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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>10</volume_number>
		<issue_number>5</issue_number>
		<publication_year>2010</publication_year>
	</journal>
	<doi>10.5194/acpd-10-11615-2010</doi>
	<article_url>http://www.atmos-chem-phys-discuss.net/10/11615/2010/</article_url>
	<abstract_html>http://www.atmos-chem-phys-discuss.net/10/11615/2010/acpd-10-11615-2010.html</abstract_html>
	<fulltext_pdf>http://www.atmos-chem-phys-discuss.net/10/11615/2010/acpd-10-11615-2010.pdf</fulltext_pdf>
	<start_page>11615</start_page>
	<end_page>11657</end_page>
	<publication_date>2010-05-03</publication_date>
	<article_title content_type="html">Particle formation and growth at five rural and urban sites</article_title>
	<authors>
		<author numeration="1" affiliations="1">
			<name>C.-H. Jeong</name>
		</author>
		<author numeration="2" affiliations="1">
			<name>G. J. Evans</name>
			<email>greg.evans@utoronto.ca</email>
		</author>
		<author numeration="3" affiliations="1">
			<name>M. L. McGuire</name>
		</author>
		<author numeration="4" affiliations="1,4">
			<name>R. Y.-W. Chang</name>
		</author>
		<author numeration="5" affiliations="1,4">
			<name>J. P. D. Abbatt</name>
		</author>
		<author numeration="6" affiliations="2">
			<name>K. Zeromskiene</name>
		</author>
		<author numeration="7" affiliations="2">
			<name>M. Mozurkewich</name>
		</author>
		<author numeration="8" affiliations="3">
			<name>S.-M. Li</name>
		</author>
		<author numeration="9" affiliations="3">
			<name>W. R. Leaitch</name>
		</author>
	</authors>
	<affiliations>
		<affiliation numeration="1" content_type="html">Southern Ontario Centre for Atmospheric Aerosol Research, University of Toronto, 200 College Street, Toronto, Ontario, M5S 3E5, Canada</affiliation>
		<affiliation numeration="2" content_type="html">Chemistry Department and Centre for Atmospheric Chemistry, York University, 4700 Keele Street, Toronto, Ontario, M3J 1P3, Canada</affiliation>
		<affiliation numeration="3" content_type="html">Science and Technology Branch, Environment Canada, 4905 Dufferin Street, Toronto, Ontario, M3H 5T4, Canada</affiliation>
		<affiliation numeration="4" content_type="html">Department of Chemistry, University of Toronto, 80 St. George Street, Toronto,\newline Ontario M5S 3H6, Canada</affiliation>
	</affiliations>
	<abstract content_type="html">Ultrafine particle (UFP) number and size distributions were simultaneously
measured at five urban and rural sites in Southern Ontario, Canada as part
of the Border Air Quality and Meteorology Study (BAQS-Met 2007). Particle
formation and growth events at these five sites were classified based on
their strength and persistence as well as the variation in geometric mean
diameter. Regional nucleation and growth events and local short-lived strong
nucleation events were frequently observed at the near-border rural sites,
upwind of industrial sources. Surprisingly, the particle number
concentrations at one of these sites were higher than the concentrations at
a downtown site in a major city, despite its high traffic density. Regional
nucleation and growth events were favored at intense solar irradiance and
less polluted cooler drier air. The most distinctive regional particle
nucleation and growth event during the campaign was observed simultaneously
at all five sites, which were up to 350 km apart. Although the ultrafine
particle concentrations and size distributions generally were spatially
heterogeneous across the region, a more uniform spatial distribution of UFP
across the five areas was observed during this regional nucleation event.
Thus, nucleation events can cover large regions, contributing to the burden
of UFP in cities and potentially to the associated health impacts on urban
populations. In addition, particle formation in southwestern Ontario appears
to more often be related to anthropogenic gaseous emissions, although
biogenic emissions may at times contribute. Local short-lived nucleation
events at the near-border sites during this three-week campaign were
associated with high SO&lt;sub&gt;2&lt;/sub&gt;, which likely originated from US and
Canadian industrial sources. These particle formation events may contribute
to the production of cloud condensation nuclei, thus potentially influencing
regional climate. Longer-term studies are needed to help resolve the
relative contributions of anthropogenic and biogenic emissions to nucleation
and growth in this region.</abstract>
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