Skip to main content
Log in

Consequences and causes of geographic variation in the body size of a keystone predator,Notophthalmus viridescens

  • Original Paper
  • Published:
Oecologia Aims and scope Submit manuscript

Abstract

Two subspecies of the predatory aquatic salamanderNotophthalmus, N. viridescens viridescens andN. v. dorsalis, differ in adult body size and geographic distribution. We tested whether experimental populations of the two predator subspecies differed in their effects on prey populations ofB. americanus, and whether observed differences in predator body size were genetic and/or environmentally induced. We compared the effects of predation by bothNotophthalmus subspecies on larvalBufo americanus by experimentally manipulating the densities (0, 2, or 4 newts/m3) and subspecies ofNotophthalmus (N. v. viridescens orN. v. dorsalis) added to artificial ponds. BothNotophthalmus subspecies significantly reducedB. americanus survival, but differed significantly in this effect. FewerBufo survived with the larger subspecies,N. v. viridescens, than with the smallerNotophthalmus subspecies,N. v. dorsalis. TheNotophthalmus subspecies differed in their patterns of adult and larval growth. Adults of the smaller subspecies,N. v. dorsalis, had a significantly higher growth rate than the larger subspecies,N. v. viridescens, under common environmental conditions, suggesting that differences in predator size were partly genetic, rather than entirely environmentally induced. LarvalN. v. dorsalis metamorphosed significantly later in the season than larvae ofN. v. viridescens, suggesting that larvalN. v. dorsalis had a lower growth rate than larvalN. v. viridescens. Differences in adult and larval growth, together with differences in the minimum adult size observed in natural populations, suggest that differences in the rate or duration of pre-adult growth may contribute substantially to observed differences in size.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Institutional subscriptions

Similar content being viewed by others

References

  • Alford RA (1989) Variation in predator phenology affects predator performance and prey community composition. Ecology 70:206–219

    Google Scholar 

  • Andrews RM (1982) Patterns of growth in reptiles. In: Gans C, Pough FH (eds) Biology of the reptiles, vol 13: Physiological ecology. Academic Press, London, pp 273–320

    Google Scholar 

  • Arnold SJ (1981) Behavioral variation in natural populations. II. The inheritance of a feeding response in crosses between geographic races of the garter snake,Thamnophis elegans. Evolution 35:510–515

    Google Scholar 

  • Berven KA, Gill DE (1983) Interpreting geographic variation in life-history traits. Amer Zool 23:85–97

    Google Scholar 

  • Briand F (1983) Environmental control of food web structure. Ecology 64:253–263

    Google Scholar 

  • Bristow CE (1991) Interactions between phylogenetically distant predators:Notophthalmus viridescens andEnneacanthus obesus. Copeia 1991:1–8

    Google Scholar 

  • Brockelman WY (1969) An analysis of density effects and predation inBufo americanus tadpoles. Ecology 50:632–644

    Google Scholar 

  • Brophy TE (1980) Food habits of sympatric larvalAmbystoma tigrinum andNotophthalmus viridescens. J Herpetol 14:1–6

    Google Scholar 

  • Bruce RC (1990) An explanation for differences in body size between two desmognathine salamanders. Copeia 1990:1–9

    Google Scholar 

  • Clausen J, Keck DD, Heisey WM (1948) Experimental studies on the nature of species. III. Environmental responses of climatic races ofAchillea. Carnegie Inst Wash Publ 581:1–129

    Google Scholar 

  • Conant R, Collins JT (1991) A field guide to the reptiles and amphibians of eastern and central North America, 3rd edn. Houghton Miflin, Boston

    Google Scholar 

  • Fauth JE, Resetarits WJ Jr (1991) Interactions between the salamanderSiren intermedia and the keystone predatorNotophthalmus viridescens. Ecology 72:827–838

    Google Scholar 

  • Forester DC, Lykens DV (1991) Age structure in a population of red-spotted newts from the Allegheny Plateau of Maryland. J Herpetol 25:373–376

    Google Scholar 

  • Freund RJ, Littell RC (1981) SAS for linear models: a guide to the ANOVA and GLM procedures. SAS Institute Inc., Cary, NC

    Google Scholar 

  • Gerwien RW, John-Alder HB (1992) Growth and behavior of thyroid-deficient lizards (Sceloporus undulatus). Gen Comp Endocrinol 87:312–324

    Google Scholar 

  • Gill DE (1978) The metapopulation ecology of the red-spotted newt,Notophthalmus viridescens (Rafinesque). Ecol Monogr 48:145–166

    Google Scholar 

  • Gill DE (1979) Density dependence and homing behavior in adult red-spotted newtsNotophthalmus viridescens (Rafinesque). Ecology 60:800–813

    Google Scholar 

  • Hairston NG (1980) Evolution under interspecific competition: field experiments on terrestrial salamanders. Evolution 34:409–420

    Google Scholar 

  • Harris RN (1987a) Density-dependent paedomorphosis in the salamanderNotophthalmus viridescens dorsalis. Ecology 68:705–712

    Google Scholar 

  • Harris RN (1987b) An experimental study of population regulation in the salamander,Notophthalmus viridescens dorsalis (Urodela: Salamandridae). Oecologia 71:280–285

    Google Scholar 

  • Harris RN, Alford RA, Wilbur HM (1988) Density and phenology of adult and larvalNotophthalmus viridescens dorsalis in a natural pond. Herpetologica 44:234–242

    Google Scholar 

  • Healy WR (1973) Life history variation and the growth of juvenileNotophthalmus viridescens from Massachusetts. Copeia 1973:641–647

    Google Scholar 

  • Healy WR (1974) Population consequences of alternative life histories inNotophthalmus v. viridescens. Copeia 1974:221–229

    Google Scholar 

  • MacArthur RH (1972) Geographical ecology. Harper and Row, New York

    Google Scholar 

  • Martof BS, Palmer WM, Bailey RJ, Harrison JR III (1980) Amphibians and reptiles of the Carolinas and Virginia. The University of North Carolina Press, Chapel Hill, NC

    Google Scholar 

  • May RM (1974) Stability and complexity in model ecosystems. Princeton University Press, Princeton, NJ

    Google Scholar 

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

    Google Scholar 

  • Morin PJ (1983a) Predation, competition, and the composition of larval anuran guilds. Ecol Monogr 53:119–138

    Google Scholar 

  • Morin PJ (1983b) Competitive and predatory interactions in natural and experimental populations ofNotophthalmus viridescens dorsalis andAmbystoma tigrinum. Copeia 1983:628–639

    Google Scholar 

  • Morin PJ (1986) Interactions between intraspecific competition and predation in an amphibian predator-prey system. Ecology 67:713–720

    Google Scholar 

  • Morin PJ (1987) Predation, breeding asynchrony, and the outcome of competition among treefrog tadpoles. Ecology 68:675–683

    Google Scholar 

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

    Google Scholar 

  • Paine RT (1976) Size-limited predation: an observational and experimental approach with theMytilus-Pisaster interaction. Ecology 57:858–873

    Google Scholar 

  • Paine RT (1980) Food webs: linkage, interaction strength and community infrastructure. J Anim Ecol 49:667–685

    Google Scholar 

  • Persson L (1988) Asymmetries in competitive and predatory interactions in fish populations. In: Ebenman B, Persson L (eds) Size-structured populations. Springer, Berlin Heidelberg New York, pp 203–218

    Google Scholar 

  • Pianka ER (1966) Latitudinal gradients in species diversity: a review of the concepts. Am Nat 100:33–46

    Google Scholar 

  • Polis GA (1988) Exploitation competition and the evolution of interference, cannibalism, and intraguild predation in age/sizestructured populations. In: Ebenman B, Persson L (eds) Sizestructured populations. Springer, Berlin Heidelberg New York, pp 185–202

    Google Scholar 

  • Reilly SM (1990) Biochemical systematics and evolution of the eastern North American newts, genusNotophthalmus (Caudata: Salamandridae). Herpetologica 46:51–59

    Google Scholar 

  • Reznick DA, Bryga H, Endler JA (1990) Experimentally induced life-history evolution in a natural population. Nature 346:357–35

    Google Scholar 

  • Rice WR (1990) A consensus combined p-value test and the family-wide significance of component tests. Biometrics 46:303–308

    Google Scholar 

  • Roughgarden JR, Gaines S, Possingham H (1988) Recruitment dynamics and complex life cycles. Science 241:1460–1466

    Google Scholar 

  • Scheiner SM (1993) MANOVA: multiple response variables and multiple species interactions. In: Scheiner SM, Gurevitch J, (eds) Design and analysis of ecological experiments. Chapman and Hall, New York, pp 95–112

    Google Scholar 

  • Semlitsch RD, Gibbons JW (1988) Fish predation in size-structured populations of treefrog tadpoles. Oecologia 75:321–326

    Google Scholar 

  • Semlitsch RD, Gibbons JW (1990) Effects of egg size on success of larval salamanders in complex aquatic environments. Ecology 71:1789–1795

    Google Scholar 

  • Smith DC (1983) Factors controlling tadpole populations of the chorus frog (Pseudacris triseriata) on Isle Royale, Michigan. Ecology 64:501–510

    Google Scholar 

  • Sokal RR, Rohlf FJ (1981) Biometry, 2nd edn. W.H. Freeman and company, New York

    Google Scholar 

  • Tabachnik WJ (1977) Geographic variation of five biochemical polymorphisms inNotophthalmus viridescens. J Hered 68:117–122

    Google Scholar 

  • Travis J, Keen WH, Juilianna J (1985) The role of relative body size in a predator-prey relationship between dragonfly naiads and larval anurans. Oikos 45:59–65

    Google Scholar 

  • Underwood AJ, Fairweather PG (1989) Supply-side ecology and benthic marine assemblages. Trends Ecol Evol 4:16–20

    Google Scholar 

  • Werner EE (1986) Amphibian metamorphosis: growth rate, predation risk, and the optimal size at transformation. Am Nat 128:319–341

    Google Scholar 

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

    Google Scholar 

  • Wilbur HM (1988) Interactions in size-structured populations: from individual behavior to ecosystem dynamics. In: Ebenman B, Persson L (eds) Size-structured populations. Springer, Berlin Heidelberg, New York, pp 157–183

    Google Scholar 

  • Wilbur HM, Fauth JE (1990) Experimental aquatic food webs: interactions between two predators and two prey. Am Nat 135:176–204

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Kurzava, L.M., Morin, P.J. Consequences and causes of geographic variation in the body size of a keystone predator,Notophthalmus viridescens . Oecologia 99, 271–280 (1994). https://doi.org/10.1007/BF00627739

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00627739

Key words

Navigation