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Drought perception by plants Do cells of droughted plants experience water stress?

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Abstract

Because of regulations at the whole-plant level, cells of droughted plants do not necessarily experience dehydration. In fact, recent data suggest that they usually do not in the range of water deficits compatible with agriculture. In this range, leaf water potential and cell turgor are frequently maintained at high values in spite of decreasing soil water status. As a consequence, ‘water stress’ cannot be defined by plant water status, except when very rapid and severe water deficits cause catastrophic events such as xylem embolism or severe cell dehydration. In water deficits compatible with agricultural situations, plant water status is in many cases tightly controlled by the plant. ‘Water stress’ should then be defined by water statuses at plant boundaries, i.e. soil and air. Partial maintenance of plant water status under water deficit is allowed by controls of stomatal conductance, root and leaf expansions and leaf senescence. These processes involve both chemical and hydraulic signallings from roots. All these controls tend to reduce transpiration (stomatal closure, reduced leaf growth or leaf senescence) or to increase water uptake (maintenance of root growth or increase in root/shoot ratio). During relatively mild stresses, the role of abscisic acid, frequently considered as a ‘stress hormone’, in fact appears to be to avoid dehydration at the cellular level. In the cases described here, selecting plants for better resistance to cell dehydration may not be the best strategy for improving ‘drought resistance’ of crops.

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References

  • Aguirrezabal LAN, Deléens E and Tardieu F (1994) Root elongation rate is accounted for by intercepted PPFD and source-sink relations in field and laboratory-grown sunflower. Plant, Cell and Environment 17: 443–450

    Google Scholar 

  • Bartels D and Nelson D (1994) Approaches to improve stress tolerance using molecular genetics. Plant, Cell and Environment 17: 659–667

    Google Scholar 

  • Bates LM and Hall AE (1981) Stomatal closure with soil depletion not associated with changes in bulk leaf water status. Oecologia 50: 62–65

    Google Scholar 

  • Becker W and Apels K (1993) Differences in gene expressin between natural and artificially induced leaf senescence. Planta 189: 74–79

    Article  Google Scholar 

  • Bohnert HJ, Nelson DE and Jensen RG (1995) Adaptation to environmental stresses. The Plant Cell 7: 1099–1111

    Article  PubMed  Google Scholar 

  • Bolanos J, Edmeades GO and Martinez L (1993) Eight cycles of selection for drought tolerance in lowand tropical maize. III Response in drought-adaptative physiological and morphological traits. Field Crop Research 31: 269–286

    Article  Google Scholar 

  • Boyer JS (1970) Leaf enlargement and metabolic rates in corn, soybean and sunflower at various leaf water potentials. Plant Physiol 46: 233–235

    Google Scholar 

  • Brouwer R (1966) Root growth of grasses and cereals. In: Milthorpe FL and Ivins JD (eds) The Growth of Cereals and Grasses, pp 153–156. London, UK: Butterworth

    Google Scholar 

  • Bruckler L, Lafolie F and Tardieu F (1991) Modelling the root water potential and water extraction in the two-dimensional case. II Field comparisons. Soil Sci Am J 55: 1213–1220

    Google Scholar 

  • Cornic G and Briantais JM (1991) Partitioning of photosynthetic electron flow between CO2 and O2 reduction in a C3 leaf (Phaseolus vulgaris L.) at different CO2 concentrations and during drought stress. Planta 183: 178–184

    Article  Google Scholar 

  • Cornish K and Zeevaart JAD (1985) Abscisic acid accumulation by roots of Xanthium strumarium L. and Lycopersicon esculentum Mill. in relation to water stress. Plant Physiol 79: 653–658

    Google Scholar 

  • Cosgrove DJ (1993) How do plant cells extend? Plant Physiol 102: 1–6

    PubMed  Google Scholar 

  • Davidson DJ and Chevalier PM (1987) Influence of polyethylene glycol-induced water deficits on tiller production in spring wheat. Crop Sci 27: 1185–1187

    Google Scholar 

  • Davies WJ and Zhang J (1991) Root signals and the regulation of growth and development of plants in drying soil. Annual Review of Plant Physiology and Molecular Biology 42: 55–76

    Article  Google Scholar 

  • Fambrini M, Pugliesi C, Vernieri P, Pardossi A and Baroncelli S (1994) Characterization of a wilty sunflower (Helianthus annuus L) mutant. II. Water relations, stomatal conductance, abscisic acid content in leaves and xylem sap of plants subjected to water deficiency. Journal of Experimental Botany 45: 1809–1815

    Google Scholar 

  • Fry SC, Smith RC, Renwick KF, Martin DJ, Hodge SK, and Matthews LJ (1992) Xyloglucan Endotransglycosylase, a new wall-loosening enzyme activity from plants. Biochem J 282: 821–828

    PubMed  Google Scholar 

  • Girma FD and Krieg DR (1992) Osmotic adjustment in sorghum. II Relationship to gas exchange rates. Plant Physiol 99: 583–588

    Google Scholar 

  • Gowing DJG, Davies WJ and Jones HG (1990) A positive root-sourced signal as an indicator of soil drying in apple Malus Domestica. Journal of Experimental Botany 41: 1535–1540

    Google Scholar 

  • Gowing DJG, Jones HG and Davies WJ (1993) Xylem-transported abscisic acid: the relative importance of its mass and its concentration in the control of stomatal aperture. Plant, Cell and Environment 16: 453–459

    Google Scholar 

  • Hall AE (1993) Is dehydration tolerance relevant to genotypic differences in leaf senescence and crop adaptation to dry environments? In Plant responses to cellular dehydration during environmental stress. In: Close TJ and Bray EA (eds) The American Society of Plant Physiologist

  • Hartung W and Davis WJ (1991) Drought-induced changes in physiology and ABA. In: Davies WJ and Jones HG (eds) Abscisic Acid, Physiology and Biochemistry, pp 63–79. Oxford, UK: Bios Scientific Publishers

    Google Scholar 

  • Hensel L, Vojislava G, Baumgarten DA and Bleeker AB (1993) Developmental and age related processes that influence the longevity and senescence of photosynthetic tissues in Arabidopsis. The Plant Cell 5: 553–564

    Article  PubMed  Google Scholar 

  • Hormann H, Neubauer C, Asada K and Schreiber U (1993) Intact chloroplasts display pH-5 optimum of O2-reduction in the absence of methyl viologen — Indirect evidence for a regulatory role of superoxide protonation. Photosynthesis Research 37: 69–80

    Google Scholar 

  • Hsiao TC (1973) Plant response to water stress. Ann Rev Plant Physiol 24: 519–570

    Article  Google Scholar 

  • Jones HG (1992) Plants and microclimate, a quantitative approach to environmental plant physiology. Cambridge University Press

  • Jones HG and Sutherland RA (1991) Stomatal control of xylem embolism. Plant, Cell Environ 14: 607–612

    Google Scholar 

  • Lockart JA (1965) An analysis of irreversible plant cell elongation. J Theor Biol 8: 453–470

    Google Scholar 

  • Matthews MA, VanVolkenburgh E and Boyer JS (1984) Acclimation of leaf growth to low water potentials in sunflower. Plant, Cell and Environment 7: 199–206

    Google Scholar 

  • Muller B and Farrar JF (1995) Can altered carbon balance at the whole plant level explain differences in root growth during water stress? Stressnet report, in the press

  • Ney B, Duthion C and Turc O (1994) Phenological response of pea to water stress during reproductive development. Crop Science 34: 141–146

    Google Scholar 

  • Nonami H and Boyer JS (1990) Wall extensibility and cell hydraulic conductivity decrease in enlarging stem tissues at low water potentials. Plant Physiology 93: 1610–1619

    Google Scholar 

  • Norris IB (1982) Soil moisture and growth of contrasting varieties of Lolium, Dactylis and Festuca species. Grass and Forage science 37: 273–283

    Google Scholar 

  • Pardossi A, Pritchard J and Tomos AD (1994) Leaf illumination and root cooling inhibit bean leaf expansion by decreasing turgor pressure. Journal of Experimental Botany 45: 415–422

    Google Scholar 

  • Passioura JB (1988) Root signals control leaf expansion in wheat seedlings growing in dry soil. Aust J Plant Physiol 15: 687–693

    Google Scholar 

  • Passioura JB and Fry SC (1992) Turgor and cell expansion: Beyond the Lockhart equation. Aust J Plant Physiol 19: 565–576

    Google Scholar 

  • Petrie CL and Hall AE (1992) Water relations in cowpea and pearl millet under soil water deficits. I Contrasting leaf water relations. Aust J Plant Physiol 19: 577–589

    Google Scholar 

  • Pritchard J, Wyn RG Jones and Tomos AD (1991) Turgor, growth and rheological gradients of cereal roots and the effect of osmotic stress. Journal of Experimental Botany 42: 1043–1049

    Google Scholar 

  • Ribaut JW and Pilet PE (1991) Effects of water stress on growth, osmotic potential and abscisic acid content of maize roots. Physilogia Plantarum 81: 156–162

    Article  Google Scholar 

  • Saab IN and Sharp RE (1989) Non-hydraulic signals from maize roots in drying soil: inhibition of leaf elongation but not stomatal conductance. Planta: 466–474

  • Saab IN, Sharp RE and Pritchard J (1990) Increased endogenous abscisic acid maintains primary root growth and inhibits shoot growth of maize seedlings at low water potentials. Plant Physiol 93: 1329–1336

    Google Scholar 

  • Saab IN, Ho THD and Sharp RE (1995) Translatable RNA populations associated with maintenance of primary root elongation and inhibition of mesocotyl elongation by abscisic acid in maize seedlings at low water potentials. Plant Physiol 109: 593–601

    PubMed  Google Scholar 

  • Schurr U, Gollan T and Schulze E-D (1992) Stomatal response to drying soil in relation to changes in the sap composition of Helianthus annuus. II Stomatal sensitivity to abscisic acid imported from the xylem sap. Plant, Cell and Environment 15: 561–567

    Google Scholar 

  • Shackel KA, Matthews MA and Morrison JC (1987) Dynamic relation between expansion and cellular turgor in growing grape (Vitis vinifera L.) leaves. Plant Physiol 84: 1166–1171

    Google Scholar 

  • Simonneau Th, Tardieu F and Barrieu Ph (1995) Accumulation of ABA in detached roots of maize. Stressnet report, in the press

  • Slovik S and Hartung W (1992) Compartmental distribution and redistribution of abscisic acid in intact leaves, II Model analysis, III Analysis of the stress-signal chain. Planta 187: 26–47

    Google Scholar 

  • Smart C (1994) Gene expression during leaf senescence. New Phytol 126: 419–446

    Google Scholar 

  • Spollen WG and Sharp RE (1991) Spatial distribution of turgor and root growth at low water potentials. Plant Physiol 96: 438–443

    Google Scholar 

  • Steinberg SL, Miller JC and McFarland MJ (1990) Dry matter partitioning and vegetative growth of young peach trees under water stress. Aust J Plant Physiol 17: 23–36

    Google Scholar 

  • Stocker O (1956) Die Abhängigkeit des Transpiration von den Umweltfaktoren. Encyclopedia of Plant Physiology, W.Ruhland. III 436–488, Springer-Verlag, Berlin

    Google Scholar 

  • Tal M and Imber D (1972) The effect of abscisic acid on stomatal behaviour in flacca, a wilty mutant of tomato, in darkness. New Phytol 71: 21–28

    Google Scholar 

  • Tardieu F (1993) Will progresses in understanding soil-root relations and root signalling substantially alter water flux models? Ph Trans Royal Soc London 341: 57–66

    Google Scholar 

  • Tardieu F and Katerji N (1991) Plant response to the soil water reserve: consequences of the root system environment. Irrigation Science 12: 145–152

    Article  Google Scholar 

  • Tardieu F and Davies WJ (1992) Stomatal response to ABA is a function of current plant water status. Plant Physiol 98: 540–545

    Google Scholar 

  • Tardieu F, Zhang J and Davies WJ (1992) What information is conveyed by an ABA signal from maize roots in drying field soil? Plant, Cell and Environment 15: 185–191

    Google Scholar 

  • Tardieu F, Zhang J and Gowing DJG (1993) Stomatal control by both [ABA] in the xylem sap and leaf water status: test of a model and of alternative hypotheses for droughted or ABA-fed field-grown maize. Plant, Cell and Environment 16: 413–420

    Google Scholar 

  • Tardieu F, Lafarge T and Simonneau Th (1996) Stomatal control by by fed or endogenous xylem ABA in sunflower: interpretation of observed correlations between leaf water potential and stomatal conductance in anisohydric species. Plant, Cell and Environment 19: 75–84

    Google Scholar 

  • Tourneux C and Peltier G (1995) Effect of water deficit on the photosynthetic oxygen exchange measured using 18O2 and mass spectrometry in Solanum tuberosum leaf disks. Planta 195: 570–577

    Article  Google Scholar 

  • Trejo CL, Davies WJ and Del Mar L (1993) Sensitivity of stomata to abscisic acid. An effect of the mesophyll. Plant Physiol 102: 497–502

    PubMed  Google Scholar 

  • Tyree MT and Sperry JS (1989) The vulnerability of xylem to cavitation and embolism. Ann Rev Plant Physiol Mol Biol 40: 19–38

    Article  Google Scholar 

  • Van deHonert TH (1948) Water transport in plants as a catenary process. Disc Faraday soc 3: 146–153

    Article  Google Scholar 

  • Voetberg GS and Sharp RE (1991) Growth of the maize primaty root at low water potentials. III Role of increased proline deposition in osmotic adjustment. Plant Physiol 96: 1125–1130

    Google Scholar 

  • Walton DC, Harrison MA and Cote P (1976) The effects of water stress on abscisic acid levels and metabolism in roots of Phaseolus vulgaris and other plants. Planta 131: 141–144

    Google Scholar 

  • Wartinger A, Heilmeier H, Hartung W and Schultze ED (1990) Daily and seasonal courses of leaf conductance and abscisic acid in the xylme sap of almond trees (Prunus dulcis M.) under desert conditions. New Phytologist 116: 581–587

    Google Scholar 

  • Wolfe DW, Henderson DW, Hsiao TC and Alvino A (1988) Interactive water and nitrogen effects on senescence of maize. I Leaf area duration, nitrogen distribution and yield. Agron J 80: 859–864

    Google Scholar 

  • Zeevaart JAD, Rock CD, Fantauzzo F, Heath TG and Gage DA (1991) Metabolism of ABA and its physiological implications. In: Davies WJ, HG Jones HG (eds) Abscisic acid: Physiology and Biochemistry. Bios Scientific Publishers, Oxford, England, pp 39–52

    Google Scholar 

  • Zhang J and Davies WJ (1989) Abscisic acid produced in dehydrating roots may enable the plant to measure the water status of the soil. Plant cell and environment 12: 73–81

    Google Scholar 

  • Zhang J and Davies WJ (1990) Does ABA in the xylem control the rate of leaf growth in soil-dried maize and sunflower plants? Journal of Experimental Botany 41: 1125–1132

    Google Scholar 

  • Zhang J and Davies WJ (1991) Antitranspirant activity in xylem sap of maize plants. Journal of Experimental Botany 42: 317–321

    Google Scholar 

  • Zhu GL and Boyer JS (1992) Enlargement in Chara studied with a turgor clamp. Growth rate is not determined by turgor. Plant Physiology 100: 2071–2080

    Google Scholar 

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Tardieu, F. Drought perception by plants Do cells of droughted plants experience water stress?. Plant Growth Regul 20, 93–104 (1996). https://doi.org/10.1007/BF00024005

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