Behaviour of hybrid male Tetrao tetrix male X T. urogallus female on black grouse leks.

Life span, dispersal and age of nesting Great Grey Owls (Strix nebulosa lapponica) in Sweden.

3,073 Great Grey Owls were banded in Sweden in 1955–2012. 416 were controlled at least once (54.6%) or recovered dead (45.4%). Three birds banded as nestlings were recovered in their 17th calendar year. Most birds were recovered during first year of life. Only 4 females were controlled breeding as 2CY birds. 91.3% of birds controlled as first time breeders were at least 4CY. Birds banded as nestlings and recovered dead between September and July moved 100.8 km (mean) with a median distance of 64 km. Juveniles controlled alive moved 45.9 km (mean) with a median distance of 23 km during first year of life. Maximum natal dispersal was 650 km. Median natal dispersal for females was 40 km, betwe…

Molt pattern of primaries and secondaries during first and second flight feather molt in Great Grey Owls Strix nebulosa.

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Home range and excursive post-breeding movements of Eurasian Eagle-owls revealed by GPS satellite transmitters

Investigating space use of wild birds provides important knowledge of bird behavior and ecology, which is crucial in the management and conservation of threatened species. In the present study, we used GPS satellite telemetry to investigate space use and movements of seven adult Eurasian Eagle-Owls (Bubo bubo) in Norway during breeding and post-breeding seasons. Breeding adults had a mean home range size of 42.9 km2 (SD ± 35.1 km2; 95% kernel density estimation Had hoc), and five individuals performed long (>20 km) excursive movements away from their breeding territories during autumn. Such wide-ranging behavior has not previously been reported for adults of the nominate subspecies B. b. bu…

Age structure in a newly established and increasing population: initially high proportion of young birds among nesting Great Grey Owls

AbstractThe mechanisms behind expansions of the distribution of a bird species and the ensuing establishment of new populations are poorly known. The distribution of Great Grey Owl (Strix nebulosa) in the western Palearctic has generally expanded towards southwest during the past fifty years, and particularly so in Fennoscandia. In the past decade, the recorded breeding population in Norway, confined to Hedmark county bordering Sweden, increased from 1 pair in 2009 to > 100 pairs in 2017–2018, extending the southwestern border of the distribution > 100 km. We studied the age structure of this expanding population based on the molting pattern of the wing feathers of birds captured at t…

No phylogeographic structure in the circumpolar snowy owl (Bubo scandiacus)

The snowy owl (Bubo scandiacus) is a nomadic species with a circumpolar distribution. It has recently declined in the western Palearctic and may thus be worthy of special consideration for conservation. We investigated genetic structure in three well separated geographic regions within the snowy owls’ breeding range. We sequenced two mitochondrial genes; the control region and cytochrome b, and two Z-chromosome introns; VLDLR-9 and BRM-15. We found no phylogeographic structure among the sampled regions, indicating high levels of gene flow in the recent past and possibly still today. Intra-population diversity did not vary between regions for the control region, but for Cyt b, North American…

Individual identification of Snowy Owls (Bubo scandiacus) and Great Grey Owls (Strix nebulosa) based on wing bar patterns.

Wing feather moult and age determination of Snowy Owls Bubo scandiacus.

Moult of primary and secondary flight feathers of Snowy Owls Bubo scandiacus was studied from 53 museum specimens retaining some juvenile feathers. There were no ringed Snowy Owls of known age in the skin material, and the moult pattern has thus been interpreted using the moult of Eagle Owls Bubo bubo as a model. The difference between juvenile and adult primaries is described. Greater coverts may facilitate age determination of single flight feathers. Snowy Owls start their first flight feather moult M1 by shedding the innermost 2-6 secondaries during their second summer (as 2C birds). A majority of the owls also shed primary P7 during this first moult, occasionally also P8. This moult pro…

Density-dependent winter survival of immatures in an irruptive raptor with pulsed breeding

Highly mobile predators can show strong numerical responses to pulsed resources, sometimes resulting in irruptions where large numbers of young invade landscapes at a continental scale. High production of young in irruption years may have a strong influence on the population dynamics unless immature survival is reduced compared to non-irruption years. This could occur if subordinate individuals (mainly immatures) are forced into suboptimal habitats due to density-dependent effects in irruption years. To test whether irruptive individuals had lower survival than non-irruptive ones, we combined necropsy results (N = 365) with telemetry (N = 185) from more than 20 years to record timing and ca…

Range extension of Great Grey Owl in Europe.

Arctic avian predators synchronise their spring migration with the northern progression of snowmelt

AbstractMigratory species display a range of migration patterns between irruptive (facultative) to regular (obligate), as a response to different predictability of resources. In the Arctic, snow directly influences resource availability. The causes and consequences of different migration patterns of migratory species as a response to the snow conditions remains however unexplored. Birds migrating to the Arctic are expected to follow the spring snowmelt to optimise their arrival time and select for snow-free areas to maximise prey encounter en-route. Based on large-scale movement data, we compared the migration patterns of three top predator species of the tundra in relation to the spatio-te…

Age of Great Grey Owls Strix nebulosa observed in Scandinavia in 2012 as revealed by digital photos in the national species report archives.

Record breaking numbers of breeding Great Grey Owls Strix nebulosa were reported in Sweden and Norway in 2010 and 2011, followed by 4,105 observations in 2012 as revealed by the national Species archives. Based on locality id numbers, at least 144 individuals were reported with photos which could be used to age the individuals. The majority (76%) of these birds were young birds hatched in 2011 (83% including birds aged probably 2CY). Among dead owls brought to the Natural History Museum in Stockholm, the percentages of owls hatched in 2011 were similar (78% and 88%). The high percentage of young owls could be caused by young birds hunting closer to human settlement than older birds, but mor…

Behaviour of hybrid male Tetrao tetrix male x T. urogallus female on black grouse and capercaillie display grounds.

Effects of satellite transmitters on survival in Snowy Owls Bubo scandiacus

The use of tracking devices to monitor birds is extensive, but the effects of such instruments on equipped individuals are still insufficiently taken into account. Here we evaluate potential effects of backpack-mounted satellite transmitters (platform terminal transmitters; PTTs) on survival of 28 Snowy Owls Bubo scandiacus. Six confirmed deaths were all probably related to natural and human-induced causes. Although PTT operational time was significantly shorter than expected lifetime of Snowy Owls, five owls were observed alive after transmissions ceased. Additionally four PTTs stopped due to low battery levels, indicating end of transmitter life and not owl mortality. We found no evidence…

The origin of Swedish and Norwegian populations of the Eurasian harvest mouse (Micromys minutus).

The harvest mouse (Micromys minutus) occurs throughout most of continental Europe. There are also two isolated and recently discovered populations on the Scandinavian peninsula, in Sweden and Norway. Here, we investigate the origin of these populations through analyses of mitochondrial DNA. We found that the two populations on the Scandinavian peninsula have different mtDNA haplotypes. A comparison of our haplotypes to published sequences from most of Europe showed that all Swedish and Norwegian haplotypes are most closely related to the haplotypes in harvest mice from Denmark. Hence, the two populations seem to represent independent colonisations but originate from the same geographical ar…