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	<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>9</volume_number>
		<issue_number>12</issue_number>
		<publication_year>2009</publication_year>
	</journal>
	<doi>10.5194/acp-9-4157-2009</doi>
	<article_url>http://www.atmos-chem-phys.net/9/4157/2009/</article_url>
	<abstract_html>http://www.atmos-chem-phys.net/9/4157/2009/acp-9-4157-2009.html</abstract_html>
	<fulltext_pdf>http://www.atmos-chem-phys.net/9/4157/2009/acp-9-4157-2009.pdf</fulltext_pdf>
	<start_page>4157</start_page>
	<end_page>4175</end_page>
	<publication_date>2009-06-23</publication_date>
	<article_title content_type="html">Surface ozone at the Caucasian site Kislovodsk High Mountain Station and the Swiss Alpine site Jungfraujoch: data analysis and trends (1990â€“2006)</article_title>
	<authors>
		<author numeration="1" affiliations="1,6">
			<name>O. A. Tarasova</name>
			<email>tarasova@mpch-mainz.mpg.de</email>
		</author>
		<author numeration="2" affiliations="2">
			<name>I. A. Senik</name>
		</author>
		<author numeration="3" affiliations="3">
			<name>M. G. Sosonkin</name>
		</author>
		<author numeration="4" affiliations="4">
			<name>J. Cui</name>
		</author>
		<author numeration="5" affiliations="4">
			<name>J. Staehelin</name>
		</author>
		<author numeration="6" affiliations="5">
			<name>A. S. H. PrÃ©vÃ´t</name>
		</author>
	</authors>
	<affiliations>
		<affiliation numeration="1" content_type="html">Max-Planck Institute for Chemistry, Mainz, Germany</affiliation>
		<affiliation numeration="2" content_type="html">Obukhov Institute of Atmosphere Physics RAS, Moscow, Russia</affiliation>
		<affiliation numeration="3" content_type="html">International Center for Astronomical, Medical and Ecological Research NAS, Kiev, Ukraine</affiliation>
		<affiliation numeration="4" content_type="html">Institute for Atmospheric and Climate Science, Swiss Federal Institute of Technology ZÃ¼rich, Switzerland</affiliation>
		<affiliation numeration="5" content_type="html">Paul Scherrer Institute, Villigen, Switzerland</affiliation>
		<affiliation numeration="6" content_type="html">currently at: WMO, Atmospheric Environment Research Department, Switzerland</affiliation>
	</affiliations>
	<abstract content_type="html">Long-term ozone measurements of two background mountain sites, namely the
Kislovodsk High Mountain Station in Caucasus, Russia (KHMS, 43.70&amp;deg; N,
42.70&amp;deg; E, 2070 m a.s.l.) and the Jungfraujoch in Switzerland (JFJ,
46.55&amp;deg; N, 7.98&amp;deg; E, 3580 m a.s.l.) are compared. Despite of more than
1.5 km altitude difference ozone mixing ratios are comparable at JFJ an
KHMS in the beginning of measurements (1990â€“1993) while the annually
averaged levels at JFJ are around 15 ppb higher than the ones at KHMS for
the most recent years (1997â€“2006). The seasonal cycle of the surface ozone
mixing ratios is characterized by a double spring-summer maximum at both
sites with a spring one being more pronounced for the air masses with the
longest contact with the upper free troposphere and stratosphere. Ozone
mixing ratio increased at JFJ but decreased at KHMS for the period
1990â€“2006. Trends are more pronounced for the 1990s (+0.73&amp;plusmn;0.20 ppb/year
at JFJ and &amp;minus;0.91&amp;plusmn;0.17 ppb/year at KHMS for the period
1991â€“2001) in comparison with the later years (+0.04&amp;plusmn;0.21 ppb/year at
JFJ and &amp;minus;0.37&amp;plusmn;0.14 ppb/year at KHMS for the period 1997â€“2006). Trends
show a distinct seasonality, which is different for the different periods.
To investigate possible reasons for this remarkable trends difference 3-D
trajectories using LAGRANTO trajectory model are used. Effects of horizontal
and vertical transport on ozone trends are considered. No substantial
systematic changes in the transport patterns were detected which could lead
to strong changes in the trend magnitude between 1991â€“2001 and 1997â€“2006.
The geographical position of the sites relative to the main topographic
features and emission sources as well as distance from the coast are
interpreted to be among the main reasons for the opposite surface ozone
trends. During the 90s the JFJ trend reflects increase of the ozone in the
upper free troposphere/lower stratosphere, while KHMS is not sensitive to
this change or even showing the opposite tendency. The analysis provided
evidence for a stronger influence of processes in the lower troposphere, in
particular the dramatic emission decrease in the earlier 1990s in former
USSR and emissions regulations in Western Europe on the surface ozone trend at KHMS.</abstract>
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