Physiological and Growth Responses of Castor (Ricinus Communis L) Under Cadmium Stressed Environment

Authors

  • Muhammad Afzal Chhajro Office of Research Inovation & Commercialization (ORIC) SMIU
  • Hongqing Hu Key Laboratory of Arable Land Conservation (Middle and Lower Reaches of Yangtze River), Ministry of Agriculture, College of Resources and Environment, Huazhong Agricultural University, Wuhan 430070, China.
  • Kashif Ali Kubar Faculty of Agriculture, Lasbela University of Agriculture, Water and Marine Sciences, Uthal, Pakistan
  • Shahmir Ali Kalhoro Faculty of Agriculture, Lasbela University of Agriculture, Water and Marine Sciences, Uthal, Pakistan
  • Mehar un Nisa Narejo Faculty of Crop Production, Sindh Agriculture University, Tandojam
  • Qamar Sarfaraz Faculty of Agriculture, Lasbela University of Agriculture, Water and Marine Sciences, Uthal, Pakistan
  • Naimatullah Koondhar Faculty of Agriculture, Lasbela University of Agriculture, Water and Marine Sciences, Uthal, Pakistan
  • Sanaullah Magsi Department of Land and Water Management Faculty of Agricultural Engineering Sindh Agriculture University Tandojam

DOI:

https://doi.org/10.38211/joarps.2022.3.2.30

Abstract

Cadmium (Cd) is considered as phytotoxic in nature, its toxicity on the plant development decrease the antioxidative enzymes activities under stress environment. Castor (Ricinus Communis L.) is a metal tolerant plant and its ability to survive in highly polluted soils. Castor plant exhibited the high level of the Cd stress in the soil and buildup the antioxidants i.e., super oxide dismutase (SOD), peroxidase (POD) and malondialdehyde (MAD) on the top of the ground parts under Cd stress. Castor plant grown in the treated soil for 30 days in various levels of Cd 0, 10, 25 and 50 mg kg-1 soil treatments. Stress caused by heavy metal toxicity effects on reduced the plant growth, biomass, of castor plant respectively under 25- 50 mg kg-1 stress as against to control treatment. Our results indicated that castor significantly enhanced the Cd contents in root, stem and leaves. The POD and SOD enzyme activities were significantly increased 215.30 µmol/g-1 and 53.20 U/g respectively under 50 mg kg-1 stress as against control. While, MAD and chlorophyll content 3.11% and 0.48%, proline content 2.23 to 1.75 µg-1 were decreased under 25 and 50 mg kg-1 Cd stress as against control. According to Pearson’s correlation the our research work exposed strongly positive relationship with root, shoot, proline and malionaldihyde.  Although the destructive relationship was demonstrated by PoD and SOD enzyme activities. Hence, this study recommended that castor can grow in highly polluted soils for phytoremediation

Downloads

Download data is not yet available.

Metrics

Metrics Loading ...

Author Biography

Hongqing Hu, Key Laboratory of Arable Land Conservation (Middle and Lower Reaches of Yangtze River), Ministry of Agriculture, College of Resources and Environment, Huazhong Agricultural University, Wuhan 430070, China.

*Corresponding author

References

Adriano, D. C. (2001). Trace elements in terrestrial environments: biogeochemistry, bioavailability, and risks of metals (Vol. 860). New York: Springer. https://doi.org/10.1007/978-0-387-21510-5

Arshad, M., Ali, S., Noman, A., Ali, Q., Rizwan, M., Farid, M., & Irshad, M. K. (2016). Phosphorus amendment decreased cadmium (Cd) uptake and ameliorates chlorophyll contents, gas exchange attributes, antioxidants, and mineral nutrients in wheat (Triticum aestivum L.) under Cd stress. Archives of Agronomy and Soil Science, 62(4), 533-546.

Bauddh, K., & Singh, R. P. (2012). Growth, tolerance efficiency and phytoremediation potential of Ricinus communis (L.) and Brassica juncea (L.) in salinity and drought affected cadmium contaminated soil. Ecotoxicology and Environmental safety, 85, 13-22.

Chaoui, A., Mazhoudi, S., Ghorbal, M. H., & El Ferjani, E. (1997). Cadmium and zinc induction of lipid peroxidation and effects on antioxidant enzyme activities in bean (Phaseolus vulgaris L.). Plant Science, 127(2), 139-147.

Chhajro, M. A., Rizwan, M. S., Guoyong, H., Jun, Z., Kubar, K. A., & Hongqing, H. (2016). Enhanced accumulation of Cd in castor (Ricinus communis L) by soil-applied chelators. International journal of phytoremediation, 18(7), 664-670.

Chhajro, M. A., Fu, Q., Shaaban, M., Rizwan, M. S., Jun, Z., Salam, A., & Jamro, G. M. (2018). Identifying the functional groups and the influence of synthetic chelators on Cd availability and microbial biomass carbon in Cd-contaminated soil. International journal of phytoremediation, 20(2), 168-174.

Ci, D., Jiang, D., Dai, T., Jing, Q., & Cao, W. (2009). Effects of cadmium on plant growth and physiological traits in contrast wheat recombinant inbred lines differing in cadmium tolerance. Chemosphere, 77(11), 1620-1625.

Farooq, M. A., Ali, S., Hameed, A., Ishaque, W., Mahmood, K., & Iqbal, Z. (2013). Alleviation of cadmium toxicity by silicon is related to elevated photosynthesis, antioxidant enzymes; suppressed cadmium uptake and oxidative stress in cotton. Ecotoxicology and environmental safety, 96, 242-249.

Gallego, S. M., Benavides, M. P., & Tomaro, M. L. (1996). Effect of heavy metal ion excess on sunflower leaves: evidence for involvement of oxidative stress. Plant Science, 121(2), 151-159.

Guo, H., Hong, C., Chen, X., Xu, Y., Liu, Y., Jiang, D., & Zheng, B. (2016). Different growth and physiological responses to cadmium of the three Miscanthus species. PloS one, 11(4), e0153475.

Heath, R. L., & Packer, L. (1968). Photoperoxidation in isolated chloroplasts: I. Kinetics and stoichiometry of fatty acid peroxidation. Archives of biochemistry and biophysics, 125(1), 189-198.

Huang, H., Yu, N., Wang, L., Gupta, D. K., He, Z., Wang, K., & Yang, X. E. (2011). The phytoremediation potential of bioenergy crop Ricinus communis for DDTs and cadmium co-contaminated soil. Bioresource Technology, 102(23), 11034-11038.

Khan, N. A., Samiullah, Singh, S., & Nazar, R. (2007). Activities of antioxidative enzymes, sulphur assimilation, photosynthetic activity and growth of wheat (Triticum aestivum) cultivars differing in yield potential under cadmium stress. Journal of Agronomy and Crop Science, 193(6), 435-444.

Lacan, D., & Baccou, J. C. (1998). High levels of antioxidant enzymes correlate with delayed senescence in nonnetted muskmelon fruits. Planta, 204(3), 377-382.

Liu, S. L., Yang, R. J., Ma, M. D., Dan, F., Zhao, Y., Jiang, P., & Wang, M. H. (2015). Effects of exogenous NO on the growth, mineral nutrient content, antioxidant system, and ATPase activities of Trifolium repens L. plants under cadmium stress. Acta Physiologiae Plantarum, 37(1), 1-16.

Roychoudhury, A., Basu, S., & Sengupta, D. N. (2012). Antioxidants and stress-related metabolites in the seedlings of two indica rice varieties exposed to cadmium chloride toxicity. Acta Physiologiae Plantarum, 34(3), 835-847.

Shi, G., & Cai, Q. (2009). Cadmium tolerance and accumulation in eight potential energy crops. Biotechnology Advances, 27(5), 555-561.

Shi, G., Xia, S., Ye, J., Huang, Y., Liu, C., & Zhang, Z. (2015). PEG-simulated drought stress decreases cadmium accumulation in castor bean by altering root morphology. Environmental and Experimental Botany, 111, 127-134.

Szőllősi, R., Varga, I. S., Erdei, L., & Mihalik, E. (2009). Cadmium-induced oxidative stress and antioxidative mechanisms in germinating Indian mustard (Brassica juncea L.) seeds. Ecotoxicology and environmental safety,72(5), 1337-1342.

Bor, M., Özdemir, F., & Türkan, I. (2003). The effect of salt stress on lipid peroxidation and antioxidants in leaves of sugar beet Beta vulgaris L. and wild beet Beta maritima L. Plant science, 164(1), 77-84.

Vaculík, M., Lux, A., Luxová, M., Tanimoto, E., & Lichtscheidl, I. (2009). Silicon mitigates cadmium inhibitory effects in young maize plants. Environmental and Experimental Botany, 67(1), 52-58.

Wu, Z., Zhao, X., Sun, X., Tan, Q., Tang, Y., Nie, Z., ... & Hu, C. (2015). Antioxidant enzyme systems and the ascorbate–glutathione cycle as contributing factors to cadmium accumulation and tolerance in two oilseed rape cultivars (Brassica napus L.) under moderate cadmium stress. Chemosphere, 138, 526-536.

Xi, T., Xing, H., Shi, W., Wu, Y., & Zhou, P. (2012). Preparation and characterization of artificial antigens for cadmium and lead. Biological trace element research, 150(1), 411-417.

Xu, X., Liu, C., Zhao, X., Li, R., & Deng, W. (2014). Involvement of an antioxidant defense system in the adaptive response to cadmium in maize seedlings (Zea mays L.). Bulletin of environmental contamination and toxicology, 93(5), 618-624.

Zhang, H., Guo, Q., Yang, J., Shen, J., Chen, T., Zhu, G., & Shao, C. (2015). Subcellular cadmium distribution and antioxidant enzymatic activities in the leaves of two castor (Ricinus communis L.) cultivars exhibit differences in Cd accumulation. Ecotoxicology and environmental safety, 120, 184-192.

Zhang, X., Chen, D., Zhong, T., Zhang, X., Cheng, M., & Li, X. (2015). Assessment of cadmium (Cd) concentration in arable soil in China. Environmental Science and Pollution Research, 22(7), 4932-4941.

Zhou, W., & Qiu, B. (2005). Effects of cadmium hyperaccumulation on physiological characteristics of Sedum alfredii Hance (Crassulaceae). Plant Science, 169(4), 737-745.

Downloads

Published

2022-09-01

How to Cite

Chhajro, M. A., Hu, H., Kubar, K. A., Kalhoro, S. A., Narejo, M. un N., Sarfaraz, Q., … Magsi, S. (2022). Physiological and Growth Responses of Castor (Ricinus Communis L) Under Cadmium Stressed Environment. Journal of Applied Research in Plant Sciences , 3(02), 242–247. https://doi.org/10.38211/joarps.2022.3.2.30

Funding data

Most read articles by the same author(s)