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Physiological Responses and Phytoextraction Potential of Pinus thunbergii on Cd-contaminated Soil  

Han, Sim-Hee (Department of Forest Resources & Development, Korea Forest Research Institute)
Kim, Du-Hyun (Department of Forest Resources & Development, Korea Forest Research Institute)
Ultra, Venecio U. Jr. (Department of Forest Resources & Development, Korea Forest Research Institute)
Lee, Jae-Cheon (Department of Forest Resources & Development, Korea Forest Research Institute)
Publication Information
Journal of Korean Society of Forest Science / v.99, no.5, 2010 , pp. 711-719 More about this Journal
Abstract
We investigated physiological responses and phytoextraction ability of Pinus thunbergii in cadmium contaminated soil as part of our efforts in identifying plant materials for the restoration and revegetation of forest soil contaminated by heavy metals. Thirty seedlings (ten per treatment) were assigned to three treatments (control, 0.3 and 0.6 mM $CdSO_4$ solution) at first year experiment. At second year, ten seedlings per treatment treated with Cd during the first year experiment were divided by two groups (no Cd-treated and consecutive Cd-treated group). At first experiment, photosynthetic pigment content, and superoxide dismutase (SOD) and glutathione reductase (GR) activities have significantly reduced by Cd application, and the reduction rate was increased much higher as the rate of Cd application increased. On the other hand, thiol and malondialdehyde (MDA) content were significantly increased at the application of 0.6 mM of Cd. At the second year experiment, a general increase in chlorophyll and carotenoid content was observed with Cd treatment while SOD and GR activities showed a relative reduction compared to the control. Similar to the first year measurement, thiol and MDA contents also increased considerably due to Cd treatment. At harvest, dry matter was significantly reduced by Cd treatment especially at the rate of 0.6 mM Cd, but dry yield of P. thunbergii treated with 0.3 mM Cd was less affected and it was comparable with the control seedling. Cadmium concentration in seedling tissues increased with increasing Cd application rate while Cd uptake was higher in seedlings supplied with 0.3 mM Cd, which could be ascribed to their high dry matter. Overall, our study has demonstrated the unique physiological response of P. thunbergii to Cd-prolonged exposure by showing that the changes in photosynthetic pigment content and antioxidative enzyme activities were dependent on the concentration and duration of treatment. In addition, our results have demonstrated the potential of P. thunbergii to withstand up to 0.3 mM Cd (equivalent to cumulative Cd concentration of 134.4 to 268 mg $kg^{-1}$) without showing growth reduction, hence it might be used for phytoremediation of Cd contaminated areas.
Keywords
cadmium; photosynthetic pigments; physiological response; phytoextraction; Pinus thunbergii;
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1 Han, S.H., Lee, J.C., Oh, C.Y. and Kim, P.G. 2006b. Antioxidant characteristics and phytoremediation potential of 27 taxa of roadside trees at industrial complex area. Korean Journal of Agricultural and Forest Meteorology 8: 159-168.   과학기술학회마을
2 Beauchamp, C. and Fridovichi, I. 1971. Superoxide dismutase: Improved assays and an assay applicable to acrylamide gels. Analytical Biochemistry 44: 276-297.   DOI   ScienceOn
3 Ding, X., Jiang, J., Wang, Y., Wang, W. and Ru, B. 1994. Bioconcentration of cadmium in water hyacinth (Eichhornia crassipes) in relation to thiol group content. Environmental Pollution 84: 93-96.   DOI   ScienceOn
4 Schoch, S. and Brown, J. 1987. The action of chlorophyllase on chlorophyll-protein complexs. Journal of Plant Physiology 129: 242-249.
5 Seth, C.S., Chaturvedi, P.K. and Misra, V. 2008. The role of phytochelatins and antioxidants in tolerance to Cd accumulation in Brassica juncea L. Eco-Environment Safety 71: 76-85.   DOI   ScienceOn
6 Skorzynska-Polit, E., Bednara, J. and Baszynski, T. 1995. Some aspects of runner bean plant response to cadmium at different stages of the primary leaf growth. Acta Societatis Botanicorum Poloniae 64: 165-170.   DOI
7 SAS Institute Inc. 1996. SAS Software Proprietary Release 6.12. Cary (NC): SAS Institute Inc.
8 Padmaja, K., Parsad, D.D.K. and Parsad, A.R.K. 1990. Inhibiton of chlorophyll synthesis in Phaseolus vulgaris L. seedling by cadmium acetate. Photosynthetica 24: 399-404.
9 Rice-Evans, C., Sampson, J., Bramley, P.M. and Holloway, D.E. 1997. Why do we expect carotenoids to be antioxidants in vivo. Free Radical Research 26: 381-398.   DOI   ScienceOn
10 Rodryguez, L., Ruiz, E., Alonso-Azcarate, J. and Rincon, J. 2009. Heavy metal distribution and chemical speciation in tailings and soils around a Pb-Zn mine in Spain. Journal of Environmental Management 90: 1106-1116.   DOI   ScienceOn
11 Mishra, S., Srivastava, S., Tripathi, R.D., Govindarajan, R., Kuriakose, S.V. and Prasad, M.N.V. 2006. Phytochelatin synthesis and response of antioxidants during cadmium stress in Bacopa monnieri L. Plant Physiology and Biochemistry 44: 25-37.   DOI   ScienceOn
12 Lichtenthaler HK. 1987. Chlorophylls and carotenoids: pigments of photosynthetic biomembranes. Methods in Enzymology 148: 350-382.   DOI
13 Lima, A.I., Pereira, S.I., Figueira, A., Caldeira, G. and Caldeira, H. 2006. Cadmium detoxification in roots of Pisum sativum seedlings: relationship between toxicity levels, thiol pool alterations and growth. Environmental and Experimental Botany 55: 149-162.   DOI   ScienceOn
14 Marchiol, L., Leita, L., Martin, M. and Peressotti, Z.G. 1996. Physiological responses of two soybean cultivars to cadmium. Journal of Environmental Quality 25: 562-566.
15 Heath, R.L. and Parker, L. 1968. Photoperoxidation in isolated chloroplasts. I. Kinetics and stoichiometry of fatty acid peroxidation. Archives of Biochemistry and Biophysics 125: 189-198.   DOI   ScienceOn
16 Hendry, G.A.F., Baker, A.J.M. and Ewart, C.F. 1992. Cadmium tolerance and toxicity, oxygen radical processes and molecular damage in cadmium-tolerant and cadmium sensitive clones of Holcus lanatus L. Acta Botanica Neerlandica 41: 271-281.   DOI
17 Horst, W.J. 1995. The role of the apoplast in Al toxicity and resistance of higher plants: a review. Zeitschrift fur Pflanzenernabrung und Bodenkunde 158: 419-428.   DOI   ScienceOn
18 Jarup, L. 2003. Hazards of heavy metal contamination. British Medical Bulletin 68:167-182.   DOI   ScienceOn
19 Kim, C.G., Power, S.A. and Bell, J.N.B. 2004. Effects of host plant exposure to cadmium on mycorrhizal infection and soluble carbohydrate levels of Pinus sylvestris seedlings. Environment Pollution 131: 287-294.   DOI   ScienceOn
20 Han, S.H., Lee, J.C., Oh, C.Y. and Kim, P.G. 2006a. Alleviation of Cd toxicity by composted sewage sludge in Cd-treated Schmidt birch (Betula schmidtii) seedlings. Chemosphere 65: 5421-546.
21 Drazkiewicz, M. 1994. Chlorophyllase: occurrence, functions, mechanisms of action, effects of external and internal factors. Phytosynthetica 30: 321-331.
22 Cobbett, C.S., May, M.J., Howden, R. and Rolls, B. 1998. The glutathione-deficient cadmium-sensitive mutant, cad 2-1, of Arabidopsis thaliana is deficient in gammaglutamylcysteine synthetase. The Plant Journal 16: 73- 78.   DOI   ScienceOn
23 Das, P., Samantaray, S. and Rout, G.R. 1997. Studies on cadmium toxicity in plants: A review. Environmental Pollution 98: 29-36.   DOI   ScienceOn
24 Dickinson N.M. 2000. Strategies for sustainable woodland on contaminated soils. Chemosphere 41: 259-263.   DOI   ScienceOn
25 Ewais, E.A. 1997. Effects of cadmium, nickel and lead on growth, chlorophyll content and proteins of weeds. Biologia Plantarum 39: 403-410.   DOI   ScienceOn
26 Abdel-Basset, R., Issa, A.A. and Adam, M.S. 1995. Chlorophyllase activity: effect of heavy metals and calcium. Photosynthetica 31: 421-425.
27 Foyer, C.H. and Noctor, G. 2005. Oxidant and antioxidant signaling in plants: a re-evaluation of the concept of oxidative stress in a physiological context. Plant Cell Environment 28: 1056-1071.   DOI   ScienceOn
28 Hall, J.L. 2002. Cellular mechanism of heavy metal detoxification and tolerance. Journal of Experimental Botany 53: 1-11.   DOI   ScienceOn
29 Halliwell, B. and Gutteridge, J.M.C. 1989. Free radicals in biology and medicine. Oxford: clarendon Press p. 188-206.
30 Abad, A.K.J. and Khara, J. 2007. Effect of cadmium toxicity on the level of lipid peroxidation and antioxidarive enzymes activities in wheat plants colonized by arbuscular mycorrhizal fungi. Pakistan Journal of Biological Sciences10: 2413-2417.   DOI
31 Baryla, A., Carrier, P., Franck, F., Coulomb, C., Sahut, C. and Havaux, M. 2001. Leaf chlorosis in oilseed rape plants (Brassica napus) grown on cadmium-polluted soil: causes and consequences for photosynthesis and growth. Planta 212: 696-709.   DOI   ScienceOn
32 Carlberg, I. and Mannervik, B. 1985. Glutathione reductase. Methods in Enzymology 113: 485-490.
33 Cho, U.H. and Seo, N.H. 2005. Oxidative stress in Arabidopsis thaliana exposed to cadmium is due to hydrogen peroxide accumulation. Plant Science 168: 113-120.   DOI   ScienceOn
34 Young, A.J. 1991. The photoprotective role of carotenoids in higher plants. Physiologia Plantarum 83: 702-708.   DOI
35 Wagner, G.J. 1993. Accumulation of cadmium in crop plants and its consequences to human health. Advances in Agronomy 52: 173-212.
36 Wu, F., Zhang, G. and Dominy, P. 2003. Four barley genotypes respond differently to cadmium: lipid peroxidation and activities of antioxidant capacity. Environmental and Experimental Botany 50: 67-78.   DOI   ScienceOn
37 Yang, X.E., Long, X.X., Ye, H.B., He, Z.L., Calvert, D.V. and Stoffella, P.J. 2004. Cadmium tolerance and hyperaccumulation in a new Zn-hyperaccumulating plant species (Sedum alfredii Hance). Plant and Soil 259: 181-189.   DOI
38 Zhou, W. and Qiu, B. 2005. Effects of cadmium hyperaccumulation on physiological characteristics of Sedum alfredii Hance (Crassulaceae). Plant Science 169: 737-745.   DOI   ScienceOn
39 Tsukahara, H., Kozlowski, T.T. and Shanklin, J. 1985. Tolerance of Pinus densiflora, Pinus thunbergii, and Larix leptolepis seedlings to $SO_{2}$. Plant and Soil 88: 385-397.   DOI
40 Tadaki, Y. 1992. The ecological succession in coasts and coastal forests. pp. 52-57. In: Murai, H., Ishikawa, M., Endo, J.and Tadaki, Y. (Eds). Japanese coastal forests: the many sided environmental functions and the applications (in Japanese). Soft Science, Tokyo.
41 Tukendorf, A. and Rauser, W.E. 1990. Changes in glutathione and phytochelatins in roots of maize seedlings exposed to cadmium. Plant Science 70: 155-166.   DOI   ScienceOn