Skip to main content
Log in

Prey vulnerability in relation to sexual coloration of prey

  • Original Article
  • Published:
Behavioral Ecology and Sociobiology Aims and scope Submit manuscript

Abstract

Sexual selection that results in the evolution of exaggerated secondary sexual characters has been hypothesized to impose production and maintenance costs of such traits on their bearers. Costs arising from sexual selection could increase the intensity of predator-mediated natural selection, leading to the prediction that species with exaggerated secondary sexual characters should be particularly susceptible to predation. We tested this prediction in a comparative analysis based on 31,745 prey individuals belonging to 66 species of birds collected from a total of 937 breeding events by 33 to 66 different pairs of European sparrowhawks Accipiter nisus annually during a period of 21 years. To assess vulnerability of different species we estimated a prey vulnerability index based on the difference in the logarithmically transformed absolute abundance of prey minus the logarithmically transformed expected abundance as determined by population density of breeding birds. The prey vulnerability index was predicted by sexual dichromatism, accounting for 23% of the variance in risk of predation among species, even when considering similarity in phenotype among species due to common descent (in the latter case explaining 12% of the variance). This finding suggests that sexual selection is an important evolutionary force-affecting predator–prey interactions.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1

Similar content being viewed by others

References

  • Allen JA (1988) Frequency-dependent selection by predators. Phil Trans R Soc Lond B 319:485–503

    Article  CAS  Google Scholar 

  • Amundsen T (2000) Why are female birds ornamented? Trends Ecol Evol 15:149–155

    Article  PubMed  Google Scholar 

  • Andersson M (1994) Sexual selection. Princeton Univ Press, Princeton, NJ

    Google Scholar 

  • Badyaev AV (1997) Altitudinal variation in sexual dimorphism: a new pattern and alternative hypotheses. Behav Ecol 8:675–690

    Article  Google Scholar 

  • Baker RR, Bibby CJ (1987) Merlin Falco columbarius predation and theories of the evolution of bird coloration. Ibis 129:259–263

    Article  Google Scholar 

  • Baker RR, Parker GA (1979) The evolution of bird coloration. Phil Trans R Soc Lond B 287:63–130

    Article  Google Scholar 

  • Barker FK, Barrowclough GF, Groth JG (2001) A phylogenetic hypothesis for passerine birds: Taxonomic and biogeographic implications of an analysis of nuclear DNA sequence data. Proc R Soc Lond B 269:295–308

    Article  CAS  Google Scholar 

  • Barker FK, Cibois A, Schikler P, Feinstein J, Cracraft J (2004) Phylogeny and diversification of the largest avian radiation. Proc Natl Acad Sci USA 101:11040–11045

    Article  PubMed  CAS  Google Scholar 

  • Blondel J, Catzeflis F, Perret P (1996) Molecular phylogeny and thehistorical biogeography of the warblers of the genus Sylvia (Aves). J Evol Biol 9:871–891

    Article  Google Scholar 

  • Burnham KP, Anderson DR (1998) Model selection and inference. Springer, Berlin Heidelberg New York

    Google Scholar 

  • Cibois A, Pasquet E (1999) Molecular analysis of the phylogeny of 11 genera of the Corvidae. Ibis 141:297–306

    Article  Google Scholar 

  • Cott HB (1947) The edibility of birds: Illustrated by five years’ experiments and observations (1941–1946) on the food preferences of the hornet, cat and man; and considered with special reference to the theories of adaptive coloration. Proc Zool Soc Lond 116:371–524

    Google Scholar 

  • Crawley MJ (1992) Natural enemies: The population biology of predators, parasites and diseases. Blackwell, Oxford

    Google Scholar 

  • Darwin C (1871) The descent of man and selection in relation to sex. Murray, London

    Google Scholar 

  • Dunning Jr JB (1993) CRC handbook of avian body masses. CRC, Boca Raton

    Google Scholar 

  • Eaton MD (2005) Human vision fails to distinguish widespread sexual dichromatism among sexually “monochromatic” birds. Proc Natl Acad Sci USA 102:10942–10946

    Article  PubMed  CAS  Google Scholar 

  • Endler JA (1986) Natural selection in the wild. Princeton Univ Press, Princeton, NJ

    Google Scholar 

  • Endler JA (1991) Interactions between predators and prey. In: JR Krebs, NB Davies (eds) Behavioural ecology. Blackwell, Oxford, pp 169–196

    Google Scholar 

  • Felsenstein J (1985) Phylogenies and the comparative method. Am Nat 125:1–15

    Article  Google Scholar 

  • Garland Jr T, Harvey PH, Ives AR (1992) Procedures for the analysis of comparative data using phylogenetically independent contrasts. Syst Biol 41:18–32

    Article  Google Scholar 

  • Götmark F (1992) Anti-predator effects of conspicuous plumage in a male birds. Anim Behav 44:51–55

    Article  Google Scholar 

  • Götmark F (1993) Conspicuous coloration in male birds: favoured by predation in some species, disfavoured in others. Proc R Soc Lond B 253:143–146

    Article  Google Scholar 

  • Götmark F, Post P (1996) Prey selection by sparrowhawks, Accipiter nisus: relative predation risk for breeding passerine birds in relation to their size, ecology and behaviour. Phil Trans R Soc Lond 351:1559–1577

    Article  Google Scholar 

  • Green R (1979) Sampling design and statistical methods for environmental biologists. Wiley, New York

    Google Scholar 

  • Grell MB (1998) Fuglenes Danmark. Gad, Copenhagen

    Google Scholar 

  • Holling CS (1965) The functional response of predators to prey density and its role in mimicry and population regulation. Mem Entomol Soc Can 45:1–60

    Google Scholar 

  • Huhta E, Rytkönen S, Solonen T (2003) Plumage brightness of prey increases predation risk: an among-species comparison. Ecology 84:1793–1799

    Article  Google Scholar 

  • JMP (2000) JMP. SAS Institute Inc., Cary

    Google Scholar 

  • Jones KE, Purvis A (1997) An optimum body size for mammals? Comparative evidence from bats. Funct Ecol 11:751–756

    Article  Google Scholar 

  • Møller AP, Birkhead TR (1994) The evolution of plumage brightness in birds is related to extra-pair paternity. Evolution 48:1089–1100

    Article  Google Scholar 

  • Møller AP, Nielsen JT (1997) Differential predation cost of a secondary sexual character: Sparrowhawk predation on barn swallows. Anim Behav 54:1545–1551

    Article  PubMed  Google Scholar 

  • Møller AP, Merino S, Brown CR, Robertson RJ (2001) Immune defense and host sociality: A comparative study of swallows and martins. Am Nat 158:136–145

    Article  Google Scholar 

  • Møller AP, Marzal, A, Navarro C, de Lope F (2004) Predation risk, host immune response and parasitism. Behav Ecol 15:629–635

    Article  Google Scholar 

  • Mullarney T, Svensson L, Zetterström D, Grant PJ (2000) The complete guide to the birds of Europe. Harper Collins, London

    Google Scholar 

  • Newton I (1986) The sparrowhawk. Poyser, Berkhamstead

    Google Scholar 

  • Newton I, Marquiss M (1982) Food, predation and breeding season in sparrowhawks (Accipiter nisus). J Zool 197:221–240

    Google Scholar 

  • Nielsen JT (2004) A population study of sparrowhawks Accipiter nisus in Vendsyssel, Denmark, 1977–1997. Dan Ornithol Foren Tidsskr 98:147–162 (Danish, with English summary)

    Google Scholar 

  • Nielsen JT (2004) Prey selection of sparrowhawks in Vendsyssel, Denmark. Dan Ornithol Foren Tidsskr 98:164–173 (Danish, with English summary)

    Google Scholar 

  • Opdam P (1978) Feeding ecology of a sparrowhawk population (Accipiter nisus). Ardea 66:137–155

    Google Scholar 

  • Petrie M (1992) Peacocks with low mating success are more likely to suffer predation. Anim Behav 44:585–586

    Article  Google Scholar 

  • Purvis A, Rambaut A (1995) Comparative analysis by independent contrasts (CAIC). Comput Appl Biosci 11:247–251

    PubMed  CAS  Google Scholar 

  • Read AF (1987) Comparative evidence supports the Hamilton and Zuk hypothesis on parasites and sexual selection. Nature 328:68–70

    Article  Google Scholar 

  • Rytkönen S, Kuokkanen P, Hukkanen M, Huhtala K (1998) Prey selection by sparrowhawks Accipiter nisus and characteristics of vulnerable prey. Ornis Fenn 75:77–87

    Google Scholar 

  • Selås V (1993) Selection of avian prey by breeding sparrowhawks Accipiter nisus in southern Norway: the importance of size and foraging behaviour of prey. Ornis Fenn 70:144–154

    Google Scholar 

  • Sheldon FH, Slikas B, Kinnarney M, Gill FB, Zhao E, Silverin B (1992) DNA–DNA hybridization evidence of phylogenetic relationships among major lineages of Parus. Auk 109:173–185

    Google Scholar 

  • Sibley CG, Ahlquist JE (1990) Phylogeny and classification of birds, a study in molecular evolution. Yale Univ Press, New Haven and London

    Google Scholar 

  • Sibley CG, Monroe Jr BL (1990) Distribution and taxonomy of birds of the World. Yale Univ Press, New Haven and London

    Google Scholar 

  • Slagsvold T, Dale S, Kruszewics A (1995) Predation favours cryptic coloration in breeding male pied flycatchers, Ficedula hypoleuca. Anim Behav 50:1109–1121

    Article  Google Scholar 

  • Slikas B, Sheldon FH, Gill FB (1996) Phylogeny of titmice (Paridae): I. Estimate of relationships among subgenera based on DNA–DNA hybridization. J Avian Biol 27:70–82

    Article  Google Scholar 

  • Sokal RR, Rohlf FJ (1995) Biometry. 3rd edn. Freeman, New York

    Google Scholar 

  • Svensson L (1984) Identification guide to European passerines. L. Svensson, Stockholm

    Google Scholar 

  • van Beusekom CF (1972) Ecological isolation with respect to food between sparrowhawk and goshawk. Ardea 60:72 — 96

    Google Scholar 

  • Vermeij GJ (1987) Evolution and escalation: An ecological history of life. Princeton Univ Press, Princeton

    Google Scholar 

  • Viitala J, Korpimäki E, Palokangas P, Koivula M (1995) Attraction of kestrels to vole scent marks visible in ultraviolet-light. Nature 373:425–427

    Article  CAS  Google Scholar 

Download references

Acknowledgements

We would like to thank all landowners who provided access to their properties. H. Grunnet and J. K. Jensen helped collect some of the material. S. Rytkönen kindly provided constructive criticism.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Anders Pape Møller.

Additional information

Communicated by P. Bednekoff

Electronic supplementary materials

Rights and permissions

Reprints and permissions

About this article

Cite this article

Møller, A.P., Nielsen, J.T. Prey vulnerability in relation to sexual coloration of prey. Behav Ecol Sociobiol 60, 227–233 (2006). https://doi.org/10.1007/s00265-006-0160-x

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00265-006-0160-x

Keywords

Navigation