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      Illuminating plant water dynamics: the role of light in leaf hydraulic regulation

      1 , 2 , 1 , 1
      New Phytologist
      Wiley

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          Summary

          Light intensity and quality influence photosynthesis directly but also have an indirect effect by increasing stomatal apertures and enhancing gas exchange. Consequently, in areas such as the upper canopy, a high water demand for transpiration and temperature regulation is created. This paper explores how light intensity and the natural high Blue‐Light (BL) : Red‐Light (RL) ratio in these areas, is important for controlling leaf hydraulic conductance ( K leaf) by BL signal transduction, increasing water permeability in cells surrounding the vascular tissue, in supporting the enormous water demands. Conversely, shaded inner‐canopy areas receive less radiation, have lower water and cooling demands, and exhibit reduced K leaf due to diminished intensity and BL induction. Intriguingly, shaded leaves display higher water‐use efficiency (compared with upper‐canopy) due to decreased transpiration and cooling requirements while the presence of RL supports photosynthesis.

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          Most cited references66

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          Leaf hydraulics.

          Leaves are extraordinarily variable in form, longevity, venation architecture, and capacity for photosynthetic gas exchange. Much of this diversity is linked with water transport capacity. The pathways through the leaf constitute a substantial (>or=30%) part of the resistance to water flow through plants, and thus influence rates of transpiration and photosynthesis. Leaf hydraulic conductance (K(leaf)) varies more than 65-fold across species, reflecting differences in the anatomy of the petiole and the venation architecture, as well as pathways beyond the xylem through living tissues to sites of evaporation. K(leaf) is highly dynamic over a range of time scales, showing circadian and developmental trajectories, and responds rapidly, often reversibly, to changes in temperature, irradiance, and water supply. This review addresses how leaf structure and physiology influence K(leaf), and the mechanisms by which K(leaf) contributes to dynamic functional responses at the level of both individual leaves and the whole plant.
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            Phot1 and phot2 mediate blue light regulation of stomatal opening.

            The stomatal pores of higher plants allow for gaseous exchange into and out of leaves. Situated in the epidermis, they are surrounded by a pair of guard cells which control their opening in response to many environmental stimuli, including blue light. Opening of the pores is mediated by K(+) accumulation in guard cells through a K(+) channel and driven by an inside-negative electrical potential. Blue light causes phosphorylation and activation of the plasma membrane H(+)-ATPase that creates this potential. Thus far, no blue light receptor mediating stomatal opening has been identified, although the carotenoid, zeaxanthin, has been proposed. Arabidopsis mutants deficient in specific blue-light-mediated responses have identified four blue light receptors, cryptochrome 1 (cry1), cryptochrome 2 (cry2), phot1 and phot2. Here we show that in a double mutant of phot1 and phot2 stomata do not respond to blue light although single mutants are phenotypically normal. These results demonstrate that phot1 and phot2 act redundantly as blue light receptors mediating stomatal opening.
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              Signal transduction in maize and Arabidopsis mesophyll protoplasts.

              Plant protoplasts show physiological perceptions and responses to hormones, metabolites, environmental cues, and pathogen-derived elicitors, similar to cell-autonomous responses in intact tissues and plants. The development of defined protoplast transient expression systems for high-throughput screening and systematic characterization of gene functions has greatly contributed to elucidating plant signal transduction pathways, in combination with genetic, genomic, and transgenic approaches.
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                Author and article information

                Contributors
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                Journal
                New Phytologist
                New Phytologist
                Wiley
                0028-646X
                1469-8137
                December 28 2023
                Affiliations
                [1 ] The Robert H. Smith Institute of Plant Sciences and Genetics in Agriculture, The Robert H. Smith Faculty of Agriculture, Food and Environment The Hebrew University of Jerusalem Rehovot 7610001 Israel
                [2 ] The Plant & Environmental Sciences Department Weizmann Institute of Science Rehovot 7632706 Israel
                Article
                10.1111/nph.19497
                b427d16b-38e4-47e3-bb57-e48171daa10d
                © 2023

                http://creativecommons.org/licenses/by-nc-nd/4.0/

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