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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>
</journal-title-group>
<issn pub-type="epub">1680-7324</issn>
<publisher><publisher-name>Copernicus GmbH</publisher-name>
<publisher-loc>GÃ¶ttingen, Germany</publisher-loc>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="doi">10.5194/acp-11-7491-2011</article-id>
<title-group>
<article-title>Modeling chemical and aerosol processes in the transition from closed to open cells during VOCALS-REx</article-title>
</title-group>
<contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Kazil</surname>
<given-names>J.</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>Wang</surname>
<given-names>H.</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>Feingold</surname>
<given-names>G.</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>Clarke</surname>
<given-names>A. D.</given-names>
</name>
<xref ref-type="aff" rid="aff4">
<sup>4</sup>
</xref>
</contrib>
<contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Snider</surname>
<given-names>J. R.</given-names>
</name>
<xref ref-type="aff" rid="aff5">
<sup>5</sup>
</xref>
</contrib>
<contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Bandy</surname>
<given-names>A. R.</given-names>
</name>
<xref ref-type="aff" rid="aff6">
<sup>6</sup>
</xref>
</contrib>
</contrib-group><aff id="aff1">
<label>1</label>
<addr-line>Cooperative Institute for Research in Environmental Sciences (CIRES), University of Colorado, Boulder, CO, USA</addr-line>
</aff>
<aff id="aff2">
<label>2</label>
<addr-line>NOAA Earth System Research Laboratory, Chemical Sciences Division, Boulder, CO, USA</addr-line>
</aff>
<aff id="aff3">
<label>3</label>
<addr-line>Pacific Northwest National Laboratory, Atmospheric Sciences &amp; Global Change Division, Richland, WA, USA</addr-line>
</aff>
<aff id="aff4">
<label>4</label>
<addr-line>School of Ocean and Earth Science and Technology, University of Hawaii, Honolulu, HI, USA</addr-line>
</aff>
<aff id="aff5">
<label>5</label>
<addr-line>Department of Atmospheric Science, University of Wyoming, Laramie, WY, USA</addr-line>
</aff>
<aff id="aff6">
<label>6</label>
<addr-line>Chemistry Department, Drexel University, Philadelphia, PA, USA</addr-line>
</aff>
<pub-date pub-type="epub">
<day>01</day>
<month>08</month>
<year>2011</year>
</pub-date>
<volume>11</volume>
<issue>15</issue>
<fpage>7491</fpage>
<lpage>7514</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>
<self-uri xlink:href="http://www.atmos-chem-phys.net/11/7491/2011/acp-11-7491-2011.html">This article is available from http://www.atmos-chem-phys.net/11/7491/2011/acp-11-7491-2011.html</self-uri>
<self-uri xlink:href="http://www.atmos-chem-phys.net/11/7491/2011/acp-11-7491-2011.pdf">The full text article is available as a PDF file from http://www.atmos-chem-phys.net/11/7491/2011/acp-11-7491-2011.pdf</self-uri>
<abstract>
<p>Chemical and aerosol processes in the transition from closed- to open-cell circulation in
      the remote, cloudy marine boundary layer are explored. It has previously been shown that
      precipitation can initiate a transition from the closed- to the open-cellular state, but
      that the boundary layer cannot maintain this open-cell state without a resupply of cloud
      condensation nuclei (CCN). Potential sources of CCN include wind-driven production of sea salt
      from the ocean, nucleation from the gas phase, and entrainment from the free
      troposphere.  In order to investigate CCN sources in the marine boundary layer and their
      role in supplying new particles, we have coupled in detail chemical, aerosol, and cloud
      processes in the WRF/Chem model, and added state-of-the-art representations of sea salt
      emissions and aerosol nucleation. We conduct numerical simulations of the marine boundary layer in the transition from a closed- to an
open-cell
      state. Results are compared with observations in the Southeast Pacific boundary layer during
      the VAMOS Ocean-Cloud-Atmosphere-Land Study Regional Experiment (VOCALS-REx). The transition
      from the closed- to the open-cell state generates conditions that are conducive to
      nucleation by forming a cloud-scavenged, ultra-clean layer below the inversion base. Open
      cell updrafts loft dimethyl sulfide from the ocean surface into the ultra-clean layer,
      where it is oxidized during daytime to SO&lt;sub&gt;2&lt;/sub&gt; and subsequently to H&lt;sub&gt;2&lt;/sub&gt;SO&lt;sub&gt;4&lt;/sub&gt;. Low
      H&lt;sub&gt;2&lt;/sub&gt;SO&lt;sub&gt;4&lt;/sub&gt; condensation sink values in the ultra-clean layer allow H&lt;sub&gt;2&lt;/sub&gt;SO&lt;sub&gt;4&lt;/sub&gt; to
      rise to concentrations at which aerosol nucleation produces new aerosol in significant numbers. The existence of
      the ultra-clean layer is confirmed by observations. We find that the observed DMS flux from
      the ocean in the VOCALS-REx region can support a nucleation source of aerosol in open cells
      that exceeds sea salt emissions in terms of the number of particles produced. The freshly
      nucleated, nanometer-sized aerosol particles need, however, time to grow to sizes large enough
      to act as CCN. In contrast, mechanical production of particles from the ocean surface by
      near-surface winds provides a steady source of larger particles that are effective CCN at
      a rate exceeding a threshold for maintenance of open-cell circulation. Entrainment of aerosol
      from the free troposphere contributes significantly to boundary layer aerosol for the
      considered VOCALS-REx case, but less than sea salt aerosol emissions.</p>
</abstract>
<counts><page-count count="24"/></counts>
</article-meta>
</front>
<body/>
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