Global CO2 rise leads to reduced maximum stomatal conductance in Florida vegetation
- aPalaeoecology, Laboratory of Palaeobotany and Palynology, Institute of Environmental Biology, Utrecht University, 3584 CD, Utrecht, The Netherlands;
- bDepartment of Environmental Sciences, Copernicus Institute, Utrecht University, 3508 TC, Utrecht, The Netherlands; and
- cDepartment of Biology, Indiana University, Bloomington, IN 47405
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Contributed by David L. Dilcher, January 11, 2011 (sent for review October 19, 2010)

Abstract
A principle response of C3 plants to increasing concentrations of atmospheric CO2 (CO2) is to reduce transpirational water loss by decreasing stomatal conductance (gs) and simultaneously increase assimilation rates. Via this adaptation, vegetation has the ability to alter hydrology and climate. Therefore, it is important to determine the adaptation of vegetation to the expected anthropogenic rise in CO2. Short-term stomatal opening–closing responses of vegetation to increasing CO2 are described by free-air carbon enrichments growth experiments, and evolutionary adaptations are known from the geological record. However, to date the effects of decadal to centennial CO2 perturbations on stomatal conductance are still largely unknown. Here we reconstruct a 34% (±12%) reduction in maximum stomatal conductance (gsmax) per 100 ppm CO2 increase as a result of the adaptation in stomatal density (D) and pore size at maximal stomatal opening (amax) of nine common species from Florida over the past 150 y. The species-specific gsmax values are determined by different evolutionary development, whereby the angiosperms sampled generally have numerous small stomata and high gsmax, and the conifers and fern have few large stomata and lower gsmax. Although angiosperms and conifers use different D and amax adaptation strategies, our data show a coherent response in gsmax to CO2 rise of the past century. Understanding these adaptations of C3 plants to rising CO2 after decadal to centennial environmental changes is essential for quantification of plant physiological forcing at timescales relevant for global warming, and they are likely to continue until the limits of their phenotypic plasticity are reached.
Footnotes
- 1To whom correspondence may be addressed. E-mail: e.i.lammertsma{at}uu.nl or dilcher{at}indiana.edu.
Author contributions: E.I.L., H.J.d.B., S.C.D., D.L.D., A.F.L., and F.W.-C. designed research; E.I.L., H.J.d.B., and F.W.-C. performed research; E.I.L. and F.W.-C. analyzed data; and E.I.L., H.J.d.B., and F.W.-C. wrote the paper.
The authors declare no conflict of interest.
This article contains supporting information online at www.pnas.org/lookup/suppl/doi:10.1073/pnas.1100371108/-/DCSupplemental.
Freely available online through the PNAS open access option.














