MODELING CARBON FLUX OF THE SUNDARBANS: A THEORETICAL FRAMEWORK FOR PREDICTION OF THE SUNDARBANS’ CONTRIBUTION AND VULNERABILITY TO CLIMATE CHANGE

Authors

  • Md. Golam Rakkibu Forestry and Wood Technology Discipline, Khulna University, Khulna 9208, Bangladesh

DOI:

https://doi.org/10.53808/KUS.SI.SESB.2010.141-148-ls

Keywords:

Modeling, photosynthesis, respiration, Sundarbans, climate change

Abstract

Models of canopy gas exchange provide a theoretical framework for thorough analysis and interpretation of the scaling of physiological processes, enabling physiologist to extend their work to larger scales. They also fit the requirements of assessing effects of climate change on vegetation. Process-based models of forest canopy carbon uptake predict fluxes from individual leaves and canopies, and have been extended to provide estimates of carbon uptake at national and global scales. Fundamental to such models is the scaling of leaf photosynthesis to canopies by considering interception of solar radiation and leaf photosynthetic capacity. The net carbon gain of a tree canopy is the balance between carbon assimilated through photosynthesis and carbon lost through respiration. The within-canopy distribution of photosynthetic capacity is related to the distribution of leaf nitrogen, which can determine canopy-level carbon assimilation because of the nitrogen-rich photosynthetic enzyme Rubisco (ribulose-1,5-bisphosphate carboxylase/ oxygenase) and electron-transport capacity. Photosynthesis of a canopy element depends, amongst other things, on the biochemical capacity for photosynthesis of that element, its temperature, its carbon dioxide at the sites of carboxylation, and its absorbed irradiance. During the last decade, process-based simulation models have been increasingly used to deepen the understanding of tree growth and development. Of the processes controlling tree growth and yield represented in these models, photosynthetic capacities are always of prime importance, because they determine (along with foliage distribution) potential tree carbon gains. Furthermore, environmental variables largely control actual photosynthetic rates. Thus, developing a process-based canopy photosynthesis model for the Sundarbans calls for reliable and comprehensive information on functional relationships between leaf CO2 assimilation and plant and environmental variables of the ecosystem.  Such models can be useful to predict the Sundarbans growth and carbon sequestration potential and their vulnerability to the change in climatic variables. 

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References

Cao, B.; Dang, Q.L. and Zhang, S. 2007. Relationship between photosynthesis and leaf nitrogen concentration in ambient and elevated [CO2] in white birch seedlings. Tree Physiology, 27: 891-899

De Pury, D.G.G. and Farquhar, G.D. 1997. Simple scaling of photosynthesis from leaves to canopies without the errors of big-leaf models. Plant Cell and Environment, 20:, 537-557

Dungan, R.J., Whitehead, D. and Duncan, R.P. 2003. Seasonal and temperature dependence of photosynthesis and respiration for two co-occurring broad-leaved tree species with contrasting leaf phenology. Tree Physiology, 23: 561-568

Evans, J.R. 1989. Photosynthesis and nitrogen relationships in leaves of C3 plants. Oecologia, 78: 9-19

Farquhar, G.D.; Caemmerer, S. Von and Berry, J.A. 1980. A biochemical model of photosynthetic CO2 assimilation in leaves of C3 species. Planta,149: 78-90

Fearnside, P.M. 2000. Global worming and tropical land-use change: greenhouse gas emissions from biomass burning, decomposition and soils in forest conversion, shifting cultivation and secondary vegetation. Climate Change, 46: 115-158

Field, C. and Mooney, H. 1986. The photosynthesis-nitrogen relationship in wild plants. In Givnish, T.J. (ed) On the Economy of Plant Form and Function, Cambridge Press: 25-55

Field, C. and Mooney, H.A. 1983. Leaf age and seasonal effects on light, water and nitrogen use efficiency in a California shrub. Oecologia, 56: 348-355

Gash, J.H.C.; Nobre, C.A.; Roberts, J.M. and Victoria, R.L. 1996. Amazonian deforestation and climate. John Wiley & Sons, Chichester: 611 pp

Grace, J. 2004. Understanding and managing the global carbon cycle. Journal of Ecology, 92: 189-202

Harrington, R.A.; Brown, B.J.; Reich, P.B. and Fownes, J.H. 1989. Ecophysiology of exotic and native shrubs in southern Wisconsin. II. Annual growth and carbon gain. Oecologia, 80: 368-373

Hirose, T. and Werger, M.J.A. 1987. Maximising daily canopy photosynthesis with respect to leaf nitrogen allocation pattern in the canopy. Oecologia, 72: 520-526

Ibrom, A.; Jarvis, P.G.; Clement, R.; Morgenstern, K.; Oltchev, A.; Medlyn, B.E.; Wang, Y.P.; Wingate, L.; Moncrieff, J.B. and Gravenhorst, G. 2006. A comparative analysis of simulated and observed photosynthetic CO2 uptake in two coniferous forest canopies. Tree physiology, 26: 845-864

Jarvis, P.G. 1976. The interpretation of the variations in leaf water potential and stomatal conductance found in canopies in the field. Philos. Trans. R. Soc. Lond. B, 273: 593-610

Jarvis, P.G. 1989. Atmospheric carbon dioxide and forests. Philos. Trans. R. Soc. Lond. B, 324: 369-392

Lambers, H.; Chapin, F.S. III, and Pons, T.L. 1998. Plant physiological ecology. Springer-Verlag, New York: 540 pp.

Larcher, W. 2003. Physiological plant ecology. Fourth edition, Springer-Verlag, New York: 540pp.

Lloyd, J. 1999. The CO2 dependence of photosynthesis, plant growth responses to elevated CO2 concentrations and their interactions with soil nutrient status. II. Temperate and boreal forest productivity and the combined effects of increasing CO2 concentrations and increased nitrogen deposition at a global scale. Functional Ecology,13: 439-459

Malhi, Y., Baldocchi, D.D. and Jarvis, P.G. 1999. The carbon balance of tropical, temperate and boreal forests. Plant Cell and Environment, 22: 715-740

Medlyn, B.E. 2004. A MAESTRO retrospective. In: Mencuccini, M.; Moncrieff, J.; McNaughton, K.G. and Grace, J., (eds) Forests at the land-Atmosphere Interface. CABI Publishing, Wallingford, U.K.: 105-121

Medlyn, B.E.; Dreyer, E.; Ellsworth, D.; Forstreuter, M.; Harley, P.C.; Kirschbaum, M.U.F.; Leroux, X.; Montpied, P.; Strassemeyer, J.; Walcroft, A.; Wang, K. and Loustau, D. 2002. Temperature response of parameters of a biochemically based model of photosynthesis. II. A review of experimental data. Plant, Cell and Enviroment, 25: 1167-1179

Meir, P.; Grace, J. and Miranda, A.C. 2001. Leaf respiration in two tropical rainforests: constraints on physiology by phosphorus, nitrogen and temperature. Functional Ecology, 15: 378-387

Meir, P.; Kruijt, B.; Broadmeadow, M.; Barbosa, E.; Kull, O.; Carswell, F.; Nobre, A. and Jarvis, P.G. 2002. Acclimation of photosynthetic capacity to irradiance in tree canopies in relation to leaf nitrogen concentration and leaf mass per unit area. Plant, Cell and Environment, 25: 343-357

Niinemets, U. and Tenhunen, J.D. 1997. A model separating leaf structural and physiological effects on carbon gain along light gradients for the shade tolerant species Acer saccharum. Plant Cell Environment, 20: 845-866

Poorter, H. and Evans J.R. 1998. Photosynthetic nitrogen-use efficiency of species that differ inherently in specific leaf area. Oecologia, 116: 26-37

Reich, P.B.; Walters M.B. and Ellsworth, D.S. 1991. Leaf age and season influence the relationships between leaf nitrogen, leaf mass per area and photosynthesis in maple and oak trees. Plant Cell Environment, 14: 251-259

Reich, P.B.; Walters, M.B. and Ellsworth, D.S. 1997. From tropics to tundra: global convergence in plant functioning. Proc. Nat. Acad. Sci., 94: 13730-13734

Rey, A. and Jarvis, P.G. 1998. Long-term photosynthetic acclimation to increased atmospheric CO2 concentration in young birch (Betula pendula) trees. Tree physiology, 8: 441-450

Roux, X.L.; Grand, S.; Dreyer, E. and Daudet, F.A. 1999. Parameterization and testing of a biochemically based photosynthesis model for walnut (Juglans regia) trees and seedlings. Tree Physiology, 19: 481-492

Sellers, P.J.; Dickinson, R.E. and Randall, D.A. 1997. Modeling the exchanges of energy, water and carbon between continents and the atmosphere. Science, 275: 502-509

von Caemmerer, S. and Farquhar, G.D. 1981. Some relationships between the biochemistry of photosynthesis and the gas exchange of leaves. Planta, 153: 367-387

von Caemmerer, S.; Evans, J.R.; Hudson, G.S. and Andrews, T.J. 1994. The kinetics of Rubisco inferred from measurements of photosynthesis in leaves of transgenic tobaco with reduced Rubisco content. Planta, 195: 88-97

Wang, Y.P. 1998. Crown structure, radiation absorption, photosynthesis and transpiration. In: IERM. University of Edinburg, Edinburg: 188 pp

Wang, Y.P. and Jarvis, P.G. 1990. Description and validation of an array model – MAESTRO. Agricultural and forest meteorology, 51: 257-280

Wessman, C. 1990. Evaluation of canopy biochemistry. In Hobbs, R.J. and Mooney, H.A. (eds) Remote Sensing and Biosphere Functioning. Springer-Verlag, New York: 135-154

Williams, M.; Malhi, Y.; Nobre, A.D.; Rastetter, E.B.; Grace, J. and Pereira, M.G.P. 1998. Seasonal variation in net carbon exchange and evapotranspiration in a Brazilian rain forest: a modeling analysis. Plant, Cell and Environment, 21: 953-968

Wilson, K.B.; Baldocchi, D.D. and Hanson, P.J. 2000. Spatial and seasonal variability of photosynthetic parameters and their relationship to leaf nitrogen in a deciduous forest. Tree Physiology, 20: 565-578

Yoda, K. 1983. Community respiration in a lowland rainforest in Pasoh, Peninsular Malayasia. Japanese Journal of Ecology, 33: 183-197

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Published

27-05-2010

How to Cite

[1]
M. G. . Rakkibu, “MODELING CARBON FLUX OF THE SUNDARBANS: A THEORETICAL FRAMEWORK FOR PREDICTION OF THE SUNDARBANS’ CONTRIBUTION AND VULNERABILITY TO CLIMATE CHANGE”, Khulna Univ. Stud., pp. 141–148, May 2010.

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