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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>9</volume_number>
		<issue_number>3</issue_number>
		<publication_year>2009</publication_year>
	</journal>
	<doi>10.5194/acpd-9-13523-2009</doi>
	<article_url>http://www.atmos-chem-phys-discuss.net/9/13523/2009/</article_url>
	<abstract_html>http://www.atmos-chem-phys-discuss.net/9/13523/2009/acpd-9-13523-2009.html</abstract_html>
	<fulltext_pdf>http://www.atmos-chem-phys-discuss.net/9/13523/2009/acpd-9-13523-2009.pdf</fulltext_pdf>
	<start_page>13523</start_page>
	<end_page>13567</end_page>
	<publication_date>2009-06-18</publication_date>
	<article_title content_type="html">Origin of aerosol particles in the mid latitude and subtropical upper troposphere and lowermost stratosphere from cluster analysis of CARIBIC data</article_title>
	<authors>
		<author numeration="1" affiliations="1">
			<name>M. KÃ¶ppe</name>
		</author>
		<author numeration="2" affiliations="1">
			<name>M. Hermann</name>
			<email>hermann@tropos.de</email>
		</author>
		<author numeration="3" affiliations="2">
			<name>C. A. M. Brenninkmeijer</name>
		</author>
		<author numeration="4" affiliations="1">
			<name>J. Heintzenberg</name>
		</author>
		<author numeration="5" affiliations="3">
			<name>H. Schlager</name>
		</author>
		<author numeration="6" affiliations="2">
			<name>T. Schuck</name>
		</author>
		<author numeration="7" affiliations="2">
			<name>F. Slemr</name>
		</author>
		<author numeration="8" affiliations="4">
			<name>D. Sprung</name>
		</author>
		<author numeration="9" affiliations="5">
			<name>P. F. J. van Velthoven</name>
		</author>
		<author numeration="10" affiliations="1">
			<name>A. Wiedensohler</name>
		</author>
		<author numeration="11" affiliations="4">
			<name>A. Zahn</name>
		</author>
		<author numeration="12" affiliations="3">
			<name>H. Ziereis</name>
		</author>
	</authors>
	<affiliations>
		<affiliation numeration="1" content_type="html">Leibniz Institute for Tropospheric Research, Permoserstr. 15, 04318 Leipzig, Germany</affiliation>
		<affiliation numeration="2" content_type="html">Atmospheric Chemistry Division, Max Planck Institute for Chemistry, P.O. Box 3060,  55020 Mainz, Germany</affiliation>
		<affiliation numeration="3" content_type="html">Institute of Atmospheric Physics, German Aerospace Center, Oberpfaffenhofen,  82230 Wessling, Germany</affiliation>
		<affiliation numeration="4" content_type="html">Institute for Meteorology and Climate Research, Karlsruhe Institute of Technology,  P.O. Box 3640, 76021 Karlsruhe, Germany</affiliation>
		<affiliation numeration="5" content_type="html">Royal Netherlands Meteorological Institute, P.O. Box 201, 3730 AE de Bilt, The Netherlands</affiliation>
	</affiliations>
	<abstract content_type="html">The origin of aerosol particles in the upper troposphere and lowermost stratosphere
over the Eurasian continent was investigated by applying cluster analysis methods to
in situ measured data. Number concentrations of submicrometer aerosol
particles and trace gas mixing ratios derived by the CARIBIC (Civil Aircraft for
Regular Investigation of the Atmosphere Based on an Instrument Container)
measurement system on flights between Germany and South-East Asia were
used for this analysis. Four cluster analysis methods were applied to a
test data set and their capability of separating the data points into
scientifically reasonable clusters was assessed. The best method was
applied to seasonal data subsets for summer and winter resulting in five
cluster or air mass types: stratosphere, tropopause, free troposphere,
high clouds, and boundary layer influenced. Other source clusters,
like aircraft emissions could not be resolved in the present data set
with the used methods. While the cluster separation works satisfactory
well for the summer data, in winter interpretation is more difficult,
which is attributed to either different vertical transport pathways or
different chemical lifetimes in the two seasons. The geographical
 distribution of the clusters together with histograms for nucleation
 and Aitken mode particles within each cluster are presented. Aitken
 mode particle number concentrations show a clear vertical
 gradient with the lowest values in the lowermost stratosphere (750â€“2820 particles/cm&lt;sup&gt;3&lt;/sup&gt;
 STP, minimum of the two 25%- and maximum of the two 75%-percentiles of both seasons)
 and the highest values for the boundary-layer-influenced air (4290â€“22 760 particles/cm&lt;sup&gt;3&lt;/sup&gt;
 STP). Nucleation mode particles are also highest in the boundary-layer-influenced air
 (1260â€“29 500 particles/cm&lt;sup&gt;3&lt;/sup&gt; STP, but are lowest in the free troposphere
 (0â€“450 particles/cm3 STP). The given submicrometer particle number
 concentrations represent the first statistically sound data set
 for the upper troposphere and lowermost stratosphere over the Eurasian continent.</abstract>
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</article>

