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Wood preservative leachates from docks in an estuarine environment

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Abstract

Environmental concentrations and biological effects of certain metals and organic compounds found in wood preservatives were examined. The study focused on leachates from private residential docks in South Carolina tidal creeks. Copper, chromium, arsenic, and polynuclear aromatic hydrocarbons (PAHs) were measured in composite samples of surficial sediments and naturally occurring oyster populations (Crassostrea virginica) from creeks with high densities of docks, and from nearby reference creeks with no docks. In some cases, metal concentrations in sediments and oysters were higher immediately adjacent to dock pilings than they were elsewhere in the same creek. Sediments from most sites had concentrations of metals and total PAHs which were below levels reported to cause biological effects, however. Solid-phase Microtox® bioassays using whole sediments and rotifer bioassays using sediment pore water showed no significant differences in acute toxicity between creeks with and without docks. Oysters growing directly on dock pilings had significantly higher concentrations of copper than oysters growing at least 10 m away; however, there was no significant difference in the physiological condition of these oysters. Four-day field bioassays measuring percent survival of mummichogs (Fundulus heteroclitus), mud snails (Ilyanassa obsoleta), juvenile red drum (Sciaenops ocellatus), and juvenile white shrimp (Penaeus setiferus) showed no significant differences between sites near to and distant from newly constructed docks. Hatchery-reared oysters showed no significant differences between dock and reference sites in percent survival, growth, or bioaccumulation of metals after six weeks of exposure. The results suggest that, in estuarine environments with a moderate tidal range (1.5–2.0 m), wood preservative leachates from dock pilings have no acutely toxic effects on four common estuarine species, nor do they affect the short-term survival or growth of juvenile oysters.

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References

  • Abbe GR, Sanders JG (1988) Rapid decline in oyster condition in the Patuxent River, Maryland. J Shellfish Res 7:57–59

    Google Scholar 

  • Baldwin WJ, Pasek EA, Osborne PD (1994) Sediment toxicity study of CCA-C treated marine piles. In: Annual Proceedings of the American Wood-Preservers' Association, pp 300–316

  • Breteler RJ (1992) Critique provided on behalf of the American Wood Preservers Institute. The Coalition to Preserve the Availability of Treated Wood. c/o The Tri-Star Group, Inc., Long Island, New York

    Google Scholar 

  • Brooks KM (1994) Literature review and assessment of the environmental risks associated with the use of CCA and ACZA treated wood products in aquatic environments. Draft Report prepared for: Western Wood Preservers Institute, Vancouver, WA, 61 pp

    Google Scholar 

  • Bulich AA (1979) Use of luminescent bacteria for determining toxicity in aquatic environments. In: Marking LL, Kimerle RA (eds) Aquatic Toxicology. ASTM STP 667, pp 98–106

  • Bulich AA, Isenberg DL (1981) Use of the luminescent bacterial system for the rapid assessment of aquatic toxicity. ISA Transactions 20:29–33

    CAS  PubMed  Google Scholar 

  • Burrell VG Jr, Manzi JJ, Carson WZ (1981) Growth and mortality of two types of seed oysters from the Wando River, South Carolina. J Shellfish Res 1:1–7

    Google Scholar 

  • Cheng TC (1989) Immunodeficiency diseases in marine mollusks: measurements of some variables. J Aquatic Animal Health 1:209–216

    Google Scholar 

  • Chmura GL, Ross NW (1978) The environmental impacts of marinas and their boats: a literature review with management considerations. Memorandum 45, University of Rhode Island, Marine Advisory Service, Naragansett, RI, 32 pp

  • Cunningham PA (1979) The use of bivalve molluscs in heavy metal pollution research. In: Vernberg WB, Calabrese A, Thurberg FP, Vernberg FJ (eds) Proceedings of the Symposium “Pollution and Physiology of Marine Organisms”, Nov. 14–17, 1977, Hobcaw Barony, Georgetown, South Carolina, pp 183–221

    Google Scholar 

  • Dame RF, Spurrier JD, Williams TM, Kjerfve B, Zingmark RG, Wolaver TG, Chrzanowski TH, McKellar HN, Vernberg FJ (1991) Annual material processing by a salt marsh-estuarine basin in South Carolina, USA. Mar Ecol Prog Ser 72:153–166

    Google Scholar 

  • De Zwart D, Slooff W (1983) The Microtox as an alternate assay in the acute toxicity assessment of water pollutants. Aquat Toxicol 4:129–138

    Google Scholar 

  • Frazier JM (1976) The dynamics of metals in the American oyster, Crassostrea virginica. II. Environmental effects. Ches Sci 17:188–197

    Google Scholar 

  • Galtsoff PS (1964) The American oyster Crassostrea virginica (Gmelin). U.S. Fish Wildlife Serv Fish Bull 64:1–480

    Google Scholar 

  • Greig RA, Wenzloff DR (1978) Metal accumulation and depuration by the American oyster, Crassostrea virginica. Bull Environ Contam Toxicol 20:499–504

    Google Scholar 

  • Lawrence DR, Scott GI (1982) The determination and use of condition index of oysters. Estuaries 5:23–27

    Google Scholar 

  • Long ER, Morgan LG (1990) The potential for biological effects of sediment-sorbed contaminants tested in the National Status and Trends Program. NOAA Tech Mem NOS OMA 52. Seattle, WA, 175 pp

    Google Scholar 

  • Long ER, Mac Donald DD, Smith SL, Calder FD (1995) Incidence of adverse biological effects within ranges of chemical concentrations in marine and estuarine sediments. Environ Management 19:81–97

    Google Scholar 

  • Marcus JM, Scott GI, Heizer DD (1989) The use of oyster shell thickness and condition index measurements as physiological indicators of no heavy metal pollution around three coastal marinas. J Shellfish Res 8:87–94

    Google Scholar 

  • Marcus JM, Stokes TP (1985) Polynuclear aromatic hydrocarbons in oyster tissue around three coastal marinas. Bull Environ Contam Toxicol 35:835–844

    Google Scholar 

  • Marcus JM, Swearingen GR, Williams AD, Heizer DD (1988) Polynuclear aromatic hydrocarbon and heavy metal concentrations in sediments at South Carolina marinas. Arch Environ Contam Toxicol 17:103–113

    Google Scholar 

  • Mathews TD, Boyne JV, Davis RA, Simmons DR (1979) The distribution of copper and iron in South Carolina oysters. J Environ Sci Health A14(8):683–694

    Google Scholar 

  • Microbics Corporation (1992a) Detailed solid-phase test protocol. In: Microtox® manual, Volume 2, Detailed Protocols, 1992 Edition. Microbics Corp, Carlsbad, CA, pp 153–178

    Google Scholar 

  • — (1992b) Condensed protocol for solid-phase test. In: Microtox® Update Manual, December 92. Microbics Corp, Carlsbad, CA, pp 53–59

    Google Scholar 

  • National Oceanic and Atmospheric Administration (1987) National Status and Trends Program progress report: a summary of selected data on chemical contaminants in tissues collected during 1984, 1985, and 1986. NOAA Tech Mem NOS OMA 38. Rockville, MD, 21 pp

    Google Scholar 

  • — (1989) National Status and Trends Program progress report: A summary of data on tissue contamination from the first three years (1986–1988) of the Mussel Watch Project. NOAA Tech Mem NOS OMA 49. Rockville, MD, 22 pp

    Google Scholar 

  • — (1991) National Status and Trends Program progress report: second summary of data on chemical contaminants in sediments from the National Status and Trends Program. NOAA Tech Mem NOS OMA 59. Rockville, MD, 29 pp

    Google Scholar 

  • Phelps HL, Hetzel EW (1987) Oyster size, age, and copper and zinc accumulation. J Shellfish Res 6:67–70

    Google Scholar 

  • Plumb RH Jr (1981) Procedures for handling and chemical analysis of sediment and water samples. Tech Rept EPA/CE-81-1. U.S. Army Engineer Waterways Experiment Station, Vicksburg, MS

  • Pringle BH, Hissong DE, Katz EL, Mulawka ST (1968) Trace metal accumulation by estuarine mollusks. J Sanit Engineering Div, Proc Amer Soc Civil Engineers. 94(SA3):455–475

    Google Scholar 

  • Pringle BH, Shuster CN Jr (1967) A guide to trace metal levels in shellfish. Shellfish Sanit Tech Rept. USDHEW, Public Health Service, 19 pp

  • Roberts MH Jr, Hargis WJ Jr, Strobel CJ, De Lisle PF (1989) Acute toxicity of PAH contaminated sediments to the estuarine fish, Leiostomus xanthurus. Bull Environ Contam Toxicol 42(1):142–149

    Google Scholar 

  • Roosenberg WH (1969) Greening and copper accumulation in the American oyster, Crassostrea virginica, in the vicinity of a steam electric generating station. Ches Sci 10:241–252

    Google Scholar 

  • Ross PE, Burnett LC, Kermode C, Timme M (1991) Miniaturizing a toxicity test battery for screening contaminated sediments. In: Chapman P, Power E, Hall K, Harding L, McLeay D, Nassichuk M, Knapp W (eds) Proceedings of the Seventeenth Annual Aquatic Toxicity Workshop, November 5–7, 1990, Vancouver, BC, pp 331–335

  • Ross PE, Henebry MS (1989) Use of four microbial tests to assess the ecotoxicological hazard of contaminated sediments. Toxicity Assessment: An International Journal 4:1–21

    Google Scholar 

  • Rostad CE, Pereira WE (1987) Creosote compounds in snails obtained from Pensacola Bay, Florida, near an onshore hazardous-waste site. Chemosphere 16:2397–2404

    Google Scholar 

  • Sami SM, Faisal M, Huggett RJ (1992) Alterations in cytomeric characteristics of hemocytes from the American oyster Crassostrea virginica exposed to a polycyclic aromatic hydrocarbon (PAH) contaminated environment. Mar Biol 113:247–252

    Google Scholar 

  • Schiewe MH, Hawk EG, Actor DI, Krahn MM (1985) Use of a bacterial bioluminescence assay to assess toxicity of contaminated marine sediments. Can J Fish Aquat Sci 42:1244–1248

    Google Scholar 

  • Schropp SJ, Lewis FG, Windom HL, Ryan JD, Calder FD, Burney LC (1990) Interpretation of metal concentrations in estuarine sediments of Florida using aluminum as a reference element. Estuaries 13:227–235

    Google Scholar 

  • Snell TW, Persoone G (1989) Acute toxicity bioassays using rotifers. I. A test for brackish and marine environments with Brachionus plicatilis. Aquat Toxicol 14:65–80

    Google Scholar 

  • Swartz RC, Kemp PF, Schults DW, Ditsworth GR, Ozretich RJ (1989) Acute toxicity of sediment from Eagle Harbor, Washington, to the infaunal amphipod Rhepoxynius abronius. Environ Toxicol Chem 8(3):215–222

    Google Scholar 

  • Tagatz ME, Plaia GR, Deans CH, Lores EM (1983) Toxicity of creosote-contaminated sediment to field- and laboratory-colonized estuarine benthic communities. Environ Toxicol Chem 2(4):441–450

    Google Scholar 

  • U.S. Environmental Protection Agency (1991) Methods for the determination of metals in environmental samples. EPA/600/4-91/010. Office of Research and Development, Washington D.C.

  • Van Dolah RF, Bobo MY, Levisen ML, Wendt PH, Manzi JJ (1992) Effects of marina proximity on the physiological condition, reproduction, and settlement of oyster populations. J Shellfish Res 11:41–48

    Google Scholar 

  • Van Dolah RF, Maier PP, Fulton MH, Scott GI (1995) Comparison of azinphosmethyl toxicity on juvenile red drum, Sciaenops ocellatus, versus the mummichog, Fundulus heteroclitus. Final Report for Project No. F-56 submitted to U.S. Department of Interior, Fish and Wildlife Service. 46 pp

  • Vogelbein WK, Fournie JW, van Veld PA, Huggett RJ (1990) Hepatic neoplasms in the mummichog Fundulus heteroclitus from a creosote-contaminated site. Cancer Res. 50(18):5978–5986

    Google Scholar 

  • Weis JS, Weis P (1992a) Construction materials in estuaries: reduction in the epibiotic community on chromated copper arsenate (CCA) treated wood. Mar Ecol Prog Ser 83:45–53

    Google Scholar 

  • —, — (1992b) Transfer of contaminants from CCA-treated to aquatic biota. J Exper Mar Biol Ecol 161:189–199

    Google Scholar 

  • —, — (1993) Trophic transfer of contaminants from organisms living by chromated-copper-arsenate (CCA)-treated wood to their predators. J Exper Mar Biol Ecol 168:25–34

    Google Scholar 

  • --, -- (1994) The marine hard substrate community as an assay for toxicity of CCA-treated wood. Abstract. In: Proceedings of the 15th Annual Meeting of the Society of Environmental Toxicology and Chemistry, Oct. 30–Nov. 3, Denver, CO

  • Weis P, Weis JS, Coohill LM (1991) Toxicity to estuarine organisms of leachates from chromated copper arsenate treated wood. Arch Environ Contam Toxicol 20:118–124

    Google Scholar 

  • Weis P, Weis JS, Couch J (1993a) Histopathology and bioaccumulation in Crassostrea virginica living on wood preserved with chromated copper arsenate. Diseases Aquat Org 17:41–46

    Google Scholar 

  • Weis P, Weis JS, Lores E (1993b) Uptake of matals from chromated-copper-arsenate (CCA)-treated lumber by epibiota. Mar Pollut Bull 26:428–430

    Google Scholar 

  • Weis P, Weis JS, Proctor T (1993c) Copper, chromium, and arsenic in estuarine sediments adjacent to wood treated with chromated-copper-arsenate (CCA). Estuar Coast Shelf Sci 36:71–79

    Google Scholar 

  • Weis P, Weis JS, Greenberg A, Nosker TJ (1992) Toxicity of construction materials in the marine environment: a comparison of chromated-copper-arsenate-treated wood and recycled plastic. Arch Environ Contam Toxicol 22:99–106

    Google Scholar 

  • Wendt PH, Van Dolah RF, Bobo MY, Manzi JJ (1990) Effects of marina proximity on certain aspects of the biology of oysters and other benthic macrofauna in a South Carolina estuary. S.C. Marine Resources Center Tech. Rept. No. 74. South Carolina Wildlife and Marine Resources Department, Charleston, SC, 50 pp

    Google Scholar 

  • Windom HL, Smith RG (1972) Distribution of iron, magnesium, copper, zinc, and silver in oysters along the Georgia coast. J Fish Res Bd Can 29:450–452

    Google Scholar 

  • Windom HL, Schropp SJ, Calder FD, Ryan JD, Smith RG Jr, Burney LC, Lewis FG, Rawlinson CH (1989) Natural trace metal concentrations in estuarine and coastal marine sediments of the southeastern United States. Environ Sci Technol 23:314–320

    Google Scholar 

  • Winger PV, Lasier PJ (1994) Sediment toxicity in Savannah Harbor. Final Report to the Georgia Department of Natural Resources, Coastal Resources Division, Brunswick, GA

    Google Scholar 

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Wendt, P.H., Van Dolah, R.F., Bobo, M.Y. et al. Wood preservative leachates from docks in an estuarine environment. Arch. Environ. Contam. Toxicol. 31, 24–37 (1996). https://doi.org/10.1007/BF00203904

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