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Persistent Organochlorine Pollutants (POPs) and DNA Damage in Giant Toads (Rhinella marina) from an Industrial Area at Coatzacoalcos, Mexico

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Abstract

Coatzacoalcos River Basin is one of the most important hydrological and ecological regions of Mexico. Persistent organic pollutants (POPs) and other contaminants have been detected in several environmental matrices in the region. So far, there have been a few efforts to evaluate exposure and effects on wildlife in the area. The purpose of this research work is to measure exposure to POPs and deoxyribonucleic acid (DNA) damage in specimens of giant toads (Rhinella marina) taken from two zones near the industrial complex by the lower Coatzacoalcos River. Total POPs levels in soil and toads' tissues are between 660.5 and 2,712.9 ng/g d.w. and 55.6 and 1,2471.9 ng/g l.w., respectively. We found differences between the body burdens of POPs from different toad tissues evaluated but it did not happen by site type. DNA damage in blood varies from 0.7 to 4.8 (olive tail moment) and 7.4 to 16.7 μm (tail length). DNA damage is found to be higher at industrial zones compared with urban zones. This study provides a data baseline about the POPs pollution status in soil and giant toads of the lower Coatzacoalcos River in Veracruz.

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References

  • ATSDR. (2002a). Toxicological profile for hexachlorobenzene. Atlanta: Agency for Toxic Substances and Disease Registry. 447 pp.

  • ATSDR. (2002b). Toxicological profile for DDT, DDE, and DDD. Atlanta: Agency for Toxic Substances and Disease Registry. 497 pp.

  • ATSDR. (2004). Toxicological profile for polybrominated biphenyls and polybrominated diphenyl ethers (PBBs and PBDEs). Atlanta: Agency for Toxic Substances and Disease Registry. 618 pp.

  • Bahena-Manjarrez, J. L., Rosales-Hoz, L., & Carranza-Edwards, A. (2002). Spatial and temporal variation of heavy metals in a tropical estuary. Environmental Geology, 42, 575–582.

    Article  CAS  Google Scholar 

  • Bernanke, J., & Köhler, H. R. (2009). The impact of environmental chemicals on wildlife vertebrates. Reviews of Environmental Contamination and Toxicology, 198, 1–47.

    Article  CAS  Google Scholar 

  • Bonin, J., DesGranges, J. L., Bishop, C. A., Rodrigue, J., Gendron, A., & Elliott, J. E. (1995). Comparative study of contaminants in the mudpuppy (Amphibia) and the common snapping turtle (Reptilia), St. Lawrence River, Canada. Archives of Environmental Contamination and Toxicology, 28, 184–194.

    Article  CAS  Google Scholar 

  • Buccini, J. (2003). The development of a global treaty on persistent organic pollutants (POPs). In H. Fiedler (Ed.), The handbook of environmental chemistry, Vol. 3, part O: persistent organic pollutants (pp. 13–30). Berlin: Springer.

    Chapter  Google Scholar 

  • Clarke, K. R. (1993). Non-parametric multivariate analyses of changes in community structure. Australian Journal of Ecology, 18, 117–143.

    Article  Google Scholar 

  • Collins, J. P., & Storfer, A. (2003). Global amphibian declines: sorting the hypotheses. Diversity and Distributions, 9, 89–98.

    Article  Google Scholar 

  • Collins, A. R., Azqueta, A. O., Brunborg, G., Gaivão, I., Giovannelli, L., Kruszewski, M., Smith, C. C., & Štětina, R. (2008). Comet assay: topical issues. Mutagenesis, 23, 143–151.

    Article  CAS  Google Scholar 

  • Cotelle, S., & Férard, J. F. (1999). Comet assay in genetic ecotoxicology: a review. Environmental and Molecular Mutagenesis, 34, 246–55.

    Article  CAS  Google Scholar 

  • DeGarady, C. J., & Halbrook, R. S. (2003). Impacts from PCB accumulation on amphibians inhabiting streams flowing from the Paducah gaseous diffusion plant. Archives of Environmental Contamination and Toxicology, 45, 525–532.

    Article  CAS  Google Scholar 

  • Dhawan, A., Bajpayee, M., & Parmar, D. (2009). Comet assay: a reliable tool for the assessment of DNA damage in different model. Cell Biology and Toxicology, 25, 5–32.

    Article  CAS  Google Scholar 

  • Díaz-Barriga, F., Borja-Aburto, V., Waliszewski, S., & Yáñez, L. (2003). DDT in Mexico. In H. Fiedler (Ed.), The handbook of environmental chemistry vol. 3, part O: persistent organic pollutants (pp. 371–388). Berlin: Springer.

    Chapter  Google Scholar 

  • Dohm, M. R., Mautz, W. J., Doratt, R. E., & Stevens, J. R. (2008). Ozone exposure affects feeding and locomotor behavior of adult Bufo marinus. Environmental Toxicology and Chemistry, 27, 1209–1216.

    Article  CAS  Google Scholar 

  • Espinosa-Reyes, G., Ilizaliturri, C. A., González-Mille, D. J., Costilla, R., Díaz-Barriga, F., Cuevas, M. C., et al. (2010). DNA damage in earthworms (Eisenia spp.) as an indicator of environmental stress in the industrial zone of Coatzacoalcos, Veracruz, Mexico. Journal of Environmental Science and Health, Part A, 45, 49–55.

    Article  CAS  Google Scholar 

  • Fellers, G. M., McConnell, L. L., Pratt, D., & Datta, S. (2004). Pesticides in mountain yellow-leggend frogs (Rana muscosa) from the Sierra Nevada Mountains of California, USA. Environmental Toxicology and Chemistry, 23, 2170–2177.

    Article  CAS  Google Scholar 

  • Frenzilli, G., Nigro, M., & Lyons, B. P. (2009). The comet assay for the evaluation of genotoxic impact in aquatic environments. Mutation Research, Reviews in Mutation Research, 681, 80–92.

    Article  CAS  Google Scholar 

  • Gillilland, C. D., Summer, C. L., Gillilland, M. G., Kannan, K., Villeneuve, D. L., Coady, K. K., Muzzall, P., Mehne, C., & Giesy, J. P. (2001). Organochloride insecticides, polychlorinated biphenyls, and metals in water, sediment, and green frogs from southwestern Michigan. Chemosphere, 44, 327–339.

    Article  CAS  Google Scholar 

  • Glennemeier, K. A., & Begnoche, L. J. (2002). Impact of organochlorine contamination on amphibian populations in southwestern Michigan. Journal of Herpetology, 36, 233–244.

    Google Scholar 

  • Gonzalez-Mille, D. J., Ilizaliturri-Hernández, C. A., Espinosa-Reyes, G., Costilla-Salazar, R., Díaz-Barriga, F., Ize-Lema, I., & Mejía-Saavedra, J. (2010). Exposure to persistent organic pollutants (POPs) and DNA damage as an indicator of environmental stress in fish of different feeding habits of Coatzacoalcos, Veracruz, Mexico. Ecotoxicology, 19, 1238–1248.

    Article  CAS  Google Scholar 

  • Hall, R. J., Driscoll, C. T., Likens, G. E., & Pratt, J. M. (1985). Physical, chemical, and biological consequences of episodic aluminum additions to a stream. Limnology and Oceanography, 30, 212–220.

    Article  CAS  Google Scholar 

  • Huang, D., Zhang, Y., Wang, Y., Xie, Z., & Ji, W. (2007). Assessment of the genotoxicity in toad Bufo raddei exposed to petrochemical contaminants in Lanzhou Region, China. Mutation Research, 629, 81–88.

    Article  CAS  Google Scholar 

  • Ilizaliturri-Hernández, C. A., González-Mille, D. J., Mejía-Saavedra, J., Espinosa-Reyes, G., Torres-Dosal, A., & Pérez-Maldonado, I. (2013). Blood lead levels, δ-ALAD inhibition, and hemoglobin content in blood of giant toad (Rhinella marina) to assess lead exposure in three areas surrounding an industrial complex in Coatzacoalcos, Veracruz, Mexico. Environmental Monitoring Assessment, 85, 1685–98.

    Article  Google Scholar 

  • INEGI. (2013). Anuario estadístico de Veracruz de Ignacio de la Llave: ganadería. Instituto Nacional de Estadística y Geografía (INEGI). Available in: http://www.inegi.org.mx/sistemas/biblioteca/detalle.aspx?c=265&upc=702825045258&s=inegi&tg=13&f=2&pf=prod&ef=30&cl=0. Accessed May 2013.

  • Jofré, M. B., Antón, R. I., & Caviedes-Vidal, E. (2008). Organochlorine contamination in anuran amphibians of an artificial lake in the semiarid midwest of Argentina. Archives of Environmental Contamination and Toxicology, 55, 471–80.

    Article  Google Scholar 

  • Karasov, W. H., Jung, R. E., Vanden Langenberg, S., & Bergenson, T. L. E. (2005). Field exposure of frog embryos and tadpoles along a pollution gradient in the Fox River and Green Bay ecosystem in Wisconsin, USA. Archives of Environmental Contamination and Toxicology, 24, 942–953.

    CAS  Google Scholar 

  • Kirk, J. J. (1988). Western spotted frog (Rana pretiosa) mortality following forest spraying of DDT. Herpetological Review, 19, 51–53.

    Google Scholar 

  • Kruskal, J. B. (1964). Multidimensional scaling by optimizing goodness of fit to a nonmetric hypothesis. Psychometrika, 29, 1–27.

    Article  Google Scholar 

  • Kumaravel, T. S., Vilhar, B., Faux, S. P., & Jha, A. N. (2009). Comet assay measurements: a perspective. Cell Biology and Toxicology, 25, 53–6.

    Article  CAS  Google Scholar 

  • Lee, R. F., & Steinert, S. (2003). Use of the single cell gel electrophoresis/comet assay for detecting DNA damage in aquatic (marine and freshwater) animals. Mutation Research, 544, 43–64.

    Article  CAS  Google Scholar 

  • Li, X., Li, S., & Liu, G. Z. (2010). Lethal effect and in vivo genotoxicity of profenofos to Chinese native amphibian (Rana spinosa) tadpoles. Archives of Environmental Contamination and Toxicology, 59, 478–483.

    Article  CAS  Google Scholar 

  • Linzey, D. W., Burroughs, J., Hudson, L., Marini, M., Robertson, J., Bacon, J. P., Nagarkatti, M., & Nagarkatti, P. S. (2003). Role of environmental pollutants on immune functions, parasitic infections and limp malformations in marine toads and whistling frogs from Bermuda. International Journal of Environmental Health Research, 13, 125–148.

    Article  CAS  Google Scholar 

  • Loveridge, A. R., Bishop, C. A., Elliot, J. E., & Kennedy, C. J. (2007). Polychlorinated biphenyls and organochlorine pesticides bioaccumulated in green frogs, Rana clamitans, from the lower Fraser Valley, British Columbia, Canada. Bulletin of Environmental Contamination and Toxicology, 79, 315–8.

    Article  CAS  Google Scholar 

  • Maselli, V., Polese, G., Rippa, D., Ligrone, R., Rastogi, R. K., & Fulgione, D. (2010). Frogs, sentinels of DNA damage induced by pollution in Naples and the neighbouring provinces. Ecotoxicology and Environmental Safety, 73, 1525–1529.

    Article  CAS  Google Scholar 

  • McCoy, K. A., Bortnick, L. J., Campbell, C. M., Hamlin, H. J., Guillette, L. J., & St Mary, C. M. (2008). Agriculture alters gonadal form and function in the toad Bufo marinus. Environmental Health Perspectives, 116, 1526–1532.

    Article  Google Scholar 

  • Pastor, D., Sanpera, C., Gonzalez-Solis, J., Ruiz, X., & Albaiges, J. (2004). Factors affecting the organochlorine pollutant load in biota of a rice field ecosystem (Ebro Delta, NE Spain). Chemosphere, 55, 567–576.

    Article  CAS  Google Scholar 

  • Pelallo-Martínez, N. A., Ilizaliturri-Hernández, C. A., Espinosa-Reyes, G., Carrizales-Yáñez, L., & González-Mille, D. J. (2011). Assessment of exposure to lead in humans and turtles living in an industrial site in Coatzacoalcos, Veracruz, Mexico. Bulletin of Environmental Contamination and Toxicology, 86, 642–645.

    Article  Google Scholar 

  • Phaneuf, D., DesGrandes, J. L., Plante, N., & Rodrigue, J. (1995). Contamination of local wildlife following a fire at a polychlorinated-biphenyls warehouse in St Basile Le Grand, Quebec, Canada. Archives of Environmental Contamination and Toxicology, 28, 145–153.

    Article  CAS  Google Scholar 

  • Ralph, S., & Petras, M. (1997). Genotoxicity monitoring of small bodies of water using two species of tadpoles and the alkaline single cell gel (comet) assay. Environmental and Molecular Mutagenesis, 29, 418–30.

    Article  CAS  Google Scholar 

  • Rico, C., Hernandez, L. M., Gonzalez, J., Fernandez, M. A., & Montero, M. C. (1987). Organochlorine and metal pollution in aquatic organisms sampled in the Donna National Park during the period 1983–1986. Bulletin of Environmental Contamination and Toxicology, 39, 1076–1083.

    Article  CAS  Google Scholar 

  • Rosales-Hoz, L., & Carranza-Edwards, A. (1998). Heavy metals in sediments from Coatzacoalcos River, Mexico. Bulletin of Environmental Contamination and Toxicology, 60, 553–561.

    Article  CAS  Google Scholar 

  • Rosales-Hoz, L., Cundy, A. B., & Bahena-Manjarrez, J. L. (2003). Heavy metals in sediment cores from a tropical estuary affected by anthropogenic discharges: Coatzacoalcos estuary, Mexico. Estuarine, Coastal and Shelf Science, 58, 117–126.

    Article  CAS  Google Scholar 

  • Russell, R. W., Hecnar, S. J., & Haffner, G. D. (1995). Organochlorine pesticide residues in southern Ontario spring peepers. Archives of Environmental Contamination and Toxicology, 14, 815–818.

    CAS  Google Scholar 

  • Russell, R. W., Gillan, K. A., & Haffner, G. D. (1997). Polychlorinated biphenyls and chlorinated pesticides in southerm Ontario, Canada, green frogs. Archives of Environmental Contamination and Toxicology, 16, 2258–2263.

    CAS  Google Scholar 

  • Russell, R. W., Lipps, G. J., Hecnar, S. J., & Haffner, G. D. (2002). Persistent organic pollutants in Blanchard's cricket frogs (Acris crepitans blanchardi) from Ohio. The Ohio Journal of Science, 102, 119–122.

    CAS  Google Scholar 

  • Singh, N. P., McCoy, M. T., Tice, R. R., & Schneider, E. L. (1988). A simple technique for quantitation of low levels of DNA damage in individual cells. Experimental Cell Research, 175, 184–191.

    Article  CAS  Google Scholar 

  • Sparling, D. W., Linder, G., Bishop, C. A. (2010). Ecotoxicology of amphibians and reptiles. 2nd ed. Pensacola, FL: Society of Environmental Toxicology and Chemistry (SETAC). 944 pp.

  • Stringer, R., Labunska, I., & Brigden, K. (2001). Organochlorine and heavy metal contaminants in the environment around the complejo petroquimicos Paharitos, Coatzacoalcos. Mexico. Technique note Greenpeace Research Laboratories: University of Exeter, UK. 60 pp.

    Google Scholar 

  • Trejo-Acevedo, A., Díaz-Barriga, F., Carrizales, L., Domínguez, G., Costilla, R., Ize-Lema, I., et al. (2009). Exposure assessment of persistent organic pollutants and metals in Mexican children. Chemosphere, 74, 974–980.

    Article  CAS  Google Scholar 

  • Walker, C. H. (2009). Organic pollutants: an ecotoxicological perspective (2nd ed.). Boca Raton: CRC. 408 pp.

    Google Scholar 

  • Wang, M. Z., & Jia, X. Y. (2009). Low levels of lead exposure induce oxidative damage and DNA damage in the testes of the frog Rana nigromaculata. Ecotoxicology, 18, 94–99.

    Article  Google Scholar 

  • Willett, K. L., Ulrich, E. M., & Hites, R. A. (1998). Differential toxicity and environmental fates of hexachlorocyclohexane isomers. Environmental Science & Technology, 32, 2197–2207.

    Article  CAS  Google Scholar 

  • Yim, U. H., Hong, S. H., Shim, W. J., & Oh, J. R. (2005). Levels of persistent organochlorine contaminants in fish from Korea and their potential health risk. Archives of Environmental Contamination and Toxicology, 48, 358–366.

    Article  CAS  Google Scholar 

  • Yin, X. H., Li, S. N., Zhang, L., Zhu, G. N., & Zhuang, H. S. (2008). Evaluation of DNA damage in Chinese toad (Bufo bufo gargarizans) after in vivo exposure to sublethal concentrations of four herbicides using the comet assay. Ecotoxicology, 17, 280–286.

    Article  CAS  Google Scholar 

  • Yin, X. H., Zhu, G. N., Li, X. B., & Liu, S. Y. (2009). Genotoxicity evaluation of chlorpyrifos to amphibian Chinese toad (Amphibian: Anura) by comet assay and micronucleus test. Mutation Research/Genetic Toxicology and Environmental Mutagenesis, 680, 2–6.

    Article  CAS  Google Scholar 

  • Zug, G. R., Zug, P. B. (1979). The marine toad, Bufo marinus: a natural history resume of native populations. Washington, D.C: Smithsonian Contribution to Zoology No, 284, Smithsonian Institution Press, 58 pp.

  • Zupanovic, Z., Musso, C., Lopez, G., Louriero, C. L., Hyatt, A. D., Hengstberger, S., & Robinson, A. J. (1998). Isolation and characterization of iridoviruses from the giant toad Bufo marinus in Venezuela. Diseases of Aquatic Organisms, 33, 1–9.

    Article  CAS  Google Scholar 

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Acknowledgments

This work was supported by a grant from the Dirección General de Investigación sobre la Contaminación Urbana y Regional del Instituto Nacional de Ecología [No. de convenio INE/A1-047/2007] SEMARNAT and Commission For Environmental Cooperation as part of the National Program for Environmental Monitoring and Assessment [No. de convenio N/D 241.0261 File 2011–1014] coordinated by the Dirección General del Centro Nacional de Investigación y Capacitación Ambiental del Instituto Nacional de Ecología y Cambio Climático. Special thanks to Prof. J. Jesus Guerrero Cabrera from the language center of San Luis Potosí Autonomous University and Mark Blackman for English language editing of the manuscript. We also would like to thank PhD. María del Carmen Cuevas Díaz of the Veracruz University Campus at Coatzacoalcos for providing laboratory facilities.

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Correspondence to César A. Ilizaliturri-Hernández.

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Gonzalez-Mille, D.J., Espinosa-Reyes, G., Rivero-Pérez, N.E. et al. Persistent Organochlorine Pollutants (POPs) and DNA Damage in Giant Toads (Rhinella marina) from an Industrial Area at Coatzacoalcos, Mexico. Water Air Soil Pollut 224, 1781 (2013). https://doi.org/10.1007/s11270-013-1781-0

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