Skip to main content
Proceedings of the Royal Society B: Biological Sciences logoLink to Proceedings of the Royal Society B: Biological Sciences
. 2003 Nov 7;270(1530):2215–2222. doi: 10.1098/rspb.2003.2490

Forest fragmentation is associated with primary brood sex ratio in the treecreeper (Certhia familiaris).

Petri Suorsa 1, Heikki Helle 1, Esa Huhta 1, Ari Jäntti 1, Ari Nikula 1, Harri Hakkarainen 1
PMCID: PMC1691495  PMID: 14613607

Abstract

We studied the primary brood sex ratio of an old-growth forest passerine, the Eurasian treecreeper (Certhia familiaris), along a gradient of forest fragmentation. We found evidence that male nestlings were more costly to produce, since they suffered twofold higher nestling mortality and were larger in body size than females. Furthermore, the proportion of males in the brood was positively associated with the provisioning rate and the amount of food delivered to the nestlings. During the first broods, a high edge density and a high proportion of pine forests around the nests were related to a decreased production of males. The densities of spiders, the main food of the treecreeper, were 38% higher on spruce trunks than on pine trunks. This suggests that pine-dominated territories with female-biased broods may have contained less food during the first broods. The observation was further supported by the fact that the feeding frequencies were lower in territories with high proportions of pines. In the second broods, territories with a high forest patch density produced female-biased broods, whereas high-quality territories with a large amount of deciduous trees and mixed forests produced male-biased broods. Our results suggest that habitat quality as measured by habitat characteristics is associated with sex allocation in free-living birds.

Full Text

The Full Text of this article is available as a PDF (230.1 KB).

Selected References

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

  1. Kilner R. Primary and secondary sex ratio manipulation by zebra finches. Anim Behav. 1998 Jul;56(1):155–164. doi: 10.1006/anbe.1998.0775. [DOI] [PubMed] [Google Scholar]
  2. Komdeur Jan, Magrath Michael J. L., Krackow Sven. Pre-ovulation control of hatchling sex ratio in the Seychelles warbler. Proc Biol Sci. 2002 May 22;269(1495):1067–1072. doi: 10.1098/rspb.2002.1965. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Nager R. G., Monaghan P., Griffiths R., Houston D. C., Dawson R. Experimental demonstration that offspring sex ratio varies with maternal condition. Proc Natl Acad Sci U S A. 1999 Jan 19;96(2):570–573. doi: 10.1073/pnas.96.2.570. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. doi: 10.1098/rspb.1997.0153. [DOI] [PMC free article] [Google Scholar]
  5. doi: 10.1098/rspb.1998.0375. [DOI] [PMC free article] [Google Scholar]
  6. Suorsa Petri, Huhta Esa, Nikula Ari, Nikinmaa Mikko, Jäntti Ari, Helle Heikki, Hakkarainen Harri. Forest management is associated with physiological stress in an old-growth forest passerine. Proc Biol Sci. 2003 May 7;270(1518):963–969. doi: 10.1098/rspb.2002.2326. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Trivers R. L., Willard D. E. Natural selection of parental ability to vary the sex ratio of offspring. Science. 1973 Jan 5;179(4068):90–92. doi: 10.1126/science.179.4068.90. [DOI] [PubMed] [Google Scholar]
  8. Watridge C. B., Todd M. A., Boyd A. S., DeSaussure R., Friedman H., Robertson J. T. Nervous system metastasis from carcinoma of the lung: three unusual cases. South Med J. 1981 Nov;74(11):1313–1316. doi: 10.1097/00007611-198111000-00007. [DOI] [PubMed] [Google Scholar]
  9. Williams G. C. The question of adaptive sex ratio in outcrossed vertebrates. Proc R Soc Lond B Biol Sci. 1979 Sep 21;205(1161):567–580. doi: 10.1098/rspb.1979.0085. [DOI] [PubMed] [Google Scholar]

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

RESOURCES