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Organochlorine contaminants in a coastal lagoon in Argentina: Analysis of sediment, crabs, and cordgrass from two different habitats

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Abstract

Burrowing crabs (Chasmagnathus granulata), sediment collected from inside and outside crab burrows as well as outside the crab bed, and cordgrass (Spartina densiflora) were collected from intertidal mudflat and cordgrass marsh habitats and analyzed for concentrations of polychlorinated biphenyl (PCB) congeners and organochlorine (OC) compounds to test the hypothesis that there are differences in the distribution and bioaccumulation of OC contaminants in coastal lagoon habitats in Argentina. PCB concentrations were relatively low, although the penta- and hexachlorobiphenyl detected in sediments and biota indicated that there had been direct inputs of PCBs into the ecosystem. Heptachlor epoxide, dieldrin, endosulfan sulphate, chlordane compounds, DDT and metabolites, and hexachlorocyclohexanes (HCHs) were the major pesticides detected in sediment and biota samples. When lipid-normalized concentration data for all OC pesticides in crabs were summed together (ΣOCC), there were higher concentrations in crabs from the cordgrass habitat in comparison to crabs from the mudflat. In sediment samples, there were no significant differences in percent organic matter of marsh and mudflat sediments, but the concentrations of ΣOCC normalized to organic carbon were higher in the sediments collected in the cordgrass marsh. Samples of rhizomes and roots from the cordgrass contained high concentrations of OC compounds and it was estimated that 2.4 kg of heptachlor epoxide, the most abundant OC pesticide, may be present in the total cordgrass root biomass in Mar Chiquita lagoon. These data indicated that the cordgrass in coastal lagoon environments is an important factor in determining the distribution of persistent contaminants, and that a significant portion of the total burden of these hydrophobic compounds may be deposited in cordgrass biomass.

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Literature Cited

  • Adams, P. 1990. Saltmarsh Ecology. Cambridge Studies in Ecology. Cambridge University Press, Cambridge, England.

    Google Scholar 

  • Berril, M., D. Coulson, L. McGillivray, andB. Pauli. 1998. Toxicity of endosulfan to aquatic stages of anuran amphibians.Environmental Toxicology and Chemistry 17:1738–1744.

    Article  Google Scholar 

  • Bilyard, G. R. 1987. The value of benthic infauma in marine pollution monitoring studies.Marine Pollution Bulletin 18:581–585.

    Article  CAS  Google Scholar 

  • Black, C. A. 1965. Methods of Soil Analysis. American Society of Agronomy, Madison, Wisconsin.

    Google Scholar 

  • Bortolus, A. andO. Iribarne. 1999. Effects of the burrowing crabChasmagnathus granulata on aSpartina salt marsh.Marine Ecology Progress Series 178:78–88.

    Article  Google Scholar 

  • Botto, F. andO. Iribarne. 1999. The effect of the burrowing crabChasmagnathus granulata on the benthic community of a SW Atlantic coastal lagoon.Journal of Experimental marine Biology and Ecology 241:263–284.

    Article  Google Scholar 

  • Colombo, J. L., M. F. Khalil, M. Arnac, A. C. Horth, andJ. A. Catoggio. 1990. Distribution of chlorinated pesticides and individual polychlorinated biphenyls in biotic and abiotic compartments of the Río de la Plata, Argentina.Environmental Science Technology 24:498–505.

    Article  CAS  Google Scholar 

  • Connell, D. W. 1997. Basic Concepts of Environmental Chemistry. Lewis Publishers, New York.

    Google Scholar 

  • Dannenberger, D. 1996. Chlorinated microcontaminants in surface sediments of the Baltic Sea—Investigations in the Belt Sea, the Arkona Sea and the Pomeranian Bight.Marine Pollution Bulletin 32:772–781.

    Article  CAS  Google Scholar 

  • Duinker, J. C., M. T. J. Hillebrand, andJ. P. Boon. 1983. Organochlorines in benthic invertebrates and sediments from the Dutch Wadden Sea.Netherland Journal of Sea Research 17: 19–38.

    Article  CAS  Google Scholar 

  • Everaarts, J. M., R. Heesters, C. V. Fischer, and M. T. J. Hillebrand. 1993. Baseline levels of cyclic pesticides and PCBs in benthic invertebrates from the continental slope of the Bane d’Arguin (Mauritania).Marine Pollution Bulletin 26:515–521.

    Article  CAS  Google Scholar 

  • Everaarts, J. M., B. Nasreen, C. Swennen, andT. J. Hillebrand. 1991. Cyclic chlorinated hydrocarbons in benthic invertebrates from three coastal areas in Thailand and Malaysia.Journal of Science Society of Thailand 17:31–49.

    Article  CAS  Google Scholar 

  • Faggi, A. M., M. Cagnoli, and P. Otero. 1997. Mar Chiquito: Nueva Reserva de la Biosfera. Actas 6° Encuentro de Geógrafos de América Latina. Buenos Aires. Argentina.

  • Farrington, J. W. andJ. Westal. 1986. Organic chemical pollutants in the oceans and groundwater: A review of fundamental chemical properties and biogeochemistry, p. 361–426.In G. Kullenberg (ed.), Scientific Basis for the Role of the Oceans as a Waste Disposal Option. North Atlantic Treaty Organization Advanced Research Workshop Proceedings. Riedel Publishing Co., Dordrecht, Netherlands.

    Google Scholar 

  • Fasano, J. L., M. A. Hernandez, F. J. Isla, and E. J. Schnack. 1982. Aspectos evolutivos y ambientales de la laguna Mar Chiquita (provincia de Buenos Aires, Argentina).Oceanologica Acta No SP:285–292.

    Google Scholar 

  • Feng, H., J. K. Cochran, H. Lwiza, B. J. Brownawell, andD. J. Hirschberg. 1998. Distribution of heavy metal and PCB contaminant in the sediments of an urban estuary: The Hudson river.Marine Environmental Research 45:69–88.

    Article  CAS  Google Scholar 

  • Froese, K. L., D. A. Verbrugge, G. T. Ankley, G. J. Niemi, C. P. Larsen, andJ. P. Giesy. 1998. Bioaccumulation of polychlorinated biphenyls from sediments to aquatic insects and tree swallow eggs and nestlings in Saginaw Bay, Michigan, USA.Environmental Toxicology and Chemistry 17:484–492.

    Article  CAS  Google Scholar 

  • Gobas, F. A. P. C., E. J. McNeil, L. Loveit-Doust, andD. Haffner. 1991. Bioconcentration of chlorinated aromatic hydrocarbons in aquatic macrophytes.Environmental Science Technology 25:924–929.

    Article  CAS  Google Scholar 

  • Hendy, E. J. andB. M. Peake. 1996. Organochlorine pesticides in a dated sediment core from Mapua, Waimea Inlet, New Zealand.Marine Pollution Bulletin 32:751–754.

    Article  CAS  Google Scholar 

  • Iribarne, O., A. Bortolus, andF. Botto. 1997. Between-habitats differences in burrow characteristics and trophic modes in the southwestern Atlantic burrowing crabChasmagnathus granulata.Marine Ecology Progress Series 155:132–145.

    Article  Google Scholar 

  • Keith, L. H., W. Crummett, J. Deegan, R. A. Libby, J. K. Taylor, andG. Wentler. 1983. Principles of environmental analysis.Analytical Chemistry 55:2210–2218.

    Article  CAS  Google Scholar 

  • Kukkonen, J. andP. F. Landrum. 1996. Distribution of organic carbon and organic xenobiotics among different particle-size fractions in sediments.Chemosphere 32:1063–1076.

    Article  CAS  Google Scholar 

  • Lanfranchi, A. L., J. E. A. de Moreno, V. J. Moreno, T. Metcalfe, andM. L. Menone. 1998. Distribution of organochlorine compounds in tissues of croaker (Micropogonias furnieri) from Samborombón bay, Argentina.Environmental Sciences 6: 055–067.

    CAS  Google Scholar 

  • Lanfredi, N. W., C. F. Balestrini, C. A. Mazio, andS. A. Schmidt. 1987. Tidal sandbanks in Mar Chiquita coastal lagoon, Argentina.Journal Coastal Research 3:515–520.

    Google Scholar 

  • Maruya, K. A., G. Loganathan, K. Kannan, S. McCumber-Kahn, andR. F. Lee. 1997a. Organic and organometallic compounds in estuarine sediments from the Gulf of Mexico (1993–1994).Estuaries 20:700–709.

    Article  CAS  Google Scholar 

  • Maruya, K. A., R. W. Risebrough, andA. J. Horne. 1997b. The bioaccumulation of polynuclear aromatic hydrocarbons by benthic invertebrates in an intertidal marsh.Environmental Toxicology and Chemistry 16:1087–1097.

    Article  CAS  Google Scholar 

  • Menone, M. L., J. E. Aizpún de Moreno, V. J. Moreno, A. L. Lanfranchi, T. L. Metcalfe, andC. D. Metcalfe. 2000. PCBs and organochlorines in tissues of silverside (Odontesthes bonariensis) from a coastal lagoon in Argentina.Archives of Environmental Contamionation and Toxicology 38:202–208.

    Article  CAS  Google Scholar 

  • Metcalfe, T. L. andC. D. Metcalfe. 1997. The trophodynamics of PCBs, including mono- and non-ortho congeners in the food web of north-central Lake Ontario.Science of the Total Environment 201:245–272.

    Article  CAS  Google Scholar 

  • Olivier, S., A. Escofet, P. Penchaszadeh, andJ. Orensanz. 1972. Estudios ecológicos de la región estuarial de Mar Chiquita (Bs. As., Argentina). I. Las comunidades bentónicas.Anales de la Sociedad Científica Argentina 193:237–262.

    Google Scholar 

  • Piérard, C., H. Budzinski, andP. Garrigues. 1996. Grain-size distribution of polyclorobyphenyls in coastal sediments.Environmental Science Technology 30:2776–2783.

    Article  Google Scholar 

  • Porte, C. andJ. Albaigés. 1993. Bioaccumulation patterns of hydrocarbons and polychlorinated biphenyls in bivalves, crustaceans and fishes.Archives of Environmental Contamination and Toxicology 26:273–281.

    Google Scholar 

  • Sociedad Rural de Mar del Plata. 1995. Agroquímicos prohibidos, restringidos o suspendidos.ESEBE Productiones gráficas 7:1–24.

    Google Scholar 

  • Spivak, E., K. Anger, T. Luppi, C. Bas, andD. Ismael. 1994. Distribution and habitat preferences of two grapsid species in Mar Chiquita lagoon (Province of Buenos Aires, Argentina).Helgolander Meeresuntersuchungen 48:59–78.

    Article  Google Scholar 

  • Van Zoest, R. andG. T. M. Van Eck. 1990. Behaviour of particulate polychlorinated biphenyls and polycyclic aromatic hydrocarbons in the Scheldt estuary.Netherlands Journal of Sea Research 26:89–96.

    Article  Google Scholar 

  • Waish, G. E., D. E. Weber, T. L. Simon, L. K. Brashes, and J. C. Moore. 1991. Use of Marsh Plants for Toxicity Testing of Water and Sediment. Water Resources Division. Technical Report NPS/NRWRD/NRTR-91/03. Appendix 2. 1–29. Washington, D.C.

  • Zarenko, D. T., R. W. Griffiths, andN. K. Kaushik. 1997. Biomagnification of polychlorinated biphenyls through a riverine food web.Environmental Toxicology and Chemistry 16:1463–1471.

    Article  Google Scholar 

  • Zar, J. H. 1984. Biostatistical Analysis. 2nd edition. Prentice-Hall Inc., Englewood Cliffs, New Jersey.

    Google Scholar 

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Correspondence to M. L. Menone.

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Menone, M.L., Bortolus, A., Botto, F. et al. Organochlorine contaminants in a coastal lagoon in Argentina: Analysis of sediment, crabs, and cordgrass from two different habitats. Estuaries 23, 583–592 (2000). https://doi.org/10.2307/1353148

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  • DOI: https://doi.org/10.2307/1353148

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