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The photosynthetic responses of marine phytoplankton, periphyton and epipsammon to the herbicides paraquat and simazine

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Abstract

Short-term toxicity tests using photosynthesis (incorporation of 14C) as a test parameter were performed in order to compare the sensitivities of three marine microalgal communities (phytoplankton, periphyton and epipsammon) to two herbicides, paraquat and simazine. Thirty minutes of pre-exposure to simazine were sufficient to obtain the full effect in all communities, while for paraquat 4 h was required. The bioavailability of paraquat and simazine was not limited by adsorption to sediment in the epipsammon samples. Simazine was more toxic than paraquat for the three communities at similar concentrations. Phytoplankton was slightly more sensitive for both herbicides (EC50 ranges of 9--23 mu m for paraquat and 0.37--0.99 mu m for simazine) than periphyton and epipsammon. These attached communities exhibited different results for each toxicant, periphyton being more sensitive to paraquat (EC50 range 9--21 mu m) and epipsammon to simazine (EC50 range 0.44--1.17 mu m). The three communities presented EC ranges comparable to those found in single species tests, suggesting that different levels of biological organization can exhibit a similar sensibility to toxicants, thus indicating that natural communities are suitable for use in these kinds of toxicity tests

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References

  • Blanck, H. (1983) On the impact of long-chained aliphatic amines on photosynthesis and algal growth in ecotoxicological test systems. PhD thesis, Department of Plant Physiology, University of Göteborg.

    Google Scholar 

  • Blanck, H. (1985) A simple, community level, ecotoxicological test system using samples of periphyton. Hydrobiologia 124, 251–61.

    Google Scholar 

  • Blanck, H. and Wängberg, S-Å. (1988) Validity of an ecotoxicological test system: short-term and long-term effects of arsenate on marine periphyton communities in laboratory systems. Can. J. Fish. Aquatic Sci. 45, 1807–15.

    Google Scholar 

  • Blanck, H., Wallin, G. and Wängberg, S-Å. (1984) Species dependent variation in algal sensitivity to chemical compounds. Ecotoxicol. Environ. Safety 8, 339–51.

    PubMed  Google Scholar 

  • Bozeman, J., Koopman, B. and Bitton, B. (1989) Toxicity testing using mobilized algae. Aquatic Toxicol. 14, 345–52.

    Article  Google Scholar 

  • Cairns, J. (1986) The myth of the most sensitive species. BioScience 36, 670–2.

    Google Scholar 

  • Cairns, J. and Pratt, J.R. (1989) The scientific basis of bioassays. Hydrobiologia 188/189, 5–20.

    Google Scholar 

  • Clements, W.H. and Kiffney, P.M. (1994) Assessing contaminant effects at higher levels of biological organization. Environ. Toxicol. Chem. 13, 357–9.

    Google Scholar 

  • Couture, P., Thellen, C. and Thompson, P. (1989) Phytoplankton recovery responses at the population and community levels in a hazard and risk assessment study. Hydrobiologia 188/189, 269–76.

    Google Scholar 

  • Cserháti, T. (1993) Interaction of diquat and paraquat with humic acid and the influence of salt concentration and pH on the strength on interaction. Fresenius J. Anal. Chem. 345, 541–4.

    Article  Google Scholar 

  • Dahl, B. and Blanck, H. (1996) The use of sand-living microalgal communities (epipsammon) in ecotoxicological testing. Mar. Ecol.-Prog. Ser. 144, 163–73.

    Google Scholar 

  • DeNoyelles, F., Kettle, W.D. and Sinn, D.E. (1982) The responses of plankton communities in experimental ponds to atrazine, the most heavily used pesticide in the United States. Ecology 63, 1285–93.

    Google Scholar 

  • Elliot, J.M. (1983) Some Methods for the Statistical Analysis of Samples of Benthic Invertebrates. Scientific Publication No. 25, Freshwater Biological Association.

  • Erickson, L.E. and Lee, K.H. (1989) Degradation of atrazine and related s-triazines. Crit. Rev. Environ. Control 19, 1–13.

    Google Scholar 

  • Fedtke, C. (1982) Biochemistry and Physiology of Herbicide Action. New York: Springer-Verlag.

    Google Scholar 

  • Francois, D.L. and Robinson, G.C. (1990) Indices of triazine toxicity in Chlamydomonas geitleri. Aquatic Toxicol. 16, 205–28.

    Article  Google Scholar 

  • Goldsborough, L. and Robinson, G.C. (1986) Changes in periphytic algal community structure as a consequence of short herbicide exposures. Hydrobiologia 139, 177–92.

    Google Scholar 

  • Goldsborough, L. and Robinson, G.C. (1988) Functional responses of freshwater periphyton to short simazine exposures. Verh. Int. Verein. Limnol. 23, 1586–93.

    Google Scholar 

  • Gurney, S.E. and Robinson, G.C. (1989) The influence of two triazine herbicides on the productivity, biomass and community composition of freshwater marsh periphyton. Aquatic Bot. 36, 1–22.

    Article  Google Scholar 

  • Hakansson, L. and Jansson, M. (1993) Principles of Lake Sedimentology. Berlin: Springer-Verlag.

    Google Scholar 

  • Hansson, O. and Wydrzynski, T. (1990) Current perceptions of photosystem II. Photosystem Res. 23, 131–62.

    Google Scholar 

  • Hiraprandit, H. and Foy, C.L. (1992) Effect of four triazine herbicides on growth of nontarget green algae. Weed Sci. 40, 134–42.

    Google Scholar 

  • Ibrahim, E.A. (1990) The influence of the herbicide paraquat “Gramaxon” on growth and metabolic activity of three chlorophytes. Water, Air Soil Pollut. 51, 89–93.

    Google Scholar 

  • Kookana, R.S. and Aylmore, A.G. (1993) Retention and release of diquat and paraquat herbicides in soil. Aust. J. Soil. Res. 31, 97–109.

    Google Scholar 

  • Lagoutte, B. and Mathis, P. (1989) The photosystem I reaction center: structure and photochemistry. Photochem. Photobiol. 49, 833–44.

    Google Scholar 

  • Landner, L., Blanck, H., Heyman, U., Lundgren, A., Notini, M., Rosemarin, A. and Sundelin, A. (1989) Community testing, microcosm and mesocosm experiments: ecotoxicological tools with high ecological realism. In Chemicals in the Aquatic Environment — Advanced Hazard Assessment, p. 216–54 (L. Landner, ed). Berlin: Springer-Verlag.

    Google Scholar 

  • Lanno, R.P., Hickie, H.E. and Dixon, D.G. (1989) Feeding and nutritional considerations in aquatic toxicology. Hydrobiologia 188/189, 525–31.

    Google Scholar 

  • Mauck, W.L., Mayer, F.L. and Holz, D.D. (1976) Simazine residue dynamics in small ponds. Bull. Environ. Contam. Toxicol. 16, 1–8.

    PubMed  Google Scholar 

  • Munawar, M., Munawar, I.F. and Leppard, G.G. (1989) Early warning assays: an overview of toxicity testing with phytoplankton in the North American Great Lakes. Hydrobiologia 188/189, 237–46.

    Google Scholar 

  • Naqvi, S.M., Leung, T.S. and Naqvi, N.Z. (1981) Toxicities of paraquat and metribuzin (Sencor) herbicides to the freshwater copepods, Eucyclops agilis and Diaptomus mississippiensis. Environ. Pollut. (Ser A) 26, 275–80.

    Google Scholar 

  • Nicholls, P.H., Briggs, G.C. and Evans, A.A. (1984) The influence of water solubility on the movement and degradation of simazine in fallow soil. Weed Res. 24, 37–49.

    Google Scholar 

  • O'Neill, R.V., Gardner, R.H., Barnthouse, L.W., Suter, G.W., Hildebrand, S.G. and Gehrs, C.W. (1982) Ecosystem risk analysis: a new methodology. Environ. Toxicol. Chem. 1, 167–77.

    Google Scholar 

  • Rochaix, J-D. and Erickson, J. (1988) Function and assembly of photosystem II: genetic and molecular analysis. TIBS 13, 56–9.

    PubMed  Google Scholar 

  • Smith, L.L. (1988) The toxicity of paraquat. Adv. Drug. React. Ac. Poison Rev. 1, 1–17.

    Google Scholar 

  • Svansson, A. (1984) Hydrography of Gullmar Fjord. Sweden: Institute of Hydrography Research (23), Fishery Board of Sweden.

    Google Scholar 

  • Tubbing, D.M.J., Admiraal, W., Blanck, H., Sabater, S. and Guasch, H. (1996) Can periphyton communities be used to detect pollution with chemicals? In Use of Algae to Monitoring Rivers II, pp. 59–62 (B. Whitton, ed). Innsbruck: Institut für Botanik, Universität Innsbruck.

    Google Scholar 

  • Turbak, S.C., Olson, S.B. and McFeters, G.A. (1986) Comparison of algal assay systems for detecting waterborne herbicides and metals. Water. Res. 20, 91–6.

    Article  Google Scholar 

  • Wängberg, S.Å. (1989) Arsenate tolerance in periphyton and phytoplankton, PhD thesis. Göteborg: Department of Plant Physiology, University of Göteborg.

    Google Scholar 

  • Weber, A. (1981) An uncomplicated screening test to evaluate toxicity of environmentally hazardous compounds in water. Environ. Technol. Lett. 2, 323–8.

    Google Scholar 

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Bonilla, S., Conde, D. & Blanck, H. The photosynthetic responses of marine phytoplankton, periphyton and epipsammon to the herbicides paraquat and simazine. Ecotoxicology 7, 99–105 (1998). https://doi.org/10.1023/A:1008867920179

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