Skip to main content

Advertisement

Log in

Locomotor performance in an invasive species: cane toads from the invasion front have greater endurance, but not speed, compared to conspecifics from a long-colonised area

  • Behavioral ecology - Original Paper
  • Published:
Oecologia Aims and scope Submit manuscript

Abstract

Cane toads (Bufo marinus) are now moving about 5 times faster through tropical Australia than they did a half-century ago, during the early phases of toad invasion. Radio-tracking has revealed higher daily rates of displacement by toads at the invasion front compared to those from long-colonised areas: toads from frontal populations follow straighter paths, move more often, and move further per displacement than do toads from older (long-established) populations. Are these higher movement rates of invasion-front toads associated with modified locomotor performance (e.g. speed, endurance)? In an outdoor raceway, toads collected from the invasion front had similar speeds, but threefold greater endurance, compared to conspecifics collected from a long-established population. Thus, increased daily displacement in invasion-front toads does not appear to be driven by changes in locomotor speed. Instead, increased dispersal is associated with higher endurance, suggesting that invasion-front toads tend to spend more time moving than do their less dispersive conspecifics. Whether this increased endurance is a cause or consequence of behavioural shifts associated with rapid dispersal is unclear. Nonetheless, shifts in endurance between frontal and core populations of this invasive species point to the complex panoply of traits affected by selection for increased dispersal ability on expanding population fronts.

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.

Fig. 1
Fig. 2

Similar content being viewed by others

References

  • Alford RA, Brown GP, Schwarzkopf L, Phillips BL, Shine R (2009) Comparisons through time and space suggest rapid evolution of dispersal behaviour in an invasive species. Wildl Res 36:23–28

    Article  Google Scholar 

  • Aubret F, Shine R, Bonnet X (2004) Adaptive developmental plasticity in snakes. Nature 431:261–262

    Article  CAS  PubMed  Google Scholar 

  • Battisti A, Stastny M, Netherer S, Robinet C, Schopf A, Roques A, Larsson S (2005) Expansion of geographic range in the pine processionary moth caused by increased winter temperatures. Ecol Appl 15:2084–2096

    Article  Google Scholar 

  • Bernays EA (1986) Diet-induced head allometry among foliage-chewing insects and its importance for graminivores. Science 231:495–497

    Article  PubMed  Google Scholar 

  • Brown GP, Shilton C, Phillips BL, Shine R (2007) Invasion stress and spinal arthritis in cane toads. Proc Natl Acad Sci USA 104:17698–17700

    Article  CAS  PubMed  Google Scholar 

  • Byers JE, Reichard S, Randall JM, Parker IM, Smith CS, Lonsdale WM, Atkinson IAE, Seastedt TR, Williamson M, Chornesky E, Hayes D (2002) Directing research to reduce the impacts of nonindigenous species. Conserv Biol 16:630–640

    Article  Google Scholar 

  • Carey JR (1996) The future of the Mediterranean fruit fly Ceratitis capitata invasion of California: a predictive framework. Biol Conserv 78:35–50

    Article  Google Scholar 

  • Crozier L (2004) Warmer winters drive butterfly range expansion by increasing survivorship. Ecology 85:231–241

    Article  Google Scholar 

  • Cummings JW (1979) Physiological and biochemical adaptations to training in Rana pipiens. J Comp Physiol B 134:345–350

    Article  CAS  Google Scholar 

  • Cwynar LC, MacDonald GM (1987) Geographical variation of lodgepole pine in relation to population history. Am Nat 129:463–469

    Article  Google Scholar 

  • Freeman DB (1992) Prickly Pear menace in eastern Australia 1880–1940. Geogr Rev 82:413–429

    Article  Google Scholar 

  • Goodman BA, Miles DB, Schwarzkopf L (2008) Life on the rocks: habitat use drives morphological and performance evolution in lizards. Ecology 89:3462–3471

    Article  PubMed  Google Scholar 

  • Grosholz ED (1996) Contrasting rates of spread for introduced species in terrestrial and marine systems. Ecology 77:1680–1686

    Article  Google Scholar 

  • Hastings A, Cuddington K, Davies KF, Dugaw CJ, Elmendorf S, Freestone A, Harrison S, Holland M, Lambrinos J, Malvadkar U, Melbourne BA, Moore K, Taylor C, Thomson D (2005) The spatial spread of invasions: new developments in theory and evidence. Ecol Lett 8:91–101

    Article  Google Scholar 

  • Hughes CL, Dytham C, Hill JK (2007) Modelling and analysing evolution of dispersal in populations at expanding range boundaries. Ecol Entomol 32:437–445

    Article  Google Scholar 

  • Johnson LE, Carlton JT (1996) Post-establishment spread in large-scale invasions: dispersal mechanisms of the zebra mussel Dreissena polymorpha. Ecology 77:1686–1690

    Article  Google Scholar 

  • Knowles TW, Weigl PD (1990) Thermal dependence of anuran burst locomotor performance. Copeia 1990:796–802

    Article  Google Scholar 

  • Kraus F, Campbell EW (2004) Human-mediated escalation of a formerly eradicable problem: the invasion of Caribbean frogs in the Hawaiian Islands. Biol Invas 4:327–332

    Article  Google Scholar 

  • Lever C (2001) The cane toad: the history and ecology of a successful colonist. Westbury Academic and Scientific Publishing, UK

    Google Scholar 

  • Losos JB, Creer DA, Glossip D, Goellner R, Hampton A, Roberts G, Haskell N, Taylor P, Ettling J (2000) Evolutionary implications of phenotypic plasticity in the hindlimb of the lizard Anolis sagrei. Evolution 54:301–305

    CAS  PubMed  Google Scholar 

  • Miller K, Camilliere JJ (1981) Physical training improves swimming performance of the African clawed frog Xenopus laevis. Herpetologica 37:1–10

    Google Scholar 

  • Phillips BL, Brown GP, Webb JK, Shine R (2006) Invasion and the evolution of speed in toads. Nature 439:803

    Article  CAS  PubMed  Google Scholar 

  • Phillips BL, Brown GP, Greenlees M, Webb JK, Shine R (2007) Rapid expansion of the cane toad (Bufo marinus) invasion front in tropical Australia. Austral Ecol 32:169–176

    Article  Google Scholar 

  • Phillips BL, Brown GP, Travis JMJ, Shine R (2008) Reid’s paradox revisited: the evolution of dispersal in range-shifting populations. Am Nat 172:S34–S48

    Article  PubMed  Google Scholar 

  • Schwarzkopf L, Alford RA (2002) Nomadic movement in tropical toads. Oikos 96:492–506

    Article  Google Scholar 

  • Sharov AA, Liebhold AM (1998) Bioeconomics of managing the spread of exotic pest species with barrier zones. Ecol Appl 8:833–845

    Google Scholar 

  • Simmons AD, Thomas CD (2004) Changes in dispersal during species’ range expansions. Am Nat 164:378–395

    Article  PubMed  Google Scholar 

  • Thebaud C, Debussche M (1991) Rapid invasion of Fraxinus ornus L. along the Herault River system in southern France: the importance of seed dispersal by water. J Biogeogr 18:7–12

    Article  Google Scholar 

  • Travis JMJ, Dytham C (2002) Dispersal evolution during invasions. Evol Ecol Res 4:1119–1129

    Google Scholar 

  • Urban MC, Phillips BL, Skelly DK, Shine R (2008) A toad more traveled: the heterogeneous invasion dynamics of cane toads in Australia. Am Nat 171:E134–E148

    Article  PubMed  Google Scholar 

  • West-Eberhard MJ (1989) Phenotypic plasticity and the origins of diversity. Annu Rev Ecol Syst 20:249–278

    Article  Google Scholar 

  • West-Eberhard MJ (2002) Developmental plasticity and evolution. Oxford University Press, New York

    Google Scholar 

  • Zug GR (1972) Anuran locomotion: structure and function. I. Preliminary observations on relation between jumping and osteometrics of appendicular and postaxial skeleton. Copeia 1972:613–624

    Article  Google Scholar 

Download references

Acknowledgments

We thank Travis Child, Matthew Greenlees and Greg Brown for their help collecting cane toads. We also thank Melanie Elphick for her feedback on this manuscript. The work was supported financially by the Invasive Animals Cooperative Research Centre, and by the Australian Research Council.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Richard Shine.

Additional information

Communicated by Janne Sundell.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Llewelyn, J., Phillips, B.L., Alford, R.A. et al. Locomotor performance in an invasive species: cane toads from the invasion front have greater endurance, but not speed, compared to conspecifics from a long-colonised area. Oecologia 162, 343–348 (2010). https://doi.org/10.1007/s00442-009-1471-1

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00442-009-1471-1

Keywords

Navigation