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Environmental contaminants in redheads wintering in coastal Louisiana and Texas

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Abstract

Whole body and liver analyses indicated that wintering redheads (Aythya americana; n=70) in coastal Louisiana (one site) and Texas (two sites) were relatively free of contamination with common trace elements, organochlorines, and hydrocarbons. Most trace elements, including As, Cr, Hg, Mg, Mn, Ni, Pb, Se, Sr, and Zn, were within background concentrations in livers; levels of B, Cd, Cu, and Fe were elevated in some specimens. Only one organochlorine, DDE, was detected in redhead carcasses, but its concentration was below reported toxic levels in waterfowl. Body burdens of aliphatic and aromatic hydrocarbons were generally low, but levels of pristane, total hydrocarbons, and the ratios of phytane:n-octadecane and pristane:n-heptadecane were indicative of possible chronic exposure to petroleum. Based on brain cholinesterase assays, redheads were not recently exposed to organophosphorous or carbamate pesticides. Of 30 elements or compounds tested for seasonal differences, only Se increased from early to late winter at one of the three sites. Eight of 57 contaminants differed among the three sites; no sex or age differences were found.

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References

  • Adair SE (1990) Factors influencing wintering diving duck use of coastal ponds in south Texas. MSc Thesis, Texas A&M Univ, College Station, TX

    Google Scholar 

  • Bellrose FC (1980) Ducks, geese and swans of North America. Stackpole Books, Harrisburg, PA

    Google Scholar 

  • Benson WW, Brock DW, Gabica J, Loomis M (1976) Swan mortality due to certain heavy metals in the Mission Lake area, Idaho. Bull Environ Contam Toxicol 15:171–174

    Google Scholar 

  • Boesch DF, Rabalais NN (eds) (1989) Produced waters in sensitive coastal habitats: An analysis of impacts, central coastal Gulf of Mexico. US Dept Int Minerals Manage Serv OCS Rep/MMS 89-0031, Washington, DC

  • Brealey CJ, Walker CH, Baldwin BC (1980) A-esterase activities in relation to the differential toxicity of pirimiphos-methyl to birds and mammals. Pest Sci 11:546–554

    Google Scholar 

  • Cornelius SE (1977) Food and resource utilization of wintering redheads on lower Laguna Madre. J Wildl Manage 41:374–385

    Google Scholar 

  • Cowardin LM, Carter V, Golet FC, LaRoe ET (1979) Classification of wetlands and deepwater habitats of the United States. US Fish Wildl Serv FWS/OBS 79/31

  • Cromartie EW, Reichel WL, Locke LN, Belisle AA, Kaiser TE, Lamont TG, Mulhern BM, Prouty RM, Swineford DM (1975) Residues of organochlorine pesticides and polychlorinated biphenyls and autopsy data for bald eagles, 1971–72. Pest Monit J 9:11–14

    Google Scholar 

  • Custer TW, Hohman WL (1993) Trace elements in canvasbacks from Louisiana, 1987–88. Environ Pollut (in press)

  • Custer TW, Mitchell CA (1987) Exposure to insecticides of brushland wildlife within the Lower Rio Grande Valley, Texas, USA. Environ Pollut 45:207–220

    Google Scholar 

  • —, — (1991) Contaminant exposure of willets feeding in agricultural drainages of the Lower Rio Grande Valley of South Texas. Environ Monitor Assess 16:189–200

    Google Scholar 

  • —, — (1993) Trace elements and organochlorines in the shoalgrass community of the lower Laguna Madre, Texas. Environ Monit Assess 25:235–246

    Google Scholar 

  • Davison KL, Sell JL (1974) Dieldrin and DDT effects on reproduction and some hepatic mixed-function oxidases in the mallard duck. Arch Environ Contam 2(4):302–314

    Google Scholar 

  • Day RW, Quinn GP (1989) Comparisons of treatments after an analysis of variance in ecology. Ecol Mono 58(4):433–463

    Google Scholar 

  • Demas CR (1983) Hydrology, water quality, and biology of Baptiste Collette Bayou in relation to the lower Mississippi River at Venice, Louisiana. US Geol Surv Tech Rep No 31

  • DiGiulio RT (1982) The occurrence and toxicology of heavy metals in Chesapeake Bay waterfowl. PhD Thesis, Virginia Polytech Inst State Univ, Blacksburg, VA

    Google Scholar 

  • DiGiulio RT, Scanlon PF (1984) Heavy metals in tissues of waterfowl from the Chesapeake Bay, USA. Environ Pollut 35:29–48

    Google Scholar 

  • Eisler R (1988) Arsenic hazards to fish, wildlife, and invertebrates: A synoptic review. US Fish Wildl Serv Biol Rep 85(1. 12)

  • Elliot JE, Scheuhammer AM, Leighton FA, Pearce PA (1992) Heavy metal and metallothionein concentrations in Atlantic Canadian seabirds. Arch Environ Contam Toxicol 22:63–73

    Google Scholar 

  • Ellman GL, Courtney KD, Andres Jr V, Featherstone MR (1961) A new and rapid calorimetric determination of acetylcholinesterase activity. Biochem Pharmacol 7:88–98

    Article  CAS  PubMed  Google Scholar 

  • Fleming WJ, O'Shea TJ (1980) Influence of a local source of DDT pollution on statewide DDT residues in waterfowl wings, northern Alabama, 1978–79. Pest Monit J 14:86–89

    Google Scholar 

  • Ford WM, Hill EP (1990) Organochlorine contaminants in eggs and tissue of wood ducks from Mississippi. Bull Environ Contam Toxicol 45:870–875

    Google Scholar 

  • Friend M (1985) Interpretation of criteria commonly used to determine lead poisoning problem areas. US Fish Wildl Serv, Fish Wildl Leafl 2

  • Gilbert RO (1987) Statistical methods for environmental pollution monitoring. Van Nostrand Reinhold Company, NY

    Google Scholar 

  • Haegele MA, Hudson RH (1974) Eggshell thinning and residues in mallards one year after DDE exposure. Arch Environ Contam Toxicol 2:356–363

    Article  CAS  PubMed  Google Scholar 

  • Hall RJ, Coon NC (1988) Interpreting residues of petroleum hydrocarbons in wildlife tissues. US Fish Wildl Serv Bio Rep 88(15)

  • Hill EF (1988) Brain cholinesterase activity of apparently normal wild birds. J Wildl Dis 24:51–61

    Google Scholar 

  • — (1989) Divergent effects of postmortem ambient temperature on organophosphorus-and carbamate-inhibited brain cholinesterase activity in birds. Pest Biochem Physiol 33:264–275

    Google Scholar 

  • — (1992) Avian toxicology of anticholinesterases. In: Ballantyne B and Marrs TC (eds) Clinical and experimental toxicology of organophosphates and carbamates. Butterworth-Heinemann Ltd, Oxford, pp 272–294

    Google Scholar 

  • Hill EF, Fleming WJ (1982) Anticholinesterase poisoning of birds: Field monitoring and diagnosis of acute poisoning. Environ Toxicol Chem 1:27–38

    Google Scholar 

  • Hill EF, Murray HC (1987) Seasonal variation in diagnostic enzymes and biochemical constituents of captive northern bobwhites and passerines. Comp Biochem Physiol 87B:933–940

    Google Scholar 

  • Hoffman DJ, Heinz GH (1988) Embryotoxic and teratogenic effects of selenium in the diets of mallards. J Toxicol Environ Health 24:477–490

    Google Scholar 

  • Hoffman DJ, Camardese MB, Lecaptain LJ, Pendleton GW (1990) Effects of boron on growth and physiology in mallard ducklings. Environ Toxicol Chem 9:335–346

    Google Scholar 

  • Irby HD, Locke LN, Bagley GE (1967) Relative toxicity of lead and selected substitute shot types to game farm mallards. J Wildl Manage 31:253–257

    Google Scholar 

  • Kaiser TE, Reichel WL, Locke LN, Cromartie E, Krynitsky AJ, Lamont TG, Mulhern BM, Prouty RM, Stafford CJ, Swineford DM (1980) Organochlorine pesticides, PCB, and PBB residues and necropsy data for bald eagles from 29 states—1975–77. Pest Monit J 13:145–149

    Google Scholar 

  • King KA, Stafford CJ, Cain BW, Mueller AJ, Hall HD (1987) Industrial, agricultural, and petroleum contaminants in cormorants wintering near the Houston ship channel, Texas, USA. Colonial Waterbirds 10(1):93–99

    Google Scholar 

  • Lande E (1977) Heavy metal pollution in Trondheimsfjorden, Norway, and recorded effects on the fauna and flora. Environ Pollut 12:187–198

    Google Scholar 

  • Lawler, GC, Loong W, Laseter JL (1978) Accumulation of saturated hydrocarbons in tissues of petroleum-exposed mallard ducks (Anas platyrhynchos). Environ Sci Technol 12:47–51

    Google Scholar 

  • Locke LN, Irby HD, Bagley GE (1967) Histopathology of mallards dosed with lead and selected substitute shot. Bull Wildl Dis Assoc 3:143–147

    Google Scholar 

  • Longcore JR, Stendell RC (1977) Shell thinning and reproductive impairment in black ducks after cessation of DDE dosage. Arch Environ Contam Toxicol 6:293–304

    Google Scholar 

  • Lowenstine LJ, Petrak ML (1980) Iron pigment in the livers of birds. In: Montali RJ, Migaki G (eds) The comparative pathology of zoo animals. Smithsonian Institution Press, Washington, DC

    Google Scholar 

  • Ludke JL, Hill EF, Dieter MP (1975) Cholinesterase (ChE) response and related mortality among birds fed ChE inhibitors. Arch Environ Contam Toxicol 3:1–21

    Google Scholar 

  • McMahan CA (1970) Food habits of ducks wintering on Laguna Madre, Texas. J Wildl Manage 34:946–949

    Google Scholar 

  • Michot TC, Nault AJ (1993) Diet differences in redheads from nearshore and offshore zones in Louisiana. J Wildl Manage 57:238–244

    Google Scholar 

  • Michot TC, Moser EB, Norling W (1994) Effects of weather and tides on feeding and flock positions of wintering redheads in Chandeleur Sound, Louisiana. Hydrobiologia (in press)

  • Mitchell, CA (1992) Water depth predicts redhead distribution in the lower Laguna Madre, Texas. Wildl Soc Bull 20:420–424

    Google Scholar 

  • Mitchell CA, Custer TW, and Zwank PJ (1992) Redhead duck behavior on Lower Laguna Madre and adjacent ponds of southern Texas. Southwest Nat 37:65–72

    Google Scholar 

  • Moore JL (1991) Habitat-related activities and body mass of wintering redhead ducks on coastal ponds in South Texas. MSc Thesis, Texas A&M Univ, College Station, TX

    Google Scholar 

  • Mora MA, Anderson DW, Mount ME (1987) Seasonal variation of body condition and organochlorines in wild ducks from California and Mexico. J Wildl Manage 51:132–141

    Article  CAS  Google Scholar 

  • Ohlendorf HM (1989) Bioaccumulation and effects of selenium in wildlife. In: Jacobs LW (ed) Selenium in agriculture and the environment. SSSA Spec Pub No 23, Am Soc of Agronomy and Soil Sci, Madison, WI

    Google Scholar 

  • Ohlendorf HM, Miller MR (1984) Organochlorine contaminants in California waterfowl. J Wildl Manage 48:867–877

    Google Scholar 

  • Ohlendorf HM, Lowe RW, Kelly PR, Harvey TE (1986) Selenium and heavy metals in San Francisco Bay diving ducks. J Wildl Manage 50:64–71

    Google Scholar 

  • Pacheco PA, Farrow DRG, Manuelides T, Rohmann SO, Katz M, McLeod J (1990) Point source discharges in coastal areas of Texas: a summary by estuarine watershed for 1987. Draft Report. US Dept Comm, Nat Oceanic Atmos Admn, Rockville, MD

    Google Scholar 

  • Paasivirta J (1991) Chemical ecotoxicology. Lewis Publishers, Chelsea, MI

    Google Scholar 

  • Paveglio FL, Bunck CM, Heinz GH (1992) Selenium and boron in aquatic birds from central California. J Wildl Manage 56(1):31–42

    Google Scholar 

  • Rattner BA, Flickinger EL, Hoffman DJ (1993) Morphological, biochemical, and histopathological indices and contaminant burdens of cotton rats (Sigmodon hispidus) at three hazardous waste sites near Houston, Texas, USA. Environ Pollut 79:85–93

    Google Scholar 

  • Rhodes RC (1981) Much ado about next to nothing, or what to do with measurements below the detection limit. Environmetrics 81: selected papers, SIAM-SIMS conference series no. 8. Society for industrial and applied mathematics, Philadelphia, pp 157–162

    Google Scholar 

  • Risebrough RW, Anderson DW (1975) Some effects of DDE and PCB on mallards and their eggs. J Wildl Manage 39:508–513

    Google Scholar 

  • Sabourin TD, Stickle WB, Michot TC, Villars CE, Garton DW, Mushinsky HR (1984) Organochlorine residue levels in Mississippi River water snakes in southern Louisiana. Bull Environ Contam Toxicol 32:460–468

    Google Scholar 

  • St. Pé KM (ed) (1990) An assessment of produced water impacts to low-energy, brackish water systems in Southeast Louisiana. Louisiana Dept Environ Qual, Water Pollut Control Div, Baton Rouge, LA

    Google Scholar 

  • SAS Institute Inc (1987) SAS/STAT guide for personal computers, version 6 ed. SAS Inst Inc, Cary, NC

    Google Scholar 

  • Scheuhammer AM (1987) The chronic toxicity of aluminum, cadmium, mercury, and lead in birds: A review. Environ Pollut 46:263–295

    Google Scholar 

  • Scott ML, Nesheim MC, Young RJ (1976) Nutrition of the chicken. ML Scott & Assoc, Ithaca, NY

    Google Scholar 

  • Shumway RH, Azari AS, Johnson P (1989) Estimating mean concentrations under transformation for environmental data with detection limits. Technometrics 31(3):347–356

    CAS  PubMed  Google Scholar 

  • Smith GJ, Anders VP (1989) Toxic effects of boron on mallard reproduction. Environ Toxicol Chem 8:943–950

    Google Scholar 

  • Smith VE, Spurr JM, Filkins JC, Jones JJ (1985) Organochlorine contaminants of wintering ducks foraging on Detroit river sediments. J Great Lakes Res 11:231–246

    Google Scholar 

  • Vermeer K, Castilla JC (1991) High cadmium residues observed during a pilot study in shorebirds and their prey downstream from El Salvador copper mine, Chile. Bull Environ Contam Toxicol 46:242–248

    Google Scholar 

  • Walker CH, El Zorgani GA (1974) The comparative metabolism and excretion of HCE, a biodegradable analogue of dieldrin, by vertebrate species. Arch Environ Contam Toxicol 2:97–116

    Google Scholar 

  • Westlake GE, Martin AD, Stanley PI, Walker CH (1983) Control enzyme levels in the plasma, brain, and liver from wild birds and mammals in Britain. Comp Biochem Physiol 76C:15–24

    Google Scholar 

  • White DH, Stendell RC, Mulhern BM (1979) Relations of wintering canvasbacks to environmental pollutants—Chesapeake Bay, Maryland. Wilson Bull 91:279–287

    Google Scholar 

  • Woodin MC (1994) Use of saltwater and freshwater habitats by wintering redheads in southern Texas. Hydrobiologia (in press)

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Michot, T.C., Custer, T.W., Nault, A.J. et al. Environmental contaminants in redheads wintering in coastal Louisiana and Texas. Arch. Environ. Contam. Toxicol. 26, 425–434 (1994). https://doi.org/10.1007/BF00214143

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