Fróðskaparrit - 01.01.2009, Side 105

Fróðskaparrit - 01.01.2009, Side 105
í EITT ÁR VÓRÐU REIÐURSTAÐIR HJÁ HAVHESTI (FULMARUS CLACIALIS) í FØROYUM EYCLEIDDIR VIÐ VAKMYNDATÓLI 103 could be applicable, where some prospec- tors are first attracted to a relatively old and large colony but due to competition go else- where (see also Coulson and Horobin, 1972). However, the surveillance cameras did not record any behaviours that indicated com- petition for nest-sites (no other cliff-breed- ing species nested within the colony area), which of course could be due to the fact that the colony was small. For the Northern Ful- mar, and other long-lived seabird species, prospecting for information regarding suit- able feeding areas, breeding colonies, nest- sites, and breeding success of conspecifics (the „public information" hypothesis) is probably a significant element of the species' life-history strategy (see Forbes and Kaiser, 1994). MacDonald (1980) suggested that breeding adults and other potential recruits might use the „winter assembly" to look for, and form pair-bonds with unmated birds. Al- though the divorce and mortality rates among fulmars are low, approximately 5% of the breeders will lose their mates annually and therefore have to search for a new part- ner (MacDonald, 1977a; Ollason and Dun- net, 1978). Despite scanty data, the present study indicates that divorce rate may have been higher and nest-site fidelty lower at Sund (see Results and Table 4) than previ- ously reported for other colonies, (Ollason and Dunnet, 1978,1988). This may be due to disturbance and a subsequent low breeding success (Table 3) or some other environ- mental unpredictability. In the context of the „success-stay/failure-leave" concept (Schmidt, 2004), breeding performance is thought to influence both mate and site fi- delity in long-lived seabirds (Naves et al„ 2006); though with regard to site fidelity the- ory predicts that it should be inversely re- lated to lifespan and that individuals should be site-faithful in unpredictable habitats pro- vided there is equal site-quality (Switzer, 1993, 1997). However, not surprisingly in view of the small sample-size, no significant differences in first arrival dates and atten- dance patterns between nest-sites and years, or between successful and failed breeders, are discernible in the present data (Table 5). Almost invariably the first landfall occurred in December though the attendance at the individual nest-sites varied considerably from a single day (and one minute to an hour) to 9-10 days (Table 5). The fulmars continued to visit the nest-sites intermit- tently and with two individuals present throughout the months January-March and with two-bird-attendance reachinga peak in April (Fig. 1); thus coinciding with the period when all copulations were recorded (Table 6). According to Hatch (1987a) fulmars copulate only at the nest-site and in his stud- ies of the species in Alaska, the pairs began to copulate immediately upon first landfall (c. 50 days prior to first eggs) and on average every 2-4 hours in daylight. Furthermore, the frequency of copulations peaked about 3 weeks before the egg is laid and the female is inseminated 30-40 times before she departs for the pre-laying exodus (Hatch, 1987a). This is in sharp contrast to our study where all copulations recorded by the cameras took place during a relatively short period (11 April to 1 May), although the birds had been attending the colony since in December or January. In a study of albatrosses 96% of the observed copulations occurred in one day (Astheimer etal., 1985). In our fulmarcolony
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