<?xml version="1.0" encoding="utf-8" standalone="no"?>
<!DOCTYPE article SYSTEM "http://www.atmos-chem-phys-discuss.net/inc/acpd/copernicus.dtd">
<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>5</volume_number>
		<issue_number>2</issue_number>
		<publication_year>2005</publication_year>
	</journal>
	<doi>10.5194/acpd-5-2469-2005</doi>
	<article_url>http://www.atmos-chem-phys-discuss.net/5/2469/2005/</article_url>
	<abstract_html>http://www.atmos-chem-phys-discuss.net/5/2469/2005/acpd-5-2469-2005.html</abstract_html>
	<fulltext_pdf>http://www.atmos-chem-phys-discuss.net/5/2469/2005/acpd-5-2469-2005.pdf</fulltext_pdf>
	<start_page>2469</start_page>
	<end_page>2501</end_page>
	<publication_date>2005-04-22</publication_date>
	<article_title content_type="html">Characterization of aerosol particle episodes in Finland caused by wildfires in Eastern Europe</article_title>
	<authors>
		<author numeration="1" affiliations="1">
			<name>J. V. Niemi</name>
		</author>
		<author numeration="2" affiliations="2,3">
			<name>H. Tervahattu</name>
		</author>
		<author numeration="3" affiliations="4">
			<name>H. Vehkamäki</name>
		</author>
		<author numeration="4" affiliations="4">
			<name>J. Martikainen</name>
		</author>
		<author numeration="5" affiliations="4">
			<name>L. Laakso</name>
		</author>
		<author numeration="6" affiliations="4">
			<name>M. Kulmala</name>
		</author>
		<author numeration="7" affiliations="5">
			<name>P. Aarnio</name>
		</author>
		<author numeration="8" affiliations="5">
			<name>T. Koskentalo</name>
		</author>
		<author numeration="9" affiliations="6">
			<name>M. Sillanpää</name>
		</author>
		<author numeration="10" affiliations="6">
			<name>U. Makkonen</name>
		</author>
	</authors>
	<affiliations>
		<affiliation numeration="1" content_type="html">Department of Biological and Environmental Sciences, University of Helsinki, P.O. Box 27, FIN-00014 Helsinki, Finland</affiliation>
		<affiliation numeration="2" content_type="html">Nordic Envicon Ltd., Koetilantie 3, FIN-00790 Helsinki, Finland</affiliation>
		<affiliation numeration="3" content_type="html">Cooperative Institute for Research in Environmental Sciences, University of Colorado, Campus Box 216, Boulder, CO 80309, USA</affiliation>
		<affiliation numeration="4" content_type="html">Department of Physical Sciences, University of Helsinki, P.O. Box 64, FIN-00014 Helsinki, Finland</affiliation>
		<affiliation numeration="5" content_type="html">Helsinki Metropolitan Area Council (YTV), Opastinsilta 6 A, FIN-00520 Helsinki, Finland</affiliation>
		<affiliation numeration="6" content_type="html">Finnish Meteorological Institute, Sahaajankatu 20 E, FIN-00880 Helsinki, Finland</affiliation>
	</affiliations>
	<abstract content_type="html">We studied the sources, compositions and size distributions of aerosol
particles during long-range transport (LRT) PM&lt;sub&gt;2.5&lt;/sub&gt; episodes occurred on
12&amp;ndash;15 August, 26&amp;ndash;28 August and 5&amp;ndash;6 September 2002 in Finland. Backward air mass trajectories,
satellite detections of fire areas, and dispersion modelling results
indicate that emissions from wildfires in Russia and other Eastern European
countries arrived to Finland during the episodes. Individual particle
analyses using scanning electron microscopy (SEM) coupled with energy
dispersive X-ray analyses (EDX) showed that the proportion of S-rich
particles increased during the episodes and they contained elevated
fractions of K, which indicates emissions from biomass burning. These
aerosols were mixed with S-rich emissions from fossil fuel burning during
the transport, since air masses came through polluted areas of Europe. Minor
amounts of coarse Ca-rich particles were also brought by LRT during the
episodes, and they probably originated from wildfires and/or from Estonian
and Russian oil-shale burning industrial areas. The ion chromatography
analysis showed that concentrations of sulphate (SO&lt;sub&gt;4&lt;/sub&gt;&lt;sup&gt;2-&lt;/sup&gt;), total
nitrate (NO&lt;sub&gt;3&lt;/sub&gt;&lt;sup&gt;-&lt;/sup&gt;+HNO&lt;sub&gt;3&lt;/sub&gt;(g)) and total ammonium (NH&lt;sub&gt;4&lt;/sub&gt;&lt;sup&gt;+&lt;/sup&gt;+NH&lt;sub&gt;3&lt;/sub&gt;(g))
increased during the episodes, but the ratio of total amount of
these ions to PM&lt;sub&gt;10&lt;/sub&gt; concentration decreased indicating unusually high
fractions of other chemical components. The particle number size
distribution measurements with differential mobility particle sizer (DMPS)
showed that the concentrations of 90&amp;ndash;500 nm particles increased during the
episodes, but the concentrations of particles smaller than 90nm decreased.
The reduction of the smallest particles was caused by suppressed new
particle formation due to the vapour and molecular cluster uptake of LRT
particles. Our results show that the emissions from wildfires in Russian and
other Eastern European deteriorated air quality on very large areas, even at
the distance of over 1000 km from the fire areas.</abstract>
	<references>
	</references>
</article>

