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Exclusion of the Jefferson salamander, Ambystoma jeffersonianum, from some potential breeding ponds in Pennsylvania: Effects of pH, temperature, and metals on embryonic development

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Abstract

A field survey revealed that Al, SO4, H+, and Zn were significantly higher in 40 ponds lacking successful breeding of the Jefferson salamander, A. jeffersonianum, whereas alkalinity, Cu, DOC, K, Mg, Na, and NO3 were significantly higher in 10 ponds that supported successful breeding. In a second smaller set of ponds used for transplant studies, Al, conductivity, H+, and SiO2 were significantly higher in five ponds lacking reproduction of A. jeffersonianum; alkalinity, Ca, and K were significantly higher in three ponds with successful reproduction. Survival and hatching success were significantly greater for egg masses transplanted into ponds supporting viable Jefferson salamander populations than into those that did not. Survival and hatching success were greater at 15°C than at 10°C. Low pH slowed developmental rate, consequently increasing the time until hatching. Low pH decreased hatching success of the embryos at 10 and 15°C. Copper was acutely toxic to embryos at pH 4.50 (96 h LC50=315 μg/L); chronic exposure levels in the field were much lower (approximately 0.01 times). Since successful ponds actually contained more Cu than unsuccessful ones, Cu does not appear to be toxic in the field. Aluminum ameliorated the acute 96 h toxicity of pH 4.50; at [Al]'s between 250 and 500 μg/L mortality at pH 4.50 was greatly reduced. This effect of Al occurred at concentrations comparable to those found in the field. Lead and zinc, at concentrations up to 2,000 μg/L, had no apparent effects on the developing embryos of A. jeffersonianum. Aluminum, Pb, and Zn did not afect developmental rate, as did low pH and Cu. Based on these findings, low pH and its interaction with Al are likely to be major factors responsible for the success or failure of the Jefferson salamander in breeding ponds in Pennsylvania. Further investigation is needed into interations among pH, metals, dissolved organics, and non-toxic cations to further clarify the mechanisms of toxicity of the complex mixture of which pond water consists.

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References

  • Andren C, Henrikson L, Olsson M, Nilson G (1988) Effects of pH and aluminum on embryonic and early larval stages of the Swedish brown frogs Rana arvalis, Rana temporaria, and Rana dalmatina. Holarctic Ecology 11:127–135

    Google Scholar 

  • Barinaga M (1990) Where have all the froggies gone? Science 247:1033–1034

    Google Scholar 

  • Beattie RC, Aston RJ, Milner AJP (1991) A field study of fertilization and embryonic development in the common frog (Rana temporaria) with particular reference to acidity and temperature. J Appl Ecol 28:346–357

    Google Scholar 

  • Blaustein AR (1990) Declining amphibian populations—a global phenomenon? Bull Ecol Soc Am 71(2):127–128

    Google Scholar 

  • Blem CR, Blem LB (1989) Tolerance of acidity in a Virginia population of the spotted salamander Ambystoma maculatum (Amphibia: Ambystomatidae). Brimleyana 15:37–45

    Google Scholar 

  • Burton TM, Likens GE (1975) Energy flow and nutrient cycling in salamander populations in the Hubbard Brook Experimental Forest, New Hampshire. Ecology 56:1068–1080

    Google Scholar 

  • Clark KL (1986) Responses of spotted salamander, Ambystoma maculatum, population in central Ontario to habitat acidity. Can Field-Naturalist 100(4):463–469

    Google Scholar 

  • Clark KL, Hall RJ (1985) Effects of elevated hydrogen ion and aluminum concentration on the survival of amphibian embryos and larvae. Can J Sci 42:116–123

    Google Scholar 

  • Clark KL, LaZerte BD (1985) A laboratory study of the effects of aluminum and pH on amphibian eggs and tadpoles. Can J Fish Aquat Sci 42:1544–1551

    Google Scholar 

  • —, — (1987) Interspecific variation in hydrogen ion and aluminum toxicity in Bufo americanus and Ambystoma maculatum. Can J Fish Aqua Sci 44:1622–1628

    Google Scholar 

  • Cusimano RF, Brakke DF, Chapman GA (1986) Effects of pH on the toxicities of cadmium, copper, and zinc to steelhead trout (Salmo gairdneri). Can J Fish Aquat Sci 43:1497–1503

    Google Scholar 

  • Dale JM, Freedman B, Kerekes J (1985) Experimental studies of the effects of acidity and associated water chemistry on amphibians. Proc N S Inst Sci 35:35–54

    Google Scholar 

  • Dougan WK, Wilson AL (1974) The absorptimetric determination of aluminum in water. A comparison of some chromogenic reagents and the development of an improved method. Analyst 99:413–430

    Google Scholar 

  • Dunson WA, Connell J (1982) Specific inhibition of hatching in amphibian embryos by low pH. J Herp 3:314–316

    Google Scholar 

  • Dunson WA, Wyman RL, Corbett ES (1992) A symposium on amphibian declines and habitat acidification. J Herp 26(4):349–352

    Google Scholar 

  • Flemming CA, Trevors JT (1989) Copper toxicity and chemistry in the environment: A review. Water Air Soil Pollut 44:143–158

    Google Scholar 

  • Freda J (1986) The influence of acidic pond water on amphibians: A review. Water Air Soil Pollut 20:439–450

    Google Scholar 

  • — (1991) The effects of aluminum and other metals on amphibians. Environ POllu 71:305–328

    Google Scholar 

  • Freda J, Dunson WA (1985a) The influence of external cation concentration on the hatching of amphibian embryos in water of low pH. Can J Zool 63:2649–2656

    Google Scholar 

  • --, -- (1985b) The effect of acidic precipitation on amphibian breeding in temporary ponds of Pennsylgania. US Fish and Wildlife Service, Eastern Energy and Land Use Team. Biol Rep 80(40.22), 85 pp

  • —, — (1986) Effects of low pH and other chemical variables on the local distribution of amphibians. Copeia 2:454–466

    Google Scholar 

  • Freda J, McDonald DG (1989) Effects of Al on the leopard frog Rana pipiens: Lifestage comparisons and aluminum uptake. Can J Fish Aquat Sci 47:210–216

    Google Scholar 

  • Freda J, Cavdek V, McDonald DG (1990) Role of organic complexation in the toxicity of aluminum to Rana pipiens embryos and Bufo americanus tadpoles. Can J Fish Aquat Sci 47:217–224

    Google Scholar 

  • Freda J, Sadinski WJ, Dunson WA (1991) Long term monitoring of amphibian populations to the effects of acidic deposition. Water Air Soil Pollut 55:445–462

    Google Scholar 

  • Gad SC, Weil CS (1989) Statistics for Toxicologists. In Hayes AW (ed) Principles and methods of toxicology. Raven Press, NY, pp 435–483

    Google Scholar 

  • Hairston NG Sr (1987) Community ecology and salamander guilds. Cambridge University Press, Cambridge, pp 198–200

    Google Scholar 

  • Harfenist A, Power T, Clark KL, Peakall DB (1989) A review and evaluation of the amphibian toxicological literature. Technical Report #61, Canadian Wildlife Service, Headquarters

  • Lauren DJ, McDonald DG (1987) Acclimation to copper by rainbow trout, Salmo gairdneri, physiology. Can J Fish Aquat Sci 44:99–104

    Google Scholar 

  • Ling RW, Van Amberg JW, Werner JK (1986) Pond acidity and its relationship to larval development of Ambystoma maculatum and Rana sylvatica in upper Michigan. J Herp 20:453–458

    Google Scholar 

  • Lynch JA, Corbett ES (1983) Atmospheric deposition: Spatial and temporal variation in Pennsylvania 1982. Institute for Research on Land and Water Resources, Publ No. LW8313. The Pennsylvania State University, University Park, PA 73 pp

    Google Scholar 

  • Lynch JA, Corbett ES, Rishel GB (1984) Atmospheric deposition: Spatial and temporal variation in Pennsylvania 1983. Institute for Research on Land and Water Resources, Publ No. LW8405. The Pennsylvania State University, University Park, PA, 85 pp

    Google Scholar 

  • McCoy CJ (1982) Amphibians and reptiles in Pennsylvania: Checklist, bibliography, and atlas of distribution. Special Publication of Carnegie Museum of Natural History, Pittsburgh, PA

    Google Scholar 

  • McDonald DG, Reeder JP, Dalziel TRK (1989) The combined effects of pH and trace metals on rish ionoregulation. In: Morris R (ed) Acid toxicity and aquatic animals. Cambridge Univ Press, Cambridge

    Google Scholar 

  • Pagenkopf GK (1983) Gill surface interaction model for trace-metal toxicity to fishes: Role of complexation, pH, and water hardness. Environ Sci Technol 17:342–347

    Google Scholar 

  • Pascoe D, Evans SA, Woodworth J (1986) Heavy metal toxicity to fish and the influence of water hardness. Arch Environ Contam Toxicol 15:481–487

    Google Scholar 

  • Pechman JHK, Scott DE, Semlitsch RD, Caldwell JP, Vitt LJ, Gibbons JW (1991) Declining amphibian populations: The problem of separating human impacts from natural fluctuations. Science 253:892–895

    Google Scholar 

  • Pierce BA (1985) Acid tolerances in amphibians. Bioscience 35:239–243

    Google Scholar 

  • — (1989) Effects of short-term acidification on growth rates of tadpoles. J Herp 23:97–102

    Google Scholar 

  • Playle RC, Wood CM (1991) Mechanisms of aluminum extraction and accumulation at the gills of the rainbow trout, Oncorhynchus mykiss (Walbaum), in acidic soft water. J Fish Biol 38:791–805

    Google Scholar 

  • Playle RC, Gensemer RW, Dixon DG (1992) Copper accumulation on gills of fathead minnows: Influence of water hardness, complexation and pH of the gill micro-environment. Environ Toxicol Chem 11:381–391

    Google Scholar 

  • Pough FH, Wilson RE (1977) Acid precipitation and reproductive success of Ambystoma salamanders. Water Air Soil Pollut 7:531–544

    Google Scholar 

  • Reid SD, McDonald DG (1988) Effects of cadmium, copper, and low pH on ion fluxes in the rainbow trout, Salmo gairdneri. Can J Aquat Sci 45:244–253

    Google Scholar 

  • Rowe CL, Sadinski WJ, Dunson WA (1992) Effects of acute and chronic acidification on three larval amphibians that breed in temporary ponds. Arch Environ Contam Toxicol 23:339–350

    Google Scholar 

  • Rowe CL, Dunson WA (in press) Relationship among abiotic parameters and breeding effort by three amphibians in temporary wetlands of central Pennsylvania. Wetlands

  • Rugh R (1962) Experimental embryology. Burgess Publ Co, Minneapolis, MN, 501 pp

    Google Scholar 

  • Sadinski WJ (1991) Direct and indirect effects of low pH on the communities of temporary ponds. PhD thesis in ecology. The Pennsylvania State University, University Park, PA 253 pp

    Google Scholar 

  • Sadinski WJ, Dunson WA (1992) A multilevel study of the effects of low pH on amphibians of temporary ponds. J Herp 26:413–422

    Google Scholar 

  • Sayer MDJ, Reader JP, Morris R, (1989) The effect of calcium concentration on the toxicity of copper, lead and zinc to yolk-sac fry of brown trout, Salmo trutta L., in soft, acid water. J Fish Biol 35:323–332

    Google Scholar 

  • —, —, —, (1991) Embryonic and larval development of brown trout, Salmo trutta L.: exposure to aluminum, copper, lead or zinc in soft, acid water. J Fish Biol 38:431–455

    Google Scholar 

  • Tyler-Jones R, Beattie RC, Aston RJ (1989) The effects of acid water and aluminum on the embryonic development of the common frog, Rana temporaria. J Zool London 219:355–372

    Google Scholar 

  • Wake DB (1991) Declining amphibian populations. Science 253:860

    Google Scholar 

  • Williams DD (1987) The ecology of temporary waters. Timber Press, Portland, OR

    Google Scholar 

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Horne, M.T., Dunson, W.A. Exclusion of the Jefferson salamander, Ambystoma jeffersonianum, from some potential breeding ponds in Pennsylvania: Effects of pH, temperature, and metals on embryonic development. Arch. Environ. Contam. Toxicol. 27, 323–330 (1994). https://doi.org/10.1007/BF00213167

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  • DOI: https://doi.org/10.1007/BF00213167

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