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6 - Behaviour on Invasion Fronts, and the Behaviour of Invasion Fronts

from Part I - Behaviour and the Invasion Process

Published online by Cambridge University Press:  27 October 2016

By
Ben L. Phillips
Edited by
Judith S. Weis  and
Daniel Sol
Judith S. Weis
Affiliation:
Rutgers University, New Jersey
Daniel Sol
Affiliation:
National Spanish Research Council (CSIC)
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Biological Invasions and Animal Behaviour , pp. 82 - 95
Publisher: Cambridge University Press
Print publication year: 2016

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References

Agrawal, A.F. and Lively, C.M. (2001). Parasites and the evolution of self-fertilization. Evolution, 55, 869–879.CrossRefGoogle ScholarPubMed
Alford, R.A. (1994). Interference and exploitation competition in larval Bufo marinus. Advances in Ecology and Environmental Sciences, 297–306.Google Scholar
Alford, R.A., Brown, G.P., Schwarzkopf, L., Phillips, B.L. and Shine, R. (2009). Comparisons through time and space suggest rapid evolution of dispersal behaviour in an invasive species. Wildlife Research, 36, 23–28.CrossRefGoogle Scholar
Amundsen, P.-A., Salonen, E., Niva, T., et al. (2012). Invader population speeds up life history during colonization. Biological Invasions, 14, 1501–1513.CrossRefGoogle Scholar
Barber, I. and Dingemanse, N.J. (2010). Parasitism and the evolutionary ecology of animal personality. Philosophical Transactions of the Royal Society B: Biological Sciences, 365, 4077–4088.CrossRefGoogle ScholarPubMed
Benichou, O., Calvez, V., Meunier, N. and Voituriez, R. (2012). Front acceleration by dynamic selection in Fisher population waves. Physical Review E, 86, 041908.CrossRefGoogle ScholarPubMed
Berthouly-Salazar, C., van Rensburg, B.J., Le Roux, J.J., van Vuuren, B.J. and Hui, C. (2012). Spatial sorting drives morphological variation in the invasive bird, Acridotheris tristis. PLoS ONE, 7, e38145.CrossRefGoogle ScholarPubMed
Biro, P.A. and Stamps, J.A. (2008). Are animal personality traits linked to life-history productivity? Trends in Ecology and Evolution, 23, 361–368.CrossRefGoogle ScholarPubMed
Blackburn, T.M. and Duncan, R.P. (2001). Establishment patterns of exotic birds are constrained by non-random patterns in introduction. Journal of Biogeography, 28, 927–939.CrossRefGoogle Scholar
Bøhn, T., Terje Sandlund, O., Amundsen, P.-A. and Primicerio, R. (2004). Rapidly changing life history during invasion. Oikos, 106, 138–150.CrossRefGoogle Scholar
Bouin, E., Calvez, V., Meunier, N., et al. (2012). Invasion fronts with variable motility: phenotype selection, spatial sorting and wave acceleration. Comptes Rendus Mathematique, 350, 761–766.CrossRefGoogle Scholar
Bridge, E.S., Thorup, K., Bowlin, M.S., et al. (2011). Technology on the move: recent and forthcoming innovations for tracking migratory birds. BioScience, 61, 689–698.CrossRefGoogle Scholar
Brook, B.W. and Bradshaw, C.J.A. (2006). Strength of evidence for density dependence in abundance time series of 1198 species. Ecology, 87, 1445–1451.CrossRefGoogle ScholarPubMed
Brown, G.P., Kelehear, C. and Shine, R. (2013). The early toad gets the worm: cane toads at an invasion front benefit from higher prey availability. Journal of Animal Ecology, 82, 854–862.CrossRefGoogle ScholarPubMed
Brown, G.P., Phillips, B.L. and Shine, R. (2014). The straight and narrow path: the evolution of straight-line dispersal at a cane toad invasion front. Proceedings of the Royal Society B: Biological Sciences, 281, 20141385.CrossRefGoogle Scholar
Brown, G.P., Phillips, B.L. and Shine, R. (2015). Directional dispersal has not evolved during the cane toad invasion. Functional Ecology, 29, 830–838.CrossRefGoogle Scholar
Burton, O.J., Travis, J.M.J. and Phillips, B.L. (2010). Trade-offs and the evolution of life-histories during range expansion. Ecology Letters, 13, 1210–1220.CrossRefGoogle ScholarPubMed
Chapple, D.G., Simmonds, S.M. and Wong, B. (2012). Can behavioral and personality traits influence the success of unintentional species introductions? Trends in Ecology and Evolution, 27, 57–64.CrossRefGoogle ScholarPubMed
Crossland, M.R. and Shine, R. (2011a). Cues for cannibalism: cane toad tadpoles use chemical signals to locate and consume conspecific eggs. Oikos, 120, 327–332.CrossRefGoogle Scholar
Crossland, M.R. and Shine, R. (2011b). Embryonic exposure to conspecific chemicals suppresses cane toad growth and survival. Biology Letters, rsbl20110794.CrossRefGoogle Scholar
Dingemanse, N.J. and Réale, D. (2005). Natural selection and animal personality. Behaviour, 142, 1159–1184.CrossRefGoogle Scholar
Duckworth, R.A. and Badyaev, A.V. (2007). Coupling of dispersal and aggression facilitates the rapid range expansion of a passerine bird. Proceedings of the National Academy of Sciences, USA, 104, 15017–15022.CrossRefGoogle ScholarPubMed
Elliott, E.C. and Cornell, S.J. (2013). Are anomalous invasion speeds robust to demographic stochasticity? PLoS ONE, 8, e67871.CrossRefGoogle ScholarPubMed
Elton, C.S. (1958). The Ecology of Invasions by Animals and Plants. London: Methuen.CrossRefGoogle Scholar
Excoffier, L. and Ray, N. (2008). Surfing during population expansions promotes genetic revolutions and structuration. Trends in Ecology and Evolution, 23, 347–351.CrossRefGoogle ScholarPubMed
Excoffier, L., Foll, M. and Petit, R.J. (2009). Genetic consequences of range expansions. Annual Review of Ecology and Systematics, 2009, 40.Google Scholar
Facon, B., Hufbauer, R.A., Tayeh, A., et al. (2011). Inbreeding depression is purged in the invasive insect Harmonia axyridis. Current Biology, 21, 424–427.CrossRefGoogle ScholarPubMed
Feiner, Z., Aday, D.D. and Rice, J. (2012). Phenotypic shifts in white perch life history strategy across stages of invasion. Biological Invasions, 14, 2315–2329.CrossRefGoogle Scholar
Fisher, R.A. (1937). The wave advance of advantageous genes. Annals of Eugenics, 7, 355–369.CrossRefGoogle Scholar
Florance, D., Webb, J.K., Dempster, T., et al. (2011). Excluding access to invasion hubs can contain the spread of an invasive vertebrate. Proceedings of the Royal Society B: Biological Sciences, 278, 2900–2908.CrossRefGoogle ScholarPubMed
Gutowsky, L.F.G. and Fox, M.G. (2012). Intra-population variability of life-history traits and growth during range expansion of the invasive round goby, Neogobius melanostomus. Fisheries Management and Ecology, 19, 78–88.CrossRefGoogle Scholar
Hallatschek, O., Hersen, P., Ramanathan, S. and Nelson, D.R. (2007). Genetic drift at expanding frontiers promotes gene segregation. Proceedings of the National Academy of Sciences, 104, 19926–19930.CrossRefGoogle ScholarPubMed
Hamilton, W.D. and May, R.M. (1977). Dispersal in stable habitats. Nature, 269, 578–581.CrossRefGoogle Scholar
Hastings, A., Cuddington, K., Davies, K.F., et al. (2005). The spatial spread of invasions: new developments in theory and evidence. Ecology Letters, 8, 91–101.CrossRefGoogle Scholar
Hudson, P.J., Dobson, A.P. and Newborn, D. (1998). Prevention of population cycles by parasite removal. Science, 282, 2256–2258.CrossRefGoogle ScholarPubMed
Hughes, C.L., Dytham, C. and Hill, J.K. (2007). Modelling and analysing evolution of dispersal in populations at expanding range boundaries. Ecological Entomology, 32, 437–445.CrossRefGoogle Scholar
Klopfstein, S., Currat, M. and Excoffier, L. (2006). The fate of mutations surfing on the wave of range expansion. Molecular Biology and Evolution, 23, 482–490.CrossRefGoogle ScholarPubMed
Kubisch, A., Fronhofer, E.A., Poethke, H.J. and Hovestadt, T. (2013). Kin competition as a major driving force for invasions. The American Naturalist, 181, 700–706.CrossRefGoogle Scholar
Léotard, G., Debout, G., Dalecky, A., et al. (2009). Range expansion drives dispersal evolution in an equatorial three-species symbiosis. PLoS ONE 4:e5377.CrossRefGoogle Scholar
Lever, C. (2001). The Cane Toad. The History and Ecology of a Successful Colonist. Yorkshire, UK: Westbury Academic and Scientific Publishing.Google Scholar
Lewontin, R.C. (1965). Selection for colonizing ability. In The Genetics of Colonizing Species, ed. Baker, H. and Stebbins, G. London: Academic Press, pp. 77–94.Google Scholar
Lockwood, J.L., Hoopes, M.F. and Marchetti, M.P. (2007). Invasion Ecology. Maiden, MA: Blackwell.Google Scholar
Lombaert, E., Estoup, A. Facon, B., et al. (2014). Rapid increase in dispersal during range expansion in the invasive ladybird Harmonia axyridis. Journal of Evolutionary Biology, 27, 508–517.CrossRefGoogle ScholarPubMed
Lopez, D.P., Jungman, A.A. and Rehage, J.S. (2012). Nonnative African jewelfish are more fit but not bolder at the invasion front: a trait comparison across an Everglades range expansion. Biological Invasions, 14, 2159–2174.CrossRefGoogle Scholar
MacArthur, R.H. and Wilson, E.O. (1967). The Theory of Island Biogeography. Princeton, NJ: Princeton University Press.Google Scholar
Mitchell, C.E. and Power, A.G. (2003). Release of invasive plants from fungal and viral pathogens. Nature, 421, 625–627.CrossRefGoogle ScholarPubMed
Peischl, S., Kirkpatrick, M. and Excoffier, L. (2015). Expansion load and the evolutionary dynamics of a species range. American Naturalist, 185(4), E81–93.CrossRefGoogle ScholarPubMed
Perkins, T.A. (2012). Evolutionarily labile species interactions and spatial spread of invasive species. The American Naturalist, 179, E37–E54.CrossRefGoogle ScholarPubMed
Perkins, T.A., Phillips, B.L., Baskett, M.L. and Hastings, A. (2013). Evolution of dispersal and life-history interact to drive accelerating spread of an invasive species. Ecology Letters, 16, 1079–1087.CrossRefGoogle ScholarPubMed
Phillips, B.L. (2009). The evolution of growth rates on an expanding range edge. Biology Letters, 5, 802–804.CrossRefGoogle Scholar
Phillips, B.L. (2015). Evolutionary processes make invasion speed difficult to predict. Biological Invasions, 17, 1949–1960.CrossRefGoogle Scholar
Phillips, B.L. and Suarez, A.V. (2012). The role of behavioural variation in the invasion of new areas. In Behavioural Responses to a Changing World: Mechanisms and Consequences, ed. Candolin, U. and Wong, B.B.M. Oxford: Oxford University Press, pp. 190–200.CrossRefGoogle Scholar
Phillips, B.L., Brown, G.P., Webb, J.K. and Shine, R. (2006). Invasion and the evolution of speed in toads. Nature, 439, 803.CrossRefGoogle ScholarPubMed
Phillips, B.L., Brown, G.P., Travis, J.M.J. and Shine, R. (2008). Reid's paradox revisited: the evolution of dispersal in range-shifting populations. The American Naturalist, 172, S34–S48.CrossRefGoogle Scholar
Phillips, B.L., Brown, G.P. and Shine, R. (2010a). Evolutionarily accelerated invasions: the rate of dispersal evolves upwards during range advance of cane toads. Journal of Evolutionary Biology, 23, 2595–2601.CrossRefGoogle ScholarPubMed
Phillips, B.L., Brown, G.P. and Shine, R. (2010b). Life-history evolution in range-shifting populations. Ecology, 91, 1617–1627.CrossRefGoogle ScholarPubMed
Phillips, B.L., Kelehear, C., Pizzatto, L., et al. (2010c). Parasites and pathogens lag behind their host during periods of host range-advance. Ecology, 91, 872–881.CrossRefGoogle ScholarPubMed
Phillips, B.L., Tingley, R. and Shine, R. (2016). Genetic backburning to halt invasions. Proceedings of the Royal Society B: Biological Sciences, 283, 20153037.CrossRefGoogle Scholar
Pizzatto, L. and Shine, R. (2008). The behavioral ecology of cannibalism in cane toads (Bufo marinus). Behavioral Ecology and Sociobiology, 63, 123–133.CrossRefGoogle Scholar
Pujol, B., Zhou, S.-R., Vilas, J.S. and Pannell, J.R. (2009). Reduced inbreeding depression after species range expansion. Proceedings of the National Academy of Sciences, USA, 106, 15379–15383.CrossRefGoogle ScholarPubMed
Réale, D., Garant, D., Humphries, M.M., et al. (2010). Personality and the emergence of the pace-of-life syndrome concept at the population level. Philosophical Transactions of the Royal Society B: Biological Sciences, 365, 4051–4063.CrossRefGoogle ScholarPubMed
Reznick, D., Bryant, M.J. and Bashey, F. (2002). r- and K-selection revisited: the role of population regulation in life-history evolution. Ecology, 83, 1509–1520.CrossRefGoogle Scholar
Rodriguez, A., Hausberger, M. and Clergeau, P. (2010). Flexibility in European starlings' use of social information: experiments with decoys in different populations. Animal Behaviour, 80, 965–973.CrossRefGoogle Scholar
Shigesada, N. and Kawasaki, K. (1997). Biological Invasions: Theory and Practice. Oxford, UK: Oxford University Press.CrossRefGoogle Scholar
Shine, R., Brown, G.P. and Phillips, B.L. (2011). An evolutionary process that assembles phenotypes through space rather than through time. Proceedings of the National Academy of Sciences, USA, 108, 5708–5711.CrossRefGoogle ScholarPubMed
Sih, A., Bell, A. and Johnson, J.C. (2004a). Behavioral syndromes: an ecological and evolutionary overview. Trends in Ecology and Evolution, 19, 372–378.CrossRefGoogle ScholarPubMed
Sih, A., Bell, A.M., Johnson, J.C. and Ziemba, R.E. (2004b). Behavioral syndromes: an integrative overview. The Quarterly Review of Biology, 79, 241–277.CrossRefGoogle Scholar
Simmons, A.D. and Thomas, C.D. (2004). Changes in dispersal during species' range expansions. American Naturalist, 164, 378–395.CrossRefGoogle ScholarPubMed
Simons, A.M. (2003). Invasive aliens and sampling bias. Ecology Letters, 6, 278–280.CrossRefGoogle Scholar
Skellam, J.G. (1951). Random dispersal in theoretical populations. Biometrika, 38, 196–218.CrossRefGoogle ScholarPubMed
Stevens, V.M., Trochet, A., Blanchet, S., Moulherat, S., Clobert, J. and Baguette, M. (2013). Dispersal syndromes and the use of life-histories to predict dispersal. Evolutionary Applications, 6, 630–642.CrossRefGoogle ScholarPubMed
Therry, L., Lefevre, E., Bonte, D. and Stoks, R. (2014a). Increased activity and growth rate in the non-dispersive aquatic larval stage of a damselfly at an expanding range edge. Freshwater Biology, 59, 1266–1277.CrossRefGoogle Scholar
Therry, L., Nilsson-Örtman, V., Bonte, D. and Stoks, R. (2014b). Rapid evolution of larval life history, adult immune function and flight muscles in a poleward-moving damselfly. Journal of Evolutionary Biology, 27, 141–152.CrossRefGoogle Scholar
Tingley, R., Phillips, B.L., Letnic, M., et al. (2013). Identifying optimal barriers to halt the invasion of cane toads Rhinella marina in arid Australia. Journal of Applied Ecology, 50, 129–137.CrossRefGoogle Scholar
Torchin, M.E., Lafferty, K.D., Dobson, A.P., McKenzie, V.J. and Kuris, A.M. (2003). Introduced species and their missing parasites. Nature, 421, 628–630.CrossRefGoogle ScholarPubMed
Travis, J.M.J. and Dytham, C. (2002). Dispersal evolution during invasions. Evolutionary Ecology Research, 4, 1119–1129.Google Scholar
Travis, J.M.J., Münkemüller, T., Burton, O.J., Best, A., Dytham, C. and Johst, K. (2007). Deleterious mutations can surf to high densities on the wave front of an expanding population. Molecular Biology and Evolution, 24, 2334–2343.CrossRefGoogle ScholarPubMed
Urban, M.C., Phillips, B.L., Skelly, D.K. and Shine, R. (2008). A toad more travelled: the heterogeneous invasion dynamics of cane toads in Australia. The American Naturalist, 171, E134–E148.CrossRefGoogle ScholarPubMed
Van Dyken, J.D., Müller, M.J., Mack, K.M. and Desai, M.M. (2013). Spatial population expansion promotes the evolution of cooperation in an experimental prisoner's dilemma. Current Biology, 23, 919–923.CrossRefGoogle Scholar
Vermeij, G. (2005). Invasion as expectation: a historical fact of life. In Species Invasions: Insights into Ecology, Evolution, and Biogeography, ed. Sax, D.F., Stachowicz, J.J. and Gaines, S.D. Sunderland, MA: Sinauer Associates, pp. 315–339.Google Scholar
Williamson, M. (1996). Biological Invasions. London: Chapman and Hall.Google Scholar

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