Fróðskaparrit - 01.01.2004, Page 264

Fróðskaparrit - 01.01.2004, Page 264
262 PHILOPATRY, DISPERSAL, AND SURVIVAL OF WREN (TROGLODYTES TROGLODYTES) 1N THE FAROE ISLANDS exhibit breeding site fidelity, a majority disperse at the end of the breeding season and spend the non-breeding season in, or moving between, any places where condi- tions are favourable and in the spring mate some distance from natal areas. The islands appear to be saturated with suitable breed- ing habitats and territorial wrens (Bengt- son, 2001 and unpubl.), which may result in a lower site attachment in the females. Ecological constraints on dispersal and the benefits of philopatry may interact (Koenig et al., 1992; Ernlen, 1994) and variation in quality between territories may promote variability in dispersing behaviour (Kokko and Lundberg, 2001). Hence a justification for comparing study areas, though the fail- ure to detect any differences between them with respect to dispersal patterns was not surprising considering the small sample sizes. Conclusions In the Faroes, wrens disperse in autumn and during the non-breeding season they occur in habitats not suitable for breeding, for in- stance the littoral zone. However, the post- breeding movements seem mostly confined to the natal island, though at least one of the colour-marked fledglings dispersed at least 50 km and passed several islands and open water crossings. Dispersal is sex-biased and relatively few adult females returned to the areas where they had bred in the previ- ous year, while the males, which are ter- ritorial through most of the year, showed a high degree of philopatry. Males breeding for the first time also show a stronger at- tachment to their nalal areas than females, but appeared to be less successful in obtain- ing mates than older males were. Mean an- nual survival rate, and thus length of life span, appears to be higher than in mainland wrens. Evolutionary explanations for the patterns observed require larger samples, extended study areas, more behavioural ob- servations during critical periods of time, and experimental approaches. Acknowledgements Funding was received from the Swedish Natural Science Research Council, Dansk-svensk samfunds fond for kulturoch vetenskap, Copenhagen, Kungl. Fysiografiska Sallskapet i Lund, and Letterstedska foreningen, Stockholm. Among many local people and others who provided valuable assistance the following deserve special mentioning: Professor Dorete Bloch and her late husband Hans Ólavus Danielsen, Mr Søren Sørensen, Professor Arne Nørrevang, Ms Herdis Joensen, Dr. Pehr H. Enckell, and the ringing-team in 1984, viz. Andrew Berry, Tim Anderson, and Chris Dee. References Armstrong, E.A. 1955. The Wren. London. Armstrong, E.A. and Whitehouse, H.L.K. 1977. Behavioural adaptations of the wren (Troglodytes troglodytes). Biol. Rev. 52: 235-294. Arnold, K.E. and Owens, I.P.F. 1998. Cooperative breeding in birds: a comparative test of the life history hypothesis. Proc. R. Soc. Lond. B 265: 739- 745. Bengtson, S.-A. 2001. Breedingdistribution and numbers of wren (Troglodytes troglodytes) in the Faroe Islands. Fródskaparrit 49:127-139. Tórshavn. Bijlsma, R., Bundgaard, J. and Van Putten, W.F. 1999. Environmental dependence of inbreeding depression and purging in Drosophila melanogaster. J. Evol. Biol.. 12: 1125-1137. Brown, J.L. and Brown, E.R. 1984. Parental facilitation: parenl-offspring relations in communally breeding birds. Behav. Ecol. Sociobiol. 14: 203-209. Cramp, S. (Chief Editor). 1988. The Birds ofthe Western Palearctic Vol. 5: 525-542. Oxford and New York.
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