<?xml version="1.0" encoding="utf-8" standalone="no"?>
<!DOCTYPE article SYSTEM "http://www.atmos-chem-phys-discuss.net/inc/acpd/copernicus.dtd">
<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>5</volume_number>
		<issue_number>6</issue_number>
		<publication_year>2005</publication_year>
	</journal>
	<doi>10.5194/acpd-5-11215-2005</doi>
	<article_url>http://www.atmos-chem-phys-discuss.net/5/11215/2005/</article_url>
	<abstract_html>http://www.atmos-chem-phys-discuss.net/5/11215/2005/acpd-5-11215-2005.html</abstract_html>
	<fulltext_pdf>http://www.atmos-chem-phys-discuss.net/5/11215/2005/acpd-5-11215-2005.pdf</fulltext_pdf>
	<start_page>11215</start_page>
	<end_page>11248</end_page>
	<publication_date>2005-11-02</publication_date>
	<article_title content_type="html">The overwhelming role of soils in the global atmospheric hydrogen cycle</article_title>
	<authors>
		<author numeration="1" affiliations="1">
			<name>T. S. Rhee</name>
			<email>rhee@mpch-mainz.mpg.de</email>
		</author>
		<author numeration="2" affiliations="1">
			<name>C. A. M. Brenninkmeijer</name>
		</author>
		<author numeration="3" affiliations="2,3">
			<name>T. Röckmann</name>
		</author>
	</authors>
	<affiliations>
		<affiliation numeration="1" content_type="html">Max Planck Institute for Chemistry, Atmospheric Chemistry Division, Mainz, Germany</affiliation>
		<affiliation numeration="2" content_type="html">Max Planck Institute for Nuclear Physics, Atmospheric Physics Division, Heidelberg, Germany</affiliation>
		<affiliation numeration="3" content_type="html">now at: Institute for Marine and Atmospheric Research Utrecht, Utrecht University, Utrecht, The Netherlands</affiliation>
	</affiliations>
	<abstract content_type="html">The removal of molecular hydrogen (H&lt;sub&gt;2&lt;/sub&gt;) from the atmosphere is dominated
by the uptake in soils. Notwithstanding, estimates of the magnitude of this
important process on a global scale are highly uncertain. The CARIBIC
aircraft observations of the seasonal variations of H&lt;sub&gt;2&lt;/sub&gt; and its D/H
isotopic ratio in the northern hemisphere allow an independent, better
constrained estimate. We derive that 82% of the annual turnover of
tropospheric H&lt;sub&gt;2&lt;/sub&gt; is due to soil uptake, equaling 88 (&amp;plusmn;11) Tg a&lt;sup&gt;&amp;minus;1&lt;/sup&gt;,
of which the northern hemisphere alone accounts for 62 (&amp;plusmn;10) Tg a&lt;sup&gt;&amp;minus;1&lt;/sup&gt;.
Our calculations further show that tropospheric H&lt;sub&gt;2&lt;/sub&gt;
has a lifetime of only 1.4 (&amp;plusmn;0.2) years &amp;ndash; significantly shorter than
the recent estimate of ~2 years &amp;ndash; which is expected to decrease in the
future. In addition, our independent top-down approach, confined by the
global and hemispheric sinks of H&lt;sub&gt;2&lt;/sub&gt;, indicates 64 (&amp;plusmn;12) Tg a&lt;sup&gt;&amp;minus;1&lt;/sup&gt;
emissions from various sources of volatile organic compounds by
photochemical oxidation in the atmosphere. This estimate is as much as up to
60% larger than the previous estimates. This large airborne production
of H&lt;sub&gt;2&lt;/sub&gt; helps to explain the fairly homogeneous distribution of H&lt;sub&gt;2&lt;/sub&gt;
in the troposphere.</abstract>
	<references>
	</references>
</article>

