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<!DOCTYPE article SYSTEM "http://www.atmos-chem-phys-discuss.net/inc/acpd/copernicus.dtd">
<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>5</volume_number>
		<issue_number>1</issue_number>
		<publication_year>2005</publication_year>
	</journal>
	<doi>10.5194/acpd-5-179-2005</doi>
	<article_url>http://www.atmos-chem-phys-discuss.net/5/179/2005/</article_url>
	<abstract_html>http://www.atmos-chem-phys-discuss.net/5/179/2005/acpd-5-179-2005.html</abstract_html>
	<fulltext_pdf>http://www.atmos-chem-phys-discuss.net/5/179/2005/acpd-5-179-2005.pdf</fulltext_pdf>
	<start_page>179</start_page>
	<end_page>215</end_page>
	<publication_date>2005-01-14</publication_date>
	<article_title content_type="html">A global off-line model of size-resolved aerosol microphysics: I. Model development and prediction of aerosol properties</article_title>
	<authors>
		<author numeration="1" affiliations="1">
			<name>D. V. Spracklen</name>
		</author>
		<author numeration="2" affiliations="1">
			<name>K. J. Pringle</name>
		</author>
		<author numeration="3" affiliations="1">
			<name>K. S. Carslaw</name>
		</author>
		<author numeration="4" affiliations="1">
			<name>M. P. Chipperfield</name>
		</author>
		<author numeration="5" affiliations="1">
			<name>G. W. Mann</name>
		</author>
	</authors>
	<affiliations>
		<affiliation numeration="1" content_type="html">The School of Earth and Environment, University of Leeds, UK</affiliation>
	</affiliations>
	<abstract content_type="html">A GLObal Model of Aerosol Processes (GLOMAP) has been developed as an
extension to the TOMCAT 3-D Eulerian off-line chemical
transport model. GLOMAP simulates the evolution of the global aerosol
size distribution using a sectional
two-moment scheme and includes the processes of aerosol nucleation,
condensation, growth, coagulation, wet and  dry deposition
and cloud processing. We describe the results of a global simulation
of sulfuric acid and sea spray  aerosol. The
model captures features of the aerosol size distribution that are well
established  from observations in the marine
boundary layer and free troposphere. Modelled condensation nuclei (CN&amp;gt;3 nm)
vary between about 250&amp;ndash;500 cm&lt;sup&gt;-3&lt;/sup&gt; in remote marine boundary layer regions and between
2000 and 10 000 cm&lt;sup&gt;-3&lt;/sup&gt; (at standard
temperature and pressure) in the upper troposphere. Cloud condensation
nuclei (CCN) at 0.2% supersaturation
vary between about 1000 cm&lt;sup&gt;-3&lt;/sup&gt; in polluted regions and between
10 and 500 cm&lt;sup&gt;-3&lt;/sup&gt; in the remote
marine boundary layer. New particle formation through sulfuric
acid-water binary nucleation occurs predominantly
in the upper troposphere, but the model results show that these
particles contribute  greatly to aerosol
concentrations in the marine boundary layer. It is estimated that sea
spray emissions account for only
~10% of CCN in the tropical marine boundary layer, but between
20 and 75% in the mid-latitude
Southern Ocean.</abstract>
	<references>
	</references>
</article>

