Crosswise migration by Yellow Warblers,Nearctic‐Neotropical passerine migrants

Yellow Warblers (Setophaga petechia) are abundant breeding birds in North America, but their migratory and non‐breeding biology remain poorly understood. Studies where genetic and isotopic techniques were used identified parallel migration systems and longitudinal segregation among eastern‐ and western‐breeding populations of Yellow Warblers in North America, but these techniques have low spatial resolution. During the 2015 breeding season, we tagged male Yellow Warblers breeding in Maine (N = 10) and Wisconsin (N = 10) with light‐level geolocators to elucidate fine‐scale migratory connectivity within the eastern haplotype of this species and determine fall migration timing, routes, and wintering locations. We recovered seven of 20 geolocators (35%), including four in Maine and three in Wisconsin. The mean duration of fall migration was 49 d with departure from breeding areas in late August and early September and arrival in wintering areas in mid‐October. Most individuals crossed the Gulf of Mexico to Central America before completing the final eastward leg of their migration to northern South America. Yellow Warblers breeding in Maine wintered in north‐central Colombia, west of those breeding in Wisconsin that wintered in Venezuela and the border region between Brazil, Colombia, and Venezuela. Our results provide an example of crosswise migration, where the more easterly breeding population wintered farther west than the more westerly breeding population (and vice versa), a seldom‐documented phenomenon in birds. Our results confirm earlier work demonstrating that the eastern haplotype of northern Yellow Warblers winters in northern South America, and provide novel information about migratory strategies, timing, and wintering locations of birds from two different populations.     

Around the Mediterranean: an extreme example of loop migration in a long‐distance migratory passerine

An important issue in migration research is how small‐bodied passerines pass over vast geographical barriers; in European–African avian migration, these are represented by the Mediterranean Sea and the Sahara Desert. Eastern (passing eastern Mediterranean), central (passing Apennine Peninsula) and western (via western Mediterranean) major migration flyways are distinguished for European migratory birds. The autumn and spring migration routes may differ (loop migration) and there could be a certain level of individual flexibility in how individuals navigate themselves during a single migration cycle. We used light‐level loggers to map migration routes of barn swallows Hirundo rustica breeding in the centre of a wide putative contact zone between the northeastern and southernwestern European populations that differ in migration flyways utilised and wintering grounds. Our data documented high variation in migration patterns and wintering sites of tracked birds (n = 19 individuals) from a single breeding colony, with evidence for loop migration in all but one of the tracked swallows. In general, two migratory strategies were distinguished. In the first, birds wintering in a belt stretching from southcentral to southern Africa that used an eastern route for both the spring and autumn migration, then shifted their spring migration eastwards (anti‐clockwise loops, n = 12). In the second, birds used an eastern or central route to their wintering grounds in central Africa, shifting the spring migration route westward (clockwise loops, n = 7). In addition, we observed an extremely wide clockwise loop migration encompassing the entire Mediterranean, with one individual utilising both the eastern (autumn) and western (spring) migratory flyway during a single annual migration cycle. Further investigation is needed to ascertain whether clockwise migratory loops encircling the entire Mediterranean also occur other small long‐distance passerine species.     

Searching for potential wintering and migration areas of a Danish Barn Swallow population in South Africa by correlating NDVI with survival estimates

On the basis of correlation analyses between annual Normalised Difference Vegetation Index (NDVI) values in Africa and the annual survival rate estimated for a breeding population of barn swallows Hirundo rustica from Denmark, we identified potential wintering and migration areas in South Africa during December–February and March–May, when barn swallows commonly occur in South Africa. During December–February we identified potential wintering areas only in the western part of South Africa, in the Karoo. Potential areas in the central and eastern parts of the country were only identified during March–May. NDVI values in the Karoo during March–May explained most of the variance in annual adult survival rate of the population. The high ratio of European ringed barn swallows among controlled individuals in the Karoo was similar to the ratio that would be expected based on the number of ringed barn swallows and the population sizes of barn swallows in north-western European breeding populations. The level of this ratio in the Karoo was higher than in any other locality in the central and eastern parts of South Africa and Botswana, indicating that ringed birds from the eastern flyway are absent to a much smaller extent than ringed birds from the western flyway. This approach shows that the NDVI and survival method can focus ringing efforts to regions and areas that are likely to harbour specific breeding populations, thereby helping to identify potential wintering and migration areas for breeding populations of migratory birds.     

The pull of the Central Flyway? Veeries breeding in western Canada migrate using an ancestral eastern route

Understanding non‐breeding season movements and identifying wintering areas of different populations of migratory birds is important for establishing patterns of migratory connectivity over the annual cycle. We analyzed archival solar geolocation (N = 5) and global positioning data (N = 1) to investigate migration routes, stopover sites, and wintering areas of a western‐most breeding population of Veeries (Catharus fuscescens) in the Pemberton Valley, British Columbia, Canada. Geolocation data were analyzed using a Bayesian state‐space model to improve likely position estimates. We compared our results with those from a Veery population located ~250 km east across a mountain chain in the Okanagan Valley, British Columbia, and with an eastern population in Delaware, U.S.A. Migrating Veeries from the Pemberton Valley used an eastern trajectory through the Rocky Mountains to the Great Plains to join a central flyway during fall and spring migration, a route similar to that used by Veeries breeding in the Okanagan Valley. However, wintering destinations of Pemberton Valley birds were more varied, with inter‐individual wintering distances ~1000 km greater than birds from the Okanagan Valley population and ~500 km from the previously known winter range of Veeries. The observed eastern migration path likely follows an ancestral route that evolved following the most recent glacial retreat. Consistent with patterns observed from the Okanagan and Delaware populations, Veeries from the Pemberton Valley undertook an intra‐tropical migration on the wintering grounds, but this winter movement differed from those of previously studied populations. Such winter movements may thus be idiosyncratic or show coarse population associations. Intra‐wintering‐ground movements likely occur either in response to seasonal changes in habitat suitability or as a means of optimizing pre‐migratory fueling prior to long‐distance spring movements to North America.     

Dramatic intraspecific differences in migratory routes,stopover sites and wintering areas,revealed using light-level geolocators

Migratory divides are contact zones between breeding populations that use divergent migratory routes and have been described in a variety of species. These divides are of major importance to evolution, ecology and conservation but have been identified using limited band recovery data and/or indirect methods. Data from band recoveries and mitochondrial haplotypes suggested that inland and coastal Swainson''s thrushes (Catharus ustulatus) form a migratory divide in western North America. We attached light-level geolocators to birds at the edges of this contact zone to provide, to our knowledge, the first direct test of a putative divide using data from individual birds over the entire annual cycle. Coastal thrushes migrated along the west coast to Mexico, Guatemala and Honduras. Some of these birds used multiple wintering sites. Inland thrushes migrated across the Rocky Mountains, through central North America to Columbia and Venezuela. These birds migrated longer distances than coastal birds and performed a loop migration, navigating over the Gulf of Mexico in autumn and around this barrier in spring. These findings support the suggestion that divergent migratory behaviour could contribute to reproductive isolation between migrants, advance our understanding of their non-breeding ecology, and are integral to development of detailed conservation strategies for this group.     

Accipiter hawks of the Laurentian Upland and the Interior Plains undertake the longest migrations: insights from birds banded or recovered in Veracruz,Mexico

Bird banding has allowed us to understand diverse aspects of the life histories of migratory raptors. However, most banding stations are located at northern latitudes so what we know about the movements of these raptors is biased toward higher latitudes, primarily from Canada and the United States, leaving important gaps in our knowledge of their movements at lower latitudes. Our objective was to describe the migratory movements of Sharp-shinned (Accipiter striatus) and Cooper’s (A. cooperii) hawks based on banding and recapture records of birds that migrate through Veracruz, Mexico. More specifically, we sought to determine their breeding, migration, and non-breeding locations, estimate their migration distances, and contribute to a better understanding of their migration patterns. With a total of 80 records, we calculated migration distances and used Kernel Density Estimation analyses to identify where these hawks were recaptured or recovered by season. The distribution of recaptures and recoveries largely coincided with breeding locations in the Laurentian Upland and the Interior Plains physiographic regions. All migration records follow a trajectory that extends from the midwestern United States to the Gulf coastal plain of Mexico. The mean breeding season migration distance to Veracruz was 3374 km (a difference of 27 degrees of latitude) for Sharp-shinned Hawks and 2926 km (a difference of 25 degrees of latitude) for Cooper’s Hawks. Our non-breeding records indicate that populations of Accipiter hawks from these North American populations migrate the longest distances to reach Central America, the southernmost distribution of their migratory populations. Distances covered by both species represent round-trip migrations that may be as long as 10,000 km. Our results support those of previous studies and illustrate how continental physiography influences the migration routes, migratory behavior, and migratory connectivity of these hawks.     

Geolocator tagging reveals Pacific migration of Red‐necked Phalarope Phalaropus lobatus breeding in Scotland

The migration route of Red‐necked Phalarope populations breeding on North Atlantic islands has been subject to considerable speculation. Geolocator tags were fitted to nine Red‐necked Phalaropes breeding in northern Scotland to assess whether they migrated to Palaearctic or Nearctic wintering grounds. Of four birds known to return, two had retained their tags, of which one was recaptured. This male Phalarope left Shetland on 1 August 2012 and crossed the Atlantic Ocean to the Labrador Sea off eastern Canada in 6 days, then moved south to reach Florida during September, crossed the Gulf of Mexico into the Pacific Ocean and reached an area between the Galapagos Islands and the South American coast by mid‐October, where it remained until the end of April, returning by a similar route until the tag battery failed as the bird was crossing the Atlantic Ocean. The total migration of 22 000 km is approximately 60% longer than the previously assumed route to the western part of the Arabian Sea, and this first evidence of migration of a European breeding bird to the Pacific Ocean also helps to indicate the possible migratory route of the large autumn movements of Red‐necked Phalaropes down the east coast of North America.     

Continent-wide tracking to determine migratory connectivity and tropical habitat associations of a declining aerial insectivore

North American birds that feed on flying insects are experiencing steep population declines, particularly long-distance migratory populations in the northern breeding range. We determine, for the first time, the level of migratory connectivity across the range of a songbird using direct tracking of individuals, and test whether declining northern populations have higher exposure to agricultural landscapes at their non-breeding grounds in South America. We used light-level geolocators to track purple martins, Progne subis, originating from North American breeding populations, coast-to-coast (n = 95 individuals). We show that breeding populations of the eastern subspecies, P. s. subis, that are separated by ca. 2000 km, nevertheless have almost completely overlapping non-breeding ranges in Brazil. Most (76%) P. s. subis overwintered in northern Brazil near the Amazon River, not in the agricultural landscape of southern Brazil. Individual non-breeding sites had an average of 91 per cent forest and only 4 per cent agricultural ground cover within a 50 km radius, and birds originating from declining northern breeding populations were not more exposed to agricultural landscapes than stable southern breeding populations. Our results show that differences in wintering location and habitat do not explain recent trends in breeding population declines in this species, and instead northern populations may be constrained in their ability to respond to climate change.     

Lack of genetic differentiation between monarch butterflies with divergent migration destinations

Monarch butterflies are best known for their spectacular annual migration from eastern North America to Mexico. Monarchs also occur in the North American states west of the Rocky Mountains, from where they fly shorter distances to the California Coast. Whether eastern and western North American monarchs form one genetic population or are genetically differentiated remains hotly debated, and resolution of this debate is essential to understand monarch migration patterns and to protect this iconic insect species. We studied the genetic structure of North American migratory monarch populations, as well as nonmigratory populations in Hawaii and New Zealand. Our results show that eastern and western migratory monarchs form one admixed population and that monarchs from Hawaii and New Zealand have genetically diverged from North American butterflies. These findings suggest that eastern and western monarch butterflies maintain their divergent migrations despite genetic mixing. The finding that eastern and western monarchs form one genetic population also suggests that the conservation of overwintering sites in Mexico is crucial for the protection of monarchs in both eastern and western North America.     

Assessing migration patterns of sharp-shinned hawks Accipiter striatus using stable-isotope and band encounter analysis

Intraspecific migration patterns in birds have both spatial and temporal components. Two commonly reported spatial patterns are leap-frog and chain migration. Temporal migration patterns refer to the timing of migration of populations from different breeding latitudes. We investigated the spatial and temporal migration patterns of hatching-year (HY) sharp-shinned hawks Accipiter striatus of interior North America using stable-hydrogen isotope and band encounter analyses. Feather samples were collected from hawks migrating through New Mexico, USA and measured for their stable-hydrogen isotope ratios (δD) to distinguish individuals originating from relatively high and low natal latitudes. We then examined the relationship between feather δD values and passage dates through New Mexico, USA. We also gathered band encounter data from the Bird Banding Lab of the United States Geological Survey to determine the wintering latitudes of HY sharp-shinned hawks relative to their passage date through migration banding sites in interior North America. Combining these data, we found that during fall migration HY sharp-shinned hawks used a chain migration pattern, that is, hawks originating from lower latitudes wintered further south than those from higher latitudes. In addition, birds originating from lower latitudes passed through interior North America earlier than those from higher latitudes. We also found that hawks from higher latitudes were significantly larger than those from lower latitudes, and that females from higher latitudes had significantly higher estimated fat levels than females from lower latitudes.     

High juvenile mortality during migration in a declining population of a long‐distance migratory raptor

Many populations of long‐distance migrants are declining and there is increasing evidence that declines may be caused by factors operating outside the breeding season. Among the four vulture species breeding in the western Palaearctic, the species showing the steepest population decline, the Egyptian Vulture Neophron percnopterus, is a long‐distance migrant wintering in Africa. However, the flyways and wintering areas of the species are only known for some populations, and without knowledge of where mortality occurs, effective conservation management is not possible. We tracked 19 juvenile Egyptian Vultures from the declining breeding population on the Balkan Peninsula between 2010 and 2014 to estimate survival and identify important migratory routes and wintering areas for this species. Mortality during the first autumn migration was high (monthly survival probability 0.75) but mortality during migration was exclusively associated with suboptimal navigation. All birds from western breeding areas and three birds from central and eastern breeding areas attempted to fly south over the Mediterranean Sea, but only one in 10 birds survived this route, probably due to stronger tailwind. All eight birds using the migratory route via Turkey and the Middle East successfully completed their first autumn migration. Of 14 individual and environmental variables examined to explain why juvenile birds did or did not successfully complete their first migration, the natal origin of the bird was the most influential. We speculate that in a declining population with fewer experienced adults, an increasing proportion of juvenile birds are forced to migrate without conspecific guidance, leading to high mortality as a consequence of following sub‐optimal migratory routes. Juvenile Egyptian Vultures wintered across a vast range of the Sahel and eastern Africa, and had large movement ranges with core use areas at intermediate elevations in savannah, cropland or desert. Two birds were shot in Africa, where several significant threats exist for vultures at continental scales. Given the broad distribution of the birds and threats, effective conservation in Africa will be challenging and will require long‐term investment. We recommend that in the short term, more efficient conservation could target narrow migration corridors in southern Turkey and the Middle East, and known congregation sites in African wintering areas.     

Energy reserves stored by migrating Gray‐cheeked Thrushes Catharus minimus at a spring stopover site in northern Colombia are sufficient for a long‐distance flight to North America

Stopover sites used to accumulate the energy that fuels migration, especially those used prior to crossing ecological barriers, are regarded as critically important for the survival of Nearctic?Neotropical migratory birds. To assess whether South American stopover sites are used to store the energy required to cross the Caribbean Sea and the Gulf of Mexico to North America by a Neotropical migratory landbird, we studied Gray‐cheeked Thrushes in northern Colombia through constant effort mist‐netting during spring migration in 2010 and 2011. We combined stopover duration estimates and models of body mass change based on recaptures to estimate departure body mass and potential flight range from our study site. We recaptured 62 birds, the majority of which gained mass. Models indicated significant differences in rates of mass gain between years and age groups and with arrival date. Estimated total stopover durations varied between 15.4 (2010) and 12.5 days (2011). Predicted departure mass ranged between 41.3 and 44.9 g, and potential flight range was estimated at between 2727 and 4270 km. Gray‐cheeked Thrushes therefore departed our study site with sufficient energy reserves to cross the Caribbean Sea and the Gulf of Mexico (2550 km). As the first demonstration that birds departing from South American stopover sites can reach North America without refuelling, this has important implications for stopover site protection. Strategic conservation measures in the Sierra Nevada de Santa Marta could protect habitats in which up to 40% of the energy required to complete spring migration is stored by a Neotropical migratory land bird.     

Population structure of Purple Sandpipers (Calidris maritima) as revealed by mitochondrial DNA and microsatellites

The Purple Sandpiper (Calidris maritima) is a medium‐sized shorebird that breeds in the Arctic and winters along northern Atlantic coastlines. Migration routes and affiliations between breeding grounds and wintering grounds are incompletely understood. Some populations appear to be declining, and future management policies for this species will benefit from understanding their migration patterns. This study used two mitochondrial DNA markers and 10 microsatellite loci to analyze current population structure and historical demographic trends. Samples were obtained from breeding locations in Nunavut (Canada), Iceland, and Svalbard (Norway) and from wintering locations along the coast of Maine (USA), Nova Scotia, New Brunswick, and Newfoundland (Canada), and Scotland (UK). Mitochondrial haplotypes displayed low genetic diversity, and a shallow phylogeny indicating recent divergence. With the exception of the two Canadian breeding populations from Nunavut, there was significant genetic differentiation among samples from all breeding locations; however, none of the breeding populations was a monophyletic group. We also found differentiation between both Iceland and Svalbard breeding populations and North American wintering populations. This pattern of divergence is consistent with a previously proposed migratory pathway between Canadian breeding locations and wintering grounds in the United Kingdom, but argues against migration between breeding grounds in Iceland and Svalbard and wintering grounds in North America. Breeding birds from Svalbard also showed a genetic signature intermediate between Canadian breeders and Icelandic breeders. Our results extend current knowledge of Purple Sandpiper population genetic structure and present new information regarding migration routes to wintering grounds in North America.     

Connectivity in piping plovers: Do breeding populations have distinct winter distributions?

Resightings of uniquely marked birds from 2001 to 2008 were used to determine winter distributions of 4 breeding populations of a species at risk, the piping plover (Charadrius melodus). Although considerable overlap exists, a distinct pattern in winter distributions was evident. Birds originating from eastern Canada wintered farthest north compared to other populations. Most individuals from the United States Great Lakes were found in South Carolina and Georgia in winter, whereas birds from eastern Canada were found primarily in North Carolina. Although the great majority of birds marked in Prairie Canada were observed wintering in Texas, particularly southern Texas, breeding plovers from the United States Great Plains were more widely distributed on the gulf coast from Florida to Texas. Very few large-scale movements of individuals in winter were reported either within or between years. This study highlights the significance of geographic regions for eastern Canada, the United States Great Lakes, the United States Great Plains, and Prairie Canada populations, and demonstrates relatively high winter site fidelity. This information will help focus conservation efforts for specific breeding populations during the winter. © 2011 The Wildlife Society.     

Migratory movements and wintering areas of Leach's Storm‐Petrels tracked using geolocators

Accumulating evidence suggests that Atlantic populations of Leach's Storm‐Petrels (Oceanodroma leucorhoa) are experiencing significant declines. To better understand possible causes of these declines, we used geolocators to document movements of these small (～50‐g) pelagic seabirds during migration and the non‐breeding period. During 2012 and 2013, movement tracks were obtained from two birds that traveled in a clock‐wise direction from two breeding colonies in eastern Canada (Bon Portage Island, Nova Scotia, and Gull Island, Newfoundland) to winter in tropical waters. The bird from Bon Portage Island started its migration towards Cape Verde in October, arrived at its wintering area off the coast of eastern Brazil in January, and started migration back to Nova Scotia in April. The bird from Gull Island staged off Newfoundland in November and then again off Cape Verde in January before its geolocator stopped working. Movements of Leach's Storm‐Petrels in our study and those of several other procellariiforms during the non‐breeding period are likely facilitated by the prevailing easterly trade winds and the Antilles and Gulf Stream currents. Although staging and wintering areas used by Leach's Storm‐Petrels in our study were characterized by low productivity, the West Africa and northeastern Brazilian waters are actively used by fisheries and discards can attract Leach's Storm‐Petrels. Our results provide an initial step towards understanding movements of Leach's Storm‐Petrels during the non‐breeding period, but further tracking is required to confirm generality of their migratory routes, staging areas, and wintering ranges.     

Light‐level geolocators reveal migratory connectivity in European populations of pied flycatchers Ficedula hypoleuca

Understanding what drives or prevents long‐distance migrants to respond to environmental change requires basic knowledge about the wintering and breeding grounds, and the timing of movements between them. Both strong and weak migratory connectivity have been reported for Palearctic passerines wintering in Africa, but this remains unknown for most species. We investigated whether pied flycatchers Ficedula hypoleuca from different breeding populations also differ in wintering locations in west‐Africa. Light‐level geolocator data revealed that flycatchers from different breeding populations travelled to different wintering sites, despite similarity in routes during most of the autumn migration. We found support for strong migratory connectivity showing an unexpected pattern: individuals breeding in Fennoscandia (S‐Finland and S‐Norway) wintered further west compared to individuals breeding at more southern latitudes in the Netherlands and SW‐United Kingdom. The same pattern was found in ring recovery data from sub‐Saharan Africa of individuals with confirmed breeding origin. Furthermore, population‐specific migratory connectivity was associated with geographical variation in breeding and migration phenology: birds from populations which breed and migrate earlier wintered further east than birds from ‘late’ populations. There was no indication that wintering locations were affected by geolocation deployment, as we found high repeatability and consistency in δ¹³C and δ¹⁵N stable isotope ratios of winter grown feathers of individuals with and without a geolocator. We discuss the potential ecological factors causing such an unexpected pattern of migratory connectivity. We hypothesise that population differences in wintering longitudes of pied flycatchers result from geographical variation in breeding phenology and the timing of fuelling for spring migration at the wintering grounds. Future research should aim at describing how temporal dynamics in food availability across the wintering range affects migration, wintering distribution and populations’ capacity to respond to environmental changes.     

Seasonal variation in the regulation of redox state and some biotransformation enzyme activities in the barn swallow (Hirundo rustica L.)

Little is known of the normal seasonal variation in redox state and biotransformation activities in birds. In long-distance migratory birds, in particular, seasonal changes could be expected to occur because of the demands of migration and reproduction. In this study, we measured several redox parameters in the barn swallow (Hirundo rustica L.) during the annual cycle. We captured the wintering barn swallows before spring migration in South Africa, and we captured the barn swallows that arrived in spring, bred in summer, and migrated in autumn in Finland. The redox status and biotransformation activities of barn swallows varied seasonally. Wintering birds in South Africa had high biotransformation activities and appeared to experience oxidative stress, whereas in spring and summer, they showed relatively low redox (superoxide dismutase [SOD], catalase [CAT], and glutathione reductase [GR]) and biotransformation enzyme activities. Autumn birds had very low biotransformation enzyme activities and low indication of oxidative stress but high activity of some redox enzymes (GR and glucose 6-phosphate dehydrogenase [G6PDH]). High activities of some redox enzymes (SOD, GR, and G6PDH) seem to be related to migration, whereas low activities of some redox enzymes (SOD, CAT, and GR) may be associated with breeding. Barn swallows in South Africa may experience pollution-related oxidative stress, which may hamper interpretation of normal seasonal variation in redox parameters.     

Connecting breeding and wintering grounds of Neotropical migrant songbirds using stable hydrogen isotopes: a call for an isotopic atlas of migratory connectivity

There is an overdue and urgent need to establish patterns of migratory connectivity linking breeding grounds, stopover sites, and wintering grounds of migratory birds. Such information allows more effective application of conservation efforts by applying focused actions along movement trajectories at the population level. Stable isotope methods, especially those using stable hydrogen isotope abundance in feathers (δ²H_f) combined with Bayesian assignment techniques incorporating prior information such as relative abundance of breeding birds, now provide a fast and reliable means of establishing migratory connectivity, especially for Neotropical migrants that breed in North America and molt prior to fall migration. Here we demonstrate how opportunistic sampling of feathers of 30 species of wintering birds in Cuba, Venezuela, Guatemala, Puerto Rico, and Mexico, regions that have typically been poorly sampled for estimating migratory connectivity, can be assigned to breeding areas in North America through both advanced spatial assignment to probability surfaces and through simpler map lookup approaches. Incorporating relative abundance information from the North American Breeding Bird Survey in our Bayesian assignment models generally resulted in a reduction in potential assignment areas on breeding grounds. However, additional tools to constrain longitude such as DNA markers or other isotopes would be desirable for establishing breeding or molt origins of species with broad longitudinal distributions. The isotope approach could act as a rapid means of establishing basic patterns of migratory connectivity across numerous species and populations. We propose a large‐scale coordinated sampling effort on the wintering grounds to establish an isotopic atlas of migratory connectivity for North American Neotropical migrants and suggest that isotopic variance be considered as a valuable metric to quantify migratory connectivity. This initiative could then act as a strategic template to guide further efforts involving stable isotopes, light‐sensitive geolocators, and other technologies.     

Migration timing and routes,and wintering areas of Flammulated Owls

Determining patterns in annual movements of animals is an important component of population ecology, particularly for migratory birds where migration timing and routes, and wintering habitats have key bearing on population dynamics. From 2009 to 2011, we used light‐level geolocators to document the migratory movements of Flammulated Owls (Psiloscops flammeolus). Four males departed from breeding areas in Colorado for fall migration between ≤5 and 21 October, arrived in wintering areas in Mexico between 11 October and 3 November, departed from wintering areas from ≤6 to 21 April, and returned to Colorado between 15 and 21 May. Core wintering areas for three males were located in the Trans‐Mexican Volcanic Belt Mountains in the states of Jalisco, Michoacán, and Puebla in central and east‐central Mexico, and the core area for the other male was in the Sierra Madre Oriental Mountains in Tamaulipas. The mean distance from breeding to wintering centroids was 2057 ± 128 km (SE). During fall migration, two males took a southeastern path to eastern Mexico, and two males took a path due south to central Mexico. In contrast, during spring migration, all four males traveled north from Mexico along the Sierra Madre Oriental Mountains to the Rio Grande Valley and north through New Mexico. The first stopovers in fall and last stopovers in spring were the longest in duration for all males and located 300–400 km from breeding areas. Final spring stopovers may have allowed male Flammulated Owls to fine tune the timing of their return to high‐elevation breeding areas where late snows are not uncommon. One male tracked in both years had similar migration routes, timing, and wintering areas each year. Core wintering and final stopover areas were located primarily in coniferous forests and woodlands, particularly pine‐oak forests, suggesting that these are important habitats for Flammulated Owls throughout their annual cycle.     

Comparative migration strategies of wild and captive‐bred Asian Houbara Chlamydotis macqueenii

For migratory species, the success of population reintroduction or reinforcement through captive‐bred released individuals depends on survivors undertaking appropriate migrations. We assess whether captive‐bred Asian Houbara Chlamydotis macqueenii from a breeding programme established with locally sourced individuals and released into suitable habitat during spring or summer undertake similar migrations to those of wild birds. Using satellite telemetry, we compare the migrations of 29 captive‐bred juveniles, 10 wild juveniles and 39 wild adults (including three birds first tracked as juveniles), examining migratory propensity (proportion migrating), timing, direction, stopover duration and frequency, efficiency (route deviation), and wintering and breeding season locations. Captive‐bred birds initiated autumn migration an average of 20.6 (±4.6 se) days later and wintered 470.8 km (±76.4) closer to the breeding grounds, mainly in Turkmenistan, northern Iran and Afghanistan, than wild birds, which migrated 1217.8 km (±76.4), predominantly wintering in southern Iran and Pakistan (juveniles and adults were similar). Wintering locations of four surviving captive‐bred birds were similar in subsequent years (median distance to first wintering site = 70.8 km, range 6.56–221.6 km), suggesting that individual captive‐bred birds (but not necessarily their progeny) remain faithful to their first wintering latitude. The migratory performance of captive‐bred birds was otherwise similar to that of wild juveniles. Although the long‐term fitness consequences for captive‐bred birds establishing wintering sites at the northern edge of those occupied by wild birds remain to be quantified, it is clear that the pattern of wild migrations established by long‐term selection is not replicated. If the shorter migration distance of young captive‐bred birds has a physiological rather than a genetic basis, then their progeny may still exhibit wild‐type migration. However, as there is a considerable genetic component to migration, captive breeding management must respect migratory population structure as well as natal and release‐site fidelity.