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<front>
<journal-meta>
<journal-id journal-id-type="publisher">ACP</journal-id>
<journal-title-group>
<journal-title>Atmospheric Chemistry and Physics</journal-title>
<abbrev-journal-title abbrev-type="publisher">ACP</abbrev-journal-title>
</journal-title-group>
<issn pub-type="epub">1680-7324</issn>
<publisher><publisher-name>Copernicus GmbH</publisher-name>
<publisher-loc>Göttingen, Germany</publisher-loc>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="doi">10.5194/acp-6-1495-2006</article-id>
<title-group>
<article-title>The origin of ozone</article-title>
</title-group>
<contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Grewe</surname>
<given-names>V.</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
</contrib>
</contrib-group><aff id="aff1">
<label>1</label>
<addr-line>Institut für Physik der Atmosphäre, DLR-Oberpfaffenhofen, Wessling, Germany</addr-line>
</aff>
<pub-date pub-type="epub">
<day>10</day>
<month>05</month>
<year>2006</year>
</pub-date>
<volume>6</volume>
<issue>6</issue>
<fpage>1495</fpage>
<lpage>1511</lpage>
<permissions>
<license xlink:type="simple">
<license-p>This is an open-access article ditributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.</license-p>
</license>
</permissions>
<self-uri xlink:href="http://www.atmos-chem-phys.net/6/1495/2006/acp-6-1495-2006.html">This article is available from http://www.atmos-chem-phys.net/6/1495/2006/acp-6-1495-2006.html</self-uri>
<self-uri xlink:href="http://www.atmos-chem-phys.net/6/1495/2006/acp-6-1495-2006.pdf">The full text article is available as a PDF file from http://www.atmos-chem-phys.net/6/1495/2006/acp-6-1495-2006.pdf</self-uri>
<abstract>
<p>Highest atmospheric ozone production rates can be found at around 30 km
in the tropical stratosphere, leading to ozone mixing ratios of about 10 ppmv.
Those stratospheric air masses are then transported to extra-tropical
latitudes via the Brewer-Dobson circulation. This is considered the main
mechanism to generate mid- and high latitude ozone.
By applying the climate-chemistry models E39/C and MAECHAM4/CHEM,
this view is investigated in more detail.
The origin of ozone in the troposphere and stratosphere is analysed, by
incorporating a diagnostics (&quot;marked ozone origin tracers&quot;) into the models,
which allows to identify the origin of ozone.
In most regions the simulated local ozone concentration is dominated by local ozone
production, i.e.&amp;nbsp;less than 50% of the ozone at higher latitudes
of the stratosphere is
produced in the tropics, which conflicts with the idea that the tropics
are the global source for stratospheric ozone.
Although episodic stratospheric intrusions occur basically everywhere,
the main ozone stratosphere-to-troposphere exchange is connected
to exchange processes at the sub-tropical jet-stream.
The simulated tropospheric influx of ozone amounts to 420 Tg per year, and originates
in the Northern Hemisphere from the extra-tropical stratosphere, whereas
in the Southern Hemisphere a re-circulation of tropical tropospheric ozone
contributes most to the influx of ozone into the troposphere.
In the model E39/C, the upper troposphere of both hemispheres is clearly dominated by tropical
tropospheric ozone (40%&amp;ndash;50%) except for northern summer hemisphere, where the tropospheric
contribution (from the tropics as well as from the Northern Hemisphere) does not
exceed 20%.</p>
</abstract>
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