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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-9-27611-2009</doi>
	<article_url>http://www.atmos-chem-phys-discuss.net/9/27611/2009/</article_url>
	<abstract_html>http://www.atmos-chem-phys-discuss.net/9/27611/2009/acpd-9-27611-2009.html</abstract_html>
	<fulltext_pdf>http://www.atmos-chem-phys-discuss.net/9/27611/2009/acpd-9-27611-2009.pdf</fulltext_pdf>
	<start_page>27611</start_page>
	<end_page>27648</end_page>
	<publication_date>2009-12-21</publication_date>
	<article_title content_type="html">Can a global model chemical mechanism reproduce NO, NO&lt;sub&gt;2&lt;/sub&gt;, and O&lt;sub&gt;3&lt;/sub&gt; measurements above a tropical rainforest?</article_title>
	<authors>
		<author numeration="1" affiliations="1">
			<name>R. C. Pike</name>
			<email>rachel.pike@atm.ch.cam.ac.uk</email>
		</author>
		<author numeration="2" affiliations="2">
			<name>J. D. Lee</name>
		</author>
		<author numeration="3" affiliations="1,9">
			<name>P. J. Young</name>
		</author>
		<author numeration="4" affiliations="3">
			<name>S. Moller</name>
		</author>
		<author numeration="5" affiliations="1,4">
			<name>G. D. Carver</name>
		</author>
		<author numeration="6" affiliations="1">
			<name>X. Yang</name>
		</author>
		<author numeration="7" affiliations="5,6">
			<name>P. Misztal</name>
		</author>
		<author numeration="8" affiliations="7">
			<name>B. Langford</name>
		</author>
		<author numeration="9" affiliations="8,10">
			<name>D. Stewart</name>
		</author>
		<author numeration="10" affiliations="8">
			<name>C. E. Reeves</name>
		</author>
		<author numeration="11" affiliations="7">
			<name>C. N. Hewitt</name>
		</author>
		<author numeration="12" affiliations="1,4">
			<name>J. A. Pyle</name>
		</author>
	</authors>
	<affiliations>
		<affiliation numeration="1" content_type="html">Centre for Atmospheric Science, Department of Chemistry, University of Cambridge, Lensfield Road, Cambridge, CB2 1EW, UK</affiliation>
		<affiliation numeration="2" content_type="html">National Centre for Atmospheric Science (NCAS), University of York, Heslington, York, YO10 5DD, UK</affiliation>
		<affiliation numeration="3" content_type="html">Department of Chemistry, University of York, Heslington, York, YO10 5DD, UK</affiliation>
		<affiliation numeration="4" content_type="html">National Centre for Atmospheric Science�Climate, University of Cambridge, Lensfield Road, Cambridge, CB2 1EW, UK</affiliation>
		<affiliation numeration="5" content_type="html">Centre for Ecology and Hydrology Edinburgh, Bush Estate, Penicuik, Midlothian, EH26 0QB, UK</affiliation>
		<affiliation numeration="6" content_type="html">The University of Edinburgh, School of Chemistry, Joseph Black Building, West Mains Road, Edinburgh, EH9 3JJ, UK</affiliation>
		<affiliation numeration="7" content_type="html">Lancaster Environment Centre, Lancaster University, Lancaster, LA1 4YQ, UK</affiliation>
		<affiliation numeration="8" content_type="html">School of Environmental Sciences, University of East Anglia, Norwich, NR4 7TJ, UK</affiliation>
		<affiliation numeration="9" content_type="html">now at: NOAA Earth System Research Laboratory, 325 Broadway, Boulder, CO, 80501, USA</affiliation>
		<affiliation numeration="10" content_type="html">now at: Department of Chemistry, University of Reading, Whiteknights, Reading, RG6 6AH, UK</affiliation>
	</affiliations>
	<abstract content_type="html">A cross-platform field campaign, OP3, was conducted in the state of Sabah in
Malaysian Borneo between April and July of 2008.  Among the suite of
observations recorded, the campaign included measurements of NO&lt;sub&gt;x&lt;/sub&gt; and
O&lt;sub&gt;3&lt;/sub&gt;–crucial outputs of any model chemistry mechanism.  We describe the
measurements of these species made from both the ground site and aircraft.
We examine the output from the global model p-TOMCAT at two resolutions for
this location during the April campaign period.  The models exhibit reasonable
ability in capturing the NO&lt;sub&gt;x&lt;/sub&gt; diurnal cycle, but ozone is overestimated.
We use a box model containing the same chemical mechanism to explore the
weaknesses in the global model and the ability of the simplified global
model chemical mechanism to capture the chemistry at the rainforest site.
We achieve a good fit to the data for all three species (NO, NO&lt;sub&gt;2&lt;/sub&gt;, and O&lt;sub&gt;3&lt;/sub&gt;),
though the model is much more sensitive to changes in the treatment of physical
processes than to changes in the chemical mechanism.  Indeed, without some
parameterization of the nighttime boundary layer-free troposphere mixing, a
time dependent box model will not reproduce the observations.  The final
simulation uses this mixing parameterization for NO and NO&lt;sub&gt;2&lt;/sub&gt; but not O&lt;sub&gt;3&lt;/sub&gt;,
as determined by the vertical structure of each species, and matches the
measurements well.</abstract>
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</article>

