Skip to main content
Proceedings of the Royal Society B: Biological Sciences logoLink to Proceedings of the Royal Society B: Biological Sciences
. 1998 Mar 7;265(1394):397–407. doi: 10.1098/rspb.1998.0308

Sexual dimorphism in birds: why are there so many different forms of dimorphism?

I P F Owens, I R Hartley
PMCID: PMC1688905

Abstract

Variation in the extent of sexual dimorphism among bird species is traditionally attributed to differences in social mating system. However, there are many different forms of dimorphism among birds, and not all of them show an obvious correlation with social mating system. For example, recent work has shown that many highly polygamous species are, in fact, monomorphic, whereas many putatively monogamous species are dimorphic. In this paper we break up sexual dimorphism into subcomponents and then use comparative analyses to examine the pattern of covariation between these subcomponents and various aspects of sexual, social, and parental behaviour. Our first finding is that size dimorphism and plumage-colour dimorphism do not show the same pattern of covariation. Differences in size dimorphism are associated with variation in social mating system and sex differences in parental care, whereas differences in plumage-colour dimorphism are associated with variation in the frequency of extra-bond paternity. These results suggest that size dimorphism is associated with the sort of intrasexual competition described by traditional classifications of social mating system, whereas plumage-colour dimorphism is associated with cryptic female choice. However, when we break up plumage-colour dimorphism according to whether it is due to melanins, carotenoids or structural colours, we find that each category of plumage-colour dimorphism shows a different pattern of covariation. The correlation between overall plumage-colour dimorphism and the rate of extra-bond paternity is due to structural colours, whereas melanin-based dimorphism is associated with sex differences in parental care. The former result is particularly interesting given that new work suggests structural colours are associated with active sexual displays and the reflection of ultraviolet light.

Full Text

The Full Text of this article is available as a PDF (213.8 KB).

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Bennett A. T., Cuthill I. C., Partridge J. C., Lunau K. Ultraviolet plumage colors predict mate preferences in starlings. Proc Natl Acad Sci U S A. 1997 Aug 5;94(16):8618–8621. doi: 10.1073/pnas.94.16.8618. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Gibbs H. L., Weatherhead P. J., Boag P. T., White B. N., Tabak L. M., Hoysak D. J. Realized reproductive success of polygynous red-winged blackbirds revealed by DNA markers. Science. 1990 Dec 7;250(4986):1394–1397. doi: 10.1126/science.250.4986.1394. [DOI] [PubMed] [Google Scholar]
  3. Gyllensten U. B., Jakobsson S., Temrin H. No evidence for illegitimate young in monogamous and polygynous warblers. Nature. 1990 Jan 11;343(6254):168–170. doi: 10.1038/343168a0. [DOI] [PubMed] [Google Scholar]
  4. Herrera D. G., Robertson H. A. N-methyl-D-aspartate receptors mediate activation of the c-fos proto-oncogene in a model of brain injury. Neuroscience. 1990;35(2):273–281. doi: 10.1016/0306-4522(90)90081-e. [DOI] [PubMed] [Google Scholar]
  5. doi: 10.1098/rspb.1997.0152. [DOI] [PMC free article] [Google Scholar]
  6. doi: 10.1098/rspb.1997.0221. [DOI] [PMC free article] [Google Scholar]
  7. Primmer C. R., Møller A. P., Ellegren H. Resolving genetic relationships with microsatellite markers: a parentage testing system for the swallow Hirundo rustica. Mol Ecol. 1995 Aug;4(4):493–498. doi: 10.1111/j.1365-294x.1995.tb00243.x. [DOI] [PubMed] [Google Scholar]
  8. Purvis A., Rambaut A. Comparative analysis by independent contrasts (CAIC): an Apple Macintosh application for analysing comparative data. Comput Appl Biosci. 1995 Jun;11(3):247–251. doi: 10.1093/bioinformatics/11.3.247. [DOI] [PubMed] [Google Scholar]
  9. Schulze C., Firth J. A. Junctions between pericytes and the endothelium in rat myocardial capillaries: a morphometric and immunogold study. Cell Tissue Res. 1993 Jan;271(1):145–154. doi: 10.1007/BF00297552. [DOI] [PubMed] [Google Scholar]
  10. Warkentin I. G., Curzon A. D., Carter R. E., Wetton J. H., James P. C., Oliphant L. W., Parkin D. T. No evidence for extrapair fertilizations in the merlin revealed by DNA fingerprinting. Mol Ecol. 1994 Jun;3(3):229–234. doi: 10.1111/j.1365-294x.1994.tb00056.x. [DOI] [PubMed] [Google Scholar]

Articles from Proceedings of the Royal Society B: Biological Sciences are provided here courtesy of The Royal Society

RESOURCES