We manipulated the primary brood size of Eurasian treecreepers (Certhia familiaris) breeding in different sized forest patches (0.5-12.8 ha) in moderately fragmented landscapes. We examined the effects of brood size manipulation (reduced, control, enlarged) and forest patch size on physiological stress (heterophillymphocyte ratios; H/L), body condition and cell-mediated immunocompetence (phytohaemagglutinin test). Nestlings' H/L ratios were negatively related to forest patch area in control and enlarged broods, whereas no effects were found in reduced broods. The effects of forest patch area were strongest in enlarged broods, which had, in general, twofold higher H/L ratios than control and reduced broods. The elevated H/L ratios were positively related to nestling mortality and negatively correlated with bodycondition indices suggesting that the origin of stress in nestlings was mainly nutritional. Cell-mediated immunity of nestlings was not related to brood manipulation or to forest patch size. Also, the H/L ratios of adults were not related to brood manipulation or forest patch size. In addition, parental H/L ratios and body condition were not related to nestling H/L ratios. Our results suggest that during the breeding period the deleterious effects of habitat loss are seen explicitly in growing young.

No abstract

Koivunen, V. 2003. Habitat composition as a determinant of reproductive success of Tengmalm's owls under fluctuating food conditions. -Oikos 100: 162-171.The effect of landscape composition on the breeding success of vole-eating Tengmalm's owl (Aegolius funereus) was studied in western Finland at five different spatial scales (250-4000 m) around the nests during two consecutive three-year population cycles of voles. Landscape composition had strongest effects on owl breeding in the decrease phase of vole cycles. Significant variation in owl breeding occurred along the productivity gradient from farmland predominated areas to barren hinterland. Owls tended to produce earlier clutches on territories predominated by agricultural areas in increasing vole years. A similar trend was observed in the decreasing phase of the vole cycle; owls breeding on barren hinterland seemed to delay breeding compared to owls breeding near agricultural areas. Surprisingly, nestling survival and fledgling production in the decreasing phase declined steeply with increasing proportion of farmland. Clutch size was not significantly related to landscape composition. The number of fledglings decreased with increases in clear-cut and sapling areas in the decrease phase. During the declining years of vole abundance nestling survival increased from western farmland areas towards the eastern outlying district. These results indicate sudden summer decline of vole populations on farmland predominated habitats. This is probably due to that the number of vole-eating predators, and hence their impact on vole populations is apparently higher in farmland areas than on forested hinterland. This finding gives support for the 'spill-over' hypothesis, which states that predators and their exploitation tends to 'spill over' from luxuriant habitats to the barren habitats.

No abstract

Nest predation and its avoidance are critical components of an individual's fitness and play an important role in life history evolution. Almost all studies on this topic have been observational, and thus have not been able to separate the effects of individual quality, habitat selection and predation risk of given nest sites from each other. More experimental studies on nest predation and breeding dispersal, therefore, are needed to avoid confusing interpretations of the results. In western Finland, pine marten (Martes martes) predation risk was experimentally simulated at the nests of Tengmalm's owls (Aegolius funereus) by using a caged American mink (Mustela vison) as a predator. Nests without exposure to a mink served as controls. In accordance with our predictions and earlier observational studies, males exposed to simulated predation risk increased nest-hole shift and breeding dispersal distances compared to control males. Nest-hole shift and long breeding dispersal distances probably decrease the risk of nest predation, because pine martens are known to revisit nest-holes they have found.