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	<journal>
		<journal_title>Atmospheric Chemistry and Physics</journal_title>
		<journal_url>www.atmos-chem-phys.net</journal_url>
		<issn>1680-7316</issn>
		<eissn>1680-7324</eissn>
		<volume_number>7</volume_number>
		<issue_number>10</issue_number>
		<publication_year>2007</publication_year>
	</journal>
	<doi>10.5194/acp-7-2705-2007</doi>
	<article_url>http://www.atmos-chem-phys.net/7/2705/2007/</article_url>
	<abstract_html>http://www.atmos-chem-phys.net/7/2705/2007/acp-7-2705-2007.html</abstract_html>
	<fulltext_pdf>http://www.atmos-chem-phys.net/7/2705/2007/acp-7-2705-2007.pdf</fulltext_pdf>
	<start_page>2705</start_page>
	<end_page>2720</end_page>
	<publication_date>2007-05-23</publication_date>
	<article_title content_type="html">Sub-micron atmospheric aerosols in the surroundings of Marseille and Athens: physical characterization and new particle formation</article_title>
	<authors>
		<author numeration="1" affiliations="1">
			<name>T. Petäjä</name>
			<email>tuukka.petaja@helsinki.fi</email>
		</author>
		<author numeration="2" affiliations="2">
			<name>V.-M. Kerminen</name>
		</author>
		<author numeration="3" affiliations="1">
			<name>M. Dal Maso</name>
		</author>
		<author numeration="4" affiliations="1">
			<name>H. Junninen</name>
		</author>
		<author numeration="5" affiliations="1,3">
			<name>I. K. Koponen</name>
		</author>
		<author numeration="6" affiliations="1,4">
			<name>T. Hussein</name>
		</author>
		<author numeration="7" affiliations="1">
			<name>P. P. Aalto</name>
		</author>
		<author numeration="8" affiliations="5">
			<name>S. Andronopoulos</name>
		</author>
		<author numeration="9" affiliations="6">
			<name>D. Robin</name>
		</author>
		<author numeration="10" affiliations="1,7">
			<name>K. Hämeri</name>
		</author>
		<author numeration="11" affiliations="5,8">
			<name>J. G. Bartzis</name>
		</author>
		<author numeration="12" affiliations="1">
			<name>M. Kulmala</name>
		</author>
	</authors>
	<affiliations>
		<affiliation numeration="1" content_type="html">Division of Atmospheric Sciences, Dept. of Physical  Sciences, University of Helsinki, Finland</affiliation>
		<affiliation numeration="2" content_type="html">Finnish  Meteorological Institute, Climate and Global Change, Helsinki,  Finland</affiliation>
		<affiliation numeration="3" content_type="html">Department of Chemistry, University of  Copenhagen, Denmark</affiliation>
		<affiliation numeration="4" content_type="html">Dept. of Applied Environmental  Sciences (ITM), Stockholm University, Stockholm, Sweden</affiliation>
		<affiliation numeration="5" content_type="html">National Centre for Scientific Research &quot;Demokritos&quot;,  Athens, Greece</affiliation>
		<affiliation numeration="6" content_type="html">AIRMARAIX, Marseille, France</affiliation>
		<affiliation numeration="7" content_type="html">Finnish Institute of Occupational Health, Helsinki,  Finland</affiliation>
		<affiliation numeration="8" content_type="html">Department of Engineering and Management of  Energy Resources, University of West Macedonia, Kozani, Greece</affiliation>
	</affiliations>
	<abstract content_type="html">The properties of atmospheric aerosol particles in Marseille and Athens
were investigated. The studies were performed in Marseille, France,
during July 2002 and in Athens, Greece, during June 2003. The aerosol
size distribution and the formation and growth rates of newly formed
particles were characterized using Differential Mobility Particle
Sizers. Hygroscopic properties were observed using a Hygroscopic Tandem
Differential Mobility Analyzer setup. During both campaigns, the
observations were performed at suburban, almost rural sites, and the
sites can be considered to show general regional background behavior
depending on the wind direction. At both sites there were clear pattern
for both aerosol number concentration and hygroscopic properties.
Nucleation mode number concentration increased during the morning hours
indicating new particle formation, which was observed during more than
30% of the days. The observed formation rate was typically more than
1 cm&lt;sup&gt;&amp;minus;3&lt;/sup&gt; s&lt;sup&gt;&amp;minus;1&lt;/sup&gt;, and the growth rate was between
1.2&amp;ndash;9.9 nm h&lt;sup&gt;&amp;minus;1&lt;/sup&gt;. Based on hygroscopicity measurements in Athens,
the nucleation mode size increase was due to condensation of both water
insoluble and water soluble material. However, during a period of less
anthropogenic influence, the growth was to a larger extent due to water
insoluble components. When urban pollution was more pronounced, growth
due to condensation of water soluble material dominated.</abstract>
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</article>

