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Using modern plant trait relationships between observed and theoretical maximum stomatal conductance and vein density to examine patterns of plant macroevolution
Author(s) -
McElwain Jennifer C.,
Yiotis Charilaos,
Lawson Tracy
Publication year - 2016
Publication title -
new phytologist
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.742
H-Index - 244
eISSN - 1469-8137
pISSN - 0028-646X
DOI - 10.1111/nph.13579
Subject(s) - macroevolution , biology , photosynthesis , niche , stomatal conductance , botany , taxon , ecology , phylogenetics , gene , biochemistry
Summary 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 ( g max ) and leaf vein density ( D v ) and physiological measurements including operational stomatal conductance ( g op ), saturated ( A sat ) and maximum ( A max ) assimilation rates were investigated for 18 extant taxa in order to improve understanding of angiosperm diversification in the Cretaceous. Our study demonstrated significant relationships between g op , g max and D v that together can be used to estimate gas exchange and the photosynthetic capacities of fossils. We showed that acquisition of high g max 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 g max (> 1400 mmol m −2 s −1 ) would have been capable of maintaining a high A max as the atmospheric CO 2 declined through the Cretaceous, whereas gymnosperms with a low g max would experience severe photosynthetic penalty. Expansion of the ecophysiological niche space in angiosperms, afforded by coordinated evolution of high g max , D v and increased plasticity in g op , adds further functional insights into the mechanisms driving angiosperm speciation.