Natal dispersal and its consequences in Black Grouse Tetrao tetrix

Data on dispersal distances of juveniles are important for understanding the genetic structure of populations, population regulation processes and the effects of landscape ecology on metapopulation dynamics. We studied dispersal in juvenile Black Grouse Tetrao tetrix in the French Alps between 1990 and 1998, by radiotracking 39 young grouse captured in August or autumn in a study area of 836 ha. Natal dispersal occurred in two discrete phases, autumn (October) and spring (mid-April to early May), with periods of reduced mobility between. The mean distance travelled by females exceeded that of males in autumn but not in spring. The natal dispersal distance of females was greater than that of males, and resulted in 81% of females leaving the study area to nest 5–29 km from their site of capture. This emigration must have been compensated for by immigrants because the number of hens in the study area increased during the study. Males were more philopatric. By the summer after capture, only 9% had emigrated from the study area. Despite the longer dispersal distances of females, there was no difference in the survival functions of the sexes between the ages of 6 weeks and 13 months.     

Dispersal distances of juvenile radiotagged Red Grouse Lagopus lagopus scoticus on moors in northern England

Radio-transmitters were fitted on 146 juvenile Red Grouse Lagopus lagopus scoticus (116 hens, 30 cocks) to study the timing, frequency and distances of dispersal on managed grouse moors in northern England between 1999 and 2002. A third of the radiotagged birds were shot. Disturbance on shoot days meant that radiotagged birds were shot at points more than twice as far from the catch location as the points when they were last recorded alive. For birds that were shot, the distance from the catch location to the place they were shot was more than twice the natal dispersal distances of the survivors. Therefore, shot birds were excluded from the dispersal analysis. Juvenile hens dispersed significantly further (mean 861 m, range 50–4660 m) than juvenile cocks (mean 343 m, range 90–660 m). Dispersal distances were not related to predispersal Grouse densities at the catch area in summer or to Grouse densities in the following spring. The mean date of dispersal for juvenile hens was 6 October ± 4 days (se), with only one record of spring dispersal (14 March) of 1490 m.     

DISPERSAL, ROOKERY FIDELITY, AND METAPOPULATION STRUCTURE OF STELLER SEA LIONS (EUMETOPIAS JUBATUS) IN AN INCREASING AND A DECREASING POPULATION IN ALASKA

Over the past 24 yr, 8,596 Steller sea lion ( Eumetopias jubatus ) pups were branded on their natal rookeries throughout Alaska with the objectives of determining survival rates, recruitment, movements, and site fidelity. Our objectives here were to examine the extent of dispersal of Steller sea lions away from their natal rookeries, movements between stocks, and degree of natal rookery fidelity. Pups (<1 yr old) usually remained within 500 km of their natal rookery. Branded juveniles dispersed widely and were resighted at distances up to 1,785 km from their natal rookeries. Adults generally remained within 500 km of their natal rookeries. No interchange of breeding animals between the ES (eastern stock) and WS (western stock) was observed. Although natal rookery fidelity was prevalent, 33% of the 12 observations of females branded in the WS during 1987–1988 and 19% of the 29 observations of females branded in the ES during 1994–1995 were observed with newly born pups at sites other than their natal rookeries. Steller sea lions generally conformed to the metapopulation concept as depicted by Hanski and Simberloff (1997), with local breeding populations (rookeries) and movements among these local populations having the potential of affecting local dynamics.     

Dispersal, interpatch movements, and survival in a shrubland breeding bird community

ABSTRACT Dispersal events can affect the distribution, abundance, population structure, and gene flow of animal populations, but little is known about long‐distance movements due to the difficulty of tracking individuals across space. We documented the natal and breeding dispersal of shrubland birds among 13 study sites in a 1000 km² area in southeastern Ohio. In addition, we radio‐marked and tracked 37 adult males of one shrubland specialist, the Yellow‐breasted Chat (Icteria virens). We banded 1925 juveniles and 2112 adults of nine shrubland species from 2002 to 2005. Of these, 33 (1.7%) juveniles were encountered in subsequent years (2003–2006) as adults (natal dispersal) and 442 (20.9%) birds initially banded as breeding adults were re‐encountered in subsequent years (breeding dispersal). Apparent survival of juvenile shrubland birds on their natal patches was 0.024 (95% CI 0.016–0.036). After accounting for the probability of detection, we found that 21% of birds banded as juveniles and recaptured as adults returned to their natal patches, whereas 78% of adult birds showed fidelity to the patch where they were originally captured. Moreover, natal dispersers tended to move farther than breeding dispersers (corrected natal median = 1.7 km ± 0.37; corrected breeding median = 0.23 km ± 0.10). We used our estimates of natal dispersal and annual apparent survival to estimate true survival at 0.11 (95% CI 0.07–0.18) for juveniles in their first year. However, this estimate was only applicable for birds dispersing within 7 km of their natal patches. Interpatch movements of radio‐marked Yellow‐breasted Chats were not uncommon, with 13 of 37 males located in more than one habitat patch. Overall, we observed low natal philopatry, but high adult site fidelity for shrubland birds in our study area. Considering the frequency of short‐distance movements observed (median = 531 m, range = 88–1045 m), clustering of patches within 1 km might facilitate use of shrubland habitat.     

DIFFERENTIAL MOVEMENTS BY HARBOR SEAL PUPS IN CONTRASTING ALASKA ENVIRONMENTS

Movement patterns of Alaska harbor seal pups were studied using satellite telemetry during 1997–2000. Mean tracking duration was 277.3 d (SD = 105.8) for Tugidak Island pups ( n = 26) and 171.2 d (108.3) for Prince William Sound (PWS) pups ( n = 27). Movements were similar for males and females and were largely restricted to the continental shelf. Multiple return trips of > 75 km from the natal area and up to ∼3 wk duration were most common, followed by movements restricted to <25 km from the natal area; one way movements from the natal site were rare. Distances moved and home range sizes remained relatively stable or increased gradually from July through winter, then decreased markedly through spring. Monthly movements (maximum distance from tagging location, mean distance from haul-outs to at-sea locations, and home range size) were significantly greater for Tugidak vs . PWS pups. Six of seven pups from each region that traveled farthest and were tracked the longest had returned to their tagging site when their last location was recorded, indicating philopatry or limited dispersal during their first year of life. Seal pups exhibited similar movement patterns in the distinct habitats of the two regions, but differed in the spatial extent of their movements.     

Dispersal,ranging and settling behaviour of Marsh Tits Poecile palustris in a fragmented landscape in lowland England

Capsule Natal dispersal was rapid and distances were short. Winter ranging and breeding dispersal were limited. Few birds undertook large movements.

Aims To investigate the natal and breeding dispersal of Marsh Tits, including the timing of dispersal movements.

Methods Nestlings, juveniles and adults were ringed and searched for over 4500 ha during summer, autumn–winter, and spring over six years. Dispersal distances were measured as metric distances and multiples of territory widths. Ranging distances were compared with dispersal distances.

Results Median distances of natal dispersal were 2.6 territory widths for males (704.5 m) and 3.1 territory widths for females (1065.0 m). Median distances of breeding dispersal were 0.2 territory widths for males and females (58.6 and 53.1 m respectively). Most natal dispersal was completed soon after independence, with further movement in spring. Breeding dispersal was also detected during these periods. Median ranging distances were short, and some winter floaters were identified.

Conclusion Marsh Tits had short dispersal distances, with most dispersal activity occurring in June. Results suggested that dispersal behaviour was sensitive to habitat fragmentation, resulting in poor settling success outside of the natal wood. Habitat fragmentation may, therefore, be a contributory factor in the decline of the Marsh Tit population in Britain.     

Role of breeding and natal movements in lifetime dispersal of a forest‐dwelling rodent

The lifetime movements of an individual determine the gene flow and invasion potential of the species. However, sex dependence of dispersal and selective pressures driving dispersal have gained much more attention than dispersal at different life and age stages. Natal dispersal is more common than dispersal between breeding attempts, but breeding dispersal may be promoted by resource availability and competition. Here, we utilize mark–recapture data on the nest‐box population of Siberian flying squirrels to analyze lifetime dispersal patterns. Natal dispersal means the distance between the natal nest and the nest used the following year, whereas breeding movements refer to the nest site changes between breeding attempts. The movement distances observed here were comparable to distances reported earlier from radio‐telemetry studies. Breeding movements did not contribute to lifetime dispersal distance and were not related to variation in food abundance or habitat patch size. Breeding movements of males were negatively, albeit not strongly, related to male population size. In females, breeding movement activity was low and was not related to previous breeding success or to competition between females for territories. Natal philopatry was linked to apparent death of a mother; that is, we did not find evidence for mothers bequeathing territories for offspring, like observed in some other rodent species. Our results give an example of a species in which breeding movements are not driven by environmental variability or nest site quality. Different evolutionary forces often operate in natal and breeding movements, and our study supports the view that juveniles are responsible for redistributing individuals within and between populations. This emphasizes the importance of knowledge on natal dispersal, if we want to understand consequences of movement ecology of the species at the population level.     

Natal dispersal in great bustards: the effect of sex, local population size and spatial isolation

1. We investigated the causes of natal dispersal in four Spanish areas where 35 breeding groups of the polygynous great bustard Otis tarda were monitored intensively. A total of 392 juveniles were radio-tracked between 1991 and 2006 by ground and via aeroplane to avoid potential biases derived from the non-detection of long-distance dispersers. 2. We explored 10 explanatory variables that were related to individual phenotypic features, habitat and conspecific traits in terms of group size and breeding performance, and spatial distribution of available breeding groups. Probability of group change and natal dispersal distances were investigated separately through multifactorial analyses. 3. Natal dispersal occurred in 47.8% of the birds and median natal dispersal distance of dispersers was 18.1 km (range 4.97-178.42 km). Sex largely determined the dispersal probability, with 75.6% of males being dispersers and 80.0% of females being philopatric, in contrast to the general pattern of female-biased dispersal found in most avian species. 4. Both the frequency of natal dispersal and dispersal distances were affected by the spatial distribution of breeding groups. More isolated groups showed a higher proportion of philopatric individuals, the effect being more evident in males than in females. This implies a reduction in gene flow in fragmented populations, as most genetic exchange is achieved through male dispersal. Additionally, dispersers hatched in more isolated groups tended to exhibit longer dispersal distances, which increases the associated energetic costs and mortality risks. 5. The dispersal decision was influenced by the number of conspecifics in the natal group. The individual probability of natal dispersal was related inversely to the size of the natal group, which supports the balanced dispersal model and the conspecific attraction hypothesis. 6. Overall, our results provide a good example of phenotypic plasticity and reinforce the current view that dispersal is an evolutionary complex trait conditioned by the interaction of individual, social and environmental causes that vary between individuals and populations.     

Radio-telemetric monitoring of dispersing stag beetles: implications for conservation

Migratory movements of the endangered stag beetles Lucanus cervus (18 males, 38 females) were monitored radio-telemetrically for three reproductive periods (2003–2005). The aim of the study was to estimate the migratory range of free-ranging individuals as a measure of connectivity among neighbouring populations for future conservation measures. Miniature transmitters of c . 350 mg (battery life: 10–15 days) were attached externally to the pronotum. Transmitter/beetle mass ratio was 12.8% on average (7.1–28.0%). Male dispersal behaviour consisted of frequent flights directed to sites with reproductive females and rarely of on-ground movement. Total displacement distance recorded was up to 2065 m, the maximum distance of a single flight being 1720 m. Flights always began at elevated structures such as trees and shrubs and took place in an air temperature range of 11–27°C. Within this range, temperature did not influence flight distance. Female dispersal behaviour consisted mostly of a single flight, followed by mating and consequent ground movements towards oviposition sites. Total displacement distance recorded was up to 762.6 m, the maximum distance of a single flight being 701 m. Climatic constraints of flights were the same as in males. Modelling the dispersal behaviour suggests that about 1% of males are capable of maintaining gene flux among nest sites within a radius of about 3 km. However, the colonization of new nest sites depends on the dispersal ability of females and amounts to less than 1 km. Thus, isolated populations (distance to the next population greater than 3 km) have an increased probability of local extinction.     

How do birds search for breeding areas at the landscape level? Interpatch movements of male ortolan buntings

Animal movements at large spatial scales are of great importance in population ecology, yet little is known due to practical problems following individuals across landscapes. We studied the whole Norwegian population of a small songbird (ortolan bunting, Emberiza hortulana ) occupying habitat patches dispersed over nearly 500 km². Movements of colour-ringed males were monitored during ten years, and extensive long-distance dispersal was recorded. More than half of all cases of breeding dispersal took place within one breeding season, and males moved up to 43 km between singing territories, using 1–22 d. Natal dispersal was usually to a habitat patch close to the natal patch, or within the natal patch if it was large. Breeding dispersal movements were often long-distance, beyond neighbouring patches, and up to 11–19 patches were overflown. Movements of at least 6–9 km across areas of unsuitable habitat occurred regularly. The number of patches visited was low (1–4) even though search costs in terms of time spent moving from one site to another were relatively low (often only a few days even for distances >10 km). Most males seemed to use a threshold tactic when choosing a patch, but returns to previously visited patches were recorded, including some cases of commuting. In conclusion, male ortolan buntings have a surprising ability to move quickly at the landscape level, and this resulted in a high connectivity of patches. We discuss our results in relation to optimal searching strategies, in particular the use of within-breeding season versus post-breeding season search, conspecific attraction and adaptive late arrival of young birds.     

Dispersal and migration of juvenile African Black Oystercatchers Haematopus moquini

African Black Oystercatchers Haematopus moquini are sedentary as adults. However, colour-ringing of more than 700 juveniles has revealed complex post-fledging movements that vary geographically. Young from the western part of the breeding range either remain within 150 km of their natal site or migrate 1500–2000 km to one of five discrete nursery areas on the Namib Desert coast of central and northern Namibia, and southern Angola. These nurseries all lie north of the species' breeding range. We calculate that 36–46% of all juveniles born in South Africa migrate to nurseries. Birds return to their natal sites from nurseries at 2–3 years old, but never migrate again. Juveniles from the eastern part of the range undertake 'diffusion dispersal', regularly up to 1000 km, but these journeys mostly end within the breeding range, where there are no nurseries. Very few eastern birds reach nurseries. There is no evidence that movements of western birds are density-dependent responses to hatching date, but long-distance migrants are significantly heavier as chicks than are short-distance dispersers. We hypothesize that a genetic basis exists to these movements, possibly triggered by body condition, that could account not only for the highly dichotomous behaviour of western birds, but also for the intermediate behaviour of eastern birds.     

Dispersal and migration of juvenile African Black Oystercatchers Haematopus moquini

African Black Oystercatchers Haematopus moquini are sedentary as adults. However, colour-ringing of more than 700 juveniles has revealed complex post-fledging movements that vary geographically. Young from the western part of the breeding range either remain within 150 km of their natal site or migrate 1500–2000 km to one of five discrete nursery areas on the Namib Desert coast of central and northern Namibia, and southern Angola. These nurseries all lie north of the species' breeding range. We calculate that 36–46% of all juveniles born in South Africa migrate to nurseries. Birds return to their natal sites from nurseries at 2–3 years old, but never migrate again. Juveniles from the eastern part of the range undertake 'diffusion dispersal', regularly up to 1000 km, but these journeys mostly end within the breeding range, where there are no nurseries. Very few eastern birds reach nurseries. There is no evidence that movements of western birds are density-dependent responses to hatching date, but long-distance migrants are significantly heavier as chicks than are short-distance dispersers. We hypothesize that a genetic basis exists to these movements, possibly triggered by body condition, that could account not only for the highly dichotomous behaviour of western birds, but also for the intermediate behaviour of eastern birds.     

Restricted dispersal in a long-distance migrant bird with patchy distribution,the great reed warbler

In patchily distributed species dispersal connects local populations into metapopulations. Reliable quantifications of dispersal are therefore crucial to understanding the population dynamics and genetic structure of such metapopulation systems. The great reed warbler (Acrocephalus arundinaceus) inhabits eutrophic lakes and has a patchy breeding distribution. In this study we investigated the dispersal pattern of the great reed warbler based on an extensive capture-recapture effort covering a large census area (22,500 km²). At two adjacent breeding sites (10 km apart) in southern Central Sweden, the "main study area", we ringed the majority of adult and nestling great reed warblers between 1992 and 1999. In 1998 and 1999, we opportunistically searched for territorial males at the majority of the Swedish breeding sites, and were able to examine about 56% of all males in the region. Analyses of recaptured males demonstrated that philopatry predominated. Sixty-nine percent of the recruiting nestlings returned to breed in the main study area (their natal area), and 92% of the resighted adults were found at the same breeding locality in both study years. Breeding dispersal was significantly more restricted than natal dispersal. Additional data on natal and breeding dispersal within the main study area in 1992-1999 suggested that females were as philopatric as males. The overall high level of philopatry, with only occasional longer dispersal distances documented, yielded a root-mean-square dispersal distance of 33 km per generation. High philopatry, short dispersal distances and similar dispersal patterns of male and female great reed warblers contrast the findings among birds in general, but conform to data of species having patchy breeding habitat and isolated populations. Restricted dispersal suggests limited gene flow even among several Swedish populations, which is in line with some previous findings of the population ecology of the great reed warbler: (1) structured mtDNA lineages among European populations; (2) small-scale population differences in song patterns; and (3) low genetic variation and occurrence of inbreeding depression in our main study population.     

Inversely density-dependent natal dispersal in brown bears Ursus arctos

There is considerable controversy in the literature about the presence of density dependence in dispersal. In this study, we exploit a data series from a long-term study (>18 years) on radio-marked brown bears (Ursus arctos L.) in two study areas in Scandinavia to investigate how individual-based densities influence the probability of natal dispersal and natal dispersal distances. Cumulatively, 32% and 46% of the females and 81% and 92% of the males dispersed before reaching 5 years of age in the northern and southern study area, respectively. Density had a negative effect on both the probability of dispersal and dispersal distances for the dispersing animals, when controlling for study area, sex and age, making this the first study to show that natal dispersal probability and distances are inversely density dependent in a large carnivore. We suggest that female–female competition for space caused females in higher density areas to settle closer to their natal area. For males, however, merging of demes, resulting in decreased relatedness and increased heterozygosity in an expanding population, might be the reason for shorter dispersal distances in males living at higher densities. This has been hypothesised for small mammals. The high proportion of dispersing female brown bears in Scandinavian compared with North American studies might be due to lower densities in Scandinavia and recent population expansion, with unoccupied areas available at the edges of the population. The longer dispersal distances in female Scandinavian brown bears suggest less social constraints on movements than for North American females. The longer dispersal distances by Scandinavian males may be due to increased searching for potential mates in peripheral areas with lower densities of females. These results, in addition to results of other brown bear studies, suggest that brown bears might be more territorial than previously thought, and that density is regulated by social interactions.     

Movement and dispersal patterns in the bush cricket Pholidoptera griseoaptera: the role of developmental stage and sex

Abstract.  1. To persist in a highly fragmented environment, such as the intensively used agricultural landscapes of Europe, species may need to successfully disperse between sub-populations. This paper describes a capture – mark – resight experiment to investigate movement and dispersal patterns of the flightless bush cricket species Pholidoptera griseoaptera .
2. Movement parameters showed little difference between juveniles and imagos as well as between males and females. Both developmental stages and sexes moved considerable distances, were cap\able of crossing habitat boundaries, and showed successful inter-patch dispersal through the agricultural matrix.
3. The results suggest that P. griseoaptera exhibits movement behaviours that compensate for its inability to fly. It was concluded that the good dispersal ability exhibited by animals of both sexes and developmental stage is an important factor allowing P. griseoaptera to persist in fragmented agricultural landscapes.     

Comparing red deer (Cervus elaphus L.) and wild boar (Sus scrofa L.) dispersal patterns in southern Belgium

This study analyses the natal dispersal of red deer and wild boar in order to compare their dispersal capabilities in southern Belgium and to evaluate the relevance of management unit areas (MUA) designed for their monitoring. Dispersal was studied thanks to a mark-recovery method based on 111 red deer fawns and 1,613 piglets. The recovery rate of ear-tagged animals was 68 and 40 %, respectively. In both species, sub-adult males moved on longer distances ( $ \mathop{x}\limits^{-} $ red deer?=?4.82+/?4.17 km and $ \mathop{x}\limits^{-} $ wild boar?=?4.90+/?5.65 km) than females and juveniles $ \mathop{x}\limits^{-} $ (red deer?=?1.84+/?1.46 km and $ \mathop{x}\limits^{-} $ wild boar?=?2.49+/?3.74 km). Taking into account the age and sex categories, we found no difference between species in dispersal mean distance. But we observed higher maximal dispersal distances in wild boar compared to red deer. The natal home range mean sizes were 5.29 km² (+/?4.87) for red deer and 6.23 km² (+/?4.60) for wild boar. Red deer and wild boar showed similar dispersal rates according to age and sex category: 53 and 42 % in sub-adult males and 14 and 16 % in females and juveniles. Our results confirmed the higher proportion of philopatry in females and juveniles of both species compared to sub-adult males more likely to disperse. Wild boar of any sex or age seemed to be less sensitive than red deer to infrastructure (road, rail, river) network on which the management unit area limits are currently based.     

Tracking Natal Dispersal in a Coastal Population of a Migratory Songbird Using Feather Stable Isotope (δ2H, δ34S) Tracers

Adult birds tend to show high fidelity to their breeding territory or disperse over relatively short distances. Gene flow among avian populations is thus expected to occur primarily through natal dispersal. Although natal dispersal is a critical demographic process reflecting the area over which population dynamics take place, low recapture rates of birds breeding for the first time have limited our ability to reliably estimate dispersal rates and distances. Stable isotope approaches can elucidate origins of unmarked birds and so we generated year- and age-specific δ²H and δ³⁴S feather isoscapes (ca. 180 000 km²) of coastal-breeding Ovenbirds (Seiurus aurocapilla) and used bivariate probability density functions to assign the likely natal areas of 35 males recruited as first-year breeders into a population located in northwestern New Brunswick, Canada. Most individuals (80–94% depending on the magnitude of an age correction factor used; i.e. 28–33 out of 35) were classified as residents (i.e. fledged within our study area) and estimated minimum dispersal distances of immigrants were between 40 and 240 km. Even when considering maximum dispersal distances, the likely origin of most first-year breeders was<200 km from our study area. Our method identified recruitment into our population from large geographic areas with relatively few samples whereas previous mark-recapture based methods have required orders of magnitude more individuals to describe dispersal at such geographic scales. Natal dispersal movements revealed here suggest the spatial scale over which many population processes are taking place and we suggest that conservation plans aiming to maintain populations of Ovenbirds and ecologically-similar species should consider management units within 100 or at most 200 km of target breeding populations.     

Female-biased natal and breeding dispersal in an alpine lizard, Niveoscincus microlepidotus

We measured two aspects of dispersal in the alpine Australian scincid lizard, Niveoscincus micolepidotus : (1) natal dispersal, i.e. shift in home range over the lizard's first year of life, and (2) breeding dispersal, i.e. shifts of home ranges between breeding attempts as adults. On average, displacements were surprisingly small. Female neonates dispersed about twice as far as did males in the same cohort (means of 12 m vs. 6 m). A female's natal dispersal distance was not correlated with her body size or our estimate of physiological performance (sprint speed). However, larger, faster-running male neonates dispersed further than did smaller, slower males. As was the case for neonates, adult females moved significantly further between breeding seasons than did adult males (14.2 m vs. 9.6 m). Because of a female's long gestation period (more than 1 year), two groups of females occur simultaneously in the population, non-ovulated (i.e. with yolking folicles) and pregnant females (i.e. approaching parturition). Females that were not yet ovulated showed a markedly stronger dispersal in response to high reproductive effort (i.e. clutch size in relation to body condition) than did pregnant females. In adult males, body size was negatively correlated with dispersal distance, suggesting that although males have overlapping territories, they exhibit an increasing level of site tenacity with age and/or size. Thus, selection for the relatively more pronounced site tenacity in adult males may have resulted in the more marked philopatric behaviour compared to females also as neonates.  © 2003 The Linnean Society of London, Biological Journal of the Linnean Society , 2003, 79 , 277–283.     

Limited dispersal by Nazca boobies Sula granti

We documented natal and breeding dispersal at several spatial scales by Galápagos Nazca boobies Sula granti , a wide-ranging pelagic seabird. We found exceptionally low degrees of both types of dispersal despite these birds' vagility. Median natal dispersal distances were 26 m and 105 m for males and females, respectively. Median breeding dispersal distances for both sexes were 0 m. No natal or breeding dispersals occurred from our study site at Punta Cevallos, Isla Española to six other colonies in the Galápagos, but we did document four long-distance natal dispersals from Punta Cevallos to islands near the South American coast. Recaptures and dead recoveries of ringed birds showed long distance non-breeding movements to the Central American coast and elsewhere in the eastern Pacific, contrasting with the very limited dispersal to breeding sites.