Warming winter effects,fat store accumulation and timing of spring departure of Greenland White-fronted Geese <Emphasis Type="Italic">Anser albifrons flavirostris</Emphasis> from their winter quarters

Migratory geese accumulate energy and nutrient stores in winter to fly to refuelling spring staging areas before onward migration to breeding areas. Mean ground temperatures at two important Greenland White-fronted Geese wintering sites rose in winter and spring by 1.0–1.3°C during 1973–2007. Greenland White-fronted Geese departed the Wexford winter quarters on 3rd April 2007 for Icelandic spring staging areas, the earliest on record, representing a mean advancement of 15 days since 1973, mirrored amongst mean dates of departure amongst Scottish wintering birds that have advanced by 12 days during 1973–2007. Icelandic temperatures at critical midway staging areas en route to Greenland showed no significant change since 1973, suggesting that it is warming on the winter quarters that enable geese to depart earlier, rather than elevated temperatures at ultimate spring staging areas. However, Wexford departure date did not correlate with spring temperature. Data presented here show that Greenland White-fronted Geese have accumulated threshold body stores progressively earlier in spring migration, especially during 1995–2007. Although this did not correlate with ambient temperature, the mean degree of accumulated fat stored by 1st April in each year was a statistically significant predictor of departure date for the wintering population at Wexford. These data support the hypothesis that it is intrinsic factors (i.e. improvements in internal body state resulting from better feeding conditions) that has permitted progressively earlier departure of these geese from Wexford on spring migration, rather than amelioration of spring conditions in Iceland or solely the result of warming of the winter quarters.     

Earlier spring staging in Iceland amongst Greenland White-fronted Geese <Emphasis Type="Italic">Anser albifrons flavirostris</Emphasis> achieved without cost to refuelling rates

Greenland White-fronted Geese wintering in Ireland and Britain stage for 3 weeks in Iceland in spring before migrating onwards to breeding areas in west Greenland. The geese now depart their wintering quarters 12–15 days earlier than in 1973 because they attain necessary fat stores earlier than in previous years. Icelandic temperatures at critical midway staging areas have shown no significant change since 1973, creating a potential mismatch in food availability along the migratory route. Greenland White-fronted Geese have shifted from consuming below-ground plant storage organs in Iceland in spring to grazing managed hayfields created since the 1950s where fresh grass shoot growth occurs despite sub-zero temperatures, when traditional natural foods are physically inaccessible to staging geese due to frozen substrates. Rates of fat accumulation (measured by field scores of abdominal profiles) and mass change (measured in captured geese) were the same in the springs of 1997, 1998 and 1999 as in that of 2007 when the migration episode was 10 days earlier. Hence, earlier arrival in Iceland in 2007 did not occur at cost to refuelling rates there. The shift to acquiring energy from artificial grasslands has enabled Greenland White-fronted Geese to arrive in Iceland earlier, but has apparently not impaired their ability to accumulate fat reserves required for onwards migration, which occurs at the same rate, only earlier in the spring.     

The spring migration pattern of arctic birds in southwest Iceland, as recorded by radar

A surveillance radar in southwest Iceland was recorded by time-lapse filming in order to monitor the migration pattern of birds departing from or passing Iceland on their way to high-arctic breeding grounds in late May and early June 1988–1990. An overwhelming majority of the radar echoes from migrating bird flocks departed from Iceland but a few seemed to pass over from further south. Timing of movements and supplementary field observations indicated that mainly four species were involved, i.e. Knot Calidris canutus , Turnstone Arenaria interpres. Sanderling C. alba and Brent Goose Branta bernicla. Departures in late May from stopover sites in Iceland took place mainly in the afternoons, peaking between 1700 and 1900h in all 3 years. The departure intensity was lowest between 0100 and 1300h. Flight paths were generally straight, and the average track direction was towards the northwest (315°), suggesting that the majority of birds were heading for a transglacial migration across the Greenland icecap on their way to breeding grounds in northwest Greenland and northern Canada. Track directions varied with wind, although to a rather small degree, indicating partial drift or pseudodrift. More echoes were registered in easterly winds (tailwinds) and fewer in northerly winds than expected from random. Airspeeds were significantly slower than groundspeeds (average 17.0 and 18.7 m/s, respectively), showing that the birds more often than not benefited from tail wind assistance.     

Staging site fidelity of Greenland White-fronted Geese Anser albifrons flavirostris in Iceland

Capsule Based upon resighting histories of marked individuals, a high level of site loyalty was found for Greenland White-fronted Geese staging in Icelandic stopover areas in spring and autumn.

Aims To determine levels of within- and between-season staging site fidelity, to assess whether offspring adopt the staging areas of their parents and to determine relationships between Icelandic staging areas and winter provenance of individuals.

Methods Sequential resighting histories and recoveries (2658 observations) of 415 different individually marked geese were analysed from the period 1986–99.

Results In spring, > 90% of goslings associated with parents and siblings and all goslings were subsequently seen <4 km from where they were first sighted with parents in spring. Ninety-six percent of all multiple within-spring resightings of 192 marked individuals were within 4 km of each other; three geese moved 88 km from the southern to the western staging areas. Four percent of the 45 marked geese seen in two consecutive springs and none of the 27 birds seen in consecutive autumns moved more than 4 km between years. By contrast, significantly more (12%) moved greater than 4 km in subsequent seasons between spring/autumn (n = 56) and autumn/spring (n = 49). All these individuals shifted to Hvanneyri Agricultural College in autumn, the only declared hunting-free area for Greenland White-fronted Geese. Based upon resighting histories and recoveries of shot birds, Scottish wintering birds were more likely to use southern staging areas, and Wexford (Ireland) wintering birds were generally more likely to be seen staging in the western lowlands in Iceland.

Conclusions Given the apparent cultural reinforcement of patterns of use of staging areas in Iceland, the high levels of site loyalty and the relatively limited exchange between southern and western staging areas, we argue for strategic refuge designation throughout both staging areas to protect the population.     

Spring ice formation on goose neck collars: effects on body condition and survival in Greenland white-fronted geese Anser albifrons flavirostris

During sub-zero temperatures and strong winds on 10–11 April 2013, we witnessed ice accumulation on plastic collars of staging Greenland white-fronted geese Anser albifrons flavirostris in Iceland. Ice affected 19 of 77 collared individuals seen, all of which had lost ice by 12 April, despite continuing freezing temperatures. Temperatures exceeded freezing after 14 April; daily observations found no recurrence of ice formation before geese left for Greenland in early May. Abdominal profile scores (a field assessment of accumulated body fat) did not differ significantly between geese with and without ice before departure from Iceland. There was no significant difference in return rates between geese with iced (79 %) or un-iced collars (83 %) reported the following autumn. These first reports of collar icing in over 30 years of the project give cause for concern and vigilance, but we recommend continued use of collars given exceptional weather conditions and lack of effects.     

Seasonal movements of Gyrfalcons Falco rusticolus include extensive periods at sea

Little information exists on the movements of Gyrfalcons Falco rusticolus outside the breeding season, particularly amongst High Arctic populations, with almost all current knowledge based on Low Arctic populations. This study is the first to provide data on summer and winter ranges and migration distances. We highlight a behaviour previously unknown in Gyrfalcons, in which birds winter on sea ice far from land. During 2000–2004, data were collected from 48 Gyrfalcons tagged with satellite transmitters in three parts of Greenland: Thule (northwest), Kangerlussuaq (central‐west) and Scoresbysund (central‐east). Breeding home‐range size for seven adult females varied from 140 to 1197 km² and was 489 and 503 km² for two adult males. Complete outward migrations from breeding to wintering areas were recorded for three individuals: an adult male which travelled 3137 km over a 38‐day period (83 km/day) from northern Ellesmere Island to southern Greenland, an adult female which travelled 4234 km from Thule to southern Greenland (via eastern Canada) over an 83‐day period (51 km/day), and an adult female which travelled 391 km from Kangerlussuaq to southern Greenland over a 13‐day period (30 km/day). Significant differences were found in winter home‐range size between Falcons tagged on the west coast (383–6657 km²) and east coast (26 810–63 647 km²). Several Falcons had no obvious winter home‐ranges and travelled continually during the non‐breeding period, at times spending up to 40 consecutive days at sea, presumably resting on icebergs and feeding on seabirds. During the winter, one juvenile female travelled over 4548 km over an approximately 200‐day period, spending over half that time over the ocean between Greenland and Iceland. These are some of the largest winter home‐ranges ever documented in raptors and provide the first documentation of the long‐term use of pelagic habitats by any falcon. In general, return migrations were faster than outward ones. This study highlights the importance of sea ice and fjord regions in southwest Greenland as winter habitat for Gyrfalcons, and provides the first detailed insights into the complex and highly variable movement patterns of the species.     

Body condition and wind support initiate the shift of migratory direction and timing of nocturnal departure in a songbird

1.?An innate migration strategy guides birds through space and time. Environmental variation further modulates individual behaviour within a genetically determined frame. In particular, ecological barriers could influence departure direction and its timing. A shift in the migratory direction in response to an ecological barrier could reveal how birds adjust their individual trajectories to environmental cues and body condition. 2.?Northern wheatears of the Greenland/Iceland subspecies Oenanthe oenanthe leucorhoa arrive in Western Europe en route from their West African winter range. They then undergo an endogenously controlled shift in migratory direction from north to north-west to cross a large ecological barrier, the North Atlantic. We radiotracked these songbirds departing from Helgoland, a small island in the North Sea, over an unprecedented range of their journey. 3.?Here, we show that both birds' body condition and the wind conditions that they encountered influenced the departure direction significantly. Jointly high fuel loads and favourable wind conditions enabled migrants to cross large stretches of sea. Birds in good condition departed early in the night heading to the sea towards their breeding areas, while birds with low fuel loads and/or flying in poor weather conditions departed in directions leading towards nearby mainland areas during the entire night. These areas could be reached even after setting off late at night. 4.?Behavioural adjustment of migratory patterns is a critical adaptation for crossing ecological barriers. The observed variation in departure direction and time in relation to fuel load and wind revealed that these birds have an innate ability to respond by jointly incorporating internal information (body condition) and external information (wind support).     

Patterns in departure phenology and mass gain on African non‐breeding territories prior to the Sahara crossing in a long‐distance migrant

Afro‐Palaearctic migrants are declining to a greater degree than other European species, suggesting that processes occurring in Africa or on migration may be driving these trends. Constraints on food availability on the wintering grounds may contribute to these declines but little is known about when and where these resource constraints may occur. Sufficient resources are particularly important prior to spring migration, when migrants must cross the Sahara Desert. We examined mass gain and departure phenology in a long‐distance Palaearctic passerine migrant to determine the degree to which pre‐migratory fattening occurs in their long‐term non‐breeding territories in the Guinea Savannah region of Africa. We monitored 75 Whinchats Saxicola rubetra for departure from their non‐breeding territories in one spring, and analysed mass data of 377 Whinchats collected over three non‐breeding seasons plus 141 migrating Whinchats caught in April over 8 years, all within the same few square kilometres of human‐modified Guinea Savannah in central Nigeria. Whinchats left their winter territories throughout April, with males departing on average 8 days earlier than females. However, there was no evidence that time of departure from territory was linked to age, body size or mass at capture. Whinchats departed their territories with a predicted mass of 16.8 ± 0.3 g, considerably less than the c. 24 g required for the average Whinchat to cross the Sahara directly. Comparing departure dates with arrival dates in southern Europe showed a discrepancy of at least 2 weeks, suggesting that many Whinchats spend considerable time on pre‐migratory fuelling outside their winter territory prior to crossing the Sahara. Overwintering birds gained mass slowly during February and March (0.03 g/day), and non‐territorial or migrating birds at a much higher rate in April (at least 0.23 g/day), with up to 20% of migrating Whinchats in April potentially having sufficient fuel loads to cross the Sahara directly from central Nigeria. Our results suggest that most Whinchats leave their winter territories to fatten up locally or, possibly, by staging further north, closer to the southern limit of the Sahara. Resource constraints are therefore likely to be particularly focused in West Africa during mid‐April and possibly at staging areas before the crossing of the Sahara Desert.     

Travel schedules to the high arctic: barnacle geese trade-off the timing of migration with accumulation of fat deposits

On their way from the wintering area to the breeding grounds in Spitsbergen, barnacle geese Branta leucopsis stage on islands off the coast of Norway. The aim of this study was to describe when the geese migrate in relation to the body stores deposited and explore questions related to the concept of optimal migration schedules and on the possible mechanisms involved. We estimated fat stores by repeated assessments of the abdominal profile index of individually marked females throughout staging. Reproductive success was derived from observations of the same individuals later in the annual cycle. Females arriving late, or with low fat stores at arrival, achieved higher fat deposition rates, probably by spending more time foraging. But they were unable to match final fat scores of birds that arrived earlier or with larger fat stores. Reproductive success was correlated with the timing of migration and individuals departing at intermediate dates achieved highest success. The exact date of peak reproductive success depended on the size of fat stores accumulated, such that low-quality birds (depositing less fat) benefited most from an early departure to the breeding grounds. Observations in the breeding colonies showed that these birds did not initiate a nest earlier but they spent a longer time in Spitsbergen before settling. The length of stay in Norway was close to the prediction derived from an optimisation model relating spring events to eventual breeding success. Poorest performing birds stayed longer than expected, perhaps depositing more fat to avoid the risk of starvation. Two possible mechanisms of the timing of migration were contrasted and it seemed that the geese departed for migration as soon as they were unable to accumulate any more fat stores.     

Population structure,biometrics and moult of migrant Purple Sandpipers Calidris maritima in southwest Iceland in spring

Capsule Iceland is a stop‐over site for a population of Purple Sandpipers that winter in Britain. Here, they accumulate fuel loads for onward migration along with birds that have wintered in Iceland.

Aims To establish whether Purple Sandpipers from Britain stop‐over in Iceland during spring migration and, if so, to describe their population structure, changes in mass and moult.

Methods Purple Sandpipers were cannon‐netted on the coast of the Reykjanes Peninsula in southwest Iceland during May 2003 and 2005. Birds were aged, sexed (some by DNA) and standard biometric measurements made. Active body moult was scored.

Results Bill and wing lengths showed that the Purple Sandpipers we caught were similar to one of the populations that winter in Britain rather than Icelandic breeding birds. There were more males than females throughout the migration period (63% males for first‐year‐birds and 67% for adult birds). Accounting for a bias due to a higher percentage of males in a less usual habitat (muddy/sandy bays), the values for rocky sites were 52% males for first‐year birds and 62% for adults. The percentage of first‐year birds was 19% in 2003 and 32% in 2005, though the latter figure was biased by catches in muddy/sandy bays where there was a higher percentage of young birds. The percentage of first‐year birds was 25% on just the rocky shores in 2005. Many birds were in latter stages of body moult, and males were slightly in advance of females. Increasing mass showed that they were preparing for onward migration. The average increase of 0.58 g per day was similar to the rate measured in Orkney at an earlier point on the migration route. However, a high turnover of birds could be the reason for these low values. By late May, and close to the assumed departure date, the Purple Sandpipers of the different age/sex classes had fuel indices of 24–29% (33–42% of the lean mass). This was lower than that for the high Arctic sandpipers (Knots and Sanderlings) leaving southwest Iceland for Greenland and Canada.

Conclusions Our study confirmed that Purple Sandpipers do stop‐over in Iceland, and the possible lower rate of fuel accumulation and smaller amount stored, compared with Knots and Sanderlings, suggests a different migration pattern.     

Temperature and precipitation at migratory grounds influence demographic trends of an Arctic‐breeding bird

Anthropogenic climate disruption, including temperature and precipitation regime shifts, has been linked to animal population declines since the mid‐20th century. However, some species, such as Arctic‐breeding geese, have thrived during this period. An increased understanding of how climate disruption might link to demographic rates in thriving species is an important perspective in quantifying the impact of anthropogenic climate disruption on the global state of nature. The Greenland barnacle goose (Branta leucopsis) population has increased tenfold in abundance since the mid‐20th century. A concurrent weather regime shift towards warmer, wetter conditions occurred throughout its range in Greenland (breeding), Ireland and Scotland (wintering) and Iceland (spring and autumn staging). The aim of this study was to determine the relationship between weather and demographic rates of Greenland barnacle geese to discern the role of climate shifts in the population trend. We quantified the relationship between temperature and precipitation and Greenland barnacle goose survival and productivity over a 50 year period from 1968 to 2018. We detected significant positive relationships between warmer, wetter conditions on the Icelandic spring staging grounds and survival. We also detected contrasting relationships between warmer, wetter conditions during autumn staging and survival and productivity, with warm, dry conditions being the most favourable for productivity. Survival increased in the latter part of the study period, supporting the possibility that spring weather regime shifts contributed to the increasing population trend. This may be related to improved forage resources, as warming air temperatures have been shown to improve survival rates in several other Arctic and northern terrestrial herbivorous species through indirect bottom‐up effects on forage availability.     

Wind conditions affect stopover decisions and fuel stores of shorebirds migrating through the south Yellow Sea

We assessed the effects of wind conditions on stopover decisions and fuel stores of migratory shorebirds at Chongming Dongtan in the south Yellow Sea along the East Asian–Australasian Flyway. In spring and autumn, wind directions differed among altitudes and wind speed generally increased with altitude. Numbers of shorebirds were related to wind effects at low altitudes (on the ground and at 300 and 800 m above the ground), wind effects at 300 m being the best predictor of shorebird numbers. In spring, total number of shorebirds and numbers of the four most abundant shorebird species were negatively related to wind assistance at low altitudes, more birds departing when tailwinds prevailed and more arriving when headwinds prevailed. In autumn, however, total number of shorebirds and numbers of the four most abundant species were positively related to wind assistance at low altitudes, more birds departing and more arriving with tailwinds than with headwinds. When tailwinds prevailed, the number of arriving birds was higher than the number of departing birds. The fuel stores of captured shorebirds, represented by their body mass, was related to wind effects and change in wind conditions between two consecutive days in both spring and autumn, captured birds being heavier when headwinds prevailed than in tailwind conditions, and when the wind conditions became less favourable for flight between two consecutive days. Our results suggest that wind conditions affect stopover decisions and fuel stores, and thus the optimal migration and fuel deposition strategies of migratory shorebirds.     

Non‐breeding areas and timing of migration in relation to weather of Scottish‐breeding common sandpipers Actitis hypoleucos

The number of breeding common sandpipers has declined in Britain due to poorer return rates from non‐breeding areas. To investigate little known aspects of their annual cycle, breeding common sandpipers were fitted with geolocators to track their migrations and determine their non‐breeding areas. Ten tagged birds left Scotland on 9 July (median dates and durations are given throughout the abstract). Short‐term staging was carried out by some birds in England and Ireland, then for longer by most birds in Iberia before continuing to West Africa, arriving on 28 July. Six birds spent most of the non‐breeding season (October–February) on the coast of Guinea‐Bissau, suggesting that this is a key area. Single birds occurred in Sierra Leone, Guinea, the Canary Islands and western Sahara. The southward migration from Scotland took 17.5 d (range 1.5–24 d), excluding the initial fuelling period. The first northward movement from Africa was on 12 April. Staging occurred in either Morocco, Iberia or France. Arrival in Scotland was on 2 May. The northward migration took 16 d (range 13.5–20.5 d). The main migration strategy involved short‐ and medium‐range flights, using tail‐winds in most cases. Variation in strategy was associated with departure date; birds that left later staged for shorter durations. Coastal West Africa provides two major habitats for common sandpipers: mudflats associated with mangroves and rice fields. Although the area of mangrove has been depleted, the scale of loss has probably been insufficient to account for the decline in sandpiper numbers. Rice fields are expanding, providing feeding areas for water‐birds. Meteorological data during the migrations suggest that the weather during the southward migration is unlikely to contribute to a population decline but strong cross‐winds or head‐winds during the northward migration to the breeding grounds may do so.     

Changes in nutrient dynamics of midcontinent greater white-fronted geese during spring migration

Waterfowl and other migratory birds commonly store nutrients at traditional staging areas during spring for later use during migration and reproduction. We investigated nutrient-storage dynamics in the midcontinent population of greater white-fronted geese (Anser albifrons; hereafter white-fronted geese) at spring staging sites in the Rainwater Basin of Nebraska during February–April and in southern Saskatchewan during April–May, 1998 and 1999. In Nebraska, lipid content of white-fronted geese did not increase, and protein content changed little over time for most age and sex categories. In Saskatchewan, lipids increased 11.4 g/day (SE = 1.7) and protein content increased 1.6 g/day (SE = 0.6) in the sample of adult geese collected over a 3-week period. A study conducted during 1979–1980 in the Rainwater Basin reported that white-fronted geese gained 8.8–17.7 g of lipids per day during spring, differing greatly from our results 2 decades later. In addition, lipid levels were less in the 1990s compared to spring 1980 for adult geese nearing departure from staging sites in Saskatchewan. This shift in where geese acquired nutrient stores from Nebraska to more northern staging sites coincided with a decrease in availability of waste corn in Nebraska, their primary food source while staging at that stopover site, and an increase in cultivation of high-energy pulse crops in Saskatchewan. White-fronted geese exhibited flexibility in nutrient dynamics during spring migration, likely in response to landscape-level variation in food availability caused by changes in agricultural trends and practices. Maintaining a wide distribution of wetlands in the Great Plains may allow spring-staging waterfowl to disperse across the region and facilitate access to high-energy foods over a larger cropland base. © 2011 The Wildlife Society.     

Temperature‐related increases in grass growth and greater competition for food drive earlier migrational departure of wintering Whooper Swans

Understanding the departure decisions of migratory birds is critical for determining how changing climatic conditions will influence subsequent arrival times on the breeding grounds. A long‐term dataset (1972–2008) of Whooper Swan Cygnus cygnus departure dates from a wintering site in Ireland was used to assess the factors determining the timing of migration. Early and late migrating swans showed different departure patterns. Earlier wintering ground departure was more pronounced for the first 50% of the population than the last 10% of departing individuals. Earlier departure was associated with an increase in February temperatures at the wintering site for all departure phases except the date when the last individual departed. The date by which the first 50% of Swans had departed was earlier with increasing numbers of wintering Swans, suggesting that competition on the wintering grounds may further influence the timing of departure. The results also suggested that departure is mediated by the influence of spring temperature on food resources, with increased February grass growth in warmer years enabling earlier departure of migrating Swans. To determine why arrival dates in the breeding ground have altered, environmental conditions in the wintering grounds must be taken into account.     

Effects of agricultural change on abundance, fitness components and distribution of two arctic-nesting goose populations

Intensification of agriculture since the 1950s has enhanced the availability, competitive ability, crude protein content, digestibility and extended growing seasons of forage grasses. Spilled cereal grain also provides a rich food source in autumn and in winter. Long‐distance migratory herbivorous geese have rapidly exploited these feeding opportunities and most species have shown expansions in range and population size in the last 50 years. Results of long‐term studies are presented from two Arctic‐breeding populations, the Svalbard pink‐footed goose and the Greenland white‐fronted goose (GWFG). GWFGs have shown major habitat shifts since the 1950s from winter use of plant storage organs in natural wetlands to feeding on intensively managed farmland. Declines in local density on, and abandonment of, unmodified traditional wintering habitat and increased reproductive success among those birds wintering on farmland suggest that density‐dependent processes were not the cause of the shift in this winter‐site‐faithful population. Based on enhanced nutrient and energy intake rates, we argue that observed shifts in both species from traditionally used natural habitats to intensively managed farmland on spring staging and wintering areas have not necessarily been the result of habitat destruction. Increased food intake rates and potential demographic benefits resulting from shifts to highly profitable foraging opportunities on increasingly intensively managed farmland, more likely explain increases in goose numbers in these populations. The geographically exploratory behaviour of subdominant individuals enables the discovery and exploitation of new winter feeding opportunities and hence range expansion. Recent destruction of traditional habitats and declines in farming at northern latitudes present fresh challenges to the well being of both populations. More urgently, Canada geese colonizing breeding and moulting habitats of white‐fronted geese in Greenland are further affecting their reproductive output.     

The role of migration for spatial turnover of arctic bird species in a circumpolar perspective

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.     

THE MIGRATION PATTERNS OF THE PURPLE SANDPIPER CALIDRIS MARITIMA

Summers, R. W. 1994. The migration patterns of the Purple Sandpiper Calidris maritima. Ostrich 65: 167–173.

The Purple Sandpiper breeds largely in the Arctic, and winters (boreal season) on the rocky shores of the north Atlantic, further north than any other sandpiper. As the populations from Canada, Greenland, Iceland, Svalbard, Norway and Russia differ in wing and bill lengths it is possible to match measurements taken from breeding birds with samples of birds caught in winter. Ringing recoveries, especially from colour marked birds, have also helped to determine migration routes and wintering areas. Four populations move to the nearest ice-free coast. Two populations move south of the nearest ice-free coast, being replaced by larger birds from a more northerly population (“chain migration”). Only the north Canadian population is believed to migrate a long distance, “leap-frogging” other winter populations. These patterns are discussed in relation to theories for the migration patterns of waders.     

Does migration promote or restrict circumpolar breeding ranges of arctic birds?

Aim Migration has been suggested to promote large breeding ranges among birds because of the greater mobility of migratory compared with non‐migratory species, but migration has also been suggested to restrict breeding ranges because of evolutionary constraints imposed by the genetically based migration control programme. We aim to investigate the association between migration and the breeding ranges of both land birds and pelagic birds breeding in the Arctic region. Location The Arctic region. Methods Information on breeding and wintering ranges and migratory status of bird species breeding in the arctic tundra biome was compiled from the literature. The association between breeding range, migration distance and primary winter habitat was tested using multivariate generalized linear models and pair‐wise Mann–Whitney U‐tests. Phylogenetic effects were tested for using Mantel’s permutation tests. Results We found different relationships depending on the species’ major winter habitat. Among birds that are pelagic during winter, long‐distance migrants have the largest breeding ranges, while among terrestrial birds, residents and short‐distance migrants have the largest breeding ranges. Breeding ranges of coastal birds of all migratory distance classes are comparatively restricted. Main conclusions As a new explanation for this pattern we suggest that the possibility of colonizing large winter ranges is a key factor for the subsequent expansion of breeding ranges in arctic bird communities and possibly also in bird communities of other regions of the world. Because of the reversal in the relative extent of continents and oceans between the hemispheres, longitudinally wide winter ranges are more likely for long‐distance than short‐distance migrants among pelagic birds, while the reverse holds true for birds that use terrestrial winter habitats. For coastal birds both continents and oceans form barriers restricting colonization of extensive winter quarters and consequently also of extensive breeding ranges, regardless of the distance to the winter quarters.     

Incidence of embedded shotgun pellets and inferred hunting kill amongst Russian/Baltic barnacle geese Branta leucopsis

X-rays of wild caught barnacle geese from the Russian/Baltic population were taken in Denmark in the springs of 2009 and 2011 to determine the incidence of embedded shotgun pellets and to estimate the annual hunting kill. On average, 13 % of adult geese (n?=?212) and 6 % of first year geese (n?=?35) examined contained pellets in their tissue. Assuming that these birds represented a random sample, extrapolation to the entire population of c. 770,000 individuals indicates that 96,000 barnacle geese carry embedded pellets. Based on the assumption that the ratio between the number of birds with embedded shot and the total number of birds harvested per season is similar to that found in pink-footed geese Anser brachyrhynchus (recorded as 3.6:1 during 1990–1996 and 1.7:1 during 2009–2011), the annual kill of barnacle geese was estimated at 26,300–58,300 birds. The Russian/Baltic barnacle geese are protected from hunting on their winter quarters (The Netherlands, Germany and Denmark), but are quarry in Russia and are shot under license to protect agricultural crops in Estonia, Germany, Sweden and Denmark (amounting to a total of c. 1,800–3,000 geese shots per year). Barnacle geese are known to be shot illegally (accidentally and deliberately) along the migration route, but in the absence of Russian bag statistics, the contribution of illegal hunting to the overall harvest cannot be substantiated. Although the population is currently increasing at an annual rate of 8 %, the indirectly estimated hunting pressure (3–7 %) is not insubstantial and should be taken into account in future population management models.