Diurnal changes and effect of elevated CO2 on gas exchange under individual and interactive salt and water stress in wheat (Triticum aestivum)
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Keywords:
Diurnal changes, Elevated CO2, Gas exchange attributes, Photosynthesis, Wheat varietiesAbstract
To evaluate the individual and interactive effects of drought and salt stress on diurnal stomatal behaviour and gas exchange parameters, two salt tolerant (Kharchia 65, KRL 210) and two salt sensitive (HD 2851, HD 2009) wheat (Triticum aestivum L.) varieties were subjected to drought (25% and 50% water deficit) and salt (50 mM and 100 mM NaCl) stresses, imposed separately and in combination. Diurnal changes in photosynthetic rate (Pn), stomatal conductance (gS) and transpiration rates (E) of wheat leaves were measured at 4 h intervals under field conditions, using an infrared open gas exchange system. Photosynthetic rate was also measured across a range of variable intercellular CO2 concentrations (50 – 800 ppm). Kharchia 65 (salt tolerant) and KRL 210 (moderately salt tolerant) wheat varieties showed photosynthetic rate of 19.74 and 9.19 μmol/m2/s, while HD 2009 and HD 2851 (salt sensitive) showed photosynthetic rate of -27.65 and -17.65 μmol/m2/s at 50 ppm intercellular CO2 concentration which increased with increasing CO2 concentration. Up to 200 ppm intercellular CO2 concentration, these sensitive varieties showed negative Pn values. Diurnal photosynthetic activities of wheat varieties significantly differed under stressful environment but these differences could not be expressed in control conditions. Pn was low in the early morning, increasing with time and reached maximum (μmol/m2/s) between 10:00 AM to 2:00 PM, thereafter, Pn decreased. Similar trends of increase and decrease were observed for gS and E.Downloads
References
Abdul Q, Razzaq A, Muhammad A and Matthew A. 2001. Water stress causes differential effects on germination indices, total soluble sugar and proline content in wheat (Triticum aestivum L.) genotypes. African Journal of Biotechnology 10: 14038–45. DOI: https://doi.org/10.5897/AJB11.2220
Ball M C and Anderson J M. 1986. Sensitivity of photosystem II to NaCl in relation to salinity tolerance. Comparative studies with thylakoids of the salt-tolerant mangrove (Avicennia marina) and the salt-sensitive pea (Pisum sativum). Australian Journal of Plant Physiology 13: 689–98. DOI: https://doi.org/10.1071/PP9860689
Boyer J S. 1982. Plant productivity and environment. Science 218: 443–8. DOI: https://doi.org/10.1126/science.218.4571.443
Campbell W J, Allen L H and Bowes G. 1988. Effects of CO2 concentration on RuBisCO activity, amount and photosynthesis in soybean leaves. Plant Physiology 88: 1310–6. DOI: https://doi.org/10.1104/pp.88.4.1310
Chaves M M, Flexas J and Pinheiro C. 2009. Photosynthesis under drought and salt stress: regulation mechanisms from whole plant to cell. Annals of Botany 103: 551–6. DOI: https://doi.org/10.1093/aob/mcn125
Chedlia B A, Bechi B R and Boukhris M. 2007. Effect of water deficit on olive trees cv. Chemlali under field conditions in arid region in Tunisia. Scientia Horticulturae 113: 267–77. DOI: https://doi.org/10.1016/j.scienta.2007.03.020
FAO. 2009. High level expert forum - how to feed the world in 2050. Economic and Social Development Department, Food and Agricultural Organization of the United Nations, Rome.
Fereres E and Soriano A. 2006. Deficit irrigation for reducing agricultural water use. Journal of Experimental Botany 58(2): 147–59. DOI: https://doi.org/10.1093/jxb/erl165
Fernandez J E, Green S R, Caspari H W, Diaz-Espejo A and Cuevas M V. 2008. The use of sap flow measurements for scheduling irrigation in olive, apple and Asian pear trees and in grapevines. Plant and Soil 305: 91–104. DOI: https://doi.org/10.1007/s11104-007-9348-8
Fischer G, Shah M, van Velthuizen H and Nachtergaele F O. 2001. Global agro-ecological assessment for agriculture in the 21st century. IIASA and FAO, Laxenburg, Austria.
Flagella Z, Campanile R G, Stoppelli M C, De Caro A and Di Fonzo N. 1998. Drought tolerance of photosynthetic electron transport under CO2-enriched and normal air in cereal species. Physiologia Plantarum 104: 753–9. DOI: https://doi.org/10.1034/j.1399-3054.1998.1040434.x
Flanagan L B and Jefferies R L. 1988. Stomatal limitation of photosynthesis and reduced growth of the halophyte, Plantago maritima L., at high salinity. Plant Cell Environment 11: 239–46. DOI: https://doi.org/10.1111/j.1365-3040.1988.tb01142.x
Flexas J and Medrano H. 2002. Drought-inhibition of photosynthesis in C-3 plants: Stomatal and non-stomatal limitation revisited. Annals of Botany 89: 183–9. DOI: https://doi.org/10.1093/aob/mcf027
Gong H, Zhu X, Chen K, Wang S and Zhang C. 2005. Silicon alleviates oxidative damage of wheat plants in pots under drought. Plant Science 169: 131–321. DOI: https://doi.org/10.1016/j.plantsci.2005.02.023
Hattori T, Inanaga S, Araki H, Morita S, Luxova M and Lux A. 2005. Application of silicon enhanced drought tolerance in Sorghum bicolor. Physiologia Plantarum 123: 459–66. DOI: https://doi.org/10.1111/j.1399-3054.2005.00481.x
He J X, Wang J and Liang H G. 1995. Effects of water stress on photochemical function and protein metabolism of photosystem II in wheat leaves. Physiologia Plantarum. 93: 771–7. DOI: https://doi.org/10.1111/j.1399-3054.1995.tb05130.x
Hirasawa T and Hsiao T C. 1999. Some characteristics of reduced leaf photosynthesis at midday in maize growing in the field. Field Crops Research 62: 53–62. DOI: https://doi.org/10.1016/S0378-4290(99)00005-2
Kumar A, Kumar A, Lata C and Kumar S. 2016. Eco-physiological responses of Aeluropus lagopoides (grass halophyte) and Suaeda nudiflora (non-grass halophyte) under individual and interactive sodic and salt stress. South African Journal of Botany 105: 36–44. DOI: https://doi.org/10.1016/j.sajb.2015.12.006
Kumar A, Krishnamurthy S L, Lata C, Kumar P, Devi R, Kulshrestha N, Yadav R K and Sharma S K. 2016. Effect of dual stress (salinity and drought) on gas exchange attributes and chlorophyll fluorescence characteristics in rice. Indian Journal of Agricultural Sciences 86(6): 19–27.
Kumar A, Lata C, Krishnamurthy S L, Kumar A, Prasad K R K and Kulshreshtha N. 2017. Physiological and biochemical characterization of rice varieties under salt and drought stresses. Journal of Soil Salinity and Water Quality 9(2): 167–77.
Kumar A, Sharma S K, Lata C, Devi R, Kulshreshtha N, Krishnamurthy S L, Singh K and Yadav R K. 2018. Impact of water deficit (salt and drought) stress on physiological, biochemical and yield attributes on wheat varieties. Indian Journal of Agriculture Sciences.
Levitt J. 1980. Responses of Plants to Environmental Stresses. Academic Press, New York.
Makino' A and Mae T. 1999. Photosynthesis and Plant Growth at Elevated Levels of CO2. Plant Cell Physiology 40(10): 999–1006. DOI: https://doi.org/10.1093/oxfordjournals.pcp.a029493
Munns R and Tester M. 2008. Mechanisms of salinity tolerance. Annual Review of Plant Biology 59: 651–81. DOI: https://doi.org/10.1146/annurev.arplant.59.032607.092911
Prasad R. 2005. Rice-wheat cropping system. Advances in Agronomy 86: 285–339. DOI: https://doi.org/10.1016/S0065-2113(05)86006-7
Ribeiro R V, Machado E C, Santos M G and Oliveira R F. 2009. Seasonal and diurnal changes in photosynthetic limitation of young sweet orange trees. Environmental and Experimental Botany 66: 203–11. DOI: https://doi.org/10.1016/j.envexpbot.2009.03.011
Riveli A R, James R A, Munns R and Condon A G. 2002. Effect of salinity on water relations and growth of wheat genotypes with contrasting sodium uptake. Functional Plant Biology 29: 1065–74. DOI: https://doi.org/10.1071/PP01154
Shanker A K and Venkateswarlu B. 2011. Abiotic Stress in Plants–Mechanisms and Adaptations, p 428. Tech Publisher, Rijeka, Croatia. DOI: https://doi.org/10.5772/895
Sharma D K and Singh A. 2015. Salinity research in India-achievements, challenges and future prospects. Water Energy International 58(6): 35–45.
Yang X S and Chen G X. 2015. Diurnal changes in gas exchange and chlorophyll fluorescence in ginkgo leaves under field conditions. Journal of Animal and Plant Science 25(1): 309–13.
Ziska L H and Bunce J A. 1997. Influence of increasing carbon dioxide concentration on the photosynthetic and growth stimulation of selected C4 crops and weeds. Photosynthetic Research 54: 199–208. DOI: https://doi.org/10.1023/A:1005947802161
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