Fróðskaparrit - 01.01.2002, Qupperneq 141

Fróðskaparrit - 01.01.2002, Qupperneq 141
VISTFRØÐIN HJÁ INNVORTIS SNÍKUM í LUNDA 139 ductive stages of the birds’ lives. In migrat- ing birds, females typically have longer na- tal dispersal than males. (Møller and Erritzøe, 2001). The hypothesis is that the development of the immune system is pos- itively correlated with the diversity of the parasitic fauna to which the host is ex- posed, which is again positively correlated to the dispersal distance of the host (Møller and Erritzøe, 2001). Further investigations are necessary to explore this hypothesis, es- pecially as knowledge is sparse about the migration behaviour of pre-mature puffins. Hoberg (1987); Bakke (1972); and Bockeler and Vauk-Hentzelt (1979) report- ed sludies on a total of 265 birds; a total of 8 females and 7 males were infested with pentastomes. Whilst the present study ap- pears to show a tendency for females being the more heavily infested with pentas- tomes, this is not supported by the litera- ture. Host age The reason for adult birds tending to have a higher relative intensity of infestation with trematodes may reflect immunological suppression at a cost to reproductive effort, a phenomenon that may impose not only immediate effects but also possibly life- long negative consequences for viability (Nordling et al., 1998). An alternative or complementary cause might lie in the dif- ferences in the functional response of the immune system, in which information on immune responses is stored in memory cells in adult birds, rather than in the func- tion of the Bursa Fabricii in juvenile birds (Møller and Erritzøe, 2001), the functional response of the adult being less efficient perhaps. Regarding pentastomes, other investiga- tors (Bakke, 1972; Bðckeler and Vauk- Hentzelt, 1979; Bockeler, 1984) have shown a higher prevalence of infestation in juvenile than in adult birds; the converse was found in the present study, in which all pentastome-infested birds were adults. Seasonal effects The helminth fauna of migrating birds is generally seasonal, a natural consequence of seasonal and regional fiuctuations in food supply (Bykhovskaya-Pavlovskaya, 1953; 1962; Bezubik, 1956; Jarecka, 1958; Polozhentsev and Negrobov, 1958; Kassi- mov et al., 1962; Rysavy, 1962; 1964 in Wallace and Pence, 1986). A lack of re- placement might also be an influence, when prey species change in connection with migration, and longevity of the para- sites is limited (Avery, 1969). The helminth fauna of auks is also seasonal and related to the breeding areas (Hoberg, 1981), as there is a seasonal occurrence of pentastomes (Bockeler, 1984). Parasites usually adapt their reproductive period to the annual cy- cle of the host, with parasite population densities peaking late during the hosts’ re- productive season (Cox, 1993). Such peaks may be in part at least to a consequence of the immunological cost of reproduction during the breeding season (Nordling, 1998). In addition, the risk of infestation is usually density-dependent (Begon et ai, 1986), and the puffin density is clearly highest in the breeding period. The great dispersion of the birds outside the breeding
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