Photosynthetica 2004, 42(1):93-97 | DOI: 10.1023/B:PHOT.0000040575.92512.ab

Significance of the Leaf Area Ratio in Hevea brasiliensis Under High Irradiance and Low Temperature Stress

D. Ray1, S.K. Dey1, G. Das1
1 Regional Research Station, Rubber Research Institute of India, Rubber Board Kunjaban PO, Agartala, Tripura, India, e-mail

Adjustment in leaf area : mass ratio called leaf area ratio (LAR) is one of the strategies to optimize photon harvesting. LAR was recorded for 10 genotypes of Hevea brasiliensis under high irradiance and low temperature and the genotypes were categorized into two groups, i.e. high LAR and low LAR types. Simultaneously, the growth during summer as well as winter periods, photosynthetic characteristics, and in-vitro oxidative damage were studied. Low LAR (19.86±0.52 m2 kg-1) types, recorded an average of 18.0 % chlorophyll (Chl) degradation under high irradiance and 7.1 % Chl degradation under low temperature. These genotypes maintained significantly higher net photosynthetic rate (PN) of 10.4 μmol(CO2) m-2 s-1 during winter season. On the contrary, the high LAR (24.33±0.27 m2 kg-1) types recorded significantly lower PN of 4 μmol(CO2) m-2 s-1 and greater Chl degradation of 37.7 and 13.9 % under high irradiance and low temperature stress, respectively. Thus LAR may be one of the physiological traits, which are possibly involved in plant acclimation process under both stresses studied.

Additional key words: CO2 concentration in sub-stomatal spaces; net photosynthetic rate; Paraquat; photo-oxidative damage; stomatal conductance

Published: March 1, 2004  Show citation

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Ray, D., Dey, S.K., & Das, G. (2004). Significance of the Leaf Area Ratio in Hevea brasiliensis Under High Irradiance and Low Temperature Stress. Photosynthetica42(1), 93-97. doi: 10.1023/B:PHOT.0000040575.92512.ab
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References

  1. Ackerly, D.D.: Light, leaf age and leaf nitrogen concentration in a tropical vine.-Oecologia 89: 596-600, 1992. Go to original source...
  2. Anten, N.P.R., Werger, M.J.A.: Canopy structure and nitrogen distribution in dominant and subordinate plants in a dense stand of Amaranthus dubius L. with size hierarchy of individuals.-Oecologia 105: 30-37, 1996. Go to original source...
  3. Arnon, D.I.: Copper enzymes in isolated chloroplasts. Polyphe-noloxidase in Beta vulgaris.-Plant Physiol. 24: 1-15, 1949. Go to original source...
  4. Björkman, O.: Responses to different quantum flux densities.-In: Lange, O.L., Nobel, P.S., Osmond, C.B., Ziegler, H. (ed.): Physiological Plant Ecology I. Pp. 57-107. Springer-Verlag, Berlin-Heidelberg-New York 1981. Go to original source...
  5. Boardman, N.K.: Comparative photosynthesis of sun and shade plants.-Annu. Rev. Plant Physiol. 28: 355-377, 1977. Go to original source...
  6. Brooks, A., Portis, A.R., Jr., Sharkey, T.D.: Effects of irradi-ance and methyl viologen treatment on ATP, ADP, and acti-vation of ribulose-bisphosphate carboxylase in spinach leaves.-Plant Physiol. 88: 850-853, 1988. Go to original source...
  7. Chazdon, R.L., Kaufmann, S.: Plasticity of leaf anatomy of two rain forest shrubs in relation to photosynthetic light accli-mation.-Funct. Ecol. 7: 385-394, 1993. Go to original source...
  8. Collins, G.G., Nie, X., Saltveit, M.E.: Heat shock increases chil-ling tolerance of mung bean hypocotyls tissue.-Physiol. Plant. 89: 117-124, 1993. Go to original source...
  9. Collins, G.G., Nie, X., Saltveit, M.E.: Heat shock protein and chilling sensitivity of mung bean hypocotyls.-J. exp. Bot. 16: 795-802, 1995. Go to original source...
  10. DeJong, T.M., Doyle, J.F.: Seasonal relationships between leaf nitrogen content (photosynthetic capacity) and leaf canopy light exposure in peach (Prunus persica).-Plant Cell Environ. 8: 701-706, 1985. Go to original source...
  11. Dey, S.K., Sobhana, P., Sethuraj, M.R., Vijaykumar, K.R.: Pho-tosynthetic rate and its relation with leaf characteristics in seedlings of Hevea brasiliensis.-Indian J. nat. Rubber Res. 8: 66-69, 1995.
  12. Evans, J.R.: Partitioning of nitrogen between and within leaves under different irradiances.-Aust. J. Plant Physiol. 16: 533-548, 1989. Go to original source...
  13. Field, C., Mooney, H.A.: The photosynthesis-nitrogen relation-ship in wild plants.-In: Givnish, G.T. (ed.): On the Economy of Plant Form and Function. Pp. 25-55. Cambridge University Press, Cambridge-London-New York-New Rochelle-Melbourne-Sydney 1986.
  14. He, R., China, Z.: Preliminary studies on cold resistance of rubber trees determined by electric conductometer.-In: Pro-ceeding of the IRRDB Rubber Physiology and Exploitation. Pp. 98-105. SCATC, Hainan 1986.
  15. Hirose, T., Werger, M.J.A.: Maximizing daily canopy photo-synthesis with respect to leaf nitrogen allocation pattern in the canopy.-Oecologia 72: 520-526, 1987. Go to original source...
  16. Jacob, J., Annamalainathan, K., Alam, B., Sathik, M.B., Thapliyal, A.P., Devakumar, A.S.: Physiological constraints for cultivation of Hevea brasisliensis in certain unfavorable agro-climatic regions of India.-Indian J. nat. Rubber. Res. 12: 1-16, 1999.
  17. Le Roux, X., Sinoquet, H., Vandame, M.: Spatial distribution of leaf dry weight per area and leaf nitrogen concentration in re-lation to local radiation regime.-Tree Physiol. 19: 181-188, 1999. Go to original source...
  18. Le Roux, X., Walcroft, A.S., Daudet, F.A., Sinoquet, H., Chaves, M.M., Rodrigues, A., Osorio, L.: Photosynthetic light acclimation in peach leaves: importance of changes in mass:area ratio, nitrogen concentration, and leaf nitrogen partitioning.-Tree Physiol. 21: 377-386, 2001. Go to original source...
  19. Marini, R.P., Marini, M.C.: Seasonal changes in specific leaf weight, net photosynthesis and chlorophyll content of leaves of peach leaves as affected by light penetration and canopy position.-J. amer. Soc. hort. Sci. 108: 609-613, 1983. Go to original source...
  20. Reich, P.B., Uhl, C., Walters, M.B., Ellsworth, D.A.: Leaf lifespan as a determinant of leaf structure and function among 23 Amazonian tree species.-Oecologia 86: 16-24, 1991. Go to original source...
  21. Rosati, A., Esparza, G., DeJong, T.M., Pearcy, R.W.: Influence of canopy light environment and nitrogen availability on leaf photosynthetic characteristics and photosynthetic nitrogen use efficiency of field-grown nectarine trees.-Tree Physiol. 19: 173-180, 1999. Go to original source...
  22. Sathik, M.B.M., Vijayakumar, K.R., Jacob, J., Sethuraj, M.R.: Membrane stability as measured by electrolyte leakage: A tool for screening Hevea clones for cold tolerance.-In: Mathew, N.M., Jacob, K. (ed.): Developments in Plantation Crop Research. Pp. 136-138. Rubber Research Institute of India, Kottayam 1998.
  23. Sharkey, T.D., Vanderveer, P.J.: Stromal phosphate concen-tration is low during feedback limited photosynthesis.-Plant Physiol. 91: 679-684, 1989. Go to original source...
  24. Sharkey, T.D., Vassey, T.L.: Low oxygen inhibition of photo-synthesis is caused by inhibition of starch synthesis.-Plant Physiol. 90: 385-387, 1989. Go to original source...
  25. Sullivan, C.Y., Ross, W.M.: Selecting for drought and heat resistance in grain sorghum.-In: Mussel, H., Staples, R.C. (ed.): Stress Physiology in Crop Plants. Pp. 264-281. John Wiley, New York 1979.
  26. Waller, D.M.: The dynamics of growth and form.-In: Crawles, M.J. (ed.): Plant Ecology. P. 496. Oxford University Press, Oxford-London 1986.