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Distribution, biomagnification, and elimination of butyltin compound residues in common cormorants (Phalacrocorax carbo) from Lake Biwa, Japan

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Abstract

Concentrations of butyltin compounds (BTs) were determined in various body tissues of common cormorants (Phalacrocorax carbo) collected from the Lake Biwa, Japan. Elevated concentrations of butyltins were detected in the feathers of cormorants. Among other organs and tissues, butyltin levels were also higher in the kidney (290±150 ng/g) and liver (270±260 ng/g), ranging from 115 to 544 ng/g and 142 to 1007 ng/g (wet wt basis), respectively. The accumulation of BTs in cormorant bodies was in the order of MBT > DBT > TBT and their organ specific burdens were in the order of muscle ≥ feathers > skin > liver > rest of the tissues and organs. The higher levels of BTs residues in feather suggested the excretion of about one fourth of their body burden during a complete molting cycle, which has been a natural detoxification mechanism in these birds. Based on the whole body concentrations of BTs in cormorants (42–160 ng/g wet wt) and fish (10–55 ng/g wet wt) biomagnification factors were assessed to be in the range of 1.1–4.1. To our knowledge, this is the first fundamental study to substantially indicate the contamination and kinetics of BTs in wild birds.

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References

  • Alzieu C, Sanjuan J, Deltreil JP, Borel M (1986) Tin contamination in Aracachon Bay: effects on oyster shell anomalies. Mar Pollut Bull 17:494–498

    Google Scholar 

  • Becker PH (1989) Seabird as monitor organisms of contaminants along the German North Sea coast. Helgolander Meersunter 43:395–403

    Google Scholar 

  • Champ MA (1986) Organotin symposium: introduction and overview. Oceans 86 Proceedings, vol. 4

  • Coenen TMM, Brouwer A, Enninga IC and Koeman JH (1992) Subchronic toxicity and reproduction effects of tri-n-butyltin oxide in Japanese Quail. Arch Environ Contam Toxicol 23:457–463

    Google Scholar 

  • Crewther WG, Fraser RDB, Lennox FG, Lindley H (1965) The chemistry of keratins. Adv Prot Chem 20:191–346

    Google Scholar 

  • Dowson PH, Bubb JM, Lester JN (1992) Organotin distribution in sediments and waters of selected east coast estuaries in the UK. Mar Pollut Bull 24:492–498

    Google Scholar 

  • Environment Agency (1993) Office of Health Studies, Environmental Health Department, Japan, 257–258

  • Epstein RL, Phillippo ET, Harr R, Koscinski W, Vasco G (1991) Organotin residue determination in poultry and turkey sample survey in the United States. J Agric Food Chem 39:917–921

    Google Scholar 

  • Evans DW, Laughlin RB (1984) Accumulation of bis(tributyltin) oxide by the mud crab, Rhithropanopeus harrisii. Chemosphere 13: 213–219

    Google Scholar 

  • Fleming WJ, Hill EF, Momot JJ, Pang VF (1991) Toxicity of trimethyltin and triethyltin to mallard ducklings. Environ Toxicol Chem 10:255–260

    Google Scholar 

  • Furness RW, Muirhead SJ, Woodburn M (1986) Using bird feathers to measure mercury in the environment: Relationships between mercury content and moult. Mar Pollut Bull 17:27–30

    Google Scholar 

  • Ginn HB, Melville DS (1983) Moult in birds. British trust for ornithology guide number 19. 38 pp

  • Garcia-Romero B, Wade TL, Salata GG, Brooks JM (1993) Butyltin concentrations in oysters from the Gulf of Mexico from 1989 to 1991. Environ Pollut 81:103–111

    Google Scholar 

  • Gibbs PE, Bryan GW (1986) Reproductive failure in populations of the dog-whelk, Nucella Lapillus, caused by imposex induced by tributyltin from antifouling paints. J Mar Biol Ass UK 66: 767–777

    Google Scholar 

  • Higashiyama T, Shiraishi H, Otsuki A, Hashimoto S (1991) Concentrations of organotin compounds in blue mussels from the wharves of Tokyo Bay. Mar Pollut Bull 22:585–587

    Google Scholar 

  • Honda K, Min BY, Tatsukawa R, Ogi H (1986a) Distribution of heavy metals and their age-related changes in the eastern great white, Egretta alba modesta, in Korea. Arch Environ Contam Toxicol 15:185–197

    Google Scholar 

  • Honda K, Nasu T, Tatsukawa R (1986b) Seasonal changes in mercury accumulation in the black-eared Kite, Milvus migrans lineatus. 42:325–334

  • Itami T, Ema M, Amano H, Murai T, Kawasaki H (1990) Teratogenic evaluation of tributyltin chloride in rats following oral exposure. Drug Chem Toxicol 13:283–295

    Google Scholar 

  • Iwata H, Tanabe S, Miyazaki N, Tatsukawa R (1994) Detection of butyltin compound residues in the blubber of marine mammals. Mar Pollut Bull 28:607–612

    Google Scholar 

  • Iwata H, Tanabe S, Mizuno T, Tatsukawa R (1995) High accumulation of toxic butyltins in marine mammals from Japanese coastal waters. Environ Sci Technol 29:2959–2962

    Google Scholar 

  • Kannan K, Iwata H, Tanabe S, Tatsukawa R (1995) Butyltins in muscle and liver of fish collected from certain Asian and Oceanian countries. Environ Pollut 90:279–290

    Google Scholar 

  • Kjellen N (1994) Moult in relation to migration in birds—a review. Ornis Svecica 4:1–24

    Google Scholar 

  • Langston WJ, Burt GR, Mingjiang Z (1987) Tin and organotin on water, sediments, and benthic organisms of Poole Harbour. Mar Pollut Bull 18:634–639

    Google Scholar 

  • Lewis SA, Furness RW (1991) Mercury accumulation and excretion in laboratory reared Black-Headed Gull Larus ridibundus chicks. Arch Environ Contam Toxicol 21:316–320

    Google Scholar 

  • Maguire RJ (1986) Review of the occurrence, persistence and degradation of tributyltin in fresh water ecosystems in Canada. Organotin symposium. Oceans 86 proceedings. 4:1252–1255

    Google Scholar 

  • Mercier A, Pelletier E, Hamel JF (1994) Metabolism and toxic effects of butyltin compounds in starfish. Aqua Toxicol 28:259–273

    Google Scholar 

  • Osborn D, Harris MP, Nicholson JK (1979) Comparative tissue distribution of mercury, cadmium and zinc in three species of pelagic seabirds. Com Biochem Physiol 64C:61–67

    Google Scholar 

  • Osborn D, Leach DV (1987) Organotin in birds: Pilot survey (Final report to the UK Department of the Environment), 15 pp

  • Quevauviller P, Lavigne R, Pinel R, Astruc M (1989) Organotins in sediments and mussels from the Sado estuarine system (Portugal). Environ Pollut 57:149–166

    Google Scholar 

  • Rexrode M (1987) Ecotoxicity of tributyltin. Organotin symposium. Oceans 87 Proceedings, pp 1443–1455

  • Schlatterer B, Coenon TMM, Ebert E, Grau R, Hilbig V, Munk R (1993) Effect of Bis(tri-n-butyltin)oxide in Japanese quail exposed during egg laying period: An interlaboratory comparison study. Arch Environ Contam Toxicol 24:440–448

    Google Scholar 

  • Seinen W, Vos JG, Spanje I, Snoek M, Brands R, Hooykaas H (1977) Toxicity of organotin compound. II. Comparative in vivo and in vitro studies with various organotin and organolead compound in different animal species with special emphasis on Lymphocyte cytotoxicity. Toxicol Appl Pharmocol 42:197–212

    Google Scholar 

  • Seligman PF, Grovhoug JG, Valkirs AO, Stang PM, Fransham R, Stallard MO, Davidson B, Lee RF (1989) Distribution and fate of tributyltin in the United States marine environment. Appl Organomet Chem 3:31–47

    Google Scholar 

  • Short JW, Thrower FP (1986) Accumulation of butyltins in muscle tissue of Chinook Salmon reared in sea pens treated with tri-n-butyltin. Mar Pollut Bull 17:542–545

    Google Scholar 

  • Smith PJ, Crowe AJ, Kumar Das VG, Duncan J (1979) Structure-activity relationships for some organotin molluscicides. Pestic Sci 10:419–422

    Google Scholar 

  • Snoeij NJ, Van Iersel AAJ, Penninks AS, Seinen W (1986) Triorganotin-induced cytotoxicity to rat thymus, bone marrow and red blood cells as determined by several in vitro assays. Toxicology 39:71–83

    Google Scholar 

  • Suzuki T, Matsuda R, Saito Y (1992) Molecular species of tri-n-butyltin compounds in marine products. J Agric Food Chem 40:1437–1443

    CAS  Google Scholar 

  • Tanabe S, Tatsukawa R, Tanaka H, Maruyama K, Miyazaki N, Fujiyama T (1981) Distribution and total burdens of chlorinated hydrocarbons in bodies of striped dolphins (Stenella coeruleoalba). Agric Biol Chem 45:2569–2578

    Google Scholar 

  • Thompson DR, Furness RW (1989) The chemical form of mercury stored in south Atlantic seabirds. Environ. Pollut 60:305–317

    Google Scholar 

  • Thompson DR, Stewart FM, Furness RW (1990) Using seabirds to monitor mercury in marine environments—The validity of conversion ratios for tissue comparison. Mar Pollut Bull 21:339–342

    Google Scholar 

  • Tsuda T, Nakanishi H, Morita T, Takebayashi J (1986) Simultaneous gas chromatographic determination of dibutyltin and tributyltin compounds in biological and sediment samples. Assoc Anal Chem 69:6:981–984

    Google Scholar 

  • Wade TL, Garcia-Romero B, Brooks JM (1988) Tributyltin contamination in bivalves from United States coastal estuaries. Environ Sci Technol 22:1488–1493

    Google Scholar 

  • Yamada H, Tateishi M, Takayanagi K (1994) Bioaccumulation of organotin compounds in the red sea bream (Pagrus major) by two uptake and direct uptake from water. Environ Toxicol Chem 13:1415–1422

    Google Scholar 

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Guruge, K.S., Tanabe, S., Iwata, H. et al. Distribution, biomagnification, and elimination of butyltin compound residues in common cormorants (Phalacrocorax carbo) from Lake Biwa, Japan. Arch. Environ. Contam. Toxicol. 31, 210–217 (1996). https://doi.org/10.1007/BF00212368

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  • DOI: https://doi.org/10.1007/BF00212368

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