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At least 325 records · Page 18Linked to original sources
USGS1998

Forage site selection by lesser snow geese during autumn staging on the Arctic National Wildlife Refuge, Alaska

Lesser snow geese ( Chen caerulescens caerulescens ) of the Western Canadian Arctic Population feed intensively for 2-4 weeks on the coastal plain of the Beaufort Sea in Canada and Alaska at the beginning of their autumn migration. Petroleum leasing proposed for the Alaskan portion of the staging area on the Arctic National Wildlife Refuge (ANWR) could affect staging habitats and their use by geese. Therefore we studied availability, distribution, and use by snow geese of tall and russett cotton-grass ( Eriophorum angustifolium and E. russeolum , respectively) feeding habitats on the ANWR. We studied selection of feeding habitats at 3 spatial scales (feeding sites [0.06 m 2 ], feeding patches [ca. 100 m 2 ], and feeding areas [>1 ha]) during 1990-93. We used logistic regression analysis to discriminate differences in soil moisture and vegetation between 1,548 feeding sites where snow geese exploited individual cotton-grass plants and 1,143 unexploited sites at 61 feeding patches in 1990. Feeding likelihood increased with greater soil moisture and decreased where nonforage species were present. We tested the logistic regression model in 1991 by releasing human-imprinted snow geese into 4 10 × 20-m enclosed plots where plant communities had been mapped, habitats sampled, and feeding probabilities calculated. Geese selected more feeding sites per square meter in areas of predicted high quality feeding habitat (feeding probability ≥ 0.6) than in medium (feeding probability = 0.3-0.59) or poor (feeding probability < 0.3) quality habitat (P < 0.0001). Geese increasingly used medium quality areas and spent more time feeding as trials progressed and forage was presumably reduced in high quality habitats. We examined relationships between underground biomass of plants, feeding probability, and surface microrelief at 474 0.06- m 2 sites in 20 thermokarst pits in 1992. Feeding probability was correlated with the percentage of underground biomass composed of cotton-grass (r = 0.56). Feeding probability and relative availability of cotton-grass forage were highest in flooded soils along the ecotone of flooded and upland habitats. In 1992, we also used the logistic regression model to estimate availability of high quality feeding sites on 192 80 × 90-m plots that were randomly located on 24 study areas. A mean of 1.6% of the area sampled in each plot was classified as high quality feeding habitat at 23 of the study areas. Relative availability of high quality sites was highest in troughs, thermokarst pits, and water tracks because saturated soils in those microreliefs were dominated by cotton-grass. Relative availability of high quality sites was lower in saturated soils of basins (low-centered polygons, wet meadows, and strangmoor) because that microrelief was dominated by Carex spp. Most (63%) of the saturated area on the ANWR coastal plain was in basins. We examined distribution of feeding patches relative to microrelief in 49 snow goose feeding areas in 1993. Only 2.5% of the tundra in each feeding area was exploited by snow geese. Snow geese preferentially fed in thermokarst pits, water tracks, and troughs, and avoided basins and uplands. Feeding areas had more thermokarst pit but less basin microrelief than adjacent randomly-selected areas. Thermokarst pits and water tracks occurred most frequently in regions of the coastal plain where geese were observed most often during aerial surveys (1982-93). Microrelief influenced selection of feeding patches and feeding areas and may have affected snow goose distribution on the ANWR. Potential feeding patches were widely distributed but composed a small percentage (≤2.5%) of the tundra landscape and were highly interspersed with less suitable habitat. The Western Canadian Arctic Population probably used a large staging area on the Beaufort Sea coastal plain because snow geese exploited a spatially and temporally heterogeneous resource.

Alaska↗
USGS2012

Appendix A: other methods for estimating trends of Arctic birds

The Arctic PRISM was designed to determine shorebird population size and trend. During an extensive peer review of PRISM, some reviewers suggested that measuring demographic rates or monitoring shorebirds on migration would be more appropriate than estimating population size on the breeding grounds. However, each method has its own limitations. For demographic monitoring, an unbiased estimate based on a large sample of first-year survivorship would be extremely difficult for shorebirds in the arctic because the needed sample size would be unobtainable (in Canada at least) and the level of effort that would need to be expended (both financial and human resource-wise) would far exceed that of the current Arctic PRISM methodology. For migration monitoring, issues such as changes in use of monitored to non-monitored sites, residency times, and detection rates introduce bias that has not yet been resolved. While we believe demographic and migration monitoring are very valuable and are already components of the PRISM approach (e.g., Tier 2 sites focus on the collection of demographic data), we do not believe that either is likely to achieve the PRISM accuracy target of an 80% power to detect a 50% decline.

Book chapter↗
USGS1973

Permian paleogeography of the Arctic

Three large land areas were dominant in the Arctic during the Permian: Fennoscandia, central and southern Siberia (Angara), and Canada. Smaller landmasses were in China, the Seward-Chukotskiy region, northern and eastern Siberia, and near Alaska. Coal deposits and strata bearing land plants covered a large area in central Siberia; saline basins containing red beds formed in the Zechstein, Perm, and West Texas basins as the seas withdrew, generally in the later Permian. Eugeosynclinal troughs, apparently limited to the Pacific border regions, were marked by volcanism and deposition of predominantly clastic sediments in many areas. Platform and miogeosynclinal deposits, dominated by carbonate rocks, preceded saline deposition in the basins and persisted on shallow shelves adjacent to the geosynclines. The Arctic Permian marine fauna evolved in middle Permian time because of partial isolation of the Arctic areas from the southern ocean. Endemism, latitudinal temperature controls, and the effect of ocean currents explain in large part the faunal patterns in Permian seas. Post-Permian tectonic movements account for anomalies in the present positions of some rock sequences and fossils. Northeasterly drift and counterclockwise rotation of the northern landmasses are suggested. Right-lateral shear along the southern edge of Asia is supported, followed by northward movement of peninsular India.

Journal of Research of the U.S. Geological Survey↗
USGS1979

Nesting ecology of Arctic loons

Arctic Loons were studied on the Yukon-Kuskokwim Delta, Alaska, from the time of their arrival in May to their departure in September, in 1974 and 1975. Pairs arrived on breeding ponds as soon as sufficient meltwater was available to allow their take-off and landing. Loons apparently do not initiate nests immediately after their arrival, even when nest-sites are available. Delayed egg-laying may be dependent on a period of yolk formation. Delaying yolk formation until after arrival on nest ponds is an adaptation by loons to the variable time suitable habitat becomes available for nesting. Predation of eggs by Glaucous Gulls, Long-tailed and Parasitic jaegers and foxes varied in relation to the location of the nest-site, and the availability of alternate prey. Hatching success was the lowest recorded for Arctic Loons (5%) in 1974, when eggs of both loons and Cackling Geese were taken in large numbers by predators. Hatching success increased to 32% in 1975 when an abundance of tundra voles was observed. No loon eggs hatched after the hatching of the Cackling Goose eggs when this alternate prey was no longer available. Nests destroyed by foxes were predominantly along shorelines, and those by gulls and jaegers were predominantly on islands. Nest-site selection by Arctic Loons may reflect an adaptive response to varying selective pressures by their predators.

Alaska↗
USGS2023

Vulnerability and resilience of ice-rich permafrost to thermal erosion gullying in the Arctic Foothills infrastructure corridor, Alaska

The Arctic and its permafrost terrains are inherently dynamic, complex, and sensitive environments. Understanding the past and current changes occurring in these systems is key in predicting future variations, including the response of permafrost to climate change and to surface disturbances resulting from natural processes or anthropogenic activities. Here, we focus on advancing our understanding of the drivers controlling terrain vulnerability and resilience to thermal erosion gullying proximal to linear infrastructure in the lowlands of the Arctic Foothills (Alaska). This builds upon our previous work (Stephani et al. 2023) in the infrastructure corridor that includes the Dalton Highway and Trans Alaska Pipeline System (TAPS). To identify locations affected by thermal erosion gullying and recognize changes in the ~80-km long corridor section that travels through the Arctic Foothills, we compared time series of high-resolution satellite imagery from 2001 to 2023. When we captured the timing of gullying onset and/or growth, we examined prevailing climatic conditions (Sagwon Station) prior to these terrain changes. We integrated our findings with our field-based data (e.g., drilling) described in Stephani et al. (2023).

Alaska↗
USGS2018

Post-breeding movement and habitat use by wood frogs along an Arctic–Subarctic ecotone

By altering essential micro- and macrohabitat conditions for many organisms, climate change is already causing disproportionately greater impacts on Arctic and Subarctic ecosystems. Yet there is a lack of basic information about many species in northern latitudes, including amphibians. We used radio telemetry to study the post-breeding movements and habitat use of wood frogs ( Rana [= Lithobates ] sylvatica ) in the Hudson Bay Lowlands near Churchill, Manitoba, Canada. We tracked fifty-seven frogs (thirty-five males, twenty-two females; mean duration = 16.8 d) from three wetlands during the summers of 2015 and 2016. The three wetlands were representative of the Arctic–Subarctic ecotone, with each wetland surrounded by different proportions of boreal forest and tundra. Our results indicate that at the landscape scale, movement distances increased with temperature, and all frogs spent more time in the tundra habitat than in boreal forests, relative to the availability of each habitat type. At the microhabitat scale (1 m 2 plots), frogs selected areas with greater amounts of standing water, sedge, and shrubs. These results provide information on terrestrial movement patterns and critical habitat data for northern populations of wood frogs in a Subarctic environment, which will aid in understanding how climate change will affect amphibians in this rapidly changing ecosystem.

Manitoba↗
USGS2021

Arctic insect emergence timing and composition differs across thaw ponds of varying morphology

Freshwater ponds provide habitats for aquatic insects that emerge and subsidize consumers in terrestrial ecosystems. In the Arctic, insects provide an important seasonal source of energy to birds that breed and rear young on the tundra. The abundance and timing of insect emergence from arctic thaw ponds is poorly understood, but understanding these fluxes is important, given the role of insects in food webs and current rates of environmental change at high latitudes. We aimed to evaluate emerging insect communities from thaw ponds with different morphologies, identify environmental covariates influencing insect composition, and describe temporal changes in insect abundance. We collected environmental information and insects that emerged over two growing seasons and examined the phenology and taxonomic composition of insects arising from different pond classes: low centered polygon, small coalescent, large coalescent, and trough ponds. Our findings indicated no differences in the timing of total emergence across ponds of varying morphology. Community dissimilarity was primarily associated with center or margin habitat and variables that differed strongly among pond classes. These insects, which provide important provisions for various species of birds, are likely to experience changes in emergence phenology and composition due to ongoing, rapid warming in the region.

Alaska↗
USGS1969

Heat flow in the Arctic

Defines heat flow as the flux at the earth's solid surface of heat conducted from the interior; the heat-flow-unit (hfu) is on the order of 1-millionth calorie through each sq cm of the surface/sec, which is enough to melt a 4-mm layer of ice over the earth's surface/yr. Earth heat originates from radioactive decay of U, Th and K in the crust and mantle. Although land heat-flow measurements in the Arctic are too few for regional interpretation, those from Cape Thompson, Barrow and Cape Simpson, Northern Alaska are discussed and figured to show what they contribute to understanding of permafrost, climatic change and shoreline movements. Measuring thermal conductivity and gradient is much simpler in ocean basins than on land. Locations of such measurements are mapped, the results for the Alaskan quadrant in more detail. The sharp change in heat flow at the edge of the Alpha Cordillera, shown in a geothermal model, suggests that this feature is a huge accumulation of basalt, rather than mantle material or remnant of a foundering continent as previously postulated. Future Arctic heat flow studies are discussed.

Arctic↗
USGS2010

Central Arctic caribou and petroleum development: Distributional, nutritional, and reproductive implications

We synthesize findings from cooperative research on effects of petroleum development on caribou ( Rangifer tarandus granti ) of the Central Arctic Herd (CAH). The CAH increased from about 6000 animals in 1978 to 23000 in 1992, declined to 18 000 by 1995, and again increased to 27 000 by 2000. Net calf production was consistent with changes in herd size. In the Kuparuk Development Area (KDA), west of Prudhoe Bay, abundance of calving caribou was less than expected within 4 km of roads and declined exponentially with road density. With increasing infrastructure, high-density calving shifted from the KDA to inland areas with lower forage biomass. During July and early August, caribou were relatively unsuccessful in crossing road/pipeline corridors in the KDA, particularly when in large, insect-harassed aggregations; and both abundance and movements of females were lower in the oil field complex at Prudhoe Bay than in other areas along the Arctic coast. Female caribou exposed to petroleum development west of the Sagavanirktok River may have consumed less forage during the calving period and experienced lower energy balance during the midsummer insect season than those under disturbance-free conditions east of the river. The probable consequences were poorer body condition at breeding and lower parturition rates for western females than for eastern females (e.g., 1988–94: 64% vs. 83% parturient, respectively; p = 0.003), which depressed the productivity of the herd. Assessments of cumulative effects of petroleum development on caribou must incorporate the complex interactions with a variable natural environment.

Arctic↗
USGS2010

Decline and recovery of a high Arctic wolf-prey system

A long-existing system of wolves ( Canis lupus ), muskoxen ( Ovibos moschatus ), and arctic hares ( Lepus arcticus ) in a 2600 km2 area of Canada’s High Arctic (80° N latitude) began collapsing in 1997 because of unusual adverse summer weather but recovered to a level at which all three species were reproducing by 2004. Recovery of wolf presence and reproduction appeared to be more dependent on muskox increase than on hare increase.

Nunavit↗
USGS2000

Lack of reproduction in muskoxen and arctic hares caused by early winter?

A lack of young muskoxen ( Ovibos moschatus ) and arctic hares ( Lepus arcticus ) in the Eureka area of Ellesmere Island, Northwest Territories (now Nunavut), Canada, was observed during summer 1998, in contrast to most other years since 1986. Evidence of malnourished muskoxen was also found. Early winter weather and a consequent 50% reduction of the 1997 summer replenishment period appeared to be the most likely cause, giving rise to a new hypothesis about conditions that might cause adverse demographic effects in arctic herbivores.

Arctic↗
USGS1999

Long-term experimental manipulation of winter snow regime and summer temperature in arctic and alpine tundra

Three 60 m long, 2·8 m high snowfences have been erected to study long-term effects of changing winter snow conditions on arctic and alpine tundra. This paper describes the experimental design and short-term effects. Open-top fiberglass warming chambers are placed along the experimental snow gradients and in controls areas outside the fences; each warming plot is paired with an unwarmed plot. The purpose of the experiment is to examine short- and long-term changes to the integrated physical-biological systems under simultaneous changes of winter snow regime and summer temperature, as part of the Long-Term Ecological Research network and the International Tundra Experiment. The sites were at Niwot Ridge, Colorado, a temperate high altitude site in the Colorado Rockies, and Toolik Lake, Alaska, a high-latitude site. Initial results indicate that although experimental designs are essentially identical at the arctic and alpine sites, experimental effects are different. The drift at Niwot Ridge lasts much longer than do the Toolik Lake drifts, so that the Niwot Ridge fence affects both summer and winter conditions, whereas the Toolik Lake fence affects primarily winter conditions. The temperature experiment also differs in effect between the sites. Although the average temperature increase at the two sites is similar (daily increase 1·5 °C at Toolik and 1·9 °C at Niwot Ridge), at Toolik Lake there is only minor diurnal variation, whereas at Niwot Ridge the daytime increases are extreme on sunny days (as much as 7–10 °C), and minimum nighttime temperatures in the chambers are often slightly cooler than ambient (by about 1 °C). The experimental drifts resulted in wintertime increases in temperature and CO 2 flux. Temperatures under the deep drifts were much more consistent and warmer than in control areas, and at Niwot Ridge remained very close to 0 °C all winter. These increased temperatures were likely responsible for observed increases in system carbon loss. Initial changes to the aboveground biotic system included an increase in growth in response to both snow and warming, despite a reduced growing season. This is expected to be a transient response that will eventually be replaced by reduced growth. At least one species, Kobresia myosuroides , had almost completely died at Niwot Ridge three years after fence construction, whereas other species were increasing. We expect in both the short- and long-term to see the strongest effects of snow at the Niwot Ridge site, and stronger effects of temperature at Toolik Lake.

Hydrological Processes↗
USGS2014

InSAR detects increase in surface subsidence caused by an Arctic tundra fire

Wildfire is a major disturbance in the Arctic tundra and boreal forests, having a significant impact on soil hydrology, carbon cycling, and permafrost dynamics. This study explores the use of the microwave Interferometric Synthetic Aperture Radar (InSAR) technique to map and quantify ground surface subsidence caused by the Anaktuvuk River fire on the North Slope of Alaska. We detected an increase of up to 8 cm of thaw-season ground subsidence after the fire, which is due to a combination of thickened active layer and permafrost thaw subsidence. Our results illustrate the effectiveness and potential of using InSAR to quantify fire impacts on the Arctic tundra, especially in regions underlain by ice-rich permafrost. Our study also suggests that surface subsidence is a more comprehensive indicator of fire impacts on ice-rich permafrost terrain than changes in active layer thickness alone.

Alaska↗
USGS2014

Radiocarbon age-offsets in an arctic lake reveal the long-term response of permafrost carbon to climate change

Continued warming of the Arctic may cause permafrost to thaw and speed the decomposition of large stores of soil organic carbon (OC), thereby accentuating global warming. However, it is unclear if recent warming has raised the current rates of permafrost OC release to anomalous levels or to what extent soil carbon release is sensitive to climate forcing. Here we use a time series of radiocarbon age-offsets ( 14 C) between the bulk lake sediment and plant macrofossils deposited in an arctic lake as an archive for soil and permafrost OC release over the last 14,500 years. The lake traps and archives OC imported from the watershed and allows us to test whether prior warming events stimulated old carbon release and heightened age-offsets. Today, the age-offset (2 ka; thousand of calibrated years before A.D. 1950) and the depositional rate of ancient OC from the watershed into the lake are relatively low and similar to those during the Younger Dryas cold interval (occurring 12.9–11.7 ka). In contrast, age-offsets were higher (3.0–5.0 ka) when summer air temperatures were warmer than present during the Holocene Thermal Maximum (11.7–9.0 ka) and Bølling-Allerød periods (14.5–12.9 ka). During these warm times, permafrost thaw contributed to ancient OC depositional rates that were ~10 times greater than today. Although permafrost OC was vulnerable to climate warming in the past, we suggest surface soil organic horizons and peat are presently limiting summer thaw and carbon release. As a result, the temperature threshold to trigger widespread permafrost OC release is higher than during previous warming events.

Alaska↗
USGS2019

Geographic variation in the intensity of warming and phenological mismatch between Arctic shorebirds and invertebrates

Responses to climate change can vary across functional groups and trophic levels, leading to a temporal decoupling of trophic interactions or ‘phenological mismatches.’ Despite a growing number of single-species studies that identified phenological mismatches as a nearly universal consequence of climate change, we have a limited understanding of the spatial variation in the intensity of this phenomenon nor what influences this variation. In this study, we tested for geographic patterns in phenological mismatches between six species of shorebirds and their invertebrate prey at ten sites spread across ~13º latitude and ~84º longitude in the Arctic over three years. At each site, we quantified the phenological mismatch between shorebirds and their invertebrate prey at: 1) an individual nest level, as the difference in days between the seasonal peak in food and the peak demand by chicks, and 2) a population level, as the overlapped area under fitted curves for total daily biomass of invertebrates and dates of the peak demand by chicks. We tested whether the intensity of past climatic change observed at each site corresponded with the extent of phenological mismatch and used Structural Equation Modeling to test for causal relationships among: 1) environmental factors, including geographic location and current climatic conditions, 2) the timing of invertebrate emergence and the breeding phenology of shorebirds, and 3) the phenological mismatch between the two trophic levels. The extent of phenological mismatch varied more among different sites than among different species within each site. A greater extent of phenological mismatch at both the individual-nest and population-levels coincided with changes in the timing of snowmelt as well as the potential dissociation of long-term snow phenology from changes in temperature. The timing of snowmelt also affected the shape of the food and demand curves, which determined the extent of phenological mismatch at the population level. Finally, we found larger mismatches at more easterly longitudes, which may be affecting the population dynamics of shorebirds, as two of our study species show regional population declines in only the eastern part of their range. This suggests that phenological mismatches may be resulting in demographic consequences for arctic-nesting birds.

Alaska↗
USGS2021

Response of forage plants to alteration of temperature and spring thaw date: Implications for geese in a warming Arctic

Changes in summer temperatures in Arctic Alaska have led to longer and warmer growing seasons over the last three decades. Corresponding with these changes in climate, the abundance and distributions of geese have increased and expanded over the same period. We used an experimental approach to assess the response of goose forage plants to simulated environmental change. We subjected Carex subspathacea , a preferred goose forage growing on the Arctic Coastal Plain (ACP) of Alaska, to manipulations of temperature and timing of spring thaw to measure potential effects in terms of plant nitrogen concentration, aboveground biomass, and total nitrogen availability. Carex subspathacea responded to warming in a dynamic fashion. Increases in temperature led to decreases in leaf nitrogen concentration but increases in aboveground biomass. The increase in biomass was stronger than the decline in nitrogen concentration such that total nitrogen availability was increased with temperature for the first 35–40 d of the season. Grazing removal accounted for only minimal offtake of biomass, and we found no indication that grazing maintained elevated levels of nitrogen concentration longer in the season as reported in other studies. Based on demonstrated relationships in the literature between forage nitrogen concentrations and gosling growth rates, we conclude that there is currently abundant high-quality forage available across the ACP. This finding fits with recent evidence of high gosling growth rates and increasing trends in goose abundance on the ACP. Our results suggest that with climate warming of a few degrees, nitrogen concentration of forage may decrease, but forage biomass and total nitrogen availability will increase. Our data suggest that nitrogen concentration will not fall below the minimum threshold required by geese in the near future. As such, we suggest that there is currently no bottom-up limitation to goose numbers on the ACP.

Alaska↗
USGS2020

Co-producing knowledge: The Integrated Ecosystem Model for resource management in Arctic Alaska

Assessments of climate-change effects on ecosystem processes and services in high-latitude regions are hindered by a lack of decision-support tools capable of forecasting possible future landscapes. We describe a collaborative effort to develop and apply the Integrated Ecosystem Model (IEM) for Alaska and northwestern Canada to explore how climate change influences interactions among disturbance regimes, permafrost integrity, hydrology, and vegetation, and how these dynamics in turn influence resource management decisions. This process emphasizes co-production of knowledge among decision makers, scientists, major funders, partners, and stakeholders. We highlight research findings based on IEM applications in Arctic Alaska, as well as successes and challenges of the co-production process. The overall framework and lessons from our work with the IEM are relevant to other collaborative efforts outside the Arctic that aim to develop a decision-support tool or an undertaking of equivalent scope.

Alaska↗
USGS2021

Understanding the effects of climate change via disturbance on pristine arctic lakes — Multitrophic level response and recovery to a 12-yr, low-level fertilization experiment

Effects of climate change-driven disturbance on lake ecosystems can be subtle; indirect effects include increased nutrient loading that could impact ecosystem function. We designed a low-level fertilization experiment to mimic persistent, climate change-driven disturbances (deeper thaw, greater weathering, or thermokarst failure) delivering nutrients to arctic lakes. We measured responses of pelagic trophic levels over 12 yr in a fertilized deep lake with fish and a shallow fishless lake, compared to paired reference lakes, and monitored recovery for 6 yr. Relative to prefertilization in the deep lake, we observed a maximum pelagic response in chl a (+201%), dissolved oxygen (DO, −43%), and zooplankton biomass (+88%) during the fertilization period (2001–2012). Other responses to fertilization, such as water transparency and fish relative abundance, were delayed, but both ultimately declined. Phyto- and zooplankton biomass and community composition shifted with fertilization. The effects of fertilization were less pronounced in the paired shallow lakes, because of a natural thermokarst failure likely impacting the reference lake. In the deep lake there was (a) moderate resistance to change in ecosystem functions at all trophic levels, (b) eventual responses were often nonlinear, and (c) postfertilization recovery (return) times were most rapid at the base of the food web (2–4 yr) while higher trophic levels failed to recover after 6 yr. The timing and magnitude of responses to fertilization in these arctic lakes were similar to responses in other lakes, suggesting indirect effects of climate change that modify nutrient inputs may affect many lakes in the future.

Alaska↗