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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>2</issue_number>
		<publication_year>2008</publication_year>
	</journal>
	<doi>10.5194/acpd-8-7217-2008</doi>
	<article_url>http://www.atmos-chem-phys-discuss.net/8/7217/2008/</article_url>
	<abstract_html>http://www.atmos-chem-phys-discuss.net/8/7217/2008/acpd-8-7217-2008.html</abstract_html>
	<fulltext_pdf>http://www.atmos-chem-phys-discuss.net/8/7217/2008/acpd-8-7217-2008.pdf</fulltext_pdf>
	<start_page>7217</start_page>
	<end_page>7262</end_page>
	<publication_date>2008-04-14</publication_date>
	<article_title content_type="html">Consistent simulation of bromine chemistry from the marine boundary   layer to the stratosphere, Part I: model description, sea salt aerosols   and pH</article_title>
	<authors>
		<author numeration="1" affiliations="1,2">
			<name>A. Kerkweg</name>
			<email>akerkweg@mpch-mainz.mpg.de</email>
		</author>
		<author numeration="2" affiliations="1">
			<name>P. Jöckel</name>
		</author>
		<author numeration="3" affiliations="1">
			<name>A. Pozzer</name>
		</author>
		<author numeration="4" affiliations="1">
			<name>H. Tost</name>
		</author>
		<author numeration="5" affiliations="1">
			<name>R. Sander</name>
		</author>
		<author numeration="6" affiliations="3">
			<name>M. Schulz</name>
		</author>
		<author numeration="7" affiliations="4">
			<name>P. Stier</name>
		</author>
		<author numeration="8" affiliations="5">
			<name>E. Vignati</name>
		</author>
		<author numeration="9" affiliations="5">
			<name>J. Wilson</name>
		</author>
		<author numeration="10" affiliations="1">
			<name>J. Lelieveld</name>
		</author>
	</authors>
	<affiliations>
		<affiliation numeration="1" content_type="html">Atmospheric Chemistry Department, Max Planck Institute of Chemistry, P.O. Box 3060, 55020 Mainz, Germany</affiliation>
		<affiliation numeration="2" content_type="html">Institute for Atmospheric Physics, University of Mainz, Germany</affiliation>
		<affiliation numeration="3" content_type="html">Laboratoire des Sciences du Climat et de l&apos;Environnement, CEA-IPSL, Saclay, France</affiliation>
		<affiliation numeration="4" content_type="html">Atmospheric, Oceanic and Planetary Physics, University of Oxford, UK</affiliation>
		<affiliation numeration="5" content_type="html">Joint Research Centre, Institute of Environment and Sustainability, Ispra, Italy</affiliation>
	</affiliations>
	<abstract content_type="html">This is the first article of a series presenting a detailed analysis
of bromine chemistry simulated with the atmospheric chemistry general
circulation model ECHAM5/MESSy.
 Release from sea salt is an important bromine source, hence the model
 explicitly calculates aerosol chemistry and phase partitioning for coarse
 mode aerosol particles.
 Many processes including chemical reaction rates are
 influenced by the particle size distribution, and aerosol associated water
 strongly affects the aerosol pH. Knowledge of the aerosol pH is
 important as it determines the aerosol chemistry, e.g., the efficiency of
 sulphur oxidation and bromine release.
 Here, we focus on the simulated sea salt aerosol size distribution and the
 coarse mode aerosol pH.
&lt;br&gt;&lt;br&gt;
 A comparison with available field data shows that the simulated aerosol
 distributions agree reasonably well within the range of measurements.
 In spite of the small number of aerosol pH measurements and the uncertainty
 in its experimental determination, the simulated aerosol pH compares
 well with  the observations.
 The aerosol pH ranges from alkaline aerosol in areas of strong production
 down to
 pH values of 1 over regions of medium sea salt production and high levels of
 gas phase acids, mostly polluted regions over the oceans in the northern
 hemisphere.</abstract>
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