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	<journal>
		<journal_title>Biogeosciences</journal_title>
		<journal_url>www.biogeosciences.net</journal_url>
		<issn>1726-4170</issn>
		<eissn>1726-4189</eissn>
		<volume_number>5</volume_number>
		<issue_number>3</issue_number>
		<publication_year>2008</publication_year>
	</journal>
	<doi>10.5194/bg-5-875-2008</doi>
	<article_url>http://www.biogeosciences.net/5/875/2008/</article_url>
	<abstract_html>http://www.biogeosciences.net/5/875/2008/bg-5-875-2008.html</abstract_html>
	<fulltext_pdf>http://www.biogeosciences.net/5/875/2008/bg-5-875-2008.pdf</fulltext_pdf>
	<start_page>875</start_page>
	<end_page>889</end_page>
	<publication_date>2008-06-02</publication_date>
	<article_title content_type="html">Impact of variable air-sea O&lt;sub&gt;2&lt;/sub&gt; and CO&lt;sub&gt;2&lt;/sub&gt; fluxes on atmospheric potential oxygen (APO) and land-ocean carbon sink partitioning</article_title>
	<authors>
		<author numeration="1" affiliations="1">
			<name>C. D. Nevison</name>
		</author>
		<author numeration="2" affiliations="1,4">
			<name>N. M. Mahowald</name>
		</author>
		<author numeration="3" affiliations="2">
			<name>S. C. Doney</name>
		</author>
		<author numeration="4" affiliations="2">
			<name>I. D. Lima</name>
		</author>
		<author numeration="5" affiliations="3">
			<name>N. Cassar</name>
		</author>
	</authors>
	<affiliations>
		<affiliation numeration="1" content_type="html">National Center for Atmospheric Research, Boulder, Colorado, USA</affiliation>
		<affiliation numeration="2" content_type="html">Dept. of Marine Chemistry and Geochemistry, Woods Hole Oceanographic Institution, Woods Hole, MA, USA</affiliation>
		<affiliation numeration="3" content_type="html">Dept. of Geoscience, Princeton University, Princeton, NJ, USA</affiliation>
		<affiliation numeration="4" content_type="html">now at: Cornell University, Ithaca, NY, USA</affiliation>
	</affiliations>
	<abstract content_type="html">A three dimensional, time-evolving field of atmospheric potential oxygen
(APO ~O&lt;sub&gt;2&lt;/sub&gt;/N&lt;sub&gt;2&lt;/sub&gt;+CO&lt;sub&gt;2&lt;/sub&gt;) was estimated using surface
O&lt;sub&gt;2&lt;/sub&gt;, N&lt;sub&gt;2&lt;/sub&gt; and CO&lt;sub&gt;2&lt;/sub&gt; fluxes from the WHOI ocean ecosystem model to
force the MATCH atmospheric transport model. Land and fossil carbon fluxes
were also run in MATCH and translated into O&lt;sub&gt;2&lt;/sub&gt; tracers using assumed
O&lt;sub&gt;2&lt;/sub&gt;:CO&lt;sub&gt;2&lt;/sub&gt; stoichiometries. The modeled seasonal cycles in APO agree
well with the observed cycles at 13 global monitoring stations, with
agreement helped by including oceanic CO&lt;sub&gt;2&lt;/sub&gt; in the APO calculation. The
modeled latitudinal gradient in APO is strongly influenced by seasonal
rectifier effects in atmospheric transport. An analysis of the
APO-vs.-CO&lt;sub&gt;2&lt;/sub&gt; mass-balance method for partitioning land and ocean carbon
sinks was performed in the controlled context of the MATCH simulation, in
which the true surface carbon and oxygen fluxes were known exactly. This
analysis suggests uncertainty of up to &amp;plusmn;0.2 PgC in the inferred sinks
due to variability associated with sparse atmospheric sampling. It also
shows that interannual variability in oceanic O&lt;sub&gt;2&lt;/sub&gt; fluxes can cause large
errors in the sink partitioning when the method is applied over short
timescales. However, when decadal or longer averages are used, the
variability in the oceanic O&lt;sub&gt;2&lt;/sub&gt; flux is relatively small, allowing carbon
sinks to be partitioned to within a standard deviation of 0.1 Pg C/yr of the
true values, provided one has an accurate estimate of long-term mean O&lt;sub&gt;2&lt;/sub&gt;
outgassing.</abstract>
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