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<article language="en">
	<journal>
		<journal_title>Atmospheric Chemistry and Physics Discussions</journal_title>
		<journal_url>www.atmos-chem-phys-discuss.net</journal_url>
		<issn>1680-7367</issn>
		<eissn>1680-7375</eissn>
		<volume_number>8</volume_number>
		<issue_number>4</issue_number>
		<publication_year>2008</publication_year>
	</journal>
	<doi>10.5194/acpd-8-16445-2008</doi>
	<article_url>http://www.atmos-chem-phys-discuss.net/8/16445/2008/</article_url>
	<abstract_html>http://www.atmos-chem-phys-discuss.net/8/16445/2008/acpd-8-16445-2008.html</abstract_html>
	<fulltext_pdf>http://www.atmos-chem-phys-discuss.net/8/16445/2008/acpd-8-16445-2008.pdf</fulltext_pdf>
	<start_page>16445</start_page>
	<end_page>16471</end_page>
	<publication_date>2008-08-27</publication_date>
	<article_title content_type="html">Evaluation of the global oceanic isoprene source and its impacts on marine organic carbon aerosol</article_title>
	<authors>
		<author numeration="1" affiliations="1">
			<name>S. R. Arnold</name>
			<email>s.arnold@see.leeds.ac.uk</email>
		</author>
		<author numeration="2" affiliations="1">
			<name>D. V. Spracklen</name>
		</author>
		<author numeration="3" affiliations="2">
			<name>J. Williams</name>
		</author>
		<author numeration="4" affiliations="2">
			<name>N. Yassaa</name>
		</author>
		<author numeration="5" affiliations="3">
			<name>J. Sciare</name>
		</author>
		<author numeration="6" affiliations="3">
			<name>B. Bonsang</name>
		</author>
		<author numeration="7" affiliations="3">
			<name>V. Gros</name>
		</author>
		<author numeration="8" affiliations="4">
			<name>I. Peeken</name>
		</author>
		<author numeration="9" affiliations="5">
			<name>A. C. Lewis</name>
		</author>
		<author numeration="10" affiliations="3">
			<name>S. Alvain</name>
		</author>
		<author numeration="11" affiliations="3">
			<name>C. Moulin</name>
		</author>
	</authors>
	<affiliations>
		<affiliation numeration="1" content_type="html">Institute for Climate and Atmospheric Science, School of Earth and Environment, University of Leeds, Leeds, UK</affiliation>
		<affiliation numeration="2" content_type="html">Max Planck Institute for Chemistry, Mainz, Germany</affiliation>
		<affiliation numeration="3" content_type="html">IPSL/LSCE, CEA Saclay, Gif-sur-Yvette, France</affiliation>
		<affiliation numeration="4" content_type="html">Ifm GEOMAR, Kiel, Germany</affiliation>
		<affiliation numeration="5" content_type="html">Department of Chemistry, University of York, York, UK</affiliation>
	</affiliations>
	<abstract content_type="html">We have combined the first satellite maps of the global
distribution of phytoplankton functional type and new measurements of
phytoplankton-specific isoprene productivities, with available remote marine
isoprene observations and a global model, to evaluate our understanding of the
marine isoprene source and its impacts on organic aerosol abundances. Using
satellite products to scale up data on phytoplankton-specific isoprene
productivity to the global oceans, we infer a mean &quot;bottom-up&quot; oceanic
isoprene emission of 0.31&amp;plusmn;0.08 (1 Ïƒ) Tg/yr. By minimising the mean
bias between the model and isoprene observations in the marine atmosphere remote
from the continents, we produce a &quot;top-down&quot; oceanic isoprene source estimate
of 1.9 Tg/yr. We suggest our reliance on limited atmospheric isoprene data,
and limited knowledge of isoprene productivity across the broad range of
phytoplankton communities in the oceans as contributors
to this difference between the two estimates. Inclusion of secondary organic
aerosol (SOA) production from oceanic isoprene in the model with a 2% yield
produces small contributions (0.01â€“1.6%) to observed organic carbon (OC)
aerosol mass at three remote marine sites in the Northern and Southern
Hemispheres. In addition, we find the seasonal cycle of the isoprene SOA
source is out of phase with the observed cycle in OC in the remote Southern
Ocean. Based on these findings we suggest an insignificant role for isoprene
in modulating remote marine aerosol abundances, giving further support to a
recently postulated primary OC source in the remote marine atmosphere.</abstract>
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