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<front>
<journal-meta>
<journal-id journal-id-type="publisher">ACP</journal-id>
<journal-title-group>
<journal-title>Atmospheric Chemistry and Physics</journal-title>
<abbrev-journal-title abbrev-type="publisher">ACP</abbrev-journal-title>
</journal-title-group>
<issn pub-type="epub">1680-7324</issn>
<publisher><publisher-name>Copernicus GmbH</publisher-name>
<publisher-loc>Göttingen, Germany</publisher-loc>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="doi">10.5194/acp-8-389-2008</article-id>
<title-group>
<article-title>N&lt;sub&gt;2&lt;/sub&gt;O release from agro-biofuel production negates global warming reduction by replacing fossil fuels</article-title>
</title-group>
<contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Crutzen</surname>
<given-names>P. J.</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
<xref ref-type="aff" rid="aff2">
<sup>2</sup>
</xref>
<xref ref-type="aff" rid="aff3">
<sup>3</sup>
</xref>
</contrib>
<contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Mosier</surname>
<given-names>A. R.</given-names>
</name>
<xref ref-type="aff" rid="aff4">
<sup>4</sup>
</xref>
</contrib>
<contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Smith</surname>
<given-names>K. A.</given-names>
</name>
<xref ref-type="aff" rid="aff5">
<sup>5</sup>
</xref>
</contrib>
<contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Winiwarter</surname>
<given-names>W.</given-names>
</name>
<xref ref-type="aff" rid="aff3">
<sup>3</sup>
</xref>
<xref ref-type="aff" rid="aff6">
<sup>6</sup>
</xref>
</contrib>
</contrib-group><aff id="aff1">
<label>1</label>
<addr-line>Max Planck Institute for Chemistry, Department of Atmospheric Chemistry, Mainz, Germany</addr-line>
</aff>
<aff id="aff2">
<label>2</label>
<addr-line>Scripps Institution of Oceanography, University of California, La Jolla, USA</addr-line>
</aff>
<aff id="aff3">
<label>3</label>
<addr-line>International Institute for Applied Systems Analysis (IIASA), Laxenburg, Austria</addr-line>
</aff>
<aff id="aff4">
<label>4</label>
<addr-line>Mount Pleasant, SC, USA</addr-line>
</aff>
<aff id="aff5">
<label>5</label>
<addr-line>School of Geosciences, University of Edinburgh, Edinburgh, UK</addr-line>
</aff>
<aff id="aff6">
<label>6</label>
<addr-line>Austrian Research Centers - ARC, Vienna, Austria</addr-line>
</aff>
<pub-date pub-type="epub">
<day>29</day>
<month>01</month>
<year>2008</year>
</pub-date>
<volume>8</volume>
<issue>2</issue>
<fpage>389</fpage>
<lpage>395</lpage>
<permissions>
<license xlink:type="simple">
<license-p>This is an open-access article ditributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.</license-p>
</license>
</permissions>
<self-uri xlink:href="http://www.atmos-chem-phys.net/8/389/2008/acp-8-389-2008.html">This article is available from http://www.atmos-chem-phys.net/8/389/2008/acp-8-389-2008.html</self-uri>
<self-uri xlink:href="http://www.atmos-chem-phys.net/8/389/2008/acp-8-389-2008.pdf">The full text article is available as a PDF file from http://www.atmos-chem-phys.net/8/389/2008/acp-8-389-2008.pdf</self-uri>
<abstract>
<p>The relationship, on a global basis, between the amount of N fixed by
chemical, biological or atmospheric processes entering the terrestrial
biosphere, and the total emission of nitrous oxide (N&lt;sub&gt;2&lt;/sub&gt;O), has been
re-examined, using known global atmospheric removal rates and concentration
growth of N&lt;sub&gt;2&lt;/sub&gt;O as a proxy for overall emissions. For both the
pre-industrial period and in recent times, after taking into account the
large-scale changes in synthetic N fertiliser production, we find an overall
conversion factor of 3&amp;ndash;5% from newly fixed N to N&lt;sub&gt;2&lt;/sub&gt;O-N. We assume the
same factor to be valid for biofuel production systems. It is covered only
in part by the default conversion factor for &quot;direct&quot; emissions from
agricultural crop lands (1%) estimated by IPCC (2006), and the default
factors for the &quot;indirect&quot; emissions (following volatilization/deposition
and leaching/runoff of N: 0.35&amp;ndash;0.45%) cited therein. However, as we
show in the paper, when additional emissions included in the IPCC
methodology, e.g. those from livestock production, are included, the total
may not be inconsistent with that given by our &quot;top-down&quot; method. When the
extra N&lt;sub&gt;2&lt;/sub&gt;O emission from biofuel production is calculated in
&quot;CO&lt;sub&gt;2&lt;/sub&gt;-equivalent&quot; global warming terms, and compared with the
quasi-cooling effect of &quot;saving&quot; emissions of fossil fuel derived
CO&lt;sub&gt;2&lt;/sub&gt;, the outcome is that the production of commonly used biofuels, such
as biodiesel from rapeseed and bioethanol from corn (maize), depending on N
fertilizer uptake efficiency by the plants, can contribute as much or more
to global warming by N&lt;sub&gt;2&lt;/sub&gt;O emissions than cooling by fossil fuel savings.
Crops with less N demand, such as grasses and woody coppice species, have
more favourable climate impacts. This analysis only considers the conversion
of biomass to biofuel. It does not take into account the use of fossil fuel
on the farms and for fertilizer and pesticide production, but it also
neglects the production of useful co-products. Both factors partially
compensate each other. This needs to be analyzed in a full life cycle
assessment.</p>
</abstract>
<counts><page-count count="7"/></counts>
</article-meta>
</front>
<body/>
<back>
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