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<article language="en">
	<journal>
		<journal_title>Atmospheric Chemistry and Physics</journal_title>
		<journal_url>www.atmos-chem-phys.net</journal_url>
		<issn>1680-7316</issn>
		<eissn>1680-7324</eissn>
		<volume_number>10</volume_number>
		<issue_number>3</issue_number>
		<publication_year>2010</publication_year>
	</journal>
	<doi>10.5194/acp-10-931-2010</doi>
	<article_url>http://www.atmos-chem-phys.net/10/931/2010/</article_url>
	<abstract_html>http://www.atmos-chem-phys.net/10/931/2010/acp-10-931-2010.html</abstract_html>
	<fulltext_pdf>http://www.atmos-chem-phys.net/10/931/2010/acp-10-931-2010.pdf</fulltext_pdf>
	<start_page>931</start_page>
	<end_page>945</end_page>
	<publication_date>2010-02-01</publication_date>
	<article_title content_type="html">First remote sensing measurements of ClOOCl along with ClO and ClONO&lt;sub&gt;2&lt;/sub&gt; in activated and deactivated Arctic vortex conditions using new ClOOCl IR absorption cross sections</article_title>
	<authors>
		<author numeration="1" affiliations="1">
			<name>G. Wetzel</name>
			<email>gerald.wetzel@kit.edu</email>
		</author>
		<author numeration="2" affiliations="1">
			<name>H. Oelhaf</name>
		</author>
		<author numeration="3" affiliations="1">
			<name>O. Kirner</name>
		</author>
		<author numeration="4" affiliations="1">
			<name>R. Ruhnke</name>
		</author>
		<author numeration="5" affiliations="1">
			<name>F. Friedl-Vallon</name>
		</author>
		<author numeration="6" affiliations="1">
			<name>A. Kleinert</name>
		</author>
		<author numeration="7" affiliations="1">
			<name>G. Maucher</name>
		</author>
		<author numeration="8" affiliations="1">
			<name>H. Fischer</name>
		</author>
		<author numeration="9" affiliations="2">
			<name>M. Birk</name>
		</author>
		<author numeration="10" affiliations="2">
			<name>G. Wagner</name>
		</author>
		<author numeration="11" affiliations="3">
			<name>A. Engel</name>
		</author>
	</authors>
	<affiliations>
		<affiliation numeration="1" content_type="html">Karlsruhe Institute of Technology, Institute for Meteorology and Climate Research, Karlsruhe, Germany</affiliation>
		<affiliation numeration="2" content_type="html">Deutsches Zentrum für Luft und Raumfahrt, Institut für Methodik der Fernerkundung, Wessling, Germany</affiliation>
		<affiliation numeration="3" content_type="html">Institut für Atmosphäre und Umwelt, J. W. Goethe Universität Frankfurt, Frankfurt, Germany</affiliation>
	</affiliations>
	<abstract content_type="html">Active chlorine species play a dominant role in the catalytic destruction of
stratospheric ozone in the polar vortices during the late winter and early
spring seasons. Recently, the correct understanding of the ClO dimer cycle
was challenged by the release of new laboratory absorption cross sections
(Pope et al., 2007) yielding significant model underestimates of observed
ClO and ozone loss (von Hobe et al., 2007). Under this aspect, nocturnal
Arctic stratospheric limb emission measurements carried out by the balloon
version of the Michelson Interferometer for Passive Atmospheric Sounding
(MIPAS-B) from Kiruna (Sweden) on 11 January 2001 and 20/21 March 2003 have
been reanalyzed with regard to the chlorine reservoir species ClONO&lt;sub&gt;2&lt;/sub&gt;
and the active species, ClO and ClOOCl (Cl&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;2&lt;/sub&gt;). New laboratory
measurements of IR absorption cross sections of ClOOCl for various
temperatures and pressures allowed for the first time the retrieval of
ClOOCl mixing ratios from remote sensing measurements. High values of active
chlorine (ClO&lt;sub&gt;x&lt;/sub&gt;) of roughly 2.3 ppbv at 20 km were observed by MIPAS-B
in the cold mid-winter Arctic vortex on 11 January 2001. While nighttime
ClOOCl shows enhanced values of nearly 1.1 ppbv at 20 km, ClONO&lt;sub&gt;2&lt;/sub&gt; mixing
ratios are less than 0.1 ppbv at this altitude. In contrast, high
ClONO&lt;sub&gt;2&lt;/sub&gt; mixing ratios of nearly 2.4 ppbv at 20 km have been observed in
the late winter Arctic vortex on 20 March 2003. No significant ClO&lt;sub&gt;x&lt;/sub&gt;
amounts are detectable on this date since most of the active chlorine has
already recovered to its main reservoir species ClONO&lt;sub&gt;2&lt;/sub&gt;. The observed
values of ClO&lt;sub&gt;x&lt;/sub&gt; and ClONO&lt;sub&gt;2&lt;/sub&gt; are in line with the established polar
chlorine chemistry. The thermal equilibrium constants between the dimer
formation and its dissociation, as derived from the balloon measurements,
are on the lower side of reported data and in good agreement with values
recommended by von Hobe et al. (2007). Calculations with the ECHAM/MESSy
Atmospheric Chemistry model (EMAC) using established kinetics show similar
chlorine activation and deactivation, compared to the measurements in
January 2001 and March 2003, respectively.</abstract>
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