Stomatal Movement in Response to Root Zone Temperature in Purple Heart (Tradescantia pallida)
الموضوعات : مجله گیاهان زینتیNabiyollah Ashrafi 1 , Abdolhossein Rezaei Nejad 2
1 - Ph.D Student, Department of Horticultural Sciences, Faculty of Agriculture, Lorestan University, P.O. Box 465, Khorramabad, Iran.
2 - Associate Professor, Department of Horticultural Sciences, Faculty of Agriculture, Lorestan University, P.O. Box 465, Khorramabad, Iran
الکلمات المفتاحية: Photosynthesis, Heat shock, Root zone temperature, Stomatal Conductance,
ملخص المقالة :
The effects of root temperatures (25, 35 and 45°C) and temperature duration (30, 60 and 90 min) on net photosynthesis rate, stomatal conductance and transpiration rate in Tradescantia pallida were investigated. The experiment was conducted under controlled conditions with factorial arrangement based on a completely randomized design (CRD) and four replications. Result showed that, net photosynthesis rate was not significantly different between plants treated with 25 and 35°C. However, aperture area and width increased at 35°C and declined sharply at 45 °C as compared with that at 25 °C. Net photosynthesis rate and stomata1 conductance of plants treated with 45°C decreased to 76 and 68%, respectively, as compared with those at 35°C. Stomatal aperture area of plants treated with 35°C was 27% and 320% higher than those treated with 25 and 45°C, respectively. Stomatal resistance of plants treated with high temperature (45°C) were higher (174%) than those treated with 35°C. In 35 °C, aperture area of plants after 30 min was 61% and 45% higher than those after 60 and 90 min exposure, respectively. The results revealed that, a heat shock of roots at 45°C could lead to a significant decrease in stomatal conductance (by 81%) and transpiration rate (by 60%) as compared with those at 35°C. Overall, the results suggest that the root temperature affects leaf gas exchange and stomatal behavior and has to be taken into account in plant production system, in particular, hydroponics.
Brownlee, C. 2001. The long and the short of stomatal density signals. Trends in Plant Science. 6 (10): 441-442.
Davies, W. J. and Zhang, J. 1991. Root signals and the regulation of growth and development of plants in drying soil. Annual Review of Plant Biology. 42 (1): 55-76.
Feller, U. 2006. Stomatal opening at elevated temperature: An underestimated regulatory mechanism. Gen. Appl. Plant Physiol. 32: 19-31.
Haldimann, P. and Feller, U. 2004. Inhibition of photosynthesis by high temperature in oak (Quercus pubescens L.) leaves grown under natural conditions closely correlates with a reversible heat‐dependent reduction of the activation state of ribulose‐1, 5‐bisphosphate carboxylase/oxygenase. Plant, Cell and Environment. 27 (9): 1169-1183.
Iriti, M., Picchi, V., Rossoni, M., Gomarasca, S., Ludwig, N., Gargano, M. and Faoro, F. 2009. Chitosan antitranspirant activity is due to abscisic acid-dependent stomatal closure. Environmental and Experimental Botany. 66 (3): 493-500.
Liang, J. and Zhang, J. 1999. Xylem-carried ABA in plant response to soil drying. Current Topics in Plant Biology. 1: 89-96.
Marchi, S., Tognetti, R., Minnocci, A., Borghi, M. and Sebastiani, L. 2008. Variation in mesophyll anatomy and photosynthetic capacity during leaf development in a deciduous mesophyte fruit tree (Prunus persica) and an evergreen sclerophyllous Mediterranean shrub (Olea europaea). Trees. 22 (4): 559-571.
Reynolds-Henne, C. E., Langenegger, A., Mani, J., Schenk, N., Zumsteg, A. and Feller, U. 2010. Interactions between temperature, drought and stomatal opening in legumes. Environmental and Experimental Botany. 68 (1): 37-43.
Roblin, G. and Bonnemain, J. L. 1985. Propagation in Vicia faba stem of a potential variation induced by wounding. Plant and Cell Physiology. 26 (7): 1273-1283.
Rouhi, V., Samson, R., Lemeur, R. and Van Damme, P. 2007. Photosynthetic gas exchange characteristics in three different almond species during drought stress and subsequent recovery. Environmental and Experimental Botany. 59 (2): 117-129.
Schroeder, J. I., Allen, G. J., Hugouvieux, V., Kwak, J. M. and Waner, D. 2001. Guard cell signal transduction. Annual Review of Plant Biology. 52 (1): 627-658.
Smith, S., Weyers, J. and Berry, W. 1989. Variation in stomatal characteristics over the lower surface of Commelina communis leaves. Plant, Cell and Environment. 12 (6): 653-659.
Veselova, S., Farkhutdinov, R., Veselov, D. and Kudoyarova, G. 2006. Role of cytokinins in the regulation of stomatal conductance of wheat seedlings under conditions of rapidly changing local temperature. Russian Journal of Plant Physiology. 53 (6): 756-761.
Wilkinson, S., Clephan, A. L. and Davies, W. J. 2001. Rapid low temperature-induced stomatal closure occurs in cold-tolerant Commelina communis leaves but not in cold-sensitive tobacco leaves, via a mechanism that involves apoplastic calcium but not abscisic acid. Plant Physiology. 126 (4): 1566-1578.
Yang, S., Huang, C., Wu, Z., Hu, J., Li, T., Liu, S. and Jia, W. 2006. Stomatal movement in response to long distance-communicated signals initiated by heat shock in partial roots of Commelina communis L. Science China Life Sciences. 49 (1): 18-25.
Yordanov, I., Velikova, V. and Tsonev, T. 2000. Plant responses to drought, acclimation, and stress tolerance. Photosynthetica. 38 (2): 171-186.