Encyclopedia of Animal Cognition and Behavior

Living Edition
| Editors: Jennifer Vonk, Todd Shackelford

Adaptedness of Behavior

  • Ulrika CandolinEmail author
Living reference work entry
DOI: https://doi.org/10.1007/978-3-319-47829-6_366-1

Synonyms

Definition

The adaptedness of behavior depends on the effects behavior has on individual fitness, i.e., how it influences survival and reproductive success. This hinges in turn on how well suited to environmental conditions the behaviors are.

Introduction

Behavior is a major determinant of fitness. It influences foraging success, the ability to avoid predators, success in the competition for resources, and reproductive success. Similarly to other traits, behavior evolves through natural selection; individuals with behaviors that allow them to produce more viable offspring than other individuals pass more copies of their genes onto the next generations, and thereby also the genes for their behaviors, which then increase in frequency in the population.

Evolution consequently gradually changes the behavior of individuals so that they become better and better adapted to local environmental...

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References

  1. Aplin, L. M., Farine, D. R., Morand-Ferron, J., et al. (2013). Individual personalities predict social behaviour in wild networks of great tits (Parus major). Ecology Letters, 16, 1365–1372.CrossRefGoogle Scholar
  2. Bauder, J. A. S., Morawetz, L., Warren, A. D., & Krenn, H. W. (2015). Functional constraints on the evolution of long butterfly proboscides: Lessons from Neotropical skippers (Lepidoptera: Hesperiidae). Journal of Evolutionary Biology, 28, 678–687.CrossRefGoogle Scholar
  3. Benazzo, A., Trucchi, E., Cahill, J. A., et al. (2017). Survival and divergence in a small group: The extraordinary genomic history of the endangered Apennine brown bear stragglers. Proceedings of the National Academy of Sciences of the United States of America, 114, E9589–E9597.CrossRefGoogle Scholar
  4. Both, C., & Visser, M. E. (2001). Adjustment to climate change is constrained by arrival date in a long-distance migrant bird. Nature, 411, 296–298.CrossRefGoogle Scholar
  5. Botsch, Y., Tablado, Z., & Jenni, L. (2017). Experimental evidence of human recreational disturbance effects on bird-territory establishment. Proceedings of the Royal Society B-Biological Sciences, 284, 8.CrossRefGoogle Scholar
  6. Candolin, U. (1998). Reproduction under predation risk and the trade-off between current and future reproduction in the threespine stickleback. Proceedings of the Royal Society B-Biological Sciences, 265, 1171–1175.CrossRefGoogle Scholar
  7. Candolin, U. (2000). Changes in expression and honesty of sexual signalling over the reproductive lifetime of sticklebacks. Proceedings of the Royal Society B-Biological Sciences, 267, 2425–2430.CrossRefGoogle Scholar
  8. Candolin, U., & Wong, B. B. M. (2012). Behavioural responses to a changing world. Mechanisms and consequences. Oxford: Oxford University Press.CrossRefGoogle Scholar
  9. DiRienzo, N., & Montiglio, P. O. (2016). The contribution of developmental experience vs. condition to life history, trait variation and individual differences. Journal of Animal Ecology, 85, 915–926.CrossRefGoogle Scholar
  10. Duckworth, R. A., Belloni, V., & Anderson, S. R. (2015). Cycles of species replacement emerge from locally induced maternal effects on offspring behavior in a passerine bird. Science, 347, 875–877.CrossRefGoogle Scholar
  11. Emlen, D. J. (1994). Environmental control of horn length dimorphism in the beetle Onthophagus acuminatus (Coleoptera, Scarabaeidae). Proceedings of the Royal Society of London Series B-Biological Sciences, 256, 131–136.CrossRefGoogle Scholar
  12. Frid, A., & Dill, L. (2002). Human-caused disturbance stimuli as a form of predation risk. Conservation Ecology, 6, 16.CrossRefGoogle Scholar
  13. Gross, M. R. (1985). Disruptive selection for alternative life histories in salmon. Nature, 313, 47–48.CrossRefGoogle Scholar
  14. Gross, M. R. (1996). Alternative reproductive strategies and tactics: Diversity within sexes. Trends in Ecology & Evolution, 11, 92–98.CrossRefGoogle Scholar
  15. Gruber, J., Brown, G., Whiting, M. J., & Shine, R. (2017). Is the behavioural divergence between range-core and range-edge populations of cane toads (Rhinella marina) due to evolutionary change or developmental plasticity? Royal Society Open Science, 4, 9.CrossRefGoogle Scholar
  16. Guillette, L. M., Scott, A. C. Y., & Healy, S. D. (2016). Social learning in nest-building birds: A role for familiarity. Proceedings of the Royal Society B-Biological Sciences, 283, 6.CrossRefGoogle Scholar
  17. Jirotkul, M. (1999). Operational sex ratio influences female preference and male-male competition in guppies. Animal Behaviour, 58, 287–294.CrossRefGoogle Scholar
  18. Jukema, J., & Piersma, T. (2006). Permanent female mimics in a lekking shorebird. Biology Letters, 2, 161–164.CrossRefGoogle Scholar
  19. Levis, N. A., Serrato-Capuchina, A., & Pfennig, D. W. (2017). Genetic accommodation in the wild: Evolution of gene expression plasticity during character displacement. Journal of Evolutionary Biology, 30, 1712–1723.CrossRefGoogle Scholar
  20. Napper, C. J., & Hatchwell, B. J. (2016). Social dynamics in nonbreeding flocks of a cooperatively breeding bird: Causes and consequences of kin associations. Animal Behaviour, 122, 23–35.CrossRefGoogle Scholar
  21. Oliveira, R. F., Canario, A. V. M., Grober, M. S., & Santos, R. S. (2001). Endocrine correlates of male polymorphism and alternative reproductive tactics in the Azorean rock-pool blenny, Parablennius sanguinolentus parvicornis. General and Comparative Endocrinology, 121, 278–288.CrossRefGoogle Scholar
  22. Reed, J. M. (1999). The role of behavior in recent avian extinctions and endangerments. Conservation Biology, 13, 232–241.CrossRefGoogle Scholar
  23. Robertson, B. A., Rehage, J. S., & Sih, A. (2013). Ecological novelty and the emergence of evolutionary traps. Trends in Ecology & Evolution, 28, 552–560.CrossRefGoogle Scholar
  24. Sachser, N., Kaiser, S., & Hennessy, M. B. (2013). Behavioural profiles are shaped by social experience: When, how and why. Philosophical Transactions of the Royal Society B-Biological Sciences, 368, 11.CrossRefGoogle Scholar
  25. Sherley, R. B., Ludynia, K., Dyer, B. M., et al. (2017). Metapopulation tracking juvenile penguins reveals an ecosystem-wide ecological trap. Current Biology, 27, 563–568.CrossRefGoogle Scholar
  26. Sih, A. (2013). Understanding variation in behavioural responses to human-induced rapid environmental change: A conceptual overview. Animal Behaviour, 85, 1077–1088.CrossRefGoogle Scholar
  27. Tuomainen, U., & Candolin, U. (2011). Behavioural responses to human-induced environmental change. Biological Reviews, 86, 640–657.CrossRefGoogle Scholar
  28. van Beest, F. M., McLoughlin, P. D., Mysterud, A., & Brook, R. K. (2016). Functional responses in habitat selection are density dependent in a large herbivore. Ecography, 39, 515–523.CrossRefGoogle Scholar
  29. Welch, M. J., & Munday, P. L. (2017). Heritability of behavioural tolerance to high CO2 in a coral reef fish is masked by nonadaptive phenotypic plasticity. Evolutionary Applications, 10, 682–693.CrossRefGoogle Scholar
  30. Wong, B. B. M., & Candolin, U. (2015). Behavioral responses to changing environments. Behavioral Ecology, 26, 665–673.CrossRefGoogle Scholar

Copyright information

© Springer International Publishing AG, part of Springer Nature 2018

Authors and Affiliations

  1. 1.University of HelsinkiHelsinkiFinland

Section editors and affiliations

  • Marieke Cassia Gartner
    • 1
  1. 1.Philadelphia ZooPhiladelphiaUSA