Genetic and demographic responses of mosquitofish (Gambusia holbrooki girard 1859) populations stressed by mercury
Corresponding Author
Margaret Mulvey
University of Georgia, Savannah River Ecology Laboratory, P.O. Drawer E, Aiken, South Carolina 29802
University of Georgia, Savannah River Ecology Laboratory, P.O. Drawer E, Aiken, South Carolina 29802Search for more papers by this authorMichael C. Newman
University of Georgia, Savannah River Ecology Laboratory, P.O. Drawer E, Aiken, South Carolina 29802
Search for more papers by this authorAnn Chazal
University of Georgia, Savannah River Ecology Laboratory, P.O. Drawer E, Aiken, South Carolina 29802
Search for more papers by this authorM. Michele Keklak
University of Georgia, Savannah River Ecology Laboratory, P.O. Drawer E, Aiken, South Carolina 29802
Search for more papers by this authorM. Gay Heagler
University of Georgia, Savannah River Ecology Laboratory, P.O. Drawer E, Aiken, South Carolina 29802
Search for more papers by this authorL. Stan Hales Jr.
Zoology Department, University of Georgia, Athens, Georgia 30602
Search for more papers by this authorCorresponding Author
Margaret Mulvey
University of Georgia, Savannah River Ecology Laboratory, P.O. Drawer E, Aiken, South Carolina 29802
University of Georgia, Savannah River Ecology Laboratory, P.O. Drawer E, Aiken, South Carolina 29802Search for more papers by this authorMichael C. Newman
University of Georgia, Savannah River Ecology Laboratory, P.O. Drawer E, Aiken, South Carolina 29802
Search for more papers by this authorAnn Chazal
University of Georgia, Savannah River Ecology Laboratory, P.O. Drawer E, Aiken, South Carolina 29802
Search for more papers by this authorM. Michele Keklak
University of Georgia, Savannah River Ecology Laboratory, P.O. Drawer E, Aiken, South Carolina 29802
Search for more papers by this authorM. Gay Heagler
University of Georgia, Savannah River Ecology Laboratory, P.O. Drawer E, Aiken, South Carolina 29802
Search for more papers by this authorL. Stan Hales Jr.
Zoology Department, University of Georgia, Athens, Georgia 30602
Search for more papers by this authorAbstract
Genetic and demographic changes in mosquitofish populations are reported after chronic (111 d) exposure to mercury. Sex ratios, normally female-biased in field populations, were also female-biased in control mesocosms. However, the sex ratio was male-biased in the mercury treatments. Frequencies of glucosephosphate isomerase-2 (Gpi-2) allozymes for fish exposed to mercury differed from initial frequencies and from those of control fish. In a selection-component analysis, female sexual selection was statistically significant for the mercury-treated fish; the proportion of females that were gravid differed among Gpi-2 genotypes. The number of developing embryos per female also differed among Gpi-2 genotypes. Mercury had genotype-specific effects on mosquitofish reproduction in addition to genotype-specific effects on mortality reported earlier. These effects may reflect metabolic qualities of the Gpi-2 genotypes or loci closely linked to the Gpi-2 locus.
References
- 1 Bouquegneau, J. M. 1979 Evidence for the protective effect of metallothioneins against inorganic mercury injuries to fish. Bull Environ Contam Toxicol 23 218–219
- 2 Bensen, W. H. and W. J. Birge. 1985 Heavy metal tolerance and metallothionein induction in fathead minnows Results from field and laboratory investigations. Environ Toxicol Chem 4 209–217
- 3 Kynard, B. 1974 Avoidance behavior of insecticide susceptible and resistant populations of mosquitofish to four insecticides. Trans Am Fish Soc 3 557–561
- 4 Brown, B. E. 1977 Uptake of copper and lead by a metal-tolerant isopod. Asellus meridianus Freshwater Biol 7 235–244
- 5 Klerks, P. L. and J. S. Levinton 1989 Rapid evolution of metal resistance in a benthic oligochaete inhabiting a metal polluted site. Biol Bull 176 135–141
- 6
Olafson, R. W.,
A. Kearns and
R. G. Sim.
1979
Heavy metal induction of metallothionein synthesis in the hepatopancreas of the crab, Scylla serrata
Comp. Biochem. Physiol. B
62
417–424
10.1016/0305-0491(79)90112-3 Google Scholar
- 7 Hamilton, S. J. and P. M. Mehrle. 1986. Metallothionein in fish: Review of its importance in assessing stress from metal contaminants. Trans. Am. Fish. Soc. 115: 596–609.
- 8 Pynnonen, K., D. A. Holwerda and D. I. Zandee. 1987. Occurrence of calcium concretions in various tissues of freshwater mussels and their capacity for cadmium sequestration. Aquat. Toxicol. 10: 101–114.
- 9 Calow, P. and R. M. Sibly. 1990. A physiological basis of population processes: Ecotoxicological implications. Funct. Ecol. 4: 283–288.
- 10 Burton, R. S. and M. W. Feldman. 1983. Physiological effects of an allozyme polymorphism: Glutamate-pyruvate transaminase and response to hyperosmotic stress in the copepod Tigriopus californicus. Biochem. Genet. 21: 239–251.
- 11 Watt, W. B., P. A. Carter and S. M. Blower. 1985. Adaptation at specific loci: IV. Differential mating success among glycolytic allozyme genotypes of Colias butterflies. Genetics 109: 157–175.
- 12 Nevo, E., R. Ben-Shlomo and B. Lavie. 1984. Mercury selection of allozymes in marine organisms: Predictions and verification in nature. Proc. Natl. Acad. Sci. USA 81: 1258–1259.
- 13 Nevo, E., R. Noy, B. Lavie, A. Beiles and S. Muchtar. 1986. Genetic diversity and resistance to marine pollution. Biol. J. Linn. Soc. 29: 139–144.
- 14 Koehn, R. K. 1978. Physiology and biochemistry of enzyme variation: The interface of ecology and population genetics. In P. F. Brussard, ed., Ecological Genetics: The Interface. Springer-Verlag, New York, NY, pp. 51–72.
- 15 Frati, F., P. P. Fanciulli and L. Posthuma. 1992. Allozyme variation in reference and metal-exposed natural populations of Orchesella cinta (Insecta: Collembola). Biochem. Syst. Ecol. 20: 297–310.
- 16 Diamond, S. A., M. C. Newman, M. Mulvey, P. M. Dixon and D. Martinson. 1989. Allozyme genotype and time to death of mosquitofish, Gambusia affinis (Baird and Girard), during acute exposure to inorganic mercury. Environ. Toxicol. Chem. 8: 613–622.
- 17 Heagler, M. G., M. C. Newman, M. Mulvey and P. M. Dixon. 1993. Allozyme genotype in mosquitofish, Gambusia holbrooki, during mercury exposure: Temporal stability, concentration effects and field verification. Environ. Toxicol. Chem. 12: 385–395.
- 18 Kramer, V. J., M. C. Newman and G. R. Ultsch. 1992. Changes in concentration of glycolysis and Krebs cycle metabolites in mosquitofish, Gambusia holbrooki, induced by mercuric chloride and starvation. Environ. Biol. Fishes 34: 315–320.
- 19 Kramer, V. J., M. C. Newman, M. Mulvey and G. R. Ultsch. 1992. Glycolysis and Krebs cycle metabolites in mosquitofish, Gambusia holbrooki Girard 1859, exposed to mercuric chloride: Allozyme genotype effects. Environ. Toxicol. Chem. 11: 357–364.
- 20 Kramer, V. J. and M. C. Newman. 1994. Inhibition of glucose-phosphate isomerase allozymes of the mosquitofish, Gambusia holbrooki, by mercury. Environ. Toxicol. Chem. 13: 9–14.
- 21 Newman, M. C. 1986. Comprehensive cooling water report, Vol. 2—Water quality. Publication 28–II. Savannah River Ecology Laboratory, University of Georgia, Aiken, SC.
- 22 Pannella, G. 1971. Fish otoliths: Daily layers and periodic patterns. Science 173: 1124–1127.
- 23 Haake, P. W., C. A. Wilson and J. M. Dean. 1981. A technique for the examination of otoliths by SEM with application to larval fishes. Proceedings, Fifth Annual Larval Fish Conference, Baton Rouge, LA, March 2–3, pp. 12–15.
- 24 Spurr, A. R. 1969. A low-viscosity epoxy resin embedding medium for electron microscopy. J. Ultrastruct. Res. 26: 31–43.
- 25 Hales, L. S., Jr. and K. W. Able. 1995. Effects of oxygen concentration on somatic and otolith growth rates of juvenile black sea bass, Centropristis striata. In D. H. Secor, J. M. Dean and M. Campana, eds., Recent Developments in Fish Otolith Research. University of South Carolina Press, Columbia, SC, pp. 135–153.
- 26 Newman, M. C., S. A. Diamond, M. Mulvey and P. Dixon. 1989. Allozyme genotype and time to death of mosquitofish, Gambusia affinis (Baird and Girard), during acute toxicant exposure: A comparison of arsenate and inorganic mercury. Aquat. Toxicol. 15: 141–156.
- 27 SAS Institute, Inc. 1987. SASr̀ User's Guide: Statistics, Version 5. Cary, NC.
- 28 Sokal, R. R. and F. J. Rohlf. 1981. Biometry: The Principles and Practice of Statistics in Biological Research, 2nd ed. W. H. Freeman, New York, NY.
- 29
Swofford, D. L. and
R. B. Selander.
1981.
BIOSYS-1: A FORTRAN program for the comprehensive analysis of electrophoretic data in population genetics and systematics.
J. Hered.
72:
282–283.
10.1093/oxfordjournals.jhered.a109497 Google Scholar
- 30 Christiansen, F. B., O. Frydenberg and V. Simonsen. 1973. Genetics of Zoarces populations: IV. Selection component analysis of an esterase polymorphism using population samples including mother-offspring combinations. Hereditas 73: 291–304.
- 31 Weis, J. S., P. Weis and M. Heber. 1982. Variation in response to methylmercury by killifish (Fundulus heteroclitus) embryos. In J. G. Pearson, R. Foster and W. E. Bishop, eds., Aquatic Toxicology and Hazard Assessment: 5th Volume. STP 766. American Society for Testing and Materials, Philadelphia, PA, pp. 109–119.
- 32 Krumholz, L. A. 1948. Reproduction in the western mosquitofish, Gambusia affinis (Baird and Girard) and its use in mosquito control. Ecol. Monogr. 18: 1–43.
- 33 Newman, M. C. and M. Aplin. 1992. Enhancing toxicity data interpretation and prediction of ecological risk with survival time modeling: An illustration using sodium chloride toxicity to mosquitofish (Gambusia holbrooki). Aquat. Toxicol. 23: 85–96.
- 34 Newman, M. C., M. M. Keklak and S. M. Doggett. 1994. Quantifying animal size effects on toxicity: A general approach. Aquat. Toxicol. 28: 1–13.
- 35 Duncan, D. A. and J. F. Klaverkamp. 1983. Tolerance and resistance to cadmium in white suckers (Catostomus commersoni) previously exposed to cadmium, zinc or selenium. Can. J. Fish. Aquat. Sci. 40: 128–138.
- 36 Chapman, G. A. 1985. Acclimation as a factor influencing metal criteria. In R. C. Bahner and D. J. Hansen, eds., Aquatic Toxicology and Hazard Assessment: 8th Volume. STP 891. American Society for Testing and Materials, Philadelphia, PA, pp. 119–136.
- 37 Hughes, J. M., D. A. Harrison and J. M. Arthur. 1991. Genetic variation at the Pgi locus in the mosquitofish Gambusia affinis (Poecilidae) and a possible effect on susceptibility to an insecticide. Biol. J. Linn. Soc. 44: 153–167.
- 38 Mulvey, M., G. Keller and G. K. Meffe. 1994. Single- and multiple-locus genotypes and life history responses of Gambusia holbrooki reared at two temperatures. Evolution (in press).
- 39 Watt, W. B. 1985. Bioenergetics and evolutionary genetics: Opportunities for new synthesis. Am. Nat. 125: 118–143.