Water uptake by roots: effects of water deficit.

By E. Steudle. Journal of Experimental Botany, 2000

650 citations recorded by the source corpus.

Subfields: Global and Planetary Change, Plant Science

View Paper: https://www.semanticscholar.org/paper/b6ede2c902207a2625bc04b7362a6cc55074ab44

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Citations in the corpus

The role of aquaporins in root water uptake. (2002, background): “This increase in Lp may facilitate osmotic water transport and the capture of remaining soil water under conditions of reduced transpiration, with plant water uptake relying mostly on the solute pumping capacity of the root (Steudle, 2000).”
Plant aquaporins: multifunctional water and solute channels with expanding roles. (2002, methodology): “…there is evidence for permeation via MIPs in plants and other organisms, include boron (Dordas, Chrispeels & Brown 2000), antimonite (Sanders et al. 1997), H2O2 (Henzler & Steudle 2000), small alcohols (Hertel & Steudle 1997; Schütz & Tyerman 1997) and compatible solutes (Gerbeau et al. 1999).”
Plant Responses to Salt Stress: Adaptive Mechanisms (2017, background): “Other root characteristics, such as the number and diameter of xylem vessels, width of the root cortex, number of root hairs, and the suberin deposition in both the root exodermis and endodermis, also determine the permeability of roots to water [36,37].”
A vertically extended stochastic model of soil moisture in the root zone (2006, background): “Here we neglect this compensating ability because it involves mechanisms that are complex and still not completely understood [e.g., Steudle, 2000; Cruziat et al., 2002], and its modeling adds parameters that are not easy to determine.”
Root anatomy and soil resource capture (2021, neutral): “4; McCully 1999a; Steudle 2000; Strock et al. 2018).”
Morpho-Anatomical Traits for Plant Adaptation to Drought (2012, background): “The relevance of the apoplastic barriers in controlling water flow depends on root developmental stage: in young unstressed roots, most of the radial hydraulic resistance is more evenly distributed across cortical layers, while in water-stressed old plants it is mainly due to exodermis and endodermi”
Plant Response to Salt Stress and Role of Exogenous Protectants to Mitigate Salt-Induced Damages (2013, background): “Steudle ( 2000 ) reported that in transpiring plants, water is thought to come from the soil to the root xylem through apoplastic pathway due to hydrostatic pressure gradient.”
Physiological parameters in sugarcane cultivars submitted to water deficit (2010, background): “Physiological responses can vary according to plant genotype, but in general, modifications related to water deficit include lower water potential in the soil and in the leaves (Steudle, 2000; Liberato et al., 2006), increases in osmoprotectors such as proline and sugars (Molinari et al.”
Morphological traits and water use strategies in seedlings of Mediterranean coexisting species (2010, positive): “The root morphology and distribution is related to the ability of plants to access water and nutrients (Steudle 2000; Green et al. 2005).”
Root traits contributing to plant productivity under drought (2013, background): “Roots increase apoplastic barriers and take up less water with age and exposure to dry soil (Steudle, 2000), which may appear unfavorable.”
Osmolytes and Plants Acclimation to Changing Environment: Emerging Omics Technologies (2016, background): “Although initially it was thought that osmotic adjustment was specifi c for plants subjected to high salinities, later studies proved that this response is also common in plants grown in conditions of water stress (Cushman 2001 ; Steudle 2000 ).”
Genome-wide identification and characterization of the aquaporin gene family in Sorghum bicolor (L.) (2015, background): “The movement of water through the root cylinder occurs through three parallel paths (i.e., apoplastic, symplastic, or transcellular) (Steudle, 2000).”
Water Flow in the Roots of Crop Species: The Influence of Root Structure, Aquaporin Activity, and Waterlogging (2007, background): “a highly significant and important resistance to overall flow of water in the plant (Steudle, 2000).”
Partial rootzone drying and deficit irrigation increase stomatal sensitivity to vapour pressure deficit in anisohydric grapevines (2010, positive): “In grapevines, changes in root hydraulic conductivity in response to water deficits may be the result of aquaporin activity (Vandeleur et al. 2009) with ABA being associated with increased aquaporin activity in other plants ( Steudle 2000 ).”