A hydromechanical and biochemical model of stomatal conductance

By Thomas N. Buckley, Keith A. Mott, G. Farquhar. 2003

356 citations recorded by the source corpus.

Subfields: Global and Planetary Change, Plant Science

View Paper: https://www.semanticscholar.org/paper/6e0251ab9b052e64f60e91ee408008453e0c1483

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Citations in the corpus

Hydraulic and environmental limitations to leaf water relations in trees with respect to canopy position (2006, background): “One cannot exclude partial stomatal closure as a result of increased epidermal backpressure due to high turgor of the epidermal cells at improved water supply (Buckley et al., 2003).”
Different ability of three Mediterranean oak species to tolerate progressive water stress (2006, background): “Modulation of gas exchange in relation to the variation of hydraulic resistances of leaves, stem, and roots pointed out a well-triggered above- and under-ground mechanism allowing a good water balance for oak species (Bucci et al. 2003, Buckley et al. 2003, Katul et al. 2003, Lo Gullo et al. 2003).”
Xylem hydraulic physiology: the functional backbone of terrestrial plant productivity. (2009, background): “Therefore in this review I will respect the greater evidence and proceed with the view of stomata as ‘‘hydromechanical’’ valves [23], restricting discussion of ABAmediated stomatal control until the last section that examines drought.”
Modelling C3 and C4 photosynthesis under water-stressed conditions (2008, background): “…stress and other factor possibly relevant to stomatal functioning, such as solar radiation, vapour pressure deficit (VPD) and abscisic acid (ABA) dynamics (e.g., Buckley et al. 2003; Dewar 2002; Gao et al. 2002; Jarvis 1976; Leuning 1995; Norman 1982; Tardieu and Davies 1993; Tuzet et al. 2003).”
Biological constraints on water transport in the soil–plant–atmosphere system (2013, background): “More mechanistic approaches detail the mechanical movement of guard cells in response to changes in the local pressure [21,96–98], or account for long-distance control from root-derived phyto-hormones, like abscisic acid (ABA) [58,97,99].”
Photosynthetic physiology of eucalypts along a sub-continental rainfall gradient in northern Australia (2011, background): “Several authors have formulated models that apply this concept (Ball et al., 1987; Buckley et al., 2003; Farquhar and Wong, 1984; Jarvis and Davies, 1998; Leuning, 1990; Leuning, 1995), although the mechanistic basis for coupling between photosynthetic capacity and gs is still uncertain (von Caemmer”
Rising atmospheric carbon dioxide: plants FACE the future. (2004, methodology): “A simple phenomenological model, which holds that stomatal conductance is linearly proportional to the product of assimilation rate and humidity, and inversely proportional to [CO2], is highly effective in predicting stomatal response to [CO 2] in the absence of water and humidity stress (19).”
Morphological plasticity, photosynthesis and chlorophyll fluorescence of Athyrium pachyphlebium at different shade levels (2011, unknown): “Before the PPFD increased to 100 μmol m–2 s–1, the values of gs, E and Ci varied dramatically which may be due to the quick light induction of the enzymes involved in the Calvin cycle and forming a metabolism center (Sassenrath et al. 1994, Buckley et al. 2003).”