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Effects of acute and chronic acidification on three larval amphibians that breed in temporary ponds

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Abstract

This study explored the effects of acute (7 days) and chronic (4 months) exposure to pH 4.2 on three species of larval amphibians, Ambystoma jeffersonianum, Ambystoma maculatum, and Rana sylvatica. Acute tests were conducted in 24 impermeable enclosures in three temporary ponds. Total dissolved aluminum was higher in acidified enclosures in comparison with controls (pH 4.2, [Al]≈10–30 μM and pH>4.7, [Al]≈5–15 μM, respectively). Greater mortality of A. jeffersonianum occurred at pH 4.2 than at pH>4.7, whereas survival of A. maculatum and R. sylvatica were unaffected by pH. Mean wet masses of R. sylvatica were significantly lower at pH 4.2 than at pH>4.7, but mean wet masses of surviving A. jeffersonianum and A. maculatum were not influenced by pH. There were no pH-related differences in body sodium concentration in larval R. sylvatica.

Chronic acidification of mesocosms to pH 4.2 ([Al]≈16 μM) (controls=pH>6, [Al]≈0.1 μM) resulted in total mortality of A. jeffersonianum. Survival of A. maculatum and R. sylvatica were not associated with pH, but survival of A. maculatum was low at both pH levels. Time to metamorphosis was longer for R. sylvatica maintained at pH 4.2, but not for A. maculatum. No differences in wet masses at metamorphosis were observed for R. sylvatica or A. maculatum. These results indicate that short and long term acidification of temporary wetlands could dramatically affect amphibians which rely upon them as breeding sites, either by causing mortality or by decreasing growth rates.

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References

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

    Google Scholar 

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

    Google Scholar 

  • Cronin JT, Travis J (1986) Size-limited predation on larval Rana areolata (Anura: Ranidae) by two species of backswimmer (Insecta: Hemiptera:Notonectidae). Herpetologica 42(2):171–174

    Google Scholar 

  • Cummins CP (1989) Interaction between the effects of pH and density on growth and development in Rana temporaria L. tadpoles. Funct Ecol 3:45–52

    Google Scholar 

  • Day RW, Quinn GP (1989) Comparisons of treatments after an analysis of variance in ecology. Ecol Monog 59(4):433–463

    Google Scholar 

  • Dougan WK, Wilson AL (1974) The absorptiometric determination of aluminum in water. A comparison of some chromographic 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 Herpetol 16:314–316

    Google Scholar 

  • Freda J (1986) The influence of acidic pond water on amphibians: a review. Water Air Soil Pollut 30:439–450

    Google Scholar 

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

    Google Scholar 

  • Freda J, Dunson WA (1984) Sodium balance of amphibian larvae exposed to low environmental pH. Physiol Zool 57(4):435–443

    Google Scholar 

  • —, — (1985a) Field and laboratory studies of ion balance and growth rates of ranid tadpoles chronically exposed to low pH. Copeia 1985(2):415–423

    Google Scholar 

  • —, — (1985b) 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 

  • —, — (1986a) The effect of prior exposure on sodium uptake in tadpoles exposed to low pH water. J Comp Physiol B: 156:649–654

    Google Scholar 

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

    Google Scholar 

  • Freda J, McDonald DG (1990) Effects of aluminum on the leopard frog, Rana pipiens: life stage comparisons and aluminum uptake. Can J Fish Aquat Sci 47:210–216

    Google Scholar 

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

    Google Scholar 

  • Gosner KL (1960) A simplified table for staging anuran embryos and larvae with notes on identification. Herpetologica 16:183–190

    Google Scholar 

  • Harrison RG (1969) Stages and description of the normal development of the spotted salamander Ambystoma punctatum (Linn.). In: Wiles S (ed) Organization and development of the embryo. Yale University Press, New Haven, pp 44–46

    Google Scholar 

  • Keeley JE, Sandquist DR (1991) Diurnal photosynthesis cycle in cam and non-cam seasonal pool aquatic macrophytes. Ecology 72(2):716–727

    Google Scholar 

  • Leuven RSEW, den Hartog C, Christiaans MMC, Heijligers WHC (1986) Effects of water acidification on the distribution pattern and the reproductive success of amphibians. Experentia 42:495–503

    Google Scholar 

  • Ling RW, VanAmberg JP, Werner JK (1986) Pond acidity and its relationship to larval development of Ambystoma maculatum and Rana sylvatica in upper Michigan. J Herpetol 20(2):230–236

    Google Scholar 

  • McDonald DG, Ozog JL, Simons BP (1984) The influence of low pH environments on ion regulation in the larval stages of the anuran amphibian, Rana clamitans. Can J Zool 62:2171–2177

    Google Scholar 

  • Minitab Reference Manual, Release 7 (1989) Minitab Inc., State College, PA

  • Morin, PJ (1981) Predatory salamanders reverse the outcome of competition among three species of anuran tadpoles. Science 212:1284–1286

    Google Scholar 

  • — (1983) Predation, competition, and the composition of larval anuran guilds. Ecol Monog 53(2):119–138

    Google Scholar 

  • Morin PJ, Wilbur HM, Harris RN (1983) Salamander predation and the structure of experimental communities: Responses of Notophthalamus and microcrustacea. Ecology 64(6):1430–1436

    Google Scholar 

  • Morin PJ, Lawler SP, Johnson EA (1988) Competition between aquatic insects and vertebrates: Interaction strength and higher order interactions. Ecology 69(5):1401–1409

    Google Scholar 

  • Neter J, Wasserman W, Kutner MH (1990) Applied linear statistical models: Regression, analysis of variance, and experimental designs, 3rd ed. Richard D. Irwin, Inc, Homewood, IL, 1181 pp

    Google Scholar 

  • Packer RK, Dunson WA (1972) Anoxia and sodium loss associated with the death of brook trout at low pH. Comp Biochem Physiol 41A:17–26

    Google Scholar 

  • Pechmann JHK, Scott DE, Semlitsh RD, Caldwell JP, Vitt LJ, Gibbons JW (1991) Declining amphibian populations: The problem of separating human impacts from natural fluctuations. Science 253:893–895

    Google Scholar 

  • Rice WR (1989) Analyzing tables of statistical tests. Evolution 43(1):223–225

    Google Scholar 

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

    Google Scholar 

  • Sadinski WJ, Dunson WA. A multilevel study of the effects of low pH on amphibians of temporary ponds. J Herpetol (in press)

  • Streams FA (1987) Within-habitat spatial separation of two Notonecta species: Interactive vs. noninteractive resource partitioning. Ecology 68(4):935–945

    Google Scholar 

  • Warner SC, Dunson WA, Travis J (1991) Interaction of pH, density, and priority effects on the survivorship and growth of two species of hylid tadpoles. Oecologia 88:331–339

    Google Scholar 

  • Warner SC, Travis J, Dunson WA. The effect of pH level on the interspecific competition between two species of hylid tadpoles. Ecology (in press)

  • Wilbur HM, Morin PJ, Harris RN (1983) Salamander predation and the structure of experimental communities: Anuran responses. Ecology 64(6):1423–1429

    Google Scholar 

  • Wilbur HM (1987) Regulation of structure in complex systems: Experimental temporary pond communities. Ecology 68(5):1437–1452

    Google Scholar 

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Rowe, C.L., Sadinski, W.J. & Dunson, W.A. Effects of acute and chronic acidification on three larval amphibians that breed in temporary ponds. Arch. Environ. Contam. Toxicol. 23, 339–350 (1992). https://doi.org/10.1007/BF00216243

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  • DOI: https://doi.org/10.1007/BF00216243

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