Bioaccumulation and dietary exposure of the Red-Crowned Cranes (Grus japonensis) to arsenic in Zhalong Wetland, northeastern China
Keywords:
arsenic contamination, habitat of Red-Crowned Crane, aquatic animal, food chain, risk, geo-accumulation indexAbstract
Arsenic concentrations in the habitat and the prey of the Red-Crowned Crane (i.e. reed rhizomes and three aquatic animal families [Perccottus glehni Dybowski, Cybister japonicus Sharp and Viviparidae]) were analyzed to examine the bioaccumulation of arsenic in Red-Crowned Cranes in northeastern China. The results indicated that arsenic concentrations in the prey of the Red-Crowned Cranes were elevated via food chain. Most of the detected arsenic contents in the sediments were below the natural background level (7.49 ppm) and ranged from 0.34 to 8.32 ppm (dry weight). The geo-accumulation indices at all sites were less than 0, which suggests the region had only background concentrations of arsenic. Three aquatic animal families were observed to contain some arsenic, with the following order of increasing concentrations: primary consumer < secondary consumers. The arsenic concentrations of sediments and water animals in the buffer zone were significantly higher than those in the core area, and increased in higher trophic level animals. The highest arsenic metal concentrations were found in the livers of the Red-Crowned Cranes (in a range of 145.46 ppb to 367.78 ppb) compared with the kidneys (116.44 ppb to 257.46 ppb) and muscles (63.45 ppb to 94.26 ppb). By contrast, the feathers had the lowest concentrations, with an average of 32.25 ppb. The dietary exposure level of arsenic to the Red-Crowned Crane population in Zhalong wetland of northeastern China appeared to be below arsenic toxicity threshold concentrations.
References
Abedin, M. J., Feldmann, J., Meharg, A. A., 2002. Uptake kinetics of arsenic species in rice plants. Plant Physiology 128, 1120–1128.
Agah, H., Leermakers, M., Elskens, M., Mohamad Rez Fatemi, S., Baeyens, W., 2009. Accumulation of trace metals in the muscle and liver tissues of five fish species from the Persian Gulf. Environ. Monit. Assess. 157, 499–514.
BirdLife International, 2012. Grus monacha: IUCN 2012. IUCN Red List of Threatened Species. Version 2012. 4. http://www.birdlife.org/datazone/speciesfactsheet.
Burger, J., Gochfeld, M., 1997. Risk, Mercury Levels, and Birds: Relating Adverse Laboratory Effects to Field Biomonitoring. Environmental Research, 75, 160–172.
Burger, J., Gochfeld, M., Jeitner, C., Snigaroff, D., Snigaroff, D., Stamm, T., Volz, C., 2008. Assessment of metals in down feathers of female common eiders and their eggs from Aleutians: arsenic, cadmium, chromium, lead,manganese, mercury, and selenium. Environ.Monit. Assess. 143, 247–256.
Canli, M., Ay, O., Kalay, M., 1998. Levels of heavy metals (Cd, Pb, Cu, Cr and Ni) in tissue of Cyprinus carpio, Barbus capito and Chondrostoma regium from the Seyhan River, Turkey. Turkish Journal of Zoology, 22, 149–157.
Eisler, R., 1988. Arsenic hazards to fish, wildlife, and invertebrates: a synoptic review. Contaminant hazard reviews: U.S. Fish Wildl. Serv. Biol. Rep., 85(1.12).
EPA., 1980. Ambient water quality criteria for arsenic. U.S. Environ. Protection Agency Rep. 440/5-80-021.
Fasola, M., Movalli, P. A., Gandini, C., 1998. Heavy Metal, Organochlorine Pesticide, and PCB Residues in Eggs and Feathers of Herons Breeding in Northern Italy. Arch. Environ. Contam. Toxicol.. 34, 87–93.
Fisk A, deWit C, Wayland M, Kuzyk Z Z, Burgess N, Lethcer R, Branue B, Norstrom R, Blum S P, Sandau C, Lie E, Larsen H J S, Skaare J U., 2005. Assessment of toxicological significance of anthropogenic contaminants in Canadian artic wildlife. Science of the total Enviroment, 351-352, 57–93.
Fleischer, M., Sarofim, A. F., Fassett, D. W., Hammond, P., Shacklette, H. T., Nisbet, I. C. T., and Epstein, S., 1974. Environmental impact of cadmium, Environ. Health Perspect. 5, 253.
Gulz, P. A., Gupta, S. K., Schulin, R., 2005. Arsenic accumulation of common plants from contaminated soil. Plant and Soil, 272, 337–347.
Hansan, S. A., Fariduddin, Q., Ali, B., 2009. Cadmium: Toxicity and tolerance in plants. Journal of Environmental Biology 20(2), 165–174.
Harris, J., 2008. Cranes respond to climate change. ICF Bugle 34, 1-3, 14–15.
Hughes, M. K., Lepp, N. W., and Phipps, D. A., 1980. Aerial heavy metal pollution and terrestrial ecosystems. Adv. Ecol. Res., 11, 217.
Kabata-Pendias, A., Pendias, H. (Eds), 2001. Trace elements in soils and plants, 3rd Edition. CRC Press, Boca Raton, London, New York, Washington, D. C.
Koller, L. D., 1980. Immunotoxicology of heavy metals. Int. J. Immunopharmacol 2, 269–279.
Li, J. and Zheng, C. J. (Eds), 2008. Handbook of environmental background concentration of heavy metals in China., China Environmental Science Press, Beijing, P.R. China (In Chinese).
Ma, Y. and Li, X. (Eds), 2002. Research on the Red-Crowned Crane. Shanghai Scientific & Technological Education Press, Shanghai, P.R.China (In Chinese).
Malik, N., Biswas, A. K., Qureshi, T. A., Borana, K., Virha, R., 2010. Bioaccumulation of heavy metals in fish tissues of a freshwater lake of Bhopal. Environ Monit Assess. 160, 267–276.
Martínez-Villegas, N., Flores-Vélez, L. M., Domínguez, O., 2004. Sorption of lead in soil as a function of pH: a study case in México. Chemosphere, 57, 1537–1542.
Muller, G.., 1969. Index of geo-accumulation in sediments of the Rhine River. Geo. J. 2 (3), 108–118.
Nsikak, U. B., Joseph, P. E., Akan, B. W., David, E. B., 2007. Mercury accumulation in fishes from tropical aquatic ecosystems in the Niger Delta, Nigeria. Current Science, 92(6), 781–785.
Sekabira, K., Oryem Origa, H., Basamba, T. A., Mutumba, G., Kakudidi, E., 2010. Assessment of heavy metal pollution in the urban stream sediments and its tributaries. Int. J. Environ. Sci. Tech. 7(3), 435–446.
Shaw, J.R., Jackson, B., Garor, K., Stanton, S., Hamilton, J. W., Stanton, B., 2007. The influence of exposure history on arsenic accumulation and toxicity in the Killifish, Fundulus Heteroclitus. Environmental Toxicology and Chemistry 26(12), 2704–2709.
Takazawa, Y., Kitamura, K., Yoshikane, Y., Morita, M., 2004. Discovery of Fenthion poisoning in two Japanese cranes (Grus japonensis) found dead in Hokkaida, Japan. Bull. Environ. Contam. Toxicol. 73, 947–954.
Teraoka, H., Kumagai, Y., Iwai, H., Haraguchi, K., Ohba, T., Nakai, K., Satoh, H., Sakamoto, M., Momose, K., Masatomi, H., Hiraga, T., 2007. Heavy metal contamination status of Japanese cranes (Grus japonensis) in east Hokkaido,Japan-extensive mercury pollution. Environ Toxicol Chem. 26, 307–312.
USEPA, 1996. Method 3050B-Acid digestion of sediments, sludges, and soils. U.S. Environmental Protection Agency, Washington, USA.
Viklander, M. 1998. Particle Size Distribution and Metal Content in Street Sediments. J. Environ. Eng. 124, 761–766.
Williams, P. N, Villada, A., Deacon, C., Raab, A., Figuerola, J., Green, A. J., Feldmann, J. Meharg, A. A., 2007. Greatly enhanced arsenic shoot assimilation in rice leads to elevated grain levels compared to wheat and barley. Environmental Science & Technology 41, 6854–6859.
Zhang, Y., Ruan, L., Fasola, M., Boncompagni, E., Dong, Y., Dai. N., Gandini, C., Orvin, E., and Ruiz, X., 2006. Little Egrets (Egretta Garzetta) and trace metal contamination in wetlands of China. Environ. Monit. Assess. 118, 355–368.
Zuo, P., Zhao, S., Zhao, X., Teng, H., Geng, J., Gao, X., 2010. Distribution characteristics of heavy metals in surface sediments in original salt marshes in Yancheng, Jiangsu Province, China. Marine Sci. Bul. 29, 372–377 (In Chinese).
Published
Issue
Section
License
Manuscripts must be original. They must not be published or be under consideration for publication elsewhere, in whole or in part. It is required that the lead author of accepted papers complete and sign the MSU Press AEHM Author Publishing Agreement and provide it to the publisher upon acceptance.