Water deficits and hydraulic limits to leaf water supply.

By J. Sperry, Uwe G Hacke, Ram Oren, J. Comstock. Plant, Cell and Environment, 2002

825 citations recorded by the source corpus.

Subfields: Global and Planetary Change, Plant Science, Soil Science

View Paper: https://www.semanticscholar.org/paper/c867ecfd9448bdccd8c45e720e3558c64f37019c

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Citations in the corpus

Growth, carbon‐isotope discrimination, and drought‐associated mortality across a Pinus ponderosa elevational transect (2010, background): “, 2002), and more complex hydraulic models exist (e.g. Williams et al., 2001; Sperry et al., 2002); however, the simple framework in Eqn (2) allows interpretation of gross level impacts of chronic differences in Cs and VPD on whole-tree gas exchange in the absence of detailed parameterization data (”
Leaf hydraulics. (2006, background): “low plants to maintain gas exchange closer to the level of irreversible Kleaf decline (19, 120).”
Biological constraints on water transport in the soil–plant–atmosphere system (2013, background): “Hence, it is reasonable to hypothesize that the maximum conductances (under well-watered conditions) in different parts of the SPAC are inter-related or coordinated, such that a relatively more efficient stem water transport system corresponds to hydraulically-efficient leaves and higher maximum sto”
High competitiveness of a resource demanding invasive acacia under low resource supply (2009, background): “sponding stomatal closure to avoid runaway cavitations (Sperry et al. 2002).”
Leaf water status and stem xylem flux in relation to soil drought in five temperate broad-leaved tree species with contrasting water use strategies (2011, background): “Long-term plastic responses to drought include regulation strategies like growing a deep rooting system, reducing leaf area or developing stems with high hydraulic conductivity and low cavitation risk (Sperry et al., 2002).”
Rhizosphere: biophysics, biogeochemistry and ecological relevance (2009, background): “This is likely to occur under high evaporative demand, a small root-shoot ratio and a coarse soil texture (Gardner 1960; Sperry et al. 2002) and was demonstrated experimentally (Hainsworth and Aylmore 1989; MacFall et al. 1990).”
Morphological traits and water use strategies in seedlings of Mediterranean coexisting species (2010, positive): “Species with greater KAs displayed greater leaf gas exchange values consistent with previously reported correlations (Bond and Kavanagh 1999; Sperry et al. 2002; Hernández et al. 2009).”
The control of stomata by water balance. (2005, background): “Taken together, these considerations may help to explain further why stomatal behaviour tends to operate so close to the edge of water-supply catastrophe (Tyree & Sperry, 1988; Sperry et al., 2002; Brodribb & Holbrook, 2003).”
Plant morphology and root hydraulics are altered by nutrient deficiency in Pistacia lentiscus (L.) (2006, background): “Several works have analyzed the relationship between changes in plant hydraulic conductance, and stomatal conductance and transpiration (Nardini et al. 2000; Sperry et al. 2002).”
Stomatal Closure during Leaf Dehydration, Correlation with Other Leaf Physiological Traits1 (2003, background): “The evolution of internal conduits for water transport added a level of complexity to optimizing gas exchange during photosynthesis, because of the dependence of water supply capacity upon the water potential in the plant (Sperry et al., 2002).”
The hydraulic architecture of Pinaceae – a review (2004, background): “This explains the role of xylem embolism in limiting gas exchange and drought-resistance in plants (Sperry et al. 2002).”
Adjustment of structure and function of Hawaiian Metrosideros polymorpha at high vs. low precipitation (2007, background): “The plant may build xylem tissue that is less vulnerable to embolism at highly negative water potentials (Sperry et al. 2002).”
Understanding plant responses to drought - from genes to the whole plant. (2003, background): “A revived interest in the hydraulic component of signalling is apparent (Jackson et al. 2000; Sperry et al. 2002), but we are still far from understanding where and how chemical and hydraulic signals are integrated to regulate plant response to dehydration (Comstock 2002).”
Plasticity of morphological and physiological traits in response to different levels of irradiance in seedlings of silver fir (Abies alba Mill) (2003, background): “Such phenotypic differences in vulnerability to cavitation may be of consequence for the drought induced stomatal closure (Cochard et al. 1996; Sperry et al. 2002) that is expected to occur at higher water potential in”