Journal of Experimental Botany, Vol 50, 391-398, Copyright © 1999 by Oxford University Press
D Thomas, D Eamus and D Bell
In a companion paper several methods of calculating the marginal unit water
cost of plant carbon gain (
ARTICLES
Optimization theory of stomatal behaviour II. Stomatal responses of several tree species of north Australia to changes in light, soil and atomospheric water content and temperature
School of Biological and Environmental Sciences, and School of Mathematical and Physical Sciences, Northern Territory University, Darwin, NT Australia, 9090; Corresponding author e-mail: dane.thomas@ntu.edu.au
E/
A) were tested to determine
whether stomata were behaving optimally in relation to regulating leaf gas
exchange. In this paper one method is applied to several tropical tree
species when leaf-to-air vapour pressure difference (D), photosynthetic
photon flux density, leaf temperature, and atmospheric soil water
availability were manipulated. The response of leaves that had expanded
during the dry season were also compared to that of leaves that had
expanded in the wet season. Few differences in absolute value of
E/
A, or the form of the relationship, were observed
between species or between seasons. In the majority of species,
E/
A increased significantly as either leaf-to-air vapour
pressure difference increased, at a leaf temperature of either 33
C or 38
C, or as in
photosynthetic photon flux density increased. In contrast, as leaf
temperature increased at constant D,
E/
A was generally
constant. As pre-dawn water potential declined,
E/
A
declined. The relationship between
E/
A and D did not
differ whether internal or ambient carbon dioxide concentration were kept
constant. It is concluded that stomata are only behaving optimally over a
very small range of D. If a larger range of D is used, to incorporate
values that more closely reflect those experienced by tropical trees in a
savanna environment optimization is incomplete.Key
words: Stomatal optimization theory, marginal unit water cost.
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