Skip to main content
Log in

Changes in the photosynthetic characteristics of Plantago major plants caused by soil drought stress

  • Published:
Plant Growth Regulation Aims and scope Submit manuscript

Abstract

Changes in net photosynthetic rate (PN), stomatal conductance (gs), intercellular CO2 concentrations (Ci), transpiration rate (E) and water use efficiency (WUE) were measured in Plantago major L. plants grown under sufficient soil water supply or under soil water stress conditions. The plants had high PN in a wide range of soil water potential and temperature regimes. Soil water had little effect on PN under ambient CO2 concentrations, which was explained by a high carboxylation rate, but increased the dark respiration rate. Carboxylation activity at low Ci depended on RuBP regeneration, whereas at high Ci it depended on the phosphate regeneration rate. The gs and E values were low in plants under stress as compared to the controls that resulted in an increase of WUE. The results obtained show that Plantago major plants have different ways of adaptation to soil water deficit conditions.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  • Berkowitz G.A. and Gibbs M. 1983. Reduced osmotic potential inhibition of photosynthesis. Plant Physiol. 72: 1100–1109.

    Google Scholar 

  • Caemmerer C.S. von and Farquhar G.D. 1983. Some relationships between the biochemistry of photosynthesis and the gas exchange rates of leaves. Planta 153: 376–387.

    Google Scholar 

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

    Google Scholar 

  • Cornic G., Le Goualles J.L., Briantais J.M. and Hodges M. 1989. Effect of dehydration and high light on photosynthesis of two C3 plants (Phaseolus vulgaris L. and Elatosperma repens (Lour) Hall f.). Planta 77: 84–90.

    Google Scholar 

  • Epron D. and Dreyer E. 1990. Photosynthesis of oak leaves under water stress: maintenance of high photochemical efficiency of photosystem II and occurrence of nonuniform CO2 assimilation. Tree Physiol. 13: 107–117.

    Google Scholar 

  • Farquhar G.D. and Sharkey T.D. 1982. Stomatal conductance and photosynthesis. Annu. Rev. Plant Physiol. 33: 317–345.

    Google Scholar 

  • Farquhar G.D., von C.S. and Berry J. 1980. A biochemical model of photosynthetic CO2 assimilation in leaves of C3 species. Planta 149: 78–90.

    Google Scholar 

  • Harley P.C. and Sharkey T.D. 1991. An improved model of C3 photosynthesis at high CO2: Reverses O2 sensitivity explained by lack of glycerate re-entry into the chloroplast. Photosynthesis Research 27: 169–178.

    Google Scholar 

  • Harley P.C., Thomas R.B., Reynolds J.F. and Strain B.R. 1992. Modelling photosynthesis of cotton grown in elevated CO2. Plant Cell Environ. 15: 271–282.

    Google Scholar 

  • Hsiao T.C. 1973. Plant responses to water stress. Annu. Rev. Plant Physiol. 24: 519–570.

    Google Scholar 

  • Kaiser W.M. 1987. Effect of water deficit on photosynthetic capacity. J. Physiol Plant. 71: 142–149.

    Google Scholar 

  • Kelly G.J. and Latzko E. 1993. Photosynthesis: carbon metabolism twenty years of following carbon cycles in photosynthetic cells. In: Behnke H.D., Luttge U., Esser K., Kadereit J.W. and Runge M. (eds), Progress in Botany. Springer-Verlag, Berlin, pp. 174–200.

    Google Scholar 

  • Lauer M.J. and Boyer J.S. 1992. Internal CO2 measures directly in leaves abscisic acid and low leaf water potential cause opposing effects. J. Plant Physiol. 8: 1010–1016.

    Google Scholar 

  • Mudrik V.A., Romanova A.K., Ivanov B.N., Novichkova N.S. and Polyakova V.A. 1997. Effect of increased CO2 concentration on growth, photosynthesis and composition of Pisum sativum L. plants. Fiziologiya Rastenii 44: 141–146.

    Google Scholar 

  • Panković D., Sakač Z., Kevrešan S. and Plesnič M. 1999. Acclimation to long term water deficit in the leaves of two sunflower hybrids: photosynthesis, electron transport and carbon metabolism. J. Exp. Bot. 50: 127–138.

    Google Scholar 

  • Parson R. and Ogstone S.A. 1997. Photosyn Assistant Windows software for analysis of photosynthesis. Dundee Scientific, Scotland, UK.

    Google Scholar 

  • Prioul J.L. and Chartier P. 1977. Partition of transfer and carboxylation components of intracellular resistance to photosynthetic CO2 fixation: A critical analysis of the methods used. Ann. of Bot. 41: 789–800.

    Google Scholar 

  • Quick P., Siegl G., Neuhaus E., Feil R. and Stitt M. 1989. Shortterm water stress leads to stimulation of sucrose synthesis by activating sucrose-phosphate synthase. Planta 177: 535–546.

    Google Scholar 

  • Saccardy K., Cornic G., Brulfeld J. and Reyss A. 1996. Effect of drought stress on net CO2 uptake by Zea mays leaves. Planta 199: 589–595.

    Google Scholar 

  • Shangguan Z., Shao M. and Dyckmans J. 1999. Interaction of osmotic adjustment and photosynthesis in winter heat under soil drought. J. Plant Physiol. 154: 735–758.

    Google Scholar 

  • Sharkey T.D. 1985. Photosynthesis of intact leaves of C3 plants: physics, physiology and rate limitations. Bot. Rev. 51: 53–105.

    Google Scholar 

  • Stitt M., Wilke J., Feil R. and Held H.W. 1988. Coarse control of sucrose-phosphate synthase in leaves: Alterations of the kinetic properties in response to the rate of photosynthesis and the accumulation of sucrose. Planta 174: 217–230.

    Google Scholar 

  • Tezara W. and Lawlor D.W. 1995. Effect of water stress on the biochemistry and physiology of photosynthesis in sunflower. In: Mathis P. (ed.), Photosynthesis: From Light to Biosphere. Kluwer Academic Publishers, Dordrecht, Boston, London, pp. 625–628.

    Google Scholar 

  • Walker D.A. 1989. Automated measurement of leaf photosynthetic O2 evolution as a function of photon flux density. Phil. Trans. Roy. Soc. Bot. Res. 26: 317–352.

    Google Scholar 

  • Wise R.R., Ortis-Lorez A. and Ort D.R. 1991. Spatial distribution of photosynthesis during drought in field-grown and acclimated and nonacclimated growth chamber-grown cotton. Plant Physiol. 100: 26–32.

    Google Scholar 

  • Woodrow I.E. and Mott K.A. 1989. Rate limitation of non-steadystate photosynthesis by ribulose-1,5-bisphosphate carboxylase in spinach. Aust. J. Plant Physiol. 16: 487–500.

    Google Scholar 

  • Yordanov I., Velikova V. and Tsonev T. 2000. Plant responses to drought, acclimation, and water tolerance. Photosynthetica 38: 171–186.

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Mudrik, V., Kosobrukhov, A., Knyazeva, I. et al. Changes in the photosynthetic characteristics of Plantago major plants caused by soil drought stress. Plant Growth Regulation 40, 1–6 (2003). https://doi.org/10.1023/A:1023009025426

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1023/A:1023009025426

Navigation