Skip to main content

Advertisement

Log in

Photosynthesis and photoinhibition in two xerophytic shrubs during drought

  • Published:
Photosynthetica

Abstract

Seasonal changes in water relations, net photosynthetic rate (P N), and fluorescence of chlorophyll (Chl) a of two perennial C3 deciduous shrubs, Ipomoea carnea and Jatropha gossypifolia, growing in a thorn scrub in Venezuela were studied in order to establish the possible occurrence of photoinhibition during dry season and determine whether changes in photochemical activity of photosystem 2 (PS2) may explain variations of P N in these species. Leaf water potential (ψ) decreased from −0.2 to −2.1 MPa during drought in both species. The P N decreased with ψ in I. carnea and J. gossypifolia by 64 and 74 %, respectively. Carboxylation efficiency (CE) decreased by more than 50 and 70 % in I. carnea and J. gossypifolia, respectively. In I. carnea, relative stomatal limitation (Ls) increased by 17 % and mesophyll limitation (Lm) by 65 % during drought, while in J. gossypifolia Ls decreased by 27 % and Lm increased by 51 %. Drought caused a reduction in quantum yield of PS2 (ϕPS2) in both species. Drought affected the capacity of energy dissipation of leaves, judging from the changes in the photochemical (qP) and non-photochemical quenching (NPQ) coefficients. Photoinhibition during drought in I. carnea and J. gossypifolia was evidenced in the field by a drop in the maximum quantum yield of PS2 (Fv/Fm) below 0.8 and also by non-coordinated changes in ϕPS2 and quantum yield of non-photochemical excitation quenching (Yn). Total soluble protein content on an area basis increased with ψ but the ribulose-1,5-bisphosphate carboxylase/oxygenase content remained unchanged. A reduction of total Chl content with drought was observed. Hence in the species studied photoinhibition occurred, which imposed an important limitation on carbon assimilation during drought.

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

Abbreviations

C i :

intercellular CO2 concentration

CE:

carboxylation efficiency

Chl:

chlorophyll

Fv/Fm :

maximum quantum yield of photosystem 2

g s :

stomatal conductance

J:

total electron-transport rate in leaves

Ls :

relative stomatal limitation

Lm :

relative mesophyll limitation

NPQ:

non-photochemical quenching coefficient

PS:

photosystem

qP :

photochemical quenching coefficient of chlorophyll a fluorescence

P N :

net photosynthetic rate

P Nsat :

CO2-saturated P N

PPFD:

photosynthetic photon flux density

RuBPCO:

ribulose-1,5-bisphosphate carboxylase/oxygenase

TSP:

total soluble protein

Yn :

quantum yield of non-photochemical quenching

ϕPS2 :

relative quantum yield of photosystem 2

ψ:

morning leaf water potential

ψs :

osmotic potential

References

  • Ball, M.C., Butterworth, J.A., Roben, J.S., Christian, R., Egerton, J.J.G.: Applications of chlorophyll fluorescence to forest ecology. — Aust. J. Plant Physiol. 22: 311–319, 1994.

    Google Scholar 

  • Biehler, K., Fock, H.P.: P700 contributes to the dissipation of excessive light energy in water-stressed wheat. — Photosynthetica 4: 555–558, 1993.

    Google Scholar 

  • Biehler, K., Fock, H.: Evidence for the contribution of the Mehler-peroxidase reaction in dissipating excess electrons in drought-stressed wheat. — Plant Physiol. 112: 265–272, 1996.

    Google Scholar 

  • Björkman, O., Demmig-Adams, B.: Regulation of photosynthetic light energy capture, conversion and dissipation in leaves of higher plants. — In: Schulze, E.-D., Caldwell, M.M. (ed.): Ecophysiology of Photosynthesis. Pp. 17–47. Springer-Verlag, Berlin 1994.

    Google Scholar 

  • Bradford, M.M.: A rapid and sensitive method for the quantification of microgram quantities of protein utilising the principle of protein-dye binding. — Anal. Biochem. 72: 248–254, 1976.

    Google Scholar 

  • Bruinsma, J.: The quantitative analysis of chlorophylls a and b in plant extracts. — Photochem. Photobiol. 2: 241–249, 1963.

    Google Scholar 

  • Buschmann, C.: Photochemical and non-photochemical quenching coefficients of the chlorophyll fluorescence: comparison of variation and limits. — Photosynthetica 37: 217–224, 1999.

    Google Scholar 

  • Centritto, M., Loreto, F., Chartzoulakis, K.: The use of low [CO2] to estimate diffusional and nondiffusional limitations of photosynthetic capacity of salt-stressed olive saplings. — Plant Cell Environ. 26: 585–594, 2003.

    Google Scholar 

  • Cornic, G.: Drought stress and high light effects on leaf photosynthesis. — In: Baker, N.R., Bowyer, J.R. (ed.): Photoinhibition of Photosynthesis: From Molecular Mechanisms to the Field. Pp. 297–313. Bios Scientific Publishers, Oxford 1994.

    Google Scholar 

  • Cornic, G.: Drought stress inhibits photosynthesis by decreasing stomatal aperture — not by affecting ATP synthesis. — Trends Plant Sci. 5: 187–188, 2000.

    Google Scholar 

  • Downton, W.J.S., Loveys, B.R., Grant, W.J.R.: Non-uniform stomatal closure induced by water stress putative non-stomatal inhibition of photosynthesis. — New Phytol. 110: 503–509, 1988.

    Google Scholar 

  • Epron, D., Dreyer, E., Breda, N.: Photosynthesis of oak trees (Quercus petraea (Matt.) Liebl.) during drought under field conditions: diurnal course of net CO2 assimilation and photochemical efficiency of photosystem II. — Plant Cell Environ. 15: 809–820, 1992.

    Google Scholar 

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

    Google Scholar 

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

    Google Scholar 

  • Flexas, J., Bota, J., Escalona, J.M., Sampol, B., Medrano H.: Effects of drought on light-energy dissipation mechanism in high-light-acclimated, field-grown grapevines. — Funct. Plant Biol. 29: 1197–1207, 2002.

    Google Scholar 

  • Flexas, J., Medrano, H.: Energy dissipation in C3 plants under drought. — Funct. Plant Biol. 29: 1209–1215, 2002.

    Google Scholar 

  • Franco, A.C., Herzog, B., Hübner, C., de Matos, E.A., Scarano, F.R., Ball, E., Lüttge, U.: Diurnal changes in chlorophyll a fluorescence, CO2-exchange and organic acid decarboxylation in the tropical CAM tree Clusia hilariana. — Tree Physiol. 19: 635–644, 1999.

    Google Scholar 

  • Genty, B., Briantais, J.-M., Baker, N.R.: The relationship between the quantum yield of photosynthetic electron transport and quenching of chlorophyll fluorescence. — Biochim. biophys. Acta 990: 87–92, 1989.

    Google Scholar 

  • Giménez, C., Mitchell, V.J., Lawlor, D.W.: Regulation of photosynthetic rate of two sunflower hybrids under water stress. — Plant Physiol. 98: 516–524, 1992.

    Google Scholar 

  • Herrera, A., Tezara, W., Urich, R., Cuberos, M., Montes, G.: Mechanisms of drought tolerance in the C3 deciduous shrub, Ipomoea carnea. — Ecotrópicos 7: 35–47, 1994.

    Google Scholar 

  • Horton, P., Ruban, A., Walters, R.G.: Regulation of light harvesting in green plants. Indication by nonphotochemical quenching of chlorophyll fluorescence. — Plant Physiol. 106: 415–420, 1994.

    Google Scholar 

  • Jacob, J., Lawlor, D.W.: Stomatal and mesophyll limitations of photosynthesis in phosphate deficient sunflower, maize and wheat plants. — J. exp. Bot. 42: 1003–1011, 1991.

    Google Scholar 

  • Krall, J.P., Edwards, G.E.: Relationship between photosystem II activity and CO2 fixation in leaves. — Physiol. Plant. 86: 180–187, 1992.

    Google Scholar 

  • Krause, G.H., Weis, E.: Chlorophyll fluorescence and photosynthesis: The basics. — Annu. Rev. Plant Physiol. Plant mol. Biol. 42: 313–349, 1991.

    Google Scholar 

  • Kozaki, A., Takeba, G.: Photorespiration protects C3 plants from photooxidation. — Nature 384: 557–560, 1996.

    Google Scholar 

  • Laisk, A., Oja, V., Rasulov, B., Eichelmann, H., Sumberg, A.: Quantum yields and rate constants of photochemical and non-photochemical excitation quenching. — Plant Physiol. 115: 803–815, 1997.

    Google Scholar 

  • Lawlor, D.W.: The effects of water deficit on photosynthesis. — In: Smirnoff, N. (ed.): Environment and Plant Metabolism. Flexibility and Acclimation. Pp.129–161. Bios Scientific Publishers, Oxford 1995.

    Google Scholar 

  • Lawlor, D.W.: Limitation to photosynthesis in water-stressed leaves: Stomata vs. metabolism and the role of ATP. — Ann. Bot. 89: 871–885, 2002.

    Google Scholar 

  • Lawlor, D.W., Cornic, G.: Photosynthetic carbon assimilation and associated metabolism in relation to water deficits in higher plants. — Plant Cell Environ. 25: 275–294, 2002.

    Google Scholar 

  • Lawlor, D.W., Kontturi, M., Young, A.T.: Photosynthesis by flag leaves of wheat in relation to protein, ribulose bisphosphate carboxylase activity and nitrogen supply. — J. exp. Bot. 40: 43–52, 1989.

    Google Scholar 

  • Long, S.P., Humphries, S., Falkowski, P.G.: Photoinhibition of photosynthesis in nature. — Annu. Rev. Plant Physiol. Plant mol. Biol. 45: 633–662, 1994.

    Google Scholar 

  • Osmond, C.B., Grace, S.C.: Perspectives on photoinhibition and photorespiration in the field: quintessential inefficiencies of the light and dark reaction of photosynthesis? — J. exp. Bot. 46: 1351–1362, 1995.

    Google Scholar 

  • Powles, S.B.: Photoinhibition of photosynthesis induced by visible light. — Annu. Rev. Plant Physiol. 35: 15–44, 1984.

    Google Scholar 

  • Scheuermann, R., Biehler, K., Stuhlfauth, T., Fock, H.P.: Simultaneous gas exchange and fluorescence measurements indicate differences in the response of sunflower, bean and maize to water stress. — Photosynth. Res. 27: 188–197, 1991.

    Google Scholar 

  • Schreiber, U., Bilger, W.: Rapid assessment of stress effects on plant leaves by chlorophyll fluorescence measurements. — In: Tenhunen, J.D., Catarino, F.M., Lange, O.L., Oechel, W.D. (ed.): Plant Response to Stress. Pp. 27–53. Springer-Verlag, Berlin — Heidelberg — New York — London — Paris — Tokyo 1987.

    Google Scholar 

  • Schreiber, U., Bilger, W., Neubauer, C.: Chlorophyll fluorescence as a nonintrusive indicator for rapid assessment of in vivo photosynthesis. — In: Schulze, E.-D., Caldwell, M.M. (ed.): Ecophysiology of Photosynthesis. Pp. 49–70. Springer-Verlag, Berlin 1994.

    Google Scholar 

  • Solhaugh, K.A. Haugen, J.: Seasonal variation of photoinhibition of photosynthesis in bark from Populus tremula L. — Photosynthetica 35: 411–417, 1998.

    Google Scholar 

  • Stuhlfauth, T., Scheuermann, R., Fock, H.P.: Light energy dissipation under water stress conditions. Contribution of reassimilation and evidence for additional processes. — Plant Physiol. 92: 1053–1061, 1990.

    Google Scholar 

  • Terashima, I., Wong, S.-C., Osmond, C.B., Farquhar, G.D.: Characterisation of non-uniform photosynthesis induced by abscisic acid in leaves having different mesophyll anatomies. — Plant Cell Physiol. 29: 385–394, 1988.

    Google Scholar 

  • Tezara, W., Fernández, M.D., Donoso, C., Herrera, A.: Seasonal changes in photosynthesis and stomatal conductance of five plant species from a semiarid ecosystem. — Photosynthetica 35: 399–410, 1998.

    Google Scholar 

  • Tezara, W., Lawlor, D.W.: Effects of water stress on the biochemistry and physiology of photosynthesis in sunflower. — In: Mathis, P. (ed.): Photosynthesis: from Light to Biosphere. Vol. IV. Pp. 625–628. Kluwer Academic Publishers, Dordrecht 1995.

    Google Scholar 

  • Tezara, W., Martïnez, D., Rengifo, E., Herrera, A.: Photosynthetic responses of the tropical spiny shrub Lycium nodosum (Solanaceae) to drought, soil salinity and saline spray. — Ann. Bot. 92: 757–765, 2003.

    Google Scholar 

  • Tezara, W., Mitchell, V.J., Driscoll, S.D., Lawlor, D.W.: Water stress inhibits plant photosynthesis by decreasing coupling factor and ATP. — Nature 401: 914–917, 1999.

    Google Scholar 

  • Weis, E., Berry, J.A.: Quantum efficiency of photosystem II in relation to “energy”-dependent quenching of chlorophyll fluorescence. — Biochim. biophys. Acta 894: 198–208, 1987.

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to W. Tezara.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Tezara, W., Marín, O., Rengifo, E. et al. Photosynthesis and photoinhibition in two xerophytic shrubs during drought. Photosynthetica 43, 37–45 (2005). https://doi.org/10.1007/s11099-005-7045-5

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s11099-005-7045-5

Additional key words

Navigation