Geology topics

K.S. Bollinger

Publications and source records attributed to K.S. Bollinger.

8 recordsLinked to original sources

USGS2007

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. ?? 2007 Springer-Verlag.

Polar Biology↗

USGS2007

Reproductive strategies of northern geese: Why wait?

Migration and reproductive strategies in waterbirds are tightly linked, with timing of arrival and onset of nesting having important consequences for reproductive success. Whether migratory waterbirds are capital or income breeders is predicated by their spring migration schedule, how long they are on breeding areas before nesting, and how adapted they are to exploiting early spring foods at northern breeding areas. However, for most species, we know little about individual migration schedules, arrival times, and duration of residence on breeding areas before nesting. To document these relationships in a northern nesting goose, we radiotracked winter-marked Tule Greater White-fronted Geese ( Anser albifrons elgasi ; hereafter “Tule Geese”; n = 116) from the time of their arrival in Alaska through nesting. Tule Geese arrived on coastal feeding areas in mid-April and moved to nesting locations a week later. They initiated nests 15 days (range: 6–24 days) after arrival, a period roughly equivalent to the duration of rapid follicle growth. Tule Geese that arrived the earliest were more likely to nest than geese that arrived later; early arrivals also spent more time on the breeding grounds and nested earlier than geese that arrived later. The length of the prenesting period was comparable to that of other populations of this species, but longer than for goose species that initiate rapid follicle growth before arrival on the breeding grounds. We suggest that Tule Geese nesting in more temperate climates are more likely to delay breeding to exploit local food resources than Arctic-nesting species that may be constrained by short growing seasons.

The Auk↗

USGS2006

Traversing a boreal forest landscape: Summer movements of Tule Greater White-fronted Geese

We monitored the movement, distribution and site affinities of radio-marked Tule Greater White-fronted Geese (Anser albifrons elgasi) during spring and summer in Alaska, 1994-1997 and 2004. Our assessment of summer movements was comprehensive, as locations were obtained during prenesting, nesting, and molt for over 90% of geese with active radios captured during winter or the previous summer in Alaska. Geese arrived to coastal and interior marshes in the Cook Inlet Basin (CIB) from mid April to early May, after which they moved to nesting areas in the upper CIB. Nesting birds used coastal staging areas in close proximity to eventual nest site location. Molting sites included a sub-glacial lake system in the upper CIB, although up to 50% of geese underwent a molt migration to wetlands across the Alaska Range, 400-600 km west of the CIB. Geese that molted at distant sites returned to the CIB before autumn migration. Length of stay in the CIB varied among years from 108-119 days, and averaged 116 days. Summer home-range sizes, exclusive of molting areas, averaged >273,000 ha, and were substantially larger than reported for other northern-nesting waterfowl. No radio-marked geese were found nesting in the vicinity of Redoubt Bay on the west side of Cook Inlet, and few nested near the Susitna Flats, the only other previously known nesting areas. The absence of nesting geese from Redoubt Bay corroborates aerial survey data showing a precipitous decline in the use of the west side of Cook Inlet between the early 1980s and early 1990s. The change in distribution of geese is likely related to a major eruption of Redoubt Volcano in 1989 that significantly altered landscapes used by nesting, brood rearing, and molting geese in the vicinity of Redoubt Bay. High inter-site movements of Greater White-fronted Geese throughout summer in south central Alaska likely increases exposure to predation, but also promotes social interactions and facilitates pioneering of distant, and diverse habitats in a vast, patchy, and often unpredictable landscape.

Alaska↗

USGS2006

Nesting habitat of the Tule Greater White-fronted Goose Anser albifrons elgasi

This paper presents the first information on the availability and use of nesting habitat by the rare Tule Greater White-fronted Goose Anser albifrons elgasi. The breeding range was sampled by marking geese with radio transmitters on wintering and moulting areas, and tracking them to nest sites in Alaska. Nesting habitat was described at the scales of ecoregion, wetland ecosystem (National Wetlands Inventory (NWI) maps), vegetation type within wetland (Alaska Vegetation Classification (AVC) maps based on satellite imagery), and nest site. Tule Greater White-fronted Goose nests were located in boreal forest wetlands in the upper Cook Inlet Basin ecoregion. Nesting Tule Greater White-fronted Geese selected NWT Palustrine Seasonally Flooded wetlands and used NWI Palustrine Saturated wetlands in proportion to availability. Within these wetlands, Tule Greater White-fronted Geese used Needleleaf Forest, Low Shrub and Herbaceous (mostly graminoid) AVC classes for nest sites in proportion to availability Most (93%) Tule Greater White-fronted Geese nested > 75 m from open water ponds or lakes, and many nested in wetlands with little or no open water. Tule Greater White-fronted Geese nest only in a small breeding area near the most human-impacted area of the state, and continued development may limit the use of suitable nesting habitat.

Alaska↗

USGS2003

Phylogeography of Canada Geese ( Branta canadensis ) in western North America

Using molecular genetic markers that differ in mode of inheritance and rate of evolution, we examined levels and partitioning of genetic variation for seven nominal subspecies (11 breeding populations) of Canada Geese (Branta canadensis) in western North America. Gene trees constructed from mtDNA control region sequence data show that subspecies of Canada Geese do not have distinct mtDNA. Large- and small-bodied forms of Canada Geese were highly diverged (0. 077 average sequence divergence) and represent monophyletic groups. A majority (65%) of 20 haplotypes resolved were observed in single breeding locales. However, within both large- and small-bodied forms certain haplotypes occurred across multiple subspecies. Population trees for both nuclear (microsatellites) and mitochondrial markers were generally concordant and provide resolution of population and subspecific relationships indicating incomplete lineage sorting. All populations and subspecies were genetically diverged, but to varying degrees. Analyses of molecular variance, nested-clade and coalescence-based analyses of mtDNA suggest that both historical (past fragmentation) and contemporary forces have been important in shaping current spatial genetic distributions. Gene flow appears to be ongoing though at different rates, even among currently recognized subspecies. The efficacy of current subspecific taxonomy is discussed in light of hypothesized historical vicariance and current demographic trends of management and conservation concern.

The Auk↗

USGS2002

Sources of variation in breeding-ground fidelity of mallards (Anas platyrhynchos)

Generalizations used to support hypotheses about the evolution of fidelity to breeding areas in birds include the tendency for fidelity to be greater in adult birds than in yearlings. In ducks, in contrast to most bird species, fidelity is thought to be greater among females than males. Researchers have suggested that fidelity in ducks is positively correlated with pond availability. However, most estimates of fidelity on which these inferences have been based represent functions of survival and recapture-resighting probabilities in addition to fidelity. We applied the modeling approach developed by Burnham to recapture and band recovery data of mallard ducks to test the above hypotheses about fidelity. We found little evidence of sex differences in adult philopatry, with females being slightly more philopatric than males in one study area, but not in a second study area. However, yearling females were more philopatric than yearling males in both study areas. We found that adults were generally more philopatric than yearlings. We could find no relationship between fidelity and pond availability. Our results, while partially supporting current theory concerning sex and age differences in philopatry, suggest that adult male mallards are more philopatric than once thought, and we recommend that other generalizations about philopatry be revisited with proper estimation techniques.

Behavioral Ecology↗

USGS1996

Black brant from Alaska staging and wintering in Japan

Black brant (Branta bernicla nigricans) nest in colonies in arctic Canada, Alaska, and Russia (Derksen and Ward 1993, Sedinger et al. 1993). Virtually the entire population stages in fall at Izembek Lagoon near the tip of the Alaska Peninsula (Bellrose 1976) before southward migration (Dau 1992) to winter habitats in British Columbia, Washington, Oregon, California, and Baja California (Subcommittee on Black Brant 1992). A small number of black brant winter in Japan, Korea, and China (Owen 1980). In Japan 3,000–5,000 brant of unknown origin stop over in fall, and a declining population (<1,000) of birds winter here, primarily in the northern islands (Brazil 1991, Miyabayashi et al. 1994). Here, we report sightings of brant in Japan that were marked in Alaska and propose a migration route based on historical and recent observations and weather patterns.

Alaska↗

USGS1996

Demographic characteristics of molting black brant near Teshekpuk Lake, Alaska

Molting Brant in the Teshekpuk Lake Special Area (TLSA) on the Arctic Coastal Plain of Alaska were studied from 1987 to 1992 using capture-mark-recapture techniques to determine origin, age and sex composition, return rates and site fidelity. Brant originated from 10 nesting colonies in Canada and Alaska. The captured birds were 76% adults and 57% males. Ninety-one percent of known-age recaptures were

Journal of Field Ornithology↗