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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-9-13439-2009</doi>
	<article_url>http://www.atmos-chem-phys-discuss.net/9/13439/2009/</article_url>
	<abstract_html>http://www.atmos-chem-phys-discuss.net/9/13439/2009/acpd-9-13439-2009.html</abstract_html>
	<fulltext_pdf>http://www.atmos-chem-phys-discuss.net/9/13439/2009/acpd-9-13439-2009.pdf</fulltext_pdf>
	<start_page>13439</start_page>
	<end_page>13474</end_page>
	<publication_date>2009-06-18</publication_date>
	<article_title content_type="html">Chemical apportionment of southern African aerosol mass and optical depth</article_title>
	<authors>
		<author numeration="1" affiliations="1">
			<name>B. I. Magi</name>
			<email>brian.magi@noaa.gov</email>
		</author>
	</authors>
	<affiliations>
		<affiliation numeration="1" content_type="html">Princeton University, Princeton, New Jersey, USA</affiliation>
	</affiliations>
	<abstract content_type="html">We investigate the aerosol mass apportionment and derive aerosol
      optical properties that characterize the aerosol over extratropical
      and tropical southern Africa during the biomass burning season. We
      find that 54% and 83% of the extratropical and tropical aerosol
      mass, respectively, is composed of carbonaceous species, consistent
      with the fact that the major source of particulate matter in southern
      Africa is biomass burning. This mass apportionment implies that
      carbonaceous species in the form of organic carbon (OC) and black
      carbon (BC) play a critical role in the aerosol optical properties. By
      combining the in situ measurements of aerosol mass concentrations with
      concurrent measurements of aerosol optical properties at a wavelength
      of 550 nm, we find that 80–90% of the aerosol scattering
      is due to carbonaceous aerosol, where our derived mass scattering
      cross sections (MSC) for OC and BC are 3.9&amp;plusmn;0.6 m&lt;sup&gt;2&lt;/sup&gt;/g
      and 1.6&amp;plusmn;0.2 m&lt;sup&gt;2&lt;/sup&gt;/g, respectively. Our derived values of
      mass absorption cross sections (MAC) for OC and BC are
      0.7&amp;plusmn;0.6 m&lt;sup&gt;2&lt;/sup&gt;/g and 8.2&amp;plusmn;1.1 m&lt;sup&gt;2&lt;/sup&gt;/g,
      respectively. The values of MAC imply that 26–27% of the aerosol
      absorption in southern Africa is due to OC, with the remainder due to
      BC. Our results provide important constraints for aerosol properties
      in a region dominated by biomass burning and should be integrated into
      climate models to improve aerosol simulations.</abstract>
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