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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>2</issue_number>
		<publication_year>2009</publication_year>
	</journal>
	<doi>10.5194/acp-9-383-2009</doi>
	<article_url>http://www.atmos-chem-phys.net/9/383/2009/</article_url>
	<abstract_html>http://www.atmos-chem-phys.net/9/383/2009/acp-9-383-2009.html</abstract_html>
	<fulltext_pdf>http://www.atmos-chem-phys.net/9/383/2009/acp-9-383-2009.pdf</fulltext_pdf>
	<start_page>383</start_page>
	<end_page>411</end_page>
	<publication_date>2009-01-19</publication_date>
	<article_title content_type="html">Effects of regional-scale and convective transports on tropospheric ozone chemistry revealed by aircraft observations during the wet season of the AMMA campaign</article_title>
	<authors>
		<author numeration="1" affiliations="1">
			<name>G. Ancellet</name>
			<email>gerard.ancellet@aero.jussieu.fr</email>
		</author>
		<author numeration="2" affiliations="1">
			<name>J. Leclair de Bellevue</name>
		</author>
		<author numeration="3" affiliations="2">
			<name>C. Mari</name>
		</author>
		<author numeration="4" affiliations="2">
			<name>P. Nedelec</name>
		</author>
		<author numeration="5" affiliations="1">
			<name>A. Kukui</name>
		</author>
		<author numeration="6" affiliations="3">
			<name>A. Borbon</name>
		</author>
		<author numeration="7" affiliations="3">
			<name>P. Perros</name>
		</author>
	</authors>
	<affiliations>
		<affiliation numeration="1" content_type="html">Service d&apos;AÃ©ronomie, UniversitÃ© Paris 6, UniversitÃ© Versailles-St-Quentin, CNRS, France</affiliation>
		<affiliation numeration="2" content_type="html">UniversitÃ© de Toulouse, CNRS, LA (Laboratoire d&apos;AÃ©rologie), France</affiliation>
		<affiliation numeration="3" content_type="html">Laboratoire Interuniversitaire des SystÃ¨mes AtmosphÃ©riques, UniversitÃ© Paris 12, CNRS, France</affiliation>
	</affiliations>
	<abstract content_type="html">The African Monsoon Multidisciplinary Analyses (AMMA) fourth airborne
campaign was conducted in Julyâ€“August 2006 to study the chemical
composition
of the middle and upper troposphere in West Africa with the major objective
to better understand the processing of chemical emissions by the West
African
Monsoon (WAM) and its associated regional-scale and vertical transports.
In particular, the french airborne experiment was organized around two
goals.
The first was to characterize the impact of Mesoscale Convective Systems
(MCSs)
 on the ozone budget in the upper troposphere and the evolution of the
chemical composition of these convective plumes as they move westward
toward
the Atlantic Ocean. The second objective was to discriminate the impact of
remote sources of pollution over West Africa, including transport from the
middle east, Europe, Asia and from southern hemispheric fires.
Observations of O&lt;sub&gt;3&lt;/sub&gt;, CO, NO&lt;sub&gt;x&lt;/sub&gt;, H&lt;sub&gt;2&lt;/sub&gt;O and hydroperoxide above West Africa along
repeated meridional transects were coupled with transport analysis
based on the FLEXPART lagrangian model. The cross analysis of trace gas
concentrations and
transport pathways revealed 5 types of air masses:
convective uplift of industrial and urban emissions,
convective uplift of biogenic emissions,
slow advection from Cotonou polluted plumes near the coast,
meridional transport of upper
tropospheric air from the subtropical barrier region,
and meridional transport of Southern Hemisphere (SH) biomass burning
emissions.
O&lt;sub&gt;3&lt;/sub&gt;/CO
correlation plots and the correlation plots of H&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;2&lt;/sub&gt; with a OH proxy
revealed not only a control of the trace gas variability by transport
processes but also significant photochemical reactivity in the mid- and upper
troposphere.
The study of four MCSs outflow showed contrasted chemical composition
and air mass origins depending on the MCSs lifetime and latitudinal position.
Favorables conditions for ozone production were found for MCSs with
increased MCS lifetime (&amp;gt;1.5 days), which allowed for more H&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;2&lt;/sub&gt; formation,
and
with trajectories crossing the 10&amp;deg; N latitude, which increased
CO transport to the upper troposphere.
The upper tropospheric concentrations sampled in the MCS outflow regions
showed mixed origins including local vertical convective transport,
and uplifting of air from the low troposphere over the middle-east
related to the summer Asian low pressure system or from the southern
hemispheric fires.</abstract>
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</article>

