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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>1</issue_number>
		<publication_year>2009</publication_year>
	</journal>
	<doi>10.5194/acpd-9-4417-2009</doi>
	<article_url>http://www.atmos-chem-phys-discuss.net/9/4417/2009/</article_url>
	<abstract_html>http://www.atmos-chem-phys-discuss.net/9/4417/2009/acpd-9-4417-2009.html</abstract_html>
	<fulltext_pdf>http://www.atmos-chem-phys-discuss.net/9/4417/2009/acpd-9-4417-2009.pdf</fulltext_pdf>
	<start_page>4417</start_page>
	<end_page>4488</end_page>
	<publication_date>2009-02-17</publication_date>
	<article_title content_type="html">Evaluation of new secondary organic aerosol models for a case study in Mexico City</article_title>
	<authors>
		<author numeration="1" affiliations="1,2,3">
			<name>K. Dzepina</name>
		</author>
		<author numeration="2" affiliations="2">
			<name>R. M. Volkamer</name>
		</author>
		<author numeration="3" affiliations="3">
			<name>S. Madronich</name>
		</author>
		<author numeration="4" affiliations="1,3,4">
			<name>P. Tulet</name>
		</author>
		<author numeration="5" affiliations="1,2">
			<name>I. M. Ulbrich</name>
		</author>
		<author numeration="6" affiliations="5">
			<name>Q. Zhang</name>
		</author>
		<author numeration="7" affiliations="6">
			<name>C. D. Cappa</name>
		</author>
		<author numeration="8" affiliations="7">
			<name>P. J. Ziemann</name>
		</author>
		<author numeration="9" affiliations="1,2">
			<name>J. L. Jimenez</name>
			<email>jose.jimenez@colorado.edu</email>
		</author>
	</authors>
	<affiliations>
		<affiliation numeration="1" content_type="html">Cooperative Institute for Research in the Environmental Sciences (CIRES), University of Colorado at Boulder, Boulder, CO, USA</affiliation>
		<affiliation numeration="2" content_type="html">Department of Chemistry and Biochemistry, Univ. of Colorado at Boulder, Boulder, CO, USA</affiliation>
		<affiliation numeration="3" content_type="html">National Center for Atmospheric Research â€“ Atmospheric Chemistry Division, Boulder, CO, USA</affiliation>
		<affiliation numeration="4" content_type="html">Meteo France/CNRM-GREI, Toulouse, France</affiliation>
		<affiliation numeration="5" content_type="html">Atmospheric Sciences Research Center, University at Albany, SUNY, Albany, NY, USA</affiliation>
		<affiliation numeration="6" content_type="html">Dept. of Civil and Environmental Engineering, Univ. of California at Davis, Davis, CA, USA</affiliation>
		<affiliation numeration="7" content_type="html">Air Pollution Research Center, Univ. of California, Riverside, CA, USA</affiliation>
	</affiliations>
	<abstract content_type="html">Recent field studies have found large discrepancies in the measured vs.
modeled SOA mass loadings in both urban and regional polluted atmospheres.
The reasons for these large differences are unclear. Here we revisit a case
study of SOA formation in Mexico City described by Volkamer et al. (2006),
during a photochemically active period when the impact of regional biomass
burning is minor or negligible, and show that the observed increase in
OA/Î”CO is consistent with results from several groups during
MILAGRO 2006. Then we use the case study to evaluate three new SOA
models: 1) the update of aromatic SOA yields from recent chamber experiments
(Ng et al., 2007); 2) the formation of SOA from glyoxal (Volkamer et al.,
2007a); and 3) the formation of SOA from primary semivolatile and
intermediate volatility species (P-S/IVOC) (Robinson et al., 2007). We also
evaluate the effect of reduced partitioning of SOA into POA (Song et al.,
2007). Traditional SOA precursors (mainly aromatics) by themselves still fail
to produce enough SOA to match the observations by a factor of  7. The
new low-NO&lt;sub&gt;x&lt;/sub&gt; aromatic pathways with very high SOA yields make a very
small contribution in this high-NO&lt;sub&gt;x&lt;/sub&gt; urban environment as the
RO&lt;sub&gt;2&lt;/sub&gt;&lt;sup&gt;.&lt;/sup&gt;+NO reaction dominates the fate of the RO&lt;sub&gt;2&lt;/sub&gt;&lt;sup&gt;.&lt;/sup&gt; radicals. Glyoxal
contributes several &amp;mu;g m&lt;sup&gt;&amp;minus;3&lt;/sup&gt; to SOA formation, with similar timing
as the measurements. P-S/IVOC are estimated from equilibrium with emitted
POA, and introduce a large amount of gas-phase oxidizable carbon that was not
in models before. With the formulation in Robinson et al. (2007) these
species have a high SOA yield, and this mechanism can close the gap in SOA
mass between measurements and models in our case study. However the
volatility of SOA produced in the model is too high and the O/C ratio is
lower than observations. Glyoxal SOA helps to bring the O/C ratio of
predicted and observed SOA into better agreement. The sensitivities of the
model to some key uncertain parameters are evaluated.</abstract>
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</article>

