Skip to main content

Advertisement

Log in

Photosynthetic limitations caused by different rates of water-deficit induction in Glycine max and Vigna unguiculata

  • Published:
Photosynthetica

Abstract

Plants are constantly subjected to variations in their surrounding environment, which affect their functioning in different ways. The influence of environmental factors on the physiology of plants depends on several factors including the intensity, duration and frequency of the variation of the external stimulus. Water deficit is one of the main limiting factors for agricultural production worldwide and affects many physiological processes in plants. The aim of this study was to analyse the effects of different rates of induced water deficit on the leaf photosynthetic responses of soybean (Glycine max L.) and cowpea (Vigna unguiculata L.). The plants were subjected to two types of water deficit induction: a rapid induction (RD) by which detached leaves were dehydrated by the exposure to air under controlled conditions and a slow induction (SD) by suspending irrigation under greenhouse conditions. The leaf gas exchange, chlorophyll (Chl) a fluorescence, and relative water content (RWC) were analysed throughout the water-deficit induction. V. unguiculata and G. max demonstrated similar dehydration as the soil water percentage declined under SD, with V. unguiculata showing a greater stomatal sensitivity to reductions in the RWC. V. unguiculata plants were more sensitive to water deficit, as determined by all of the physiological parameters when subjected to RD, and the net photosynthetic rate (P N) was sharply reduced in the early stages of dehydration. After the plants exposed to the SD treatment were rehydrated, V. unguiculata recovered 65% of the P N in relation to the values measured under the control conditions (initial watering state), whereas G. max recovered only 10% of the P N. Thus, the better stomatal control of V. unguiculata could enable the maintenance of the RWC and a more efficient recovery of the P N than G. max.

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

E :

transpiration rate

ETR:

electron transport rate

F0 :

minimal fluorescence of dark-adapted state

F0′:

minimal fluorescence of light-adapted state

Fm :

maximal fluorescence of dark-adapted state

Fm′:

maximal fluorescence of light-adapted state

Fs :

steady-state fluorescence

Fv :

variable fluorescence

Fv/Fm :

maximum quantum yield of PSII photochemistry

g s :

stomatal conductance

H2Osoil% :

soil water percentage

NPQ:

nonphotochemical quenching

P N :

net photosynthetic rate

qP :

photochemical quenching coefficient

RD:

rapid water-deficit induction

RWC:

relative water content

SD:

slow water-deficit induction

WUE:

water-use efficiency

ΦPSII :

effective quantum yield of PSII photochemistry

References

  • Biehler, K., Fock, H.: Evidence for the contribution of mehlerperoxidase reaction in dissipating excess electrons in droughtstressed wheat. — Plant Physiol. 112: 265–272, 1996.

    PubMed  CAS  Google Scholar 

  • Bilger, W., Björkman, O.: Role of the xanthophyll cycle in photoprotection elucidated by measurements of light-induced absorbance changes, fluorescence and photosynthesis in leaves of Hedera canariensis. — Photosynth. Res. 25: 173–185, 1990.

    Article  CAS  Google Scholar 

  • Bota, J., Medrano, H., Flexas, J.: Is photosynthesis limited by decreased Rubisco activity and RuBP content under progressive water stress? — New Phytol.. 162: 671–681, 2004.

    Article  CAS  Google Scholar 

  • Câmara, G.M.S., Heiffig, L.S.: [Physiology, environment and yield of soybean.] — In: Câmara, G.M.S (ed.): Soybean: Production Technology. II.: ESALQ/LPV, Piracicaba 2000. [In Portuguese.]

  • Čatský, J.: Determination of water deficit in discs cut out from leaf blades. — Biol. Plant. 2: 76–77, 1960.

    Article  Google Scholar 

  • Catuchi, T. A., Vitolo, H. F., Bertolli, S. C. et al.: Tolerance to water deficiency between two soybean cultivars: transgenic versus conventional. — Ciência Rural 41: 373–378, 2011. [In Portuguese.]

    Article  Google Scholar 

  • Chaves, M.M., Oliveira, M.M.: Mechanisms underlying plant resilience to water deficit: prospects for water-saving agriculture. — J. Exp. Bot. 55: 2365–2384, 2004.

    Article  PubMed  CAS  Google Scholar 

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

    Article  Google Scholar 

  • Demmig, B., Björkman, O.: Comparison of the effect of excessive light on chlorophyll fluorescence (77K) and photon yield of O2 evolution in leaves of higher plants. — Planta 171: 171–184, 1987.

    Article  CAS  Google Scholar 

  • Doss, B.D., Thulow, D.L.: Irrigation, row width and plant population in relation to growth characteristics of two soybean varieties. — Agron. J. 65: 620–623, 1974.

    Article  Google Scholar 

  • Flexas, J., Bota, J., Galmés, J., Medrano, H., Ribas-Carbo, M.: Keeping positive carbon balance under adverse conditions: responses of photosynthesis and respiration to water stress. — Physiol. Plant. 127: 343–352, 2006.

    Article  CAS  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. — Bioch. Biophys. Acta 990: 87–92, 1989.

    Article  CAS  Google Scholar 

  • Gopefert, H., Rossetti, L.A., Souza, J.: [Generalized events and agricultural security.] — IPEA, Ministério do Planejamento, Brasília 1993. [In Portuguese.]

    Google Scholar 

  • Harbison, J., Genty, B., Baker, N.R.: The relationship between CO2 assimilation and electron transport in leaves. — Photosyn. Res. 25: 199–212, 1990.

    Article  Google Scholar 

  • Kaiser, W.M.: Effects of water deficit on photosynthetic capacity. — Physiol. Plant. 71: 142–149, 1987.

    Article  CAS  Google Scholar 

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

    Article  CAS  Google Scholar 

  • Krause, G.H.: Photoinhibition of photosynthesis: an evaluation of damaging and protective mechanisms. — Physiol. Plant. 74: 566–574, 1988.

    Article  CAS  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.

    Article  PubMed  CAS  Google Scholar 

  • Lawlor, D.W., Tezara, W.: Causes of decreased photosynthetic rate and metabolic capacity in water-deficient leaf cells: a critical evaluation of mechanisms and integration of processes. — Ann. Bot. 103: 561–579, 2009

    Article  PubMed  CAS  Google Scholar 

  • Leshem, Y.Y., Shewfelt, R.L., Willmer, C.M. et al.: Plant membranes: A biophysical approach to structure, development and senescence. — Kluwer Acad. Publ., Dordrecht 1992.

    Google Scholar 

  • Matos, M.C., Campos, P.S., Passarinho, J.A. et al.: Drought effect on photosynthetic activity, osmolyte accumulation and membrane integrity of two Cicer arietinum genotypes. — Photosynthetica 48: 303–312, 2010.

    Article  Google Scholar 

  • Miyashita, K., Tanakamaru, S., Maitani, T., Kimura, K.: Recovery responses of photosynthesis, transpiration, and stomatal conductance in kidney bean following drought stress. — Environ. Exp. Bot. 53: 205–214, 2005.

    Article  CAS  Google Scholar 

  • Ögren, E.: Evaluation of chlorophyll fluorescence as a probe for drought stress in willow leaves. — Plant Physiol. 93: 1280–1285, 1990.

    Article  PubMed  Google Scholar 

  • Oliveira, M.N.S., Oliva, M.A., Martinez, C.A. et al.: [Stomatal sensitivity to ABA related to pH and NO−3, PO4 −3 and Ca+2 levels of xylem sap.] — Braz. J. Plant Physiol. 14: 117–123, 2002. [In Portuguese.]

    Google Scholar 

  • Parry, M.A. J., Andralojc, P.J., Khan, S. et al.: Rubisco activity: effects of drought stress. — Ann. Bot. 89: 833–839, 2002.

    Article  PubMed  CAS  Google Scholar 

  • Pinheiro, C., Chaves, M.M.: Photosynthesis and drought: can we make metabolic connections from avaiable data? — J. Exp. Bot. 62: 869–882, 2011.

    Article  PubMed  CAS  Google Scholar 

  • Raven, J.A.: The cost of photoinhibition. — Physiol. Plant. 142: 87–104, 2011.

    Article  PubMed  CAS  Google Scholar 

  • Reynolds, M.P., Mujeeb-Kazi, A., Sawkins, M.: Prospects for utilizing plant-adaptive mechanisms to improve wheat and other crops in drought- and salinity-prone environments. — Ann. Appl. Biol. 146: 239–259, 2005.

    Article  CAS  Google Scholar 

  • Saccardy, K., Pineau, B., Roche, O. et al.: Photochemical efficiency of photosystem II and xanthophyll cycle components in Zea mays leaves exposed to water stress and high light. — Photosynth. Res. 56: 57–66, 1998.

    Article  CAS  Google Scholar 

  • Scholes, J.D., Press, M.C., Zipperlen, S.W.: Differences in light energy utilisation and dissipation between dipterocarp rain forest tree seedlings. — Oecologia. 109: 41–48, 1997.

    Article  Google Scholar 

  • Shangguan, Z.P., Shao, M.G., Dyckmans, J.: Effects of nitrogen nutrition and water deficit on net photosynthetic rate and chlorophyll fluorescence in winter wheat. — J. Plant Physiol. 156: 46–51, 2000.

    Article  CAS  Google Scholar 

  • Silva, J.M., Arrabaça, M.C.: Photosynthesis in the waterstressed C4 grass Setaria sphacelata is mainly limited by stomata with both rapidly and slowly imposed water deficits. — Physiol. Plant. 121: 409–420, 2004.

    Article  Google Scholar 

  • Singh, S. K., Reddy, K. R.: Regulation of photosynthesis, fluorescence, stomatal conductance and water-use efficiency of cowpea (Vigna unguiculata [L.] Walp.) under drought. — J. Photochem. Photobiol. B: Biol. 105: 40–50, 2011.

    Article  CAS  Google Scholar 

  • Souza, R.P., Machado, E.C., Silva, J.A. et al.: Photosynthetic gas exchange, chlorophyll fluorescence and some associated metabolic changes in cowpea (Vigna unguiculata) during water stress and recovery. — Environ. Exp. Bot. 51: 45–56, 2004.

    Article  CAS  Google Scholar 

  • Subbarao, G.V., Johansen, C., Slinkard, A.E. et al.: Strategies for improving drought resistance in grain legumes. — Critical Rev. Plant Sci. 14: 469–529, 1995.

    Google Scholar 

  • Tezara, W., Martínez, 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.

    Article  PubMed  CAS  Google Scholar 

  • Wingler, A., Quick, W.P., Bungard, R.A. et al.: The role of photorespiration during drought stress: an analysis utilizing barley mutants with reduced activities of photorespiratory enzymes. — Plant Cell Environ. 22: 361–373, 1999.

    Article  CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to G. M. Souza.

Additional information

Acknowledgments: This study was supported by Fundação de Amparo a Pesquisa do Estado de São Paulo, Brazil (FAPESP 2008/57571-1). GM Souza was supported by fellowship granted by CNPq (Conselho Nacional de Pesquisa e Desenvolvimento Tecnológico, Brazil) and SC Bertolli and GL Rapchan were supported by fellowships granted by FAPESP.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Bertolli, S.C., Rapchan, G.L. & Souza, G.M. Photosynthetic limitations caused by different rates of water-deficit induction in Glycine max and Vigna unguiculata . Photosynthetica 50, 329–336 (2012). https://doi.org/10.1007/s11099-012-0036-4

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s11099-012-0036-4

Additional key words

Navigation