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Breeding Range (breeding + range)
Selected AbstractsPopulation structure and migratory directions of Scandinavian bluethroats Luscinia svecica, a molecular, morphological and stable isotope analysisECOGRAPHY, Issue 1 2008Olof Hellgren Many species of birds show evidence of secondary contact zones and subspeciation in their Scandinavian distribution range, presumably resulting from different post-glacial recolonization routes. We investigated whether this is the case also in the Scandinavian bluethroat Luscinia svecica, a species that has been suggested to consist of two separate populations: one SW-migrating and long-winged (L. s. gaetkei) breeding in southern Norway, and one shorter-winged ESE-migrating (L. s. svecica) in northern Scandinavia. We sampled males at eleven breeding sites from southern Norway to northernmost Sweden. There were no morphological differences or latitudinal trends within the sample, neither were there any genetic differences or latitudinal trends as measured by variation in AFLP and microsatellite markers. Stable isotope ratios of throat feathers moulted on the wintering grounds showed no, or possibly marginal differences between birds from southern Norway and northern Sweden. We also re-measured old museum skins that in previous studies were classified as L. s.gaetkei, and found marginally longer wings in birds from the southern part of the Scandinavian breeding range. The difference, however, was much smaller than proposed in earlier studies. We conclude that there is no evidence of a genetic population structure among Scandinavian bluethroats that would suggest the presence of a zone of secondary contact. Finally we discuss whether the presumed subspecies gaetkei ever existed. [source] The ability to mount multiple immune responses simultaneously varies across the range of the tree swallowECOGRAPHY, Issue 1 2007Daniel R. Ardia Variation in immune responses is an important part of life history variation. When correlations between multiple immune measures are reported, studies report different patterns. I tested whether the correlation between levels of immune response was consistent across a species range. The ability of tree swallows Tachycineta bicolor to simultaneously produce immune responses to both a humoral immune response and T-cell mediated local inflammation to PHA was tested at three sites that span the breeding range. Females in Tennessee maintained stronger PHA responses than did females in either New York or Alaska. In New York and Alaska, individuals that produced strong PHA responses produced low levels of antibodies to a humoral challenge of sheep red blood cells (SRBC). However, in Tennessee, individuals that showed strong local PHA inflammation also mounted strong responses to SRBC. Increasing daily daytime temperatures led to increased PHA response, but there were no differences in the effect of temperature among sites. These results indicate spatial and/or temporal variation occurs in the ability to produce multiple immune responses simultaneously; this pattern suggests important geographic (or temporal) differences in factors driving investment in immune activity. In addition, these results suggest that studies extrapolating results across populations should be careful to consider geographic variation in immune activity. [source] Effect of abiotic factors on reproduction in the centre and periphery of breeding ranges: a comparative analysis in sympatric harriersECOGRAPHY, Issue 4 2001J. T. García Variables such as weather or other abiotic factors should have a higher influence on demographic rates in border areas than in central areas, given that climatic adaptation might be important in determining range borders. Similarly, for a given area, the relationship between weather and reproduction should be dissimilar for species which are in the centre of their breeding range and those that are near the edge. We tested this hypothesis on two sympatric ground-nesting raptors, the hen harrier Circus cyaneus and the Montagu's harrier Circus pygargus in Madrid, central Spain, where the hen harrier is at the southern edge of its breeding range in the western Palearctic and the Montagu's harrier is central in its distribution. We examined the reproductive success of both species during an 8-yr period, and looked at the influence of the most stressful abiotic factors in the study area (between-year variation in rainfall and within-year variation in temperature) on reproductive parameters. In the hen harrier, low levels of rainfall during the breeding season had a negative influence on annual fledging success and thus on population fledgling production. The relationship between rainfall and reproduction was probably mediated through food abundance, which in Mediterranean habitat depends directly on rainfall levels. In the Montagu's harrier, no negative effect of dry seasons on productivity was found. Additionally, in the hen harrier, the proportion of eggs that did not hatch in each clutch increased with higher temperatures during the incubation period. No such relationship was found in the Montagu's harrier. We interpret these between-species differences in terms of differences of breeding range and adaptations to the average conditions existing there. Hen harriers, commonest at northern latitudes, are probably best adapted to the most typical conditions at those latitudes, and have probably not developed thermoregulatory or behavioural mechanisms to cope with drought and high temperatures in Mediterranean habitats, in contrast to Montagu's harrier. Thus hen harrier distribution might be constrained by these variables, due to lower reproductive success or higher reproductive costs. Accordingly, a logistic regression analysis of the presence or absence of both species in 289 random points throughout the western Palearctic showed that the distribution of both species was related to temperature, but the relationship was in opposite directions for the two species: hen harriers had lower probability of breeding in areas with higher temperature (as expected in a species with a more northerly distribution). [source] Mating Call Discrimination in Female European (Coturnix c. coturnix) and Japanese Quail (Coturnix c. japonica)ETHOLOGY, Issue 2 2003Sébastien Derégnaucourt Each year, thousands of domestic Japanese and hybrid quails are released within the breeding range of the European quail. We showed recently that no post-zygotic isolating mechanisms have yet been established between these subspecies. The aim of this study was to investigate whether pre-zygotic mechanisms are strong enough to prevent hybridization. We tested the level of subspecies selectivity in females of European and Japanese quail respectively using playbacks of European, hybrid and Japanese male mating calls. European quail females emitted the greatest number of rally calls in response to mating calls by conspecific males. Their responses were the weakest to mating calls produced by males of the other subspecies and intermediate to mating calls by hybrid males. In contrast, Japanese quails produced similar responses to all types of mating calls. These results suggest that mixed pairs could form in the wild. The European quail could thus become one of the most endangered galliforms of the Western Palearctic. [source] Habitat selection by Ortolan Buntings Emberiza hortulana in post-fire succession in Catalonia: implications for the conservation of farmland populationsIBIS, Issue 4 2009MYLES H. M. MENZ The Ortolan Bunting Emberiza hortulana is a long-distance migrant that has suffered major population declines across much of its European breeding range. While northern populations are bound largely to farmland, Mediterranean populations are largely confined to habitats subject to recurrent wildfires. Habitat selection of the Ortolan Bunting was assessed in a recently burnt area in Catalonia at landscape and habitat scales. A Zero-inflated Poisson procedure was used to model the abundance of birds in relation to landscape and habitat variables. The most parsimonious landscape model predicted the highest abundance on south-facing slopes, with a gradient above 10°. The most parsimonious habitat model showed a positive quadratic effect of bare ground and regenerating oak Quercus spp., with predicted optima for abundance around 20,30% and 20% cover, respectively. There was a clear relationship between predicted abundance of the Ortolan Bunting and post-fire regenerating oak shrubs. South-facing, moderately sloping areas were favoured and bare ground was a key feature of the species' habitat. A matrix combining patches of sparse oak shrubs and patches of bare ground appears to be the optimal breeding habitat in the Mediterranean. The maintenance or provision of similar habitat features, especially patches of bare ground, may prove crucial for the conservation of rapidly declining Ortolan Bunting populations on farmland across temperate Europe. [source] Is nest-site availability limiting Lesser Kestrel populations?IBIS, Issue 4 2005A multiple scale approach The Lesser Kestrel, a colonial migratory falcon, is one of the most endangered birds in Europe and, due to a sharp population decline across much of the breeding range, is globally threatened. The reasons for this decline are unclear, but reduced nest-site availability might be a major cause. To test this hypothesis we looked at nest-site availability within Portuguese colonies in rural and urban buildings. Nest holes were larger, longer, higher and older than unoccupied cavities. A typical nest cavity was approximately 29,30 cm long, 300,340 cm high and had an inner chamber 16.5,18 cm wide. Large-scale surveys of existing buildings in Portuguese villages suggested that 85% of sites lacked suitable nest cavities. The model for selection of buildings indicated that Lesser Kestrels prefer buildings with many roof and wall cavities, and that are surrounded by extensive cereal and fallow fields. The villages selected had many old buildings and monuments, were located in areas with few rivers, and a low percentage cover of cereal, olive groves and forest. The conservation implications of these results are discussed. [source] Dispersal and migration of juvenile African Black Oystercatchers Haematopus moquiniIBIS, Issue 3 2003Philip A. R. Hockey 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. [source] Metabolic correlates of leg length in breeding arctic shorebirds: the cost of getting highJOURNAL OF BIOGEOGRAPHY, Issue 3 2005Ralph V. Cartar Abstract Aim, We test the hypothesis that tarsus length in all shorebirds breeding in the Canadian arctic shows an evolutionary response to average metabolic stress encountered across the breeding range, such that birds nesting in metabolically stressful environments have relatively shorter legs. Longer-legged birds living in colder environments will experience greater metabolic costs because their torsos are elevated farther away from the ground's wind-dampening boundary layer. Methods, We use weather data (temperature, wind speed, global solar radiation) from 27 arctic weather stations measured over 37 years, and a previously published model of heat transfer, to characterize the metabolic harshness over the breeding season of the ranges of each of the 17 shorebirds of the family Charadriidae nesting in the Canadian arctic. Results, After controlling for the lengths of two other body extremities (wing and bill), there was a significant negative relationship between tarsus length and mean metabolic harshness. This result was obtained whether species were treated as independent data points, or in a comparative analysis using standardized independent contrasts. Main conclusions, We support a unique extension of Allen's rule: body-supporting appendages of homeotherms may be shorter in colder environments so as to take advantage of a boundary layer effect, thereby reducing metabolic costs. [source] Genetic divergence and migration patterns in a North American passerine bird: implications for evolution and conservationMOLECULAR ECOLOGY, Issue 8 2006LESLIE A. DAVIS Abstract Like many other migratory birds, the black-throated blue warbler (Dendroica caerulescens) shows pronounced differences in migratory behaviour and other traits between populations: birds in the southern part of the breeding range have darker plumage and migrate to the eastern Caribbean during the winter, whereas those in the north have lighter plumage and migrate to the western Caribbean. We examined the phylogeography of this species, using samples collected from northern and southern populations, to determine whether differentiation between these populations dates to the Pleistocene or earlier, or whether differences in plumage and migratory behaviour have arisen more recently. We analysed variation at 369 bp of the mitochondrial control region domain I and also at seven nuclear microsatellites. Analyses revealed considerable genetic variation, but the vast majority of this variation was found within rather than between populations, and there was little differentiation between northern and southern populations. Phylogeographic analyses revealed a very shallow phylogenetic tree, a star-like haplotype network, and a unimodal mismatch distribution, all indicative of a recent range expansion from a single refugium. Coalescent modelling approaches also indicated a recent common ancestor for the entire group of birds analysed, no split between northern and southern populations, and high levels of gene flow. These results show that Pleistocene or earlier events have played little role in creating differences between northern and southern populations, suggesting that migratory and other differences between populations have arisen very recently. The implications of these results for the evolution of migration and defining taxonomic groups for conservation efforts are discussed. [source] Winter commingling of populations of migratory species can cause breeding range underpopulationOIKOS, Issue 12 2007Alexander M. Mills We build a model with large-scale demographic consequences for migratory species. The model operates where four elements co-occur, and we rely on empirical research using migratory birds to demonstrate them. First, breeding ranges have internal structure flowing from natal philopatry. Second, fecundity varies geographically. Third, populations of different breeding provenances commingle during winter. And fourth, a population-limiting carrying capacity operates during winter. In the absence of breeding season population-limitation, only the breeding population with maximum fecundity persists. Consequently, some potential breeding areas that offer suitable and productive habitat are bereft of breeding birds because of the interplay between the geographical fecundity gradient and the shared winter quarters. Where breeding season population-limitation also plays a role for at least one population, one (or more) breeding population becomes permanently depressed, resulting in a density well below the carrying capacity of the productive breeding habitat that is occupied. In either case, not all populations fare equally well, despite net positive breeding season productivity. Changes in winter carrying capacity, for example habitat degradation in winter quarters, can lead to uneven effects on geographically defined breeding populations, even though there has been no change in the circumstances of the breeding range. [source] Process in the evolution of bird migration and pattern in avian ecogeographyJOURNAL OF AVIAN BIOLOGY, Issue 2 2000Christopher P. Bell Current ideas about the evolution of bird migration equate its origin with the first appearance of fully migratory populations, and attribute its evolution to a selective advantage generated by increased breeding success, gained through temporary emigration from resident populations to breed in under-exploited seasonal areas. I propose an alternative hypothesis in which migration first appears as a temporary directional shift away from the breeding site outside the reproductive period, in response to seasonal variation in the direction and/or severity of environmental gradients. Fully migratory populations then appear through either extinction of sedentary phenotypes, or colonisation of vacant seasonal areas by migrants. Where colonisation occurs, resident ancestral populations can be driven to extinction by competition from migrants which invade their range outside the breeding season, resulting in fully migratory species. An analogous process drives the evolution of migration between high latitudes and the tropics, since extension of breeding range into higher latitudes may drive low latitude populations to extinction, resulting in an overall shift of breeding range. This process can explain reverse latitudinal gradients in avian diversity in the temperate zone, since the breeding ranges of migratory species concentrate in latitudes where they enjoy the highest breeding success. Near absence of forest-dwelling species among Palaearctic-African migrants is attributable to the lack of forest in northern Africa for much of the Tertiary, which has precluded selection both for southward extension of migration by west Palaearctic forest species, and northward breeding colonisation by African forest species. [source] The role of migration for spatial turnover of arctic bird species in a circumpolar perspectiveOIKOS, Issue 11 2008Sara Henningsson Several different factors may determine where species range limits are located within regions of otherwise continuously available habitat and suitable climate. Within the Arctic tundra biome many bird species are migratory and their breeding distributions are affected by migration routes that are in turn limited by factors such as suitable winter habitat, migratory stopover sites, geographical barriers and historical routes of colonization. We identified longitudinal zones in the circumpolar Arctic of pronounced changes in the avian species composition (high species spatial turnover; ,species divides'). We tested for the association between migratory status and the geographical location and numbers of such species divides for species with non-breeding habitats mainly within terrestrial, pelagic and coastal ecosystems. Our results demonstrate that migration is of profound importance for both the number and locations of species divides in the Arctic. Long-distance migration is associated with a large number of divides among terrestrial and coastal arctic birds but with a reduced number of divides among pelagic birds. We suggest that long-distance migration permits pelagic but not terrestrial and coastal birds to colonize large winter ranges, which in turn causes expansion of breeding ranges, with more homogenous communities and reduction of species divides as consequences, among the long-distance migrants of pelagic but not of terrestrial and coastal birds. Furthermore, the divides among long-distance migrants are situated in two main regions, the Beringia and Greenland zones, while divides among short-distance migrants are more evenly spaced throughout the circumpolar Arctic. The Beringia and Greenland divides result largely from inter-continental colonization of new breeding ranges but retainment of original winter quarters in a process of evolution through extension of migration routes, leading to aggregated divides in the meeting zones of major global flyways. [source] | |||||||||||||||||||