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.     

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 migration routes and timing of Greenland white-fronted geese – results from satellite telemetry

Greenland white‐fronted geese accumulate body mass throughout late winter in preparation for migration after mid‐April to spring staging areas in Iceland. This analysis presents field assessment of abdominal fat deposits (API) from large samples of marked birds which showed increasing rates of fuel deposition throughout January–April. Historical records show that geese rarely depart en masse before 17 April, a pattern followed by all but one of the tagged birds. Timed positions obtained from 12 geese fitted with satellite transmitters in 1997, 1998 and 1999 suggested that all geese departed winter quarters on tailwinds between 16 and 19 April. Tracked geese flew directly to staging areas in Iceland, although one staged for 10 days in Northern Ireland in 1997 and another may have stopped briefly in western Scotland. Average migration duration of all tagged birds departing Ireland (including the 1997 bird that stopped over within Ireland) was 25 hours (range 13–77). Four geese apparently overshot and returned to Iceland during strong E to ESE winds. APIs in Iceland showed more rapid and linear increases in stores during the mean 19‐day (range 13–22) staging period there than on the winter quarters. Geese continued their migration to Greenland when APIs attained or exceeded levels at departure from Ireland and all departed on assisting tailwinds between 1 and 11 May. Tracked birds continued the journey to West Greenland in between 24 and 261 (mean 82) hours, although one bird turned back during the traverse of the Greenland Ice Cap and summered on the east coast. Seven of the birds staged for 1–20 hours at, or near, the East Greenland coast and several made slow progress crossing the inland ice, all in the direction of their ultimate destination (i.e. not necessarily taking the lowest or shortest crossing routes). It is suggested that the energy‐savings of departing on tailwinds may favour geese to wait for such conditions once threshold fat storage levels have been reached, but more research is needed to confirm this.     

Interactions between land use,habitat use,and population increase in greater snow geese: what are the consequences for natural wetlands?

The North American greater snow goose population has increased dramatically during the last 40 years. We evaluated whether refuge creation, changes in land use on the wintering and staging grounds, and climate warming have contributed to this expansion by affecting the distribution, habitat use, body condition, and migration phenology of birds. We also reviewed the effects of the increasing population on marshes on the wintering grounds, along the migratory routes and on the tundra in summer. Refuges established before 1970 may have contributed to the initial demographic increase. The most important change, however, was the switch from a diet entirely based on marsh plants in spring and winter (rhizomes of Scirpus/Spartina) to one dominated by crops (corn/young grass shoots) during the 1970s and 1980s. Geese now winter further north along the US Atlantic coast, leading to reduced hunting mortality. Their migratory routes now include portions of southwestern Québec where corn production has increased exponentially. Since the mid‐1960s, average temperatures have increased by 1–2.4°C throughout the geographic range of geese, which may have contributed to the northward shift in wintering range and an earlier migration in spring. Access to spilled corn in spring improved fat reserves upon departure for the Arctic and may have contributed to a high fecundity. The population increase has led to intense grazing of natural wetlands used by geese although these habitats are still largely undamaged. The foraging in fields allowed the population to exceed limits imposed by natural marshes in winter and spring, but also prevented permanent damage because of their overgrazing.     

Central European Greylag Geese Anser anser show a shortening of migration distance and earlier spring arrival over 60 years

Global climate change can cause pronounced changes in species? migratory behaviour. Numerous recent studies have demonstrated climate‐driven changes in migration distance and spring arrival date in waterbirds, but detailed studies based on long‐term records of individual recapture or re‐sighting events are scarce. Using re‐sighting data from 430 marked individuals spanning a 60‐year period (winters 1956/1957 to 2015/2016), we assessed patterns in migration distance and spring arrival date, wintering‐site fidelity and survival in the increasing central European breeding population of Greylag Geese Anser anser. We demonstrate a long‐term decrease in migration distance, changes in the wintering range caused by winter partial short‐stopping, and the earlier arrival of geese on their breeding grounds. Greylag Geese marked on central Europe moulting grounds have not been recorded wintering in Spain since 1986 or in Tunisia and Algeria since 2004. The migration distance and spring arrival of geese indicated an effect of temperature at the breeding site and values of the NAO index. Greylag Geese migrate shorter distances and arrive earlier in milder winters. We suggest that shifts in the migratory behaviour of Central European Greylag Geese are individual temperature‐dependent decisions to take advantage of wintering grounds becoming more favourable closer to their breeding grounds, allowing birds to acquire breeding territories earlier.     

Circumpolar variation in morphological characteristics of Greater White-fronted Geese Anser albifrons

Capsule Greater White-fronted Geese show significant variation in body size from sampling locations throughout their circumpolar breeding range.

Aims To determine the degree of geographical variation in body size of Greater White-fronted Geese and identify factors contributing to any apparent patterns in variation.

Methods Structural measures of >3000 geese from 16 breeding areas throughout the Holarctic breeding range of the species were compared statistically.

Results Palearctic forms varied clinally, and increased in size from the smallest forms on the Kanin and Taimyr peninsulas in western Eurasia to the largest forms breeding in the Anadyr Lowlands of eastern Chukotka. Clinal variation was less apparent in the Nearctic, as both the smallest form in the Nearctic and the largest form overall (the Tule Goose) were from different breeding areas in Alaska. The Tule Goose was 25% larger than the smallest form. Birds from Greenland (A. a. flavirostris) were the second largest, although only slightly larger than geese from several North American populations. Body size was not correlated with breeding latitude but was positively correlated with temperature on the breeding grounds, breeding habitat, and migration distance. Body mass of Greater White-fronted Geese from all populations remained relatively constant during the period of wing moult. Morphological distinctness of eastern and western Palearctic forms concurs with earlier findings of complete range disjunction.

Conclusions Patterns of morphological variation in Greater White-fronted Geese across the Holarctic can be generally attributed to adaptation to variable breeding environments, migration requirements, and phylo-geographical histories.     

The onset of spring and timing of migration in two arctic nesting goose populations: the pink‐footed goose Anser bachyrhynchus and the barnacle goose Branta leucopsis

An earlier onset of spring has been recorded for many parts of Eurasia in recent decades. This has consequences for migratory species, both in changing the conditions encountered by individuals on reaching migratory sites and in affecting cues regulating the timing of migration where decisions to migrate are influenced by local environmental variables. Here we examine the timing of spring migration for two arctic goose populations, the pink‐footed goose Anser brachyrhynchus (during 1990–2003) and barnacle goose Branta leucopsis (during 1982–2003), which both breed on Svalbard. The satellite‐derived Normalised Difference Vegetation Index (NDVI) was used to express the onset of spring at their wintering and spring staging sites. Pink‐footed geese use several sites during spring migration, ranging from the southernmost wintering areas in Belgium to two spring staging areas in Norway, and distances between sites used along the flyway are relatively short. There was a positive correlation in the onset of spring between neighbouring sites, and the geese migrated earlier in early springs. Barnacle geese, on the other hand, have a long overseas crossing from their wintering grounds in Britain to spring staging areas in Norway. Although spring advanced in both regions, there was no corresponding correlation in the timing of onset of spring between their wintering and spring staging sites, and little evidence for barnacle geese migrating earlier over the whole study period. Hence, where geese can use spring conditions at one site as an indicator of the conditions they might encounter at the next, they have responded quickly to the advancement of spring, whereas in a situation where they cannot predict, they have not yet responded, despite the advancement of spring in the spring staging area.     

Seasonal variation in nutritional characteristics of the diet of greater white-fronted geese

We studied diet and habitat use of greater white-fronted geese (Anser albifrons) from autumn through spring on their primary staging and wintering areas in the Pacific Flyway, 1979–1982. There have been few previous studies of resource use and forage quality of wintering greater white-fronted geese in North America, and as a consequence there has been little empirical support for management practices pertaining to habitat conservation of this broadly distributed species. Observations of >2,500 flocks of geese and collections of foraging birds revealed seasonal and geographic variation in resource use reflective of changes in habitat availability, selection, and fluctuating physiological demands. Autumn migrants from Alaska arrived first in the Klamath Basin of California and southern Oregon, where they fed on barley, oats, wheat, and potatoes. Geese migrated from the Klamath Basin into the Central Valley of California in late autumn where they exploited agricultural crops rich in soluble carbohydrates, with geese in the Sacramento Valley feeding almost exclusively on rice and birds on the Sacramento–San Joaquin Delta primarily utilizing corn. White-fronted geese began their northward migration in late winter, and by early spring most had returned to the Klamath Basin where 37% of flocks were found in fields of new growth cultivated and wild grasses. Cereal grains and potatoes ingested by geese were low in protein (7–14%) and high in soluble nutrients (17–47% neutral detergent fiber [NDF]), whereas grasses were low in available energy (47–49% NDF) but high in protein (26–42%). Greater white-fronted geese are generalist herbivores and can exploit a variety of carbohydrate-rich cultivated crops, likely making these geese less susceptible to winter food shortages than prior to the agriculturalization of the North American landscape. However, agricultural landscapes can be extremely dynamic and may be less predictable in the long-term than the historic environments to which geese are adapted. Thus far greater white-fronted geese have proved resilient to changes in land cover in the Pacific Flyway and by altering their migration regime have even been able to adapt to changes in the availability of suitable forage crops. © 2010 The Wildlife Society.     

Does snowmelt constrain spring migration progression in sympatric wintering Arctic-nesting geese? Results from a Far East Asia telemetry study

Telemetry data from sympatric Eastern Tundra Bean Geese Anser serrirostris captured on their winter quarters in the Yangtze River Floodplain, China, tracked to two discrete breeding areas (the Anadyr Region (AR) at 65°N and Central Russian Arctic (CRA) at 75°N) showed that, despite longer migration distance (6300 vs. 5300 km), AR geese reached their destination 23 days earlier than CRA geese as a result of increasingly delayed date of 50% snow cover along the route of CRA geese (based on satellite imagery data). Both groups arrived at breeding areas 8–9 days prior to the local date of 50% snow cover thaw, suggesting optimal timing of arrival for subsequent reproduction. Despite small sample sizes from one season of tracking, these intra-specific data are the first to suggest that, in time-limited Arctic-nesting geese, snowmelt conditions regulated the individual progress and duration of spring migration along the flyway to coincide with arrival at optimal spring conditions on breeding areas.     

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 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.     

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.     

Survival of Svalbard pink-footed geese Anser brachyrhynchus in relation to winter climate, density and land-use

1. Global change may strongly affect population dynamics, but mechanisms remain elusive. Several Arctic goose species have increased considerably during the last decades. Climate, and land-use changes outside the breeding area have been invoked as causes but have not been tested. We analysed the relationships between conditions on wintering and migration staging areas, and survival in Svalbard pink-footed geese Anser brachyrhynchus. Using mark-recapture data from 14 winters (1989-2002) we estimated survival rates and tested for time trends, and effects of climate, goose density and land-use. 2. Resighting rates differed for males and females, were higher for birds recorded during the previous winter and changed smoothly over time. Survival rates did not differ between sexes, varied over time with a nonsignificant negative trend, and were higher for the first interval after marking (0.88-0.97) than afterwards (0.74-0.93). Average survival estimates were 0.967 (SE 0.026) for the first and 0.861 (SE 0.023) for all later survival intervals. 3. We combined 16 winter and spring climate covariates into two principal components axes. F1 was related to warm/wet winters and an early spring on the Norwegian staging areas and F2 to dry/cold winters. We expected that F1 would be positively related to survival and F2 negatively. F1 explained 23% of survival variation (F1,10=3.24; one-sided P=0.051) when alone in a model and 28% (F1,9=4.50; one-sided P=0.031) in a model that assumed a trend for survival. In contrast, neither F2 nor density, land-use, or scaring practices on important Norwegian spring staging areas had discernible effects on survival. 4. Climate change may thus affect goose population dynamics, with warmer winters and earlier springs enhancing survival and fecundity. A possible mechanism is increased food availability on Danish wintering and Norwegian staging areas. As geese are among the main herbivores in Arctic ecosystems, climate change, by increasing goose populations, may have important indirect effects on Arctic vegetation. Our study also highlights the importance of events outside the breeding area for the population dynamics of migrant species.     

Long-term changes in numbers of geese stopping over and wintering in south-western Poland

South-western Poland belongs to the key staging areas for geese in Europe, supporting some 100000 birds in recent years. We compared goose counts conducted in the 1970s, 1990s and during 2009–2011 in this region, and linked the findings to the recent assessments of trends in the flyway-populations. Numbers increased several dozen times between the first two counts and have stabilized to the present. More than 14% of the flyway Tundra Bean Goose (Anser fabalis rossicus) stopped over in SW Poland on passage. Smaller numbers of White-fronted Goose (A. albifrons), Greylag Goose (A. anser), and four other rarer species, have all increased since the 1970s. The likely factors responsible for these changes are mild weather conditions, increased availability of large water bodies and shifts in winter ranges of particular species. Temporal mismatch between SW Poland and the total flyways in Bean and White-fronted Geese was recorded when we compared the long-term and the short-term population trends. Increasing reports of other species in SW Poland match the general tendencies in Europe. These data document that regional trends are not a simple reflection of those in flyways as a whole. To understand changes in goose populations a re-established international count network is desired.     

No evidence for sex bias in winter inter‐site movements in an Arctic‐nesting goose population

Understanding movement of individuals between sites is necessary to quantify emigration and immigration, yet previous analyses exploring sex biases in site fidelity among birds have not evaluated remigration (the return of marked birds that moved to alternative areas from the site at which they were marked). Using novel Bayesian multistate models, we tested whether between‐winter emigration, remigration and survival rates were sex‐biased among 851 Greenland White‐fronted Geese Anser albifrons flavirostris marked at Wexford, Ireland. We found no evidence for sex biases in emigration, remigration or survival. Thus, sex biases in winter site fidelity do not occur in any form in this population; these techniques for modelling sex‐biased movement will be useful for a better understanding of site fidelity and connectivity in other marked animal populations.     

Food constraints explain the restricted distribution of wintering Lesser White‐fronted Geese Anser erythropus in China

More than 90% of the Lesser White‐fronted Geese Anser erythropus in the Eastern Palearctic flyway population winter at East Dongting Lake, China. To explain this restricted distribution and to understand better the winter feeding ecology and habitat requirements of this poorly known species, we assessed their food availability, diet and energy budgets at this site through two winters. Lesser White‐fronted Geese maintained a positive energy budget when feeding on above‐ground green production of Eleocharis and Alopecurus in recessional grasslands in autumn and spring to accumulate fat stores. Such food was severely depleted by late November and showed no growth in mid‐winter. Geese fed on more extensive old‐growth Carex sedge meadows in mid‐winter where they were in energy deficit and depleted endogenous fat stores. Geese failed to accumulate autumn fat stores in one year when high water levels prevented the Geese from using recessional grassland feeding areas. Fat stores remained lower throughout that winter and Geese left for breeding areas later in spring than in the previous year, perhaps reflecting the need to gain threshold fat stores for migration. Sedge meadows are widespread at other Yangtze River floodplain wetlands, but recessional grasslands are rare and perhaps restricted to parts of East Dongting Lake, which would explain the highly localized distribution of Lesser White‐fronted Geese in China and their heavy use of these habitats at this site. Sympathetic management of water tables is essential to maintain the recessional grasslands in the best condition for Geese. Regular depletion of fat stores whilst grazing sedge meadows in mid‐winter also underlines the need to protect the species from unnecessary anthropogenic disturbances that enhance energy expenditure. The specialized diet of the Lesser White‐fronted Goose may explain its highly restricted winter distribution and global rarity.     

Seasonal migrations of four individual bar-headed geese Anser indicus from Kyrgyzstan followed by satellite telemetry

The Kyrgyz population of the bar-headed goose Anser indicus has declined dramatically during the past decades. Human persecution during migration and habitat loss at stopover and wintering sites are commonly regarded as most serious threats. However, little is known about seasonal movements, migration routes, and wintering sites of the bar-headed geese from Kyrgyzstan, which represent the westernmost geographical population of the species. As part of a conservation project, which also included reinforcement of the wild population by the release of hand-reared juveniles, in late summer of 1998, five bar-headed geese, three wild adults and two hand-reared goslings, were fitted with sun-powered satellite transmitters in order to track their movements from Lake Son Kul and Lake Chatyr Kul in Kyrgyzstan. The five individuals contributed very unevenly to the more than 5,000 signals in total that were received from the French ARGOS system: one failed after 8 weeks, while another one was tracked for more than 2 years. The four geese contributing to this study followed three completely different migration routes leading to their wintering areas in Pakistan, India and Uzbekistan, while stopover areas were situated in southern Tajikistan and in western Tibet. Both in autumn and spring the adult birds migrated distances of 1,280–1,550 km in two steps, with stopover periods of 32–46 days (autumn) and 16–23 days (spring). Flight speeds of up to 680 km per actual migration day were recorded regularly, even during crossings of very high summits. A hand-reared juvenile flew non-stop for 790 km to southern Uzbekistan and even visited southernmost Turkmenistan, where the species is very rarely seen. The timing of migration varied considerably between individuals but also for the same individual between years. We compare our tracking results with previous findings (field observations, ring recoveries, and satellite tracking results) and discuss them with respect to migration over high-mountain habitats and a general migration strategy of the species.     

Favorable spring conditions can buffer the impact of winter carryover effects on a key breeding decision in an Arctic‐breeding seabird

1. The availability and investment of energy among successive life‐history stages is a key feature of carryover effects. In migratory organisms, examining how both winter and spring experiences carryover to affect breeding activity is difficult due to the challenges in tracking individuals through these periods without impacting their behavior, thereby biasing results.
2. Using common eiders Somateria mollissima, we examined whether spring conditions at an Arctic breeding colony (East Bay Island, Nunavut, Canada) can buffer the impacts of winter temperatures on body mass and breeding decisions in birds that winter at different locations (Nuuk and Disko Bay, Greenland, and Newfoundland, Canada; assessed by analyzing stable isotopes of 13‐carbon in winter‐grown claw samples). Specifically, we used path analysis to examine how wintering and spring environmental conditions interact to affect breeding propensity (a key reproductive decision influencing lifetime fitness in female eiders) within the contexts of the timing of colony arrival, pre‐breeding body mass (body condition), and a physiological proxy for foraging effort (baseline corticosterone).
3. We demonstrate that warmer winter temperatures predicted lower body mass at arrival to the nesting colony, whereas warmer spring temperatures predicted earlier arrival dates and higher arrival body mass. Both higher body mass and earlier arrival dates of eider hens increased the probability that birds would initiate laying (i.e., higher breeding propensity). However, variation in baseline corticosterone was not linked to either winter or spring temperatures, and it had no additional downstream effects on breeding propensity.
4. Overall, we demonstrate that favorable pre‐breeding conditions in Arctic‐breeding common eiders can compensate for the impact that unfavorable wintering conditions can have on breeding investment, perhaps due to greater access to foraging areas prior to laying.

     

The influence of wind conditions in Europe on the advance in timing of the spring migration of the song thrush (<Emphasis Type="Italic">Turdus philomelos</Emphasis>) in the south-east Baltic region

Some of the factors that could influence changes in phenology of the song thrush (Turdus philomelos) during spring migration have been analyzed in relation to the timing of their return to the south-east Baltic region over the last 40 years. These include wind direction and velocity, temperature and precipitation in the wintering areas and along the migratory route. In March, a significant correlation was found between the timing of passage in the Baltic region and both the air temperatures in wintering area and winds over the migratory route. In April, when mass migration of thrushes occurs, the timing of passage was correlated with temperature, winds and, partly, precipitation over the route of migration. In this month, the frequency of tailwinds increased significantly along the route of migration from south-west France to the Baltic region over the last 40 years. The tailwind frequency was correlated with the beginning, middle and end of spring passage, accounting for 51% of the variance of median dates of the passage. The higher ambient temperatures over the migratory route explain nearly 20% of the variance in the timing of passage. Our results suggest that the advance in the timing of spring migration is primarily due to (1) the increased frequency of tailwinds favorable for migratory flights over the migratory route, and (2) the earlier emergence of the conditions enhancing migration due to higher spring temperatures in the winter quarters and on the migratory route.     

Expensive Traditions: Energy Expenditure of Aleutian Geese in Traditional and Recently Colonized Habitats

ABSTRACT In an effort to reduce goose depredation at a traditional spring migratory stopover site, private landowners implemented a coordinated hazing plan to scare Aleutian cackling geese (Branta hutchinsii leucopareia) from private lands to adjacent public pastures that were cultivated and set aside specifically for geese. Coincidentally, some Aleutian geese began using a new stopover site 150 km farther south in their spring migratory range; numbers at the new site continue to increase. We tested the idea that when their ability to acquire resources deteriorates geese are likely to seek improved foraging conditions, especially during spring migration when individuals strive to maximize nutrient stores and minimize energy expenditure. We quantified measures of goose foraging performance in traditional and new spring staging sites by calculating foraging opportunity, foraging effort, body condition, and daily energy expenditure. Geese staging at the site with higher levels of human disturbance had less foraging opportunity and, despite increased foraging effort and more nutritious food-plants at the site, birds there experienced an elevated energy expenditure and poorer body condition than birds at the new stopover site. Reduced foraging time and increased energy expenditure at the traditional spring staging site may have triggered the colonization process. Suitability assessment of habitat for migratory geese should include measures of foraging opportunity, disturbance risks, and daily energy expenditure in addition to quantity and quality of foods.