Studying capability of soil cadmium phytoremediation by sorghum in the presence of mycorrhiza fungi

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Research Paper 01/10/2013
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Studying capability of soil cadmium phytoremediation by sorghum in the presence of mycorrhiza fungi

Mehdi Moradi, Mojtaba Yousefi Rad, Adeleh Darbani
Int. J. Biosci. 3(10), 233-239, October 2013.
Copyright Statement: Copyright 2013; The Author(s).
License: CC BY-NC 4.0

Abstract

This study was designed to investigate the capability of Sorghum plant to purify the cadmium-contaminated soil in the presence of mycorrhiza fungi. This study was performed in Farm of Agriculture Research of Saveh Islamic Azad University as a factorial experiment based on randomized complete blocks design with three replications. Seeds were cultivated in certain pots. In this study, two factors were considered including: the concentrations of cadmium nitrate at four levels (0, 100, 200 and 300 ppm) which was considered as the first factor, the contamination as well as the lack of contamination with mycorrhiza fungi (Glomus Intraradices) which was considered as the second factor. The results showed that the presence of mycorrhiza fungi has increased the concentration of cadmium in all plant organs. It was also observed that increasing the concentration of cadmium in the soil has increased the cadmium concentrations in various organs of the sorghum plant. The mycorrhiza inoculation at all levels of the cadmium intake has significantly increased the cadmium concentration in different organs of the sorghum plant. According to this study, the presence of mycorrhiza fungi has increased the absorption of cadmium toxic elements. It also resulted in purification of the soil by sorghum.

Alipur H. 1990. Agriculture and Plant Breeding in Forage Crops (Sorghum). Karaj, Iran: Islamic Azad University of Karaj Publications, 175 pages. (In Persian).

Auge RM, Schekel KA, Wample RL. 1986. Greater leaf conductance of well-watered VA mycorrhizal Rose plants is not related to phosphorus nutrition. New Phytologist 103, 107-116. http://dx.doi.org/10.1111/j.14698137.1986.tb00600.X

Boominathan R, Doran PM. 2003. Cadmium tolerance and antioxidative defenses in hairy roots of the cadmium hyperaccumulator, Thlaspi caerulescens. Biotechnology and Bioengineerging 83, 158-167. http://dx.doi.org/10.1002/bit.10656

Boumman LA, Bloem J, Romkens PFAM, Boon GT, Vangronsveld J. 200l. Beneficial effects of the growth of metal tolerant grass on biological and chemical parameters in copper- and zinc-contaminated sandy soils. Minerva Biotechnologica 13(1), 19-26.

Casio C, Martinoia E, Keller C. 2004. Hyperaccumulation of cadmium and zinc in Thlaspi caerulescense and Arabidopsis halleri at the leaf cellular level. Plant Physiology 134, 716-725. http://dx.doi.org/10.1104/p.103.031948

Chaney RL, Angle JS, McIntosh MS, Reeves RD, Li YM, Brewer EP, Chen KY, Roseberg RJ, Perner H, Synkowski EC, Broadhurst CL, Wang S, Baker AJ. 2005. Using Hyperaccumulator plants to phytoextraction of soil Ni and Cd. Zeitschrift für Naturforschung C 60(3-4), 190-198. http://dx.doi.org/10.1371/journal.pone.0062941

Cunningham SD, Ow DW. 1996. Promises and prospects for phytoremediation. Plant Physiology 110, 715-719. http://dx.doi.org/10.1104/pp.110.3.715

Davies Jr FT, Puryear JD, Newton RJ, Egilla JN, Saravia Grossi JA. 2001 Mycorrhiza fungi enhance accumulation and tolerance of chromium in sunflower (Helianthus annuus ). Journal of plant physiology 158(6), 777-786. http://dx.doi.org/10.1078/0176-1617-00311

Danielson RM. 1985. Mycorrhizae and reclamation of stressed terrestrial environments. In: Tate Ill RL, Klein DA, eds. Soil reclamation processes: microbiological analysis and applications. New York, NY, Marcel Dekker, 173- 201.

Davies FT, Potter JR, Linderman RG. 1993. Drought resistance of mycorrhizal pepper plants independent of leaf P-concentration response in gas exchange and water relations. Physiology Plant 87, 45-53.

Dogget H. I985. Sorghum tropical. Agriculture series. London.

Fischer RA. 1975. Yield potential of dwarf spring wheat and the effects of shading. Crop Science 15, 607- 613.

Halim M, Conte P, Piccolo A. 2003. Potential availability of heavy metals to phytoextraction from contaminated soils induced by exogenous humic substances. Chemosphere 52(1), 265-275. http://dx.doi.org/10.1016/S0045-6535(03)00185-1

Kotrba P, Najmanova J, Macek T, Ruml T, Mackova M. 2009. Genetically modified plants in phytoremediation of heavy metal and metalloid soil and sediment pollution. Biotechnology advance 27(6), 799-810. http://dx.doi.org/10.1016/j.biotechadv.2009.06.003

Revathi S, Subhashree Venugopal. 2013. Physiological and biochemical mechanisms of heavy metal tolerance.International Journal of Environment Science 3(5), 1339-1354. http://dx.doi.org/10.6088/ijes.2013030500004

Vierheilig H, Lerat S, Piche Y. 2003. Systemic inhibition of arbuscular mycorrhiza development by root exudates of cucumber plants colonized by Glomus mosseae. Mycorrhiza 13, 167-70. http://dx.doi.org/10.1007/s00572-002-0219-0

Yang XE, Long XX, Ni WZ. 2002. Physiological and molecular mechanisms of heavy metal uptake by hyperaccumulating plant species. Journal of Plant Nutrition and Fertilization 8, 8-15.

Yang XE, Long XX, Ye FLB. Fle ZL, Stoffella PJ, Calvert DV. 2004. Cadmium tolerance and hyperaccumulation in a new Zn-hyperaccumulating plant species (Sedum alfredjj Hance). Plant and Soil 259(l-2), 181-9.

Zand B. 1997. Evaluation and Qualitative as well as Quantitative Estimation of Forage Sorghum and Millet Intercropping under different Planting Models. Master’s thesis of Department of Agriculture and Plant Breeding, University of Tehran, Iran, 150 page.(In Persian).

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