>
     <p>
         对于本教程，为了缩短导入所需的时间：
@@ -660,7 +660,7 @@ <h2>从多样品 WIFF 文件导入数据</h2>
         Skyline 应显示以下消息，允许您从用于显示有关这些重复测定的信息中移除在所有名称中重复的前缀 “7_3_”：
     </p>
     <p>
-        <img src="image-24.png" />
+        <img src="s-20.png" />
     </p>
     <ul>
         <li>单击<b>删除</b>按钮以接受这项操作。</li>
@@ -681,7 +681,7 @@ <h2>检查和调整色谱峰积分</h2>
         <li>调整视图比例，使之如下图所示。</li>
     </ul>
     <p>
-        <img src="image-25.png" />
+        <img src="s-21.png" />
     </p>
     <p>
         目前选择的肽段是 “YEVQGEVFTKPQ<b><span class="blue">L</span></b>WP”（此为 CRP 蛋白质的 C- 末端肽段），事实上给 Study 7 中验证工作组的分析带来了一些麻烦。在导入数据时，您可以看到
@@ -728,7 +728,7 @@ <h2>检查和调整色谱峰积分</h2>
         此时 Skyline 将显示如下：
     </p>
     <p>
-        <img src="image-26.png" />
+        <img src="s-22.png" />
     </p>
     <h2>用峰面积视图检查数据</h2>
     <p>
@@ -764,7 +764,7 @@ <h2>用峰面积视图检查数据</h2>
         选择肽段 SSDLVALSGGHTFG<b><span class="blue">K</span></b>，您会看到如下所示的归一化图表：
     </p>
     <p>
-        <img src="image-27.png" />
+        <img src="s-23.png" />
     </p>
     <p>
         确实，您将发现每一种浓度下的重复检测所获得结果之间的精确度得到了提高。
@@ -783,7 +783,7 @@ <h2>用峰面积视图检查数据</h2>
         对于 6 个行为正常的肽段，您会看到如下所示的图表（选取了 ESDTSYVSL<b><span class="blue">K</span></b> 肽段轻母离子 564.7746++）：
     </p>
     <p>
-        <img src="image-28.png" />
+        <img src="s-24.png" />
     </p>
     <p>
         不出所料，这些比值非常相似。第二个和第三个肽段（INDISHTQSVSA<b><span class="blue">K</span></b> 和 LFTGHPETLE<b><span
@@ -796,7 +796,7 @@ <h2>用峰面积视图检查数据</h2>
         峰面积图表将显示如下：
     </p>
     <p>
-        <img src="image-29.png" />
+        <img src="s-25.png" />
     </p>
     <p>
         看起来 y3 的离子对中存在干扰，因为其低浓度下比值与此肽段其它离子对差异较大。
@@ -811,13 +811,13 @@ <h2>用峰面积视图检查数据</h2>
         图表将发生如下变化：
     </p>
     <p>
-        <img src="image-30.png" />
+        <img src="s-26.png" />
     </p>
     <p>
         此图表再次清晰地显示出 y3（棕色）的离子对存在干扰，随着内源性肽的浓度增加至超出 E组重复测定时的浓度，其影响变小。移动峰面积视图，以便看到色谱图，您这时可以单击各个条以查看存在干扰的峰值。本例中可以非常清楚地看到 y3 的色谱峰存在干扰（重复检测 E_03）：
     </p>
     <p>
-        <img src="image-31.png" />
+        <img src="s-27.png" />
     </p>
     <p>
         与 MRMer 文档中的情况一样，您可能为了排除干扰峰而尽力调整积分界线，但删除 y3 离子对或将它作为非定量离子对或许是一种更好的办法，尤其是因为该离子对对肽段的总的峰面积贡献不大。如要深入了解这些测定结果的精确性，请执行以下操作：
@@ -831,7 +831,7 @@ <h2>用峰面积视图检查数据</h2>
         <b>峰值面积</b>图表将发生变化：
     </p>
     <p>
-        <img src="image-32.png" />
+        <img src="s-28.png" />
     </p>
     <p>
         如果该肽段未按照这个顺序出现，请执行以下操作：
@@ -907,7 +907,7 @@ <h2>设置浓度值</h2>
         输入这些值后，<b>文档网格</b>应如下所示：
     </p>
     <p>
-        <img src="image-33.png" />
+        <img src="s-29.png" />
     </p>
     <p>
         现在您可以执行以下操作，以在<b>峰面积：重复检测比较</b>图中使用新输入的浓度：
@@ -923,7 +923,7 @@ <h2>设置浓度值</h2>
         <b>峰面积</b>图表将显示如下：
     </p>
     <p>
-        <img src="image-34.png" />
+        <img src="s-30.png" />
     </p>
     <p>
         该图显示出 CV 值都非常小（最低浓度的CV值除外）。通过执行以下操作，您可以轻易切换到显示平均比值和标准偏差的图表：
@@ -935,7 +935,7 @@ <h2>设置浓度值</h2>
         视图将发生如下变化：
     </p>
     <p>
-        <img src="image-35.png" />
+        <img src="s-31.png" />
     </p>
     <ul>
         <li>在<b>文件</b>菜单中单击<b>保存</b>，该部分至此结束。 </li>
@@ -957,7 +957,7 @@ <h2>进一步探索</h2>
         此文件会快速打开，并且您会看到重同位素标记参考肽段的 CV 值不尽相同，如下图所示：
     </p>
     <p>
-        <img src="image-36.png" />
+        <img src="s-32.png" />
     </p>
     <p>
         在第一组数据中，有 4 个肽段CV值偏大（40%至50%）；其中，INDISHTQSVSA<b><span class="blue">K</span></b> 是唯一一个在此数据集的变异系数仍然约为40%的肽段。同时，
@@ -970,7 +970,7 @@ <h2>进一步探索</h2>
         如果您查看<b>保留时间：重复检测比较</b>图表，会发现 Skyline 为 3 次“空白”的重复检测选择了错误的峰（尽管很久以前就已经解决了该问题，但却是在导入和保存文档数据之后）：
     </p>
     <p>
-        <img src="image-37.png" />
+        <img src="s-33.png" />
     </p>
     <p>
         如果您通过单击并向右拖动 X 轴的方式纠正这些错误，LSEPAELTDAV<b><span class="blue">K</span></b> 的重母离子变异系数可以下降至类似其它大多数肽段的 10% 左右。
@@ -989,7 +989,7 @@ <h2>进一步探索</h2>
         <li>单击 "INDISHTQSVSA<b><span class="blue">K</span></b>" 肽段。</li>
     </ul>
     <p>
-        <img src="image-38.png" />
+        <img src="s-34.png" />
     </p>
     <p>
         这似乎显示出内标对此肽段检测结果的差异起到了补偿作用。查看归一化前的数据：
@@ -1001,7 +1001,7 @@ <h2>进一步探索</h2>
         如果不是这张图表，我们很难想象到归一化会如此有效：
     </p>
     <p>
-        <img src="image-39.png" />
+        <img src="s-35.png" />
     </p>
     <p>
         最后，回到我们在第一组数据集中发现的存在干扰的肽段上来：
@@ -1015,13 +1015,13 @@ <h2>进一步探索</h2>
         在这里您会看到 y3 离子对中存在干扰的明显证据：
     </p>
     <p>
-        <img src="image-40.png" />
+        <img src="s-36.png" />
     </p>
     <p>
         然而，和第一组数据集不同，在这组数据里检查此肽段色谱图来发现干扰作用显得更困难。在这种情况下，由于稍微改变了色谱条件，几乎不可能在y3的积分范围中找到此肽段两个峰，如下面所示（重复检测 E_03）：
     </p>
     <p>
-        <img src="image-41.png" />
+        <img src="s-37.png" />
     </p>
     <p>
         NCI CPTAC Study 7 提供了更多的数据，现在这些数据均已公开。Skyline 可以帮助您迅速批量了解这些数据，即使参与此研究的人员并不知道 Skyline 会面世。
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/zh-CHS/invariant.html b/pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/zh-CHS/invariant.html
index 1c9178dede..fc796010dc 100644
--- a/pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/zh-CHS/invariant.html
+++ b/pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/zh-CHS/invariant.html
@@ -113,7 +113,7 @@ <h1>Preparing a Document to Accept a Transition List</h1>
         The <b>Peptide Settings</b> form should now look something like:
     </p>
     <p>
-        <img src="image-0.png" />
+        <img src="s-1.png" />
     </p>
     <p>
         To set up the background proteome for the MRMer document now, perform the following steps:
@@ -132,7 +132,7 @@ <h1>Preparing a Document to Accept a Transition List</h1>
         The <b>Peptide Settings</b> form should now look something like this:
     </p>
     <p>
-        <img src="image-1.png" />
+        <img src="s-2.png" />
     </p>
     <p>
         Finally, before you can insert the transition list from the MRMer experiment into the current document, you will need to define the isotope
@@ -159,7 +159,7 @@ <h1>Preparing a Document to Accept a Transition List</h1>
         The <b>Edit Isotope Modification</b> form should now look like this:
     </p>
     <p>
-        <img src="image-2.png" />
+        <img src="s-3.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button</li>
@@ -181,7 +181,7 @@ <h1>Preparing a Document to Accept a Transition List</h1>
         The <b>Edit Isotope Modification</b> form should now look like this:
     </p>
     <p>
-        <img src="image-3.png" />
+        <img src="s-4.png" />
     </p>
     <p>
         Skyline automatically calculates both the monoisotopic and average masses, approximately 8 Daltons for Lysine (K) and 10 Daltons for Arginine
@@ -236,7 +236,7 @@ <h1>Inserting a Transition List with Associated Proteins</h1>
         The <b>Insert Transition List</b> form appears:
     </p>
     <p>
-        <img src="image-4.png" />
+        <img src="s-5.png" />
     </p>
     <ul>
         <li>Press Ctrl-V to paste the copied cells into the <b>Insert Transition List</b> form.</li>
@@ -245,7 +245,7 @@ <h1>Inserting a Transition List with Associated Proteins</h1>
         This will bring up the <b>Import Transition List: Identify Columns</b> form, which should look like this:
     </p>
     <p>
-        <img src="image-5.png" />
+        <img src="s-6.png" />
     </p>
     <ul>
         <li>Make sure the <b>Associate Proteins</b> checkbox is ticked.</li>
@@ -267,12 +267,12 @@ <h1>Inserting a Transition List with Associated Proteins</h1>
     </ul>
     <p>
         The main Skyline window should show a number of peptides grouped within their proteins. The peptide icons should contain 3 vertical lines and a
-        baseline (<img src="image-6.png" />), like a very small MS/MS spectrum, in the lower right corner (<img src="image-7.png" />). The presence of
+        baseline (<img src="../../shared/peptide-icon.png" />), like a very small MS/MS spectrum, in the lower right corner (<img src="../../shared/peptide-with-spectrum-lines-icon.png" />). The presence of
         this image indicates the peptide has an associated MS/MS library spectrum. The peptide label should highlight in blue the C-terminal Lysine or
         Arginine, indicating the stable isotope labeled amino acid in the heavy, labeled form:
     </p>
     <p>
-        <img src="image-8.png" />
+        <img src="s-7.png" />
     </p>
     <p>
         You can also see at the bottom right corner of the window, in the status bar, the indicator “1/296 tran”, confirming that all 296 transitions
@@ -297,7 +297,7 @@ <h1>Inserting a Transition List with Associated Proteins</h1>
         show the spectrum that matches the current peptide, and the peak matching the selected transition will be highlighted in red:
     </p>
     <p>
-        <img src="image-9.png" />
+        <img src="s-8.png" />
     </p>
     <p>
         You will notice that not all of the peptides have the most abundant product ions chosen for transitions, like the one shown in the image above,
@@ -365,7 +365,7 @@ <h1>Importing Data</h1>
         This should leave Skyline looking something like:
     </p>
     <p>
-        <img src="image-10.png" />
+        <img src="s-9.png" />
     </p>
     <p>
         You can also change the proportions allocated to the various panes by clicking and dragging the light gray splitter bars between them.
@@ -386,7 +386,7 @@ <h1>Importing Data</h1>
         This should change Skyline to look like:
     </p>
     <p>
-        <img src="image-11.png" />
+        <img src="s-10.png" />
     </p>
     <p>
         If you do not see chromatograms for all three transitions, as shown above, do the following:
@@ -413,7 +413,7 @@ <h1>Importing Data</h1>
         the following before starting the next section:
     </p>
     <ul>
-        <li>Click the pushpin <img src="image-12.png" /> to the left of the X in the upper right corner of the <b>Library Match</b> title
+        <li>Click the pushpin <img src="../../shared/pushpin-icon.png" /> to the left of the X in the upper right corner of the <b>Library Match</b> title
             bar.</li>
     </ul>
     <h2>Removing a Transition Peak with Interference</h2>
@@ -436,7 +436,7 @@ <h2>Removing a Transition Peak with Interference</h2>
         The precursor total area ratio is a weighted mean, using the internal standard peak area as the weights, which simplifies algebraically to:
     </p>
     <p>
-        <img src="image-13.png" />
+        <img src="s-precursor-total-area-ratio-formula.png" />
     </p>
     <p>
         Removing either a light or heavy peak removes the peak for its matching transition. Hence, when only one pair of transitions remain, as with y7
@@ -457,7 +457,7 @@ <h2>Adjusting Peak Boundaries to Exclude Interference</h2>
         This should leave Skyline showing something like:
     </p>
     <p>
-        <img src="image-14.png" />
+        <img src="s-11.png" />
     </p>
     <p>
         In this case, y4 and y3 show ratios of 0.31 and 0.35 respectively and y7 shows 0.23, yielding a weighted mean, precursor total ratio of 0.27.
@@ -502,7 +502,7 @@ <h1>Preparing a Document to Accept the Study 7 Transition List</h1>
         You should be presented with a spreadsheet that looks something like this:
     </p>
     <p>
-        <img src="image-15.png" />
+        <img src="s-transition-list-spreadsheet.png" />
     </p>
     <p>
         You can tell that this is a spreadsheet created manually by someone who put significant effort, using borders, merged cells and highlighting,
@@ -545,7 +545,7 @@ <h1>Preparing a Document to Accept the Study 7 Transition List</h1>
         The <b>Edit Isotope Modification</b> form should now look like this:
     </p>
     <p>
-        <img src="image-16.png" />
+        <img src="s-12.png" />
     </p>
     <p>
         To finish preparing the document for the Study 7 transition list, do the following:
@@ -595,7 +595,7 @@ <h2>Pasting a Transition List into the Document </h2>
         This will bring up the <b>Import Transition List: Identify Columns</b> form, which should look like this:
     </p>
     <p>
-        <img src="image-17.png" />
+        <img src="s-13.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -604,7 +604,7 @@ <h2>Pasting a Transition List into the Document </h2>
         Skyline should present the following error message:
     </p>
     <p>
-        <img src="image-18.png" /> 
+        <img src="s-14.png" /> 
     </p>
     <p>
         Messages like this are not uncommon when working with transition lists created outside Skyline. Others are presented in the Skyline
@@ -637,7 +637,7 @@ <h2>Pasting a Transition List into the Document </h2>
         This should leave the Skyline peptide view looking like:
     </p>
     <p>
-        <img src="image-19.png" />
+        <img src="s-15.png" />
     </p>
     <h2>Adjusting Modifications Manually</h2>
     <p>
@@ -661,7 +661,7 @@ <h2>Adjusting Modifications Manually</h2>
         The <b>Edit Isotope Modification</b> form should look like:
     </p>
     <p>
-        <img src="image-20.png" />
+        <img src="s-16.png" />
     </p>
     <p>
         This modification will apply a varying mass shift to any amino acid, depending on how many Carbon atoms it contains.
@@ -670,7 +670,7 @@ <h2>Adjusting Modifications Manually</h2>
         <li>Click the <b>OK</b> button to return to the <b>Edit Modifications</b> form, which should now look like:</li>
     </ul>
     <p>
-        <img src="image-21.png" />
+        <img src="s-17.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button on the <b>Edit Modifications</b> form to return to the document.</li>
@@ -688,7 +688,7 @@ <h2>Adjusting Modifications Manually</h2>
         The peptide view should now look like this:
     </p>
     <p>
-        <img src="image-22.png" />
+        <img src="s-18.png" />
     </p>
     <p>
         Now expand both the “744.8398++” precursor and the <b>“</b>747.3481++ (heavy)” precursor: 
@@ -741,7 +741,7 @@ <h2>Importing Data from a Multiple Sample WIFF File</h2>
         present you with a form that looks like this:
     </p>
     <p>
-        <img src="image-23.png" />
+        <img src="s-19.png" />
     </p>
     <p>
         For this tutorial, to reduce the time that will be required to complete the import:
@@ -756,7 +756,7 @@ <h2>Importing Data from a Multiple Sample WIFF File</h2>
         use to display information about these replicates:
     </p>
     <p>
-        <img src="image-24.png" />
+        <img src="s-20.png" />
     </p>
     <ul>
         <li>Click the <b>Remove</b> button to accept this operation.</li>
@@ -780,7 +780,7 @@ <h2>Inspecting and Adjusting Peak Integration</h2>
         <li>Adjust the view proportions to look something like the image below.</li>
     </ul>
     <p>
-        <img src="image-25.png" />
+        <img src="s-21.png" />
     </p>
     <p>
         The currently selected peptide “YEVQGEVFTKPQ<b><span class="blue">L</span></b>WP”, which was the peptide at the C-terminal end of CRP
@@ -840,7 +840,7 @@ <h2>Inspecting and Adjusting Peak Integration</h2>
         Skyline should now look something like:
     </p>
     <p>
-        <img src="image-26.png" />
+        <img src="s-22.png" />
     </p>
     <h2>Data Inspection with Peak Areas View</h2>
     <p>
@@ -884,7 +884,7 @@ <h2>Data Inspection with Peak Areas View</h2>
                 class="blue">K</span></b> selected:
     </p>
     <p>
-        <img src="image-27.png" />
+        <img src="s-23.png" />
     </p>
     <p>
         You will see that, indeed, precision among the replicates for each concentration appears to have improved.
@@ -904,7 +904,7 @@ <h2>Data Inspection with Peak Areas View</h2>
         For the 6 well behaved peptides, you should see a chart like the one below, with the ESDTSYVSL<b><span class="blue">K</span></b> peptide light precursor 564.7746++ selected:
     </p>
     <p>
-        <img src="image-28.png" />
+        <img src="s-24.png" />
     </p>
     <p>
         As expected, the ratios are quite similar. The second and third peptides (INDISHTQSVSA<b><span class="blue">K</span></b> and
@@ -917,7 +917,7 @@ <h2>Data Inspection with Peak Areas View</h2>
         This should cause the peak area graph to look like:
     </p>
     <p>
-        <img src="image-29.png" />
+        <img src="s-25.png" />
     </p>
     <p>
         This seems to indicate some interference in the transition for y3, since its ratio, at low concentrations, is so different from the others for
@@ -934,7 +934,7 @@ <h2>Data Inspection with Peak Areas View</h2>
         The chart should change to something like:
     </p>
     <p>
-        <img src="image-30.png" />
+        <img src="s-26.png" />
     </p>
     <p>
         Again, this chart clearly indicates interference on the transition for y3 (brown) that becomes less of a factor as the concentration of the
@@ -942,7 +942,7 @@ <h2>Data Inspection with Peak Areas View</h2>
         charts, you can click on the individual bars to see the interfering peak, which, in this case, is pretty clear, as in replicate E_03 below:
     </p>
     <p>
-        <img src="image-31.png" />
+        <img src="s-27.png" />
     </p>
     <p>
         As with the case in the MRMer document, you might attempt to adjust the integration boundaries to exclude the interfering peak, but it is
@@ -958,7 +958,7 @@ <h2>Data Inspection with Peak Areas View</h2>
         The <b>Peak Areas</b> chart should have changed to look something like:
     </p>
     <p>
-        <img src="image-32.png" />
+        <img src="s-28.png" />
     </p>
     <p>
         If the peptides do not appear in this order, do the following:
@@ -1046,7 +1046,7 @@ <h2>Settings Concentration Values</h2>
         When you are done entering these values, the <b>Document Grid</b> should look like this:
     </p>
     <p>
-        <img src="image-33.png" />
+        <img src="s-29.png" />
     </p>
     <p>
         You can now use the newly entered concentrations in the <b>Peak Areas: Replicate Comparison</b> graph by doing the following:
@@ -1062,7 +1062,7 @@ <h2>Settings Concentration Values</h2>
         The <b>Peak Areas</b> graph should now look like:
     </p>
     <p>
-        <img src="image-34.png" />
+        <img src="s-30.png" />
     </p>
     <p>
         This graph shows that the CVs are quite low until the very lowest concentrations. You can easily switch to a graph showing the mean ratios with
@@ -1075,7 +1075,7 @@ <h2>Settings Concentration Values</h2>
         This should change the graph to look like:
     </p>
     <p>
-        <img src="image-35.png" />
+        <img src="s-31.png" />
     </p>
     <ul>
         <li>On the <b>File</b> menu, click <b>Save</b>, to end this section. </li>
@@ -1100,7 +1100,7 @@ <h2>Further Exploration</h2>
         appearing as in the chart below:
     </p>
     <p>
-        <img src="image-36.png" />
+        <img src="s-32.png" />
     </p>
     <p>
         The peptide INDISHTQSVSA<b><span class="blue">K</span></b> is the only one of the 4 from the first data set that still has a CV
@@ -1114,7 +1114,7 @@ <h2>Further Exploration</h2>
         for 3 of the “Blank” replicates (though this issue was fixed a long time ago – but after the document data was imported and saved):
     </p>
     <p>
-        <img src="image-37.png" />
+        <img src="s-33.png" />
     </p>
     <p>
         If you correct these by clicking and dragging beneath the x-axis, the CV for the heavy precursor of LSEPAELTDAV<b><span
@@ -1135,7 +1135,7 @@ <h2>Further Exploration</h2>
         <li>Click the “INDISHTQSVSA<b><span class="blue">K</span></b>” peptide.</li>
     </ul>
     <p>
-        <img src="image-38.png" />
+        <img src="s-34.png" />
     </p>
     <p>
         This seems to indicate that the internal standard is doing its job of compensating for variance in measurements of this peptide. To review the
@@ -1148,7 +1148,7 @@ <h2>Further Exploration</h2>
         It would be hard to guess from this chart that the normalization would be so effective:
     </p>
     <p>
-        <img src="image-39.png" />
+        <img src="s-35.png" />
     </p>
     <p>
         Finally, returning to the peptide in which we detected interference in the first data set:
@@ -1162,7 +1162,7 @@ <h2>Further Exploration</h2>
         Here also, you will see clear evidence of interference on the y3 transition:
     </p>
     <p>
-        <img src="image-40.png" />
+        <img src="s-36.png" />
     </p>
     <p>
         Unlike the first data set, however, it is much harder to see the interference by inspecting the individual chromatograms. In this case, due to
@@ -1170,7 +1170,7 @@ <h2>Further Exploration</h2>
         replicate E_03 shown below:
     </p>
     <p>
-        <img src="image-41.png" />
+        <img src="s-37.png" />
     </p>
     <p>
         The NCI CPTAC Study 7 provided quite a lot more data, all of which is now public. Skyline can help you learn a lot about this data quickly,
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/GroupedStudies/en/index.html b/pwiz_tools/Skyline/Documentation/Tutorials/GroupedStudies/en/index.html
index 74606a2ca8..204135e129 100644
--- a/pwiz_tools/Skyline/Documentation/Tutorials/GroupedStudies/en/index.html
+++ b/pwiz_tools/Skyline/Documentation/Tutorials/GroupedStudies/en/index.html
@@ -96,7 +96,7 @@ <h1>Differential analysis after method refinement</h1>
         very much prior knowledge of the targeted proteins or peptides and without aid of stable isotope labeled reference peptides.
     </p>
     <p>
-        <img src="image-0.png" />
+        <img src="s-detection-and-differentiation-phases.png" />
     </p>
     <p>
         <b>Figure 1</b>: A schematic showing proposed “Detection” and “Differentiation” phases of targeted method refinement in a heart
@@ -113,7 +113,7 @@ <h1>Differential analysis after method refinement</h1>
         peptides and 789 transitions.
     </p>
     <p>
-        <img src="image-1.png" />
+        <img src="s-1.png" />
     </p>
     <p>
         This is not quite what is promised in the figure above (from a manuscript draft that was never published), but the document also contains one
@@ -123,8 +123,8 @@ <h1>Differential analysis after method refinement</h1>
     </p>
     <p>
         You will notice that some of the peptides have matching library spectra. You can see this in the <b>Targets</b> view. The peptide
-        icons with spectrum lines in the lower right corner (<img src="image-2.png" />) have matching spectra and those without these lines (<img
-            src="image-3.png" />) do not. The spectra come from two different public spectral libraries: one from NIST and one from the Global
+        icons with spectrum lines in the lower right corner (<img src="../../shared/peptide-with-spectrum-lines-icon.png" />) have matching spectra and those without these lines (<img
+            src="../../shared/peptide-without-spectrum-lines-icon.png" />) do not. The spectra come from two different public spectral libraries: one from NIST and one from the Global
         Proteome Machine (GPM). You can explore their coverage by doing the following:
     </p>
     <ul>
@@ -139,7 +139,7 @@ <h1>Differential analysis after method refinement</h1>
         (GPM) library (31). Note that the row number of the selected cell is shown in the toolbar above the grid.
     </p>
     <p>
-        <img src="image-4.png" />
+        <img src="s-2.png" />
     </p>
     <p>
         For the current example, this information gives you a sense of the sparse prior knowledge on which the experiment was based. Modern knowledge
@@ -164,7 +164,7 @@ <h2>Setting up to process multi-replicate data without reference standards</h2>
         The files should begin loading, and Skyline will display progress in a window like the one shown below:
     </p>
     <p>
-        <img src="image-5.png" />
+        <img src="s-3.png" />
     </p>
     <p>
         To continue preparing for data processing while Skyline imports the SRM chromatograms, do the following:
@@ -179,7 +179,7 @@ <h2>Setting up to process multi-replicate data without reference standards</h2>
         <li>Drag the cursor into the bottom docking indicator to see a blue rectangle fill the bottom edge of the Skyline window, as shown below.</li>
     </ul>
     <p>
-        <img src="image-6.png" />
+        <img src="s-4.png" />
     </p>
     <ul>
         <li>Release the left mouse button to dock the <b>Retention Times</b> view.</li>
@@ -188,7 +188,7 @@ <h2>Setting up to process multi-replicate data without reference standards</h2>
             share the bottom edge with the <b>Peak Areas</b> view.</li>
     </ul>
     <p>
-        <img src="image-7.png" />
+        <img src="s-5.png" />
     </p>
     <ul>
         <li>Release the left mouse button to dock the <b>Peak Areas</b> view.</li>
@@ -196,7 +196,7 @@ <h2>Setting up to process multi-replicate data without reference standards</h2>
             to the left edge of the Skyline window.</li>
     </ul>
     <p>
-        <img src="image-8.png" />
+        <img src="s-6.png" />
     </p>
     <ul>
         <li>Close any other windows left floating outside the main Skyline window.</li>
@@ -209,7 +209,7 @@ <h2>Setting up to process multi-replicate data without reference standards</h2>
         The form should look like this:
     </p>
     <p>
-        <img src="image-9.png" />
+        <img src="s-7.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -220,7 +220,7 @@ <h2>Setting up to process multi-replicate data without reference standards</h2>
         Your Skyline window should now look something like this:
     </p>
     <p>
-        <img src="image-10.png" />
+        <img src="s-8.png" />
     </p>
     <p>
         <b>Note</b>: This image was taken on a 24” monitor at 1920x1080. If you are viewing this tutorial digitally, you may want to zoom in
@@ -232,7 +232,7 @@ <h2>Setting up to process multi-replicate data without reference standards</h2>
         not very consistent. Most of the chosen peaks elute around 19 minutes. However, nearly one third (12) elute closer to 22 minutes.
     </p>
     <p>
-        <img src="image-11.png" />
+        <img src="s-9.png" />
     </p>
     <p>
         The integration for this peptide is quite poor. While the peak at around 19 minutes appears to be the better peak, it is hard to have much
@@ -247,7 +247,7 @@ <h2>Scheduled SRM and peak truncation</h2>
         Just by looking at the retention time plot for the second peptide, you can see that it is much more consistently integrated.
     </p>
     <p>
-        <img src="image-12.png" />
+        <img src="s-10.png" />
     </p>
     <p>
         However, you can still see that the peak apexes for all transitions (shown by the horizontal lines in the bars) are not very consistent. If you
@@ -270,13 +270,13 @@ <h2>Scheduled SRM and peak truncation</h2>
         This changes the <b>Peak Areas</b> plot from:
     </p>
     <p>
-        <img src="image-13.png" />
+        <img src="s-11.png" />
     </p>
     <p class="keep-next">
         To:
     </p>
     <p>
-        <img src="image-14.png" />
+        <img src="s-12.png" />
     </p>
     <p>
         This makes it possible to see differences in relative ion abundance across multiple runs in a single glance and adds to the information you are
@@ -294,13 +294,13 @@ <h2>Scheduled SRM and peak truncation</h2>
         This will activate the chromatogram graph for the peak, which looks like:
     </p>
     <p>
-        <img src="image-15.png" />
+        <img src="s-13.png" />
     </p>
     <p>
         While plots for the correctly integrated peaks look more like this:
     </p>
     <p>
-        <img src="image-16.png" />
+        <img src="s-14.png" />
     </p>
     <p>
         Since the scheduled acquisition window did not capture the entire elution profile for the peptide, Skyline has picked the wrong peak. However,
@@ -344,7 +344,7 @@ <h2>Scheduled SRM and peak truncation</h2>
         The <b>Find</b> form should look like this:
     </p>
     <p>
-        <img src="image-17.png" />
+        <img src="s-15.png" />
     </p>
     <ul>
         <li>Click the <b>Find All</b> button.</li>
@@ -355,7 +355,7 @@ <h2>Scheduled SRM and peak truncation</h2>
         any line to see the corresponding chromatogram graph activated.
     </p>
     <p>
-        <img src="image-18.png" />
+        <img src="s-16.png" />
     </p>
     <p>
         You can also use the <b>Document Grid</b> to create a list of all precursors with any peak truncation by doing the following:
@@ -366,7 +366,7 @@ <h2>Scheduled SRM and peak truncation</h2>
         <li>On the <b>Reports</b> menu in the <b>Document Grid</b> view, click <b>Customize Report</b>.</li>
         <li>In the <b>Report name</b> field, enter “Truncated Precursors”.</li>
         <li>In the right side list, select all column names (using click and shift-click) after the first two (Precursor and Peptide).</li>
-        <li>Click the <img src="image-19.png" /> button near the right edge to delete all but the first two columns.</li>
+        <li>Click the <img src="../../shared/red-x-icon.png" /> button near the right edge to delete all but the first two columns.</li>
         <li>Check “Replicates” in the tree on the left side.</li>
         <li>Expand the tree to check Proteins &gt; Peptides &gt; Precursors &gt; PrecursorResults &gt; Count Truncated.</li>
     </ul>
@@ -374,7 +374,7 @@ <h2>Scheduled SRM and peak truncation</h2>
         The <b>Customize Report</b> form should look something like this:
     </p>
     <p>
-        <img src="image-20.png" />
+        <img src="s-17.png" />
     </p>
     <ul>
         <li>In the right side list, double-click “Count Truncated”.</li>
@@ -387,7 +387,7 @@ <h2>Scheduled SRM and peak truncation</h2>
         The <b>Customize Report</b> form should look something like this:
     </p>
     <p>
-        <img src="image-21.png" />
+        <img src="s-18.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -397,7 +397,7 @@ <h2>Scheduled SRM and peak truncation</h2>
         The <b>Document Grid</b> will show 221 truncated peaks that Skyline has already chosen automatically:
     </p>
     <p>
-        <img src="image-22.png" />
+        <img src="s-19.png" />
     </p>
     <p>
         To view these peaks:
@@ -410,7 +410,7 @@ <h2>Scheduled SRM and peak truncation</h2>
         Skyline will activate chromatogram graphs that look like the following:
     </p>
     <p>
-        <img src="image-23.png" />
+        <img src="s-20.png" />
     </p>
     <ul>
         <li>Close the <b>Document Grid</b>.</li>
@@ -423,7 +423,7 @@ <h2>Beginning multi-replicate data processing</h2>
         peak apex lines match up for almost all transitions in each replicate.
     </p>
     <p>
-        <img src="image-24.png" />
+        <img src="s-21.png" />
     </p>
     <p>
         The relative ion abundances shown in the <b>Peak Areas</b> view also appear relatively stable. You might notice that there is a
@@ -440,7 +440,7 @@ <h2>Beginning multi-replicate data processing</h2>
         measured peak areas ranging from 1 (best) to zero (worst).
     </p>
     <p>
-        <img src="image-25.png" />
+        <img src="s-22.png" />
     </p>
     <p>
         Return the <b>Peak Areas</b> view to its former state by doing the following:
@@ -461,13 +461,13 @@ <h2>Beginning multi-replicate data processing</h2>
         You might notice that some of the transitions show a signal around the edges of the main peak that is not well matched by the other peaks.
     </p>
     <p>
-        <img src="image-26.png" />
+        <img src="s-23.png" />
     </p>
     <p>
         There is frequently signal on y5 and y6 around 13.1 minutes, which is clearly not from the same peptide.
     </p>
     <p>
-        <img src="image-27.png" />
+        <img src="s-24.png" />
     </p>
     <p>
         When an interfering signal like this occurs inside the integration boundaries, it will add error to the quantitative measurements. For critical
@@ -477,13 +477,13 @@ <h2>Beginning multi-replicate data processing</h2>
         For the current tutorial, however, continue to the next peptide. There you will find strong, clean, and co-eluting peaks for all 7 transitions.
     </p>
     <p>
-        <img src="image-28.png" />
+        <img src="s-25.png" />
     </p>
     <p>
         Relative ion abundance is also extremely consistent.
     </p>
     <p>
-        <img src="image-29.png" />
+        <img src="s-26.png" />
     </p>
     <p>
         The peak area in y3 is stronger than what was seen for the library spectrum. This might be explained by secondary fragmentation occurring in a
@@ -506,14 +506,14 @@ <h2>Beginning multi-replicate data processing</h2>
         not coincide with the peptide of interest can add information to the chromatogram “landscape” you see.
     </p>
     <p>
-        <img src="image-30.png" />
+        <img src="s-27.png" />
     </p>
     <p class="keep-next">
         In D_103_REP3, you will see the integrated peak at 33.9 minutes with signal mostly on y4 and y5, but no other candidate peak
         to the left.
     </p>
     <p>
-        <img src="image-31.png" />
+        <img src="s-28.png" />
     </p>
     <p>
         In this case, the scheduling window has failed to capture any signal from the targeted peptide. To remove the incorrect peak do the following:
@@ -525,7 +525,7 @@ <h2>Beginning multi-replicate data processing</h2>
         This should leave a blank spot in the <b>Peak Areas</b> graph.
     </p>
     <p>
-        <img src="image-32.png" />
+        <img src="s-29.png" />
     </p>
     <p>
         Continuing through the chromatogram plots, you will see this pattern repeated several times. Keep removing the missing peaks. You will even
@@ -533,20 +533,20 @@ <h2>Beginning multi-replicate data processing</h2>
         but part of the correct peak is still visible.
     </p>
     <p>
-        <img src="image-33.png" />
+        <img src="s-30.png" />
     </p>
     <p>
         You can simply integrate this as a truncated peak, as you did above, by clicking and dragging beneath the x-axis. You should end up with a
         <b>Peak Areas</b> plot that looks like this:
     </p>
     <p>
-        <img src="image-34.png" />
+        <img src="s-31.png" />
     </p>
     <p class="keep-next">
         And a retention times plot that looks like this:
     </p>
     <p>
-        <img src="image-35.png" />
+        <img src="s-32.png" />
     </p>
     <ul>
         <li>Continue to the peptide R.DIPVNPM<b><u>C</u></b>IYR.S [46, 56].</li>
@@ -570,7 +570,7 @@ <h2>Beginning multi-replicate data processing</h2>
         For the peptide TSDQIHFFFAK the retention times look like this:
     </p>
     <p>
-        <img src="image-36.png" />
+        <img src="s-33.png" />
     </p>
     <p>
         However, it may also be quite helpful to see the runs in the order they were acquired on the instrument. You can achieve this by doing the
@@ -583,7 +583,7 @@ <h2>Beginning multi-replicate data processing</h2>
         The graph will change to look like the following:
     </p>
     <p>
-        <img src="image-37.png" />
+        <img src="s-34.png" />
     </p>
     <p>
         This retention time pattern is now a little less erratic. If you now select through the next two peptides (LQPLDFK, SQLPGIIAEGR), you will see
@@ -598,10 +598,10 @@ <h2>Beginning multi-replicate data processing</h2>
     <table class="comp-fig">
         <tr>
             <td class="comp-fig">
-                <img src="image-38.png" />
+                <img src="s-35.png" />
             </td>
             <td class="comp-fig">
-                <img src="image-39.png" />
+                <img src="s-36.png" />
             </td>
         </tr>
     </table>
@@ -615,7 +615,7 @@ <h2>Beginning multi-replicate data processing</h2>
         peak close to 19 minutes. However, the <b>Peak Areas</b> view shows very poor consistency in relative ion abundance.
     </p>
     <p>
-        <img src="image-40.png" />
+        <img src="s-37.png" />
     </p>
     <p>
         If you examine a few of the chromatogram graphs, you will find it hard to imagine consistently integrating the signal at 18.8 minutes with any
@@ -638,17 +638,17 @@ <h2>Global normalization standards</h2>
         consistent.
     </p>
     <p>
-        <img src="image-41.png" />
+        <img src="s-38.png" />
     </p>
     <p>
-        <img src="image-42.png" />
+        <img src="s-39.png" />
     </p>
     <p>
         Moving to the peptide HLNGFSVPR, you will observe consistent retention times. However, there is much more variance in the peak areas. The
         relative area for y4 and sometimes y3 seems to vary throughout the data set.
     </p>
     <p>
-        <img src="image-43.png" />
+        <img src="s-40.png" />
     </p>
     <p>
         If you click on some of the peak area bars where y4 is most abundant, you will see obvious interference on y4 and sometimes y3.
@@ -657,7 +657,7 @@ <h2>Global normalization standards</h2>
         <li>On the <b>View</b> menu, choose <b>Auto-Zoom</b> and click <b>Best Peak</b> (F11).</li>
     </ul>
     <p>
-        <img src="image-44.png" />
+        <img src="s-41.png" />
     </p>
     <p>
         To gain an even clearer understanding of the performance of these injected peptides as potential normalization standards, you should do the
@@ -679,13 +679,13 @@ <h2>Global normalization standards</h2>
         To see where these peptides elute relative to each other do the following:
     </p>
     <ul>
-        <li>Select the “S” element preceded by the <img src="image-45.png" /> icon.</li>
+        <li>Select the “S” element preceded by the <img src="../../shared/protein-icon-2.png" /> icon.</li>
     </ul>
     <p>
         The chromatogram graphs will change to show all three peptides in the “S” list together.
     </p>
     <p>
-        <img src="image-46.png" />
+        <img src="s-42.png" />
     </p>
     <p>
         Now to see all the peptides in the document together:
@@ -694,7 +694,7 @@ <h2>Global normalization standards</h2>
         <li>On the <b>Edit</b> menu, click <b>Select All</b> (Ctrl-A).</li>
     </ul>
     <p>
-        <img src="image-47.png" />
+        <img src="s-43.png" />
     </p>
     <p>
         This makes it clear that the two problematic peptides are both hydrophilic and early eluting. In fact, they are the 3<sup>rd</sup> and
@@ -726,7 +726,7 @@ <h2>Global normalization standards</h2>
         more hydrophobic and later eluting, is 108<sup>th</sup> or in the 80<sup>th</sup> percentile with 18.6% CV.)
     </p>
     <p>
-        <img src="image-48.png" />
+        <img src="s-44.png" />
     </p>
     <p>
         If you do the following, you should be able to convince yourself that the LGP peptide has a problem very similar to the HLN peptide.
@@ -739,7 +739,7 @@ <h2>Global normalization standards</h2>
         Remember that there are supposed to be three cycles or technical replicates:
     </p>
     <p>
-        <img src="image-49.png" />
+        <img src="s-45.png" />
     </p>
     <p class="keep-next">
         To convince yourself that the peaks are correctly integrated, do the following:
@@ -753,7 +753,7 @@ <h2>Global normalization standards</h2>
         extremely stable.
     </p>
     <p>
-        <img src="image-50.png" />
+        <img src="s-46.png" />
     </p>
     <p>
         Although this one peptide seems to have similar issues, you should exclude a peptide like HLNGFSVPR from consideration as a global
@@ -780,7 +780,7 @@ <h2>Continuing multi-replicate data processing</h2>
         H_146_REP1 was not fully captured by the 5-minute scheduling window. (You might need to turn off x-axis zooming – Shift-F11 – to see this.)
     </p>
     <p>
-        <img src="image-51.png" />
+        <img src="s-47.png" />
     </p>
     <p>
         As you did before, you can correct this by clicking and dragging beneath the x-axis to integrate the truncated peak, or by using the
@@ -791,7 +791,7 @@ <h2>Continuing multi-replicate data processing</h2>
         unusual differences in the ranges of time being integrated.
     </p>
     <p>
-        <img src="image-52.png" />
+        <img src="s-48.png" />
     </p>
     <p>
         If you review some of the chromatograms for this peptide, you will see that many show a single, very nice peak eluting over 0.2 minutes.
@@ -799,7 +799,7 @@ <h2>Continuing multi-replicate data processing</h2>
         distinct peaks.
     </p>
     <p>
-        <img src="image-53.png" />
+        <img src="s-49.png" />
     </p>
     <p>
         A peptide like this may be very difficult to use for quantification, especially without a matching SIL peptide. You should probably delete this
@@ -813,7 +813,7 @@ <h2>Continuing multi-replicate data processing</h2>
         When you reach the peptide MLSGFIPLKPTVK, however, you will see much more variance in the <b>Peak Areas</b> graph.
     </p>
     <p>
-        <img src="image-54.png" />
+        <img src="s-50.png" />
     </p>
     <p>
         The total peak area for this peptide is dominated by the y7 ion. Although this is also reflected in the library spectrum (as shown at the far
@@ -821,7 +821,7 @@ <h2>Continuing multi-replicate data processing</h2>
         ion (see below).
     </p>
     <p>
-        <img src="image-55.png" />
+        <img src="s-51.png" />
     </p>
     <p>
         However, it is also clear that Skyline is, for the most part, integrating the same peak for the same molecule in each run. To convince yourself
@@ -836,20 +836,20 @@ <h2>Continuing multi-replicate data processing</h2>
         minutes does, in fact, cause the co-eluting signals on all 6 monitored transitions when peptide abundance is high enough.
     </p>
     <p>
-        <img src="image-56.png" />
+        <img src="s-52.png" />
     </p>
     <p>
         Rather than deleting this peptide, you will want to correct the one case where Skyline has chosen the wrong peak. You can see this in the
         <b>Retention Times</b> plot, as a narrower band occurring below 22.5 minutes.
     </p>
     <p>
-        <img src="image-57.png" />
+        <img src="s-53.png" />
     </p>
     <p class="keep-next">
         And also in the <b>Peak Areas</b> plot, as the run with no visible integrated signal.
     </p>
     <p class="keep-next">
-        <img src="image-58.png" />
+        <img src="s-54.png" />
     </p>
     <p>
         You can click on the bar in the <b>Retention Times</b> view to activate the chromatogram graph for this run. You will see that the
@@ -857,7 +857,7 @@ <h2>Continuing multi-replicate data processing</h2>
         knowledge you have gained from the surrounding runs.
     </p>
     <p>
-        <img src="image-59.png" />
+        <img src="s-55.png" />
     </p>
     <p>
         To correct the integration of this run, do the following:
@@ -900,7 +900,7 @@ <h2>Continuing multi-replicate data processing</h2>
         This gives you added confidence in the consistency of the integrated peak.
     </p>
     <p>
-        <img src="image-60.png" />
+        <img src="s-56.png" />
     </p>
     <p>
         Continuing up the <b>Targets</b> list, you will find several peptides (YANVIAYDHSR and TDEDVPSGPPR) where the difference between the
@@ -908,14 +908,14 @@ <h2>Continuing multi-replicate data processing</h2>
         <b>Peak Areas</b> graph:
     </p>
     <p>
-        <img src="image-61.png" />
+        <img src="s-57.png" />
     </p>
     <p>
         You can also observe this in the chromatogram graphs where Skyline displays the low dot product values “(dotp 0.28)” beneath the peak retention
         times.
     </p>
     <p>
-        <img src="image-62.png" />
+        <img src="s-58.png" />
     </p>
     <p>
         Skyline displays the “dotp” value like this when there is another peak on the graph with a higher dotp value. In the case above, you cannot see
@@ -950,7 +950,7 @@ <h2>Continuing multi-replicate data processing</h2>
         below), you may initially be tempted to delete this peptide and move on:
     </p>
     <p>
-        <img src="image-63.png" />
+        <img src="s-59.png" />
     </p>
     <p>
         However, if you look closely you will see that there are regions of consistency among the healthy subjects. To see this expressed more clearly,
@@ -963,10 +963,10 @@ <h2>Continuing multi-replicate data processing</h2>
         This will change the graphs to look like:
     </p>
     <p>
-        <img src="image-64.png" />
+        <img src="s-60.png" />
     </p>
     <p>
-        <img src="image-65.png" />
+        <img src="s-61.png" />
     </p>
     <p>
         Making it clearer that a consistent peak is being integrated for the healthy subjects but not for the diseased subjects. If you review the peak
@@ -982,11 +982,11 @@ <h2>Continuing multi-replicate data processing</h2>
         <tr>
             <td class="comp-fig">
                 D_102_REP3<br />
-                <img src="image-66.png" />
+                <img src="s-62.png" />
             </td>
             <td class="comp-fig">
                 D_108_REP1<br />
-                <img src="image-67.png" />
+                <img src="s-63.png" />
             </td>
         </tr>
     </table>
@@ -999,7 +999,7 @@ <h2>Continuing multi-replicate data processing</h2>
         after runs of healthy subjects (D_102_REP2 and D_102_REP3). This observation might suggest a carryover effect.
     </p>
     <p>
-        <img src="image-68.png" />
+        <img src="s-64.png" />
     </p>
     <p>
         In the end, these transitions may represent one of the strongest biomarker candidates in this document. You could now order a synthetic peptide
@@ -1039,7 +1039,7 @@ <h2>Preparing for statistical analysis with replicate annotations</h2>
         The form should look like this:
     </p>
     <p>
-        <img src="image-69.png" />
+        <img src="s-65.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button in the <b>Define Annotation</b> form.</li>
@@ -1050,7 +1050,7 @@ <h2>Preparing for statistical analysis with replicate annotations</h2>
         The <b>Document Settings</b> form should look like:
     </p>
     <p>
-        <img src="image-70.png" />
+        <img src="s-66.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -1069,7 +1069,7 @@ <h2>Preparing for statistical analysis with replicate annotations</h2>
         The <b>Install from Tool Store</b> form should look like:
     </p>
     <p>
-        <img src="image-71.png" />
+        <img src="s-67.png" />
     </p>
     <ul>
         <li>Click the <b>Install</b> button and follow the prompts until MSstats installation is completed.</li>
@@ -1090,10 +1090,10 @@ <h2>Preparing for statistical analysis with replicate annotations</h2>
     <table class="comp-fig">
         <tr>
             <td class="comp-fig" style="padding: 5px;">
-                <img src="image-72.png" />
+                <img src="s-68.png" />
             </td>
             <td class="comp-fig" style="padding: 5px;">
-                <img src="image-73.png" />
+                <img src="s-69.png" />
             </td>
         </tr>
     </table>
@@ -1105,7 +1105,7 @@ <h2>Preparing for statistical analysis with replicate annotations</h2>
         The <b>Document Settings</b> form should look like this:
     </p>
     <p>
-        <img src="image-74.png" />
+        <img src="s-70.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -1122,7 +1122,7 @@ <h2>Preparing for statistical analysis with replicate annotations</h2>
         The <b>Document Grid</b> should look something like this:
     </p>
     <p>
-        <img src="image-75.png" />
+        <img src="s-71.png" />
     </p>
     <p>
         You can now manually enter the annotations for all 42 replicates into this grid. You can also paste values from a spreadsheet directly into
@@ -1142,7 +1142,7 @@ <h2>Preparing for statistical analysis with replicate annotations</h2>
         The <b>Document Grid</b> should look like this:
     </p>
     <p>
-        <img src="image-76.png" />
+        <img src="s-72.png" />
     </p>
     <ul>
         <li>Press Ctrl-V to paste into the <b>Document Grid</b>.</li>
@@ -1151,7 +1151,7 @@ <h2>Preparing for statistical analysis with replicate annotations</h2>
         Skyline should fill in the cells in the <b>Document Grid</b> with the values from the spreadsheet as follows:
     </p>
     <p>
-        <img src="image-77.png" />
+        <img src="s-73.png" />
     </p>
     <h2>Annotating Peptides with Problem Peaks</h2>
     <p>
@@ -1171,7 +1171,7 @@ <h2>Annotating Peptides with Problem Peaks</h2>
         The <b>Define Annotation</b> form should look like:
     </p>
     <p>
-        <img src="image-78.png" />
+        <img src="s-74.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -1182,7 +1182,7 @@ <h2>Annotating Peptides with Problem Peaks</h2>
         The <b>Document Settings</b> form should look like:
     </p>
     <p>
-        <img src="image-79.png" />
+        <img src="s-75.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -1201,7 +1201,7 @@ <h2>Annotating Peptides with Problem Peaks</h2>
         The <b>Customize Report</b> form should look like this:
     </p>
     <p>
-        <img src="image-80.png" />
+        <img src="s-76.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -1211,7 +1211,7 @@ <h2>Annotating Peptides with Problem Peaks</h2>
         The <b>Document Grid</b> should look like this:
     </p>
     <p>
-        <img src="image-81.png" />
+        <img src="s-77.png" />
     </p>
     <p>
         Depending on how you processed the rest of your document, there may or may not be exactly 223 truncated precursor peak groups. You could check
@@ -1226,7 +1226,7 @@ <h2>Annotating Peptides with Problem Peaks</h2>
         The <b>Document Grid</b> should now look like this:
     </p>
     <p>
-        <img src="image-82.png" />
+        <img src="s-78.png" />
     </p>
     <p>
         You can also use Excel and the <b>Document Grid</b> support for pasting values to set all 163 rows in a single paste as follows:
@@ -1250,7 +1250,7 @@ <h2>Annotating Peptides with Problem Peaks</h2>
         marked with a small red triangle above and right of the peptide name.
     </p>
     <p>
-        <img src="image-83.png" />
+        <img src="s-79.png" />
     </p>
     <p>
         If you hover the mouse cursor over one of these triangles, you will see a tip appear with the text “<b>Missing Data</b> True”.
@@ -1264,7 +1264,7 @@ <h2>Annotating Peptides with Problem Peaks</h2>
         <li>Select the “Truncated Precursors” report you have been using.</li>
         <li>Click the <b>Copy</b> button.</li>
         <li>In the <b>Report Name</b> field of the <b>Customize Report</b> form, enter “Missing Peaks”.</li>
-        <li>Remove the <b>Precursors</b> and <b>Count Truncated</b> columns using the <img src="image-84.png" /> button to the
+        <li>Remove the <b>Precursors</b> and <b>Count Truncated</b> columns using the <img src="../../shared/red-x-icon.png" /> button to the
             right of the columns list.</li>
         <li>Check the <b>Pivot Replicate Name</b> checkbox.</li>
     </ul>
@@ -1272,11 +1272,11 @@ <h2>Annotating Peptides with Problem Peaks</h2>
         The <b>Customize Report</b> form should look like this:
     </p>
     <p>
-        <img src="image-85.png" />
+        <img src="s-80.png" />
     </p>
     <ul>
         <li>Click the <b>Filter</b> tab.</li>
-        <li>Click the <img src="image-86.png" /> button to remove the existing filter on <b>Count Truncated</b>.</li>
+        <li>Click the <img src="../../shared/red-x-icon.png" /> button to remove the existing filter on <b>Count Truncated</b>.</li>
         <li>Expand the columns tree to check Proteins &gt; Peptides &gt; Precursors &gt; Precursor Results, to add a filter for the <b>Total Area</b> column.</li>
         <li>In the <b>Operation</b> column, choose “Is Blank”.</li>
     </ul>
@@ -1284,7 +1284,7 @@ <h2>Annotating Peptides with Problem Peaks</h2>
         The <b>Customize Report</b> form should look like this:
     </p>
     <p>
-        <img src="image-87.png" />
+        <img src="s-81.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -1295,7 +1295,7 @@ <h2>Annotating Peptides with Problem Peaks</h2>
         The <b>Document Grid</b> should look like the following:
     </p>
     <p>
-        <img src="image-88.png" />
+        <img src="s-82.png" />
     </p>
     <p>
         <b>NOTE</b>: If you did not fully process your document, you may instead see only one line for the peptide GSYNLQDLLAQ. The next note
@@ -1343,7 +1343,7 @@ <h2>Initial multi-replicate inspection in Skyline</h2>
         This should leave the <b>Peak Areas</b> graph looking something like:
     </p>
     <p>
-        <img src="image-89.png" />
+        <img src="s-83.png" />
     </p>
     <p>
         You can now select through several more peptides to review the coefficients of variation (CV) among the technical replicates for each subject.
@@ -1367,13 +1367,13 @@ <h2>Initial multi-replicate inspection in Skyline</h2>
     <table class="comp-fig">
         <tr>
             <td class="comp-fig">
-                <img src="image-90.png" />
+                <img src="s-84.png" />
             </td>
             <td class="comp-fig">
-                <img src="image-91.png" />
+                <img src="s-85.png" />
             </td>
             <td class="comp-fig">
-                <img src="image-92.png" />
+                <img src="s-86.png" />
             </td>
         </tr>
     </table>
@@ -1416,10 +1416,10 @@ <h2>Initial multi-replicate inspection in Skyline</h2>
     <table class="comp-fig">
         <tr>
             <td class="comp-fig">
-                <img src="image-93.png" />
+                <img src="s-87.png" />
             </td>
             <td class="comp-fig">
-                <img src="image-94.png" />
+                <img src="s-88.png" />
             </td>
         </tr>
     </table>
@@ -1435,10 +1435,10 @@ <h2>Initial multi-replicate inspection in Skyline</h2>
     <table class="comp-fig">
         <tr>
             <td class="comp-fig">
-                <img src="image-95.png" />
+                <img src="s-89.png" />
             </td>
             <td class="comp-fig">
-                <img src="image-96.png" />
+                <img src="s-90.png" />
             </td>
         </tr>
     </table>
@@ -1474,7 +1474,7 @@ <h2>Simple group comparisons in Skyline</h2>
         The <b>Edit Group Comparison Form</b> should look like this:
     </p>
     <p>
-        <img src="image-97.png" />
+        <img src="s-91.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -1483,7 +1483,7 @@ <h2>Simple group comparisons in Skyline</h2>
         The <b>Document Settings</b> form should look like this:
     </p>
     <p>
-        <img src="image-98.png" />
+        <img src="s-92.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -1498,7 +1498,7 @@ <h2>Simple group comparisons in Skyline</h2>
         Skyline will show a grid view that looks like this:
     </p>
     <p>
-        <img src="image-99.png" />
+        <img src="s-93.png" />
     </p>
     <p>
         If the “Fold Change Result” column does not show the full confidence interval, double-click the vertical line between the Fold Change Result
@@ -1514,7 +1514,7 @@ <h2>Simple group comparisons in Skyline</h2>
         Skyline adds a graph pane beside the <b>Healthy v. Diseased:Grid</b> view that looks like this:
     </p>
     <p>
-        <img src="image-100.png" />
+        <img src="s-94.png" />
     </p>
     <ul>
         <li>On the grid, click the “Fold Change Result” header, and click <b>Sort Ascending</b> in the menu that appears.</li>
@@ -1538,7 +1538,7 @@ <h2>Simple group comparisons in Skyline</h2>
         You will see the number of rows indicated in the grid toolbar drop from 48 to 11, and the graph should now look like this:
     </p>
     <p>
-        <img src="image-101.png" />
+        <img src="s-95.png" />
     </p>
     <p>
         Note that more of the proteins that displayed significant change have positive fold-change means, indicating they were more intense in the
@@ -1592,7 +1592,7 @@ <h2>Refinement by differentiation</h2>
         like this:
     </p>
     <p>
-        <img src="image-102.png" />
+        <img src="s-96.png" />
     </p>
     <p class="keep-next">
         To delete these peptides from the document do the following:
@@ -1607,20 +1607,20 @@ <h2>Refinement by differentiation</h2>
         The grid should look like this:
     </p>
     <p>
-        <img src="image-103.png" />
+        <img src="s-97.png" />
     </p>
     <p>
         Note that the VVLSGSDATLAYSAFK peptide has a fold-change of 1, with a 99% confidence interval of 1 to 1. This is the single peptide used as the
         Global Standard for normalization. You do not want to delete this peptide from the document. That is why you deselected it.
     </p>
     <ul>
-        <li>Click the <img src="image-104.png" /> button in the grid toolbar.</li>
+        <li>Click the <img src="../../shared/red-x-icon.png" /> button in the grid toolbar.</li>
     </ul>
     <p class="keep-next">
         Skyline will show the following message to confirm you really want to delete the selected rows:
     </p>
     <p>
-        <img src="image-105.png" />
+        <img src="s-98.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/GroupedStudies/en/image-1.png b/pwiz_tools/Skyline/Documentation/Tutorials/GroupedStudies/en/s-1.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/GroupedStudies/en/image-1.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/GroupedStudies/en/s-1.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/GroupedStudies/en/image-12.png b/pwiz_tools/Skyline/Documentation/Tutorials/GroupedStudies/en/s-10.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/GroupedStudies/en/image-12.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/GroupedStudies/en/s-10.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/GroupedStudies/en/image-13.png b/pwiz_tools/Skyline/Documentation/Tutorials/GroupedStudies/en/s-11.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/GroupedStudies/en/image-13.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/GroupedStudies/en/s-11.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/GroupedStudies/en/image-14.png b/pwiz_tools/Skyline/Documentation/Tutorials/GroupedStudies/en/s-12.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/GroupedStudies/en/image-14.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/GroupedStudies/en/s-12.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/GroupedStudies/en/image-15.png b/pwiz_tools/Skyline/Documentation/Tutorials/GroupedStudies/en/s-13.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/GroupedStudies/en/image-15.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/GroupedStudies/en/s-13.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/GroupedStudies/en/image-16.png b/pwiz_tools/Skyline/Documentation/Tutorials/GroupedStudies/en/s-14.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/GroupedStudies/en/image-16.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/GroupedStudies/en/s-14.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/GroupedStudies/en/image-17.png b/pwiz_tools/Skyline/Documentation/Tutorials/GroupedStudies/en/s-15.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/GroupedStudies/en/image-17.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/GroupedStudies/en/s-15.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/GroupedStudies/en/image-18.png b/pwiz_tools/Skyline/Documentation/Tutorials/GroupedStudies/en/s-16.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/GroupedStudies/en/image-18.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/GroupedStudies/en/s-16.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/GroupedStudies/en/image-20.png b/pwiz_tools/Skyline/Documentation/Tutorials/GroupedStudies/en/s-17.png
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--- a/pwiz_tools/Skyline/Documentation/Tutorials/GroupedStudies/ja/index.html
+++ b/pwiz_tools/Skyline/Documentation/Tutorials/GroupedStudies/ja/index.html
@@ -67,7 +67,7 @@ <h1>メソッド最適化後の差分解析 </h1>
         本研究の全体的な目標は、ターゲットタンパク質／ペプチドの予備知識をあまり多く持っていなくても、しかも安定同位体標識した参照ペプチドを使用せずに、ターゲット解析から役立つ科学的洞察が得られるかどうかを判定することです。
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     <p>
-        <img src="image-0.png" />
+        <img src="s-detection-and-differentiation-phases.png" />
     </p>
     <p>
         <b>図1</b>：塩分感受性ラットモデルの心不全研究において、ターゲットメソッド最適化の「検出」および「差分」フェーズを示す概略図。
@@ -82,14 +82,14 @@ <h1>メソッド最適化後の差分解析 </h1>
         Skylineウィンドウの右下角の数値をチェックすると、開いたファイルには49のタンパク質、137のペプチド、および789のトランジションが含まれていることが分かります。
     </p>
     <p>
-        <img src="image-1.png" />
+        <img src="s-1.png" />
     </p>
     <p>
         これは上記の図（発表されていない論文からの図）で示されたものとは大きく異なり、またドキュメントには追加のペプチドリストが1つ含まれています（下の方に「S」と名付けられているもの）。同リストにはグローバル正規化ペプチドが3つ含まれています。これらは、試料内のすべてのペプチドに影響を与えてしまう、分析における体系的変動の影響を低減させることを目的としています。これについては、後で詳しく触れます。また、ペプチドを1つ持つタンパク質が1つ、上記で説明したファイルからなくなってしまっています。
     </p>
     <p>
-        一部のペプチドにはライブラリスペクトルと一致するものがあることに気づかれるでしょう。これは、[ <b>ターゲット</b> ] ビューで見ることができます。右下角のスペクトルラインのあるペプチドアイコン（<img src="image-2.png" />
-        ）には一致スペクトルがあり、ラインなしのペプチドアイコン（<img src="image-3.png" /> ） には一致スペクトルはありません。当該スペクトルは2つの異なる公共スペクトルライブラリからのもので、1つはNIST、もう1つはグローバルプロテオームマシン（Global
+        一部のペプチドにはライブラリスペクトルと一致するものがあることに気づかれるでしょう。これは、[ <b>ターゲット</b> ] ビューで見ることができます。右下角のスペクトルラインのあるペプチドアイコン（<img src="../../shared/peptide-with-spectrum-lines-icon.png" />
+        ）には一致スペクトルがあり、ラインなしのペプチドアイコン（<img src="../../shared/peptide-without-spectrum-lines-icon.png" /> ） には一致スペクトルはありません。当該スペクトルは2つの異なる公共スペクトルライブラリからのもので、1つはNIST、もう1つはグローバルプロテオームマシン（Global
         Proteome Machine、GPM）からのものです。以下を行ってこれらの範囲を探索できます。
     </p>
     <ul>
@@ -101,7 +101,7 @@ <h1>メソッド最適化後の差分解析 </h1>
         ここでグリッドをスクロールダウンすると、ライブラリスペクトルを用いたペプチドの数（80個）を確認できます。これらは、ラット（NIST）ライブラリ（49個）とラット（GPM）ライブラリ（31個）の各スペクトルデータに由来します。選択したセルの行番号がグリッドの上にあるツールバー内に表示されていることに注意してください。
     </p>
     <p>
-        <img src="image-4.png" />
+        <img src="s-2.png" />
     </p>
     <p>
         現在の例については、この情報により、この実験の基となった予備知識がわずかに得られます。タンパク質に関する知識は今日、高度化しており、<a
@@ -123,7 +123,7 @@ <h2>参照標準なしで複数の繰り返し測定データ処理を設定す
         ファイルの読み込みが始まり、Skylineはウィンドウに、進行状況を以下のように表示します。
     </p>
     <p>
-        <img src="image-5.png" />
+        <img src="s-3.png" />
     </p>
     <p>
         SkylineがSRMクロマトグラムをインポートしている間にデータ処理の準備を続行するには、以下の操作を行います。
@@ -138,7 +138,7 @@ <h2>参照標準なしで複数の繰り返し測定データ処理を設定す
         <li>以下のように、青い長方形の枠がSkylineウィンドウの下端を覆うまでカーソルを下部ドッキングインジケーターへドラッグします。</li>
     </ul>
     <p>
-        <img src="image-6.png" />
+        <img src="s-4.png" />
     </p>
     <ul>
         <li>マウスの左ボタンから指を離し、[ <b>保持時間</b> ] ビューを ドッキングします。</li>
@@ -146,14 +146,14 @@ <h2>参照標準なしで複数の繰り返し測定データ処理を設定す
         <li>[ <b>ピーク領域</b> ] ビューを、マウスカーソルがドッキングインジケーター内に入るまでドラッグすると、青い長方形枠が表示され、 [ <b>ピーク領域</b> ] ビューの下端を共有することを示します。</li>
     </ul>
     <p>
-        <img src="image-7.png" />
+        <img src="s-5.png" />
     </p>
     <ul>
         <li>マウスの左ボタンから指を離し、[ <b>ピーク領域</b> ] ビューをドッキングします。</li>
         <li>[ <b>ターゲット</b> ] ビューを、マウスカーソルがドッキングインジケーター内に入るまでドラッグすると、青い長方形枠が表示され、Skylineウィンドウの左端とドッキングすることを示します。</li>
     </ul>
     <p>
-        <img src="image-8.png" />
+        <img src="s-6.png" />
     </p>
     <ul>
         <li>メインのSkylineウィンドウの外側で表示されている、その他のウィンドウを閉じます。</li>
@@ -166,7 +166,7 @@ <h2>参照標準なしで複数の繰り返し測定データ処理を設定す
         フォームは以下のようになります。
     </p>
     <p>
-        <img src="image-9.png" />
+        <img src="s-7.png" />
     </p>
     <ul>
         <li>[ <b>OK</b> ] ボタンをクリックします。</li>
@@ -177,7 +177,7 @@ <h2>参照標準なしで複数の繰り返し測定データ処理を設定す
         Skylineウィンドウは以下のようになります。
     </p>
     <p>
-        <img src="image-10.png" />
+        <img src="s-8.png" />
     </p>
     <p>
         <b>注：</b>この画像は、解像度1920x1080の24インチのモニタ上でキャプチャしたものです。本チュートリアルをデジタル方式でご覧になっている場合、200%以上ズームインしてこの画像を見ることをお薦めします。これ以降、本チュートリアルでは元通り、8½ x
@@ -188,7 +188,7 @@ <h2>参照標準なしで複数の繰り返し測定データ処理を設定す
         積分領域があまり一貫していないことが分かります。選択されたピークのほとんどは約19分で溶出します。しかし、3分の1ほど（12）は22分付近で溶出します。
     </p>
     <p>
-        <img src="image-11.png" />
+        <img src="s-9.png" />
     </p>
     <p>
         これでも、このペプチドの積分はあまり良くありません。19分前後のピークはより良いピークに見えますが、単一ペプチドの結果なのであまり信頼できません。更に、積分を調整しても、すべての分析で一貫して測定可能な単一ペプチドとなる可能性は低くなっています。したがって、更に調整を行って時間を無駄にすることはせず、次の操作を行ってく
@@ -202,7 +202,7 @@ <h2>スケジュール化SRMおよびピーク切断</h2>
         2番目のペプチドの保持時間プロットを見るだけで、同ペプチドがより一貫して積分されてい ることが分かります。
     </p>
     <p>
-        <img src="image-12.png" />
+        <img src="s-10.png" />
     </p>
     <p>
         しかし、すべてのトランジションのピーク頂点（バー内の水平ラインで表示）は一定していません。いくつかのクロマトグラムグラフに注目してみると、形状がギザギザで強度が中～低のピークも見られます。
@@ -223,13 +223,13 @@ <h2>スケジュール化SRMおよびピーク切断</h2>
         これにより [ <b>ピーク領域</b> ] プロットが以下から
     </p>
     <p>
-        <img src="image-13.png" />
+        <img src="s-11.png" />
     </p>
     <p class="keep-next">
         次のプロットへと変わります。
     </p>
     <p>
-        <img src="image-14.png" />
+        <img src="s-12.png" />
     </p>
     <p>
         これにより、複数の分析にわたる相対イオン存在量の差を一瞥して見分けることが可能となり、 [ <b>保持時間</b> ]
@@ -246,13 +246,13 @@ <h2>スケジュール化SRMおよびピーク切断</h2>
         これにより当該ピークのクロマトグラムグラフが有効化され、以下のようになります。
     </p>
     <p>
-        <img src="image-15.png" />
+        <img src="s-13.png" />
     </p>
     <p>
         一方、正しく積分されたピークのプロットはこのようになります。
     </p>
     <p>
-        <img src="image-16.png" />
+        <img src="s-14.png" />
     </p>
     <p>
         スケジュール化取得ウィンドウが当該ペプチドの全溶出プロファイルをキャプチャしなかったため、Skylineにより誤ったピークが選択されていますが、正しいピークが30.2分付近で終わっているのが見えます。これは「切断ピーク」と呼ばれます。このペプチドの積分は、切断ピークを使用し以下の操作を行うことで修正できます。
@@ -288,7 +288,7 @@ <h2>スケジュール化SRMおよびピーク切断</h2>
         [ <b>検索</b> ] フォームは以下のようになります。
     </p>
     <p>
-        <img src="image-17.png" />
+        <img src="s-15.png" />
     </p>
     <ul>
         <li>[ <b>すべて検索</b> ] ボタンをクリックします。</li>
@@ -298,7 +298,7 @@ <h2>スケジュール化SRMおよびピーク切断</h2>
         Skylineに切断プリカーサーおよびトランジションの長いリストが表示され、先に検査したばかりの3つのピークが冒頭に記載されています。ラインをダブルクリックすると、対応するクロマトグラムグラフが有効化されます。
     </p>
     <p>
-        <img src="image-18.png" />
+        <img src="s-16.png" />
     </p>
     <p>
         また<b>ドキュメントグリッド</b>を使用して以下の操作を行うと、ピークが切断されているすべてのプリカーサーのリストを作成できます。
@@ -309,7 +309,7 @@ <h2>スケジュール化SRMおよびピーク切断</h2>
         <li>[ <b>ドキュメントグリッド</b> ] ビューの [ <b>レポート</b> ] メニューで、[ <b>レポートをカスタマイズ</b> ] をクリックします。</li>
         <li>[ <b>レポート名</b> ] フィールドに「Truncated Precursor」と入力します。</li>
         <li>リストの右側で、最初の2つ（プリカーサーおよびペプチド）を除くすべての列名を選択します（クリックおよびシフト-クリックを利用）。</li>
-        <li>右縁付近の <img src="image-19.png" /> ボタンをクリックして、最初の2つを除くすべての列を削除します。</li>
+        <li>右縁付近の <img src="../../shared/red-x-icon.png" /> ボタンをクリックして、最初の2つを除くすべての列を削除します。</li>
         <li>左側のツリー内の「繰り返し測定」のチェックボックスをオンにします。</li>
         <li>ツリーを展開して、タンパク質 &gt; ペプチド &gt; プリカーサー &gt; プリカーサー結果 &gt; 切断数とチェックします。</li>
     </ul>
@@ -317,7 +317,7 @@ <h2>スケジュール化SRMおよびピーク切断</h2>
         [ <b>レポートをカスタマイズ</b> ] フォームは次のようになります。
     </p>
     <p>
-        <img src="image-20.png" />
+        <img src="s-17.png" />
     </p>
     <ul>
         <li>右側のリストで「切断数」をダブルクリックします。</li>
@@ -330,7 +330,7 @@ <h2>スケジュール化SRMおよびピーク切断</h2>
         [ <b>レポートをカスタマイズ</b> ] フォームは次のようになります。
     </p>
     <p>
-        <img src="image-21.png" />
+        <img src="s-18.png" />
     </p>
     <ul>
         <li>[ <b>OK</b> ] ボタンをクリックします。</li>
@@ -340,7 +340,7 @@ <h2>スケジュール化SRMおよびピーク切断</h2>
         [ <b>ドキュメントグリッド</b> ] に、Skylineがすでに自動的に選択した221の切断ピークが表示されます。
     </p>
     <p>
-        <img src="image-22.png" />
+        <img src="s-19.png" />
     </p>
     <p>
         これらのピークを表示するには、以下の操作を行います。
@@ -353,7 +353,7 @@ <h2>スケジュール化SRMおよびピーク切断</h2>
         Skylineにより以下のクロマトグラムグラフが有効化されます。
     </p>
     <p>
-        <img src="image-23.png" />
+        <img src="s-20.png" />
     </p>
     <ul>
         <li>[ <b>ドキュメントグリッド</b> ] を閉じます。</li>
@@ -365,7 +365,7 @@ <h2>複数の繰り返し測定データの処理を開始する</h2>
         ペプチドLGGEEVSVACKは、これまで見てきた他の2つのペプチドよりもかなり良い結果となっています。保持時間は非常に安定しており、水平ピーク頂点ラインは各繰り返し測定内のほとんどすべてのトランジションに対して一致しています。
     </p>
     <p>
-        <img src="image-24.png" />
+        <img src="s-21.png" />
     </p>
     <p>
         [ <b>ピーク領域</b> ] ビューに表示されている相対イオン存在量も比較的安定して見えます。このペプ
@@ -379,7 +379,7 @@ <h2>複数の繰り返し測定データの処理を開始する</h2>
         Skylineに、1（最良）～0（最悪）の範囲のライブラリスペクトルピーク強度と測定ピーク領域との間の類似性測定値であるドット積（dotp）関係が表示されます。
     </p>
     <p>
-        <img src="image-25.png" />
+        <img src="s-22.png" />
     </p>
     <p>
         以下の操作を行って [ <b>ピーク領域</b> ] ビューを元の状態に戻します。
@@ -400,13 +400,13 @@ <h2>複数の繰り返し測定データの処理を開始する</h2>
         一部のトランジションでは、メインピークの端付近に他のピークとあまり一致しないシグナルが表れていることに気付かれるかもしれません。
     </p>
     <p>
-        <img src="image-26.png" />
+        <img src="s-23.png" />
     </p>
     <p>
         13.1分付近のy5およびy6に明確なシグナルが見られるため、これは明らかに同一ペプチドからのものではありません。
     </p>
     <p>
-        <img src="image-27.png" />
+        <img src="s-24.png" />
     </p>
     <p>
         このような干渉シグナルが積分境界内で起こる場合、定量的測定にエラーが増えます。重要な定量的データについては、このペプチドの5つのトランジションすべてが必要かどうか検討してみてください。
@@ -415,13 +415,13 @@ <h2>複数の繰り返し測定データの処理を開始する</h2>
         本チュートリアルでは次のペプチドへと続行します。7個のトランジションすべてにおいて、強いシグナルで形状が整っており、かつ共溶出のピークが見られます。
     </p>
     <p>
-        <img src="image-28.png" />
+        <img src="s-25.png" />
     </p>
     <p>
         相対イオン存在量も非常に一定しています。
     </p>
     <p>
-        <img src="image-29.png" />
+        <img src="s-26.png" />
     </p>
     <p>
         y3のピーク領域は、ライブラリスペクトルで見たものより強力です。これは、三連四重極装置内で起こる二次断片化により、説明可能かもしれません。ライブラリスペクトルを生成した際に用いたイオントラップでは、装置内での共鳴励起では二次断片化は起こらない場合があります。このケースでは、スペクトルはNIST公共ライブラリからのものですので、ライブラリ作成に使用した装置のタイプについての情報はありません。
@@ -438,13 +438,13 @@ <h2>複数の繰り返し測定データの処理を開始する</h2>
         最初の5つの繰り返し測定については、選択されたピークが約32.5分～33.5分にあり、5つのトランジションすべてにシグナルがあります。しかし、35分付近で主にy4およびy5のシグナルを示すもう1つのピークがあり、これらは明らかに別のペプチドにより引き起こされたものです。このようなケースでは、目的ペプチドと共溶出しない干渉シグナルの情報が表示中のクロマトグラム「環境」に追加される場合があります。
     </p>
     <p>
-        <img src="image-30.png" />
+        <img src="s-27.png" />
     </p>
     <p class="keep-next">
         D_103_REP3では、主にy4およびy5上にシグナルを持つ積分ピークが33.9分に見られますが、左側にはその他の候補ピークは見られません。
     </p>
     <p>
-        <img src="image-31.png" />
+        <img src="s-28.png" />
     </p>
     <p>
         このケースでは、スケジュールウィンドウによるターゲットペプチドのシグナルキャプチャが失敗に終わっています。不正確なピークを削除するには、以下の操作を行います。
@@ -456,25 +456,25 @@ <h2>複数の繰り返し測定データの処理を開始する</h2>
         [ <b>ピーク領域</b> ] グラフが空白になります。
     </p>
     <p>
-        <img src="image-32.png" />
+        <img src="s-29.png" />
     </p>
     <p>
         クロマトグラムプロットを続行すると、このパターンが何回か繰り返されることがわかります。欠損ピークを削除し続けてください。ピーク切断のケースも一部見られます。H_148_REP2に目を向けると、Skylineは33.9分のピークを選択しているものの正しいピークの一部を視認できます。
     </p>
     <p>
-        <img src="image-33.png" />
+        <img src="s-30.png" />
     </p>
     <p>
         これは単に、上記で行ったようにx軸の下をクリック＆ドラッグすることで、切断ピークとして積分可能です。<b>ピーク領域</b>プロットは以下のようになるはずです。
     </p>
     <p>
-        <img src="image-34.png" />
+        <img src="s-31.png" />
     </p>
     <p class="keep-next">
         また保持時間プロットは以下のようになるはずです。
     </p>
     <p>
-        <img src="image-35.png" />
+        <img src="s-32.png" />
     </p>
     <ul>
         <li>ペプチドR.DIPVNPM<b><u>C</u></b>IYR.S [46, 56]へと続けていくと、</li>
@@ -495,7 +495,7 @@ <h2>複数の繰り返し測定データの処理を開始する</h2>
         ペプチドTSDQIHFFFAKについては、保持時間はこのようになります。
     </p>
     <p>
-        <img src="image-36.png" />
+        <img src="s-33.png" />
     </p>
     <p>
         しかし、装置上で取得された順に分析を見ることができれば便利な場合もあります。これは、以下の操作によって実行可能です。
@@ -507,7 +507,7 @@ <h2>複数の繰り返し測定データの処理を開始する</h2>
         グラフが以下のように変更されます。
     </p>
     <p>
-        <img src="image-37.png" />
+        <img src="s-34.png" />
     </p>
     <p>
         この保持時間パターンは、一貫性がやや向上しています。ここで、次の2つのペプチド（LQPLDFK、SQLPGIIAEGR）から選択すると、一貫したパターンを確認できます。
@@ -519,10 +519,10 @@ <h2>複数の繰り返し測定データの処理を開始する</h2>
     <table class="comp-fig">
         <tr>
             <td class="comp-fig">
-                <img src="image-38.png" />
+                <img src="s-35.png" />
             </td>
             <td class="comp-fig">
-                <img src="image-39.png" />
+                <img src="s-36.png" />
             </td>
         </tr>
     </table>
@@ -534,7 +534,7 @@ <h2>複数の繰り返し測定データの処理を開始する</h2>
         ビューは、相対イオン存在量の一貫性が非常に乏しいことを示しています。
     </p>
     <p>
-        <img src="image-40.png" />
+        <img src="s-37.png" />
     </p>
     <p>
         いくつかのクロマトグラムグラフを分析すると、18.8分の信号は、積分シグナルすべてが単一ペプチドに由来していると信頼した上で、一定して積分されているとは考えにくいということが分かります。このケースでは、当該ペプチドを消去して先に進みます。
@@ -553,16 +553,16 @@ <h2>グローバル正規化標準</h2>
         、VVLSGSDATLAYSAFKとAFGLSSPRは、本実験で注入された合成ペプチドです。これまで検査してきた2つの概要プロットからの最後の2つのペプチドの自動積分は精度が高いと確信できます。保持時間およびピーク領域は比較的一貫しています。
     </p>
     <p>
-        <img src="image-41.png" />
+        <img src="s-38.png" />
     </p>
     <p>
-        <img src="image-42.png" />
+        <img src="s-39.png" />
     </p>
     <p>
         ペプチドHLNGFSVPRへ移ると、一貫した保持時間を観察できます。しかし、ピーク面積にはより多くの変動が見られます。y4、そしてy3の相対面積は、時折データセットを通してむらがあるように見えます。
     </p>
     <p>
-        <img src="image-43.png" />
+        <img src="s-40.png" />
     </p>
     <p>
         y4が最も豊富なピーク領域バーを複数クリックすると、y4、そして時にはy3への明らかな干渉が見られます。
@@ -571,7 +571,7 @@ <h2>グローバル正規化標準</h2>
         <li>[ <b>ビュー</b> ] メニューで、 [ <b>自動ズーム</b> ] を選択し [ <b>最適ピーク</b> ]（F11）をクリックします。</li>
     </ul>
     <p>
-        <img src="image-44.png" />
+        <img src="s-41.png" />
     </p>
     <p>
         これら注入ペプチドが正規化標準として使用できるかについて明確な情報を得るには、 以下の操作を行います。
@@ -588,13 +588,13 @@ <h2>グローバル正規化標準</h2>
         これらのペプチドが相互に比較してどこで溶出してくるかを見るには、以下の操作を行います。
     </p>
     <ul>
-        <li>この <img src="image-45.png" /> アイコンが先頭にある「S」エレメントを選択します。</li>
+        <li>この <img src="../../shared/protein-icon-2.png" /> アイコンが先頭にある「S」エレメントを選択します。</li>
     </ul>
     <p>
         クロマトグラムグラフが変更され、「S」リスト内の3つのペプチドすべてがまとめて表示されます。
     </p>
     <p>
-        <img src="image-46.png" />
+        <img src="s-42.png" />
     </p>
     <p>
         ここでドキュメント内のすべてのペプチドをまとめて見るには、以下の操作を行います。
@@ -603,7 +603,7 @@ <h2>グローバル正規化標準</h2>
         <li>[ <b>編集</b> ] メニューで [ <b>すべて選択</b> ]（Ctrl+A）をクリックします。</li>
     </ul>
     <p>
-        <img src="image-47.png" />
+        <img src="s-43.png" />
     </p>
     <p>
         これにより、問題があった2つのペプチドはどちらも親水性で早く溶出することが明確となります。実際のところ、これらは本実験の3番目および10番目の溶出ペプチドです。こ れをSkylineで見るには、以下の操作を行います。
@@ -629,7 +629,7 @@ <h2>グローバル正規化標準</h2>
         表示内容を理解しようとする前に、すべての非標準ペプチドには、14個の被験体で測定されたためにより大きな誤差が出ると予想されると考えてください。また積分は、すべてのペプチドについて完全に調整されているわけではありません。現在のデータセットについては、当該標準に関して自動的に選択されたピークは正しいように見えます。しかし、HLNGFSVPRペプチドは約160%で2番目に高いCV値を持ち、またAFGLSSPRペプチドのCV値は約50%で、最初の15個のペプチドの中央値に近くなっています。（より疎水性で遅く溶出するVVLSGSDATLAYSAFKペプチドは108番目、またはCV値18.6%で80パーセンタイルに入ります。）
     </p>
     <p>
-        <img src="image-48.png" />
+        <img src="s-44.png" />
     </p>
     <p>
         以下を行うと、LGPペプチドにはHLNペプチドと非常に似た問題があると確信できるはずです。
@@ -642,7 +642,7 @@ <h2>グローバル正規化標準</h2>
         3サイクルまたは技術的繰り返し測定があるはずですので留意してください。
     </p>
     <p>
-        <img src="image-49.png" />
+        <img src="s-45.png" />
     </p>
     <p class="keep-next">
         ピークが正しく積分されていることを確認するには、以下の操作を行います。
@@ -655,7 +655,7 @@ <h2>グローバル正規化標準</h2>
         最小から最大まで200倍の範囲（1億4000万～70万）であるにも関わらず、分析間の相対プロダクトイオン存在量は非常に安定しています。
     </p>
     <p>
-        <img src="image-50.png" />
+        <img src="s-46.png" />
     </p>
     <p>
         このペプチドには同様の問題があるように見えますが、HLNGFSVPRのようなペプチドはグロ
@@ -678,7 +678,7 @@ <h2>複数の繰り返し測定データ処理を続行する</h2>
         x軸ズーム（Shift+F11）をオフにする必要があります。）
     </p>
     <p>
-        <img src="image-51.png" />
+        <img src="s-47.png" />
     </p>
     <p>
         この問題については、以前行ったように、x軸の下をクリック＆ドラッグして切断ピークを積分するか、または右クリックメニューを利用してピークを完全に削除することで修正できます。
@@ -687,13 +687,13 @@ <h2>複数の繰り返し測定データ処理を続行する</h2>
         しかし、これはこのペプチドに限った問題ではありません。[ <b>保持時間</b> ] グラフに注目すると、積分される時間の範囲に、通常とは異なった差異が複数見られます。
     </p>
     <p>
-        <img src="image-52.png" />
+        <img src="s-48.png" />
     </p>
     <p>
         このペプチドに関するいくつかのクロマトグラムを再確認すると、多くのものが0.2分間に溶出する単一の非常に優良なピークを示しているのが分かります。しかしその他については、溶出が約0.5分間にわたってテーリングしているピークや、2分間にわたる溶出で2つの明白なピークを持つペプチドが存在します。
     </p>
     <p>
-        <img src="image-53.png" />
+        <img src="s-49.png" />
     </p>
     <p>
         このようなペプチドは、特に一致SILペプチドがなければ、定量化に使用することは非常に困難です。本実験からこのペプチドを消去した方がよいかもしれません。せめて、二重溶出プロファイルを示すピークは削除した方が良いでしょう。 
@@ -705,13 +705,13 @@ <h2>複数の繰り返し測定データ処理を続行する</h2>
         しかしペプチドMLSGFIPLKPTVKまで来ると、大きな変動があることが [ <b>ピーク領域</b> ] グラフから分かります。
     </p>
     <p>
-        <img src="image-54.png" />
+        <img src="s-50.png" />
     </p>
     <p>
         このペプチドの総ピーク領域では、y7イオンが優位となっています。これは、ライブラリスペクトルにも反映されていますが（上記グラフの左端に表示）、実際にy7イオンと共溶出するものがあるかどうかについてクロマトグラムを見ただけで識別することは困難です（以下を参照）。
     </p>
     <p>
-        <img src="image-55.png" />
+        <img src="s-51.png" />
     </p>
     <p>
         しかしSkylineはほとんどの場合、各ランにおいて同一分子に対する同一ピークを積分していることも明らかです。y7ピーク以外のものがあるかを確認するには、最高強度の測定値に注目してください。以下の手順でこれを行うことができます。
@@ -724,26 +724,26 @@ <h2>複数の繰り返し測定データ処理を続行する</h2>
         これらの3つのプロット内で見られるクロマトグラムピークから、ペプチド存在量が十分に高い場合、23～24分でy7ピークを持つペプチドでは6つのトランジションすべてで共溶出信号が得られていることが十分に理解できます。
     </p>
     <p>
-        <img src="image-56.png" />
+        <img src="s-52.png" />
     </p>
     <p>
         このペプチドを消去するよりは、Skylineによって誤ったピークが選択されているデータを修正する方が良策でしょう。これは、[ <b>保持時間</b> ] プロットにおいて、22.5分未満に現れる短いバンドとして確認できます。
     </p>
     <p>
-        <img src="image-57.png" />
+        <img src="s-53.png" />
     </p>
     <p class="keep-next">
         また [ <b>ピーク領域</b> ] プロットでも、このランには視認できる積分信号がないことが分かります。
     </p>
     <p>
-        <img src="image-58.png" />
+        <img src="s-54.png" />
     </p>
     <p>
         [ <b>保持時間</b> ]
         ビュー内のバーをクリックして、このランのクロマトグラムグラフを有効化します。このランがy7トランジションにおいて非常に低い信号を有しているのが分かります。周辺のランから得たデータを確認せずに、ペプチドを代表するトランジションとしてこのトランジションのみを選択することはまずないでしょう。
     </p>
     <p>
-        <img src="image-59.png" />
+        <img src="s-55.png" />
     </p>
     <p>
         このランの積分を修正するには、以下の操作を行います。
@@ -781,20 +781,20 @@ <h2>複数の繰り返し測定データ処理を続行する</h2>
         多くのグラフで、選択したピークの約1.5分前のy3およびy4トランジションでペプチドが干渉しているのが分かります。これにより、積分ピークの一貫性における信頼度が高まります。
     </p>
     <p>
-        <img src="image-60.png" />
+        <img src="s-56.png" />
     </p>
     <p>
         [ <b>ターゲット</b> ] リストを続行していくと、複数のペプチド（YANVIAYDHSRとTDEDVPSGPPR）で測定ピークの相対イオン存在量と一致ライブラリスペクトルとの間の差が明白となっていることがわかります。これらの差は [
         <b>ピーク領域</b> ] グラフ内で見ることができます。
     </p>
     <p>
-        <img src="image-61.png" />
+        <img src="s-57.png" />
     </p>
     <p>
         これはクロマトグラムグラフ内でも観察でき、Skylineではピーク保持時間の下に低いドット積値「（dotp 0.28）」が表示されます。
     </p>
     <p>
-        <img src="image-62.png" />
+        <img src="s-58.png" />
     </p>
     <p>
         Skylineは、dotp値が高いグラフに別のピークがある場合に、このような「dotp」値を表示します。上記のケースでは、選択したピークに対してノイズレベル付近の低いピークしか見られないため、より良いdotp値を持つピークを見つけることはできません。上記を見るためには、以下の操作を行います。
@@ -822,7 +822,7 @@ <h2>複数の繰り返し測定データ処理を続行する</h2>
         ペプチド<b><u>C</u></b>SSLLWAGAAWLRへと移ります。サマリープロットで観察される変動から判断して（以下を参照）、最初はこのペプチドを削除して先に進みたいと思われるかもしれません。
     </p>
     <p>
-        <img src="image-63.png" />
+        <img src="s-59.png" />
     </p>
     <p>
         しかし注視してみると、健常被験体の中には一貫性のある領域があります。これを明確に示すため、以下の操作を行います。
@@ -834,10 +834,10 @@ <h2>複数の繰り返し測定データ処理を続行する</h2>
         そこでグラフは以下のように変更されます。
     </p>
     <p>
-        <img src="image-64.png" />
+        <img src="s-60.png" />
     </p>
     <p>
-        <img src="image-65.png" />
+        <img src="s-61.png" />
     </p>
     <p>
         健常被験体では一定のピークが積分され、罹患被験体についてはそうではないことが明確になります。健常被験体のピークを再確認すると、強度はかなり低く、主にy4、y5、およびy6イオンの共溶出に依存しているのが分かります。この共溶出はおそらく、1つのペプチドに起因しています。しかし、このペプチドが実際に<b><u>C</u></b>SSLLWAGAAWLRであるかどうかを判定することは困難です。
@@ -849,11 +849,11 @@ <h2>複数の繰り返し測定データ処理を続行する</h2>
         <tr>
             <td class="comp-fig">
                 D_102_REP3<br />
-                <img src="image-66.png" />
+                <img src="s-62.png" />
             </td>
             <td class="comp-fig">
                 D_108_REP1<br />
-                <img src="image-67.png" />
+                <img src="s-63.png" />
             </td>
         </tr>
     </table>
@@ -861,7 +861,7 @@ <h2>複数の繰り返し測定データ処理を続行する</h2>
         しかし、罹患被験体のクロマトグラム内には、健常被験体で観察されたのと同じようなピーク領域を作り出せるピークは見つかりません。これまでにピークドリフトや切断の操作で得てきた経験を用いれば、このピークは単にすべての罹患被験体の測定範囲外に横滑りしているわけではないと確信できますが、健常被験体に関しては違います。注入のランダム化により、上記の信頼度が増す可能性もあります。しかし現在の研究については、3つの繰り返し測定サイクルで十分なはずです。可能な限り積分を修正した後、このペプチドについてより多くの視認できるピークを持つ罹患群のランのうち2つが、健常被験体のランのすぐ後に続いていることにも気付くかもしれません（D_102_REP2およびD_102_REP3）。これは、キャリーオーバー効果を示唆している可能性があります。
     </p>
     <p>
-        <img src="image-68.png" />
+        <img src="s-64.png" />
     </p>
     <p>
         結局のところ、これらのトランジションは本研究におけるバイオマーカーの最有力候補の1つを表している可能性があります。合成ペプチドを使うことで、<b><u>C</u></b>SSLLWAGAAWLRペプチドを正しく測定しているという信頼性を向上させることができます。また、ペプチド検索エンジンでこのペプチドが同定されるかどうか確かめるために、このピークのMS/MSスペクトルを取得（並列反応モニタリング（PRM）を使用）することもできます。最後に、上記の操作が失敗した場合、健常被験体で見られるピークがどのようなペプチドかを同定するため、MS/MSスペクトル上で<i>de
@@ -890,7 +890,7 @@ <h2>繰り返し注釈のある統計分析を作成する</h2>
         フォームは以下のようになります。
     </p>
     <p>
-        <img src="image-69.png" />
+        <img src="s-65.png" />
     </p>
     <ul>
         <li>[ <b>注釈を定義</b> ] フォームで [ <b>OK</b> ] ボタンをクリックします。</li>
@@ -901,7 +901,7 @@ <h2>繰り返し注釈のある統計分析を作成する</h2>
         [ <b>ドキュメント設定</b> ] フォームは以下のようになります。
     </p>
     <p>
-        <img src="image-70.png" />
+        <img src="s-66.png" />
     </p>
     <ul>
         <li>[ <b>OK</b> ] ボタンをクリックします。</li>
@@ -917,7 +917,7 @@ <h2>繰り返し注釈のある統計分析を作成する</h2>
         [ <b>ツールストアからインストール</b> ] フォームは次のようになります。
     </p>
     <p>
-        <img src="image-71.png" />
+        <img src="s-67.png" />
     </p>
     <ul>
         <li>[ <b>インストール</b> ] ボタンをクリックし、MSstatsのインストールが完了するまでプロンプトに従います。</li>
@@ -937,10 +937,10 @@ <h2>繰り返し注釈のある統計分析を作成する</h2>
     <table class="comp-fig">
         <tr>
             <td class="comp-fig" style="padding: 5px;">
-                <img src="image-72.png" />
+                <img src="s-68.png" />
             </td>
             <td class="comp-fig" style="padding: 5px;">
-                <img src="image-73.png" />
+                <img src="s-69.png" />
             </td>
         </tr>
     </table>
@@ -952,7 +952,7 @@ <h2>繰り返し注釈のある統計分析を作成する</h2>
         [ <b>ドキュメント設定</b> ] フォームは以下のようになります。
     </p>
     <p>
-        <img src="image-74.png" />
+        <img src="s-70.png" />
     </p>
     <ul>
         <li>[ <b>OK</b> ] ボタンをクリックします。</li>
@@ -968,7 +968,7 @@ <h2>繰り返し注釈のある統計分析を作成する</h2>
         [ <b>ドキュメントグリッド</b> ] は以下のようになります。
     </p>
     <p>
-        <img src="image-75.png" />
+        <img src="s-71.png" />
     </p>
     <p>
         これで、42個の繰り返し測定すべての注釈をこのグリッドに手動入力できます。スプレッドシートからこのフォームに直接貼り付けることも可能です。これを行うには、以下の手順に従います。
@@ -986,7 +986,7 @@ <h2>繰り返し注釈のある統計分析を作成する</h2>
         [ <b>ドキュメントグリッド</b> ] は以下のようになります。
     </p>
     <p>
-        <img src="image-76.png" />
+        <img src="s-72.png" />
     </p>
     <ul>
         <li>Ctrl+Vを押して [ <b>ドキュメントグリッド</b> ] に貼り付けます。</li>
@@ -995,7 +995,7 @@ <h2>繰り返し注釈のある統計分析を作成する</h2>
         スプレッドシートの値が [ <b>ドキュメントグリッド</b> ] 内のセルに以下のように入力されます。
     </p>
     <p>
-        <img src="image-77.png" />
+        <img src="s-73.png" />
     </p>
     <h2>問題ピークのあるペプチドに注釈を付ける</h2>
     <p>
@@ -1014,7 +1014,7 @@ <h2>問題ピークのあるペプチドに注釈を付ける</h2>
         [ <b>注釈を定義</b> ] フォームは以下のようになります。
     </p>
     <p>
-        <img src="image-78.png" />
+        <img src="s-74.png" />
     </p>
     <ul>
         <li>[ <b>OK</b> ] ボタンをクリックします。</li>
@@ -1025,7 +1025,7 @@ <h2>問題ピークのあるペプチドに注釈を付ける</h2>
         [ <b>ドキュメント設定</b> ] フォームは以下のようになります。
     </p>
     <p>
-        <img src="image-79.png" />
+        <img src="s-75.png" />
     </p>
     <ul>
         <li>[ <b>OK</b> ] ボタンをクリックします。</li>
@@ -1042,7 +1042,7 @@ <h2>問題ピークのあるペプチドに注釈を付ける</h2>
         [ <b>レポートをカスタマイズ</b> ] フォームは以下のようになります。
     </p>
     <p>
-        <img src="image-80.png" />
+        <img src="s-76.png" />
     </p>
     <ul>
         <li>[ <b>OK</b> ] ボタンをクリックします。</li>
@@ -1052,7 +1052,7 @@ <h2>問題ピークのあるペプチドに注釈を付ける</h2>
         [ <b>ドキュメントグリッド</b> ] は以下のようになります。
     </p>
     <p>
-        <img src="image-81.png" />
+        <img src="s-77.png" />
     </p>
     <p>
         残りのドキュメントの処理方法によっては、切断プリカーサーピークグループの数は223個ちょうどとなったり、ならない場合があります。ペプチドの「MissingData」チェックボックスは1個ずつオンにすることが可能です。任意ペプチドのボックスをオンにすると、残りは自動的にオンになります。なぜならこの注釈は、どのペプチドにも一度だけ適用されるからです。以下の操作を行って、これを試してみましょう。
@@ -1065,7 +1065,7 @@ <h2>問題ピークのあるペプチドに注釈を付ける</h2>
         [ <b>ドキュメントグリッド</b> ] は以下のようになります。
     </p>
     <p>
-        <img src="image-82.png" />
+        <img src="s-78.png" />
     </p>
     <p>
         また以下の操作を行うことで、Excelおよび [ <b>ドキュメントグリッド</b> ] の値貼り付け機能を利用して1回の貼り付けで163行すべてを設定できます。
@@ -1086,7 +1086,7 @@ <h2>問題ピークのあるペプチドに注釈を付ける</h2>
         上記手順を実行すると、[ <b>ターゲット</b> ] リスト上位の多くのペプチドの名前の上／右側に、小さな赤い三角形マークが付いているのが分かります。
     </p>
     <p>
-        <img src="image-83.png" />
+        <img src="s-79.png" />
     </p>
     <p>
         これらの三角形の上にマウスをポイントすると、テキスト「<b>Missing Data</b> True」とともにヒントが表示されます。
@@ -1099,18 +1099,18 @@ <h2>問題ピークのあるペプチドに注釈を付ける</h2>
         <li>これまで使用していた「切断プリカーサー」レポートを選択します。</li>
         <li>[ <b>コピー</b> ] ボタンをクリックします。</li>
         <li>[ <b>レポートをカスタマイズ</b> ] フォームの [ <b>レポート名</b> ] フィールドに「Missing Peaks」と入力します。</li>
-        <li>[ <b>プリカーサー</b> ] 列および [ <b>切断数</b> ] 列を削除するには、列リストの右側の <img src="image-84.png" /> ボタンを使用します。</li>
+        <li>[ <b>プリカーサー</b> ] 列および [ <b>切断数</b> ] 列を削除するには、列リストの右側の <img src="../../shared/red-x-icon.png" /> ボタンを使用します。</li>
         <li>[<b>ピボット繰り返し測定名</b>] チェックボックスをオンにします。</li>
     </ul>
     <p class="keep-next">
         [ <b>レポートをカスタマイズ</b> ] フォームは以下のようになります。
     </p>
     <p>
-        <img src="image-85.png" />
+        <img src="s-80.png" />
     </p>
     <ul>
         <li>[ <b>フィルタ</b> ] タブをクリックします。</li>
-        <li>次に <img src="image-86.png" /> ボタンをクリックして、[ <b>切断数</b> ] の既存のフィルタを削除します。</li>
+        <li>次に <img src="../../shared/red-x-icon.png" /> ボタンをクリックして、[ <b>切断数</b> ] の既存のフィルタを削除します。</li>
         <li>列ツリーを展開して、タンパク質 &gt; ペプチド &gt; プリカーサー &gt; プリカーサー結果をチェックした後、[ <b>総面積</b> ] 列のフィルタを追加します。</li>
         <li>[ <b>操作</b> ] 列で、「空白」を選択します。</li>
     </ul>
@@ -1118,7 +1118,7 @@ <h2>問題ピークのあるペプチドに注釈を付ける</h2>
         [ <b>レポートをカスタマイズ</b> ] フォームは以下のようになります。
     </p>
     <p>
-        <img src="image-87.png" />
+        <img src="s-81.png" />
     </p>
     <ul>
         <li>[ <b>OK</b> ] ボタンをクリックします。</li>
@@ -1129,7 +1129,7 @@ <h2>問題ピークのあるペプチドに注釈を付ける</h2>
         [ <b>ドキュメントグリッド</b> ] は以下のようになります。
     </p>
     <p>
-        <img src="image-88.png" />
+        <img src="s-82.png" />
     </p>
     <p>
         <b>注</b>：ドキュメントを完全に処理しなかった場合、ペプチドGSYNLQDLLAQには1行しか表示されない可能性があります。完全に処理されたドキュメントを開く手順については、次の注で説明します。
@@ -1169,7 +1169,7 @@ <h2>Skyline内での最初の複数の繰り返し測定検査</h2>
         これにより、[ <b>ピーク領域</b> ] グラフは以下のようになります。
     </p>
     <p>
-        <img src="image-89.png" />
+        <img src="s-83.png" />
     </p>
     <p>
         ここでさらに多くのペプチドを選択して、各被験体の技術的繰り返し測定間での変動係数（CV）を再確認できます。ほとんどが25%未満であることが分かります。しかし理想的には、本実験よりも低いCVが見られることが望ましいでしょう。3個の測定値から得られた低いCV
@@ -1189,13 +1189,13 @@ <h2>Skyline内での最初の複数の繰り返し測定検査</h2>
     <table class="comp-fig">
         <tr>
             <td class="comp-fig">
-                <img src="image-90.png" />
+                <img src="s-84.png" />
             </td>
             <td class="comp-fig">
-                <img src="image-91.png" />
+                <img src="s-85.png" />
             </td>
             <td class="comp-fig">
-                <img src="image-92.png" />
+                <img src="s-86.png" />
             </td>
         </tr>
     </table>
@@ -1225,10 +1225,10 @@ <h2>Skyline内での最初の複数の繰り返し測定検査</h2>
     <table class="comp-fig">
         <tr>
             <td class="comp-fig">
-                <img src="image-93.png" />
+                <img src="s-87.png" />
             </td>
             <td class="comp-fig">
-                <img src="image-94.png" />
+                <img src="s-88.png" />
             </td>
         </tr>
     </table>
@@ -1241,10 +1241,10 @@ <h2>Skyline内での最初の複数の繰り返し測定検査</h2>
     <table class="comp-fig">
         <tr>
             <td class="comp-fig">
-                <img src="image-95.png" />
+                <img src="s-89.png" />
             </td>
             <td class="comp-fig">
-                <img src="image-96.png" />
+                <img src="s-90.png" />
             </td>
         </tr>
     </table>
@@ -1274,7 +1274,7 @@ <h2>Skyline内での簡単なグループ比較</h2>
         [ <b>グループ比較を編集</b> ] フォームは以下のようになります。
     </p>
     <p>
-        <img src="image-97.png" />
+        <img src="s-91.png" />
     </p>
     <ul>
         <li>[ <b>OK</b> ] ボタンをクリックします。</li>
@@ -1283,7 +1283,7 @@ <h2>Skyline内での簡単なグループ比較</h2>
         [ <b>ドキュメント設定</b> ] フォームは以下のようになります。
     </p>
     <p>
-        <img src="image-98.png" />
+        <img src="s-92.png" />
     </p>
     <ul>
         <li>[ <b>OK</b> ] ボタンをクリックします。</li>
@@ -1298,7 +1298,7 @@ <h2>Skyline内での簡単なグループ比較</h2>
         Skylineに以下のようなグリッドビューが表示されます。
     </p>
     <p>
-        <img src="image-99.png" />
+        <img src="s-93.png" />
     </p>
     <p>
         「倍率変化結果」列に信頼区間が表示されていない場合、倍率変化結果と調整されたP値の両ヘッダー間の縦線をダブルクリックします。
@@ -1313,7 +1313,7 @@ <h2>Skyline内での簡単なグループ比較</h2>
         Skylineにより、以下のように [ <b>Healthy v. Diseased：グリッド</b> ] ビューの横にグラフパネルが追加されます。
     </p>
     <p>
-        <img src="image-100.png" />
+        <img src="s-94.png" />
     </p>
     <ul>
         <li>当該グリッドで「倍率変化結果」ヘッダーをクリックして、表示されたメニュー内の [ <b>昇順に並べ替え</b> ] をクリックします。</li>
@@ -1334,7 +1334,7 @@ <h2>Skyline内での簡単なグループ比較</h2>
         グリッドツールバーに示す行数が48から11に減少し、当該グラフは以下のようになります。
     </p>
     <p>
-        <img src="image-101.png" />
+        <img src="s-95.png" />
     </p>
     <p>
         ここで、有意の変化を示したタンパク質の多くには正の倍率変化平均値があり、これは羅患群ではこの値がさらに強いことを意味します。ただし、試料順序のランダム化の失敗による影響を考慮することが重要です。測定の全3サイクルにおいて罹患被験体は健常被験体に先行していたため、正規化において考慮しなかった劣化が倍率変化を引き起こして罹患群の上方調節のように見えてしまうと予測されます。
@@ -1376,7 +1376,7 @@ <h2>差分による最適化</h2>
         [ <b>Healthy v. Diseased：グリッド</b> ] には、1% FDRカットオフを超えている92行が表示され、グラフはこのようになります。
     </p>
     <p>
-        <img src="image-102.png" />
+        <img src="s-96.png" />
     </p>
     <p class="keep-next">
         これらのペプチドをドキュメントから削除するには、以下の操作を行います。
@@ -1390,19 +1390,19 @@ <h2>差分による最適化</h2>
         グリッドは以下のようになります。
     </p>
     <p>
-        <img src="image-103.png" />
+        <img src="s-97.png" />
     </p>
     <p>
         VVLSGSDATLAYSAFKペプチドの倍率変化は1であり、信頼区間は1から1の99%であることに注意してください。これは、正規化のグローバル標準として使用されている単一ペプチドです。このペプチドはドキュメントから削除しない方がいいでしょう。それが非選択にした理由です。
     </p>
     <ul>
-        <li>グリッドツールバー内の <img src="image-104.png" /> ボタンをクリックします。</li>
+        <li>グリッドツールバー内の <img src="../../shared/red-x-icon.png" /> ボタンをクリックします。</li>
     </ul>
     <p class="keep-next">
         Skylineに、選択した行の削除を確認する以下のメッセージが表示されます。
     </p>
     <p>
-        <img src="image-105.png" />
+        <img src="s-98.png" />
     </p>
     <ul>
         <li>[ <b>OK</b> ] ボタンをクリックします。</li>
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/GroupedStudies/ja/invariant.html b/pwiz_tools/Skyline/Documentation/Tutorials/GroupedStudies/ja/invariant.html
index cb8413c3d6..b2c8a3c599 100644
--- a/pwiz_tools/Skyline/Documentation/Tutorials/GroupedStudies/ja/invariant.html
+++ b/pwiz_tools/Skyline/Documentation/Tutorials/GroupedStudies/ja/invariant.html
@@ -96,7 +96,7 @@ <h1>Differential analysis after method refinement</h1>
         very much prior knowledge of the targeted proteins or peptides and without aid of stable isotope labeled reference peptides.
     </p>
     <p>
-        <img src="image-0.png" />
+        <img src="s-detection-and-differentiation-phases.png" />
     </p>
     <p>
         <b>Figure 1</b>: A schematic showing proposed “Detection” and “Differentiation” phases of targeted method refinement in a heart
@@ -113,7 +113,7 @@ <h1>Differential analysis after method refinement</h1>
         peptides and 789 transitions.
     </p>
     <p>
-        <img src="image-1.png" />
+        <img src="s-1.png" />
     </p>
     <p>
         This is not quite what is promised in the figure above (from a manuscript draft that was never published), but the document also contains one
@@ -123,8 +123,8 @@ <h1>Differential analysis after method refinement</h1>
     </p>
     <p>
         You will notice that some of the peptides have matching library spectra. You can see this in the <b>Targets</b> view. The peptide
-        icons with spectrum lines in the lower right corner (<img src="image-2.png" />) have matching spectra and those without these lines (<img
-            src="image-3.png" />) do not. The spectra come from two different public spectral libraries: one from NIST and one from the Global
+        icons with spectrum lines in the lower right corner (<img src="../../shared/peptide-with-spectrum-lines-icon.png" />) have matching spectra and those without these lines (<img
+            src="../../shared/peptide-without-spectrum-lines-icon.png" />) do not. The spectra come from two different public spectral libraries: one from NIST and one from the Global
         Proteome Machine (GPM). You can explore their coverage by doing the following:
     </p>
     <ul>
@@ -139,7 +139,7 @@ <h1>Differential analysis after method refinement</h1>
         (GPM) library (31). Note that the row number of the selected cell is shown in the toolbar above the grid.
     </p>
     <p>
-        <img src="image-4.png" />
+        <img src="s-2.png" />
     </p>
     <p>
         For the current example, this information gives you a sense of the sparse prior knowledge on which the experiment was based. Modern knowledge
@@ -164,7 +164,7 @@ <h2>Setting up to process multi-replicate data without reference standards</h2>
         The files should begin loading, and Skyline will display progress in a window like the one shown below:
     </p>
     <p>
-        <img src="image-5.png" />
+        <img src="s-3.png" />
     </p>
     <p>
         To continue preparing for data processing while Skyline imports the SRM chromatograms, do the following:
@@ -179,7 +179,7 @@ <h2>Setting up to process multi-replicate data without reference standards</h2>
         <li>Drag the cursor into the bottom docking indicator to see a blue rectangle fill the bottom edge of the Skyline window, as shown below.</li>
     </ul>
     <p>
-        <img src="image-6.png" />
+        <img src="s-4.png" />
     </p>
     <ul>
         <li>Release the left mouse button to dock the <b>Retention Times</b> view.</li>
@@ -188,7 +188,7 @@ <h2>Setting up to process multi-replicate data without reference standards</h2>
             share the bottom edge with the <b>Peak Areas</b> view.</li>
     </ul>
     <p>
-        <img src="image-7.png" />
+        <img src="s-5.png" />
     </p>
     <ul>
         <li>Release the left mouse button to dock the <b>Peak Areas</b> view.</li>
@@ -196,7 +196,7 @@ <h2>Setting up to process multi-replicate data without reference standards</h2>
             to the left edge of the Skyline window.</li>
     </ul>
     <p>
-        <img src="image-8.png" />
+        <img src="s-6.png" />
     </p>
     <ul>
         <li>Close any other windows left floating outside the main Skyline window.</li>
@@ -209,7 +209,7 @@ <h2>Setting up to process multi-replicate data without reference standards</h2>
         The form should look like this:
     </p>
     <p>
-        <img src="image-9.png" />
+        <img src="s-7.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -220,7 +220,7 @@ <h2>Setting up to process multi-replicate data without reference standards</h2>
         Your Skyline window should now look something like this:
     </p>
     <p>
-        <img src="image-10.png" />
+        <img src="s-8.png" />
     </p>
     <p>
         <b>Note</b>: This image was taken on a 24” monitor at 1920x1080. If you are viewing this tutorial digitally, you may want to zoom in
@@ -232,7 +232,7 @@ <h2>Setting up to process multi-replicate data without reference standards</h2>
         not very consistent. Most of the chosen peaks elute around 19 minutes. However, nearly one third (12) elute closer to 22 minutes.
     </p>
     <p>
-        <img src="image-11.png" />
+        <img src="s-9.png" />
     </p>
     <p>
         The integration for this peptide is quite poor. While the peak at around 19 minutes appears to be the better peak, it is hard to have much
@@ -247,7 +247,7 @@ <h2>Scheduled SRM and peak truncation</h2>
         Just by looking at the retention time plot for the second peptide, you can see that it is much more consistently integrated.
     </p>
     <p>
-        <img src="image-12.png" />
+        <img src="s-10.png" />
     </p>
     <p>
         However, you can still see that the peak apexes for all transitions (shown by the horizontal lines in the bars) are not very consistent. If you
@@ -270,13 +270,13 @@ <h2>Scheduled SRM and peak truncation</h2>
         This changes the <b>Peak Areas</b> plot from:
     </p>
     <p>
-        <img src="image-13.png" />
+        <img src="s-11.png" />
     </p>
     <p class="keep-next">
         To:
     </p>
     <p>
-        <img src="image-14.png" />
+        <img src="s-12.png" />
     </p>
     <p>
         This makes it possible to see differences in relative ion abundance across multiple runs in a single glance and adds to the information you are
@@ -294,13 +294,13 @@ <h2>Scheduled SRM and peak truncation</h2>
         This will activate the chromatogram graph for the peak, which looks like:
     </p>
     <p>
-        <img src="image-15.png" />
+        <img src="s-13.png" />
     </p>
     <p>
         While plots for the correctly integrated peaks look more like this:
     </p>
     <p>
-        <img src="image-16.png" />
+        <img src="s-14.png" />
     </p>
     <p>
         Since the scheduled acquisition window did not capture the entire elution profile for the peptide, Skyline has picked the wrong peak. However,
@@ -346,7 +346,7 @@ <h2>Scheduled SRM and peak truncation</h2>
         The <b>Find</b> form should look like this:
     </p>
     <p>
-        <img src="image-17.png" />
+        <img src="s-15.png" />
     </p>
     <ul>
         <li>Click the <b>Find All</b> button.</li>
@@ -357,7 +357,7 @@ <h2>Scheduled SRM and peak truncation</h2>
         any line to see the corresponding chromatogram graph activated.
     </p>
     <p>
-        <img src="image-18.png" />
+        <img src="s-16.png" />
     </p>
     <p>
         You can also use the <b>Document Grid</b> to create a list of all precursors with any peak truncation by doing the following:
@@ -368,7 +368,7 @@ <h2>Scheduled SRM and peak truncation</h2>
         <li>On the <b>Reports</b> menu in the <b>Document Grid</b> view, click <b>Customize Report</b>.</li>
         <li>In the <b>Report name</b> field, enter “Truncated Precursors”.</li>
         <li>In the right side list, select all column names (using click and shift-click) after the first two (Precursor and Peptide).</li>
-        <li>Click the <img src="image-19.png" /> button near the right edge to delete all but the first two columns.</li>
+        <li>Click the <img src="../../shared/red-x-icon.png" /> button near the right edge to delete all but the first two columns.</li>
         <li>Check “Replicates” in the tree on the left side.</li>
         <li>Expand the tree to check Proteins &gt; Peptides &gt; Precursors &gt; PrecursorResults &gt; Count Truncated.</li>
     </ul>
@@ -376,7 +376,7 @@ <h2>Scheduled SRM and peak truncation</h2>
         The <b>Customize Report</b> form should look something like this:
     </p>
     <p>
-        <img src="image-20.png" />
+        <img src="s-17.png" />
     </p>
     <ul>
         <li>In the right side list, double-click “Count Truncated”.</li>
@@ -389,7 +389,7 @@ <h2>Scheduled SRM and peak truncation</h2>
         The <b>Customize Report</b> form should look something like this:
     </p>
     <p>
-        <img src="image-21.png" />
+        <img src="s-18.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -399,7 +399,7 @@ <h2>Scheduled SRM and peak truncation</h2>
         The <b>Document Grid</b> will show 221 truncated peaks that Skyline has already chosen automatically:
     </p>
     <p>
-        <img src="image-22.png" />
+        <img src="s-19.png" />
     </p>
     <p>
         To view these peaks:
@@ -412,7 +412,7 @@ <h2>Scheduled SRM and peak truncation</h2>
         Skyline will activate chromatogram graphs that look like the following:
     </p>
     <p>
-        <img src="image-23.png" />
+        <img src="s-20.png" />
     </p>
     <ul>
         <li>Close the <b>Document Grid</b>.</li>
@@ -425,7 +425,7 @@ <h2>Beginning multi-replicate data processing</h2>
         peak apex lines match up for almost all transitions in each replicate.
     </p>
     <p>
-        <img src="image-24.png" />
+        <img src="s-21.png" />
     </p>
     <p>
         The relative ion abundances shown in the <b>Peak Areas</b> view also appear relatively stable. You might notice that there is a
@@ -442,7 +442,7 @@ <h2>Beginning multi-replicate data processing</h2>
         measured peak areas ranging from 1 (best) to zero (worst).
     </p>
     <p>
-        <img src="image-25.png" />
+        <img src="s-22.png" />
     </p>
     <p>
         Return the <b>Peak Areas</b> view to its former state by doing the following:
@@ -463,13 +463,13 @@ <h2>Beginning multi-replicate data processing</h2>
         You might notice that some of the transitions show a signal around the edges of the main peak that is not well matched by the other peaks.
     </p>
     <p>
-        <img src="image-26.png" />
+        <img src="s-23.png" />
     </p>
     <p>
         There is frequently signal on y5 and y6 around 13.1 minutes, which is clearly not from the same peptide.
     </p>
     <p>
-        <img src="image-27.png" />
+        <img src="s-24.png" />
     </p>
     <p>
         When an interfering signal like this occurs inside the integration boundaries, it will add error to the quantitative measurements. For critical
@@ -479,13 +479,13 @@ <h2>Beginning multi-replicate data processing</h2>
         For the current tutorial, however, continue to the next peptide. There you will find strong, clean, and co-eluting peaks for all 7 transitions.
     </p>
     <p>
-        <img src="image-28.png" />
+        <img src="s-25.png" />
     </p>
     <p>
         Relative ion abundance is also extremely consistent.
     </p>
     <p>
-        <img src="image-29.png" />
+        <img src="s-26.png" />
     </p>
     <p>
         The peak area in y3 is stronger than what was seen for the library spectrum. This might be explained by secondary fragmentation occurring in a
@@ -508,14 +508,14 @@ <h2>Beginning multi-replicate data processing</h2>
         not coincide with the peptide of interest can add information to the chromatogram “landscape” you see.
     </p>
     <p>
-        <img src="image-30.png" />
+        <img src="s-27.png" />
     </p>
     <p class="keep-next">
         In D_103_REP3, you will see the integrated peak at 33.9 minutes with signal mostly on y4 and y5, but no other candidate peak
         to the left.
     </p>
     <p>
-        <img src="image-31.png" />
+        <img src="s-28.png" />
     </p>
     <p>
         In this case, the scheduling window has failed to capture any signal from the targeted peptide. To remove the incorrect peak do the following:
@@ -527,7 +527,7 @@ <h2>Beginning multi-replicate data processing</h2>
         This should leave a blank spot in the <b>Peak Areas</b> graph.
     </p>
     <p>
-        <img src="image-32.png" />
+        <img src="s-29.png" />
     </p>
     <p>
         Continuing through the chromatogram plots, you will see this pattern repeated several times. Keep removing the missing peaks. You will even
@@ -535,20 +535,20 @@ <h2>Beginning multi-replicate data processing</h2>
         where Skyline has chosen the peak at 33.9 minutes, but part of the correct peak is still visible.
     </p>
     <p>
-        <img src="image-33.png" />
+        <img src="s-30.png" />
     </p>
     <p>
         You can simply integrate this as a truncated peak, as you did above, by clicking and dragging beneath the x-axis. You should end up with a
         <b>Peak Areas</b> plot that looks like this:
     </p>
     <p>
-        <img src="image-34.png" />
+        <img src="s-31.png" />
     </p>
     <p class="keep-next">
         And a retention times plot that looks like this:
     </p>
     <p>
-        <img src="image-35.png" />
+        <img src="s-32.png" />
     </p>
     <ul>
         <li>Continue to the peptide R.DIPVNPM<b><u>C</u></b>IYR.S [46, 56].</li>
@@ -573,7 +573,7 @@ <h2>Beginning multi-replicate data processing</h2>
         like this:
     </p>
     <p>
-        <img src="image-36.png" />
+        <img src="s-33.png" />
     </p>
     <p>
         However, it may also be quite helpful to see the runs in the order they were acquired on the instrument. You can achieve this by doing the
@@ -586,7 +586,7 @@ <h2>Beginning multi-replicate data processing</h2>
         The graph will change to look like the following:
     </p>
     <p>
-        <img src="image-37.png" />
+        <img src="s-34.png" />
     </p>
     <p>
         This retention time pattern is now a little less erratic. If you now select through the next two peptides (LQPLDFK, SQLPGIIAEGR), you will see
@@ -601,10 +601,10 @@ <h2>Beginning multi-replicate data processing</h2>
     <table class="comp-fig">
         <tr>
             <td class="comp-fig">
-                <img src="image-38.png" />
+                <img src="s-35.png" />
             </td>
             <td class="comp-fig">
-                <img src="image-39.png" />
+                <img src="s-36.png" />
             </td>
         </tr>
     </table>
@@ -618,7 +618,7 @@ <h2>Beginning multi-replicate data processing</h2>
         poor consistency in relative ion abundance.
     </p>
     <p>
-        <img src="image-40.png" />
+        <img src="s-37.png" />
     </p>
     <p>
         If you examine a few of the chromatogram graphs, you will find it hard to imagine consistently integrating the signal at 18.8 minutes with any
@@ -641,17 +641,17 @@ <h2>Global normalization standards</h2>
         peptides from the two summary plots we have been examining. The retention times and peak areas are relatively consistent.
     </p>
     <p>
-        <img src="image-41.png" />
+        <img src="s-38.png" />
     </p>
     <p>
-        <img src="image-42.png" />
+        <img src="s-39.png" />
     </p>
     <p>
         Moving to the peptide HLNGFSVPR, you will observe consistent retention times. However, there is
         much more variance in the peak areas. The relative area for y4 and sometimes y3 seems to vary throughout the data set.
     </p>
     <p>
-        <img src="image-43.png" />
+        <img src="s-40.png" />
     </p>
     <p>
         If you click on some of the peak area bars where y4 is most abundant, you will see obvious interference on y4 and sometimes y3.
@@ -660,7 +660,7 @@ <h2>Global normalization standards</h2>
         <li>On the <b>View</b> menu, choose <b>Auto-Zoom</b> and click <b>Best Peak</b> (F11).</li>
     </ul>
     <p>
-        <img src="image-44.png" />
+        <img src="s-41.png" />
     </p>
     <p>
         To gain an even clearer understanding of the performance of these injected peptides as potential normalization standards, you should do the
@@ -682,13 +682,13 @@ <h2>Global normalization standards</h2>
         To see where these peptides elute relative to each other do the following:
     </p>
     <ul>
-        <li>Select the “S” element preceded by the <img src="image-45.png" /> icon.</li>
+        <li>Select the “S” element preceded by the <img src="../../shared/protein-icon-2.png" /> icon.</li>
     </ul>
     <p>
         The chromatogram graphs will change to show all three peptides in the “S” list together.
     </p>
     <p>
-        <img src="image-46.png" />
+        <img src="s-42.png" />
     </p>
     <p>
         Now to see all the peptides in the document together:
@@ -697,7 +697,7 @@ <h2>Global normalization standards</h2>
         <li>On the <b>Edit</b> menu, click <b>Select All</b> (Ctrl-A).</li>
     </ul>
     <p>
-        <img src="image-47.png" />
+        <img src="s-43.png" />
     </p>
     <p>
         This makes it clear that the two problematic peptides are both hydrophilic and early eluting. In fact, they are the 3<sup>rd</sup> and
@@ -729,7 +729,7 @@ <h2>Global normalization standards</h2>
         more hydrophobic and later eluting, is 108<sup>th</sup> or in the 80<sup>th</sup> percentile with 18.6% CV.)
     </p>
     <p>
-        <img src="image-48.png" />
+        <img src="s-44.png" />
     </p>
     <p>
         If you do the following, you should be able to convince yourself that the LGP peptide has a problem very similar to the HLN peptide.
@@ -742,7 +742,7 @@ <h2>Global normalization standards</h2>
         Remember that there are supposed to be three cycles or technical replicates:
     </p>
     <p>
-        <img src="image-49.png" />
+        <img src="s-45.png" />
     </p>
     <p class="keep-next">
         To convince yourself that the peaks are correctly integrated, do the following:
@@ -756,7 +756,7 @@ <h2>Global normalization standards</h2>
         extremely stable.
     </p>
     <p>
-        <img src="image-50.png" />
+        <img src="s-46.png" />
     </p>
     <p>
         Although this one peptide seems to have similar issues, you should exclude a peptide like HLNGFSVPR from consideration as a global
@@ -783,7 +783,7 @@ <h2>Continuing multi-replicate data processing</h2>
         scheduling window. (You might need to turn off x-axis zooming – Shift-F11 – to see this.)
     </p>
     <p>
-        <img src="image-51.png" />
+        <img src="s-47.png" />
     </p>
     <p>
         As you did before, you can correct this by clicking and dragging beneath the x-axis to integrate the truncated peak, or by using the
@@ -794,7 +794,7 @@ <h2>Continuing multi-replicate data processing</h2>
         unusual differences in the ranges of time being integrated.
     </p>
     <p>
-        <img src="image-52.png" />
+        <img src="s-48.png" />
     </p>
     <p>
         If you review some of the chromatograms for this peptide, you will see that many show a single, very nice peak eluting over 0.2 minutes.
@@ -802,7 +802,7 @@ <h2>Continuing multi-replicate data processing</h2>
         distinct peaks.
     </p>
     <p>
-        <img src="image-53.png" />
+        <img src="s-49.png" />
     </p>
     <p>
         A peptide like this may be very difficult to use for quantification, especially without a matching SIL peptide. You should probably delete this
@@ -817,7 +817,7 @@ <h2>Continuing multi-replicate data processing</h2>
         <b>Peak Areas</b> graph.
     </p>
     <p>
-        <img src="image-54.png" />
+        <img src="s-50.png" />
     </p>
     <p>
         The total peak area for this peptide is dominated by the y7 ion. Although this is also reflected in the library spectrum (as shown at the far
@@ -825,7 +825,7 @@ <h2>Continuing multi-replicate data processing</h2>
         ion (see below).
     </p>
     <p>
-        <img src="image-55.png" />
+        <img src="s-51.png" />
     </p>
     <p>
         However, it is also clear that Skyline is, for the most part, integrating the same peak for the same molecule in each run. To convince yourself
@@ -840,20 +840,20 @@ <h2>Continuing multi-replicate data processing</h2>
         minutes does, in fact, cause the co-eluting signals on all 6 monitored transitions when peptide abundance is high enough.
     </p>
     <p>
-        <img src="image-56.png" />
+        <img src="s-52.png" />
     </p>
     <p>
         Rather than deleting this peptide, you will want to correct the one case where Skyline has chosen the wrong peak. You can see this in the
         <b>Retention Times</b> plot, as a narrower band occurring below 22.5 minutes.
     </p>
     <p>
-        <img src="image-57.png" />
+        <img src="s-53.png" />
     </p>
     <p class="keep-next">
         And also in the <b>Peak Areas</b> plot, as the run with no visible integrated signal.
     </p>
     <p>
-        <img src="image-58.png" />
+        <img src="s-54.png" />
     </p>
     <p>
         You can click on the bar in the <b>Retention Times</b> view to activate the chromatogram graph for this run. You will see that the
@@ -861,7 +861,7 @@ <h2>Continuing multi-replicate data processing</h2>
         knowledge you have gained from the surrounding runs.
     </p>
     <p>
-        <img src="image-59.png" />
+        <img src="s-55.png" />
     </p>
     <p>
         To correct the integration of this run, do the following:
@@ -904,7 +904,7 @@ <h2>Continuing multi-replicate data processing</h2>
         This gives you added confidence in the consistency of the integrated peak.
     </p>
     <p>
-        <img src="image-60.png" />
+        <img src="s-56.png" />
     </p>
     <p>
         Continuing up the <b>Targets</b> list, you will find several peptides (YANVIAYDHSR and
@@ -912,14 +912,14 @@ <h2>Continuing multi-replicate data processing</h2>
         the matching library spectrum is pronounced. You can see these differences in the <b>Peak Areas</b> graph:
     </p>
     <p>
-        <img src="image-61.png" />
+        <img src="s-57.png" />
     </p>
     <p>
         You can also observe this in the chromatogram graphs where Skyline displays the low dot product values “(dotp 0.28)” beneath the peak retention
         times.
     </p>
     <p>
-        <img src="image-62.png" />
+        <img src="s-58.png" />
     </p>
     <p>
         Skyline displays the “dotp” value like this when there is another peak on the graph with a higher dotp value. In the case above, you cannot see
@@ -953,7 +953,7 @@ <h2>Continuing multi-replicate data processing</h2>
         summary plots (see below), you may initially be tempted to delete this peptide and move on:
     </p>
     <p>
-        <img src="image-63.png" />
+        <img src="s-59.png" />
     </p>
     <p>
         However, if you look closely you will see that there are regions of consistency among the healthy subjects. To see this expressed more clearly,
@@ -966,10 +966,10 @@ <h2>Continuing multi-replicate data processing</h2>
         This will change the graphs to look like:
     </p>
     <p>
-        <img src="image-64.png" />
+        <img src="s-60.png" />
     </p>
     <p>
-        <img src="image-65.png" />
+        <img src="s-61.png" />
     </p>
     <p>
         Making it clearer that a consistent peak is being integrated for the healthy subjects but not for the diseased subjects. If you review the peak
@@ -985,11 +985,11 @@ <h2>Continuing multi-replicate data processing</h2>
         <tr>
             <td class="comp-fig">
                 D_102_REP3<br />
-                <img src="image-66.png" />
+                <img src="s-62.png" />
             </td>
             <td class="comp-fig">
                 D_108_REP1<br />
-                <img src="image-67.png" />
+                <img src="s-63.png" />
             </td>
         </tr>
     </table>
@@ -1002,7 +1002,7 @@ <h2>Continuing multi-replicate data processing</h2>
         after runs of healthy subjects (D_102_REP2 and D_102_REP3). This observation might suggest a carryover effect.
     </p>
     <p>
-        <img src="image-68.png" />
+        <img src="s-64.png" />
     </p>
     <p>
         In the end, these transitions may represent one of the strongest biomarker candidates in this document. You could now order a synthetic peptide
@@ -1042,7 +1042,7 @@ <h2>Preparing for statistical analysis with replicate annotations</h2>
         The form should look like this:
     </p>
     <p>
-        <img src="image-69.png" />
+        <img src="s-65.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button in the <b>Define Annotation</b> form.</li>
@@ -1053,7 +1053,7 @@ <h2>Preparing for statistical analysis with replicate annotations</h2>
         The <b>Document Settings</b> form should look like:
     </p>
     <p>
-        <img src="image-70.png" />
+        <img src="s-66.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -1072,7 +1072,7 @@ <h2>Preparing for statistical analysis with replicate annotations</h2>
         The <b>Install from Tool Store</b> form should look like:
     </p>
     <p>
-        <img src="image-71.png" />
+        <img src="s-67.png" />
     </p>
     <ul>
         <li>Click the <b>Install</b> button and follow the prompts until MSstats installation is completed.</li>
@@ -1093,10 +1093,10 @@ <h2>Preparing for statistical analysis with replicate annotations</h2>
     <table class="comp-fig">
         <tr>
             <td class="comp-fig" style="padding: 5px;">
-                <img src="image-72.png" />
+                <img src="s-68.png" />
             </td>
             <td class="comp-fig" style="padding: 5px;">
-                <img src="image-73.png" />
+                <img src="s-69.png" />
             </td>
         </tr>
     </table>
@@ -1108,7 +1108,7 @@ <h2>Preparing for statistical analysis with replicate annotations</h2>
         The <b>Document Settings</b> form should look like this:
     </p>
     <p>
-        <img src="image-74.png" />
+        <img src="s-70.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -1125,7 +1125,7 @@ <h2>Preparing for statistical analysis with replicate annotations</h2>
         The <b>Document Grid</b> should look something like this:
     </p>
     <p>
-        <img src="image-75.png" />
+        <img src="s-71.png" />
     </p>
     <p>
         You can now manually enter the annotations for all 42 replicates into this grid. You can also paste values from a spreadsheet directly into
@@ -1145,7 +1145,7 @@ <h2>Preparing for statistical analysis with replicate annotations</h2>
         The <b>Document Grid</b> should look like this:
     </p>
     <p>
-        <img src="image-76.png" />
+        <img src="s-72.png" />
     </p>
     <ul>
         <li>Press Ctrl-V to paste into the <b>Document Grid</b>.</li>
@@ -1154,7 +1154,7 @@ <h2>Preparing for statistical analysis with replicate annotations</h2>
         Skyline should fill in the cells in the <b>Document Grid</b> with the values from the spreadsheet as follows:
     </p>
     <p>
-        <img src="image-77.png" />
+        <img src="s-73.png" />
     </p>
     <h2>Annotating Peptides with Problem Peaks</h2>
     <p>
@@ -1174,7 +1174,7 @@ <h2>Annotating Peptides with Problem Peaks</h2>
         The <b>Define Annotation</b> form should look like:
     </p>
     <p>
-        <img src="image-78.png" />
+        <img src="s-74.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -1185,7 +1185,7 @@ <h2>Annotating Peptides with Problem Peaks</h2>
         The <b>Document Settings</b> form should look like:
     </p>
     <p>
-        <img src="image-79.png" />
+        <img src="s-75.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -1204,7 +1204,7 @@ <h2>Annotating Peptides with Problem Peaks</h2>
         The <b>Customize Report</b> form should look like this:
     </p>
     <p>
-        <img src="image-80.png" />
+        <img src="s-76.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -1214,7 +1214,7 @@ <h2>Annotating Peptides with Problem Peaks</h2>
         The <b>Document Grid</b> should look like this:
     </p>
     <p>
-        <img src="image-81.png" />
+        <img src="s-77.png" />
     </p>
     <p>
         Depending on how you processed the rest of your document, there may or may not be exactly 223 truncated precursor peak groups. You could check
@@ -1229,7 +1229,7 @@ <h2>Annotating Peptides with Problem Peaks</h2>
         The <b>Document Grid</b> should now look like this:
     </p>
     <p>
-        <img src="image-82.png" />
+        <img src="s-78.png" />
     </p>
     <p>
         You can also use Excel and the <b>Document Grid</b> support for pasting values to set all 163 rows in a single paste as follows:
@@ -1253,7 +1253,7 @@ <h2>Annotating Peptides with Problem Peaks</h2>
         marked with a small red triangle above and right of the peptide name.
     </p>
     <p>
-        <img src="image-83.png" />
+        <img src="s-79.png" />
     </p>
     <p>
         If you hover the mouse cursor over one of these triangles, you will see a tip appear with the text “<b>Missing Data</b> True”.
@@ -1267,7 +1267,7 @@ <h2>Annotating Peptides with Problem Peaks</h2>
         <li>Select the “Truncated Precursors” report you have been using.</li>
         <li>Click the <b>Copy</b> button.</li>
         <li>In the <b>Report Name</b> field of the <b>Customize Report</b> form, enter “Missing Peaks”.</li>
-        <li>Remove the <b>Precursors</b> and <b>Count Truncated</b> columns using the <img src="image-84.png" /> button to the
+        <li>Remove the <b>Precursors</b> and <b>Count Truncated</b> columns using the <img src="../../shared/red-x-icon.png" /> button to the
             right of the columns list.</li>
         <li>Check the <b>Pivot Replicate Name</b> checkbox.</li>
     </ul>
@@ -1275,11 +1275,11 @@ <h2>Annotating Peptides with Problem Peaks</h2>
         The <b>Customize Report</b> form should look like this:
     </p>
     <p>
-        <img src="image-85.png" />
+        <img src="s-80.png" />
     </p>
     <ul>
         <li>Click the <b>Filter</b> tab.</li>
-        <li>Click the <img src="image-86.png" /> button to remove the existing filter on <b>Count Truncated</b>.</li>
+        <li>Click the <img src="../../shared/red-x-icon.png" /> button to remove the existing filter on <b>Count Truncated</b>.</li>
         <li>Expand the columns tree to check Proteins &gt; Peptides &gt; Precursors &gt; Precursor Results, to add a filter for the <b>Total Area</b> column.</li>
         <li>In the <b>Operation</b> column, choose “Is Blank”.</li>
     </ul>
@@ -1287,7 +1287,7 @@ <h2>Annotating Peptides with Problem Peaks</h2>
         The <b>Customize Report</b> form should look like this:
     </p>
     <p>
-        <img src="image-87.png" />
+        <img src="s-81.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -1298,7 +1298,7 @@ <h2>Annotating Peptides with Problem Peaks</h2>
         The <b>Document Grid</b> should look like the following:
     </p>
     <p>
-        <img src="image-88.png" />
+        <img src="s-82.png" />
     </p>
     <p>
         <b>NOTE</b>: If you did not fully process your document, you may instead see only one line for the peptide GSYNLQDLLAQ. The next note
@@ -1346,7 +1346,7 @@ <h2>Initial multi-replicate inspection in Skyline</h2>
         This should leave the <b>Peak Areas</b> graph looking something like:
     </p>
     <p>
-        <img src="image-89.png" />
+        <img src="s-83.png" />
     </p>
     <p>
         You can now select through several more peptides to review the coefficients of variation (CV) among the technical replicates for each subject.
@@ -1370,13 +1370,13 @@ <h2>Initial multi-replicate inspection in Skyline</h2>
     <table class="comp-fig">
         <tr>
             <td class="comp-fig">
-                <img src="image-90.png" />
+                <img src="s-84.png" />
             </td>
             <td class="comp-fig">
-                <img src="image-91.png" />
+                <img src="s-85.png" />
             </td>
             <td class="comp-fig">
-                <img src="image-92.png" />
+                <img src="s-86.png" />
             </td>
         </tr>
     </table>
@@ -1418,10 +1418,10 @@ <h2>Initial multi-replicate inspection in Skyline</h2>
     <table class="comp-fig">
         <tr>
             <td class="comp-fig">
-                <img src="image-93.png" />
+                <img src="s-87.png" />
             </td>
             <td class="comp-fig">
-                <img src="image-94.png" />
+                <img src="s-88.png" />
             </td>
         </tr>
     </table>
@@ -1437,10 +1437,10 @@ <h2>Initial multi-replicate inspection in Skyline</h2>
     <table class="comp-fig">
         <tr>
             <td class="comp-fig">
-                <img src="image-95.png" />
+                <img src="s-89.png" />
             </td>
             <td class="comp-fig">
-                <img src="image-96.png" />
+                <img src="s-90.png" />
             </td>
         </tr>
     </table>
@@ -1476,7 +1476,7 @@ <h2>Simple group comparisons in Skyline</h2>
         The <b>Edit Group Comparison Form</b> should look like this:
     </p>
     <p>
-        <img src="image-97.png" />
+        <img src="s-91.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -1485,7 +1485,7 @@ <h2>Simple group comparisons in Skyline</h2>
         The <b>Document Settings</b> form should look like this:
     </p>
     <p>
-        <img src="image-98.png" />
+        <img src="s-92.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -1500,7 +1500,7 @@ <h2>Simple group comparisons in Skyline</h2>
         Skyline will show a grid view that looks like this:
     </p>
     <p>
-        <img src="image-99.png" />
+        <img src="s-93.png" />
     </p>
     <p>
         If the “Fold Change Result” column does not show the full confidence interval, double-click the vertical line between the Fold Change Result
@@ -1516,7 +1516,7 @@ <h2>Simple group comparisons in Skyline</h2>
         Skyline adds a graph pane beside the <b>Healthy v. Diseased:Grid</b> view that looks like this:
     </p>
     <p>
-        <img src="image-100.png" />
+        <img src="s-94.png" />
     </p>
     <ul>
         <li>On the grid, click the “Fold Change Result” header, and click <b>Sort Ascending</b> in the menu that appears.</li>
@@ -1540,7 +1540,7 @@ <h2>Simple group comparisons in Skyline</h2>
         You will see the number of rows indicated in the grid toolbar drop from 48 to 11, and the graph should now look like this:
     </p>
     <p>
-        <img src="image-101.png" />
+        <img src="s-95.png" />
     </p>
     <p>
         Note that more of the proteins that displayed significant change have positive fold-change means, indicating they were more intense in the
@@ -1594,7 +1594,7 @@ <h2>Refinement by differentiation</h2>
         like this:
     </p>
     <p>
-        <img src="image-102.png" />
+        <img src="s-96.png" />
     </p>
     <p class="keep-next">
         To delete these peptides from the document do the following:
@@ -1609,20 +1609,20 @@ <h2>Refinement by differentiation</h2>
         The grid should look like this:
     </p>
     <p>
-        <img src="image-103.png" />
+        <img src="s-97.png" />
     </p>
     <p>
         Note that the VVLSGSDATLAYSAFK peptide has a fold-change of 1, with a 99% confidence interval of 1 to 1. This is the single peptide used as the
         Global Standard for normalization. You do not want to delete this peptide from the document. That is why you deselected it.
     </p>
     <ul>
-        <li>Click the <img src="image-104.png" /> button in the grid toolbar.</li>
+        <li>Click the <img src="../../shared/red-x-icon.png" /> button in the grid toolbar.</li>
     </ul>
     <p class="keep-next">
         Skyline will show the following message to confirm you really want to delete the selected rows:
     </p>
     <p>
-        <img src="image-105.png" />
+        <img src="s-98.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/GroupedStudies/zh-CHS/index.html b/pwiz_tools/Skyline/Documentation/Tutorials/GroupedStudies/zh-CHS/index.html
index 7bb5faf455..139c4ac800 100644
--- a/pwiz_tools/Skyline/Documentation/Tutorials/GroupedStudies/zh-CHS/index.html
+++ b/pwiz_tools/Skyline/Documentation/Tutorials/GroupedStudies/zh-CHS/index.html
@@ -74,7 +74,7 @@ <h1>方法调整后的差异分析</h1>
         本研究的总体目标，是确定能否从无需事先具备关于目标蛋白质或肽段的知识，也不要求具备稳定同位素标记的肽段作为参考的靶向研究得出有用的科学结论。
     </p>
     <p>
-        <img src="image-0.png" />
+        <img src="s-detection-and-differentiation-phases.png" />
     </p>
     <p>
         <b>图 1：</b>盐敏感性大鼠心力衰竭研究中靶向方法调整的原理示意图，包含“检测(Detction)”和“差异分析(Differentiation)”两个阶段。
@@ -89,14 +89,14 @@ <h1>方法调整后的差异分析</h1>
         通过观查 Skyline 窗口右下角的显示栏，您会看到您打开的文件包括 49 个蛋白质、137 个肽段和 789 个离子对。
     </p>
     <p>
-        <img src="image-1.png" />
+        <img src="s-1.png" />
     </p>
     <p>
         这并不是通过图1应得出的最理想情况（来自一份未发表的手稿中的分析结论）。虽然如此，介理该文档同时包括了一份额外的肽段列表（在文档底部，命名为“S”），其中包括了 3
         个全球标准化肽段。它们旨在减小测量中系统方差对肽段样品的影响。对于这一点，您会在稍后的过程了解更清楚。另外，该文件肯定比上述文件少了 1 个单肽段的蛋白质。
     </p>
     <p>
-        您会发现，一些肽段有匹配的库谱图。您可以在<b>目标</b>视图中查看相关结果。在右下角肽段图标中，有谱图线标记的 (<img src="image-2.png" />) 表示有相应匹配的谱图，没有的 (<img src="image-3.png" />)
+        您会发现，一些肽段有匹配的库谱图。您可以在<b>目标</b>视图中查看相关结果。在右下角肽段图标中，有谱图线标记的 (<img src="../../shared/peptide-with-spectrum-lines-icon.png" />) 表示有相应匹配的谱图，没有的 (<img src="../../shared/peptide-without-spectrum-lines-icon.png" />)
         则表示没有匹配谱图。这些谱图来自两个不同的公共谱图库：一个来自 NIST，一个来自全球蛋白质组机构 (GPM)。您可以按以下步骤探索其覆盖范围：
     </p>
     <ul>
@@ -108,7 +108,7 @@ <h1>方法调整后的差异分析</h1>
         现在，您可以向下滚动就可以看到有相应匹配谱图的肽段数量（总共80，其中49来自于NIST，31来源于GPM）。请注意，所选单元的行编号显示在网格上方的工具栏中。
     </p>
     <p>
-        <img src="image-4.png" />
+        <img src="s-2.png" />
     </p>
     <p>
         在当前的例子中，您将会了解一些与这个实验相关的的基础知识。现代人对蛋白质的认识可能高得多，并且 Prosit 等谱图预测工具现在集成在 Skyline 中，可以完全覆盖目标肽段。
@@ -129,7 +129,7 @@ <h2>无参考标准下多平行实验组数据处理的设置</h2>
         文件将开始加载，Skyline 会显示一个如下的进度窗口：
     </p>
     <p>
-        <img src="image-5.png" />
+        <img src="s-3.png" />
     </p>
     <p>
         按以下操作可在 Skyline 导入 SRM 色谱图时，继续准备其它数据处理操作：
@@ -144,7 +144,7 @@ <h2>无参考标准下多平行实验组数据处理的设置</h2>
         <li>拖拽光标至底部对接指示器，看到一个蓝色的矩形填满了 Skyline 窗口的底部，如下所示：</li>
     </ul>
     <p>
-        <img src="image-6.png" />
+        <img src="s-4.png" />
     </p>
     <ul>
         <li>松开鼠标左键来对接<b>保留时间</b>视图。</li>
@@ -152,14 +152,14 @@ <h2>无参考标准下多平行实验组数据处理的设置</h2>
         <li>拖拽<b>峰面积</b>视图直到鼠标光标位于一个对接指示器内，蓝色矩形说明它将与<b>峰面积</b>视图共享底边。</li>
     </ul>
     <p>
-        <img src="image-7.png" />
+        <img src="s-5.png" />
     </p>
     <ul>
         <li>松开鼠标左键来对接<b>峰面积</b>视图。</li>
         <li>拖拽<b>目标</b>视图直到鼠标光标位于一个对接指示器内，蓝色矩形说明它将对接 Skyline 窗口左边缘。</li>
     </ul>
     <p>
-        <img src="image-8.png" />
+        <img src="s-6.png" />
     </p>
     <ul>
         <li>关闭悬浮在主 Skyline 窗口外左边的其他任何窗口。</li>
@@ -172,7 +172,7 @@ <h2>无参考标准下多平行实验组数据处理的设置</h2>
         此分组窗口应如下图所示：
     </p>
     <p>
-        <img src="image-9.png" />
+        <img src="s-7.png" />
     </p>
     <ul>
         <li>单击<b>确定</b>按钮。</li>
@@ -183,7 +183,7 @@ <h2>无参考标准下多平行实验组数据处理的设置</h2>
         您的 Skyline 窗口现在应看起来像这样：
     </p>
     <p>
-        <img src="image-10.png" />
+        <img src="s-8.png" />
     </p>
     <p>
         <b>注意：</b>此图片取自分辨率 1920x1080 的 24 英寸显示屏。如果您正使用本教程的电子版，您可以将其放大到 200% 或更多来查看此图片。本教程之后的内容，会返回至使用更适合 8½ x 11 英寸页面排版的图片。许多 Skyline 培训使用的是
@@ -193,7 +193,7 @@ <h2>无参考标准下多平行实验组数据处理的设置</h2>
         查看第一个肽段 K.GILAADESVGSMAK.R [28, 41] 的<b>保留时间</b>视图，您会看到整合分布不是非常一致。大部分考查的峰洗脱时间约为 19 分钟。但将近三分之一 的(12) 洗脱时间接近 22 分钟。
     </p>
     <p>
-        <img src="image-11.png" />
+        <img src="s-9.png" />
     </p>
     <p>
         这个肽段的整合相当差。虽然 19 分钟左右处的峰看似较好，但很难让人相信它由单肽段生成。此外，任何整合调整都不可能在所有测试中都一致地测量到单一的肽段。所以，您不应浪费时间尝试做更多的调整，而应：
@@ -206,7 +206,7 @@ <h2>预定的 SRM 和峰截短</h2>
         仅通过查看第二个肽段的保留时间图，您便能看出，它的整合一致性更高。
     </p>
     <p>
-        <img src="image-12.png" />
+        <img src="s-10.png" />
     </p>
     <p>
         但您仍可以看出，所有离子对的峰顶点（由条状图中的水平线显示）不是很一致。如果您查看其中一些色谱图，您会看出这些峰的强度也是从中到低，参差不齐的。
@@ -227,13 +227,13 @@ <h2>预定的 SRM 和峰截短</h2>
         这样，<b>峰面积</b>绘图会从如下：
     </p>
     <p>
-        <img src="image-13.png" />
+        <img src="s-11.png" />
     </p>
     <p class="keep-next">
         改变成这样：
     </p>
     <p>
-        <img src="image-14.png" />
+        <img src="s-12.png" />
     </p>
     <p>
         这样您便可能一眼看在出多个运行中相对离子丰度值的差异，并将这些结合到您从<b>保留时间</b>视图获取的信息中。从这些信息中，您可能注意到了 D_103_REP3 和 D_108_REP2 有很显著的差异，且 H_162_REP3
@@ -249,13 +249,13 @@ <h2>预定的 SRM 和峰截短</h2>
         这将会激活这个峰的色谱图，显示如下：
     </p>
     <p>
-        <img src="image-15.png" />
+        <img src="s-13.png" />
     </p>
     <p>
         而正确整合的峰的图形更应该像这样：
     </p>
     <p>
-        <img src="image-16.png" />
+        <img src="s-14.png" />
     </p>
     <p>
         由于预先设定的采集窗口不能捕获到完整的峰洗脱图，所以 Skyline 拣选了错误的峰。但您仍能查看到正确的峰型，直到约 30.2 分钟峰洗脱结束。这被称为“截短的峰”。但是，您仍可以通过校正这个肽段的积分整合来使用这个不完整的峰，具体步骤如下所述：
@@ -291,7 +291,7 @@ <h2>预定的 SRM 和峰截短</h2>
         此<b>查找</b>分类应看起来如下图所示：
     </p>
     <p>
-        <img src="image-17.png" />
+        <img src="s-15.png" />
     </p>
     <ul>
         <li>单击<b>查找全部</b>按钮。</li>
@@ -301,7 +301,7 @@ <h2>预定的 SRM 和峰截短</h2>
         Skyline 会显示一份被截短过的母离子和子离子列表，前三个是您刚刚查看过的。您可以双击任何行来查看相应的色谱图图形。
     </p>
     <p>
-        <img src="image-18.png" />
+        <img src="s-16.png" />
     </p>
     <p>
         您也可以使用<b>文档网格</b>创建一份包含所有截短的峰的所有母离子的列表，具体步骤如下：
@@ -312,7 +312,7 @@ <h2>预定的 SRM 和峰截短</h2>
         <li>在<b>文档网格</b>视图的<b>报告</b>菜单上单击<b>自定义报告</b>。</li>
         <li>在<b>报告名称</b>字段中输入“Truncated Precursors”。</li>
         <li>在右侧列表，选择除了前两个（母离子和肽段）的所有栏名称（使用单击和按 shift 单击）。</li>
-        <li>单击右侧附近的 <img src="image-19.png" /> 按钮来删除除了前两栏的所有栏。</li>
+        <li>单击右侧附近的 <img src="../../shared/red-x-icon.png" /> 按钮来删除除了前两栏的所有栏。</li>
         <li>勾选左边目录树中的“重复测定”。</li>
         <li>展开树目录来勾选蛋白质&gt;肽段&gt;母离子&gt;母离子结果&gt;截尾计数。</li>
     </ul>
@@ -320,7 +320,7 @@ <h2>预定的 SRM 和峰截短</h2>
         <b>自定义报告</b>表单应显示如下： 
     </p>
     <p>
-        <img src="image-20.png" />
+        <img src="s-17.png" />
     </p>
     <ul>
         <li>在右边列表中双击“截尾计数”。</li>
@@ -333,7 +333,7 @@ <h2>预定的 SRM 和峰截短</h2>
         <b>自定义报告</b>表单应显示如下：
     </p>
     <p>
-        <img src="image-21.png" />
+        <img src="s-18.png" />
     </p>
     <ul>
         <li>单击<b>确定</b>按钮。</li>
@@ -343,7 +343,7 @@ <h2>预定的 SRM 和峰截短</h2>
         <b>文档网格</b>将显示 Skyline 已自动选择的 221 个截短的峰：
     </p>
     <p>
-        <img src="image-22.png" />
+        <img src="s-19.png" />
     </p>
     <p>
         若要查看这些峰：
@@ -356,7 +356,7 @@ <h2>预定的 SRM 和峰截短</h2>
         Skyline 会激活类似如下的色谱图图形：
     </p>
     <p>
-        <img src="image-23.png" />
+        <img src="s-20.png" />
     </p>
     <ul>
         <li>关闭<b>文档网格</b>。</li>
@@ -368,7 +368,7 @@ <h2>开始多平行实验组数据处理</h2>
         肽段 LGGEEVSVACK 看起来比我们目前已看到的其他两个肽段好很多。在所有平行实验组中，其保留时间相当稳定，所有离子对的水平峰顶点线也几乎彼此匹配。
     </p>
     <p>
-        <img src="image-24.png" />
+        <img src="s-21.png" />
     </p>
     <p>
         在<b>峰面积</b>视图中显示的相对离子丰度值也看起来相对稳定。您可能会注意到，这个肽段在标准图库有一个对应的谱图，且这个标准谱图的相对离子丰度值（显示在绘图中最左边的条带）与测量峰的丰度值基本相似。按以下步骤可更好地理解肽段与其相应的图库谱图的匹配程度：
@@ -381,7 +381,7 @@ <h2>开始多平行实验组数据处理</h2>
         Skyline 将向您显示点积 (dotp) 关系，它是衡量库谱图峰强度和测量的峰面积之间相似度的指标，范围从 1（最好）至 0（最差）。
     </p>
     <p>
-        <img src="image-25.png" />
+        <img src="s-22.png" />
     </p>
     <p>
         如要返回<b>峰面积</b>视图之前的状态， 请按以下步骤执行：
@@ -402,13 +402,13 @@ <h2>开始多平行实验组数据处理</h2>
         您可能注意到，一些离子对在这个主峰的边缘显示出了信号，但与其它峰并没有很好地匹配度。
     </p>
     <p>
-        <img src="image-26.png" />
+        <img src="s-23.png" />
     </p>
     <p>
         在大约 13.1 分钟左右，y5 和 y6 频繁地出现信号，但很明显这些不是来自同一个肽段。
     </p>
     <p>
-        <img src="image-27.png" />
+        <img src="s-24.png" />
     </p>
     <p>
         当在积分边界内出现像这样干扰信号时，定量测量出错的机率会更大。对于关键的定量数据，您可能需要考虑这个肽段是否需要所有 5 个离子对。
@@ -417,13 +417,13 @@ <h2>开始多平行实验组数据处理</h2>
         但仅就当前的教程，我们可继续进行下一个肽段的处理。您会在那里看到高强度、无干扰的所有7 个离子对的共洗脱峰。
     </p>
     <p>
-        <img src="image-28.png" />
+        <img src="s-25.png" />
     </p>
     <p>
         相对离子丰度值亦高度一致。
     </p>
     <p>
-        <img src="image-29.png" />
+        <img src="s-26.png" />
     </p>
     <p>
         y3 中的峰面积比在标准库谱图中看到的更强。这可能是因为离子在三重四极杆仪器中会产生二次碎片，而在使用共振激发的离子阱仪器中，这是不会发生的。我们的标准谱图来自于一个 NIST 公共库，而我们无法查询至生成它的仪器类型的信息。
@@ -441,13 +441,13 @@ <h2>开始多平行实验组数据处理</h2>
         离子对。这个峰肯定是由另一个肽段造成的。在这样的情况下，与目标肽段不匹配的干扰信息会导致您看到的色谱图“风景”含有额外的内容。
     </p>
     <p>
-        <img src="image-30.png" />
+        <img src="s-27.png" />
     </p>
     <p class="keep-next">
         在 D_103_REP3 中，您会看到整合峰出现在 33.9 分钟，信号几乎全部集中在 y4 和 y5，但它左边却没有其它候选峰。
     </p>
     <p>
-        <img src="image-31.png" />
+        <img src="s-28.png" />
     </p>
     <p>
         在此情况中，调度窗口将无法捕获到目标肽段的任何信号。要移除谱图中错误的峰，可按以下步骤：
@@ -459,25 +459,25 @@ <h2>开始多平行实验组数据处理</h2>
         这样在<b>峰面积</b>图形中会留出一个空白处。
     </p>
     <p>
-        <img src="image-32.png" />
+        <img src="s-29.png" />
     </p>
     <p>
         继续查看余下的色谱图，您会看到这个情况会重复出现几次。您需删除所有问题峰。同时，您将甚至会看到出现峰截短的现象。当您查看到 H_148_REP2 时，您会看到这样的情况，即 Skyline 选中了 33.9 分钟的错误峰，但目标峰的部分在谱图中仍是可见的。 
     </p>
     <p>
-        <img src="image-33.png" />
+        <img src="s-30.png" />
     </p>
     <p>
         您可以按它作为截短的峰的情况，并按照之前所述的方法进行相应处理（单击并拖拽 x 轴下方）。然后，您会得到如下所示的一幅<b>峰面积</b>示图：
     </p>
     <p>
-        <img src="image-34.png" />
+        <img src="s-31.png" />
     </p>
     <p class="keep-next">
         以及一幅如下所示的保留时间示图：
     </p>
     <p>
-        <img src="image-35.png" />
+        <img src="s-32.png" />
     </p>
     <ul>
         <li>继续查看肽段 R.DIPVNPM<b><u>C</u></b>IYR.S [46, 56]。</li>
@@ -498,7 +498,7 @@ <h2>开始多平行实验组数据处理</h2>
         对于肽段 TSDQIHFFFAK，保留时间显示如下： 
     </p>
     <p>
-        <img src="image-36.png" />
+        <img src="s-33.png" />
     </p>
     <p>
         但您也可以按照在仪器中采集的顺序查看运行，这有时也会非常有帮助。操作步骤如下所述：
@@ -510,7 +510,7 @@ <h2>开始多平行实验组数据处理</h2>
         图形会变为如下所示：
     </p>
     <p>
-        <img src="image-37.png" />
+        <img src="s-34.png" />
     </p>
     <p>
         现在这个保留时间看起来会稍微稳定一些。如果您现在选择下两个肽段（LQPLDFK、SQLPGIIAEGR），则您会看到个模式的一致性如何。
@@ -522,10 +522,10 @@ <h2>开始多平行实验组数据处理</h2>
     <table class="comp-fig">
         <tr>
             <td class="comp-fig">
-                <img src="image-38.png" />
+                <img src="s-35.png" />
             </td>
             <td class="comp-fig">
-                <img src="image-39.png" />
+                <img src="s-36.png" />
             </td>
         </tr>
     </table>
@@ -536,7 +536,7 @@ <h2>开始多平行实验组数据处理</h2>
         本章节最后来看肽段 FGLYSDQMR，在<b>保留时间</b>视图中，您可以看到Skyline 主要挑选了在 19 分钟附近的一个峰。但是在<b>峰面积</b>视图里，这些峰的相对离子丰度值非常不一致。
     </p>
     <p>
-        <img src="image-40.png" />
+        <img src="s-37.png" />
     </p>
     <p>
         如果您查看几个色谱图图形，您会发现很难有效地积分整合在18.8 分钟的峰， 以确认这些信号来自于同一肽段。这种情况下，您应该直接删除此肽段并继续下一步。
@@ -554,16 +554,16 @@ <h2>全球标准化标准</h2>
         AFGLSSPR，就是为实验注入的合成肽段。从我们已经查看的两个汇总图中，您可以完全信任最后两个肽段的自动积分整合结果。它们的保留时间和峰面积相对来说会很一致。
     </p>
     <p>
-        <img src="image-41.png" />
+        <img src="s-38.png" />
     </p>
     <p>
-        <img src="image-42.png" />
+        <img src="s-39.png" />
     </p>
     <p>
         进行到肽段 HLNGFSVPR 时，您将观察到很一致的保留时间分布。但它的峰面积仍有一定的方差。y4 和部分 y3 峰的相对面积似乎在整个数据集中变化不定。
     </p>
     <p>
-        <img src="image-43.png" />
+        <img src="s-40.png" />
     </p>
     <p>
         如果您单击一些 y4 峰度最强的的峰面积条带，您将看到在 y4 和 y3（有时）有明显的干扰。
@@ -572,7 +572,7 @@ <h2>全球标准化标准</h2>
         <li>在<b>视图</b>菜单，单击<b>自动缩放</b>并选择<b>最佳峰值</b> (F11)。</li>
     </ul>
     <p>
-        <img src="image-44.png" />
+        <img src="s-41.png" />
     </p>
     <p>
         为了更清楚地了解这些作为潜在标准化标准的肽段的表现，您应执行以下操作：
@@ -589,13 +589,13 @@ <h2>全球标准化标准</h2>
         按以步骤可查看这些相互关联的肽段的洗脱位置：
     </p>
     <ul>
-        <li>选择 <img src="image-45.png" /> 图标后边的“S”元素。</li>
+        <li>选择 <img src="../../shared/protein-icon-2.png" /> 图标后边的“S”元素。</li>
     </ul>
     <p>
         色谱图图形将会变更如下所示，在同一图谱中显示“S”列表里的所有三个肽段。
     </p>
     <p>
-        <img src="image-46.png" />
+        <img src="s-42.png" />
     </p>
     <p>
         现在来一起查看文档中的所有肽段：
@@ -604,7 +604,7 @@ <h2>全球标准化标准</h2>
         <li>在<b>编辑</b>菜单中，单击<b>选择全部</b> (Ctrl-A)。</li>
     </ul>
     <p>
-        <img src="image-47.png" />
+        <img src="s-43.png" />
     </p>
     <p>
         这清楚表明两个有问题的肽段均表现出亲水性，并在早期洗脱。事实上，它们是此实验中第 3 个和第 10 个洗脱的肽段。您可以按以下步骤在 Skyline 中对此查看：
@@ -631,7 +631,7 @@ <h2>全球标准化标准</h2>
         而AFGLSSPR 肽段的CV值约为接近前 15 个肽段的中位数，50%。（VVLSGSDATLAYSAFK 肽段更具疏水性并为晚期洗脱，CV 为 18.6%，排在第 108 位或第 80 个百分位。）
     </p>
     <p>
-        <img src="image-48.png" />
+        <img src="s-44.png" />
     </p>
     <p>
         按以下步骤，您会发现LGP 肽段有着与 HLN 肽段非常相似的问题。
@@ -644,7 +644,7 @@ <h2>全球标准化标准</h2>
         请记住，应该有三个循环周期测试或技术重复测定：
     </p>
     <p>
-        <img src="image-49.png" />
+        <img src="s-45.png" />
     </p>
     <p class="keep-next">
         为确保这些峰的积分整合是正确的，请按以下步骤：
@@ -657,7 +657,7 @@ <h2>全球标准化标准</h2>
         您可以看到，尽管离子丰度绝对值从最低到最高有着 200倍差距 的分布范围（1.4 亿至 70 万），但各测试之间的相对离子丰度值是高度稳定的。
     </p>
     <p>
-        <img src="image-50.png" />
+        <img src="s-46.png" />
     </p>
     <p>
         尽管这个肽段有相似的问题，您仍应该只将 HLNGFSVPR 这样的肽段排除在作为全球标准化标准的考虑范围之外。在理想情况下，在您将标准肽段加进重要的定量数据很久之前就应该这样做。在此例中，您应当仅使用 VVLSGSDATLAYSAFK
@@ -678,7 +678,7 @@ <h2>继续多重复测定数据处理</h2>
         分钟时序安排的窗口所捕获。（您可能要关闭 x 轴缩放才能看到 — 按 Shift 加 F11。）
     </p>
     <p>
-        <img src="image-51.png" />
+        <img src="s-47.png" />
     </p>
     <p>
         如您在前面所做一样，您可以通过单击并拖拽 x 轴下方来积分截短的峰，或右键单击菜单来完全删除这个峰。
@@ -687,13 +687,13 @@ <h2>继续多重复测定数据处理</h2>
         然而这不并是此肽段的唯一问题。在观看<b>保留时间</b>图形时，您会观察到在被整合的时间范围内有些异常的差异。
     </p>
     <p>
-        <img src="image-52.png" />
+        <img src="s-48.png" />
     </p>
     <p>
         如果您查看这个肽段的一些色谱图，您会看到许多色谱图显示了一个单独、状态很好的峰，其洗脱超过了 0.2 分钟。但其他色谱图带有一些延长至大约 0.5 分钟的拖尾，而其他仍显示了洗脱超过 2 分钟、有两个不同峰的肽段。
     </p>
     <p>
-        <img src="image-53.png" />
+        <img src="s-49.png" />
     </p>
     <p>
         这样的肽段可能很难用于定量，尤其是没有匹配 SIL 的肽段。也许您应该从此实验中删除这个肽段。至少您应该从显示双重洗脱分布图的运行中删除这些峰。 
@@ -705,13 +705,13 @@ <h2>继续多重复测定数据处理</h2>
         但当您进行到肽段 MLSGFIPLKPTVK 时，您会在<b>峰面积</b>图中看到更多的方差。
     </p>
     <p>
-        <img src="image-54.png" />
+        <img src="s-50.png" />
     </p>
     <p>
         这个肽段的的总峰面积主要由 y7 离子占据。尽管这在库谱图中也有显示（在上方图形的最左边显示），但想要通过视觉观察色谱图中是否有任何肽段实际上与 y7 离子共洗脱是很困难的（见下方）。
     </p>
     <p>
-        <img src="image-55.png" />
+        <img src="s-51.png" />
     </p>
     <p>
         但很明显的是，在大部分情况下 Skyline 在每一次运行中均整合相同分子的相同的峰。若要证实图中不只有 y7 峰，则您应该查看强度最高的一次测量。您可以按以下步骤执行：
@@ -724,25 +724,25 @@ <h2>继续多重复测定数据处理</h2>
         这三张图中的色谱峰可证实，在 23 至 24 分钟之间y7峰对应的肽段事实上就是导致在肽段丰度值足够高时在所有 6 个受监控离子对上生形成共洗脱信号的肽段。
     </p>
     <p>
-        <img src="image-56.png" />
+        <img src="s-52.png" />
     </p>
     <p>
         相较删除这个肽段之外，您可能更想更正 Skyline 选错色谱峰的这个事实。您可以在<b>保留时间</b>图中看到，在 22.5 分钟下方产生了一条更窄的条带，
     </p>
     <p>
-        <img src="image-57.png" />
+        <img src="s-53.png" />
     </p>
     <p class="keep-next">
         同样情况在出现在<b>峰面积</b>图中，其中该运行没有可见的已积分信号。
     </p>
     <p>
-        <img src="image-58.png" />
+        <img src="s-54.png" />
     </p>
     <p>
         您可以单击<b>保留时间</b>视图中的条带以激活该运行的色谱图。您会看到运行在 y7 离子对保留的信号非常低。在没有其它运行获取的信息作为参考时，不要单独选择这个离子对来代表一个肽段。
     </p>
     <p>
-        <img src="image-59.png" />
+        <img src="s-55.png" />
     </p>
     <p>
         按以下步骤可更正该运行的积分：
@@ -780,19 +780,19 @@ <h2>继续多重复测定数据处理</h2>
         在许多图形中您会看到，在被选中的峰前大约 1.5 分钟处，y3 和 y4 离子对有一个肽段干扰。这让您对已积分的峰的一致性更有把握。
     </p>
     <p>
-        <img src="image-60.png" />
+        <img src="s-56.png" />
     </p>
     <p>
         继续在<b>目标</b>列表中操作，您会发现有些肽段（YANVIAYDHSR 和 TDEDVPSGPPR）显示出实际测量的相对离子丰度值和匹配库谱图的差异。您可以在<b>峰面积</b>图形中看到这些差异：
     </p>
     <p>
-        <img src="image-61.png" />
+        <img src="s-57.png" />
     </p>
     <p>
         您也会在色谱图中观察到这些差异，而在这些色谱图中 Skyline 在峰保留时间下边显示了较低的点积值“（点积 0.28）”。
     </p>
     <p>
-        <img src="image-62.png" />
+        <img src="s-58.png" />
     </p>
     <p>
         当在图形上有另一个点积值较高的峰时，Skyline 便会显示这样的“点积”值。在上述情况中，您无法看到点积值更高的峰，这是因为它接近被选中峰的噪声级别。按以下步骤可查看这个峰：
@@ -819,7 +819,7 @@ <h2>继续多重复测定数据处理</h2>
         之后您会看到肽段 <b><u>C</u></b>SSLLWAGAAWLR。根据您将在汇总图（见下方）看到的方差，最初您可能想删除这个肽段并继续前进：
     </p>
     <p>
-        <img src="image-63.png" />
+        <img src="s-59.png" />
     </p>
     <p>
         但是如果您仔细查看，您会发现在健康受试对象中存在一致的区域。按以下步骤可更清晰地查看此内容：
@@ -831,10 +831,10 @@ <h2>继续多重复测定数据处理</h2>
         图形会变为这样：
     </p>
     <p>
-        <img src="image-64.png" />
+        <img src="s-60.png" />
     </p>
     <p>
-        <img src="image-65.png" />
+        <img src="s-61.png" />
     </p>
     <p>
         这样可更明显地看出在健康受试对象中有一个一致的峰可被积分，而在患病受试对象中并没有。如果查看健康受试对象的峰，您会看出它的强度相当低，且主要依靠 y4、y5 和 y6 离子的共洗脱。这个共洗脱很可能由一个肽段引起，但要确定这个肽段是否为
@@ -847,11 +847,11 @@ <h2>继续多重复测定数据处理</h2>
         <tr>
             <td class="comp-fig">
                 D_102_REP3<br />
-                <img src="image-66.png" />
+                <img src="s-62.png" />
             </td>
             <td class="comp-fig">
                 D_108_REP1<br />
-                <img src="image-67.png" />
+                <img src="s-63.png" />
             </td>
         </tr>
     </table>
@@ -860,7 +860,7 @@ <h2>继续多重复测定数据处理</h2>
         和 D_102_REP3）。您所观察到的内容可能暗示存在延滞效应。
     </p>
     <p>
-        <img src="image-68.png" />
+        <img src="s-64.png" />
     </p>
     <p>
         最后，这些离子对可能代表着本文档中最强的生物标记候选者之一。现在您可以订购一个合成肽段，让您更有把握您事实上是在测量 <b><u>C</u></b>SSLLWAGAAWLR 肽段。您也可以尝试在这个峰范围内采集 MS/MS 谱图（使用平行反应监测 —
@@ -888,7 +888,7 @@ <h2>准备使用重复测定注释的统计分析</h2>
         窗口如下所示：
     </p>
     <p>
-        <img src="image-69.png" />
+        <img src="s-65.png" />
     </p>
     <ul>
         <li>单击<b>定义注释</b>窗口中的<b>确定</b>按钮。</li>
@@ -899,7 +899,7 @@ <h2>准备使用重复测定注释的统计分析</h2>
         <b>文档设置</b>窗口如下所示：
     </p>
     <p>
-        <img src="image-70.png" />
+        <img src="s-66.png" />
     </p>
     <ul>
         <li>单击<b>确定</b>按钮。</li>
@@ -916,7 +916,7 @@ <h2>准备使用重复测定注释的统计分析</h2>
         <b>从工具商店安装</b>窗口如下所示：
     </p>
     <p>
-        <img src="image-71.png" />
+        <img src="s-67.png" />
     </p>
     <ul>
         <li>单击<b>安装</b>按钮并遵循提示，直到 MSstats 安装完成。</li>
@@ -936,10 +936,10 @@ <h2>准备使用重复测定注释的统计分析</h2>
     <table class="comp-fig">
         <tr>
             <td class="comp-fig" style="padding: 5px;">
-                <img src="image-72.png" />
+                <img src="s-68.png" />
             </td>
             <td class="comp-fig" style="padding: 5px;">
-                <img src="image-73.png" />
+                <img src="s-69.png" />
             </td>
         </tr>
     </table>
@@ -951,7 +951,7 @@ <h2>准备使用重复测定注释的统计分析</h2>
         <b>文档设置</b>窗口如下所示：
     </p>
     <p>
-        <img src="image-74.png" />
+        <img src="s-70.png" />
     </p>
     <ul>
         <li>单击<b>确定</b>按钮。</li>
@@ -967,7 +967,7 @@ <h2>准备使用重复测定注释的统计分析</h2>
         <b>文档网格</b>窗口如下所示：
     </p>
     <p>
-        <img src="image-75.png" />
+        <img src="s-71.png" />
     </p>
     <p>
         现在您可以手动将所有 42 个重复测定的注释输入到网格中。您也可以将电子表格中的值直接粘贴到这个表中。您可以按以下步骤执行：
@@ -985,7 +985,7 @@ <h2>准备使用重复测定注释的统计分析</h2>
         <b>文档网格</b>窗口如下所示：
     </p>
     <p>
-        <img src="image-76.png" />
+        <img src="s-72.png" />
     </p>
     <ul>
         <li>按 Ctrl 加 V 键粘贴到<b>文档网格</b>中。</li>
@@ -994,7 +994,7 @@ <h2>准备使用重复测定注释的统计分析</h2>
         Skyline 会使用电子表格中的值填写<b>文档网格</b>中的单元格，如下所示：
     </p>
     <p>
-        <img src="image-77.png" />
+        <img src="s-73.png" />
     </p>
     <h2>注释问题峰的肽段</h2>
     <p>
@@ -1013,7 +1013,7 @@ <h2>注释问题峰的肽段</h2>
         <b>定义注释</b>窗口如下所示：
     </p>
     <p>
-        <img src="image-78.png" />
+        <img src="s-74.png" />
     </p>
     <ul>
         <li>单击<b>确定</b>按钮。</li>
@@ -1024,7 +1024,7 @@ <h2>注释问题峰的肽段</h2>
         <b>文档设置</b>窗口如下所示：
     </p>
     <p>
-        <img src="image-79.png" />
+        <img src="s-75.png" />
     </p>
     <ul>
         <li>单击<b>确定</b>按钮。</li>
@@ -1041,7 +1041,7 @@ <h2>注释问题峰的肽段</h2>
         <b>自定义报告</b>表单应显示如下：
     <p>
     </p>
-        <img src="image-80.png" />
+        <img src="s-76.png" />
     </p>
     <ul>
         <li>单击<b>确定</b>按钮。</li>
@@ -1051,7 +1051,7 @@ <h2>注释问题峰的肽段</h2>
         <b>文档网格</b>窗口如下所示：
     </p>
     <p>
-        <img src="image-81.png" />
+        <img src="s-77.png" />
     </p>
     <p>
         是否恰好存在 223 个截短的母离子峰组取决于您处理剩余文档的方式。您可以一次勾选一个肽段的“MissingData”复选框。当您勾选了任一肽段的方框后，其余会自动勾选，因为注释仅会应用于任一肽段一次。按以下步骤来立即尝试一下：
@@ -1064,7 +1064,7 @@ <h2>注释问题峰的肽段</h2>
         <b>文档网格</b>窗口如下所示：
     </p>
     <p>
-        <img src="image-82.png" />
+        <img src="s-78.png" />
     </p>
     <p>
         您也可以使用 Excel 和<b>文档网格</b>支持按如下所示在一次粘贴中设置所有 163 行：
@@ -1085,7 +1085,7 @@ <h2>注释问题峰的肽段</h2>
         当您完成了上述步骤后您会注意到，<b>目标</b>列表顶部的许多肽段均在肽段名称的右上角被标记了一小块红色的三角形。
     </p>
     <p>
-        <img src="image-83.png" />
+        <img src="s-79.png" />
     </p>
     <p>
         如果您将鼠标光标悬浮在这些三角形上，您会看到一则消息显示“<b>Missing Data</b> 真”。
@@ -1098,18 +1098,18 @@ <h2>注释问题峰的肽段</h2>
         <li>选择您一直使用的“Truncated Precursors”报告。</li>
         <li>单击<b>复制</b>按钮。</li>
         <li>在<b>自定义报告</b>表单的<b>报告名称</b>字段中，输入“Missing Peaks”。</li>
-        <li>使用每列列表右边的 <img src="image-84.png" /> 按钮删除<b>母离子</b>和<b>截尾计数</b>列。</li>
+        <li>使用每列列表右边的 <img src="../../shared/red-x-icon.png" /> 按钮删除<b>母离子</b>和<b>截尾计数</b>列。</li>
         <li>勾选<b>枢轴重复测定名称</b>复选框。</li>
     </ul>
     <p class="keep-next">
         <b>自定义报告</b>表单应显示如下：
     </p>
     <p>
-        <img src="image-85.png" />
+        <img src="s-80.png" />
     </p>
     <ul>
         <li>单击<b>过滤器</b>标签。</li>
-        <li>单击 <img src="image-86.png" /> 按钮来删除<b>截尾计数</b>的现有过滤器。</li>
+        <li>单击 <img src="../../shared/red-x-icon.png" /> 按钮来删除<b>截尾计数</b>的现有过滤器。</li>
         <li>展开列树状目录，勾选蛋白质&gt;肽段&gt;母离子&gt;母离子结果，为<b>总面积</b>列添加一个过滤器。</li>
         <li>在<b>操作</b>列选择“为空白”。</li>
     </ul>
@@ -1117,7 +1117,7 @@ <h2>注释问题峰的肽段</h2>
         <b>自定义报告</b>表单应显示如下：
     </p>
     <p>
-        <img src="image-87.png" />
+        <img src="s-81.png" />
     </p>
     <ul>
         <li>单击<b>确定</b>按钮。</li>
@@ -1128,7 +1128,7 @@ <h2>注释问题峰的肽段</h2>
         <b>文档网格</b>窗口如下所示：
     </p>
     <p>
-        <img src="image-88.png" />
+        <img src="s-82.png" />
     </p>
     <p>
         <b>注意：</b>如果您没有完全成功处理您的文档，则您仅会看到肽段 GSYNLQDLLAQ 的一行。下一个注释说明了如何打开一个全处理完全的文档。
@@ -1168,7 +1168,7 @@ <h2>Skyline 初始多重复测定检查</h2>
         这样<b>峰面积</b>图形如下所示：
     </p>
     <p>
-        <img src="image-89.png" />
+        <img src="s-83.png" />
     </p>
     <p>
         现在您可查看更多肽段在每个受试对象的技术重复测定中的变异系数 (CV)。您会看到大部分在 25% 以下。然而在理想情况下，CV 应比在本实验中观察到的更低。值得说明的一点是，3 组测量相比 10 组测量更容易获取相同且较低的CV。这是因为，在统计学上，我们容易低估小型样本的标准偏差。
@@ -1187,13 +1187,13 @@ <h2>Skyline 初始多重复测定检查</h2>
     <table class="comp-fig">
         <tr>
             <td class="comp-fig">
-                <img src="image-90.png" />
+                <img src="s-84.png" />
             </td>
             <td class="comp-fig">
-                <img src="image-91.png" />
+                <img src="s-85.png" />
             </td>
             <td class="comp-fig">
-                <img src="image-92.png" />
+                <img src="s-86.png" />
             </td>
         </tr>
     </table>
@@ -1223,10 +1223,10 @@ <h2>Skyline 初始多重复测定检查</h2>
     <table class="comp-fig">
         <tr>
             <td class="comp-fig">
-                <img src="image-93.png" />
+                <img src="s-87.png" />
             </td>
             <td class="comp-fig">
-                <img src="image-94.png" />
+                <img src="s-88.png" />
             </td>
         </tr>
     </table>
@@ -1239,10 +1239,10 @@ <h2>Skyline 初始多重复测定检查</h2>
     <table class="comp-fig">
         <tr>
             <td class="comp-fig">
-                <img src="image-95.png" />
+                <img src="s-89.png" />
             </td>
             <td class="comp-fig">
-                <img src="image-96.png" />
+                <img src="s-90.png" />
             </td>
         </tr>
     </table>
@@ -1272,7 +1272,7 @@ <h2>Skyline 中的简单群组比较</h2>
         <b>编辑群组比较</b>窗口如下所示：
     </p>
     <p>
-        <img src="image-97.png" />
+        <img src="s-91.png" />
     </p>
     <ul>
         <li>单击<b>确定</b>按钮。</li>
@@ -1281,7 +1281,7 @@ <h2>Skyline 中的简单群组比较</h2>
         <b>文档设置</b>窗口如下所示：
     </p>
     <p>
-        <img src="image-98.png" />
+        <img src="s-92.png" />
     </p>
     <ul>
         <li>单击<b>确定</b>按钮。</li>
@@ -1296,7 +1296,7 @@ <h2>Skyline 中的简单群组比较</h2>
         Skyline 会显示如下的网格：
     </p>
     <p>
-        <img src="image-99.png" />
+        <img src="s-93.png" />
     </p>
     <p>
         如果“倍数变化结果”列不显示完整的置信区间，则双击倍数变化结果和已调整的 p 值标题之间的垂直线。
@@ -1311,7 +1311,7 @@ <h2>Skyline 中的简单群组比较</h2>
         Skyline 会在 Healthy v. Diseased<b>：网格</b>视图旁边添加一个图形窗格，如下所示：
     </p>
     <p>
-        <img src="image-100.png" />
+        <img src="s-94.png" />
     </p>
     <ul>
         <li>在网格上单击“倍数变化结果”标题，在出现的菜单上单击<b>升序排序</b>。</li>
@@ -1332,7 +1332,7 @@ <h2>Skyline 中的简单群组比较</h2>
         您会看到网格工具栏显示的行数从 48 减少到 11，图形如下所示：
     </p>
     <p>
-        <img src="image-101.png" />
+        <img src="s-95.png" />
     </p>
     <p>
         请注意，更多显著变化的蛋白质的倍数变化平均值为正，表明它们在患病组的受试对象中表现更为强烈。不过，重要的是要考虑未能使样本顺序随机化可能引起的问题。因为在所有三组测量周期中，是先测定患病组受试对象，后测定健康组受试对象，您应考虑到任何不计入标准化的降解会使得倍数变化在患病组中上调。
@@ -1373,7 +1373,7 @@ <h2>按区分调整</h2>
         <b>Healthy v. Diseased：网格</b>会在 1% FDR 阈值上方显示 92 行，图形如下所示：
     </p>
     <p>
-        <img src="image-102.png" />
+        <img src="s-96.png" />
     </p>
     <p class="keep-next">
         按以下步骤可将这些肽段从文档中删除：
@@ -1387,19 +1387,19 @@ <h2>按区分调整</h2>
         此网格如下所示：
     </p>
     <p>
-        <img src="image-103.png" />
+        <img src="s-97.png" />
     </p>
     <p>
         请注意，VVLSGSDATLAYSAFK 肽段的倍数变化为 1，99% 的置信区间为 1 至 1。这是作为标准化全局标准的单一肽段。建议您不要从文档中删除这个肽段。这就是取消选定它的原因。
     </p>
     <ul>
-        <li>单击网格工具栏中的 <img src="image-104.png" /> 按钮。</li>
+        <li>单击网格工具栏中的 <img src="../../shared/red-x-icon.png" /> 按钮。</li>
     </ul>
     <p class="keep-next">
         Skyline 将显示以下消息用以确定您是否真想删除所选的行：
     </p>
     <p>
-        <img src="image-105.png" />
+        <img src="s-98.png" />
     </p>
     <ul>
         <li>单击<b>确定</b>按钮。</li>
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/GroupedStudies/zh-CHS/invariant.html b/pwiz_tools/Skyline/Documentation/Tutorials/GroupedStudies/zh-CHS/invariant.html
index aaadc34a32..22791b5ea7 100644
--- a/pwiz_tools/Skyline/Documentation/Tutorials/GroupedStudies/zh-CHS/invariant.html
+++ b/pwiz_tools/Skyline/Documentation/Tutorials/GroupedStudies/zh-CHS/invariant.html
@@ -96,7 +96,7 @@ <h1>Differential analysis after method refinement</h1>
         very much prior knowledge of the targeted proteins or peptides and without aid of stable isotope labeled reference peptides.
     </p>
     <p>
-        <img src="image-0.png" />
+        <img src="s-detection-and-differentiation-phases.png" />
     </p>
     <p>
         <b>Figure 1</b>: A schematic showing proposed “Detection” and “Differentiation” phases of targeted method refinement in a heart
@@ -113,7 +113,7 @@ <h1>Differential analysis after method refinement</h1>
         peptides and 789 transitions.
     </p>
     <p>
-        <img src="image-1.png" />
+        <img src="s-1.png" />
     </p>
     <p>
         This is not quite what is promised in the figure above (from a manuscript draft that was never published), but the document also contains one
@@ -123,8 +123,8 @@ <h1>Differential analysis after method refinement</h1>
     </p>
     <p>
         You will notice that some of the peptides have matching library spectra. You can see this in the <b>Targets</b> view. The peptide
-        icons with spectrum lines in the lower right corner (<img src="image-2.png" />) have matching spectra and those without these lines (<img
-            src="image-3.png" />) do not. The spectra come from two different public spectral libraries: one from NIST and one from the Global
+        icons with spectrum lines in the lower right corner (<img src="../../shared/peptide-with-spectrum-lines-icon.png" />) have matching spectra and those without these lines (<img
+            src="../../shared/peptide-without-spectrum-lines-icon.png" />) do not. The spectra come from two different public spectral libraries: one from NIST and one from the Global
         Proteome Machine (GPM). You can explore their coverage by doing the following:
     </p>
     <ul>
@@ -139,7 +139,7 @@ <h1>Differential analysis after method refinement</h1>
         (GPM) library (31). Note that the row number of the selected cell is shown in the toolbar above the grid.
     </p>
     <p>
-        <img src="image-4.png" />
+        <img src="s-2.png" />
     </p>
     <p>
         For the current example, this information gives you a sense of the sparse prior knowledge on which the experiment was based. Modern knowledge
@@ -164,7 +164,7 @@ <h2>Setting up to process multi-replicate data without reference standards</h2>
         The files should begin loading, and Skyline will display progress in a window like the one shown below:
     </p>
     <p>
-        <img src="image-5.png" />
+        <img src="s-3.png" />
     </p>
     <p>
         To continue preparing for data processing while Skyline imports the SRM chromatograms, do the following:
@@ -179,7 +179,7 @@ <h2>Setting up to process multi-replicate data without reference standards</h2>
         <li>Drag the cursor into the bottom docking indicator to see a blue rectangle fill the bottom edge of the Skyline window, as shown below.</li>
     </ul>
     <p>
-        <img src="image-6.png" />
+        <img src="s-4.png" />
     </p>
     <ul>
         <li>Release the left mouse button to dock the <b>Retention Times</b> view.</li>
@@ -188,7 +188,7 @@ <h2>Setting up to process multi-replicate data without reference standards</h2>
             share the bottom edge with the <b>Peak Areas</b> view.</li>
     </ul>
     <p>
-        <img src="image-7.png" />
+        <img src="s-5.png" />
     </p>
     <ul>
         <li>Release the left mouse button to dock the <b>Peak Areas</b> view.</li>
@@ -196,7 +196,7 @@ <h2>Setting up to process multi-replicate data without reference standards</h2>
             to the left edge of the Skyline window.</li>
     </ul>
     <p>
-        <img src="image-8.png" />
+        <img src="s-6.png" />
     </p>
     <ul>
         <li>Close any other windows left floating outside the main Skyline window.</li>
@@ -209,7 +209,7 @@ <h2>Setting up to process multi-replicate data without reference standards</h2>
         The form should look like this:
     </p>
     <p>
-        <img src="image-9.png" />
+        <img src="s-7.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -220,7 +220,7 @@ <h2>Setting up to process multi-replicate data without reference standards</h2>
         Your Skyline window should now look something like this:
     </p>
     <p>
-        <img src="image-10.png" />
+        <img src="s-8.png" />
     </p>
     <p>
         <b>Note</b>: This image was taken on a 24” monitor at 1920x1080. If you are viewing this tutorial digitally, you may want to zoom in
@@ -232,7 +232,7 @@ <h2>Setting up to process multi-replicate data without reference standards</h2>
         not very consistent. Most of the chosen peaks elute around 19 minutes. However, nearly one third (12) elute closer to 22 minutes.
     </p>
     <p>
-        <img src="image-11.png" />
+        <img src="s-9.png" />
     </p>
     <p>
         The integration for this peptide is quite poor. While the peak at around 19 minutes appears to be the better peak, it is hard to have much
@@ -247,7 +247,7 @@ <h2>Scheduled SRM and peak truncation</h2>
         Just by looking at the retention time plot for the second peptide, you can see that it is much more consistently integrated.
     </p>
     <p>
-        <img src="image-12.png" />
+        <img src="s-10.png" />
     </p>
     <p>
         However, you can still see that the peak apexes for all transitions (shown by the horizontal lines in the bars) are not very consistent. If you
@@ -270,13 +270,13 @@ <h2>Scheduled SRM and peak truncation</h2>
         This changes the <b>Peak Areas</b> plot from:
     </p>
     <p>
-        <img src="image-13.png" />
+        <img src="s-11.png" />
     </p>
     <p class="keep-next">
         To:
     </p>
     <p>
-        <img src="image-14.png" />
+        <img src="s-12.png" />
     </p>
     <p>
         This makes it possible to see differences in relative ion abundance across multiple runs in a single glance and adds to the information you are
@@ -294,13 +294,13 @@ <h2>Scheduled SRM and peak truncation</h2>
         This will activate the chromatogram graph for the peak, which looks like:
     </p>
     <p>
-        <img src="image-15.png" />
+        <img src="s-13.png" />
     </p>
     <p>
         While plots for the correctly integrated peaks look more like this:
     </p>
     <p>
-        <img src="image-16.png" />
+        <img src="s-14.png" />
     </p>
     <p>
         Since the scheduled acquisition window did not capture the entire elution profile for the peptide, Skyline has picked the wrong peak. However,
@@ -346,7 +346,7 @@ <h2>Scheduled SRM and peak truncation</h2>
         The <b>Find</b> form should look like this:
     </p>
     <p>
-        <img src="image-17.png" />
+        <img src="s-15.png" />
     </p>
     <ul>
         <li>Click the <b>Find All</b> button.</li>
@@ -357,7 +357,7 @@ <h2>Scheduled SRM and peak truncation</h2>
         any line to see the corresponding chromatogram graph activated.
     </p>
     <p>
-        <img src="image-18.png" />
+        <img src="s-16.png" />
     </p>
     <p>
         You can also use the <b>Document Grid</b> to create a list of all precursors with any peak truncation by doing the following:
@@ -368,7 +368,7 @@ <h2>Scheduled SRM and peak truncation</h2>
         <li>On the <b>Reports</b> menu in the <b>Document Grid</b> view, click <b>Customize Report</b>.</li>
         <li>In the <b>Report name</b> field, enter “Truncated Precursors”.</li>
         <li>In the right side list, select all column names (using click and shift-click) after the first two (Precursor and Peptide).</li>
-        <li>Click the <img src="image-19.png" /> button near the right edge to delete all but the first two columns.</li>
+        <li>Click the <img src="../../shared/red-x-icon.png" /> button near the right edge to delete all but the first two columns.</li>
         <li>Check “Replicates” in the tree on the left side.</li>
         <li>Expand the tree to check Proteins &gt; Peptides &gt; Precursors &gt; PrecursorResults &gt; Count Truncated.</li>
     </ul>
@@ -376,7 +376,7 @@ <h2>Scheduled SRM and peak truncation</h2>
         The <b>Customize Report</b> form should look something like this:
     </p>
     <p>
-        <img src="image-20.png" />
+        <img src="s-17.png" />
     </p>
     <ul>
         <li>In the right side list, double-click “Count Truncated”.</li>
@@ -389,7 +389,7 @@ <h2>Scheduled SRM and peak truncation</h2>
         The <b>Customize Report</b> form should look something like this:
     </p>
     <p>
-        <img src="image-21.png" />
+        <img src="s-18.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -399,7 +399,7 @@ <h2>Scheduled SRM and peak truncation</h2>
         The <b>Document Grid</b> will show 221 truncated peaks that Skyline has already chosen automatically:
     </p>
     <p>
-        <img src="image-22.png" />
+        <img src="s-19.png" />
     </p>
     <p>
         To view these peaks:
@@ -412,7 +412,7 @@ <h2>Scheduled SRM and peak truncation</h2>
         Skyline will activate chromatogram graphs that look like the following:
     </p>
     <p>
-        <img src="image-23.png" />
+        <img src="s-20.png" />
     </p>
     <ul>
         <li>Close the <b>Document Grid</b>.</li>
@@ -425,7 +425,7 @@ <h2>Beginning multi-replicate data processing</h2>
         peak apex lines match up for almost all transitions in each replicate.
     </p>
     <p>
-        <img src="image-24.png" />
+        <img src="s-21.png" />
     </p>
     <p>
         The relative ion abundances shown in the <b>Peak Areas</b> view also appear relatively stable. You might notice that there is a
@@ -442,7 +442,7 @@ <h2>Beginning multi-replicate data processing</h2>
         measured peak areas ranging from 1 (best) to zero (worst).
     </p>
     <p>
-        <img src="image-25.png" />
+        <img src="s-22.png" />
     </p>
     <p>
         Return the <b>Peak Areas</b> view to its former state by doing the following:
@@ -463,13 +463,13 @@ <h2>Beginning multi-replicate data processing</h2>
         You might notice that some of the transitions show a signal around the edges of the main peak that is not well matched by the other peaks.
     </p>
     <p>
-        <img src="image-26.png" />
+        <img src="s-23.png" />
     </p>
     <p>
         There is frequently signal on y5 and y6 around 13.1 minutes, which is clearly not from the same peptide.
     </p>
     <p>
-        <img src="image-27.png" />
+        <img src="s-24.png" />
     </p>
     <p>
         When an interfering signal like this occurs inside the integration boundaries, it will add error to the quantitative measurements. For critical
@@ -479,13 +479,13 @@ <h2>Beginning multi-replicate data processing</h2>
         For the current tutorial, however, continue to the next peptide. There you will find strong, clean, and co-eluting peaks for all 7 transitions.
     </p>
     <p>
-        <img src="image-28.png" />
+        <img src="s-25.png" />
     </p>
     <p>
         Relative ion abundance is also extremely consistent.
     </p>
     <p>
-        <img src="image-29.png" />
+        <img src="s-26.png" />
     </p>
     <p>
         The peak area in y3 is stronger than what was seen for the library spectrum. This might be explained by secondary fragmentation occurring in a
@@ -508,14 +508,14 @@ <h2>Beginning multi-replicate data processing</h2>
         not coincide with the peptide of interest can add information to the chromatogram “landscape” you see.
     </p>
     <p>
-        <img src="image-30.png" />
+        <img src="s-27.png" />
     </p>
     <p class="keep-next">
         In D_103_REP3, you will see the integrated peak at 33.9 minutes with signal mostly on y4 and y5, but no other candidate peak
         to the left.
     </p>
     <p>
-        <img src="image-31.png" />
+        <img src="s-28.png" />
     </p>
     <p>
         In this case, the scheduling window has failed to capture any signal from the targeted peptide. To remove the incorrect peak do the following:
@@ -527,7 +527,7 @@ <h2>Beginning multi-replicate data processing</h2>
         This should leave a blank spot in the <b>Peak Areas</b> graph.
     </p>
     <p>
-        <img src="image-32.png" />
+        <img src="s-29.png" />
     </p>
     <p>
         Continuing through the chromatogram plots, you will see this pattern repeated several times. Keep removing the missing peaks. You will even
@@ -535,20 +535,20 @@ <h2>Beginning multi-replicate data processing</h2>
         where Skyline has chosen the peak at 33.9 minutes, but part of the correct peak is still visible.
     </p>
     <p>
-        <img src="image-33.png" />
+        <img src="s-30.png" />
     </p>
     <p>
         You can simply integrate this as a truncated peak, as you did above, by clicking and dragging beneath the x-axis. You should end up with a
         <b>Peak Areas</b> plot that looks like this:
     </p>
     <p>
-        <img src="image-34.png" />
+        <img src="s-31.png" />
     </p>
     <p class="keep-next">
         And a retention times plot that looks like this:
     </p>
     <p>
-        <img src="image-35.png" />
+        <img src="s-32.png" />
     </p>
     <ul>
         <li>Continue to the peptide R.DIPVNPM<b><u>C</u></b>IYR.S [46, 56].</li>
@@ -573,7 +573,7 @@ <h2>Beginning multi-replicate data processing</h2>
         like this:
     </p>
     <p>
-        <img src="image-36.png" />
+        <img src="s-33.png" />
     </p>
     <p>
         However, it may also be quite helpful to see the runs in the order they were acquired on the instrument. You can achieve this by doing the
@@ -586,7 +586,7 @@ <h2>Beginning multi-replicate data processing</h2>
         The graph will change to look like the following:
     </p>
     <p>
-        <img src="image-37.png" />
+        <img src="s-34.png" />
     </p>
     <p>
         This retention time pattern is now a little less erratic. If you now select through the next two peptides (LQPLDFK, SQLPGIIAEGR), you will see
@@ -601,10 +601,10 @@ <h2>Beginning multi-replicate data processing</h2>
     <table class="comp-fig">
         <tr>
             <td class="comp-fig">
-                <img src="image-38.png" />
+                <img src="s-35.png" />
             </td>
             <td class="comp-fig">
-                <img src="image-39.png" />
+                <img src="s-36.png" />
             </td>
         </tr>
     </table>
@@ -618,7 +618,7 @@ <h2>Beginning multi-replicate data processing</h2>
         poor consistency in relative ion abundance.
     </p>
     <p>
-        <img src="image-40.png" />
+        <img src="s-37.png" />
     </p>
     <p>
         If you examine a few of the chromatogram graphs, you will find it hard to imagine consistently integrating the signal at 18.8 minutes with any
@@ -641,17 +641,17 @@ <h2>Global normalization standards</h2>
         peptides from the two summary plots we have been examining. The retention times and peak areas are relatively consistent.
     </p>
     <p>
-        <img src="image-41.png" />
+        <img src="s-38.png" />
     </p>
     <p>
-        <img src="image-42.png" />
+        <img src="s-39.png" />
     </p>
     <p>
         Moving to the peptide HLNGFSVPR, you will observe consistent retention times. However, there is
         much more variance in the peak areas. The relative area for y4 and sometimes y3 seems to vary throughout the data set.
     </p>
     <p>
-        <img src="image-43.png" />
+        <img src="s-40.png" />
     </p>
     <p>
         If you click on some of the peak area bars where y4 is most abundant, you will see obvious interference on y4 and sometimes y3.
@@ -660,7 +660,7 @@ <h2>Global normalization standards</h2>
         <li>On the <b>View</b> menu, choose <b>Auto-Zoom</b> and click <b>Best Peak</b> (F11).</li>
     </ul>
     <p>
-        <img src="image-44.png" />
+        <img src="s-41.png" />
     </p>
     <p>
         To gain an even clearer understanding of the performance of these injected peptides as potential normalization standards, you should do the
@@ -682,13 +682,13 @@ <h2>Global normalization standards</h2>
         To see where these peptides elute relative to each other do the following:
     </p>
     <ul>
-        <li>Select the “S” element preceded by the <img src="image-45.png" /> icon.</li>
+        <li>Select the “S” element preceded by the <img src="../../shared/protein-icon-2.png" /> icon.</li>
     </ul>
     <p>
         The chromatogram graphs will change to show all three peptides in the “S” list together.
     </p>
     <p>
-        <img src="image-46.png" />
+        <img src="s-42.png" />
     </p>
     <p>
         Now to see all the peptides in the document together:
@@ -697,7 +697,7 @@ <h2>Global normalization standards</h2>
         <li>On the <b>Edit</b> menu, click <b>Select All</b> (Ctrl-A).</li>
     </ul>
     <p>
-        <img src="image-47.png" />
+        <img src="s-43.png" />
     </p>
     <p>
         This makes it clear that the two problematic peptides are both hydrophilic and early eluting. In fact, they are the 3<sup>rd</sup> and
@@ -729,7 +729,7 @@ <h2>Global normalization standards</h2>
         more hydrophobic and later eluting, is 108<sup>th</sup> or in the 80<sup>th</sup> percentile with 18.6% CV.)
     </p>
     <p>
-        <img src="image-48.png" />
+        <img src="s-44.png" />
     </p>
     <p>
         If you do the following, you should be able to convince yourself that the LGP peptide has a problem very similar to the HLN peptide.
@@ -742,7 +742,7 @@ <h2>Global normalization standards</h2>
         Remember that there are supposed to be three cycles or technical replicates:
     </p>
     <p>
-        <img src="image-49.png" />
+        <img src="s-45.png" />
     </p>
     <p class="keep-next">
         To convince yourself that the peaks are correctly integrated, do the following:
@@ -756,7 +756,7 @@ <h2>Global normalization standards</h2>
         extremely stable.
     </p>
     <p>
-        <img src="image-50.png" />
+        <img src="s-46.png" />
     </p>
     <p>
         Although this one peptide seems to have similar issues, you should exclude a peptide like HLNGFSVPR from consideration as a global
@@ -783,7 +783,7 @@ <h2>Continuing multi-replicate data processing</h2>
         scheduling window. (You might need to turn off x-axis zooming – Shift-F11 – to see this.)
     </p>
     <p>
-        <img src="image-51.png" />
+        <img src="s-47.png" />
     </p>
     <p>
         As you did before, you can correct this by clicking and dragging beneath the x-axis to integrate the truncated peak, or by using the
@@ -794,7 +794,7 @@ <h2>Continuing multi-replicate data processing</h2>
         unusual differences in the ranges of time being integrated.
     </p>
     <p>
-        <img src="image-52.png" />
+        <img src="s-48.png" />
     </p>
     <p>
         If you review some of the chromatograms for this peptide, you will see that many show a single, very nice peak eluting over 0.2 minutes.
@@ -802,7 +802,7 @@ <h2>Continuing multi-replicate data processing</h2>
         distinct peaks.
     </p>
     <p>
-        <img src="image-53.png" />
+        <img src="s-49.png" />
     </p>
     <p>
         A peptide like this may be very difficult to use for quantification, especially without a matching SIL peptide. You should probably delete this
@@ -817,7 +817,7 @@ <h2>Continuing multi-replicate data processing</h2>
         <b>Peak Areas</b> graph.
     </p>
     <p>
-        <img src="image-54.png" />
+        <img src="s-50.png" />
     </p>
     <p>
         The total peak area for this peptide is dominated by the y7 ion. Although this is also reflected in the library spectrum (as shown at the far
@@ -825,7 +825,7 @@ <h2>Continuing multi-replicate data processing</h2>
         ion (see below).
     </p>
     <p>
-        <img src="image-55.png" />
+        <img src="s-51.png" />
     </p>
     <p>
         However, it is also clear that Skyline is, for the most part, integrating the same peak for the same molecule in each run. To convince yourself
@@ -840,20 +840,20 @@ <h2>Continuing multi-replicate data processing</h2>
         minutes does, in fact, cause the co-eluting signals on all 6 monitored transitions when peptide abundance is high enough.
     </p>
     <p>
-        <img src="image-56.png" />
+        <img src="s-52.png" />
     </p>
     <p>
         Rather than deleting this peptide, you will want to correct the one case where Skyline has chosen the wrong peak. You can see this in the
         <b>Retention Times</b> plot, as a narrower band occurring below 22.5 minutes.
     </p>
     <p>
-        <img src="image-57.png" />
+        <img src="s-53.png" />
     </p>
     <p class="keep-next">
         And also in the <b>Peak Areas</b> plot, as the run with no visible integrated signal.
     </p>
     <p>
-        <img src="image-58.png" />
+        <img src="s-54.png" />
     </p>
     <p>
         You can click on the bar in the <b>Retention Times</b> view to activate the chromatogram graph for this run. You will see that the
@@ -861,7 +861,7 @@ <h2>Continuing multi-replicate data processing</h2>
         knowledge you have gained from the surrounding runs.
     </p>
     <p>
-        <img src="image-59.png" />
+        <img src="s-55.png" />
     </p>
     <p>
         To correct the integration of this run, do the following:
@@ -904,7 +904,7 @@ <h2>Continuing multi-replicate data processing</h2>
         This gives you added confidence in the consistency of the integrated peak.
     </p>
     <p>
-        <img src="image-60.png" />
+        <img src="s-56.png" />
     </p>
     <p>
         Continuing up the <b>Targets</b> list, you will find several peptides (YANVIAYDHSR and
@@ -912,14 +912,14 @@ <h2>Continuing multi-replicate data processing</h2>
         the matching library spectrum is pronounced. You can see these differences in the <b>Peak Areas</b> graph:
     </p>
     <p>
-        <img src="image-61.png" />
+        <img src="s-57.png" />
     </p>
     <p>
         You can also observe this in the chromatogram graphs where Skyline displays the low dot product values “(dotp 0.28)” beneath the peak retention
         times.
     </p>
     <p>
-        <img src="image-62.png" />
+        <img src="s-58.png" />
     </p>
     <p>
         Skyline displays the “dotp” value like this when there is another peak on the graph with a higher dotp value. In the case above, you cannot see
@@ -953,7 +953,7 @@ <h2>Continuing multi-replicate data processing</h2>
         summary plots (see below), you may initially be tempted to delete this peptide and move on:
     </p>
     <p>
-        <img src="image-63.png" />
+        <img src="s-59.png" />
     </p>
     <p>
         However, if you look closely you will see that there are regions of consistency among the healthy subjects. To see this expressed more clearly,
@@ -966,10 +966,10 @@ <h2>Continuing multi-replicate data processing</h2>
         This will change the graphs to look like:
     </p>
     <p>
-        <img src="image-64.png" />
+        <img src="s-60.png" />
     </p>
     <p>
-        <img src="image-65.png" />
+        <img src="s-61.png" />
     </p>
     <p>
         Making it clearer that a consistent peak is being integrated for the healthy subjects but not for the diseased subjects. If you review the peak
@@ -985,11 +985,11 @@ <h2>Continuing multi-replicate data processing</h2>
         <tr>
             <td class="comp-fig">
                 D_102_REP3<br />
-                <img src="image-66.png" />
+                <img src="s-62.png" />
             </td>
             <td class="comp-fig">
                 D_108_REP1<br />
-                <img src="image-67.png" />
+                <img src="s-63.png" />
             </td>
         </tr>
     </table>
@@ -1002,7 +1002,7 @@ <h2>Continuing multi-replicate data processing</h2>
         after runs of healthy subjects (D_102_REP2 and D_102_REP3). This observation might suggest a carryover effect.
     </p>
     <p>
-        <img src="image-68.png" />
+        <img src="s-64.png" />
     </p>
     <p>
         In the end, these transitions may represent one of the strongest biomarker candidates in this document. You could now order a synthetic peptide
@@ -1042,7 +1042,7 @@ <h2>Preparing for statistical analysis with replicate annotations</h2>
         The form should look like this:
     </p>
     <p>
-        <img src="image-69.png" />
+        <img src="s-65.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button in the <b>Define Annotation</b> form.</li>
@@ -1053,7 +1053,7 @@ <h2>Preparing for statistical analysis with replicate annotations</h2>
         The <b>Document Settings</b> form should look like:
     </p>
     <p>
-        <img src="image-70.png" />
+        <img src="s-66.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -1072,7 +1072,7 @@ <h2>Preparing for statistical analysis with replicate annotations</h2>
         The <b>Install from Tool Store</b> form should look like:
     </p>
     <p>
-        <img src="image-71.png" />
+        <img src="s-67.png" />
     </p>
     <ul>
         <li>Click the <b>Install</b> button and follow the prompts until MSstats installation is completed.</li>
@@ -1093,10 +1093,10 @@ <h2>Preparing for statistical analysis with replicate annotations</h2>
     <table class="comp-fig">
         <tr>
             <td class="comp-fig" style="padding: 5px;">
-                <img src="image-72.png" />
+                <img src="s-68.png" />
             </td>
             <td class="comp-fig" style="padding: 5px;">
-                <img src="image-73.png" />
+                <img src="s-69.png" />
             </td>
         </tr>
     </table>
@@ -1108,7 +1108,7 @@ <h2>Preparing for statistical analysis with replicate annotations</h2>
         The <b>Document Settings</b> form should look like this:
     </p>
     <p>
-        <img src="image-74.png" />
+        <img src="s-70.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -1125,7 +1125,7 @@ <h2>Preparing for statistical analysis with replicate annotations</h2>
         The <b>Document Grid</b> should look something like this:
     </p>
     <p>
-        <img src="image-75.png" />
+        <img src="s-71.png" />
     </p>
     <p>
         You can now manually enter the annotations for all 42 replicates into this grid. You can also paste values from a spreadsheet directly into
@@ -1145,7 +1145,7 @@ <h2>Preparing for statistical analysis with replicate annotations</h2>
         The <b>Document Grid</b> should look like this:
     </p>
     <p>
-        <img src="image-76.png" />
+        <img src="s-72.png" />
     </p>
     <ul>
         <li>Press Ctrl-V to paste into the <b>Document Grid</b>.</li>
@@ -1154,7 +1154,7 @@ <h2>Preparing for statistical analysis with replicate annotations</h2>
         Skyline should fill in the cells in the <b>Document Grid</b> with the values from the spreadsheet as follows:
     </p>
     <p>
-        <img src="image-77.png" />
+        <img src="s-73.png" />
     </p>
     <h2>Annotating Peptides with Problem Peaks</h2>
     <p>
@@ -1174,7 +1174,7 @@ <h2>Annotating Peptides with Problem Peaks</h2>
         The <b>Define Annotation</b> form should look like:
     </p>
     <p>
-        <img src="image-78.png" />
+        <img src="s-74.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -1185,7 +1185,7 @@ <h2>Annotating Peptides with Problem Peaks</h2>
         The <b>Document Settings</b> form should look like:
     </p>
     <p>
-        <img src="image-79.png" />
+        <img src="s-75.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -1204,7 +1204,7 @@ <h2>Annotating Peptides with Problem Peaks</h2>
         The <b>Customize Report</b> form should look like this:
     </p>
     <p>
-        <img src="image-80.png" />
+        <img src="s-76.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -1214,7 +1214,7 @@ <h2>Annotating Peptides with Problem Peaks</h2>
         The <b>Document Grid</b> should look like this:
     </p>
     <p>
-        <img src="image-81.png" />
+        <img src="s-77.png" />
     </p>
     <p>
         Depending on how you processed the rest of your document, there may or may not be exactly 223 truncated precursor peak groups. You could check
@@ -1229,7 +1229,7 @@ <h2>Annotating Peptides with Problem Peaks</h2>
         The <b>Document Grid</b> should now look like this:
     </p>
     <p>
-        <img src="image-82.png" />
+        <img src="s-78.png" />
     </p>
     <p>
         You can also use Excel and the <b>Document Grid</b> support for pasting values to set all 163 rows in a single paste as follows:
@@ -1253,7 +1253,7 @@ <h2>Annotating Peptides with Problem Peaks</h2>
         marked with a small red triangle above and right of the peptide name.
     </p>
     <p>
-        <img src="image-83.png" />
+        <img src="s-79.png" />
     </p>
     <p>
         If you hover the mouse cursor over one of these triangles, you will see a tip appear with the text “<b>Missing Data</b> True”.
@@ -1267,7 +1267,7 @@ <h2>Annotating Peptides with Problem Peaks</h2>
         <li>Select the “Truncated Precursors” report you have been using.</li>
         <li>Click the <b>Copy</b> button.</li>
         <li>In the <b>Report Name</b> field of the <b>Customize Report</b> form, enter “Missing Peaks”.</li>
-        <li>Remove the <b>Precursors</b> and <b>Count Truncated</b> columns using the <img src="image-84.png" /> button to the
+        <li>Remove the <b>Precursors</b> and <b>Count Truncated</b> columns using the <img src="../../shared/red-x-icon.png" /> button to the
             right of the columns list.</li>
         <li>Check the <b>Pivot Replicate Name</b> checkbox.</li>
     </ul>
@@ -1275,11 +1275,11 @@ <h2>Annotating Peptides with Problem Peaks</h2>
         The <b>Customize Report</b> form should look like this:
     </p>
     <p>
-        <img src="image-85.png" />
+        <img src="s-80.png" />
     </p>
     <ul>
         <li>Click the <b>Filter</b> tab.</li>
-        <li>Click the <img src="image-86.png" /> button to remove the existing filter on <b>Count Truncated</b>.</li>
+        <li>Click the <img src="../../shared/red-x-icon.png" /> button to remove the existing filter on <b>Count Truncated</b>.</li>
         <li>Expand the columns tree to check Proteins &gt; Peptides &gt; Precursors &gt; Precursor Results, to add a filter for the <b>Total Area</b> column.</li>
         <li>In the <b>Operation</b> column, choose “Is Blank”.</li>
     </ul>
@@ -1287,7 +1287,7 @@ <h2>Annotating Peptides with Problem Peaks</h2>
         The <b>Customize Report</b> form should look like this:
     </p>
     <p>
-        <img src="image-87.png" />
+        <img src="s-81.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -1298,7 +1298,7 @@ <h2>Annotating Peptides with Problem Peaks</h2>
         The <b>Document Grid</b> should look like the following:
     </p>
     <p>
-        <img src="image-88.png" />
+        <img src="s-82.png" />
     </p>
     <p>
         <b>NOTE</b>: If you did not fully process your document, you may instead see only one line for the peptide GSYNLQDLLAQ. The next note
@@ -1346,7 +1346,7 @@ <h2>Initial multi-replicate inspection in Skyline</h2>
         This should leave the <b>Peak Areas</b> graph looking something like:
     </p>
     <p>
-        <img src="image-89.png" />
+        <img src="s-83.png" />
     </p>
     <p>
         You can now select through several more peptides to review the coefficients of variation (CV) among the technical replicates for each subject.
@@ -1370,13 +1370,13 @@ <h2>Initial multi-replicate inspection in Skyline</h2>
     <table class="comp-fig">
         <tr>
             <td class="comp-fig">
-                <img src="image-90.png" />
+                <img src="s-84.png" />
             </td>
             <td class="comp-fig">
-                <img src="image-91.png" />
+                <img src="s-85.png" />
             </td>
             <td class="comp-fig">
-                <img src="image-92.png" />
+                <img src="s-86.png" />
             </td>
         </tr>
     </table>
@@ -1418,10 +1418,10 @@ <h2>Initial multi-replicate inspection in Skyline</h2>
     <table class="comp-fig">
         <tr>
             <td class="comp-fig">
-                <img src="image-93.png" />
+                <img src="s-87.png" />
             </td>
             <td class="comp-fig">
-                <img src="image-94.png" />
+                <img src="s-88.png" />
             </td>
         </tr>
     </table>
@@ -1437,10 +1437,10 @@ <h2>Initial multi-replicate inspection in Skyline</h2>
     <table class="comp-fig">
         <tr>
             <td class="comp-fig">
-                <img src="image-95.png" />
+                <img src="s-89.png" />
             </td>
             <td class="comp-fig">
-                <img src="image-96.png" />
+                <img src="s-90.png" />
             </td>
         </tr>
     </table>
@@ -1476,7 +1476,7 @@ <h2>Simple group comparisons in Skyline</h2>
         The <b>Edit Group Comparison Form</b> should look like this:
     </p>
     <p>
-        <img src="image-97.png" />
+        <img src="s-91.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -1485,7 +1485,7 @@ <h2>Simple group comparisons in Skyline</h2>
         The <b>Document Settings</b> form should look like this:
     </p>
     <p>
-        <img src="image-98.png" />
+        <img src="s-92.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -1500,7 +1500,7 @@ <h2>Simple group comparisons in Skyline</h2>
         Skyline will show a grid view that looks like this:
     </p>
     <p>
-        <img src="image-99.png" />
+        <img src="s-93.png" />
     </p>
     <p>
         If the “Fold Change Result” column does not show the full confidence interval, double-click the vertical line between the Fold Change Result
@@ -1516,7 +1516,7 @@ <h2>Simple group comparisons in Skyline</h2>
         Skyline adds a graph pane beside the <b>Healthy v. Diseased:Grid</b> view that looks like this:
     </p>
     <p>
-        <img src="image-100.png" />
+        <img src="s-94.png" />
     </p>
     <ul>
         <li>On the grid, click the “Fold Change Result” header, and click <b>Sort Ascending</b> in the menu that appears.</li>
@@ -1540,7 +1540,7 @@ <h2>Simple group comparisons in Skyline</h2>
         You will see the number of rows indicated in the grid toolbar drop from 48 to 11, and the graph should now look like this:
     </p>
     <p>
-        <img src="image-101.png" />
+        <img src="s-95.png" />
     </p>
     <p>
         Note that more of the proteins that displayed significant change have positive fold-change means, indicating they were more intense in the
@@ -1594,7 +1594,7 @@ <h2>Refinement by differentiation</h2>
         like this:
     </p>
     <p>
-        <img src="image-102.png" />
+        <img src="s-96.png" />
     </p>
     <p class="keep-next">
         To delete these peptides from the document do the following:
@@ -1609,20 +1609,20 @@ <h2>Refinement by differentiation</h2>
         The grid should look like this:
     </p>
     <p>
-        <img src="image-103.png" />
+        <img src="s-97.png" />
     </p>
     <p>
         Note that the VVLSGSDATLAYSAFK peptide has a fold-change of 1, with a 99% confidence interval of 1 to 1. This is the single peptide used as the
         Global Standard for normalization. You do not want to delete this peptide from the document. That is why you deselected it.
     </p>
     <ul>
-        <li>Click the <img src="image-104.png" /> button in the grid toolbar.</li>
+        <li>Click the <img src="../../shared/red-x-icon.png" /> button in the grid toolbar.</li>
     </ul>
     <p class="keep-next">
         Skyline will show the following message to confirm you really want to delete the selected rows:
     </p>
     <p>
-        <img src="image-105.png" />
+        <img src="s-98.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/GroupedStudies/zh-CHS/image-1.png b/pwiz_tools/Skyline/Documentation/Tutorials/GroupedStudies/zh-CHS/s-1.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/HiResMetabolomics/en/index.html b/pwiz_tools/Skyline/Documentation/Tutorials/HiResMetabolomics/en/index.html
index 20fbabedc0..3c3c0df1cd 100644
--- a/pwiz_tools/Skyline/Documentation/Tutorials/HiResMetabolomics/en/index.html
+++ b/pwiz_tools/Skyline/Documentation/Tutorials/HiResMetabolomics/en/index.html
@@ -103,7 +103,7 @@ <h1>Importing a Molecule Transition List into a Skyline Document</h1>
         In Excel, it will look something like this:
     </p>
     <p>
-        <img src="image-0.png" />
+        <img src="s-transition-list-spreadsheet.png" />
     </p>
     <p>
         But again, the .csv version will work just as well.
@@ -139,7 +139,7 @@ <h1>Adding Isotopic Peaks</h1>
         The <b>Transitions Settings</b> form should look like this:
     </p>
     <p>
-        <img src="image-1.png" />
+        <img src="s-1.png" />
     </p>
     <table>
         <tr>
@@ -162,7 +162,7 @@ <h1>Adding Isotopic Peaks</h1>
         The <b>Transitions Settings</b> form should look like this:
     </p>
     <p>
-        <img src="image-2.png" />
+        <img src="s-2.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -178,7 +178,7 @@ <h1>Adding Isotopic Peaks</h1>
         Skyline will show the <b>Insert Transition List</b> form, looking something like this: 
     </p>
     <p>
-        <img src="image-3.png" />
+        <img src="s-3.png" />
     </p>
     <ul>
         <li>Press <b>Ctrl-V</b> to paste the information you placed on the clipboard into Skyline.</li>
@@ -187,7 +187,7 @@ <h1>Adding Isotopic Peaks</h1>
         Skyline will show the <b>Import Transition List: Identify Columns</b> form:
     </p>
     <p>
-        <img src="image-4.png" />
+        <img src="s-4.png" />
     </p>
     <p>
         Make sure that the <b>Molecules</b> radio button is selected.
@@ -200,7 +200,7 @@ <h1>Adding Isotopic Peaks</h1>
         declared as +1. 
     </p>
     <p>
-        <img src="image-5.png" />
+        <img src="s-5.png" />
     </p>
     <p>
         This is easy to correct:
@@ -213,7 +213,7 @@ <h1>Adding Isotopic Peaks</h1>
         The precursor adduct is all the information that is needed.
     </p>
     <p>
-        <img src="image-6.png" />
+        <img src="s-6.png" />
     </p>
     <p>
         Notice that the first two entries are a heavy/light labeled pair based on having the same name and formulas that differ only in isotopic
@@ -227,7 +227,7 @@ <h1>Adding Isotopic Peaks</h1>
         input transition list, and offers you a choice:
     </p>
     <p>
-        <img src="image-7.png" />
+        <img src="s-7.png" />
     </p>
     <p>
         The additional seven precursor transitions are the M+1 isotopes of the targets in the input transition list that Skyline can generate based on
@@ -251,7 +251,7 @@ <h1>Adding Isotopic Peaks</h1>
         stable-isotope internal standards (as applicable):
     </p>
     <p>
-        <img src="image-8.png" /> 
+        <img src="s-8.png" /> 
     </p>
     <p>
         Note that for the molecules with a heavy labeled precursor, the label is expressed as part of the adduct description for the heavy variant. The
@@ -268,7 +268,7 @@ <h1>Surrogate Standards</h1>
         <li>Right-click the “DHA” target, choose <b>Set Standard Type</b>, and click <b>Surrogate Standard</b>.</li>
     </ul>
     <p>
-        <img src="image-9.png" />
+        <img src="s-9.png" />
     </p>
     <p>
         Now the experimental mass spectrometer results can be imported.
@@ -292,7 +292,7 @@ <h1>Importing Mass Spectrometer Runs</h1>
         The <b>Import Results Files</b> form should look like this:
     </p>
     <p>
-        <img src="image-10.png" />
+        <img src="s-10.png" />
     </p>
     <ul>
         <li>Click the <b>Open</b> button.</li>
@@ -301,7 +301,7 @@ <h1>Importing Mass Spectrometer Runs</h1>
         The files should import within 30 seconds or so, leaving your Skyline window looking like this:
     </p>
     <p>
-        <img src="image-11.png" /> 
+        <img src="s-11.png" /> 
     </p>
     <p>
         To take advantage of the Skyline summary graphs for viewing individual targets, do the following:
@@ -319,7 +319,7 @@ <h1>Importing Mass Spectrometer Runs</h1>
         The Skyline window should now look like this:
     </p>
     <p>
-        <img src="image-12.png" />
+        <img src="s-12.png" />
     </p>
     <h1>Checking Peak Integration</h1>
     <p>
@@ -344,7 +344,7 @@ <h1>Preparing for ‘Single Point Quantification’</h1>
         The <b>Molecule Settings</b> form should look like this: 
     </p>
     <p>
-        <img src="image-13.png" />
+        <img src="s-13.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -360,7 +360,7 @@ <h1>Preparing for ‘Single Point Quantification’</h1>
         edit the Sample Type and Analyte Concentration cells for each row as necessary so the grid looks like this:
     </p>
     <p>
-        <img src="image-14.png" />
+        <img src="s-14.png" />
     </p>
     <p>
         In this situation, the concentration given for the NIST sample (NIST-SRM-1950) is entered as “1”, since all analytes have a different
@@ -374,7 +374,7 @@ <h1>Preparing for ‘Single Point Quantification’</h1>
         <li>Set the Concentration Multiplier and Normalization Method cells for each target as shown below.</li>
     </ul>
     <p>
-        <img src="image-15.png" />
+        <img src="s-15.png" />
     </p>
     <p>
         The default normalization method is “Ratio to Heavy” when using stable-isotope internal standards, but you need to set the “FA 18:3” analyte to
@@ -392,7 +392,7 @@ <h1>Inspecting the Calibration Curves</h1>
         The <b>Calibration Curve</b> view will appear looking like this:
     </p>
     <p>
-        <img src="image-16.png" />
+        <img src="s-16.png" />
     </p>
     <p>
         Note that the calibration curve by default has an intercept of 0, as defined by the method of quantification (<b>Settings</b> menu,
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/HiResMetabolomics/en/image-1.png b/pwiz_tools/Skyline/Documentation/Tutorials/HiResMetabolomics/en/s-1.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/HiResMetabolomics/en/image-1.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/HiResMetabolomics/en/s-1.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/HiResMetabolomics/en/image-10.png b/pwiz_tools/Skyline/Documentation/Tutorials/HiResMetabolomics/en/s-10.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/HiResMetabolomics/en/image-10.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/HiResMetabolomics/en/s-10.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/HiResMetabolomics/en/image-11.png b/pwiz_tools/Skyline/Documentation/Tutorials/HiResMetabolomics/en/s-11.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/HiResMetabolomics/en/image-11.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/HiResMetabolomics/en/s-11.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/HiResMetabolomics/en/image-12.png b/pwiz_tools/Skyline/Documentation/Tutorials/HiResMetabolomics/en/s-12.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/HiResMetabolomics/en/image-12.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/HiResMetabolomics/en/s-12.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/HiResMetabolomics/en/image-13.png b/pwiz_tools/Skyline/Documentation/Tutorials/HiResMetabolomics/en/s-13.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/HiResMetabolomics/en/image-13.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/HiResMetabolomics/en/s-13.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/HiResMetabolomics/en/image-14.png b/pwiz_tools/Skyline/Documentation/Tutorials/HiResMetabolomics/en/s-14.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/HiResMetabolomics/en/image-14.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/HiResMetabolomics/en/s-14.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/HiResMetabolomics/en/image-15.png b/pwiz_tools/Skyline/Documentation/Tutorials/HiResMetabolomics/en/s-15.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/HiResMetabolomics/en/image-15.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/HiResMetabolomics/en/s-15.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/HiResMetabolomics/en/image-16.png b/pwiz_tools/Skyline/Documentation/Tutorials/HiResMetabolomics/en/s-16.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/HiResMetabolomics/en/image-16.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/HiResMetabolomics/en/s-16.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/HiResMetabolomics/en/image-2.png b/pwiz_tools/Skyline/Documentation/Tutorials/HiResMetabolomics/en/s-2.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/HiResMetabolomics/en/image-2.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/HiResMetabolomics/en/s-2.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/HiResMetabolomics/en/image-3.png b/pwiz_tools/Skyline/Documentation/Tutorials/HiResMetabolomics/en/s-3.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/HiResMetabolomics/en/image-3.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/HiResMetabolomics/en/s-3.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/HiResMetabolomics/en/image-4.png b/pwiz_tools/Skyline/Documentation/Tutorials/HiResMetabolomics/en/s-4.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/HiResMetabolomics/en/image-4.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/HiResMetabolomics/en/s-4.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/HiResMetabolomics/en/image-5.png b/pwiz_tools/Skyline/Documentation/Tutorials/HiResMetabolomics/en/s-5.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/HiResMetabolomics/en/image-5.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/HiResMetabolomics/en/s-5.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/HiResMetabolomics/en/image-6.png b/pwiz_tools/Skyline/Documentation/Tutorials/HiResMetabolomics/en/s-6.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/HiResMetabolomics/en/image-6.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/HiResMetabolomics/en/s-6.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/HiResMetabolomics/en/image-7.png b/pwiz_tools/Skyline/Documentation/Tutorials/HiResMetabolomics/en/s-7.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/HiResMetabolomics/en/image-7.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/HiResMetabolomics/en/s-7.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/HiResMetabolomics/en/image-8.png b/pwiz_tools/Skyline/Documentation/Tutorials/HiResMetabolomics/en/s-8.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/HiResMetabolomics/en/image-8.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/HiResMetabolomics/en/s-8.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/HiResMetabolomics/en/image-9.png b/pwiz_tools/Skyline/Documentation/Tutorials/HiResMetabolomics/en/s-9.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/HiResMetabolomics/en/image-9.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/HiResMetabolomics/en/s-9.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/HiResMetabolomics/en/image-0.png b/pwiz_tools/Skyline/Documentation/Tutorials/HiResMetabolomics/en/s-transition-list-spreadsheet.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/HiResMetabolomics/en/image-0.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/HiResMetabolomics/en/s-transition-list-spreadsheet.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/IMSFiltering/en/image-14.png b/pwiz_tools/Skyline/Documentation/Tutorials/IMSFiltering/en/image-14.png
deleted file mode 100644
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/IMSFiltering/en/index.html b/pwiz_tools/Skyline/Documentation/Tutorials/IMSFiltering/en/index.html
index 18056d3241..92eb6f2b37 100644
--- a/pwiz_tools/Skyline/Documentation/Tutorials/IMSFiltering/en/index.html
+++ b/pwiz_tools/Skyline/Documentation/Tutorials/IMSFiltering/en/index.html
@@ -81,7 +81,7 @@ <h1>Start Skyline and Open the Example Skyline Document</h1>
         The document has no mass spec results loaded yet, and looks like this: 
     </p>
     <p>
-        <img src="image-0.png" />
+        <img src="s-1.png" />
     </p>
     <p>
         This document is the result of importing a peptide search that included a BSA digest. It is set up for full gradient chromatogram extraction
@@ -96,7 +96,7 @@ <h1>Start Skyline and Open the Example Skyline Document</h1>
         like this:
     </p>
     <p>
-        <img src="image-1.png" />
+        <img src="s-2.png" />
     </p>
     <p>
         This instructs Skyline to extract 3 precursor isotope peaks from MS1 (low-energy) spectra and fragment ions from MS/MS (high energy) spectra
@@ -125,7 +125,7 @@ <h1>Import the Results Data</h1>
         Which should bring up the <b>Import Results</b> form:
     </p>
     <p>
-         <img src="image-2.png" />
+         <img src="s-3.png" />
     </p>
     <ul>
         <li>Set the <b>File to import simultaneous field</b> to “Many”.</li>
@@ -137,7 +137,7 @@ <h1>Import the Results Data</h1>
         tutorial folder:
     </p>
     <p class="keep-next">
-         <img src="image-3.png" />
+         <img src="s-4.png" />
     </p>
     <ul>
         <li>Select both .d files.</li>
@@ -147,7 +147,7 @@ <h1>Import the Results Data</h1>
         This should start the import and cause Skyline to show the <b>Importing Results</b> progress form:
     </p>
     <p>
-        <img src="image-4.png" />
+        <img src="s-5.png" />
     </p>
     <h1>Reviewing the Extracted Ion Chromatograms</h1>
     <p class="keep-next">
@@ -167,7 +167,7 @@ <h1>Reviewing the Extracted Ion Chromatograms</h1>
         ion appears more intense in the yeast background sample:
     </p>
     <p>
-        <img src="image-5.png" />
+        <img src="s-6.png" />
     </p>
     <p>
         The difference is even more pronounced, if you view the entire gradient range by doing the following:
@@ -176,7 +176,7 @@ <h1>Reviewing the Extracted Ion Chromatograms</h1>
         <li>On the <b>View</b> menu, choose <b>Auto-Zoom</b> and click <b>None</b> (shift-F11).</li>
     </ul>
     <p>
-        <img src="image-6.png" />
+        <img src="s-7.png" />
     </p>
     <p>
         Since there are only 38 peptide precursors in this document, you may want to review all 38 to get an overall feel for how the extracted ion
@@ -201,7 +201,7 @@ <h1>Reviewing the Extracted Ion Chromatograms</h1>
         You should end up with a layout that looks something like this:
     </p>
     <p>
-        <img src="image-7.png" />
+        <img src="s-8.png" />
     </p>
     <p>
         This will help make it obvious how the retention times in the two replicates compare with each other. As you review, you should become
@@ -233,7 +233,7 @@ <h1>Reviewing the Extracted Ion Chromatograms</h1>
         The form should look like this:
     </p>
     <p>
-        <img src="image-8.png" />
+        <img src="s-9.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -245,7 +245,7 @@ <h1>Reviewing the Extracted Ion Chromatograms</h1>
         peak.
     </p>
     <p>
-        <img src="image-9.png" />
+        <img src="s-10.png" />
     </p>
     <h1>Understanding Ion Mobility Separation</h1>
     <p>
@@ -257,28 +257,28 @@ <h1>Understanding Ion Mobility Separation</h1>
             mouse movement, and click on it.</li>
     </ul>
     <p>
-        <img src="image-10.png" />
+        <img src="s-11.png" />
     </p>
     <p class="keep-next">
         This should bring up the <b>Full-Scan</b> view showing a normal two-dimensional spectrum in profile mode:
     </p>
     <p>
-        <img src="image-11.png" />
+        <img src="s-12.png" />
     </p>
     <ul>
-        <li>Click the <b>Show 2D Spectrum</b> button <img src="image-12.png" /> to change the plot to a 3D spectrum with drift time.</li>
+        <li>Click the <b>Show 2D Spectrum</b> button <img src="../../shared/show-2d-spectrum-button.png" /> to change the plot to a 3D spectrum with drift time.</li>
     </ul>
     <p>
-        <img src="image-13.png" />
+        <img src="s-13.png" />
     </p>
     <p>
         You can see that only one peptide precursor is visible in this plot at 634.6 <i>m/z</i> and 25 ms drift time.
     </p>
     <ul>
-        <li>Click the <b>Zoom to Selection</b> button <img src="image-14.png" /> to see the entire 3D MS1 spectrum.</li>
+        <li>Click the <b>Zoom to Selection</b> button <img src="../../shared/magnifying-glass-icon.png" /> to see the entire 3D MS1 spectrum.</li>
     </ul>
     <p>
-        <img src="image-15.png" />
+        <img src="s-14.png" />
     </p>
     <p>
         This is a typical MS1 spectrum for IM-MS data, with separate distributions of ions showing correlation between <i>m/z</i> and drift time for
@@ -306,7 +306,7 @@ <h1>Understanding Ion Mobility Separation</h1>
         The <b>Full-Scan</b> graph should change to look like this:
     </p>
     <p>
-        <img src="image-16.png" />
+        <img src="s-15.png" />
     </p>
     <p>
         You can see the most intense visible ion is also at 25 <i>msec</i>, consistent with its precursor, with 1 <i>m/z</i> isotope spacing,
@@ -319,7 +319,7 @@ <h1>Understanding Ion Mobility Separation</h1>
         <li>Click the <b>Zoom to Selection</b> button again to see the entire 3D MS/MS spectrum.</li>
     </ul>
     <p>
-        <img src="image-17.png" />
+        <img src="s-16.png" />
     </p>
     <p>
         This is also a typical MS/MS spectrum, where you can imagine each horizontal stripe as a top-down view of a normal 2D spectrum. You can also
@@ -333,7 +333,7 @@ <h1>Understanding Ion Mobility Separation</h1>
         more complicated these spectra are in the yeast sample and more evidence of the peptide at 30 ms drift time.
     </p>
     <p>
-        <img src="image-18.png" />
+        <img src="s-17.png" />
     </p>
     <h1>Creating an Ion Mobility Library</h1>
     <p>
@@ -372,7 +372,7 @@ <h1>Creating an Ion Mobility Library</h1>
         <li>Click the <b>Ion Mobility</b> tab.</li>
     </ul>
     <p>
-        <img src="image-19.png" />
+        <img src="s-18.png" />
     </p>
     <ul>
         <li>Set the ion mobility filtering <b>Window type</b> to “Resolving power”.</li>
@@ -400,7 +400,7 @@ <h1>Creating an Ion Mobility Library</h1>
         When the training is complete, the form should look like this:
     </p>
     <p>
-        <img src="image-20.png" />
+        <img src="s-19.png" />
     </p>
     <p>
         Note that the peptide NE<b><u>C</u></b>FLSHKDDSPDLPK you have been looking at was found to yield peak intensity at 24.5064 ms, about
@@ -420,7 +420,7 @@ <h1>Creating an Ion Mobility Library</h1>
         form should look like this:
     </p>
     <p>
-        <img src="image-21.png" />
+        <img src="s-20.png" />
     </p>
     <p>
         Before reimporting the yeast sample data do the following to also limit the retention time ranges for chromatogram extraction:
@@ -434,7 +434,7 @@ <h1>Creating an Ion Mobility Library</h1>
         The form should look like this:
     </p>
     <p>
-        <img src="image-22.png" />
+        <img src="s-21.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -451,7 +451,7 @@ <h1>Creating an Ion Mobility Library</h1>
         The form should look like this:
     </p>
     <p>
-        <img src="image-23.png" />
+        <img src="s-22.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -474,7 +474,7 @@ <h1>Reimport the Yeast Data with Ion Mobility Filtering</h1>
         requested chromatogram extraction and allowing you to choose which replicates:
     </p>
     <p>
-        <img src="image-24.png" />
+        <img src="s-23.png" />
     </p>
     <ul>
         <li>Check <b>Select / deselect all</b>.</li>
@@ -488,7 +488,7 @@ <h1>Reimport the Yeast Data with Ion Mobility Filtering</h1>
         extracted. If you left the NE<b><u>C</u></b>FLSHKDDSPDLPK peptide selected you will see the difference immediately:
     </p>
     <p>
-        <img src="image-25.png" />
+        <img src="s-24.png" />
     </p>
     <p>
         To better understand what happened, do the following:
@@ -501,7 +501,7 @@ <h1>Reimport the Yeast Data with Ion Mobility Filtering</h1>
         The <b>Full-Scan</b> graph should look something like this:
     </p>
     <p>
-        <img src="image-26.png" />
+        <img src="s-25.png" />
     </p>
     <p>
         You can now see the horizontal violet range showing the filter imposed by filtering with the ion mobility library you trained. Signal outside
@@ -520,7 +520,7 @@ <h1>Reimport the Yeast Data with Ion Mobility Filtering</h1>
         the fragment ions of the first peptide in the document FKDLGEEHFK:
     </p>
     <p>
-        <img src="image-27.png" />
+        <img src="s-26.png" />
     </p>
     <p>
         Interference that coelutes as nicely some of the chromatograms in this file could easily be coming from other charge states of the same
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/IMSFiltering/en/image-0.png b/pwiz_tools/Skyline/Documentation/Tutorials/IMSFiltering/en/s-1.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/IMSFiltering/en/image-0.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/IMSFiltering/en/s-1.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/IMSFiltering/en/image-9.png b/pwiz_tools/Skyline/Documentation/Tutorials/IMSFiltering/en/s-10.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/IMSFiltering/en/image-9.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/IMSFiltering/en/s-10.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/IMSFiltering/en/image-10.png b/pwiz_tools/Skyline/Documentation/Tutorials/IMSFiltering/en/s-11.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/IMSFiltering/en/image-10.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/IMSFiltering/en/s-11.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/IMSFiltering/en/image-11.png b/pwiz_tools/Skyline/Documentation/Tutorials/IMSFiltering/en/s-12.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/IMSFiltering/en/image-11.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/IMSFiltering/en/s-12.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/IMSFiltering/en/image-13.png b/pwiz_tools/Skyline/Documentation/Tutorials/IMSFiltering/en/s-13.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/IMSFiltering/en/image-13.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/IMSFiltering/en/s-13.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/IMSFiltering/en/image-15.png b/pwiz_tools/Skyline/Documentation/Tutorials/IMSFiltering/en/s-14.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/IMSFiltering/en/image-15.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/IMSFiltering/en/s-14.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/IMSFiltering/en/image-16.png b/pwiz_tools/Skyline/Documentation/Tutorials/IMSFiltering/en/s-15.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/IMSFiltering/en/image-16.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/IMSFiltering/en/s-15.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/IMSFiltering/en/image-17.png b/pwiz_tools/Skyline/Documentation/Tutorials/IMSFiltering/en/s-16.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/IMSFiltering/en/image-17.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/IMSFiltering/en/s-16.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/IMSFiltering/en/image-18.png b/pwiz_tools/Skyline/Documentation/Tutorials/IMSFiltering/en/s-17.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/IMSFiltering/en/image-18.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/IMSFiltering/en/s-17.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/IMSFiltering/en/image-19.png b/pwiz_tools/Skyline/Documentation/Tutorials/IMSFiltering/en/s-18.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/IMSFiltering/en/image-19.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/IMSFiltering/en/s-18.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/IMSFiltering/en/image-20.png b/pwiz_tools/Skyline/Documentation/Tutorials/IMSFiltering/en/s-19.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/IMSFiltering/en/image-20.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/IMSFiltering/en/s-19.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/IMSFiltering/en/image-1.png b/pwiz_tools/Skyline/Documentation/Tutorials/IMSFiltering/en/s-2.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/IMSFiltering/en/image-1.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/IMSFiltering/en/s-2.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/IMSFiltering/en/image-21.png b/pwiz_tools/Skyline/Documentation/Tutorials/IMSFiltering/en/s-20.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/IMSFiltering/en/image-21.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/IMSFiltering/en/s-20.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/IMSFiltering/en/image-22.png b/pwiz_tools/Skyline/Documentation/Tutorials/IMSFiltering/en/s-21.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/IMSFiltering/en/image-22.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/IMSFiltering/en/s-21.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/IMSFiltering/en/image-23.png b/pwiz_tools/Skyline/Documentation/Tutorials/IMSFiltering/en/s-22.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/IMSFiltering/en/image-23.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/IMSFiltering/en/s-22.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/IMSFiltering/en/image-24.png b/pwiz_tools/Skyline/Documentation/Tutorials/IMSFiltering/en/s-23.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/IMSFiltering/en/image-24.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/IMSFiltering/en/s-23.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/IMSFiltering/en/image-25.png b/pwiz_tools/Skyline/Documentation/Tutorials/IMSFiltering/en/s-24.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/IMSFiltering/en/image-25.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/IMSFiltering/en/s-24.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/IMSFiltering/en/image-26.png b/pwiz_tools/Skyline/Documentation/Tutorials/IMSFiltering/en/s-25.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/IMSFiltering/en/image-26.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/IMSFiltering/en/s-25.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/IMSFiltering/en/image-27.png b/pwiz_tools/Skyline/Documentation/Tutorials/IMSFiltering/en/s-26.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/IMSFiltering/en/image-27.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/IMSFiltering/en/s-26.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/IMSFiltering/en/image-2.png b/pwiz_tools/Skyline/Documentation/Tutorials/IMSFiltering/en/s-3.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/IMSFiltering/en/image-2.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/IMSFiltering/en/s-3.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/IMSFiltering/en/image-3.png b/pwiz_tools/Skyline/Documentation/Tutorials/IMSFiltering/en/s-4.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/IMSFiltering/en/image-3.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/IMSFiltering/en/s-4.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/IMSFiltering/en/image-4.png b/pwiz_tools/Skyline/Documentation/Tutorials/IMSFiltering/en/s-5.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/IMSFiltering/en/image-4.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/IMSFiltering/en/s-5.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/IMSFiltering/en/image-5.png b/pwiz_tools/Skyline/Documentation/Tutorials/IMSFiltering/en/s-6.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/IMSFiltering/en/image-5.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/IMSFiltering/en/s-6.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/IMSFiltering/en/image-6.png b/pwiz_tools/Skyline/Documentation/Tutorials/IMSFiltering/en/s-7.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/IMSFiltering/en/image-6.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/IMSFiltering/en/s-7.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/IMSFiltering/en/image-7.png b/pwiz_tools/Skyline/Documentation/Tutorials/IMSFiltering/en/s-8.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/IMSFiltering/en/image-7.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/IMSFiltering/en/s-8.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/IMSFiltering/en/image-8.png b/pwiz_tools/Skyline/Documentation/Tutorials/IMSFiltering/en/s-9.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/IMSFiltering/en/image-8.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/IMSFiltering/en/s-9.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/ImportingAssayLibraries/en/index.html b/pwiz_tools/Skyline/Documentation/Tutorials/ImportingAssayLibraries/en/index.html
index 25d78124f3..33174b792c 100644
--- a/pwiz_tools/Skyline/Documentation/Tutorials/ImportingAssayLibraries/en/index.html
+++ b/pwiz_tools/Skyline/Documentation/Tutorials/ImportingAssayLibraries/en/index.html
@@ -76,7 +76,7 @@ <h1>Transition List Format</h1>
         The file should look like this:
     </p>
     <p>
-        <img src="image-0.png" />
+        <img src="s-experiment-assay-library.png" />
     </p>
     <p>
         Notice that the file has columns for precursor m/z, product m/z, peptide sequence, protein name, iRT value (“Tr_recalibrated”), and spectral
@@ -168,7 +168,7 @@ <h1>Pasting or Importing the Assay Library</h1>
         You should see the following window, which informs you that Skyline has detected iRT values for the transitions you have pasted in:
     </p>
     <p>
-        <img src="image-1.png" />
+        <img src="s-1.png" />
     </p>
     <ul>
         <li>Click the <b>Create</b> button.</li>
@@ -177,7 +177,7 @@ <h1>Pasting or Importing the Assay Library</h1>
         You should now see the following window:
     </p>
     <p>
-        <img src="image-2.png" />
+        <img src="s-2.png" />
     </p>
     <p>
         The empty document you opened does not yet have an iRT calculator or iRT standard peptides specified. Therefore, the iRT values in the assay
@@ -200,7 +200,7 @@ <h1>Pasting or Importing the Assay Library</h1>
         You should now see the following window:
     </p>
     <p>
-        <img src="image-3.png" />
+        <img src="s-3.png" />
     </p>
     <p>
         This informs you that Skyline has detected transition intensities in the assay library you have pasted in. 
@@ -213,14 +213,14 @@ <h1>Pasting or Importing the Assay Library</h1>
         345 of the experiment peptides and also all 10 of the iRT standard peptides. The document tree should look as follows:
     </p>
     <p>
-        <img src="image-4.png" />
+        <img src="s-4.png" />
     </p>
     <p>
         Click on the first peptide (ADSTGTLVITDPT<b><span class="blue">R</span></b>) in the document tree. The newly created library spectrum
         for this peptide should appear in the <b>Library Match</b> view, with four peaks from the ions y7-y10:
     </p>
     <p>
-        <img src="image-5.png" />
+        <img src="s-5.png" />
     </p>
     <p>
         You can also browse this newly generated spectral library in the Spectral Library Explorer by doing the following:
@@ -247,7 +247,7 @@ <h1>Pasting or Importing the Assay Library</h1>
         Skyline should show the <b>Edit iRT Calculator</b> form like this:
     </p>
     <p>
-        <img src="image-6.png" />
+        <img src="s-6.png" />
     </p>
     <p>
         As you can see, the 10 standard peptides and the 345 experiment peptides have both been added to the iRT database.
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/ImportingAssayLibraries/en/image-1.png b/pwiz_tools/Skyline/Documentation/Tutorials/ImportingAssayLibraries/en/s-1.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/ImportingAssayLibraries/en/image-1.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/ImportingAssayLibraries/en/s-1.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/ImportingAssayLibraries/en/image-2.png b/pwiz_tools/Skyline/Documentation/Tutorials/ImportingAssayLibraries/en/s-2.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/ImportingAssayLibraries/en/image-2.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/ImportingAssayLibraries/en/s-2.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/ImportingAssayLibraries/en/image-3.png b/pwiz_tools/Skyline/Documentation/Tutorials/ImportingAssayLibraries/en/s-3.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/ImportingAssayLibraries/en/image-3.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/ImportingAssayLibraries/en/s-3.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/ImportingAssayLibraries/en/image-4.png b/pwiz_tools/Skyline/Documentation/Tutorials/ImportingAssayLibraries/en/s-4.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/ImportingAssayLibraries/en/image-4.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/ImportingAssayLibraries/en/s-4.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/ImportingAssayLibraries/en/image-5.png b/pwiz_tools/Skyline/Documentation/Tutorials/ImportingAssayLibraries/en/s-5.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/ImportingAssayLibraries/en/image-5.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/ImportingAssayLibraries/en/s-5.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/ImportingAssayLibraries/en/image-6.png b/pwiz_tools/Skyline/Documentation/Tutorials/ImportingAssayLibraries/en/s-6.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/ImportingAssayLibraries/en/image-6.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/ImportingAssayLibraries/en/s-6.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/ImportingAssayLibraries/en/image-0.png b/pwiz_tools/Skyline/Documentation/Tutorials/ImportingAssayLibraries/en/s-experiment-assay-library.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/ImportingAssayLibraries/en/image-0.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/ImportingAssayLibraries/en/s-experiment-assay-library.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/ImportingIntegrationBoundaries/en/index.html b/pwiz_tools/Skyline/Documentation/Tutorials/ImportingIntegrationBoundaries/en/index.html
index a8613caf0d..03abb792b0 100644
--- a/pwiz_tools/Skyline/Documentation/Tutorials/ImportingIntegrationBoundaries/en/index.html
+++ b/pwiz_tools/Skyline/Documentation/Tutorials/ImportingIntegrationBoundaries/en/index.html
@@ -85,7 +85,7 @@ <h1 class="document-title">Skyline Importing Integration Boundaries from Other T
         importing, and is based on a text file output by the OpenSWATH tool:
     </p>
     <p>
-        <img src="image-0.png" />
+        <img src="s-peak-boundary-csv.png" />
     </p>
     <p>
         This text file is tab-separated, but Skyline will also accept space, comma, or (if European language settings are enabled) semicolon as a
@@ -107,7 +107,7 @@ <h1 class="document-title">Skyline Importing Integration Boundaries from Other T
         A progress bar should appear, and when it is done, the document’s peak boundaries will be adjusted to match those specified in the file:
     </p>
     <p>
-        <img src="image-1.png" />
+        <img src="s-1.png" />
     </p>
     <p>
         At present, only peak boundaries exported from OpenSWATH or Skyline itself can be imported without any change to the file. Other tools
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/ImportingIntegrationBoundaries/en/image-1.png b/pwiz_tools/Skyline/Documentation/Tutorials/ImportingIntegrationBoundaries/en/s-1.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/ImportingIntegrationBoundaries/en/image-1.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/ImportingIntegrationBoundaries/en/s-1.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/ImportingIntegrationBoundaries/en/image-0.png b/pwiz_tools/Skyline/Documentation/Tutorials/ImportingIntegrationBoundaries/en/s-peak-boundary-csv.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/ImportingIntegrationBoundaries/en/image-0.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/ImportingIntegrationBoundaries/en/s-peak-boundary-csv.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/LibraryExplorer/en/index.html b/pwiz_tools/Skyline/Documentation/Tutorials/LibraryExplorer/en/index.html
index e1f27e4b74..b9cd0331c7 100644
--- a/pwiz_tools/Skyline/Documentation/Tutorials/LibraryExplorer/en/index.html
+++ b/pwiz_tools/Skyline/Documentation/Tutorials/LibraryExplorer/en/index.html
@@ -90,7 +90,7 @@ <h1>Exploring a Library</h1>
         The <b>Peptide Settings</b> form should now look something like this:
     </p>
     <p>
-        <img src="image-0.png" />
+        <img src="s-1.png" />
     </p>
     <p>
         Next, ensure that peptide modifications are set to the default values:
@@ -102,7 +102,7 @@ <h1>Exploring a Library</h1>
         The form should look like this: 
     </p>
     <p>
-        <img src="image-1.png" />
+        <img src="s-2.png" />
     </p>
     <ul>
         <li>If you have other modifications that do not appear here, uncheck all but the ‘Carbamidomethyl (C)’ modification shown above.</li>
@@ -125,7 +125,7 @@ <h1>Exploring a Library</h1>
         The library explorer should look something like this:
     </p>
     <p>
-        <img src="image-2.png" />
+        <img src="s-3.png" />
     </p>
     <p>
         On the left side of the explorer, the <b>Library</b> list should show that you are currently viewing the Experiment 15N library. The
@@ -159,7 +159,7 @@ <h1>Exploring a Library</h1>
         that the single Q is enough to reduce the list to the various modified states for the two peptides QVLFSADDR++ and QVLFSADDRVK+++.
     </p>
     <p>
-        <img src="image-3.png" />
+        <img src="s-4.png" />
     </p>
     <p>
         Hover the cursor over the one displayed as <b><u>Q</u></b>VLFSADDR++, and you will see that the glutamine modification is displayed
@@ -188,7 +188,7 @@ <h1>Exploring a Library</h1>
         The library explorer should now look something like this:
     </p>
     <p>
-        <img src="image-4.png" />
+        <img src="s-5.png" />
     </p>
     <p>
         The chart is pretty crowded in a window small enough to paste into this document. Hopefully you are using a larger window, but you can also
@@ -225,7 +225,7 @@ <h1>Matching Modifications</h1>
         should look like this:
     </p>
     <p>
-        <img src="image-5.png" />
+        <img src="s-6.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button on the <b>Edit Structural Modification</b> form.</li>
@@ -245,7 +245,7 @@ <h1>Matching Modifications</h1>
         The <b>Edit Isotope Modification</b> form should look like this:
     </p>
     <p>
-        <img src="image-6.png" />
+        <img src="s-7.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button on the <b>Edit Isotope Modification</b> form. </li>
@@ -256,7 +256,7 @@ <h1>Matching Modifications</h1>
         The <b>Peptide Settings</b> form should now look like this:
     </p>
     <p>
-        <img src="image-7.png" />
+        <img src="s-8.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button for the <b>Peptide Settings</b> form. </li>
@@ -267,7 +267,7 @@ <h1>Matching Modifications</h1>
         You should find the peptide list looking like this:
     </p>
     <p>
-        <img src="image-8.png" />
+        <img src="s-9.png" />
     </p>
     <p>
         All of the peptides now display icons to the left, indicating your document modifications match those found in the library, and modifications
@@ -289,7 +289,7 @@ <h1>Adding Library Peptides to the Document</h1>
         The following form may appear: 
     </p>
     <p>
-        <img src="image-9.png" />
+        <img src="s-10.png" />
     </p>
     <p>
         This form appears because the peptide <b><span class="blue">AEVNGLAAQGKYEGSGEDGGAAAQSLYIANHAY</span></b> contains a missed cleavage,
@@ -318,7 +318,7 @@ <h1>Adding Library Peptides to the Document</h1>
         <b>Spectrum</b> dropdown list.
     </p>
     <p>
-        <img src="image-10.png" />
+        <img src="s-11.png" />
     </p>
     <p>
         By default, Skyline uses the light spectrum if both the heavy and light spectra are available. You can still view the heavy spectrum by
@@ -366,7 +366,7 @@ <h1>Neutral Losses</h1>
         The <b>Peptide Settings</b> form should now something look like this:
     </p>
     <p>
-        <img src="image-11.png" />
+        <img src="s-12.png" />
     </p>
     <p>
         To add the second library, do the following:
@@ -388,7 +388,7 @@ <h1>Neutral Losses</h1>
         The <b>Peptide Settings</b> form should now look something like this:
     </p>
     <p>
-        <img src="image-12.png" />
+        <img src="s-13.png" />
     </p>
     <p>
         You are now ready to explore the Human Phospho library.
@@ -400,7 +400,7 @@ <h1>Neutral Losses</h1>
         Skyline will present the following message:
     </p>
     <p>
-        <img src="image-13.png" />
+        <img src="s-14.png" />
     </p>
     <ul>
         <li>Click the <b>Yes</b> button, to save the new settings and open the <b>Spectral Library Explorer</b>.</li>
@@ -426,10 +426,10 @@ <h1>Neutral Losses</h1>
     <table class="comp-fig">
         <tr>
             <td class="comp-fig">
-                <img src="image-14.png" />
+                <img src="s-15.png" />
             </td>
             <td class="comp-fig">
-                <img src="image-15.png" />
+                <img src="s-16.png" />
             </td>
         </tr>
     </table>
@@ -454,7 +454,7 @@ <h1>Neutral Losses</h1>
         The <b>Edit Structural Modification</b> form should now look like this:
     </p>
     <p>
-        <img src="image-16.png" />
+        <img src="s-17.png" />
     </p>
     <p>
         Note: You could have also simply chosen the “Phospho (ST)” modification from the <b>Name</b> dropdown list to get the same end
@@ -475,10 +475,10 @@ <h1>Neutral Losses</h1>
     <table class="comp-fig">
         <tr>
             <td class="comp-fig">
-                <img src="image-17.png" />
+                <img src="s-18.png" />
             </td>
             <td class="comp-fig">
-                <img src="image-18.png" />
+                <img src="s-19.png" />
             </td>
         </tr>
     </table>
@@ -519,7 +519,7 @@ <h1>Matching Library Peptides to Proteins</h1>
         The <b>Edit Background Proteome</b> form should now look like this:
     </p>
     <p>
-        <img src="image-19.png" />
+        <img src="s-20.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button on the <b>Edit Background Proteome</b> form.</li>
@@ -543,7 +543,7 @@ <h1>Matching Library Peptides to Proteins</h1>
         This should bring up a form that looks like this:
     </p>
     <p>
-        <img src="image-20.png" />
+        <img src="s-21.png" />
     </p>
     <ul>
         <li>For the <b>163 peptides matching multiple proteins</b>, choose/change to <b>Add to only the first matching
@@ -556,7 +556,7 @@ <h1>Matching Library Peptides to Proteins</h1>
         Skyline will display a message that looks like this:
     </p>
     <p>
-        <img src="image-21.png" />
+        <img src="s-22.png" />
     </p>
     <p>
         This form gives you a preview of the changes that will be made to your document. The 40 unmatched library entries refer to the spectra for
@@ -569,7 +569,7 @@ <h1>Matching Library Peptides to Proteins</h1>
         This should leave the main Skyline window looking something like this:
     </p>
     <p>
-        <img src="image-22.png" />
+        <img src="s-23.png" />
     </p>
     <p>
         As you can see from inspecting the status bar at the bottom-right of the window, Skyline has added all of the proteins, peptides, precursors
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/LibraryExplorer/en/image-0.png b/pwiz_tools/Skyline/Documentation/Tutorials/LibraryExplorer/en/s-1.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/LibraryExplorer/en/image-0.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/LibraryExplorer/en/s-1.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/LibraryExplorer/en/image-9.png b/pwiz_tools/Skyline/Documentation/Tutorials/LibraryExplorer/en/s-10.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/LibraryExplorer/en/image-9.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/LibraryExplorer/en/s-10.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/LibraryExplorer/en/image-10.png b/pwiz_tools/Skyline/Documentation/Tutorials/LibraryExplorer/en/s-11.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/LibraryExplorer/en/image-10.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/LibraryExplorer/en/s-11.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/LibraryExplorer/en/image-11.png b/pwiz_tools/Skyline/Documentation/Tutorials/LibraryExplorer/en/s-12.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/LibraryExplorer/en/image-11.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/LibraryExplorer/en/s-12.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/LibraryExplorer/en/image-12.png b/pwiz_tools/Skyline/Documentation/Tutorials/LibraryExplorer/en/s-13.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/LibraryExplorer/en/image-12.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/LibraryExplorer/en/s-13.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/LibraryExplorer/en/image-13.png b/pwiz_tools/Skyline/Documentation/Tutorials/LibraryExplorer/en/s-14.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/LibraryExplorer/en/image-13.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/LibraryExplorer/en/s-14.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/LibraryExplorer/en/image-14.png b/pwiz_tools/Skyline/Documentation/Tutorials/LibraryExplorer/en/s-15.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/LibraryExplorer/en/image-14.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/LibraryExplorer/en/s-15.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/LibraryExplorer/en/image-15.png b/pwiz_tools/Skyline/Documentation/Tutorials/LibraryExplorer/en/s-16.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/LibraryExplorer/en/image-15.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/LibraryExplorer/en/s-16.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/LibraryExplorer/en/image-16.png b/pwiz_tools/Skyline/Documentation/Tutorials/LibraryExplorer/en/s-17.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/LibraryExplorer/en/image-16.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/LibraryExplorer/en/s-17.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/LibraryExplorer/en/image-17.png b/pwiz_tools/Skyline/Documentation/Tutorials/LibraryExplorer/en/s-18.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/LibraryExplorer/en/image-17.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/LibraryExplorer/en/s-18.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/LibraryExplorer/en/image-18.png b/pwiz_tools/Skyline/Documentation/Tutorials/LibraryExplorer/en/s-19.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/LibraryExplorer/en/image-18.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/LibraryExplorer/en/s-19.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/LibraryExplorer/en/image-1.png b/pwiz_tools/Skyline/Documentation/Tutorials/LibraryExplorer/en/s-2.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/LibraryExplorer/en/image-1.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/LibraryExplorer/en/s-2.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/LibraryExplorer/en/image-19.png b/pwiz_tools/Skyline/Documentation/Tutorials/LibraryExplorer/en/s-20.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/LibraryExplorer/en/image-19.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/LibraryExplorer/en/s-20.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/LibraryExplorer/en/image-20.png b/pwiz_tools/Skyline/Documentation/Tutorials/LibraryExplorer/en/s-21.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/LibraryExplorer/en/image-20.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/LibraryExplorer/en/s-21.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/LibraryExplorer/en/image-21.png b/pwiz_tools/Skyline/Documentation/Tutorials/LibraryExplorer/en/s-22.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/LibraryExplorer/en/image-21.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/LibraryExplorer/en/s-22.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/LibraryExplorer/en/image-22.png b/pwiz_tools/Skyline/Documentation/Tutorials/LibraryExplorer/en/s-23.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/LibraryExplorer/en/image-22.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/LibraryExplorer/en/s-23.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/LibraryExplorer/en/image-2.png b/pwiz_tools/Skyline/Documentation/Tutorials/LibraryExplorer/en/s-3.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/LibraryExplorer/en/image-2.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/LibraryExplorer/en/s-3.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/LibraryExplorer/en/image-3.png b/pwiz_tools/Skyline/Documentation/Tutorials/LibraryExplorer/en/s-4.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/LibraryExplorer/en/image-3.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/LibraryExplorer/en/s-4.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/LibraryExplorer/en/image-4.png b/pwiz_tools/Skyline/Documentation/Tutorials/LibraryExplorer/en/s-5.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/LibraryExplorer/en/image-4.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/LibraryExplorer/en/s-5.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/LibraryExplorer/en/image-5.png b/pwiz_tools/Skyline/Documentation/Tutorials/LibraryExplorer/en/s-6.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/LibraryExplorer/en/image-5.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/LibraryExplorer/en/s-6.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/LibraryExplorer/en/image-6.png b/pwiz_tools/Skyline/Documentation/Tutorials/LibraryExplorer/en/s-7.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/LibraryExplorer/en/image-6.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/LibraryExplorer/en/s-7.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/LibraryExplorer/en/image-7.png b/pwiz_tools/Skyline/Documentation/Tutorials/LibraryExplorer/en/s-8.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/LibraryExplorer/en/image-7.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/LibraryExplorer/en/s-8.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/LibraryExplorer/en/image-8.png b/pwiz_tools/Skyline/Documentation/Tutorials/LibraryExplorer/en/s-9.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/LibraryExplorer/en/image-8.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/LibraryExplorer/en/s-9.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/en/index.html b/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/en/index.html
index 32cb7d5bdd..626b747b49 100644
--- a/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/en/index.html
+++ b/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/en/index.html
@@ -112,7 +112,7 @@ <h1>Importing a Data Dependent Peptide Search into a Skyline Document</h1>
         Skyline should present a form that looks like this:
     </p>
     <p>
-        <img src="image-0.png" />
+        <img src="s-1.png" />
     </p>
     <p>
         Next, you will use this wizard to create a spectral library from the output of one of the many peptide search engines supported by Skyline. For
@@ -133,7 +133,7 @@ <h1>Importing a Data Dependent Peptide Search into a Skyline Document</h1>
         The wizard form should now look like this:
     </p>
     <p>
-        <img src="image-1.png" />
+        <img src="s-2.png" />
     </p>
     <ul>
         <li>Click the <b>Next</b> button.</li>
@@ -147,7 +147,7 @@ <h1>Importing a Data Dependent Peptide Search into a Skyline Document</h1>
         <li>The redundant library called “MS1FilteringTutorial.redundant.blib” containing all matching spectra.</li>
     </ul>
     <p>
-        <img src="image-2.png" />
+        <img src="s-ms1-filtering-folder.png" />
     </p>
     <p>
         You may also find a file ‘MS1FilterTutorial.slc’, which is a ‘Skyline Library Cache’ file to improve library load time. It can be deleted, and
@@ -163,7 +163,7 @@ <h1>Importing a Data Dependent Peptide Search into a Skyline Document</h1>
         When library building has completed, Skyline will present the next page in the wizard as shown below:
     </p>
     <p>
-        <img src="image-3.png" />
+        <img src="s-3.png" />
     </p>
     <p>
         In this case, Skyline has found original WIFF data files matching the spectrum source files used to build your library, and the library appears
@@ -180,7 +180,7 @@ <h1>Importing a Data Dependent Peptide Search into a Skyline Document</h1>
         A form should appear asking you how to handle the prefix shared by the two WIFF files:
     </p>
     <p>
-        <img src="image-4.png" />
+        <img src="s-4.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -195,7 +195,7 @@ <h1>Importing a Data Dependent Peptide Search into a Skyline Document</h1>
         and the wizard should look like this:
     </p>
     <p>
-        <img src="image-5.png" />
+        <img src="s-5.png" />
     </p>
     <p>
         It is possible that your document will already have one or more of these modifications defined (e.g. Oxidation (M)), in which case the list
@@ -215,7 +215,7 @@ <h1>Importing a Data Dependent Peptide Search into a Skyline Document</h1>
         this:
     </p>
     <p>
-        <img src="image-6.png" />
+        <img src="s-6.png" />
     </p>
     <p>
         In the <b>MS1 filtering</b> section, you will see the following default settings.
@@ -240,13 +240,13 @@ <h1>Importing a Data Dependent Peptide Search into a Skyline Document</h1>
         </table>
     </div>
     <p>
-        <img src="image-7.png" />
+        <img src="s-relative-abundance-graph.png" />
     </p>
     <p class="keep-next">
         A series of these intensities extracted over time make up the chromatograms you will see in Skyline:
     </p>
     <p>
-        <img src="image-8.png" />
+        <img src="s-chromatogram.png" />
     </p>
     <p>
         In the <b>Retention time filtering</b> section, note the choice to <b>Use only scans within [5] minutes of MS/MS IDs</b>.
@@ -273,7 +273,7 @@ <h1>Importing a Data Dependent Peptide Search into a Skyline Document</h1>
         The wizard should now look like this:
     </p>
     <p>
-        <img src="image-9.png" />
+        <img src="s-7.png" />
     </p>
     <ul>
         <li>Click the <b>Finish</b> button.</li>
@@ -283,7 +283,7 @@ <h1>Importing a Data Dependent Peptide Search into a Skyline Document</h1>
         FASTA file with matching spectra in the peptide search results which you imported.
     </p>
     <p>
-        <img src="image-10.png" />
+        <img src="s-8.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button in the <b>Associate Proteins</b> form.</li>
@@ -295,7 +295,7 @@ <h1>Importing a Data Dependent Peptide Search into a Skyline Document</h1>
         You should see a progress graph like this:
     </p>
     <p>
-        <img src="image-11.png" />
+        <img src="s-9.png" />
     </p>
     <p>
         Once the import has completed, first have an in-depth look at the spectral library you created before inspecting the chromatogram data.
@@ -319,7 +319,7 @@ <h2>Verifying Library Retention Time Information</h2>
         during the <b>Import Peptide Search</b> wizard.
     </p>
     <p>
-        <img src="image-12.png" />
+        <img src="s-10.png" />
     </p>
     <p>
         Choosing to use them now in the <b>Spectral Library Explorer</b> will not add them to the current document unless you use the
@@ -333,7 +333,7 @@ <h2>Verifying Library Retention Time Information</h2>
         The <b>Spectral Library Explorer</b> will appear, looking something like this:
     </p>
     <p>
-        <img src="image-13.png" />
+        <img src="s-11.png" />
     </p>
     <p>
         In the peptide list, the peptides without an icon to the left of the sequence text are ones that contain any of the modifications you just
@@ -378,7 +378,7 @@ <h1>Peptide Targets, Spectra and Chromatograms</h1>
         Your Skyline document should look like the following:
     </p>
     <p>
-        <img src="image-14.png" />
+        <img src="s-12.png" />
     </p>
     <p>
         The document is now fully configured for MS1 Filtering with two DDA runs imported. You will see that the chromatogram in this view is
@@ -398,7 +398,7 @@ <h1>Peptide Targets, Spectra and Chromatograms</h1>
         <li>In the <b>Peak Areas</b> window, right-click, choose <b>Show Dot Product</b>, and click <b>Labels</b>.</li>
     </ul>
     <p>
-        <img src="image-15.png" />
+        <img src="s-13.png" />
     </p>
     <p>
         You can dock the <b>Peak Areas</b> window to your desired location by doing the following:
@@ -415,7 +415,7 @@ <h1>Peptide Targets, Spectra and Chromatograms</h1>
         Your Skyline file should look something like this:
     </p>
     <p>
-        <img src="image-16.png" />
+        <img src="s-14.png" />
     </p>
     <p>
         The chromatogram views show the MS1 extracted ion chromatogram for all precursor isotope ions M (blue), M+1 (purple), M+2 (brown). Below the
@@ -465,7 +465,7 @@ <h1>Peptide Targets, Spectra and Chromatograms</h1>
         The chromatogram graphs should look something like this:
     </p>
     <p>
-        <img src="image-17.png" />
+        <img src="s-15.png" />
     </p>
     <p>
         To gain some insight into how the retention time alignment works, do the following:
@@ -477,7 +477,7 @@ <h1>Peptide Targets, Spectra and Chromatograms</h1>
         Skyline will present a window that looks like this:
     </p>
     <p>
-        <img src="image-18.png" />
+        <img src="s-16.png" />
     </p>
     <p>
         This window shows you the points for a linear regression used to align times between runs. Skyline calculates a linear regression like this
@@ -514,7 +514,7 @@ <h1>Reviewing the Data</h1>
         out of the 50 is currently selected, you can look in the status bar at the bottom right of the Skyline window:
     </p>
     <p>
-        <img src="image-19.png" />
+        <img src="s-17.png" />
     </p>
     <p>
         After the peptide I<b><u>S</u></b>MSEVDLNVAAPK, you will see 4 peptides with acceptable peak integration, though
@@ -530,11 +530,11 @@ <h2>Basic understanding of a chromatographic landscape</h2>
         <tr>
             <td  class="comp-fig">
                 <b>5b_MCF7_TiTip3</b><br />
-                <img src="image-20.png" />
+                <img src="s-18.png" />
             </td>
             <td  class="comp-fig">
                 <b>1_MCF7_TiB_L</b><br />
-                <img src="image-21.png" />
+                <img src="s-19.png" />
             </td>
         </tr>
     </table>
@@ -543,7 +543,7 @@ <h2>Basic understanding of a chromatographic landscape</h2>
         see in the 5b_MCF7_TiTip3 graph:
     </p>
     <p>
-        <img src="image-22.png" />
+        <img src="s-20.png" />
     </p>
     <p>
         This is an extremely important aspect of working with chromatographic data: just as your target peptides can be expected to elute at highly
@@ -576,7 +576,7 @@ <h2>Basic understanding of a chromatographic landscape</h2>
         previously selected peaks (0.86 and 0.87 versus 0.9 and 0.99):
     </p>
     <p>
-        <img src="image-23.png" />
+        <img src="s-21.png" />
     </p>
     <p>
         You can see from the distribution in the column marked Expected that this is because the M+1 and M+2 peaks are smaller than the predicted
@@ -601,7 +601,7 @@ <h2>Basic understanding of a chromatographic landscape</h2>
         Skyline will show a pop-up that looks like:
     </p>
     <p>
-        <img src="image-24.png" />
+        <img src="s-22.png" />
     </p>
     <p>
         If you see only these three precursor transitions:
@@ -613,7 +613,7 @@ <h2>Basic understanding of a chromatographic landscape</h2>
         This causes Skyline to show all possible transitions for this peptide precursor:
     </p>
     <p>
-        <img src="image-25.png" />
+        <img src="s-23.png" />
     </p>
     <p>
         The green dots indicate the transitions for which Skyline already has chromatogram data. Skyline automatically extracts chromatograms for all
@@ -630,7 +630,7 @@ <h2>Basic understanding of a chromatographic landscape</h2>
         kind in Skyline.
     </p>
     <p>
-        <img src="image-26.png" />
+        <img src="s-24.png" />
     </p>
     <p>
         You can now feel fairly confident that the peak at 33 minutes is caused by another peptide of very similar elemental composition to the target
@@ -653,7 +653,7 @@ <h2>Inspecting the MS1 spectra</h2>
         This will cause Skyline to display the <b>Full Scan</b> view with a plot like the one below:
     </p>
     <p>
-        <img src="image-27.png" />
+        <img src="s-25.png" />
     </p>
     <ul>
         <li>Repeat this hover and click operation for the peak at 33.2 minutes.</li>
@@ -662,7 +662,7 @@ <h2>Inspecting the MS1 spectra</h2>
         The graph should change to something like this:
     </p>
     <p>
-        <img src="image-28.png" />
+        <img src="s-26.png" />
     </p>
     <p>
         The differences observed in the chromatograms should also be clear in these spectra.
@@ -677,11 +677,11 @@ <h2>Detecting and understanding interference</h2>
         <tr>
             <td class="comp-fig">
                 <b>5b_MCF7_TiTip3</b><br />
-                <img src="image-29.png" />
+                <img src="s-27.png" />
             </td>
             <td class="comp-fig">
                 <b>1_MCF7_TiB_L</b><br />
-                <img src="image-30.png" />
+                <img src="s-28.png" />
             </td>
         </tr>
     </table>
@@ -702,7 +702,7 @@ <h2>Detecting and understanding interference</h2>
         Da greater mass:
     </p>
     <p>
-        <img src="image-31.png" />
+        <img src="s-29.png" />
     </p>
     <ul>
         <li>Click the <b>Undo</b> button to revert this change and continue exploring.</li>
@@ -715,11 +715,11 @@ <h2>Detecting and understanding interference</h2>
         <tr>
             <td class="comp-fig">
                 <b>5b_MCF7_TiTip3</b><br />
-                <img src="image-32.png" />
+                <img src="s-30.png" />
             </td>
             <td class="comp-fig">
                 <b>1_MCF7_TiB_L</b><br />
-                <img src="image-33.png" />
+                <img src="s-31.png" />
             </td>
         </tr>
     </table>
@@ -731,11 +731,11 @@ <h2>Detecting and understanding interference</h2>
         <tr>
             <td class="comp-fig">
                 <b>5b_MCF7_TiTip3</b><br />
-                <img src="image-34.png" />
+                <img src="s-32.png" />
             </td>
             <td class="comp-fig">
                 <b>1_MCF7_TiB_L</b><br />
-                <img src="image-35.png" />
+                <img src="s-33.png" />
             </td>
         </tr>
     </table>
@@ -765,11 +765,11 @@ <h2>Differently modified forms of a peptide</h2>
         <tr>
             <td class="comp-fig">
                 <b>5b_MCF7_TiTip3</b><br />
-                <img src="image-36.png" />
+                <img src="s-34.png" />
             </td>
             <td class="comp-fig">
                 <b>1_MCF7_TiB_L</b><br />
-                <img src="image-37.png" />
+                <img src="s-35.png" />
             </td>
         </tr>
     </table>
@@ -790,14 +790,14 @@ <h2>More tools for data analysis</h2>
         idotp values of 1.0 and 0.99 with the expected distribution:
     </p>
     <p>
-        <img src="image-38.png" />
+        <img src="s-36.png" />
     </p>
     <p>
         Using the transition pick-list, as you have been doing, you can add the chromatograms for M+3 through M+7, all of which should contain greater
         than 1% of the entire isotope distribution, and see that the idotp values remain quite high at 0.98:
     </p>
     <p>
-        <img src="image-39.png" />
+        <img src="s-37.png" />
     </p>
     <p>
         In the chromatogram graphs, you can see that this is the only peptide in the document that was identified multiple times in a single run (3 in
@@ -819,7 +819,7 @@ <h2>More tools for data analysis</h2>
         The chromatogram graphs should now look like this:
     </p>
     <p>
-        <img src="image-40.png" />
+        <img src="s-38.png" />
     </p>
     <p>
         To see the isotope distribution in an MS1 spectrum from which the chromatogram points were extracted:
@@ -831,7 +831,7 @@ <h2>More tools for data analysis</h2>
         The <b>Full Scan</b> view will appear with a plot like this:
     </p>
     <p>
-        <img src="image-41.png" />
+        <img src="s-39.png" />
     </p>
     <ul>
         <li>Click the X in the upper right corner of the <b>Full Scan</b> view to close it.</li>
@@ -849,13 +849,13 @@ <h2>More tools for data analysis</h2>
         <b>5b_MCF7_TiTip3 (37.61 Min)</b>
     </p>
     <p>
-        <img src="image-42.png" />
+        <img src="s-40.png" />
     </p>
     <p class="keep-next">
         <b>1_MCF_TiB_L (37.03 min)</b>
     </p>
     <p>
-        <img src="image-43.png" />
+        <img src="s-41.png" />
     </p>
     <p>
         But you should feel pretty confident that the chromatogram peaks in the two runs measure the same peptide molecule.
@@ -868,11 +868,11 @@ <h2>More fun with interference</h2>
         <tr>
             <td class="comp-fig">
                 <b>5b_MCF7_TiTip3</b><br />
-                <img src="image-44.png" />
+                <img src="s-42.png" />
             </td>
             <td class="comp-fig">
                 <b>1_MCF7_TiB_L</b><br />
-                <img src="image-45.png" />
+                <img src="s-43.png" />
             </td>
         </tr>
     </table>
@@ -924,7 +924,7 @@ <h1>Minimizing a Chromatogram Cache File</h1>
         The <b>Minimize Results</b> form should now look like:
     </p>
     <p>
-        <img src="image-46.png" />
+        <img src="s-44.png" />
     </p>
     <p>
         The form indicates that this operation is expected to reduce the size of the cache file from about 947 KB to 49% of its current size, or about
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rename from pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/en/image-2.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/en/s-ms1-filtering-folder.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/en/image-7.png b/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/en/s-relative-abundance-graph.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/en/image-7.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/en/s-relative-abundance-graph.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/index.html b/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/index.html
index 041d2fe6a0..c4a4737220 100644
--- a/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/index.html
+++ b/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/index.html
@@ -103,7 +103,7 @@ <h1>DDA （data dependent acquisition: データ依存的取得）モードの
         以下のようなフォームが表示されます。
     </p>
     <p>
-        <img src="image-0.png" />
+        <img src="s-1.png" />
     </p>
     <p>
         このウィザードを使用して複数のペプチド検索エンジンの<br />1つからスペクトルライブラリを作成します。サポートされている検索パイプラインの詳細については「<a
@@ -121,7 +121,7 @@ <h1>DDA （data dependent acquisition: データ依存的取得）モードの
         ウィザードフォームは以下のようになります。
     </p>
     <p>
-        <img src="image-1.png" />
+        <img src="s-2.png" />
     </p>
     <ul>
         <li>[ <b>次へ</b> ] ボタンをクリックします。</li>
@@ -134,7 +134,7 @@ <h1>DDA （data dependent acquisition: データ依存的取得）モードの
         <li>すべての一致スペクトルを含むライブラリ（Redundant library）「MS1FilteringTutorial.redundant.blib」。</li>
     </ul>
     <p>
-        <img src="image-2.png" />
+        <img src="s-ms1-filtering-folder.png" />
     </p>
     <p>
         ファイル「MS1FilterTutorial.slc」も表示されます。 これはライブラリの読み込み時間を短縮するためのCacheファイルとなります。これは削除可能ですが必要であれば再度作成もできます。
@@ -146,7 +146,7 @@ <h1>DDA （data dependent acquisition: データ依存的取得）モードの
         ライブラリ構築が完了すると以下のように表示されます。
     </p>
     <p>
-        <img src="image-3.png" />
+        <img src="s-3.png" />
     </p>
     <p>
         この場合は自動的にライブラリ構築に利用したスペクトルのソースファイルと一致するWIFFデータファイルが見つかります。ライブラリにはMS/MSスペクトル同定の際に必要なクロマトグラムの保持時間情報（retention
@@ -159,7 +159,7 @@ <h1>DDA （data dependent acquisition: データ依存的取得）モードの
         2つのWIFFファイルに共通のプリフィックスをどう取り扱うかを尋ねるフォームが表示されます。
     </p>
     <p>
-        <img src="image-4.png" />
+        <img src="s-4.png" />
     </p>
     <ul>
         <li>[ <b>OK</b> ] ボタンをクリックします。</li>
@@ -176,7 +176,7 @@ <h1>DDA （data dependent acquisition: データ依存的取得）モードの
         (M)」（Methionine残基の酸化）のみです。リストでこれらのチェックをオンにすると、ウィザードは以下のようになります。
     </p>
     <p>
-        <img src="image-5.png" />
+        <img src="s-5.png" />
     </p>
     <p>
         ドキュメントによっては、いくつかの修飾（例: Oxidation (M)）がすでに定義済みで表示が異なる可能性があります。
@@ -194,7 +194,7 @@ <h1>DDA （data dependent acquisition: データ依存的取得）モードの
         このページの他のフィールドはデフォルト設定のままにしてください。ウィザードは以下のようになります。
     </p>
     <p>
-        <img src="image-6.png" />
+        <img src="s-6.png" />
     </p>
     <p>
         [ <b>MS1フィルタ</b> ]セクションのデフォルト設定は以下のようになります。
@@ -215,13 +215,13 @@ <h1>DDA （data dependent acquisition: データ依存的取得）モードの
         </table>
     </div>
     <p>
-        <img src="image-7.png" />
+        <img src="s-relative-abundance-graph.png" />
     </p>
     <p class="keep-next">
         Skylineに表示されるクロマトグラム（Extracted ion chromatogram）は各保持時間における選択されたフラグメントイオン（<i>m/z</i> 521.27）の強度となっています。
     </p>
     <p>
-        <img src="image-8.png" />
+        <img src="s-chromatogram.png" />
     </p>
     <p>
         [ <b>保持時間のフィルタ</b> ] セクションが[<b>MS/MS ID のスキャンの中で [5] 分前後のスキャンのもののみを使用</b> ]
@@ -244,7 +244,7 @@ <h1>DDA （data dependent acquisition: データ依存的取得）モードの
         ウィザードは以下のようになります。
     </p>
     <p>
-        <img src="image-9.png" />
+        <img src="s-7.png" />
     </p>
     <ul>
         <li>[ <b>完了</b> ] ボタンをクリックします。</li>
@@ -253,7 +253,7 @@ <h1>DDA （data dependent acquisition: データ依存的取得）モードの
         Skylineはコンピュータを使ってこのファイルにある11個のタンパク質を消化し、インポートしたペプチド検索結果での一致スペクトルを使ってFASTAファイルから50個のペプチドとペプチド価を持つ51個のプリカーサーの追加を提案します。
     </p>
     <p>
-        <img src="image-10.png" />
+        <img src="s-8.png" />
     </p>
     <ul>
         <li>[<b>タンパク質の関連付け</b> ] の[ <b>OK</b> ] ボタンをクリックします。</li>
@@ -265,7 +265,7 @@ <h1>DDA （data dependent acquisition: データ依存的取得）モードの
         進行状況は以下のように表示されます。
     </p>
     <p>
-        <img src="image-11.png" />
+        <img src="s-9.png" />
     </p>
     <p>
         インポートが完了したらクロマトグラムデータを吟味する前に、まず今回作成したスペクトルライブラリの詳細を見てみましょう。
@@ -285,7 +285,7 @@ <h2>ライブラリ保持時間の検証</h2>
         ここでライブラリでヒットしたタンパク質の修飾候補リストが表示されます。これらは [ <b>ペプチド検索のインポート</b> ] ウィザードではドキュメントに追加されてなかった修飾です。
     </p>
     <p>
-        <img src="image-12.png" />
+        <img src="s-10.png" />
     </p>
     <p>
         [ <b>スペクトルライブラリエクスプローラー</b> ] でこれらの修飾情報を使用するにしても[ <b>スペクトルライブラリエクスプローラー</b> ]
@@ -298,7 +298,7 @@ <h2>ライブラリ保持時間の検証</h2>
         [ <b>スペクトルライブラリエクスプローラー</b> ] は以下のように表示されます。
     </p>
     <p>
-        <img src="image-13.png" />
+        <img src="s-11.png" />
     </p>
     <p>
         ペプチドリストの中でシークエンス文字列の左側にアイコンの付いていないペプチドは<br />上記リストで選択しなかった修飾を含むペプチドになります。
@@ -334,7 +334,7 @@ <h1>ターゲットペプチドとそのクロマトグラム、MSスペクト
         Skylineドキュメントは以下のようになります。
     </p>
     <p>
-        <img src="image-14.png" />
+        <img src="s-12.png" />
     </p>
     <p>
         このドキュメントはMS1フィルタ向けの設定で、DDAモードでの測定結果2件がインポートされています。インポートウィザードで [ <b>MS/MSのIDの時間（5分）のスキャンのみを使用します</b>
@@ -351,7 +351,7 @@ <h1>ターゲットペプチドとそのクロマトグラム、MSスペクト
         <li>[ <b>ピーク面積</b> ] ウィンドウで右クリックし、[ <b>内積を表示</b> ] を選択し、[ <b>ラベル</b> ] をクリックします。</li>
     </ul>
     <p>
-        <img src="image-15.png" />
+        <img src="s-13.png" />
     </p>
     <p>
         以下の操作で[ <b>ピーク面積</b> ] ウィンドウを好きな場所にドッキングすることができます。
@@ -367,7 +367,7 @@ <h1>ターゲットペプチドとそのクロマトグラム、MSスペクト
         Skylineファイルは以下のようになります。
     </p>
     <p>
-        <img src="image-16.png" />
+        <img src="s-14.png" />
     </p>
     <p>
         クロマトグラム表示には、すべてのプリカーサーとその同位体イオンM（青）、M+1（紫）、M+2（赤茶）のMS1イオンクロマトグラム（Extracted ion
@@ -408,7 +408,7 @@ <h1>ターゲットペプチドとそのクロマトグラム、MSスペクト
         クロマトグラム表示は以下のようになります。
     </p>
     <p>
-        <img src="image-17.png" />
+        <img src="s-15.png" />
     </p>
     <p>
         保持時間アライメントがどのように動作しているのかを知るため、以下の操作を行います。
@@ -420,7 +420,7 @@ <h1>ターゲットペプチドとそのクロマトグラム、MSスペクト
         Skylineには以下のようなウィンドウが表示されます。
     </p>
     <p>
-        <img src="image-18.png" />
+        <img src="s-16.png" />
     </p>
     <p>
         このウィンドウに保持時間のアライメントに使用した線形回帰の（各測定間での）各ポイントが<br />表示されます。スペクトルライブラリ内の各スペクトルのソースファイルやその他すべてのスペクトルソースファイルからこのような線形回帰が計算されます。測定結果が2つ以上存在する場合ですが[
@@ -446,7 +446,7 @@ <h1>データの再確認（レビュー）</h1>
         Skylineウィンドウ右下にあるステータスバーで確認できます（下図の場合は4番目のペプチド（51個中）、4番目のプリカーサー（52個中）、10番目のトランジション（156個中）が選択されていることになります）。
     </p>
     <p>
-        <img src="image-19.png" />
+        <img src="s-17.png" />
     </p>
     <p>
         ペプチドISMSEVDLNVAAPKの下には、
@@ -461,11 +461,11 @@ <h2>クロマトグラフィー環境の基礎知識</h2>
         <tr>
             <td  class="comp-fig">
                 <b>5b_MCF7_TiTip3</b><br />
-                <img src="image-20.png" />
+                <img src="s-18.png" />
             </td>
             <td  class="comp-fig">
                 <b>1_MCF7_TiB_L</b><br />
-                <img src="image-21.png" />
+                <img src="s-19.png" />
             </td>
         </tr>
     </table>
@@ -473,7 +473,7 @@ <h2>クロマトグラフィー環境の基礎知識</h2>
         スクロールホイール（マウスホイール）で（手前にスクロール）、5b_MCF7_TiTip3のグラフと同じピークが見えるまで、1_MCF_TiB_Lのグラフをズームアウトします。
     </p>
     <p>
-        <img src="image-22.png" />
+        <img src="s-20.png" />
     </p>
     <p>
         これはクロマトグラフィーデータを扱う際に非常に重要なことです。ターゲットペプチドが一連の測定において毎回同じような時間に溶出すると予想されるますが、これは他のペプチドでも同じです。一方で、共溶出の可能性にも注意しましょう。ターゲット（37分）の両側（33分および40.5分）にある2つのピークは実は2つの他のペプチドによるピークとなりますが、もしターゲットペプチドと共溶出した場合には干渉を考慮せねばいけません。また逆に共溶出しない場合でも、他のペプチドの由来で再現性あるピークが、ピーク強度の低いターゲットペプチドの保持時間判別に役だつことがあります。クロマトグラム抽出範囲内に検出されるペプチドがより多くなるため、MS1フィルタのような選択性が低いメソッドでは特に効果を発揮します。
@@ -497,7 +497,7 @@ <h2>クロマトグラフィー環境の基礎知識</h2>
         Skylineはこれらのピークを選択し、[ <b>ピーク面積</b> ] のidotp値が以前に選択されたピークよりも低い（0.9および0.99に対して0.86および0.87）ことが表示されます。
     </p>
     <p>
-        <img src="image-23.png" />
+        <img src="s-21.png" />
     </p>
     <p>
         棒グラフ上の[ 期待値 ]分布をみるとM+1ピークとM+2ピークがターゲットペプチドに対して予測される同位体分布より小さいことがわかります。このピークのペプチドは、約37分にもMS/MS IDがあるターゲットペプチドより炭素数が少なく13Cの取り込み数が小さいためと予想されます。
@@ -518,7 +518,7 @@ <h2>クロマトグラフィー環境の基礎知識</h2>
         Skylineに以下のようなポップアップが表示されます。
     </p>
     <p>
-        <img src="image-24.png" />
+        <img src="s-22.png" />
     </p>
     <p>
         これら3つのプリカーサートランジションしか表示されない場合は以下の操作を行います。
@@ -530,7 +530,7 @@ <h2>クロマトグラフィー環境の基礎知識</h2>
         この操作でこのペプチドプリカーサーについて考えられるすべてのトランジションがSkylineに表示されます。
     </p>
     <p>
-        <img src="image-25.png" />
+        <img src="s-23.png" />
     </p>
     <p>
         緑の丸はクロマトグラムデータがSkylineに存在するトランジションを意味します。同位体分布があると予測されるピーク（すくなくても全体の1％以上のピークとなります）に対してクロマトグラムが自動的に抽出されます。また[M-1]のクロマトグラムも自動的に抽出されますが、干渉を受けていない正しく選択されたピークでは通常この<i>m/z</i>のシグナルは検出されません。
@@ -543,7 +543,7 @@ <h2>クロマトグラフィー環境の基礎知識</h2>
         これにより、M+3とM+4のクロマトグラムが追加表示され、33分のピークで37分のピークより多くのシグナルが表示されるようになります。Skylineでのあらゆるクロマトグラムデータ解析作業で保持時間再現性がどれだけ重要かは言うまでもありません。
     </p>
     <p>
-        <img src="image-26.png" />
+        <img src="s-24.png" />
     </p>
     <p>
         33分のピークはターゲットに非常によく似た元素組成の別のペプチドであり、モノアイソトピック質量が1ダルトン大きい3価のペプチド（M+3のデータから見て）であることがわかります。
@@ -563,7 +563,7 @@ <h2>MS1スペクトル精査</h2>
         Skyline上で以下のようなプロットの<b>フルスキャン</b>が表示されます。
     </p>
     <p>
-        <img src="image-27.png" />
+        <img src="s-25.png" />
     </p>
     <ul>
         <li>この操作を33.2分のピークについても同様に行います。</li>
@@ -572,7 +572,7 @@ <h2>MS1スペクトル精査</h2>
         表示が以下のように変化します。
     </p>
     <p>
-        <img src="image-28.png" />
+        <img src="s-26.png" />
     </p>
     <p>
         クロマトグラフで観測された違いもこのMSスペクトル上で明確になります。
@@ -585,11 +585,11 @@ <h2>干渉の検知と理解</h2>
         <tr>
             <td class="comp-fig">
                 <b>5b_MCF7_TiTip3</b><br />
-                <img src="image-29.png" />
+                <img src="s-27.png" />
             </td>
             <td class="comp-fig">
                 <b>1_MCF7_TiB_L</b><br />
-                <img src="image-30.png" />
+                <img src="s-28.png" />
             </td>
         </tr>
     </table>
@@ -604,7 +604,7 @@ <h2>干渉の検知と理解</h2>
         上記M+3とM+4の追加を利用すると、干渉ピークはおそらく質量が2 Da大きい3価ペプチドであろうと予想できます。
     </p>
     <p>
-        <img src="image-31.png" />
+        <img src="s-29.png" />
     </p>
     <ul>
         <li>[ <b>元に戻す</b> ] ボタンをクリックしてこの変更を元に戻します。</li>
@@ -616,11 +616,11 @@ <h2>干渉の検知と理解</h2>
         <tr>
             <td class="comp-fig">
                 <b>5b_MCF7_TiTip3</b><br />
-                <img src="image-32.png" />
+                <img src="s-30.png" />
             </td>
             <td class="comp-fig">
                 <b>1_MCF7_TiB_L</b><br />
-                <img src="image-33.png" />
+                <img src="s-31.png" />
             </td>
         </tr>
     </table>
@@ -631,11 +631,11 @@ <h2>干渉の検知と理解</h2>
         <tr>
             <td class="comp-fig">
                 <b>5b_MCF7_TiTip3</b><br />
-                <img src="image-34.png" />
+                <img src="s-32.png" />
             </td>
             <td class="comp-fig">
                 <b>1_MCF7_TiB_L</b><br />
-                <img src="image-35.png" />
+                <img src="s-33.png" />
             </td>
         </tr>
     </table>
@@ -657,11 +657,11 @@ <h2>翻訳後修飾が特殊なペプチドの解析</h2>
         <tr>
             <td class="comp-fig">
                 <b>5b_MCF7_TiTip3</b><br />
-                <img src="image-36.png" />
+                <img src="s-34.png" />
             </td>
             <td class="comp-fig">
                 <b>1_MCF7_TiB_L</b><br />
-                <img src="image-37.png" />
+                <img src="s-35.png" />
             </td>
         </tr>
     </table>
@@ -675,13 +675,13 @@ <h2>その他のデータ解析ツール</h2>
         ペプチド25まで下がっていくと、このドキュメントで最長かつ初めての4価のペプチドプリカーサーであるYGPADVEDTTGSGATDSKDDDDIDLFG<b><u>S</u></b>DDEEESEEAKRが見つかります。このペプチドは非常に大きく、その同位体分布も今まで見てきた典型的な2価のペプチドや3価ペプチドとかなり異なります。この場合13C原子取り込みのないモノアイソトピックペプチドM+はM+1やM+2よりも存在率が低くなると予測できます。実際クロマトグラムでも予測される分布のidotp値が1.0および0.99になっています。
     </p>
     <p>
-        <img src="image-38.png" />
+        <img src="s-36.png" />
     </p>
     <p>
         今までと同じようにトランジション選択リストを利用し、M+3からM+7までのクロマトグラムを追加します。これらのイオンはすべて同位体分布全体で1%以上となっており、idotp値も高めの0.98であることがわかります。
     </p>
     <p>
-        <img src="image-39.png" />
+        <img src="s-37.png" />
     </p>
     <p>
         （クロマトグラムグラフをみると）このペプチドは本ドキュメント内で唯一、1回の測定で複数回検出、同定されたものであることがわかります（5b_MCF7_TiTip3において3回）。
@@ -701,7 +701,7 @@ <h2>その他のデータ解析ツール</h2>
         クロマトグラムは以下のようになります。
     </p>
     <p>
-        <img src="image-40.png" />
+        <img src="s-38.png" />
     </p>
     <p>
         クロマトグラフの抽出元MS1スペクトル内の同位体分布を確認するため以下の操作を行います。
@@ -713,7 +713,7 @@ <h2>その他のデータ解析ツール</h2>
         以下のプロットで[ <b>フルスキャン</b> ]ビューが表示されます。
     </p>
     <p>
-        <img src="image-41.png" />
+        <img src="s-39.png" />
     </p>
     <ul>
         <li>[ <b>フルスキャン</b> ] 表示の右上隅のXをクリックし表示を閉じます。</li>
@@ -729,13 +729,13 @@ <h2>その他のデータ解析ツール</h2>
         <b>5b_MCF7_TiTip3（37.61分）</b>
     </p>
     <p>
-        <img src="image-42.png" />
+        <img src="s-40.png" />
     </p>
     <p class="keep-next">
         <b>1_MCF_TiB_L（37.03分）</b>
     </p>
     <p>
-        <img src="image-43.png" />
+        <img src="s-41.png" />
     </p>
     <p>
         ただし、2つの測定のクロマトグラムピークは同一のペプチド分子を測定していると大いに確信できるはずです。
@@ -748,11 +748,11 @@ <h2>干渉に関する詳細</h2>
         <tr>
             <td class="comp-fig">
                 <b>5b_MCF7_TiTip3</b><br />
-                <img src="image-44.png" />
+                <img src="s-42.png" />
             </td>
             <td class="comp-fig">
                 <b>1_MCF7_TiB_L</b><br />
-                <img src="image-45.png" />
+                <img src="s-43.png" />
             </td>
         </tr>
     </table>
@@ -796,7 +796,7 @@ <h1>クロマトグラムキャッシュファイルの最小化</h1>
         [ <b>結果を最小化</b> ] フォームは以下のようになります。
     </p>
     <p>
-        <img src="image-46.png" />
+        <img src="s-44.png" />
     </p>
     <p>
         フォームはこの操作によってキャッシュファイルのサイズが約947KBから約464KB、つまり現在のサイズの49%に縮小される見込みであることを示します。
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/invariant.html b/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/invariant.html
index cbef36ba1f..e627f13b8f 100644
--- a/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/invariant.html
+++ b/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/invariant.html
@@ -112,7 +112,7 @@ <h1>Importing a Data Dependent Peptide Search into a Skyline Document</h1>
         Skyline should present a form that looks like this:
     </p>
     <p>
-        <img src="image-0.png" />
+        <img src="s-1.png" />
     </p>
     <p>
         Next, you will use this wizard to create a spectral library from the output of one of the many peptide search engines supported by Skyline. For
@@ -133,7 +133,7 @@ <h1>Importing a Data Dependent Peptide Search into a Skyline Document</h1>
         The wizard form should now look like this:
     </p>
     <p>
-        <img src="image-1.png" />
+        <img src="s-2.png" />
     </p>
     <ul>
         <li>Click the <b>Next</b> button.</li>
@@ -147,7 +147,7 @@ <h1>Importing a Data Dependent Peptide Search into a Skyline Document</h1>
         <li>The redundant library called “MS1FilteringTutorial.redundant.blib” containing all matching spectra.</li>
     </ul>
     <p>
-        <img src="image-2.png" />
+        <img src="s-ms1-filtering-folder.png" />
     </p>
     <p>
         You may also find a file ‘MS1FilterTutorial.slc’, which is a ‘Skyline Library Cache’ file to improve library load time. It can be deleted, and
@@ -163,7 +163,7 @@ <h1>Importing a Data Dependent Peptide Search into a Skyline Document</h1>
         When library building has completed, Skyline will present the next page in the wizard as shown below:
     </p>
     <p>
-        <img src="image-3.png" />
+        <img src="s-3.png" />
     </p>
     <p>
         In this case, Skyline has found original WIFF data files matching the spectrum source files used to build your library, and the library appears
@@ -180,7 +180,7 @@ <h1>Importing a Data Dependent Peptide Search into a Skyline Document</h1>
         A form should appear asking you how to handle the prefix shared by the two WIFF files:
     </p>
     <p>
-        <img src="image-4.png" />
+        <img src="s-4.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -198,7 +198,7 @@ <h1>Importing a Data Dependent Peptide Search into a Skyline Document</h1>
         and the wizard should look like this:
     </p>
     <p>
-        <img src="image-5.png" />
+        <img src="s-5.png" />
     </p>
     <p>
         It is possible that your document will already have one or more of these modifications defined (e.g. Oxidation (M)), in which case the list
@@ -218,7 +218,7 @@ <h1>Importing a Data Dependent Peptide Search into a Skyline Document</h1>
         this:
     </p>
     <p>
-        <img src="image-6.png" />
+        <img src="s-6.png" />
     </p>
     <p>
         In the <b>MS1 filtering</b> section, you will see the following default settings.
@@ -243,13 +243,13 @@ <h1>Importing a Data Dependent Peptide Search into a Skyline Document</h1>
         </table>
     </div>
     <p>
-        <img src="image-7.png" />
+        <img src="s-relative-abundance-graph.png" />
     </p>
     <p class="keep-next">
         A series of these intensities extracted over time make up the chromatograms you will see in Skyline:
     </p>
     <p>
-        <img src="image-8.png" />
+        <img src="s-chromatogram.png" />
     </p>
     <p>
         In the <b>Retention time filtering</b> section, note the choice to <b>Use only scans within [5] minutes of MS/MS IDs</b>.
@@ -276,7 +276,7 @@ <h1>Importing a Data Dependent Peptide Search into a Skyline Document</h1>
         The wizard should now look like this:
     </p>
     <p>
-        <img src="image-9.png" />
+        <img src="s-7.png" />
     </p>
     <ul>
         <li>Click the <b>Finish</b> button.</li>
@@ -286,7 +286,7 @@ <h1>Importing a Data Dependent Peptide Search into a Skyline Document</h1>
         FASTA file with matching spectra in the peptide search results which you imported.
     </p>
     <p>
-        <img src="image-10.png" />
+        <img src="s-8.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button in the <b>Associate Proteins</b> form.</li>
@@ -298,7 +298,7 @@ <h1>Importing a Data Dependent Peptide Search into a Skyline Document</h1>
         You should see a progress graph like this:
     </p>
     <p>
-        <img src="image-11.png" />
+        <img src="s-9.png" />
     </p>
     <p>
         Once the import has completed, first have an in-depth look at the spectral library you created before inspecting the chromatogram data.
@@ -322,7 +322,7 @@ <h2>Verifying Library Retention Time Information</h2>
         during the <b>Import Peptide Search</b> wizard.
     </p>
     <p>
-        <img src="image-12.png" />
+        <img src="s-10.png" />
     </p>
     <p>
         Choosing to use them now in the <b>Spectral Library Explorer</b> will not add them to the current document unless you use the
@@ -336,7 +336,7 @@ <h2>Verifying Library Retention Time Information</h2>
         The <b>Spectral Library Explorer</b> will appear, looking something like this:
     </p>
     <p>
-        <img src="image-13.png" />
+        <img src="s-11.png" />
     </p>
     <p>
         In the peptide list, the peptides without an icon to the left of the sequence text are ones that contain any of the modifications you just
@@ -381,7 +381,7 @@ <h1>Peptide Targets, Spectra and Chromatograms</h1>
         Your Skyline document should look like the following:
     </p>
     <p>
-        <img src="image-14.png" />
+        <img src="s-12.png" />
     </p>
     <p>
         The document is now fully configured for MS1 Filtering with two DDA runs imported. You will see that the chromatogram in this view is
@@ -401,7 +401,7 @@ <h1>Peptide Targets, Spectra and Chromatograms</h1>
         <li>In the <b>Peak Areas</b> window, right-click, choose <b>Show Dot Product</b>, and click <b>Labels</b>.</li>
     </ul>
     <p>
-        <img src="image-15.png" />
+        <img src="s-13.png" />
     </p>
     <p>
         You can dock the <b>Peak Areas</b> window to your desired location by doing the following:
@@ -418,7 +418,7 @@ <h1>Peptide Targets, Spectra and Chromatograms</h1>
         Your Skyline file should look something like this:
     </p>
     <p>
-        <img src="image-16.png" />
+        <img src="s-14.png" />
     </p>
     <p>
         The chromatogram views show the MS1 extracted ion chromatogram for all precursor isotope ions M (blue), M+1 (purple), M+2 (brown). Below the
@@ -468,7 +468,7 @@ <h1>Peptide Targets, Spectra and Chromatograms</h1>
         The chromatogram graphs should look something like this:
     </p>
     <p>
-        <img src="image-17.png" />
+        <img src="s-15.png" />
     </p>
     <p>
         To gain some insight into how the retention time alignment works, do the following:
@@ -480,7 +480,7 @@ <h1>Peptide Targets, Spectra and Chromatograms</h1>
         Skyline will present a window that looks like this:
     </p>
     <p>
-        <img src="image-18.png" />
+        <img src="s-16.png" />
     </p>
     <p>
         This window shows you the points for a linear regression used to align times between runs. Skyline calculates a linear regression like this
@@ -517,7 +517,7 @@ <h1>Reviewing the Data</h1>
         out of the 50 is currently selected, you can look in the status bar at the bottom right of the Skyline window:
     </p>
     <p>
-        <img src="image-19.png" />
+        <img src="s-17.png" />
     </p>
     <p>
         After the peptide I<b><u>S</u></b>MSEVDLNVAAPK, you will see 4 peptides with acceptable peak integration, though
@@ -533,11 +533,11 @@ <h2>Basic understanding of a chromatographic landscape</h2>
         <tr>
             <td  class="comp-fig">
                 <b>5b_MCF7_TiTip3</b><br />
-                <img src="image-20.png" />
+                <img src="s-18.png" />
             </td>
             <td  class="comp-fig">
                 <b>1_MCF7_TiB_L</b><br />
-                <img src="image-21.png" />
+                <img src="s-19.png" />
             </td>
         </tr>
     </table>
@@ -546,7 +546,7 @@ <h2>Basic understanding of a chromatographic landscape</h2>
         see in the 5b_MCF7_TiTip3 graph:
     </p>
     <p>
-        <img src="image-22.png" />
+        <img src="s-20.png" />
     </p>
     <p>
         This is an extremely important aspect of working with chromatographic data: just as your target peptides can be expected to elute at highly
@@ -579,7 +579,7 @@ <h2>Basic understanding of a chromatographic landscape</h2>
         previously selected peaks (0.86 and 0.87 versus 0.9 and 0.99):
     </p>
     <p>
-        <img src="image-23.png" />
+        <img src="s-21.png" />
     </p>
     <p>
         You can see from the distribution in the column marked Expected that this is because the M+1 and M+2 peaks are smaller than the predicted
@@ -604,7 +604,7 @@ <h2>Basic understanding of a chromatographic landscape</h2>
         Skyline will show a pop-up that looks like:
     </p>
     <p>
-        <img src="image-24.png" />
+        <img src="s-22.png" />
     </p>
     <p>
         If you see only these three precursor transitions:
@@ -616,7 +616,7 @@ <h2>Basic understanding of a chromatographic landscape</h2>
         This causes Skyline to show all possible transitions for this peptide precursor:
     </p>
     <p>
-        <img src="image-25.png" />
+        <img src="s-23.png" />
     </p>
     <p>
         The green dots indicate the transitions for which Skyline already has chromatogram data. Skyline automatically extracts chromatograms for all
@@ -633,7 +633,7 @@ <h2>Basic understanding of a chromatographic landscape</h2>
         kind in Skyline.
     </p>
     <p>
-        <img src="image-26.png" />
+        <img src="s-24.png" />
     </p>
     <p>
         You can now feel fairly confident that the peak at 33 minutes is caused by another peptide of very similar elemental composition to the target
@@ -656,7 +656,7 @@ <h2>Inspecting the MS1 spectra</h2>
         This will cause Skyline to display the <b>Full Scan</b> view with a plot like the one below:
     </p>
     <p>
-        <img src="image-27.png" />
+        <img src="s-25.png" />
     </p>
     <ul>
         <li>Repeat this hover and click operation for the peak at 33.2 minutes.</li>
@@ -665,7 +665,7 @@ <h2>Inspecting the MS1 spectra</h2>
         The graph should change to something like this:
     </p>
     <p>
-        <img src="image-28.png" />
+        <img src="s-26.png" />
     </p>
     <p>
         The differences observed in the chromatograms should also be clear in these spectra.
@@ -680,11 +680,11 @@ <h2>Detecting and understanding interference</h2>
         <tr>
             <td class="comp-fig">
                 <b>5b_MCF7_TiTip3</b><br />
-                <img src="image-29.png" />
+                <img src="s-27.png" />
             </td>
             <td class="comp-fig">
                 <b>1_MCF7_TiB_L</b><br />
-                <img src="image-30.png" />
+                <img src="s-28.png" />
             </td>
         </tr>
     </table>
@@ -705,7 +705,7 @@ <h2>Detecting and understanding interference</h2>
         Da greater mass:
     </p>
     <p>
-        <img src="image-31.png" />
+        <img src="s-29.png" />
     </p>
     <ul>
         <li>Click the <b>Undo</b> button to revert this change and continue exploring.</li>
@@ -718,11 +718,11 @@ <h2>Detecting and understanding interference</h2>
         <tr>
             <td class="comp-fig">
                 <b>5b_MCF7_TiTip3</b><br />
-                <img src="image-32.png" />
+                <img src="s-30.png" />
             </td>
             <td class="comp-fig">
                 <b>1_MCF7_TiB_L</b><br />
-                <img src="image-33.png" />
+                <img src="s-31.png" />
             </td>
         </tr>
     </table>
@@ -734,11 +734,11 @@ <h2>Detecting and understanding interference</h2>
         <tr>
             <td class="comp-fig">
                 <b>5b_MCF7_TiTip3</b><br />
-                <img src="image-34.png" />
+                <img src="s-32.png" />
             </td>
             <td class="comp-fig">
                 <b>1_MCF7_TiB_L</b><br />
-                <img src="image-35.png" />
+                <img src="s-33.png" />
             </td>
         </tr>
     </table>
@@ -768,11 +768,11 @@ <h2>Differently modified forms of a peptide</h2>
         <tr>
             <td class="comp-fig">
                 <b>5b_MCF7_TiTip3</b><br />
-                <img src="image-36.png" />
+                <img src="s-34.png" />
             </td>
             <td class="comp-fig">
                 <b>1_MCF7_TiB_L</b><br />
-                <img src="image-37.png" />
+                <img src="s-35.png" />
             </td>
         </tr>
     </table>
@@ -793,14 +793,14 @@ <h2>More tools for data analysis</h2>
         idotp values of 1.0 and 0.99 with the expected distribution:
     </p>
     <p>
-        <img src="image-38.png" />
+        <img src="s-36.png" />
     </p>
     <p>
         Using the transition pick-list, as you have been doing, you can add the chromatograms for M+3 through M+7, all of which should contain greater
         than 1% of the entire isotope distribution, and see that the idotp values remain quite high at 0.98:
     </p>
     <p>
-        <img src="image-39.png" />
+        <img src="s-37.png" />
     </p>
     <p>
         In the chromatogram graphs, you can see that this is the only peptide in the document that was identified multiple times in a single run (3 in
@@ -822,7 +822,7 @@ <h2>More tools for data analysis</h2>
         The chromatogram graphs should now look like this:
     </p>
     <p>
-        <img src="image-40.png" />
+        <img src="s-38.png" />
     </p>
     <p>
         To see the isotope distribution in an MS1 spectrum from which the chromatogram points were extracted:
@@ -834,7 +834,7 @@ <h2>More tools for data analysis</h2>
         The <b>Full Scan</b> view will appear with a plot like this:
     </p>
     <p>
-        <img src="image-41.png" />
+        <img src="s-39.png" />
     </p>
     <ul>
         <li>Click the X in the upper right corner of the <b>Full Scan</b> view to close it.</li>
@@ -852,13 +852,13 @@ <h2>More tools for data analysis</h2>
         <b>5b_MCF7_TiTip3 (37.61 Min)</b>
     </p>
     <p>
-        <img src="image-42.png" />
+        <img src="s-40.png" />
     </p>
     <p class="keep-next">
         <b>1_MCF_TiB_L (37.03 min)</b>
     </p>
     <p>
-        <img src="image-43.png" />
+        <img src="s-41.png" />
     </p>
     <p>
         But you should feel pretty confident that the chromatogram peaks in the two runs measure the same peptide molecule.
@@ -871,11 +871,11 @@ <h2>More fun with interference</h2>
         <tr>
             <td class="comp-fig">
                 <b>5b_MCF7_TiTip3</b><br />
-                <img src="image-44.png" />
+                <img src="s-42.png" />
             </td>
             <td class="comp-fig">
                 <b>1_MCF7_TiB_L</b><br />
-                <img src="image-45.png" />
+                <img src="s-43.png" />
             </td>
         </tr>
     </table>
@@ -927,7 +927,7 @@ <h1>Minimizing a Chromatogram Cache File</h1>
         The <b>Minimize Results</b> form should now look like:
     </p>
     <p>
-        <img src="image-46.png" />
+        <img src="s-44.png" />
     </p>
     <p>
         The form indicates that this operation is expected to reduce the size of the cache file from about 947 KB to 49% of its current size, or about
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/image-0.png b/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/s-1.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/image-0.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/s-1.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/image-12.png b/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/s-10.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/image-12.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/s-10.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/image-13.png b/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/s-11.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/image-13.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/s-11.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/image-14.png b/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/s-12.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/image-14.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/s-12.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/image-15.png b/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/s-13.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/image-15.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/s-13.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/image-16.png b/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/s-14.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/image-16.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/s-14.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/image-17.png b/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/s-15.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/image-17.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/s-15.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/image-18.png b/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/s-16.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/image-18.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/s-16.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/image-19.png b/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/s-17.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/image-19.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/s-17.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/image-20.png b/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/s-18.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/image-20.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/s-18.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/image-21.png b/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/s-19.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/image-21.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/s-19.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/image-1.png b/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/s-2.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/image-1.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/s-2.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/image-22.png b/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/s-20.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/image-22.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/s-20.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/image-23.png b/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/s-21.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/image-25.png b/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/s-23.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/image-26.png b/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/s-24.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/image-27.png b/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/s-25.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/image-28.png b/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/s-26.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/image-29.png b/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/s-27.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/image-30.png b/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/s-28.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/image-31.png b/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/s-29.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/image-3.png b/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/s-3.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/image-32.png b/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/s-30.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/image-33.png b/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/s-31.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/image-34.png b/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/s-32.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/image-35.png b/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/s-33.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/image-36.png b/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/s-34.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/image-37.png b/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/s-35.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/image-38.png b/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/s-36.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/image-39.png b/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/s-37.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/image-41.png b/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/s-39.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/image-4.png b/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/s-4.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/image-42.png b/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/s-40.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/image-43.png b/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/s-41.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/image-44.png b/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/s-42.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/image-45.png b/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/s-43.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/image-46.png b/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/s-44.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/image-5.png b/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/s-5.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/image-6.png b/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/s-6.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/image-9.png b/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/s-7.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/image-10.png b/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/s-8.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/image-11.png b/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/s-9.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/image-8.png b/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/s-chromatogram.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/image-2.png b/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/s-ms1-filtering-folder.png
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rename to pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/s-ms1-filtering-folder.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/image-7.png b/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/s-relative-abundance-graph.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/ja/image-7.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/zh-CHS/index.html b/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/zh-CHS/index.html
index 1995f5435b..06926e65b2 100644
--- a/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/zh-CHS/index.html
+++ b/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/zh-CHS/index.html
@@ -102,7 +102,7 @@ <h1>将数据依赖型肽段搜索结果导入 Skyline 文档</h1>
         Skyline 将呈现如下所示的表单：
     </p>
     <p>
-        <img src="image-0.png" />
+        <img src="s-1.png" />
     </p>
     <p>
         接下来，您就可以使用本向导从Skyline可支持的诸多肽段搜索引擎的输出结果来创建一个谱图库。关于受支持的搜索管道的完整列表，请参考<a
@@ -121,7 +121,7 @@ <h1>将数据依赖型肽段搜索结果导入 Skyline 文档</h1>
         此时向导表单将显示如下：
     </p>
     <p>
-        <img src="image-1.png" />
+        <img src="s-2.png" />
     </p>
     <ul>
         <li>单击<b>下一步</b>按钮。</li>
@@ -134,7 +134,7 @@ <h1>将数据依赖型肽段搜索结果导入 Skyline 文档</h1>
         <li>包含所有匹配谱图的冗余库“MS1FilteringTutorial.redundant.blib”。</li>
     </ul>
     <p>
-        <img src="image-2.png" />
+        <img src="s-ms1-filtering-folder.png" />
     </p>
     <p>
         您还可以看到文件“MS1FilterTutorial.slc”，这是一个旨在改善库的加载时间的“Skyline 库缓存”文件。您可以将其删除，必要时 Skyline 会重新创建此文件。
@@ -147,7 +147,7 @@ <h1>将数据依赖型肽段搜索结果导入 Skyline 文档</h1>
         创建完库后，Skyline 将显示向导中的下一页，如下所示：
     </p>
     <p>
-        <img src="image-3.png" />
+        <img src="s-3.png" />
     </p>
     <p>
         在这种情况下，Skyline 已找到了与用于创建谱图库所使用的与源文件相匹配的原始 WIFF数据 文件，并且谱图库似乎包含了保留时间信息。该信息是 Skyline 将鉴定的串联质谱谱图定位于其即将提取的色谱上所需要的。如果 Skyline
@@ -160,7 +160,7 @@ <h1>将数据依赖型肽段搜索结果导入 Skyline 文档</h1>
         此时将显示一个表单，询问您如何处理这两个 WIFF 文件的相同前缀：
     </p>
     <p>
-        <img src="image-4.png" />
+        <img src="s-4.png" />
     </p>
     <ul>
         <li>单击<b>确定</b>按钮。</li>
@@ -172,7 +172,7 @@ <h1>将数据依赖型肽段搜索结果导入 Skyline 文档</h1>
         在本教程中，您只需要“Phospho (ST)”、“Phospho (Y)”和“Oxidation (M)”修饰。在列表中选中这些修饰，向导应显示如下：
     </p>
     <p>
-        <img src="image-5.png" />
+        <img src="s-5.png" />
     </p>
     <p>
         您的文档可能已有其中一个或多个已定义的修饰（例如 Oxidation (M)），这种情况下列表看起来可能会有所不同。
@@ -190,7 +190,7 @@ <h1>将数据依赖型肽段搜索结果导入 Skyline 文档</h1>
         本页面中所有其它字段应设置为默认值，向导显示如下：
     </p>
     <p>
-        <img src="image-6.png" />
+        <img src="s-6.png" />
     </p>
     <p>
         在 <b>MS1 筛选</b>部分中，您将看到下列默认设置。
@@ -210,13 +210,13 @@ <h1>将数据依赖型肽段搜索结果导入 Skyline 文档</h1>
         </table>
     </div>
     <p>
-        <img src="image-7.png" />
+        <img src="s-relative-abundance-graph.png" />
     </p>
     <p class="keep-next">
         在某一时间范围内提取的一系列强度将构成您在 Skyline 中看到的色谱图：
     </p>
     <p>
-        <img src="image-8.png" />
+        <img src="s-chromatogram.png" />
     </p>
     <p>
         在<b>保留时间筛选</b>部分，注意选择<b>仅使用 MS/MS ID 5 分钟之内的扫描</b>。这表明，对于只具有 1 个 ID 的肽段，Skyline 将围绕此 ID 提取 10 分钟的色谱图。对 3 分钟以上范围的一组
@@ -239,7 +239,7 @@ <h1>将数据依赖型肽段搜索结果导入 Skyline 文档</h1>
         此时向导将显示如下：
     </p>
     <p>
-        <img src="image-9.png" />
+        <img src="s-7.png" />
     </p>
     <ul>
         <li>单击<b>完成</b>按钮。</li>
@@ -248,7 +248,7 @@ <h1>将数据依赖型肽段搜索结果导入 Skyline 文档</h1>
         Skyline 将模拟消化此文件中的 11 个蛋白质，并建议从您导入的具有肽段搜索结果中的匹配谱图的 FASTA 文件中添加 50 个肽段和 51 个肽段电荷态母离子。
     </p>
     <p>
-        <img src="image-10.png" />
+        <img src="s-8.png" />
     </p>
     <ul>
         <li>单击<b>关联蛋白质</b>表单中的<b>确定</b>按钮。</li>
@@ -260,7 +260,7 @@ <h1>将数据依赖型肽段搜索结果导入 Skyline 文档</h1>
         您将看到如下所示的进度图：
     </p>
     <p>
-        <img src="image-11.png" />
+        <img src="s-9.png" />
     </p>
     <p>
         导入完成后，在检验色谱图数据前先仔细检查您创建的谱图库。
@@ -280,7 +280,7 @@ <h2>验证谱图库保留时间信息</h2>
         Skyline 将再次提出使用在谱图库中检测到的但在<b>导入肽段搜索</b>向导中您选择不添加的修饰。
     </p>
     <p>
-        <img src="image-12.png" />
+        <img src="s-10.png" />
     </p>
     <p>
         现在选择在<b>谱图库浏览器</b>中使用这些修饰并不会将其加入目前的文档，除非您使用<b>谱图库浏览器</b>将使用这些修饰的肽段添加到您的文档。但是，这些修饰对于本教程并不重要。您可以执行下列操作，在不使用这些修饰的情况下继续本教程：
@@ -292,7 +292,7 @@ <h2>验证谱图库保留时间信息</h2>
         将出现如下所示的<b>谱图库浏览器</b>：
     </p>
     <p>
-        <img src="image-13.png" />
+        <img src="s-11.png" />
     </p>
     <p>
         在肽段列表中，序列文本左侧没有图标的肽段包含有您未选择使用的某种修饰。
@@ -327,7 +327,7 @@ <h1>肽段目标、谱图和色谱图</h1>
         您的 Skyline 文档将显示如下：
     </p>
     <p>
-        <img src="image-14.png" />
+        <img src="s-12.png" />
     </p>
     <p>
         现在文档已通过所导入的两项 DDA 运行完成了 MS1 筛选的全部配置。由于在导入向导中选择了<b>仅使用 MS/MS ID 5 分钟之内的扫描</b>设置，本视图中的色谱图长度约为 10 分钟（31 至 41 分钟）。请注意，在为 MS1 筛选进行 Skyline
@@ -344,7 +344,7 @@ <h1>肽段目标、谱图和色谱图</h1>
         <li>在<b>峰面积</b>窗口中单击右键，选择<b>显示点积</b>，然后单击<b>标签</b>。</li>
     </ul>
     <p>
-        <img src="image-15.png" />
+        <img src="s-13.png" />
     </p>
     <p>
         您可以通过下列操作将<b>峰面积</b>窗口停靠在您需要的位置：
@@ -359,7 +359,7 @@ <h1>肽段目标、谱图和色谱图</h1>
         您的 Skyline 文件将显示如下：
     </p>
     <p>
-        <img src="image-16.png" />
+        <img src="s-14.png" />
     </p>
     <p>
         色谱图视图显示了所有母离子同位素离子的 MS1 提取离子色谱图，包括 M（蓝色）、M+1（紫色）、M+2（棕色）。如果您使用过 Skyline 对 SRM
@@ -398,7 +398,7 @@ <h1>肽段目标、谱图和色谱图</h1>
         色谱图将显示如下：
     </p>
     <p>
-        <img src="image-17.png" />
+        <img src="s-15.png" />
     </p>
     <p>
         为深入了解保留时间校准的工作原理，请执行下列操作：
@@ -410,7 +410,7 @@ <h1>肽段目标、谱图和色谱图</h1>
         Skyline 将呈现如下所示的窗口：
     </p>
     <p>
-        <img src="image-18.png" />
+        <img src="s-16.png" />
     </p>
     <p>
         此窗口显示运行之间用于校准时间的线性回归点。Skyline 会计算谱图库中两两谱图源文件间这样的线性回归。当出现 2 个以上的运行时，会看到<b>针对以下目标校准重复测定</b>下拉列表中选定的运行以外的运行各占据一行。当某个运行中缺少对应 ID
@@ -436,7 +436,7 @@ <h1>审查数据</h1>
         在有了基本的了解并且按此方法配置 Skyline后，您现在可以快速审查本文档中的所有 50 个肽段。您只需要单击<b>目标</b>视图，并使用向下键依次选中每一个肽段。要了解目前从 50 个肽段中被选中的肽段数，可以查看 Skyline 窗口右下方的状态栏：
     </p>
     <p>
-        <img src="image-19.png" />
+        <img src="s-17.png" />
     </p>
     <p>
         在肽段 I<b><u>S</u></b>MSEVDLNVAAPK 后面，可以看到有 4 个含有可接受整合峰的肽段，它们进行峰整合是可以接受的，虽然 VSVGAPDLSLEA<b><u>S</u></b>EGSIKLPK
@@ -450,11 +450,11 @@ <h2>对色谱图的基本认识</h2>
         <tr>
             <td  class="comp-fig">
                 <b>5b_MCF7_TiTip3</b><br />
-                <img src="image-20.png" />
+                <img src="s-18.png" />
             </td>
             <td  class="comp-fig">
                 <b>1_MCF7_TiB_L</b><br />
-                <img src="image-21.png" />
+                <img src="s-19.png" />
             </td>
         </tr>
     </table>
@@ -462,7 +462,7 @@ <h2>对色谱图的基本认识</h2>
         使用鼠标上的滚轮（朝您自己回滚）缩小 1_MCF_TiB_L 图，直至能看到与 5b_MCF7_TiTip3 图相同的峰：
     </p>
     <p>
-        <img src="image-22.png" />
+        <img src="s-20.png" />
     </p>
     <p>
         这是处理色谱图数据的一个极其重要的方面：正如您的目标肽段可以在多个运行中以高度相似的时间被洗脱出来，其它肽段也如此。目标（37 分钟）两侧（33.1 分钟和 40.5
@@ -488,7 +488,7 @@ <h2>对色谱图的基本认识</h2>
         这步操作会使得 Skyline 挑选这些峰，并在<b>峰面积</b>图中显示它们的 idotp 值低于此前选择的峰（0.86 和 0.87，而此前为 0.9 和 0.99）：
     </p>
     <p>
-        <img src="image-23.png" />
+        <img src="s-21.png" />
     </p>
     <p>
         您可以查看标示“预期的”色谱柱中的分布，因为 M+2 和 M+3 同位峰比目标肽段的预期同位素分布强度小，这表明产生此峰的肽段中碳原子比目标肽段中的少（因此产生 13C 的机会较小），而目标肽段采用的是大约 37 分钟时的一个串联质谱ID。
@@ -509,7 +509,7 @@ <h2>对色谱图的基本认识</h2>
         Skyline 将弹出如下所示的窗口：
     </p>
     <p>
-        <img src="image-24.png" />
+        <img src="s-22.png" />
     </p>
     <p>
         如果仅看到这三个母离子离子对：
@@ -521,7 +521,7 @@ <h2>对色谱图的基本认识</h2>
         这样 Skyline 就会显示此肽段母离子所有可能的离子对：
     </p>
     <p>
-        <img src="image-25.png" />
+        <img src="s-23.png" />
     </p>
     <p>
         绿色虚线表示 Skyline 已获得色谱图数据的离子对。Skyline 自动提取同位素分布中所有峰的色谱图，预计至少占据整个分布的 1%。此外，Skyline 始终提取 M-1 的色谱图，因为在该<i>质荷比</i>下，没有干扰的挑选正确的峰一般不会产生信号。
@@ -534,7 +534,7 @@ <h2>对色谱图的基本认识</h2>
         这项操作将在图中增加 M+3 和 M+4 的色谱图，您将看到在 33 分钟处峰信号强度高于 37 分钟处鉴定的峰。在使用 Skyline 处理任何类型的色谱图数据时，可靠的保留时间重复性的作用相当重要，其重要性无论怎么强调也不为过。
     </p>
     <p>
-        <img src="image-26.png" />
+        <img src="s-24.png" />
     </p>
     <p>
         您现在可以相当确信，33 分钟时的峰确由另一种肽段产生，其原子组成与目标肽段非常相似，同时也带有三个电荷，不同之处仅仅在于其单一同位素峰质量比目标的大 1 Dalton。
@@ -554,7 +554,7 @@ <h2>检查 MS1 谱图</h2>
         这样 Skyline 就会显示<b>全扫描</b>视图，显示如下：
     </p>
     <p>
-        <img src="image-27.png" />
+        <img src="s-25.png" />
     </p>
     <ul>
         <li>重复悬停和单击操作，以达到 33.2 分钟时的峰值。</li>
@@ -563,7 +563,7 @@ <h2>检查 MS1 谱图</h2>
         此图应变为如下所示：
     </p>
     <p>
-        <img src="image-28.png" />
+        <img src="s-26.png" />
     </p>
     <p>
         在色谱图中观察到的差异在这些谱图中也应当一清二楚。
@@ -576,11 +576,11 @@ <h2>检测并解读干扰</h2>
         <tr>
             <td class="comp-fig">
                 <b>5b_MCF7_TiTip3</b><br />
-                <img src="image-29.png" />
+                <img src="s-27.png" />
             </td>
             <td class="comp-fig">
                 <b>1_MCF7_TiB_L</b><br />
-                <img src="image-30.png" />
+                <img src="s-28.png" />
             </td>
         </tr>
     </table>
@@ -595,7 +595,7 @@ <h2>检测并解读干扰</h2>
         您可以使用相同的方法添加 M+3 和 M+4，并发现干扰峰可能由另一个带 3 个电荷和质量大 2 Dalton 的肽段产生。
     </p>
     <p>
-        <img src="image-31.png" />
+        <img src="s-29.png" />
     </p>
     <ul>
         <li>单击<b>撤销</b>按钮恢复此变更，并继续探索。</li>
@@ -607,11 +607,11 @@ <h2>检测并解读干扰</h2>
         <tr>
             <td class="comp-fig">
                 <b>5b_MCF7_TiTip3</b><br />
-                <img src="image-32.png" />
+                <img src="s-30.png" />
             </td>
             <td class="comp-fig">
                 <b>1_MCF7_TiB_L</b><br />
-                <img src="image-33.png" />
+                <img src="s-31.png" />
             </td>
         </tr>
     </table>
@@ -622,11 +622,11 @@ <h2>检测并解读干扰</h2>
         <tr>
             <td class="comp-fig">
                 <b>5b_MCF7_TiTip3</b><br />
-                <img src="image-34.png" />
+                <img src="s-32.png" />
             </td>
             <td class="comp-fig">
                 <b>1_MCF7_TiB_L</b><br />
-                <img src="image-35.png" />
+                <img src="s-33.png" />
             </td>
         </tr>
     </table>
@@ -649,11 +649,11 @@ <h2>肽段的不同修饰形式</h2>
         <tr>
             <td class="comp-fig">
                 <b>5b_MCF7_TiTip3</b><br />
-                <img src="image-36.png" />
+                <img src="s-34.png" />
             </td>
             <td class="comp-fig">
                 <b>1_MCF7_TiB_L</b><br />
-                <img src="image-37.png" />
+                <img src="s-35.png" />
             </td>
         </tr>
     </table>
@@ -669,13 +669,13 @@ <h2>更多数据分析工具</h2>
         0.99，且与预期分布一致，如下所示：
     </p>
     <p>
-        <img src="image-38.png" />
+        <img src="s-36.png" />
     </p>
     <p>
         就像您一直在做的一样，您可以使用离子对挑选列表增加从 M+3 至 M+7 的色谱图，所有色谱图都应包含强度大于整体同位素分布 1% 的峰，并且会看到 idotp 值仍非常高，为 0.98：
     </p>
     <p>
-        <img src="image-39.png" />
+        <img src="s-37.png" />
     </p>
     <p>
         在色谱图中可以发现，这是文档中唯一在单个运行中被确认多次的肽段（在 5b_MCF7_TiTip3 被确认 3 次）。
@@ -694,7 +694,7 @@ <h2>更多数据分析工具</h2>
         色谱图现在将显示如下：
     </p>
     <p>
-        <img src="image-40.png" />
+        <img src="s-38.png" />
     </p>
     <p>
         要查看从中提取色谱图点的 MS1 谱图中的同位素分布，请执行以下操作：
@@ -706,7 +706,7 @@ <h2>更多数据分析工具</h2>
         随即<b>全扫描</b>视图将显示如下：
     </p>
     <p>
-        <img src="image-41.png" />
+        <img src="s-39.png" />
     </p>
     <ul>
         <li>单击<b>全扫描</b>视图右上角的“X”将其关闭。</li>
@@ -721,13 +721,13 @@ <h2>更多数据分析工具</h2>
         <b>5b_MCF7_TiTip3（37.61 分钟）</b>
     </p>
     <p>
-        <img src="image-42.png" />
+        <img src="s-40.png" />
     </p>
     <p class="keep-next">
         <b>1_MCF_TiB_L（37.03 分钟）</b>
     </p>
     <p>
-        <img src="image-43.png" />
+        <img src="s-41.png" />
     </p>
     <p>
         但是您应该非常确信，两个运行之间的色谱图峰测量的是相同的肽段分子。
@@ -740,11 +740,11 @@ <h2>与干扰有关的更多有趣实验</h2>
         <tr>
             <td class="comp-fig">
                 <b>5b_MCF7_TiTip3</b><br />
-                <img src="image-44.png" />
+                <img src="s-42.png" />
             </td>
             <td class="comp-fig">
                 <b>1_MCF7_TiB_L</b><br />
-                <img src="image-45.png" />
+                <img src="s-43.png" />
             </td>
         </tr>
     </table>
@@ -788,7 +788,7 @@ <h1>将色谱图缓存文件最小化</h1>
         <b>最小化结果</b>表单现在将显示如下：
     </p>
     <p>
-        <img src="image-46.png" />
+        <img src="s-44.png" />
     </p>
     <p>
         表单显示，预期此操作可将缓存文件的大小从大约 947 KB 减少为当前大小的 49%，即大约 464 KB。
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/zh-CHS/invariant.html b/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/zh-CHS/invariant.html
index af5488b4dd..942aacd2e9 100644
--- a/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/zh-CHS/invariant.html
+++ b/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/zh-CHS/invariant.html
@@ -112,7 +112,7 @@ <h1>Importing a Data Dependent Peptide Search into a Skyline Document</h1>
         Skyline should present a form that looks like this:
     </p>
     <p>
-        <img src="image-0.png" />
+        <img src="s-1.png" />
     </p>
     <p>
         Next, you will use this wizard to create a spectral library from the output of one of the many peptide search engines supported by Skyline. For
@@ -133,7 +133,7 @@ <h1>Importing a Data Dependent Peptide Search into a Skyline Document</h1>
         The wizard form should now look like this:
     </p>
     <p>
-        <img src="image-1.png" />
+        <img src="s-2.png" />
     </p>
     <ul>
         <li>Click the <b>Next</b> button.</li>
@@ -147,7 +147,7 @@ <h1>Importing a Data Dependent Peptide Search into a Skyline Document</h1>
         <li>The redundant library called “MS1FilteringTutorial.redundant.blib” containing all matching spectra.</li>
     </ul>
     <p>
-        <img src="image-2.png" />
+        <img src="s-ms1-filtering-folder.png" />
     </p>
     <p>
         You may also find a file ‘MS1FilterTutorial.slc’, which is a ‘Skyline Library Cache’ file to improve library load time. It can be deleted, and
@@ -163,7 +163,7 @@ <h1>Importing a Data Dependent Peptide Search into a Skyline Document</h1>
         When library building has completed, Skyline will present the next page in the wizard as shown below:
     </p>
     <p>
-        <img src="image-3.png" />
+        <img src="s-3.png" />
     </p>
     <p>
         In this case, Skyline has found original WIFF data files matching the spectrum source files used to build your library, and the library appears
@@ -180,7 +180,7 @@ <h1>Importing a Data Dependent Peptide Search into a Skyline Document</h1>
         A form should appear asking you how to handle the prefix shared by the two WIFF files:
     </p>
     <p>
-        <img src="image-4.png" />
+        <img src="s-4.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -195,7 +195,7 @@ <h1>Importing a Data Dependent Peptide Search into a Skyline Document</h1>
         and the wizard should look like this:
     </p>
     <p>
-        <img src="image-5.png" />
+        <img src="s-5.png" />
     </p>
     <p>
         It is possible that your document will already have one or more of these modifications defined (e.g. Oxidation (M)), in which case the list
@@ -215,7 +215,7 @@ <h1>Importing a Data Dependent Peptide Search into a Skyline Document</h1>
         this:
     </p>
     <p>
-        <img src="image-6.png" />
+        <img src="s-6.png" />
     </p>
     <p>
         In the <b>MS1 filtering</b> section, you will see the following default settings.
@@ -240,13 +240,13 @@ <h1>Importing a Data Dependent Peptide Search into a Skyline Document</h1>
         </table>
     </div>
     <p>
-        <img src="image-7.png" />
+        <img src="s-relative-abundance-graph.png" />
     </p>
     <p class="keep-next">
         A series of these intensities extracted over time make up the chromatograms you will see in Skyline:
     </p>
     <p>
-        <img src="image-8.png" />
+        <img src="s-chromatogram.png" />
     </p>
     <p>
         In the <b>Retention time filtering</b> section, note the choice to <b>Use only scans within [5] minutes of MS/MS IDs</b>.
@@ -273,7 +273,7 @@ <h1>Importing a Data Dependent Peptide Search into a Skyline Document</h1>
         The wizard should now look like this:
     </p>
     <p>
-        <img src="image-9.png" />
+        <img src="s-7.png" />
     </p>
     <ul>
         <li>Click the <b>Finish</b> button.</li>
@@ -283,7 +283,7 @@ <h1>Importing a Data Dependent Peptide Search into a Skyline Document</h1>
         FASTA file with matching spectra in the peptide search results which you imported.
     </p>
     <p>
-        <img src="image-10.png" />
+        <img src="s-8.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button in the <b>Associate Proteins</b> form.</li>
@@ -295,7 +295,7 @@ <h1>Importing a Data Dependent Peptide Search into a Skyline Document</h1>
         You should see a progress graph like this:
     </p>
     <p>
-        <img src="image-11.png" />
+        <img src="s-9.png" />
     </p>
     <p>
         Once the import has completed, first have an in-depth look at the spectral library you created before inspecting the chromatogram data.
@@ -319,7 +319,7 @@ <h2>Verifying Library Retention Time Information</h2>
         during the <b>Import Peptide Search</b> wizard.
     </p>
     <p>
-        <img src="image-12.png" />
+        <img src="s-10.png" />
     </p>
     <p>
         Choosing to use them now in the <b>Spectral Library Explorer</b> will not add them to the current document unless you use the
@@ -333,7 +333,7 @@ <h2>Verifying Library Retention Time Information</h2>
         The <b>Spectral Library Explorer</b> will appear, looking something like this:
     </p>
     <p>
-        <img src="image-13.png" />
+        <img src="s-11.png" />
     </p>
     <p>
         In the peptide list, the peptides without an icon to the left of the sequence text are ones that contain any of the modifications you just
@@ -378,7 +378,7 @@ <h1>Peptide Targets, Spectra and Chromatograms</h1>
         Your Skyline document should look like the following:
     </p>
     <p>
-        <img src="image-14.png" />
+        <img src="s-12.png" />
     </p>
     <p>
         The document is now fully configured for MS1 Filtering with two DDA runs imported. You will see that the chromatogram in this view is
@@ -398,7 +398,7 @@ <h1>Peptide Targets, Spectra and Chromatograms</h1>
         <li>In the <b>Peak Areas</b> window, right-click, choose <b>Show Dot Product</b>, and click <b>Labels</b>.</li>
     </ul>
     <p>
-        <img src="image-15.png" />
+        <img src="s-13.png" />
     </p>
     <p>
         You can dock the <b>Peak Areas</b> window to your desired location by doing the following:
@@ -415,7 +415,7 @@ <h1>Peptide Targets, Spectra and Chromatograms</h1>
         Your Skyline file should look something like this:
     </p>
     <p>
-        <img src="image-16.png" />
+        <img src="s-14.png" />
     </p>
     <p>
         The chromatogram views show the MS1 extracted ion chromatogram for all precursor isotope ions M (blue), M+1 (purple), M+2 (brown). Below the
@@ -465,7 +465,7 @@ <h1>Peptide Targets, Spectra and Chromatograms</h1>
         The chromatogram graphs should look something like this:
     </p>
     <p>
-        <img src="image-17.png" />
+        <img src="s-15.png" />
     </p>
     <p>
         To gain some insight into how the retention time alignment works, do the following:
@@ -477,7 +477,7 @@ <h1>Peptide Targets, Spectra and Chromatograms</h1>
         Skyline will present a window that looks like this:
     </p>
     <p>
-        <img src="image-18.png" />
+        <img src="s-16.png" />
     </p>
     <p>
         This window shows you the points for a linear regression used to align times between runs. Skyline calculates a linear regression like this
@@ -514,7 +514,7 @@ <h1>Reviewing the Data</h1>
         out of the 50 is currently selected, you can look in the status bar at the bottom right of the Skyline window:
     </p>
     <p>
-        <img src="image-19.png" />
+        <img src="s-17.png" />
     </p>
     <p>
         After the peptide I<b><u>S</u></b>MSEVDLNVAAPK, you will see 4 peptides with acceptable peak integration, though
@@ -530,11 +530,11 @@ <h2>Basic understanding of a chromatographic landscape</h2>
         <tr>
             <td  class="comp-fig">
                 <b>5b_MCF7_TiTip3</b><br />
-                <img src="image-20.png" />
+                <img src="s-18.png" />
             </td>
             <td  class="comp-fig">
                 <b>1_MCF7_TiB_L</b><br />
-                <img src="image-21.png" />
+                <img src="s-19.png" />
             </td>
         </tr>
     </table>
@@ -543,7 +543,7 @@ <h2>Basic understanding of a chromatographic landscape</h2>
         see in the 5b_MCF7_TiTip3 graph:
     </p>
     <p>
-        <img src="image-22.png" />
+        <img src="s-20.png" />
     </p>
     <p>
         This is an extremely important aspect of working with chromatographic data: just as your target peptides can be expected to elute at highly
@@ -576,7 +576,7 @@ <h2>Basic understanding of a chromatographic landscape</h2>
         previously selected peaks (0.86 and 0.87 versus 0.9 and 0.99):
     </p>
     <p>
-        <img src="image-23.png" />
+        <img src="s-21.png" />
     </p>
     <p>
         You can see from the distribution in the column marked Expected that this is because the M+1 and M+2 peaks are smaller than the predicted
@@ -601,7 +601,7 @@ <h2>Basic understanding of a chromatographic landscape</h2>
         Skyline will show a pop-up that looks like:
     </p>
     <p>
-        <img src="image-24.png" />
+        <img src="s-22.png" />
     </p>
     <p>
         If you see only these three precursor transitions:
@@ -613,7 +613,7 @@ <h2>Basic understanding of a chromatographic landscape</h2>
         This causes Skyline to show all possible transitions for this peptide precursor:
     </p>
     <p>
-        <img src="image-25.png" />
+        <img src="s-23.png" />
     </p>
     <p>
         The green dots indicate the transitions for which Skyline already has chromatogram data. Skyline automatically extracts chromatograms for all
@@ -630,7 +630,7 @@ <h2>Basic understanding of a chromatographic landscape</h2>
         kind in Skyline.
     </p>
     <p>
-        <img src="image-26.png" />
+        <img src="s-24.png" />
     </p>
     <p>
         You can now feel fairly confident that the peak at 33 minutes is caused by another peptide of very similar elemental composition to the target
@@ -653,7 +653,7 @@ <h2>Inspecting the MS1 spectra</h2>
         This will cause Skyline to display the <b>Full Scan</b> view with a plot like the one below:
     </p>
     <p>
-        <img src="image-27.png" />
+        <img src="s-25.png" />
     </p>
     <ul>
         <li>Repeat this hover and click operation for the peak at 33.2 minutes.</li>
@@ -662,7 +662,7 @@ <h2>Inspecting the MS1 spectra</h2>
         The graph should change to something like this:
     </p>
     <p>
-        <img src="image-28.png" />
+        <img src="s-26.png" />
     </p>
     <p>
         The differences observed in the chromatograms should also be clear in these spectra.
@@ -677,11 +677,11 @@ <h2>Detecting and understanding interference</h2>
         <tr>
             <td class="comp-fig">
                 <b>5b_MCF7_TiTip3</b><br />
-                <img src="image-29.png" />
+                <img src="s-27.png" />
             </td>
             <td class="comp-fig">
                 <b>1_MCF7_TiB_L</b><br />
-                <img src="image-30.png" />
+                <img src="s-28.png" />
             </td>
         </tr>
     </table>
@@ -702,7 +702,7 @@ <h2>Detecting and understanding interference</h2>
         Da greater mass:
     </p>
     <p>
-        <img src="image-31.png" />
+        <img src="s-29.png" />
     </p>
     <ul>
         <li>Click the <b>Undo</b> button to revert this change and continue exploring.</li>
@@ -715,11 +715,11 @@ <h2>Detecting and understanding interference</h2>
         <tr>
             <td class="comp-fig">
                 <b>5b_MCF7_TiTip3</b><br />
-                <img src="image-32.png" />
+                <img src="s-30.png" />
             </td>
             <td class="comp-fig">
                 <b>1_MCF7_TiB_L</b><br />
-                <img src="image-33.png" />
+                <img src="s-31.png" />
             </td>
         </tr>
     </table>
@@ -731,11 +731,11 @@ <h2>Detecting and understanding interference</h2>
         <tr>
             <td class="comp-fig">
                 <b>5b_MCF7_TiTip3</b><br />
-                <img src="image-34.png" />
+                <img src="s-32.png" />
             </td>
             <td class="comp-fig">
                 <b>1_MCF7_TiB_L</b><br />
-                <img src="image-35.png" />
+                <img src="s-33.png" />
             </td>
         </tr>
     </table>
@@ -765,11 +765,11 @@ <h2>Differently modified forms of a peptide</h2>
         <tr>
             <td class="comp-fig">
                 <b>5b_MCF7_TiTip3</b><br />
-                <img src="image-36.png" />
+                <img src="s-34.png" />
             </td>
             <td class="comp-fig">
                 <b>1_MCF7_TiB_L</b><br />
-                <img src="image-37.png" />
+                <img src="s-35.png" />
             </td>
         </tr>
     </table>
@@ -790,14 +790,14 @@ <h2>More tools for data analysis</h2>
         idotp values of 1.0 and 0.99 with the expected distribution:
     </p>
     <p>
-        <img src="image-38.png" />
+        <img src="s-36.png" />
     </p>
     <p>
         Using the transition pick-list, as you have been doing, you can add the chromatograms for M+3 through M+7, all of which should contain greater
         than 1% of the entire isotope distribution, and see that the idotp values remain quite high at 0.98:
     </p>
     <p>
-        <img src="image-39.png" />
+        <img src="s-37.png" />
     </p>
     <p>
         In the chromatogram graphs, you can see that this is the only peptide in the document that was identified multiple times in a single run (3 in
@@ -819,7 +819,7 @@ <h2>More tools for data analysis</h2>
         The chromatogram graphs should now look like this:
     </p>
     <p>
-        <img src="image-40.png" />
+        <img src="s-38.png" />
     </p>
     <p>
         To see the isotope distribution in an MS1 spectrum from which the chromatogram points were extracted:
@@ -831,7 +831,7 @@ <h2>More tools for data analysis</h2>
         The <b>Full Scan</b> view will appear with a plot like this:
     </p>
     <p>
-        <img src="image-41.png" />
+        <img src="s-39.png" />
     </p>
     <ul>
         <li>Click the X in the upper right corner of the <b>Full Scan</b> view to close it.</li>
@@ -849,13 +849,13 @@ <h2>More tools for data analysis</h2>
         <b>5b_MCF7_TiTip3 (37.61 Min)</b>
     </p>
     <p>
-        <img src="image-42.png" />
+        <img src="s-40.png" />
     </p>
     <p class="keep-next">
         <b>1_MCF_TiB_L (37.03 min)</b>
     </p>
     <p>
-        <img src="image-43.png" />
+        <img src="s-41.png" />
     </p>
     <p>
         But you should feel pretty confident that the chromatogram peaks in the two runs measure the same peptide molecule.
@@ -868,11 +868,11 @@ <h2>More fun with interference</h2>
         <tr>
             <td class="comp-fig">
                 <b>5b_MCF7_TiTip3</b><br />
-                <img src="image-44.png" />
+                <img src="s-42.png" />
             </td>
             <td class="comp-fig">
                 <b>1_MCF7_TiB_L</b><br />
-                <img src="image-45.png" />
+                <img src="s-43.png" />
             </td>
         </tr>
     </table>
@@ -924,7 +924,7 @@ <h1>Minimizing a Chromatogram Cache File</h1>
         The <b>Minimize Results</b> form should now look like:
     </p>
     <p>
-        <img src="image-46.png" />
+        <img src="s-44.png" />
     </p>
     <p>
         The form indicates that this operation is expected to reduce the size of the cache file from about 947 KB to 49% of its current size, or about
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/zh-CHS/image-0.png b/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/zh-CHS/s-1.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/zh-CHS/image-6.png b/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/zh-CHS/s-6.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/zh-CHS/image-6.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/zh-CHS/s-6.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/zh-CHS/image-9.png b/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/zh-CHS/s-7.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/zh-CHS/image-9.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/zh-CHS/s-7.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/zh-CHS/image-10.png b/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/zh-CHS/s-8.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/zh-CHS/image-10.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/zh-CHS/s-8.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/zh-CHS/image-11.png b/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/zh-CHS/s-9.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/zh-CHS/image-11.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/zh-CHS/s-9.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/zh-CHS/image-8.png b/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/zh-CHS/s-chromatogram.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/zh-CHS/image-8.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/zh-CHS/s-chromatogram.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/zh-CHS/image-2.png b/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/zh-CHS/s-ms1-filtering-folder.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/zh-CHS/image-2.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/zh-CHS/s-ms1-filtering-folder.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/zh-CHS/image-7.png b/pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/zh-CHS/s-relative-abundance-graph.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/zh-CHS/image-7.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MS1Filtering/zh-CHS/s-relative-abundance-graph.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/en/index.html b/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/en/index.html
index 4060d6d58d..92893dc249 100644
--- a/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/en/index.html
+++ b/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/en/index.html
@@ -153,7 +153,7 @@ <h1>Creating a MS/MS Spectral Library</h1>
         The Library tab should now look like this:
     </p>
     <p>
-        <img src="image-0.png" />
+        <img src="s-1.png" />
     </p>
     <h1>Creating a Background Proteome File:</h1>
     <p>
@@ -181,7 +181,7 @@ <h1>Creating a Background Proteome File:</h1>
         file you created. The Background Proteome form should look like this:
     </p>
     <p>
-        <img src="image-1.png" />
+        <img src="s-2.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -191,7 +191,7 @@ <h1>Creating a Background Proteome File:</h1>
         look like this:
     </p>
     <p>
-        <img src="image-2.png" />
+        <img src="s-3.png" />
     </p>
     <p>
         Skyline provides many editable lists like the two you just modified. The Enzyme list at the top of the <b>Digestion</b> tab is
@@ -224,7 +224,7 @@ <h1>Pasting FASTA Sequences</h1>
         This should leave Skyline looking something like this:
     </p>
     <p>
-        <img src="image-3.png" />
+        <img src="s-4.png" />
     </p>
     <ul>
         <li>On the <b>View</b> menu, choose <b>Ion Types</b>, and then click <b>B</b>.</li>
@@ -241,7 +241,7 @@ <h1>Pasting FASTA Sequences</h1>
         Skyline highlights ions in the graph as you select the corresponding transitions to present the following view:
     </p>
     <p>
-        <img src="image-4.png" />
+        <img src="s-5.png" />
     </p>
     <p>
         By default, Skyline has only chosen the 3 most intense charge 1 product y-ions as the transitions it will measure for the charge 2 precursor.
@@ -258,7 +258,7 @@ <h1>Pasting FASTA Sequences</h1>
         The <b>Transition Settings</b> form should look like this:
     </p>
     <p>
-        <img src="image-5.png" />
+        <img src="s-6.png" />
     </p>
     <ul>
         <li>Click the <b>Library</b> tab.</li>
@@ -268,7 +268,7 @@ <h1>Pasting FASTA Sequences</h1>
         The <b>Transition Settings</b> form should look like:
     </p>
     <p>
-        <img src="image-6.png" />
+        <img src="s-7.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -277,7 +277,7 @@ <h1>Pasting FASTA Sequences</h1>
         The Skyline document tree should update to look like the following:
     </p>
     <p>
-        <img src="image-7.png" />
+        <img src="s-8.png" />
     </p>
     <p>
         Skyline has added the rank 4 and rank 5 ions for the VDIIANDQGNR peptide, including its b5 ion. A new peptide has been added as the first
@@ -310,7 +310,7 @@ <h1>Using a Public Spectral Library</h1>
         The Peptide Settings form should now look like the following:
     </p>
     <p>
-         <img src="image-8.png" />
+         <img src="s-9.png" />
     </p>
     <p>
         Since Skyline can only choose a single spectrum to inform its product-ion decisions, and the value by which to rank these matches remains blank
@@ -395,7 +395,7 @@ <h1>Inserting a Protein List</h1>
         So that the form looks like:
     </p>
     <p>
-        <img src="image-9.png" />
+        <img src="s-10.png" />
     </p>
     <ul>
         <li>Click the <b>Insert</b> button.</li>
@@ -439,7 +439,7 @@ <h1>Inserting a Peptide List</h1>
         peptides. The Skyline document should now look something like this:
     </p>
     <p>
-        <img src="image-10.png" />
+        <img src="s-11.png" />
     </p>
     <p>
         To insert the same list so that each peptide is associated with its respective protein in the background proteome, you need to use the
@@ -454,7 +454,7 @@ <h1>Inserting a Peptide List</h1>
         Skyline populates the protein fields for each peptide to present the form looking like this:
     </p>
     <p>
-        <img src="image-11.png" />
+        <img src="s-12.png" />
     </p>
     <ul>
         <li>Click the <b>Insert</b> button to insert the peptides into the document.</li>
@@ -477,7 +477,7 @@ <h1>Simple Refinement</h1>
         This spectrum shows only 1 matching y-ion and 1 matching b-ion, and looks like:
     </p>
     <p>
-        <img src="image-12.png" />
+        <img src="s-13.png" />
     </p>
     <p>
         Measuring these two ions is unlikely to produce useful information about this peptide.
@@ -494,7 +494,7 @@ <h1>Simple Refinement</h1>
         The status bar indicators at the bottom-right corner of the Skyline window show that the number of peptides has been reduced from 70 to 64:
     </p>
     <p>
-        <img src="image-13.png" />
+        <img src="s-14.png" />
     </p>
     <h1>Checking Peptide Uniqueness</h1>
     <p>
@@ -514,7 +514,7 @@ <h1>Checking Peptide Uniqueness</h1>
         Skyline displays the <b>Unique Peptides</b> form with the following information:
     </p>
     <p>
-        <img src="image-14.png" />
+        <img src="s-15.png" />
     </p>
     <p>
         A close review of these 6 proteins shows that some are similar to each other, but there is certainly enough variation that this one peptide
@@ -555,7 +555,7 @@ <h2>Protein Name Auto-Completion</h2>
         Skyline will offer to complete this by adding a protein as shown below:
     </p>
     <p>
-        <img src="image-15.png" />
+        <img src="s-16.png" />
     </p>
     <ul>
         <li>Press the Enter key to add the protein to your document.</li>
@@ -572,7 +572,7 @@ <h2>Protein Description Auto-Completion</h2>
         <li>Press the down-arrow key once to select the first protein listed, as shown:</li>
     </ul>
     <p>
-        <img src="image-16.png" />
+        <img src="s-17.png" />
     </p>
     <ul>
         <li>Press the Enter key to add the protein to your document.</li>
@@ -593,7 +593,7 @@ <h2>Peptide Sequence Auto-Completion</h2>
         should now look like:
     </p>
     <p>
-        <img src="image-17.png" />
+        <img src="s-18.png" />
     </p>
     <h2>Pop-up Pick-Lists</h2>
     <p>
@@ -618,7 +618,7 @@ <h2>Pop-up Pick-Lists</h2>
         This should leave the pick-list looking like:
     </p>
     <p>
-        <img src="image-18.png" />
+        <img src="s-19.png" />
     </p>
     <ul>
         <li>Press the Enter key or click the button with the green check image to commit the change to your document.</li>
@@ -648,7 +648,7 @@ <h2>Pop-up Pick-Lists</h2>
         The pick-list should now look like this:
     </p>
     <p>
-        <img src="image-19.png" />
+        <img src="s-20.png" />
     </p>
     <ul>
         <li>Press the Enter key or click the button with the green check image to commit the change to your document.</li>
@@ -661,10 +661,10 @@ <h2>Bigger Picture</h2>
         for elements which match the filter but are not included in the document.
     </p>
     <p>
-        <img src="image-20.png" />
+        <img src="s-21.png" />
     </p>
     <p>
-        <img src="image-21.png" />
+        <img src="s-22.png" />
     </p>
     <h2>Drag and Drop</h2>
     <p>
@@ -726,7 +726,7 @@ <h1>Preparing to Measure</h1>
         This should leave the Export Transition List form looking like:
     </p>
     <p>
-        <img src="image-22.png" />
+        <img src="s-23.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -738,13 +738,13 @@ <h1>Preparing to Measure</h1>
         The contents of the MethodEdit folder should now look like:
     </p>
     <p>
-        <img src="image-23.png" />
+        <img src="s-method-edit-file-explorer.png" />
     </p>
     <p class="keep-next">
         Open the first of the five new files, and you should find a transition list that looks like:
     </p>
     <p>
-        <img src="image-24.png" />
+        <img src="s-transition-list-spreadsheet.png" />
     </p>
     <p>
         The columns are in the order: precursor <i>m/z</i>, product <i>m/z</i>, dwell time, extended peptide, declustering potential, and collision
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/en/image-0.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/en/s-1.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/en/image-0.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/en/s-1.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/en/image-9.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/en/s-10.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/en/image-9.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/en/s-10.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/en/image-10.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/en/s-11.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/en/image-10.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/en/s-11.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/en/image-11.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/en/s-12.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/en/image-11.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/en/s-12.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/en/image-12.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/en/s-13.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/en/image-12.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/en/s-13.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/en/image-13.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/en/s-14.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/en/image-13.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/en/s-14.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/en/image-14.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/en/s-15.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/en/image-14.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/en/s-15.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/en/image-15.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/en/s-16.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/en/image-15.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/en/s-16.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/en/image-16.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/en/s-17.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/en/image-16.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/en/s-17.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/en/image-17.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/en/s-18.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/en/image-17.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/en/s-18.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/en/image-18.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/en/s-19.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/en/image-18.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/en/s-19.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/en/image-1.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/en/s-2.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/en/image-1.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/en/s-2.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/en/image-19.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/en/s-20.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/en/image-19.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/en/s-20.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/en/image-20.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/en/s-21.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/en/image-20.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/en/s-21.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/en/image-21.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/en/s-22.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/en/image-21.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/en/s-22.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/en/image-22.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/en/s-23.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/en/image-22.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/en/s-23.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/en/image-2.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/en/s-3.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/en/image-2.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/en/s-3.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/en/image-3.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/en/s-4.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/en/image-3.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/en/s-4.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/en/image-4.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/en/s-5.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/en/image-4.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/en/s-5.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/en/image-5.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/en/s-6.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/en/image-5.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/en/s-6.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/en/image-6.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/en/s-7.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/en/image-6.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/en/s-7.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/en/image-7.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/en/s-8.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/en/image-7.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/en/s-8.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/en/image-8.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/en/s-9.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/en/image-8.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/en/s-9.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/en/image-23.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/en/s-method-edit-file-explorer.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/en/image-23.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/en/s-method-edit-file-explorer.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/en/image-24.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/en/s-transition-list-spreadsheet.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/en/image-24.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/en/s-transition-list-spreadsheet.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/ja/index.html b/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/ja/index.html
index e6763037d6..f61791c591 100644
--- a/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/ja/index.html
+++ b/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/ja/index.html
@@ -139,7 +139,7 @@ <h1>MS/MS スペクトルライブラリの作成</h1>
         [ ライブラリ ] タブは次のようになっています。
     </p>
     <p>
-        <img src="image-0.png" />
+        <img src="s-1.png" />
     </p>
     <h1>バックグラウンドプロテオームファイルの作成:</h1>
     <p>
@@ -164,7 +164,7 @@ <h1>バックグラウンドプロテオームファイルの作成:</h1>
         Skylineはこのファイル内にある5801個のタンパク質シークエンスをスキャンし、ペプチドシークエンス検索のためのインデックスを作成し、このインデックスを作成したファイルに保存します。[バックグラウンドプロテオーム] の画面は次のようになります。
     </p>
     <p>
-        <img src="image-1.png" />
+        <img src="s-2.png" />
     </p>
     <ul>
         <li>[ <b>OK</b> ] ボタンをクリックします。</li>
@@ -173,7 +173,7 @@ <h1>バックグラウンドプロテオームファイルの作成:</h1>
         [ <b>ペプチド設定</b> ] の [ <b>消化</b> ] タブに戻りますので、次のような画面を確認します。
     </p>
     <p>
-        <img src="image-2.png" />
+        <img src="s-3.png" />
     </p>
     <p>
         Skylineには、ここまでで変更した2つの設定項目を始め、多数の設定項目があります。[ <b>消化</b> ] タブの上部にある酵素リストを含めて[ ペプチド設定 ] の各タブには他にもいろいろな設定項目があります。後で確認してみてください。 
@@ -203,7 +203,7 @@ <h1>FASTAシークエンスの貼り付け</h1>
         これにより以下のような画面が表示されます。
     </p>
     <p>
-        <img src="image-3.png" />
+        <img src="s-4.png" />
     </p>
     <ul>
         <li>[ <b>表示</b> ] メニューで、[ <b>イオンタイプ</b> ] を選択して [ <b>B</b> ] をクリックします。</li>
@@ -219,7 +219,7 @@ <h1>FASTAシークエンスの貼り付け</h1>
         対応するトランジションを選択すると、グラフ内のイオンがハイライトされ、次のようなグラフが表示されます。
     </p>
     <p>
-        <img src="image-4.png" />
+        <img src="s-5.png" />
     </p>
     <p>
         デフォルトでは、2価のプリカーサーに対して測定するトランジションとして最も強度の高い1価のプロダクトyイオン3つのみが選択されていますが、この設定は以下の操作で変更できます。デフォルト設定から変更するには、次の手順を実行します。
@@ -235,7 +235,7 @@ <h1>FASTAシークエンスの貼り付け</h1>
         [ <b>トランジション設定</b> ] の画面は次のようになります。
     </p>
     <p>
-        <img src="image-5.png" />
+        <img src="s-6.png" />
     </p>
     <ul>
         <li>[ <b>ライブラリ</b> ] タブをクリックします。</li>
@@ -245,7 +245,7 @@ <h1>FASTAシークエンスの貼り付け</h1>
         [ <b>トランジション設定</b> ] の画面は次のようになります。
     </p>
     <p>
-        <img src="image-6.png" />
+        <img src="s-7.png" />
     </p>
     <ul>
         <li>[ <b>OK</b> ] ボタンをクリックします。</li>
@@ -254,7 +254,7 @@ <h1>FASTAシークエンスの貼り付け</h1>
         Skylineドキュメントツリーは次のように更新されます。
     </p>
     <p>
-        <img src="image-7.png" />
+        <img src="s-8.png" />
     </p>
     <p>
         VDIIANDQGNRペプチドに、rank 4とrank
@@ -281,7 +281,7 @@ <h1>公開スペクトルライブラリの使用</h1>
         [ペプチド設定 ] の画面は次のようになります。
     </p>
     <p>
-         <img src="image-8.png" />
+         <img src="s-9.png" />
     </p>
     <p>
         Skylineではプロダクトイオン決定の情報としてスペクトルを1つしか選択できないこと、一致する結果をランクする基準を示す [ ペプチドをランク ]
@@ -352,7 +352,7 @@ <h1>タンパク質リストの挿入</h1>
         画面は次のようになります。
     </p>
     <p>
-        <img src="image-9.png" />
+        <img src="s-10.png" />
     </p>
     <ul>
         <li>[ <b>挿入</b> ] ボタンをクリックします。</li>
@@ -392,7 +392,7 @@ <h1>ペプチドリストの挿入</h1>
         GPMライブラリには追加されたすべてのペプチドのスペクトルがあり、下向き矢印キーを押して貼り付けられたペプチドを選択するとそれぞれの対応するスペクトルが見られます。Skylineドキュメントは次のようになります。
     </p>
     <p>
-        <img src="image-10.png" />
+        <img src="s-11.png" />
     </p>
     <p>
         各ペプチドがバックグラウンドプロテオーム内のタンパク質に関連付けられるように同じリストを挿入するには、[ <b>ペプチドリストを挿入</b> ] を使用する必要があります。ここで以下の手順を実行します。
@@ -406,7 +406,7 @@ <h1>ペプチドリストの挿入</h1>
         各ペプチドのタンパク質フィールドが自動入力され、フォームが次のようになります。
     </p>
     <p>
-        <img src="image-11.png" />
+        <img src="s-12.png" />
     </p>
     <ul>
         <li>[ <b>挿入</b> ] ボタンをクリックして、ドキュメントにペプチドを挿入します。</li>
@@ -427,7 +427,7 @@ <h1>簡易修正</h1>
         下に示すように、このスペクトルには一致するyイオンが1つとbイオンが1つしか表示されません。
     </p>
     <p>
-        <img src="image-12.png" />
+        <img src="s-13.png" />
     </p>
     <p>
         これら2つのイオンを測定しても、このペプチドについての有用な情報は得られないと思われます。
@@ -444,7 +444,7 @@ <h1>簡易修正</h1>
         Skylineウィンドウの右下角にあるステータスバーインジケーターの、ペプチド数が70から64に減ったことがわかります。
     </p>
     <p>
-        <img src="image-13.png" />
+        <img src="s-14.png" />
     </p>
     <h1>ペプチドの特異性（ユニーク性）チェック</h1>
     <p>
@@ -461,7 +461,7 @@ <h1>ペプチドの特異性（ユニーク性）チェック</h1>
         以下の情報と共に、[ <b>ユニークペプチド</b> ] フォームが開きます。
     </p>
     <p>
-        <img src="image-14.png" />
+        <img src="s-15.png" />
     </p>
     <p>
         これら6つのタンパク質を詳細に確認すると、一部のシークエンスは類似していますが、十分にばらつきがありますので、この1つのペプチドだけでは対象のタンパク質を十分な信頼性をもって測定できません。グリッド表示の列を選択すると、各タンパク質のシークエンスを表示できます。
@@ -496,7 +496,7 @@ <h2>タンパク質名のオートコンプリーション</h2>
         Skylineは、タンパク質の追加が下記のように補助されます。
     </p>
     <p>
-        <img src="image-15.png" />
+        <img src="s-16.png" />
     </p>
     <ul>
         <li>Enterキーを押すと、このタンパク質がドキュメントに追加されます。</li>
@@ -512,7 +512,7 @@ <h2>タンパク質の説明のオートコンプリーション</h2>
         <li>下向き矢印キーを1回押して、下に示すように1つ目のタンパク質を選択します。</li>
     </ul>
     <p>
-        <img src="image-16.png" />
+        <img src="s-17.png" />
     </p>
     <ul>
         <li>Enterキーを押すと、このタンパク質がドキュメントに追加されます。</li>
@@ -531,7 +531,7 @@ <h2>ペプチドシークエンスのオートコンプリーション</h2>
         ペプチドがドキュメントに追加されますが、それは最後のブランク要素のすぐ上にある既存のタンパク質YDR385Wに追加されます。追加されたタンパク質は次のようになります。
     </p>
     <p>
-        <img src="image-17.png" />
+        <img src="s-18.png" />
     </p>
     <h2>ポップアップ選択リスト</h2>
     <p>
@@ -553,7 +553,7 @@ <h2>ポップアップ選択リスト</h2>
         これによって、選択リストは次のようになります。
     </p>
     <p>
-        <img src="image-18.png" />
+        <img src="s-19.png" />
     </p>
     <ul>
         <li>Enterキーを押すか、緑のチェック印のアイコンをクリックして、ドキュメントへの変更を確定します。</li>
@@ -581,7 +581,7 @@ <h2>ポップアップ選択リスト</h2>
         選択リストは次のようになります。
     </p>
     <p>
-        <img src="image-19.png" />
+        <img src="s-20.png" />
     </p>
     <ul>
         <li>Enterキーを押すか、緑のチェック印のアイコンをクリックして、ドキュメントへの変更を確定します。</li>
@@ -591,10 +591,10 @@ <h2>広い視点での情報</h2>
         ドキュメント内の情報をより広い視野から確認する方がいいこともあります。ドキュメント上でマウスを動かしたときに気づかれたかもしれませんが、気づかれていない方のために、この機能を説明します。マウスカーソルをドキュメントツリー内の要素上にポイントすると、下図で示すようなデータヒントが表示されます。これらのヒントでは、選択した要素が赤で強調表示され、ドキュメント内に含まれる要素は青で、またフィルタに一致するがドキュメントに含まれていない要素は太字で表示されます。
     </p>
     <p>
-        <img src="image-20.png" />
+        <img src="s-21.png" />
     </p>
     <p>
-        <img src="image-21.png" />
+        <img src="s-22.png" />
     </p>
     <h2>ドラッグアンドドロップ</h2>
     <p>
@@ -646,7 +646,7 @@ <h1>測定準備</h1>
         これによって、[ トランジションリストをエクスポート ] の画面は次のようになります。
     </p>
     <p>
-        <img src="image-22.png" />
+        <img src="s-23.png" />
     </p>
     <ul>
         <li>[ <b>OK</b> ] ボタンをクリックします。</li>
@@ -657,13 +657,13 @@ <h1>測定準備</h1>
         Windowsエクスプローラーウィンドウに切り替えて、MethodEditフォルダに移動し、作成したトランジションリストファイルを見てみましょう。MethodEditフォルダの内容は次のようになります。
     </p>
     <p>
-        <img src="image-23.png" />
+        <img src="s-method-edit-file-explorer.png" />
     </p>
     <p class="keep-next">
         5つの新しいファイルのうちの最初のファイルを開いてください。下に示すようなトランジションリストが表示されます。
     </p>
     <p>
-        <img src="image-24.png" />
+        <img src="s-transition-list-spreadsheet.png" />
     </p>
     <p>
         プリカーカーサー<i>m/z</i>、プロダクト<i>m/z</i>、ドウェル時間、拡張ペプチド情報、デクラスタリングポテンシャル、コリジョンエネルギーの順です。この情報をAnalystソフトウェアメソッド作成ユーザーインターフェイスに貼り付けることで、酵母サンプルを用いたペプチドの測定に使用できるメソッドが作成できます。
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/ja/invariant.html b/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/ja/invariant.html
index 93613c5ebf..47020e1fbe 100644
--- a/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/ja/invariant.html
+++ b/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/ja/invariant.html
@@ -153,7 +153,7 @@ <h1>Creating a MS/MS Spectral Library</h1>
         The Library tab should now look like this:
     </p>
     <p>
-        <img src="image-0.png" />
+        <img src="s-1.png" />
     </p>
     <h1>Creating a Background Proteome File:</h1>
     <p>
@@ -181,7 +181,7 @@ <h1>Creating a Background Proteome File:</h1>
         file you created. The Background Proteome form should look like this:
     </p>
     <p>
-        <img src="image-1.png" />
+        <img src="s-2.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -191,7 +191,7 @@ <h1>Creating a Background Proteome File:</h1>
         look like this:
     </p>
     <p>
-        <img src="image-2.png" />
+        <img src="s-3.png" />
     </p>
     <p>
         Skyline provides many editable lists like the two you just modified. The Enzyme list at the top of the <b>Digestion</b> tab is
@@ -224,7 +224,7 @@ <h1>Pasting FASTA Sequences</h1>
         This should leave Skyline looking something like this:
     </p>
     <p>
-        <img src="image-3.png" />
+        <img src="s-4.png" />
     </p>
     <ul>
         <li>On the <b>View</b> menu, choose <b>Ion Types</b>, and then click <b>B</b>.</li>
@@ -241,7 +241,7 @@ <h1>Pasting FASTA Sequences</h1>
         Skyline highlights ions in the graph as you select the corresponding transitions to present the following view:
     </p>
     <p>
-        <img src="image-4.png" />
+        <img src="s-5.png" />
     </p>
     <p>
         By default, Skyline has only chosen the 3 most intense charge 1 product y-ions as the transitions it will measure for the charge 2 precursor.
@@ -258,7 +258,7 @@ <h1>Pasting FASTA Sequences</h1>
         The <b>Transition Settings</b> form should look like this:
     </p>
     <p>
-        <img src="image-5.png" />
+        <img src="s-6.png" />
     </p>
     <ul>
         <li>Click the <b>Library</b> tab.</li>
@@ -268,7 +268,7 @@ <h1>Pasting FASTA Sequences</h1>
         The <b>Transition Settings</b> form should look like:
     </p>
     <p>
-        <img src="image-6.png" />
+        <img src="s-7.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -277,7 +277,7 @@ <h1>Pasting FASTA Sequences</h1>
         The Skyline document tree should update to look like the following:
     </p>
     <p>
-        <img src="image-7.png" />
+        <img src="s-8.png" />
     </p>
     <p>
         Skyline has added the rank 4 and rank 5 ions for the VDIIANDQGNR peptide, including its b5 ion. A new peptide has been added as the first
@@ -310,7 +310,7 @@ <h1>Using a Public Spectral Library</h1>
         The Peptide Settings form should now look like the following:
     </p>
     <p>
-         <img src="image-8.png" />
+         <img src="s-9.png" />
     </p>
     <p>
         Since Skyline can only choose a single spectrum to inform its product-ion decisions, and the value by which to rank these matches remains blank
@@ -395,7 +395,7 @@ <h1>Inserting a Protein List</h1>
         So that the form looks like:
     </p>
     <p>
-        <img src="image-9.png" />
+        <img src="s-10.png" />
     </p>
     <ul>
         <li>Click the <b>Insert</b> button.</li>
@@ -439,7 +439,7 @@ <h1>Inserting a Peptide List</h1>
         peptides. The Skyline document should now look something like this:
     </p>
     <p>
-        <img src="image-10.png" />
+        <img src="s-11.png" />
     </p>
     <p>
         To insert the same list so that each peptide is associated with its respective protein in the background proteome, you need to use the
@@ -454,7 +454,7 @@ <h1>Inserting a Peptide List</h1>
         Skyline populates the protein fields for each peptide to present the form looking like this:
     </p>
     <p>
-        <img src="image-11.png" />
+        <img src="s-12.png" />
     </p>
     <ul>
         <li>Click the <b>Insert</b> button to insert the peptides into the document.</li>
@@ -477,7 +477,7 @@ <h1>Simple Refinement</h1>
         This spectrum shows only 1 matching y-ion and 1 matching b-ion, and looks like:
     </p>
     <p>
-        <img src="image-12.png" />
+        <img src="s-13.png" />
     </p>
     <p>
         Measuring these two ions is unlikely to produce useful information about this peptide.
@@ -494,7 +494,7 @@ <h1>Simple Refinement</h1>
         The status bar indicators at the bottom-right corner of the Skyline window show that the number of peptides has been reduced from 70 to 64:
     </p>
     <p>
-        <img src="image-13.png" />
+        <img src="s-14.png" />
     </p>
     <h1>Checking Peptide Uniqueness</h1>
     <p>
@@ -514,7 +514,7 @@ <h1>Checking Peptide Uniqueness</h1>
         Skyline displays the <b>Unique Peptides</b> form with the following information:
     </p>
     <p>
-        <img src="image-14.png" />
+        <img src="s-15.png" />
     </p>
     <p>
         A close review of these 6 proteins shows that some are similar to each other, but there is certainly enough variation that this one peptide
@@ -555,7 +555,7 @@ <h2>Protein Name Auto-Completion</h2>
         Skyline will offer to complete this by adding a protein as shown below:
     </p>
     <p>
-        <img src="image-15.png" />
+        <img src="s-16.png" />
     </p>
     <ul>
         <li>Press the Enter key to add the protein to your document.</li>
@@ -572,7 +572,7 @@ <h2>Protein Description Auto-Completion</h2>
         <li>Press the down-arrow key once to select the first protein listed, as shown:</li>
     </ul>
     <p>
-        <img src="image-16.png" />
+        <img src="s-17.png" />
     </p>
     <ul>
         <li>Press the Enter key to add the protein to your document.</li>
@@ -593,7 +593,7 @@ <h2>Peptide Sequence Auto-Completion</h2>
         should now look like:
     </p>
     <p>
-        <img src="image-17.png" />
+        <img src="s-18.png" />
     </p>
     <h2>Pop-up Pick-Lists</h2>
     <p>
@@ -618,7 +618,7 @@ <h2>Pop-up Pick-Lists</h2>
         This should leave the pick-list looking like:
     </p>
     <p>
-        <img src="image-18.png" />
+        <img src="s-19.png" />
     </p>
     <ul>
         <li>Press the Enter key or click the button with the green check image to commit the change to your document.</li>
@@ -648,7 +648,7 @@ <h2>Pop-up Pick-Lists</h2>
         The pick-list should now look like this:
     </p>
     <p>
-        <img src="image-19.png" />
+        <img src="s-20.png" />
     </p>
     <ul>
         <li>Press the Enter key or click the button with the green check image to commit the change to your document.</li>
@@ -661,10 +661,10 @@ <h2>Bigger Picture</h2>
         for elements which match the filter but are not included in the document.
     </p>
     <p>
-        <img src="image-20.png" />
+        <img src="s-21.png" />
     </p>
     <p>
-        <img src="image-21.png" />
+        <img src="s-22.png" />
     </p>
     <h2>Drag and Drop</h2>
     <p>
@@ -726,7 +726,7 @@ <h1>Preparing to Measure</h1>
         This should leave the Export Transition List form looking like:
     </p>
     <p>
-        <img src="image-22.png" />
+        <img src="s-23.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -738,13 +738,13 @@ <h1>Preparing to Measure</h1>
         The contents of the MethodEdit folder should now look like:
     </p>
     <p>
-        <img src="image-23.png" />
+        <img src="s-method-edit-file-explorer.png" />
     </p>
     <p class="keep-next">
         Open the first of the five new files, and you should find a transition list that looks like:
     </p>
     <p>
-        <img src="image-24.png" />
+        <img src="s-transition-list-spreadsheet.png" />
     </p>
     <p>
         The columns are in the order: precursor <i>m/z</i>, product <i>m/z</i>, dwell time, extended peptide, declustering potential, and collision
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/ja/image-0.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/ja/s-1.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/ja/image-0.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/ja/s-1.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/ja/image-9.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/ja/s-10.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/ja/image-9.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/ja/s-10.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/ja/image-10.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/ja/s-11.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/ja/image-10.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/ja/s-11.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/ja/image-11.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/ja/s-12.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/ja/image-11.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/ja/s-12.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/ja/image-12.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/ja/s-13.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/ja/image-12.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/ja/s-13.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/ja/image-13.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/ja/s-14.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/ja/image-13.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/ja/s-14.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/ja/image-14.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/ja/s-15.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/ja/image-14.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/ja/s-15.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/ja/image-15.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/ja/s-16.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/ja/image-15.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/ja/s-16.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/ja/image-16.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/ja/s-17.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/ja/image-16.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/ja/s-17.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/ja/image-17.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/ja/s-18.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/ja/image-17.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/ja/s-18.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/ja/image-18.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/ja/s-19.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/ja/image-18.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/ja/s-19.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/ja/image-1.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/ja/s-2.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/ja/image-1.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/ja/s-2.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/ja/image-19.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/ja/s-20.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/ja/image-19.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/ja/s-20.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/ja/image-20.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/ja/s-21.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/ja/image-20.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/ja/s-21.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/ja/image-21.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/ja/s-22.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/ja/image-21.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/ja/s-22.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/ja/image-22.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/ja/s-23.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/ja/image-22.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/ja/s-23.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/ja/image-2.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/ja/s-3.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/ja/image-2.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/ja/s-3.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/ja/image-3.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/ja/s-4.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/ja/image-3.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/ja/s-4.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/ja/image-4.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/ja/s-5.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/ja/image-4.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/ja/s-5.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/ja/image-5.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/ja/s-6.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/ja/image-5.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/ja/s-6.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/ja/image-6.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/ja/s-7.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/ja/image-6.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/ja/s-7.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/ja/image-7.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/ja/s-8.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/ja/image-7.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/ja/s-8.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/ja/image-8.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/ja/s-9.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/ja/image-8.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/ja/s-9.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/ja/image-23.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/ja/s-method-edit-file-explorer.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/ja/image-23.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/ja/s-method-edit-file-explorer.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/ja/image-24.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/ja/s-transition-list-spreadsheet.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/ja/image-24.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/ja/s-transition-list-spreadsheet.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/zh-CHS/index.html b/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/zh-CHS/index.html
index c37075ddbd..730f1c885c 100644
--- a/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/zh-CHS/index.html
+++ b/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/zh-CHS/index.html
@@ -137,7 +137,7 @@ <h1>创建 MS/MS 谱图库</h1>
         “库”选项卡现在应显示如下：
     </p>
     <p>
-        <img src="image-0.png" />
+        <img src="s-1.png" />
     </p>
     <h1>创建一个背景蛋白质组文件：</h1>
     <p>
@@ -162,7 +162,7 @@ <h1>创建一个背景蛋白质组文件：</h1>
         Skyline 将扫描此文件中的 5801 蛋白序列，为肽段序列查找创建索引，并将其保存到所创建的文件中。背景蛋白质组表单应显示如下：
     </p>
     <p>
-        <img src="image-1.png" />
+        <img src="s-2.png" />
     </p>
     <ul>
         <li>单击<b>确定</b>按钮。</li>
@@ -171,7 +171,7 @@ <h1>创建一个背景蛋白质组文件：</h1>
         此时将返回<b>肽段设置</b>表单的<b>酶解</b>选项卡，该选项卡现在看起来类似于如下：
     </p>
     <p>
-        <img src="image-2.png" />
+        <img src="s-3.png" />
     </p>
     <p>
         Skyline 可提供许多可编辑的列表，正如您刚编辑过的两个列表那样。<b>酶解</b>选项卡顶部的“酶”列表是另一个列表，并且“肽段设置”表单中的每个选项卡上都有其他列表，您可以稍后了解这些列表。 
@@ -201,7 +201,7 @@ <h1>粘贴 FASTA 序列</h1>
         执行此操作后，Skyline 应显示如下：
     </p>
     <p>
-        <img src="image-3.png" />
+        <img src="s-4.png" />
     </p>
     <ul>
         <li>在<b>视图</b>菜单上选择<b>离子类型</b>，然后单击 <b>B</b>。</li>
@@ -217,7 +217,7 @@ <h1>粘贴 FASTA 序列</h1>
         在您选择相应的离子对的过程中，Skyline 将在图中突出显示离子，以呈现如下视图：
     </p>
     <p>
-        <img src="image-4.png" />
+        <img src="s-5.png" />
     </p>
     <p>
         通过设置默认值，Skyline 已选择 3 个强度最高的电荷数为 1 的产物 y- 离子作为其将针对电荷数为 2的母离子测量的离子对。然而，所有这些设置都可以被调整。需要更改设置的默认值时，请执行如下步骤：
@@ -233,7 +233,7 @@ <h1>粘贴 FASTA 序列</h1>
         <b>离子对设置</b>表单现在应显示如下：
     </p>
     <p>
-        <img src="image-5.png" />
+        <img src="s-6.png" />
     </p>
     <ul>
         <li>单击<b>库</b>选项卡。</li>
@@ -243,7 +243,7 @@ <h1>粘贴 FASTA 序列</h1>
         <b>离子对设置</b>表单现在应显示如下：
     </p>
     <p>
-        <img src="image-6.png" />
+        <img src="s-7.png" />
     </p>
     <ul>
         <li>单击<b>确定</b>按钮。</li>
@@ -252,7 +252,7 @@ <h1>粘贴 FASTA 序列</h1>
         Skyline 文档树应更新为如下所示：
     </p>
     <p>
-        <img src="image-7.png" />
+        <img src="s-8.png" />
     </p>
     <p>
         Skyline 已针对 VDIIANDQGNR 肽段添加排名 4 和排名 5 离子，包括 b 离子。新肽段如 YAL005C 蛋白质中的第一个肽段一样被添加至蛋白质。展开后，可以看到该肽段的新谱图库仅包含一个电荷数为 3 的肽段谱图匹配，同时库中明显不含有电荷数为 3 的
@@ -280,7 +280,7 @@ <h1>使用公共谱图库</h1>
         “肽段设置”表单现在应显示如下：
     </p>
     <p>
-         <img src="image-8.png" />
+         <img src="s-9.png" />
     </p>
     <p>
         由于 Skyline 只能选择单一的谱图来选择其子离子，并且“按下列内容排列肽”中字段保持为空白，因此这些库将按其在列表中出现的顺序被依次搜索。Skyline 将使用其发现的第一个谱图匹配来选择离子对。要在操作中查看此项： 
@@ -349,7 +349,7 @@ <h1>插入蛋白质列表</h1>
         表单将显示为这样：
     </p>
     <p>
-        <img src="image-9.png" />
+        <img src="s-10.png" />
     </p>
     <ul>
         <li>单击<b>插入</b>按钮。</li>
@@ -389,7 +389,7 @@ <h1>插入肽段列表</h1>
         GPM 库拥有所添加的全部肽段的谱图，您可以按向下箭头键来选择粘贴的每个肽段，从而查看这些谱图。Skyline 文档现在应显示如下：
     </p>
     <p>
-        <img src="image-10.png" />
+        <img src="s-11.png" />
     </p>
     <p>
         如要插入相同的列表，以便每个肽都与背景蛋白质组中各自的蛋白质相关，您需要使用<b>插入肽段列表</b>分类。请执行下列步骤来操作：
@@ -403,7 +403,7 @@ <h1>插入肽段列表</h1>
         Skyline 会为每个肽段填充蛋白质字段，填充后的表单应如下所示：
     </p>
     <p>
-        <img src="image-11.png" />
+        <img src="s-12.png" />
     </p>
     <ul>
         <li>单击<b>插入</b>按钮，将肽段插入文档。</li>
@@ -424,7 +424,7 @@ <h1>简单优化</h1>
         此谱图仅显示 1 个匹配的 y- 离子和 1 个匹配的 b- 离子，并且看起来类似于如下：
     </p>
     <p>
-        <img src="image-12.png" />
+        <img src="s-13.png" />
     </p>
     <p>
         测量这两个离子不太可能获得有关此肽段的有用信息。
@@ -441,7 +441,7 @@ <h1>简单优化</h1>
         Skyline 窗口右下角的状态栏指示器显示出肽段数目已从 70 减少到 64：
     </p>
     <p>
-        <img src="image-13.png" />
+        <img src="s-14.png" />
     </p>
     <h1>查看肽段独特性</h1>
     <p>
@@ -458,7 +458,7 @@ <h1>查看肽段独特性</h1>
         Skyline 随即在<b>序列特异的肽段</b>表单中显示如下信息：
     </p>
     <p>
-        <img src="image-14.png" />
+        <img src="s-15.png" />
     </p>
     <p>
         对这 6 个蛋白质的详细检查显示它们相互间非常相似，但当然还是存在微弱的却是足够的差异，可以通过测量某一肽段实现对目标蛋白质可能的区分性测量。您可以在网格视图中选择蛋白质序列所在的列，从而查看每个蛋白质的序列。
@@ -493,7 +493,7 @@ <h2>蛋白质名称自动完成</h2>
         Skyline 将如下所示添加蛋白质，从而完成此目的。
     </p>
     <p>
-        <img src="image-15.png" />
+        <img src="s-16.png" />
     </p>
     <ul>
         <li>按 Enter 键向您的文档中添加蛋白质。</li>
@@ -509,7 +509,7 @@ <h2>蛋白质描述自动完成</h2>
         <li>按一次下箭头键，以选择列出的第一个蛋白质，如下所示：</li>
     </ul>
     <p>
-        <img src="image-16.png" />
+        <img src="s-17.png" />
     </p>
     <ul>
         <li>按 Enter 键向您的文档中添加蛋白质。</li>
@@ -528,7 +528,7 @@ <h2>肽段序列自动完成</h2>
         肽段已添加至文档，但它被添加至现有蛋白质 YDR385W 中，就在最终的空白要素之上。已添加的蛋白质应看起来如此：
     </p>
     <p>
-        <img src="image-17.png" />
+        <img src="s-18.png" />
     </p>
     <h2>弹出式选择列表</h2>
     <p>
@@ -550,7 +550,7 @@ <h2>弹出式选择列表</h2>
         这样选择列表应如下显示：
     </p>
     <p>
-        <img src="image-18.png" />
+        <img src="s-19.png" />
     </p>
     <ul>
         <li>按 Enter 键或单击带有绿色选中图标的按钮，以提交对文档所做的更改。</li>
@@ -578,7 +578,7 @@ <h2>弹出式选择列表</h2>
         选择列表现在应如下所示：
     </p>
     <p>
-        <img src="image-19.png" />
+        <img src="s-20.png" />
     </p>
     <ul>
         <li>按 Enter 键或单击带有绿色选中图标的按钮，以提交对文档所做的更改。</li>
@@ -589,10 +589,10 @@ <h2>较大的图</h2>
         将显示出类似下述内容的数据提示。在这些提示中，选定的元素以红色突出显示，文档中的元素以蓝色显示，粗体用于标示满足过滤条件但却未纳入文档的元素。
     </p>
     <p>
-        <img src="image-20.png" />
+        <img src="s-21.png" />
     </p>
     <p>
-        <img src="image-21.png" />
+        <img src="s-22.png" />
     </p>
     <h2>拖放</h2>
     <p>
@@ -645,7 +645,7 @@ <h1>准备测量</h1>
         执行此操作后，“导出离子对列表”表单应显示如下：
     </p>
     <p>
-        <img src="image-22.png" />
+        <img src="s-23.png" />
     </p>
     <ul>
         <li>单击<b>确定</b>按钮。</li>
@@ -656,13 +656,13 @@ <h1>准备测量</h1>
         切换至 Windows Explorer 窗口并导航至 MethodEdit 文件夹，以查看您刚刚创建的离子对列表。MethodEdit 文件夹中的内容现在应看起来如下所示：
     </p>
     <p>
-        <img src="image-23.png" />
+        <img src="s-method-edit-file-explorer.png" />
     </p>
     <p class="keep-next">
         打开五个新文件中的第一个，会看到第一个离子对列表显示如下：
     </p>
     <p>
-        <img src="image-24.png" />
+        <img src="s-transition-list-spreadsheet.png" />
     </p>
     <p>
         各列顺序如下：母离子<i>质荷比</i>、子离子<i>质荷比</i>、质谱驻留时间、扩展的肽段标识、去簇电压和碰撞能量。这些内容应该足够粘贴到 Analyst 软件方法创建用户界面，并且创建一种可用于在酵母样品上运行仪器的方法，以尝试靶向测量这些肽段。
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/zh-CHS/invariant.html b/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/zh-CHS/invariant.html
index 93613c5ebf..47020e1fbe 100644
--- a/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/zh-CHS/invariant.html
+++ b/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/zh-CHS/invariant.html
@@ -153,7 +153,7 @@ <h1>Creating a MS/MS Spectral Library</h1>
         The Library tab should now look like this:
     </p>
     <p>
-        <img src="image-0.png" />
+        <img src="s-1.png" />
     </p>
     <h1>Creating a Background Proteome File:</h1>
     <p>
@@ -181,7 +181,7 @@ <h1>Creating a Background Proteome File:</h1>
         file you created. The Background Proteome form should look like this:
     </p>
     <p>
-        <img src="image-1.png" />
+        <img src="s-2.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -191,7 +191,7 @@ <h1>Creating a Background Proteome File:</h1>
         look like this:
     </p>
     <p>
-        <img src="image-2.png" />
+        <img src="s-3.png" />
     </p>
     <p>
         Skyline provides many editable lists like the two you just modified. The Enzyme list at the top of the <b>Digestion</b> tab is
@@ -224,7 +224,7 @@ <h1>Pasting FASTA Sequences</h1>
         This should leave Skyline looking something like this:
     </p>
     <p>
-        <img src="image-3.png" />
+        <img src="s-4.png" />
     </p>
     <ul>
         <li>On the <b>View</b> menu, choose <b>Ion Types</b>, and then click <b>B</b>.</li>
@@ -241,7 +241,7 @@ <h1>Pasting FASTA Sequences</h1>
         Skyline highlights ions in the graph as you select the corresponding transitions to present the following view:
     </p>
     <p>
-        <img src="image-4.png" />
+        <img src="s-5.png" />
     </p>
     <p>
         By default, Skyline has only chosen the 3 most intense charge 1 product y-ions as the transitions it will measure for the charge 2 precursor.
@@ -258,7 +258,7 @@ <h1>Pasting FASTA Sequences</h1>
         The <b>Transition Settings</b> form should look like this:
     </p>
     <p>
-        <img src="image-5.png" />
+        <img src="s-6.png" />
     </p>
     <ul>
         <li>Click the <b>Library</b> tab.</li>
@@ -268,7 +268,7 @@ <h1>Pasting FASTA Sequences</h1>
         The <b>Transition Settings</b> form should look like:
     </p>
     <p>
-        <img src="image-6.png" />
+        <img src="s-7.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -277,7 +277,7 @@ <h1>Pasting FASTA Sequences</h1>
         The Skyline document tree should update to look like the following:
     </p>
     <p>
-        <img src="image-7.png" />
+        <img src="s-8.png" />
     </p>
     <p>
         Skyline has added the rank 4 and rank 5 ions for the VDIIANDQGNR peptide, including its b5 ion. A new peptide has been added as the first
@@ -310,7 +310,7 @@ <h1>Using a Public Spectral Library</h1>
         The Peptide Settings form should now look like the following:
     </p>
     <p>
-         <img src="image-8.png" />
+         <img src="s-9.png" />
     </p>
     <p>
         Since Skyline can only choose a single spectrum to inform its product-ion decisions, and the value by which to rank these matches remains blank
@@ -395,7 +395,7 @@ <h1>Inserting a Protein List</h1>
         So that the form looks like:
     </p>
     <p>
-        <img src="image-9.png" />
+        <img src="s-10.png" />
     </p>
     <ul>
         <li>Click the <b>Insert</b> button.</li>
@@ -439,7 +439,7 @@ <h1>Inserting a Peptide List</h1>
         peptides. The Skyline document should now look something like this:
     </p>
     <p>
-        <img src="image-10.png" />
+        <img src="s-11.png" />
     </p>
     <p>
         To insert the same list so that each peptide is associated with its respective protein in the background proteome, you need to use the
@@ -454,7 +454,7 @@ <h1>Inserting a Peptide List</h1>
         Skyline populates the protein fields for each peptide to present the form looking like this:
     </p>
     <p>
-        <img src="image-11.png" />
+        <img src="s-12.png" />
     </p>
     <ul>
         <li>Click the <b>Insert</b> button to insert the peptides into the document.</li>
@@ -477,7 +477,7 @@ <h1>Simple Refinement</h1>
         This spectrum shows only 1 matching y-ion and 1 matching b-ion, and looks like:
     </p>
     <p>
-        <img src="image-12.png" />
+        <img src="s-13.png" />
     </p>
     <p>
         Measuring these two ions is unlikely to produce useful information about this peptide.
@@ -494,7 +494,7 @@ <h1>Simple Refinement</h1>
         The status bar indicators at the bottom-right corner of the Skyline window show that the number of peptides has been reduced from 70 to 64:
     </p>
     <p>
-        <img src="image-13.png" />
+        <img src="s-14.png" />
     </p>
     <h1>Checking Peptide Uniqueness</h1>
     <p>
@@ -514,7 +514,7 @@ <h1>Checking Peptide Uniqueness</h1>
         Skyline displays the <b>Unique Peptides</b> form with the following information:
     </p>
     <p>
-        <img src="image-14.png" />
+        <img src="s-15.png" />
     </p>
     <p>
         A close review of these 6 proteins shows that some are similar to each other, but there is certainly enough variation that this one peptide
@@ -555,7 +555,7 @@ <h2>Protein Name Auto-Completion</h2>
         Skyline will offer to complete this by adding a protein as shown below:
     </p>
     <p>
-        <img src="image-15.png" />
+        <img src="s-16.png" />
     </p>
     <ul>
         <li>Press the Enter key to add the protein to your document.</li>
@@ -572,7 +572,7 @@ <h2>Protein Description Auto-Completion</h2>
         <li>Press the down-arrow key once to select the first protein listed, as shown:</li>
     </ul>
     <p>
-        <img src="image-16.png" />
+        <img src="s-17.png" />
     </p>
     <ul>
         <li>Press the Enter key to add the protein to your document.</li>
@@ -593,7 +593,7 @@ <h2>Peptide Sequence Auto-Completion</h2>
         should now look like:
     </p>
     <p>
-        <img src="image-17.png" />
+        <img src="s-18.png" />
     </p>
     <h2>Pop-up Pick-Lists</h2>
     <p>
@@ -618,7 +618,7 @@ <h2>Pop-up Pick-Lists</h2>
         This should leave the pick-list looking like:
     </p>
     <p>
-        <img src="image-18.png" />
+        <img src="s-19.png" />
     </p>
     <ul>
         <li>Press the Enter key or click the button with the green check image to commit the change to your document.</li>
@@ -648,7 +648,7 @@ <h2>Pop-up Pick-Lists</h2>
         The pick-list should now look like this:
     </p>
     <p>
-        <img src="image-19.png" />
+        <img src="s-20.png" />
     </p>
     <ul>
         <li>Press the Enter key or click the button with the green check image to commit the change to your document.</li>
@@ -661,10 +661,10 @@ <h2>Bigger Picture</h2>
         for elements which match the filter but are not included in the document.
     </p>
     <p>
-        <img src="image-20.png" />
+        <img src="s-21.png" />
     </p>
     <p>
-        <img src="image-21.png" />
+        <img src="s-22.png" />
     </p>
     <h2>Drag and Drop</h2>
     <p>
@@ -726,7 +726,7 @@ <h1>Preparing to Measure</h1>
         This should leave the Export Transition List form looking like:
     </p>
     <p>
-        <img src="image-22.png" />
+        <img src="s-23.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -738,13 +738,13 @@ <h1>Preparing to Measure</h1>
         The contents of the MethodEdit folder should now look like:
     </p>
     <p>
-        <img src="image-23.png" />
+        <img src="s-method-edit-file-explorer.png" />
     </p>
     <p class="keep-next">
         Open the first of the five new files, and you should find a transition list that looks like:
     </p>
     <p>
-        <img src="image-24.png" />
+        <img src="s-transition-list-spreadsheet.png" />
     </p>
     <p>
         The columns are in the order: precursor <i>m/z</i>, product <i>m/z</i>, dwell time, extended peptide, declustering potential, and collision
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/zh-CHS/image-0.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/zh-CHS/s-1.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/zh-CHS/image-0.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/zh-CHS/s-1.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/zh-CHS/image-9.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/zh-CHS/s-10.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/zh-CHS/image-9.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/zh-CHS/s-10.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/zh-CHS/image-10.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/zh-CHS/s-11.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/zh-CHS/image-10.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/zh-CHS/s-11.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/zh-CHS/image-11.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/zh-CHS/s-12.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/zh-CHS/image-11.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/zh-CHS/s-12.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/zh-CHS/image-12.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/zh-CHS/s-13.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/zh-CHS/image-12.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/zh-CHS/s-13.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/zh-CHS/image-13.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/zh-CHS/s-14.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/zh-CHS/image-13.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/zh-CHS/s-14.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/zh-CHS/image-14.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/zh-CHS/s-15.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/zh-CHS/image-14.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/zh-CHS/s-15.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/zh-CHS/image-15.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/zh-CHS/s-16.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/zh-CHS/image-15.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/zh-CHS/s-16.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/zh-CHS/image-16.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/zh-CHS/s-17.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/zh-CHS/image-16.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/zh-CHS/s-17.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/zh-CHS/image-17.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/zh-CHS/s-18.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/zh-CHS/image-17.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/zh-CHS/s-18.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/zh-CHS/image-18.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/zh-CHS/s-19.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/zh-CHS/image-18.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/zh-CHS/s-19.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/zh-CHS/image-1.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/zh-CHS/s-2.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/zh-CHS/image-1.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/zh-CHS/s-2.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/zh-CHS/image-19.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/zh-CHS/s-20.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/zh-CHS/image-19.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/zh-CHS/s-20.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/zh-CHS/image-20.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/zh-CHS/s-21.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/zh-CHS/image-20.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/zh-CHS/s-21.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/zh-CHS/image-21.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/zh-CHS/s-22.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/zh-CHS/image-21.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/zh-CHS/s-22.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/zh-CHS/image-22.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/zh-CHS/s-23.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/zh-CHS/image-22.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/zh-CHS/s-23.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/zh-CHS/image-2.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/zh-CHS/s-3.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/zh-CHS/image-2.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/zh-CHS/s-3.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/zh-CHS/image-3.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/zh-CHS/s-4.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/zh-CHS/image-3.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/zh-CHS/s-4.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/zh-CHS/image-4.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/zh-CHS/s-5.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/zh-CHS/image-4.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/zh-CHS/s-5.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/zh-CHS/image-5.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/zh-CHS/s-6.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/zh-CHS/image-5.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/zh-CHS/s-6.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/zh-CHS/image-6.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/zh-CHS/s-7.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/zh-CHS/image-6.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/zh-CHS/s-7.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/zh-CHS/image-7.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/zh-CHS/s-8.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/zh-CHS/image-7.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/zh-CHS/s-8.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/zh-CHS/image-8.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/zh-CHS/s-9.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/zh-CHS/image-8.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/zh-CHS/s-9.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/zh-CHS/image-23.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/zh-CHS/s-method-edit-file-explorer.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/zh-CHS/image-23.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/zh-CHS/s-method-edit-file-explorer.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/zh-CHS/image-24.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/zh-CHS/s-transition-list-spreadsheet.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/zh-CHS/image-24.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MethodEdit/zh-CHS/s-transition-list-spreadsheet.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/en/index.html b/pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/en/index.html
index ad882faba7..0d80e8f3a4 100644
--- a/pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/en/index.html
+++ b/pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/en/index.html
@@ -22,7 +22,7 @@ <h1 class="document-title">Skyline Targeted Method Refinement</h1>
         We call this the Targeted Method Refinement Cycle and often present the idea as shown below:
     </p>
     <p>
-        <img src="image-0.png" />
+        <img src="s-targeted-method-refinement-cycle.png" />
     </p>
     <p>
         By iterating over this cycle, you can start with a broad hypothesis including dozens to thousands of proteins you are interested in monitoring,
@@ -104,7 +104,7 @@ <h1>Results Data</h1>
         product ions y3 – y15 of this peptide on an instrument in the MacCoss lab:
     </p>
     <p>
-        <img src="image-1.png" />
+        <img src="s-1.png" />
     </p>
     <p>
         Note that the MS/MS library spectrum associated with each peptide was derived from experiments conducted on an ion trap mass spectrometer.
@@ -143,7 +143,7 @@ <h1>Unrefined Methods</h1>
         The <b>Export Transition List</b> form should look like:
     </p>
     <p>
-        <img src="image-2.png" />
+        <img src="s-2.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -219,7 +219,7 @@ <h1>Importing Multiple Injection Data</h1>
         form like the one below:
     </p>
     <p>
-        <img src="image-3.png" />
+        <img src="s-3.png" />
     </p>
     <p>
         While Skyline stores this data into its high-performance data file, you are free to continue reviewing the results. You could even begin
@@ -268,7 +268,7 @@ <h1>Simple Manual Refinement</h1>
         For the first peptide in the document, that full range looks like:
     </p>
     <p>
-        <img src="image-4.png" />
+        <img src="s-4.png" />
     </p>
     <p>
         This looks like pretty noisy data at first glance, but if you would like to look deeper, you can click and drag a box around any of the large
@@ -296,7 +296,7 @@ <h1>Retention Time Prediction</h1>
         Skyline will display a graph like this:
     </p>
     <p>
-        <img src="image-5.png" />
+        <img src="s-5.png" />
     </p>
     <p>
         Notice the red point positioned on the current Regression Refined line. This point shows the SSRCalc score and measured time for the currently
@@ -315,7 +315,7 @@ <h1>Retention Time Prediction</h1>
         Skyline recalculates the regression, marking more peptides as outliers to change the graph to:
     </p>
     <p>
-        <img src="image-6.png" />
+        <img src="s-6.png" />
     </p>
     <p>
         You can create a new linear equation for retention time prediction by doing the following:
@@ -341,7 +341,7 @@ <h1>Retention Time Prediction</h1>
         to move the regression graph out of the way to see this):
     </p>
     <p>
-        <img src="image-7.png" />
+        <img src="s-7.png" />
     </p>
     <p>
         The shaded rectangle around this indicator shows the window (15.7 minutes) you accepted in the <b>Edit Retention Time Predictor</b>
@@ -361,7 +361,7 @@ <h1>Missing Data</h1>
         Escape key to return to the <b>Targets</b> view, which should now look something like:
     </p>
     <p>
-        <img src="image-8.png" />
+        <img src="s-8.png" />
     </p>
     <p>
         The absence of even a red dot peak quality icon indicates that no measurements were present for these 7 peptides in the RAW files imported into
@@ -378,7 +378,7 @@ <h1>Missing Data</h1>
         The chromatogram graph should now look something like:
     </p>
     <p>
-        <img src="image-9.png" />
+        <img src="s-9.png" />
     </p>
     <p>
         Notice the toolbar that has been added at the top, with the <b>File</b> choice list. If you click on this list, it will show that
@@ -421,19 +421,19 @@ <h1>Picking Measurable Peptides and Transitions</h1>
         The peptide view should now look like this:
     </p>
     <p>
-        <img src="image-10.png" />
+        <img src="s-10.png" />
     </p>
     <p class="keep-next">
         The dot-product (0.57) of the selected peptide is not that good, but all 11 y-ions measured have nicely co-eluting peaks:
     </p>
     <p>
-        <img src="image-11.png" />
+        <img src="s-11.png" />
     </p>
     <p class="keep-next">
         If you look at the MS/MS library spectrum graph, you can see an issue that might be causing the poor dot-product:
     </p>
     <p>
-        <img src="image-12.png" />
+        <img src="s-12.png" />
     </p>
     <p>
         Notice that the two most intense peaks in the MS/MS library spectrum are annotated with both y- and b-ions (y10, b10 and y12, b12). The Thermo
@@ -444,7 +444,7 @@ <h1>Picking Measurable Peptides and Transitions</h1>
         <li>Expand the precursor 1160.5434++ to have a closer look at the transitions, and you will see:</li>
     </ul>
     <p>
-        <img src="image-13.png" />
+        <img src="s-13.png" />
     </p>
     <p>
         The rank numbers on the left are the MS/MS library spectrum peak ranks, while the bracketed numbers to the far right are the SRM peak ranks.
@@ -487,10 +487,10 @@ <h1>Picking Measurable Peptides and Transitions</h1>
     <table class="comp-fig">
         <tr>
             <td class="comp-fig">
-                <img src="image-14.png" />
+                <img src="s-14.png" />
             </td>
             <td class="comp-fig">
-                <img src="image-15.png" />
+                <img src="s-15.png" />
             </td>
         </tr>
     </table>
@@ -606,7 +606,7 @@ <h2>Measuring Retention Times</h2>
         The <b>Export Transition List</b> form should look like this:
     </p>
     <p>
-        <img src="image-16.png" />
+        <img src="s-16.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -630,7 +630,7 @@ <h3>Reviewing Retention Time Runs</h3>
         Skyline should be showing charts for both replicates you created, as shown below:
     </p>
     <p>
-        <img src="image-17.png" />
+        <img src="s-17.png" />
     </p>
     <ul>
         <li>Press Shift-F11 to see the full range of the data acquired.</li>
@@ -646,7 +646,7 @@ <h3>Reviewing Retention Time Runs</h3>
         Skyline presents a graph like:
     </p>
     <p>
-        <img src="image-18.png" />
+        <img src="s-18.png" />
     </p>
     <p>
         From this graph, you can see the number of concurrent transitions the instrument will measure over your full chromatography run using several
@@ -674,7 +674,7 @@ <h2>Creating a Scheduled Transition List</h2>
         The <b>Peptide Settings</b> form should look like:
     </p>
     <p>
-        <img src="image-19.png" />
+        <img src="s-19.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -686,7 +686,7 @@ <h2>Creating a Scheduled Transition List</h2>
         The <b>Export Transition List</b> form should look like:
     </p>
     <p>
-        <img src="image-20.png" />
+        <img src="s-20.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -700,7 +700,7 @@ <h2>Creating a Scheduled Transition List</h2>
         at the file in Excel, you can see that start and stop times, 4 minutes apart, have been added in columns D and E:
     </p>
     <p>
-        <img src="image-21.png" />
+        <img src="s-transition-list-spreadsheet.png" />
     </p>
     <h1>Reviewing Multi-Replicate Data</h1>
     <p>
@@ -761,7 +761,7 @@ <h1>Reviewing Multi-Replicate Data</h1>
         Adjust splitters and window sizing until the Skyline window looks like this:
     </p>
     <p>
-        <img src="image-22.png" />
+        <img src="s-21.png" />
     </p>
     <p>
         You can now use the Down-Arrow key to review the data collected for these peptides. Other tutorials give more attention to analysis of
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/en/image-1.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/en/s-1.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/en/image-1.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/en/s-1.png
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similarity index 100%
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rename to pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/en/s-11.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/en/image-12.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/en/s-12.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/en/image-12.png
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rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/en/image-13.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/en/image-14.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/en/s-14.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/en/image-14.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/en/image-15.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/en/s-15.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/en/image-16.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/en/s-16.png
similarity index 100%
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/en/image-17.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/en/s-17.png
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rename to pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/en/s-17.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/en/image-18.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/en/s-18.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/en/image-18.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/en/image-19.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/en/s-19.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/en/image-19.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/en/image-2.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/en/s-2.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/en/image-2.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/en/image-20.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/en/s-20.png
similarity index 100%
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rename to pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/en/s-20.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/en/image-22.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/en/s-21.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/en/image-22.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/en/s-21.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/en/image-3.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/en/s-3.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/en/image-3.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/en/s-3.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/en/image-4.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/en/s-4.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/en/image-4.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/en/s-4.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/en/image-5.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/en/s-5.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/en/image-5.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/en/s-5.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/en/image-6.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/en/s-6.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/en/image-6.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/en/s-6.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/en/image-7.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/en/s-7.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/en/image-7.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/en/s-7.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/en/image-8.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/en/s-8.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/en/image-8.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/en/s-8.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/en/image-9.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/en/s-9.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/en/image-9.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/en/s-9.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/en/image-0.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/en/s-targeted-method-refinement-cycle.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/en/image-0.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/en/s-targeted-method-refinement-cycle.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/en/image-21.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/en/s-transition-list-spreadsheet.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/en/image-21.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/en/s-transition-list-spreadsheet.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/ja/index.html b/pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/ja/index.html
index 3b3b4a8792..c15f7c7754 100644
--- a/pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/ja/index.html
+++ b/pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/ja/index.html
@@ -19,7 +19,7 @@ <h1 class="document-title">Skylineターゲットメソッドの最適化</h1>
         これをターゲットメソッド最適化サイクルと呼び、下図に示すような考え方を表すことが多くあります。
     </p>
     <p>
-        <img src="image-0.png" />
+        <img src="s-targeted-method-refinement-cycle.png" />
     </p>
     <p>
         このサイクルを繰り返すことで、同時に数十から数千のタンパク質を対象とした最適なターゲットメソッド構築ができます。また実験目的に沿った最良のペプチド、プロダクトイオン、および装置設定をメソッドに組み込むことができます。ただしサイクル開始時のリストが大きいときには、他のチュートリアルで紹介されているグループ比較や詳細ピーク検出モデルといった統計メソッドを用いてサイクルを開始することもできます。
@@ -95,7 +95,7 @@ <h1>測定結果</h1>
         ライブラリから、MacCossラボの装置で測定されたこのペプチドのMS/MSスペクトルおよび、プロダクトイオンy3～y15についての時間-強度クロマトグラムが表示されます。
     </p>
     <p>
-        <img src="image-1.png" />
+        <img src="s-1.png" />
     </p>
     <p>
         注：各ペプチドに関連付けられたライブラリ内のMS/MSスペクトルは、イオントラップ型質量分析計を用いた測定結果から得られたものです。
@@ -128,7 +128,7 @@ <h1>未最適化メソッド</h1>
         [ <b>トランジションリストをエクスポート</b> ] は以下のように表示されます。
     </p>
     <p>
-        <img src="image-2.png" />
+        <img src="s-2.png" />
     </p>
     <ul>
         <li>[ <b>OK</b> ] ボタンをクリックします。</li>
@@ -197,7 +197,7 @@ <h1>複数の測定結果をインポートする</h1>
         Skylineが15個のファイルのインポートを開始します。インポートの進捗状況は、以下のように [ <b>結果をインポート</b> ] に表示されます。
     </p>
     <p>
-        <img src="image-3.png" />
+        <img src="s-3.png" />
     </p>
     <p>
         Skylineがこのデータを高性能なデータファイル形式に変換している間も、結果の確認が可能です。ドキュメントの修正を始めることも可能ですが、このチュートリアルでは、以下の手順に従って先に39個の結果ファイルすべてのインポートを完了してください。（ただし、最近のコンピュータは非常に高速なため、みなさんが他の作業を始める前にインポートが完了すると思います。）
@@ -239,7 +239,7 @@ <h1>手動最適化</h1>
         ドキュメント内の最初のペプチドのトランジションの保持時間範囲の全体図は、以下の通りです。
     </p>
     <p>
-        <img src="image-4.png" />
+        <img src="s-4.png" />
     </p>
     <p>
         一見ノイズの多いデータであるように見えます。より詳細に見るには、保持時間でラベルされたどの大きなピークも、その周辺をマウスでドラッグすると拡大できます。
@@ -262,7 +262,7 @@ <h1>保持時間予測</h1>
         Skylineに、以下のようなグラフが表示されます。
     </p>
     <p>
-        <img src="image-5.png" />
+        <img src="s-5.png" />
     </p>
     <p>
         「回帰の改良 refined regression」直線上に、赤色の点がハイライト表示されています。この点は、現在選択されているペプチドに対するSSRCalcスコアおよび測定時間を表しています。ハイライト表示された点は、Skyline [ <b>ターゲット</b>
@@ -280,7 +280,7 @@ <h1>保持時間予測</h1>
         Skylineが再度線形回帰を行い、より多くのペプチドを異常値としてマークしてグラフを以下のように変更します。
     </p>
     <p>
-         <img src="image-6.png" />
+         <img src="s-6.png" />
     </p>
     <p>
         以下の手順を行うことにより、保持時間予測のための新たな線形方程式を作成することも可能です。
@@ -303,7 +303,7 @@ <h1>保持時間予測</h1>
         下図のように、クロマトグラムにペプチドの予測保持時間が追加されます。
     </p>
     <p>
-        <img src="image-7.png" />
+        <img src="s-7.png" />
     </p>
     <p>
         保持時間予測値周辺の影がついた部分は、[ <b>保持時間予測を編集</b> ] で承認したウィンドウ幅（15.7分）を示します。影がついた部分の外側にあるピークはすべて、保持時間が予測値から標準偏差の2倍以上外れたものです。
@@ -321,7 +321,7 @@ <h1>データの欠落</h1>
         表示に戻ると、以下のように表示されます。
     </p>
     <p>
-        <img src="image-8.png" />
+        <img src="s-8.png" />
     </p>
     <p>
         赤いドットのピーク品質アイコンがないということは、このドキュメントにインポートしたRAWファイルの中には、これら7つのペプチドの測定値が存在しないということを表しています。最初にRAWファイルをインポートしたとき、39のトランジションリストと39のRAWファイルがありました。いったい何が起こったのでしょうか?
@@ -336,7 +336,7 @@ <h1>データの欠落</h1>
         クロマトグラムグラフが以下のように表示されます。
     </p>
     <p>
-        <img src="image-9.png" />
+        <img src="s-9.png" />
     </p>
     <p>
         上部に追加された、[ <b>ファイル</b> ] 選択リスト付きのツールバーに注目してください。このリストをクリックすると、worm_0027.RAWおよびworm_0028.RAWの両方がこのペプチドの測定値を含んでいると表示されます。
@@ -370,19 +370,19 @@ <h1>測定可能なペプチドおよびトランジションを選択する</h1
         ペプチド表示は以下のように表示されます。
     </p>
     <p>
-        <img src="image-10.png" />
+        <img src="s-10.png" />
     </p>
     <p class="keep-next">
         選択したペプチドはピーク品質アイコンが緑色であることから、プロダクトイオン（y1-y11）のピークすべてがほぼ同じ時間に観測されているとわかります。しかし、dotp値（0.57）はあまりよくありません。
     </p>
     <p>
-        <img src="image-11.png" />
+        <img src="s-11.png" />
     </p>
     <p class="keep-next">
         ライブラリのMS/MSスペクトルを見てみると、dotp値がよくない原因が理解できます。
     </p>
     <p>
-        <img src="image-12.png" />
+        <img src="s-12.png" />
     </p>
     <p>
         ライブラリのMS/MSスペクトル内で最も強度が高いピーク2つに、y-およびb-イオン（y10、b10およびy12、b12）両方の注釈が付いていることに注目してください。SRM測定に使用したThermo
@@ -392,7 +392,7 @@ <h1>測定可能なペプチドおよびトランジションを選択する</h1
         <li>トランジションの詳細を見るためプリカーサーイオンのm/z=1160.5434++を展開します。</li>
     </ul>
     <p>
-        <img src="image-13.png" />
+        <img src="s-13.png" />
     </p>
     <p>
         左側の( )に囲まれた数字はライブラリ内のMS/MSスペクトルにおける強度のランクを示します。右端の[
@@ -430,10 +430,10 @@ <h1>測定可能なペプチドおよびトランジションを選択する</h1
     <table class="comp-fig">
         <tr>
             <td class="comp-fig">
-                <img src="image-14.png" />
+                <img src="s-14.png" />
             </td>
             <td class="comp-fig">
-                <img src="image-15.png" />
+                <img src="s-15.png" />
             </td>
         </tr>
     </table>
@@ -533,7 +533,7 @@ <h2>保持時間を測定する</h2>
         [ <b>トランジションリストをエクスポート</b> ] は以下のように表示されます。
     </p>
     <p>
-        <img src="image-16.png" />
+        <img src="s-16.png" />
     </p>
     <ul>
         <li>[ <b>OK</b> ] ボタンをクリックします。</li>
@@ -556,7 +556,7 @@ <h3>保持時間情報を再確認する</h3>
         2回の繰り返し測定の両方のクロマトグラムが、以下のように表示されます。
     </p>
     <p>
-        <img src="image-17.png" />
+        <img src="s-17.png" />
     </p>
     <ul>
         <li>Shift+F11を押すと取得データの全範囲が表示されます。</li>
@@ -572,7 +572,7 @@ <h3>保持時間情報を再確認する</h3>
         Skylineに以下のようなグラフが表示されます。
     </p>
     <p>
-        <img src="image-18.png" />
+        <img src="s-18.png" />
     </p>
     <p>
         このグラフより、測定中のある時間（横軸）において同時に測定する必要のあるトランジション数（縦軸）が、トランジションの測定時間ごとにわかります。1トランジションの測定時間ウィンドウが長くなるほど、より多くのトランジションを同時に測定する必要が発生します。今回の場合は、各トランジションの測定時間ウィンドウを5分に設定すると、最大で約60のトランジションを同時に測定する必要があります。使用する装置のスピードに応じて1トランジションあたりの測定時間を設定することにより、1回の測定で各ペプチドの全トランジションで溶出曲線を描くのに充分なデータを取得することができるでしょう。
@@ -594,7 +594,7 @@ <h2>スケジュール化されたトランジションリストを作成する<
         [ <b>ペプチド設定</b> ] は以下のように表示されます。
     </p>
     <p>
-        <img src="image-19.png" />
+        <img src="s-19.png" />
     </p>
     <ul>
         <li>[ <b>OK</b> ] ボタンをクリックします。</li>
@@ -606,7 +606,7 @@ <h2>スケジュール化されたトランジションリストを作成する<
         [ <b>トランジションリストをエクスポート</b> ] フォームは以下のように表示されます。
     </p>
     <p>
-        <img src="image-20.png" />
+        <img src="s-20.png" />
     </p>
     <ul>
         <li>[ <b>OK</b> ] ボタンをクリックします。</li>
@@ -619,7 +619,7 @@ <h2>スケジュール化されたトランジションリストを作成する<
         MethodRefineフォルダ内に、新たにスケジュール化されたSRMトランジションリストファイル（Scheduled.csv）が作成されます。当該ファイルをExcelで開くと、4分間の測定の開始・停止時間がD列およびE列に追加されていることが確認できます。
     </p>
     <p>
-        <img src="image-21.png" />
+        <img src="s-transition-list-spreadsheet.png" />
     </p>
     <h1>複数繰り返し測定結果を確認する</h1>
     <p>
@@ -675,7 +675,7 @@ <h1>複数繰り返し測定結果を確認する</h1>
         Skylineウィンドウが以下のように見えるまで、スプリッターおよびウィンドウサイズを調整します。
     </p>
     <p>
-        <img src="image-22.png" />
+        <img src="s-21.png" />
     </p>
     <p>
         ここで下向き矢印キーを使用すると、これらのペプチドについて収集したデータを確認することが可能です。複数の繰り返し測定により最適化したSRMメソッドの詳細については、その他のチュートリアルで説明いたします。
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/ja/invariant.html b/pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/ja/invariant.html
index e0cfeacbf9..821ae56e37 100644
--- a/pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/ja/invariant.html
+++ b/pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/ja/invariant.html
@@ -22,7 +22,7 @@ <h1 class="document-title">Skyline Targeted Method Refinement</h1>
         We call this the Targeted Method Refinement Cycle and often present the idea as shown below:
     </p>
     <p>
-        <img src="image-0.png" />
+        <img src="s-targeted-method-refinement-cycle.png" />
     </p>
     <p>
         By iterating over this cycle, you can start with a broad hypothesis including dozens to thousands of proteins you are interested in monitoring,
@@ -104,7 +104,7 @@ <h1>Results Data</h1>
         product ions y3 – y15 of this peptide on an instrument in the MacCoss lab:
     </p>
     <p>
-        <img src="image-1.png" />
+        <img src="s-1.png" />
     </p>
     <p>
         Note that the MS/MS library spectrum associated with each peptide was derived from experiments conducted on an ion trap mass spectrometer.
@@ -143,7 +143,7 @@ <h1>Unrefined Methods</h1>
         The <b>Export Transition List</b> form should look like:
     </p>
     <p>
-        <img src="image-2.png" />
+        <img src="s-2.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -219,7 +219,7 @@ <h1>Importing Multiple Injection Data</h1>
         form like the one below:
     </p>
     <p>
-        <img src="image-3.png" />
+        <img src="s-3.png" />
     </p>
     <p>
         While Skyline stores this data into its high-performance data file, you are free to continue reviewing the results. You could even begin
@@ -268,7 +268,7 @@ <h1>Simple Manual Refinement</h1>
         For the first peptide in the document, that full range looks like:
     </p>
     <p>
-        <img src="image-4.png" />
+        <img src="s-4.png" />
     </p>
     <p>
         This looks like pretty noisy data at first glance, but if you would like to look deeper, you can click and drag a box around any of the large
@@ -296,7 +296,7 @@ <h1>Retention Time Prediction</h1>
         Skyline will display a graph like this:
     </p>
     <p>
-        <img src="image-5.png" />
+        <img src="s-5.png" />
     </p>
     <p>
         Notice the red point positioned on the current Regression Refined line. This point shows the SSRCalc score and measured time for the currently
@@ -315,7 +315,7 @@ <h1>Retention Time Prediction</h1>
         Skyline recalculates the regression, marking more peptides as outliers to change the graph to:
     </p>
     <p>
-        <img src="image-6.png" />
+        <img src="s-6.png" />
     </p>
     <p>
         You can create a new linear equation for retention time prediction by doing the following:
@@ -341,7 +341,7 @@ <h1>Retention Time Prediction</h1>
         to move the regression graph out of the way to see this):
     </p>
     <p>
-        <img src="image-7.png" />
+        <img src="s-7.png" />
     </p>
     <p>
         The shaded rectangle around this indicator shows the window (15.7 minutes) you accepted in the <b>Edit Retention Time Predictor</b>
@@ -361,7 +361,7 @@ <h1>Missing Data</h1>
         Escape key to return to the <b>Targets</b> view, which should now look something like:
     </p>
     <p>
-        <img src="image-8.png" />
+        <img src="s-8.png" />
     </p>
     <p>
         The absence of even a red dot peak quality icon indicates that no measurements were present for these 7 peptides in the RAW files imported into
@@ -378,7 +378,7 @@ <h1>Missing Data</h1>
         The chromatogram graph should now look something like:
     </p>
     <p>
-        <img src="image-9.png" />
+        <img src="s-9.png" />
     </p>
     <p>
         Notice the toolbar that has been added at the top, with the <b>File</b> choice list. If you click on this list, it will show that
@@ -421,19 +421,19 @@ <h1>Picking Measurable Peptides and Transitions</h1>
         The peptide view should now look like this:
     </p>
     <p>
-        <img src="image-10.png" />
+        <img src="s-10.png" />
     </p>
     <p class="keep-next">
         The dot-product (0.57) of the selected peptide is not that good, but all 11 y-ions measured have nicely co-eluting peaks:
     </p>
     <p>
-        <img src="image-11.png" />
+        <img src="s-11.png" />
     </p>
     <p class="keep-next">
         If you look at the MS/MS library spectrum graph, you can see an issue that might be causing the poor dot-product:
     </p>
     <p>
-        <img src="image-12.png" />
+        <img src="s-12.png" />
     </p>
     <p>
         Notice that the two most intense peaks in the MS/MS library spectrum are annotated with both y- and b-ions (y10, b10 and y12, b12). The Thermo
@@ -444,7 +444,7 @@ <h1>Picking Measurable Peptides and Transitions</h1>
         <li>Expand the precursor 1160.5434++ to have a closer look at the transitions, and you will see:</li>
     </ul>
     <p>
-        <img src="image-13.png" />
+        <img src="s-13.png" />
     </p>
     <p>
         The rank numbers on the left are the MS/MS library spectrum peak ranks, while the bracketed numbers to the far right are the SRM peak ranks.
@@ -487,10 +487,10 @@ <h1>Picking Measurable Peptides and Transitions</h1>
     <table class="comp-fig">
         <tr>
             <td class="comp-fig">
-                <img src="image-14.png" />
+                <img src="s-14.png" />
             </td>
             <td class="comp-fig">
-                <img src="image-15.png" />
+                <img src="s-15.png" />
             </td>
         </tr>
     </table>
@@ -605,7 +605,7 @@ <h2>Measuring Retention Times</h2>
         The <b>Export Transition List</b> form should look like this:
     </p>
     <p>
-        <img src="image-16.png" />
+        <img src="s-16.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -629,7 +629,7 @@ <h3>Reviewing Retention Time Runs</h3>
         Skyline should be showing charts for both replicates you created, as shown below:
     </p>
     <p>
-        <img src="image-17.png" />
+        <img src="s-17.png" />
     </p>
     <ul>
         <li>Press Shift-F11 to see the full range of the data acquired.</li>
@@ -645,7 +645,7 @@ <h3>Reviewing Retention Time Runs</h3>
         Skyline presents a graph like:
     </p>
     <p>
-        <img src="image-18.png" />
+        <img src="s-18.png" />
     </p>
     <p>
         From this graph, you can see the number of concurrent transitions the instrument will measure over your full chromatography run using several
@@ -673,7 +673,7 @@ <h2>Creating a Scheduled Transition List</h2>
         The <b>Peptide Settings</b> form should look like:
     </p>
     <p>
-        <img src="image-19.png" />
+        <img src="s-19.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -685,7 +685,7 @@ <h2>Creating a Scheduled Transition List</h2>
         The <b>Export Transition List</b> form should look like:
     </p>
     <p>
-        <img src="image-20.png" />
+        <img src="s-20.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -699,7 +699,7 @@ <h2>Creating a Scheduled Transition List</h2>
         at the file in Excel, you can see that start and stop times, 4 minutes apart, have been added in columns D and E:
     </p>
     <p>
-        <img src="image-21.png" />
+        <img src="s-transition-list-spreadsheet.png" />
     </p>
     <h1>Reviewing Multi-Replicate Data</h1>
     <p>
@@ -759,7 +759,7 @@ <h1>Reviewing Multi-Replicate Data</h1>
         Adjust splitters and window sizing until the Skyline window looks like this:
     </p>
     <p>
-        <img src="image-22.png" />
+        <img src="s-21.png" />
     </p>
     <p>
         You can now use the Down-Arrow key to review the data collected for these peptides. Other tutorials give more attention to analysis of
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/ja/image-1.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/ja/s-1.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/ja/image-1.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/ja/s-1.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/ja/image-10.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/ja/s-10.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/ja/image-10.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/ja/s-10.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/ja/image-11.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/ja/s-11.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/ja/image-11.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/ja/s-11.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/ja/image-12.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/ja/s-12.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/ja/image-12.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/ja/s-12.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/ja/image-13.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/ja/s-13.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/ja/image-13.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/ja/s-13.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/ja/image-14.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/ja/s-14.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/ja/image-14.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/ja/s-14.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/ja/image-15.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/ja/s-15.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/ja/image-15.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/ja/s-15.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/ja/image-16.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/ja/s-16.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/ja/image-16.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/ja/s-16.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/ja/image-17.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/ja/s-17.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/ja/image-17.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/ja/s-17.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/ja/image-18.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/ja/s-18.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/ja/image-18.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/ja/s-18.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/ja/image-19.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/ja/s-19.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/ja/image-19.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/ja/s-19.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/ja/image-2.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/ja/s-2.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/ja/image-2.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/ja/s-2.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/ja/image-20.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/ja/s-20.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/ja/image-20.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/ja/s-20.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/ja/image-22.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/ja/s-21.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/ja/image-22.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/ja/image-3.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/ja/s-3.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/ja/image-3.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/ja/s-3.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/ja/image-4.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/ja/s-4.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/ja/image-4.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/ja/s-4.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/ja/image-5.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/ja/s-5.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/ja/image-5.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/ja/image-6.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/ja/s-6.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/ja/image-6.png
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similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/ja/image-7.png
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similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/ja/image-8.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/ja/image-9.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/ja/s-9.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/ja/image-9.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/ja/s-9.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/ja/image-0.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/ja/s-targeted-method-refinement-cycle.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/ja/image-0.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/ja/s-targeted-method-refinement-cycle.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/ja/image-21.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/ja/s-transition-list-spreadsheet.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/ja/image-21.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/ja/s-transition-list-spreadsheet.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/zh-CHS/index.html b/pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/zh-CHS/index.html
index 986a4e1ad8..c2fe64ef29 100644
--- a/pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/zh-CHS/index.html
+++ b/pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/zh-CHS/index.html
@@ -18,7 +18,7 @@ <h1 class="document-title">Skyline 靶向方法优化</h1>
         我们将这个过程称为“靶向方法优化周期”，该过程经常以下图体现：
     </p>
     <p>
-        <img src="image-0.png" />
+        <img src="s-targeted-method-refinement-cycle.png" />
     </p>
     <p>
         通过循环此周期，您可以从比较笼统的假设开始，包括您想监测的几十到几千个不等的蛋白质，快速缩小清单至最佳肽段、子离子和仪器设置，以便达到您的实验目标。但如果您的起始列表含有很多蛋白质，那么从其它教程中介绍的统计方法（例如分组比较和高级峰值检测模型）着手会更好。
@@ -93,7 +93,7 @@ <h1>结果数据</h1>
         然后Skyline 会显示一些图，包括来自谱图库中的相应 MS/MS 谱图，以及在 MacCoss 实验室仪器上对该肽段的子离子 y3 – y15 测得的时间-强度色谱图数据：
     </p>
     <p>
-        <img src="image-1.png" />
+        <img src="s-1.png" />
     </p>
     <p>
         请注意，与每个肽段相关联的来自于谱图库中的 MS/MS谱图是在离子阱质谱仪上采集的。
@@ -127,7 +127,7 @@ <h1>未优化的方法</h1>
         <b>导出离子对列表</b>表单如下所示：
     </p>
     <p>
-        <img src="image-2.png" />
+        <img src="s-2.png" />
     </p>
     <ul>
         <li>单击<b>确定</b>按钮。</li>
@@ -195,7 +195,7 @@ <h1>导入多个进样数据</h1>
         Skyline 将开始导入这 15 个文件，在<b>导入结果</b>表单中可以看到如下所示的结果：
     </p>
     <p>
-        <img src="image-3.png" />
+        <img src="s-3.png" />
     </p>
     <p>
         Skyline 将该数据存储至高性能数据文件后，日后随时可以检查结果。您甚至可以开始优化文档，但是对于本教程，您应当执行下列步骤来完成导入所有 39 个结果文件（不过在现代计算机上的运行速度非常之快，其它工作尚未开始便已完成导入）：
@@ -236,7 +236,7 @@ <h1>简单手动优化</h1>
         对于文档中的第一个肽段，整个范围如下所示：
     </p>
     <p>
-        <img src="image-4.png" />
+        <img src="s-4.png" />
     </p>
     <p>
         乍一看这很像有大量噪音的数据，但是如果您想看更多的细节，您可以对标有保留时间的任何较大峰附近单击并拖曳出一个方框来放大该区域。
@@ -259,7 +259,7 @@ <h1>保留时间预测</h1>
         Skyline 将显示如下图形：
     </p>
     <p>
-        <img src="image-5.png" />
+        <img src="s-5.png" />
     </p>
     <p>
         注意位于当前已优化的回归线上的红色点。该点显示了 SSRCalc 分值和当前所选肽段的出峰时间。您在 Skyline <b>目标</b>视图中选择不同的肽段时，突出点将会相应改变。
@@ -276,7 +276,7 @@ <h1>保留时间预测</h1>
         Skyline 将重新计算回归，将更多的肽段标记为异常值，将图变成：
     </p>
     <p>
-        <img src="image-6.png" />
+        <img src="s-6.png" />
     </p>
     <p>
         您可通过执行如下操作来创建新的线性方程式以进行保留时间预测：
@@ -299,7 +299,7 @@ <h1>保留时间预测</h1>
         Skyline 会将所选肽段的预测的保留时间的指示符添加至色谱图中，如下所示（您可能需要将回归图移开以便进行观察）：
     </p>
     <p>
-        <img src="image-7.png" />
+        <img src="s-7.png" />
     </p>
     <p>
         该指示符周围的阴影矩形显示了您在<b>编辑保留时间预测器</b>表单中选择的窗口（15.7 分钟）。任何阴影矩形外的值均大于预测值的 2 个标准偏差。
@@ -316,7 +316,7 @@ <h1>缺失数据</h1>
         Skyline 将以红色突出显示该点并滚动<b>目标</b>视图，以显示新选择的肽段 (YLAEVASEDR)。按 Esc 键返回<b>目标</b>视图，现在应显示如下：
     </p>
     <p>
-        <img src="image-8.png" />
+        <img src="s-8.png" />
     </p>
     <p>
         这里有 7 个肽段没有红点峰质量图标，表示这些肽段在导入的 RAW 文件中无法进行定量。如果我们是首次将原始文件导入本文档，这可能会令人觉得奇怪。39 个离子对列表对应 39 个原始文件。这是怎么回事呢？
@@ -331,7 +331,7 @@ <h1>缺失数据</h1>
         色谱图现在将显示如下：
     </p>
     <p>
-        <img src="image-9.png" />
+        <img src="s-9.png" />
     </p>
     <p>
         注意已经使用<b>文件</b>下拉列表将工具栏添加到顶部。如果您单击该列表，将会显示 worm_0027.RAW 和 worm_0028.RAW 这两个文件都包含该肽段测量值。
@@ -365,19 +365,19 @@ <h1>选择可测量肽段和离子对</h1>
         肽段视图现在将如下所示：
     </p>
     <p>
-        <img src="image-10.png" />
+        <img src="s-10.png" />
     </p>
     <p class="keep-next">
         所选肽段的点积值 (0.57) 并不好，但是所有测量的 11 个 y-离子具有较好的共洗脱峰：
     </p>
     <p>
-        <img src="image-11.png" />
+        <img src="s-11.png" />
     </p>
     <p class="keep-next">
         如果您查看 MS/MS谱图库，您可以看到导致较差的点积值的问题所在：
     </p>
     <p>
-        <img src="image-12.png" />
+        <img src="s-12.png" />
     </p>
     <p>
         请注意在 MS/MS谱图库中的两个最强峰标注有 y-离子和 b-离子（y10, b10 和 y12, b12）。我们已经知道用于 SRM 测量的 Thermo TSQ 仪器不能很好地保留 b-离子，这意味着这些峰的 b10 和 b12 离子不会在 SRM 测量中出现。
@@ -386,7 +386,7 @@ <h1>选择可测量肽段和离子对</h1>
         <li>展开母离子 1160.5434++ 来进一步查看离子对，您将看到：</li>
     </ul>
     <p>
-        <img src="image-13.png" />
+        <img src="s-13.png" />
     </p>
     <p>
         左侧的排名序号是 MS/MS谱图库峰排名，而最右边方括号内的数字是 SRM 峰排名。这些数字可能会帮助您决定是否相信这些离子对的测量值对应于MS/MS 谱图库中的肽段。不过在本教程中需要移除该肽段： 
@@ -423,10 +423,10 @@ <h1>选择可测量肽段和离子对</h1>
     <table class="comp-fig">
         <tr>
             <td class="comp-fig">
-                <img src="image-14.png" />
+                <img src="s-14.png" />
             </td>
             <td class="comp-fig">
-                <img src="image-15.png" />
+                <img src="s-15.png" />
             </td>
         </tr>
     </table>
@@ -526,7 +526,7 @@ <h2>测量保留时间</h2>
         <b>导出离子对列表</b>表单应当如下所示：
     </p>
     <p>
-        <img src="image-16.png" />
+        <img src="s-16.png" />
     </p>
     <ul>
         <li>单击<b>确定</b>按钮。</li>
@@ -549,7 +549,7 @@ <h3>查看保留时间运行</h3>
         Skyline 将显示您创建的两个重复检测的图表，如下所示：
     </p>
     <p>
-        <img src="image-17.png" />
+        <img src="s-17.png" />
     </p>
     <ul>
         <li>按 Shift-F11 查看所获取的全部数据。</li>
@@ -565,7 +565,7 @@ <h3>查看保留时间运行</h3>
         Skyline 将显示下图：
     </p>
     <p>
-        <img src="image-18.png" />
+        <img src="s-18.png" />
     </p>
     <p>
         从该图中，您可以查看仪器在整个色谱运行中使用先前测量的保留时间附近的多个可能的时间窗口测量的并行离子对的数量。时间窗口越大，您看到的同时出现的离子对就越多。在此文档中，时间窗口为 5 分钟时，同时测量的离子对的最大数量大约为
@@ -588,7 +588,7 @@ <h2>创建安排时序的离子对列表</h2>
         <b>肽段设置</b>表单应如下所示：
     </p>
     <p>
-        <img src="image-19.png" />
+        <img src="s-19.png" />
     </p>
     <ul>
         <li>单击<b>确定</b>按钮。</li>
@@ -600,7 +600,7 @@ <h2>创建安排时序的离子对列表</h2>
         <b>导出离子对列表</b>表单如下所示：
     </p>
     <p>
-        <img src="image-20.png" />
+        <img src="s-20.png" />
     </p>
     <ul>
         <li>单击<b>确定</b>按钮。</li>
@@ -613,7 +613,7 @@ <h2>创建安排时序的离子对列表</h2>
         在 MethodRefine 文件夹中，您将看到剩余肽段的已安排时序的 SRM 新离子对列表文件 (Scheduled.csv)。如果您用 Excel 查看这个文件，您可以看到在 D 栏和 E 栏中添加了起始时间和结束时间，两者间隔时间为 4 分钟。
     </p>
     <p>
-        <img src="image-21.png" />
+        <img src="s-transition-list-spreadsheet.png" />
     </p>
     <h1>查看多次平行测定数据</h1>
     <p>
@@ -669,7 +669,7 @@ <h1>查看多次平行测定数据</h1>
         调节分离条和窗口尺寸，直至 Skyline 窗口如下所示：
     </p>
     <p>
-        <img src="image-22.png" />
+        <img src="s-21.png" />
     </p>
     <p>
         您现在可以使用下箭头键，查看为这些肽段采集的数据。其它教程会着重分析为多次平行测定优化的 SRM 方法。
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/zh-CHS/invariant.html b/pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/zh-CHS/invariant.html
index e0cfeacbf9..821ae56e37 100644
--- a/pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/zh-CHS/invariant.html
+++ b/pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/zh-CHS/invariant.html
@@ -22,7 +22,7 @@ <h1 class="document-title">Skyline Targeted Method Refinement</h1>
         We call this the Targeted Method Refinement Cycle and often present the idea as shown below:
     </p>
     <p>
-        <img src="image-0.png" />
+        <img src="s-targeted-method-refinement-cycle.png" />
     </p>
     <p>
         By iterating over this cycle, you can start with a broad hypothesis including dozens to thousands of proteins you are interested in monitoring,
@@ -104,7 +104,7 @@ <h1>Results Data</h1>
         product ions y3 – y15 of this peptide on an instrument in the MacCoss lab:
     </p>
     <p>
-        <img src="image-1.png" />
+        <img src="s-1.png" />
     </p>
     <p>
         Note that the MS/MS library spectrum associated with each peptide was derived from experiments conducted on an ion trap mass spectrometer.
@@ -143,7 +143,7 @@ <h1>Unrefined Methods</h1>
         The <b>Export Transition List</b> form should look like:
     </p>
     <p>
-        <img src="image-2.png" />
+        <img src="s-2.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -219,7 +219,7 @@ <h1>Importing Multiple Injection Data</h1>
         form like the one below:
     </p>
     <p>
-        <img src="image-3.png" />
+        <img src="s-3.png" />
     </p>
     <p>
         While Skyline stores this data into its high-performance data file, you are free to continue reviewing the results. You could even begin
@@ -268,7 +268,7 @@ <h1>Simple Manual Refinement</h1>
         For the first peptide in the document, that full range looks like:
     </p>
     <p>
-        <img src="image-4.png" />
+        <img src="s-4.png" />
     </p>
     <p>
         This looks like pretty noisy data at first glance, but if you would like to look deeper, you can click and drag a box around any of the large
@@ -296,7 +296,7 @@ <h1>Retention Time Prediction</h1>
         Skyline will display a graph like this:
     </p>
     <p>
-        <img src="image-5.png" />
+        <img src="s-5.png" />
     </p>
     <p>
         Notice the red point positioned on the current Regression Refined line. This point shows the SSRCalc score and measured time for the currently
@@ -315,7 +315,7 @@ <h1>Retention Time Prediction</h1>
         Skyline recalculates the regression, marking more peptides as outliers to change the graph to:
     </p>
     <p>
-        <img src="image-6.png" />
+        <img src="s-6.png" />
     </p>
     <p>
         You can create a new linear equation for retention time prediction by doing the following:
@@ -341,7 +341,7 @@ <h1>Retention Time Prediction</h1>
         to move the regression graph out of the way to see this):
     </p>
     <p>
-        <img src="image-7.png" />
+        <img src="s-7.png" />
     </p>
     <p>
         The shaded rectangle around this indicator shows the window (15.7 minutes) you accepted in the <b>Edit Retention Time Predictor</b>
@@ -361,7 +361,7 @@ <h1>Missing Data</h1>
         Escape key to return to the <b>Targets</b> view, which should now look something like:
     </p>
     <p>
-        <img src="image-8.png" />
+        <img src="s-8.png" />
     </p>
     <p>
         The absence of even a red dot peak quality icon indicates that no measurements were present for these 7 peptides in the RAW files imported into
@@ -378,7 +378,7 @@ <h1>Missing Data</h1>
         The chromatogram graph should now look something like:
     </p>
     <p>
-        <img src="image-9.png" />
+        <img src="s-9.png" />
     </p>
     <p>
         Notice the toolbar that has been added at the top, with the <b>File</b> choice list. If you click on this list, it will show that
@@ -421,19 +421,19 @@ <h1>Picking Measurable Peptides and Transitions</h1>
         The peptide view should now look like this:
     </p>
     <p>
-        <img src="image-10.png" />
+        <img src="s-10.png" />
     </p>
     <p class="keep-next">
         The dot-product (0.57) of the selected peptide is not that good, but all 11 y-ions measured have nicely co-eluting peaks:
     </p>
     <p>
-        <img src="image-11.png" />
+        <img src="s-11.png" />
     </p>
     <p class="keep-next">
         If you look at the MS/MS library spectrum graph, you can see an issue that might be causing the poor dot-product:
     </p>
     <p>
-        <img src="image-12.png" />
+        <img src="s-12.png" />
     </p>
     <p>
         Notice that the two most intense peaks in the MS/MS library spectrum are annotated with both y- and b-ions (y10, b10 and y12, b12). The Thermo
@@ -444,7 +444,7 @@ <h1>Picking Measurable Peptides and Transitions</h1>
         <li>Expand the precursor 1160.5434++ to have a closer look at the transitions, and you will see:</li>
     </ul>
     <p>
-        <img src="image-13.png" />
+        <img src="s-13.png" />
     </p>
     <p>
         The rank numbers on the left are the MS/MS library spectrum peak ranks, while the bracketed numbers to the far right are the SRM peak ranks.
@@ -487,10 +487,10 @@ <h1>Picking Measurable Peptides and Transitions</h1>
     <table class="comp-fig">
         <tr>
             <td class="comp-fig">
-                <img src="image-14.png" />
+                <img src="s-14.png" />
             </td>
             <td class="comp-fig">
-                <img src="image-15.png" />
+                <img src="s-15.png" />
             </td>
         </tr>
     </table>
@@ -605,7 +605,7 @@ <h2>Measuring Retention Times</h2>
         The <b>Export Transition List</b> form should look like this:
     </p>
     <p>
-        <img src="image-16.png" />
+        <img src="s-16.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -629,7 +629,7 @@ <h3>Reviewing Retention Time Runs</h3>
         Skyline should be showing charts for both replicates you created, as shown below:
     </p>
     <p>
-        <img src="image-17.png" />
+        <img src="s-17.png" />
     </p>
     <ul>
         <li>Press Shift-F11 to see the full range of the data acquired.</li>
@@ -645,7 +645,7 @@ <h3>Reviewing Retention Time Runs</h3>
         Skyline presents a graph like:
     </p>
     <p>
-        <img src="image-18.png" />
+        <img src="s-18.png" />
     </p>
     <p>
         From this graph, you can see the number of concurrent transitions the instrument will measure over your full chromatography run using several
@@ -673,7 +673,7 @@ <h2>Creating a Scheduled Transition List</h2>
         The <b>Peptide Settings</b> form should look like:
     </p>
     <p>
-        <img src="image-19.png" />
+        <img src="s-19.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -685,7 +685,7 @@ <h2>Creating a Scheduled Transition List</h2>
         The <b>Export Transition List</b> form should look like:
     </p>
     <p>
-        <img src="image-20.png" />
+        <img src="s-20.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -699,7 +699,7 @@ <h2>Creating a Scheduled Transition List</h2>
         at the file in Excel, you can see that start and stop times, 4 minutes apart, have been added in columns D and E:
     </p>
     <p>
-        <img src="image-21.png" />
+        <img src="s-transition-list-spreadsheet.png" />
     </p>
     <h1>Reviewing Multi-Replicate Data</h1>
     <p>
@@ -759,7 +759,7 @@ <h1>Reviewing Multi-Replicate Data</h1>
         Adjust splitters and window sizing until the Skyline window looks like this:
     </p>
     <p>
-        <img src="image-22.png" />
+        <img src="s-21.png" />
     </p>
     <p>
         You can now use the Down-Arrow key to review the data collected for these peptides. Other tutorials give more attention to analysis of
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/zh-CHS/image-1.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/zh-CHS/s-1.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/zh-CHS/image-1.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/zh-CHS/s-1.png
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rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/zh-CHS/image-8.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/zh-CHS/s-8.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/zh-CHS/image-9.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/zh-CHS/s-9.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/zh-CHS/image-9.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/zh-CHS/s-9.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/zh-CHS/image-0.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/zh-CHS/s-targeted-method-refinement-cycle.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/zh-CHS/image-0.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/zh-CHS/s-targeted-method-refinement-cycle.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/zh-CHS/image-21.png b/pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/zh-CHS/s-transition-list-spreadsheet.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/zh-CHS/image-21.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/MethodRefine/zh-CHS/s-transition-list-spreadsheet.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/OptimizeCE/en/index.html b/pwiz_tools/Skyline/Documentation/Tutorials/OptimizeCE/en/index.html
index b37b493db7..f882776418 100644
--- a/pwiz_tools/Skyline/Documentation/Tutorials/OptimizeCE/en/index.html
+++ b/pwiz_tools/Skyline/Documentation/Tutorials/OptimizeCE/en/index.html
@@ -90,7 +90,7 @@ <h1>Deriving a New Linear Equation</h1>
         You should be presented with a form that looks like this:
     </p>
     <p>
-        <img src="image-0.png" />
+        <img src="s-1.png" />
     </p>
     <p>
         In it you can see the slope and y-intercept values used for both charge 2 and charge 3 precursors. Any precursor charges that are not covered
@@ -123,7 +123,7 @@ <h2>Measuring Retention Times for Method Scheduling</h2>
         Make sure the form looks like this:
     </p>
     <p>
-        <img src="image-1.png" />
+        <img src="s-2.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -228,7 +228,7 @@ <h2>Measuring Retention Times for Method Scheduling</h2>
         After the import is completed, Skyline should look like this:
     </p>
     <p>
-        <img src="image-2.png" />
+        <img src="s-3.png" />
     </p>
     <p>
         You can select a few of the peptides in the tree-view to see their chromatograms in the chart on the right.
@@ -242,7 +242,7 @@ <h2>Creating Optimization Methods</h2>
         <li>Edit the form to look like this:</li>
     </ul>
     <p>
-        <img src="image-3.png" />
+        <img src="s-4.png" />
     </p>
     <p>
         NOTE: We eventually realized that 132 was a better value for <b>Max concurrent transitions</b>, because it allows 3 precursors * 4
@@ -261,7 +261,7 @@ <h2>Creating Optimization Methods</h2>
         something like the following for your OptimizeCE folder:
     </p>
     <p>
-        <img src="image-4.png" />
+        <img src="s-5.png" />
     </p>
     <p>
         If you open one of the CSV files in Excel, it should contain a transition list like the one below, with 9 columns in the order precursor m/z,
@@ -490,7 +490,7 @@ <h2>Analyzing Optimization Data</h2>
         Once the data is loaded, Skyline should look something like this:
     </p>
     <p>
-        <img src="image-5.png" />
+        <img src="s-6.png" />
     </p>
     <p>
         The red bar in the middle of the <b>Peak Areas</b> view and the red curve among the chromatograms is the measurement for the
@@ -517,7 +517,7 @@ <h2>Analyzing Optimization Data</h2>
         but not that bad.
     </p>
     <p>
-        <img src="image-6.png" />
+        <img src="s-7.png" />
     </p>
     <p>
         For this tutorial, however, remove this peptide before calculating the new equation for the Thermo TSQ Vantage.
@@ -562,7 +562,7 @@ <h2>Creating a New Equation for CE</h2>
         Skyline will present the following graphs:
     </p>
     <p>
-        <img src="image-7.png" />
+        <img src="s-8.png" />
     </p>
     <p>
         The points correlate very well to the new linear equation, and appear to be on average 3-4 volts below the CE values chosen by the default
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/OptimizeCE/en/image-0.png b/pwiz_tools/Skyline/Documentation/Tutorials/OptimizeCE/en/s-1.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/OptimizeCE/en/image-0.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/OptimizeCE/en/s-1.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/OptimizeCE/en/image-1.png b/pwiz_tools/Skyline/Documentation/Tutorials/OptimizeCE/en/s-2.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/OptimizeCE/en/image-1.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/OptimizeCE/en/s-2.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/OptimizeCE/en/image-2.png b/pwiz_tools/Skyline/Documentation/Tutorials/OptimizeCE/en/s-3.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/OptimizeCE/en/image-2.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/OptimizeCE/en/s-3.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/OptimizeCE/en/image-3.png b/pwiz_tools/Skyline/Documentation/Tutorials/OptimizeCE/en/s-4.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/OptimizeCE/en/image-3.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/OptimizeCE/en/s-4.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/OptimizeCE/en/image-4.png b/pwiz_tools/Skyline/Documentation/Tutorials/OptimizeCE/en/s-5.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/OptimizeCE/en/image-4.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/OptimizeCE/en/s-5.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/OptimizeCE/en/image-5.png b/pwiz_tools/Skyline/Documentation/Tutorials/OptimizeCE/en/s-6.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/OptimizeCE/en/image-5.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/OptimizeCE/en/s-6.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/OptimizeCE/en/image-6.png b/pwiz_tools/Skyline/Documentation/Tutorials/OptimizeCE/en/s-7.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/OptimizeCE/en/image-6.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/OptimizeCE/en/s-7.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/OptimizeCE/en/image-7.png b/pwiz_tools/Skyline/Documentation/Tutorials/OptimizeCE/en/s-8.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/OptimizeCE/en/image-7.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/OptimizeCE/en/s-8.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/PRM/en/index.html b/pwiz_tools/Skyline/Documentation/Tutorials/PRM/en/index.html
index 899d2446d6..ae80d65dbf 100644
--- a/pwiz_tools/Skyline/Documentation/Tutorials/PRM/en/index.html
+++ b/pwiz_tools/Skyline/Documentation/Tutorials/PRM/en/index.html
@@ -20,27 +20,27 @@ <h1 class="document-title">Skyline Parallel Reaction Monitoring</h1>
         the practice of SRM with triple quadrupole mass spectrometers, where Skyline got its start:
     </p>
     <p>
-        <img style="width: 500px;" src="image-0.png" />
+        <img style="width: 500px;" src="s-triple-quadrupole-mass-spectrometer.png" />
     </p>
     <p>
         As SRM scans through precursor and product ion pairs, collecting single intensity measurements for each in a cycle over time, PRM scans through
         a data independent list of precursor ions collecting full MS/MS spectra for each in a cycle over time. 
     </p>
     <p>
-        <img style="width: 500px;" src="image-1.png" />
+        <img style="width: 500px;" src="s-single-intensity-measurements.png" />
     </p>
     <p>
         Time-intensity chromatograms are extracted by Skyline from the full spectra acquired in this manner.
     </p>
     <p>
-        <img src="image-2.png" />
+        <img src="s-full-spectrum-chromatogram.png" />
     </p>
     <p>
         The resulting chromatograms provide quantitative data similar to the SRM data from triple quadrupole experiments, in the now familiar Skyline
         user interface.
     </p>
     <p>
-        <img src="image-3.png" /> 
+        <img src="s-intensity-retention-time-graph.png" /> 
     </p>
     <p>
         PRM can be used to provide an alternative for a triple quadrupole when time on such an instrument is not an option. Though, filtering high
@@ -78,7 +78,7 @@ <h1>Getting Started</h1>
         Select the first peptide in the document, and Skyline should look something like this:
     </p>
     <p>
-        <img src="image-4.png" />
+        <img src="s-1.png" />
     </p>
     <p>
         This is a relatively small document. The indicators in the lower right corner, on the status bar, tell you that it contains 10 peptide
@@ -127,7 +127,7 @@ <h1>Configuring a Skyline Document for PRM</h1>
         will need to make some changes to prepare it for importing full-scan data files. The <b>Full-Scan</b> tab will look like this:
     </p>
     <p>
-        <img src="image-5.png" />
+        <img src="s-2.png" />
     </p>
     <p>
         To extract chromatograms from full-scan data, Skyline needs a little more information.
@@ -141,7 +141,7 @@ <h1>Configuring a Skyline Document for PRM</h1>
         The <b>Full-Scan</b> tab should now look like this:
     </p>
     <p>
-        <img src="image-6.png" />
+        <img src="s-3.png" />
     </p>
     <p>
         Note that when both MS1 and MS/MS filtering are enabled, all precursor ion chromatograms will be extracted exclusively from MS1 spectra, and
@@ -175,7 +175,7 @@ <h1>Configuring a Skyline Document for PRM</h1>
         The <b>Library</b> tab should look like this:
     </p>
     <p>
-        <img src="image-7.png" />
+        <img src="s-4.png" />
     </p>
     <p>
         The library ion match window is now the same as the chromatogram extraction window. This can be a little more complicated with high resolution
@@ -195,7 +195,7 @@ <h1>Configuring a Skyline Document for PRM</h1>
         The <b>Filter</b> tab should now look like this:
     </p>
     <p>
-        <img src="image-8.png" />
+        <img src="s-5.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -218,7 +218,7 @@ <h1>Configuring a Skyline Document for PRM</h1>
         The form should now look like this:
     </p>
     <p>
-        <img src="image-9.png" />
+        <img src="s-6.png" />
     </p>
     <ul>
         <li>Click the green check button (Enter).</li>
@@ -256,7 +256,7 @@ <h1>PRM Method Export</h1>
         The <b>Export Method</b> form should now look like:
     </p>
     <p>
-        <img src="image-10.png" />
+        <img src="s-7.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -269,13 +269,13 @@ <h1>PRM Method Export</h1>
         you specified. If you double-click on the file, then the LTQ Instrument Setup software should show you something like this:
     </p>
     <p>
-        <img src="image-11.png" />
+        <img src="s-ltq-instrument-setup-software.png" />
     </p>
     <p>
         Otherwise, Skyline will show you the following error message:
     </p>
     <p>
-        <img src="image-12.png" />
+        <img src="s-8.png" />
     </p>
     <p>
         Simply click the <b>OK</b> button to continue the rest of the tutorial, but remember that similar steps will work for Thermo Ion Trap
@@ -303,7 +303,7 @@ <h1>PRM Method Export</h1>
         The <b>Edit Report</b> form should now look like this:
     </p>
     <p>
-        <img src="image-13.png" />
+        <img src="s-9.png" />
     </p>
     <ul>
         <li>Click the <b>Preview</b> button.</li>
@@ -313,7 +313,7 @@ <h1>PRM Method Export</h1>
         The <b>Preview Report</b> form should now look like this:
     </p>
     <p>
-        <img src="image-14.png" />
+        <img src="s-10.png" />
     </p>
     <p>
         With the precursor <i>m/z</i> values presented in this form, it should not take long to set up a PRM method for this document, even on an
@@ -333,7 +333,7 @@ <h1>Importing and Inspecting Full-Scan Data</h1>
         Skyline presents a wizard form that looks like this:
     </p>
     <p>
-        <img src="image-15.png" />
+        <img src="s-11.png" />
     </p>
     <p>
         The first page of this form can be used to build a spectral library for your Skyline document. To do this now, perform the following steps:
@@ -350,7 +350,7 @@ <h1>Importing and Inspecting Full-Scan Data</h1>
         The form should now look like this:
     </p>
     <p>
-        <img src="image-16.png" />
+        <img src="s-12.png" />
     </p>
     <ul>
         <li>In one of the <b>Score Threshold</b> field, enter ‘0.01’. Both score thresholds will change because they have the same score
@@ -367,7 +367,7 @@ <h1>Importing and Inspecting Full-Scan Data</h1>
         The wizard form should now look like the following, showing you the files Skyline will use for chromatogram extraction:
     </p>
     <p>
-        <img src="image-17.png" />
+        <img src="s-13.png" />
     </p>
     <ul>
         <li>Click the <b>Next</b> button.</li>
@@ -377,7 +377,7 @@ <h1>Importing and Inspecting Full-Scan Data</h1>
         like this:
     </p>
     <p>
-        <img src="image-18.png" />
+        <img src="s-14.png" />
     </p>
     <p>
         Because Skyline will show these replicate names in graph labels and other UI elements, it is often a good idea to accept these shortened names,
@@ -405,7 +405,7 @@ <h1>Importing and Inspecting Full-Scan Data</h1>
             chromatograms</b> form.
     </p>
     <p>
-        <img src="image-19.png" />
+        <img src="s-15.png" />
     </p>
     <h1>Reviewing the Data</h1>
     <p>
@@ -420,7 +420,7 @@ <h1>Reviewing the Data</h1>
         When the import has completed, the Skyline window should look something like this:
     </p>
     <p>
-        <img src="image-20.png" />
+        <img src="s-16.png" />
     </p>
     <p>
         It may be a little difficult to see the chromatograms in this view because of the large number of spectrum IDs, which are annotated with dark
@@ -441,7 +441,7 @@ <h1>Reviewing the Data</h1>
         This should cause the chromatogram graphs to look like this:
     </p>
     <p>
-        <img src="image-21.png" />
+        <img src="s-17.png" />
     </p>
     <p>
         Now you can see the individual lines for spectra that were identified as the target peptide, and if you look closely, you can see one red line
@@ -453,7 +453,7 @@ <h1>Reviewing the Data</h1>
         beyond the peak integration boundaries, you will see that they have very low signal-to-noise.
     </p>
     <p>
-        <img src="image-22.png" />
+        <img src="s-18.png" />
     </p>
     <p>
         And yet, the search was performed with unspecified cleavage on a FASTA file containing the three expected proteins followed by the entire
@@ -470,7 +470,7 @@ <h1>Reviewing the Data</h1>
     </ul>
     <p>
         Turning your attention to the <b>Targets</b> view, you can see that all of the target peptides now have matching MS/MS spectra and
-        show an icon <img src="image-23.png" /> with a small spectrum in the lower right corner. You can see 0.84 is the lowest dot-product score
+        show an icon <img src="../../shared/target-peptide-with-spectrum-icon.png" /> with a small spectrum in the lower right corner. You can see 0.84 is the lowest dot-product score
         (labeled ‘dotp’) which provides a correlation score between the measured product ion peak areas and the fragment ion intensities in the
         library spectra, for the precursor ‘417.8946+++ (dotp 0.84)’. The <b>Targets</b> view shows only the dot-product scores for the
         active replicate, which is ‘20fmol’. You can tell the active replicate because its tab text is bold, and it is selected in the drop list at
@@ -488,7 +488,7 @@ <h1>Reviewing the Data</h1>
         The <b>Peak Areas</b> graph should now look like this:
     </p>
     <p>
-        <img src="image-24.png" />
+        <img src="s-19.png" />
     </p>
     <p>
         But, if it does not, you may still need to perform some of the following steps:
@@ -505,7 +505,7 @@ <h1>Reviewing the Data</h1>
         area graph for the LVNELTEFAK peptide shown above looks like:
     </p>
     <p>
-        <img src="image-25.png" />
+        <img src="s-20.png" />
     </p>
     <p>
         Next, turn your attention to the human peptide DRVYIHPF, where you should expect to see the 4:1 concentration ratio implied by the sample names
@@ -519,7 +519,7 @@ <h1>Reviewing the Data</h1>
         The <b>Peak Areas</b> graph should now look something like:
     </p>
     <p>
-        <img src="image-26.png" />
+        <img src="s-21.png" />
     </p>
     <p>
         The 80 fmol product ions sum to about 3 x 10<sup>6</sup> and the 20 fmol product ions sum to about 0.7 x 10<sup>6</sup>, which is not far from
@@ -527,7 +527,7 @@ <h1>Reviewing the Data</h1>
         is about 0.9 x 10<sup>6</sup>, or a 9:1 ratio. Turn your attention to the chromatogram graphs to understand the source of the discrepancy.
     </p>
     <p>
-        <img src="image-27.png" />
+        <img src="s-22.png" />
     </p>
     <p>
         You can see that the product ion chromatograms experience much less noise than the chromatograms extracted from MS1. With the background
@@ -558,11 +558,11 @@ <h1>Reviewing the Data</h1>
         <tr>
             <td  class="comp-fig">
                 R.IKNLQ<b><u>S</u></b>LDPSH.- [80, 90]<br />
-                <img src="image-28.png" />
+                <img src="s-23.png" />
             </td>
             <td class="comp-fig">
                 K.HLVDEPQNLIK.Q [401, 411]<br />
-                <img src="image-29.png" />
+                <img src="s-24.png" />
             </td>
         </tr>
     </table>
@@ -584,7 +584,7 @@ <h1>Configuring a Skyline Document for High-Resolution PRM</h1>
         tutorial, you will get the following error message:
     </p>
     <p>
-        <img src="image-30.png" />
+        <img src="s-25.png" />
     </p>
     <p>
         If you actually tried this, get the document back to its original state by doing the following:
@@ -618,7 +618,7 @@ <h1>Configuring a Skyline Document for High-Resolution PRM</h1>
         The <b>Full-Scan</b> tab should now look like this:
     </p>
     <p>
-        <img src="image-31.png" />
+        <img src="s-26.png" />
     </p>
     <p>
         For this data set, there are no peptide search results from which to get MS/MS IDs, which is why this option appears in red. Nor do you have
@@ -648,7 +648,7 @@ <h1>Configuring a Skyline Document for High-Resolution PRM</h1>
         MS1 scans. The transitions in the <b>Targets</b> view should look something like this:
     </p>
     <p>
-        <img src="image-32.png" />
+        <img src="s-27.png" />
     </p>
     <p>
         The precursor transitions were added automatically, because none of the peptides have been edited manually, leaving them in auto-select mode.
@@ -683,7 +683,7 @@ <h1>Importing and Inspecting High-Resolution Full-Scan Data</h1>
         When the import has completed, the Skyline window should look something like this:
     </p>
     <p>
-        <img src="image-33.png" />
+        <img src="s-28.png" />
     </p>
     <p>
         First, you should notice that the chromatograms in the chromatogram graph cover only a range of 3 minutes, in the image above 12 to 15 minutes.
@@ -694,7 +694,7 @@ <h1>Importing and Inspecting High-Resolution Full-Scan Data</h1>
         very good correlation between the chromatogram peaks and the expected relative intensities.
     </p>
     <p>
-        <img src="image-34.png" />
+        <img src="s-29.png" />
     </p>
     <p>
         To zoom into the chosen peaks on all graphs, do the following:
@@ -706,7 +706,7 @@ <h1>Importing and Inspecting High-Resolution Full-Scan Data</h1>
         This should make the chromatograms look like:
     </p>
     <p>
-        <img src="image-35.png" />
+        <img src="s-30.png" />
     </p>
     <p>
         One thing you might notice from the six chromatogram graphs is that the 50 amol sample has a more intense (700) and better formed peak group
@@ -727,7 +727,7 @@ <h1>Importing and Inspecting High-Resolution Full-Scan Data</h1>
         This should make the <b>Peak Areas</b> graph look like:
     </p>
     <p>
-        <img src="image-36.png" />
+        <img src="s-31.png" />
     </p>
     <p>
         In this view, the 50 amol sample appears to match more closely to 10 fmol sample than the 100 amol sample. If you review the 4 other peptides,
@@ -765,7 +765,7 @@ <h1>Importing and Inspecting High-Resolution Full-Scan Data</h1>
         <tr>
             <td  class="comp-fig">
                 K.LVNELTEFAK.T (500 fmol)<br />
-                <img src="image-37.png" />
+                <img src="s-32.png" />
             </td>
         </tr>
     </table>
@@ -783,13 +783,13 @@ <h1>Importing and Inspecting High-Resolution Full-Scan Data</h1>
         This should leave Skyline looking like:
     </p>
     <p>
-        <img src="image-38.png" />
+        <img src="s-33.png" />
     </p>
     <p class="keep-next">
         The <b>Peak Areas</b> graph should look like:
     </p>
     <p>
-        <img src="image-39.png" />
+        <img src="s-34.png" />
     </p>
     <p>
         If you review each of the 5 peptides again, you will see that the relative intensities of the concentration points are very similar to what you
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/PRM/en/image-4.png b/pwiz_tools/Skyline/Documentation/Tutorials/PRM/en/s-1.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/PRM/en/image-4.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/PRM/en/s-1.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/PRM/en/image-14.png b/pwiz_tools/Skyline/Documentation/Tutorials/PRM/en/s-10.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/PRM/en/image-14.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/PRM/ja/image-23.png b/pwiz_tools/Skyline/Documentation/Tutorials/PRM/ja/image-23.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/PRM/ja/index.html b/pwiz_tools/Skyline/Documentation/Tutorials/PRM/ja/index.html
index dbc0f4e5b2..17deabee5f 100644
--- a/pwiz_tools/Skyline/Documentation/Tutorials/PRM/ja/index.html
+++ b/pwiz_tools/Skyline/Documentation/Tutorials/PRM/ja/index.html
@@ -15,25 +15,25 @@ <h1 class="document-title">Skyline並列反応モニタリング</h1>
         本チュートリアルではSkylineを使用して、並列反応モニタリング（PRM）と呼ばれるターゲットアプローチで取得したMS/MSスペクトルを分析する方法を習得します。この方法はpseudo-SRMやMRM-HR™とも呼ばれます。これらの別名が示唆するとおり、PRMはSkylineが使用し始めた三連四重極質量分析計でのSRMに最も類似しているフルスキャンメソッドです。
     </p>
     <p>
-        <img style="width: 500px;" src="image-0.png" />
+        <img style="width: 500px;" src="s-triple-quadrupole-mass-spectrometer.png" />
     </p>
     <p>
         SRMがプリカーサーイオンとプロダクトイオンの複数のペアをスキャンして、経時的にサイクル内のそれぞれに対する単一強度の測定を収集していくのに対し、PRMはプリカーサーイオンのデータ非依存リストをスキャンして、経時的にサイクル内のそれぞれに対するすべてのMS/MSスペクトルを収集していきます。
     </p>
     <p>
-        <img style="width: 500px;" src="image-1.png" />
+        <img style="width: 500px;" src="s-single-intensity-measurements.png" />
     </p>
     <p class="keep-next">
         Skylineにより、この分析法で取得されたフルスキャンデータから時間強度クロマトグラムが抽出されます。
     </p>
     <p class="keep-next">
-        <img src="image-2.png" />
+        <img src="s-full-spectrum-chromatogram.png" />
     </p>
     <p>
         結果として抽出されたクロマトグラムは、今ではすっかり慣れ親しまれているSkylineのユー<br />ザーインターフェイスで、三連四重極質量分析計から得られたSRMデータに類似した定量的<br />データを提供します。
     </p>
     <p>
-        <img src="image-3.png" />
+        <img src="s-intensity-retention-time-graph.png" />
     </p>
     <p>
         PRMは、三連四重極質量分析計で時間がないときに代替法として使用できます。一方で、高分解能MS/MSでのフィルタリングは、従来のSRMよりも選択性に優れていることがあり、収集されたスキャンデータをペプチド検索で処理すると積分されたクロマトグラムのピークを検証できます。またPRMは、主にペプチドスペクトルマッチングパイプラインのためのMS/MSスペクトルのdata
@@ -67,7 +67,7 @@ <h1>はじめに</h1>
         ドキュメント内の最初のペプチドを選択すると、Skylineは以下のようになります。
     </p>
     <p>
-        <img src="image-4.png" />
+        <img src="s-1.png" />
     </p>
     <p>
         これは比較的小さなドキュメントです。ステータスバー上の右下隅にあるインジケーターには、合計78個のプロダクトイオンまたはターゲットトランジションを有する10個のペプチドのプリカーサーイオンが含まれていることが示されています。このプリカーサーイオンの中には、ウシ血清アルブミン（BSA）について公開されているNSTライブラリのMS/MSライブラリスペクトルと関連付けられているものもあります。また、他の2つのペプチド（ヒトとウシと1つずつ）ではMS/MSライブラリスペクトルにはない非修飾体とリン酸化修飾体として観測されています。
@@ -109,7 +109,7 @@ <h1>PRM用のSkylineドキュメントの設定</h1>
         タブは以下のようになります。
     </p>
     <p>
-        <img src="image-5.png" />
+        <img src="s-2.png" />
     </p>
     <p>
         フルスキャンデータからクロマトグラムを抽出するには、Skylineにさらに情報を入力する必要があります。
@@ -123,7 +123,7 @@ <h1>PRM用のSkylineドキュメントの設定</h1>
         [ <b>フルスキャン</b>] タブは以下のようになります。
     </p>
     <p>
-        <img src="image-6.png" />
+        <img src="s-3.png" />
     </p>
     <p>
         MS1とMS/MSフィルタの両方が有効化されている場合、すべてのプリカーサーイオンのクロマトグラムはMS1スペクトルからのみ抽出され、すべてのフラグメントイオンのクロマトグラムはMS/MSスペクトルからのみ抽出されます。MS/MSスキャン内でプリカーサーイオンがどのように表示されるかを見るには、MS1フィルタが無効になっているドキュメントを使用する必要があります。
@@ -151,7 +151,7 @@ <h1>PRM用のSkylineドキュメントの設定</h1>
         [ <b>ライブラリ</b> ] タブは以下のようになります。
     </p>
     <p>
-        <img src="image-7.png" />
+        <img src="s-4.png" />
     </p>
     <p>
         これでライブラリイオン一致ウィンドウはクロマトグラム抽出ウィンドウと同じになります。クロマトグラム抽出ウィンドウはm/zで変化するため、高分解能データではこれがもう少し複雑になることがあります。今後はチェックボックスを追加してこれら2つの設定を一致させていくことを検討中ですが、現時点では0.05～0.01の間の値が高分解能データに最も適しています（MS/MS質量アナライザーの分解能設定による）。
@@ -167,7 +167,7 @@ <h1>PRM用のSkylineドキュメントの設定</h1>
         [ <b>フィルタ</b> ] タブは以下のようになります。
     </p>
     <p>
-        <img src="image-8.png" />
+        <img src="s-5.png" />
     </p>
     <ul>
         <li>[ <b>OK</b> ] ボタンをクリックします。</li>
@@ -189,7 +189,7 @@ <h1>PRM用のSkylineドキュメントの設定</h1>
         フォームは以下のようになります。
     </p>
     <p>
-        <img src="image-9.png" />
+        <img src="s-6.png" />
     </p>
     <ul>
         <li>緑のチェックボタン（Enter）をクリックします。</li>
@@ -221,7 +221,7 @@ <h1>PRMメソッドのエクスポート</h1>
         [ <b>メソッドをエクスポート</b> ] フォームは以下のようになります。
     </p>
     <p>
-        <img src="image-10.png" />
+        <img src="s-7.png" />
     </p>
     <ul>
         <li>[ <b>OK</b> ] ボタンをクリックします。</li>
@@ -233,13 +233,13 @@ <h1>PRMメソッドのエクスポート</h1>
         実際にこの手順をThermo LTQ上で行った場合、この操作で指定した新しい「TargetedMSMS_BSA_Protea.meth」ファイルが作成されます。当該ファイルをダブルクリックすると、その後、LTQ装置の設定ソフト上では以下のような画面が表示されます。
     </p>
     <p>
-        <img src="image-11.png" />
+        <img src="s-ltq-instrument-setup-software.png" />
     </p>
     <p class="keep-next">
         または、Skylineによって以下のエラーメッセージが表示されます。
     </p>
     <p class="keep-next">
-        <img src="image-12.png" />
+        <img src="s-8.png" />
     </p>
     <p>
         [ <b>OK</b> ] ボタンをクリックしてチュートリアルの残りの操作を続けます。Thermo Ion Trap and Fusion、Bruker QTOFおよびSCIEX QTOFの装置制御用コンピュータでも同様の手順が動作します。 [ ファイル ]
@@ -264,7 +264,7 @@ <h1>PRMメソッドのエクスポート</h1>
         [ <b>レポートを編集</b> ] フォームは以下のようになります。
     </p>
     <p>
-        <img src="image-13.png" />
+        <img src="s-9.png" />
     </p>
     <ul>
         <li>[ <b>プレビュー</b> ] ボタンをクリックします。</li>
@@ -274,7 +274,7 @@ <h1>PRMメソッドのエクスポート</h1>
         [ <b>レポートをプレビュー</b> ] フォームは以下のようになります。
     </p>
     <p>
-        <img src="image-14.png" />
+        <img src="s-10.png" />
     </p>
     <p>
         このフォームにはプリカーサー<i>m/z</i>が表示されており、現在、直接メソッドエクスポートをサポートしていない装置であっても、このドキュメントのPRMメソッドの設定に時間はかからないはずです。実際に、これから調べようとしているデータの元のメソッドはこの方法で作成されています。多くのPRM実験は、Skylineにおいてもスケジューリングアルゴリズムが急速に重要となったSRMと同様、スケジュール化されたデータ取得に依存するようになってきていることに注意してください。
@@ -291,7 +291,7 @@ <h1>フルスキャンデータのインポートと確認</h1>
         Skylineには以下のようなウィザードが表示されます。
     </p>
     <p>
-        <img src="image-15.png" />
+        <img src="s-11.png" />
     </p>
     <p>
         このフォームの最初のページは、Skylineドキュメントのスペクトルライブラリの構築に使用可能です。これを行うには、以下の手順を実施します。
@@ -309,7 +309,7 @@ <h1>フルスキャンデータのインポートと確認</h1>
         フォームは以下のようになります。
     </p>
     <p>
-        <img src="image-16.png" />
+        <img src="s-12.png" />
     </p>
     <ul>
         <li>[ <b>次へ</b> ] ボタンをクリックします。</li>
@@ -322,7 +322,7 @@ <h1>フルスキャンデータのインポートと確認</h1>
         ウィザードフォームは以下のようになり、Skylineがクロマトグラム抽出に使用するファイルが表示されます。
     </p>
     <p>
-        <img src="image-17.png" />
+        <img src="s-13.png" />
     </p>
     <ul>
         <li>[ <b>次へ</b> ] ボタンをクリックします。</li>
@@ -331,7 +331,7 @@ <h1>フルスキャンデータのインポートと確認</h1>
         Skylineはこれらの長いファイル名に共通のプレフィックスやサフィックスがあることを検知し、それを削除するように提案して以下のようなフォームを表示します。
     </p>
     <p>
-        <img src="image-18.png" />
+        <img src="s-14.png" />
     </p>
     <p>
         Skylineはこのような繰り返し測定名をグラフラベルやその他のUI要素で表示するため、このように短い名前にしてしまう方が良いでしょう。ここでは短くなった名前で続けます。
@@ -356,7 +356,7 @@ <h1>フルスキャンデータのインポートと確認</h1>
         ファイルのインポートが開始され、Skylineウィンドウおよび [ <b>クロマトグラムの読み込み</b> ] <br />フォームの下部にあるステータスバーに進行状況が表示されます。
     </p>
     <p>
-        <img src="image-19.png" />
+        <img src="s-15.png" />
     </p>
     <h1>データの確認</h1>
     <p>
@@ -370,7 +370,7 @@ <h1>データの確認</h1>
         インポートが完了すると、Skylineウィンドウは以下のようになります。
     </p>
     <p>
-        <img src="image-20.png" />
+        <img src="s-16.png" />
     </p>
     <p>
         この表示には濃い青の縦線、「ID」の文字および同定されたスペクトルの分単位の時間が注釈付けられたスペクトルIDが多数あるため、クロマトグラムを確認しづらいことがあります。選択したクロマトグラムピークが、その頂点を示す黒の矢印ポインタ付きで、これらのIDの<br />真ん中に表示されます。
@@ -389,7 +389,7 @@ <h1>データの確認</h1>
         クロマトグラムグラフは以下のようになります。
     </p>
     <p>
-        <img src="image-21.png" />
+        <img src="s-17.png" />
     </p>
     <p>
         これでターゲットペプチドとして同定されたスペクトルの個々の線が見えるようになりました。よく見てみると、20fmol試料のクロマトグラムピークの真ん中に赤い線が見えます。これは、[ <b>ライブラリの一致</b> ]
@@ -398,7 +398,7 @@ <h1>データの確認</h1>
         表示にある他のスペクトルも見ることができます。ペプチド検索エンジンが、明確なクロマトグラムピークからこの存在量のペプチドを含むスペクトルとしてここまで同定できることに少し驚かれるかもしれません。ピーク積分境界外のスペクトルを見てみると、シグナルノイズ比が非常に低いことがわかります。
     </p>
     <p>
-        <img src="image-22.png" />
+        <img src="s-18.png" />
     </p>
     <p>
         それでもなお、すべてのUniprot FASTAを反転させた後、3つの予想タンパク質を含むFASTAファイルに対して未指定開裂での検索が行われました。
@@ -414,7 +414,7 @@ <h1>データの確認</h1>
     </ul>
     <p>
         [ <b>ターゲット</b> ] 表示に注目してみると、すべてのターゲットペプチドに一致するMS/MSスペクトルがあり、小さなスペクトル付きのアイコン <img
-            src="image-23.png" />が右下隅に表示されます。ここでは最低内積スコア（「dotp」という標識）が0.84であることがわかります。 これにより、プリカーサー「417.8946+++ (dotp
+            src="../../shared/target-peptide-with-spectrum-icon.png" />が右下隅に表示されます。ここでは最低内積スコア（「dotp」という標識）が0.84であることがわかります。 これにより、プリカーサー「417.8946+++ (dotp
         0.84)」に対する観測されたプロダクトイオンピーク面積とライブラリスペクトル内のフラグメントイオン強度間の相関度スコアが出ます。[ <b>ターゲット</b> ]
         表示には有効な繰り返し測定である「20fmol」の内積スコアのみが表示されています。有効な繰り返し測定は、タブテキストが太字になっており、[<b>ターゲット</b>]
         表示上部のドロップリスト内で選択されていることからわかります。「80fmol」繰り返し測定の内積スコアは、そのクロマトグラムをクリックするか、ドロップリスト内で選択すると見ることができます。
@@ -430,7 +430,7 @@ <h1>データの確認</h1>
         [ <b>ピーク面積</b> ] グラフは以下のようになります。
     </p>
     <p>
-        <img src="image-24.png" />
+        <img src="s-19.png" />
     </p>
     <p>
         そのように表示されない場合は、以下の手順のうち複数を実施する必要があります。
@@ -445,7 +445,7 @@ <h1>データの確認</h1>
         fmolの試料に対して高くなっているものもありますが、これは単に測定値のばらつきによるものです。全5ポイント希釈曲線については、上記LVNELTEFAKペプチドのピーク面積グラフは以下のようになります。
     </p>
     <p>
-        <img src="image-25.png" />
+        <img src="s-20.png" />
     </p>
     <p>
         次に、ヒトペプチドDRVYIHPFに注目してみましょう。 ここでは、試料名80 fmolおよび<br />20 fmolで4:1の濃度比が見られると予測されます。Skylineが実際に行った測定値の詳細を見るには、以下の操作を行います。
@@ -458,7 +458,7 @@ <h1>データの確認</h1>
         [ <b>ピーク面積</b> ] グラフは以下のようになります。
     </p>
     <p>
-        <img src="image-26.png" />
+        <img src="s-21.png" />
     </p>
     <p>
         80 fmolプロダクトイオンは合計約3 x 10<sup>6</sup>、および20 fmolプロダクトイオンは合計約0.7 x 10<sup>6</sup>となります。
@@ -466,7 +466,7 @@ <h1>データの確認</h1>
         10<sup>6</sup>、9:1の比率となっています。この相違の原因を見つけるためにクロマトグラムに注目してみましょう。
     </p>
     <p>
-        <img src="image-27.png" />
+        <img src="s-22.png" />
     </p>
     <p>
         プロダクトイオンクロマトグラムのノイズは、MS1から抽出したクロマトグラムと比較してかなり少ないということがわかります。Skylineによってバックグラウンドが差し引かれると、<br />バックグラウンドを超える20
@@ -493,11 +493,11 @@ <h1>データの確認</h1>
         <tr>
             <td  class="comp-fig">
                 R.IKNLQ<strong><u>S</u></strong>LDPSH.- [80, 90]<br />
-                <img src="image-28.png" />
+                <img src="s-23.png" />
             </td>
             <td class="comp-fig">
                 K.HLVDEPQNLIK.Q [401, 411]<br />
-                <img src="image-29.png" />
+                <img src="s-24.png" />
             </td>
         </tr>
     </table>
@@ -514,7 +514,7 @@ <h1>高分解能PRM用のSkylineドキュメントの設定</h1>
         繰り返しになりますが、これは「TOF」フォルダ内の生データファイルにより測定された実験の全Skylineドキュメントであり、その設定では現在SRMデータしかインポートできません。この時点で、このチュートリアルに含まれているTOF質量分析計データファイルをインポートしようとすると、以下のエラーメッセージが表示されます。
     </p>
     <p>
-        <img src="image-30.png" />
+        <img src="s-25.png" />
     </p>
     <p>
         実際にこれを行った場合、以下の操作を行ってドキュメントを元の状態に戻します。
@@ -547,7 +547,7 @@ <h1>高分解能PRM用のSkylineドキュメントの設定</h1>
         [ <b>フルスキャン</b> ] タブは以下のようになります。
     </p>
     <p>
-        <img src="image-31.png" />
+        <img src="s-26.png" />
     </p>
     <p>
         このデータセットでは、MS/MS
@@ -573,7 +573,7 @@ <h1>高分解能PRM用のSkylineドキュメントの設定</h1>
         この場合には、すべてのペプチドが3つのプリカーサートランジション（M、M+1、およびM+2）を含んでいることがわかります。 そしてこれは高分解能MS1スキャンでのみ可能です。<br />[ <b>ターゲット</b> ] 表示のトランジションは以下のようになります。
     </p>
     <p>
-        <img src="image-32.png" />
+        <img src="s-27.png" />
     </p>
     <p>
         プリカーサートランジションが自動的に追加されます。これはどのペプチドも手動で編集されておらず、自動選択モードのままになっているからです。ここでも、Skylineは [ <b>フィルタ</b> ]
@@ -605,7 +605,7 @@ <h1>高分解能フルスキャンデータのインポートと確認</h1>
         インポートが完了すると、Skylineウィンドウは以下のようになります。
     </p>
     <p>
-        <img src="image-33.png" />
+        <img src="s-28.png" />
     </p>
     <p>
         まず、グラフ内のクロマトグラムは3分の範囲のみ表示していることに注意します。上図では12分から15分です。
@@ -615,7 +615,7 @@ <h1>高分解能フルスキャンデータのインポートと確認</h1>
         fmolの場合、これらの値はクロマトグラムピークと予測相対強度との間の非常に良好な相関度があることを示しています。
     </p>
     <p>
-        <img src="image-34.png" />
+        <img src="s-29.png" />
     </p>
     <p>
         すべてグラフにおいて選択したピークを拡大するには、以下の操作を行います。
@@ -627,7 +627,7 @@ <h1>高分解能フルスキャンデータのインポートと確認</h1>
         これにより、クロマトグラムは以下のようになります。
     </p>
     <p>
-        <img src="image-35.png" />
+        <img src="s-30.png" />
     </p>
     <p>
         6つのクロマトグラムグラフからわかるのは、100 amolの試料ピーク（40）よりも50 amolの試料ピークの方が、高強度（700）で形状が優れていることです。すべてのピークの保持時間は非常に近く、Skylineが100
@@ -644,7 +644,7 @@ <h1>高分解能フルスキャンデータのインポートと確認</h1>
         これにより、[ <b>ピーク面積</b> ] グラフは以下のようになります。
     </p>
     <p>
-        <img src="image-36.png" />
+        <img src="s-31.png" />
     </p>
     <p>
         この表示では、50 amolの試料は100 amolの試料より10
@@ -678,7 +678,7 @@ <h1>高分解能フルスキャンデータのインポートと確認</h1>
         <tr>
             <td  class="comp-fig">
                 K.LVNELTEFAK.T (500 fmol)<br />
-                <img src="image-37.png" />
+                <img src="s-32.png" />
             </td>
         </tr>
     </table>
@@ -695,13 +695,13 @@ <h1>高分解能フルスキャンデータのインポートと確認</h1>
         これによりSkylineは以下のようになります。
     </p>
     <p>
-        <img src="image-38.png" />
+        <img src="s-33.png" />
     </p>
     <p class="keep-next">
         [ <b>ピーク面積</b> ] グラフは以下のようになります。
     </p>
     <p>
-        <img src="image-39.png" />
+        <img src="s-34.png" />
     </p>
     <p>
         5つのペプチドをそれぞれもう一度確認すると、濃度ポイントの相対強度はプロダクトイオンでの比較で見られたものと非常に似ていることがわかります。
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/PRM/ja/invariant.html b/pwiz_tools/Skyline/Documentation/Tutorials/PRM/ja/invariant.html
index 948a52e168..9343b81b01 100644
--- a/pwiz_tools/Skyline/Documentation/Tutorials/PRM/ja/invariant.html
+++ b/pwiz_tools/Skyline/Documentation/Tutorials/PRM/ja/invariant.html
@@ -20,27 +20,27 @@ <h1 class="document-title">Skyline Parallel Reaction Monitoring</h1>
         the practice of SRM with triple quadrupole mass spectrometers, where Skyline got its start:
     </p>
     <p>
-        <img style="width: 500px;" src="image-0.png" />
+        <img style="width: 500px;" src="s-triple-quadrupole-mass-spectrometer.png" />
     </p>
     <p>
         As SRM scans through precursor and product ion pairs, collecting single intensity measurements for each in a cycle over time, PRM scans through
         a data independent list of precursor ions collecting full MS/MS spectra for each in a cycle over time. 
     </p>
     <p>
-        <img style="width: 500px;" src="image-1.png" />
+        <img style="width: 500px;" src="s-single-intensity-measurements.png" />
     </p>
     <p>
         Time-intensity chromatograms are extracted by Skyline from the full spectra acquired in this manner.
     </p>
     <p>
-        <img src="image-2.png" />
+        <img src="s-full-spectrum-chromatogram.png" />
     </p>
     <p>
         The resulting chromatograms provide quantitative data similar to the SRM data from triple quadrupole experiments, in the now familiar Skyline
         user interface.
     </p>
     <p>
-        <img src="image-3.png" />
+        <img src="s-intensity-retention-time-graph.png" />
     </p>
     <p>
         PRM can be used to provide an alternative for a triple quadrupole when time on such an instrument is not an option. Though, filtering high
@@ -78,7 +78,7 @@ <h1>Getting Started</h1>
         Select the first peptide in the document, and Skyline should look something like this:
     </p>
     <p>
-        <img src="image-4.png" />
+        <img src="s-1.png" />
     </p>
     <p>
         This is a relatively small document. The indicators in the lower right corner, on the status bar, tell you that it contains 10 peptide
@@ -127,7 +127,7 @@ <h1>Configuring a Skyline Document for PRM</h1>
         will need to make some changes to prepare it for importing full-scan data files. The <b>Full-Scan</b> tab will look like this:
     </p>
     <p>
-        <img src="image-5.png" />
+        <img src="s-2.png" />
     </p>
     <p>
         To extract chromatograms from full-scan data, Skyline needs a little more information.
@@ -141,7 +141,7 @@ <h1>Configuring a Skyline Document for PRM</h1>
         The <b>Full-Scan</b> tab should now look like this:
     </p>
     <p>
-        <img src="image-6.png" />
+        <img src="s-3.png" />
     </p>
     <p>
         Note that when both MS1 and MS/MS filtering are enabled, all precursor ion chromatograms will be extracted exclusively from MS1 spectra, and
@@ -175,7 +175,7 @@ <h1>Configuring a Skyline Document for PRM</h1>
         The <b>Library</b> tab should look like this:
     </p>
     <p>
-        <img src="image-7.png" />
+        <img src="s-4.png" />
     </p>
     <p>
         The library ion match window is now the same as the chromatogram extraction window. This can be a little more complicated with high resolution
@@ -195,7 +195,7 @@ <h1>Configuring a Skyline Document for PRM</h1>
         The <b>Filter</b> tab should now look like this:
     </p>
     <p>
-        <img src="image-8.png" />
+        <img src="s-5.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -218,7 +218,7 @@ <h1>Configuring a Skyline Document for PRM</h1>
         The form should now look like this:
     </p>
     <p>
-        <img src="image-9.png" />
+        <img src="s-6.png" />
     </p>
     <ul>
         <li>Click the green check button (Enter).</li>
@@ -256,7 +256,7 @@ <h1>PRM Method Export</h1>
         The <b>Export Method</b> form should now look like:
     </p>
     <p>
-        <img src="image-10.png" />
+        <img src="s-7.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -269,13 +269,13 @@ <h1>PRM Method Export</h1>
         you specified. If you double-click on the file, then the LTQ Instrument Setup software should show you something like this:
     </p>
     <p>
-        <img src="image-11.png" />
+        <img src="s-ltq-instrument-setup-software.png" />
     </p>
     <p>
         Otherwise, Skyline will show you the following error message:
     </p>
     <p>
-        <img src="image-12.png" />
+        <img src="s-8.png" />
     </p>
     <p>
         Simply click the <b>OK</b> button to continue the rest of the tutorial, but remember that similar steps will work for Thermo Ion Trap
@@ -303,7 +303,7 @@ <h1>PRM Method Export</h1>
         The <b>Edit Report</b> form should now look like this:
     </p>
     <p>
-        <img src="image-13.png" />
+        <img src="s-9.png" />
     </p>
     <ul>
         <li>Click the <b>Preview</b> button.</li>
@@ -313,7 +313,7 @@ <h1>PRM Method Export</h1>
         The <b>Preview Report</b> form should now look like this:
     </p>
     <p>
-        <img src="image-14.png" />
+        <img src="s-10.png" />
     </p>
     <p>
         With the precursor <i>m/z</i> values presented in this form, it should not take long to set up a PRM method for this document, even on an
@@ -333,7 +333,7 @@ <h1>Importing and Inspecting Full-Scan Data</h1>
         Skyline presents a wizard form that looks like this:
     </p>
     <p>
-        <img src="image-15.png" />
+        <img src="s-11.png" />
     </p>
     <p>
         The first page of this form can be used to build a spectral library for your Skyline document. To do this now, perform the following steps:
@@ -351,7 +351,7 @@ <h1>Importing and Inspecting Full-Scan Data</h1>
         The form should now look like this:
     </p>
     <p>
-        <img src="image-16.png" />
+        <img src="s-12.png" />
     </p>
     <ul>
         <li>Click the <b>Next</b> button.</li>
@@ -366,7 +366,7 @@ <h1>Importing and Inspecting Full-Scan Data</h1>
         The wizard form should now look like the following, showing you the files Skyline will use for chromatogram extraction:
     </p>
     <p>
-        <img src="image-17.png" />
+        <img src="s-13.png" />
     </p>
     <ul>
         <li>Click the <b>Next</b> button.</li>
@@ -376,7 +376,7 @@ <h1>Importing and Inspecting Full-Scan Data</h1>
         like this:
     </p>
     <p>
-        <img src="image-18.png" />
+        <img src="s-14.png" />
     </p>
     <p>
         Because Skyline will show these replicate names in graph labels and other UI elements, it is often a good idea to accept these shortened names,
@@ -404,7 +404,7 @@ <h1>Importing and Inspecting Full-Scan Data</h1>
             chromatograms</b> form.
     </p>
     <p>
-        <img src="image-19.png" />
+        <img src="s-15.png" />
     </p>
     <h1>Reviewing the Data</h1>
     <p>
@@ -419,7 +419,7 @@ <h1>Reviewing the Data</h1>
         When the import has completed, the Skyline window should look something like this:
     </p>
     <p>
-        <img src="image-20.png" />
+        <img src="s-16.png" />
     </p>
     <p>
         It may be a little difficult to see the chromatograms in this view because of the large number of spectrum IDs, which are annotated with dark
@@ -440,7 +440,7 @@ <h1>Reviewing the Data</h1>
         This should cause the chromatogram graphs to look like this:
     </p>
     <p>
-        <img src="image-21.png" />
+        <img src="s-17.png" />
     </p>
     <p>
         Now you can see the individual lines for spectra that were identified as the target peptide, and if you look closely, you can see one red line
@@ -452,7 +452,7 @@ <h1>Reviewing the Data</h1>
         beyond the peak integration boundaries, you will see that they have very low signal-to-noise.
     </p>
     <p>
-        <img src="image-22.png" />
+        <img src="s-18.png" />
     </p>
     <p>
         And yet, the search was performed with unspecified cleavage on a FASTA file containing the three expected proteins followed by the entire
@@ -469,7 +469,7 @@ <h1>Reviewing the Data</h1>
     </ul>
     <p>
         Turning your attention to the <b>Targets</b> view, you can see that all of the target peptides now have matching MS/MS spectra and
-        show an icon <img src="image-23.png" /> with a small spectrum in the lower right corner. You can see 0.84 is the lowest dot-product score
+        show an icon <img src="../../shared/target-peptide-with-spectrum-icon.png" /> with a small spectrum in the lower right corner. You can see 0.84 is the lowest dot-product score
         (labeled ‘dotp’) which provides a correlation score between the measured product ion peak areas and the fragment ion intensities in the
         library spectra, for the precursor ‘417.8946+++ (dotp 0.84)’. The <b>Targets</b> view shows only the dot-product scores for the
         active replicate, which is ‘20fmol’. You can tell the active replicate because its tab text is bold, and it is selected in the drop list at
@@ -487,7 +487,7 @@ <h1>Reviewing the Data</h1>
         The <b>Peak Areas</b> graph should now look like this:
     </p>
     <p>
-        <img src="image-24.png" />
+        <img src="s-19.png" />
     </p>
     <p>
         But, if it does not, you may still need to perform some of the following steps:
@@ -504,7 +504,7 @@ <h1>Reviewing the Data</h1>
         area graph for the LVNELTEFAK peptide shown above looks like:
     </p>
     <p>
-        <img src="image-25.png" />
+        <img src="s-20.png" />
     </p>
     <p>
         Next, turn your attention to the human peptide DRVYIHPF, where you should expect to see the 4:1 concentration ratio implied by the sample names
@@ -518,7 +518,7 @@ <h1>Reviewing the Data</h1>
         The <b>Peak Areas</b> graph should now look something like:
     </p>
     <p>
-        <img src="image-26.png" />
+        <img src="s-21.png" />
     </p>
     <p>
         The 80 fmol product ions sum to about 3 x 10<sup>6</sup> and the 20 fmol product ions sum to about 0.7 x 10<sup>6</sup>, which is not far from
@@ -526,7 +526,7 @@ <h1>Reviewing the Data</h1>
         is about 0.9 x 10<sup>6</sup>, or a 9:1 ratio. Turn your attention to the chromatogram graphs to understand the source of the discrepancy.
     </p>
     <p>
-        <img src="image-27.png" />
+        <img src="s-22.png" />
     </p>
     <p>
         You can see that the product ion chromatograms experience much less noise than the chromatograms extracted from MS1. With the background
@@ -557,11 +557,11 @@ <h1>Reviewing the Data</h1>
         <tr>
             <td  class="comp-fig">
                 R.IKNLQ<strong><u>S</u></strong>LDPSH.- [80, 90]<br />
-                <img src="image-28.png" />
+                <img src="s-23.png" />
             </td>
             <td class="comp-fig">
                 K.HLVDEPQNLIK.Q [401, 411]<br />
-                <img src="image-29.png" />
+                <img src="s-24.png" />
             </td>
         </tr>
     </table>
@@ -583,7 +583,7 @@ <h1>Configuring a Skyline Document for High-Resolution PRM</h1>
         tutorial, you will get the following error message:
     </p>
     <p>
-        <img src="image-30.png" />
+        <img src="s-25.png" />
     </p>
     <p>
         If you actually tried this, get the document back to its original state by doing the following:
@@ -617,7 +617,7 @@ <h1>Configuring a Skyline Document for High-Resolution PRM</h1>
         The <b>Full-Scan</b> tab should now look like this:
     </p>
     <p>
-        <img src="image-31.png" />
+        <img src="s-26.png" />
     </p>
     <p>
         For this data set, there are no peptide search results from which to get MS/MS IDs, which is why this option appears in red. Nor do you have
@@ -647,7 +647,7 @@ <h1>Configuring a Skyline Document for High-Resolution PRM</h1>
         MS1 scans. The transitions in the <b>Targets</b> view should look something like this:
     </p>
     <p>
-        <img src="image-32.png" />
+        <img src="s-27.png" />
     </p>
     <p>
         The precursor transitions were added automatically, because none of the peptides have been edited manually, leaving them in auto-select mode.
@@ -682,7 +682,7 @@ <h1>Importing and Inspecting High-Resolution Full-Scan Data</h1>
         When the import has completed, the Skyline window should look something like this:
     </p>
     <p>
-        <img src="image-33.png" />
+        <img src="s-28.png" />
     </p>
     <p>
         First, you should notice that the chromatograms in the chromatogram graph cover only a range of 3 minutes, in the image above 12 to 15 minutes.
@@ -693,7 +693,7 @@ <h1>Importing and Inspecting High-Resolution Full-Scan Data</h1>
         very good correlation between the chromatogram peaks and the expected relative intensities.
     </p>
     <p>
-        <img src="image-34.png" />
+        <img src="s-29.png" />
     </p>
     <p>
         To zoom into the chosen peaks on all graphs, do the following:
@@ -705,7 +705,7 @@ <h1>Importing and Inspecting High-Resolution Full-Scan Data</h1>
         This should make the chromatograms look like:
     </p>
     <p>
-        <img src="image-35.png" />
+        <img src="s-30.png" />
     </p>
     <p>
         One thing you might notice from the six chromatogram graphs is that the 50 amol sample has a more intense (700) and better formed peak group
@@ -726,7 +726,7 @@ <h1>Importing and Inspecting High-Resolution Full-Scan Data</h1>
         This should make the <b>Peak Areas</b> graph look like:
     </p>
     <p>
-        <img src="image-36.png" />
+        <img src="s-31.png" />
     </p>
     <p>
         In this view, the 50 amol sample appears to match more closely to 10 fmol sample than the 100 amol sample. If you review the 4 other peptides,
@@ -764,7 +764,7 @@ <h1>Importing and Inspecting High-Resolution Full-Scan Data</h1>
         <tr>
             <td  class="comp-fig">
                 K.LVNELTEFAK.T (500 fmol)<br />
-                <img src="image-37.png" />
+                <img src="s-32.png" />
             </td>
         </tr>
     </table>
@@ -782,13 +782,13 @@ <h1>Importing and Inspecting High-Resolution Full-Scan Data</h1>
         This should leave Skyline looking like:
     </p>
     <p>
-        <img src="image-38.png" />
+        <img src="s-33.png" />
     </p>
     <p class="keep-next">
         The <b>Peak Areas</b> graph should look like:
     </p>
     <p>
-        <img src="image-39.png" />
+        <img src="s-34.png" />
     </p>
     <p>
         If you review each of the 5 peptides again, you will see that the relative intensities of the concentration points are very similar to what you
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/PRM/ja/image-4.png b/pwiz_tools/Skyline/Documentation/Tutorials/PRM/ja/s-1.png
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rename to pwiz_tools/Skyline/Documentation/Tutorials/PRM/ja/s-triple-quadrupole-mass-spectrometer.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/image-23.png b/pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/image-23.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/index.html b/pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/index.html
index 1e604d115f..ff85b80e03 100644
--- a/pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/index.html
+++ b/pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/index.html
@@ -16,25 +16,25 @@ <h1 class="document-title">Skyline 平行反应监测</h1>
         在本教程中，您将学习如何使用 Skyline 来分析一种叫做平行反应监测 (PRM)的靶向质谱方法（这种方法亦称伪 SRM 或 MRM-HR™）采集的数据。顾名思义，PRM 是一种与基于三重四级杆质谱仪的 SRM 非常相似的一种扫描方法：
     </p>
     <p>
-        <img style="width: 500px;" src="image-0.png" />
+        <img style="width: 500px;" src="s-triple-quadrupole-mass-spectrometer.png" />
     </p>
     <p>
         在 SRM 扫描成对的母离子和子离子时， 将随时间的推移收集每一对的单个强度测量值；PRM 扫描不依赖数据的母离子列表，从而收集每一个母离子在每个周期的完整 MS/MS 谱图。
     </p>
     <p>
-        <img style="width: 500px;" src="image-1.png" />
+        <img style="width: 500px;" src="s-single-intensity-measurements.png" />
     </p>
     <p>
         Skyline 可以对以这种方式采集的完整MS/MS谱图进行提取，来获得时间-强度色谱图。
     </p>
     <p>
-        <img src="image-2.png" />
+        <img src="s-full-spectrum-chromatogram.png" />
     </p>
     <p>
         由此产生的色谱图提供的定量数据，与目前在 Skyline 中分析的SRM数据类似。
     </p>
     <p>
-        <img src="image-3.png" />
+        <img src="s-intensity-retention-time-graph.png" />
     </p>
     <p>
         当三重四极杆质谱仪不可用时，可将PRM作为一种替代方法。虽然如此，这种高分辨率串联质谱相比传统 SRM 在选择性上有其优势，而且完整的MS/MS数据可以进行肽段搜索，从而帮助验证色谱峰提取的正确性。PRM 还可以用于对多种全扫描质谱仪进行系统适用性测试，即便是在进行数据依赖的采集
@@ -67,7 +67,7 @@ <h1>入门指南</h1>
         选择文档中的第一个肽段，Skyline 将显示如下：
     </p>
     <p>
-        <img src="image-4.png" />
+        <img src="s-1.png" />
     </p>
     <p>
         这是一个相对较小的文档。右下角状态栏显示其中包含 10 个肽段母离子，总共 78 个子离子或目标离子对。其中有些母离子具有源自公共 NIST 库的牛血清白蛋白 (BSA)
@@ -108,7 +108,7 @@ <h1>为 PRM 配置 Skyline 文档</h1>
         当前的参数设置仅支持 SRM 数据分析，尚需要进行一些修改才能导入全扫描数据。<b>全扫描</b>选项卡将显示如下：
     </p>
     <p>
-        <img src="image-5.png" />
+        <img src="s-2.png" />
     </p>
     <p>
         Skyline 需要更多信息才能从全扫描数据中提取色谱图。
@@ -122,7 +122,7 @@ <h1>为 PRM 配置 Skyline 文档</h1>
         此时，<b>全扫描</b>选项卡将显示如下：
     </p>
     <p>
-        <img src="image-6.png" />
+        <img src="s-3.png" />
     </p>
     <p>
         请注意，同时启用 MS1 和串联质谱筛选时，所有母离子色谱图将会从 MS1 谱图中提取出来，而所有子离子色谱图从串联质谱谱图中提取出来。如果您想在串联质谱扫描中查看母离子的色谱图，需要禁用 MS1 筛选选项。
@@ -149,7 +149,7 @@ <h1>为 PRM 配置 Skyline 文档</h1>
         <b>库</b>选项卡现在应显示如下：
     </p>
     <p>
-        <img src="image-7.png" />
+        <img src="s-4.png" />
     </p>
     <p>
         此时，离子匹配窗口与色谱提取窗口相同。这对于高分辨率数据而言可能稍显复杂，因为色谱提取窗口将随着质荷比变化。我们希望日后添加一个复选框来强制两种设置相互匹配，但就目前而言，介于 0.05 和 0.01 之间的值通常最适合高分辨率数据，具体取决于串联质谱质量分析仪上的分辨能力设置。
@@ -165,7 +165,7 @@ <h1>为 PRM 配置 Skyline 文档</h1>
         此时，<b>过滤器</b>选项卡应显示如下：
     </p>
     <p>
-        <img src="image-8.png" />
+        <img src="s-5.png" />
     </p>
     <ul>
         <li>单击<b>确定</b>按钮。</li>
@@ -187,7 +187,7 @@ <h1>为 PRM 配置 Skyline 文档</h1>
         此时，表单将显示如下：
     </p>
     <p>
-        <img src="image-9.png" />
+        <img src="s-6.png" />
     </p>
     <ul>
         <li>单击绿色复选按钮 (Enter)。</li>
@@ -219,7 +219,7 @@ <h1>PRM 方法导出</h1>
         <b>导出方法</b>表单将显示为：
     </p>
     <p>
-        <img src="image-10.png" />
+        <img src="s-7.png" />
     </p>
     <ul>
         <li>单击<b>确定</b>按钮。</li>
@@ -231,13 +231,13 @@ <h1>PRM 方法导出</h1>
         如果在 Thermo LTQ 仪器上执行这些步骤，此操作应该会成功，并会创建您指定的新的“TargetedMSMS_BSA_Protea.meth”文件。双击此文件，LTQ 仪器设置软件应显示如下：
     </p>
     <p>
-        <img src="image-11.png" />
+        <img src="s-ltq-instrument-setup-software.png" />
     </p>
     <p>
         否则，Skyline 将显示以下错误消息：
     </p>
     <p>
-        <img src="image-12.png" />
+        <img src="s-8.png" />
     </p>
     <p>
         单击<b>确定</b>按钮即可继续教程的其余部分。但请记住，类似的步骤对 Thermo Ion Trap、Fusion、Bruker TOF 以及 SCIEX QTOF 仪器控制电脑也适用。或者，对于 Agilent TOF、Thermo Q Exactive 和
@@ -262,7 +262,7 @@ <h1>PRM 方法导出</h1>
         此时<b>编辑报告</b>表单将显示如下：
     </p>
     <p>
-        <img src="image-13.png" />
+        <img src="s-9.png" />
     </p>
     <ul>
         <li>单击<b>预览</b>按钮。</li>
@@ -272,7 +272,7 @@ <h1>PRM 方法导出</h1>
         此时<b>预览新报告</b>表单将显示如下：
     </p>
     <p>
-        <img src="image-14.png" />
+        <img src="s-10.png" />
     </p>
     <p>
         借助此表单中显示的母离子<i>质荷比</i>值，可以加快 PRM 方法的设置过程，即使在目前缺乏直接方法导出支持的仪器上也能做到这一点。实际上，下面将要检查的数据的初始方法就是通过这种方式建立的。不过需要注意的是，越来越多的 PRM 实验变得和 SRM
@@ -290,7 +290,7 @@ <h1>导入并检查全扫描数据</h1>
         Skyline 将显示如下向导表单：
     </p>
     <p>
-        <img src="image-15.png" />
+        <img src="s-11.png" />
     </p>
     <p>
         此表单的首页可用于针对您的 Skyline 文档建立一个谱图库。若要现在执行此操作，请执行下列<br />步骤：
@@ -308,7 +308,7 @@ <h1>导入并检查全扫描数据</h1>
         此时，表单将显示如下：
     </p>
     <p>
-        <img src="image-16.png" />
+        <img src="s-12.png" />
     </p>
     <ul>
         <li>单击<b>下一步</b>按钮。</li>
@@ -321,7 +321,7 @@ <h1>导入并检查全扫描数据</h1>
         向导表单现在将显示如下，其中显示 Skyline 用于色谱图提取的文件：
     </p>
     <p>
-        <img src="image-17.png" />
+        <img src="s-13.png" />
     </p>
     <ul>
         <li>单击<b>下一步</b>按钮。</li>
@@ -330,7 +330,7 @@ <h1>导入并检查全扫描数据</h1>
         Skyline 检测到这些长文件名有共同的前缀和后缀，并提出删除它们，显示的表单如下：
     </p>
     <p>
-        <img src="image-18.png" />
+        <img src="s-14.png" />
     </p>
     <p>
         由于 Skyline 会在图形标签和其它 UI 元素中显示这些重复测定名称，所以接受这些缩写名称不失为好主意，在这里您就会这样做。
@@ -354,7 +354,7 @@ <h1>导入并检查全扫描数据</h1>
         文件导入开始，底部 Skyline 窗口的状态栏中将显示进度和<b>加载色谱图</b>表单。
     </p>
     <p>
-        <img src="image-19.png" />
+        <img src="s-15.png" />
     </p>
     <h1>检查数据</h1>
     <p>
@@ -368,7 +368,7 @@ <h1>检查数据</h1>
         导入完成后，Skyline 窗口将显示如下：
     </p>
     <p>
-        <img src="image-20.png" />
+        <img src="s-16.png" />
     </p>
     <p>
         查看此视图中的色谱图可能有些困难，因为谱图 ID 数量较多。这些谱图用深蓝色的垂直线表示，并标注了字母“ID”和以分钟为单位的色谱保留时间。被选中的色谱峰显示在这些 ID 中间，在其顶点有一个黑色箭头指示。
@@ -386,14 +386,14 @@ <h1>检查数据</h1>
         执行此操作后色谱图显示如下：
     </p>
     <p>
-        <img src="image-21.png" />
+        <img src="s-17.png" />
     </p>
     <p>
         现在，您可以看到一条条竖线，每一条竖线代表一个被鉴定为目标肽段的谱图，仔细观察会发现 20fmol 样品的色谱峰中间有一条红线。这是<b>库匹配</b>视图中当前显示的谱图，并且是 BiblioSpec
         库生成工具所认为的“最佳谱图”。您可以单击色谱图中的竖线，或单击<b>库匹配</b>视图顶部的下拉列表并从长长的谱图时间列表中进行选择，以查看<b>库匹配</b>视图中的其它谱图。你可以发现，有些谱图已经距离色谱峰边界较远，但仍然可被肽段搜索引擎鉴定出来，这点有些令人惊奇。而且，从色谱峰边界以外的谱图来看，其信噪比其实是非常低的。
     </p>
     <p>
-        <img src="image-22.png" />
+        <img src="s-18.png" />
     </p>
     <p>
         不过，它是通过未指定的酶切执行搜索的，该 FASTA 文件包含三种预期蛋白质以及整个Uniprot FASTA反库。
@@ -408,7 +408,7 @@ <h1>检查数据</h1>
         <li>右键单击色谱图，选择<b>肽段 ID 次数</b>并单击<b>匹配</b>（如果已选中）。</li>
     </ul>
     <p>
-        将您的注意力转移到<b>目标</b>视图，此时会看到所有目标肽段均有匹配的串联质谱谱图， 并在右下角显示带有小谱图的图标<img src="image-23.png" />。您会看到 0.84 为最低点积分数（标有“点积”），其为母离子“417.8946+++
+        将您的注意力转移到<b>目标</b>视图，此时会看到所有目标肽段均有匹配的串联质谱谱图， 并在右下角显示带有小谱图的图标<img src="../../shared/target-peptide-with-spectrum-icon.png" />。您会看到 0.84 为最低点积分数（标有“点积”），其为母离子“417.8946+++
         (dotp
         0.84)”的子离子实际测定峰面积与谱图库中碎片离子的强度之间的相关分数。<br /><b>目标</b>视图仅显示当前样品“20fmol”的点积分数。当前样品的选项卡文本采用粗体，可从<b>目标</b>视图顶部的下拉列表中选择。单击样品“80fmol”的色谱图，或在下拉列表中选择它，以查看其点积分数。
     </p>
@@ -423,7 +423,7 @@ <h1>检查数据</h1>
         <b>峰面积</b>图将显示如下：
     </p>
     <p>
-        <img src="image-24.png" />
+        <img src="s-19.png" />
     </p>
     <p>
         可执行以下某个步骤改变显示：
@@ -438,7 +438,7 @@ <h1>检查数据</h1>
         个浓度稀释点，上述BSA肽段 LVNELTEFAK 的峰面积图显示如下：
     </p>
     <p>
-        <img src="image-25.png" />
+        <img src="s-20.png" />
     </p>
     <p>
         接下来，对于人源肽段 DRVYIHPF，可以看到在样品80 fmol 和 20 fmol 中的峰面积为 4:1 ，与其浓度比值结果相一致。为了更好地查看 Skyline结果，请执行以下步骤：
@@ -451,14 +451,14 @@ <h1>检查数据</h1>
         <b>峰面积</b>图显示如下：
     </p>
     <p>
-        <img src="image-26.png" />
+        <img src="s-21.png" />
     </p>
     <p>
         80 fmol 样品的子离子峰面积之和约为 3 x 10<sup>6</sup>，20 fmol 样品的子离子峰面积之和约为 0.7 x 10<sup>6</sup>，接近预期的 4:1 的比例，但对于从 MS1 扫描提取的母离子而言，80 fmol 面积约为 8 x
         10<sup>6</sup>，20 fmol 面积接近 0.9 x 10<sup>6</sup>，其比例约为 9:1。我们来看一下色谱图，以了解出现比例差异的来源。
     </p>
     <p>
-        <img src="image-27.png" />
+        <img src="s-22.png" />
     </p>
     <p>
         可以看到，子离子色谱图比从 MS1 中提取的色谱图的噪音少得多。通过 Skyline 应用的背景扣减法， 20 fmol样品的母离子色谱峰面积相当低。来自串联质谱的子离子色谱图比来自相同分辨率的 MS1 的母离子色谱图更具选择性，并且子离子色谱峰的背景非常低。
@@ -483,11 +483,11 @@ <h1>检查数据</h1>
         <tr>
             <td  class="comp-fig">
                 R.IKNLQ<strong><u>S</u></strong>LDPSH.- [80, 90]<br />
-                <img src="image-28.png" />
+                <img src="s-23.png" />
             </td>
             <td class="comp-fig">
                 K.HLVDEPQNLIK.Q [401, 411]<br />
-                <img src="image-29.png" />
+                <img src="s-24.png" />
             </td>
         </tr>
     </table>
@@ -504,7 +504,7 @@ <h1>为高分辨率 PRM 配置 Skyline 文档</h1>
         这是针对“TOF”文件夹中包含的原始数据文件的完整 Skyline文档，但当前设置仅允许导入 SRM 数据，如果您在此尝试导入本教程中包含的任何 TOF 质谱数据文件，系统会出现以下错误消息：
     </p>
     <p>
-        <img src="image-30.png" />
+        <img src="s-25.png" />
     </p>
     <p>
         如果您确实尝试了该操作，则请执行以下操作将文档恢复到原始状态。
@@ -537,7 +537,7 @@ <h1>为高分辨率 PRM 配置 Skyline 文档</h1>
         此时，<b>全扫描</b>选项卡将显示如下：
     </p>
     <p>
-        <img src="image-31.png" />
+        <img src="s-26.png" />
     </p>
     <p>
         对于此数据集，没有肽段搜索结果可供从中获取串联质谱 ID，这就是为什么该选项显示为红色的原因。在导入任何数据之前，您也无法预测肽段的洗脱保留时间。由于缺乏串联质谱 ID，如果按照这样的设置，Skyline 将从所有匹配的扫描中提取色谱图。您可以执行以下操作明确选择此项：
@@ -562,7 +562,7 @@ <h1>为高分辨率 PRM 配置 Skyline 文档</h1>
         此时，您会看到所有肽段包含 3 个母离子（M、M+1、M+2），只有高分辨率 MS1 扫描才可能出现这种情况。<b>目标</b>视图中的离子对应显示如下：
     </p>
     <p>
-        <img src="image-32.png" />
+        <img src="s-27.png" />
     </p>
     <p>
         因为未手动编辑肽段，它们均处于自动选择模式，因此将自动添加母离子。同样，Skyline 自动在<b>过滤器</b>选项卡中添加了“p”离子类型，因为您选择了 MS1 筛选。
@@ -593,7 +593,7 @@ <h1>导入并检查高分辨率全扫描数据</h1>
         导入完成后，Skyline 窗口将显示如下：
     </p>
     <p>
-        <img src="image-33.png" />
+        <img src="s-28.png" />
     </p>
     <p>
         首先，您会发现色谱图保留时间为12min- 15 min，共 3 分钟的范围。
@@ -602,7 +602,7 @@ <h1>导入并检查高分辨率全扫描数据</h1>
         将<b>目标</b>视图放大，可以看到此时已为母离子同位素分布和子离子强度分别添加了两个正交点积值：同位素点积和点积。这些值表明最高浓度 (500 fmol) 数据中肽段色谱峰与预期的相对强度之间具有良好的相关性。
     </p>
     <p>
-        <img src="image-34.png" />
+        <img src="s-29.png" />
     </p>
     <p>
         若要放大所有图上的所选峰值，请执行下列操作：
@@ -614,7 +614,7 @@ <h1>导入并检查高分辨率全扫描数据</h1>
         执行这项操作后色谱图将显示如下：
     </p>
     <p>
-        <img src="image-35.png" />
+        <img src="s-30.png" />
     </p>
     <p>
         您可能会发现，在 6 个色谱图中，50 amol样品的峰强度更大 (700)，且比 100 amol 样品 (40) 形成的峰图更佳。由于所有峰值的保留时间都非常接近，因此发生这种情况的原因不大可能是 Skyline 选择了错误的峰值。另外请注意，对于高分辨率数据，Skyline
@@ -631,7 +631,7 @@ <h1>导入并检查高分辨率全扫描数据</h1>
         执行这项操作后<b>峰面积</b>图将显示如下：
     </p>
     <p>
-        <img src="image-36.png" />
+        <img src="s-31.png" />
     </p>
     <p>
         在此视图中，50 amol 样品似乎比 100 amol 样品更加接近 10 fmol 样品。如果查看其它 4 个肽段，会发现其中2条肽段（SLHTLFGDEL<b><u>C</u></b>K 和 KVPQVSTPTLVEVSR）在50 amol
@@ -663,7 +663,7 @@ <h1>导入并检查高分辨率全扫描数据</h1>
         <tr>
             <td  class="comp-fig">
                 K.LVNELTEFAK.T (500 fmol)<br />
-                <img src="image-37.png" />
+                <img src="s-32.png" />
             </td>
         </tr>
     </table>
@@ -680,13 +680,13 @@ <h1>导入并检查高分辨率全扫描数据</h1>
         此操作过后 Skyline 应显示如下：
     </p>
     <p>
-        <img src="image-38.png" />
+        <img src="s-33.png" />
     </p>
     <p class="keep-next">
         <b>峰面积</b>图将显示如下：
     </p>
     <p>
-        <img src="image-39.png" />
+        <img src="s-34.png" />
     </p>
     <p>
         此时再次分别查看这 5 个肽段，可以发现各浓度点的相对强度与通过子离子比较得到的强度非常接近。
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/invariant.html b/pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/invariant.html
index 3db54d6bbf..f19b25b1fd 100644
--- a/pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/invariant.html
+++ b/pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/invariant.html
@@ -20,27 +20,27 @@ <h1 class="document-title">Skyline Parallel Reaction Monitoring</h1>
         the practice of SRM with triple quadrupole mass spectrometers, where Skyline got its start:
     </p>
     <p>
-        <img style="width: 500px;" src="image-0.png" />
+        <img style="width: 500px;" src="s-triple-quadrupole-mass-spectrometer.png" />
     </p>
     <p>
         As SRM scans through precursor and product ion pairs, collecting single intensity measurements for each in a cycle over time, PRM scans through
         a data independent list of precursor ions collecting full MS/MS spectra for each in a cycle over time. 
     </p>
     <p>
-        <img style="width: 500px;" src="image-1.png" />
+        <img style="width: 500px;" src="s-single-intensity-measurements.png" />
     </p>
     <p>
         Time-intensity chromatograms are extracted by Skyline from the full spectra acquired in this manner.
     </p>
     <p>
-        <img src="image-2.png" />
+        <img src="s-full-spectrum-chromatogram.png" />
     </p>
     <p>
         The resulting chromatograms provide quantitative data similar to the SRM data from triple quadrupole experiments, in the now familiar Skyline
         user interface.
     </p>
     <p>
-        <img src="image-3.png" />
+        <img src="s-intensity-retention-time-graph.png" />
     </p>
     <p>
         PRM can be used to provide an alternative for a triple quadrupole when time on such an instrument is not an option. Though, filtering high
@@ -78,7 +78,7 @@ <h1>Getting Started</h1>
         Select the first peptide in the document, and Skyline should look something like this:
     </p>
     <p>
-        <img src="image-4.png" />
+        <img src="s-1.png" />
     </p>
     <p>
         This is a relatively small document. The indicators in the lower right corner, on the status bar, tell you that it contains 10 peptide
@@ -127,7 +127,7 @@ <h1>Configuring a Skyline Document for PRM</h1>
         will need to make some changes to prepare it for importing full-scan data files. The <b>Full-Scan</b> tab will look like this:
     </p>
     <p>
-        <img src="image-5.png" />
+        <img src="s-2.png" />
     </p>
     <p>
         To extract chromatograms from full-scan data, Skyline needs a little more information.
@@ -141,7 +141,7 @@ <h1>Configuring a Skyline Document for PRM</h1>
         The <b>Full-Scan</b> tab should now look like this:
     </p>
     <p>
-        <img src="image-6.png" />
+        <img src="s-3.png" />
     </p>
     <p>
         Note that when both MS1 and MS/MS filtering are enabled, all precursor ion chromatograms will be extracted exclusively from MS1 spectra, and
@@ -175,7 +175,7 @@ <h1>Configuring a Skyline Document for PRM</h1>
         The <b>Library</b> tab should look like this:
     </p>
     <p>
-        <img src="image-7.png" />
+        <img src="s-4.png" />
     </p>
     <p>
         The library ion match window is now the same as the chromatogram extraction window. This can be a little more complicated with high resolution
@@ -195,7 +195,7 @@ <h1>Configuring a Skyline Document for PRM</h1>
         The <b>Filter</b> tab should now look like this:
     </p>
     <p>
-        <img src="image-8.png" />
+        <img src="s-5.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -218,7 +218,7 @@ <h1>Configuring a Skyline Document for PRM</h1>
         The form should now look like this:
     </p>
     <p>
-        <img src="image-9.png" />
+        <img src="s-6.png" />
     </p>
     <ul>
         <li>Click the green check button (Enter).</li>
@@ -256,7 +256,7 @@ <h1>PRM Method Export</h1>
         The <b>Export Method</b> form should now look like:
     </p>
     <p>
-        <img src="image-10.png" />
+        <img src="s-7.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -269,13 +269,13 @@ <h1>PRM Method Export</h1>
         you specified. If you double-click on the file, then the LTQ Instrument Setup software should show you something like this:
     </p>
     <p>
-        <img src="image-11.png" />
+        <img src="s-ltq-instrument-setup-software.png" />
     </p>
     <p>
         Otherwise, Skyline will show you the following error message:
     </p>
     <p>
-        <img src="image-12.png" />
+        <img src="s-8.png" />
     </p>
     <p>
         Simply click the <b>OK</b> button to continue the rest of the tutorial, but remember that similar steps will work for Thermo Ion Trap
@@ -303,7 +303,7 @@ <h1>PRM Method Export</h1>
         The <b>Edit Report</b> form should now look like this:
     </p>
     <p>
-        <img src="image-13.png" />
+        <img src="s-9.png" />
     </p>
     <ul>
         <li>Click the <b>Preview</b> button.</li>
@@ -313,7 +313,7 @@ <h1>PRM Method Export</h1>
         The <b>Preview Report</b> form should now look like this:
     </p>
     <p>
-        <img src="image-14.png" />
+        <img src="s-10.png" />
     </p>
     <p>
         With the precursor <i>m/z</i> values presented in this form, it should not take long to set up a PRM method for this document, even on an
@@ -333,7 +333,7 @@ <h1>Importing and Inspecting Full-Scan Data</h1>
         Skyline presents a wizard form that looks like this:
     </p>
     <p>
-        <img src="image-15.png" />
+        <img src="s-11.png" />
     </p>
     <p>
         The first page of this form can be used to build a spectral library for your Skyline document. To do this now, perform the following steps:
@@ -351,7 +351,7 @@ <h1>Importing and Inspecting Full-Scan Data</h1>
         The form should now look like this:
     </p>
     <p>
-        <img src="image-16.png" />
+        <img src="s-12.png" />
     </p>
     <ul>
         <li>Click the <b>Next</b> button.</li>
@@ -366,7 +366,7 @@ <h1>Importing and Inspecting Full-Scan Data</h1>
         The wizard form should now look like the following, showing you the files Skyline will use for chromatogram extraction:
     </p>
     <p>
-        <img src="image-17.png" />
+        <img src="s-13.png" />
     </p>
     <ul>
         <li>Click the <b>Next</b> button.</li>
@@ -376,7 +376,7 @@ <h1>Importing and Inspecting Full-Scan Data</h1>
         like this:
     </p>
     <p>
-        <img src="image-18.png" />
+        <img src="s-14.png" />
     </p>
     <p>
         Because Skyline will show these replicate names in graph labels and other UI elements, it is often a good idea to accept these shortened names,
@@ -404,7 +404,7 @@ <h1>Importing and Inspecting Full-Scan Data</h1>
             chromatograms</b> form.
     </p>
     <p>
-        <img src="image-19.png" />
+        <img src="s-15.png" />
     </p>
     <h1>Reviewing the Data</h1>
     <p>
@@ -419,7 +419,7 @@ <h1>Reviewing the Data</h1>
         When the import has completed, the Skyline window should look something like this:
     </p>
     <p>
-        <img src="image-20.png" />
+        <img src="s-16.png" />
     </p>
     <p>
         It may be a little difficult to see the chromatograms in this view because of the large number of spectrum IDs, which are annotated with dark
@@ -440,7 +440,7 @@ <h1>Reviewing the Data</h1>
         This should cause the chromatogram graphs to look like this:
     </p>
     <p>
-        <img src="image-21.png" />
+        <img src="s-17.png" />
     </p>
     <p>
         Now you can see the individual lines for spectra that were identified as the target peptide, and if you look closely, you can see one red line
@@ -452,7 +452,7 @@ <h1>Reviewing the Data</h1>
         beyond the peak integration boundaries, you will see that they have very low signal-to-noise.
     </p>
     <p>
-        <img src="image-22.png" />
+        <img src="s-18.png" />
     </p>
     <p>
         And yet, the search was performed with unspecified cleavage on a FASTA file containing the three expected proteins followed by the entire
@@ -469,7 +469,7 @@ <h1>Reviewing the Data</h1>
     </ul>
     <p>
         Turning your attention to the <b>Targets</b> view, you can see that all of the target peptides now have matching MS/MS spectra and
-        show an icon <img src="image-23.png" /> with a small spectrum in the lower right corner. You can see 0.84 is the lowest dot-product score
+        show an icon <img src="../../shared/target-peptide-with-spectrum-icon.png" /> with a small spectrum in the lower right corner. You can see 0.84 is the lowest dot-product score
         (labeled ‘dotp’) which provides a correlation score between the measured product ion peak areas and the fragment ion intensities in the
         library spectra, for the precursor ‘417.8946+++ (dotp 0.84)’. The <b>Targets</b> view shows only the dot-product scores for the
         active replicate, which is ‘20fmol’. You can tell the active replicate because its tab text is bold, and it is selected in the drop list at
@@ -487,7 +487,7 @@ <h1>Reviewing the Data</h1>
         The <b>Peak Areas</b> graph should now look like this:
     </p>
     <p>
-        <img src="image-24.png" />
+        <img src="s-19.png" />
     </p>
     <p>
         But, if it does not, you may still need to perform some of the following steps:
@@ -504,7 +504,7 @@ <h1>Reviewing the Data</h1>
         area graph for the LVNELTEFAK peptide shown above looks like:
     </p>
     <p>
-        <img src="image-25.png" />
+        <img src="s-20.png" />
     </p>
     <p>
         Next, turn your attention to the human peptide DRVYIHPF, where you should expect to see the 4:1 concentration ratio implied by the sample names
@@ -518,7 +518,7 @@ <h1>Reviewing the Data</h1>
         The <b>Peak Areas</b> graph should now look something like:
     </p>
     <p>
-        <img src="image-26.png" />
+        <img src="s-21.png" />
     </p>
     <p>
         The 80 fmol product ions sum to about 3 x 10<sup>6</sup> and the 20 fmol product ions sum to about 0.7 x 10<sup>6</sup>, which is not far from
@@ -526,7 +526,7 @@ <h1>Reviewing the Data</h1>
         is about 0.9 x 10<sup>6</sup>, or a 9:1 ratio. Turn your attention to the chromatogram graphs to understand the source of the discrepancy.
     </p>
     <p>
-        <img src="image-27.png" />
+        <img src="s-22.png" />
     </p>
     <p>
         You can see that the product ion chromatograms experience much less noise than the chromatograms extracted from MS1. With the background
@@ -557,11 +557,11 @@ <h1>Reviewing the Data</h1>
         <tr>
             <td  class="comp-fig">
                 R.IKNLQ<strong><u>S</u></strong>LDPSH.- [80, 90]<br />
-                <img src="image-28.png" />
+                <img src="s-23.png" />
             </td>
             <td class="comp-fig">
                 K.HLVDEPQNLIK.Q [401, 411]<br />
-                <img src="image-29.png" />
+                <img src="s-24.png" />
             </td>
         </tr>
     </table>
@@ -583,7 +583,7 @@ <h1>Configuring a Skyline Document for High-Resolution PRM</h1>
         tutorial, you will get the following error message:
     </p>
     <p>
-        <img src="image-30.png" />
+        <img src="s-25.png" />
     </p>
     <p>
         If you actually tried this, get the document back to its original state by doing the following:
@@ -617,7 +617,7 @@ <h1>Configuring a Skyline Document for High-Resolution PRM</h1>
         The <b>Full-Scan</b> tab should now look like this:
     </p>
     <p>
-        <img src="image-31.png" />
+        <img src="s-26.png" />
     </p>
     <p>
         For this data set, there are no peptide search results from which to get MS/MS IDs, which is why this option appears in red. Nor do you have
@@ -647,7 +647,7 @@ <h1>Configuring a Skyline Document for High-Resolution PRM</h1>
         MS1 scans. The transitions in the <b>Targets</b> view should look something like this:
     </p>
     <p>
-        <img src="image-32.png" />
+        <img src="s-27.png" />
     </p>
     <p>
         The precursor transitions were added automatically, because none of the peptides have been edited manually, leaving them in auto-select mode.
@@ -682,7 +682,7 @@ <h1>Importing and Inspecting High-Resolution Full-Scan Data</h1>
         When the import has completed, the Skyline window should look something like this:
     </p>
     <p>
-        <img src="image-33.png" />
+        <img src="s-28.png" />
     </p>
     <p>
         First, you should notice that the chromatograms in the chromatogram graph cover only a range of 3 minutes, in the image above 12 to 15 minutes.
@@ -693,7 +693,7 @@ <h1>Importing and Inspecting High-Resolution Full-Scan Data</h1>
         very good correlation between the chromatogram peaks and the expected relative intensities.
     </p>
     <p>
-        <img src="image-34.png" />
+        <img src="s-29.png" />
     </p>
     <p>
         To zoom into the chosen peaks on all graphs, do the following:
@@ -705,7 +705,7 @@ <h1>Importing and Inspecting High-Resolution Full-Scan Data</h1>
         This should make the chromatograms look like:
     </p>
     <p>
-        <img src="image-35.png" />
+        <img src="s-30.png" />
     </p>
     <p>
         One thing you might notice from the six chromatogram graphs is that the 50 amol sample has a more intense (700) and better formed peak group
@@ -726,7 +726,7 @@ <h1>Importing and Inspecting High-Resolution Full-Scan Data</h1>
         This should make the <b>Peak Areas</b> graph look like:
     </p>
     <p>
-        <img src="image-36.png" />
+        <img src="s-31.png" />
     </p>
     <p>
         In this view, the 50 amol sample appears to match more closely to 10 fmol sample than the 100 amol sample. If you review the 4 other peptides,
@@ -764,7 +764,7 @@ <h1>Importing and Inspecting High-Resolution Full-Scan Data</h1>
         <tr>
             <td  class="comp-fig">
                 K.LVNELTEFAK.T (500 fmol)<br />
-                <img src="image-37.png" />
+                <img src="s-32.png" />
             </td>
         </tr>
     </table>
@@ -782,13 +782,13 @@ <h1>Importing and Inspecting High-Resolution Full-Scan Data</h1>
         This should leave Skyline looking like:
     </p>
     <p>
-        <img src="image-38.png" />
+        <img src="s-33.png" />
     </p>
     <p class="keep-next">
         The <b>Peak Areas</b> graph should look like:
     </p>
     <p>
-        <img src="image-39.png" />
+        <img src="s-34.png" />
     </p>
     <p>
         If you review each of the 5 peptides again, you will see that the relative intensities of the concentration points are very similar to what you
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/image-4.png b/pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/s-1.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/image-4.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/s-1.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/image-14.png b/pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/s-10.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/image-14.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/s-10.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/image-15.png b/pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/s-11.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/image-15.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/s-11.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/image-16.png b/pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/s-12.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/image-16.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/s-12.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/image-17.png b/pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/s-13.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/image-17.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/s-13.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/image-18.png b/pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/s-14.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/image-18.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/s-14.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/image-19.png b/pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/s-15.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/image-19.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/s-15.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/image-20.png b/pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/s-16.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/image-20.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/s-16.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/image-21.png b/pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/s-17.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/image-21.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/s-17.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/image-22.png b/pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/s-18.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/image-22.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/s-18.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/image-24.png b/pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/s-19.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/image-24.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/s-19.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/image-5.png b/pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/s-2.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/image-5.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/s-2.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/image-25.png b/pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/s-20.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/image-25.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/s-20.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/image-26.png b/pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/s-21.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/image-26.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/s-21.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/image-27.png b/pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/s-22.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/image-27.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/s-22.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/image-28.png b/pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/s-23.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/image-28.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/s-23.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/image-29.png b/pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/s-24.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/image-29.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/s-24.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/image-30.png b/pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/s-25.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/image-30.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/s-25.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/image-31.png b/pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/s-26.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/image-31.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/s-26.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/image-32.png b/pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/s-27.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/image-32.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/s-27.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/image-33.png b/pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/s-28.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/image-33.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/s-28.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/image-34.png b/pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/s-29.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/image-34.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/s-29.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/image-6.png b/pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/s-3.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/image-6.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/s-3.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/image-35.png b/pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/s-30.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/image-35.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/s-30.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/image-36.png b/pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/s-31.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/image-36.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/s-31.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/image-37.png b/pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/s-32.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/image-37.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/s-32.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/image-38.png b/pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/s-33.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/image-38.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/s-33.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/image-39.png b/pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/s-34.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/image-39.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/s-34.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/image-7.png b/pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/s-4.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/image-7.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/s-4.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/image-8.png b/pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/s-5.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/image-8.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/s-5.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/image-9.png b/pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/s-6.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/image-9.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/s-6.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/image-10.png b/pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/s-7.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/image-10.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/s-7.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/image-12.png b/pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/s-8.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/image-12.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/s-8.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/image-13.png b/pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/s-9.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/image-13.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/s-9.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/image-2.png b/pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/s-full-spectrum-chromatogram.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/image-2.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/s-full-spectrum-chromatogram.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/image-3.png b/pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/s-intensity-retention-time-graph.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/image-3.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/s-intensity-retention-time-graph.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/image-11.png b/pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/s-ltq-instrument-setup-software.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/image-11.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/s-ltq-instrument-setup-software.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/image-1.png b/pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/s-single-intensity-measurements.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/image-1.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/s-single-intensity-measurements.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/image-0.png b/pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/s-triple-quadrupole-mass-spectrometer.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/image-0.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/PRM/zh-CHS/s-triple-quadrupole-mass-spectrometer.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/index.html b/pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/index.html
index e454808a39..7c85014d99 100644
--- a/pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/index.html
+++ b/pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/index.html
@@ -83,7 +83,7 @@ <h3>Peptide settings</h3>
             about 6 repeated sequences in the fasta file. Click “OK”.</li>
     </ul>
     <p>
-        <img src="image-0.png" />
+        <img src="s-1.png" />
     </p>
     <ul>
         <li>The generated proteome file should contain 16,800 proteins. Confirm by clicking “OK”. The mouse-proteome.protdb background proteome file
@@ -103,7 +103,7 @@ <h3>Peptide settings</h3>
         Now the “Digestion” tab should look like this:
     </p>
     <p>
-        <img src="image-1.png" />
+        <img src="s-2.png" />
     </p>
     <p>
         <b><i>Prediction tab</i></b>
@@ -125,7 +125,7 @@ <h3>Peptide settings</h3>
         The “Prediction” tab should look like this:
     </p>
     <p>
-        <img src="image-2.png" />
+        <img src="s-3.png" />
     </p>
     <p>
         <b><i>Filter tab</i></b>
@@ -156,7 +156,7 @@ <h3>Peptide settings</h3>
         The “Filter” tab should look like this:
     </p>
     <p>
-        <img src="image-3.png" />
+        <img src="s-4.png" />
     </p>
     <p>
         <b><i>Library tab</i></b>
@@ -236,7 +236,7 @@ <h3>Peptide settings</h3>
         Now the “Library” tab should look like this:
     </p>
     <p>
-        <img src="image-4.png" />
+        <img src="s-5.png" />
     </p>
     <p>
         <b><i>Modifications tab</i></b>
@@ -279,7 +279,7 @@ <h3>Peptide settings</h3>
         Now the “Modifications” tab should look like this:
     </p>
     <p>
-        <img src="image-5.png" />
+        <img src="s-6.png" />
     </p>
     <p>
         <b>Tip!</b> This tab might be slightly different in your case (you might have less or more modifications than the displayed in the
@@ -335,7 +335,7 @@ <h3>Peptide settings</h3>
         The “Quantification” tab should look like this:
     </p>
     <p>
-        <img src="image-6.png" />
+        <img src="s-7.png" />
     </p>
     <p>
         <b>Finally</b>, click “OK” to confirm all peptide settings.
@@ -373,7 +373,7 @@ <h3>Transition settings</h3>
         Now the “Prediction” tab should look like this:
     </p>
     <p>
-        <img src="image-7.png" />
+        <img src="s-8.png" />
     </p>
     <p class="keep-next">
         <b><i>Filter tab</i></b>
@@ -410,7 +410,7 @@ <h3>Transition settings</h3>
         Now the Filter tab should look like this:
     </p>
     <p>
-        <img src="image-8.png" />
+        <img src="s-9.png" />
     </p>
     <p class="keep-next">
         <b><i>Library tab</i></b>
@@ -445,7 +445,7 @@ <h3>Transition settings</h3>
         Now the “Library” tab should look like this:
     </p>
     <p>
-        <img src="image-9.png" />
+        <img src="s-10.png" />
     </p>
     <p>
         <b><i>Instrument tab</i></b>
@@ -478,7 +478,7 @@ <h3>Transition settings</h3>
         Now the “Instrument” tab should look like this:
     </p>
     <p class="keep-next">
-        <img src="image-10.png" />
+        <img src="s-11.png" />
     </p>
     <p class="keep-next">
         <b><i>Full-Scan tab</i></b>
@@ -497,7 +497,7 @@ <h3>Transition settings</h3>
         Now the “Full-Scan” tab should look like this:
     </p>
     <p>
-        <img src="image-11.png" />
+        <img src="s-12.png" />
     </p>
     <p>
         <b><i>Ion mobility tab</i></b>
@@ -507,7 +507,7 @@ <h3>Transition settings</h3>
         <li>We are not using ion mobility data in this course and therefore we select “None”. </li>
     </ul>
     <p>
-        <img src="image-12.png" />
+        <img src="s-13.png" />
     </p>
     <p>
         <b>Save</b> the Skyline document to Webinar17_data folder with the name PRM_Settings.sky
@@ -589,7 +589,7 @@ <h2>Create a precursor list in Skyline</h2>
         Your Skyline document should now look like this:
     </p>
     <p>
-        <img src="image-13.png" />
+        <img src="s-14.png" />
     </p>
     <ul>
         <li>Go through all target peptides and check the automatically selected transitions and the quality of the MS2 library spectra.</li>
@@ -628,7 +628,7 @@ <h2>Export your list of precursors from Skyline as an acquisition method.</h2>
         Your “Edit Report” tab should now look like this: 
     </p>
     <p>
-        <img src="image-14.png" />
+        <img src="s-15.png" />
     </p>
     <ul>
         <li>Click “Preview” to check report appears with 106 rows (one for each precursor).</li>
@@ -661,7 +661,7 @@ <h2>Export your list of precursors from Skyline into a scheduled method</h2>
         </li>
     </ul>
     <p>
-        <img src="image-15.png" />
+        <img src="s-16.png" />
     </p>
     <ul>
         <li>Click OK.</li>
@@ -683,7 +683,7 @@ <h2>Export your list of precursors from Skyline into a scheduled method</h2>
         The Skyline Window should look like this:
     </p>
     <p>
-        <img src="image-16.png" />
+        <img src="s-17.png" />
     </p>
     <p>
         The document should now contain 62 precursors (two per peptide, one for the light version and one for the heavy version). 
@@ -709,7 +709,7 @@ <h2>Export your list of precursors from Skyline into a scheduled method</h2>
             the window size onto the number of concurrent precursors.</li>
     </ul>
     <p>
-        <img src="image-17.png" />
+        <img src="s-18.png" />
     </p>
     <p>
         <b>Note</b>: The size of the window that you finally will select in your instrument depends on different factors like the
@@ -725,7 +725,7 @@ <h2>Export your list of precursors from Skyline into a scheduled method</h2>
         <li>Add the “<b>Peptide Retention Time</b>” field in “Proteins → Peptides → Peptide Results → Peptide Retention Time.</li>
     </ul>
     <p>
-        <b>Tip!</b> You can click the binoculars button (<img src="image-18.png" />) above “Report Name” to find any field by name.
+        <b>Tip!</b> You can click the binoculars button (<img src="../../shared/black-binocular-button.png" />) above “Report Name” to find any field by name.
     </p>
     <ul>
         <li>Click “Preview” to check report appears with 62 rows with each retention time appearing twice, once for the light and heavy precursor of
@@ -751,7 +751,7 @@ <h2>Export your list of precursors from Skyline into a scheduled method</h2>
         Your precursor list should now look like this:
     </p>
     <p>
-        <img src="image-19.png" />
+        <img src="s-precursor-list-spreadsheet.png" />
     </p>
     <ul>
         <li>Close the “Retention Times – Scheduling” window.</li>
@@ -816,7 +816,7 @@ <h2>Importing data results into Skyline</h2>
         Your Skyline document should now look like this:
     </p>
     <p>
-        <img src="image-20.png" />
+        <img src="s-19.png" />
     </p>
     <p>
         In this view you can visualize together the heavy and the light traces. This layout is good to check the peak integration.
@@ -831,7 +831,7 @@ <h2>Importing data results into Skyline</h2>
         The Skyline main window should look something like this:
     </p>
     <p>
-        <img src="image-21.png" />
+        <img src="s-20.png" />
     </p>
     <p>
         This layout is good to check interferences in individual transitions.
@@ -848,7 +848,7 @@ <h2>Importing data results into Skyline</h2>
         The Skyline main window should look something like this:
     </p>
     <p>
-        <img src="image-22.png" />
+        <img src="s-21.png" />
     </p>
     <h2>Manual exploration and refinement of the picked PRM chromatograms</h2>
     <p>
@@ -873,13 +873,13 @@ <h3>Peak picking (identification)</h3>
         <li>For example in the first peptide GVDCQEVSQEK remove y9, y8 and b6 ions.</li>
     </ul>
     <p>
-        <img src="image-23.png" />
+        <img src="s-22.png" />
     </p>
     <p>
         You should do the same for all 31 peptides.
     </p>
     <p>
-        <b>Tip!</b> A quicker way to remove most of the things in your document marked with a red dot (<img src="image-24.png" />) is to:
+        <b>Tip!</b> A quicker way to remove most of the things in your document marked with a red dot (<img src="../../shared/red-dot-icon.png" />) is to:
     </p>
     <ul>
         <li>“Refine” 🡪 “Advanced” – “Results” tab</li>
@@ -967,7 +967,7 @@ <h2>Protein quantitation using single point calibration </h2>
         <li>In the Document Grid window: <b>Go</b> to “Reports” → “Peptide Ratio Results”.</li>
     </ul>
     <p>
-        <img src="image-25.png" />
+        <img src="s-23.png" />
     </p>
     <p>
         We have a table with the ratio light-to-heavy (“Ratio To Standard”) for each peptide in each replicate. The Quantification shows the same value
@@ -994,7 +994,7 @@ <h2>Protein quantitation using single point calibration </h2>
             selecting the cell in the top row of this column and pressing Ctrl-V.</li>
     </ul>
     <p>
-        <img src="image-26.png" />
+        <img src="s-24.png" />
     </p>
     <p>
         Now, again from the “Document Grid” window
@@ -1007,7 +1007,7 @@ <h2>Protein quantitation using single point calibration </h2>
         point calibration method.
     </p>
     <p>
-        <img src="image-27.png" />
+        <img src="s-25.png" />
     </p>
     <h1>Statistical comparison between conditions</h1>
     <h3>Annotating samples with group information</h3>
@@ -1027,7 +1027,7 @@ <h3>Annotating samples with group information</h3>
         <li>Applies To: “Replicates” </li>
     </ul>
     <p>
-        <img src="image-28.png" />
+        <img src="s-26.png" />
     </p>
     <ul>
         <li>Click “OK”.</li>
@@ -1037,14 +1037,14 @@ <h3>Annotating samples with group information</h3>
         <li>Applies To: “Replicates”</li>
     </ul>
     <p>
-        <img src="image-29.png" />
+        <img src="s-27.png" />
     </p>
     <ul>
         <li>Click the “OK” button.</li>
         <li>Select both “Annotations” in the “Annotations” tab.</li>
     </ul>
     <p>
-        <img src="image-30.png" />
+        <img src="s-28.png" />
     </p>
     <ul>
         <li>Click the “OK” button.</li>
@@ -1057,7 +1057,7 @@ <h3>Annotating samples with group information</h3>
         <li>Annotate “Condition”, “BioReplicate” as shown in the table below.</li>
     </ul>
     <p>
-        <img src="image-31.png" />
+        <img src="s-29.png" />
     </p>
     <p>
         <b>Tip! You can use your keyboard to type directly into the Document Grid, using Enter to move to the next line, Tab to the next column,
@@ -1080,7 +1080,7 @@ <h3>Annotating samples with group information</h3>
         (K.GVD<b><u>C</u></b>QEVSQE<b><span class="blue">K</span></b>.N [593, 603]):
     </p>
     <p>
-        <img src="image-32.png" /> <img src="image-33.png" />
+        <img src="s-30.png" /> <img src="s-31.png" />
     </p>
     <p>
         <b>Save</b> the Skyline file as PRM_Annotated.sky in the Webinar17_data folder.
@@ -1114,7 +1114,7 @@ <h3>Group Comparison in Skyline</h3>
         The “Edit Group Comparison” form should look like this:
     </p>
     <p>
-        <img src="image-34.png" />
+        <img src="s-32.png" />
     </p>
     <ul>
         <li>Click the “OK” button. </li>
@@ -1127,14 +1127,14 @@ <h3>Group Comparison in Skyline</h3>
         The second group comparison should look like this:
     </p>
     <p>
-        <img src="image-35.png" />
+        <img src="s-33.png" />
     </p>
     <ul>
         <li>Click the “OK” button. </li>
         <li>Make sure both of your new group comparisons are checked.</li>
     </ul>
     <p>
-        <img src="image-36.png" />
+        <img src="s-34.png" />
     </p>
     <ul>
         <li>Click the “OK” button. </li>
@@ -1149,7 +1149,7 @@ <h3>Group Comparison in Skyline</h3>
         Skyline will show a grid view that looks like this:
     </p>
     <p>
-        <img src="image-37.png" />
+        <img src="s-35.png" />
     </p>
     <p>
         Be aware that numbers can be different in your document depending on which peptides/transitions you have selected for the refined file.
@@ -1164,7 +1164,7 @@ <h3>Group Comparison in Skyline</h3>
         Skyline adds a graph pane to the view that looks like this:
     </p>
     <p>
-        <img src="image-38.png" />
+        <img src="s-36.png" />
     </p>
     <ul>
         <li>On the grid, click the “Fold Change Result” header, and click Sort Ascending in the menu that appears. </li>
@@ -1173,7 +1173,7 @@ <h3>Group Comparison in Skyline</h3>
         This will sort the grid, and the graph like this: 
     </p>
     <p>
-        <img src="image-39.png" />
+        <img src="s-37.png" />
     </p>
     <p>
         <b>Save</b> the Skyline file as PRM_ttest.sky in Webinar17_data folder.
@@ -1221,7 +1221,7 @@ <h1>Export a custom-defined report </h1>
         Your Edit Report tab should now look like this: 
     </p>
     <p>
-        <img src="image-40.png" />
+        <img src="s-38.png" />
     </p>
     <ul>
         <li>Click “Preview” to check report appears with 31 rows, and the last 2 columns pivoted by replicate name.</li>
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/image-0.png b/pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/s-1.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/image-0.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/s-1.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/image-9.png b/pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/s-10.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/image-9.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/image-10.png b/pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/s-11.png
similarity index 100%
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/image-11.png b/pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/s-12.png
similarity index 100%
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/image-12.png b/pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/s-13.png
similarity index 100%
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/image-13.png b/pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/s-14.png
similarity index 100%
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/image-14.png b/pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/s-15.png
similarity index 100%
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/image-15.png b/pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/s-16.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/image-15.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/image-16.png b/pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/s-17.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/image-16.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/image-17.png b/pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/s-18.png
similarity index 100%
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/image-20.png b/pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/s-19.png
similarity index 100%
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/image-1.png b/pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/s-2.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/image-1.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/s-2.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/image-21.png b/pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/s-20.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/image-21.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/s-20.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/image-22.png b/pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/s-21.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/image-22.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/s-21.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/image-23.png b/pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/s-22.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/image-23.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/s-22.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/image-25.png b/pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/s-23.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/image-25.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/s-23.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/image-26.png b/pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/s-24.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/image-26.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/s-24.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/image-27.png b/pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/s-25.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/image-27.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/s-25.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/image-28.png b/pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/s-26.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/image-28.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/s-26.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/image-29.png b/pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/s-27.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/image-29.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/s-27.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/image-30.png b/pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/s-28.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/image-30.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/s-28.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/image-31.png b/pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/s-29.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/image-31.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/s-29.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/image-2.png b/pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/s-3.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/image-2.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/s-3.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/image-32.png b/pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/s-30.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/image-32.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/image-33.png b/pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/s-31.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/image-33.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/image-34.png b/pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/s-32.png
similarity index 100%
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/image-35.png b/pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/s-33.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/image-35.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/image-36.png b/pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/s-34.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/image-36.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/image-37.png b/pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/s-35.png
similarity index 100%
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/image-38.png b/pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/s-36.png
similarity index 100%
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/image-39.png b/pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/s-37.png
similarity index 100%
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/image-40.png b/pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/s-38.png
similarity index 100%
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/image-3.png b/pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/s-4.png
similarity index 100%
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/image-4.png b/pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/s-5.png
similarity index 100%
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/image-5.png b/pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/s-6.png
similarity index 100%
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/image-6.png b/pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/s-7.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/image-6.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/image-7.png b/pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/s-8.png
similarity index 100%
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/image-8.png b/pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/s-9.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/image-8.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/s-9.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/image-19.png b/pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/s-precursor-list-spreadsheet.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/image-19.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/s-precursor-list-spreadsheet.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap/en/index.html b/pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap/en/index.html
index 1e375ff3da..daf09a4a70 100644
--- a/pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap/en/index.html
+++ b/pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap/en/index.html
@@ -47,7 +47,7 @@ <h1>Getting Started</h1>
         <li>On the <b>Start Page</b>, click <b>Import Peptide List</b> which looks like this: </li>
     </ul>
     <p>
-        <img src="image-0.png" />
+        <img src="s-1.png" />
     </p>
     <ul>
         <li>If you do not see this option,<br />Click the user interface button in the upper right-hand corner of the <b>Start Page</b> and
@@ -63,7 +63,7 @@ <h1>Getting Started</h1>
         <li>In the <b>Experiment Type</b> box, click <b>Quantifications</b>.</li>
     </ul>
     <p>
-        <img src="image-1.png" />
+        <img src="s-2.png" />
     </p>
     <p>
         For a consistent and reliable set of steps through this tutorial, it is simplest to start from default settings. Otherwise, Skyline will
@@ -115,7 +115,7 @@ <h2>Peptide Settings – Digestion tab</h2>
         When the file is generated a warning message will appear to warn you about 6 repeated sequences in the FASTA file:
     </p>
     <p>
-        <img src="image-2.png" />
+        <img src="s-3.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -145,7 +145,7 @@ <h2>Peptide Settings – Digestion tab</h2>
         The <b>Peptide Settings – Digestion</b> tab should now look like this:
     </p>
     <p>
-        <img src="image-3.png" />
+        <img src="s-4.png" />
     </p>
     <ul>
         <li>Click the <b>Prediction</b> tab.</li>
@@ -172,7 +172,7 @@ <h2>Peptide Settings – Prediction tab</h2>
         The <b>Peptide Settings – Prediction</b> tab should now look like this:
     </p>
     <p>
-        <img src="image-4.png" />
+        <img src="s-5.png" />
     </p>
     <ul>
         <li>Click the <b>Filter</b> tab.</li>
@@ -216,7 +216,7 @@ <h2>Peptide Settings – Filter tab</h2>
         The <b>Peptide Settings - Filter</b> tab should look like this:
     </p>
     <p>
-        <img src="image-5.png" />
+        <img src="s-6.png" />
     </p>
     <ul>
         <li>Click the <b>Library</b> tab.</li>
@@ -300,7 +300,7 @@ <h2>Peptide Settings – Library tab</h2>
         The <b>Library</b> tab should look like this:
     </p>
     <p>
-        <img src="image-6.png" />
+        <img src="s-7.png" />
     </p>
     <ul>
         <li>Click the <b>Modifications</b> tab.</li>
@@ -338,7 +338,7 @@ <h2>Peptide Settings – Modifications tab</h2>
         The <b>Modifications</b> tab should now look like this:
     </p>
     <p>
-        <img src="image-7.png" />
+        <img src="s-8.png" />
     </p>
     <h1>Conclusion</h1>
     <p>
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap/en/image-0.png b/pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap/en/s-1.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap/en/image-0.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap/en/s-1.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap/en/image-1.png b/pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap/en/s-2.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap/en/image-1.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap/en/s-2.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap/en/image-2.png b/pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap/en/s-3.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap/en/image-2.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap/en/image-3.png b/pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap/en/s-4.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap/en/image-3.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap/en/image-4.png b/pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap/en/s-5.png
similarity index 100%
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap/en/image-5.png b/pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap/en/s-6.png
similarity index 100%
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap/en/image-6.png b/pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap/en/s-7.png
similarity index 100%
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zO?fq+vu;j155Ipu+Kr9qpx%atNb{tE+xRbn@24{iMk6X#e;EqMJX^gJRtCQi4r)a@
z?vm5?R@^prb<}BI2ZF17+t{^^^0%RTQ@#%Fc(Bd?CH(aZeoA;EuKDvph^^q}V5IH)
d_D}d)`wPL%*<nn-&6xlI002ovPDHLkV1jdj3wHnj

diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/PeakPicking/en/index.html b/pwiz_tools/Skyline/Documentation/Tutorials/PeakPicking/en/index.html
index a79d6c19b2..76af83f24e 100644
--- a/pwiz_tools/Skyline/Documentation/Tutorials/PeakPicking/en/index.html
+++ b/pwiz_tools/Skyline/Documentation/Tutorials/PeakPicking/en/index.html
@@ -77,7 +77,7 @@ <h1>Creating Decoys</h1>
         The <b>Add Decoy Peptides</b> form should now look like this: 
     </p>
     <p>
-         <img src="image-0.png" />
+         <img src="s-1.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -86,7 +86,7 @@ <h1>Creating Decoys</h1>
         A set of decoy peptides should appear below the real peptides in the <b>Targets</b> view of the main Skyline window:
     </p>
     <p>
-        <u><img src="image-1.png" /></u>
+        <u><img src="s-2.png" /></u>
     </p>
     <h2>Importing SRM Data</h2>
     <p>
@@ -123,7 +123,7 @@ <h2>Importing SRM Data</h2>
         Skyline will show a form suggesting that it can remove the common prefix on these files:
     </p>
     <p>
-         <img src="image-2.png" />
+         <img src="s-3.png" />
     </p>
     <ul>
         <li>Delete the 0 at the end of the <b>Common prefix</b> field.</li>
@@ -143,7 +143,7 @@ <h2>Importing SRM Data</h2>
         actually at 18.0 minutes, close to the predicted retention time, annotated at 18.2 minutes in the graph.
     </p>
     <p>
-         <img src="image-3.png" />
+         <img src="s-4.png" />
     </p>
     <h2>Training a Peak Scoring Model</h2>
     <p>
@@ -156,7 +156,7 @@ <h2>Training a Peak Scoring Model</h2>
         You should see the following form:
     </p>
     <p>
-         <img src="image-4.png" />
+         <img src="s-5.png" />
     </p>
     <ul>
         <li>From the <b>Peak Scoring Model</b> dropdown list, choose <b>&lt;Add…&gt;</b>.</li>
@@ -171,7 +171,7 @@ <h2>Training a Peak Scoring Model</h2>
         You should be presented with a screen that looks like this:
     </p>
     <p>
-         <img src="image-5.png" />
+         <img src="s-6.png" />
     </p>
     <p>
         This form allows you to create and customize new peak scoring models, rather than always relying on the default heuristic Skyline Legacy
@@ -191,7 +191,7 @@ <h2>Training a Peak Scoring Model</h2>
         This will show the distribution of p values according to the Gaussian model to which the decoys were fit:
     </p>
     <p>
-         <img src="image-6.png" />
+         <img src="s-7.png" />
     </p>
     <p>
         This graph is another way to assess whether decoys are Gaussian: if they are, the p values of the decoys should be uniformly distributed over
@@ -206,7 +206,7 @@ <h2>Training a Peak Scoring Model</h2>
         This will show a graph of the q values assigned to all the targets:
     </p>
     <p>
-         <img src="image-7.png" />
+         <img src="s-8.png" />
     </p>
     <p>
         For a given FDR cut-off, any q value below the FDR value will be declared a true peak, and any q value above the FDR value will be declared a
@@ -313,7 +313,7 @@ <h2>Training a Peak Scoring Model</h2>
         The graph should change to the following: 
     </p>
     <p>
-        <img src="image-8.png" /> 
+        <img src="s-9.png" /> 
     </p>
     <p>
         Note that the library dot-product is “unknown” for several of the target values, and for this reason the score is grayed and not used in the
@@ -328,10 +328,10 @@ <h1>Handling Missing Values</h1>
         <li>Move the mouse over the bar labeled <b><i>unknown</i></b> in the <b>Feature Scores</b> graph.</li>
     </ul>
     <p>
-        A find button (<img src="image-9.png" />) should appear.
+        A find button (<img src="../../shared/blue-binocular-button.png" />) should appear.
     </p>
     <p>
-        <img src="image-10.png" />
+        <img src="s-10.png" />
     </p>
     <ul>
         <li>Click the find button.</li>
@@ -355,7 +355,7 @@ <h1>Handling Missing Values</h1>
         On the <b>Find Results</b> dialog, there should be 6 peptides in the list.
     </p>
     <p>
-        <b><img src="image-11.png" /></b> 
+        <b><img src="s-11.png" /></b> 
     </p>
     <ul>
         <li>Double-click on the first peptide in the list, LGGNEQVTR.</li>
@@ -371,7 +371,7 @@ <h1>Handling Missing Values</h1>
         disabled when one or more values are missing, you must deal with all 6 peptides shown in the <b>Find Results</b> view to make the
         <b>Library intensity dot-product</b> score active. This first peptide appears under the ‘iRTpeptides’ list. While it is one of the
         11 peptides in the iRT mix used in this experiment, it was obviously not included in the iRT calculator for this document. In the
-        <b>Targets</b> view, it lacks the tiny clock icon <img src="image-12.png" /> (in the upper-right corner of the peptide icon)
+        <b>Targets</b> view, it lacks the tiny clock icon <img src="../../shared/peptide-with-spectrum-lines-and-clock-icon.png" /> (in the upper-right corner of the peptide icon)
         indicating an iRT standard peptide. Skyline automatically excludes standard peptides from scoring consideration. Although, in this document,
         all of the other iRT peptides have matching library spectra. To handle this case now, delete this peptide:
     </p>
@@ -429,7 +429,7 @@ <h1>Handling Missing Values</h1>
         improved. The <b>Edit Peak Scoring Model</b> form should look like this:
     </p>
     <p>
-         <img src="image-13.png" /> 
+         <img src="s-12.png" /> 
     </p>
     <p>
         The <b>Q Values</b> plot will now be improved as well:
@@ -441,7 +441,7 @@ <h1>Handling Missing Values</h1>
         You should see a graph like the following:
     </p>
     <p>
-         <b><img src="image-14.png" /></b>
+         <b><img src="s-13.png" /></b>
     </p>
     <p>
         As you can see, most of the q values are now smaller after adding the new scores, indicating higher confidence in the picked peaks.
@@ -489,7 +489,7 @@ <h1>Customizing the Model</h1>
         The graphs should now update and the scores that were unchecked should be removed. The model should look like this:
     </p>
     <p>
-         <img src="image-15.png" />
+         <img src="s-14.png" />
     </p>
     <p>
         You will not use this modified model. To return to the original model, simply cancel the form:
@@ -514,7 +514,7 @@ <h1>Applying the Model to Improve Peak Picking</h1>
         The <b>Reintegrate</b> dialog box should look like this:
     </p>
     <p>
-         <img src="image-16.png" /> 
+         <img src="s-15.png" /> 
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -532,7 +532,7 @@ <h1>Applying the Model to Improve Peak Picking</h1>
         Note that after reintegration, the chosen peak for this peptide/replicate is now at the correct position of 18.0 minutes. 
     </p>
     <p>
-         <img src="image-17.png" />
+         <img src="s-16.png" />
     </p>
     <p>
         Now try reintegrating in a slightly different way by doing the following:
@@ -551,14 +551,14 @@ <h1>Applying the Model to Improve Peak Picking</h1>
         <b>Targets</b> view, a peptide with no chosen peak will have a red dot left of its sequence:
     </p>
     <p>
-        <img src="image-18.png" />
+        <img src="s-17.png" />
     </p>
     <p>
         This is now the case for the peptide LPDGNGIEL<b><u>C</u><span class="blue">R</span></b> in the replicate 006_StC-DosR_B2. You will
         also see that the chromatogram graph now lacks the right-pointing arrowheads, indicating the chosen peak:
     </p>
     <p>
-         <img src="image-19.png" />
+         <img src="s-18.png" />
     </p>
     <p>
         This can be different for each replicate, however, and if you use the <b>Replicates</b> dropdown list at the top of the
@@ -567,7 +567,7 @@ <h1>Applying the Model to Improve Peak Picking</h1>
         precursor, which you can see better, if you select it (622.3086++) in the <b>Targets</b> view and zoom in a little:
     </p>
     <p>
-         <img src="image-20.png" />
+         <img src="s-19.png" />
     </p>
     <p>
         Any peak picking algorithm might do better with this peak, if the y10 ion were removed.
@@ -587,7 +587,7 @@ <h1>Exporting Peak Scoring Results (mProphet)</h1>
         The <b>Export mProphet Features</b> form should look like this:
     </p>
     <p>
-         <img src="image-21.png" /><u> </u>
+         <img src="s-20.png" /><u> </u>
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -623,7 +623,7 @@ <h1>Exporting Peak Scoring Results (Skyline report)</h1>
         The form should look like this:
     </p>
     <p>
-         <img src="image-22.png" />
+         <img src="s-21.png" />
     </p>
     <ul>
         <li>Click the <b>Edit</b> button.</li>
@@ -632,7 +632,7 @@ <h1>Exporting Peak Scoring Results (Skyline report)</h1>
         The <b>Edit Report</b> form should appear as follows:
     </p>
     <p>
-         <img src="image-23.png" />
+         <img src="s-22.png" />
     </p>
     <ul>
         <li>On the left side of the form, click on the plus icon by <b>Peptides</b> to expand the list.</li>
@@ -644,7 +644,7 @@ <h1>Exporting Peak Scoring Results (Skyline report)</h1>
         The <b>Edit Report</b> form should now look like this:
     </p>
     <p>
-        <img src="image-24.png" />
+        <img src="s-23.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -713,7 +713,7 @@ <h1>Training a Peak Scoring Model for DIA Data</h1>
         A form like the following should appear:
     </p>
     <p>
-         <img src="image-25.png" />
+         <img src="s-24.png" />
     </p>
     <ul>
         <li>Click the <b>Re-score</b> button</li>
@@ -722,7 +722,7 @@ <h1>Training a Peak Scoring Model for DIA Data</h1>
         The following form should appear:
     </p>
     <p>
-         <img src="image-26.png" />
+         <img src="s-25.png" />
     </p>
     <ul>
         <li>Click the <b>Re-score in place</b> button.</li>
@@ -743,7 +743,7 @@ <h1>Training a Peak Scoring Model for DIA Data</h1>
         This will show the model from the previous dataset, applied to the peptides in the present dataset. 
     </p>
     <p>
-         <img src="image-27.png" />
+         <img src="s-26.png" />
     </p>
     <p>
         A model trained on one dataset can be applied to another, or you can train a new model for each dataset, provided your dataset contains enough
@@ -766,7 +766,7 @@ <h1>Training a Peak Scoring Model for DIA Data</h1>
         The model should look like this:
     </p>
     <p>
-        <img src="image-28.png" /> 
+        <img src="s-27.png" /> 
     </p>
     <p>
         Note that some of the scores that were unavailable in the SRM model are available here, such as <b>Product mass error</b>. This is
@@ -777,7 +777,7 @@ <h1>Training a Peak Scoring Model for DIA Data</h1>
         <li>Above the graph on the right side, click the <b>Feature Scores</b> tab.</li>
         <li>Click on the <b>Library intensity dot-product</b> row in the <b>Available feature scores</b> grid</li>
         <li>Move the mouse over the bar labeled <b><i>unknown</i></b> in the <b>Feature Scores</b> graph.</li>
-        <li>A find button (<img src="image-29.png" />) should appear – click it.</li>
+        <li>A find button (<img src="../../shared/blue-binocular-button.png" />) should appear – click it.</li>
     </ul>
     <p>
         A <b>Find Results Form</b> should appear behind the <b>Edit Peak Scoring Model</b> window, showing many peptides that lack
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/PeakPicking/en/image-0.png b/pwiz_tools/Skyline/Documentation/Tutorials/PeakPicking/en/s-1.png
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rename from pwiz_tools/Skyline/Documentation/Tutorials/PeakPicking/en/image-0.png
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rename to pwiz_tools/Skyline/Documentation/Tutorials/PeakPicking/en/s-9.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/SmallMolecule/en/index.html b/pwiz_tools/Skyline/Documentation/Tutorials/SmallMolecule/en/index.html
index 4e01aac1d8..3da2f78c12 100644
--- a/pwiz_tools/Skyline/Documentation/Tutorials/SmallMolecule/en/index.html
+++ b/pwiz_tools/Skyline/Documentation/Tutorials/SmallMolecule/en/index.html
@@ -397,7 +397,7 @@ <h2>Transition list insert</h2>
         Skyline will show the <b>Insert Transition List</b> form which should look like this:
     </p>
     <p>
-        <img src="image-0.png" />
+        <img src="s-1.png" />
     </p>
     <ul>
         <li>Press <b>Ctrl-V</b> to paste the information you placed on the clipboard into Skyline.</li>
@@ -406,7 +406,7 @@ <h2>Transition list insert</h2>
         Skyline will show <b>the Import Transition List: Identify Columns</b> form:
     </p>
     <p>
-        <img src="image-1.png" />
+        <img src="s-2.png" />
     </p>
     <ul>
         <li>Make sure the <b>Molecules</b> button is pressed.</li>
@@ -438,7 +438,7 @@ <h2>Further notes on ion formulas and adduct descriptions</h2>
         Your Skyline window should now look like this: 
     </p>
     <p>
-        <img src="image-2.png" />
+        <img src="s-3.png" />
     </p>
     <p>
         At this point, either a native instrument method, precursor isolation list (for PRM) or transition list (for SRM) can be exported. For more
@@ -466,7 +466,7 @@ <h1>Importing Mass Spectrometer Runs</h1>
         The <b>Import Results Files</b> form should look like this:
     </p>
     <p>
-         <img src="image-3.png" />
+         <img src="s-4.png" />
     </p>
     <ul>
         <li>Click the <b>Open</b> button.</li>
@@ -539,7 +539,7 @@ <h1>Importing Mass Spectrometer Runs</h1>
         The files should import within a matter of seconds, leaving your Skyline window looking like this:
     </p>
     <p>
-        <img src="image-4.png" />
+        <img src="s-5.png" />
     </p>
     <p>
         To take advantage of the Skyline summary graphs for viewing individual targets, do the following:
@@ -554,7 +554,7 @@ <h1>Importing Mass Spectrometer Runs</h1>
         The Skyline window should now look like this:
     </p>
     <p>
-        <img src="image-5.png" />
+        <img src="s-6.png" />
     </p>
     <h1>Conclusion</h1>
     <p>
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/SmallMolecule/en/image-0.png b/pwiz_tools/Skyline/Documentation/Tutorials/SmallMolecule/en/s-1.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/SmallMolecule/en/image-0.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/SmallMolecule/en/s-1.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/SmallMolecule/en/image-1.png b/pwiz_tools/Skyline/Documentation/Tutorials/SmallMolecule/en/s-2.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/SmallMolecule/en/image-1.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/SmallMolecule/en/s-2.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/SmallMolecule/en/image-2.png b/pwiz_tools/Skyline/Documentation/Tutorials/SmallMolecule/en/s-3.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/SmallMolecule/en/image-2.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/SmallMolecule/en/s-3.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/SmallMolecule/en/image-3.png b/pwiz_tools/Skyline/Documentation/Tutorials/SmallMolecule/en/s-4.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/SmallMolecule/en/image-3.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/SmallMolecule/en/s-4.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/SmallMolecule/en/image-4.png b/pwiz_tools/Skyline/Documentation/Tutorials/SmallMolecule/en/s-5.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/SmallMolecule/en/image-4.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/SmallMolecule/en/s-5.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/SmallMolecule/en/image-5.png b/pwiz_tools/Skyline/Documentation/Tutorials/SmallMolecule/en/s-6.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/SmallMolecule/en/image-5.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/SmallMolecule/en/s-6.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/SmallMolecule/ja/index.html b/pwiz_tools/Skyline/Documentation/Tutorials/SmallMolecule/ja/index.html
index 7b5984113c..bed2d73c49 100644
--- a/pwiz_tools/Skyline/Documentation/Tutorials/SmallMolecule/ja/index.html
+++ b/pwiz_tools/Skyline/Documentation/Tutorials/SmallMolecule/ja/index.html
@@ -376,7 +376,7 @@ <h2>トランジションリストの挿入</h2>
         Skylineが以下のような [ <b>トランジションリストの挿入</b> ] フォームを表示します。
     </p>
     <p>
-        <img src="image-0.png" />
+        <img src="s-1.png" />
     </p>
     <ul>
         <li>[ <b>貼り付け</b> ] （Ctrl-V）をクリックして、クリックボードにコピーした情報を Skyline にはり付けます。</li>
@@ -385,7 +385,7 @@ <h2>トランジションリストの挿入</h2>
         Skyline に[<b>トランジションリストのインポート：列の識別</b> ] フォームが次のように表示されます。
     </p>
     <p>
-        <img src="image-1.png" />
+        <img src="s-2.png" />
     </p>
     <ul>
         <li>[ <b>分子</b> ] ボタンがオンになっていることを確認します。</li>
@@ -411,7 +411,7 @@ <h2>イオン組成および付加物の説明についてのその他の注意<
         これでSkylineウィンドウは以下のようになります。 
     </p>
     <p>
-        <img src="image-2.png" />
+        <img src="s-3.png" />
     </p>
     <p>
         この時点で、装置メソッド、プリカーサー単離リスト（PRM用）、またはトランジションリスト（SRM用）のいずれかをエクスポート可能です。この手順の実行方法の詳細については、<a
@@ -436,7 +436,7 @@ <h1>rawデータファイルのインポート</h1>
         [ <b>結果ファイルをインポート</b> ] フォームは以下のようになります。
     </p>
     <p>
-         <img src="image-3.png" />
+         <img src="s-4.png" />
     </p>
     <ul>
         <li>[ <b>開く</b> ] ボタンをクリックします。</li>
@@ -507,7 +507,7 @@ <h1>rawデータファイルのインポート</h1>
         当該ファイルは瞬時にインポートされ、Skylineウィンドウは以下のようになります。
     </p>
     <p>
-        <img src="image-4.png" />
+        <img src="s-5.png" />
     </p>
     <p>
         Skyline概要グラフを利用して個別のターゲットを表示するには、以下の操作を行います。
@@ -522,7 +522,7 @@ <h1>rawデータファイルのインポート</h1>
         これでSkylineウィンドウは以下のようになります。
     </p>
     <p>
-        <img src="image-5.png" />
+        <img src="s-6.png" />
     </p>
     <h1>まとめ</h1>
     <p>
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/SmallMolecule/ja/invariant.html b/pwiz_tools/Skyline/Documentation/Tutorials/SmallMolecule/ja/invariant.html
index 49e1f6e788..b9967111b0 100644
--- a/pwiz_tools/Skyline/Documentation/Tutorials/SmallMolecule/ja/invariant.html
+++ b/pwiz_tools/Skyline/Documentation/Tutorials/SmallMolecule/ja/invariant.html
@@ -396,7 +396,7 @@ <h2>Transition list insert</h2>
         Skyline will show the <b>Insert Transition List</b> form which should look like this:
     </p>
     <p>
-        <img src="image-0.png" />
+        <img src="s-1.png" />
     </p>
     <ul>
         <li>Press <b>Ctrl-V</b> to paste the information you placed on the clipboard into Skyline.</li>
@@ -405,7 +405,7 @@ <h2>Transition list insert</h2>
         Skyline will show <b>the Import Transition List: Identify Columns</b> form:
     </p>
     <p>
-        <img src="image-1.png" />
+        <img src="s-2.png" />
     </p>
     <ul>
         <li>Make sure the <b>Molecules</b> button is pressed.</li>
@@ -437,7 +437,7 @@ <h2>Further notes on ion formulas and adduct descriptions</h2>
         Your Skyline window should now look like this: 
     </p>
     <p>
-        <img src="image-2.png" />
+        <img src="s-3.png" />
     </p>
     <p>
         At this point, either a native instrument method, precursor isolation list (for PRM) or transition list (for SRM) can be exported. For more
@@ -465,7 +465,7 @@ <h1>Importing Mass Spectrometer Runs</h1>
         The <b>Import Results Files</b> form should look like this:
     </p>
     <p>
-         <img src="image-3.png" />
+         <img src="s-4.png" />
     </p>
     <ul>
         <li>Click the <b>Open</b> button.</li>
@@ -538,7 +538,7 @@ <h1>Importing Mass Spectrometer Runs</h1>
         The files should import within a matter of seconds, leaving your Skyline window looking like this:
     </p>
     <p>
-        <img src="image-4.png" />
+        <img src="s-5.png" />
     </p>
     <p>
         To take advantage of the Skyline summary graphs for viewing individual targets, do the following:
@@ -553,7 +553,7 @@ <h1>Importing Mass Spectrometer Runs</h1>
         The Skyline window should now look like this:
     </p>
     <p>
-        <img src="image-5.png" />
+        <img src="s-6.png" />
     </p>
     <h1>Conclusion</h1>
     <p>
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/SmallMolecule/ja/image-0.png b/pwiz_tools/Skyline/Documentation/Tutorials/SmallMolecule/ja/s-1.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/SmallMolecule/ja/image-0.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/SmallMolecule/ja/s-1.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/SmallMolecule/ja/image-1.png b/pwiz_tools/Skyline/Documentation/Tutorials/SmallMolecule/ja/s-2.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/SmallMolecule/ja/image-1.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/SmallMolecule/ja/s-2.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/SmallMolecule/ja/image-2.png b/pwiz_tools/Skyline/Documentation/Tutorials/SmallMolecule/ja/s-3.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/SmallMolecule/ja/image-2.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/SmallMolecule/ja/s-3.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/SmallMolecule/ja/image-3.png b/pwiz_tools/Skyline/Documentation/Tutorials/SmallMolecule/ja/s-4.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/SmallMolecule/ja/image-3.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/SmallMolecule/ja/s-4.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/SmallMolecule/ja/image-4.png b/pwiz_tools/Skyline/Documentation/Tutorials/SmallMolecule/ja/s-5.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/SmallMolecule/ja/image-4.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/SmallMolecule/ja/s-5.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/SmallMolecule/ja/image-5.png b/pwiz_tools/Skyline/Documentation/Tutorials/SmallMolecule/ja/s-6.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/SmallMolecule/ja/image-5.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/SmallMolecule/ja/s-6.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/SmallMolecule/zh-CHS/index.html b/pwiz_tools/Skyline/Documentation/Tutorials/SmallMolecule/zh-CHS/index.html
index 2e3cbaf07f..699ef35045 100644
--- a/pwiz_tools/Skyline/Documentation/Tutorials/SmallMolecule/zh-CHS/index.html
+++ b/pwiz_tools/Skyline/Documentation/Tutorials/SmallMolecule/zh-CHS/index.html
@@ -379,7 +379,7 @@ <h2>插入离子对列表</h2>
         Skyline 将显示<b>插入离子对列表</b>表单，如下所示：
     </p>
     <p>
-        <img src="image-0.png" />
+        <img src="s-1.png" />
     </p>
     <ul>
         <li>按 <b>Ctrl-V</b> 将剪贴板上的信息粘贴到 Skyline 中。</li>
@@ -388,7 +388,7 @@ <h2>插入离子对列表</h2>
         Skyline 将显示<b>导入离子对列表：标识列</b>表单：
     </p>
     <p>
-        <img src="image-1.png" />
+        <img src="s-2.png" />
     </p>
     <ul>
         <li>确保按下<b>分子</b>按钮。</li>
@@ -415,7 +415,7 @@ <h2>关于离子的分子式和加合物描述的进一步注释</h2>
         现在 Skyline 窗口将显示如下： 
     </p>
     <p>
-        <img src="image-2.png" />
+        <img src="s-3.png" />
     </p>
     <p>
         此时可以导出原生仪器方法、母离子分离列表（用于 PRM）或离子对列表（用于 SRM）。有关如何执行此步的更多详细信息，请参见<a href="https://skyline.ms/tutorial_method_edit_zh.url">靶向方法编辑</a>、<a
@@ -439,7 +439,7 @@ <h1>导入质谱仪运行结果</h1>
         <b>导入结果文件</b>表单应显示如下：
     </p>
     <p>
-         <img src="image-3.png" />
+         <img src="s-4.png" />
     </p>
     <ul>
         <li>单击<b>打开</b>按钮。</li>
@@ -510,7 +510,7 @@ <h1>导入质谱仪运行结果</h1>
         这些文件应在短短数秒内导入，之后 Skyline 窗口将显示如下：
     </p>
     <p>
-        <img src="image-4.png" />
+        <img src="s-5.png" />
     </p>
     <p>
         要利用 Skyline 摘要图查看各个目标，请执行以下操作：
@@ -525,7 +525,7 @@ <h1>导入质谱仪运行结果</h1>
         此时 Skyline 窗口将显示如下：
     </p>
     <p>
-        <img src="image-5.png" />
+        <img src="s-6.png" />
     </p>
     <h1>结语</h1>
     <p>
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/SmallMolecule/zh-CHS/invariant.html b/pwiz_tools/Skyline/Documentation/Tutorials/SmallMolecule/zh-CHS/invariant.html
index ff385b9d73..e11516d0cc 100644
--- a/pwiz_tools/Skyline/Documentation/Tutorials/SmallMolecule/zh-CHS/invariant.html
+++ b/pwiz_tools/Skyline/Documentation/Tutorials/SmallMolecule/zh-CHS/invariant.html
@@ -396,7 +396,7 @@ <h2>Transition list insert</h2>
         Skyline will show the <b>Insert Transition List</b> form which should look like this:
     </p>
     <p>
-        <img src="image-0.png" />
+        <img src="s-1.png" />
     </p>
     <ul>
         <li>Press <b>Ctrl-V</b> to paste the information you placed on the clipboard into Skyline.</li>
@@ -405,7 +405,7 @@ <h2>Transition list insert</h2>
         Skyline will show <b>the Import Transition List: Identify Columns</b> form:
     </p>
     <p>
-        <img src="image-1.png" />
+        <img src="s-2.png" />
     </p>
     <ul>
         <li>Make sure the <b>Molecules</b> button is pressed.</li>
@@ -437,7 +437,7 @@ <h2>Further notes on ion formulas and adduct descriptions</h2>
         Your Skyline window should now look like this: 
     </p>
     <p>
-        <img src="image-2.png" />
+        <img src="s-3.png" />
     </p>
     <p>
         At this point, either a native instrument method, precursor isolation list (for PRM) or transition list (for SRM) can be exported. For more
@@ -465,7 +465,7 @@ <h1>Importing Mass Spectrometer Runs</h1>
         The <b>Import Results Files</b> form should look like this:
     </p>
     <p>
-         <img src="image-3.png" />
+         <img src="s-4.png" />
     </p>
     <ul>
         <li>Click the <b>Open</b> button.</li>
@@ -538,7 +538,7 @@ <h1>Importing Mass Spectrometer Runs</h1>
         The files should import within a matter of seconds, leaving your Skyline window looking like this:
     </p>
     <p>
-        <img src="image-4.png" />
+        <img src="s-5.png" />
     </p>
     <p>
         To take advantage of the Skyline summary graphs for viewing individual targets, do the following:
@@ -553,7 +553,7 @@ <h1>Importing Mass Spectrometer Runs</h1>
         The Skyline window should now look like this:
     </p>
     <p>
-        <img src="image-5.png" />
+        <img src="s-6.png" />
     </p>
     <h1>Conclusion</h1>
     <p>
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/SmallMolecule/zh-CHS/image-0.png b/pwiz_tools/Skyline/Documentation/Tutorials/SmallMolecule/zh-CHS/s-1.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/SmallMolecule/zh-CHS/image-0.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/SmallMolecule/zh-CHS/s-1.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/SmallMolecule/zh-CHS/image-1.png b/pwiz_tools/Skyline/Documentation/Tutorials/SmallMolecule/zh-CHS/s-2.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/SmallMolecule/zh-CHS/image-1.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/SmallMolecule/zh-CHS/s-2.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/SmallMolecule/zh-CHS/image-2.png b/pwiz_tools/Skyline/Documentation/Tutorials/SmallMolecule/zh-CHS/s-3.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/SmallMolecule/zh-CHS/image-2.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/SmallMolecule/zh-CHS/s-3.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/SmallMolecule/zh-CHS/image-3.png b/pwiz_tools/Skyline/Documentation/Tutorials/SmallMolecule/zh-CHS/s-4.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/SmallMolecule/zh-CHS/image-3.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/SmallMolecule/zh-CHS/s-4.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/SmallMolecule/zh-CHS/image-4.png b/pwiz_tools/Skyline/Documentation/Tutorials/SmallMolecule/zh-CHS/s-5.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/SmallMolecule/zh-CHS/image-4.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/SmallMolecule/zh-CHS/s-5.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/SmallMolecule/zh-CHS/image-5.png b/pwiz_tools/Skyline/Documentation/Tutorials/SmallMolecule/zh-CHS/s-6.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/SmallMolecule/zh-CHS/image-5.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/SmallMolecule/zh-CHS/s-6.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeIMSLibraries/en/image-11.png b/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeIMSLibraries/en/image-11.png
deleted file mode 100644
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeIMSLibraries/en/index.html b/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeIMSLibraries/en/index.html
index 0696678a2a..0fbfea44ec 100644
--- a/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeIMSLibraries/en/index.html
+++ b/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeIMSLibraries/en/index.html
@@ -119,7 +119,7 @@ <h1>Transition Settings</h1>
         The <b>Transition Settings</b> form should now look like this:
     </p>
     <p>
-        <img src="image-0.png" />
+        <img src="s-1.png" />
     </p>
     <ul>
         <li>Click the <b>Full-Scan</b> tab in the <b>Transition Settings</b> form.</li>
@@ -135,7 +135,7 @@ <h1>Transition Settings</h1>
         The <b>Transition Settings</b> form should look like this:
     </p>
     <p>
-        <img src="image-1.png" />
+        <img src="s-2.png" />
     </p>
     <p>
         The <b>Transition Settings</b> form instructs Skyline to extract 3 precursor isotope peaks from MS1 (low-energy) spectra and fragment
@@ -187,7 +187,7 @@ <h1>Adding and Exploring a Spectral Library</h1>
         The <b>Molecule Settings</b> form should now look like this:
     </p>
     <p>
-        <img src="image-2.png" />
+        <img src="s-3.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button in the <b>Molecule Settings</b> form.</li>
@@ -202,7 +202,7 @@ <h1>Adding and Exploring a Spectral Library</h1>
         The library explorer should now look like this:
     </p>
     <p>
-        <img src="image-3.png" />
+        <img src="s-4.png" />
     </p>
     <p>
         On the left side of the explorer, the <b>Library</b> list illustrates that you are currently viewing the Drosophila_Lipids library.
@@ -254,7 +254,7 @@ <h1>Adding and Exploring a Spectral Library</h1>
         Your Skyline window should now look like this:
     </p>
     <p>
-        <img src="image-4.png" />
+        <img src="s-5.png" />
     </p>
     <h1>Importing Results Data</h1>
     <p>
@@ -272,7 +272,7 @@ <h1>Importing Results Data</h1>
         The <b>Import Results</b> form will appear as follows:
     </p>
     <p>
-        <img src="image-5.png" />
+        <img src="s-6.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -281,7 +281,7 @@ <h1>Importing Results Data</h1>
         The <b>Import Results Files</b> form will now show the .d files you have extracted into the tutorial folder:
     </p>
     <p>
-        <img src="image-6.png" />
+        <img src="s-7.png" />
     </p>
     <ul>
         <li>Select both .d files.</li>
@@ -293,7 +293,7 @@ <h1>Importing Results Data</h1>
         This should start the import and cause Skyline to show the <b>Importing Results</b> progress form:
     </p>
     <p>
-        <img src="image-7.png" />
+        <img src="s-8.png" />
     </p>
     <h1>Reviewing the Extracted Ion Chromatograms</h1>
     <p>
@@ -323,7 +323,7 @@ <h1>Reviewing the Extracted Ion Chromatograms</h1>
         Your chromatogram graphs should appear as follows:
     </p>
     <p>
-        <img src="image-8.png" />
+        <img src="s-9.png" />
     </p>
     <p>
         Note that while the precursor extracted ion chromatogram (XIC) is clean, the transitions for FA 16:0(+O) and FA 18:1(+O) are highly abundant
@@ -345,26 +345,26 @@ <h1>Reviewing the Extracted Ion Chromatograms</h1>
         This should leave the <b>Library Match</b> view showing an MS/MS spectrum like this:
     </p>
     <p>
-        <img src="image-9.png" />
+        <img src="s-10.png" />
     </p>
     <ul>
         <li>Attach the <b>Library Match</b> view beneath the <b>Targets</b> view by clicking in the title bar and dragging over
-            the <b>Targets</b> view until the mouse cursor is inside the bottom docking icon. <img src="image-10.png" /></li>
+            the <b>Targets</b> view until the mouse cursor is inside the bottom docking icon. <img src="../../shared/bottom-side-docking-icon.png" /></li>
         <li>On the <b>View</b> menu, choose <b>Retention Times</b> and click <b>Replicate Comparison</b> (F8).</li>
         <li>Attach the <b>Retention Times</b> view to the right edge of the main window by clicking in the title bar and dragging until the
-            mouse cursor is inside the right-side docking icon. <img src="image-11.png" /></li>
+            mouse cursor is inside the right-side docking icon. <img src="../../shared/right-side-docking-icon.png" /></li>
         <li>Right-click in the <b>Retention Times</b> view and click <b>Legend</b> to hide the legend in this graph.</li>
         <li>From the <b>View</b> menu, choose <b>Peak Areas</b> and click <b>Replicate Comparison</b> (F7).</li>
         <li>Attach the <b>Peak Areas</b> view to the left of the <b>Retention Times</b> view by clicking in the title bar and
             dragging over the <b>Retention Times</b> view until the` mouse cursor is inside the left side docking icon. <img
-                src="image-12.png" /></li>
+                src="../../shared/left-side-docking-icon.png" /></li>
         <li>Adjust the view sizing using the splitter bar regions between them.</li>
     </ul>
     <p class="keep-next">
         You should end up with a similar layout to the one shown below:
     </p>
     <p>
-        <img src="image-13.png" />
+        <img src="s-11.png" />
     </p>
     <p>
         To adjust the zooming on the chromatogram graphs:
@@ -419,20 +419,20 @@ <h1>Understanding and Utilizing the IMS Separation</h1>
             it.</li>
     </ul>
     <p>
-        <img src="image-14.png" />
+        <img src="s-12.png" />
     </p>
     <p class="keep-next">
         This should bring up the <b>Full-Scan</b> view showing a familiar two-dimensional spectrum in profile mode:
     </p>
     <p>
-        <img src="image-15.png" />
+        <img src="s-13.png" />
     </p>
     <ul class="keep-next">
-        <li>Click the <b>Show 2D Spectrum</b> button <img src="image-16.png" /> to change the plot to a three-dimensional spectrum with
+        <li>Click the <b>Show 2D Spectrum</b> button <img src="../../shared/show-2d-spectrum-button.png" /> to change the plot to a three-dimensional spectrum with
             drift time.</li>
     </ul>
     <p>
-        <img src="image-17.png" />
+        <img src="s-14.png" />
     </p>
     <p>
         You can see that there is a small interference above the most intense visible ion. 
@@ -448,7 +448,7 @@ <h1>Understanding and Utilizing the IMS Separation</h1>
         <li>Click the <b>Zoom to Selection</b> button to see the entire 3D MS1 spectrum.</li>
     </ul>
     <p>
-        <img src="image-18.png" />
+        <img src="s-15.png" />
     </p>
     <p>
         This is a fairly typical MS1 spectrum for IMS-MS lipidomics data. You can get a better sense of the data by zooming into multiple areas on this
@@ -469,7 +469,7 @@ <h1>Understanding and Utilizing the IMS Separation</h1>
         The Full-Scan graph should change to:
     </p>
     <p>
-        <img src="image-19.png" />
+        <img src="s-16.png" />
     </p>
     <p>
         You can see that at least three visible ions are contributing to the extracted intensities at 33, 37, and 44 ms. This goes back to the nature
@@ -482,7 +482,7 @@ <h1>Understanding and Utilizing the IMS Separation</h1>
         <li>Click the <b>Zoom to Selection</b> button again to see the entire 3D MS/MS spectrum.</li>
     </ul>
     <p>
-        <img src="image-20.png" />
+        <img src="s-17.png" />
     </p>
     <p>
         This is also a typical IMS-MS/MS spectrum, where you can imagine each horizontal stripe as a top-down view of a normal 2D spectrum. Clearly,
@@ -525,7 +525,7 @@ <h1>Reimporting Data with Drift Time Filtering</h1>
         The <b>Transition Settings</b> should now look like this:
     </p>
     <p>
-        <img src="image-21.png" />
+        <img src="s-18.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -556,7 +556,7 @@ <h1>Reimporting Data with Drift Time Filtering</h1>
         The <b>Full-Scan</b> graph should now look something like this:
     </p>
     <p>
-        <img src="image-22.png" />
+        <img src="s-19.png" />
     </p>
     <p>
         The horizontal violet range showing the filter imposed by the CCS (261 Å<sup>2</sup>) is now visible and stored in the Skyline document. The
@@ -584,7 +584,7 @@ <h1>Reimporting Data with Drift Time Filtering</h1>
         <li>Select <b>LipidCreator</b> in the list of available tools.</li>
     </ul>
     <p>
-        <img src="image-23.png" />
+        <img src="s-20.png" />
     </p>
     <ul>
         <li>Click the <b>Install</b> button.</li>
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeIMSLibraries/en/image-0.png b/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeIMSLibraries/en/s-1.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeIMSLibraries/en/image-0.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeIMSLibraries/en/s-1.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeIMSLibraries/en/image-9.png b/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeIMSLibraries/en/s-10.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeIMSLibraries/en/image-9.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeIMSLibraries/en/s-10.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeIMSLibraries/en/image-13.png b/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeIMSLibraries/en/s-11.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeIMSLibraries/en/image-13.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeIMSLibraries/en/s-11.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeIMSLibraries/en/image-14.png b/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeIMSLibraries/en/s-12.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeIMSLibraries/en/image-14.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeIMSLibraries/en/s-12.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeIMSLibraries/en/image-15.png b/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeIMSLibraries/en/s-13.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeIMSLibraries/en/image-15.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeIMSLibraries/en/s-13.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeIMSLibraries/en/image-17.png b/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeIMSLibraries/en/s-14.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeIMSLibraries/en/image-17.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeIMSLibraries/en/s-14.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeIMSLibraries/en/image-18.png b/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeIMSLibraries/en/s-15.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeIMSLibraries/en/image-18.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeIMSLibraries/en/s-15.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeIMSLibraries/en/image-19.png b/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeIMSLibraries/en/s-16.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeIMSLibraries/en/image-19.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeIMSLibraries/en/s-16.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeIMSLibraries/en/image-20.png b/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeIMSLibraries/en/s-17.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeIMSLibraries/en/image-20.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeIMSLibraries/en/s-17.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeIMSLibraries/en/image-21.png b/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeIMSLibraries/en/s-18.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeIMSLibraries/en/image-21.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeIMSLibraries/en/s-18.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeIMSLibraries/en/image-22.png b/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeIMSLibraries/en/s-19.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeIMSLibraries/en/image-22.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeIMSLibraries/en/s-19.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeIMSLibraries/en/image-1.png b/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeIMSLibraries/en/s-2.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeIMSLibraries/en/image-1.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeIMSLibraries/en/s-2.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeIMSLibraries/en/image-23.png b/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeIMSLibraries/en/s-20.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeIMSLibraries/en/image-23.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeIMSLibraries/en/s-20.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeIMSLibraries/en/image-2.png b/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeIMSLibraries/en/s-3.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeIMSLibraries/en/image-2.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeIMSLibraries/en/s-3.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeIMSLibraries/en/image-3.png b/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeIMSLibraries/en/s-4.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeIMSLibraries/en/image-3.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeIMSLibraries/en/s-4.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeIMSLibraries/en/image-4.png b/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeIMSLibraries/en/s-5.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeIMSLibraries/en/image-4.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeIMSLibraries/en/s-5.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeIMSLibraries/en/image-5.png b/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeIMSLibraries/en/s-6.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeIMSLibraries/en/image-5.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeIMSLibraries/en/s-6.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeIMSLibraries/en/image-6.png b/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeIMSLibraries/en/s-7.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeIMSLibraries/en/image-6.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeIMSLibraries/en/s-7.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeIMSLibraries/en/image-7.png b/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeIMSLibraries/en/s-8.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeIMSLibraries/en/image-7.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeIMSLibraries/en/s-8.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeIMSLibraries/en/image-8.png b/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeIMSLibraries/en/s-9.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeIMSLibraries/en/image-8.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeIMSLibraries/en/s-9.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeMethodDevCEOpt/en/index.html b/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeMethodDevCEOpt/en/index.html
index 5a005f04f8..0c47a03572 100644
--- a/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeMethodDevCEOpt/en/index.html
+++ b/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeMethodDevCEOpt/en/index.html
@@ -105,7 +105,7 @@ <h1>Importing a Small Molecule Transition List into a Skyline Document</h1>
         This is the published transition list:
     </p>
     <p>
-        <img src="image-0.png" />
+        <img src="s-published-transition-list.png" />
     </p>
     <p>
         It provides information about light (12C) and heavy (13C) precursor and fragment <i>m/z</i> and charge for each molecule. For the purposes of
@@ -132,7 +132,7 @@ <h1>Importing a Small Molecule Transition List into a Skyline Document</h1>
         Skyline will present a window confirming its understanding of your column headers:
     </p>
     <p>
-        <img src="image-1.png" />
+        <img src="s-1.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -141,7 +141,7 @@ <h1>Importing a Small Molecule Transition List into a Skyline Document</h1>
         Your Skyline window should now look something like this:
     </p>
     <p>
-        <img src="image-2.png" />
+        <img src="s-2.png" />
     </p>
     <table>
         <tr>
@@ -161,7 +161,7 @@ <h1>Transition Settings</h1>
         <li>On the <b>Prediction</b> tab, in the <b>Collision energy</b> dropdown list, choose “Waters Xevo”.</li>
     </ul>
     <p>
-        <img src="image-3.png" />
+        <img src="s-3.png" />
     </p>
     <p>
         Later you will perform a collision energy optimization refinement on a Waters Xevo as part of method development and optimization, since the
@@ -172,7 +172,7 @@ <h1>Transition Settings</h1>
         <li>In the <b>Precursor adducts</b> and <b>Fragment adducts</b> fields, change the text to “[M-]”.</li>
     </ul>
     <p>
-        <img src="image-4.png" />
+        <img src="s-4.png" />
     </p>
     <p>
         This experiment measures only negatively charged transitions, as you have just indicated in the transition settings. Skyline adduct
@@ -218,7 +218,7 @@ <h1>Exporting an Unscheduled Method</h1>
         The <b>Export Method</b> form should now look like this:
     </p>
     <p>
-        <img src="image-5.png" />
+        <img src="s-5.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -241,7 +241,7 @@ <h1>Exporting an Unscheduled Transition List</h1>
         The <b>Export Method</b> form should now look like this:
     </p>
     <p>
-        <img src="image-6.png" />
+        <img src="s-6.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -273,7 +273,7 @@ <h1>Importing Mass Spectrometer Runs</h1>
         The <b>Import Results Files</b> form should look like this:
     </p>
     <p>
-        <img src="image-7.png" />
+        <img src="s-7.png" />
     </p>
     <ul>
         <li>Click the <b>Open</b> button.</li>
@@ -282,7 +282,7 @@ <h1>Importing Mass Spectrometer Runs</h1>
         Skyline will notice that these file names share a common prefix and suffix and present the following form:
     </p>
     <p>
-        <img src="image-8.png" />
+        <img src="s-8.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button to accept the shortened replicate names “1” and “2”.</li>
@@ -291,7 +291,7 @@ <h1>Importing Mass Spectrometer Runs</h1>
         The files should import relatively quickly, leaving your Skyline main window looking something like this:
     </p>
     <p>
-        <img src="image-9.png" /> 
+        <img src="s-9.png" /> 
     </p>
     <p>
         The replicate names “1” and “2” are not very meaningful, but you can change them to something more descriptive by doing the following:
@@ -302,7 +302,7 @@ <h1>Importing Mass Spectrometer Runs</h1>
         <li>In the <b>Name</b> field of the <b>Rename Replicate</b> form, enter “2 min”.</li>
     </ul>
     <p>
-        <img src="image-10.png" />
+        <img src="s-10.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -313,7 +313,7 @@ <h1>Importing Mass Spectrometer Runs</h1>
         This should leave the main Skyline window looking like this:
     </p>
     <p>
-        <img src="image-11.png" />
+        <img src="s-11.png" />
     </p>
     <p>
         To take advantage of the Skyline summary graphs for viewing statistics for multiple replicates on a single screen, do the following:
@@ -329,7 +329,7 @@ <h1>Importing Mass Spectrometer Runs</h1>
         The Skyline window should now look something like this:
     </p>
     <p>
-        <img src="image-12.png" />
+        <img src="s-12.png" />
     </p>
     <h1>Comparing Peak Areas and Resolution</h1>
     <p>
@@ -351,7 +351,7 @@ <h1>Comparing Peak Areas and Resolution</h1>
         peak separation. This is not surprising, and combined with improved signal intensity it justifies the choice of the longer gradient.
     </p>
     <p>
-        <img src="image-13.png" />
+        <img src="s-13.png" />
     </p>
     <h1>Producing a Scheduled Method</h1>
     <p>
@@ -372,7 +372,7 @@ <h1>Producing a Scheduled Method</h1>
         The <b>Molecule Settings</b> form should now look like this:
     </p>
     <p>
-        <img src="image-14.png" />
+        <img src="s-14.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -389,7 +389,7 @@ <h1>Producing a Scheduled Method</h1>
         Which should leave the <b>Export Transition List</b> form looking like this:
     </p>
     <p>
-        <img src="image-15.png" />
+        <img src="s-15.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -405,7 +405,7 @@ <h1>Producing a Scheduled Method</h1>
         The <b>Scheduling Data</b> form should look like this:
     </p>
     <p>
-        <img src="image-16.png" />
+        <img src="s-16.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -434,7 +434,7 @@ <h1>Collecting and Importing Scheduled Runs</h1>
         Skyline will use for the replicate names, as shown below:
     </p>
     <p>
-        <img src="image-17.png" />
+        <img src="s-17.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -447,7 +447,7 @@ <h1>Collecting and Importing Scheduled Runs</h1>
         <li>Select the “2 min” replicate.</li>
     </ul>
     <p>
-        <img src="image-18.png" />
+        <img src="s-18.png" />
     </p>
     <ul>
         <li>Click the <b>Remove</b> button.</li>
@@ -474,7 +474,7 @@ <h1>Collecting and Importing Scheduled Runs</h1>
         When you are done, the <b>Manage Results</b> form should look like this:
     </p>
     <p>
-        <img src="image-19.png" />
+        <img src="s-19.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -495,7 +495,7 @@ <h1>Evaluating Imported Runs</h1>
         especially consistent among the scheduled runs.
     </p>
     <p>
-        <img src="image-20.png" />
+        <img src="s-20.png" />
     </p>
     <h1>Evaluating Linearity in Response</h1>
     <p>
@@ -513,7 +513,7 @@ <h1>Evaluating Linearity in Response</h1>
         When you are don the <b>Document Grid</b> should look like this:
     </p>
     <p>
-        <img src="image-21.png" />
+        <img src="s-21.png" />
     </p>
     <p>
         You also need to specify some quantification settings before inspecting a calibration curve for these runs by doing the following:
@@ -529,7 +529,7 @@ <h1>Evaluating Linearity in Response</h1>
         The <b>Molecule Settings</b> form should now look like this:
     </p>
     <p>
-        <img src="image-22.png" />
+        <img src="s-22.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -545,7 +545,7 @@ <h1>Evaluating Linearity in Response</h1>
         You should see a graph like this:
     </p>
     <p>
-        <img src="image-23.png" />
+        <img src="s-23.png" />
     </p>
     <p>
         The three dilution ratios evaluated here clearly are not as linear as one might hope. Therefore, you should expect some additional work to be
@@ -578,7 +578,7 @@ <h1>Collision Energy Optimization</h1>
         <li>In the <b>Step count</b> field, enter “5” (which should already be set).</li>
     </ul>
     <p>
-        <img src="image-24.png" />
+        <img src="s-24.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -601,7 +601,7 @@ <h1>Collision Energy Optimization</h1>
         The <b>Transition Settings</b> form should now look like this:
     </p>
     <p>
-        <img src="image-25.png" />
+        <img src="s-25.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -630,7 +630,7 @@ <h1>Collision Energy Optimization</h1>
         The <b>Export Transition List</b> form should now look like this:
     </p>
     <p>
-        <img src="image-26.png" />
+        <img src="s-26.png" />
     </p>
     <p>
         Note that the <b>Max transitions per sample injection</b> field name changed to <b>Max concurrent transitions</b> when you
@@ -654,7 +654,7 @@ <h1>Collision Energy Optimization</h1>
         The <b>Scheduling Data</b> form should look like this:
     </p>
     <p>
-        <img src="image-27.png" />
+        <img src="s-27.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -697,7 +697,7 @@ <h1>Collision Energy Optimization</h1>
         The form should now look like this:
     </p>
     <p>
-        <img src="image-28.png" />
+        <img src="s-28.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -707,7 +707,7 @@ <h1>Collision Energy Optimization</h1>
         The <b>Import Results Files</b> form should look like this:
     </p>
     <p>
-        <img src="image-29.png" />
+        <img src="s-29.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -718,7 +718,7 @@ <h1>Collision Energy Optimization</h1>
         chromatogram plots, as shown below:
     </p>
     <p>
-        <img src="image-30.png" />
+        <img src="s-30.png" />
     </p>
     <p>
         But you still need to do the following to be able to visualize the 11 different measurements made at 11 different CE voltages for each
@@ -734,7 +734,7 @@ <h1>Collision Energy Optimization</h1>
         The main Skyline window should look like this:
     </p>
     <p>
-        <img src="image-31.png" />
+        <img src="s-31.png" />
     </p>
     <p>
         The <b>Peak Areas – Replicate Comparison</b> view now shows the heavy and light transitions in separate panes with the light above
@@ -750,7 +750,7 @@ <h1>Collision Energy Optimization</h1>
         Skyline should look like this:
     </p>
     <p>
-        <img src="image-32.png" />
+        <img src="s-32.png" />
     </p>
     <p>
         Now you can explore the other molecules to see how close to optimal the original collision energies were. You can do the following to achieve
@@ -766,7 +766,7 @@ <h1>Collision Energy Optimization</h1>
         this molecule on the Waters Xevo TQ-S. The best CE value (Step -5, the blue bar on the far left) is the lowest CE value measured.
     </p>
     <p>
-        <img src="image-33.png" />
+        <img src="s-33.png" />
     </p>
     <p>
         Given the trend toward that end of the range, futher investigation may be warranted to arrive at a truly optimal CE for that compound. For that
@@ -791,7 +791,7 @@ <h1>Collision Energy Optimization</h1>
         The <b>Export Transition List</b> form should now look like this:
     </p>
     <p>
-        <img src="image-34.png" />
+        <img src="s-34.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -813,7 +813,7 @@ <h1>Collision Energy Optimization</h1>
         The <b>Scheduling Data</b> form should look like this:
     </p>
     <p>
-        <img src="image-35.png" />
+        <img src="s-35.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeMethodDevCEOpt/en/image-1.png b/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeMethodDevCEOpt/en/s-1.png
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rename from pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeMethodDevCEOpt/en/image-0.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeMethodDevCEOpt/en/s-published-transition-list.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeMethodDevCEOpt/ja/index.html b/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeMethodDevCEOpt/ja/index.html
index 1acb358e17..124202c737 100644
--- a/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeMethodDevCEOpt/ja/index.html
+++ b/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeMethodDevCEOpt/ja/index.html
@@ -93,7 +93,7 @@ <h1>低分子化合物のトランジションリストのインポート</h1>
         公開されているトランジションリストは以下の通りです。
     </p>
     <p>
-        <img src="image-0.png" />
+        <img src="s-published-transition-list.png" />
     </p>
     <p>
         各分子のライト（12C）およびヘビー（13C: 安定同位体標識）プリカーサーやフラグメントの<i>m/z</i>、電荷に関する情報がすべて記載されています。ここではネガティブモードのエントリのみを使って作業します。CE（Collison
@@ -115,7 +115,7 @@ <h1>低分子化合物のトランジションリストのインポート</h1>
         Skylineウィンドウは以下のようになります。
     </p>
     <p>
-        <img src="image-1.png" />
+        <img src="s-1.png" />
     </p>
     <table>
         <tr>
@@ -132,7 +132,7 @@ <h1>トランジション設定</h1>
         <li>[ <b>予測</b> ] タブの [ <b>衝突エネルギー</b> ] ドロップダウンリストで、「Waters Xevo」を選択します。</li>
     </ul>
     <p>
-        <img src="image-2.png" />
+        <img src="s-2.png" />
     </p>
     <p>
         衝突エネルギーの値はAgilentの装置由来ですすが、RawデータはWaters Xevoなので衝突エネルギー最適化をこのように実施します。
@@ -142,7 +142,7 @@ <h1>トランジション設定</h1>
         <li>ネガティブモードでの解析なので[ <b>プリカーサー付加イオン</b> ] および [ <b>フラグメント付加イオン</b> ] フィールドで「[M-]」に変更します。</li>
     </ul>
     <p>
-        <img src="image-3.png" />
+        <img src="s-3.png" />
     </p>
     <p>
         この実験ではトランジション設定で指定したように、負の電荷をもつトランジションのみのネガティブモードでの測定となります。Skylineでの付加物の説明は通常よく
@@ -187,7 +187,7 @@ <h1>Unscheduled（スケジュール化されていない）メソッドのエ
         [ <b>メソッドをエクスポート</b> ] は以下のようになります。
     </p>
     <p>
-        <img src="image-4.png" />
+        <img src="s-4.png" />
     </p>
     <ul>
         <li>[ <b>OK</b> ] ボタンをクリックします。</li>
@@ -208,7 +208,7 @@ <h1>Unscheduled（スケジュール化されていない）トランジショ
         [ <b>メソッドをエクスポート</b> ] フォームは以下のようになります。
     </p>
     <p>
-        <img src="image-5.png" />
+        <img src="s-5.png" />
     </p>
     <ul>
         <li>[ <b>OK</b> ] ボタンをクリックします。</li>
@@ -237,7 +237,7 @@ <h1>測定結果ファイルのインポート</h1>
         [ <b>結果ファイルをインポート</b> ] フォームは以下のようになります。
     </p>
     <p>
-        <img src="image-6.png" />
+        <img src="s-6.png" />
     </p>
     <ul>
         <li>[ <b>開く</b> ] ボタンをクリックします。</li>
@@ -246,7 +246,7 @@ <h1>測定結果ファイルのインポート</h1>
         これらのファイル名で共通のプリフィックス（ID33140_0）とサフィックス（a_WAA253_4814_092017）があるので以下のフォームが表示されます（ファイル名の短縮を提案されます）。
     </p>
     <p>
-        <img src="image-7.png" />
+        <img src="s-7.png" />
     </p>
     <ul>
         <li>[ <b>OK</b> ] ボタンをクリックして、短くなった繰り返し測定名「1」と「2」を承認します。</li>
@@ -255,7 +255,7 @@ <h1>測定結果ファイルのインポート</h1>
         当該ファイルは素早くインポートされ、Skylineメインウィンドウは以下のようになります。
     </p>
     <p>
-        <img src="image-8.png" /> 
+        <img src="s-8.png" /> 
     </p>
     <p>
         繰り返し測定名「1」と「2」はただの番号にすぎないため、以下のようにしてグラジエント情報を含む名前に変えることができます。
@@ -266,7 +266,7 @@ <h1>測定結果ファイルのインポート</h1>
         <li>[ <b>繰り返し測定の名前を変更</b> ] フォームの [ <b>名前</b> ] フィールドに、「2 min」と入力します。</li>
     </ul>
     <p>
-        <img src="image-9.png" />
+        <img src="s-9.png" />
     </p>
     <ul>
         <li>[ <b>OK</b> ] ボタンをクリックします。</li>
@@ -277,7 +277,7 @@ <h1>測定結果ファイルのインポート</h1>
         これでメインSkylineウィンドウは以下のようになります。
     </p>
     <p>
-        <img src="image-10.png" />
+        <img src="s-10.png" />
     </p>
     <p>
         概要グラフで複数の繰り返し測定の統計結果を1画面表示するには以下の操作を行います。
@@ -292,7 +292,7 @@ <h1>測定結果ファイルのインポート</h1>
         Skylineウィンドウは以下のようになり繰り返し測定間の比較が可能となります。
     </p>
     <p>
-        <img src="image-11.png" />
+        <img src="s-11.png" />
     </p>
     <h1>感度（ピーク面積）とクロマト分解能の比較</h1>
     <p>
@@ -312,7 +312,7 @@ <h1>感度（ピーク面積）とクロマト分解能の比較</h1>
         Skylineは下図のようになります。5分のグラジエントはピーク分離が良好でアナライト（代謝物）が重なっていないことが分かります。信号強度（ピーク面積値）の改善を考慮すればやはりより長いグラジエントでクロマト分離を良好にしておくことは理にかなっているということがわかります。
     </p>
     <p>
-        <img src="image-12.png" />
+        <img src="s-12.png" />
     </p>
     <h1>Scheduled（スケジュール化された）メソッドの作成</h1>
     <p>
@@ -331,7 +331,7 @@ <h1>Scheduled（スケジュール化された）メソッドの作成</h1>
         [ <b>分子設定</b> ] フォームは以下のようになります。
     </p>
     <p>
-        <img src="image-13.png" />
+        <img src="s-13.png" />
     </p>
     <ul>
         <li>[ <b>OK</b> ] ボタンをクリックします。</li>
@@ -348,7 +348,7 @@ <h1>Scheduled（スケジュール化された）メソッドの作成</h1>
          [ <b>トランジションリストをエクスポート</b> ] フォームは以下のようになります。
     </p>
     <p>
-        <img src="image-14.png" />
+        <img src="s-14.png" />
     </p>
     <ul>
         <li>[ <b>OK</b> ] ボタンをクリックします。</li>
@@ -364,7 +364,7 @@ <h1>Scheduled（スケジュール化された）メソッドの作成</h1>
         [ <b>スケジュールデータ</b> ] フォームは以下のようになります。
     </p>
     <p>
-        <img src="image-15.png" />
+        <img src="s-15.png" />
     </p>
     <ul>
         <li>[ <b>OK</b> ] ボタンをクリックします。</li>
@@ -390,7 +390,7 @@ <h1>Scheduled（スケジュールされた）測定のデータ収集とイン
         これにより [ <b>結果をインポート</b> ] フォームでは繰り返し測定名として使用するファイル名がフルファイル名（拡張子は除く）で表示されるようになります。
     </p>
     <p>
-        <img src="image-16.png" />
+        <img src="s-16.png" />
     </p>
     <ul>
         <li>[ <b>OK</b> ] ボタンをクリックします。</li>
@@ -403,7 +403,7 @@ <h1>Scheduled（スケジュールされた）測定のデータ収集とイン
         <li>「2 min」の繰り返し測定を選択します。</li>
     </ul>
     <p>
-        <img src="image-17.png" />
+        <img src="s-17.png" />
     </p>
     <ul>
         <li>[ <b>削除</b> ] ボタンをクリックします。</li>
@@ -428,7 +428,7 @@ <h1>Scheduled（スケジュールされた）測定のデータ収集とイン
         完了すると、[ <b>結果を管理</b> ] フォームは以下のようになります。
     </p>
     <p>
-        <img src="image-18.png" />
+        <img src="s-18.png" />
     </p>
     <ul>
         <li>[ <b>OK</b> ] ボタンをクリックします。</li>
@@ -448,7 +448,7 @@ <h1>インポートされた結果データのの解析</h1>
         ビューで、Acetyl-CoAは溶出時間が約1.55分で安定していることもわかります。これはスケジュール化メソッドでの測定間でも安定しています。
     </p>
     <p>
-        <img src="image-19.png" />
+        <img src="s-19.png" />
     </p>
     <h1>検量線の線形性評価</h1>
     <p>
@@ -464,7 +464,7 @@ <h1>検量線の線形性評価</h1>
         完了すると、[ <b>ドキュメントグリッド</b> ] は以下のようになります。
     </p>
     <p>
-        <img src="image-20.png" />
+        <img src="s-20.png" />
     </p>
     <p>
         検量線の線形性を調べる前に定量化設定を指定する必要があります。
@@ -480,7 +480,7 @@ <h1>検量線の線形性評価</h1>
         [ <b>分子設定</b> ] フォームは以下のようになります。
     </p>
     <p>
-        <img src="image-21.png" />
+        <img src="s-21.png" />
     </p>
     <ul>
         <li>[ <b>OK</b> ] ボタンをクリックします。</li>
@@ -496,7 +496,7 @@ <h1>検量線の線形性評価</h1>
         以下のようなグラフが表示されます。
     </p>
     <p>
-        <img src="image-22.png" />
+        <img src="s-22.png" />
     </p>
     <p>
         R-Squareの値から線形性は低いと評価されました。それゆえアナライトの濃度を変えて再度測定し線形性のある濃度範囲を探す必要があるということになります。
@@ -523,7 +523,7 @@ <h1>CE（衝突エネルギー）の最適化</h1>
         <li>[ <b>ステップ数</b> ] フィールドは「5」に設定されています（されていなければ5を入力）。</li>
     </ul>
     <p>
-        <img src="image-23.png" />
+        <img src="s-23.png" />
     </p>
     <ul>
         <li>[ <b>OK</b> ] ボタンをクリックします。</li>
@@ -542,7 +542,7 @@ <h1>CE（衝突エネルギー）の最適化</h1>
         [ <b>トランジション設定</b> ] フォームは以下のようになります。
     </p>
     <p>
-        <img src="image-24.png" />
+        <img src="s-24.png" />
     </p>
     <ul>
         <li>[ <b>OK</b> ] ボタンをクリックします。</li>
@@ -568,7 +568,7 @@ <h1>CE（衝突エネルギー）の最適化</h1>
         [ <b>トランジションリストをエクスポート</b> ] フォームは以下のようになります。
     </p>
     <p>
-        <img src="image-25.png" />
+        <img src="s-25.png" />
     </p>
     <p>
         このスケジュール化された取得を選択することで[ <b>試料インジェクションごとの最大トランジション数</b> ] フィールド名が[ <b>最大同時トランジション数</b> ]
@@ -589,7 +589,7 @@ <h1>CE（衝突エネルギー）の最適化</h1>
         [ <b>スケジュールデータ</b> ] フォームは以下のようになります。
     </p>
     <p>
-        <img src="image-26.png" />
+        <img src="s-26.png" />
     </p>
     <ul>
         <li>[ <b>OK</b> ] ボタンをクリックします。</li>
@@ -629,7 +629,7 @@ <h1>CE（衝突エネルギー）の最適化</h1>
         フォームは以下のようになります。
     </p>
     <p>
-        <img src="image-27.png" />
+        <img src="s-27.png" />
     </p>
     <ul>
         <li>[ <b>OK</b> ] ボタンをクリックします。</li>
@@ -639,7 +639,7 @@ <h1>CE（衝突エネルギー）の最適化</h1>
         [ <b>結果ファイルをインポート</b> ] フォームは以下のようになります。
     </p>
     <p>
-        <img src="image-28.png" />
+        <img src="s-28.png" />
     </p>
     <ul>
         <li>[ <b>OK</b> ] ボタンをクリックします。</li>
@@ -649,7 +649,7 @@ <h1>CE（衝突エネルギー）の最適化</h1>
         <b>繰り返し測定の比較</b> ] プロットの一番右端の値として、また以下のようにクロマトグラムプロットの一番右のタブとして表示されます。
     </p>
     <p>
-        <img src="image-29.png" />
+        <img src="s-29.png" />
     </p>
     <p>
         ここで [ <b>ターゲット</b> ] ビューにて11個の異なるCE電圧で測定された11個の測定値を各トランジションについて表示できるようにするために以下の操作を行う必要がいます。
@@ -664,7 +664,7 @@ <h1>CE（衝突エネルギー）の最適化</h1>
         メインSkylineウィンドウは以下のようになります。
     </p>
     <p>
-        <img src="image-30.png" />
+        <img src="s-30.png" />
     </p>
     <p>
         [ <b>ピーク領域 – 繰り返し測定の比較</b> ] ビューには、ライトとヘビー（安定同位体ラベル）のトランジションがそれぞれライトが上段に、ヘビーが下段に表示されます。CE
@@ -678,7 +678,7 @@ <h1>CE（衝突エネルギー）の最適化</h1>
         Skylineウィンドウは以下のようになります。
     </p>
     <p>
-        <img src="image-31.png" />
+        <img src="s-31.png" />
     </p>
     <p>
         これで他の低分子化合物に対しても文献のCE値（衝突エネルギー）が最適かどうかを調べられます。これには、以下の操作が行えます。
@@ -691,7 +691,7 @@ <h1>CE（衝突エネルギー）の最適化</h1>
         Pentose-Pの場合は文献のCE値はWaters Xevo TQ-S上では最適でなく、最適CE値（Step-5、一番左の青い棒）は測定されたCE値の中で最小のものとなります。
     </p>
     <p>
-        <img src="image-32.png" />
+        <img src="s-32.png" />
     </p>
     <p>
         このPentoseの場合は最小のCE値なのでさらにCE値を下げて最適値を調べてもよいでしょう。こういう場合はもっと広いステップサイズ（3ボルトなど）で行うのもよいでしょう。いずれにしても、「Step
@@ -715,7 +715,7 @@ <h1>CE（衝突エネルギー）の最適化</h1>
         [ <b>トランジションリストをエクスポート</b> ] フォームは以下のようになります。
     </p>
     <p>
-        <img src="image-33.png" />
+        <img src="s-33.png" />
     </p>
     <ul>
         <li>[ <b>OK</b> ] ボタンをクリックします。</li>
@@ -734,7 +734,7 @@ <h1>CE（衝突エネルギー）の最適化</h1>
         [ <b>スケジュールデータ</b> ] フォームは以下のようになります。
     </p>
     <p>
-        <img src="image-34.png" />
+        <img src="s-34.png" />
     </p>
     <ul>
         <li>[ <b>OK</b> ] ボタンをクリックします。</li>
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeMethodDevCEOpt/ja/invariant.html b/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeMethodDevCEOpt/ja/invariant.html
index 9dd2fb8efb..31a7649988 100644
--- a/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeMethodDevCEOpt/ja/invariant.html
+++ b/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeMethodDevCEOpt/ja/invariant.html
@@ -105,7 +105,7 @@ <h1>Importing a Small Molecule Transition List into a Skyline Document</h1>
         This is the published transition list:
     </p>
     <p>
-        <img src="image-0.png" />
+        <img src="s-published-transition-list.png" />
     </p>
     <p>
         It provides information about light (12C) and heavy (13C) precursor and fragment <i>m/z</i> and charge for each molecule. For the purposes of
@@ -133,7 +133,7 @@ <h1>Importing a Small Molecule Transition List into a Skyline Document</h1>
         Your Skyline window should now look something like this:
     </p>
     <p>
-        <img src="image-1.png" />
+        <img src="s-1.png" />
     </p>
     <table>
         <tr>
@@ -153,7 +153,7 @@ <h1>Transition Settings</h1>
         <li>On the <b>Prediction</b> tab, in the <b>Collision energy</b> dropdown list, choose “Waters Xevo”.</li>
     </ul>
     <p>
-        <img src="image-2.png" />
+        <img src="s-2.png" />
     </p>
     <p>
         Later you will perform a collision energy optimization refinement on a Waters Xevo as part of method development and optimization, since the
@@ -164,7 +164,7 @@ <h1>Transition Settings</h1>
         <li>In the <b>Precursor adducts</b> and <b>Fragment adducts</b> fields, change the text to “[M-]”.</li>
     </ul>
     <p>
-        <img src="image-3.png" />
+        <img src="s-3.png" />
     </p>
     <p>
         This experiment measures only negatively charged transitions, as you have just indicated in the transition settings. 
@@ -213,7 +213,7 @@ <h1>Exporting an Unscheduled Method</h1>
         The <b>Export Method</b> form should now look like this:
     </p>
     <p>
-        <img src="image-4.png" />
+        <img src="s-4.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -236,7 +236,7 @@ <h1>Exporting an Unscheduled Transition List</h1>
         The <b>Export Method</b> form should now look like this:
     </p>
     <p>
-        <img src="image-5.png" />
+        <img src="s-5.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -268,7 +268,7 @@ <h1>Importing Mass Spectrometer Runs</h1>
         The <b>Import Results Files</b> form should look like this:
     </p>
     <p>
-        <img src="image-6.png" />
+        <img src="s-6.png" />
     </p>
     <ul>
         <li>Click the <b>Open</b> button.</li>
@@ -277,7 +277,7 @@ <h1>Importing Mass Spectrometer Runs</h1>
         Skyline will notice that these file names share a common prefix and suffix and present the following form:
     </p>
     <p>
-        <img src="image-7.png" />
+        <img src="s-7.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button to accept the shortened replicate names “1” and “2”.</li>
@@ -286,7 +286,7 @@ <h1>Importing Mass Spectrometer Runs</h1>
         The files should import relatively quickly, leaving your Skyline main window looking something like this:
     </p>
     <p>
-        <img src="image-8.png" /> 
+        <img src="s-8.png" /> 
     </p>
     <p>
         The replicate names “1” and “2” are not very meaningful, but you can change them to something more descriptive by doing the following:
@@ -297,7 +297,7 @@ <h1>Importing Mass Spectrometer Runs</h1>
         <li>In the <b>Name</b> field of the <b>Rename Replicate</b> form, enter “2 min”.</li>
     </ul>
     <p>
-        <img src="image-9.png" />
+        <img src="s-9.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -308,7 +308,7 @@ <h1>Importing Mass Spectrometer Runs</h1>
         This should leave the main Skyline window looking like this:
     </p>
     <p>
-        <img src="image-10.png" />
+        <img src="s-10.png" />
     </p>
     <p>
         To take advantage of the Skyline summary graphs for viewing statistics for multiple replicates on a single screen, do the following:
@@ -324,7 +324,7 @@ <h1>Importing Mass Spectrometer Runs</h1>
         The Skyline window should now look something like this:
     </p>
     <p>
-        <img src="image-11.png" />
+        <img src="s-11.png" />
     </p>
     <h1>Comparing Peak Areas and Resolution</h1>
     <p>
@@ -346,7 +346,7 @@ <h1>Comparing Peak Areas and Resolution</h1>
         peak separation. This is not surprising, and combined with improved signal intensity it justifies the choice of the longer gradient.
     </p>
     <p>
-        <img src="image-12.png" />
+        <img src="s-12.png" />
     </p>
     <h1>Producing a Scheduled Method</h1>
     <p>
@@ -367,7 +367,7 @@ <h1>Producing a Scheduled Method</h1>
         The <b>Molecule Settings</b> form should now look like this:
     </p>
     <p>
-        <img src="image-13.png" />
+        <img src="s-13.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -384,7 +384,7 @@ <h1>Producing a Scheduled Method</h1>
         Which should leave the <b>Export Transition List</b> form looking like this:
     </p>
     <p>
-        <img src="image-14.png" />
+        <img src="s-14.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -400,7 +400,7 @@ <h1>Producing a Scheduled Method</h1>
         The <b>Scheduling Data</b> form should look like this:
     </p>
     <p>
-        <img src="image-15.png" />
+        <img src="s-15.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -429,7 +429,7 @@ <h1>Collecting and Importing Scheduled Runs</h1>
         Skyline will use for the replicate names, as shown below:
     </p>
     <p>
-        <img src="image-16.png" />
+        <img src="s-16.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -442,7 +442,7 @@ <h1>Collecting and Importing Scheduled Runs</h1>
         <li>Select the “2 min” replicate.</li>
     </ul>
     <p>
-        <img src="image-17.png" />
+        <img src="s-17.png" />
     </p>
     <ul>
         <li>Click the <b>Remove</b> button.</li>
@@ -469,7 +469,7 @@ <h1>Collecting and Importing Scheduled Runs</h1>
         When you are done, the <b>Manage Results</b> form should look like this:
     </p>
     <p>
-        <img src="image-18.png" />
+        <img src="s-18.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -490,7 +490,7 @@ <h1>Evaluating Imported Runs</h1>
         especially consistent among the scheduled runs.
     </p>
     <p>
-        <img src="image-19.png" />
+        <img src="s-19.png" />
     </p>
     <h1>Evaluating Linearity in Response</h1>
     <p>
@@ -508,7 +508,7 @@ <h1>Evaluating Linearity in Response</h1>
         When you are don the <b>Document Grid</b> should look like this:
     </p>
     <p>
-        <img src="image-20.png" />
+        <img src="s-20.png" />
     </p>
     <p>
         You also need to specify some quantification settings before inspecting a calibration curve for these runs by doing the following:
@@ -524,7 +524,7 @@ <h1>Evaluating Linearity in Response</h1>
         The <b>Molecule Settings</b> form should now look like this:
     </p>
     <p>
-        <img src="image-21.png" />
+        <img src="s-21.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -540,7 +540,7 @@ <h1>Evaluating Linearity in Response</h1>
         You should see a graph like this:
     </p>
     <p>
-        <img src="image-22.png" />
+        <img src="s-22.png" />
     </p>
     <p>
         The three dilution ratios evaluated here clearly are not as linear as one might hope. Therefore, you should expect some additional work to be
@@ -573,7 +573,7 @@ <h1>Collision Energy Optimization</h1>
         <li>In the <b>Step count</b> field, enter “5” (which should already be set).</li>
     </ul>
     <p>
-        <img src="image-23.png" />
+        <img src="s-23.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -596,7 +596,7 @@ <h1>Collision Energy Optimization</h1>
         The <b>Transition Settings</b> form should now look like this:
     </p>
     <p>
-        <img src="image-24.png" />
+        <img src="s-24.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -625,7 +625,7 @@ <h1>Collision Energy Optimization</h1>
         The <b>Export Transition List</b> form should now look like this:
     </p>
     <p>
-        <img src="image-25.png" />
+        <img src="s-25.png" />
     </p>
     <p>
         Note that the <b>Max transitions per sample injection</b> field name changed to <b>Max concurrent transitions</b> when you
@@ -649,7 +649,7 @@ <h1>Collision Energy Optimization</h1>
         The <b>Scheduling Data</b> form should look like this:
     </p>
     <p>
-        <img src="image-26.png" />
+        <img src="s-26.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -691,7 +691,7 @@ <h1>Collision Energy Optimization</h1>
         The form should now look like this:
     </p>
     <p>
-        <img src="image-27.png" />
+        <img src="s-27.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -701,7 +701,7 @@ <h1>Collision Energy Optimization</h1>
         The <b>Import Results Files</b> form should look like this:
     </p>
     <p>
-        <img src="image-28.png" />
+        <img src="s-28.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -712,7 +712,7 @@ <h1>Collision Energy Optimization</h1>
         chromatogram plots, as shown below:
     </p>
     <p>
-        <img src="image-29.png" />
+        <img src="s-29.png" />
     </p>
     <p>
         But you still need to do the following to be able to visualize the 11 different measurements made at 11 different CE voltages for each
@@ -728,7 +728,7 @@ <h1>Collision Energy Optimization</h1>
         The main Skyline window should look like this:
     </p>
     <p>
-        <img src="image-30.png" />
+        <img src="s-30.png" />
     </p>
     <p>
         The <b>Peak Areas – Replicate Comparison</b> view now shows the heavy and light transitions in separate panes with the light above
@@ -744,7 +744,7 @@ <h1>Collision Energy Optimization</h1>
         Skyline should look like this:
     </p>
     <p>
-        <img src="image-31.png" />
+        <img src="s-31.png" />
     </p>
     <p>
         Now you can explore the other molecules to see how close to optimal the original collision energies were. You can do the following to achieve
@@ -760,7 +760,7 @@ <h1>Collision Energy Optimization</h1>
         this molecule on the Waters Xevo TQ-S. The best CE value (Step -5, the blue bar on the far left) is the lowest CE value measured.
     </p>
     <p>
-        <img src="image-32.png" />
+        <img src="s-32.png" />
     </p>
     <p>
         Given the trend toward that end of the range, futher investigation may be warranted to arrive at a truly optimal CE for that compound. For that
@@ -785,7 +785,7 @@ <h1>Collision Energy Optimization</h1>
         The <b>Export Transition List</b> form should now look like this:
     </p>
     <p>
-        <img src="image-33.png" />
+        <img src="s-33.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -807,7 +807,7 @@ <h1>Collision Energy Optimization</h1>
         The <b>Scheduling Data</b> form should look like this:
     </p>
     <p>
-        <img src="image-34.png" />
+        <img src="s-34.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeMethodDevCEOpt/zh-CHS/index.html b/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeMethodDevCEOpt/zh-CHS/index.html
index 97d4568d72..5d2fed02a9 100644
--- a/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeMethodDevCEOpt/zh-CHS/index.html
+++ b/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeMethodDevCEOpt/zh-CHS/index.html
@@ -92,7 +92,7 @@ <h1>将小分子离子对列表导入 Skyline 文档 </h1>
         以下就是发布的离子对列表：
     </p>
     <p>
-        <img src="image-0.png" />
+        <img src="s-published-transition-list.png" />
     </p>
     <p>
         它提供了有关轻母离子 (12C)、重母离子 (13C)、碎片离子<i>质荷比</i>以及每个分子电荷的信息，本教程中仅使用负离子模式的条目。碰撞能量 (CE) 值来自 Agilent 6495 三重四极杆质谱仪。与过去收集所使用数据文件的操作一样，即便您要为 Waters Xevo
@@ -115,7 +115,7 @@ <h1>将小分子离子对列表导入 Skyline 文档 </h1>
         此时 Skyline 窗口将显示如下：
     </p>
     <p>
-        <img src="image-1.png" />
+        <img src="s-1.png" />
     </p>
     <table>
         <tr>
@@ -132,7 +132,7 @@ <h1>离子对设置</h1>
         <li>在<b>预测</b>选项卡上的<b>碰撞能量</b>下拉列表中，选择“Waters Xevo”。</li>
     </ul>
     <p>
-        <img src="image-2.png" />
+        <img src="s-2.png" />
     </p>
     <p>
         稍后，您将在 Waters Xevo 中进行碰撞能量优化，这是方法制定和优化过程的一部分，因为从文中粘贴的起始碰撞能量最初是用于 Agilent 仪器。 
@@ -142,7 +142,7 @@ <h1>离子对设置</h1>
         <li>在<b>母离子加合物</b>和<b>碎片加合物</b>字段中，将文本更改为“[M-]”。</li>
     </ul>
     <p>
-        <img src="image-3.png" /> 
+        <img src="s-3.png" /> 
     </p>
     <p>
         您在离子对设置中已指出，此实验仅测量负电荷离子对。Skyline支持对任何类型的加合物的电离描述（“[M-H]”、“[M+Na]”等），其中包括未知的电离模式（此处使用的“[M-]”表示“负离子模式，电荷
@@ -183,7 +183,7 @@ <h1>导出未安排时序的方法</h1>
         <b>导出方法</b>表单现在应显示如下：
     </p>
     <p>
-        <img src="image-4.png" />
+        <img src="s-4.png" />
     </p>
     <ul>
         <li>单击<b>确定</b>按钮。</li>
@@ -203,7 +203,7 @@ <h1>导出未安排时序的离子对列表</h1>
         <b>导出方法</b>表单现在应显示如下：
     </p>
     <p>
-        <img src="image-5.png" />
+        <img src="s-5.png" />
     </p>
     <ul>
         <li>单击<b>确定</b>按钮。</li>
@@ -230,7 +230,7 @@ <h1>导入质谱仪运行</h1>
         <b>导入结果文件</b>表单应显示如下：
     </p>
     <p>
-        <img src="image-6.png" />
+        <img src="s-6.png" />
     </p>
     <ul>
         <li>单击<b>打开</b>按钮。</li>
@@ -239,7 +239,7 @@ <h1>导入质谱仪运行</h1>
         Skyline 会注意到这些文件名含有共同的前缀和后缀，并显示以下表单：
     </p>
     <p>
-        <img src="image-7.png" />
+        <img src="s-7.png" />
     </p>
     <ul>
         <li>单击<b>确定</b>按钮，以接受缩短后的重复测定名称“1”和“2”。</li>
@@ -248,7 +248,7 @@ <h1>导入质谱仪运行</h1>
         这些文件会相对快速地导入，您的 Skyline 主窗口将显示如下：
     </p>
     <p>
-        <img src="image-8.png" /> 
+        <img src="s-8.png" /> 
     </p>
     <p>
         重复测定名称“1”和“2”不是很有意义，但是您可以执行以下操作，将它们更改为更具描述性的名称：
@@ -259,7 +259,7 @@ <h1>导入质谱仪运行</h1>
         <li>在<b>重命名重复测定</b>表单的<b>名称</b>字段中，输入“2 min”。</li>
     </ul>
     <p>
-        <img src="image-9.png" />
+        <img src="s-9.png" />
     </p>
     <ul>
         <li>单击<b>确定</b>按钮。</li>
@@ -270,7 +270,7 @@ <h1>导入质谱仪运行</h1>
         执行该操作后，Skyline 主窗口应显示如下：
     </p>
     <p>
-        <img src="image-10.png" />
+        <img src="s-10.png" />
     </p>
     <p>
         要利用 Skyline 摘要图在一个屏幕上查看多个重复测定的统计信息，请执行以下操作：
@@ -285,7 +285,7 @@ <h1>导入质谱仪运行</h1>
         Skyline 窗口将显示如下：
     </p>
     <p>
-        <img src="image-11.png" />
+        <img src="s-11.png" />
     </p>
     <h1>比较峰面积和分辨率</h1>
     <p>
@@ -300,7 +300,7 @@ <h1>比较峰面积和分辨率</h1>
         <li>在任一色谱图中单击并拖动，将显示时间缩放至0.8到1.8分钟的范围内。Skyline将如下图显示，从中可以看到使用 5 分钟梯度时得到的峰分离更出色。这一点不足为奇，再加上信号强度得到改善，这就证明了选择更长梯度时间的合理性。</li>
     </ul>
     <p>
-        <img src="image-12.png" />
+        <img src="s-12.png" />
     </p>
     <h1>生成已安排时序的方法</h1>
     <p>
@@ -319,7 +319,7 @@ <h1>生成已安排时序的方法</h1>
         <b>分子设置</b>表单现在应显示如下：
     </p>
     <p>
-        <img src="image-13.png" />
+        <img src="s-13.png" />
     </p>
     <ul>
         <li>单击<b>确定</b>按钮。</li>
@@ -336,7 +336,7 @@ <h1>生成已安排时序的方法</h1>
         执行此操作后，<b>导出离子对列表</b>表单应显示如下：
     </p>
     <p>
-        <img src="image-14.png" />
+        <img src="s-14.png" />
     </p>
     <ul>
         <li>单击<b>确定</b>按钮。</li>
@@ -352,7 +352,7 @@ <h1>生成已安排时序的方法</h1>
         <b>时序安排数据</b>表单应显示如下：
     </p>
     <p>
-        <img src="image-15.png" />
+        <img src="s-15.png" />
     </p>
     <ul>
         <li>单击<b>确定</b>按钮。</li>
@@ -378,7 +378,7 @@ <h1>收集和导入已安排时序的运行</h1>
         这样一来，<b>导入结果</b>表单将显示完整的文件名（已去除扩展名），与 Skyline 将使用的文件名保持一致，如下所示：
     </p>
     <p>
-        <img src="image-16.png" />
+        <img src="s-16.png" />
     </p>
     <ul>
         <li>单击<b>确定</b>按钮。</li>
@@ -391,7 +391,7 @@ <h1>收集和导入已安排时序的运行</h1>
         <li>选择“2 min”重复测定。</li>
     </ul>
     <p>
-        <img src="image-17.png" />
+        <img src="s-17.png" />
     </p>
     <ul>
         <li>单击<b>删除</b>按钮。</li>
@@ -415,7 +415,7 @@ <h1>收集和导入已安排时序的运行</h1>
         完成后，<b>管理结果</b>表单应显示如下：
     </p>
     <p>
-        <img src="image-18.png" />
+        <img src="s-18.png" />
     </p>
     <ul>
         <li>单击<b>确定</b>按钮。</li>
@@ -430,7 +430,7 @@ <h1>评估导入的运行</h1>
         <li>单击“Acetyl-Coa”及其两个子项（808 和 831）左侧的加号 (+)，将其展开，并查看下面的各个轻重离子对。</li>
     </ul>
     <p>
-        可以看到，这些峰面积的预期比率与已知的混合物比率相符。在<b>保留时间 - 重复测定比较</b>视图中，还可以看到每次运行中，Acetyl-CoA的洗脱稳定在1.55分钟左右，这在已安排时序的运行中尤其稳定。<img src="image-19.png" />
+        可以看到，这些峰面积的预期比率与已知的混合物比率相符。在<b>保留时间 - 重复测定比较</b>视图中，还可以看到每次运行中，Acetyl-CoA的洗脱稳定在1.55分钟左右，这在已安排时序的运行中尤其稳定。<img src="s-19.png" />
     </p>
     <h1>评估响应中的线性度</h1>
     <p>
@@ -446,7 +446,7 @@ <h1>评估响应中的线性度</h1>
         完成上述操作后，<b>文档网格</b>应显示如下：
     </p>
     <p>
-        <img src="image-20.png" />
+        <img src="s-20.png" />
     </p>
     <p>
         在检查这些运行的标准曲线之前，需执行以下操作来指定一些定量设置：
@@ -462,7 +462,7 @@ <h1>评估响应中的线性度</h1>
         <b>分子设置</b>表单现在应显示如下：
     </p>
     <p>
-        <img src="image-21.png" />
+        <img src="s-21.png" />
     </p>
     <ul>
         <li>单击<b>确定</b>按钮。</li>
@@ -478,7 +478,7 @@ <h1>评估响应中的线性度</h1>
         您应当看到如下所示的图：
     </p>
     <p>
-        <img src="image-22.png" />
+        <img src="s-22.png" />
     </p>
     <p>
         此处评估的三种稀释比率显然并非呈现出预想的线性。因此，需要额外执行一些工作，才能获得这项特定检测的线性动态范围信息。 
@@ -505,7 +505,7 @@ <h1>碰撞能量优化</h1>
         <li>在<b>步数</b>字段中输入“5”（应已进行此设置）<b>。</b></li>
     </ul>
     <p>
-        <img src="image-23.png" />
+        <img src="s-23.png" />
     </p>
     <ul>
         <li>单击<b>确定</b>按钮。</li>
@@ -525,7 +525,7 @@ <h1>碰撞能量优化</h1>
         <b>离子对设置</b>表单现在应显示如下：
     </p>
     <p>
-        <img src="image-24.png" />
+        <img src="s-24.png" />
     </p>
     <ul>
         <li>单击<b>确定</b>按钮。</li>
@@ -551,7 +551,7 @@ <h1>碰撞能量优化</h1>
         <b>导出离子对列表</b>表单现在应当显示如下：
     </p>
     <p>
-        <img src="image-25.png" />
+        <img src="s-25.png" />
     </p>
     <p>
         请注意，当您选择进行这种已安排时序的采集时，<b>每次进样的最大离子对数量</b>字段名称已变为<b>最大并行离子对</b>。考虑一下怎样的时序安排，可避免在每个周期运行中测量的所有离子对。 Skyline
@@ -572,7 +572,7 @@ <h1>碰撞能量优化</h1>
         <b>时序安排数据</b>表单应显示如下：
     </p>
     <p>
-        <img src="image-26.png" />
+        <img src="s-26.png" />
     </p>
     <ul>
         <li>单击<b>确定</b>按钮。</li>
@@ -611,7 +611,7 @@ <h1>碰撞能量优化</h1>
         该表单现在应显示如下：
     </p>
     <p>
-        <img src="image-27.png" />
+        <img src="s-27.png" />
     </p>
     <ul>
         <li>单击<b>确定</b>按钮。</li>
@@ -621,7 +621,7 @@ <h1>碰撞能量优化</h1>
         <b>导入结果文件</b>表单应显示如下：
     </p>
     <p>
-        <img src="image-28.png" />
+        <img src="s-28.png" />
     </p>
     <ul>
         <li>单击<b>确定</b>按钮。</li>
@@ -631,7 +631,7 @@ <h1>碰撞能量优化</h1>
         Optimization”的重复测定进行加载，如<b>重复测定比较</b>图中最右侧的值以及色谱图中最右侧选项卡中所示，该重复测定应出现在<b>目标</b>视图的<b>重复测定</b>下拉列表中，如下所示：
     </p>
     <p>
-        <img src="image-29.png" />
+        <img src="s-29.png" />
     </p>
     <p>
         但是，您仍需执行以下操作，才能在<b>目标</b>视图中直观显示于 11 种不同 CE 电压下对每个离子对进行的 11 次不同测量：
@@ -646,7 +646,7 @@ <h1>碰撞能量优化</h1>
         Skyline 主窗口应显示如下：
     </p>
     <p>
-        <img src="image-30.png" />
+        <img src="s-30.png" />
     </p>
     <p>
         <b>峰面积 - 重复测定比较</b>视图现在在单独的窗格中显示重离子对和轻离子对，并且轻离子对在重离子对上方。在“CE Optimization”重复测定中，各个条形表示逐步提高碰撞能量的效果。红色表示原始 CE 值（在与 Agilent 6495
@@ -659,7 +659,7 @@ <h1>碰撞能量优化</h1>
         Skyline 应显示如下：
     </p>
     <p>
-        <img src="image-31.png" />
+        <img src="s-31.png" />
     </p>
     <p>
         现在您可以探索其他分子，了解原始碰撞能量接近最佳状态的程度。为此，请执行以下操作：
@@ -672,7 +672,7 @@ <h1>碰撞能量优化</h1>
         查看 Pentose-P 的各种 CE 步长值的色谱图，很显然，资料中的 CE 值对于 Waters Xevo TQ-S 上测定的该分子并非最佳值。最佳 CE 值（步长为 -5，最左侧的蓝色条形）是测定的最低 CE 值。
     </p>
     <p>
-        <img src="image-32.png" />
+        <img src="s-32.png" />
     </p>
     <p>
         考虑到该范围末尾的趋势，可能需要进一步研究才能得出该化合物真正最佳的 CE 值。因此，在像这样的仪器供应商之间进行转换时，也可能需要从较大的步长（例如 3 伏）开始。即便如此，“步长 -5”（蓝色条形）CE 值相较于初始（红色条形）CE 值有了明显改善。
@@ -695,7 +695,7 @@ <h1>碰撞能量优化</h1>
         <b>导出离子对列表</b>表单现在应当显示如下：
     </p>
     <p>
-        <img src="image-33.png" />
+        <img src="s-33.png" />
     </p>
     <ul>
         <li>单击<b>确定</b>按钮。</li>
@@ -714,7 +714,7 @@ <h1>碰撞能量优化</h1>
         <b>时序安排数据</b>表单应显示如下：
     </p>
     <p>
-        <img src="image-34.png" />
+        <img src="s-34.png" />
     </p>
     <ul>
         <li>单击<b>确定</b>按钮。</li>
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeMethodDevCEOpt/zh-CHS/invariant.html b/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeMethodDevCEOpt/zh-CHS/invariant.html
index 664d3b940e..9cc323a182 100644
--- a/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeMethodDevCEOpt/zh-CHS/invariant.html
+++ b/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeMethodDevCEOpt/zh-CHS/invariant.html
@@ -105,7 +105,7 @@ <h1>Importing a Small Molecule Transition List into a Skyline Document</h1>
         This is the published transition list:
     </p>
     <p>
-        <img src="image-0.png" />
+        <img src="s-published-transition-list.png" />
     </p>
     <p>
         It provides information about light (12C) and heavy (13C) precursor and fragment <i>m/z</i> and charge for each molecule. For the purposes of
@@ -133,7 +133,7 @@ <h1>Importing a Small Molecule Transition List into a Skyline Document</h1>
         Your Skyline window should now look something like this:
     </p>
     <p>
-        <img src="image-1.png" />
+        <img src="s-1.png" />
     </p>
     <table>
         <tr>
@@ -153,7 +153,7 @@ <h1>Transition Settings</h1>
         <li>On the <b>Prediction</b> tab, in the <b>Collision energy</b> dropdown list, choose “Waters Xevo”.</li>
     </ul>
     <p>
-        <img src="image-2.png" />
+        <img src="s-2.png" />
     </p>
     <p>
         Later you will perform a collision energy optimization refinement on a Waters Xevo as part of method development and optimization, since the
@@ -164,7 +164,7 @@ <h1>Transition Settings</h1>
         <li>In the <b>Precursor adducts</b> and <b>Fragment adducts</b> fields, change the text to “[M-]”.</li>
     </ul>
     <p>
-        <img src="image-3.png" />
+        <img src="s-3.png" />
     </p>
     <p>
         This experiment measures only negatively charged transitions, as you have just indicated in the transition settings. Skyline adduct
@@ -210,7 +210,7 @@ <h1>Exporting an Unscheduled Method</h1>
         The <b>Export Method</b> form should now look like this:
     </p>
     <p>
-        <img src="image-4.png" />
+        <img src="s-4.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -233,7 +233,7 @@ <h1>Exporting an Unscheduled Transition List</h1>
         The <b>Export Method</b> form should now look like this:
     </p>
     <p>
-        <img src="image-5.png" />
+        <img src="s-5.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -265,7 +265,7 @@ <h1>Importing Mass Spectrometer Runs</h1>
         The <b>Import Results Files</b> form should look like this:
     </p>
     <p>
-        <img src="image-6.png" />
+        <img src="s-6.png" />
     </p>
     <ul>
         <li>Click the <b>Open</b> button.</li>
@@ -274,7 +274,7 @@ <h1>Importing Mass Spectrometer Runs</h1>
         Skyline will notice that these file names share a common prefix and suffix and present the following form:
     </p>
     <p>
-        <img src="image-7.png" />
+        <img src="s-7.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button to accept the shortened replicate names “1” and “2”.</li>
@@ -283,7 +283,7 @@ <h1>Importing Mass Spectrometer Runs</h1>
         The files should import relatively quickly, leaving your Skyline main window looking something like this:
     </p>
     <p>
-        <img src="image-8.png" /> 
+        <img src="s-8.png" /> 
     </p>
     <p>
         The replicate names “1” and “2” are not very meaningful, but you can change them to something more descriptive by doing the following:
@@ -294,7 +294,7 @@ <h1>Importing Mass Spectrometer Runs</h1>
         <li>In the <b>Name</b> field of the <b>Rename Replicate</b> form, enter “2 min”.</li>
     </ul>
     <p>
-        <img src="image-9.png" />
+        <img src="s-9.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -305,7 +305,7 @@ <h1>Importing Mass Spectrometer Runs</h1>
         This should leave the main Skyline window looking like this:
     </p>
     <p>
-        <img src="image-10.png" />
+        <img src="s-10.png" />
     </p>
     <p>
         To take advantage of the Skyline summary graphs for viewing statistics for multiple replicates on a single screen, do the following:
@@ -321,7 +321,7 @@ <h1>Importing Mass Spectrometer Runs</h1>
         The Skyline window should now look something like this:
     </p>
     <p>
-        <img src="image-11.png" />
+        <img src="s-11.png" />
     </p>
     <h1>Comparing Peak Areas and Resolution</h1>
     <p>
@@ -343,7 +343,7 @@ <h1>Comparing Peak Areas and Resolution</h1>
         peak separation. This is not surprising, and combined with improved signal intensity it justifies the choice of the longer gradient.
     </p>-->
     <p>
-        <img src="image-12.png" />
+        <img src="s-12.png" />
     </p>
     <h1>Producing a Scheduled Method</h1>
     <p>
@@ -364,7 +364,7 @@ <h1>Producing a Scheduled Method</h1>
         The <b>Molecule Settings</b> form should now look like this:
     </p>
     <p>
-        <img src="image-13.png" />
+        <img src="s-13.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -381,7 +381,7 @@ <h1>Producing a Scheduled Method</h1>
         Which should leave the <b>Export Transition List</b> form looking like this:
     </p>
     <p>
-        <img src="image-14.png" />
+        <img src="s-14.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -397,7 +397,7 @@ <h1>Producing a Scheduled Method</h1>
         The <b>Scheduling Data</b> form should look like this:
     </p>
     <p>
-        <img src="image-15.png" />
+        <img src="s-15.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -426,7 +426,7 @@ <h1>Collecting and Importing Scheduled Runs</h1>
         Skyline will use for the replicate names, as shown below:
     </p>
     <p>
-        <img src="image-16.png" />
+        <img src="s-16.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -439,7 +439,7 @@ <h1>Collecting and Importing Scheduled Runs</h1>
         <li>Select the “2 min” replicate.</li>
     </ul>
     <p>
-        <img src="image-17.png" />
+        <img src="s-17.png" />
     </p>
     <ul>
         <li>Click the <b>Remove</b> button.</li>
@@ -466,7 +466,7 @@ <h1>Collecting and Importing Scheduled Runs</h1>
         When you are done, the <b>Manage Results</b> form should look like this:
     </p>
     <p>
-        <img src="image-18.png" />
+        <img src="s-18.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -484,7 +484,7 @@ <h1>Evaluating Imported Runs</h1>
     <p>
         You can see that the peak areas have the expected ratios based on the known mixture ratios. In the <b>Retention Times – Replicate
             Comparison</b> view you can also see that the chromatography is stable with Acetyl-CoA eluting at around 1.55 minutes in every run,
-        especially consistent among the scheduled runs.<img src="image-19.png" />
+        especially consistent among the scheduled runs.<img src="s-19.png" />
     </p>
     <h1>Evaluating Linearity in Response</h1>
     <p>
@@ -502,7 +502,7 @@ <h1>Evaluating Linearity in Response</h1>
         When you are don the <b>Document Grid</b> should look like this:
     </p>
     <p>
-        <img src="image-20.png" />
+        <img src="s-20.png" />
     </p>
     <p>
         You also need to specify some quantification settings before inspecting a calibration curve for these runs by doing the following:
@@ -518,7 +518,7 @@ <h1>Evaluating Linearity in Response</h1>
         The <b>Molecule Settings</b> form should now look like this:
     </p>
     <p>
-        <img src="image-21.png" />
+        <img src="s-21.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -534,7 +534,7 @@ <h1>Evaluating Linearity in Response</h1>
         You should see a graph like this:
     </p>
     <p>
-        <img src="image-22.png" />
+        <img src="s-22.png" />
     </p>
     <p>
         The three dilution ratios evaluated here clearly are not as linear as one might hope. Therefore, you should expect some additional work to be
@@ -567,7 +567,7 @@ <h1>Collision Energy Optimization</h1>
         <li>In the <b>Step count</b> field, enter “5” (which should already be set).</li>
     </ul>
     <p>
-        <img src="image-23.png" />
+        <img src="s-23.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -590,7 +590,7 @@ <h1>Collision Energy Optimization</h1>
         The <b>Transition Settings</b> form should now look like this:
     </p>
     <p>
-        <img src="image-24.png" />
+        <img src="s-24.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -619,7 +619,7 @@ <h1>Collision Energy Optimization</h1>
         The <b>Export Transition List</b> form should now look like this:
     </p>
     <p>
-        <img src="image-25.png" />
+        <img src="s-25.png" />
     </p>
     <p>
         Note that the <b>Max transitions per sample injection</b> field name changed to <b>Max concurrent transitions</b> when you
@@ -643,7 +643,7 @@ <h1>Collision Energy Optimization</h1>
         The <b>Scheduling Data</b> form should look like this:
     </p>
     <p>
-        <img src="image-26.png" />
+        <img src="s-26.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -685,7 +685,7 @@ <h1>Collision Energy Optimization</h1>
         The form should now look like this:
     </p>
     <p>
-        <img src="image-27.png" />
+        <img src="s-27.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -695,7 +695,7 @@ <h1>Collision Energy Optimization</h1>
         The <b>Import Results Files</b> form should look like this:
     </p>
     <p>
-        <img src="image-28.png" />
+        <img src="s-28.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -706,7 +706,7 @@ <h1>Collision Energy Optimization</h1>
         chromatogram plots, as shown below:
     </p>
     <p>
-        <img src="image-29.png" />
+        <img src="s-29.png" />
     </p>
     <p>
         But you still need to do the following to be able to visualize the 11 different measurements made at 11 different CE voltages for each
@@ -722,7 +722,7 @@ <h1>Collision Energy Optimization</h1>
         The main Skyline window should look like this:
     </p>
     <p>
-        <img src="image-30.png" />
+        <img src="s-30.png" />
     </p>
     <p>
         The <b>Peak Areas – Replicate Comparison</b> view now shows the heavy and light transitions in separate panes with the light above
@@ -738,7 +738,7 @@ <h1>Collision Energy Optimization</h1>
         Skyline should look like this:
     </p>
     <p>
-        <img src="image-31.png" />
+        <img src="s-31.png" />
     </p>
     <p>
         Now you can explore the other molecules to see how close to optimal the original collision energies were. You can do the following to achieve
@@ -754,7 +754,7 @@ <h1>Collision Energy Optimization</h1>
         this molecule on the Waters Xevo TQ-S. The best CE value (Step -5, the blue bar on the far left) is the lowest CE value measured.
     </p>
     <p>
-        <img src="image-32.png" />
+        <img src="s-32.png" />
     </p>
     <p>
         Given the trend toward that end of the range, futher investigation may be warranted to arrive at a truly optimal CE for that compound. For that
@@ -779,7 +779,7 @@ <h1>Collision Energy Optimization</h1>
         The <b>Export Transition List</b> form should now look like this:
     </p>
     <p>
-        <img src="image-33.png" />
+        <img src="s-33.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -801,7 +801,7 @@ <h1>Collision Energy Optimization</h1>
         The <b>Scheduling Data</b> form should look like this:
     </p>
     <p>
-        <img src="image-34.png" />
+        <img src="s-34.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeMethodDevCEOpt/zh-CHS/image-1.png b/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeMethodDevCEOpt/zh-CHS/s-1.png
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rename to pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeMethodDevCEOpt/zh-CHS/s-1.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeMethodDevCEOpt/zh-CHS/image-9.png b/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeMethodDevCEOpt/zh-CHS/s-9.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeMethodDevCEOpt/zh-CHS/image-9.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeMethodDevCEOpt/zh-CHS/s-9.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeMethodDevCEOpt/zh-CHS/image-0.png b/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeMethodDevCEOpt/zh-CHS/s-published-transition-list.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeMethodDevCEOpt/zh-CHS/image-0.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeMethodDevCEOpt/zh-CHS/s-published-transition-list.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/en/index.html b/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/en/index.html
index a583674643..669dbefc98 100644
--- a/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/en/index.html
+++ b/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/en/index.html
@@ -100,7 +100,7 @@ <h1>Experimental Layout</h1>
         dataset were laid out in a 96 well plate as follows:
     </p>
     <p>
-        <img src="image-0.png" />
+        <img src="s-96-well-plate-layout.png" />
     </p>
     <p>
         Blanks, or “zero” standards, contain only the internal standard, double blanks contain no standard at all. 
@@ -124,7 +124,7 @@ <h1>Experimental Layout</h1>
         Injections were performed in this order:
     </p>
     <p>
-        <img src="image-1.png" />
+        <img src="s-injection-order.png" />
     </p>
     <p>
         In all, 113 injections were used in collecting the mass spec data for these samples.
@@ -151,7 +151,7 @@ <h1>Importing a Small Molecule Transition List into a Skyline Document</h1>
         Skyline will show the <b>Insert Transition List</b> form:
     </p>
     <p>
-        <img src="image-2.png" />
+        <img src="s-1.png" />
     </p>
     <p>
         Normally, you would copy and paste a transition list from Excel or some other external source, but in this case, the transition list is small
@@ -172,7 +172,7 @@ <h1>Importing a Small Molecule Transition List into a Skyline Document</h1>
         means.
     </p>
     <p>
-        <img src="image-3.png" />
+        <img src="s-2.png" />
     </p>
     <ul>
         <li>Make sure that the <b>Molecules</b> radio button is selected.</li>
@@ -189,7 +189,7 @@ <h1>Importing a Small Molecule Transition List into a Skyline Document</h1>
         The <b>Import Transition List: Identify Columns</b> form should now look like this:
     </p>
     <p>
-        <img src="image-4.png" />
+        <img src="s-3.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -212,7 +212,7 @@ <h1>Importing a Small Molecule Transition List into a Skyline Document</h1>
         Your Skyline window should now look like this:
     </p>
     <p>
-        <img src="image-5.png" /> 
+        <img src="s-4.png" /> 
     </p>
     <h1>Transition Settings</h1>
     <p>
@@ -229,7 +229,7 @@ <h1>Transition Settings</h1>
         The <b>Transition Settings</b> form should now look like this:
     </p>
     <p>
-        <img src="image-6.png" />
+        <img src="s-5.png" />
     </p>
     <ul>
         <li>Click the <b>Filter</b> tab.</li>
@@ -240,7 +240,7 @@ <h1>Transition Settings</h1>
         The <b>Transition Settings</b> form should now look like this: 
     </p>
     <p>
-        <img src="image-7.png" />
+        <img src="s-6.png" />
     </p>
     <p>
         In the <b>Ion types</b> field, the value “f” indicates only fragment ion transitions will be measured. If you wanted to measure
@@ -252,7 +252,7 @@ <h1>Transition Settings</h1>
         transitions that your mass spectrometer is not actually able to measure.
     </p>
     <p>
-        <img src="image-8.png" />
+        <img src="s-7.png" />
     </p>
     <p>
         The <b>Method match tolerance</b> is another important setting in the <b>Instrument</b> tab. It determines how closely the
@@ -289,7 +289,7 @@ <h1>Importing Mass Spectrometer Runs</h1>
         The <b>Import Results</b> form should now look like this: 
     </p>
     <p>
-        <img src="image-9.png" />
+        <img src="s-8.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -300,7 +300,7 @@ <h1>Importing Mass Spectrometer Runs</h1>
         The <b>Import Results Files</b> form should look like:
     </p>
     <p>
-        <img src="image-10.png" />
+        <img src="s-9.png" />
     </p>
     <ul>
         <li>Click the <b>Open</b> button.</li>
@@ -309,7 +309,7 @@ <h1>Importing Mass Spectrometer Runs</h1>
         The files should import within 30 seconds or so, leaving your Skyline window looking like this:
     </p>
     <p>
-        <img src="image-11.png" /> 
+        <img src="s-10.png" /> 
     </p>
     <p>
         To take advantage of the Skyline summary graphs for viewing individual targets, do the following:
@@ -324,7 +324,7 @@ <h1>Importing Mass Spectrometer Runs</h1>
         The Skyline window should now look like this:
     </p>
     <p>
-        <img src="image-12.png" />
+        <img src="s-11.png" />
     </p>
     <h1>Checking Peak Integration</h1>
     <p>
@@ -342,7 +342,7 @@ <h1>Checking Peak Integration</h1>
         “DoubleBlank” implies that neither is present in the sample. The chromatogram graph now shows you what peaks Skyline had to choose from:
     </p>
     <p>
-        <img src="image-13.png" />
+        <img src="s-12.png" />
     </p>
     <ul>
         <li>Click on the bars for the other two outliers in the <b>Retention Times – Replicate Comparison</b> view. </li>
@@ -360,14 +360,14 @@ <h1>Adjusting Peak Integration</h1>
     <ul>
         <li>In the <b>Targets</b> view <b>Replicates</b> dropdown list, select the “DoubleBlank1” replicate.</li>
         <li>Position the mouse cursor below the <b>Retention Time</b> axis (the cursor will change east-west arrows:<img
-                src="image-14.png" />).</li>
+                src="../../shared/vertical-split-cursor-icon.png" />).</li>
         <li>Click below the <b>Retention Time</b> axis at about 2.65 minutes and drag to about 2.75 minutes.</li>
     </ul>
     <p class="keep-next">
         The peak boundaries will change to these new values, and the original range will be marked by a shaded area, as shown below:
     </p>
     <p>
-        <img src="image-15.png" />
+        <img src="s-13.png" />
     </p>
     <p>
         Repeat the steps above for the other two “DoubleBlank” replicates.
@@ -389,7 +389,7 @@ <h1>Preparing for Quantitation</h1>
         The <b>Molecule Settings</b> form should look like this:
     </p>
     <p>
-        <img src="image-16.png" />
+        <img src="s-14.png" />
     </p>
     <p>
         This experiment uses a linear regression fit, normalizing to the heavy labeled drug. Skyline offers options for weighting across the curve as a
@@ -418,7 +418,7 @@ <h1>Declaring Sample Types for Calibration Curve Display</h1>
         The <b>Document Grid</b> should look like this:
     </p>
     <p>
-        <img src="image-17.png" />
+        <img src="s-15.png" />
     </p>
     <ul>
         <li>Expand the <b>Document Grid</b> if needed so that you can see all the replicates at once if you screen is large enough.</li>
@@ -626,7 +626,7 @@ <h1>Declaring Sample Types for Calibration Curve Display</h1>
         The <b>Document Grid</b> should look like this when done:
     </p>
     <p>
-        <img src="image-18.png" />
+        <img src="s-16.png" />
     </p>
     <h1>Inspecting the Calibration Curve</h1>
     <p>
@@ -640,7 +640,7 @@ <h1>Inspecting the Calibration Curve</h1>
         The <b>Calibration Curve</b> form should appear looking like this:
     </p>
     <p>
-        <img src="image-19.png" />
+        <img src="s-17.png" />
     </p>
     <p>
         The note about the selected replicate missing transitions is expected, when the currently selected replicate is a double blank. 
@@ -657,7 +657,7 @@ <h1>Inspecting the Calibration Curve</h1>
         <li>On the <b>View</b> menu, click <b>Document Grid</b>.</li>
         <li>Click on <b>Reports</b> in the upper left corner of the grid, and then click <b>Replicates</b>.</li>
         <li>Click again on <b>Reports</b> in the upper left corner of the grid, and then click <b>Customize Report</b>.</li>
-        <li>Click on the search button <img src="image-20.png" /> and enter “accuracy” into the <b>Find what</b> field.</li>
+        <li>Click on the search button <img src="../../shared/black-binocular-button.png" /> and enter “accuracy” into the <b>Find what</b> field.</li>
         <li>Click the <b>Find Next</b> button.</li>
         <li>Click the <b>Close</b> button on the <b>Find Column</b> form. </li>
         <li>In the <b>Customize Report</b> form, <b>Accuracy</b> should be highlighted under the <b>Quantification</b>
@@ -672,7 +672,7 @@ <h1>Inspecting the Calibration Curve</h1>
         The <b>Document Grid</b> should now look like this:
     </p>
     <p>
-        <img src="image-21.png" />
+        <img src="s-18.png" />
     </p>
     <p>
         The FDA Guidance on which this assay was based states that calibration points should have bias &lt; 15% (accuracy between 85% and 115%) between
@@ -692,7 +692,7 @@ <h1>Inspecting the Calibration Curve</h1>
         excluding the outlier “Cal_5” values. 
     </p>
     <p>
-        <img src="image-22.png" />
+        <img src="s-19.png" />
     </p>
     <p>
         Next you should import the rest of the unknowns using the following steps:
@@ -721,7 +721,7 @@ <h1>Inspecting the Calibration Curve</h1>
         The <b>Document Grid</b> should look like this:
     </p>
     <p>
-        <img src="image-23.png" />
+        <img src="s-20.png" />
     </p>
     <p>
         After removal of the two “Cal_5” datapoints, further exploration of the data reveals that one of the “Cal_7” points has accuracy &lt;85% and
@@ -740,7 +740,7 @@ <h1>Inspecting the Calibration Curve</h1>
         The calibration curve should look like this:
     </p>
     <p>
-        <img src="image-24.png" />
+        <img src="s-21.png" />
     </p>
     <p>
         This presents a view which allows you to see at a glance that the samples mostly fall between “Cal_2” (20 uM) and “Cal_3” (100 uM), and well
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rename from pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/en/image-2.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/en/image-0.png b/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/en/s-96-well-plate-layout.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/en/image-0.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/en/s-96-well-plate-layout.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/en/image-1.png b/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/en/s-injection-order.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/en/image-1.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/en/s-injection-order.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/ja/image-14.png b/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/ja/image-14.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/ja/index.html b/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/ja/index.html
index 09f4a83aab..3137e472c5 100644
--- a/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/ja/index.html
+++ b/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/ja/index.html
@@ -86,7 +86,7 @@ <h1>実験のレイアウト</h1>
             href="https://www.ncbi.nlm.nih.gov/pubmed/29039849">https://www.ncbi.nlm.nih.gov/pubmed/29039849</a>）。簡単に言うと、本データセットの試料は、以下のように96個のウェルプレートに配列されました。
     </p>
     <p>
-        <img src="image-0.png" />
+        <img src="s-96-well-plate-layout.png" />
     </p>
     <p>
         ブランク、または「ゼロ」標準には内部標準のみが含まれており、ダブルブランクには標準が一切含まれていません。 
@@ -108,7 +108,7 @@ <h1>実験のレイアウト</h1>
         注入は以下のような順序で実行されました。
     </p>
     <p>
-        <img src="image-1.png" />
+        <img src="s-injection-order.png" />
     </p>
     <p>
         これらの試料の質量分析データの収集では、全部で113回の注入が行われました。
@@ -132,7 +132,7 @@ <h1>低分子トランジションリストのSkylineドキュメントへのイ
         Skylineが [ <b>トランジションリストの挿入</b> ] フォームを表示します。
     </p>
     <p>
-        <img src="image-2.png" />
+        <img src="s-1.png" />
     </p>
     <p>
         通常は、トランジションリストをExcelや他の外部ソースからコピーして貼り付けますが、この場合はトランジションリストが十分に小さいためここに表示します。
@@ -151,7 +151,7 @@ <h1>低分子トランジションリストのSkylineドキュメントへのイ
         Skylineは、[ <b>トランジションリストのインポート：列の識別</b> ] フォームを表示します。このフォームでは、Skylineに各列が何を意味するかを指示できます。
     </p>
     <p>
-        <img src="image-3.png" />
+        <img src="s-2.png" />
     </p>
     <ul>
         <li>[ <b>分子</b> ] ラジオボタンが選択されていることを確認します。</li>
@@ -167,7 +167,7 @@ <h1>低分子トランジションリストのSkylineドキュメントへのイ
         [ <b>トランジションリストのインポート：列の識別</b> ] フォームは以下のようになります。
     </p>
     <p>
-        <img src="image-4.png" /> 
+        <img src="s-3.png" /> 
     </p>
     <ul>
         <li>[ <b>OK</b> ] ボタンをクリックします。</li>
@@ -188,7 +188,7 @@ <h1>低分子トランジションリストのSkylineドキュメントへのイ
         これでSkylineウィンドウは以下のようになります。
     </p>
     <p>
-        <img src="image-5.png" /> 
+        <img src="s-4.png" /> 
     </p>
     <h1>トランジションの設定</h1>
     <p>
@@ -204,7 +204,7 @@ <h1>トランジションの設定</h1>
         [ <b>トランジション設定</b> ] フォームは以下のようになります。
     </p>
     <p>
-        <img src="image-6.png" />
+        <img src="s-5.png" />
     </p>
     <ul>
         <li>[ <b>フィルタ</b> ] タブをクリックします。</li>
@@ -215,7 +215,7 @@ <h1>トランジションの設定</h1>
         [ <b>トランジション設定</b> ] フォームは以下のようになります。 
     </p>
     <p>
-        <img src="image-7.png" />
+        <img src="s-6.png" />
     </p>
     <p>
         [ <b>イオンタイプ</b> ] フィールドの値「f」は、フラグメントイオンのトランジションのみが測定されることを示します。プリカーサーイオンも測定したい場合には、「f, p」を使用します。
@@ -225,7 +225,7 @@ <h1>トランジションの設定</h1>
         タブは、この実験に対してはデフォルト値でうまく行きます。ただし皆さん自身の作業においては、最小/最大<i>m/z</i>値が実際の装置の状況に合うことを確認してください。この設定の目的は、使用している質量分析計が実際に測定できないターゲットトランジションを追加できないようにすることです。
     </p>
     <p>
-        <img src="image-8.png" />
+        <img src="s-7.png" />
     </p>
     <p>
         [ <b>装置</b> ] タブのもう1つの重要な設定が [ <b>メソッド許容誤差</b> ]
@@ -255,7 +255,7 @@ <h1>質量分析計実行のインポート</h1>
         [ <b>結果をインポート</b> ] フォームは以下のようになります。 
     </p>
     <p>
-        <img src="image-9.png" />
+        <img src="s-8.png" />
     </p>
     <ul>
         <li>[ <b>OK</b> ] ボタンをクリックします。</li>
@@ -266,7 +266,7 @@ <h1>質量分析計実行のインポート</h1>
         [ <b>結果ファイルをインポート</b> ] フォームは以下のようになります。
     </p>
     <p>
-        <img src="image-10.png" />
+        <img src="s-9.png" />
     </p>
     <ul>
         <li>[ <b>開く</b> ] ボタンをクリックします。</li>
@@ -275,7 +275,7 @@ <h1>質量分析計実行のインポート</h1>
         当該ファイルは30秒程度でインポートされ、Skylineウィンドウは以下のようになります。
     </p>
     <p>
-        <img src="image-11.png" /> 
+        <img src="s-10.png" /> 
     </p>
     <p>
         Skyline概要グラフを利用して個別のターゲットを表示するには、以下の操作を行います。
@@ -290,7 +290,7 @@ <h1>質量分析計実行のインポート</h1>
         これでSkylineウィンドウは以下のようになります。
     </p>
     <p>
-        <img src="image-12.png" />
+        <img src="s-11.png" />
     </p>
     <h1>ピーク積分の確認</h1>
     <p>
@@ -306,7 +306,7 @@ <h1>ピーク積分の確認</h1>
         皆さんもSkylineがこの繰り返し測定から、測定ターゲットの薬物と同位体標識物のきれいなピークを見つけるとは期待していないでしょう。なぜなら「DoubleBlank」という用語は、どちらも試料内に存在しないことを意味しているからです。現在表示しているクロマトグラムグラフには、Skylineがその代わりに選ぶしかなかったピークが示されています。
     </p>
     <p>
-        <img src="image-13.png" />
+        <img src="s-12.png" />
     </p>
     <ul>
         <li>[ <b>保持時間 – 繰り返し測定の比較</b> ] ビューで、他の2つの異常値の棒をクリックします。 </li>
@@ -320,14 +320,14 @@ <h1>ピーク積分の調整</h1>
     </p>
     <ul>
         <li>[ <b>ターゲット</b> ] ビューの [ <b>繰り返し測定</b> ] ドロップダウンリストで、「DoubleBlank1」繰り返し測定を選択します。</li>
-        <li>マウスのカーソルを<b>保持時間</b>軸の下に合わせます（カーソルは左右の矢印<img src="image-14.png" /> に変わります）。</li>
+        <li>マウスのカーソルを<b>保持時間</b>軸の下に合わせます（カーソルは左右の矢印<img src="../../shared/vertical-split-cursor-icon.png" /> に変わります）。</li>
         <li><b>保持時間</b>軸の下、2.65分あたりをクリックし、2.75分あたりにドラッグします。</li>
     </ul>
     <p class="keep-next">
         ピーク境界はこの新しい値に変わり、元の範囲は以下のように斜線部分でマークされます。
     </p>
     <p>
-        <img src="image-15.png" />
+        <img src="s-13.png" />
     </p>
     <p>
         上記の手順を、他の2つの「DoubleBlank」繰り返し測定に繰り返します。
@@ -349,7 +349,7 @@ <h1>定量の準備</h1>
         [ <b>分子設定</b> ] フォームは以下のようになります。
     </p>
     <p>
-        <img src="image-16.png" />
+        <img src="s-14.png" />
     </p>
     <p>
         この実験では、線形回帰を用いて同位体標識化合物に対する正規化を行っています。Skylineは、x：なし、1/x、1/(x*x)に応じて、曲線全体で重みを付けるオプションを提供します。本チュートリアルは、濃度の低い校正試料の重みを増加する、回帰の重み「1 / (x*x)」を使用します。[
@@ -373,7 +373,7 @@ <h1>校正曲線を表示するための試料タイプの宣言</h1>
         <b>ドキュメントグリッド</b>は以下のようになります。
     </p>
     <p>
-        <img src="image-17.png" />
+        <img src="s-15.png" />
     </p>
     <ul>
         <li>必要であれば、<b>ドキュメントグリッド</b>を拡大して画面が十分に大きければすべての繰り返し測定が同時に表示できるようにします。</li>
@@ -579,7 +579,7 @@ <h1>校正曲線を表示するための試料タイプの宣言</h1>
         完了すると、<b>ドキュメントグリッド</b>は以下のようになります。
     </p>
     <p>
-        <img src="image-18.png" />
+        <img src="s-16.png" />
     </p>
     <h1>校正曲線の検査</h1>
     <p>
@@ -593,7 +593,7 @@ <h1>校正曲線の検査</h1>
         [ <b>校正曲線</b> ] フォームは、以下のように表示されます。
     </p>
     <p>
-        <img src="image-19.png" />
+        <img src="s-17.png" />
     </p>
     <p>
         現在選択されている繰り返し測定がダブルブランクの場合は、選択されている繰り返し測定でトランジションがないものについての注記が予想されます。 
@@ -609,7 +609,7 @@ <h1>校正曲線の検査</h1>
         <li>[ <b>ビュー</b> ] メニューで、[ <b>ドキュメントグリッド</b> ] をクリックします。</li>
         <li>グリッドの左上隅にある [ <b>レポート</b> ] をクリックし、続いて [ <b>繰り返し測定</b> ] をクリックします。</li>
         <li>グリッドの左上隅にある [ <b>レポート</b> ] をもう一度クリックし、それから [ <b>レポートをカスタマイズ</b> ] をクリックします。</li>
-        <li>検索ボタン <img src="image-20.png" />をクリックし、[ <b>検索</b> ] フィールドに「精度」と入力します。</li>
+        <li>検索ボタン <img src="../../shared/black-binocular-button.png" />をクリックし、[ <b>検索</b> ] フィールドに「精度」と入力します。</li>
         <li>[ <b>次を検索</b> ] ボタンをクリックします。</li>
         <li>[ <b>列を検索</b> ] フォームの [ <b>閉じる</b> ] ボタンをクリックします。 </li>
         <li>[ <b>レポートをカスタマイズ</b> ] フォームでは、[ <b>定量化</b> ] サブカテゴリの下にある<b>精度</b>が強調表示されます。</li>
@@ -622,7 +622,7 @@ <h1>校正曲線の検査</h1>
         <b>ドキュメントグリッド</b>は以下のようになります。
     </p>
     <p>
-        <img src="image-21.png" />
+        <img src="s-18.png" />
     </p>
     <p>
         このアッセイが基にしているFDAガイダンスでは、校正点の既知濃度と校正曲線から逆に計算した濃度との間のバイアスは15%以下（精度85％から115%）であるべきと述べてきます。 [ <b>精度</b> ]
@@ -637,7 +637,7 @@ <h1>校正曲線の検査</h1>
         校正曲線は、下図のようになります。異常値である「Cal_5」値を除外することで、Rの二乗値が0.97から0.99超に改善することに注意します。 
     </p>
     <p>
-        <img src="image-22.png" />
+        <img src="s-19.png" />
     </p>
     <p>
         次に、以下の手順を実行して、不明試料の残りをインポートします。
@@ -664,7 +664,7 @@ <h1>校正曲線の検査</h1>
         <b>ドキュメントグリッド</b>は以下のようになります。
     </p>
     <p>
-        <img src="image-23.png" />
+        <img src="s-20.png" />
     </p>
     <p>
         2つの「Cal_5」データポイントの削除後、データを更に調べると、「Cal_7」の点の1つの精度が85%未満であることがわかりますので、これも削除します。「Cal_6」のレベルを超える試料はなく、また「Cal 4」と「Cal
@@ -682,7 +682,7 @@ <h1>校正曲線の検査</h1>
         校正曲線は以下のようになります。
     </p>
     <p>
-        <img src="image-24.png" />
+        <img src="s-21.png" />
     </p>
     <p>
         これを見ると、試料の大半が「Cal_2」（20 uM）と「Cal_3」（100 uM）の間にあり、アッセイの線形校正範囲に十分収まっていることが一目でわかります。品質管理 (QC) 試料（known
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/ja/invariant.html b/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/ja/invariant.html
index eaa69c9b0c..ed8c9f0aa0 100644
--- a/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/ja/invariant.html
+++ b/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/ja/invariant.html
@@ -100,7 +100,7 @@ <h1>Experimental Layout</h1>
         dataset were laid out in a 96 well plate as follows:
     </p>
     <p>
-        <img src="image-0.png" />
+        <img src="s-96-well-plate-layout.png" />
     </p>
     <p>
         Blanks, or “zero” standards, contain only the internal standard, double blanks contain no standard at all. 
@@ -124,7 +124,7 @@ <h1>Experimental Layout</h1>
         Injections were performed in this order:
     </p>
     <p>
-        <img src="image-1.png" />
+        <img src="s-injection-order.png" />
     </p>
     <p>
         In all, 113 injections were used in collecting the mass spec data for these samples.
@@ -151,7 +151,7 @@ <h1>Importing a Small Molecule Transition List into a Skyline Document</h1>
         Skyline will show the <b>Insert Transition List</b> form:
     </p>
     <p>
-        <img src="image-2.png" />
+        <img src="s-1.png" />
     </p>
     <p>
         Normally, you would copy and paste a transition list from Excel or some other external source, but in this case, the transition list is small
@@ -172,7 +172,7 @@ <h1>Importing a Small Molecule Transition List into a Skyline Document</h1>
         means.
     </p>
     <p>
-        <img src="image-3.png" />
+        <img src="s-2.png" />
     </p>
     <ul>
         <li>Make sure that the <b>Molecules</b> radio button is selected.</li>
@@ -189,7 +189,7 @@ <h1>Importing a Small Molecule Transition List into a Skyline Document</h1>
         The <b>Import Transition List: Identify Columns</b> form should now look like this:
     </p>
     <p>
-        <img src="image-4.png" />
+        <img src="s-3.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -212,7 +212,7 @@ <h1>Importing a Small Molecule Transition List into a Skyline Document</h1>
         Your Skyline window should now look like this:
     </p>
     <p>
-        <img src="image-5.png" /> 
+        <img src="s-4.png" /> 
     </p>
     <h1>Transition Settings</h1>
     <p>
@@ -229,7 +229,7 @@ <h1>Transition Settings</h1>
         The <b>Transition Settings</b> form should now look like this:
     </p>
     <p>
-        <img src="image-6.png" />
+        <img src="s-5.png" />
     </p>
     <ul>
         <li>Click the <b>Filter</b> tab.</li>
@@ -240,7 +240,7 @@ <h1>Transition Settings</h1>
         The <b>Transition Settings</b> form should now look like this: 
     </p>
     <p>
-        <img src="image-7.png" />
+        <img src="s-6.png" />
     </p>
     <p>
         In the <b>Ion types</b> field, the value “f” indicates only fragment ion transitions will be measured. If you wanted to measure
@@ -252,7 +252,7 @@ <h1>Transition Settings</h1>
         transitions that your mass spectrometer is not actually able to measure.
     </p>
     <p>
-        <img src="image-8.png" />
+        <img src="s-7.png" />
     </p>
     <p>
         The <b>Method match tolerance</b> is another important setting in the <b>Instrument</b> tab. It determines how closely the
@@ -289,7 +289,7 @@ <h1>Importing Mass Spectrometer Runs</h1>
         The <b>Import Results</b> form should now look like this: 
     </p>
     <p>
-        <img src="image-9.png" />
+        <img src="s-8.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -300,7 +300,7 @@ <h1>Importing Mass Spectrometer Runs</h1>
         The <b>Import Results Files</b> form should look like:
     </p>
     <p>
-        <img src="image-10.png" />
+        <img src="s-9.png" />
     </p>
     <ul>
         <li>Click the <b>Open</b> button.</li>
@@ -309,7 +309,7 @@ <h1>Importing Mass Spectrometer Runs</h1>
         The files should import within 30 seconds or so, leaving your Skyline window looking like this:
     </p>
     <p>
-        <img src="image-11.png" /> 
+        <img src="s-10.png" /> 
     </p>
     <p>
         To take advantage of the Skyline summary graphs for viewing individual targets, do the following:
@@ -324,7 +324,7 @@ <h1>Importing Mass Spectrometer Runs</h1>
         The Skyline window should now look like this:
     </p>
     <p>
-        <img src="image-12.png" />
+        <img src="s-11.png" />
     </p>
     <h1>Checking Peak Integration</h1>
     <p>
@@ -342,7 +342,7 @@ <h1>Checking Peak Integration</h1>
         “DoubleBlank” implies that neither is present in the sample. The chromatogram graph now shows you what peaks Skyline had to choose from:
     </p>
     <p>
-        <img src="image-13.png" />
+        <img src="s-12.png" />
     </p>
     <ul>
         <li>Click on the bars for the other two outliers in the <b>Retention Times – Replicate Comparison</b> view. </li>
@@ -360,14 +360,14 @@ <h1>Adjusting Peak Integration</h1>
     <ul>
         <li>In the <b>Targets</b> view <b>Replicates</b> dropdown list, select the “DoubleBlank1” replicate.</li>
         <li>Position the mouse cursor below the <b>Retention Time</b> axis (the cursor will change east-west arrows:<img
-                src="image-14.png" />).</li>
+                src="../../shared/vertical-split-cursor-icon.png" />).</li>
         <li>Click below the <b>Retention Time</b> axis at about 2.65 minutes and drag to about 2.75 minutes.</li>
     </ul>
     <p class="keep-next">
         The peak boundaries will change to these new values, and the original range will be marked by a shaded area, as shown below:
     </p>
     <p>
-        <img src="image-15.png" />
+        <img src="s-13.png" />
     </p>
     <p>
         Repeat the steps above for the other two “DoubleBlank” replicates.
@@ -389,7 +389,7 @@ <h1>Preparing for Quantitation</h1>
         The <b>Molecule Settings</b> form should look like this:
     </p>
     <p>
-        <img src="image-16.png" />
+        <img src="s-14.png" />
     </p>
     <p>
         This experiment uses a linear regression fit, normalizing to the heavy labeled drug. Skyline offers options for weighting across the curve as a
@@ -418,7 +418,7 @@ <h1>Declaring Sample Types for Calibration Curve Display</h1>
         The <b>Document Grid</b> should look like this:
     </p>
     <p>
-        <img src="image-17.png" />
+        <img src="s-15.png" />
     </p>
     <ul>
         <li>Expand the <b>Document Grid</b> if needed so that you can see all the replicates at once if you screen is large enough.</li>
@@ -626,7 +626,7 @@ <h1>Declaring Sample Types for Calibration Curve Display</h1>
         The <b>Document Grid</b> should look like this when done:
     </p>
     <p>
-        <img src="image-18.png" />
+        <img src="s-16.png" />
     </p>
     <h1>Inspecting the Calibration Curve</h1>
     <p>
@@ -640,7 +640,7 @@ <h1>Inspecting the Calibration Curve</h1>
         The <b>Calibration Curve</b> form should appear looking like this:
     </p>
     <p>
-        <img src="image-19.png" />
+        <img src="s-17.png" />
     </p>
     <p>
         The note about the selected replicate missing transitions is expected, when the currently selected replicate is a double blank. 
@@ -657,7 +657,7 @@ <h1>Inspecting the Calibration Curve</h1>
         <li>On the <b>View</b> menu, click <b>Document Grid</b>.</li>
         <li>Click on <b>Reports</b> in the upper left corner of the grid, and then click <b>Replicates</b>.</li>
         <li>Click again on <b>Reports</b> in the upper left corner of the grid, and then click <b>Customize Report</b>.</li>
-        <li>Click on the search button <img src="image-20.png" /> and enter “accuracy” into the <b>Find what</b> field.</li>
+        <li>Click on the search button <img src="../../shared/black-binocular-button.png" /> and enter “accuracy” into the <b>Find what</b> field.</li>
         <li>Click the <b>Find Next</b> button.</li>
         <li>Click the <b>Close</b> button on the <b>Find Column</b> form. </li>
         <li>In the <b>Customize Report</b> form, <b>Accuracy</b> should be highlighted under the
@@ -672,7 +672,7 @@ <h1>Inspecting the Calibration Curve</h1>
         The <b>Document Grid</b> should now look like this:
     </p>
     <p>
-        <img src="image-21.png" />
+        <img src="s-18.png" />
     </p>
     <p>
         The FDA Guidance on which this assay was based states that calibration points should have bias &lt; 15% (accuracy between 85% and 115%) between
@@ -692,7 +692,7 @@ <h1>Inspecting the Calibration Curve</h1>
         excluding the outlier “Cal_5” values. 
     </p>
     <p>
-        <img src="image-22.png" />
+        <img src="s-19.png" />
     </p>
     <p>
         Next you should import the rest of the unknowns using the following steps:
@@ -721,7 +721,7 @@ <h1>Inspecting the Calibration Curve</h1>
         The <b>Document Grid</b> should look like this:
     </p>
     <p>
-        <img src="image-23.png" />
+        <img src="s-20.png" />
     </p>
     <p>
         After removal of the two “Cal_5” datapoints, further exploration of the data reveals that one of the “Cal_7” points has accuracy &lt;85% and
@@ -740,7 +740,7 @@ <h1>Inspecting the Calibration Curve</h1>
         The calibration curve should look like this:
     </p>
     <p>
-        <img src="image-24.png" />
+        <img src="s-21.png" />
     </p>
     <p>
         This presents a view which allows you to see at a glance that the samples mostly fall between “Cal_2” (20 uM) and “Cal_3” (100 uM), and well
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/ja/image-2.png b/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/ja/s-1.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/ja/image-2.png
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rename from pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/ja/image-11.png
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rename from pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/ja/image-13.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/ja/image-15.png b/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/ja/s-13.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/ja/image-0.png b/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/ja/s-96-well-plate-layout.png
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rename from pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/ja/image-0.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/ja/image-1.png b/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/ja/s-injection-order.png
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rename from pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/ja/image-1.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/zh-CHS/index.html b/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/zh-CHS/index.html
index c07d16e6a6..37de8bd655 100644
--- a/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/zh-CHS/index.html
+++ b/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/zh-CHS/index.html
@@ -86,7 +86,7 @@ <h1>实验设计</h1>
             href="https://www.ncbi.nlm.nih.gov/pubmed/29039849">https://www.ncbi.nlm.nih.gov/pubmed/29039849</a>)。简单来说，该数据集的样品按如下方式分布在 96 孔检测板中：
     </p>
     <p>
-        <img src="image-0.png" />
+        <img src="s-96-well-plate-layout.png" />
     </p>
     <p>
         空白或“零”标准品仅包含内标，双空白则完全不含标准品。 
@@ -107,7 +107,7 @@ <h1>实验设计</h1>
         按以下顺序进样：
     </p>
     <p>
-        <img src="image-1.png" />
+        <img src="s-injection-order.png" />
     </p>
     <p>
         总共进样 113 次以收集这些样品的质谱数据。
@@ -131,7 +131,7 @@ <h1>将小分子离子对列表导入 Skyline 文档</h1>
         Skyline 将显示<b>插入离子对列表</b>表单:
     </p>
     <p>
-        <img src="image-2.png" />
+        <img src="s-1.png" />
     </p>
     <p>
         您通常要从 Excel 或其它外部来源复制和粘贴离子对列表，但本例中的离子对列表小到足以直接显示在这里：
@@ -150,7 +150,7 @@ <h1>将小分子离子对列表导入 Skyline 文档</h1>
          Skyline 将显示<b>导入离子对列表：标识列</b>表单，从中可以告知 Skyline 每列的含义。
     </p>
     <p>
-        <img src="image-3.png" />
+        <img src="s-2.png" />
     </p>
     <ul>
         <li>确保选中<b>分子</b>单选按钮。</li>
@@ -166,7 +166,7 @@ <h1>将小分子离子对列表导入 Skyline 文档</h1>
         <b>导入离子对列表：标识列</b>表单现在应显示如下：
     </p>
     <p>
-        <img src="image-4.png" /> 
+        <img src="s-3.png" /> 
     </p>
     <ul>
         <li>单击<b>确定</b>按钮。</li>
@@ -187,7 +187,7 @@ <h1>将小分子离子对列表导入 Skyline 文档</h1>
         此时 Skyline 窗口将显示如下：
     </p>
     <p>
-        <img src="image-5.png" /> 
+        <img src="s-4.png" /> 
     </p>
     <h1>离子对设置</h1>
     <p>
@@ -203,7 +203,7 @@ <h1>离子对设置</h1>
         <b>离子对设置</b>表单现在应显示如下：
     </p>
     <p>
-        <img src="image-6.png" />
+        <img src="s-5.png" />
     </p>
     <ul>
         <li>单击<b>过滤器</b>选项卡。</li>
@@ -214,7 +214,7 @@ <h1>离子对设置</h1>
         <b>离子对设置</b>表单现在应显示如下： 
     </p>
     <p>
-        <img src="image-7.png" />
+        <img src="s-6.png" />
     </p>
     <p>
         在<b>离子类型</b>字段中，值“f”表示将仅测量碎片离子的离子对。如果还想测量母离子，则可以使用“f，p”。
@@ -223,7 +223,7 @@ <h1>离子对设置</h1>
         <b>仪器</b>选项卡中的默认值适用于本实验。但在您自己进行实验时，请确保最小和最大<i>质荷比</i>值对您实际使用的仪器是有意义的。这些设置的目的是防止您添加质谱仪实际上无法测量的目标离子对。
     </p>
     <p>
-        <img src="image-8.png" />
+        <img src="s-7.png" />
     </p>
     <p>
         <b>方法匹配耐受性</b>是<b>仪器</b>选项卡中的另一项重要设置。它决定仪器方法（存储在原始数据文件中）中的<i>质荷比</i>值必须与 Skyline
@@ -254,7 +254,7 @@ <h1>导入质谱仪产生的原始数据</h1>
         <b>导入结果</b>表单现在应显示如下： 
     </p>
     <p>
-        <img src="image-9.png" />
+        <img src="s-8.png" />
     </p>
     <ul>
         <li>单击<b>确定</b>按钮。</li>
@@ -264,7 +264,7 @@ <h1>导入质谱仪产生的原始数据</h1>
         <b>导入结果文件</b>表单应显示如下：
     </p>
     <p>
-        <img src="image-10.png" />
+        <img src="s-9.png" />
     </p>
     <ul>
         <li>单击<b>打开</b>按钮。</li>
@@ -273,7 +273,7 @@ <h1>导入质谱仪产生的原始数据</h1>
         此文件应在 30 秒左右内导入，之后 Skyline 窗口将显示如下：
     </p>
     <p>
-        <img src="image-11.png" /> 
+        <img src="s-10.png" /> 
     </p>
     <p>
         要利用 Skyline 摘要图查看各个目标，请执行以下操作：
@@ -288,7 +288,7 @@ <h1>导入质谱仪产生的原始数据</h1>
         此时 Skyline 窗口将显示如下：
     </p>
     <p>
-        <img src="image-12.png" />
+        <img src="s-11.png" />
     </p>
     <h1>检查峰积分</h1>
     <p>
@@ -304,7 +304,7 @@ <h1>检查峰积分</h1>
         Skyline 其实并不会为该重复测定中药物的轻/重离子对找到一个良好的峰，因为“DoubleBlank”一词表示二者在该样品中都不存在。色谱图现在显示了 Skyline 不得不选择的色谱峰：
     </p>
     <p>
-        <img src="image-13.png" />
+        <img src="s-12.png" />
     </p>
     <ul>
         <li>在<b>保留时间 - 重复测定比较</b>视图中，单击另外两个离群值对应的条形。 </li>
@@ -319,14 +319,14 @@ <h1>调整峰积分</h1>
     </p>
     <ul>
         <li>在<b>目标</b>视图<b>重复测定</b>下拉列表中，选择“DoubleBlank1”重复测定。</li>
-        <li>将鼠标光标置于<b>保留时间</b>轴下方（光标变为东西双向箭头：<img src="image-14.png" />）。</li>
+        <li>将鼠标光标置于<b>保留时间</b>轴下方（光标变为东西双向箭头：<img src="../../shared/vertical-split-cursor-icon.png" />）。</li>
         <li>单击<b>保留时间</b>轴下方大约 2.65 分钟的位置，然后拖动到大约 2.75 分钟处。</li>
     </ul>
     <p class="keep-next">
         峰边界将变更为这些新值，初始范围用阴影区域标记，如下所示：
     </p>
     <p>
-        <img src="image-15.png" />
+        <img src="s-13.png" />
     </p>
     <p>
         对其他两个“DoubleBlank”重复测定重复执行上述步骤。
@@ -348,7 +348,7 @@ <h1>准备定量</h1>
         <b>分子设置</b>表单现在应显示如下：
     </p>
     <p>
-        <img src="image-16.png" />
+        <img src="s-14.png" />
     </p>
     <p>
         本实验使用线性回归拟合，对重标药物实施归一化。Skyline 提供了曲线随 x 而变化的权重选项：无、1/x 和 1/(x*x)。本教程使用“1 /
@@ -373,7 +373,7 @@ <h1>设置标准曲线样品类型</h1>
         <b>文档网格</b>应显示如下：
     </p>
     <p>
-        <img src="image-17.png" />
+        <img src="s-15.png" />
     </p>
     <ul>
         <li>需要时可以展开<b>文档网格</b>，这样在屏幕足够大时可以同时查看所有重复测定。</li>
@@ -579,7 +579,7 @@ <h1>设置标准曲线样品类型</h1>
         完成操作后，<b>文档网格</b>应显示如下：
     </p>
     <p>
-        <img src="image-18.png" />
+        <img src="s-16.png" />
     </p>
     <h1>检查标准曲线</h1>
     <p>
@@ -593,7 +593,7 @@ <h1>检查标准曲线</h1>
         <b>标准曲线</b>表单应显示如下：
     </p>
     <p>
-        <img src="image-19.png" />
+        <img src="s-17.png" />
     </p>
     <p>
         当前选择的重复测定为双空白时，会出现有关所选重复测定缺少离子对的注释。 
@@ -608,7 +608,7 @@ <h1>检查标准曲线</h1>
         <li>在<b>视图</b>菜单上，单击<b>文档网格</b>。</li>
         <li>单击网格左上角的<b>报告</b>，然后单击<b>重复测定</b>。</li>
         <li>再次单击网格左上角的<b>报告</b>，然后单击<b>自定义报告</b>。</li>
-        <li>单击搜索按钮 <img src="image-20.png" />并在<b>查找</b>字段中输入“准确性”。</li>
+        <li>单击搜索按钮 <img src="../../shared/black-binocular-button.png" />并在<b>查找</b>字段中输入“准确性”。</li>
         <li>单击<b>查找下一个</b>按钮。</li>
         <li>单击<b>查找列</b>表单中的<b>关闭</b>按钮。 </li>
         <li>在<b>自定义报告</b>表单中，<b>准确性</b>应高亮显示在<b>定量</b>子类别下。</li>
@@ -621,7 +621,7 @@ <h1>检查标准曲线</h1>
         <b>文档网格</b>现在应显示如下：
     </p>
     <p>
-        <img src="image-21.png" />
+        <img src="s-18.png" />
     </p>
     <p>
         这项分析所依据的 FDA 指南指出，校准点在已知浓度和标准曲线的反算浓度之间的偏差应小于 15％（准确性介于 85％ 和 115％
@@ -636,7 +636,7 @@ <h1>检查标准曲线</h1>
         标准曲线现在应如下图所示。请注意，通过排除“Cal_5”异常值，R 平方值从 0.97 提高到 0.99 以上。 
     </p>
     <p>
-        <img src="image-22.png" />
+        <img src="s-19.png" />
     </p>
     <p>
         接下来要执行以下步骤，导入其余的未知样品：
@@ -661,7 +661,7 @@ <h1>检查标准曲线</h1>
         <b>文档网格</b>应显示如下：
     </p>
     <p>
-        <img src="image-23.png" />
+        <img src="s-20.png" />
     </p>
     <p>
         在删除两个“Cal_5”数据点，进一步查看数据后发现，其中一个“Cal_7”点的准确性 &lt;85％，故而应将其删除。由于没有样品在级别“Cal_6”以上，并且只有四个样品的级别在“Cal 4”和“Cal 6”之间，因此这对样品的测量几乎没有影响。
@@ -678,7 +678,7 @@ <h1>检查标准曲线</h1>
         标准曲线应如下所示：
     </p>
     <p>
-        <img src="image-24.png" />
+        <img src="s-21.png" />
     </p>
     <p>
         在呈现的这种视图中，您可以一目了然地看到，样品大部分落在“Cal_2”(20 uM) 和“Cal_3”(100 uM) 之间，并且恰好位于这项分析的线性标准范围内。质量控制样品（已知的未知样品，图中的绿色菱形）的准确性介于 85％ 至 115％ 之间，符合 FDA 指导标准。
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/zh-CHS/invariant.html b/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/zh-CHS/invariant.html
index 06413066c2..1375a06ed0 100644
--- a/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/zh-CHS/invariant.html
+++ b/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/zh-CHS/invariant.html
@@ -100,7 +100,7 @@ <h1>Experimental Layout</h1>
         dataset were laid out in a 96 well plate as follows:
     </p>
     <p>
-        <img src="image-0.png" />
+        <img src="s-96-well-plate-layout.png" />
     </p>
     <p>
         Blanks, or “zero” standards, contain only the internal standard, double blanks contain no standard at all. 
@@ -124,7 +124,7 @@ <h1>Experimental Layout</h1>
         Injections were performed in this order:
     </p>
     <p>
-        <img src="image-1.png" />
+        <img src="s-injection-order.png" />
     </p>
     <p>
         In all, 113 injections were used in collecting the mass spec data for these samples.
@@ -151,7 +151,7 @@ <h1>Importing a Small Molecule Transition List into a Skyline Document</h1>
         Skyline will show the <b>Insert Transition List</b> form:
     </p>
     <p>
-        <img src="image-2.png" />
+        <img src="s-1.png" />
     </p>
     <p>
         Normally, you would copy and paste a transition list from Excel or some other external source, but in this case, the transition list is small
@@ -172,7 +172,7 @@ <h1>Importing a Small Molecule Transition List into a Skyline Document</h1>
         means.
     </p>
     <p>
-        <img src="image-3.png" />
+        <img src="s-2.png" />
     </p>
     <ul>
         <li>Make sure that the <b>Molecules</b> radio button is selected.</li>
@@ -189,7 +189,7 @@ <h1>Importing a Small Molecule Transition List into a Skyline Document</h1>
         The <b>Import Transition List: Identify Columns</b> form should now look like this:
     </p>
     <p>
-        <img src="image-4.png" />
+        <img src="s-3.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -212,7 +212,7 @@ <h1>Importing a Small Molecule Transition List into a Skyline Document</h1>
         Your Skyline window should now look like this:
     </p>
     <p>
-        <img src="image-5.png" /> 
+        <img src="s-4.png" /> 
     </p>
     <h1>Transition Settings</h1>
     <p>
@@ -229,7 +229,7 @@ <h1>Transition Settings</h1>
         The <b>Transition Settings</b> form should now look like this:
     </p>
     <p>
-        <img src="image-6.png" />
+        <img src="s-5.png" />
     </p>
     <ul>
         <li>Click the <b>Filter</b> tab.</li>
@@ -240,7 +240,7 @@ <h1>Transition Settings</h1>
         The <b>Transition Settings</b> form should now look like this: 
     </p>
     <p>
-        <img src="image-7.png" />
+        <img src="s-6.png" />
     </p>
     <p>
         In the <b>Ion types</b> field, the value “f” indicates only fragment ion transitions will be measured. If you wanted to measure
@@ -252,7 +252,7 @@ <h1>Transition Settings</h1>
         transitions that your mass spectrometer is not actually able to measure.
     </p>
     <p>
-        <img src="image-8.png" />
+        <img src="s-7.png" />
     </p>
     <p>
         The <b>Method match tolerance</b> is another important setting in the <b>Instrument</b> tab. It determines how closely the
@@ -289,7 +289,7 @@ <h1>Importing Mass Spectrometer Runs</h1>
         The <b>Import Results</b> form should now look like this: 
     </p>
     <p>
-        <img src="image-9.png" />
+        <img src="s-8.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -300,7 +300,7 @@ <h1>Importing Mass Spectrometer Runs</h1>
         The <b>Import Results Files</b> form should look like:
     </p>
     <p>
-        <img src="image-10.png" />
+        <img src="s-9.png" />
     </p>
     <ul>
         <li>Click the <b>Open</b> button.</li>
@@ -309,7 +309,7 @@ <h1>Importing Mass Spectrometer Runs</h1>
         The files should import within 30 seconds or so, leaving your Skyline window looking like this:
     </p>
     <p>
-        <img src="image-11.png" /> 
+        <img src="s-10.png" /> 
     </p>
     <p>
         To take advantage of the Skyline summary graphs for viewing individual targets, do the following:
@@ -324,7 +324,7 @@ <h1>Importing Mass Spectrometer Runs</h1>
         The Skyline window should now look like this:
     </p>
     <p>
-        <img src="image-12.png" />
+        <img src="s-11.png" />
     </p>
     <h1>Checking Peak Integration</h1>
     <p>
@@ -342,7 +342,7 @@ <h1>Checking Peak Integration</h1>
         “DoubleBlank” implies that neither is present in the sample. The chromatogram graph now shows you what peaks Skyline had to choose from:
     </p>
     <p>
-        <img src="image-13.png" />
+        <img src="s-12.png" />
     </p>
     <ul>
         <li>Click on the bars for the other two outliers in the <b>Retention Times – Replicate Comparison</b> view. </li>
@@ -360,14 +360,14 @@ <h1>Adjusting Peak Integration</h1>
     <ul>
         <li>In the <b>Targets</b> view <b>Replicates</b> dropdown list, select the “DoubleBlank1” replicate.</li>
         <li>Position the mouse cursor below the <b>Retention Time</b> axis (the cursor will change east-west arrows:<img
-                src="image-14.png" />).</li>
+                src="../../shared/vertical-split-cursor-icon.png" />).</li>
         <li>Click below the <b>Retention Time</b> axis at about 2.65 minutes and drag to about 2.75 minutes.</li>
     </ul>
     <p class="keep-next">
         The peak boundaries will change to these new values, and the original range will be marked by a shaded area, as shown below:
     </p>
     <p>
-        <img src="image-15.png" />
+        <img src="s-13.png" />
     </p>
     <p>
         Repeat the steps above for the other two “DoubleBlank” replicates.
@@ -389,7 +389,7 @@ <h1>Preparing for Quantitation</h1>
         The <b>Molecule Settings</b> form should look like this:
     </p>
     <p>
-        <img src="image-16.png" />
+        <img src="s-14.png" />
     </p>
     <p>
         This experiment uses a linear regression fit, normalizing to the heavy labeled drug. Skyline offers options for weighting across the curve as a
@@ -418,7 +418,7 @@ <h1>Declaring Sample Types for Calibration Curve Display</h1>
         The <b>Document Grid</b> should look like this:
     </p>
     <p>
-        <img src="image-17.png" />
+        <img src="s-15.png" />
     </p>
     <ul>
         <li>Expand the <b>Document Grid</b> if needed so that you can see all the replicates at once if you screen is large enough.</li>
@@ -626,7 +626,7 @@ <h1>Declaring Sample Types for Calibration Curve Display</h1>
         The <b>Document Grid</b> should look like this when done:
     </p>
     <p>
-        <img src="image-18.png" />
+        <img src="s-16.png" />
     </p>
     <h1>Inspecting the Calibration Curve</h1>
     <p>
@@ -640,7 +640,7 @@ <h1>Inspecting the Calibration Curve</h1>
         The <b>Calibration Curve</b> form should appear looking like this:
     </p>
     <p>
-        <img src="image-19.png" />
+        <img src="s-17.png" />
     </p>
     <p>
         The note about the selected replicate missing transitions is expected, when the currently selected replicate is a double blank. 
@@ -657,7 +657,7 @@ <h1>Inspecting the Calibration Curve</h1>
         <li>On the <b>View</b> menu, click <b>Document Grid</b>.</li>
         <li>Click on <b>Reports</b> in the upper left corner of the grid, and then click <b>Replicates</b>.</li>
         <li>Click again on <b>Reports</b> in the upper left corner of the grid, and then click <b>Customize Report</b>.</li>
-        <li>Click on the search button <img src="image-20.png" /> and enter “accuracy” into the <b>Find what</b> field.</li>
+        <li>Click on the search button <img src="../../shared/black-binocular-button.png" /> and enter “accuracy” into the <b>Find what</b> field.</li>
         <li>Click the <b>Find Next</b> button.</li>
         <li>Click the <b>Close</b> button on the <b>Find Column</b> form. </li>
         <li>In the <b>Customize Report</b> form, <b>Accuracy</b> should be highlighted under the
@@ -672,7 +672,7 @@ <h1>Inspecting the Calibration Curve</h1>
         The <b>Document Grid</b> should now look like this:
     </p>
     <p>
-        <img src="image-21.png" />
+        <img src="s-18.png" />
     </p>
     <p>
         The FDA Guidance on which this assay was based states that calibration points should have bias &lt; 15% (accuracy between 85% and 115%) between
@@ -692,7 +692,7 @@ <h1>Inspecting the Calibration Curve</h1>
         excluding the outlier “Cal_5” values. 
     </p>
     <p>
-        <img src="image-22.png" />
+        <img src="s-19.png" />
     </p>
     <p>
         Next you should import the rest of the unknowns using the following steps:
@@ -721,7 +721,7 @@ <h1>Inspecting the Calibration Curve</h1>
         The <b>Document Grid</b> should look like this:
     </p>
     <p>
-        <img src="image-23.png" />
+        <img src="s-20.png" />
     </p>
     <p>
         After removal of the two “Cal_5” datapoints, further exploration of the data reveals that one of the “Cal_7” points has accuracy &lt;85% and
@@ -740,7 +740,7 @@ <h1>Inspecting the Calibration Curve</h1>
         The calibration curve should look like this:
     </p>
     <p>
-        <img src="image-24.png" />
+        <img src="s-21.png" />
     </p>
     <p>
         This presents a view which allows you to see at a glance that the samples mostly fall between “Cal_2” (20 uM) and “Cal_3” (100 uM), and well
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/zh-CHS/image-2.png b/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/zh-CHS/s-1.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/zh-CHS/image-2.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/zh-CHS/s-1.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/zh-CHS/image-11.png b/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/zh-CHS/s-10.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/zh-CHS/image-11.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/zh-CHS/s-10.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/zh-CHS/image-12.png b/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/zh-CHS/s-11.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/zh-CHS/image-12.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/zh-CHS/s-11.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/zh-CHS/image-13.png b/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/zh-CHS/s-12.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/zh-CHS/image-13.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/zh-CHS/s-12.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/zh-CHS/image-15.png b/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/zh-CHS/s-13.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/zh-CHS/image-15.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/zh-CHS/s-13.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/zh-CHS/image-16.png b/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/zh-CHS/s-14.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/zh-CHS/image-16.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/zh-CHS/s-14.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/zh-CHS/image-17.png b/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/zh-CHS/s-15.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/zh-CHS/image-17.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/zh-CHS/s-15.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/zh-CHS/image-18.png b/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/zh-CHS/s-16.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/zh-CHS/image-18.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/zh-CHS/s-16.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/zh-CHS/image-19.png b/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/zh-CHS/s-17.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/zh-CHS/image-19.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/zh-CHS/s-17.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/zh-CHS/image-21.png b/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/zh-CHS/s-18.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/zh-CHS/image-21.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/zh-CHS/s-18.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/zh-CHS/image-22.png b/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/zh-CHS/s-19.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/zh-CHS/image-22.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/zh-CHS/s-19.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/zh-CHS/image-3.png b/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/zh-CHS/s-2.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/zh-CHS/image-3.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/zh-CHS/s-2.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/zh-CHS/image-23.png b/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/zh-CHS/s-20.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/zh-CHS/image-23.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/zh-CHS/s-20.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/zh-CHS/image-24.png b/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/zh-CHS/s-21.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/zh-CHS/image-24.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/zh-CHS/s-21.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/zh-CHS/image-4.png b/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/zh-CHS/s-3.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/zh-CHS/image-4.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/zh-CHS/s-3.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/zh-CHS/image-5.png b/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/zh-CHS/s-4.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/zh-CHS/image-5.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/zh-CHS/s-4.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/zh-CHS/image-6.png b/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/zh-CHS/s-5.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/zh-CHS/image-6.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/zh-CHS/s-5.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/zh-CHS/image-7.png b/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/zh-CHS/s-6.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/zh-CHS/image-7.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/zh-CHS/s-6.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/zh-CHS/image-8.png b/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/zh-CHS/s-7.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/zh-CHS/image-8.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/zh-CHS/s-7.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/zh-CHS/image-9.png b/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/zh-CHS/s-8.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/zh-CHS/image-9.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/zh-CHS/s-8.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/zh-CHS/image-10.png b/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/zh-CHS/s-9.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/zh-CHS/image-10.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/zh-CHS/s-9.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/zh-CHS/image-0.png b/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/zh-CHS/s-96-well-plate-layout.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/zh-CHS/image-0.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/zh-CHS/s-96-well-plate-layout.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/zh-CHS/image-1.png b/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/zh-CHS/s-injection-order.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/zh-CHS/image-1.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeQuantification/zh-CHS/s-injection-order.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/index.html b/pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/index.html
index ed973ce4e5..bd69a85b11 100644
--- a/pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/index.html
+++ b/pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/index.html
@@ -98,7 +98,7 @@ <h1>Calibrating an iRT Calculator</h1>
         The form looking like this:
     </p>
     <p>
-        <img src="image-0.png" />
+        <img src="s-1.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -114,7 +114,7 @@ <h1>Calibrating an iRT Calculator</h1>
         Skyline should present the <b>Retention Times</b> view showing a graph like the one below:
     </p>
     <p>
-        <img src="image-1.png" />
+        <img src="s-2.png" />
     </p>
     <p>
         This gives you a top level view of when each peptide eluted, on average, over the 30-minute gradient. Continue reviewing the data by doing the
@@ -131,7 +131,7 @@ <h1>Calibrating an iRT Calculator</h1>
         Skyline should now look something like this:
     </p>
     <p>
-        <img src="image-2.png" />
+        <img src="s-3.png" />
     </p>
     <p>
         Use the down-arrow key to review each of the 11 peptides in the Biognosys standard mix, making sure that the integration looks correct, and
@@ -148,7 +148,7 @@ <h1>Calibrating an iRT Calculator</h1>
     <ul>
         <li>On the <b>Settings</b> menu, click <b>Peptide Settings</b>.</li>
         <li>Click the <b>Prediction</b> tab.</li>
-        <li>Click the <img src="image-3.png" /> (<b>Retention time calculators</b>) button, and click <b>Add</b> in the menu it
+        <li>Click the <img src="../../shared/calculator-button.png" /> (<b>Retention time calculators</b>) button, and click <b>Add</b> in the menu it
             shows.</li>
         <li>In the <b>Name</b> field of the <b>Edit iRT Calculator</b> form, enter ‘iRT-C18’.</li>
         <li>Click the <b>Create</b> button.</li>
@@ -164,7 +164,7 @@ <h1>Calibrating an iRT Calculator</h1>
         The <b>Calibrate iRT Calculator</b> form should now look something like:
     </p>
     <p>
-        <img src="image-4.png" />
+        <img src="s-4.png" />
     </p>
     <ul>
         <li>Click the <b>Graph</b> button to the right of the <b>Calculate from</b> dropdown list to see a plot of the line from
@@ -182,7 +182,7 @@ <h1>Calibrating an iRT Calculator</h1>
         The <b>Edit iRT Calculator</b> form should now look something like:
     </p>
     <p>
-        <img src="image-5.png" />
+        <img src="s-5.png" />
     </p>
     <p>
         That is it. You have calibrated a new set of iRT standards with measured data. In this case, however, the team at Biognosys has already
@@ -190,7 +190,7 @@ <h1>Calibrating an iRT Calculator</h1>
         calibration with the canonical one, but first to see how close the two are, do the following:
     </p>
     <ul>
-        <li>Move the mouse cursor below the <b>iRT standards</b> grid until you see a horizontal split cursor <img src="image-6.png" />.
+        <li>Move the mouse cursor below the <b>iRT standards</b> grid until you see a horizontal split cursor <img src="../../shared/horizontal-split-cursor-icon.png" />.
         </li>
         <li>Click and drag the splitter until you can see all 11 standard peptides in the grid.</li>
         <li>In the dropdown list above the grid switch between the two choices:<ul>
@@ -229,7 +229,7 @@ <h1>Calibrating an iRT Calculator</h1>
         Skyline should present a graph that looks like the one below:
     </p>
     <p>
-        <img src="image-7.png" />
+        <img src="s-6.png" />
     </p>
     <p>
         In the upper left corner of the graph, you will see a Pearson’s Correlation Coefficient of 0.9991. If you do not see iRT-C18 below the x-axis,
@@ -269,7 +269,7 @@ <h1>Adding iRT Values for New Targeted Peptides</h1>
         The <b>Targets</b> view should look something like this:
     </p>
     <p>
-        <img src="image-8.png" />
+        <img src="s-7.png" />
     </p>
     <ul>
         <li>Save this document as ‘iRT Human+Standard.sky’.</li>
@@ -311,7 +311,7 @@ <h2>Creating an iRT Acquisition Method</h2>
         The form should look like the following:
     </p>
     <p>
-        <img src="image-9.png" />
+        <img src="s-8.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -331,7 +331,7 @@ <h2>Creating an iRT Acquisition Method</h2>
         The <b>Export Transition List</b> form should now look like:
     </p>
     <p>
-        <img src="image-10.png" />
+        <img src="s-9.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -385,7 +385,7 @@ <h2>Importing and Reviewing the Data</h2>
         Once the data has finished importing, you should see a graph like:
     </p>
     <p>
-        <img src="image-11.png" />
+        <img src="s-10.png" />
     </p>
     <p>
         The cluster of purple points, on the left side of the graph indicates that these peptides do not yet have calibrated iRT values. Before
@@ -411,7 +411,7 @@ <h2>Importing and Reviewing the Data</h2>
         The <b>Find</b> form should look like:
     </p>
     <p>
-        <img src="image-12.png" />
+        <img src="s-11.png" />
     </p>
     <ul>
         <li>Click the <b>Find All</b> button.</li>
@@ -422,7 +422,7 @@ <h2>Importing and Reviewing the Data</h2>
         transitions:
     </p>
     <p>
-        <img src="image-13.png" />
+        <img src="s-12.png" />
     </p>
     <p>
         To review the peptides containing these peaks, do the following:
@@ -439,10 +439,10 @@ <h2>Importing and Reviewing the Data</h2>
     <table class="comp-fig">
         <tr>
             <td class="comp-fig">
-                <img src="image-14.png" />
+                <img src="s-13.png" />
             </td>
             <td class="comp-fig">
-                <img src="image-15.png" />
+                <img src="s-14.png" />
             </td>
         </tr>
     </table>
@@ -474,7 +474,7 @@ <h2>Calculating iRT Values</h2>
         Skyline will show you the following informational message:
     </p>
     <p>
-        <img src="image-16.png" />
+        <img src="s-15.png" />
     </p>
     <p>
         Note that in producing iRT values for the two runs, Skyline has performed a separate linear regression for each run. It uses the linear
@@ -496,7 +496,7 @@ <h2>Calculating iRT Values</h2>
         The <b>Edit iRT Calculator</b> form should now look like:
     </p>
     <p>
-        <img src="image-17.png" />
+        <img src="s-16.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -505,7 +505,7 @@ <h2>Calculating iRT Values</h2>
         The <b>Retention Times</b> view should change to look like this:
     </p>
     <p>
-        <img src="image-18.png" />
+        <img src="s-17.png" />
     </p>
     <p>
         You have just calibrated iRT-C18 values for 148 new human peptides, using data acquired on a 30-minute gradient.
@@ -556,7 +556,7 @@ <h1>Using iRT to Schedule New Acquisition</h1>
         The <b>Peptide Settings</b> form should look like this:
     </p>
     <p>
-        <img src="image-19.png" />
+        <img src="s-18.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -569,7 +569,7 @@ <h1>Using iRT to Schedule New Acquisition</h1>
         When the data has finished importing, the <b>Retention Times</b> regression graph will be shown as:
     </p>
     <p>
-        <img src="image-20.png" />
+        <img src="s-19.png" />
     </p>
     <p>
         You can see that the times for the standard peptides now range from about 15 to 65 minutes, and none of the target peptides were measured in
@@ -588,7 +588,7 @@ <h1>Exporting a Scheduled Method Using an iRT Predictor</h1>
         below:
     </p>
     <p>
-        <img src="image-21.png" />
+        <img src="s-20.png" />
     </p>
     <p>
         If you do not see all three lines shown in the graph above, you can do the following:
@@ -604,7 +604,7 @@ <h1>Exporting a Scheduled Method Using an iRT Predictor</h1>
         required to capture the entire peaks of a percentage of target peptides is approximated by the function below:
     </p>
     <p>
-        <img src="image-22.png" />
+        <img src="s-window-size-formula.png" />
     </p>
     <p>
         Where “z” is a critical value for the number of standard deviations within which the desired percentage fall in a normal distribution, e.g. 95%
@@ -629,7 +629,7 @@ <h1>Exporting a Scheduled Method Using an iRT Predictor</h1>
         The <b>Export Transition List</b> form should look like:
     </p>
     <p>
-        <img src="image-23.png" />
+        <img src="s-21.png" />
     </p>
     <p>
         You could also simply click the <b>Single method</b> option, but the fact that the form shows “<b>Methods</b>: 1” confirms
@@ -677,7 +677,7 @@ <h1>Reviewing Scheduled Data</h1>
         When the data has finished loading, the <b>Retention Times</b> view should present a graph like:
     </p>
     <p>
-        <img src="image-24.png" /> 
+        <img src="s-22.png" /> 
     </p>
     <p>
         From this graph, it is immediately obvious that there are 2 outlier peptides, which could be caused by miss-integrated peaks in the current
@@ -701,7 +701,7 @@ <h1>Reviewing Scheduled Data</h1>
         The <b>Retention Times</b> graph should now look like:
     </p>
     <p>
-        <img src="image-25.png" />
+        <img src="s-23.png" />
     </p>
     <p>
         You can now click on each outlier point, causing Skyline to select it in the peptide view. Then, press Esc to give focus back to the main
@@ -737,7 +737,7 @@ <h1>Reviewing Scheduled Data</h1>
         The <b>Retention Times</b> graph should now look like this:
     </p>
     <p>
-        <img src="image-26.png" />
+        <img src="s-24.png" />
     </p>
     <p>
         This gives you a clearer sense that measured times are varying within +/- 2 minutes of the predicted times. What retention time scheduling
@@ -752,7 +752,7 @@ <h1>Reviewing Scheduled Data</h1>
         present graphs like the one below:
     </p>
     <p>
-        <img src="image-27.png" />
+        <img src="s-25.png" />
     </p>
     <p>
         You will see that all peptides, except the standards, now have light and heavy precursor pairs and generally more points across each peak than
@@ -813,7 +813,7 @@ <h1>Calculating iRT Values from MS/MS Spectra</h1>
         The <b>Add Spectral Library</b> form should look like this:
     </p>
     <p>
-        <img src="image-28.png" />
+        <img src="s-26.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -822,7 +822,7 @@ <h1>Calculating iRT Values from MS/MS Spectra</h1>
         Skyline should present a form that looks like this:
     </p>
     <p>
-        <img src="image-29.png" />
+        <img src="s-27.png" />
     </p>
     <p>
         The form tells you that Skyline was able to calculate a single valid regressions for both DDA runs in the library. When possible, Skyline will
@@ -867,7 +867,7 @@ <h1>Converting MS/MS Scan Times to Chromatogram Peak Times</h1>
         The Skyline window should look something like:
     </p>
     <p>
-        <img src="image-30.png" />
+        <img src="s-28.png" />
     </p>
     <p>
         You can double-click in the title bar of the <b>Retention Times</b> view to get a better look at the graph, and see that the
@@ -895,7 +895,7 @@ <h1>Converting MS/MS Scan Times to Chromatogram Peak Times</h1>
         Skyline presents a form that looks like this:
     </p>
     <p>
-        <img src="image-31.png" />
+        <img src="s-29.png" />
     </p>
     <p>
         To tell you that it will replace the 558 iRT values you added in the previous section. Now that you are using chromatogram peak times, you also
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/image-0.png b/pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/s-1.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/image-0.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/s-1.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/image-11.png b/pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/s-10.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/image-11.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/s-10.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/image-12.png b/pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/s-11.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/image-12.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/s-11.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/image-13.png b/pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/s-12.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/image-13.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/s-12.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/image-14.png b/pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/s-13.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/image-14.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/s-13.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/image-15.png b/pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/s-14.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/image-15.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/s-14.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/image-16.png b/pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/s-15.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/image-16.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/s-15.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/image-17.png b/pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/s-16.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/image-17.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/s-16.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/image-18.png b/pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/s-17.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/image-18.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/s-17.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/image-19.png b/pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/s-18.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/image-19.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/s-18.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/image-20.png b/pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/s-19.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/image-20.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/s-19.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/image-1.png b/pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/s-2.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/image-1.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/s-2.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/image-21.png b/pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/s-20.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/image-21.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/s-20.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/image-23.png b/pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/s-21.png
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rename from pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/image-23.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/s-21.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/image-24.png b/pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/s-22.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/image-24.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/s-22.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/image-25.png b/pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/s-23.png
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rename from pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/image-25.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/s-23.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/image-26.png b/pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/s-24.png
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rename from pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/image-26.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/s-24.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/image-27.png b/pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/s-25.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/image-27.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/s-25.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/image-28.png b/pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/s-26.png
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rename from pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/image-28.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/s-26.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/image-29.png b/pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/s-27.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/image-29.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/s-27.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/image-30.png b/pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/s-28.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/image-30.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/s-28.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/image-31.png b/pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/s-29.png
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rename from pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/image-31.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/s-29.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/image-2.png b/pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/s-3.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/image-2.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/s-3.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/image-4.png b/pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/s-4.png
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rename from pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/image-4.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/s-4.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/image-5.png b/pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/s-5.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/image-5.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/s-5.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/image-7.png b/pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/s-6.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/image-7.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/s-6.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/image-8.png b/pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/s-7.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/image-8.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/s-7.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/image-9.png b/pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/s-8.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/image-9.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/s-8.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/image-10.png b/pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/s-9.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/image-10.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/s-9.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/image-22.png b/pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/s-window-size-formula.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/image-22.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/s-window-size-formula.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/index.html b/pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/index.html
index f505c408fb..b8c1369393 100644
--- a/pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/index.html
+++ b/pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/index.html
@@ -75,7 +75,7 @@ <h1>iRTカルキュレータの校正</h1>
         フォームは以下のようになります。
     </p>
     <p>
-        <img src="image-0.png" />
+        <img src="s-1.png" />
     </p>
     <ul>
         <li>[ <b>OK</b> ] ボタンをクリックします。</li>
@@ -91,7 +91,7 @@ <h1>iRTカルキュレータの校正</h1>
         Skylineに、以下のようなグラフを示す [ <b>保持時間</b> ] が表示されます。
     </p>
     <p>
-        <img src="image-1.png" />
+        <img src="s-2.png" />
     </p>
     <p>
         ここでは、30分のグラジエント条件で各ペプチドが溶出した平均時間のトップレベルビューを示しています。以下の操作を行ってデータの確認を続けていきます。
@@ -106,7 +106,7 @@ <h1>iRTカルキュレータの校正</h1>
         Skylineは、以下のようになります。
     </p>
     <p>
-        <img src="image-2.png" />
+        <img src="s-3.png" />
     </p>
     <p>
         下向き矢印キーを使用してBiognosys社標準混合品内の11個のペプチドそれぞれについて、<br />積分が正しく表示されているか、繰り返し測定がいずれも同様の保持時間で積分ピークを表示しているかを確認します。これらのペプチドについては自動積分が良好になされているため、手動で変更を行う必要はありません。本チュートリアルには、2回の繰り返し測定のみが含まれています。自分で実際に新しいiRTカルキュレータを校正する場合には、ペプチドの平均保持時間の推定を向上させるため、より多くの繰り返し測定データを使用するとよいでしょう。保持時間のカルキュレータを校正する際に、[
@@ -118,7 +118,7 @@ <h1>iRTカルキュレータの校正</h1>
     <ul>
         <li>[ <b>設定</b> ] メニューで [ <b>ペプチド設定</b> ] をクリックします。</li>
         <li>[ <b>予測</b> ] タブをクリックします。</li>
-        <li>次に <img src="image-3.png" />（<b>保持時間カルキュレータ</b>）ボタンをクリックし、メニューの [ <b>追加</b> ] をクリックします。</li>
+        <li>次に <img src="../../shared/calculator-button.png" />（<b>保持時間カルキュレータ</b>）ボタンをクリックし、メニューの [ <b>追加</b> ] をクリックします。</li>
         <li>[ <b>iRTカルキュレータを編集</b> ] フォームの [ <b>名前</b> ] フィールドに、「iRT-C18」と入力します。</li>
         <li>[ <b>作成</b> ] ボタンをクリックします。</li>
         <li>[ <b>iRTデータベースを作成</b> ] フォームで、本チュートリアル用に作成したiRTフォルダに移動します（必要な場合）。</li>
@@ -133,7 +133,7 @@ <h1>iRTカルキュレータの校正</h1>
         [ <b>iRTカルキュレータを校正</b> ] フォームは以下のようになります。
     </p>
     <p>
-        <img src="image-4.png" />
+        <img src="s-4.png" />
     </p>
     <ul>
         <li>[ <b>計算</b> ] ドロップダウンリストの右側にある [ <b>グラフ化</b> ] ボタンをクリックし、以下に示す式「iRT = 6.7701 * RT – 105.6630」が導き出された線のプロットを確認します。</li>
@@ -147,14 +147,14 @@ <h1>iRTカルキュレータの校正</h1>
         [ <b>iRTカルキュレータを編集</b> ] フォームは以下のようになります。
     </p>
     <p>
-        <img src="image-5.png" />
+        <img src="s-5.png" />
     </p>
     <p class="keep-next">
         
         以上です。測定したデータを使って新たなiRT標準セットが校正されました。ただしこの場合は、Biognosys社のチームが、おそらく2回以上の繰り返し測定を使用してすでに独自の標準混合品を校正しています。そこで本チュートリアルでは、この校正を単に標準と置き換えますが、まずは2回の繰り返し測定値がどれだけ近いかを確認します。
     </p>
     <ul>
-        <li>[ <b>iRT標準</b> ] グリッドの下に水平方向のスプリットカーソル <img src="image-6.png" />が表示されるまでマウスカーソルを移動させます。</li>
+        <li>[ <b>iRT標準</b> ] グリッドの下に水平方向のスプリットカーソル <img src="../../shared/horizontal-split-cursor-icon.png" />が表示されるまでマウスカーソルを移動させます。</li>
         <li>11個の標準ペプチドすべてがグリッドに表示されるまでスプリッターをクリックしてドラッグします。</li>
         <li>グリッド上のドロップダウンリストで以下の2つの選択を切り替えます。<ul>
                 <li><b>Biognosys (30 min cal)</b>－今作成した値。</li>
@@ -188,7 +188,7 @@ <h1>iRTカルキュレータの校正</h1>
         Skylineに以下のようなグラフが表示されます。
     </p>
     <p>
-        <img src="image-7.png" />
+        <img src="s-6.png" />
     </p>
     <p>
         グラフの左上隅に、ピアソンの相関係数0.9991が表示されます。X軸の下にiRT-C18が表示されていない場合は、以下の操作を行う必要があります。
@@ -223,7 +223,7 @@ <h1>新しいターゲットペプチドへのiRT値の追加</h1>
         [ <b>ターゲット</b> ] 表示は以下のようになります。
     </p>
     <p>
-        <img src="image-8.png" />
+        <img src="s-7.png" />
     </p>
     <ul>
         <li>このドキュメントを「iRT Human+Standard.sky」という名前で保存します。</li>
@@ -261,7 +261,7 @@ <h2>iRT取得メソッドの作成</h2>
         フォームは以下のようになります。
     </p>
     <p>
-        <img src="image-9.png" />
+        <img src="s-8.png" />
     </p>
     <ul>
         <li>[ <b>OK</b> ] ボタンをクリックします。</li>
@@ -281,7 +281,7 @@ <h2>iRT取得メソッドの作成</h2>
         [ <b>トランジションリストをエクスポート</b> ] フォームは以下のようになります。
     </p>
     <p>
-        <img src="image-10.png" />
+        <img src="s-9.png" />
     </p>
     <ul>
         <li>[ <b>OK</b> ] ボタンをクリックします。</li>
@@ -324,7 +324,7 @@ <h2>データのインポートと確認</h2>
         データがインポートを終了すると、以下のようなグラフが表示されます。
     </p>
     <p>
-        <img src="image-11.png" />
+        <img src="s-10.png" />
     </p>
     <p>
         グラフの左側の紫色のポイントのクラスタは、これらのペプチドにまだ校正されたiRT値がないことを示しています。iRT値を計算する前に、ピーク積分を確認しておくとよいでしょう。<br />実際に自分でiRT値を校正している場合には、すべてのペプチドに対して十分に慎重に校正してください。
@@ -345,7 +345,7 @@ <h2>データのインポートと確認</h2>
         [ <b>検索</b> ] フォームは以下のようになります。
     </p>
     <p>
-        <img src="image-12.png" />
+        <img src="s-11.png" />
     </p>
     <ul>
         <li>[ <b>すべて検索</b> ] ボタンをクリックします。</li>
@@ -355,7 +355,7 @@ <h2>データのインポートと確認</h2>
         Skylineウィンドウの下には、6つの積分されていないトランジションを示す [ <b>結果を検索</b> ] が表示されます。
     </p>
     <p>
-        <img src="image-13.png" />
+        <img src="s-12.png" />
     </p>
     <p>
         これらのピークを含むペプチドを確認するには、以下の操作を行います。
@@ -371,10 +371,10 @@ <h2>データのインポートと確認</h2>
     <table class="comp-fig">
         <tr>
             <td class="comp-fig">
-                <img src="image-14.png" />
+                <img src="s-13.png" />
             </td>
             <td class="comp-fig">
-                <img src="image-15.png" />
+                <img src="s-14.png" />
             </td>
         </tr>
     </table>
@@ -403,7 +403,7 @@ <h2>iRT値の計算</h2>
         Skylineに以下の情報メッセージが表示されます。
     </p>
     <p>
-        <img src="image-16.png" />
+        <img src="s-15.png" />
     </p>
     <p>
         注：2回の実行に対するiRT値を求めるにあたり、Skylineはそれぞれに個別の線形回帰を行いました。その実行におけるペプチドのiRT値は、それぞれの線形回帰の結果を元に計算されます。複数の測定に同一のペプチドが含まれている場合、Skylineはこれらの最終的に計算されたiRT値の平均値を使用します。これは物理的に保持時間を平均する場合とは非常に異なり、測定全体でのグラジエントの変動も含んだものになります。両実行における回帰グラフは、グリッドの
@@ -422,7 +422,7 @@ <h2>iRT値の計算</h2>
         [ <b>iRTカルキュレータを編集</b> ] フォームは以下のようになります。
     </p>
     <p>
-        <img src="image-17.png" />
+        <img src="s-16.png" />
     </p>
     <ul>
         <li>[ <b>OK</b> ] ボタンをクリックします。</li>
@@ -431,7 +431,7 @@ <h2>iRT値の計算</h2>
         [ <b>保持時間</b> ] 表示は以下のように変わります。
     </p>
     <p>
-        <img src="image-18.png" />
+        <img src="s-17.png" />
     </p>
     <p>
         以上で、30分のグラジエント条件で取得されたデータを使用して、148個の新しいヒトのペプチドのiRT-C18値の校正が完了しました。
@@ -478,7 +478,7 @@ <h1>iRT値を使用した新規取得のスケジュール化</h1>
         [ <b>ペプチド設定</b> ] フォームは以下のようになります。
     </p>
     <p>
-        <img src="image-19.png" />
+        <img src="s-18.png" />
     </p>
     <ul>
         <li>[ <b>OK</b> ] ボタンをクリックします。</li>
@@ -490,7 +490,7 @@ <h1>iRT値を使用した新規取得のスケジュール化</h1>
         データがインポートを終了すると、[ <b>保持時間</b> ] 回帰グラフが以下のように表示されます。
     </p>
     <p>
-        <img src="image-20.png" />
+        <img src="s-19.png" />
     </p>
     <p>
         標準ペプチドの保持時間が約15分～65分の範囲となり、この実行においてはターゲットペプチドが一切測定されていません。ただし、これでこの新しいグラジエント条件で測定が可能になりました。
@@ -506,7 +506,7 @@ <h1>iRT Predictorによるスケジュール化されたメソッドのエクス
         [ <b>保持時間</b> ] 表示に新たな [ <b>スケジュール</b> ] タブが含まれ、以下のようなグラフが表示されます。
     </p>
     <p>
-        <img src="image-21.png" />
+        <img src="s-20.png" />
     </p>
     <p>
         上記グラフ内に3本の線すべてが表示されない場合は、以下の操作を行います。
@@ -520,7 +520,7 @@ <h1>iRT Predictorによるスケジュール化されたメソッドのエクス
         このグラフから、スケジュールに対する時間ウィンドウサイズの影響が確認できます。時間ウィンドウが小さいほど、任意の時間内で同時に測定されるトランジションの数は少なくなります。これにより、特定のドウェル時間での1回のインジェクションでより多くのトランジションが測定可能となります。ターゲットペプチドのピーク全体を割合で捉えるために必要なウィンドウサイズは、以下の関数によって概算されます。
     </p>
     <p>
-        <img src="image-22.png" />
+        <img src="s-window-size-formula.png" />
     </p>
     <p>
         ここで「z」は正規分布において希望するパーセント内に収まる標準偏差数の重要な値であり、例えば95%であれば1.96となります。保持時間の予測値が完全でありピーク幅または保持時間に分散がない場合、必要とされるウィンドウサイズはピーク幅と同じになります。一方、保持時間の予測値が完全でも、ピーク幅または保持時間の分散があった場合には、必要なウィンドウサイズが広がります。最後に、予測誤差によってサイズはさらに広がります。保持時間を<br />予測する最新の手法を用いても、ターゲットシステムにおいてスケジュール化された取得前にスケジュール化されていない測定を1回行うだけでは完璧ではないということは、注目すべきです。ここでは平均保持時間を予測しようとしています。この1回の測定では、すべてのペプチドのうち約5%は、平均値から標準偏差の2倍以上となることになります。
@@ -538,7 +538,7 @@ <h1>iRT Predictorによるスケジュール化されたメソッドのエクス
         [ <b>トランジションリストをエクスポート</b> ] フォームは以下のようになります。
     </p>
     <p>
-        <img src="image-23.png" />
+        <img src="s-21.png" />
     </p>
     <p>
         または単に [ <b>シングルメソッド</b> ] オプションを選択することも可能ですが、このフォームが [ <b>メソッド：</b> 1 ]
@@ -581,7 +581,7 @@ <h1>スケジュール化されたデータの確認</h1>
         データが読み込みを終了すると、[ <b>保持時間</b> ] 表示に以下のようなグラフが表示されます。
     </p>
     <p>
-        <img src="image-24.png" /> 
+        <img src="s-22.png" /> 
     </p>
     <p>
         このグラフから、2つの「異常値」をもつペプチドがあることがわかります。これは、現在のデータにあるきちんと積分されていないピーク、またはiRT値が計算された校正データにあるきちんと積分されていないピークによるものである可能性があります。今回の場合は、30分のグラジエントでのiRT校正の間にSkylineが自動的に選択したピークに問題があります。今表示されているデータは、上記で生成したスケジュールメソッドにより実際に収集されたものではないことに注意することが重要です。メソッドが実際に収集したデータである場合は、「異常値」を示したペプチドのクロマトグラムにここで検出されたピークが含まれることはありません。このデータは、本チュートリアルの中では割愛しましたが、校正データをより詳細に確認した後に作成されたスケジュールメソッドで収集されました。
@@ -598,7 +598,7 @@ <h1>スケジュール化されたデータの確認</h1>
         [ <b>保持時間</b> ] グラフは以下のようになります。
     </p>
     <p>
-        <img src="image-25.png" />
+        <img src="s-23.png" />
     </p>
     <p>
         ここで各「異常値」をクリックすると、Skylineがペプチド表示でその値を選択します。Escを押してメインウィンドウに戻り、Ctrl+Cを押して異常値となったペプチド標識をコピーします。<br />これらを別のエディタで収集して後で確認したり、または先ほど作成した「iRT
@@ -627,7 +627,7 @@ <h1>スケジュール化されたデータの確認</h1>
         [ <b>保持時間</b> ] グラフは以下のようになります。
     </p>
     <p>
-        <img src="image-26.png" />
+        <img src="s-24.png" />
     </p>
     <p>
         これによって、測定時間が予測時間の+/-2分で変化することがより明らかになります。この<br />場合、どのような保持時間スケジュールウィンドウを使用すればよいのでしょうか？実験では何が使用されたのでしょうか？
@@ -640,7 +640,7 @@ <h1>スケジュール化されたデータの確認</h1>
         次にここで [ <b>ターゲット</b> ] 表示内をクリックし、下向き矢印キーを利用してペプチドクロマトグラムを確認します。Skylineには以下のようなグラフが表示されます。
     </p>
     <p>
-        <img src="image-27.png" />
+        <img src="s-25.png" />
     </p>
     <p>
         標準ペプチドを除くすべてのペプチドにLightとHeavyプリカーサーのペアが見られるようになり、スケジュール化されていないデータと比較すると、概して各ピークでより多くのポイントが見られます。また、Skylineが「予測」とピークの予測時間を示します。
@@ -684,7 +684,7 @@ <h1>MS/MSスペクトルからのiRT値の計算</h1>
         [ <b>スペクトルライブラリを追加</b> ] フォームは以下のようになります。
     </p>
     <p>
-        <img src="image-28.png" />
+        <img src="s-26.png" />
     </p>
     <ul>
         <li>[ <b>OK</b> ] ボタンをクリックします。</li>
@@ -693,7 +693,7 @@ <h1>MS/MSスペクトルからのiRT値の計算</h1>
         Skylineには以下のようなフォームが表示されます。
     </p>
     <p>
-        <img src="image-29.png" />
+        <img src="s-27.png" />
     </p>
     <p>
         このフォームでは、ライブラリ内の2回のDDAの実行に対し、Skylineにて1回の有効な回帰が計算できたことが示されています。可能な場合、Skylineでは実行間で一致するすべてのペプチドを使用して内部実行間回帰が実施されます。これは標準ペプチドのみを使用した回帰よりもうまく行くことが実証されています。この最終的な校正回帰を利用して、Skylineでは新たに558個のペプチドのiRT値が計算されています。内部調整後、Skylineではペプチドに一致したすべてのMS/MSスペクトルに対して時間の中央値を使用します。これによってMS/MSスペクトルに一致した異常値が無意味なiRT値を生じないようにすることができます。また、3つのペプチドについては、クロマトグラムピークを基にしたiRT値の情報がありますので、ここでは無視されます。
@@ -730,7 +730,7 @@ <h1>MS/MSスキャン時間のクロマトグラムピーク時間への変換</
         Skylineは以下のようになります。
     </p>
     <p>
-        <img src="image-30.png" />
+        <img src="s-28.png" />
     </p>
     <p>
         [ <b>保持時間</b> ] 表示のタイトルバーをダブルクリックすると、グラフが見やすくなります。
@@ -752,7 +752,7 @@ <h1>MS/MSスキャン時間のクロマトグラムピーク時間への変換</
         Skylineには以下のようなフォームが表示されます。
     </p>
     <p>
-        <img src="image-31.png" />
+        <img src="s-29.png" />
     </p>
     <p>
         ここでは、これまでのセクションで追加した558個のiRT値が置換されることを示しています。クロマトグラムピーク時間を使用するようになったため、酵母およびヒトのサンプルで共有されている3つのペプチドを置換するオプションや、2つの値の平均値を使用するオプションもあります。
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/invariant.html b/pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/invariant.html
index 4355986755..1de24cb3e9 100644
--- a/pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/invariant.html
+++ b/pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/invariant.html
@@ -98,7 +98,7 @@ <h1>Calibrating an iRT Calculator</h1>
         The form looking like this:
     </p>
     <p>
-        <img src="image-0.png" />
+        <img src="s-1.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -114,7 +114,7 @@ <h1>Calibrating an iRT Calculator</h1>
         Skyline should present the <b>Retention Times</b> view showing a graph like the one below:
     </p>
     <p>
-        <img src="image-1.png" />
+        <img src="s-2.png" />
     </p>
     <p>
         This gives you a top level view of when each peptide eluted, on average, over the 30-minute gradient. Continue reviewing the data by doing the
@@ -131,7 +131,7 @@ <h1>Calibrating an iRT Calculator</h1>
         Skyline should now look something like this:
     </p>
     <p>
-        <img src="image-2.png" />
+        <img src="s-3.png" />
     </p>
     <p>
         Use the down-arrow key to review each of the 11 peptides in the Biognosys standard mix, making sure that the integration looks correct, and
@@ -148,7 +148,7 @@ <h1>Calibrating an iRT Calculator</h1>
     <ul>
         <li>On the <b>Settings</b> menu, click <b>Peptide Settings</b>.</li>
         <li>Click the <b>Prediction</b> tab.</li>
-        <li>Click the <img src="image-3.png" /> (<b>Retention time calculators</b>) button, and click <b>Add</b> in the menu it
+        <li>Click the <img src="../../shared/calculator-button.png" /> (<b>Retention time calculators</b>) button, and click <b>Add</b> in the menu it
             shows.</li>
         <li>In the <b>Name</b> field of the <b>Edit iRT Calculator</b> form, enter ‘iRT-C18’.</li>
         <li>Click the <b>Create</b> button.</li>
@@ -164,7 +164,7 @@ <h1>Calibrating an iRT Calculator</h1>
         The <b>Calibrate iRT Calculator</b> form should now look something like:
     </p>
     <p>
-        <img src="image-4.png" />
+        <img src="s-4.png" />
     </p>
     <ul>
         <li>Click the <b>Graph</b> button to the right of the <b>Calculate from</b> dropdown list to see a plot of the line from
@@ -182,7 +182,7 @@ <h1>Calibrating an iRT Calculator</h1>
         The <b>Edit iRT Calculator</b> form should now look something like:
     </p>
     <p>
-        <img src="image-5.png" />
+        <img src="s-5.png" />
     </p>
     <p>
         That is it. You have calibrated a new set of iRT standards with measured data. In this case, however, the team at Biognosys has already
@@ -190,7 +190,7 @@ <h1>Calibrating an iRT Calculator</h1>
         calibration with the canonical one, but first to see how close the two are, do the following:
     </p>
     <ul>
-        <li>Move the mouse cursor below the <b>iRT standards</b> grid until you see a horizontal split cursor <img src="image-6.png" />.
+        <li>Move the mouse cursor below the <b>iRT standards</b> grid until you see a horizontal split cursor <img src="../../shared/horizontal-split-cursor-icon.png" />.
         </li>
         <li>Click and drag the splitter until you can see all 11 standard peptides in the grid.</li>
         <li>In the dropdown list above the grid switch between the two choices:<ul>
@@ -229,7 +229,7 @@ <h1>Calibrating an iRT Calculator</h1>
         Skyline should present a graph that looks like the one below:
     </p>
     <p>
-        <img src="image-7.png" />
+        <img src="s-6.png" />
     </p>
     <p>
         In the upper left corner of the graph, you will see a Pearson’s Correlation Coefficient of 0.9991. If you do not see iRT-C18 below the x-axis,
@@ -269,7 +269,7 @@ <h1>Adding iRT Values for New Targeted Peptides</h1>
         The <b>Targets</b> view should look something like this:
     </p>
     <p>
-        <img src="image-8.png" />
+        <img src="s-7.png" />
     </p>
     <ul>
         <li>Save this document as ‘iRT Human+Standard.sky’.</li>
@@ -311,7 +311,7 @@ <h2>Creating an iRT Acquisition Method</h2>
         The form should look like the following:
     </p>
     <p>
-        <img src="image-9.png" />
+        <img src="s-8.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -331,7 +331,7 @@ <h2>Creating an iRT Acquisition Method</h2>
         The <b>Export Transition List</b> form should now look like:
     </p>
     <p>
-        <img src="image-10.png" />
+        <img src="s-9.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -385,7 +385,7 @@ <h2>Importing and Reviewing the Data</h2>
         Once the data has finished importing, you should see a graph like:
     </p>
     <p>
-        <img src="image-11.png" />
+        <img src="s-10.png" />
     </p>
     <p>
         The cluster of purple points, on the left side of the graph indicates that these peptides do not yet have calibrated iRT values. Before
@@ -411,7 +411,7 @@ <h2>Importing and Reviewing the Data</h2>
         The <b>Find</b> form should look like:
     </p>
     <p>
-        <img src="image-12.png" />
+        <img src="s-11.png" />
     </p>
     <ul>
         <li>Click the <b>Find All</b> button.</li>
@@ -422,7 +422,7 @@ <h2>Importing and Reviewing the Data</h2>
         transitions:
     </p>
     <p>
-        <img src="image-13.png" />
+        <img src="s-12.png" />
     </p>
     <p>
         To review the peptides containing these peaks, do the following:
@@ -439,10 +439,10 @@ <h2>Importing and Reviewing the Data</h2>
     <table class="comp-fig">
         <tr>
             <td class="comp-fig">
-                <img src="image-14.png" />
+                <img src="s-13.png" />
             </td>
             <td class="comp-fig">
-                <img src="image-15.png" />
+                <img src="s-14.png" />
             </td>
         </tr>
     </table>
@@ -474,7 +474,7 @@ <h2>Calculating iRT Values</h2>
         Skyline will show you the following informational message:
     </p>
     <p>
-        <img src="image-16.png" />
+        <img src="s-15.png" />
     </p>
     <p>
         Note that in producing iRT values for the two runs, Skyline has performed a separate linear regression for each run. It uses the linear
@@ -496,7 +496,7 @@ <h2>Calculating iRT Values</h2>
         The <b>Edit iRT Calculator</b> form should now look like:
     </p>
     <p>
-        <img src="image-17.png" />
+        <img src="s-16.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -505,7 +505,7 @@ <h2>Calculating iRT Values</h2>
         The <b>Retention Times</b> view should change to look like this:
     </p>
     <p>
-        <img src="image-18.png" />
+        <img src="s-17.png" />
     </p>
     <p>
         You have just calibrated iRT-C18 values for 148 new human peptides, using data acquired on a 30-minute gradient.
@@ -556,7 +556,7 @@ <h1>Using iRT to Schedule New Acquisition</h1>
         The <b>Peptide Settings</b> form should look like this:
     </p>
     <p>
-        <img src="image-19.png" />
+        <img src="s-18.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -569,7 +569,7 @@ <h1>Using iRT to Schedule New Acquisition</h1>
         When the data has finished importing, the <b>Retention Times</b> regression graph will be shown as:
     </p>
     <p>
-        <img src="image-20.png" />
+        <img src="s-19.png" />
     </p>
     <p>
         You can see that the times for the standard peptides now range from about 15 to 65 minutes, and none of the target peptides were measured in
@@ -588,7 +588,7 @@ <h1>Exporting a Scheduled Method Using an iRT Predictor</h1>
         below:
     </p>
     <p>
-        <img src="image-21.png" />
+        <img src="s-20.png" />
     </p>
     <p>
         If you do not see all three lines shown in the graph above, you can do the following:
@@ -604,7 +604,7 @@ <h1>Exporting a Scheduled Method Using an iRT Predictor</h1>
         required to capture the entire peaks of a percentage of target peptides is approximated by the function below:
     </p>
     <p>
-        <img src="image-22.png" />
+        <img src="s-window-size-formula.png" />
     </p>
     <p>
         Where “z” is a critical value for the number of standard deviations within which the desired percentage fall in a normal distribution, e.g. 95%
@@ -629,7 +629,7 @@ <h1>Exporting a Scheduled Method Using an iRT Predictor</h1>
         The <b>Export Transition List</b> form should look like:
     </p>
     <p>
-        <img src="image-23.png" />
+        <img src="s-21.png" />
     </p>
     <p>
         You could also simply click the <b>Single method</b> option, but the fact that the form shows “<b>Methods</b>: 1” confirms
@@ -677,7 +677,7 @@ <h1>Reviewing Scheduled Data</h1>
         When the data has finished loading, the <b>Retention Times</b> view should present a graph like:
     </p>
     <p>
-        <img src="image-24.png" /> 
+        <img src="s-22.png" /> 
     </p>
     <p>
         From this graph, it is immediately obvious that there are 2 outlier peptides, which could be caused by miss-integrated peaks in the current
@@ -701,7 +701,7 @@ <h1>Reviewing Scheduled Data</h1>
         The <b>Retention Times</b> graph should now look like:
     </p>
     <p>
-        <img src="image-25.png" />
+        <img src="s-23.png" />
     </p>
     <p>
         You can now click on each outlier point, causing Skyline to select it in the peptide view. Then, press Esc to give focus back to the main
@@ -737,7 +737,7 @@ <h1>Reviewing Scheduled Data</h1>
         The <b>Retention Times</b> graph should now look like this:
     </p>
     <p>
-        <img src="image-26.png" />
+        <img src="s-24.png" />
     </p>
     <p>
         This gives you a clearer sense that measured times are varying within +/- 2 minutes of the predicted times. What retention time scheduling
@@ -752,7 +752,7 @@ <h1>Reviewing Scheduled Data</h1>
         present graphs like the one below:
     </p>
     <p>
-        <img src="image-27.png" />
+        <img src="s-25.png" />
     </p>
     <p>
         You will see that all peptides, except the standards, now have light and heavy precursor pairs and generally more points across each peak than
@@ -813,7 +813,7 @@ <h1>Calculating iRT Values from MS/MS Spectra</h1>
         The <b>Add Spectral Library</b> form should look like this:
     </p>
     <p>
-        <img src="image-28.png" />
+        <img src="s-26.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -822,7 +822,7 @@ <h1>Calculating iRT Values from MS/MS Spectra</h1>
         Skyline should present a form that looks like this:
     </p>
     <p>
-        <img src="image-29.png" />
+        <img src="s-27.png" />
     </p>
     <p>
         The form tells you that Skyline was able to calculate a single valid regressions for both DDA runs in the library. When possible, Skyline will
@@ -867,7 +867,7 @@ <h1>Converting MS/MS Scan Times to Chromatogram Peak Times</h1>
         The Skyline window should look something like:
     </p>
     <p>
-        <img src="image-30.png" />
+        <img src="s-28.png" />
     </p>
     <p>
         You can double-click in the title bar of the <b>Retention Times</b> view to get a better look at the graph, and see that the
@@ -895,7 +895,7 @@ <h1>Converting MS/MS Scan Times to Chromatogram Peak Times</h1>
         Skyline presents a form that looks like this:
     </p>
     <p>
-        <img src="image-31.png" />
+        <img src="s-29.png" />
     </p>
     <p>
         To tell you that it will replace the 558 iRT values you added in the previous section. Now that you are using chromatogram peak times, you also
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/image-0.png b/pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/s-1.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/image-0.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/s-1.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/image-11.png b/pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/s-10.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/image-11.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/s-10.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/image-12.png b/pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/s-11.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/image-12.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/s-11.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/image-13.png b/pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/s-12.png
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rename from pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/image-13.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/s-12.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/image-14.png b/pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/s-13.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/image-14.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/s-13.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/image-15.png b/pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/s-14.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/image-15.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/s-14.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/image-16.png b/pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/s-15.png
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rename from pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/image-16.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/s-15.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/image-17.png b/pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/s-16.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/image-17.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/s-16.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/image-18.png b/pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/s-17.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/image-18.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/s-17.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/image-19.png b/pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/s-18.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/image-19.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/s-18.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/image-20.png b/pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/s-19.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/image-20.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/s-19.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/image-1.png b/pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/s-2.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/image-1.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/s-2.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/image-21.png b/pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/s-20.png
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rename from pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/image-21.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/s-20.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/image-23.png b/pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/s-21.png
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rename to pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/s-21.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/image-24.png b/pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/s-22.png
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rename to pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/s-22.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/image-25.png b/pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/s-23.png
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rename from pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/image-25.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/s-23.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/image-26.png b/pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/s-24.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/image-26.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/s-24.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/image-27.png b/pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/s-25.png
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rename from pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/image-27.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/s-25.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/image-28.png b/pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/s-26.png
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rename from pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/image-28.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/s-26.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/image-29.png b/pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/s-27.png
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rename from pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/image-29.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/s-27.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/image-30.png b/pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/s-28.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/image-30.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/s-28.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/image-31.png b/pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/s-29.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/image-31.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/s-29.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/image-2.png b/pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/s-3.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/image-2.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/s-3.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/image-4.png b/pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/s-4.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/image-4.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/s-4.png
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similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/image-5.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/s-5.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/image-7.png b/pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/s-6.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/image-7.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/s-6.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/image-8.png b/pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/s-7.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/image-8.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/s-7.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/image-9.png b/pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/s-8.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/image-9.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/s-8.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/image-10.png b/pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/s-9.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/image-10.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/s-9.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/image-22.png b/pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/s-window-size-formula.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/image-22.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/iRT/ja/s-window-size-formula.png
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diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/index.html b/pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/index.html
index 1ef32e832d..f7cfc4d3b2 100644
--- a/pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/index.html
+++ b/pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/index.html
@@ -78,7 +78,7 @@ <h1>校准 iRT 计算器</h1>
         表单应显示如下：
     </p>
     <p>
-        <img src="image-0.png" />
+        <img src="s-1.png" />
     </p>
     <ul>
         <li>单击<b>确定</b>按钮。</li>
@@ -94,7 +94,7 @@ <h1>校准 iRT 计算器</h1>
         此时 Skyline 将显示如下<b>保留时间</b>视图：
     </p>
     <p>
-        <img src="image-1.png" />
+        <img src="s-2.png" />
     </p>
     <p>
         上图呈现了30 分钟梯度条件下，每条肽段平均洗脱时间的整体视图。执行以下操作继续查看数据：
@@ -109,7 +109,7 @@ <h1>校准 iRT 计算器</h1>
         此时，Skyline 将显示如下：
     </p>
     <p>
-        <img src="image-2.png" />
+        <img src="s-3.png" />
     </p>
     <p>
         使用向下箭头键分别查看 Biognosys 标准肽段混合物中的 11 个肽段，确保整合正确无误，并且两次重复测定均在相似的保留时间出现色谱峰。其实，自动整合非常适用于这些肽段，您不必做出任何手动修改。本教程仅包括两次重复测定。如果您自行校准新的 iRT
@@ -121,7 +121,7 @@ <h1>校准 iRT 计算器</h1>
     <ul>
         <li>在<b>设置</b>菜单中单击<b>肽段设置</b>。</li>
         <li>单击<b>预测</b>选项卡。</li>
-        <li>单击（<b>保留时间计算器</b>）按钮<img src="image-3.png" />，然后单击所示菜单中的<b>添加</b>。</li>
+        <li>单击（<b>保留时间计算器</b>）按钮<img src="../../shared/calculator-button.png" />，然后单击所示菜单中的<b>添加</b>。</li>
         <li>在<b>编辑 iRT 计算器</b>表单中的<b>名称</b>字段中，输入“iRT-C18”。</li>
         <li>单击<b>创建</b>按钮。</li>
         <li>在<b>创建 iRT 数据库</b>表单中，必要时可以导航到您为本教程创建的 iRT 文件夹。</li>
@@ -136,7 +136,7 @@ <h1>校准 iRT 计算器</h1>
         此时，<b>校准 iRT 计算器</b>表单将显示如下：
     </p>
     <p>
-        <img src="image-4.png" />
+        <img src="s-4.png" />
     </p>
     <ul>
         <li>单击<b>计算方式</b>下拉列表右侧的<b>图</b>按钮，查看从中导出下面所示的公式“iRT = 6.7701 * <br />RT – 105.6630”的线性图。</li>
@@ -151,14 +151,14 @@ <h1>校准 iRT 计算器</h1>
         此时，<b>编辑 iRT 计算器</b>表单显示如下：
     </p>
     <p>
-        <img src="image-5.png" />
+        <img src="s-5.png" />
     </p>
     <p>
         整个过程就是这样。您已经利用测量数据校准了一组新的 iRT 标准。但在本案例中，Biognosys 团队很可能使用了 2 次以上的重复测定，来校准其标准肽段混合物。因此，在本教程中，您可以简单地利用 Biognosys
         提供的标准结果来替代这次的校准。但为了更好地了解两者之间的接近程度，请执行以下步骤：
     </p>
     <ul>
-        <li>将鼠标光标移到 <b>iRT 标准</b>网格下方，直至出现水平分割光标 <img src="image-6.png" />。</li>
+        <li>将鼠标光标移到 <b>iRT 标准</b>网格下方，直至出现水平分割光标 <img src="../../shared/horizontal-split-cursor-icon.png" />。</li>
         <li>单击并拖动分割条，直至这 11 个标准肽段全部出现在网格中。</li>
         <li>找到网格上方的下拉列表，并在以下两个选项之间切换：<ul>
                 <li><b>Biognosys (30 min cal)</b> – 刚才由您创建</li>
@@ -192,7 +192,7 @@ <h1>校准 iRT 计算器</h1>
         Skyline 将显示下面的图：
     </p>
     <p>
-        <img src="image-7.png" />
+        <img src="s-6.png" />
     </p>
     <p>
         在图的左上角，可以看到 Pearson 相关系数为 0.9991。如果在 x 轴下方未看到 iRT-C18，则需要执行下列操作：
@@ -226,7 +226,7 @@ <h1>为新的靶向肽段添加 iRT 值</h1>
         <b>目标</b>视图应显示如下：
     </p>
     <p>
-        <img src="image-8.png" />
+        <img src="s-7.png" />
     </p>
     <ul>
         <li>将此文档保存为“iRT Human+Standard.sky”。</li>
@@ -264,7 +264,7 @@ <h2>创建 iRT 采集方法</h2>
         表单显示如下：
     </p>
     <p>
-        <img src="image-9.png" />
+        <img src="s-8.png" />
     </p>
     <ul>
         <li>单击<b>确定</b>按钮。</li>
@@ -284,7 +284,7 @@ <h2>创建 iRT 采集方法</h2>
         此时，<b>导出离子对列表</b>表单将显示如下：
     </p>
     <p>
-        <img src="image-10.png" />
+        <img src="s-9.png" />
     </p>
     <ul>
         <li>单击<b>确定</b>按钮。</li>
@@ -328,7 +328,7 @@ <h2>导入并审核数据</h2>
         完成数据导入之后，您将看到下图：
     </p>
     <p>
-        <img src="image-11.png" />
+        <img src="s-10.png" />
     </p>
     <p>
         图中左侧的紫色散点表示这些肽段尚无校准的 iRT 值。不过在计算 iRT 值之前，最好对峰的整合情况进行检查。如果您真正希望对自己的 iRT 值进行准确校准，最好非常仔细地对所有肽段执行此操作。
@@ -349,7 +349,7 @@ <h2>导入并审核数据</h2>
         <b>查找</b>表单将显示如下：
     </p>
     <p>
-        <img src="image-12.png" />
+        <img src="s-11.png" />
     </p>
     <ul>
         <li>单击<b>查找全部</b>按钮。</li>
@@ -359,7 +359,7 @@ <h2>导入并审核数据</h2>
         在 Skyline 窗口底部可以看到<b>查找结果</b>视图，其中显示了 6 个未整合的离子对：
     </p>
     <p>
-        <img src="image-13.png" />
+        <img src="s-12.png" />
     </p>
     <p>
         要检查包含这些峰的肽段，请执行下列操作：
@@ -375,10 +375,10 @@ <h2>导入并审核数据</h2>
     <table class="comp-fig">
         <tr>
             <td class="comp-fig">
-                <img src="image-14.png" />
+                <img src="s-13.png" />
             </td>
             <td class="comp-fig">
-                <img src="image-15.png" />
+                <img src="s-14.png" />
             </td>
         </tr>
     </table>
@@ -406,7 +406,7 @@ <h2>计算 iRT 值</h2>
         Skyline 将显示以下消息：
     </p>
     <p>
-        <img src="image-16.png" />
+        <img src="s-15.png" />
     </p>
     <p>
         请注意，在对这两次运行生成 iRT 值时，Skyline 会为每次运行分别执行线性回归，然后使用每次运行的线性回归，来计算该次运行中的肽段的 iRT 值。如果多次运行中包含相同的肽段，Skyline 将采用多次计算得出的 iRT
@@ -425,7 +425,7 @@ <h2>计算 iRT 值</h2>
         此时，<b>编辑 iRT 计算器</b>表单将显示如下：
     </p>
     <p>
-        <img src="image-17.png" />
+        <img src="s-16.png" />
     </p>
     <ul>
         <li>单击<b>确定</b>按钮。</li>
@@ -434,7 +434,7 @@ <h2>计算 iRT 值</h2>
         <b>保留时间</b>视图将变为如下所示：
     </p>
     <p>
-        <img src="image-18.png" />
+        <img src="s-17.png" />
     </p>
     <p>
         您刚刚使用 30 分钟梯度采集的数据校准了 148 个新的人类肽段的 iRT-C18 值。
@@ -480,7 +480,7 @@ <h1>使用 iRT 预定新的数据采集</h1>
         <b>肽段设置</b>表单应显示如下：
     </p>
     <p>
-        <img src="image-19.png" />
+        <img src="s-18.png" />
     </p>
     <ul>
         <li>单击<b>确定</b>按钮。</li>
@@ -492,7 +492,7 @@ <h1>使用 iRT 预定新的数据采集</h1>
         完成数据导入后，<b>保留时间</b>回归图将显示如下：
     </p>
     <p>
-        <img src="image-20.png" />
+        <img src="s-19.png" />
     </p>
     <p>
         此时，可以看到标准肽段的洗脱时间范围约介于 15 至 65 分钟之间，此次运行中未对其中任何目标肽段进行测量。不过，此时您已准备好在新梯度上对肽段进行测量。
@@ -508,7 +508,7 @@ <h1>使用 iRT 预测器导出预定方法</h1>
         <b>保留时间</b>视图中将出现新的<b>时序安排</b>选项卡，并显示类似如下的图：
     </p>
     <p>
-        <img src="image-21.png" />
+        <img src="s-20.png" />
     </p>
     <p>
         如果您未能在上图中全部看到这三条线，则可执行下列操作：
@@ -522,7 +522,7 @@ <h1>使用 iRT 预测器导出预定方法</h1>
         从此图可以看到窗口大小对于预定方法的影响。时间窗口越小，则在给定时间内允许同时测定的离子对越少，这使得能够在特定驻留时间内，对单次进样中的更多离子对进行测定。捕获整个色谱峰的目标肽段百分比所需的窗口大小通过以下公式进行近似估计：
     </p>
     <p>
-        <img src="image-22.png" />
+        <img src="s-window-size-formula.png" />
     </p>
     <p>
         其中“z”为在正态分布条件下，一定百分比范围覆盖时的标准差临界值，如 z(95%)
@@ -542,7 +542,7 @@ <h1>使用 iRT 预测器导出预定方法</h1>
         <b>导出离子对列表</b>表单将显示如下：
     </p>
     <p>
-        <img src="image-23.png" />
+        <img src="s-21.png" />
     </p>
     <p>
         您可以简单地选择<b>单一方法</b>选项，但表单实际显示出“<b>方法：</b>1”，确认了在 5 分钟检测窗口以及同时测定的离子对数量不会超过 265
@@ -584,7 +584,7 @@ <h1>审查预定数据</h1>
         数据加载完成后，<b>保留时间</b>视图将显示如下：
     </p>
     <p>
-        <img src="image-24.png" />
+        <img src="s-22.png" />
     </p>
     <p>
         从此图中一眼可以看出有 2 个异常肽段，可能的原因是当前数据中的色谱峰整合错误，或用于计算 iRT 值的校准数据中的色谱峰整合错误。在本案例中，问题出在skyline在 对 30
@@ -602,7 +602,7 @@ <h1>审查预定数据</h1>
         此时，<b>保留时间</b>图将显示如下：
     </p>
     <p>
-        <img src="image-25.png" />
+        <img src="s-23.png" />
     </p>
     <p>
         现在您可以单击每个异常点，Skyline 将在肽段视图中对其进行显示。然后按下 Esc 恢复主窗口，并按下 Ctrl-C 复制肽段标记。您也可将这些内容收集到单独的编辑器中，供以后审查使用，或者为之前创建的“iRT Human+Standard
@@ -630,7 +630,7 @@ <h1>审查预定数据</h1>
         此时，<b>保留时间</b>图将显示如下：
     </p>
     <p>
-        <img src="image-26.png" />
+        <img src="s-24.png" />
     </p>
     <p>
         这样您可以更清楚地看到测量时间在预测时间的 +/-2 分钟内的变化。 在本例中，您应当使用什么保留时间时序安排窗口？实验中用的是什么？
@@ -643,7 +643,7 @@ <h1>审查预定数据</h1>
         现在单击<b>目标</b>视图，并使用向下箭头键审查肽段色谱图。Skyline 将显示如下的图：
     </p>
     <p>
-        <img src="image-27.png" />
+        <img src="s-25.png" />
     </p>
     <p>
         您会看到除标准肽段以外的所有肽段都具有轻标母离子对和重标母离子对，并且相比非预定数据，每个色谱峰的点通常更多。您还会看到 Skyline 在标记“预测的”注释下方显示了色谱峰的预测时间。
@@ -690,7 +690,7 @@ <h1>根据串联质谱谱图计算 iRT 值</h1>
         <b>添加谱图库</b>表单将显示如下：
     </p>
     <p>
-        <img src="image-28.png" />
+        <img src="s-26.png" />
     </p>
     <ul>
         <li>单击<b>确定</b>按钮。</li>
@@ -699,7 +699,7 @@ <h1>根据串联质谱谱图计算 iRT 值</h1>
         Skyline 将呈现如下所示的表单：
     </p>
     <p>
-        <img src="image-29.png" />
+        <img src="s-27.png" />
     </p>
     <p>
         该表单显示 Skyline 可以为库中的两次 DDA 运行计算出一个有效的回归系数。如若可能，Skyline 将利用运行之间所有匹配的肽段，执行运行间的内部回归运算，这被证明比只使用标准肽段的回归效果好。Skyline 利用这个最终校准回归为 558 个新肽段计算了 iRT
@@ -737,7 +737,7 @@ <h1>将串联质谱扫描时间转换为色谱峰时间</h1>
         Skyline 窗口将显示如下：
     </p>
     <p>
-        <img src="image-30.png" />
+        <img src="s-28.png" />
     </p>
     <p>
         为更好地查看该图，您可以双击<b>保留时间</b>视图中的标题栏，会看到用库谱图方法计算的 iRT 值与实际检测的保留时间的相关系数为
@@ -758,7 +758,7 @@ <h1>将串联质谱扫描时间转换为色谱峰时间</h1>
         Skyline 将显示如下表单：
     </p>
     <p>
-        <img src="image-31.png" />
+        <img src="s-29.png" />
     </p>
     <p>
         系统将替换您在上一部分添加的 558 个 iRT 值。由于您在使用色谱峰时间，因此还可以选择更换酵母和人类样品共有的 3 个肽段，或使用两者的平均值。
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/invariant.html b/pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/invariant.html
index 037d97bd83..2aa6600012 100644
--- a/pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/invariant.html
+++ b/pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/invariant.html
@@ -98,7 +98,7 @@ <h1>Calibrating an iRT Calculator</h1>
         The form looking like this:
     </p>
     <p>
-        <img src="image-0.png" />
+        <img src="s-1.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -114,7 +114,7 @@ <h1>Calibrating an iRT Calculator</h1>
         Skyline should present the <b>Retention Times</b> view showing a graph like the one below:
     </p>
     <p>
-        <img src="image-1.png" />
+        <img src="s-2.png" />
     </p>
     <p>
         This gives you a top level view of when each peptide eluted, on average, over the 30-minute gradient. Continue reviewing the data by doing the
@@ -131,7 +131,7 @@ <h1>Calibrating an iRT Calculator</h1>
         Skyline should now look something like this:
     </p>
     <p>
-        <img src="image-2.png" />
+        <img src="s-3.png" />
     </p>
     <p>
         Use the down-arrow key to review each of the 11 peptides in the Biognosys standard mix, making sure that the integration looks correct, and
@@ -148,7 +148,7 @@ <h1>Calibrating an iRT Calculator</h1>
     <ul>
         <li>On the <b>Settings</b> menu, click <b>Peptide Settings</b>.</li>
         <li>Click the <b>Prediction</b> tab.</li>
-        <li>Click the <img src="image-3.png" /> (<b>Retention time calculators</b>) button, and click <b>Add</b> in the menu it
+        <li>Click the <img src="../../shared/calculator-button.png" /> (<b>Retention time calculators</b>) button, and click <b>Add</b> in the menu it
             shows.</li>
         <li>In the <b>Name</b> field of the <b>Edit iRT Calculator</b> form, enter ‘iRT-C18’.</li>
         <li>Click the <b>Create</b> button.</li>
@@ -164,7 +164,7 @@ <h1>Calibrating an iRT Calculator</h1>
         The <b>Calibrate iRT Calculator</b> form should now look something like:
     </p>
     <p>
-        <img src="image-4.png" />
+        <img src="s-4.png" />
     </p>
     <ul>
         <li>Click the <b>Graph</b> button to the right of the <b>Calculate from</b> dropdown list to see a plot of the line from
@@ -182,7 +182,7 @@ <h1>Calibrating an iRT Calculator</h1>
         The <b>Edit iRT Calculator</b> form should now look something like:
     </p>
     <p>
-        <img src="image-5.png" />
+        <img src="s-5.png" />
     </p>
     <p>
         That is it. You have calibrated a new set of iRT standards with measured data. In this case, however, the team at Biognosys has already
@@ -190,7 +190,7 @@ <h1>Calibrating an iRT Calculator</h1>
         calibration with the canonical one, but first to see how close the two are, do the following:
     </p>
     <ul>
-        <li>Move the mouse cursor below the <b>iRT standards</b> grid until you see a horizontal split cursor <img src="image-6.png" />.
+        <li>Move the mouse cursor below the <b>iRT standards</b> grid until you see a horizontal split cursor <img src="../../shared/horizontal-split-cursor-icon.png" />.
         </li>
         <li>Click and drag the splitter until you can see all 11 standard peptides in the grid.</li>
         <li>In the dropdown list above the grid switch between the two choices:<ul>
@@ -229,7 +229,7 @@ <h1>Calibrating an iRT Calculator</h1>
         Skyline should present a graph that looks like the one below:
     </p>
     <p>
-        <img src="image-7.png" />
+        <img src="s-6.png" />
     </p>
     <p>
         In the upper left corner of the graph, you will see a Pearson’s Correlation Coefficient of 0.9991. If you do not see iRT-C18 below the x-axis,
@@ -269,7 +269,7 @@ <h1>Adding iRT Values for New Targeted Peptides</h1>
         The <b>Targets</b> view should look something like this:
     </p>
     <p>
-        <img src="image-8.png" />
+        <img src="s-7.png" />
     </p>
     <ul>
         <li>Save this document as ‘iRT Human+Standard.sky’.</li>
@@ -311,7 +311,7 @@ <h2>Creating an iRT Acquisition Method</h2>
         The form should look like the following:
     </p>
     <p>
-        <img src="image-9.png" />
+        <img src="s-8.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -331,7 +331,7 @@ <h2>Creating an iRT Acquisition Method</h2>
         The <b>Export Transition List</b> form should now look like:
     </p>
     <p>
-        <img src="image-10.png" />
+        <img src="s-9.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -385,7 +385,7 @@ <h2>Importing and Reviewing the Data</h2>
         Once the data has finished importing, you should see a graph like:
     </p>
     <p>
-        <img src="image-11.png" />
+        <img src="s-10.png" />
     </p>
     <p>
         The cluster of purple points, on the left side of the graph indicates that these peptides do not yet have calibrated iRT values. Before
@@ -411,7 +411,7 @@ <h2>Importing and Reviewing the Data</h2>
         The <b>Find</b> form should look like:
     </p>
     <p>
-        <img src="image-12.png" />
+        <img src="s-11.png" />
     </p>
     <ul>
         <li>Click the <b>Find All</b> button.</li>
@@ -422,7 +422,7 @@ <h2>Importing and Reviewing the Data</h2>
         transitions:
     </p>
     <p>
-        <img src="image-13.png" />
+        <img src="s-12.png" />
     </p>
     <p>
         To review the peptides containing these peaks, do the following:
@@ -439,10 +439,10 @@ <h2>Importing and Reviewing the Data</h2>
     <table class="comp-fig">
         <tr>
             <td class="comp-fig">
-                <img src="image-14.png" />
+                <img src="s-13.png" />
             </td>
             <td class="comp-fig">
-                <img src="image-15.png" />
+                <img src="s-14.png" />
             </td>
         </tr>
     </table>
@@ -474,7 +474,7 @@ <h2>Calculating iRT Values</h2>
         Skyline will show you the following informational message:
     </p>
     <p>
-        <img src="image-16.png" />
+        <img src="s-15.png" />
     </p>
     <p>
         Note that in producing iRT values for the two runs, Skyline has performed a separate linear regression for each run. It uses the linear
@@ -496,7 +496,7 @@ <h2>Calculating iRT Values</h2>
         The <b>Edit iRT Calculator</b> form should now look like:
     </p>
     <p>
-        <img src="image-17.png" />
+        <img src="s-16.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -505,7 +505,7 @@ <h2>Calculating iRT Values</h2>
         The <b>Retention Times</b> view should change to look like this:
     </p>
     <p>
-        <img src="image-18.png" />
+        <img src="s-17.png" />
     </p>
     <p>
         You have just calibrated iRT-C18 values for 148 new human peptides, using data acquired on a 30-minute gradient.
@@ -556,7 +556,7 @@ <h1>Using iRT to Schedule New Acquisition</h1>
         The <b>Peptide Settings</b> form should look like this:
     </p>
     <p>
-        <img src="image-19.png" />
+        <img src="s-18.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -569,7 +569,7 @@ <h1>Using iRT to Schedule New Acquisition</h1>
         When the data has finished importing, the <b>Retention Times</b> regression graph will be shown as:
     </p>
     <p>
-        <img src="image-20.png" />
+        <img src="s-19.png" />
     </p>
     <p>
         You can see that the times for the standard peptides now range from about 15 to 65 minutes, and none of the target peptides were measured in
@@ -588,7 +588,7 @@ <h1>Exporting a Scheduled Method Using an iRT Predictor</h1>
         below:
     </p>
     <p>
-        <img src="image-21.png" />
+        <img src="s-20.png" />
     </p>
     <p>
         If you do not see all three lines shown in the graph above, you can do the following:
@@ -604,7 +604,7 @@ <h1>Exporting a Scheduled Method Using an iRT Predictor</h1>
         required to capture the entire peaks of a percentage of target peptides is approximated by the function below:
     </p>
     <p>
-        <img src="image-22.png" />
+        <img src="s-window-size-formula.png" />
     </p>
     <p>
         Where “z” is a critical value for the number of standard deviations within which the desired percentage fall in a normal distribution, e.g. 95%
@@ -629,7 +629,7 @@ <h1>Exporting a Scheduled Method Using an iRT Predictor</h1>
         The <b>Export Transition List</b> form should look like:
     </p>
     <p>
-        <img src="image-23.png" />
+        <img src="s-21.png" />
     </p>
     <p>
         You could also simply click the <b>Single method</b> option, but the fact that the form shows “<b>Methods</b>: 1” confirms
@@ -677,7 +677,7 @@ <h1>Reviewing Scheduled Data</h1>
         When the data has finished loading, the <b>Retention Times</b> view should present a graph like:
     </p>
     <p>
-        <img src="image-24.png" /> 
+        <img src="s-22.png" /> 
     </p>
     <p>
         From this graph, it is immediately obvious that there are 2 outlier peptides, which could be caused by miss-integrated peaks in the current
@@ -701,7 +701,7 @@ <h1>Reviewing Scheduled Data</h1>
         The <b>Retention Times</b> graph should now look like:
     </p>
     <p>
-        <img src="image-25.png" />
+        <img src="s-23.png" />
     </p>
     <p>
         You can now click on each outlier point, causing Skyline to select it in the peptide view. Then, press Esc to give focus back to the main
@@ -737,7 +737,7 @@ <h1>Reviewing Scheduled Data</h1>
         The <b>Retention Times</b> graph should now look like this:
     </p>
     <p>
-        <img src="image-26.png" />
+        <img src="s-24.png" />
     </p>
     <p>
         This gives you a clearer sense that measured times are varying within +/- 2 minutes of the predicted times. What retention time scheduling
@@ -752,7 +752,7 @@ <h1>Reviewing Scheduled Data</h1>
         present graphs like the one below:
     </p>
     <p>
-        <img src="image-27.png" />
+        <img src="s-25.png" />
     </p>
     <p>
         You will see that all peptides, except the standards, now have light and heavy precursor pairs and generally more points across each peak than
@@ -813,7 +813,7 @@ <h1>Calculating iRT Values from MS/MS Spectra</h1>
         The <b>Add Spectral Library</b> form should look like this:
     </p>
     <p>
-        <img src="image-28.png" />
+        <img src="s-26.png" />
     </p>
     <ul>
         <li>Click the <b>OK</b> button.</li>
@@ -822,7 +822,7 @@ <h1>Calculating iRT Values from MS/MS Spectra</h1>
         Skyline should present a form that looks like this:
     </p>
     <p>
-        <img src="image-29.png" />
+        <img src="s-27.png" />
     </p>
     <p>
         The form tells you that Skyline was able to calculate a single valid regressions for both DDA runs in the library. When possible, Skyline will
@@ -867,7 +867,7 @@ <h1>Converting MS/MS Scan Times to Chromatogram Peak Times</h1>
         The Skyline window should look something like:
     </p>
     <p>
-        <img src="image-30.png" />
+        <img src="s-28.png" />
     </p>
     <p>
         You can double-click in the title bar of the <b>Retention Times</b> view to get a better look at the graph, and see that the
@@ -895,7 +895,7 @@ <h1>Converting MS/MS Scan Times to Chromatogram Peak Times</h1>
         Skyline presents a form that looks like this:
     </p>
     <p>
-        <img src="image-31.png" />
+        <img src="s-29.png" />
     </p>
     <p>
         To tell you that it will replace the 558 iRT values you added in the previous section. Now that you are using chromatogram peak times, you also
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/image-0.png b/pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/s-1.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/image-0.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/s-1.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/image-11.png b/pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/s-10.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/image-11.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/s-10.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/image-12.png b/pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/s-11.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/image-12.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/s-11.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/image-13.png b/pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/s-12.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/image-13.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/s-12.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/image-14.png b/pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/s-13.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/image-14.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/s-13.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/image-15.png b/pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/s-14.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/image-15.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/s-14.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/image-16.png b/pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/s-15.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/image-16.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/s-15.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/image-17.png b/pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/s-16.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/image-17.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/s-16.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/image-18.png b/pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/s-17.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/image-18.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/s-17.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/image-19.png b/pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/s-18.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/image-19.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/s-18.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/image-20.png b/pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/s-19.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/image-20.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/s-19.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/image-1.png b/pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/s-2.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/image-1.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/s-2.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/image-21.png b/pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/s-20.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/image-21.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/s-20.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/image-23.png b/pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/s-21.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/image-23.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/s-21.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/image-24.png b/pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/s-22.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/image-24.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/s-22.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/image-25.png b/pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/s-23.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/image-25.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/s-23.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/image-26.png b/pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/s-24.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/image-26.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/s-24.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/image-27.png b/pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/s-25.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/image-27.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/s-25.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/image-28.png b/pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/s-26.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/image-28.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/s-26.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/image-29.png b/pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/s-27.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/image-29.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/s-27.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/image-30.png b/pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/s-28.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/image-30.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/s-28.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/image-31.png b/pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/s-29.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/image-31.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/s-29.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/image-2.png b/pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/s-3.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/image-2.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/s-3.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/image-4.png b/pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/s-4.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/image-4.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/s-4.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/image-5.png b/pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/s-5.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/image-5.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/s-5.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/image-7.png b/pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/s-6.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/image-7.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/s-6.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/image-8.png b/pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/s-7.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/image-8.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/s-7.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/image-9.png b/pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/s-8.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/image-9.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/s-8.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/image-10.png b/pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/s-9.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/image-10.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/s-9.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/image-22.png b/pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/s-window-size-formula.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/image-22.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/iRT/zh-CHS/s-window-size-formula.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA/en/image-31.png b/pwiz_tools/Skyline/Documentation/Tutorials/shared/arrow-buttons.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA/en/image-31.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/shared/arrow-buttons.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/image-18.png b/pwiz_tools/Skyline/Documentation/Tutorials/shared/black-binocular-button.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/image-18.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/shared/black-binocular-button.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/PeakPicking/en/image-29.png b/pwiz_tools/Skyline/Documentation/Tutorials/shared/blue-binocular-button.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/PeakPicking/en/image-29.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/shared/blue-binocular-button.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeIMSLibraries/en/image-10.png b/pwiz_tools/Skyline/Documentation/Tutorials/shared/bottom-side-docking-icon.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeIMSLibraries/en/image-10.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/shared/bottom-side-docking-icon.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/image-3.png b/pwiz_tools/Skyline/Documentation/Tutorials/shared/calculator-button.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/image-3.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/shared/calculator-button.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/en/image-5.png b/pwiz_tools/Skyline/Documentation/Tutorials/shared/copy-button.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/CustomReports/en/image-5.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/shared/copy-button.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/image-6.png b/pwiz_tools/Skyline/Documentation/Tutorials/shared/horizontal-split-cursor-icon.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/iRT/en/image-6.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/shared/horizontal-split-cursor-icon.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeIMSLibraries/en/image-12.png b/pwiz_tools/Skyline/Documentation/Tutorials/shared/left-side-docking-icon.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/SmallMoleculeIMSLibraries/en/image-12.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/shared/left-side-docking-icon.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA/en/image-29.png b/pwiz_tools/Skyline/Documentation/Tutorials/shared/magnifying-glass-icon.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA/en/image-29.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/shared/magnifying-glass-icon.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/en/image-6.png b/pwiz_tools/Skyline/Documentation/Tutorials/shared/peptide-icon.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/en/image-6.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/shared/peptide-icon.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/PeakPicking/en/image-12.png b/pwiz_tools/Skyline/Documentation/Tutorials/shared/peptide-with-spectrum-lines-and-clock-icon.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/PeakPicking/en/image-12.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/shared/peptide-with-spectrum-lines-and-clock-icon.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/en/image-7.png b/pwiz_tools/Skyline/Documentation/Tutorials/shared/peptide-with-spectrum-lines-icon.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/en/image-7.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/shared/peptide-with-spectrum-lines-icon.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/GroupedStudies/en/image-3.png b/pwiz_tools/Skyline/Documentation/Tutorials/shared/peptide-without-spectrum-lines-icon.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/GroupedStudies/en/image-3.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/shared/peptide-without-spectrum-lines-icon.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/GroupedStudies/en/image-45.png b/pwiz_tools/Skyline/Documentation/Tutorials/shared/protein-icon-2.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/GroupedStudies/en/image-45.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/shared/protein-icon-2.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/en/image-12.png b/pwiz_tools/Skyline/Documentation/Tutorials/shared/pushpin-icon.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/ExistingQuant/en/image-12.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/shared/pushpin-icon.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/image-24.png b/pwiz_tools/Skyline/Documentation/Tutorials/shared/red-dot-icon.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/PRMOrbitrap-PRBB/en/image-24.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/shared/red-dot-icon.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/GroupedStudies/en/image-19.png b/pwiz_tools/Skyline/Documentation/Tutorials/shared/red-x-icon.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/GroupedStudies/en/image-19.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/shared/red-x-icon.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA/en/image-34.png b/pwiz_tools/Skyline/Documentation/Tutorials/shared/right-arrow-button.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA/en/image-34.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/shared/right-arrow-button.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/IMSFiltering/en/image-12.png b/pwiz_tools/Skyline/Documentation/Tutorials/shared/show-2d-spectrum-button.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/IMSFiltering/en/image-12.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/shared/show-2d-spectrum-button.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/shared/skyline.js b/pwiz_tools/Skyline/Documentation/Tutorials/shared/skyline.js
index e0d3678783..22fc245179 100644
--- a/pwiz_tools/Skyline/Documentation/Tutorials/shared/skyline.js
+++ b/pwiz_tools/Skyline/Documentation/Tutorials/shared/skyline.js
@@ -1,33 +1,68 @@
-function skylineOnload (documentRef) {
+function skylineOnload () {
     if (self != top)
       targetTop();
-    var documentRef = documentRef || document;
-    var titleElement = documentRef.getElementsByClassName("document-title")[0];
+    
+    addFigureAltText()
+    addTableOfContents()
+    scrollToAnchor()
+}
+
+function targetTop()
+{
+  document.querySelectorAll('a[href]').forEach(anchor => {
+    if (anchor.target !== '_blank') {
+        anchor.target = '_top';
+    }
+});
+}
+
+function addFigureAltText()
+{
+    const images = document.querySelectorAll('img');
+    var figureCounter = 1;
+    images.forEach((img) => {
+        if (img.src.includes("/s-")) {
+            img.title = `Figure ${figureCounter}`;
+
+            var anchor = document.createElement('a');
+            const anchorId = `figure${figureCounter}`
+            anchor.setAttribute('name', anchorId);
+            anchor.setAttribute('id', anchorId);
+            img.parentNode.parentNode.insertBefore(anchor, img.parentNode);
+
+            figureCounter++
+        }
+    });
+}
+
+function addTableOfContents(){
+    var titleElement = document.getElementsByClassName("document-title")[0];
     if(titleElement){
-        var tocElement = documentRef.getElementsByClassName("toc")[0];
+        var tocElement = document.getElementsByClassName("toc")[0];
         if(!tocElement){
-            tocElement = documentRef.createElement('div');
+            tocElement = document.createElement('div');
             tocElement.setAttribute('class', "toc");
             titleElement.insertAdjacentElement("afterend", tocElement);
         }
 
-        var headings = [].slice.call(documentRef.body.querySelectorAll('h1, h2, h3, h4, h5, h6'));
+        var headings = [].slice.call(document.body.querySelectorAll('h1, h2, h3, h4, h5, h6'));
         headings.forEach(function (heading, index) {
             if(!heading.classList.contains("document-title")){
                 var headingTextContent = heading.textContent.trim();
-                if (headingTextContent.endsWith(":")){
+                //remove English and Chinese/Japanese colons
+                if (headingTextContent.endsWith(":") || headingTextContent.endsWith("：")){
                     headingTextContent = headingTextContent.slice(0, -1);
                 }
                 var headingId = headingTextContent.replace(/ /g,"_");
 
                 //create toc link
-                var link = documentRef.createElement('a');
+                var link = document.createElement('a');
                 link.setAttribute('href', '#' + headingId);
 
                 link.textContent = headingTextContent;
 
                 //create div for toc row
-                var div = documentRef.createElement('div');
+                var div = document.createElement('div');
                 div.setAttribute('class', "toc-" +heading.tagName.toLowerCase());
 
                 //add toc row to toc
@@ -36,7 +71,7 @@ function skylineOnload (documentRef) {
 
                 //create anchor before heading for toc link
 
-                var anchor = documentRef.createElement('a');
+                var anchor = document.createElement('a');
                 anchor.setAttribute('name', headingId);
                 anchor.setAttribute('id', headingId);
                 heading.parentNode.insertBefore(anchor, heading);
@@ -45,11 +80,8 @@ function skylineOnload (documentRef) {
     }
 }
 
-function targetTop()
-{
-  document.querySelectorAll('a[href]').forEach(anchor => {
-    if (anchor.target !== '_blank') {
-        anchor.target = '_top';
+function scrollToAnchor(){
+    if(location.hash){
+        document.getElementById(location.hash.substring(1)).scrollIntoView();
     }
-});
 }
\ No newline at end of file
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/PRM/en/image-23.png b/pwiz_tools/Skyline/Documentation/Tutorials/shared/target-peptide-with-spectrum-icon.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/PRM/en/image-23.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/shared/target-peptide-with-spectrum-icon.png
diff --git a/pwiz_tools/Skyline/Documentation/Tutorials/DIA/en/image-26.png b/pwiz_tools/Skyline/Documentation/Tutorials/shared/vertical-split-cursor-icon.png
similarity index 100%
rename from pwiz_tools/Skyline/Documentation/Tutorials/DIA/en/image-26.png
rename to pwiz_tools/Skyline/Documentation/Tutorials/shared/vertical-split-cursor-icon.png