Evolution of stomatal responsiveness to CO2 and optimization of water-use efficiency among land plants

被引:192
作者
Brodribb, Timothy J. [1 ]
McAdam, Scott A. M. [1 ]
Jordan, Gregory J. [1 ]
Feild, Taylor S. [2 ]
机构
[1] Univ Tasmania, Sch Plant Sci, Hobart, Tas 7001, Australia
[2] Univ Tennessee, Dept Ecol & Evolutionary Biol, Knoxville, TN 37919 USA
基金
澳大利亚研究理事会;
关键词
angiosperm; CO2; evolution; gymnosperm; stomata; water-use efficiency; ADIANTUM-CAPILLUS-VENERIS; GAS-EXCHANGE; CARBON-DIOXIDE; CONDUCTANCE; PHOTOSYNTHESIS; RESPONSES; ACCLIMATION; HYDRAULICS; MESOPHYLL; LIGHT;
D O I
10.1111/j.1469-8137.2009.02844.x
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
P>The stomata of angiosperms respond to changes in ambient atmospheric concentrations of CO2 (C-a) in ways that appear to optimize water-use efficiency. It is unknown where in the history of land plants this important stomatal control mechanism evolved. Here, we test the hypothesis that major clades of plants have distinct stomatal sensitivities to C-a reflecting a relatively recent evolution of water-use optimization in derived angiosperms. Responses of stomatal conductance (g(s)) to step changes between elevated, ambient and low C-a (600, 380 and 100 mu mol mol(-1), respectively) were compared in a phylogenetically and ecologically diverse range of higher angiosperms, conifers, ferns and lycopods. All species responded to low C-a by increasing g(s) but only angiosperm stomata demonstrated a significant closing response when C-a was elevated to 600 mu mol mol(-1). As a result, angiosperms showed significantly greater increases in water-use efficiency under elevated C-a than the other lineages. The data suggest that the angiosperms have mechanisms for detecting and responding to increases in C-a that are absent from earlier diverging lineages, and these mechanisms impart a greater capacity to optimize water-use efficiency. New Phytologist (2009) 183: 839-847doi: 10.1111/j.1469-8137.2009.02844.x.
引用
收藏
页码:839 / 847
页数:9
相关论文
共 40 条
[1]   The response of photosynthesis and stomatal conductance to rising [CO2]:: mechanisms and environmental interactions [J].
Ainsworth, Elizabeth A. ;
Rogers, Alistair .
PLANT CELL AND ENVIRONMENT, 2007, 30 (03) :258-270
[2]   GEOCARBSULF:: A combined model for Phanerozoic atmospheric O2 and CO2 [J].
Berner, Robert A. .
GEOCHIMICA ET COSMOCHIMICA ACTA, 2006, 70 (23) :5653-5664
[3]   Contrasting physiological and structural vegetation feedbacks in climate change simulations [J].
Betts, RA ;
Cox, PM ;
Lee, SE ;
Woodward, FI .
NATURE, 1997, 387 (6635) :796-799
[4]   Projected increase in continental runoff due to plant responses to increasing carbon dioxide [J].
Betts, Richard A. ;
Boucher, Olivier ;
Collins, Matthew ;
Cox, Peter M. ;
Falloon, Peter D. ;
Gedney, Nicola ;
Hemming, Deborah L. ;
Huntingford, Chris ;
Jones, Chris D. ;
Sexton, David M. H. ;
Webb, Mark J. .
NATURE, 2007, 448 (7157) :1037-U5
[5]   Internal coordination between hydraulics and stomatal control in leaves [J].
Brodribb, Tim J. ;
Jordan, Gregory J. .
PLANT CELL AND ENVIRONMENT, 2008, 31 (11) :1557-1564
[6]   Stomatal protection against hydraulic failure: a comparison of coexisting ferns and angiosperms [J].
Brodribb, TJ ;
Holbrook, NM .
NEW PHYTOLOGIST, 2004, 162 (03) :663-670
[7]   A hydromechanical and biochemical model of stomatal conductance [J].
Buckley, TN ;
Mott, KA ;
Farquhar, GD .
PLANT CELL AND ENVIRONMENT, 2003, 26 (10) :1767-1785
[8]   How do leaf hydraulics limit stomatal conductance at high water vapour pressure deficits? [J].
Bunce, James A. .
PLANT CELL AND ENVIRONMENT, 2006, 29 (08) :1644-1650
[9]  
Cowan I R, 1977, Symp Soc Exp Biol, V31, P471
[10]   A meta-analysis of elevated CO2 effects on woody plant mass, form, and physiology [J].
Curtis, PS ;
Wang, XZ .
OECOLOGIA, 1998, 113 (03) :299-313