Skip to main content Accessibility help
×
Hostname: page-component-7c8c6479df-ws8qp Total loading time: 0 Render date: 2024-03-29T08:08:37.562Z Has data issue: false hasContentIssue false

Part I - Behaviour and the Invasion Process

Published online by Cambridge University Press:  27 October 2016

Judith S. Weis
Affiliation:
Rutgers University, New Jersey
Daniel Sol
Affiliation:
National Spanish Research Council (CSIC)
Get access

Summary

Image of the first page of this content. For PDF version, please use the ‘Save PDF’ preceeding this image.'
Type
Chapter
Information
Publisher: Cambridge University Press
Print publication year: 2016

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

References

Abbott, K.L., Greaves, S.N.J., Ritchie, P.A., et al. (2007). Behaviourally and genetically distinct populations of an invasive ant provides insight into invasion history and impacts on a tropical ant community. Biological Invasions, 9, 453463.CrossRefGoogle Scholar
Alexander, M.E., Dick, J.T.A., Weyl, O.L.F., et al. (2014). Existing and emerging high impact invasive species are characterized by higher functional responses than native. Biology Letters, 10, 20130946.CrossRefGoogle Scholar
Amiel, J.J., Tingley, R. and Shine, R. (2011). Smart moves: effects of relative brain size on establishment success of invasive amphibians and reptiles. PLoS ONE, 6, e18277.CrossRefGoogle ScholarPubMed
Aubry, S., Labaune, C., Magnin, F., et al. (2006). Active and passive dispersal of an invading land snail in Mediterranean France. Journal of Animal Ecology, 75, 802813.CrossRefGoogle ScholarPubMed
Barbaresi, S., Santini, G., Tricarico, E., et al. (2004). Ranging behaviour of the invasive crayfish, Procambarus clarkii (Girard). Journal of Natural History, 38, 28212832.CrossRefGoogle Scholar
Bell, A.M. (2007). Future directions in behavioural syndromes research. Proceedings of the Royal Society B, 274, 755761.CrossRefGoogle ScholarPubMed
Berthouly-Salazar, C., van Rensburg, B.J., Le Roux, J.J., et al. (2012). Spatial sorting drives morphological variation in the invasive bird, Acridotheres tristis. PLoS ONE, 7, e38145.Google Scholar
Bezzina, C.N., Amiel, J.J. and Shine, R. (2014). Does invasion success reflect superior cognitive ability? A case study of two congeneric lizard species (Lampropholis, Scincidae). PLoS ONE, 9, e86271.CrossRefGoogle ScholarPubMed
Biro, P.A. (2013). Are most samples of animals systematically biased? Consistent individual trait differences bias samples despite random sampling. Oecologia, 171, 339345.CrossRefGoogle ScholarPubMed
Biro, P.A. and Dingemanse, N.J. (2009). Sampling bias resulting from animal personality. Trends in Ecology and Evolution, 24, 6667.CrossRefGoogle ScholarPubMed
Blackburn, T.M., Cassey, P. and Lockwood, J.L. (2009). The role of species traits in the establishment success of exotic birds. Global Change Biology, 15, 28522860.CrossRefGoogle Scholar
Blackburn, T.M., Pyšek, P., Bacher, S., et al. (2011). A proposed unified framework for biological invasions. Trends in Ecology and Evolution, 26, 333339.CrossRefGoogle ScholarPubMed
Blackburn, T.M., Lockwood, J.L. and Cassey, P. (2015). The influence of numbers on invasion success. Molecular Ecology, 24, 19421953.CrossRefGoogle ScholarPubMed
Brodin, T. and Drotz, M.K. (2014). Individual variation in dispersal associated behavioral traits of the invasive Chinese mitten crab (Eriocheir sinensis, H. Milne Edwards, 1854) during initial invasion of Lake Vanern, Sweden. Current Zoology, 60, 410416.CrossRefGoogle 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, 13591368.CrossRefGoogle Scholar
Carpintero, S. and Reyes-Lopez, J. (2008). The role of competitive dominance in the invasive ability of the Argentine ant (Linepithema humile). Biological Invasions, 10, 2535.CrossRefGoogle Scholar
Carrete, M., Edelaar, P., Blas, J., et al. (2012). Don't neglect pre-establishment individual selection in deliberate introductions. Trends in Ecology and Evolution, 27, 6768.CrossRefGoogle ScholarPubMed
Carter, A.J., Heinsohn, R., Goldizen, A.W., et al. (2012). Boldness, trappability and sampling bias in wild lizards. Animal Behaviour, 83, 10511058.CrossRefGoogle Scholar
Carvalho, C.F., Leitao, A.V., Funghi, C., et al. (2013). Personality traits are related to ecology across a biological invasion. Behavioral Ecology, 24, 10811091.CrossRefGoogle Scholar
Cassey, P., Blackburn, T.M., Sol, D., et al. (2004). Global patterns of introduction effort and establishment success in birds. Proceedings of the Royal Society B, 271, S405S408.CrossRefGoogle ScholarPubMed
Chapple, D.G., Simmonds, S.M. and Wong, B.B.M. (2011). Know when to run, know when to hide: can behavioral differences explain the divergent invasion success of two sympatric lizards? Ecology and Evolution, 1, 278289.CrossRefGoogle ScholarPubMed
Chapple, D.G., Simmonds, S.M. and Wong, B.B.M. (2012a). Can behavioral and personality traits influence the success of unintentional species introductions? Trends in Ecology and Evolution, 27, 5764.CrossRefGoogle ScholarPubMed
Chapple, D.G., Simmonds, S.M. and Wong, B.B.M. (2012b). Intraspecific behavioral variation is important in both deliberate and unintentional species introductions: response to Carrete et al. Trends in Ecology and Evolution, 27, 6869.CrossRefGoogle Scholar
Chapple, D.G., Miller, K.A., Kraus, F., et al. (2013a). Divergent introduction histories among invasive populations of the delicate skink (Lampropholis delicata): has the importance of genetic admixture in the success of biological invasions been overemphasized? Diversity and Distributions, 19, 134146.CrossRefGoogle Scholar
Chapple, D.G., Whitaker, A.H., Chapple, S.N.J., et al. (2013b). Biosecurity interceptions of an invasive lizard: origin of stowaways and human-assisted spread within New Zealand. Evolutionary Applications, 6, 324339.CrossRefGoogle ScholarPubMed
Chapple, D.G., Miller, K.A., Chaplin, K., et al. (2014). Biology of the invasive delicate skink (Lampropholis delicata) on Lord Howe Island. Australian Journal of Zoology, 62, 498506.CrossRefGoogle Scholar
Chapple, D.G., Knegtmans, K., Kikillus, H., van Winkel, D. (2016). Biosecurity of exotic reptiles and amphibians in New Zealand: building upon Tony Whitaker's legacy. Journal of the Royal Society of New Zealand, 46, 6684.CrossRefGoogle Scholar
Cisterne, A., Vanderduys, E.P., Pike, D.A., et al. (2014). Wary invaders and clever natives: sympatric house geckos show disparate responses to predator scent. Behavioral Ecology, 25, 604611.CrossRefGoogle Scholar
Colautti, R.I., Girgorovich, I.A. and MacIsaac, H.J. (2006). Propagule pressure: a null model for biological invasions. Biological Invasions, 8, 10231037.CrossRefGoogle Scholar
Cote, J., Fogarty, S., Weinersmith, K., et al. (2010). Personality traits and dispersal tendency in the invasive mosquitofish (Gambusia affinis). Proceedings of the Royal Society B, 277, 15711579.CrossRefGoogle ScholarPubMed
Cote, J., Fogarty, S., Brodin, T., et al. (2011). Personality-dependent dispersal in the invasive mosquitofish: group composition matters. Proceedings of the Royal Society B, 278, 16701678.CrossRefGoogle ScholarPubMed
Cromie, G.L. and Chapple, D.G. (2012). Impact of tail loss on the behaviour and locomotor performance of two sympatric Lampropholis skink species. PLoS One, 7, e34732.CrossRefGoogle ScholarPubMed
Cure, K., McIlwain, J.L. and Hixon, M.A. (2014). Habitat plasticity in native Pacific red lionfish Pterois volitans facilitates successful invasion of the Atlantic. Marine Ecology Progress Series, 506, 243253.CrossRefGoogle Scholar
Dall, S.R.X., Bell, A.M., Bolnick, D.I., et al. (2012). An evolutionary ecology of individual differences. Ecology Letters, 15, 11891198.CrossRefGoogle ScholarPubMed
Davis, M.A. (2009). Invasion Biology. Oxford: Oxford University Press.CrossRefGoogle Scholar
Drake, J.M. and Lodge, D.M. (2006). Allee effects, propagule pressure and the probability of establishment: risk analysis for biological invasions. Biological Invasions, 8, 365375.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, 1501715022.CrossRefGoogle ScholarPubMed
Duckworth, R.A. and Kruuk, L.E.B. (2009). Evolution of genetic integration between dispersal and colonization ability in a bird. Evolution, 63, 968977.CrossRefGoogle ScholarPubMed
Edelaar, P., Roques, S., Hobson, E.A., Gonvalves da Silva, A., et al. (2015). Shared genetic diversity across the global invasive range of the monk parakeet suggests a common restricted geographic origin and the possibility of convergent selection. Molecular Ecology, 24, 21642176.CrossRefGoogle ScholarPubMed
Elton, C.S. (1958). The Ecology of Invasions by Animals and Plants. Chicago, IL: University of Chicago Press.CrossRefGoogle Scholar
Floerl, O. and Inglis, G.J. (2005). Starting the invasion pathway: the interaction between source populations and human transport vectors. Biological Invasions, 7, 589606.CrossRefGoogle Scholar
Fogarty, S., Cote, J. and Sih, A. (2011). Social personality polymorphism and the spread of invasive species: a model. American Naturalist, 177, 273287.CrossRefGoogle ScholarPubMed
Garamszegi, L.Z., Eens, M. and Török, J. (2009). Behavioural syndromes and trappability in free-living collared flycatchers, Ficedula albicollis. Animal Behaviour, 77, 803812.CrossRefGoogle Scholar
Gill, B.J., Bejakovich, D. and Whitaker, A.H. (2001). Records of foreign reptiles and amphibians accidentally imported to New Zealand. New Zealand Journal of Zoology, 28, 351359.CrossRefGoogle Scholar
Goldstein, E.A., Butler, F. and Lawton, C. (2015). Frontier population dynamics of an invasive squirrel species: do introduced populations function differently than those in the native range? Biological Invasions, 17, 11811197.CrossRefGoogle Scholar
González-Bernal, E., Brown, G.P. and Shine, R. (2014). Invasive cane toads: social facilitation depends upon an individual's personality. PLoS One, 9(7), e102880.CrossRefGoogle ScholarPubMed
Grangier, J. and Lester, P.J. (2012). Behavioral plasticity mediates asymmetric competition between invasive wasps and native ants. Communicative and Integrative Biology, 5, 127129.CrossRefGoogle ScholarPubMed
Hayes, K.R. and Barry, S.C. (2008). Are there any consistent predictors of invasion success? Biological Invasions, 10, 483506.CrossRefGoogle Scholar
Heavener, S.J., Carthey, A.J.R. and Banks, P.B. (2014). Competitive naiveté between a highly successful invader and a functionally similar native species. Oecologia, 175, 7384.CrossRefGoogle Scholar
Heinze, J., Cremer, S., Eckl, N., et al. (2006). Stealthy invaders: the biology of Cardiocondyla tramp ants. Insectes Sociaux, 53, 17.CrossRefGoogle Scholar
Henry, P.Y., Salgado, C.L., Muñoz, F.P., et al. (2013). Birds introduced to new areas show rest disorders. Biology Letters, 9, 20130463.CrossRefGoogle ScholarPubMed
Holway, D.A. and Suarez, A.V. (1999). Animal behavior: an essential component of invasion biology. Trends in Ecology and Evolution, 14, 328330.CrossRefGoogle ScholarPubMed
Holway, D.A., Lach, L., Suarez, A.V., et al. (2002). The causes and consequences of ant invasions. Annual Review of Ecology and Systematics, 33, 181233.CrossRefGoogle Scholar
Hudina, S., Hock, K. and Zganec, K. (2014). The role of aggression in range expansion and biological invasions. Current Zoology, 60, 401409.CrossRefGoogle Scholar
Hughes, D.P. and Cremer, S. (2007). Plasticity in antiparasite behaviours and its suggested role in invasion biology. Animal Behaviour, 74, 15931599.CrossRefGoogle Scholar
Hui, A. and Pinter-Wollman, N. (2014). Individual variation in exploratory behaviour improves speed and accuracy of collective nest selection by Argentine ants. Animal Behaviour, 93, 261266.CrossRefGoogle ScholarPubMed
Hulme, P.E. (2009). Trade, transport and trouble: managing invasive species pathways in an era of globalization. Journal of Applied Ecology, 46, 1018.CrossRefGoogle Scholar
Knop, E., Rindlisbacher, N., Ryser, S., et al. (2013). Locomotor activity of two sympatric slugs: implications for the invasion success of terrestrial invertebrates. Ecosphere, 4, 92.CrossRefGoogle Scholar
Kolar, C.S. and Lodge, D.M. (2001). Progress in invasion biology: predicting invaders. Trends in Ecology and Evolution, 16, 199204.CrossRefGoogle ScholarPubMed
Kolbe, J.J., Glor, R.E., Schettino, L.R., et al. (2004). Genetic variation increases during biological invasion by a Cuban lizard. Nature, 431, 177181.CrossRefGoogle ScholarPubMed
Kraus, F. (2009). Alien Reptiles and Amphibians. Berlin: Springer.CrossRefGoogle Scholar
Lee, C.E. and Gelembiuk, G.E. (2008). Evolutionary origins of invasive populations. Evolutionary Applications, 1, 427448.CrossRefGoogle ScholarPubMed
Liebl, A.L. and Martin, L.B. (2014). Living on the edge: range edge birds consume novel foods sooner than established ones. Behavioral Ecology, 25, 10891096.CrossRefGoogle Scholar
Lindstrom, T., Brown, G.P., Sisson, S.A., et al. (2013). Rapid shifts in dispersal behavior on an expanding range edge. Proceedings of the National Academy of Sciences, USA, 110, 1345213456.CrossRefGoogle Scholar
Liu, S.S., De Barro, P.J., Xu, J., et al. (2007). Asymmetric mating interactions drive widespread invasion and displacement in a whitefly. Science, 318, 17691772.CrossRefGoogle Scholar
Llewelyn, J., Phillips, B.L., Alford, R.A., et al. (2010). 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, 343348.CrossRefGoogle Scholar
Lockwood, J.L., Cassey, P. and Blackburn, T. (2005). The role of propagule pressure in explaining species invasions. Trends in Ecology and Evolution, 20, 223228.CrossRefGoogle ScholarPubMed
Lockwood, J.L., Hoopes, M.F. and Marchetti, M.P. (2013). Invasion Ecology, 2nd edn. Oxford, UK: Wiley-Blackwell.Google Scholar
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, 21592174.CrossRefGoogle Scholar
Luan, J.B., De Barro, P.J., Ruan, Y.M. and Liu, S.S. (2013). Distinct behavioural strategies underlying asymmetric mating interactions between invasive and indigenous whiteflies. Entomologia Experimentalis et Applicata, 146, 186194.CrossRefGoogle Scholar
Mack, R.N., Simberloff, D., Lonsdale, W.M., et al. (2000). Biotic invasions: causes, epidemiology, global consequences and control. Ecological Applications, 10, 689710.CrossRefGoogle Scholar
Martin, L.B. and Fitzgerald, L. (2005). A taste for novelty in invading house sparrows, Passer domesticus. Behavioral Ecology, 16, 702707.CrossRefGoogle Scholar
Mayr, E. (1965). The nature of colonising birds. In The Genetics of Colonizing Species, ed. Baker, H.G. and Stebbins, G.L. New York: Academic Press, pp. 2943.Google Scholar
McGrannachan, C.M. and Lester, P.J. (2012). Temperature and starvation effects on food exploitation by Argentine ants and native ants in New Zealand. Journal of Applied Entomology, 137, 550559.CrossRefGoogle Scholar
Meenken, D. (2012). Pet Biosecurity in New Zealand: Current State of the Domestic Pet Trade System and Options Going Forward. Wellington, New Zealand: Ministry for Primary Industries.Google Scholar
Minderman, J., Reid, J.M., Evans, P.G.H., et al. (2009). Personality traits in wild starlings: exploration behaviour and environmental sensitivity. Behavioral Ecology, 20, 830837.CrossRefGoogle Scholar
Monceau, K., Moreau, J., Poidatz, J., et al. (2014). Behavioural syndrome in a native and invasive hymenoptera species. Insect Science, 10.1111/1744–7917.12140.Google Scholar
Moule, H., Chaplin, K., Bray, R.D., et al. (2015). A matter of time: temporal variation in the introduction history and population genetic structuring of an invasive lizard. Current Zoology, 61, 456464.CrossRefGoogle Scholar
Mueller, J.C., Edelaar, P., Carrete, M., et al. (2014). Behaviour-related DRD4 polymorphism in invasive bird populations. Molecular Ecology, 23, 28762885.CrossRefGoogle ScholarPubMed
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. 190200.CrossRefGoogle Scholar
Phillips, B.L., Brown, G.P., Webb, J.K., et al. (2006). Invasion and the evolution of speed in toads. Nature, 439, 803.CrossRefGoogle ScholarPubMed
Pintor, L.M. and Sih, A. (2009). Differences in growth and foraging behavior of native and introduced populations in an invasive crayfish. Biological Invasions, 11, 18951902.CrossRefGoogle Scholar
Pintor, L.M., Sih, A. and Bauer, M.L. (2008). Differences in aggression, activity and boldness between native and introduced populations of an invasive crayfish. Oikos, 117, 16291636.CrossRefGoogle Scholar
Pintor, L.M., Sih, A. and Kerby, J.L. (2009). Behavioral correlations provide a mechanism for explaining high invader densities and increased impacts on native prey. Ecology, 90, 581587.CrossRefGoogle ScholarPubMed
Polo-Cavia, N., Lopez, P. and Martin, J. (2008). Interspecific differences in responses to predation risk may confer competitive advantages to invasive freshwater turtle species. Biological Invasions, 11, 17551765.CrossRefGoogle Scholar
Polo-Cavia, N., Lopez, P. and Martin, J. (2009). Interspecific differences in heat exchange rates may affect competition between introduced and native freshwater turtles. Ethology, 114, 115123.Google Scholar
Polo-Cavia, N., Lopez, P. and Martin, J. (2010). Competitive interactions during basking between native and invasive freshwater turtle species. Biological Invasions, 12, 21412152.CrossRefGoogle Scholar
Puth, L.M. and Post, D.M. (2005). Studying invasion: have we missed the boat? Ecology Letters, 8, 715721.CrossRefGoogle Scholar
Réale, D., Reader, S.M., Sol, D., et al. (2007). Integrating animal temperament within ecology and evolution. Biological Reviews, 82, 291318.CrossRefGoogle ScholarPubMed
Rehage, J.S. and Sih, A. (2004). Dispersal behavior, boldness, and the link to invasiveness: a comparison of four Gambusia species. Biological Invasions, 6, 379391.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 noninvasive relatives? Ecology of Freshwater Fish, 14, 352360.CrossRefGoogle Scholar
Rehage, J.S., Barnett, B.K. and Sih, A. (2005b). Behavioral responses to a novel predator and competitor of invasive mosquitofish and their non-invasive relatives (Gambusia sp.). Behavioral Ecology and Sociobiology, 57, 256266.CrossRefGoogle Scholar
Richardson, D.M. (ed.) (2011). Fifty Years of Invasion Ecology: The Legacy of Charles Elton. Oxford, UK: Wiley-Blackwell.Google Scholar
Rius, M. and Darling, J.A. (2014). How important is intraspecific genetic admixture to the success of colonising populations? Trends in Ecology and Evolution, 29, 233242.CrossRefGoogle Scholar
Robertson, B.A., Rehage, J.S. and Sih, A. (2013). Ecological novelty and the emergence of evolutionary traps. Trends in Ecology and Evolution, 28, 552560.CrossRefGoogle ScholarPubMed
Rowles, A.D. and O'Dowd, D.J. (2007). Interference competition by Argentine ants displaces native ants: implications for biotic resistance to invasion. Biological Invasions, 9, 7385.CrossRefGoogle Scholar
Russell, J.C., McMorland, A.J.C. and MacKay, J.W.B. (2010). Exploratory behaviour of colonizing rats in novel environments. Animal Behaviour, 79, 159164.CrossRefGoogle Scholar
Sagata, K. and Lester, P.J. (2009). Behavioural plasticity associated with propagule size, sources and the invasion success of the Argentine ant, Linepithema humile. Journal of Applied Ecology, 46, 1927.CrossRefGoogle Scholar
Short, K.H. and Petren, K. (2008). Boldness underlies foraging success of invasive Lepidodactylus lugubris geckos in the human landscape. Animal Behaviour, 76, 429437.CrossRefGoogle Scholar
Sih, A., Bell, A. and Johnson, J.C. (2004a). Behavioral syndromes: an ecological and evolutionary overview. Trends in Ecology and Evolution, 19, 372378.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, 241277.CrossRefGoogle Scholar
Sih, A., Cote, J., Evans, M., Fogarty, S. and Pruitt, J. (2012). Ecological implications of behavioural syndromes. Ecology Letters, 15, 278289.CrossRefGoogle ScholarPubMed
Simberloff, D. (2009). The role of propagule pressure in biological invasions. Annual Review of Ecology, Evolution and Systematics, 40, 81102.CrossRefGoogle Scholar
Sol, D. (2003). Behavioural flexibility: a neglected issue in the ecological and evolutionary literature. In Animal Innovation, ed. Reader, S.M. and Laland, K.N. Oxford, UK: Oxford University Press, pp. 6382.CrossRefGoogle Scholar
Sol, D. and Lefebvre, L. (2000). Behavioural flexibility predicts invasion success in birds introduced to New Zealand. Oikos, 90, 599605.CrossRefGoogle Scholar
Sol, D. and Maspons, J.M. (2015). Integrating behavior into life history theory: a comment on Wong and Candolin. Behavioral Ecology, 26, 677678.CrossRefGoogle Scholar
Sol, D., Timmermans, S. and Lefebvre, L. (2002). Behavioural flexibility and invasion success in birds. Animal Behaviour, 63, 495502.CrossRefGoogle Scholar
Sol, D., Duncan, R.P., Blackburn, T.M., et al. (2005). Big brains, enhanced cognition, and response of birds to novel environments. Proceedings of the National Academy of Sciences, USA, 102, 54605465.CrossRefGoogle ScholarPubMed
Sol, D., Bacher, S., Reader, S.M., et al. (2008). Brain size predicts the success of mammal species introduced to novel environments. American Naturalist, 172, S63S71.CrossRefGoogle ScholarPubMed
Sol, D., Griffin, A.S., Bartomeus, I., et al. (2011). Exploring or avoiding novel food resources? The novelty conflict in an invasive bird. PLoS One, 6, e19535.CrossRefGoogle ScholarPubMed
Sol, D., Maspons, J., Vall-llosera, M., et al. (2012). Unraveling the life history of successful invaders. Science, 337, 580583.CrossRefGoogle ScholarPubMed
Suarez, A.V., Holway, D.A., Liange, D., et al. (2002). Spatiotemporal patterns of intraspecific aggression in the invasive Argentine ant. Animal Behaviour, 64, 697708.CrossRefGoogle Scholar
Suarez, A.V., Holway, D.A. and Ward, P.S. (2005). The role of opportunity in the unintentional introduction of nonnative ants. Proceedings of the National Academy of Sciences, USA, 102, 1703217035.CrossRefGoogle ScholarPubMed
Suarez, A.V., Holway, D.A. and Tsutsui, N.D. (2008). Genetics and behavior of a colonizing species: the invasive Argentine ant. American Naturalist, 172, S72S84.CrossRefGoogle ScholarPubMed
Taylor, C.M. and Hastings, A. (2005). Allee effects in biological invasions. Ecology Letters, 8, 895908.CrossRefGoogle Scholar
Teixeria, C.P., Schetini de Azevado, C., Mendi, M., et al. (2007). Revisiting translocation and reintroduction programmes: the importance of considering stress. Animal Behaviour, 73, 113.CrossRefGoogle Scholar
Thibert-Plante, X. and Hendry, A.P. (2011). The consequences of phenotypic plasticity for ecological speciation. Journal of Evolutionary Biology, 24, 326342.CrossRefGoogle ScholarPubMed
Tingley, R., Romagosa, C.M., Kraus, F., et al. (2010). The frog filter: amphibian introduction bias driven by taxonomy, body size and biogeography. Global Ecology and Biogeography, 19, 496503.CrossRefGoogle Scholar
Tingley, R., Thompson, M.B., Hartley, S. and Chapple, D.G. (2016). Patterns of niche filling and expansion across the invaded ranges of an Australian lizard. Ecography, 39, 270280.CrossRefGoogle Scholar
Tobin, P.C., Berec, L. and Liebhold, A.M. (2011). Exploiting Allee effects for managing biological invasions. Ecology Letters, 14, 615624.CrossRefGoogle ScholarPubMed
Toy, S.J. and Newfield, M.J. (2010). The accidental introduction of invasive animals as hitchhikers through inanimate pathways: a New Zealand perspective. Revue Scientifique et Technique- Office International des Epizooties, 29, 123133.CrossRefGoogle ScholarPubMed
Truhlar, A.M. and Aldridge, D.C. (2015). Differences in the behavioural traits between two potentially invasive amphipods, Dikerogammarus villosus and Gammarus pulex. Biological Invasions, 17, 15691579.CrossRefGoogle Scholar
Tsutsui, N.D. and Suarez, A.V. (2003). The colony structure and population biology of invasive ants. Conservation Biology, 17, 4858.CrossRefGoogle Scholar
Tsutsui, N.D., Suarez, A.V., Holway, D.A., et al. (2000). Reduced genetic variation and the success of an invasive species. Proceedings of the National Academy of Sciences, USA, 97, 59485953.CrossRefGoogle ScholarPubMed
Ugelvig, L.V., Drijfhout, F.P., Kronauer, D.J.C., et al. (2008). The introduction history of invasive garden ants in Europe: integrating genetic, chemical and behavioural approaches. BMC Biology, 6, 11.CrossRefGoogle ScholarPubMed
Usio, N., Konishi, M. and Nakano, S. (2001). Species displacement between an introduced and a ‘vulnerable’ crayfish: the role of aggressive interactions and shelter competition. Biological Invasions, 3, 179185.CrossRefGoogle Scholar
Van Buskirk, J. (2012). Behavioural plasticity and environmental change. In Behavioural Responses to a Changing World: Mechanisms and Consequences, ed. Candolin, U. and Wong, B.B.M. Oxford: Oxford University Press, pp. 145158.CrossRefGoogle Scholar
Walsh, B. and Blows, M.W. (2009). Abundant genetic variation plus strong selection = multivariate genetic constraints: A geometric view of adaptation. Annual Reviews of Ecology, Evolution and Systematics, 40, 4159.CrossRefGoogle Scholar
Ward, D.F., Beggs, J.R., Clout, M.N., et al. (2006). The diversity and origin of exotic ants arriving in New Zealand via human-mediated dispersal. Diversity and Distributions, 12, 601609.CrossRefGoogle Scholar
Weis, J.S. (2010). The role of behavior in the success of invasive crustaceans. Marine and Freshwater Behaviour and Physiology, 43, 8398.CrossRefGoogle Scholar
White, A.W. and Shine, R. (2009). The extra-limital spread of an invasive species via ‘stowaway’ dispersal: toad to nowhere? Animal Conservation, 12, 3845.CrossRefGoogle Scholar
Witmer, G.W. Snow, N.P., Moulton, R.S., et al. (2014). Responses by wild house mice (Mus musculus) to various stimuli in a novel environment. Applied Animal Behaviour Science, 159, 99106.CrossRefGoogle Scholar
Wolf, M. and Weissing, F.J. (2012). Animal personalities: consequences for ecology and evolution. Trends in Ecology and Evolution, 27, 452461.CrossRefGoogle ScholarPubMed
Wong, B.B.M. and Candolin, U. (2015). Behavioral responses to changing environments. Behavioral Ecology, 26, 665673.CrossRefGoogle Scholar
Wright, T.F., Eberhard, J.R., Hobson, E.A., et al. (2010). Behavioral flexibility and species invasions: the adaptive flexibility hypothesis. Ethology Ecology and Evolution, 22, 393404.CrossRefGoogle Scholar

References

Allen, T. and Clarke, J. (2005). Social learning of food preferences by white-tailed ptarmigan chicks. Animal Behaviour, 70, 305310.CrossRefGoogle Scholar
Allman, J., McLaughlin, T. and Hakeem, A. (1993). Brain weight and life-span in primate species. Proceedings of the National Academy of Sciences, USA, 90, 118122.CrossRefGoogle ScholarPubMed
Amiel, J.J., Tingley, R. and Shine, R. (2011). Smart moves: effects of relative brain size on establishment success of invasive amphibians and reptiles. PLoS ONE, 6, e18277.CrossRefGoogle ScholarPubMed
Arcediano, F., Escobar, M. and Miller, R.R. (2003). Temporal integration and temporal backward associations in human and nonhuman subjects. Learning and Behavior, 31, 242256.CrossRefGoogle ScholarPubMed
Benson-Amram, S. and Holekamp, K.E. (2012). Innovative problem solving by wild spotted hyenas. Proceedings of the Royal Society of London, Series B, 279, doi: 10.1098/rspb.(2012).1450.Google ScholarPubMed
Biondi, L.M., , M.S. and Vassallo, A.I. (2010). Inter-individual and age differences in exploration, neophobia and problem-solving ability in a neotropical raptor (Milvago chimango). Animal Cognition, 13, 701710.CrossRefGoogle Scholar
Björklund, D.F. and Harnishfeger, K.K. (1995). The evolution of inhibition mechanisms and their role in human cognition and behavior. In Interference and Inhibition in Cognition, ed. Dempster, F.N. and Brainerd, C.J., pp. 142169. San Diego, CA: Academic Press.Google Scholar
Blackburn, T.M., Pyšek, P., Bacher, S., et al. (2011). A proposed unified framework for biological invasions. Trends in Ecology and Evolution, 26, 333339.CrossRefGoogle ScholarPubMed
Blaisdell, A.P., Sawa, K., Leising, K.J. and Waldmann, M.R. (2006). Causal reasoning in rats. Science, 311, 10201022.CrossRefGoogle ScholarPubMed
Bókony, V., Kulcsár, A., Tóth, Z. and Liker, A. (2012). Personality traits and behavioral syndromes in differently urbanized populations of house sparrows (Passer domesticus). PLoS one, 7, e36639.CrossRefGoogle ScholarPubMed
Boogert, N.J., Reader, S.M. and Laland, K.N. (2006). The relation between social rank, neophobia and individual learning in starlings. Animal Behaviour, 72, 12291239.CrossRefGoogle Scholar
Brown, G.E., Ferrari, M.C.O., Elvidge, C.K., Ramnarine, I. and Chivers, D.P. (2013). Phenotypically plastic neophobia: a response to variable predation risk. Proceedings of the Royal Society of London, Series B, 280, doi: 10.1098/rspb.(2012).2712.Google ScholarPubMed
Candler, S. and Bernal, X.E. (2014). Differences in neophobia between cane toads from introduced and native populations. Behavioral Ecology, 26, 97104.CrossRefGoogle Scholar
Changizi, M.A. (2003). Relationship between number of muscles, behavioral repertoire size, and encephalization in mammals. Journal of Theoretical Biology, 220, 157168.CrossRefGoogle ScholarPubMed
Chapple, D.G., Simmonds, S.M. and Wong, B.B.M. (2012). Can behavioral and personality traits influence the success of unintentional species introductions? Trends in Ecology and Evolution, 27, 5764.CrossRefGoogle ScholarPubMed
Christidis, L. and Boles, W. (2008). Systematics and Taxonomy of Australian Birds. Collingwood, Australia: CSIRO Publishing.CrossRefGoogle Scholar
Cnotka, J., Güntürkün, O., Rehkämper, G., Gray, R.D. and Hunt, G.R. (2008). Extraordinary large brains in tool-using New Caledonian crows (Corvus moneduloides). Neuroscience Letters, 433, 241245.CrossRefGoogle ScholarPubMed
Deaner, R.O., Barton, R.A. and van Schaik, C.P. (2002). Primate brains and life histories: renewing the connection. In Primate Life Histories and Socioecology, ed. Kappeler, P. M. and Pereira, M. E. Chicago, IL: The University of Chicago Press, pp. 233265.Google Scholar
Dempster, F.N. (1992). The rise and fall of the inhibitory mechanism: toward a unified theory of cognitive development and aging. Developmental Review, 12, 4575.CrossRefGoogle Scholar
Dhami, M.K. and Nagle, B. (2009). Review of the biology and ecology of the common myna (Acridotheres tristis) and some implications for management of this invasive species. Report. Auckland, New Zealand: Pacific Invasives Initiatives, pp. 128.Google Scholar
Diquelou, M., Griffin, A.S. and Sol, D. (2015). Solving new foraging problems: Motor processes are key to behavioural innovation in birds. Behavioral Ecology, doi:10.1093/beheco/arv190.CrossRefGoogle Scholar
Dukas, R. (2004). Evolutionary biology of animal cognition. Annual Review of Ecology, Evolution, and Systematics, 35, 347374.CrossRefGoogle Scholar
Duncan, R.P., Blackburn, T.M. and Sol, D. (2003). The ecology of bird introductions. Annual Review of Ecology, Evolution, and Systematics, 34, 7198.CrossRefGoogle Scholar
Elias, M.F. (1970). Spatial discrimination reversal learning for mice genetically selected for differing brain size: a supplementary report. Perceptual and Motor Skills, 30, 239245.CrossRefGoogle Scholar
Fanselow, M.S. (2000). Contextual fear, Gestalt memories, and the hippocampus. Behavioural Brain Research, 110, 7381.CrossRefGoogle ScholarPubMed
Feare, C.J. (2010). The use of Starlicide® in preliminary trials to control invasive common myna Acridotheres tristis populations on St Helena and Ascension islands, Atlantic Ocean. Conservation Evidence, 7, 5261.Google Scholar
Galef, B.G.J. (1996). Social enhancement of food preferences in Norway rats: A brief review. In Social Learning in Animals: The Roots of Culture, ed. Heyes, C.M. and Galef, B.G.J. San Diego, CA: Academic Press, pp. 4964.CrossRefGoogle Scholar
Gaser, C. and Schlaug, G. (2003). Gray matter differences between musicians and nonmusicians. Annals of the New York Academy of Sciences, 999, 514517.CrossRefGoogle ScholarPubMed
Greenberg, R.S. and Mettke-Hofmann, C. (2001). Ecological aspects of neophilia and neophobia in birds. Current Ornithology, 16, 119178.Google Scholar
Griffin, A.S. (2004). Social learning about predators: a review and prospectus. Learning and Behavior, 32, 131140.CrossRefGoogle ScholarPubMed
Griffin, A.S. (2008). Social learning in Indian mynahs, Acridotheres tristis: the role of distress calls. Animal Behaviour, 75, 7989.CrossRefGoogle Scholar
Griffin, A.S. (2009). Temporal limitations on social learning of novel predators by Indian mynahs, Acridotheres tristis. Ethology, 115, 287295.CrossRefGoogle Scholar
Griffin, A.S. (2010). Learning and conservation. In Encyclopedia of Animal Behavior, Vol. 2, ed. Breed, M.D. and Moore, J. Amsterdam: Elsevier, pp. 259264.CrossRefGoogle Scholar
Griffin, A.S. (2016). Innovativeness as an emergent property: a new alignment of comparative and experimental research on animal innovation. Philosophical Transactions of the Royal Society B: Biological Sciences, doi: 10.1098/rstb.2015.0544.Google Scholar
Griffin, A.S. and Boyce, H.M. (2009). Indian mynahs, Acridotheres tristis, learn about dangerous places by observing the fate of others. Animal Behaviour, 78, 7984.CrossRefGoogle Scholar
Griffin, A.S. and Diquelou, M. (2015). Innovative problem solving in birds: a cross-species comparison of two highly successful Passerines. Animal Behaviour, 100, 8494.CrossRefGoogle Scholar
Griffin, A.S. and Guez, D. (2014). Innovation and problem solving: a review of common mechanisms. Behavioural Processes, 109, 121134.CrossRefGoogle ScholarPubMed
Griffin, A.S. and Guez, D. (2016). Bridging the gap between cross-taxon and within-species analy-ses of behavioral innovations in birds: making sense of discrepant cognition–innovation relationships and the role of motor diversity. In Advances in the Study of Behavior, ed. Naguib, M., et al. New York, NY: Academic Press, pp. 1–40.CrossRefGoogle Scholar
Griffin, A.S. and Haythorpe, K. (2011). Learning from watching alarmed demonstrators: does the cause of alarm matter? Animal Behaviour, 81, 11631169.CrossRefGoogle Scholar
Griffin, A.S., Boyce, H.M. and MacFarlane, G.R. (2010). Social learning about places: observers may need to detect both social alarm and its cause in order to learn. Animal Behaviour, 79, 459465.CrossRefGoogle Scholar
Griffin, A.S., Lermite, F., Perea, M. and Guez, D. (2013). To innovate or not: contrasting effects of social groupings on safe and risky foraging in Indian mynahs. Animal Behaviour, 86, 12911300.CrossRefGoogle Scholar
Griffin, A.S., Diquelou, M. and Perea, M. (2014). Innovative problem solving in birds: a key role of motor diversity. Animal Behaviour, 92, 221227.CrossRefGoogle Scholar
Gronenberg, W. and Couvillon, M.J. (2010). Brain composition and olfactory learning in honey bees. Neurobiology of Learning and Memory, 93, 435443.CrossRefGoogle ScholarPubMed
Guez, D. and Audley, C. (2013). Transitive or not: a critical appraisal of transitive inference in animals. Ethology, 119, 703726.CrossRefGoogle Scholar
Healy, S.D. and Rowe, C. (2007). A critique of comparative studies of brain size. Proceedings of the Royal Society of London, Series B, 274, 453464.Google ScholarPubMed
Healy, S.D. and Rowe, C. (2013). Costs and benefits of evolving a larger brain: doubts over the evidence that large brains lead to better cognition. Animal Behaviour, 86, e1e3.CrossRefGoogle Scholar
Klopfer, P.H. 1967. Behavioural stereotypy in birds. Wilson Bulletin, 79, 290300.Google Scholar
Kotrschal, A., Rogell, B., Bundsen, A., et al. (2013a). Artificial selection on relative brain size in the guppy reveals costs and benefits of evolving a larger brain. Current Biology, 23, 168171.CrossRefGoogle ScholarPubMed
Kotrschal, A., Rogell, B., Bundsen, A., et al. (2013b). The benefit of evolving a larger brain: big-brained guppies perform better in a cognitive task. Animal Behaviour, 86, e4e6.CrossRefGoogle Scholar
Laland, K.N. (2004). Social learning strategies. Learning and Behavior, 32, 414.CrossRefGoogle ScholarPubMed
Lissek, S., Diekamp, B. and Güntürkün, O. (2002). Impaired learning of a color reversal task after NMDA receptor blockade in the pigeon (Columbia livia) associative forebrain (neostriatum caudolaterale). Behavioral Neuroscience, 116, 523529.CrossRefGoogle Scholar
Lowe, S., Browne, M., Boudjelas, S. and de Porter, M. (2000). 100 of the World's Worst Invasive Alien Species. A Selection from the Global Invasive Species Database. Auckland: The Invasive Species Specialist Group (ISSG), a specialist group of the Species Survival Commission (SSC) of the World Conservation Union (IUCN).Google Scholar
MacLean, E.L., Hare, B., Nunn, C.L. et al. (2014). The evolution of self-control. Proceedings of the National Academy of Sciences, USA, 111, E2140–8.CrossRefGoogle ScholarPubMed
Mangalam, M. and Singh, M. (2013). Flexibility in food extraction techniques in urban free-ranging bonnet macaques, Macaca radiata. PLoS ONE, 8, e85497.CrossRefGoogle ScholarPubMed
Marples, N.M. and Roper, T.J. (1997). Response of domestic chicks to methyl anthranilate odour. Animal Behaviour, 53, 12631270.CrossRefGoogle ScholarPubMed
Martin, L.B. and Fitzgerald, L. (2005). A taste for novelty in invading house sparrows, Passer domesticus. Behavioral Ecology, 16, 702707.CrossRefGoogle Scholar
Marzluff, J.M., Walls, J., Cornell, H.N., Withey, J.C. and Craig, D.P. (2010). Lasting recognition of threatening people by wild American crows. Animal Behaviour, 79, 699707.CrossRefGoogle Scholar
Mettke-Hofmann, C. (2007). Object exploration of garden and Sardinian warblers peaks in spring. Ethology, 113, 174182.CrossRefGoogle Scholar
Mettke-Hofmann, C., Winkler, H. and Leisler, B. (2002). The significance of ecological factors for exploration and neophobia in parrots. Ethology, 108, 249272.CrossRefGoogle Scholar
Mettke-Hofmann, C., Ebert, C., Schmidt, T., Steiger, S. and Stieb, S. (2005). Personality traits in resident and migratory warbler species. Behaviour, 142, 13571375.Google Scholar
Mettke-Hofmann, C., Lorentzen, S., Schlicht, E., Schneider, J. and Werner, F. (2009). Spatial neophilia and spatial neophobia in resident and migratory warblers (Sylvia). Ethology, 115, 482492.CrossRefGoogle Scholar
Miranda, A.C., Schielzeth, H., Sonntag, T. and Partecke, J. (2013). Urbanization and its effects on personality traits: a result of microevolution or phenotypic plasticity? Global Change Biology, 19, 26342644.CrossRefGoogle ScholarPubMed
Nottebohm, F. (1981). A brain for all seasons: cyclical anatomical changes in song control nuclei of the canary brain. Science, 214, 13681370.CrossRefGoogle Scholar
Overington, S.E., Cauchard, L., Côté, K.-A. and Lefebvre, L. (2011). Innovative foraging behaviour in birds: what characterizes an innovator? Behavioural Processes, 87, 274285.CrossRefGoogle ScholarPubMed
Penfield, W. and Rasmussen, T. (1950). The Cerebral Cortex of Man: A Clinical Study of Localization of Function. Oxford, UK: Macmillan Edn.Google Scholar
Phillips, B.L. and Suarez, S.D. (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, UK: Oxford University Press, pp. 190200.CrossRefGoogle Scholar
Rescorla, R.A. (2014). Pavlovian Second-Order Conditioning. Studies in Associative Learning (Psychology Revivals). New York: Psychology Press.CrossRefGoogle Scholar
Roth, G. and Dicke, U. (2005). Evolution of the brain and intelligence. Trends in Cognitive Sciences, 9, 250257.CrossRefGoogle ScholarPubMed
Sandel, A.A., MacLean, E.L. and Hare, B. (2009). Inhibitory control in an object retrieval task in five lemur species. American Journal of Primatology, 71, 80.Google Scholar
Sanes, J. and Donoghue, J. (2000). Plasticity and primary motor cortex. Annual Review of Neuroscience, 23, 393415.CrossRefGoogle ScholarPubMed
Schuppli, C., Sofia, F. and van Schaik, C.P. (2014). How sociality affects independent exploration: Evidence gathered in two populations of wild orangutans. American Journal of Physical Anthropology, 153, 234.Google Scholar
Seed, A., Emery, N. and Clayton, N. (2009). Intelligence in corvids and apes: a case of convergent evolution? Ethology, 115, 401420.CrossRefGoogle Scholar
Seok An, Y., Kriengwatana, B., MacDougall-Shackleton, E., Newman, A. and MacDougall-Shackleton, S. (2011). Social rank, neophobia and observational learning in black-capped chickadees. Behaviour, 148, 5569.Google Scholar
Shettleworth, S.J. (2010). Cognition, Evolution, and Behavior, 2nd edn. Oxford, UK: Oxford University Press.Google Scholar
Smaers, J.B. and Soligo, C. (2013). Brain reorganization, not relative brain size, primarily characterizes anthropoid brain evolution. Proceedings of the Royal Society of London, Series B, 280, doi: 10.1098/rspb.2013.0269.Google Scholar
Sol, D. (2007). Do successful invaders exist? Pre-adaptations to novel environments in terrestrial vertebrates. In Biological Invasions, ed. Nentwig, W. Berlin: Springer, pp. 127144.CrossRefGoogle Scholar
Sol, D., Duncan, R.P., Blackburn, T.M., Cassey, P. and Lefebvre, L. (2005). Big brains, enhanced cognition, and response of birds to novel environments. Proceedings of the National Academy of Sciences, USA, 102, 54605465.CrossRefGoogle ScholarPubMed
Sol, D., Bacher, S., Reader, S.M. and Lefebvre, L. (2008). Brain size predicts the success of mammal species introduced into novel environments. The American Naturalist, 172 Suppl., S6371.CrossRefGoogle ScholarPubMed
Sol, D., Griffin, A.S., Bartomeus, I. and Boyce, H. (2011). Exploring or avoiding novel food resources? The novelty conflict in an invasive bird. PLoS ONE, 6, e19535.CrossRefGoogle ScholarPubMed
Sol, D., Bartomeus, I. and Griffin, A.S. (2012a). The paradox of invasion in birds: competitive superiority or ecological opportunism? Oecologia, 169, 553564.CrossRefGoogle ScholarPubMed
Sol, D., Griffin, A.S. and Barthomeus, I. (2012b). Consumer and motor innovation in the common myna: the role of motivation and emotional responses. Animal Behaviour, 83, 179188.CrossRefGoogle Scholar
Suchail, S., Guez, D. and Belzunces, L.P. (2000). Characteristics of imidacloprid toxicity in two Apis mellifera subspecies. Environmental Toxicology and Chemistry, 19, 19011905.CrossRefGoogle Scholar
Tebbich, S., Stankewitz, S. and Teschke, I. (2012). The relationship between foraging, learning abilities and neophobia in two species of Darwin's finches. Ethology, 118, 135146.CrossRefGoogle Scholar
Thorndike, E.L. (1898). Animal intelligence: An experimental study of the associative processes in animals. Psychological Monographs: General and Applied, 2, 11251127.CrossRefGoogle Scholar
Thornton, A. and Samson, J. (2012). Innovative problem solving in wild meerkats. Animal Behaviour, 83, 14591468.CrossRefGoogle Scholar
Wright, T.F., Eberhard, J.R., Hobson, E.A., Avery, M.L. and Russello, M.A. (2010). Behavioral flexibility and species invasions: the adaptive flexibility hypothesis. Ethology Ecology and Evolution, 22, 393404.CrossRefGoogle Scholar

References

Addis, E.A., Davis, J.E., Miner, B.E. and Wingfield, J.C. (2011). Variation in circulating corticosterone levels is associated with altitudinal range expansion in a passerine bird. Oecologia, 167(2), 369378.CrossRefGoogle Scholar
Adelman, J. and Martin, L. (2009). Vertebrate sickness behavior: an adaptive and integrated neuroendocrine immune response. Integrative and Comparative Biology, 49, 202214.CrossRefGoogle Scholar
Adelman, J.S., Kirkpatrick, L., Grodio, J.L. and Hawley, D.M. (2013). House finch populations differ in early inflammatory signalling and pathogen tolerance at the peak of Mycoplasma gallisepticum infection. The American Naturalist, 181(5), 674689.CrossRefGoogle ScholarPubMed
Angelier, F. and Wingfield, J.C. (2013). Importance of the glucocorticoid stress response in a changing world: theory, hypotheses and perspectives. General and Comparative Endocrinology, 190, 118128.CrossRefGoogle Scholar
Atwell, J.W., Cardoso, G.C., Whittaker, D.J., et al. (2012). Boldness behavior and stress physiology in a novel urban environment suggest rapid correlated evolutionary adaptation. Behavioral Ecology, doi: 10.1093/beheco/ars059.CrossRefGoogle Scholar
Atwell, J.W., Cardoso, G.C., Whittaker, D.J., Price, T.D. and Ketterson, E.D. (2014). Hormonal, behavioral, and life-history traits exhibit correlated shifts in relation to population establishment in a novel environment. The American Naturalist, 184, E147160.CrossRefGoogle Scholar
Badyaev, A. (2013a). Reconciling innovation and adaptation during recurrent colonization of urban environments: molecular, genetic, and developmental bases. Avian Urban Ecology: Behavioural and Physiological Adaptations, 155.CrossRefGoogle Scholar
Badyaev, A.V. (2013b). ‘Homeostatic hitchhiking’: a mechanism for the evolutionary retention of complex adaptations. Integrative and Comparative Biology, ict084.Google Scholar
Badyaev, A.V. (2014). Epigenetic resolution of the ‘curse of complexity ’in adaptive evolution of complex traits. The Journal of Physiology, 592, 22512260.CrossRefGoogle ScholarPubMed
Badyaev, A.V. and Uller, T. (2009). Parental effects in ecology and evolution: mechanisms, processes and implications. Philosophical Transactions of the Royal Society B: Biological Sciences, 364, 11691177.CrossRefGoogle ScholarPubMed
Bonier, F. (2012). Hormones in the city: endocrine ecology of urban birds. Hormones and Behavior, 61, 763772.CrossRefGoogle ScholarPubMed
Bonneaud, C., Balenger, S.L., Russell, A.F., et al. (2011). Rapid evolution of disease resistance is accompanied by functional changes in gene expression in a wild bird. Proceedings of the National Academy of Sciences, USA, 108(19), 78667871.CrossRefGoogle Scholar
Bonneaud, C., Balenger, S.L., Hill, G.E. and Russell, A.F. (2012). Experimental evidence for distinct costs of pathogenesis and immunity against a natural pathogen in a wild bird. Molecular Ecology, 21(19), 47874796.CrossRefGoogle Scholar
Bossdorf, O., Richards, C.L. and Pigliucci, M. (2008). Epigenetics for ecologists. Ecology Letters, 11, 106115.CrossRefGoogle ScholarPubMed
Braby, C.E. and Somero, G.N. (2006). Following the heart: temperature and salinity effects on heart rate in native and invasive species of blue mussels (genus Mytilus). Journal of Experimental Biology, 209, 25542566.CrossRefGoogle ScholarPubMed
Bradley, C.A. and Altizer, S. (2007). Urbanization and the ecology of wildlife diseases. Trends in Ecology and Evolution, 22, 95102.CrossRefGoogle ScholarPubMed
Cabezas, S., Carette, M., Tella, J.L., Marchant, T.A. and Bortolotti, G.R. (2013). Differences in acute stress responses between wild-caught and captive-bred birds: a physiological mechanism contributing to current avian invasions? Biological Invasions, 15(3), 521527.CrossRefGoogle Scholar
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, 5764.CrossRefGoogle ScholarPubMed
Chown, S.L., Slabber, S., McGeoch, M.A., Janion, C. and Leinaas, H.P. (2007). Phenotypic plasticity mediates climate change responses among invasive and indigenous arthropods. Proceedings of the Royal Society B: Biological Sciences, 274, 25312537.CrossRefGoogle ScholarPubMed
Cohen, A.A., Martin, L.B., Wingfield, J.C., McWilliams, S.R. and Dunne, J.A. (2012). Physiological regulatory networks: ecological roles and evolutionary constraints. Trends in Ecology and Evolution, 27(8), 428435.CrossRefGoogle ScholarPubMed
Colautti, R.I. and MacIsaac, H.J. (2004). A neutral terminology to define ‘invasive’ species. Diversity and Distributions, 10, 135141.CrossRefGoogle Scholar
Cote, J., Clobert, J., Meylan, S. and Fitze, P.S. (2006). Experimental enhancement of corticosterone levels positively affects subsequent male survival. 49, 320327.CrossRefGoogle Scholar
Crespi, E.J., Williams, T.D., Jessop, T.S. and Delehanty, B. (2013). Life history and the ecology of stress: how do glucocorticoid hormones influence life-history variation in animals? Functional Ecology, 27, 93106.CrossRefGoogle Scholar
Dantzer, B., Newman, A.E., Boonstra, R., et al. (2013). Density triggers maternal hormones that increase adaptive offspring growth in a wild mammal. Science, 340, 12151217.CrossRefGoogle Scholar
Dell'Omo, G. and Palmery, M. (2002). Fertility control in vertebrate pest species. Contraception, 65, 273275.CrossRefGoogle ScholarPubMed
Denardo, D.F. and Sinervo, B. (1994). Effects of steroid–hormone interaction on activity and home-range size of male lizards. Hormones and Behavior, 28, 273287.CrossRefGoogle ScholarPubMed
Denver, R.J. (2009). Stress hormones mediate environment–genotype interactions during amphibian development. General and Comparative Endocrinology, 164, 2031.CrossRefGoogle ScholarPubMed
Dickens, M.J., Delehanty, D.J. and Romero, L.M. (2009). Stress and translocation: alterations in the stress physiology of translocated birds. Proceedings of the Royal Society B: Biological Sciences, 276, 20512056.CrossRefGoogle ScholarPubMed
Duckworth, R.A. and Sockman, K.W. (2012). Proximate mechanisms of behavioural inflexibility: implications for the evolution of personality traits. Functional Ecology, 26, 559566.CrossRefGoogle Scholar
Dufty, A.M., Clobert, J. and Møller, A.P. (2002). Hormones, developmental plasticity and adaptation. Trends in Ecology and Evolution, 17, 190196.CrossRefGoogle Scholar
Evans, K.L., Hatchwell, B.J., Parnell, M. and Gaston, K.J. (2010). A conceptual framework for the colonisation of urban areas: the blackbird Turdus merula as a case study. Biological Reviews, 85, 643667.CrossRefGoogle ScholarPubMed
Flatt, T. and Heyland, A. (2011). Mechanisms of Life History Evolution: The Genetics and Physiology of Life History Traits and Trade-offs. Oxford, UK: Oxford University Press.CrossRefGoogle Scholar
Francis, D., Diorio, J., Liu, D. and Meaney, M.J. (1999). Nongenomic transmission across generations of maternal behavior and stress responses in the rat. Science, 286, 11551158.CrossRefGoogle ScholarPubMed
Garland, T. and Adolph, S.C. (1994). Why not to do 2-species comparative-studies: limitations on inferring adaptation. Physiological Zoology, 67, 797828.CrossRefGoogle Scholar
Gervasi, S.S., Civitello, D.J., Kilvitis, H.J. and Martin, L.B. (2015). The context of host competence: a role for plasticity in host-parasite dynamics. Trends in Parasitology, 31, 419425.CrossRefGoogle ScholarPubMed
Ghalambor, C.K., McKay, J.K., Carroll, S.P. and Reznick, D.N. (2007). Adaptive versus non-adaptive phenotypic plasticity and the potential for contemporary adaptation in new environments. Functional Ecology, 21, 394407.CrossRefGoogle Scholar
Graham, S.P., Kelehear, C., Brown, G.P. and Shine, R. (2012). Corticosterone–immune interactions during captive stress in invading Australian cane toads (Rhinella marina). Hormones and Behavior, 62(2), 146153.CrossRefGoogle ScholarPubMed
Groothuis, T.G. and Schwabl, H. (2008). Hormone-mediated maternal effects in birds: mechanisms matter but what do we know of them? Philosophical Transactions of the Royal Society B: Biological Sciences, 363, 16471661.CrossRefGoogle ScholarPubMed
Hahn, T.P., Wingfield, J.C., Mullen, R. and Deviche, P.J. (1995). Endocrine bases of spatial and temporal opportunism in Arctic-breeding birds. American Zoologist, 35, 259273.CrossRefGoogle Scholar
Hau, M. (2007). Regulation of male traits by testosterone: implications for the evolution of vertebrate life histories. Bioessays, 29, 133144.CrossRefGoogle ScholarPubMed
Hau, M., Wikelski, M., Gwinner, H. and Gwinner, E. (2004). Timing of reproduction in a Darwin's finch: temporal opportunism under spatial constraints. Oikos, 106, 489500.CrossRefGoogle Scholar
Hau, M., Gill, S.A. and Goymann, W. (2008). Tropical field endocrinology: ecology and evolution of testosterone concentrations in male birds. General and Comparative Endocrinology, 157, 241248.CrossRefGoogle ScholarPubMed
Higgins, S.I. and Richardson, D.M. (2014). Invasive plants have broader physiological niches. Proceedings of the National Academy of Sciences, USA, 111, 1061010614.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, 949952.CrossRefGoogle ScholarPubMed
Jessop, T.S., Letnic, M., Webb, J.K. and Dempster, T. (2013). Adrenocortical stress responses influence an invasive vertebrate's fitness in an extreme environment. Proceedings of the Royal Society B: Biological Sciences, 280(1768), 20131444.CrossRefGoogle Scholar
Juliano, S.A., O'Meara, G.F., Morrill, J.R. and Cutwa, M.M. (2002). Desiccation and thermal tolerance of eggs and the coexistence of competing mosquitoes. Oecologia, 130, 458469.CrossRefGoogle ScholarPubMed
Kearney, M. and Porter, W. (2009). Mechanistic niche modelling: combining physiological and spatial data to predict species’ ranges. Ecology Letters, 12, 334350.CrossRefGoogle ScholarPubMed
Kimball, M.E., Miller, J.M., Whitfield, P.E. and Hare, J.A. (2004). Thermal tolerance and potential distribution of invasive lionfish (Pterois volitans/miles complex) on the east coast of the United States. Marine Ecology Progress Series, 283, 269278.CrossRefGoogle Scholar
Kolbe, J.J., Kearney, M. and Shine, R. (2010). Modeling the consequences of thermal trait variation for the cane toad invasion of Australia. Ecological Applications, 20, 22732285.CrossRefGoogle ScholarPubMed
Krause, S.K., Kelt, D.A., Gionfriddo, J.P. and Van Vuren, D.H. (2014). Efficacy and health effects of a wildlife immunocontraceptive vaccine on fox squirrels. The Journal of Wildlife Management, 78, 1223.CrossRefGoogle Scholar
Ledón-Rettig, C.C., Richards, C.L. and Martin, L.B. (2013). Epigenetics for behavioral ecologists. Behavioral Ecology, 24, 311324.CrossRefGoogle Scholar
Lee, K.A. and Klasing, K.C. (2004). A role for immunology in invasion biology. Trends in Ecology and Evolution, 19, 523529.CrossRefGoogle ScholarPubMed
Lee, K.A., Martin, L.B. and Wikelski, M.C. (2005). Responding to inflammatory challenges is less costly for a successful avian invader, the house sparrow (Passer domesticus), than its less-invasive congener. Oecologia, 145, 244251.CrossRefGoogle ScholarPubMed
Lee, K.A., Martin, L.B., Hasselquist, D., Ricklefs, R.E. and Wikelski, M. (2006). Contrasting adaptive immune defenses and blood parasite prevalence in closely related Passer species. Oecologia, 150, 383392.CrossRefGoogle Scholar
Lema, S.C. and Kitano, J. (2013). Hormones and phenotypic plasticity: Implications for the evolution of integrated adaptive phenotypes. Current Zoology, 59, 506525.CrossRefGoogle Scholar
Li, D.M., Wang, G., Wingfield, J.C., et al. (2008). Seasonal changes in adrenocortical responses to acute stress in Eurasian tree sparrow (Passer montanus) on the Tibetan Plateau: comparison with house sparrow (P. domesticus) in North America and with the migratory P. domesticus in Qinghai Province. General and Comparative Endocrinology, 158(1), 4753.CrossRefGoogle ScholarPubMed
Liebl, A.L. and Martin, L.B. (2012). Exploratory behaviour and stressor hyper-responsiveness facilitate range expansion of an introduced songbird. Proceedings of the Royal Society B: Biological Sciences, 279, 43754381.CrossRefGoogle ScholarPubMed
Liebl, A.L. and Martin, L.B. (2013). Stress hormone receptors change as range expansion progresses in house sparrows. Biology Letters, 9(3).CrossRefGoogle ScholarPubMed
Liebl, A.L. and Martin, L.B. (2014). Living on the edge: range edge birds consume novel foods sooner than established ones. Behavioral Ecology, 25, 10891096.CrossRefGoogle Scholar
Liebl, A.L., Schrey, A.W., Richards, C.L. and Martin, L.B. (2013). Patterns of DNA methylation throughout a range expansion of an introduced songbird. Integrative and Comparative Biology, 53, 351358.CrossRefGoogle ScholarPubMed
Love, O.P., McGowan, P.O. and Sheriff, M.J. (2013). Maternal adversity and ecological stressors in natural populations: the role of stress axis programming in individuals, with implications for populations and communities. Functional Ecology, 27, 8192.CrossRefGoogle Scholar
Lynn, S.E. (2008). Behavioral insensitivity to testosterone: why and how does testosterone alter paternal and aggressive behavior in some avian species but not others? General and Comparative Endocrinology, 157, 233240.CrossRefGoogle Scholar
MacDougall‐Shackleton, S.A., Watts, H.E. and Hahn, T.P. (2014). Biological timekeeping: individual variation, performance, and fitness. In Integrative Organismal Biology, ed. Martin, L.B., Ghalambor, C.K. and Woods, H.A. Hoboken, NJ: Wiley & Sons, Inc., pp. 235255.CrossRefGoogle Scholar
Martin, L.B. (2009). Stress and immunity in wild vertebrates: timing is everything. General and Comparative Endocrinology, 163, 7076.CrossRefGoogle ScholarPubMed
Martin, L.B. and Boruta, M. (2014). The impacts of urbanization on avian disease transmission and emergence. In Avian Urban Ecology, ed. Gil, D. and Brumm, H. Oxford, UK: Oxford University Press.Google Scholar
Martin, L.B. and Cohen, A. (2014). Physiological regulatory networks: the orchestra of life? In Integrative Organismal Biology, ed. Martin, L.B., Ghalambor, C.K. and Woods, H.A. Hoboken, NJ: Wiley & Sons, Inc., pp. 137152.CrossRefGoogle Scholar
Martin, L.B. and Liebl, A.L. (2014). Physiological flexibility in an avian range expansion. General and Comparative Endocrinology, 206, 227234.CrossRefGoogle Scholar
Martin, L.B., Alam, J.L., Imboma, T. and Liebl, A.L. (2010a). Variation in inflammation as a correlate of range expansion in Kenyan house sparrows. Oecologia, 164, 339347.CrossRefGoogle ScholarPubMed
Martin, L.B., Hopkins, W.A., Mydlarz, L. and Rohr, J.R. (2010b). The effects of anthropogenic global changes on immune functions and disease resistance. Annals of the New York Academy of Sciences, 1195, 129148.CrossRefGoogle ScholarPubMed
Martin, L.B., Liebl, A.L., Trotter, J.H., et al. (2011). Integrator networks: illuminating the black box linking genotype and phenotype. Integrative and Comparative Biology, 51, 514527.CrossRefGoogle ScholarPubMed
Martin, L.B., Coon, C.A.C., Liebl, A.L. and Schrey, A.W. (2014). Surveillance for microbes and range expansion in house sparrows. Proceedings of the Royal Society B: Biological Sciences, 281.Google ScholarPubMed
Martin, L.B., Liebl, A.L. and Kilvitis, H.J. (2015). Covariation in stress and immune gene expression in a range expanding bird. General and Comparative Endocrinology, 211, 1419.CrossRefGoogle Scholar
McGlothlin, J.W. and Ketterson, E.D. (2008). Hormone-mediated suites as adaptations and evolutionary constraints. Philosophical Transactions of the Royal Society B: Biological Sciences, 363, 16111620.CrossRefGoogle ScholarPubMed
Medzhitov, R. (2008). Origin and physiological roles of inflammation. Nature, 454, 428435.CrossRefGoogle ScholarPubMed
Moore, I.T., Greene, M.J., Lerner, D.T., et al. (2005). Physiological evidence for reproductive suppression in the introduced population of brown tree snakes (Boiga irregularis) on Guam. Biological Conservation, 121(1), 9198.CrossRefGoogle Scholar
Noble, D., Jablonka, E., Joyner, M., et al. (2014). The integration of evolutionary biology with physiological science. Journal of Physiology, 592, 22372244.CrossRefGoogle Scholar
Partecke, J., Van't Hof, T.J. and Gwinner, E. (2004). Differences in the timing of reproduction between urban and forest European blackbirds (Turdus merula): result of phenotypic flexibility or genetic differences? Proceedings of the Royal Society B, 271, 19952001.CrossRefGoogle ScholarPubMed
Phillips, B.L., Brown, G.P. and Shine, R. (2010). Life-history evolution in range-shifting populations. Ecology, 91, 16171627.CrossRefGoogle ScholarPubMed
Ricklefs, R.E. and Wikelski, M. (2002). The physiology/life-history nexus. Trends in Ecology and Evolution, 17, 462468.CrossRefGoogle Scholar
Schrey, A.W., Coon, C.A.C., Grispo, M.T., et al. (2012). Epigenetic variation may compensate for decreased genetic variation with introductions: a case study using house sparrows (Passer domesticus) on two continents. Genetics Research International, 2012, 7.CrossRefGoogle ScholarPubMed
Schrey, A.W., Liebl, A.L., Richards, C.L. and Martin, L.B. (2014). Range expansion of house sparrows (Passer domesticus) in Kenya: evidence of genetic admixture and human-mediated dispersal. Journal of Heredity, 105, 6069.CrossRefGoogle ScholarPubMed
Sheriff, M.J., Krebs, C.J. and Boonstra, R. (2009). The sensitive hare: sublethal effects of predator stress on reproduction in snowshoe hares. Journal of Animal Ecology, 78, 12491258.CrossRefGoogle ScholarPubMed
Sinervo, B. and Calsbeek, R. (2003). Physiological epistasis, ontogenetic conflict and natural selection on physiology and life history. Integrative and Comparative Biology, 43, 419430.CrossRefGoogle ScholarPubMed
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, 628630.CrossRefGoogle ScholarPubMed
Weaver, I.C.G., Cervoni, N., Champagne, F.A., et al. (2004). Epigenetic programming by maternal behavior. Nature Neuroscience, 7, 847854.CrossRefGoogle ScholarPubMed
West-Eberhard, M. (2003). Developmental Plasticity and Evolution. Oxford, UK: Oxford University Press.CrossRefGoogle Scholar
Woods, H.A. and Wilson, J.K. (2014). An elephant in the fog: unifying concepts of physiological stasis and change. In Integrative Organismal Biology, ed. Martin, L.B., Ghalambor, C.K. and Woods, H.A. Hoboken, NJ: Wiley & Sons, Inc., pp. 119136.CrossRefGoogle Scholar
Young, L.J. and Crews, D. (1995). Comparative neuroendocrinology of steroid receptor gene expression and regulation: relationship to physiology and behavior. Trends in Endocrinology and Metabolism, 6, 317323.CrossRefGoogle ScholarPubMed

References

Allman, J. (2000). Evolving Brains. New York: Scientific American Library.Google Scholar
Allman, J.M., McLaughlin, T. and Hakeem, A. (1993). Brain structures and life-span in primate species. Proceedings of the National Academy of Sciences, USA, 90, 35593563.CrossRefGoogle ScholarPubMed
Amiel, J.J., Tingley, R. and Shine, R. (2011). Smart moves: effects of relative brain size on establishment success of invasive amphibians and reptiles. PLoS ONE, 6, e18277.CrossRefGoogle ScholarPubMed
Araújo, M.S., Bolnick, D.I. and Layman, C.A. (2011). The ecological causes of individual specialisation. Ecology Letters, 14, 948958.CrossRefGoogle ScholarPubMed
Barnagaud, J., Barbaro, L. and Papaïx, J. (2013). Habitat filtering by landscape and local forest composition in native and exotic New Zealand birds. Ecology, 95, 7887.CrossRefGoogle Scholar
Barton, R.A. and Capellini, I. (2011). Maternal investment, life histories, and the costs of brain growth in mammals. Proceedings of the National Academy of Sciences, USA 108, 61696174.CrossRefGoogle ScholarPubMed
Biro, P.A. and Stamps, J.A. (2008). Are animal personality traits linked to life-history productivity? Evolution, 23, 361368.Google ScholarPubMed
Blackburn, T.M., Cassey, P. and Lockwood, J.L. (2009). The role of species traits in the establishment success of exotic birds. Global Change Biology, 15, 28522860.CrossRefGoogle Scholar
Bolnick, D.I., Amarasekare, P., Araújo, M.S., et al. (2011). Why intraspecific trait variation matters in community ecology. Trends in Ecology and Evolution, 26, 183192.CrossRefGoogle ScholarPubMed
Caceres, C.E. (1997). Temporal variation, dormancy and coexistence: A field test of the storage effect. Proceedings of the National Academy of Science, USA, 94, 91719175.CrossRefGoogle ScholarPubMed
Case, T.J. (1996). Global patterns in the establishment and distribution of exotic birds. Biological Conservation, 78, 6996.CrossRefGoogle Scholar
Cassey, P., Blackburn, T.M., Sol, D., Duncan, R.P. and Lockwood, J.L. (2004). Global patterns of introduction effort and establishment success in birds. Proceedings of the Royal Society of London, Series B, 271, S405S408.CrossRefGoogle ScholarPubMed
Chalfoun, A.D. and Martin, T.E. (2010). Facultative nest patch shifts in response to nest predation risk in the Brewer's sparrow: a ‘win-stay, lose-switch’ strategy? Oecologia, 163, 885892.CrossRefGoogle Scholar
Charlesworth, B. (1980). Evolution in Age Structured Populations. Cambridge, UK: Cambridge University Press.Google Scholar
Cubaynes, S., Doherty, P.F., Schreiber, E.A. and Gimenez, O. (2011). To breed or not to breed: a seabird's response to extreme climatic events. Biology Letters, 7, 303306.CrossRefGoogle ScholarPubMed
Danchin, E., Giraldeau, L.-A., Valone, T.J. and Wagner, R.H. (2004). Public information: from noisy neighbors to cultural evolution. Science, 305, 487491.CrossRefGoogle Scholar
Drake, J.M. (2007). Parental investment and fecundity, but not brain size, are associated with establishment success in introduced fishes. Functional Ecology, 21, 963968.CrossRefGoogle Scholar
Dukas, R. (1998). Evolutionary ecology of learning. In Cognitive Ecology: The Evolutionary Ecology of Information Processing and Decision Making, ed. Dukas, R. Chicago, IL: University of Chicago Press, pp. 129174.Google Scholar
Forcada, J., Trathan, P.N. and Murphy, E.J. (2008). Life history buffering in Antarctic mammals and birds against changing patterns of climate and environmental variation. Global Change Biology, 14, 24732488.CrossRefGoogle Scholar
Futuyma, D.J. and Moreno, G. (1988). The evolution of ecological specialization. Annual Review of Ecology and Systematics, 19, 207234.CrossRefGoogle Scholar
González-Suárez, M. and Revilla, E. (2013). Variability in life-history and ecological traits is a buffer against extinction in mammals. Ecology Letters, 16, 242251.CrossRefGoogle ScholarPubMed
Greenberg, R. (2003). The role of neophobia and neophilia in the development of innovative behaviour of birds. In Animal Innovation, ed. Reader, S.M. and Laland, K.N. Oxford, UK: Oxford University Press, pp. 176196.Google Scholar
Greggor, A.L., Clayton, N.S., Phalan, B. and Thornton, A. (2014). Comparative cognition for conservationists. Trends in Ecology and Evolution, 29, 489495.CrossRefGoogle ScholarPubMed
Griffin, A.S., Blumstein, D.T. and Evans, C.S. (2000). Training captive-bred or translocated animals to avoid predators. Conservation Biology, 14, 13171326.CrossRefGoogle Scholar
Holway, D. and Suarez, A. (1999). Animal behavior: an essential component of invasion biology. Trends in Ecology and Evolution, 5347, 1214.Google Scholar
Huey, R.B., Gilchrist, G.W., Carlson, M.L., Berrigan, D. and Serra, L. (2000). Rapid evolution of a geographic cline in size in an introduced fly. Science, 287, 308309.CrossRefGoogle Scholar
Huey, R.B., Hertz, P.E. and Sinervo, B. (2003). Behavioral drive versus behavioral inertia in evolution: a null model approach. American Naturalist, 161, 357366.CrossRefGoogle ScholarPubMed
Kokko, H. and Sutherland, W.J. (2001). Ecological traps in changing environments: Ecological and evolutionary consequences of a behaviourally mediated Allee effect. Evolutionary Ecology, 3, 537551.Google Scholar
Kolar, C.S. and Lodge, D.M. (2002). Ecological predictions and risk assessment for alien fishes in North America. Science, 298, 12331236.CrossRefGoogle ScholarPubMed
Kotrschal, A., Buechel, S.D., Zala, S.M., Corral, A., Penn, D.J. and Kolm, N. (2015). Brain size affects female but not male survival under predation threat. Ecology Letters, 8(7), 646652.CrossRefGoogle Scholar
Krams, I., Bērziņs, A., Krama, T., Wheatcroft, D., Igaune, K. and Rantala, M.J. (2010). The increased risk of predation enhances cooperation. Proceedings of the Royal Society of London B, 277, 513518.Google ScholarPubMed
Kriska, G., Horváth, G. and Andrikovics, S. (1998). Why do mayflies lay their eggs en masse on dry asphalt roads? Water-imitating polarized light reflected from asphalt attracts Ephemeroptera. The Journal of Experimental Biology, 201, 22732286.CrossRefGoogle ScholarPubMed
Lefebvre, L. (2013). Brains, innovations, tools and cultural transmission in birds, non-human primates, and fossil hominins. Frontiers in Human Neuroscience, 7, 245.CrossRefGoogle ScholarPubMed
Lefebvre, L., Whittle, P., Lascaris, E. and Finkelstein, A. (1997). Feeding innovations and forebrain size in birds. Animal Behaviour, 53, 549560.CrossRefGoogle Scholar
Leung, B., Roura-Pascual, N., Bacher, S., et al. (2012). TEASIng apart alien species risk assessments: a framework for best practices. Ecology Letters, 15, 14751493.CrossRefGoogle ScholarPubMed
Lewontin, R.C. (1965). Selection for colonizing ability. In The Genetics of Colonizing Species, ed. Baker, H. and Stebbins, G. London: Academic Press, pp. 7794.Google Scholar
Liker, A. and Bókony, V. (2009). Larger groups are more successful in innovative problem solving in house sparrows. Proceedings of the National Academy of Sciences, USA, 106, 78937898.CrossRefGoogle ScholarPubMed
Lima, S.L. (2009). Predators and the breeding bird: behavioral and reproductive flexibility under the risk of predation. Biological reviews of the Cambridge Philosophical Society, 84, 485513.CrossRefGoogle ScholarPubMed
Lockwood, J.L., Cassey, P. and Blackburn, T.M. (2005). The role of propagule pressure in explaining species invasions. Trends in Ecology and Evolution, 20, 223228.CrossRefGoogle ScholarPubMed
Losos, J.B., Schoener, T.W. and Spiller, D.A. (2004). Predator-induced behaviour shifts and natural selection in field experimental lizard populations. Nature, 432, 505508.CrossRefGoogle ScholarPubMed
Lowry, H., Lill, A. and Wong, B.B.M. (2012). Behavioural responses of wildlife to urban environments. Biological Reviews of the Cambridge Philosophical Society, 88, 537549.CrossRefGoogle ScholarPubMed
Mabry, K.E. and Stamps, J.A. (2008). Searching for a new home: decision making by dispersing brush mice. The American Naturalist, 172, 625634.CrossRefGoogle ScholarPubMed
Marchetti, C. and Drent, P. (2000). Individual differences in the use of social information in foraging by captive great tits. Animal Behaviour, 60, 131140.CrossRefGoogle ScholarPubMed
Martin, L.B. and Fitzgerald, L. (2005). A taste for novelty in invading house sparrows, Passer domesticus. Behavioral Ecology, 16, 702707.CrossRefGoogle Scholar
Mayr, E. (1965). The nature of colonising birds. In The Genetics of Colonizing Species, ed. Baker, H.G. and Stebbins, G.L. New York: Academic Press, pp. 2943.Google Scholar
Morand-Ferron, J. and Quinn, J.L. (2011). Larger groups of passerines are more efficient problem solvers in the wild. Proceedings of the National Academy of Sciences, USA, 108, 1589815903.CrossRefGoogle ScholarPubMed
Morris, W.F. and Doak, D.F. (2004). Buffering of life histories against environmental stochasticity: accounting for a spurious correlation between the variabilities of vital rates and their contributions to fitness. American Naturalist, 163, 579590.CrossRefGoogle ScholarPubMed
Moulton, M.P., Pimm, S.L., Mooney, H.A. and Drake, J.A. (1986). Species introductions to Hawaii. In Ecology of Biological Invasions in North America and Hawaii, ed. Mooney, H.A. and Drake, J.A. New York: Springer, pp. 231249.CrossRefGoogle Scholar
Overington, S.E., Morand-Ferron, J., Boogert, N.J. and Lefebvre, L. (2009). Technical innovations drive the relationship between innovativeness and residual brain size in birds. Animal Behaviour, 78, 10011010.CrossRefGoogle Scholar
Parejo, D., Danchin, É., Silva, N., White, J.F., Dreiss, A.N. and Avilés, J.M. (2008). Do great tits rely on inadvertent social information from blue tits? A habitat selection experiment. Behavioral Ecology and Sociobiology, 62, 15691579.CrossRefGoogle Scholar
Phillips, B. and Suarez, A. (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. 190200.CrossRefGoogle Scholar
Pimm, S.L. (1991). The Balance of Nature? Ecological Issues in the Conservation of Species and Communities. Chicago, UK: University of Chicago Press.Google Scholar
Pinter-Wollman, N., Isbell, L.A. and Hart, L.A. (2009). Assessing translocation outcome: comparing behavioral and physiological aspects of translocated and resident African elephants (Loxodonta africana). Biological Conservation, 142, 11161124.CrossRefGoogle Scholar
Reader, S.M. and Laland, K.N. (2002). Social intelligence, innovation, and enhanced brain size in primates. Proceedings of the National Academy of Science, USA, 99, 44364441.CrossRefGoogle ScholarPubMed
Reader, S.M., Hager, Y. and Laland, K.N. (2011). The evolution of primate general and cultural intelligence. Philosophical Transactions of the Royal Society B: Biological Sciences, 366, 10171027.CrossRefGoogle ScholarPubMed
Réale, D., Reader, S.M., Sol, D. McDougall, P.T. and Dingemanse, N.J. (2007). Integrating animal temperament within ecology and evolution. Biological Reviews of the Cambridge Philosophical Society, 82, 291318.CrossRefGoogle ScholarPubMed
Reznick, D. and Ghalambor, C. (2001). The population ecology of contemporary adaptations: what empirical studies reveal about the conditions that promote adaptive evolution. Genetica, 112–113, 183198.CrossRefGoogle ScholarPubMed
Reznick, D., Nunney, L. and Tessier, A. (2000). Big houses, big cars, superfleas and the costs of reproduction. Trends in Ecology and Evolution, 15, 421425.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, 15091520.CrossRefGoogle Scholar
Reznick, D.N., Ghalambor, C.K. and Crooks, K. (2008). Experimental studies of evolution in guppies: a model for understanding the evolutionary consequences of predator removal in natural communities. Molecular Ecology, 17, 97107.CrossRefGoogle Scholar
Ricklefs, R.E. (2004). The cognitive face of avian life histories. Wilson Bulletin, 116, 119196.CrossRefGoogle Scholar
Roff, D.A. (2002). Life History Evolution. Sunderland, MA: Sinauer Associates, Inc.Google Scholar
Sæther, B.-E. and Bakke, Ø.. (2000). Avian life history variation and contribution of demographic traits to the population growth rate. Ecology, 81, 642653.CrossRefGoogle Scholar
Saether, B.-E., Engen, S., Pape Møller, A., et al. (2004). Life history variation predicts the effects of demographic stochasticity on avian population dynamics. The American Naturalist, 164, 793802.CrossRefGoogle ScholarPubMed
Sagata, K. and Lester, P.J. (2009). Behavioural plasticity associated with propagule size, resources, and the invasion success of the Argentine ant Linepithema humile. Journal of Applied Ecology, 46, 1927.CrossRefGoogle Scholar
Schaffer, W.M. (1974). Selection for optimal life histories: the effects of age structure. Ecology, 55, 291303.CrossRefGoogle Scholar
van Schaik, C.P. and Deaner, R.O. (2003). Life history and cognitive evolution in primates. In Animal Social Complexity, ed. de Waal, F.B.M. and Tyack, P.L. Cambridge, MA: Harvard University Press, pp. 525.CrossRefGoogle Scholar
Seppänen, J.-T., Forsman, J.T., Mönkkönen, M., Krams, I. and Salmi, T. (2011). New behavioural trait adopted or rejected by observing heterospecific tutor fitness. Proceedings of the Royal Society B: Biological Sciences, 278, 17361741.CrossRefGoogle ScholarPubMed
Shultz, S. and Dunbar, R.I.M. (2007). Evolution in the social brain. Science, 317, 13441347.Google Scholar
Sih, A. and Del Giudice, M. (2012). Linking behavioural syndromes and cognition: a behavioural ecology perspective. Philosophical Transactions of the Royal Society of London B: Biological Sciences, 367, 27622772.CrossRefGoogle ScholarPubMed
Sih, A., Ferrari, M.C.O. and Harris, D.J. (2011). Evolution and behavioural responses to human-induced rapid environmental change. Evolutionary Applications, 4, 367387.CrossRefGoogle ScholarPubMed
Slagsvold, T. and Wiebe, K.L. (2007). Learning the ecological niche. Proceedings of the Royal Society of London B: Biological Sciences, 274, 1923.Google ScholarPubMed
Slagsvold, T. and Wiebe, K.L. (2011). Social learning in birds and its role in shaping a foraging niche. Philosophical Transactions of the Royal Society of London B: Biological Sciences, 366, 969977.CrossRefGoogle ScholarPubMed
Snell-Rood, E.C. (2013). An overview of the evolutionary causes and consequences of behavioural plasticity. Animal Behaviour, 85, 10041011.CrossRefGoogle Scholar
Sol, D. (2009a). The cognitive-buffer hypothesis for the evolution of large brains. In Cognitive Ecology, ed. Dukas, R. and Ratcliffe, R.M. Chicago, IL: Chicago University Press, pp. 111134.CrossRefGoogle Scholar
Sol, D. (2009b). Revisiting the cognitive buffer hypothesis for the evolution of large brains. Biology Letters, 5, 130133.CrossRefGoogle ScholarPubMed
Sol, D., Santos, D.M.M., Feria, E. and Clavell, J. (1997). Habitat selection by the Monk Parakeet during colonization of a new area in Spain. Condor, 99, 3946.CrossRefGoogle Scholar
Sol, D., Duncan, R.P., Blackburn, T. M., Cassey, P. and Lefebvre, L. (2005). Big brains, enhanced cognition, and response of birds to novel environments. Proceedings of the National Academy of Science, USA, 102, 54605465.CrossRefGoogle ScholarPubMed
Sol, D., Liker, A., Lefebvre, L. and Székely, T. (2007a). Big-brained birds survive better in nature. Proceedings of the Royal Society of London B: Biological Sciences, 274, 763769.Google ScholarPubMed
Sol, D., Vilà, M. and Kühn, I. (2007b). The comparative analysis of historical alien introductions. Biological Invasions, 10, 11191129.CrossRefGoogle Scholar
Sol, D., Bacher, S., Reader, S.M. and Lefebvre, L. (2008). Brain size predicts the success of mammal species introduced into novel environments. The American Naturalist, 172 Suppl., S6371.CrossRefGoogle ScholarPubMed
Sol, D., Griffin, A.S., Bartomeus, I. and Boyce, H. (2011). Exploring or avoiding novel food resources? The novelty conflict in an invasive bird. PLoS ONE, 6, e19535.CrossRefGoogle ScholarPubMed
Sol, D., Bartomeus, I. and Griffin, A.S. (2012a). The paradox of invasion in birds: competitive superiority or ecological opportunism? Oecologia, 169, 553564.CrossRefGoogle ScholarPubMed
Sol, D., Maspons, J. and Vall-llosera, M., et al. (2012b). Unraveling the life history of successful invaders. Science, 337, 580583.CrossRefGoogle ScholarPubMed
Sol, D., Lapiedra, O. and González-Lagos, C. (2013). Behavioural adjustments for a life in the city. Animal Behaviour, 85, 11011112.CrossRefGoogle Scholar
Sol, D., González-Lagos, C., Moreira, D., Maspons, J. and Lapiedra, O. (2014). Urbanisation tolerance and the loss of avian diversity. Ecology Letters, 17, 942995.CrossRefGoogle ScholarPubMed
Stamps, J.A. and Swaisgood, R.R. (2007). Someplace like home: experience, habitat selection and conservation biology. Applied Animal Behaviour Science, 102, 392409.CrossRefGoogle Scholar
Stamps, J., Krishnan, V. and Reid, M. (2005). Search costs and habitat selection by dispersers. Ecology, 86, 510518.CrossRefGoogle Scholar
Starrfelt, J. and Kokko, H. (2012). Bet-hedging – a triple trade-off between means, variances and correlations. Biological Reviews of the Cambridge Philosophical Society, 87, 742755.CrossRefGoogle ScholarPubMed
Stearns, S. (1983). The influence of size and phylogeny on patterns of covariation among life-history traits in the mammals. Oikos, 41, 173187.CrossRefGoogle Scholar
Stearns, S.C. (1989). Trade-offs in life-history evolution. Functional Ecology, 3, 259268.CrossRefGoogle Scholar
Stearns, S.C. (1992). The evolution of life histories. Oxford, UK: Oxford University Press.Google Scholar
Stearns, S.C. (2000). Life history evolution: successes, limitations and prospects. Die Naturwissenschaften, 87, 476486.CrossRefGoogle ScholarPubMed
Stearns, S.C. and Crandall, R. (1981). Bet-hedging and persistence as adaptations of colonizers. Evolution Today, 371383.Google Scholar
Vall-llosera, M. and Sol, D. (2009). A global risk assessment for the success of bird introductions. Journal of Applied Ecology, 46, 787795.CrossRefGoogle Scholar
Warner, R.R. and Chesson, P.L. (1985). Coexistence mediated by recruitment fluctuations: a field guide to the storage effect. American Naturalist, 125(6), 769787.CrossRefGoogle Scholar
Williams, G.C. (1966). Adaptation and Natural Selection. Princeton, NJ: Princeton University Press.Google Scholar
Williamson, M.H. (1996). Biological Invasions. London: Chapman and Hall.Google Scholar
Wolf, M., van Doorn, G.S.S., Leimar, O. and Weissing, F. J. (2007). Life-history trade-offs favour the evolution of animal personalities. Nature, 447, 581584.CrossRefGoogle ScholarPubMed
Yeh, P.J. and Price, T.D. (2004). Adaptive phenotypic plasticity and the successful colonization of a novel environment. The American Naturalist, 164, 531542.CrossRefGoogle ScholarPubMed

References

Agrawal, A.F. and Lively, C.M. (2001). Parasites and the evolution of self-fertilization. Evolution, 55, 869879.CrossRefGoogle ScholarPubMed
Alford, R.A. (1994). Interference and exploitation competition in larval Bufo marinus. Advances in Ecology and Environmental Sciences, 297306.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, 2328.CrossRefGoogle Scholar
Amundsen, P.-A., Salonen, E., Niva, T., et al. (2012). Invader population speeds up life history during colonization. Biological Invasions, 14, 15011513.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, 40774088.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, 361368.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, 927939.CrossRefGoogle Scholar
Bøhn, T., Terje Sandlund, O., Amundsen, P.-A. and Primicerio, R. (2004). Rapidly changing life history during invasion. Oikos, 106, 138150.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, 761766.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, 689698.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, 14451451.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, 854862.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, 830838.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, 12101220.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, 5764.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, 327332.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, 11591184.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, 1501715022.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, 347351.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, 424427.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, 23152329.CrossRefGoogle Scholar
Fisher, R.A. (1937). The wave advance of advantageous genes. Annals of Eugenics, 7, 355369.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, 29002908.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, 7888.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, 1992619930.CrossRefGoogle ScholarPubMed
Hamilton, W.D. and May, R.M. (1977). Dispersal in stable habitats. Nature, 269, 578581.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, 91101.CrossRefGoogle Scholar
Hudson, P.J., Dobson, A.P. and Newborn, D. (1998). Prevention of population cycles by parasite removal. Science, 282, 22562258.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, 437445.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, 482490.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, 700706.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. 7794.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, 508517.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, 21592174.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, 625627.CrossRefGoogle ScholarPubMed
Peischl, S., Kirkpatrick, M. and Excoffier, L. (2015). Expansion load and the evolutionary dynamics of a species range. American Naturalist, 185(4), E8193.CrossRefGoogle ScholarPubMed
Perkins, T.A. (2012). Evolutionarily labile species interactions and spatial spread of invasive species. The American Naturalist, 179, E37E54.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, 10791087.CrossRefGoogle ScholarPubMed
Phillips, B.L. (2009). The evolution of growth rates on an expanding range edge. Biology Letters, 5, 802804.CrossRefGoogle Scholar
Phillips, B.L. (2015). Evolutionary processes make invasion speed difficult to predict. Biological Invasions, 17, 19491960.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. 190200.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, S34S48.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, 25952601.CrossRefGoogle ScholarPubMed
Phillips, B.L., Brown, G.P. and Shine, R. (2010b). Life-history evolution in range-shifting populations. Ecology, 91, 16171627.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, 872881.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, 123133.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, 1537915383.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, 40514063.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, 15091520.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, 965973.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, 57085711.CrossRefGoogle ScholarPubMed
Sih, A., Bell, A. and Johnson, J.C. (2004a). Behavioral syndromes: an ecological and evolutionary overview. Trends in Ecology and Evolution, 19, 372378.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, 241277.CrossRefGoogle Scholar
Simmons, A.D. and Thomas, C.D. (2004). Changes in dispersal during species' range expansions. American Naturalist, 164, 378395.CrossRefGoogle ScholarPubMed
Simons, A.M. (2003). Invasive aliens and sampling bias. Ecology Letters, 6, 278280.CrossRefGoogle Scholar
Skellam, J.G. (1951). Random dispersal in theoretical populations. Biometrika, 38, 196218.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, 630642.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, 12661277.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, 141152.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, 129137.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, 628630.CrossRefGoogle ScholarPubMed
Travis, J.M.J. and Dytham, C. (2002). Dispersal evolution during invasions. Evolutionary Ecology Research, 4, 11191129.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, 23342343.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, E134E148.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, 919923.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. 315339.Google Scholar
Williamson, M. (1996). Biological Invasions. London: Chapman and Hall.Google Scholar

References

Alemadi, S.D. and Jenkins, D.G. (2008). Behavioural constraints for the spread of the eastern mosquitofish, Gambusia holbrooki (Poeciliidae). Biological Invasions, 10, 5966.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, 2328.CrossRefGoogle Scholar
Bekoff, M. (1977). Mammalian dispersal and the ontogeny of individual behavioural phenotypes. American Naturalist, 111, 715732.CrossRefGoogle Scholar
Biro, P.A. and Adriaenssens, B. (2013). Predictability as a personality trait: consistent differences in intraindividual behavioural variation. American Naturalist, 182, 621629.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, 361368.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, 333339.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, 1700017005.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, 271276.CrossRefGoogle Scholar
Bonte, D., Van Dyck, H., Bullock, J.M., et al. (2012). Costs of dispersal. Biological Reviews, 87, 290312.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, 31043111.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, 205225.CrossRefGoogle ScholarPubMed
Bowne, D.R. and Bowers, M.A. (2004). Interpatch movements in spatially structured populations: a literature review. Landscape Ecology, 19, 120.CrossRefGoogle Scholar
Brown, K.L. (1985). Demographic and genetic characteristics of dispersal in the mosquitofish, Gambusia affinis (Pisces: Poeciliidae). Copeia, 1985, 597612.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, 13591368.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, 681687.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. 190200.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, 5764.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, 343345.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, 197209.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, 721733.CrossRefGoogle Scholar
Congdon, B.C. (1994). Characteristics of dispersal in the eastern mosquitofish Gambusia holbrooki. Journal of Fish Biology, 45, 943952.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, 383390.CrossRefGoogle Scholar
Cote, J. and Clobert, J. (2007b). Social information and emigration: lessons from immigrants. Ecology Letters, 10, 411417.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, 703708.CrossRefGoogle ScholarPubMed
Cote, J., Dreiss, A. and Clobert, J. (2008). Social personality trait and fitness. Proceedings of the Royal Society B: Biological Sciences, 275, 28512858.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, 40654076.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, 15711579.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, 16701678.CrossRefGoogle ScholarPubMed
Cote, J., Fogarty, S. and Sih, A. (2012). Individual sociability and choosiness between shoal types. Animal Behaviour, 83, 14691476.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, 20132349.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. 319331.Google Scholar
Davis, J.M. and Stamps, J.A. (2004). The effect of natal experience on habitat preferences. Trends in Ecology and Evolution, 19, 411416.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, 620632.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, 973988.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, 377385.CrossRefGoogle Scholar
Duckworth, R.A. (2008). Adaptive dispersal strategies and the dynamics of a range expansion. American Naturalist, 172, S4S17.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, 1501715022.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, 24622472.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, 273287.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, 124135.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, 921924.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, 685703.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, 328330.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, 949952.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, 10331040.CrossRefGoogle ScholarPubMed
Hoysak, D.J. and Godin, J.G. (2007). Repeatability of male mate choice in the mosquitofish, Gambusia holbrooki. Ethology, 113, 10071018.CrossRefGoogle Scholar
Hudina, S., Hock, K. and Zganec, K. (2014). The role of aggression in range expansion and biological invasions. Current Zoology, 60, 401409.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, 11311138.CrossRefGoogle Scholar
Juette, T., Cucherousset, J. and Cote, J. (2014). Animal personality and the ecological impacts of freshwater non-native species. Current Zoology, 60, 417427.CrossRefGoogle Scholar
Knapp, R., Marsh-Matthews, E., Vo, L. and Rosencrans, S. (2011). Stress hormone masculinizes female morphology and behaviour. Biology Letters, 64, 598606.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, 700706.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, 23052318.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, 343348.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, 508517.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, 21592174.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, 702707.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, 619621.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, 319.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, 25952601.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, 16291636.CrossRefGoogle Scholar
Pyke, G.H. (2005). A review of the biology of Gambusia affinis and G. holbrooki. Fish Biology and Fisheries, 15, 339365.CrossRefGoogle Scholar
Rasmussen, J.E. and Belk, M.C. (2012). Dispersal behaviour correlates with personality of a North American fish. Current Zoology, 58, 260270.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, 39373946.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, 379391.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, 352360.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, 256266.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, 813822.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, 263282.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, 251253.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, 649656.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, 771776.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, 137148.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, 20632068.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, 241277.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, 367387.CrossRefGoogle ScholarPubMed
Sih, A., Cote, J., Evans, M., Fogarty, S. and Pruitt, J. (2012). Ecological implications of behavioural syndromes. Ecology Letters, 15, 278289.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, 5060.CrossRefGoogle ScholarPubMed
Sinclair, E., Noronha de Souza, C., Ward, A. and Seebacher, F. (2014). Exercise changes behaviour. Functional Ecology, 28, 652659.CrossRefGoogle Scholar
Smith, B.R. and Blumstein, D.T. (2008). Fitness consequences of personality: a meta-analysis. Behavioural Ecology, 19, 448455.CrossRefGoogle Scholar
Sol, D., Timmermans, S. and Lefebvre, L. (2002). Behavioural flexibility and invasion success in birds. Animal Behaviour, 63, 495502.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. 230242.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, 599610.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, 10391052.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, 4353.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, 946955.CrossRefGoogle ScholarPubMed
Ward, A. (2012). Social facilitation of exploration in mosquitofish (Gambusia holbrooki). Behavioural Ecology and Sociobiology, 66, 223230.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, 316324.CrossRefGoogle Scholar
Welcomme, R.L. (1992). A history of international introductions of inland aquatic species. Marine Science Symposium, 194, 314.Google Scholar
Williamson, M. and Fitter, A. (1996). The varying success of invaders. Ecology, 77, 16611666.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, 96104.CrossRefGoogle Scholar

Save book to Kindle

To save this book to your Kindle, first ensure coreplatform@cambridge.org is added to your Approved Personal Document E-mail List under your Personal Document Settings on the Manage Your Content and Devices page of your Amazon account. Then enter the ‘name’ part of your Kindle email address below. Find out more about saving to your Kindle.

Note you can select to save to either the @free.kindle.com or @kindle.com variations. ‘@free.kindle.com’ emails are free but can only be saved to your device when it is connected to wi-fi. ‘@kindle.com’ emails can be delivered even when you are not connected to wi-fi, but note that service fees apply.

Find out more about the Kindle Personal Document Service.

Available formats
×

Save book to Dropbox

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Dropbox.

Available formats
×

Save book to Google Drive

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Google Drive.

Available formats
×