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<front>
<journal-meta>
<journal-id journal-id-type="publisher">ACP</journal-id>
<journal-title-group>
<journal-title>Atmospheric Chemistry and Physics</journal-title>
<abbrev-journal-title abbrev-type="publisher">ACP</abbrev-journal-title>
<abbrev-journal-title abbrev-type="nlm-ta">Atmos. Chem. Phys.</abbrev-journal-title>
</journal-title-group>
<issn pub-type="epub">1680-7324</issn>
<publisher><publisher-name>Copernicus Publications</publisher-name>
<publisher-loc>Göttingen, Germany</publisher-loc>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="doi">10.5194/acp-2-39-2002</article-id>
<title-group>
<article-title>The influence of cloud chemistry on HO&lt;sub&gt;x&lt;/sub&gt; and NO&lt;sub&gt;x&lt;/sub&gt; in the moderately polluted marine boundary layer: a 1-D modelling study</article-title>
</title-group>
<contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Williams</surname>
<given-names>J. E.</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
<xref ref-type="aff" rid="aff2">
<sup>2</sup>
</xref>
</contrib>
<contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Dentener</surname>
<given-names>F. J.</given-names>
</name>
<xref ref-type="aff" rid="aff3">
<sup>3</sup>
</xref>
</contrib>
<contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>van den Berg</surname>
<given-names>A. R.</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
</contrib>
</contrib-group><aff id="aff1">
<label>1</label>
<addr-line>IMAU, University of Utrecht, Utrecht, The Netherlands</addr-line>
</aff>
<aff id="aff2">
<label>2</label>
<addr-line>Current Address: FOM-AMOLF, Kruislaan 107, Amsterdam, The Netherlands</addr-line>
</aff>
<aff id="aff3">
<label>3</label>
<addr-line>Joint Research Center, Environment Institute, Ispra(Va), Italy</addr-line>
</aff>
<pub-date pub-type="epub">
<day>05</day>
<month>02</month>
<year>2002</year>
</pub-date>
<volume>2</volume>
<issue>1</issue>
<fpage>39</fpage>
<lpage>54</lpage>
<permissions>
<copyright-statement>Copyright: &#x000a9; 2002 J. E. Williams et al.</copyright-statement>
<copyright-year>2002</copyright-year>
<license license-type="open-access">
<license-p>This work is licensed under the Creative Commons Attribution-NonCommercial-ShareAlike 2.5 Generic License. To view a copy of this licence, visit <ext-link ext-link-type="uri"  xlink:href="https://creativecommons.org/licenses/by-nc-sa/2.5/">https://creativecommons.org/licenses/by-nc-sa/2.5/</ext-link></license-p>
</license>
</permissions>
<self-uri xlink:href="https://acp.copernicus.org/articles/2/39/2002/acp-2-39-2002.html">This article is available from https://acp.copernicus.org/articles/2/39/2002/acp-2-39-2002.html</self-uri>
<self-uri xlink:href="https://acp.copernicus.org/articles/2/39/2002/acp-2-39-2002.pdf">The full text article is available as a PDF file from https://acp.copernicus.org/articles/2/39/2002/acp-2-39-2002.pdf</self-uri>
<abstract>
<p>A 1-D marine stratocumulus cloud model has been supplemented with
      a comprehensive and up-to-date aqueous phase chemical mechanism for the purpose of assessing the impact that the presence of
      clouds has on gas phaseHO&lt;sub&gt;x&lt;/sub&gt;, NO&lt;sub&gt;x&lt;/sub&gt; and O&lt;sub&gt;3&lt;/sub&gt; budgets in the marine boundary layer. The simulations presented
      here indicate that cloud may act as a heterogeneous source of HONO&lt;sub&gt;g&lt;/sub&gt;. The conversion of
      HNO&lt;sub&gt;4(g)&lt;/sub&gt; at moderate pH (~ 4.5) is responsible for this, and, to a lesser extent, the
      photolysis of nitrate (NO&lt;sub&gt;3&lt;/sub&gt;&lt;sup&gt;-&lt;/sup&gt;). The effect of introducing
      deliquescent aerosol on the simulated increase of HONO&lt;sub&gt;g&lt;/sub&gt; is negligible. The most important consequences of this elevation in
      HONO&lt;sub&gt;g&lt;/sub&gt; are that, in the presence of cloud, gas phase concentrations of
      NO&lt;sub&gt;x&lt;/sub&gt; species increase by a factor of 2, which minimises the simulated decrease in
      O&lt;sub&gt;3(g)&lt;/sub&gt;, and results in a regeneration of OH&lt;sub&gt;g&lt;/sub&gt;. This partly compensates
      for the removal of OH&lt;sub&gt;g&lt;/sub&gt; by direct phase transfer into the cloud and may have important implications regarding the oxidising
      capacity of the marine boundary layer.</p>
</abstract>
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