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	<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>2</issue_number>
		<publication_year>2009</publication_year>
	</journal>
	<doi>10.5194/acpd-9-9081-2009</doi>
	<article_url>http://www.atmos-chem-phys-discuss.net/9/9081/2009/</article_url>
	<abstract_html>http://www.atmos-chem-phys-discuss.net/9/9081/2009/acpd-9-9081-2009.html</abstract_html>
	<fulltext_pdf>http://www.atmos-chem-phys-discuss.net/9/9081/2009/acpd-9-9081-2009.pdf</fulltext_pdf>
	<start_page>9081</start_page>
	<end_page>9115</end_page>
	<publication_date>2009-04-06</publication_date>
	<article_title content_type="html">Black carbon over Mexico: the effect of atmospheric transport on mixing state, mass absorption cross-section, and BC/CO ratios</article_title>
	<authors>
		<author numeration="1" affiliations="1">
			<name>R. Subramanian</name>
			<email>random@dropletmeasurement.com</email>
		</author>
		<author numeration="2" affiliations="1">
			<name>G. L. Kok</name>
		</author>
		<author numeration="3" affiliations="2">
			<name>D. Baumgardner</name>
		</author>
		<author numeration="4" affiliations="3">
			<name>A. Clarke</name>
		</author>
		<author numeration="5" affiliations="3">
			<name>Y. Shinozuka</name>
		</author>
		<author numeration="6" affiliations="4">
			<name>T. L. Campos</name>
		</author>
		<author numeration="7" affiliations="4">
			<name>C. G. Heizer</name>
		</author>
		<author numeration="8" affiliations="4">
			<name>B. B. Stephens</name>
		</author>
	</authors>
	<affiliations>
		<affiliation numeration="1" content_type="html">Droplet Measurement Technologies, Boulder, CO 80301, USA</affiliation>
		<affiliation numeration="2" content_type="html">Universidad Nacional Autónoma de México, Mexico City, Mexico</affiliation>
		<affiliation numeration="3" content_type="html">University of Hawai&apos;i, Honolulu, HI 96822, USA</affiliation>
		<affiliation numeration="4" content_type="html">National Center for Atmospheric Research, Boulder, CO 80305, USA</affiliation>
	</affiliations>
	<abstract content_type="html">A single particle soot photometer (SP2) was operated on the NCAR C-130 during the MIRAGE
      campaign (part of MILAGRO), sampling black carbon (BC) over Mexico. The highest BC
      concentrations were measured over Mexico City (sometimes as much as 2&amp;mu;g/m&lt;sup&gt;3&lt;/sup&gt;)
      and over hill-fires to the south of the city. As expected, older, diluted air masses had
      lower BC concentrations. A comparison of carbon monoxide (CO) and BC suggests
      a CO background of around 65 ppbv, and a background-corrected
      BC/CO&lt;sub&gt;net&lt;/sub&gt; ratio of 3.1 (ng/m&lt;sup&gt;3&lt;/sup&gt; STP)/ppbv (&amp;plusmn;25%). This
      ratio is similar for fresh emissions over Mexico City, as well as for aged
      airmasses. Comparison of light absorption measured with a particle soot absorption
      photometer (PSAP) and the SP2 BC suggests a BC mass-normalized absorption cross-section
      (MAC) of 10.3 m&lt;sup&gt;2&lt;/sup&gt;g&lt;sup&gt;&amp;minus;1&lt;/sup&gt; (&amp;plusmn;30%) at 660 nm (or
      12.4 m&lt;sup&gt;2&lt;/sup&gt;g&lt;sup&gt;&amp;minus;1&lt;/sup&gt; @ 550 nm, assuming MAC is inversely dependent on
      wavelength). This appears independent of aging and similar to the expected absorption
      cross-section for aged BC, but values, particularly in fresh emissions, could be biased high
      due to instrument artifacts. SP2-derived BC coating indicators show a prominent
      thinly-coated BC mode over the Mexico City Metropolitan Area (MCMA), while older air masses
      show both thinly-coated and thickly-coated BC. BC mass per particle of the thinly-coated
      mode appears to increase as the air mass ages, possibly due to coagulation and/or increased
      coating of the particles containing smaller BC masses. Differences in the coating indicator
      patterns for similarly-aged air masses may be due to differences in atmospheric processing
      on each day, including mixing with non-MCMA air masses.</abstract>
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</article>

