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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>10</volume_number>
		<issue_number>2</issue_number>
		<publication_year>2010</publication_year>
	</journal>
	<doi>10.5194/acpd-10-3627-2010</doi>
	<article_url>http://www.atmos-chem-phys-discuss.net/10/3627/2010/</article_url>
	<abstract_html>http://www.atmos-chem-phys-discuss.net/10/3627/2010/acpd-10-3627-2010.html</abstract_html>
	<fulltext_pdf>http://www.atmos-chem-phys-discuss.net/10/3627/2010/acpd-10-3627-2010.pdf</fulltext_pdf>
	<start_page>3627</start_page>
	<end_page>3658</end_page>
	<publication_date>2010-02-09</publication_date>
	<article_title content_type="html">Water uptake and chemical composition of fresh aerosols generated in open burning of biomass</article_title>
	<authors>
		<author numeration="1" affiliations="1">
			<name>C. M. Carrico</name>
			<email>carrico@lamar.colostate.edu</email>
		</author>
		<author numeration="2" affiliations="1,3">
			<name>M. D. Petters</name>
		</author>
		<author numeration="3" affiliations="1">
			<name>S. M. Kreidenweis</name>
		</author>
		<author numeration="4" affiliations="1">
			<name>A. P. Sullivan</name>
		</author>
		<author numeration="5" affiliations="1,4">
			<name>G. R. McMeeking</name>
		</author>
		<author numeration="6" affiliations="1">
			<name>E. J. T. Levin</name>
		</author>
		<author numeration="7" affiliations="2">
			<name>W. C. Malm</name>
		</author>
		<author numeration="8" affiliations="1">
			<name>J. L. Collett Jr.</name>
		</author>
	</authors>
	<affiliations>
		<affiliation numeration="1" content_type="html">Department of Atmospheric Science, Colorado State University, Ft. Collins, CO 80523, USA</affiliation>
		<affiliation numeration="2" content_type="html">Cooperative Institute for Research of the Atmosphere/National Park Service, Colorado State University, Ft. Collins, CO 80523, USA</affiliation>
		<affiliation numeration="3" content_type="html">now at: Department of Marine, Earth, and Atmospheric Sciences, Campus Box 8208, North Carolina State University, Raleigh, NC 27695-8208, USA</affiliation>
		<affiliation numeration="4" content_type="html">now at: Center for Atmospheric Science, University of Manchester, Manchester, UK</affiliation>
	</affiliations>
	<abstract content_type="html">As part of the Fire Lab at Missoula Experiments (FLAME) in 2006–2007, we
examined hygroscopic properties of particles emitted from open combustion of
33 select biomass fuels. Measurements of humidification growth factors for
subsaturated water relative humidity (RH) conditions were made with a
hygroscopic tandem differential mobility analyzer (HTDMA) for dry particle
diameters of 50, 100 and 250 nm. Results were then fit to a single-parameter
model to obtain the hygroscopicity parameter, κ. Particles in
freshly emitted biomass smoke exhibited a wide range of hygroscopicity
(individual modes with 0&amp;lt;&amp;kappa;&amp;lt;1.0), spanning a range from the
hygroscopicity of fresh diesel soot emissions to that of pure inorganic
salts commonly found in the ambient aerosol. Smoke aerosols dominated by
carbonaceous species typically had a unimodal growth factor with
corresponding mean κ=0.1 (range of 0&amp;lt;&amp;kappa;&amp;lt;0.4). Those
with a substantial inorganic mass fraction typically separated into less-
and more-hygroscopic modes at high RH, the latter with mean κ=0.4
(range of 0.1&amp;lt;&amp;kappa;&amp;lt;1). The bimodal κ distributions were
indicative of smoke chemical heterogeneity at a single particle size,
whereas heterogeneity as a function of size was indicated by typically
decreasing κ values with increasing dry particle diameters.
Hygroscopicity varied strongly with biomass fuel type and, to a lesser
extent, with combustion conditions. Among the most hygroscopic smokes were
those from palmetto, rice straw, and sawgrass, while smoke particles from
coniferous species such as spruces, firs, pines, and duffs were among the
least hygroscopic. Overall, hygroscopicity decreased with increasing ratios
of total carbon to inorganic ions as measured in PM&lt;sub&gt;2.5&lt;/sub&gt; filter samples.
Despite aerosol heterogeneity, reconstructions of κ using PM&lt;sub&gt;2.5&lt;/sub&gt;
bulk chemical composition data fell along a 1:1 line with measured ensemble
κ values.</abstract>
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