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Behavioral Ecology and Sociobiology

, Volume 31, Issue 4, pp 271–277 | Cite as

Acquisition of breeding coloration depends on badge size in male house sparrows Passer domesticus

  • A. P. Møller
  • J. Erritzøe
Article

Summary

The black throat “badge” of the male house sparrow Passer domesticus, which functions as a status signal of dominance rank, changes in size during late winter because light feather tips gradually wear off. Males change the size of their visible badge earlier if their final badge size is large. The differential timing of the change from winter to breeding coloration in relation to badge size is partially controlled by the behaviour of the individual male. Feather abrasion of the badge is mainly due to preening and dust bathing. During late winter, male house sparrows preen the badge area more than females preen the homologous area, and males with large badges preen more than males with small badges. The seasonal change in size of the visible badge of male house sparrows may reflect the balance of different selection pressures. A large badge size signals dominance status in autumn and winter while predation by visually searching avian predators may constitute the main opposing selection pressure. Sexual selection causes a stronger selection pressure for a large badge in spring and summer.

Keywords

Late Winter Dominance Rank Avian Predator Strong Selection Pressure Passer Domesticus 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

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References

  1. Birkhead TR, Moller AP (1992) Sperm competition in birds: evolutionary causes and consequences. Academic Press, LondonGoogle Scholar
  2. Bogliani G, Brangi A (1990) Abrasion of the status badge in the male Italian sparrow Passer italiae. Bird Study 37:195–198Google Scholar
  3. Brown NS (1972) The effect of host beak condition on the size of Menacanthus stramineus populations of domestic chickens. Poultry Sci 51:162–164Google Scholar
  4. Brown NS (1974) The effect of louse infestation, wet feathers, and relative humidity on the grooming behavior of the domestic chicken. Poultry Sci 53:1717–1719Google Scholar
  5. Darwin C (1871) The descent of man and selection in relation to sex. John Murray, LondonGoogle Scholar
  6. Folstad I, Karter AJ (1992) Parasites, bright males and the immunocompetence handicap. Am Nat 139:603–622CrossRefGoogle Scholar
  7. Ginn HB, Melville DS (1983) Moult in birds. British Trust for Ornithology, TringGoogle Scholar
  8. Grossman CJ (1985) Interactions between the gonadal steroids and the immune system. Science 227:257–261PubMedGoogle Scholar
  9. Kartman L (1949) Preliminary observations on the relation of nutrition to pediculosis of rats and chickens. J Parasitol 25:367–374Google Scholar
  10. Kasparek M (1981) Die Mauser der Singvögel Europas: ein Feldführer. Dachverband Deutscher Avifaunisten, LengedeGoogle Scholar
  11. Møller AP (1987a) Variation in badge size in male house sparrows Passer domesticus: evidence for status signalling. Anim Behav 35:1637–1644Google Scholar
  12. Moller AP (1987b) Social control of deception among status signalling house sparrows Passer domesticus. Behav Ecol Sociobiol 20:307–311Google Scholar
  13. Møller AP (1988) Badge size in the house sparrow Passer domesticus: effects of intra- and intersexual selection. Behav Ecol Sociobiol 22:373–378Google Scholar
  14. Møller AP (1989) Natural and sexual selection on a plumage signal of status and on morphology in house sparrows Passer domesticus. J Evol Biol 2:125–140Google Scholar
  15. Møller AP (1990) Sexual behaviour is related to badge size in the house sparrow Passer domesticus. Behav Ecol Sociobiol 27:23–29Google Scholar
  16. Møller AP (1991) Sperm competition, sperm depletion, paternal care and relative testes size in birds. Am Nat 137:887–906Google Scholar
  17. Møller AP, Erritzøe J (1988) Badge, body and testes size in the house sparrow Passer domesticus. Ornis Scand 19:72–73Google Scholar
  18. Palmer RS (1972) Patterns of molting. In: Farmer DS, King JR (eds) Avian Biology. Vol 2. Academic Press, New York, pp 65–102Google Scholar
  19. Rohwer S (1975) The social significance of avian winter plumage variability. Evolution 29:593–610Google Scholar
  20. Rohwer S (1977) Status signalling in Harris sparrows: some experiments in deception. Behaviour 61:107–129Google Scholar
  21. Rohwer S, Butcher GS (1988) Winter versus summer explanations of delayed plumage maturation in temperate passerine birds. Am Nat 131:556–572Google Scholar
  22. Rohwer S, Rohwer FC (1978) Status signalling in Harris' sparrows: experimental deceptions achieved. Anim Behav 26:1012–1022Google Scholar
  23. Stresemann E, Stresemann V (1966) Die Mauser der Vögel. J Ornithol 105 (Sonderheft):1–448Google Scholar
  24. Summers-Smith JD (1963) The house sparrow. Collins, LondonGoogle Scholar
  25. Svensson L (1984) Identification guide to European passerines. L. Svensson, StockholmGoogle Scholar
  26. Zahavi A (1975) Mate selection — a selection for a handicap. J Theor Biol 53:205–214PubMedGoogle Scholar
  27. Zahavi A (1977) The cost of honesty: further remarks on the handicap principle. J Theor Biol 67:603–605Google Scholar
  28. Zahavi A (1987) The theory of signal selection and some of its implications. In: Delfino VP (ed) International Symposium of Biological Evolution. Adriatica Editrica, Bari, pp 305–327Google Scholar

Copyright information

© Springer-Verlag 1992

Authors and Affiliations

  • A. P. Møller
    • 1
  • J. Erritzøe
    • 2
  1. 1.The Galton Laboratory, Department of Genetics and BiometryUniversity College of LondonLondonUK
  2. 2.Taps GI. PræstegårdChristiansfeldDenmark

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