Factors Influencing Reporting and Harvest Probabilities in North American Geese

ABSTRACT We assessed variation in reporting probabilities of standard bands among species, populations, harvest locations, and size classes of North American geese to enable estimation of unbiased harvest probabilities. We included reward (US$10, $20, $30, $50, or $100) and control ($0) banded geese from 16 recognized goose populations of 4 species: Canada (Branta canadensis), cackling (B. hutchinsii), Ross's (Chen rossii), and snow geese (C. caerulescens). We incorporated spatially explicit direct recoveries and live recaptures into a multinomial model to estimate reporting, harvest, and band-retention probabilities. We compared various models for estimating harvest probabilities at country (United States vs. Canada), flyway (5 administrative regions), and harvest area (i.e., flyways divided into northern and southern sections) scales. Mean reporting probability of standard bands was 0.73 (95% CI = 0.69–0.77). Point estimates of reporting probabilities for goose populations or spatial units varied from 0.52 to 0.93, but confidence intervals for individual estimates overlapped and model selection indicated that models with species, population, or spatial effects were less parsimonious than those without these effects. Our estimates were similar to recently reported estimates for mallards (Anas platyrhynchos). We provide current harvest probability estimates for these populations using our direct measures of reporting probability, improving the accuracy of previous estimates obtained from recovery probabilities alone. Goose managers and researchers throughout North America can use our reporting probabilities to correct recovery probabilities estimated from standard banding operations for deriving spatially explicit harvest probabilities.     

Temporal Patterns of Apparent Leg Band Retention in North American Geese

ABSTRACT An important assumption of mark—recapture studies is that individuals retain their marks, which has not been assessed for goose reward bands. We estimated aluminum leg band retention probabilities and modeled how band retention varied with band type (standard vs. reward band), band age (1–40 months), and goose characteristics (species and size class) for Canada (Branta canadensis), cackling (Branta hutchinsii), snow (Chen caerulescens), and Ross's (Chen rossii) geese that field coordinators double-leg banded during a North American goose reward band study (N = 40,999 individuals from 15 populations). We conditioned all models in this analysis on geese that were encountered with ≥1 leg band still attached (n = 5,747 dead recoveries and live recaptures). Retention probabilities for standard aluminum leg bands were high ( = 0.9995, SE < 0.001) and constant over 1–40 months. In contrast, apparent retention probabilities for reward bands demonstrated an interactive relationship between 5 size and species classes (small cackling, medium Canada, large Canada, snow, and Ross's geese). In addition, apparent retention probabilities for each of the 5 classes varied quadratically with time, being lower immediately after banding and at older age classes. The differential retention probabilities among band type (reward vs. standard) that we observed suggests that 1) models estimating reporting probability should incorporate differential band loss if it is nontrivial, 2) goose managers should consider the costs and benefits of double-banding geese on an operational basis, and 3) the United States Geological Survey Bird Banding Lab should modify protocols for receiving recovery data.     

Using 2 Genetic Markers to Discriminate Among Canada Goose Populations in Ohio

Abstract: Canada goose (Branta canadensis) harvest management depends on reliable estimates of harvest composition, and established genetic methods provide an alternative to traditional methods. We expanded upon previous genetic studies by comparing the utility of 6 nuclear microsatellite loci and mitochondrial (mtDNA) control region sequences for discriminating among giant (B. c. maxima) and interior (B. c. interior) populations in Ohio (USA) Canada goose harvests at both individual and population levels. Subspecies and populations exhibited greater differentiation in mtDNA (F_ST = 0.202) than microsatellites (F_ST = 0.021), as would be expected based on differences in effective population size. Neither microsatellites nor mtDNA alone were sufficient for estimating harvest composition at the subspecies or population level in simulations and empirical blind tests using individuals of known origin; however, a combined microsatellite + mtDNA dataset yielded accurate and precise harvest derivations at the subspecies level. Both population-level mixed stock analysis and individual-level assignment tests provided accurate results, but a large proportion of birds could not be assigned with confidence at the individual level. We applied mixed stock analysis and the combined microsatellite + mtDNA dataset to Ohio's 2003–2004 harvest and found that interior populations accounted for 4.9% (95% CI = 1.7–8.0%) of the statewide early season and 9.3% (95% CI = 6.9–11.6%) of the regular and late-season harvested sample. These results suggest that maximum likelihood harvest derivations are highly dependent on the choice of genetic markers. Studies should only employ markers that exhibit sufficient variation and have been shown through simulations and empirical testing to accurately discriminate among the subspecies or management populations of interest.     

Long-Term Survival and Harvest of Resident Canada Geese in Virginia

Resident populations of Canada geese (Branta canadensis) are of particular management interest throughout the eastern United States given increased human-wildlife conflicts due to regional increases in the Atlantic Flyway Resident Population. Within Virginia, USA, growth rates of resident goose populations have been reduced through extended harvest seasons and increased bag limits. Our objective was to investigate spatiotemporal patterns in survival rates and harvest rates of resident geese in Virginia over the past 25 years. We estimated annual survival, recovery, and harvest rates using mark-recapture data from 1990–2015 for individuals that were banded as resident birds during summer throughout the state. We tested for differences in annual survival probability and harvest rates of resident geese banded and recovered in 3 distinct goose hunt zones: the Atlantic, Southern James Bay, and Western hunt zones, each of which had different hunting regulations. We also tested for differences in survival and harvest rates between individuals banded in rural or urban sampling locations, and between age classes (i.e., after hatch-year or hatch-year). In general, survival rates of resident geese over the past 25 years in Virginia are declining. Differences in survival among the 3 goose hunt zones also suggests that current harvest management strategies have reduced survival rates of resident geese. Upon closer examination, we found differences in survival among zones, with resident geese in the Atlantic and Southern James Bay hunt zones showing more negative declines compared to resident geese in the Western zone. Resident geese banded in rural areas had higher survival than urban-banded geese. We also investigated the effects of sampling effort on survival estimates and found no difference in survival estimates among groups when using 75%, 50%, 25%, or 5% of the data randomly sampled from the full data set, suggesting that banding efforts of resident geese could be reduced and continue to inform adaptive management strategies for these populations throughout Virginia. © 2020 The Wildlife Society.     

Demographic Parameters of Rural and Urban Adult Resident Canada Geese in Georgia

ABSTRACT In many urban metropolitan areas, resident Canada goose (Branta canadensis) populations have grown to nuisance levels in spite of increasing harvest opportunity. To document differences in demographic parameters between urban and rural geese, I estimated probabilities of survival, recapture, recovery, and fidelity for adult resident Canada geese between 2001 and 2006 using banding, live recapture, and dead recovery data from 2 distinct banding locations in Georgia, USA. Adult survival rates were higher for urban geese (0.958, SE = 0.020) than for rural geese (0.682, SE = 0.049). Using estimated recovery probabilities of 0.505 (SE = 0.107) for urban and 0.463 (SE = 0.045) for rural geese, along with current estimates of crippling loss and reporting rate, the estimated mean harvest rate for urban geese was 0.029 (SE = 0.006) and for rural geese was 0.202 (SE = 0.020). Fidelity rates were similar between urban (0.730, SE = 0.033) and rural geese (0.713, SE = 0.069). This information suggests that urban segments of the Canada goose population have substantially higher survival than rural geese and are harvested at a very low rate, and that liberalizing hunting regulations may have little impact on Georgia's urban goose population. Wildlife managers may need to consider options other than sport hunting to control nuisance goose populations in urban areas.     

Canada Goose Survival and Recovery Rates in Urban and Rural Areas of Iowa,USA

Once extirpated from much of their North American range, temperate-breeding Canada geese (Branta canadensis maxima) have reached high abundance. As a result, focus has shifted from restoration to managing harvest and addressing human-goose conflict. Conflict persists or is increasing in urban areas throughout the Mississippi Flyway. Managers need more information regarding demographic rates to determine how hunting affects geese breeding in urban areas and what management actions may be required to achieve management goals. We estimated survival, dead recovery, live recapture, and fidelity probabilities using data from 77,872 Canada geese banded in Iowa, USA, during 1999–2019 using Burnham joint live-dead band recovery models. Factors predicted to affect parameters in candidate models included age (juvenile, subadult, adult), banding site (urban, rural), time, trend, harvest regulation index, and winter severity index. We predicted Canada geese banded in urban areas would have higher survival and lower dead recovery rates than geese banded at rural sites. The top model indicated support for age and banding site effects, and trends in survival and recovery rate (Brownie parameterization). Adult survival was similar for urban (0.75; range = 0.60–0.92) and rural (0.75; range = 0.66–0.82) geese and relatively constant across years. Mean juvenile survival was lower in urban (0.74; range = 0.48–0.93) than rural (0.85; range = 0.68–0.92) areas. Survival increased for urban-banded juveniles and recovery rates increased during liberalization of harvest regulations and decreased after regulations stabilized. Recovery rates of subadults increased for the urban and rural groups. Our results suggest Canada geese breeding in urban areas contribute to harvest and specialized regulations can affect these populations. Harvest regulations in place during our analysis may not have reached a threshold required to observe substantial changes in survival. Current human-goose conflict in urban areas suggests survival has not decreased to a level required to completely address conflict via reduction in goose abundance. Managers may consider additional liberalization of harvest regulations and monitoring via banding to determine to what degree hunter harvest contributes to reducing human-goose conflict and what additional management actions will be required to achieve goals. © 2020 The Wildlife Society.     

Changes in abundance and spatial distribution of geese molting near Teshekpuk Lake,Alaska: interspecific competition or ecological change?

Goose populations molting in the Teshekpuk Lake Special Area of the National Petroleum Reserve—Alaska have changed in size and distribution over the past 30 years. Black brant (Branta bernicla nigricans) are relatively stable in numbers but are shifting from large, inland lakes to salt marshes. Concurrently, populations of greater white-fronted geese (Anser albifrons frontalis) have increased seven fold. Populations of Canada geese (Branta canadensis and/or B. hutchinsii) are stable with little indication of distributional shifts. The lesser snow goose (Anser caerulescens caerulescens) population is proportionally small, but increasing rapidly. Coastline erosion of the Beaufort Sea has altered tundra habitats by allowing saltwater intrusion, which has resulted in shifts in composition of forage plant species. We propose two alternative hypotheses for the observed shift in black brant distribution. Ecological change may have altered optimal foraging habitats for molting birds, or alternatively, interspecific competition between black brant and greater white-fronted geese may be excluding black brant from preferred habitats. Regardless of the causative mechanism, the observed shifts in species distributions are an important consideration for future resource planning.     

Molecular status of the dusky Canada goose (Branta canadensis occidentalis): A genetic assessment of a translocation effort

Until recently, the dusky Canada goose (Branta canadensis occidentalis) was managedas one breeding population from the CopperRiver Delta (CRD), Alaska. Population numberson the CRD have declined precipitously over thelast three decades, due in part to changes inhabitat. In 1981, a pair of Canada geese,presumably B.c. occidentalis, wasreported nesting on Middleton Island (MID), inthe Gulf of Alaska. Numbers of Canada geese onthe island increased in the decade subsequentto a translocation of geese from CRD to MID,but it is unclear whether the increase isattributable to the translocation effort. Weused genetic data derived from three classes ofgenetic markers to clarify relationships ofCanada geese breeding in south-coastal Alaska. Geese were sampled from 5 populations: CRD,MID, Anchorage (ANC), Admiralty Island (ADM) insoutheastern Alaska, and Green Island (GRN) inPrince William Sound (PWS). Mitochondrial DNAanalyses demonstrate Canada geese from MID arenearly monomorphic for a unique haplotype fixedon GRN but not found in CRD or any otherbreeding population. Furthermore, nuclearmarkers consistently cluster MID with GRN tothe exclusion of CRD. We suggest the currentpopulation on MID is not derived from birdstranslocated from CRD, but rather that MID wasmost likely colonised by birds inhabiting otherisland habitats within the PWS. Furthermore,since geese from the CRD share mtDNA haplotypeswith geese from other breeding locales, theyapparently share recent common ancestry and/orgene flow with populations representing othersubspecies. Our genetic data raise questionsabout the validity of current management unitsof Canada geese.     

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.     

Using a Cost-Effectiveness Model to Determine the Applicability of OvoControl G to Manage Nuisance Canada Geese

Abstract: OvoControl G is a relatively new product that reduces hatchability of Canada goose (Branta canadensis) eggs, and few data are available on its cost effectiveness. Variables such as presence of nontargets, alternative foods, and public support can affect cost efficacy. We present a model that uses these and other factors to estimate the cost of application of OvoControl G for managing nuisance Canada geese. We found that at low goose densities (<35 pairs of geese), fixed labor was a significant portion of costs. As goose densities increase, OvoControl G becomes more cost effective than other methods, such as egg oiling or addling. Managers can use this model to determine whether OvoControl G will provide a successful and cost-effective treatment for population control of Canada geese in specific management areas.     

Survival and Recovery Rate of Canada Geese Staging in Interior Alaska

Abstract: Lesser Canada geese (Branta canadensis parvipes) are indistinguishable from other subspecies of small Canada geese on the wintering grounds using current survey methods. Consequently, managers are unable to adequately measure their abundance. Without direct estimates of abundance, researchers often use estimates of vital rates that influence abundance (e.g., annual survival) to monitor potential impact of harvest on the population. Based on capture and re-sighting data records of 567 geese marked from 1994 through 1998, we calculated annual survival and recovery rates for different age and sex classes of white-cheeked geese staging in interior Alaska. We compared those survival and recovery rates with those of other neck-collared white-cheeked geese. The best approximating model allowed survival to vary by age class while holding Seber's recovery probability (r̂) constant over sex, age class, and time. We estimated annual survival to be 0.49 (SE = 0.05) for hatch-year geese and 0.68 (SE = 0.03) for after-hatch-year geese based on the weighted average of all models with a change in Akaike's Information Criterion adjusted for small sample size and lack of fit < 4. Estimates of annual survival of white-cheeked geese in this study are among the lowest and recovery estimates are among the highest for migratory populations of neck-collared geese. Low survival estimates of Canada geese in our study suggest that harvest rates may be higher than in many other populations. Surveys to estimate abundance or other population parameters such as reproductive success and recruitment are necessary to determine whether this population is self-sustaining. Furthermore, we recommend monitoring abundance and harvest of small white-cheeked geese east and west of the Cascade Mountain Range separately to better determine harvest pressure on white-cheeked geese wintering east of the Cascades.     

Survival of Dusky Canada Goose Goslings in Relation to Weather and Annual Nest Success

Abstract The dusky Canada goose (Branta canadensis occidentalis) population has been in long-term decline, likely due to reduced breeding productivity, but gosling survival of this population had not been examined. We studied gosling survival in broods of radiomarked adult females on the western Copper River Delta, Alaska, USA, during 1997–1999 and 2001–2003. Survival estimates for dusky Canada goose goslings to 45 days (x̄ = 0.32) were below estimates from most previous studies of geese. Daily survival of goslings increased with age and decreased with date of hatch. Precipitation during the first 3 days post-hatch was negatively related to gosling survival and this effect increased with date. Annual estimates of gosling survival were positively correlated with annual estimates of nest success, suggesting overlap in factors affecting nest and gosling survival. Nest success probably also directly affected gosling survival, because survival decreased with hatch date and more broods hatched from renests during years with low nest success. Gosling survival appears to play an important role in limiting current productivity of this population. Management directed at increasing nest success would likely also improve gosling survival. We recommend additional research directed at examining sources of gosling mortality and the link between nest success and gosling survival.     

Seagrass (Zostera spp.) as food for brent geese (Branta bernicla): an overview

Brent geese (called brant in North America) are among the smallest and the most marine of all goose species, and they have very long migration routes between high Arctic breeding grounds and temperate wintering grounds. Like all other geese, brent geese are almost entirely herbivorous. Because of these ecological characteristics they have a high food demand and are strongly dependent on stopover sites to ”refuel” during the migration period. Three subspecies of brent geese are distributed around the Holarctic, forming seven populations with distinct migration routes. Most or all of these populations make heavy use of Zostera spp. during migratory stopovers on spring and/or autumn migration. Examples of Zostera stopover areas being used by large numbers of brent geese for several weeks each year are Izembek Lagoon (Alaska), lagoons in Baja California, the German/Danish Wadden Sea, the Golfe du Morbihan (France), British estuaries, and the White Sea (Western Russian Arctic). Brent geese feed on Zostera wherever they can, but they can only reach the plants at low tide or in shallow water. Changes in Zostera abundance affect brent goose distribution, and the ”wasting disease” affecting Atlantic Zostera stocks during the 1930s was at least partly responsible for a steep decline in brent goose population sizes on both sides of the Atlantic. While Zostera is of outstanding importance as food for brent geese, the impact of the geese on Zostera stocks seems to be less important – at many sites, the geese consume only a small amount of the available Zostera, or, if they consume more, the seagrass can regenerate fully until the following season. Received: 6 December 1998 / Received in revised form: 6 August 1999 / Accepted: 9 August 1999     

Introduced Swedish Canada geese (Branta canadensis) have low levels of genetic variation as revealed by DNA fingerprinting

The Swedish, Finnish and Norwegian population of Canada geese (Branta canadensis), now amounting to some 30–50 000 birds, was founded by only five individuals. We used DNA fingerprinting to assess the level of genetic variability in minisatellite loci of Swedish Canada geese from two northern areas. For comparison, we estimated the minisatellite variability in lesser white-fronted geese (Anser erythropus), barnacle geese (Branta leucopsis) and a reintroduced stock of Canadian giant Canada geese (Branta canadensis maxima). The mean similarity between Swedish Canada geese was 0.76 ± 0.15, which is higher than recorded for any other natural bird population. The high similarity implies that a fourfold increase of homozygosity has taken place in this population. The probable cause for the loss of variation is the low number of birds originally introduced and a history of repeated translocations, leading to a sequence of founder events. As a consequence of the high similarity, it has not been possible to use DNA fingerprinting for determination of parenthood in the population studied.     

Evidence of Territoriality and Species Interactions from Spatial Point-Pattern Analyses of Subarctic-Nesting Geese

Quantifying spatial patterns of bird nests and nest fate provides insights into processes influencing a species’ distribution. At Cape Churchill, Manitoba, Canada, recent declines in breeding Eastern Prairie Population Canada geese (Branta canadensis interior) has coincided with increasing populations of nesting lesser snow geese (Chen caerulescens caerulescens) and Ross’s geese (Chen rossii). We conducted a spatial analysis of point patterns using Canada goose nest locations and nest fate, and lesser snow goose nest locations at two study areas in northern Manitoba with different densities and temporal durations of sympatric nesting Canada and lesser snow geese. Specifically, we assessed (1) whether Canada geese exhibited territoriality and at what scale and nest density; and (2) whether spatial patterns of Canada goose nest fate were associated with the density of nesting lesser snow geese as predicted by the protective-association hypothesis. Between 2001 and 2007, our data suggest that Canada geese were territorial at the scale of nearest neighbors, but were aggregated when considering overall density of conspecifics at slightly broader spatial scales. The spatial distribution of nest fates indicated that lesser snow goose nest proximity and density likely influence Canada goose nest fate. Our analyses of spatial point patterns suggested that continued changes in the distribution and abundance of breeding lesser snow geese on the Hudson Bay Lowlands may have impacts on the reproductive performance of Canada geese, and subsequently the spatial distribution of Canada goose nests.     

Interspecific Mate Choice Following Cross-fostering in a Mixed Colony of Greylag Geese (Anser anser) and Canada Geese (Branta canadensis). A Study on Development and Persistence of Species Preferences1

The role of early experience in mate choice and species preference of geese was studied in an experiment where young greylag geese (Anser anser) were cross-fostered by Canada geese (Branta canadensis). In two successive years, all eggs from 9 nests of wild Canada geese were removed and replaced by greylag goose eggs. The young greylag geese then followed their Canada goose foster parents on their southward migration in autumn, to return with them in spring. Of 35 returning birds, all 16 females paired with greylag goose males (100%) whereas of 19 males 5 paired with Canada goose females (14%) and the remaining 14 with greylag goose females (74%). The pair bonds generally persisted as long as both birds were present, but after loss of a partner, the remaining bird usually re-mated. Even when this happened several times during the lifetime of a male, the new mate was always a Canada goose female, showing that the males were sexually imprinted to this species. The Canada goose females which had mated with the greylag ganders also remated when widowed, but their new mate could be either a Canada goose or a greylag goose.     

Movements and Survival of Molt Migrant Canada Geese From Southern Michigan

ABSTRACT We studied movements and survival of 250 female giant Canada geese (Branta canadensis maxima) marked during incubation with either satellite-monitored platform transmitting terminals or very high frequency radiotransmitters at 27 capture areas in southern Michigan, USA, in 2000–2003. We destroyed nests of 168 radiomarked females by removing eggs after day 14 of incubation, and we left nests of 82 incubating hens undisturbed after capture and marking. Of females whose nests we experimentally destroyed, 80% subsequently migrated from breeding areas to molt remiges in Canada. Among 82 nests left undisturbed, 37 failed due to natural causes and 51% of those females departed. Migration incidence of birds that nested in urban parks was low (23%) compared with migration incidence of birds that nested in other classes of land use (87%). Departure of females from their breeding areas began during the second and third weeks of May, and most females departed during the last week of May and first week of June. Based on apparent molting locations of 227 marked geese, birds either made long-distance migratory movements >900 km, between latitudes 51° and 64° N, or they remained on breeding areas. Molting locations for 132 migratory geese indicated 4 primary destinations in Canada: Western Ungava Peninsula and offshore islands, Cape Henrietta Maria, Northeast James Bay and offshore islands, and Belcher Islands, Hudson Bay, Canada. Following molt of remiges, Canada geese began to return to their former nesting areas from 20 August through 3 September, with 37% arriving on or before 15 September and 75% arriving on or before 1 October. Migration routes of geese returning to spring breeding areas were relatively indirect compared with direct routes taken to molting sites. Although overall survival from May through November was 0.81 (95% CI: 0.74–0.88), survival of migratory geese marked on breeding sites where birds could be hunted was low (0.60; 95% CI: 0.42–0.75) compared with high survival of birds that remained resident where hunting was restricted (0.93; 95% CI: 0.84–0.97). Nest destruction can induce molt migration, increase hunting mortality of geese returning from molting areas, and reduce human-goose conflicts, but managers also should consider potential impacts of increasing numbers of molt migrants on populations of subarctic nesting Canada geese.     

Foraging preferences of Canada geese among turfgrasses: Implications for reducing human–goose conflicts

Canada geese (Branta canadensis) can cause serious damage to turfgrass areas and create human health and safety concerns (e.g., collisions with aircraft, disease transmission). We conducted a study during 2005–2007 to determine if Canada geese exhibit a feeding preference among various commercially available turfgrasses. Behavioral responses of captive geese to 9 turfgrasses, bare ground, and litter were observed over 6 4-week trials during July–September following the installation of selected turfgrasses into experimental arenas. Captive geese preferred to forage on Kentucky bluegrass, creeping bentgrass, and fine fescue sods compared to centipedegrass, St. Augustinegrass, and zoysiagrass. Forage qualities and macronutrient levels varied among the turfgrasses and might explain the foraging preferences geese exhibited during this study. Canada goose feeding rate was positively correlated with crude protein, nitrogen content, and calcium, but negatively correlated with acid detergent fiber content, within various turfgrasses. Our findings suggest careful selection of turfgrasses could be an effective method for reducing Canada goose conflicts in urban and suburban areas. © 2011 The Wildlife Society.     

Winter Fidelity and Apparent Survival of Lesser Snow Goose Populations in the Pacific Flyway

Abstract The Beringia region of the Arctic contains 2 colonies of lesser snow geese (Chen caerulescens caerulescens) breeding on Wrangel Island, Russia, and Banks Island, Canada, and wintering in North America. The Wrangel Island population is composed of 2 subpopulations from a sympatric breeding colony but separate wintering areas, whereas the Banks Island population shares a sympatric wintering area in California, USA, with one of the Wrangel Island subpopulations. The Wrangel Island colony represents the last major snow goose population in Russia and has fluctuated considerably since 1970, whereas the Banks Island population has more than doubled. The reasons for these changes are unclear, but hypotheses include independent population demographics (survival and recruitment) and immigration and emigration among breeding or wintering populations. These demographic and movement patterns have important ecological and management implications for understanding goose population structure, harvest of admixed populations, and gene flow among populations with separate breeding or wintering areas. From 1993 to 1996, we neckbanded molting birds at their breeding colonies and resighted birds on the wintering grounds. We used multistate mark-recapture models to evaluate apparent survival rates, resighting rates, winter fidelity, and potential exchange among these populations. We also compared the utility of face stain in Wrangel Island breeding geese as a predictor of their wintering area. Our results showed similar apparent survival rates between subpopulations of Wrangel Island snow geese and lower apparent survival, but higher emigration, for the Banks Island birds. Males had lower apparent survival than females, most likely due to differences in neckband loss. Transition between wintering areas was low (<3%), with equal movement between northern and southern wintering areas for Wrangel Island birds and little evidence of exchange between the Banks and northern Wrangel Island populations. Face staining was an unreliable indicator of wintering area. Our findings suggest that northern and southern Wrangel Island subpopulations should be considered a metapopulation in better understanding and managing Pacific Flyway lesser snow geese. Yet the absence of a strong population connection between Banks Island and Wrangel Island geese suggests that these breeding colonies can be managed as separate but overlapping populations. Additionally, winter population fidelity may be more important in lesser snow geese than in other species, and both breeding and wintering areas are important components of population management for sympatric wintering populations.     

Comparative survival and recovery of Ross's and lesser snow geese from Canada's central arctic

Large increases in several populations of North American arctic geese have resulted in ecosystem-level effects from associated herbivory. Consequently, some breeding populations have shown density dependence in recruitment through declines in food availability. Differences in population trajectories of lesser snow geese (Chen caerulescens caerulescens; hereafter snow geese) and Ross's geese (C. rossii) breeding in mixed-species colonies south of Queen Maud Gulf (QMG), in Canada's central arctic, suggest that density dependence may be limiting snow goose populations. Specifically, long-term declines in age ratios (immature:adult) of harvested snow geese may have resulted from declines in juvenile survival. Thus, we focused on juvenile (first-year) survival of snow and Ross's geese in relation to timing of reproduction (annual mean nest initiation date) and late summer weather. We banded Ross's and snow geese from 1991 to 2008 in the QMG Migratory Bird Sanctuary. We used age-structured mark-recapture models to estimate annual survival rates for adults and juveniles from recoveries of dead birds. Consistent with life history differences, juvenile snow geese survived at rates higher than juvenile Ross's geese. Juvenile survival of both species also was lower in late seasons, but was unrelated to arctic weather measured during a 17-day period after banding. We found no evidence of density dependence (i.e., a decline in juvenile survival over time) in either species. We also found no interspecific differences in age-specific hunting vulnerability, though juveniles were more vulnerable than adults in both species, as expected. Thus, interspecific differences in survival were unrelated to harvest. Lower survival of juvenile Ross's geese may result from natural migration mortality related to smaller body size (e.g., greater susceptibility to inclement weather or predation) compared to juvenile snow geese. Despite lower first-year survival, recruitment by Ross's geese may still be greater than that by snow geese because of earlier sexual maturity, greater breeding propensity, and higher nest success by Ross's geese. © 2012 The Wildlife Society.