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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>20</issue_number>
		<publication_year>2009</publication_year>
	</journal>
	<doi>10.5194/acp-9-7711-2009</doi>
	<article_url>http://www.atmos-chem-phys.net/9/7711/2009/</article_url>
	<abstract_html>http://www.atmos-chem-phys.net/9/7711/2009/acp-9-7711-2009.html</abstract_html>
	<fulltext_pdf>http://www.atmos-chem-phys.net/9/7711/2009/acp-9-7711-2009.pdf</fulltext_pdf>
	<start_page>7711</start_page>
	<end_page>7723</end_page>
	<publication_date>2009-10-16</publication_date>
	<article_title content_type="html">Rates and regimes of photochemical ozone production over Central East China in June 2006: a box model analysis using comprehensive measurements of ozone precursors</article_title>
	<authors>
		<author numeration="1" affiliations="1">
			<name>Y. Kanaya</name>
			<email>yugo@jamstec.go.jp</email>
		</author>
		<author numeration="2" affiliations="1">
			<name>P. Pochanart</name>
		</author>
		<author numeration="3" affiliations="1">
			<name>Y. Liu</name>
		</author>
		<author numeration="4" affiliations="1">
			<name>J. Li</name>
		</author>
		<author numeration="5" affiliations="2">
			<name>H. Tanimoto</name>
		</author>
		<author numeration="6" affiliations="3">
			<name>S. Kato</name>
		</author>
		<author numeration="7" affiliations="3">
			<name>J. Suthawaree</name>
		</author>
		<author numeration="8" affiliations="2">
			<name>S. Inomata</name>
		</author>
		<author numeration="9" affiliations="1">
			<name>F. Taketani</name>
		</author>
		<author numeration="10" affiliations="4">
			<name>K. Okuzawa</name>
		</author>
		<author numeration="11" affiliations="4">
			<name>K. Kawamura</name>
		</author>
		<author numeration="12" affiliations="1">
			<name>H. Akimoto</name>
		</author>
		<author numeration="13" affiliations="5">
			<name>Z. F. Wang</name>
		</author>
	</authors>
	<affiliations>
		<affiliation numeration="1" content_type="html">Research Institute for Global Change, Japan Agency for Marine-Earth Science and Technology, Yokohama, Japan</affiliation>
		<affiliation numeration="2" content_type="html">National Institute for Environmental Studies, Tsukuba, Japan</affiliation>
		<affiliation numeration="3" content_type="html">Tokyo Metropolitan University, Hachioji, Japan</affiliation>
		<affiliation numeration="4" content_type="html">Institute of Low Temperature Science, Hokkaido University, Sapporo, Japan</affiliation>
		<affiliation numeration="5" content_type="html">LAPC/NZC, Institute of Atmospheric Physics, Chinese Academy of Sciences, Beijing, China</affiliation>
	</affiliations>
	<abstract content_type="html">An observation-based box model approach was undertaken to estimate
concentrations of OH, HO&lt;sub&gt;2&lt;/sub&gt;, and RO&lt;sub&gt;2&lt;/sub&gt; radicals and the net
photochemical production rate of ozone at the top of Mount Tai, located in
the middle of Central East China, in June 2006. The model calculation was
constrained by the measurements of O&lt;sub&gt;3&lt;/sub&gt;, H&lt;sub&gt;2&lt;/sub&gt;O, CO, NO, NO&lt;sub&gt;2&lt;/sub&gt;,
hydrocarbon, HCHO, and CH&lt;sub&gt;3&lt;/sub&gt;CHO concentrations, and temperature and &lt;I&gt;J&lt;/I&gt;
values. The net production rate of ozone was estimated to be 6.4 ppb h&lt;sup&gt;&amp;minus;1&lt;/sup&gt;
as a 6-h average (09:00–15:00 CST), suggesting 58&amp;plusmn;37 ppb of
ozone is produced in one day. Thus the daytime buildup of ozone recorded at
the mountain top as ~23 ppb on average is likely affected by in situ
photochemistry as well as by the upward transport of polluted air mass in
the daytime. On days with high ozone concentrations (hourly values exceeding
100 ppb at least once), in situ photochemistry was more active than it was
on low ozone days, suggesting that in situ photochemistry is an important
factor controlling ozone concentrations. Sensitivity model runs for which
different NO&lt;sub&gt;x&lt;/sub&gt; and hydrocarbon concentrations were assumed suggested
that the ozone production occurred normally under NO&lt;sub&gt;x&lt;/sub&gt;-limited
conditions, with some exceptional periods (under
volatile-organic-compound-limited conditions) in which there was fresh
pollution. We also examined the possible influence of the heterogeneous loss
of gaseous HO&lt;sub&gt;2&lt;/sub&gt; radicals in contact with aerosol particle surfaces on
the rate and regimes of ozone production.</abstract>
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</article>

