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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>10</volume_number>
		<issue_number>3</issue_number>
		<publication_year>2010</publication_year>
	</journal>
	<doi>10.5194/acpd-10-6995-2010</doi>
	<article_url>http://www.atmos-chem-phys-discuss.net/10/6995/2010/</article_url>
	<abstract_html>http://www.atmos-chem-phys-discuss.net/10/6995/2010/acpd-10-6995-2010.html</abstract_html>
	<fulltext_pdf>http://www.atmos-chem-phys-discuss.net/10/6995/2010/acpd-10-6995-2010.pdf</fulltext_pdf>
	<start_page>6995</start_page>
	<end_page>7036</end_page>
	<publication_date>2010-03-12</publication_date>
	<article_title content_type="html">A linear CO chemistry parameterization in a chemistry-transport model: evaluation and application to data assimilation</article_title>
	<authors>
		<author numeration="1" affiliations="1,2">
			<name>M. Claeyman</name>
			<email>marine.claeyman@aero.obs-mip.fr</email>
		</author>
		<author numeration="2" affiliations="1,2">
			<name>J.-L. AttiÃ©</name>
		</author>
		<author numeration="3" affiliations="2">
			<name>L. El Amraoui</name>
		</author>
		<author numeration="4" affiliations="3,4">
			<name>D. Cariolle</name>
		</author>
		<author numeration="5" affiliations="2">
			<name>V.-H. Peuch</name>
		</author>
		<author numeration="6" affiliations="2">
			<name>H. TeyssÃ¨dre</name>
		</author>
		<author numeration="7" affiliations="2">
			<name>B. Josse</name>
		</author>
		<author numeration="8" affiliations="1">
			<name>P. Ricaud</name>
		</author>
		<author numeration="9" affiliations="3">
			<name>S. Massart</name>
		</author>
		<author numeration="10" affiliations="3">
			<name>A. Piacentini</name>
		</author>
		<author numeration="11" affiliations="1">
			<name>J.-P. Cammas</name>
		</author>
		<author numeration="12" affiliations="5">
			<name>N. J. Livesey</name>
		</author>
		<author numeration="13" affiliations="6">
			<name>H. C. Pumphrey</name>
		</author>
		<author numeration="14" affiliations="7">
			<name>D. P. Edwards</name>
		</author>
	</authors>
	<affiliations>
		<affiliation numeration="1" content_type="html">Laboratoire d&apos;AÃ©rologie, UniversitÃ© de Toulouse, CNRS/INSU UMR 5560, Toulouse, France</affiliation>
		<affiliation numeration="2" content_type="html">CNRM-GAME, MÃ©tÃ©o-France and CNRS URA 1357, Toulouse, France</affiliation>
		<affiliation numeration="3" content_type="html">CERFACS, CNRS URA 1875, Toulouse, France</affiliation>
		<affiliation numeration="4" content_type="html">MÃ©tÃ©o-France, Toulouse, France</affiliation>
		<affiliation numeration="5" content_type="html">Jet Propulsion Laboratory, California Institude of  Technology, Pasadena, California, USA</affiliation>
		<affiliation numeration="6" content_type="html">University of Edimburgh, Edinburgh, UK</affiliation>
		<affiliation numeration="7" content_type="html">National Center for Atmospheric Research, Boulder, Colorado, USA</affiliation>
	</affiliations>
	<abstract content_type="html">This paper presents an evaluation of a new linear parameterization valid for
the troposphere and the stratosphere, based on a first order approximation of
the carbon monoxide (CO) continuity equation. This linear scheme (hereinafter
noted LINCO) has been implemented in the 3-D Chemical Transport Model (CTM)
MOCAGE of MÃ©tÃ©o-France. On the one hand, a one and a half years of
LINCO simulation has been compared to output obtained from a detailed
chemical scheme output. In spite of small differences, the seasonal and
global CO distributions obtained by both schemes present similar general
characteristics. The mean differences between both schemes remain small
within about &amp;plusmn;25 ppbv (part per billion by volume) in the troposphere
and &amp;plusmn;15 ppbv in the stratosphere. On the other hand, LINCO has been
compared to diverse observations from satellite instruments covering the
troposphere (Measurements Of Pollution In The Troposphere: MOPITT) and the
stratosphere (Microwave Limb Sounder: MLS) and also from aircraft
(Measurements of ozone and water vapour by Airbus in-service aircraft: MOZAIC
programme) mostly flying in the upper troposphere and lower stratosphere. A
good agreement is generally found in the troposphere and the lower
stratosphere. In the troposphere, the LINCO seasonal variations as well as
the vertical and horizontal distributions are quite close to MOPITT CO
observations. However, a bias of ~&amp;minus;40 ppbv is observed at 700 hPa
between LINCO and MOPITT which is probably caused by too low emission values.
In the stratosphere, MLS and LINCO present similar large-scale patterns,
except over the poles where the CO concentration is underestimated by the
model. We suggest that the underestimation of CO at polar latitudes is not
related to the linear scheme but is induced by a too rapid transport by the
meridional circulation. In the UTLS (Upper Troposphere Lower Stratosphere),
LINCO tends to slightly overestimate the MOZAIC aircraft observations, with
general small biases less than 2%. LINCO is a simple parameterization
compared to a detailed chemical scheme, allowing very fast calculations and
thus making possible long reanalyses of MOPITT CO data. The computational
cost just corresponds to the transport of an additional passive tracer. For
this, we used a variational 3-D-FGAT (First Guess at Appropriate Time) method
in conjunction with MOCAGE for a long run of one and a half years. The data
assimilation greatly improves the vertical CO distribution in the troposphere
from 700 to 350 hPa compared to independent MOZAIC profiles. At 146 hPa, the
assimilated CO 2-D distribution is improved compared to MLS observations by
reducing the bias up to a factor of 2 in the tropics. At extratropical
latitudes, the assimilated fields tend to underestimate the CO concentrations
resulting from an excessive equator to pole circulation. This study confirms
that the linear scheme is able to simulate reasonably well the CO
distribution in the troposphere and in the lower stratosphere. Therefore, the
low computing cost of the linear scheme opens new perspectives to make free
runs and CO data assimilation runs at high resolution and over periods of
several years.</abstract>
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</article>

