https://www.coastalwiki.org/w/index.php?title=Dicofol&feed=atom&action=history
Dicofol - Revision history
2024-03-29T10:29:34Z
Revision history for this page on the wiki
MediaWiki 1.31.7
https://www.coastalwiki.org/w/index.php?title=Dicofol&diff=77584&oldid=prev
Dronkers J at 12:08, 9 August 2020
2020-08-09T12:08:19Z
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<td colspan="2" style="background-color: #fff; color: #222; text-align: center;">Revision as of 12:08, 9 August 2020</td>
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Dronkers J
https://www.coastalwiki.org/w/index.php?title=Dicofol&diff=57496&oldid=prev
Daphnisd at 15:41, 19 March 2013
2013-03-19T15:41:43Z
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<tr><td class='diff-marker'> </td><td style="background-color: #f8f9fa; color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div><references/></div></td><td class='diff-marker'> </td><td style="background-color: #f8f9fa; color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div><references/></div></td></tr>
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<tr><td class='diff-marker'> </td><td style="background-color: #f8f9fa; color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>[[Category:Coastal and marine pollution]]</div></td><td class='diff-marker'> </td><td style="background-color: #f8f9fa; color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>[[Category:Coastal and marine pollution]]</div></td></tr>
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Daphnisd
https://www.coastalwiki.org/w/index.php?title=Dicofol&diff=34836&oldid=prev
Daphnisd: /* */
2009-10-05T06:44:43Z
<p><span dir="auto"><span class="autocomment"></span></span></p>
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<td colspan="2" style="background-color: #fff; color: #222; text-align: center;">Revision as of 06:44, 5 October 2009</td>
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<tr><td class='diff-marker'> </td><td style="background-color: #f8f9fa; color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>{{Definition|title=dicofol  </div></td><td class='diff-marker'> </td><td style="background-color: #f8f9fa; color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>{{Definition|title=dicofol  </div></td></tr>
<tr><td class='diff-marker'> </td><td style="background-color: #f8f9fa; color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"></td><td class='diff-marker'> </td><td style="background-color: #f8f9fa; color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"></td></tr>
<tr><td class='diff-marker'>−</td><td style="color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div>|definition=Dicofol belongs to the group of [[organochlorine pesticides]]. It's produced from [[DDT]], therefore it has a similar chemical structure and similar properties<del class="diffchange diffchange-inline">.</del><ref name="Ospar">[http://www.ospar.org/documents%5Cdbase%5Cpublications%5Cp00150_Background%20document%20on%20Dicofol.pdf OSPAR Commission, 2004: OSPAR background document on dicofol]</ref>}}</div></td><td class='diff-marker'>+</td><td style="color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div>|definition=Dicofol belongs to the group of [[organochlorine pesticides]]. It's produced from [[DDT]], therefore it has a similar chemical structure and similar properties<ref name="Ospar">[http://www.ospar.org/documents%5Cdbase%5Cpublications%5Cp00150_Background%20document%20on%20Dicofol.pdf OSPAR Commission, 2004: OSPAR background document on dicofol]</ref><ins class="diffchange diffchange-inline">.</ins>}}</div></td></tr>
<tr><td class='diff-marker'> </td><td style="background-color: #f8f9fa; color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"></td><td class='diff-marker'> </td><td style="background-color: #f8f9fa; color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"></td></tr>
<tr><td class='diff-marker'> </td><td style="background-color: #f8f9fa; color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>== Notes ==</div></td><td class='diff-marker'> </td><td style="background-color: #f8f9fa; color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>== Notes ==</div></td></tr>
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Daphnisd
https://www.coastalwiki.org/w/index.php?title=Dicofol&diff=34835&oldid=prev
Daphnisd: /* Notes */
2009-10-05T06:44:29Z
<p><span dir="auto"><span class="autocomment">Notes</span></span></p>
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<td colspan="2" style="background-color: #fff; color: #222; text-align: center;">Revision as of 06:44, 5 October 2009</td>
</tr><tr><td colspan="2" class="diff-lineno" id="mw-diff-left-l21" >Line 21:</td>
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<tr><td class='diff-marker'> </td><td style="background-color: #f8f9fa; color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>The degradation of dicofol in soil is moderately slow, with a [[half-life]] of 30 to 60 days. In water systems and soils with a high organic matter content, the half-life can reach 84 days. Like DDT, it also has a high affinity to lipids, which causes it to [[adsorption|adsob]] to organic particles rather than dissolve in water. It's also highly [[bioaccumulation|bioaccumulative]], and [[biomagnification|biomagnifying]], therefore it poses a greater threat to high [[trophic level]] [[species]] such as [[pollution and sea birds|birds]] and [[pollution and marine mammals|mammals]].  </div></td><td class='diff-marker'> </td><td style="background-color: #f8f9fa; color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>The degradation of dicofol in soil is moderately slow, with a [[half-life]] of 30 to 60 days. In water systems and soils with a high organic matter content, the half-life can reach 84 days. Like DDT, it also has a high affinity to lipids, which causes it to [[adsorption|adsob]] to organic particles rather than dissolve in water. It's also highly [[bioaccumulation|bioaccumulative]], and [[biomagnification|biomagnifying]], therefore it poses a greater threat to high [[trophic level]] [[species]] such as [[pollution and sea birds|birds]] and [[pollution and marine mammals|mammals]].  </div></td></tr>
<tr><td class='diff-marker'> </td><td style="background-color: #f8f9fa; color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"></td><td class='diff-marker'> </td><td style="background-color: #f8f9fa; color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"></td></tr>
<tr><td class='diff-marker'>−</td><td style="color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div>Dicofol has been shown to be highly [[toxic]] for marine species. [[Pollution and pelagic fishes|<del class="diffchange diffchange-inline">Fish</del>]] die <del class="diffchange diffchange-inline">due to </del>chronic exposure to concentrations above 4,5 µg/l and concentrations above 12 µg/l can cause acute toxicity.  </div></td><td class='diff-marker'>+</td><td style="color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div>Dicofol has been shown to be highly [[toxic]] for marine species. [[Pollution and pelagic fishes|<ins class="diffchange diffchange-inline">Fishes</ins>]] <ins class="diffchange diffchange-inline">can </ins>die <ins class="diffchange diffchange-inline">by </ins>chronic exposure to concentrations above 4,5 µg/l and concentrations above 12 µg/l can cause acute toxicity.  </div></td></tr>
<tr><td class='diff-marker'>−</td><td style="color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div>In birds <del class="diffchange diffchange-inline">dicofol can cause eggshell thinning at </del>exposure 20 mg dicofol per kg body weight. It has also been shown to be a [[endocrine disrupting compounds|endocrine disrupting compound]]: male juvenile birds with a daily food intake of 5 mg dicofol per kg body weight showed effects of feminisation, which affected their mating behaviour and reproduction success<del class="diffchange diffchange-inline">.</del><ref name="Ospar">[http://www.ospar.org/documents%5Cdbase%5Cpublications%5Cp00150_Background%20document%20on%20Dicofol.pdf OSPAR Commission, 2004: OSPAR background document on dicofol]</ref></div></td><td class='diff-marker'>+</td><td style="color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div>In birds exposure <ins class="diffchange diffchange-inline">to </ins>20 mg <ins class="diffchange diffchange-inline">of </ins>dicofol per kg body weight <ins class="diffchange diffchange-inline">can cause eggshell thinning</ins>. It has also been shown to be a [[endocrine disrupting compounds|endocrine disrupting compound]]: male juvenile birds with a daily food intake of 5 mg dicofol per kg body weight showed effects of feminisation, which affected their mating behaviour and reproduction success<ref name="Ospar">[http://www.ospar.org/documents%5Cdbase%5Cpublications%5Cp00150_Background%20document%20on%20Dicofol.pdf OSPAR Commission, 2004: OSPAR background document on dicofol]</ref><ins class="diffchange diffchange-inline">.</ins></div></td></tr>
<tr><td class='diff-marker'> </td><td style="background-color: #f8f9fa; color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div><P></div></td><td class='diff-marker'> </td><td style="background-color: #f8f9fa; color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div><P></div></td></tr>
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Daphnisd
https://www.coastalwiki.org/w/index.php?title=Dicofol&diff=34834&oldid=prev
Daphnisd: /* Notes */
2009-10-05T06:38:54Z
<p><span dir="auto"><span class="autocomment">Notes</span></span></p>
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<td colspan="2" style="background-color: #fff; color: #222; text-align: center;">Revision as of 06:38, 5 October 2009</td>
</tr><tr><td colspan="2" class="diff-lineno" id="mw-diff-left-l21" >Line 21:</td>
<td colspan="2" class="diff-lineno">Line 21:</td></tr>
<tr><td class='diff-marker'> </td><td style="background-color: #f8f9fa; color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>The degradation of dicofol in soil is moderately slow, with a [[half-life]] of 30 to 60 days. In water systems and soils with a high organic matter content, the half-life can reach 84 days. Like DDT, it also has a high affinity to lipids, which causes it to [[adsorption|adsob]] to organic particles rather than dissolve in water. It's also highly [[bioaccumulation|bioaccumulative]], and [[biomagnification|biomagnifying]], therefore it poses a greater threat to high [[trophic level]] [[species]] such as [[pollution and sea birds|birds]] and [[pollution and marine mammals|mammals]].  </div></td><td class='diff-marker'> </td><td style="background-color: #f8f9fa; color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>The degradation of dicofol in soil is moderately slow, with a [[half-life]] of 30 to 60 days. In water systems and soils with a high organic matter content, the half-life can reach 84 days. Like DDT, it also has a high affinity to lipids, which causes it to [[adsorption|adsob]] to organic particles rather than dissolve in water. It's also highly [[bioaccumulation|bioaccumulative]], and [[biomagnification|biomagnifying]], therefore it poses a greater threat to high [[trophic level]] [[species]] such as [[pollution and sea birds|birds]] and [[pollution and marine mammals|mammals]].  </div></td></tr>
<tr><td class='diff-marker'> </td><td style="background-color: #f8f9fa; color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"></td><td class='diff-marker'> </td><td style="background-color: #f8f9fa; color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"></td></tr>
<tr><td class='diff-marker'>−</td><td style="color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div>Dicofol has been shown to be highly toxic for marine species. [[Pollution and pelagic fishes|Fish]] die due to chronic exposure to concentrations above 4,5 µg/l and concentrations above 12 µg/l can cause acute toxicity.  </div></td><td class='diff-marker'>+</td><td style="color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div>Dicofol has been shown to be highly <ins class="diffchange diffchange-inline">[[</ins>toxic<ins class="diffchange diffchange-inline">]] </ins>for marine species. [[Pollution and pelagic fishes|Fish]] die due to chronic exposure to concentrations above 4,5 µg/l and concentrations above 12 µg/l can cause acute toxicity.  </div></td></tr>
<tr><td class='diff-marker'> </td><td style="background-color: #f8f9fa; color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>In birds dicofol can cause eggshell thinning at exposure 20 mg dicofol per kg body weight. It has also been shown to be a [[endocrine disrupting compounds|endocrine disrupting compound]]: male juvenile birds with a daily food intake of 5 mg dicofol per kg body weight showed effects of feminisation, which affected their mating behaviour and reproduction success.<ref name="Ospar">[http://www.ospar.org/documents%5Cdbase%5Cpublications%5Cp00150_Background%20document%20on%20Dicofol.pdf OSPAR Commission, 2004: OSPAR background document on dicofol]</ref></div></td><td class='diff-marker'> </td><td style="background-color: #f8f9fa; color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>In birds dicofol can cause eggshell thinning at exposure 20 mg dicofol per kg body weight. It has also been shown to be a [[endocrine disrupting compounds|endocrine disrupting compound]]: male juvenile birds with a daily food intake of 5 mg dicofol per kg body weight showed effects of feminisation, which affected their mating behaviour and reproduction success.<ref name="Ospar">[http://www.ospar.org/documents%5Cdbase%5Cpublications%5Cp00150_Background%20document%20on%20Dicofol.pdf OSPAR Commission, 2004: OSPAR background document on dicofol]</ref></div></td></tr>
<tr><td class='diff-marker'> </td><td style="background-color: #f8f9fa; color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div><P></div></td><td class='diff-marker'> </td><td style="background-color: #f8f9fa; color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div><P></div></td></tr>
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Daphnisd
https://www.coastalwiki.org/w/index.php?title=Dicofol&diff=34833&oldid=prev
Daphnisd: /* Notes */
2009-10-05T06:36:45Z
<p><span dir="auto"><span class="autocomment">Notes</span></span></p>
<table class="diff diff-contentalign-left" data-mw="interface">
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<td colspan="2" style="background-color: #fff; color: #222; text-align: center;">← Older revision</td>
<td colspan="2" style="background-color: #fff; color: #222; text-align: center;">Revision as of 06:36, 5 October 2009</td>
</tr><tr><td colspan="2" class="diff-lineno" id="mw-diff-left-l17" >Line 17:</td>
<td colspan="2" class="diff-lineno">Line 17:</td></tr>
<tr><td class='diff-marker'> </td><td style="background-color: #f8f9fa; color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|}</div></td><td class='diff-marker'> </td><td style="background-color: #f8f9fa; color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|}</div></td></tr>
<tr><td class='diff-marker'> </td><td style="background-color: #f8f9fa; color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"></td><td class='diff-marker'> </td><td style="background-color: #f8f9fa; color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"></td></tr>
<tr><td class='diff-marker'>−</td><td style="color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div>The main source of dicofol in the environment is its use as a [[pesticide]] used on a wide variety of fruits, vegetables, ornamentals and field crops. A total amount of over 2700 tonnes of dicofol is used around the world each year, of which 290 tonnes is used in Western Europe. The only European countries which do allow its use are Belgium, Spain, Portugal and France. There are indications that through atmospheric transport dicophol used in other continents might also end up in the North Sea. <ref name="Ospar">[http://www.ospar.org/documents%5Cdbase%5Cpublications%5Cp00150_Background%20document%20on%20Dicofol.pdf OSPAR Commission, 2004: OSPAR background document on dicofol]</ref></div></td><td class='diff-marker'>+</td><td style="color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div>The main source of dicofol in the environment is its use as a [[pesticide]] used on a wide variety of fruits, vegetables, ornamentals and field crops. A total amount of over 2700 tonnes of dicofol is used around the world each year, of which 290 tonnes is used in Western Europe. The only European countries which do allow its use are Belgium, Spain, Portugal and France. There are indications that through atmospheric transport<ins class="diffchange diffchange-inline">, </ins>dicophol used in other continents might also end up in the <ins class="diffchange diffchange-inline">[[</ins>North Sea<ins class="diffchange diffchange-inline">]]</ins>. <ref name="Ospar">[http://www.ospar.org/documents%5Cdbase%5Cpublications%5Cp00150_Background%20document%20on%20Dicofol.pdf OSPAR Commission, 2004: OSPAR background document on dicofol]</ref></div></td></tr>
<tr><td class='diff-marker'> </td><td style="background-color: #f8f9fa; color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"></td><td class='diff-marker'> </td><td style="background-color: #f8f9fa; color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"></td></tr>
<tr><td class='diff-marker'> </td><td style="background-color: #f8f9fa; color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>The degradation of dicofol in soil is moderately slow, with a [[half-life]] of 30 to 60 days. In water systems and soils with a high organic matter content, the half-life can reach 84 days. Like DDT, it also has a high affinity to lipids, which causes it to [[adsorption|adsob]] to organic particles rather than dissolve in water. It's also highly [[bioaccumulation|bioaccumulative]], and [[biomagnification|biomagnifying]], therefore it poses a greater threat to high [[trophic level]] [[species]] such as [[pollution and sea birds|birds]] and [[pollution and marine mammals|mammals]].  </div></td><td class='diff-marker'> </td><td style="background-color: #f8f9fa; color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>The degradation of dicofol in soil is moderately slow, with a [[half-life]] of 30 to 60 days. In water systems and soils with a high organic matter content, the half-life can reach 84 days. Like DDT, it also has a high affinity to lipids, which causes it to [[adsorption|adsob]] to organic particles rather than dissolve in water. It's also highly [[bioaccumulation|bioaccumulative]], and [[biomagnification|biomagnifying]], therefore it poses a greater threat to high [[trophic level]] [[species]] such as [[pollution and sea birds|birds]] and [[pollution and marine mammals|mammals]].  </div></td></tr>
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Daphnisd
https://www.coastalwiki.org/w/index.php?title=Dicofol&diff=34832&oldid=prev
Daphnisd at 06:35, 5 October 2009
2009-10-05T06:35:32Z
<p></p>
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<td colspan="2" style="background-color: #fff; color: #222; text-align: center;">Revision as of 06:35, 5 October 2009</td>
</tr><tr><td colspan="2" class="diff-lineno" id="mw-diff-left-l5" >Line 5:</td>
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<tr><td class='diff-marker'> </td><td style="background-color: #f8f9fa; color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"></td><td class='diff-marker'> </td><td style="background-color: #f8f9fa; color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"></td></tr>
<tr><td class='diff-marker'> </td><td style="background-color: #f8f9fa; color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>== Notes ==</div></td><td class='diff-marker'> </td><td style="background-color: #f8f9fa; color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>== Notes ==</div></td></tr>
<tr><td class='diff-marker'>−</td><td style="color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div><del style="font-weight: bold; text-decoration: none;"></del></div></td><td colspan="2"> </td></tr>
<tr><td class='diff-marker'> </td><td style="background-color: #f8f9fa; color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"></td><td class='diff-marker'> </td><td style="background-color: #f8f9fa; color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"></td></tr>
<tr><td class='diff-marker'> </td><td style="background-color: #f8f9fa; color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>{| class="toccolours" border="1" style="float: right; clear: right; margin: 0 0 1em 1em; border-collapse: collapse;"</div></td><td class='diff-marker'> </td><td style="background-color: #f8f9fa; color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>{| class="toccolours" border="1" style="float: right; clear: right; margin: 0 0 1em 1em; border-collapse: collapse;"</div></td></tr>
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<tr><td class='diff-marker'> </td><td style="background-color: #f8f9fa; color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|-</div></td><td class='diff-marker'> </td><td style="background-color: #f8f9fa; color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|-</div></td></tr>
<tr><td class='diff-marker'> </td><td style="background-color: #f8f9fa; color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|}</div></td><td class='diff-marker'> </td><td style="background-color: #f8f9fa; color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|}</div></td></tr>
<tr><td class='diff-marker'>−</td><td style="color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div><del style="font-weight: bold; text-decoration: none;"></del></div></td><td colspan="2"> </td></tr>
<tr><td class='diff-marker'> </td><td style="background-color: #f8f9fa; color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"></td><td class='diff-marker'> </td><td style="background-color: #f8f9fa; color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"></td></tr>
<tr><td class='diff-marker'> </td><td style="background-color: #f8f9fa; color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>The main source of dicofol in the environment is its use as a [[pesticide]] used on a wide variety of fruits, vegetables, ornamentals and field crops. A total amount of over 2700 tonnes of dicofol is used around the world each year, of which 290 tonnes is used in Western Europe. The only European countries which do allow its use are Belgium, Spain, Portugal and France. There are indications that through atmospheric transport dicophol used in other continents might also end up in the North Sea. <ref name="Ospar">[http://www.ospar.org/documents%5Cdbase%5Cpublications%5Cp00150_Background%20document%20on%20Dicofol.pdf OSPAR Commission, 2004: OSPAR background document on dicofol]</ref></div></td><td class='diff-marker'> </td><td style="background-color: #f8f9fa; color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>The main source of dicofol in the environment is its use as a [[pesticide]] used on a wide variety of fruits, vegetables, ornamentals and field crops. A total amount of over 2700 tonnes of dicofol is used around the world each year, of which 290 tonnes is used in Western Europe. The only European countries which do allow its use are Belgium, Spain, Portugal and France. There are indications that through atmospheric transport dicophol used in other continents might also end up in the North Sea. <ref name="Ospar">[http://www.ospar.org/documents%5Cdbase%5Cpublications%5Cp00150_Background%20document%20on%20Dicofol.pdf OSPAR Commission, 2004: OSPAR background document on dicofol]</ref></div></td></tr>
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Daphnisd
https://www.coastalwiki.org/w/index.php?title=Dicofol&diff=34831&oldid=prev
Daphnisd: /* */
2009-10-05T06:35:11Z
<p><span dir="auto"><span class="autocomment"></span></span></p>
<table class="diff diff-contentalign-left" data-mw="interface">
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<col class="diff-marker" />
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<tr class="diff-title" lang="en">
<td colspan="2" style="background-color: #fff; color: #222; text-align: center;">← Older revision</td>
<td colspan="2" style="background-color: #fff; color: #222; text-align: center;">Revision as of 06:35, 5 October 2009</td>
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<tr><td class='diff-marker'> </td><td style="background-color: #f8f9fa; color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>{{Definition|title=dicofol  </div></td><td class='diff-marker'> </td><td style="background-color: #f8f9fa; color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>{{Definition|title=dicofol  </div></td></tr>
<tr><td class='diff-marker'> </td><td style="background-color: #f8f9fa; color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"></td><td class='diff-marker'> </td><td style="background-color: #f8f9fa; color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"></td></tr>
<tr><td class='diff-marker'>−</td><td style="color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div>|definition=Dicofol belongs to the group of [[organochlorine pesticides]]. It's produced from [[DDT]], therefore it has a <del class="diffchange diffchange-inline">simular </del>chemical structure and similar properties.<ref name="Ospar">[http://www.ospar.org/documents%5Cdbase%5Cpublications%5Cp00150_Background%20document%20on%20Dicofol.pdf OSPAR Commission, 2004: OSPAR background document on dicofol]</ref>}}</div></td><td class='diff-marker'>+</td><td style="color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div>|definition=Dicofol belongs to the group of [[organochlorine pesticides]]. It's produced from [[DDT]], therefore it has a <ins class="diffchange diffchange-inline">similar </ins>chemical structure and similar properties.<ref name="Ospar">[http://www.ospar.org/documents%5Cdbase%5Cpublications%5Cp00150_Background%20document%20on%20Dicofol.pdf OSPAR Commission, 2004: OSPAR background document on dicofol]</ref>}}</div></td></tr>
<tr><td class='diff-marker'> </td><td style="background-color: #f8f9fa; color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"></td><td class='diff-marker'> </td><td style="background-color: #f8f9fa; color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"></td></tr>
<tr><td class='diff-marker'> </td><td style="background-color: #f8f9fa; color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>== Notes ==</div></td><td class='diff-marker'> </td><td style="background-color: #f8f9fa; color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>== Notes ==</div></td></tr>
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Daphnisd
https://www.coastalwiki.org/w/index.php?title=Dicofol&diff=34830&oldid=prev
Daphnisd at 06:34, 5 October 2009
2009-10-05T06:34:58Z
<p></p>
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<td colspan="2" style="background-color: #fff; color: #222; text-align: center;">Revision as of 06:34, 5 October 2009</td>
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<tr><td class='diff-marker'> </td><td style="background-color: #f8f9fa; color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>{{Definition|title=dicofol  </div></td><td class='diff-marker'> </td><td style="background-color: #f8f9fa; color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>{{Definition|title=dicofol  </div></td></tr>
<tr><td class='diff-marker'> </td><td style="background-color: #f8f9fa; color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"></td><td class='diff-marker'> </td><td style="background-color: #f8f9fa; color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"></td></tr>
<tr><td class='diff-marker'>−</td><td style="color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div>|definition=Dicofol belongs to the group of [[organochlorine pesticides]]. It's produced from [[DDT]], <del class="diffchange diffchange-inline">its </del>chemical structure <del class="diffchange diffchange-inline">is therefore related to DDT </del>and <del class="diffchange diffchange-inline">it has </del>similar properties.<ref name="Ospar">[http://www.ospar.org/documents%5Cdbase%5Cpublications%5Cp00150_Background%20document%20on%20Dicofol.pdf OSPAR Commission, 2004: OSPAR background document on dicofol]</ref>}}</div></td><td class='diff-marker'>+</td><td style="color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div>|definition=Dicofol belongs to the group of [[organochlorine pesticides]]. It's produced from [[DDT]], <ins class="diffchange diffchange-inline">therefore it has a simular </ins>chemical structure and similar properties.<ref name="Ospar">[http://www.ospar.org/documents%5Cdbase%5Cpublications%5Cp00150_Background%20document%20on%20Dicofol.pdf OSPAR Commission, 2004: OSPAR background document on dicofol]</ref>}}</div></td></tr>
<tr><td class='diff-marker'> </td><td style="background-color: #f8f9fa; color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"></td><td class='diff-marker'> </td><td style="background-color: #f8f9fa; color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"></td></tr>
<tr><td class='diff-marker'> </td><td style="background-color: #f8f9fa; color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>== Notes ==</div></td><td class='diff-marker'> </td><td style="background-color: #f8f9fa; color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>== Notes ==</div></td></tr>
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https://www.coastalwiki.org/w/index.php?title=Dicofol&diff=33457&oldid=prev
Daphnisd: /* Notes */
2009-08-28T08:31:59Z
<p><span dir="auto"><span class="autocomment">Notes</span></span></p>
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<td colspan="2" style="background-color: #fff; color: #222; text-align: center;">Revision as of 08:31, 28 August 2009</td>
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<tr><td class='diff-marker'> </td><td style="background-color: #f8f9fa; color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"></td><td class='diff-marker'> </td><td style="background-color: #f8f9fa; color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"></td></tr>
<tr><td class='diff-marker'> </td><td style="background-color: #f8f9fa; color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"></td><td class='diff-marker'> </td><td style="background-color: #f8f9fa; color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"></td></tr>
<tr><td class='diff-marker'>−</td><td style="color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div>The main source of dicofol in the environment is its use as a pesticide used on a wide variety of fruits, vegetables, ornamentals and field crops. A total amount of over 2700 tonnes of dicofol is used around the world each year, of which 290 tonnes is used in Western Europe. The only European countries which do allow its use are Belgium, Spain, Portugal and France. There are indications that through atmospheric transport dicophol used in other continents might also end up in the North Sea. <ref name="Ospar">[http://www.ospar.org/documents%5Cdbase%5Cpublications%5Cp00150_Background%20document%20on%20Dicofol.pdf OSPAR Commission, 2004: OSPAR background document on dicofol]</ref></div></td><td class='diff-marker'>+</td><td style="color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div>The main source of dicofol in the environment is its use as a <ins class="diffchange diffchange-inline">[[</ins>pesticide<ins class="diffchange diffchange-inline">]] </ins>used on a wide variety of fruits, vegetables, ornamentals and field crops. A total amount of over 2700 tonnes of dicofol is used around the world each year, of which 290 tonnes is used in Western Europe. The only European countries which do allow its use are Belgium, Spain, Portugal and France. There are indications that through atmospheric transport dicophol used in other continents might also end up in the North Sea. <ref name="Ospar">[http://www.ospar.org/documents%5Cdbase%5Cpublications%5Cp00150_Background%20document%20on%20Dicofol.pdf OSPAR Commission, 2004: OSPAR background document on dicofol]</ref></div></td></tr>
<tr><td class='diff-marker'> </td><td style="background-color: #f8f9fa; color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"></td><td class='diff-marker'> </td><td style="background-color: #f8f9fa; color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"></td></tr>
<tr><td class='diff-marker'> </td><td style="background-color: #f8f9fa; color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>The degradation of dicofol in soil is moderately slow, with a [[half-life]] of 30 to 60 days. In water systems and soils with a high organic matter content, the half-life can reach 84 days. Like DDT, it also has a high affinity to lipids, which causes it to [[adsorption|adsob]] to organic particles rather than dissolve in water. It's also highly [[bioaccumulation|bioaccumulative]], and [[biomagnification|biomagnifying]], therefore it poses a greater threat to high [[trophic level]] [[species]] such as [[pollution and sea birds|birds]] and [[pollution and marine mammals|mammals]].  </div></td><td class='diff-marker'> </td><td style="background-color: #f8f9fa; color: #222; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>The degradation of dicofol in soil is moderately slow, with a [[half-life]] of 30 to 60 days. In water systems and soils with a high organic matter content, the half-life can reach 84 days. Like DDT, it also has a high affinity to lipids, which causes it to [[adsorption|adsob]] to organic particles rather than dissolve in water. It's also highly [[bioaccumulation|bioaccumulative]], and [[biomagnification|biomagnifying]], therefore it poses a greater threat to high [[trophic level]] [[species]] such as [[pollution and sea birds|birds]] and [[pollution and marine mammals|mammals]].  </div></td></tr>
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