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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>4</volume_number>
		<issue_number>1</issue_number>
		<publication_year>2004</publication_year>
	</journal>
	<doi>10.5194/acpd-4-533-2004</doi>
	<article_url>http://www.atmos-chem-phys-discuss.net/4/533/2004/</article_url>
	<abstract_html>http://www.atmos-chem-phys-discuss.net/4/533/2004/acpd-4-533-2004.html</abstract_html>
	<fulltext_pdf>http://www.atmos-chem-phys-discuss.net/4/533/2004/acpd-4-533-2004.pdf</fulltext_pdf>
	<start_page>533</start_page>
	<end_page>568</end_page>
	<publication_date>2004-01-26</publication_date>
	<article_title content_type="html">Single particle analysis of the accumulation mode aerosol over the northeast Amazonian tropical rain forest, Surinam, South America</article_title>
	<authors>
		<author numeration="1" affiliations="1,2">
			<name>R. Krejci</name>
		</author>
		<author numeration="2" affiliations="1">
			<name>J. Ström</name>
		</author>
		<author numeration="3" affiliations="1,3">
			<name>M. de Reus</name>
		</author>
		<author numeration="4" affiliations="4,5">
			<name>W. Sahle</name>
		</author>
	</authors>
	<affiliations>
		<affiliation numeration="1" content_type="html">Institute of Applied Environmental Research, Air Pollution Laboratory, Frescativägen 52-54, 106 91 Stockholm, Sweden</affiliation>
		<affiliation numeration="2" content_type="html">Department of Meteorology, Stockholm University, 106 91 Stockholm, Sweden</affiliation>
		<affiliation numeration="3" content_type="html">Max Planck Institute for Chemistry, Department of Air Chemistry, P. O. Box 3060, 55020 Mainz, Germany</affiliation>
		<affiliation numeration="4" content_type="html">National Institute of Working Life, 171 84 Solna, Sweden</affiliation>
		<affiliation numeration="5" content_type="html">now at: Studsvik Nuclear AB, Microstructure and microanalysis, Hot Cell Laboratory, 611 82, Nyköping, Sweden</affiliation>
	</affiliations>
	<abstract content_type="html">Single particle analysis of aerosols particles larger than 0.2 &amp;micro;m diameter was performed on 24 samples collected over Surinam tropical rain
      forest and in the adjacent marine boundary layer (MBL) during the LBA-CLAIRE
      98 campaign in March 1998. Elemental composition and morphology of 2308 particles was determined using
      SEM-EDX. The aerosol particles were divided into seven groups according to their chemical composition: organic
      particles, mineral dust, aged mineral dust, sea salt, aged sea salt, Ca-rich, and biogenic aerosol. Samples were further divided with respect to
      the distinct atmospheric layers present in the tropical troposphere including MBL, continental mixed layer, cloud convective layer, free
      troposphere and region of deep convection outflow. The organic and mineral
      dust particles are two major groups observed over the rainforest. In the MBL
      also sea salt particles represented a large fraction between 15 and 27%. The organic particles control much of the chemical characteristic of the
      aerosol in the continental tropical troposphere. Their abundance ranged from
      less than 20% in the MBL to more than 90% in the free troposphere between 4.5 and 12.6 km altitude. During the transport of the air masses
      from the MBL over the rain forest, fraction of organic aerosol particles more than doubled, reaching
      40-60% in the continental boundary layer. This increase was attributed to direct emissions of biogenic aerosols from
      the tropical vegetation. The high fraction of the organic accumulation mode
      particles in the upper tropical troposphere could be a good indicator for the air masses originated over the tropical rain forest.</abstract>
	<references>
	</references>
</article>

