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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-11-5757-2011</article-id>
<title-group>
<article-title>Effect of primary organic sea spray emissions on cloud condensation nuclei concentrations</article-title>
</title-group>
<contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Westervelt</surname>
<given-names>D. M.</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>Moore</surname>
<given-names>R. H.</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>Nenes</surname>
<given-names>A.</given-names>
</name>
<xref ref-type="aff" rid="aff2">
<sup>2</sup>
</xref>
<xref ref-type="aff" rid="aff3">
<sup>3</sup>
</xref>
</contrib>
<contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Adams</surname>
<given-names>P. J.</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
<xref ref-type="aff" rid="aff4">
<sup>4</sup>
</xref>
</contrib>
</contrib-group><aff id="aff1">
<label>1</label>
<addr-line>Department of Civil and Environmental Engineering, Carnegie Mellon University, Pittsburgh, PA, USA</addr-line>
</aff>
<aff id="aff2">
<label>2</label>
<addr-line>School of Chemical and Biomolecular Engineering, Georgia Institute of Technology, Atlanta, GA, USA</addr-line>
</aff>
<aff id="aff3">
<label>3</label>
<addr-line>School of Earth and Atmospheric Sciences, Georgia Institute of Technology, Atlanta, GA, USA</addr-line>
</aff>
<aff id="aff4">
<label>4</label>
<addr-line>Department of Engineering and Public Policy, Carnegie Mellon University, Pittsburgh, PA, USA</addr-line>
</aff>
<pub-date pub-type="epub">
<day>16</day>
<month>02</month>
<year>2011</year>
</pub-date>
<volume>11</volume>
<issue>2</issue>
<fpage>5757</fpage>
<lpage>5784</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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<self-uri xlink:href="http://www.atmos-chem-phys-discuss.net/11/5757/2011/acpd-11-5757-2011.pdf">The full text article is available as a PDF file from http://www.atmos-chem-phys-discuss.net/11/5757/2011/acpd-11-5757-2011.pdf</self-uri>
<abstract>
<p>This work quantifies the primary marine organic aerosol global emission
source and its impact on cloud condensation nuclei (CCN) concentrations by
implementing an organic sea spray source function into a series of global
aerosol simulations. The source function assumes that a fraction of the sea
spray emissions, depending on the local chlorophyll concentration, is
organic matter in place of NaCl. Effect on CCN concentrations (at 0.2%
supersaturation) is modeled using the Two-Moment Aerosol Sectional (TOMAS)
microphysics algorithm coupled to the GISS II-prime general circulation
model. The presence of organics affects CCN activity in competing ways: by
reducing the amount of solute available in the particle and decreasing
surface tension of CCN. To model surfactant effects, surface tension
depression data from seawater samples taken near the Georgia coast were
applied as a function of carbon concentrations. A global marine organic
aerosol emission rate of 17.7 Tg C yr&lt;sup&gt;&amp;minus;1&lt;/sup&gt; is estimated from the
simulations. Marine organics exert a localized influence on CCN(0.2%)
concentrations, decreasing regional concentrations by no more than 5% and
by less than 0.5% over most of the globe. The decrease in CCN
concentrations results from the fact that the decrease in particle solute
concentration outweighs the organic surfactant effects. The low sensitivity
of CCN(0.2%) to the marine organic emissions is likely due to the small
compositional changes: the mass fraction of OA in accumulation mode aerosol
increases by only  15% in a biologically active region of the
Southern Ocean.</p>
</abstract>
<counts><page-count count="28"/></counts>
</article-meta>
</front>
<body/>
<back>
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