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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>6</issue_number>
		<publication_year>2009</publication_year>
	</journal>
	<doi>10.5194/acpd-9-24085-2009</doi>
	<article_url>http://www.atmos-chem-phys-discuss.net/9/24085/2009/</article_url>
	<abstract_html>http://www.atmos-chem-phys-discuss.net/9/24085/2009/acpd-9-24085-2009.html</abstract_html>
	<fulltext_pdf>http://www.atmos-chem-phys-discuss.net/9/24085/2009/acpd-9-24085-2009.pdf</fulltext_pdf>
	<start_page>24085</start_page>
	<end_page>24143</end_page>
	<publication_date>2009-11-12</publication_date>
	<article_title content_type="html">Chemical evolution of volatile organic compounds in the outflow of the Mexico City Metropolitan area</article_title>
	<authors>
		<author numeration="1" affiliations="1">
			<name>E. C. Apel</name>
		</author>
		<author numeration="2" affiliations="1">
			<name>L. K. Emmons</name>
		</author>
		<author numeration="3" affiliations="1">
			<name>T. Karl</name>
		</author>
		<author numeration="4" affiliations="1">
			<name>F. Flocke</name>
		</author>
		<author numeration="5" affiliations="1">
			<name>A. J. Hills</name>
		</author>
		<author numeration="6" affiliations="1">
			<name>S. Madronich</name>
		</author>
		<author numeration="7" affiliations="1">
			<name>J. Lee-Taylor</name>
		</author>
		<author numeration="8" affiliations="1">
			<name>A. Fried</name>
		</author>
		<author numeration="9" affiliations="1">
			<name>P. Weibring</name>
		</author>
		<author numeration="10" affiliations="1">
			<name>J. Walega</name>
		</author>
		<author numeration="11" affiliations="1">
			<name>D. Richter</name>
		</author>
		<author numeration="12" affiliations="1">
			<name>X. Tie</name>
		</author>
		<author numeration="13" affiliations="1">
			<name>L. Mauldin</name>
		</author>
		<author numeration="14" affiliations="1">
			<name>T. Campos</name>
		</author>
		<author numeration="15" affiliations="2">
			<name>B. Sive</name>
		</author>
		<author numeration="16" affiliations="3">
			<name>L. Kleinman</name>
		</author>
		<author numeration="17" affiliations="3">
			<name>S. Springston</name>
		</author>
		<author numeration="18" affiliations="4">
			<name>R. Zaveri</name>
		</author>
		<author numeration="19" affiliations="4,12">
			<name>J. Ortega</name>
		</author>
		<author numeration="20" affiliations="5">
			<name>P. Voss</name>
		</author>
		<author numeration="21" affiliations="6">
			<name>D. Blake</name>
		</author>
		<author numeration="22" affiliations="6">
			<name>A. Baker</name>
		</author>
		<author numeration="23" affiliations="7">
			<name>C. Warneke</name>
		</author>
		<author numeration="24" affiliations="7">
			<name>D. Welsh-Bon</name>
		</author>
		<author numeration="25" affiliations="7">
			<name>J. de Gouw</name>
		</author>
		<author numeration="26" affiliations="8">
			<name>J. Zheng</name>
		</author>
		<author numeration="27" affiliations="8">
			<name>R. Zhang</name>
		</author>
		<author numeration="28" affiliations="9">
			<name>J. Rudolph</name>
		</author>
		<author numeration="29" affiliations="10">
			<name>W. Junkermann</name>
		</author>
		<author numeration="30" affiliations="11">
			<name>D. D. Riemer</name>
		</author>
	</authors>
	<affiliations>
		<affiliation numeration="1" content_type="html">Atmospheric Chemistry Division, National Center for Atmospheric Research, Boulder, CO, USA</affiliation>
		<affiliation numeration="2" content_type="html">Institute for the Study of Earth, Oceans and Space, University of New Hampshire, Durham, NH, USA</affiliation>
		<affiliation numeration="3" content_type="html">Atmospheric Sciences Division, Brookhaven National Laboratory, Upton, NY, USA</affiliation>
		<affiliation numeration="4" content_type="html">Atmospheric Sciences &amp; Global Change Division, Pacific Northwest National Laboratory, Richland, WA, USA</affiliation>
		<affiliation numeration="5" content_type="html">Picker Engineering Program, Smith College and the University of Massachusetts, Amherst, USA</affiliation>
		<affiliation numeration="6" content_type="html">Department of Chemistry, University of California, Irvine, CA, USA</affiliation>
		<affiliation numeration="7" content_type="html">Chemical Sciences Division, National Oceanic and Atmospheric Administration, Boulder, CO, USA</affiliation>
		<affiliation numeration="8" content_type="html">Department of Atmospheric Sciences, Texas A&amp;M, USA</affiliation>
		<affiliation numeration="9" content_type="html">Centre for Atmospheric Chemistry, York University, Toronto, Canada</affiliation>
		<affiliation numeration="10" content_type="html">Forschungszentrum Karlsruhe, Garmisch-Partinkirchen, Germany</affiliation>
		<affiliation numeration="11" content_type="html">University of Miami, Rosenstiel School of Marine and Atmospheric Sciences, Miami, FL, USA</affiliation>
		<affiliation numeration="12" content_type="html">currently at: Colorado School of Mines, Golden, CO, USA</affiliation>
	</affiliations>
	<abstract content_type="html">The volatile organic compound (VOC) distribution in the Mexico City
Metropolitan Area (MCMA) and its evolution as it is uplifted and transported
out of the MCMA basin was studied during the 2006 MILAGRO/MIRAGE-Mex field
campaign. The results show that in the morning hours in the city center, the
VOC distribution is dominated by non-methane hydrocarbons (NMHCs) but with a
substantial contribution from oxygenated volatile organic compounds (OVOCs),
predominantly from primary emissions. Alkanes account for a large part of the
NMHC distribution in terms of mixing ratios. In terms of reactivity, NMHCs
also dominate overall, especially in the morning hours. However, in the
afternoon, as the boundary layer lifts and air is mixed and aged within the
basin, the distribution changes as secondary products are formed. The
WRF-Chem (Weather Research and Forecasting with Chemistry) model and MOZART
(Model for Ozone and Related chemical Tracers) were able to reproduce the
general features of the daytime cycle of the VOC OH reactivity distribution
showing that NMHCs dominate the distribution except in the afternoon hours
and that the VOC OH reactivity peaks in the early morning due to high morning
emissions from the city into a shallow boundary layer. The WRF-Chem and
MOZART models showed higher reactivity than the experimental data during the
nighttime cycle, perhaps indicating problems with the modeled nighttime
boundary layer height.


In addition, a plume was studied in which air was advected out of the MCMA
and intercepted downwind with the DOE G1 on 18~March and the NCAR C130 one
day later on 19~March. A number of identical species measured aboard each
aircraft gave insight into the chemical evolution of the plume as it aged and
was transported as far as 1000 km downwind. Ozone and many OVOCs were
photochemically produced in the plume. The WRF-Chem and MOZART models were
used to examine the spatial and temporal extent of the 19~March plume and to
help interpret the OH reactivity in the downwind plume. The model results
generally showed good agreement with experimental results for the total VOC
OH reactivity downwind and gave insight into the distributions of VOC
chemical classes downwind. A box model with detailed gas phase chemistry
(NCAR Master Mechanism), initialized with concentrations observed at one of
the ground sites in the MCMA, was used to examine the expected evolution of
specific VOCs over a 1â€“2~day period. The models clearly supported the
experimental evidence for NMHC oxidation leading to the formation of OVOCs
downwind, which then become the primary fuel for ozone production far away
from the MCMA.</abstract>
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</article>

