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<front>
<journal-meta>
<journal-id journal-id-type="publisher">ACPD</journal-id>
<journal-title-group>
<journal-title>Atmospheric Chemistry and Physics Discussions</journal-title>
<abbrev-journal-title abbrev-type="publisher">ACPD</abbrev-journal-title>
</journal-title-group>
<issn pub-type="epub">1680-7375</issn>
<publisher><publisher-name>Copernicus GmbH</publisher-name>
<publisher-loc>Göttingen, Germany</publisher-loc>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="doi">10.5194/acpd-10-9647-2010</article-id>
<title-group>
<article-title>Contributions to stratospheric ozone changes from ozone depleting substances and greenhouse gases</article-title>
</title-group>
<contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Plummer</surname>
<given-names>D. A.</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
</contrib>
<contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Scinocca</surname>
<given-names>J. F.</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
</contrib>
<contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Shepherd</surname>
<given-names>T. G.</given-names>
</name>
<xref ref-type="aff" rid="aff2">
<sup>2</sup>
</xref>
</contrib>
<contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Reader</surname>
<given-names>M. C.</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
</contrib>
<contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Jonsson</surname>
<given-names>A. I.</given-names>
</name>
<xref ref-type="aff" rid="aff2">
<sup>2</sup>
</xref>
</contrib>
</contrib-group><aff id="aff1">
<label>1</label>
<addr-line>Canadian Centre for Climate Modelling and Analysis, Environment Canada, Victoria, B. C., Canada</addr-line>
</aff>
<aff id="aff2">
<label>2</label>
<addr-line>Department of Physics, University of Toronto, Toronto, Canada</addr-line>
</aff>
<pub-date pub-type="epub">
<day>15</day>
<month>04</month>
<year>2010</year>
</pub-date>
<volume>10</volume>
<issue>4</issue>
<fpage>9647</fpage>
<lpage>9694</lpage>
<permissions>
<license xlink:type="simple">
<license-p>This is an open-access article ditributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.</license-p>
</license>
</permissions>
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<abstract>
<p>A state-of-the-art chemistry climate model coupled to a three-dimensional ocean
model is used to produce three experiments, all seamlessly covering the period
1950–2100, forced by different combinations of long-lived Greenhouse Gases (GHGs)
and Ozone Depleting Substances (ODSs). The experiments are designed to investigate
the mechanisms by which GHGs and ODSs affect the evolution of ozone, including changes
in the Brewer-Dobson circulation of the stratosphere and cooling of the upper
stratosphere by CO&lt;sub&gt;2&lt;/sub&gt;. Separating the effects of GHGs and ODSs on ozone, we
find the decrease in upper stratospheric ozone from ODSs up to the year 2000 is
approximately 30% larger than the actual decrease in ozone due to the offsetting
effects of cooling by increased CO&lt;sub&gt;2&lt;/sub&gt;. Over the 21st century, as ODSs
decrease, continued cooling from CO&lt;sub&gt;2&lt;/sub&gt; is projected to account for more than
50% of the projected increase in upper stratospheric ozone. Changes below 20 hPa
show a redistribution of ozone from tropical to extra-tropical latitudes with an
increase in the Brewer-Dobson circulation, while globally averaged the amount of
ozone below 20 hPa decreases over the 21st century. Further analysis by linear
regression shows that changes associated with GHGs do not appreciably alter the
recovery of stratospheric ozone from the effects of ODSs; over much of the
stratosphere ozone recovery follows the decline of halogen concentrations within
statistical uncertainty, though the lower polar stratosphere of the Southern
Hemisphere is an exception with ozone concentrations recovering more slowly than
indicated by the halogen concentrations. These results also reveal the degree to
which climate change, and stratospheric CO&lt;sub&gt;2&lt;/sub&gt; cooling in particular, mutes
the chemical effects of N&lt;sub&gt;2&lt;/sub&gt;O on ozone in the standard future scenario used
for the WMO Ozone Assessment. Increases in the residual circulation of the
atmosphere and chemical effects from CO&lt;sub&gt;2&lt;/sub&gt; cooling more than halve the
increase in reactive nitrogen in the mid to upper stratosphere that results from
the specified increase in N&lt;sub&gt;2&lt;/sub&gt;O between 1950 and 2100.</p>
</abstract>
<counts><page-count count="48"/></counts>
</article-meta>
</front>
<body/>
<back>
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