Using modern plant trait relationships between observed and theoretical maximum stomatal conductance and vein density to examine patterns of plant macroevolution
Identifieur interne : 000378 ( Main/Exploration ); précédent : 000377; suivant : 000379Using modern plant trait relationships between observed and theoretical maximum stomatal conductance and vein density to examine patterns of plant macroevolution
Auteurs : Jennifer C. Mcelwain ; Charilaos Yiotis ; Tracy LawsonSource :
- The New Phytologist [ 0028-646X ] ; 2015.
Abstract
Understanding the drivers of geological‐scale patterns in plant macroevolution is limited by a hesitancy to use measurable traits of fossils to infer palaeoecophysiological function. Here, scaling relationships between morphological traits including maximum theoretical stomatal conductance ( Our study demonstrated significant relationships between Expansion of the ecophysiological niche space in angiosperms, afforded by coordinated evolution of high
Url:
DOI: 10.1111/nph.13579
PubMed: 26230251
PubMed Central: 5014202
Affiliations:
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<author><name sortKey="Yiotis, Charilaos" sort="Yiotis, Charilaos" uniqKey="Yiotis C" first="Charilaos" last="Yiotis">Charilaos Yiotis</name>
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<sourceDesc><biblStruct><analytic><title xml:lang="en" level="a" type="main">Using modern plant trait relationships between observed and theoretical maximum stomatal conductance and vein density to examine patterns of plant macroevolution</title>
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<author><name sortKey="Yiotis, Charilaos" sort="Yiotis, Charilaos" uniqKey="Yiotis C" first="Charilaos" last="Yiotis">Charilaos Yiotis</name>
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<author><name sortKey="Lawson, Tracy" sort="Lawson, Tracy" uniqKey="Lawson T" first="Tracy" last="Lawson">Tracy Lawson</name>
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<series><title level="j">The New Phytologist</title>
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<front><div type="abstract" xml:lang="en"><title>Summary</title>
<p><list list-type="bullet" id="nph13579-list-0001"><list-item><p>Understanding the drivers of geological‐scale patterns in plant macroevolution is limited by a hesitancy to use measurable traits of fossils to infer palaeoecophysiological function.</p>
</list-item>
<list-item><p>Here, scaling relationships between morphological traits including maximum theoretical stomatal conductance (<italic>g</italic>
<sub>max</sub>
) and leaf vein density (<italic>D</italic>
<sub>v</sub>
) and physiological measurements including operational stomatal conductance (<italic>g</italic>
<sub>op</sub>
), saturated (<italic>A</italic>
<sub>sat</sub>
<italic>)</italic>
and maximum (<italic>A</italic>
<sub>max</sub>
) assimilation rates were investigated for 18 extant taxa in order to improve understanding of angiosperm diversification in the Cretaceous.</p>
</list-item>
<list-item><p>Our study demonstrated significant relationships between <italic>g</italic>
<sub>op</sub>
, <italic>g</italic>
<sub>max</sub>
and <italic>D</italic>
<sub>v</sub>
that together can be used to estimate gas exchange and the photosynthetic capacities of fossils. We showed that acquisition of high <italic>g</italic>
<sub>max</sub>
in angiosperms conferred a competitive advantage over gymnosperms by increasing the dynamic range (plasticity) of their gas exchange and expanding their ecophysiological niche space. We suggest that species with a high <italic>g</italic>
<sub>max</sub>
(> 1400 mmol m<sup>−2</sup>
s<sup>−1</sup>
) would have been capable of maintaining a high <italic>A</italic>
<sub>max</sub>
as the atmospheric <styled-content style="fixed-case">CO</styled-content>
<sub>2</sub>
declined through the Cretaceous, whereas gymnosperms with a low <italic>g</italic>
<sub>max</sub>
would experience severe photosynthetic penalty.</p>
</list-item>
<list-item><p>Expansion of the ecophysiological niche space in angiosperms, afforded by coordinated evolution of high <italic>g</italic>
<sub>max</sub>
<italic>, D</italic>
<sub>v</sub>
and increased plasticity in <italic>g</italic>
<sub>op</sub>
<italic>,</italic>
adds further functional insights into the mechanisms driving angiosperm speciation.</p>
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