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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>5</volume_number>
		<issue_number>1</issue_number>
		<publication_year>2005</publication_year>
	</journal>
	<doi>10.5194/acpd-5-573-2005</doi>
	<article_url>http://www.atmos-chem-phys-discuss.net/5/573/2005/</article_url>
	<abstract_html>http://www.atmos-chem-phys-discuss.net/5/573/2005/acpd-5-573-2005.html</abstract_html>
	<fulltext_pdf>http://www.atmos-chem-phys-discuss.net/5/573/2005/acpd-5-573-2005.pdf</fulltext_pdf>
	<start_page>573</start_page>
	<end_page>605</end_page>
	<publication_date>2005-02-03</publication_date>
	<article_title content_type="html">The contribution of sulphuric acid to atmospheric particle formation and growth: a comparison between boundary layers in Northern and Central Europe</article_title>
	<authors>
		<author numeration="1" affiliations="1,2">
			<name>V. Fiedler</name>
		</author>
		<author numeration="2" affiliations="2">
			<name>M. Dal Maso</name>
		</author>
		<author numeration="3" affiliations="2">
			<name>M. Boy</name>
		</author>
		<author numeration="4" affiliations="1">
			<name>H. Aufmhoff</name>
		</author>
		<author numeration="5" affiliations="1">
			<name>J. Hoffmann</name>
		</author>
		<author numeration="6" affiliations="1">
			<name>T. Schuck</name>
		</author>
		<author numeration="7" affiliations="3">
			<name>W. Birmili</name>
		</author>
		<author numeration="8" affiliations="1">
			<name>F. Arnold</name>
		</author>
		<author numeration="9" affiliations="2">
			<name>M. Kulmala</name>
		</author>
	</authors>
	<affiliations>
		<affiliation numeration="1" content_type="html">Max-Planck Institute for Nuclear Physics, (MPIK), Atmospheric Physics Division, P.O. Box 103980, D-69029 Heidelberg, Germany</affiliation>
		<affiliation numeration="2" content_type="html">University of Helsinki, Dept. Physical Sciences, P.O. Box 64, FIN-00014 Univ. of Helsinki, Finland</affiliation>
		<affiliation numeration="3" content_type="html">Leibniz Institute for Tropospheric Research, Permoserstr. 15, D-04318 Leipzig, Germany</affiliation>
	</affiliations>
	<abstract content_type="html">Atmospheric gaseous sulphuric acid was measured and its influence on
particle formation and growth was investigated building on aerosol data. The
measurements were part of the EU-project QUEST and took place at two
different measurement sites in Northern and Central Europe
(Hyyti&amp;#228;l&amp;#228;, Finland, March&amp;ndash;April 2003 and Heidelberg, Germany,
March&amp;ndash;April 2004). From a comprehensive data set including particle number
size distributions, sulphuric acid, and meteorological data, particle growth
rates, particle formation rates and source rates of condensable vapors were
calculated. Growth rates were determined in two different ways, from
particle size distributions as well as from a so-called timeshift analysis.
Moreover, correlations between sulphuric acid and particle number
concentration between 3 and 6 nm were examined and the influence of
different air masses was analyzed. Measured concentrations of sulphuric acid
were in the range from 2&amp;middot;10&lt;sup&gt;6&lt;/sup&gt; to 16&amp;middot;10&lt;sup&gt;6&lt;/sup&gt; cm&lt;sup&gt;-3&lt;/sup&gt;.
The gaseous sulphuric acid lifetime with respect to condensation on aerosol
particles ranged from 2 to 33 min in Hyyti&amp;#228;l&amp;#228; and from 28 s to 8 min
in Heidelberg. Most calculated values (growth rates, formation rates, vapor
source rates) were considerably higher in Central Europe (Heidelberg), due
to the more polluted air and higher preexistent aerosol concentrations.
Close correlations between H&lt;sub&gt;2&lt;/sub&gt;SO&lt;sub&gt;4&lt;/sub&gt; and nucleation mode particles
(size range: 3&amp;ndash;6 nm) were found on many days at both sites but several
observation days also lacked such correlations. The percentage contribution
of sulphuric acid to particle growth was below 10% at both places, to
initial growth below 20%. An air mass analysis indicated that at
Heidelberg new particles were formed predominantly in air advected from
southwesterly directions.</abstract>
	<references>
	</references>
</article>

