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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-10-13557-2010</article-id>
<title-group>
<article-title>Sensitivity of a global model to the uptake of N&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;5&lt;/sub&gt; by  tropospheric aerosol</article-title>
</title-group>
<contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Macintyre</surname>
<given-names>H. L.</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>Evans</surname>
<given-names>M. J.</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
</contrib>
</contrib-group><aff id="aff1">
<label>1</label>
<addr-line>Institute for Climate and Atmospheric Science, School of Earth and Environment, University of Leeds, Leeds, LS2 9JT, UK</addr-line>
</aff>
<pub-date pub-type="epub">
<day>28</day>
<month>05</month>
<year>2010</year>
</pub-date>
<volume>10</volume>
<issue>5</issue>
<fpage>13557</fpage>
<lpage>13571</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>The uptake of N&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;5&lt;/sub&gt; on aerosol impacts atmospheric
concentrations of NO&lt;sub&gt;x&lt;/sub&gt; and so O&lt;sub&gt;3&lt;/sub&gt;, OH, and hence
CH&lt;sub&gt;4&lt;/sub&gt;. Laboratory studies show significant variation in the rate
of uptake, with a general decline in the value of
&amp;gamma;&lt;sub&gt;N&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;5&lt;/sub&gt;&lt;/sub&gt; over the last decade as increasingly relevant
tropospheric proxies have been studied. In order to understand the
implication of this decline for tropospheric composition, a global
model of tropospheric chemistry and transport (GEOS-Chem) is run with
differing values of &amp;gamma;&lt;sub&gt;N&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;5&lt;/sub&gt;&lt;/sub&gt; (0.0, 10&lt;sup&gt;&amp;minus;6&lt;/sup&gt;,
10&lt;sup&gt;&amp;minus;4&lt;/sup&gt;, 10&lt;sup&gt;−3&lt;/sup&gt;, 5&amp;times;10&lt;sup&gt;&amp;minus;3&lt;/sup&gt;, 10&lt;sup&gt;−2&lt;/sup&gt;, 2&amp;times;10&lt;sup&gt;&amp;minus;2&lt;/sup&gt;,
0.1, 0.2, 0.5, and 1.0). We identify three regimes in the model
response. At low values of &amp;gamma;&lt;sub&gt;N&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;5&lt;/sub&gt;&lt;/sub&gt;, the model shows
reduced sensitivity to the value of &amp;gamma;&lt;sub&gt;N&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;5&lt;/sub&gt;&lt;/sub&gt; as
heterogeneous uptake of N&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;5&lt;/sub&gt; does not provide a significant
pathway to perturb NO&lt;sub&gt;x&lt;/sub&gt; burdens. At high values of
&amp;gamma;&lt;sub&gt;N&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;5&lt;/sub&gt;&lt;/sub&gt; the model again shows reduced sensitivity to
the value of &amp;gamma;&lt;sub&gt;N&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;5&lt;/sub&gt;&lt;/sub&gt;, as NO&lt;sub&gt;x&lt;/sub&gt; loss through
heterogeneous removal of N&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;5&lt;/sub&gt; is limited by the rate of
production of NO&lt;sub&gt;3&lt;/sub&gt; rather than the rate of heterogeneous
uptake. At intermediate values of &amp;gamma;&lt;sub&gt;N&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;5&lt;/sub&gt;&lt;/sub&gt; the model
shows significant sensitivity to the value of
&amp;gamma;&lt;sub&gt;N&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;5&lt;/sub&gt;&lt;/sub&gt;. We find regional differences in the model&apos;s
response to changing &amp;gamma;&lt;sub&gt;N&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;5&lt;/sub&gt;&lt;/sub&gt;. Regions with high
aerosol surface area and low temperatures show NO&lt;sub&gt;3&lt;/sub&gt; production
becoming rate limiting at lower &amp;gamma;&lt;sub&gt;N&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;5&lt;/sub&gt;&lt;/sub&gt; values than
regions with lower aerosol surface area and higher temperatures. The
northern extra-tropics show significant sensitivity to the value of
&amp;gamma;&lt;sub&gt;N&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;5&lt;/sub&gt;&lt;/sub&gt; at values consistent with current literature
(0.001–0.02), thus an accurate description of
&amp;gamma;&lt;sub&gt;N&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;5&lt;/sub&gt;&lt;/sub&gt; is required for adequate simulation of
O&lt;sub&gt;3&lt;/sub&gt; burdens and long-range transport of pollutants in this
region.
&lt;br&gt;&lt;br&gt;
Our model simulations also provide insight into model sensitivity to
changes in aerosol load through changing surface area for different
values of &amp;gamma;&lt;sub&gt;N&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;5&lt;/sub&gt;&lt;/sub&gt;. We find little change in the
global sensitivity to &amp;gamma;&lt;sub&gt;N&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;5&lt;/sub&gt;&lt;/sub&gt; in the range 0.05 to
1.0, but a significant drop in sensitivity below this range. Thus
simulations of the coupled impact of both chemistry and aerosol
changes will be sensitive to the choice of &amp;gamma;&lt;sub&gt;N&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;5&lt;/sub&gt;&lt;/sub&gt;.</p>
</abstract>
<counts><page-count count="15"/></counts>
</article-meta>
</front>
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<back>
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