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<front>
<journal-meta>
<journal-id journal-id-type="publisher">CP</journal-id>
<journal-title-group>
<journal-title>Climate of the Past</journal-title>
<abbrev-journal-title abbrev-type="publisher">CP</abbrev-journal-title>
<abbrev-journal-title abbrev-type="nlm-ta">Clim. Past</abbrev-journal-title>
</journal-title-group>
<issn pub-type="epub">1814-9332</issn>
<publisher><publisher-name>Copernicus Publications</publisher-name>
<publisher-loc>Göttingen, Germany</publisher-loc>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="doi">10.5194/cp-5-431-2009</article-id>
<title-group>
<article-title>Climate and CO&lt;sub&gt;2&lt;/sub&gt; modulate the C&lt;sub&gt;3&lt;/sub&gt;/C&lt;sub&gt;4&lt;/sub&gt; balance and &amp;delta;&lt;sup&gt;13&lt;/sup&gt;C signal in simulated vegetation</article-title>
</title-group>
<contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Flores</surname>
<given-names>O.</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
</contrib>
<contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Gritti</surname>
<given-names>E. S.</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
<xref ref-type="aff" rid="aff2">
<sup>2</sup>
</xref>
</contrib>
<contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Jolly</surname>
<given-names>D.</given-names>
</name>
<xref ref-type="aff" rid="aff2">
<sup>2</sup>
</xref>
</contrib>
</contrib-group><aff id="aff1">
<label>1</label>
<addr-line>CEFE, UMR 5175 CNRS, 1919, route de Mende, 34293, Montpellier cedex 5, France</addr-line>
</aff>
<aff id="aff2">
<label>2</label>
<addr-line>ISEM, UMR 5554 CNRS/Univ. Montpellier II, Case 61, 34095 Montpellier cedex 5, France</addr-line>
</aff>
<pub-date pub-type="epub">
<day>07</day>
<month>08</month>
<year>2009</year>
</pub-date>
<volume>5</volume>
<issue>3</issue>
<fpage>431</fpage>
<lpage>440</lpage>
<permissions>
<copyright-statement>Copyright: &#x000a9; 2009 O. Flores et al.</copyright-statement>
<copyright-year>2009</copyright-year>
<license license-type="open-access">
<license-p>This work is licensed under the Creative Commons Attribution 3.0 Unported License. To view a copy of this licence, visit <ext-link ext-link-type="uri"  xlink:href="https://creativecommons.org/licenses/by/3.0/">https://creativecommons.org/licenses/by/3.0/</ext-link></license-p>
</license>
</permissions>
<self-uri xlink:href="https://cp.copernicus.org/articles/5/431/2009/cp-5-431-2009.html">This article is available from https://cp.copernicus.org/articles/5/431/2009/cp-5-431-2009.html</self-uri>
<self-uri xlink:href="https://cp.copernicus.org/articles/5/431/2009/cp-5-431-2009.pdf">The full text article is available as a PDF file from https://cp.copernicus.org/articles/5/431/2009/cp-5-431-2009.pdf</self-uri>
<abstract>
<p>Climate and atmospheric CO&lt;sub&gt;2&lt;/sub&gt; effects on the balance between C&lt;sub&gt;3&lt;/sub&gt; and C&lt;sub&gt;4&lt;/sub&gt; plants
have received conflicting interpretations based on the analysis of carbon
isotopic fractionation (&amp;delta;&lt;sup&gt;13&lt;/sup&gt;C) in sediments. But, climate and CO&lt;sub&gt;2&lt;/sub&gt; effects
on the C&lt;sub&gt;3&lt;/sub&gt;/C&lt;sub&gt;4&lt;/sub&gt; balance and &amp;delta;&lt;sup&gt;13&lt;/sup&gt;C signal are rarely addressed together. Here, we
use a process-based model (BIOME4) to disentangle these effects. We simulated
the vegetation response to climate and CO&lt;sub&gt;2&lt;/sub&gt; atmospheric concentration (&lt;i&gt;p&lt;/i&gt;CO&lt;sub&gt;2&lt;/sub&gt;)
in two sites in which vegetation changed oppositely, with respect to C&lt;sub&gt;3&lt;/sub&gt; and
C&lt;sub&gt;4&lt;/sub&gt; plants abundance, during the Last Glacial Maximum to Holocene transition.
The C&lt;sub&gt;3&lt;/sub&gt;/C&lt;sub&gt;4&lt;/sub&gt; balance and &amp;delta;&lt;sup&gt;13&lt;/sup&gt;C signal were primarily sensitive
to temperature and CO&lt;sub&gt;2&lt;/sub&gt; atmospheric partial pressure. The simulated variations
were in agreement with patterns observed in
palaeorecords. Water limitation favoured C&lt;sub&gt;4&lt;/sub&gt; plants in case of large negative
deviation in rainfall. Although a global
parameter, &lt;i&gt;p&lt;/i&gt;CO&lt;sub&gt;2&lt;/sub&gt; affected the &amp;delta;&lt;sup&gt;13&lt;/sup&gt;C signal differently from one site to the
other because of its effects on the C&lt;sub&gt;3&lt;/sub&gt;/C&lt;sub&gt;4&lt;/sub&gt; balance and on carbon isotopic
fractionation in C&lt;sub&gt;3&lt;/sub&gt; and C&lt;sub&gt;4&lt;/sub&gt; plants. Simulated Plant functional types (PFT)
also differed in their composition and response from one site to the other.
The C&lt;sub&gt;3&lt;/sub&gt;/C&lt;sub&gt;4&lt;/sub&gt; balance involved different competing C&lt;sub&gt;3&lt;/sub&gt; and C&lt;sub&gt;4&lt;/sub&gt; PFT, and not
homogeneous C&lt;sub&gt;3&lt;/sub&gt; and C&lt;sub&gt;4&lt;/sub&gt; poles as often assumed. Process-based vegetation
modelling emphasizes the need to account for multiple factors when a
palaeo-&amp;delta;&lt;sup&gt;13&lt;/sup&gt;C signal is used to reconstruct the C&lt;sub&gt;3&lt;/sub&gt;/C&lt;sub&gt;4&lt;/sub&gt; balance.</p>
</abstract>
<counts><page-count count="10"/></counts>
</article-meta>
</front>
<body/>
<back>
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