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<!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>6</volume_number>
		<issue_number>3</issue_number>
		<publication_year>2006</publication_year>
	</journal>
	<doi>10.5194/acpd-6-5505-2006</doi>
	<article_url>http://www.atmos-chem-phys-discuss.net/6/5505/2006/</article_url>
	<abstract_html>http://www.atmos-chem-phys-discuss.net/6/5505/2006/acpd-6-5505-2006.html</abstract_html>
	<fulltext_pdf>http://www.atmos-chem-phys-discuss.net/6/5505/2006/acpd-6-5505-2006.pdf</fulltext_pdf>
	<start_page>5505</start_page>
	<end_page>5542</end_page>
	<publication_date>2006-06-27</publication_date>
	<article_title content_type="html">Size distributions of non-volatile particle residuals (D&lt;sub&gt;&lt;i&gt;p&lt;/i&gt;&lt;/sub&gt;&amp;lt;800 nm) at a rural site in Germany and relation to air mass origin</article_title>
	<authors>
		<author numeration="1" affiliations="1">
			<name>C. Engler</name>
		</author>
		<author numeration="2" affiliations="1">
			<name>D. Rose</name>
		</author>
		<author numeration="3" affiliations="1">
			<name>B. Wehner</name>
		</author>
		<author numeration="4" affiliations="1">
			<name>A. Wiedensohler</name>
		</author>
		<author numeration="5" affiliations="1">
			<name>E. Brüggemann</name>
		</author>
		<author numeration="6" affiliations="1">
			<name>T. Gnauk</name>
		</author>
		<author numeration="7" affiliations="1">
			<name>G. Spindler</name>
		</author>
		<author numeration="8" affiliations="1,2">
			<name>T. Tuch</name>
		</author>
		<author numeration="9" affiliations="1">
			<name>W. Birmili</name>
		</author>
	</authors>
	<affiliations>
		<affiliation numeration="1" content_type="html">Leibniz Institute for Tropospheric Research, Leipzig, Germany</affiliation>
		<affiliation numeration="2" content_type="html">UFZ Center for Environmental Research, Department of Human Exposure Research and Epidemiology, Leipzig, Germany</affiliation>
	</affiliations>
	<abstract content_type="html">Atmospheric aerosol particle size distributions at a continental
background site in Eastern Germany were examined for a one-year
period. Particles were classified using a twin differential
mobility particle sizer in a size range between 3 and 800 nm. As a
novelty, every second measurement of this experiment involved the
removal of volatile chemical compounds in a thermodenuder at
300&amp;deg;C. This concept allowed to quantify the number size
distribution of non-volatile particle cores &amp;ndash; primarily associated
with elemental carbon, and to compare this to the original ambient
size distribution. A general result was that practically every
ambient particle in continental background air contained a
non-volatile core. The volume fraction of non-volatile particulate
matter (ambient D&lt;sub&gt;&lt;i&gt;p&lt;/i&gt;&lt;/sub&gt;&amp;lt;800 nm) varied between 10 and 30% and was
largely consistent with the experimentally determined mass
fraction of elemental carbon. The average size of the non-volatile
particle cores was estimated as a function of original ambient
size using a summation method, which showed that larger particles
(&amp;gt;200 nm) contained more non-volatile compounds than smaller
particles (&amp;lt;50 nm), thus indicating a significantly different
chemical composition. Two alternative air mass classification
schemes based on either, synoptic chart analysis (Berliner
Wetterkarte) or back trajectories showed, that the volume and
number fractions of non-volatile cores were less dependent on air
mass than the absolute concentrations in the particle size
distributions. In all air masses, the non-volatile size
distributions showed a more and a less volatile (&quot;soot&quot;) mode,
which is located in the size range of about 50 nm. During unstable
conditions and in maritime air masses, smaller values were
observed compared to continental or stable conditions. This
reflects the significant emissions of non-volatile material over
the continent and, depending on atmospheric stratification,
increased concentrations at ground level.</abstract>
	<references>
	</references>
</article>

