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<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>9</volume_number>
		<issue_number>3</issue_number>
		<publication_year>2009</publication_year>
	</journal>
	<doi>10.5194/acpd-9-13889-2009</doi>
	<article_url>http://www.atmos-chem-phys-discuss.net/9/13889/2009/</article_url>
	<abstract_html>http://www.atmos-chem-phys-discuss.net/9/13889/2009/acpd-9-13889-2009.html</abstract_html>
	<fulltext_pdf>http://www.atmos-chem-phys-discuss.net/9/13889/2009/acpd-9-13889-2009.pdf</fulltext_pdf>
	<start_page>13889</start_page>
	<end_page>13916</end_page>
	<publication_date>2009-06-25</publication_date>
	<article_title content_type="html">Clouds, photolysis and regional tropospheric ozone budgets</article_title>
	<authors>
		<author numeration="1" affiliations="1,4">
			<name>A. Voulgarakis</name>
			<email>avoulgarakis@giss.nasa.gov</email>
		</author>
		<author numeration="2" affiliations="2">
			<name>O. Wild</name>
		</author>
		<author numeration="3" affiliations="3">
			<name>N. H. Savage</name>
		</author>
		<author numeration="4" affiliations="1">
			<name>G. D. Carver</name>
		</author>
		<author numeration="5" affiliations="1">
			<name>J. A. Pyle</name>
		</author>
	</authors>
	<affiliations>
		<affiliation numeration="1" content_type="html">Centre for Atmospheric Science, University of Cambridge, UK</affiliation>
		<affiliation numeration="2" content_type="html">Lancaster Environment Centre, University of Lancaster, UK</affiliation>
		<affiliation numeration="3" content_type="html">Met Office, Exeter, UK</affiliation>
		<affiliation numeration="4" content_type="html">now at: Columbia University, Center for Climate Systems Research, NASA Goddard Institute for Space Studies, New York, USA</affiliation>
	</affiliations>
	<abstract content_type="html">We use a three-dimensional chemical transport model to examine the shortwave
radiative effects of clouds on the tropospheric ozone budget. In addition to
looking at changes in global concentrations as previous studies have done, we
examine changes in ozone chemical production and loss caused by clouds and
how these vary in different parts of the troposphere. On a global scale, we
find that clouds have a modest effect on ozone chemistry, but on a regional
scale their role is much more significant, with the size of the response
dependent on the region. The largest averaged changes in chemical budgets
(&amp;plusmn;10–14%) are found in the marine troposphere, where cloud optical
depths are high. We demonstrate that cloud effects are small on average in
the middle troposphere because this is a transition region between reduction
and enhancement in photolysis rates. We show that increases in boundary layer
ozone due to clouds are driven by large-scale changes in downward ozone
transport from higher in the troposphere rather than by decreases in in-situ
ozone chemical loss rates. Increases in upper tropospheric ozone are caused
by higher production rates due to backscattering of radiation and consequent
increases in photolysis rates, mainly J(NO&lt;sub&gt;2&lt;/sub&gt;). The global radiative effect
of clouds on isoprene is stronger than on ozone. Tropospheric isoprene
lifetime increases by 7% when taking clouds into account. We compare the
importance of clouds in contributing to uncertainties in the global ozone
budget with the role of other radiatively-important factors. The budget is
most sensitive to the overhead ozone column, while surface albedo and clouds
have smaller effects. However, uncertainty in representing the spatial
distribution of clouds may lead to a large sensitivity on regional scales.</abstract>
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</article>

