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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>9</volume_number>
		<issue_number>9</issue_number>
		<publication_year>2009</publication_year>
	</journal>
	<doi>10.5194/acp-9-3011-2009</doi>
	<article_url>http://www.atmos-chem-phys.net/9/3011/2009/</article_url>
	<abstract_html>http://www.atmos-chem-phys.net/9/3011/2009/acp-9-3011-2009.html</abstract_html>
	<fulltext_pdf>http://www.atmos-chem-phys.net/9/3011/2009/acp-9-3011-2009.pdf</fulltext_pdf>
	<start_page>3011</start_page>
	<end_page>3025</end_page>
	<publication_date>2009-05-11</publication_date>
	<article_title content_type="html">The governing processes and timescales of stratosphere-to-troposphere transport and its contribution to ozone in the Arctic troposphere</article_title>
	<authors>
		<author numeration="1" affiliations="1,2">
			<name>Q. Liang</name>
			<email>Qing.Liang@nasa.gov</email>
		</author>
		<author numeration="2" affiliations="1">
			<name>A. R. Douglass</name>
		</author>
		<author numeration="3" affiliations="1,3">
			<name>B. N. Duncan</name>
		</author>
		<author numeration="4" affiliations="1">
			<name>R. S. Stolarski</name>
		</author>
		<author numeration="5" affiliations="1,4">
			<name>J. C. Witte</name>
		</author>
	</authors>
	<affiliations>
		<affiliation numeration="1" content_type="html">NASA Goddard Space Flight Center, Atmospheric Chemistry and Dynamics Branch, Code 613.3, Greenbelt, MD 20771, USA</affiliation>
		<affiliation numeration="2" content_type="html">Oak Ridge Associated Universities, NASA Postdoctoral Program, Oak Ridge, TN 37831, USA</affiliation>
		<affiliation numeration="3" content_type="html">Goddard Earth Sciences &amp; Technology Center, University of Maryland, Baltimore County, MD, USA</affiliation>
		<affiliation numeration="4" content_type="html">Science Systems and Applications Inc., Lanham, MD, USA</affiliation>
	</affiliations>
	<abstract content_type="html">We used the seasonality of a combination of atmospheric trace gases and
idealized tracers to examine stratosphere-to-troposphere transport and its
influence on tropospheric composition in the Arctic. Maximum
stratosphere-to-troposphere transport of CFCs and O&lt;sub&gt;3&lt;/sub&gt; occurs in April as
driven by the Brewer-Dobson circulation. Stratosphere-troposphere exchange
(STE) occurs predominantly between 40&amp;deg; N to 80&amp;deg; N with stratospheric
influx in the mid-latitudes (30–70&amp;deg; N) accounting for 67–81% of the
air of stratospheric origin in the Northern Hemisphere extratropical
troposphere. Transport from the lower stratosphere to the lower troposphere
(LT) takes three months on average, one month to cross the tropopause, the
second month to travel from the upper troposphere (UT) to the middle
troposphere (MT), and the third month to reach the LT. During downward
transport, the seasonality of a trace gas can be greatly impacted by wet
removal and chemistry. A comparison of idealized tracers with varying
lifetimes suggests that when initialized with the same concentrations and
seasonal cycles at the tropopause, trace gases that have shorter lifetimes
display lower concentrations, smaller amplitudes, and earlier seasonal
maxima during transport to the LT. STE contributes to O&lt;sub&gt;3&lt;/sub&gt; in the Arctic
troposphere directly from the transport of O&lt;sub&gt;3&lt;/sub&gt; and indirectly from the
transport of NO&lt;sub&gt;y&lt;/sub&gt;. Direct transport of O&lt;sub&gt;3&lt;/sub&gt; from the stratosphere
accounts for 78% of O&lt;sub&gt;3&lt;/sub&gt; in the Arctic UT with maximum contributions
occurring from March to May. The stratospheric contribution decreases
significantly in the MT/LT (20–25% of total O&lt;sub&gt;3&lt;/sub&gt;) and shows a very
weak March–April maximum. Our NO&lt;sub&gt;x&lt;/sub&gt; budget analysis in the Arctic UT
shows that during spring and summer, the stratospheric injection of
NO&lt;sub&gt;y&lt;/sub&gt;-rich air increases NO&lt;sub&gt;x&lt;/sub&gt; concentrations above the 20 pptv
threshold level, thereby shifting the Arctic UT from a regime of net
photochemical ozone loss to one of net production with rates as high as +16 ppbv/month.</abstract>
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</article>

