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7 - The Role of Dispersal Behaviour and Personality in Post-establishment Spread

from Part I - Behaviour and the Invasion Process

Published online by Cambridge University Press:  27 October 2016

By
Jennifer S. Rehage ,
Julien Cote  and
Andrew Sih
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. 96 - 116
Publisher: Cambridge University Press
Print publication year: 2016

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References

Alemadi, S.D. and Jenkins, D.G. (2008). Behavioural constraints for the spread of the eastern mosquitofish, Gambusia holbrooki (Poeciliidae). Biological Invasions, 10, 59–66.CrossRefGoogle 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
Bekoff, M. (1977). Mammalian dispersal and the ontogeny of individual behavioural phenotypes. American Naturalist, 111, 715–732.CrossRefGoogle Scholar
Biro, P.A. and Adriaenssens, B. (2013). Predictability as a personality trait: consistent differences in intraindividual behavioural variation. American Naturalist, 182, 621–629.CrossRefGoogle Scholar
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., Pyšek, P., Bacher, S., et al. (2011). A proposed unified framework for biological invasions. Trends in Ecology and Evolution, 26, 333–339.CrossRefGoogle ScholarPubMed
Bonte, D., Travis, J.M.J., De Clercq, N., Zwertvaegher, I. and Lens, L. (2008). Thermal conditions during juvenile development affect adult dispersal in a spider. Proceedings of the National Academy of Sciences, 105, 17000–17005.CrossRefGoogle Scholar
Bonte, D., Clercq, N.D., Zwertvaegher, I. and Lens, L. (2009). Repeatability of dispersal behaviour in a common dwarf spider: evidence for different mechanisms behind short‐ and long‐distance dispersal. Ecological Entomology, 34, 271–276.CrossRefGoogle Scholar
Bonte, D., Van Dyck, H., Bullock, J.M., et al. (2012). Costs of dispersal. Biological Reviews, 87, 290–312.CrossRefGoogle ScholarPubMed
Bonte, D., De Roissart, A., Wybouw, N. and Van Leeuwen, T. (2014). Fitness maximization by dispersal: evidence from an invasion experiment. Ecology, 95, 3104–3111.CrossRefGoogle Scholar
Bowler, D.E. and Benton, T.G. (2005). Causes and consequences of animal dispersal strategies: relating individual behaviour to spatial dynamics. Biological Reviews, 80, 205–225.CrossRefGoogle ScholarPubMed
Bowne, D.R. and Bowers, M.A. (2004). Interpatch movements in spatially structured populations: a literature review. Landscape Ecology, 19, 1–20.CrossRefGoogle Scholar
Brown, K.L. (1985). Demographic and genetic characteristics of dispersal in the mosquitofish, Gambusia affinis (Pisces: Poeciliidae). Copeia, 1985, 597–612.Google Scholar
Bubb, D.H., Thom, T.J. and Lucas, M.C. (2006). Movement, dispersal and refuge use of co-occurring introduced and native crayfish. Freshwater Biology, 51, 1359–1368.CrossRefGoogle Scholar
Burgess, S.C. and Marshall, D.J. (2011). Are numbers enough? Colonizer phenotype and abundance interact to affect population dynamics. Journal of Animal Ecology, 80, 681–687.CrossRefGoogle ScholarPubMed
Burns, A.L.J., Herbert-Read, J., Morrell, L.J. and Ward, A.J.W. (2012). Consistency of leadership in shoals of mosquitofish (Gambusia holbrooki) in novel and in familiar environments. PloS ONE, 7, e36567.Google ScholarPubMed
Chapple, D.G. and Wong, B.B.M. (2015). The role of behavioural variation and behavioural syndromes across different stages of the introduction process. In Behavioural Responses to a Changing World: Mechanisms and Consequences, ed. Candolin, U. and Wong, B.B.M. Oxford, UK: Oxford University Press, pp. 190–200.Google Scholar
Chapple, D.G., Simmonds, S.M. and Wong, B.B.M. (2012). Can behavioural and personality traits influence the success of unintentional species introductions? Trends in Ecology and Evolution, 27, 57–64.CrossRefGoogle ScholarPubMed
Chen, T., Beekman, M. and Ward, A.J.W. (2010). The role of female dominance hierarchies in the mating behaviour of mosquitofish. Biology Letters, 7, 343–345.CrossRefGoogle ScholarPubMed
Clobert, J., Le Galliard, J.F., Cote, J., Meylan, S. and Massot, M. (2009). Informed dispersal, heterogeneity in animal dispersal syndromes and the dynamics of spatially structured populations. Ecology Letters, 12, 197–209.CrossRefGoogle ScholarPubMed
Colatti, R.I, Ricciardi, A., Grigorovich, I.A., and MacIsaac, H.J. (2004). Is invasion success explained by the enemy release hypothesis. Ecology Letters, 7, 721–733.CrossRefGoogle Scholar
Congdon, B.C. (1994). Characteristics of dispersal in the eastern mosquitofish Gambusia holbrooki. Journal of Fish Biology, 45, 943–952.CrossRefGoogle Scholar
Cote, J. and Clobert, J. (2007a). Social personalities influence natal dispersal in a lizard. Proceedings of the Royal Society B: Biological Sciences, 274, 383–390.CrossRefGoogle Scholar
Cote, J. and Clobert, J. (2007b). Social information and emigration: lessons from immigrants. Ecology Letters, 10, 411–417.CrossRefGoogle ScholarPubMed
Cote, J., Clobert, J. and Fitze, P.S. (2007). Mother-offspring competition promotes colonization success. Proceedings of the National Academy of Sciences, USA, 104, 703–708.CrossRefGoogle ScholarPubMed
Cote, J., Dreiss, A. and Clobert, J. (2008). Social personality trait and fitness. Proceedings of the Royal Society B: Biological Sciences, 275, 2851–2858.CrossRefGoogle ScholarPubMed
Cote, J., Clobert, J., Brodin, T., Fogarty, S. and Sih, A. (2010a). Personality dependent dispersal: characterization, ontogeny and consequences for spatially structured populations. Philosophical Transactions of the Royal Society B: Biological Sciences, 365, 4065–4076.CrossRefGoogle ScholarPubMed
Cote, J., Fogarty, S., Weinersmith, K., Brodin, T. and Sih, A. (2010b). Personality traits and dispersal tendency in the invasive mosquitofish Gambusia affinis. Proceedings of the Royal Society B: Biological Sciences, 277, 1571–1579.CrossRefGoogle ScholarPubMed
Cote, J., Fogarty, S., Brodin, T. and Sih, A. (2011). Personality-dependent dispersal in invasive mosquitofish: group composition matters. Proceedings of the Royal Society B: Biological Sciences, 278, 1670–1678.CrossRefGoogle ScholarPubMed
Cote, J., Fogarty, S. and Sih, A. (2012). Individual sociability and choosiness between shoal types. Animal Behaviour, 83, 1469–1476.CrossRefGoogle Scholar
Cote, J., Fogarty, S., Tymen, B., Sih, A. and Brodin, T. (2013). Personality dependent dispersal cancelled under predation risk. Proceedings of the Royal Society B: Biological Sciences, 280, 2013–2349.Google ScholarPubMed
Courtenay, W.R. and Meffe, G.K. (1989). Small fishes in strange places: a review of introduced poeciliids. In Ecology and Evolution of Livebearing Fishes (Poeciliidae), ed. Meffe, G.K. and Snelson, , Jr, F.F. Englewood Cliffs, NJ: Prentice-Hall, pp. 319–331.Google Scholar
Davis, J.M. and Stamps, J.A. (2004). The effect of natal experience on habitat preferences. Trends in Ecology and Evolution, 19, 411–416.CrossRefGoogle ScholarPubMed
Delgado, M.D., Penteriani, V., Revilla, E. and Nams, V.O. (2010). The effect of phenotypic traits and external cues on natal dispersal movements. Journal of Animal Ecology, 79, 620–632.CrossRefGoogle ScholarPubMed
Doligez, B., Danchin Cadet, C., Danchin, T. and Boulinier, E. (2003). When to use public information for breeding habitat selection? The role of environmental predictability and density dependence. Animal Behaviour, 66, 973–988.CrossRefGoogle Scholar
Ducatez, S., Legrand, D., Chaput-Bardy, A., et al. (2012). Inter-individual variation in movement: is there a mobility syndrome in the large white butterfly (Pieris brassicae)? Ecological Entomology, 37, 377–385.CrossRefGoogle Scholar
Duckworth, R.A. (2008). Adaptive dispersal strategies and the dynamics of a range expansion. American Naturalist, 172, S4–S17.CrossRefGoogle ScholarPubMed
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
Edelaar, P., Siepielski, A.M. and Clobert, J. (2008). Matching habitat choice causes directed gene flow: a neglected dimension in evolution and ecology. Evolution, 62, 2462–2472.CrossRefGoogle ScholarPubMed
Elliott, E.C. and Cornell, S.J. (2012). Dispersal polymorphism and the speed of biological invasions. PLoS ONE, 7, e40496.CrossRefGoogle ScholarPubMed
Fogarty, S., Cote, J. and Sih, A. (2011). Social personality polymorphism and the spread of invasive species: a model. American Naturalist, 177, 273–287.CrossRefGoogle ScholarPubMed
Fraser, D.F., Gilliam, J.F., Daley, M.J., Le, A.N. and Skalski, G.T. (2001). Explaining leptokurtic movement distributions: intrapopulation variation in boldness and exploration. American Naturalist, 158, 124–135.CrossRefGoogle ScholarPubMed
Goodsell, J.A. and Kats, L.B. (1999). Effect of introduced mosquitofish on pacific treefrogs and the role of alternative prey. Conservation Biology, 13, 921–924.CrossRefGoogle Scholar
Groen, M., Sopinka, N.M., Marentette, J.R., et al. (2012). Is there a role for aggression in round goby invasion fronts? Behaviour, 149, 685–703.Google Scholar
Herbert-Read, J.E., Krause, S., Morrell, L.J., et al. (2013). The role of individuality in collective group movement. Proceedings of the Royal Society B: Biological Sciences, 280, 20122564.Google ScholarPubMed
Holway, D.A. and Suarez, A.V. (1999). Animal behaviour: an essential component of invasion biology. Trends in Ecology and Evolution, 14, 328–330.CrossRefGoogle ScholarPubMed
Holway, D.A., Suarez, A.V. and Case, T.J. (1998). Loss of intraspecific aggression in the success of a widespread invasive social insect. Science, 282, 949–952.CrossRefGoogle ScholarPubMed
Horth, L. (2003). Melanic body colour and aggressive mating behaviour are correlated traits in male mosquitofish (Gambusia holbrooki). Proceedings of the Royal Society: Biological Sciences, 270, 1033–1040.CrossRefGoogle ScholarPubMed
Hoysak, D.J. and Godin, J.G. (2007). Repeatability of male mate choice in the mosquitofish, Gambusia holbrooki. Ethology, 113, 1007–1018.CrossRefGoogle Scholar
Hudina, S., Hock, K. and Zganec, K. (2014). The role of aggression in range expansion and biological invasions. Current Zoology, 60, 401–409.CrossRefGoogle Scholar
Huntingford, F.A. (2011). Animal Conflict. London: Chapman and Hall.Google Scholar
Johnson, J.C. and Sih, A. (2007). Fear, food, sex and parental care: a syndrome of boldness in the fishing spider, Dolomedes triton. Animal Behaviour, 74, 1131–1138.CrossRefGoogle Scholar
Juette, T., Cucherousset, J. and Cote, J. (2014). Animal personality and the ecological impacts of freshwater non-native species. Current Zoology, 60, 417–427.CrossRefGoogle Scholar
Knapp, R., Marsh-Matthews, E., Vo, L. and Rosencrans, S. (2011). Stress hormone masculinizes female morphology and behaviour. Biology Letters, 64, 598–606.Google Scholar
Kubisch, A., Fronhofer, E.A., Poethke, H.J. and Hovestadt, T. (2013). Kin competition as a major driving force for invasions. American Naturalist, 181, 700–706.CrossRefGoogle Scholar
Langerhans, R.B., Layman, C.A., Shokrollahi, A.M. and DeWitt, T.J. (2004). Predator-driven phenotypic diversification in Gambusia affinis. Evolution, 58, 2305–2318.Google ScholarPubMed
Llewelyn, J., Philips, B.L., Alford, R.A., Schwartzkopf, L. and Shine, R. (2010). Locomotor performance in an invasive species: cane toads from the invasion front have greater endurance, but not speed, compared to conspecifics from long-colonised area. Oecologia, 162, 343–348.CrossRefGoogle 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
Lowe, S., Browne, M., Boudjelas, S. and De Poorter, M. (2000). 100 of the World's Worst Invasive Alien Species: A Selection from the Global Invasive Species Database. The Invasive Species Specialist Group (ISSG), a specialist group of the Species Survival Commission (SSC) of the World Conservation Union (IUCN), Auckland.Google Scholar
Martin, L.B. and Fitzgerald, L. (2005). A taste for novelty in invading house sparrows Passer domesticus. Behavioural Ecology, 16, 702–707.CrossRefGoogle Scholar
O'Riain, M.J., Jarvis, J.U.M. and Faulkes, C.G. (1996). A dispersive morph in the naked mole-rat. Nature, 380, 619–621.CrossRefGoogle ScholarPubMed
Parker, I.M., Simberloff, D., Lonsdale, W.M., et al. (1999). Impact: toward a framework for understanding the ecological effects of invaders. Biological Invasions, 1, 3–19.CrossRefGoogle Scholar
Phillips, B.L., Brown, G.P., Webb, J.K. and Shine, R. (2006). Invasion and the evolution of speed in toads. Nature, 43:803.CrossRefGoogle Scholar
Phillips, B.L., Brown, G.P. and Shine, R. (2010). Evolutionarily accelerated invasions: the rate of dispersal evolves upwards during the range advance of cane toads. Journal of Evolutionary Biology, 23, 2595–2601.CrossRefGoogle ScholarPubMed
Pintor, L.M., Sih, A. and Bauer, M. (2008). Differences in aggression, activity and boldness between native introduced populations of an invasive crayfish. Oikos, 117, 1629–1636.CrossRefGoogle Scholar
Pyke, G.H. (2005). A review of the biology of Gambusia affinis and G. holbrooki. Fish Biology and Fisheries, 15, 339–365.CrossRefGoogle Scholar
Rasmussen, J.E. and Belk, M.C. (2012). Dispersal behaviour correlates with personality of a North American fish. Current Zoology, 58, 260–270.CrossRefGoogle Scholar
Réale, D., Dingemanse, N.J., Kazem, A.J.N. and Wright, J. (2010). Evolutionary and ecological approaches to the study of personality. Philosophical Transactions of the Royal Society B: Biological Sciences, 365, 3937–3946.CrossRefGoogle Scholar
Rehage, J.S. and Sih, A. (2004). Dispersal behaviour, boldness, and the link to invasiveness: a comparison of four Gambusia species. Biological Invasions, 6, 379–391.CrossRefGoogle Scholar
Rehage, J.S., Barnett, B.K. and Sih, A. (2005a). Foraging behaviour and invasiveness: do invasive Gambusia exhibit higher feeding rates and broader diets than their non-invasive relatives? Ecology of Freshwater Fish, 14, 352–360.CrossRefGoogle Scholar
Rehage, J.S., Barnett, B.K. and Sih, A. (2005b). Behavioural responses to a novel predator and competitor of invasive mosquitofish and their non-invasive relatives (Gambusia sp.). Behavioural Ecology and Sociobiology, 57, 256–266.CrossRefGoogle Scholar
Rémy, A., Le Galliard, J.F., Odden, M. and Andreassen, H.P. (2014). Concurrent effects of age class and food distribution on immigration success and population dynamics in a small mammal. Journal of Animal Ecology, 83, 813–822.CrossRefGoogle Scholar
Ricciardi, A., Hoopes, M. F., Marchetti, M. P. and Lockwood, J. L. (2013). Progress toward understanding the ecological impacts of nonnative species. Ecological Monographs, 83, 263–282.CrossRefGoogle Scholar
Ronce, O. (2007). How does it feel to be like a rolling stone? Ten questions about dispersal evolution. Annual Review of Ecology, Evolution, and Systematics, 38, 251–253.CrossRefGoogle Scholar
Schoepf, I. and Schradin, C. (2012). Better off alone! Reproductive competition and ecological constraints determine sociality in the African striped mouse (Rhabdomys pumilio). Journal of Animal Ecology, 81, 649–656.CrossRefGoogle ScholarPubMed
Seebacher, F., Ward, A.J.W. and Wilson, R.S. (2013). Increased aggression during pregnancy comes at a higher metabolic cost. Journal of Experimental Biology, 216, 771–776.CrossRefGoogle Scholar
Seebacher, S., Beaman, J. and Little, A.G. (2014). Regulation of thermal acclimation varies between generations of the short-lived mosquitofish that developed in different environmental conditions. Functional Ecology, 28, 137–148.CrossRefGoogle Scholar
Selonen, V., Hanski, I.K. and Desrochers, A. (2007). Natal habitat-biased dispersal in the Siberian flying squirrel. Proceedings of the Royal Society B: Biological Sciences, 274, 2063–2068.CrossRefGoogle ScholarPubMed
Sih, A., Bell, A.M., Johnson, J.C. and Ziemba, R.E. (2004). Behavioural syndromes: an integrative overview. The Quarterly Review of Biology, 79, 241–277.CrossRefGoogle Scholar
Sih, A., Ferrari, M.C.O. and Harris, D.J. (2011). Evolution and behavioural responses to human induced rapid environmental change. Evolutionary Applications, 4, 367–387.CrossRefGoogle ScholarPubMed
Sih, A., Cote, J., Evans, M., Fogarty, S. and Pruitt, J. (2012). Ecological implications of behavioural syndromes. Ecology Letters, 15, 278–289.CrossRefGoogle ScholarPubMed
Sih, A., Mathot, K.J., Moiron, M. Montiglio, P.-O. et al. (2015). Animal personality and state-behaviour feedbacks: a review and guide for empiricists. Trends in Ecology and Evolution, 30, 50–60.CrossRefGoogle ScholarPubMed
Sinclair, E., Noronha de Souza, C., Ward, A. and Seebacher, F. (2014). Exercise changes behaviour. Functional Ecology, 28, 652–659.CrossRefGoogle Scholar
Smith, B.R. and Blumstein, D.T. (2008). Fitness consequences of personality: a meta-analysis. Behavioural Ecology, 19, 448–455.CrossRefGoogle Scholar
Sol, D., Timmermans, S. and Lefebvre, L. (2002). Behavioural flexibility and invasion success in birds. Animal Behaviour, 63, 495–502.CrossRefGoogle Scholar
Stamps, J.A. (2001). Habitat selection by dispersers: integrating proximate and ultimate approaches. In Dispersal, ed. Clobert, J., Danchin, E., Dhondt, A. and Nichols, J. Oxford, UK: Oxford University Press, pp. 230–242.CrossRefGoogle Scholar
Stamps, J.A., Davis, J.M., Blozis, S.A. and Boundy-Mills, K.L. (2007). Genotypic variation in refractory periods and habitat selection by natal dispersers. Animal Behaviour, 74, 599–610.CrossRefGoogle Scholar
Stevens, V.M., Whitmee, S., Le Galliard, J.F., et al. (2014). A comparative analysis of dispersal syndromes in terrestrial and semi-terrestrial animals. Ecology Letters, 17, 1039–1052.CrossRefGoogle ScholarPubMed
Suarez, A.V., Tsutsui, N.D., Holway, D.A. and Case, T.J. (1999). Behavioural and genetic differentiation between native and introduced populations of the Argentine ant. Biological Invasions, 1, 43–53.CrossRefGoogle Scholar
Trochet, A., Legrand, D., Larranaga, N., et al. (2013). Population sex ratio and dispersal in experimental two-patch metapopulations of butterflies. Journal of Animal Ecology, 82, 946–955.CrossRefGoogle ScholarPubMed
Ward, A. (2012). Social facilitation of exploration in mosquitofish (Gambusia holbrooki). Behavioural Ecology and Sociobiology, 66, 223–230.CrossRefGoogle Scholar
Webb, C.E. and Joss, J. (1997). Does predation by the fish Gambusia holbrooki (Atheriniformes: Poecilidae) contribute to declining frog populations? Australian Zoologist, 30, 316–324.CrossRefGoogle Scholar
Welcomme, R.L. (1992). A history of international introductions of inland aquatic species. Marine Science Symposium, 194, 3–14.Google Scholar
Williamson, M. and Fitter, A. (1996). The varying success of invaders. Ecology, 77, 1661–1666.CrossRefGoogle Scholar
Wilson, A.D.M., Godin, J.G.J. and Ward, A.J.W. (2010). Boldness and reproductive fitness correlates in the eastern mosquitofish. Gambusia holbrooki. Ethology, 116, 96–104.CrossRefGoogle Scholar

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