Subscribe to RSS
DOI: 10.1055/s-2006-924280
Georg Thieme Verlag Stuttgart KG · New York
Circumvention of Over-Excitation of PSII by Maintaining Electron Transport Rate in Leaves of Four Cotton Genotypes Developed under Long-Term Drought
Publication History
Received: January 26, 2006
Accepted: May 3, 2006
Publication Date:
01 August 2006 (online)
Abstract
We investigated the patterns of response to a long-term drought in the field in cotton cultivars (genotypes) with known differences in their drought tolerance. Four cotton genotypes with varying physiological and morphological traits, suited to different cropping conditions, were grown in the field and subjected to a long-term moderate drought. In general, cotton leaves developed under drought had significantly higher area-based leaf nitrogen content (Narea) than those under well irrigation. Droughted plants showed a lower light-saturated net photosynthetic rate (Asat) with lower stomatal conductance (gs) and intercellular CO2 concentration (Ci) than irrigated ones. Based on the responses of Asat to gs and Ci, there was no decreasing trend in Asat at a given gs and Ci in droughted leaves, suggesting that the decline in Asat in field-grown cotton plants under a long-term drought can be attributed mainly to stomatal closure, but not to nonstomatal limitations. There was little evidence of an increase in thermal energy dissipation as indicated by the lack of a decrease in the photochemical efficiency of open PSII (Fv′/Fm′) in droughted plants. On the basis of electron transport (ETR) and photochemical quenching (qP), however, we found evidence indicating that droughted cotton plants can circumvent the risk of excessive excitation energy in photosystem (PS) II by maintaining higher electron transport rates associated with higher Narea, even while photosynthetic rates were reduced by stomatal closure.
Key words
Chlorophyll fluorescence - cultivars - gas exchange - Gossypium - water deficit
References
- 1 Aranda I., Castro L., Pardos M., Gil L., Pardos J. A.. Effects of the interaction between drought and shade on water relations, gas exchange and morphological traits in cork oak (Quercus suber L.) seedlings. Forest Ecology and Management. (2005); 210 117-129
- 2 Baroli I., Melis A.. Photoinhibitory damage is modulated by the rate of photosynthesis and by the photosystem II light-harvesting chlorophyll antenna size. Planta. (1998); 205 288-296
- 3 Bernacchi C. J., Singsaas E. L., Pimentel C., Portis A. R., Long S. P.. Improved temperature response functions for models of Rubisco-limited photosynthesis. Plant, Cell and Environment. (2001); 24 253-259
- 4 Biehler K., Fock H.. Evidence for the contribution of the Mehler-peroxidase reaction in dissipating excess electrons in drought-stressed wheat. Plant Physiology. (1996); 112 265-272
-
5 Björkman O., Demmig-Adams B..
Regulation of photosynthetic light energy capture, conversion, and dissipation in leaves of higher plants. Schulze, E.-D. and Caldwell, M. M., eds. Ecophysiology of Photosynthesis. Berlin; Springer-Verlag (1994): 17-47 - 6 Clough B. F., Sim R. G.. Changes in gas exchange characteristics and water use efficiency of mangroves in response to salinity and vapour pressure deficit. Oecologia. (1989); 79 38-44
- 7 Cornic G., Briantais J.-M.. 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. (1991); 183 178-184
-
8 Cornic G., Massacci A..
Leaf photosynthesis under drought stress. Baker, N. R., ed. Photosynthesis and the Environment. Dordrecht; Kluwer Academic Publishers (1996): 347-366 - 9 Cunningham S. A., Summerhayes B., Westoby M.. Evolutionary divergences in leaf structure and chemistry, comparing rainfall and soil nutrient gradients. Ecological Monograph. (1999); 69 569-588
- 10 Demmig-Adams B., Adams III., W. W.. Photoprotection and other responses of plants to high light stress. Annual Review of Plant Physiology and Plant Molecular Biology. (1992); 43 599-626
- 11 Demmig-Adams B., Adams III. W. W., Baker D. H., Logan B. A., Bowling D. R., Verhoeven A. S.. Using chlorophyll fluorescence to assess the fraction of absorbed light allocated to thermal dissipation of excess excitation. Physiologia Plantarum. (1996); 98 253-264
- 12 Epron D., Dreyer E.. Effects of severe dehydration on leaf photosynthesis in Quercus petraea (Matt.) Liebl.: photosystem II efficiency, photochemical and nonphotochemical fluorescence quenching and electrolyte leakage. Tree Physiology. (1992); 10 273-284
- 13 Evans J. R.. Photosynthesis and nitrogen relationship in leaves of C3 plants. Oecologia. (1989); 78 9-19
-
14 Evans J. R..
Developmental constraints on photosynthesis: effects of light and nutrition. Baker, N. R., ed. Photosynthesis and the Environment. Dordrecht; Kluwer Academic Publishers (1996): 281-304 - 15 Farquhar G. D., von Caemmerer S., Berry J. A.. A biochemical model of photosynthetic CO2 assimilation in leaves of C3 species. Planta. (1980); 149 78-90
- 16 Flexas J., Badger M., Chow W. S., Medrano H., Osmond C. B.. Analysis of the relative increase in photosynthetic O2 uptake when photosynthesis in grapevine leaves is inhibited following low night temperatures and/or water stress. Plant Physiology. (1999); 121 675-684
- 17 Genty B., Briantais J.-M., Baker N. R.. The relationship between the quantum yield of photosynthetic electron transport and quenching of chlorophyll fluorescence. Biochimica et Biophysica Acta. (1989); 990 87-92
-
18 Genty B., Harbinson J..
Regulation of light utilization for photosynthetic electron transport. Baker, N. R. ed. Photosynthesis and the Environment. Dordrecht; Kluwer Academic Publishers (1996): 67-99 - 19 Haupt-Herting S., Fock H. P.. Exchange of oxygen and its role in energy dissipation during drought stress in tomato plants. Physiologia Plantarum. (2000); 110 489-495
- 20 Hearn A. B.. Responses of cotton to water and nitrogen in a tropical environment. I. Frequency of watering and method of application of nitrogen. Journal of Agricultural Science. (1975 a); 84 407-417
- 21 Hearn A. B.. Response of cotton to water and nitrogen in a tropical environment. II. Date of last watering and rate of application of nitrogen fertilizer. Journal of Agricultural Science. (1975 b); 84 419-430
- 22 Jefferies R. A.. Drought and chlorophyll fluorescence in field-grown potato (Solanum tuberosum). . Physiologia Plantarum. (1994); 90 93-97
-
23 Jones H. G..
Drought tolerance and water-use efficiency. Smith, J. A. C. and Griffiths, H., eds. Water Deficit. Oxford; BIOS Scientific (1993): 193-203 - 24 Kitao M., Koike T., Tobita H., Maruyama Y.. Elevated CO2 and limited nitrogen nutrition can restrict excitation energy dissipation in photosystem II of Japanese white birch (Betula platyphylla var. japonica) leaves. Physiologia Plantarum. (2005); 125 64-73
- 25 Kitao M., Lei T. T., Koike T., Tobita H., Maruyama Y.. Higher electron transport rate observed at low intercellular CO2 concentration in long-term drought-acclimated leaves of Japanese mountain birch (Betula ermanii Cham.). Physiologia Plantarum. (2003); 109 284-290
- 26 Kitaoka S., Koike T.. Seasonal and yearly variations in light use and nitrogen use by seedlings of four deciduous broad-leaved tree species invading larch plantations. Tree Physiology. (2005); 25 467-475
- 27 Lal A., Ku M. S. B., Edwards G. E.. Analysis of inhibition of photosynthesis due to water stress in the C3 species Hordeum vulgare and Vicia faba: electron transport, CO2 fixation and carboxylation capacity. Photosynthesis Research. (1996); 49 57-69
- 28 Lawlor D. W., Cornic G.. Photosynthetic carbon assimilation and associated metabolism in relation to water deficits in higher plants. Plant, Cell and Environment. (2002); 25 275-294
- 29 Long S. P., Humphries S., Falkowski P. G.. Photoinhibition of photosynthesis in nature. Annual Review of Plant Physiology and Plant Molecular Biology. (1994); 45 633-662
- 30 Milroy S. P., Bange M. P.. Nitrogen and light responses of cotton photosynthesis and implications for crop growth. Crop Science. (2003); 43 904-913
- 31 Ögren E., Rosenqvist E.. On the significance of photoinhibition of photosynthesis in the field and its generality among species. Photosynthesis Research. (1992); 33 63-71
- 32 Öquist G., Huner N. P. A.. Cold-hardening-induced resistance to photoinhibition of photosynthesis in winter rye is dependent upon an increased capacity for photosynthesis. Planta. (1993); 189 150-156
-
33 Ort D. R., Oxborough K., Wise R. R..
Depressions of photosynthesis in crops with water deficits. Baker, N. R. and Bowyer, J. R., eds. Photoinhibition of Photosynthesis from Molecular Mechanisms to the Field. Oxford; BIOS Scientific Publishers (1994): 315-329 - 34 Panković D., Sakač Z., Kevrešan S., Plesničar M.. Acclimation to long-term water deficit in the leaves of two sunflower hybrids: photosynthesis, electron transport and carbon metabolism. Journal of Experimental Botany. (1999); 50 127-138
- 35 Park Y.-I., Chow W. S., Osmond C. B., Anderson J. M.. Electron transport to oxygen mitigates against the photoinactivation of Photosystem II in vivo. Photosynthesis Research. (1996); 50 23-32
- 36 Peterson R. B.. Effects of O2 and CO2 concentrations on quantum yields of photosystems I and II in tobacco leaf tissue. Plant Physiology. (1991); 97 1388-1394
- 37 Reich P. B., Ellsworth D. S., Walters M. B., Vose J. M., Gresham C., Volin J. C., Bowman W. D.. Generality of leaf trait relationships: a test across six biomes. Ecology. (1999); 80 1955-1969
-
38 Ritchie J. T..
Water dynamics in the soil-plant-atmosphere system. Monteith, J. and Webb, C., eds. Soil Water and Nitrogen in Mediterranean-Type Environments. The Hague; Martinus Nijhoff and Dr W. Junk (1981): 50-66 -
39 Schreiber U., Bilger W., Neubauer C..
Chlorophyll fluorescence as a non-intrusive indicator for rapid assessment of in vivo photosynthesis. Schulze, E.-D. and Caldwell, M. M., eds. Ecophysiology of Photosynthesis. Berlin; Springer-Verlag (1994): 49-70 - 40 Sharkey T. D., Seemann J. R.. Mild water stress effects on carbon-reduction-cycle intermediates, ribulose bisphosphate carboxylase activity, and spatial homogeneity of photosynthesis in intact leaves. Plant Physiology. (1989); 89 1060-1065
- 41 Tezara W., Mitchell V. J., Driscoll S. D., Lawlor D. W.. Water stress inhibits plant photosynthesis by decreasing coupling factor and ATP. Nature. (1999); 401 914-917
- 42 Turner N. C., Hearn A. B., Begg J. E., Constable G. A.. Cotton (Gossypium hirsutum L.): physiological and morphological responses to water deficits and their relationship to yield. Field Crops Research. (1986); 14 153-170
- 43 von Caemmerer S.. Biochemical models of leaf photosynthesis. Canberra, Australia; CSIRO Publishing (2000)
- 44 von Caemmerer S., Evans J. R., Hudson G. S., Andrews T. J.. The kinetics of ribulose-1,5-bisphosphate carboxylase/oxygenase in vivo inferred from measurements of photosynthesis in leaves of transgenic tobacco. Planta. (1994); 195 88-97
- 45 Wise R. R., Ortiz-Lopez A., Ort D. R.. Spatial distribution of photosynthesis during drought in field-grown and acclimated and nonacclimated growth chamber-grown cotton. Plant Physiology. (1992); 100 26-32
- 46 Wise R. R., Sparrow D. H., Ortiz-Lopez A., Ort D. R.. Biochemical regulation during the mid-day decline of photosynthesis in field-grown sunflower. Plant Science. (1991); 74 45-52
- 47 Wright I. J., Reich P. B., Westoby M.. Strategy shifts in leaf physiology, structure and nutrient content between species of high- and low-rainfall and high- and low-nutrient habitats. Functional Ecology. (2001); 15 423-434
- 48 Wright I. J., Westoby M.. Leaves at low versus high rainfall: coordination of structure, lifespan and physiology. New Phytologist. (2002); 155 403-416
T. T. Lei
Department of Environmental Solution Technology
Faculty of Science and Technology
Ryukoku University
1-5 Yokoba
Seta-Oe, 520-2194
Japan
Email: tomlei@rins.ryukoku.ac.jp
Editor: R. C. Leegood