Relationship between plant hydraulic and biochemical properties derived from a steady‐state coupled water and carbon transport model
By Gabriel G. Katul, R. Leuning, Ram Oren. 2003
227 citations recorded by the source corpus.
Subfields: Civil and Structural Engineering, Global and Planetary Change, Plant Science
View Paper: https://www.semanticscholar.org/paper/972e265e772a7edb8e8067501e10454b86c4f3c3
How researchers see this paper
The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.
In Civil and Structural Engineering
In Global and Planetary Change
- H. Cochard
- Nathan G. McDowell
- Gabriel G. Katul
- Tim J. Brodribb
- Giulia Vico
- Stefano Manzoni
- Amilcare Porporato
- R. Duursma
In Plant Science
- Tim J. Brodribb
- Amilcare Porporato
- Giulia Vico
- R. Duursma
- Gabriel G. Katul
- Stefano Manzoni
- H. Cochard
- Nathan G. McDowell
Citations in the corpus
- Mechanisms of plant survival and mortality during drought: why do some plants survive while others succumb to drought? (2008, background): “The long-term structural adjustments that maintain homeostasis between water supply, water demand, and plant metabolism (Whitehead & Jarvis, 1981; Cinnirella et al., 2002; Katul et al., 2003; Bréda et al., 2006) may all play a role in the survival or mortality of plants during drought.”
- An overview of models of stomatal conductance at the leaf level. (2010, background): “…it has been repeatedly observed that the gs-to-Anet ratio shifts in drought conditions (Brodribb 1996; Lawlor & Cornic 2002; Medrano et al. 2002; Katul et al. 2003; MacFarlane et al. 2004; Urban et al. 2006; Damour, Vandame & Urban 2008), which seriously limits the generalization of the use of…”
- Effects of stand age and tree species on canopy transpiration and average stomatal conductance of boreal forests (2005, background): “When maximum hydraulic conductance is reduced, GS and EL follow with the possibility of reduced carbon uptake (Hubbard, Bond, & Ryan 1999; Katul et al. 2003).”
- Xylem hydraulic physiology: the functional backbone of terrestrial plant productivity. (2009, background): “Not only is coordination apparently general amongst vascular plants, but the ratio of K and A seems to be conservative in C3 plants, suggesting convergence upon an optimal strategy [24,47,48].”
- Biological constraints on water transport in the soil–plant–atmosphere system (2013, methodology): “As a first approximation, the soil–root conductance per unit ground area, gS-R (m s 1 Pa (1)), can be calculated as [55]”
- Modelling C3 and C4 photosynthesis under water-stressed conditions (2008, background): “The first one is here described through a simple cylindrical model (Katul et al. 2003), including soil hydraulic conductivity, Ks (s), active soil depth, Zr, and root area index, RAI, as”
- 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).”
- Reconciling the optimal and empirical approaches to modelling stomatal conductance (2011, background): “…evidence is accumulating that photosynthetic capacity and maximal stomatal conductance are related to plant hydraulic architecture (e.g. Nardini & Salleo, 2000; Clearwater & Meinzer, 2001; Hubbard et al. 2001; Katul et al. 2003; Mencuccini, 2003; Bucci et al. 2005; Taylor & Eamus, 2008).”