<p>Males and females differ in morphology and behaviour, so that selection acts differently on the two sexes. This changes the relative reproductive success of males and females, and it is beneficial for parents to bias the sex ratio of their broods in favour of the sex with the best survival and breeding prospects. Differences between the sexes and brood sex ratio in Tengmalm’s owl (Aegolius funereus) in northern Sweden were investigated, using a molecular sexing technique based on PCRamplification of sex-linked CHD1 genes. Among owls caught during autumn migration, females were commoner than males, especially within juveniles. However, in contrast to earlier studies, it was shown that adult males sometimes undertake migratory movements indicatory of nomadism. Measurements of these owls revealed that sexual size dimorphism in Tengmalm’s owl is not as great as previously reported from studies carried out during the breeding season. Females were slightly larger (4% by mass) than males, probably owing to the different roles of males and females during breeding, when this dimorphism is greater. The size difference between male and female nestlings was found to be similar to that for adults in autumn, and to investigate whether this led to differential mortality, the effect of supplementary feeding on mortality of male and female nestlings was studied. Supplementary feeding reduced male mortality when vole abundance was low, and it was concluded that larger female nestlings out-competed their smaller brothers, who then suffered increased mortality when food was scarce. Recruitment of male nestlings into the breeding population declined with decreasing food supply at the time of fledging, a pattern not observed in females. Juvenile males were therefore more vulnerable to food shortage than females, both in the nest and after fledging. Mean brood sex ratio varied significantly among years characterized by different phases of the vole cycle and associated vole abundance. Broods were male-biased (63% males) in a year when the food supply was favourable during spring and summer, neutral (50%) in a year with an intermediate food supply, and female-biased (35% males) in a year when food was in short supply. Parents appeared to adaptively adjust the sex ratio of their broods according to the relative mortality risk and reproductive potential of sons and daughters.</p>

Males and females differ in morphology and behaviour, so that selection acts differently on the two sexes. This changes the relative reproductive success of males and females, and it is beneficial for parents to bias the sex ratio of their broods in favour of the sex with the best survival and breeding prospects. Differences between the sexes and brood sex ratio in Tengmalm’s owl (Aegolius funereus) in northern Sweden were investigated, using a molecular sexing technique based on PCRamplification of sex-linked CHD1 genes. Among owls caught during autumn migration, females were commoner than males, especially within juveniles. However, in contrast to earlier studies, it was shown that adult males sometimes undertake migratory movements indicatory of nomadism. Measurements of these owls revealed that sexual size dimorphism in Tengmalm’s owl is not as great as previously reported from studies carried out during the breeding season. Females were slightly larger (4% by mass) than males, probably owing to the different roles of males and females during breeding, when this dimorphism is greater. The size difference between male and female nestlings was found to be similar to that for adults in autumn, and to investigate whether this led to differential mortality, the effect of supplementary feeding on mortality of male and female nestlings was studied. Supplementary feeding reduced male mortality when vole abundance was low, and it was concluded that larger female nestlings out-competed their smaller brothers, who then suffered increased mortality when food was scarce. Recruitment of male nestlings into the breeding population declined with decreasing food supply at the time of fledging, a pattern not observed in females. Juvenile males were therefore more vulnerable to food shortage than females, both in the nest and after fledging. Mean brood sex ratio varied significantly among years characterized by different phases of the vole cycle and associated vole abundance. Broods were male-biased (63% males) in a year when the food supply was favourable during spring and summer, neutral (50%) in a year with an intermediate food supply, and female-biased (35% males) in a year when food was in short supply. Parents appeared to adaptively adjust the sex ratio of their broods according to the relative mortality risk and reproductive potential of sons and daughters.

No description available.

Bank voles, grey-sided voles, and field voles had synchronous 3-4 year density cycles with variable amplitudes which averaged about 200-fold in each species. Cycles of vole predators (red fox and Tengmalm's owl), and their (foxes') alternative prey (mountain hare and forest grouse) lagged behind the vole cycles. The nomadic Tengmalm's owl responded with a very rapid and strong numerical increase to the initial cyclic summer increase of voles (the owl’s staple food). Owl breeding densities in the springs were highly correlated with vole supply in the previous autumns. This suggested that the number of breeding owls was largely determined in the autumn at the time of the owl's nomadic migrations, and that immigration was crucial for the rapid rise in owl numbers. The owl's numerical response was reinforced by the laying of earlier and larger clutches when food was plentiful. In addition, the owl has an early maturation at one year of age. The transition between subsequent vole cycles was characterized by a distinct shift in rate of change in numbers from low to high or markedly higher values in both summer and winter. Regulation increased progressively throughout the cycle since the rate of change decreased continuously in the summers. Moreover, there was a similar decrease of the rate of change in winter. Rate of change was delayed density-dependent. The delayed density-dependence had an 8 month time-lag in the summers and a 4 month time-lag in the winters relative to the density in previous autumns and springs, respectively. These findings suggest that vole cycles are likely to be generated by a time-lag mechanism. On theoretical grounds, it has been found that a delayed density- dependence of population growth rate with a 9 month time-lag caused stable limit cycles with a period between 3 and 4 years. Some mechanisms for the delayed density-dependence are suggested and discussed. The mechanisms are assumed to be related to remaining effects of vole populations past interactions with predators, food supplies, and/or diseases. Unlike the other voles, the bank vole had regular and distinct seasonal declines in density over winter. These declines are proposed to be due to predation, mainly by Tengmalm's owl. Supranivean foraging for epiphytic tree lichens and conifer seeds most likely explains why this species was frequently taken by the owl under snow-rich conditions. The alternative prey hypothesis predicts that a reduction of predator numbers should increase the number of alternative prey. Alternative prey should be less effectively synchronized to the vole cycle by predation at declining and low vole (main prey) densities; they may also lose their 3-4 year cyclicity. The appearance of sarcoptic mange among foxes in northern Sweden in the mid 1970s provided an opportunity to "test" these ideas, and these were found to be supported. In areas with highest mange infection rates, foxes declined markedly from the late 1970s to mid 1980s, whereas hare numbers rose rapidly and appeared non-cyclic. / <p>Diss. (sammanfattning) Umeå : Umeå universitet, 1991, härtill 7 uppsatser</p> / digitalisering@umu