1991
DOI: 10.1111/j.1365-3040.1991.tb01379.x
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Do stomata respond to relative humidity?

Abstract: The objective of the work reported was to answer the following questions; (1) Do stomata respond to both humidity and temperature? (2) Do these responses interact in sueh a way that relative humidity at the leaf surface is a more appropriate variable than water vapour saturation deficit at the leaf surface and yields a simpler description of the cotnpound response? To answer these questions, we tneasured the response of leaf conductance to humidity under constant leaf temperature, and the response to increasin… Show more

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Cited by 205 publications
(104 citation statements)
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“…as well as a search for 'universal' relationships between photosynthesis, temperature and humidity, has led to formulations which combine the mechanistic photosynthesis model of Farquhar et al (1980) with the empirical but readily applicable 'Ball-Berry' model (Ball et al 1987;Collatz et al 1991). Although it is now understood that neither relative humidity (Aphalo & Jarvis 1991) nor external carbon dioxide concentrations (Mott 1988) are physically detected by the plant, the use of these parameters in an empirical relationship has been shown to fit a wide range of data (Ball et al 1987;Leuning 1990). In the present data, this relationship was marginally adequate (except at the very lowest LAVPD) in predicting the LAVPD responses at 35 °C and in qualitatively predicting the temperature dependence of the slope.…”
Section: Discussionmentioning
confidence: 99%
“…as well as a search for 'universal' relationships between photosynthesis, temperature and humidity, has led to formulations which combine the mechanistic photosynthesis model of Farquhar et al (1980) with the empirical but readily applicable 'Ball-Berry' model (Ball et al 1987;Collatz et al 1991). Although it is now understood that neither relative humidity (Aphalo & Jarvis 1991) nor external carbon dioxide concentrations (Mott 1988) are physically detected by the plant, the use of these parameters in an empirical relationship has been shown to fit a wide range of data (Ball et al 1987;Leuning 1990). In the present data, this relationship was marginally adequate (except at the very lowest LAVPD) in predicting the LAVPD responses at 35 °C and in qualitatively predicting the temperature dependence of the slope.…”
Section: Discussionmentioning
confidence: 99%
“…The physical limits for production of EEMT defined here correspond directly to well defined temperature and vapor pressure deficit limits on transpiration, photosynthesis, and primary production; processes mediated by a combination of biophysical controls on plant stomatal conductance and carbon assimilation, and physical controls on evaporation (Law et al, 2002;Aphalo and Jarvis, 1991;Damour et al, 2010;Oren et al, 1999;Jolly et al, 2005;Schulze et al, 1994;Jarvis and McNaughton, 1986;Pieruschka et al, 2010). While EEMT does not include the mass and energy transfer associated with evapotranspiration, the production of EEMT is closely coupled with water, energy and carbon balances as mediated by photosynthesis and evapotranspiration and thus expresses similar physical limits.…”
Section: Discussionmentioning
confidence: 99%
“…Modelling assimilation and intercellular CO 2 from measured conductance 1315 appropriate driving mechanism for stomatal response (Aphalo & Jarvis 1991;Monteith 1995;Oren et al 1999). Using similar approximation, the Leuning (1995) model reduces to:…”
Section: The Ball-berry Modelmentioning
confidence: 99%