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Research about Glacier Bay

Source-linked reports with geographic coverage including Glacier Bay.

18 recordsLinked to original sources
USGS2024

The dynamics of sea otter prey selection under population growth and expansion

Sea otters ( Enhydra lutris ) were extirpated from much of their range in the North Pacific by the early 1900s but have made a remarkable recovery in Southeast Alaska. Sea otter populations have been particularly successful in Glacier Bay, Alaska, a protected tidewater glacier fjord with a diverse and productive nearshore habitat. Collection of sea otter foraging observations in Glacier Bay began in 1993, along with high-resolution aerial surveys that provide estimates of sea otter abundance and distribution. We integrated these two data sources to investigate how sea otter diet changed in space and time as sea otters established and spread across Glacier Bay. Specifically, we developed a multilevel Bayesian model to capture how sea otter diet at a location (the number, type, and size of prey collected) changed as a function of local cumulative otter abundance and the year in which the location was first occupied. This framework enabled us to estimate the sequence of sea otter prey selection and switching as prey populations responded to sea otter foraging pressure. We found that local sea otter diet changed substantially as the population established, shifting away from large urchins, crabs, and clams to Modiolus mussels and small urchins, and lastly to small clams and Mytilus mussels. We also found that sea otter diet at newly occupied sites changed as otters spread over the main channel and into the arms of Glacier Bay. Further, by 2019, sea otters across the bay were primarily foraging on small prey, regardless of the local occupancy history. The absence of a spatial gradient in the size of prey captured late in the study suggests that feedbacks between the top-down effects of sea otter foraging, sea otter dispersal processes, and local variation in habitat productivity may have homogenized the size structure of available prey across Glacier Bay.

Alaska↗
USGS2022

Submarine landslide susceptibility mapping in recently deglaciated terrain, Glacier Bay, Alaska

Submarine mass wasting events have damaged underwater structures and propagated waves that have inundated towns and affected human populations in nearby coastal areas. Susceptibility to submarine landslides can be pronounced in degrading cryospheric environments, where existing glaciers can provide high volumes of sediment, while cycles of glaciation and ice-loss can damage and destabilize slopes. Despite their contribution to potential tsunami hazard, submarine landslides can be difficult to study because of limited access and data collection in underwater environments. Here we present a method to quantify and map the submarine landslide susceptibility of sediment-covered slopes in Glacier Bay, Glacier Bay National Park and Preserve, Alaska, using multibeam-sonar bathymetric digital elevation models (DEMs) and historical maps of glacial extents over the last ∼250 years. After mapping an inventory of >7,000 landslide scarps in submarine sediments, we filtered the inventory by size to account for limitations in DEM resolution and spatial scales relevant to tsunami hazards. We then assessed landslide concentration, accounting for the age of the initial exposure of submarine slopes by deglaciation. We found a positive correlation between landslide concentration and deglaciation age, which we interpreted as a mean landslide accumulation rate over the period of record. Local deviations from this rate indicated differences in susceptibility. Additionally, we accounted for some of the effect of material and morphometric properties by estimating the submarine bedrock-sediment distribution using a morphometric model and assessing the relationship between slope angle and landslide incidence. Finally, we supplemented our susceptibility assessment with a geomorphic component based on the propensity of active submarine fans and deltas to produce landslides. Thus, our map of submarine landslide susceptibility incorporates three components: age-adjusted landslide concentration, slope angle, and geomorphology. We find that areas of mapped high susceptibility correlate broadly with areas of high sediment input and availability, locations of fans and deltas, and steep sediment-covered glacially carved fjords and troughs. Areas of high submarine landslide susceptibility in Glacier Bay moderately correspond with locations of known high-hazard subaerial slopes, but more research on submarine and subaerial landslides in degrading cryospheric environments would be beneficial to better understand landslide and tsunami hazards.

Alaska↗
USGS2020

Using a bayesian multistate occupancy model to assess seabird and shorebird status in Glacier Bay, Alaska

The U.S. Department of Interior National Park Service is charged with both monitoring avian communities and evaluating the influence of visitors to National Parks on sensitive species; however, this task is challenging considering that sampling programs often involve multiple species, each with differing behavior, habitat requirements, and detectability. Our objectives were to build a model to describe the status of waterbirds in Glacier Bay National Park, Alaska, USA, and assess effects of area closures on these species. We used a Bayesian multistate occupancy model to describe the status of multiple species and make the best possible use of existing survey data. We modeled up to 5 states per species and evaluated predictors of occupancy, nesting, and abundance, as well as survey-related predictors of state-dependent detection probability. We found that occupancy probability varied across species and habitats (islands vs. glacial outwashes). For most species, occupancy probability was substantially greater at sites occupied in the year previous (site persistence). We found weak evidence that area closures affected the occurrence of species in the study, but this was largely because most sites were closed for the entirety of the study period. The probability of detecting occurrence, nesting, and abundance varied across species and survey methods (ground vs. vessel). Detection parameters provided valuable information for enhancing the efficiency of future surveys, by identifying preferred survey methods and sampling periods for specific waterbird species. © 2020 The Wildlife Society.

Alaska↗
USGS2019

Nonlinear reaction–diffusion process models improve inference for population dynamics

Partial differential equations (PDEs) are a useful tool for modeling spatiotemporal dynamics of ecological processes. However, as an ecological process evolves, we need statistical models that can adapt to changing dynamics as new data are collected. We developed a model that combines an ecological diffusion equation and logistic growth to characterize colonization processes of a population that establishes long-term equilibrium over a heterogeneous environment. We also developed a homogenization strategy to statistically upscale the PDE for faster computation and adopted a hierarchical framework to accommodate multiple data sources collected at different spatial scales. We highlighted the advantages of using a logistic reaction component instead of a Malthusian component when population growth demonstrates asymptotic behavior. As a case study, we demonstrated that our model improves spatiotemporal abundance forecasts of sea otters in Glacier Bay, Alaska. Furthermore, we predicted spatially varying local equilibrium abundances as a result of environmentally driven diffusion and density-regulated growth. Integrating equilibrium abundances over the study area in our application enabled us to infer the overall carrying capacity of sea otters in Glacier Bay, Alaska.

Alaska↗
USGS2019

The rise of an apex predator following deglaciation

Aim Sea otters ( Enhydra lutris ) are an apex predator of the nearshore marine community and nearly went extinct at the turn of the 20th century. Reintroductions and legal protection allowed sea otters to re‐colonize much of their former range. Our objective was to chronicle the colonization of this apex predator in Glacier Bay, Alaska, to help understand the mechanisms that governed their successful colonization. Location Glacier Bay is a tidewater glacier fjord in southeastern Alaska that was entirely covered by glaciers in the mid‐18th century. Since then, it has endured the fastest tidewater glacier retreat in recorded history. Methods We collected and analysed several data sets, spanning 20 years, to document the spatio‐temporal dynamics of an apex predator expanding into an area where they were formerly absent. We used novel quantitative tools to model the occupancy, abundance and colonization dynamics of sea otters, while accounting for uncertainty in the data collection process, the ecological process and model parameters. Results Twenty years after sea otters were first observed colonizing Glacier Bay, they became one of the most abundant and widely distributed marine mammal. The population grew exponentially at a rate of 20% per year. They colonized Glacier Bay at a maximum rate of 6 km per year, with faster colonization rates occurring early in the colonization process. During colonization, sea otters selected shallow areas, close to shore, with a steep bottom slope, and a relatively simple shoreline complexity index. Main conclusions The growth and expansion of sea otters in Glacier Bay demonstrate how legal protection and translocation of apex predators can facilitate their successful establishment into a community in which they were formerly absent. The success of sea otters was, in part, a consequence of habitat that was left largely unperturbed by humans for the past 250 years. Further, sea otters and other marine predators, whose distribution is limited by ice, have the potential to expand in distribution and abundance, reshaping future marine communities in the wake of deglaciation and global loss of sea ice.

Alaska↗
USGS2012

Structure of marine predator and prey communities along environmental gradients in a glaciated fjord

Spatial patterns of marine predator communities are influenced to varying degrees by prey distribution and environmental gradients. We examined physical and biological attributes of an estuarine fjord with strong glacier influence to determine the factors that most influence the structure of predator and prey communities. Our results suggest that some species, such as walleye pollock ( Theragra chalcogramma ), black-legged kittiwake ( Rissa tridactyla ), and glaucous-winged gull ( Larus glaucescens ), were widely distributed across environmental gradients, indicating less specialization, whereas species such as capelin ( Mallotus villosus ), harbor seal ( Phoca vitulina ), and Kittlitz's murrelet ( Brachyramphus brevirostris ) appeared to have more specialized habitat requirements related to glacial influence. We found that upper trophic level communities were well correlated with their mid trophic level prey community, but strong physical gradients in photic depth, temperature, and nutrients played an important role in community structure as well. Mid-trophic level forage fish communities were correlated with the physical gradients more closely than upper trophic levels were, and they showed strong affinity to tidewater glaciers. Silica was closely correlated with the distribution of fish communities, the mechanisms of which deserve further study.

Alaska↗
USGS2011

Status and trend of the Kittlitz's Murrelet Brachyramphus brevirostris in Glacier Bay, Alaska

We conducted standardized surveys for marine birds in Glacier Bay in seven years between 1991 and 2008. From our most recent survey, a combination of line- and strip-transect methods completed in 2008, we estimated that 4981 (95% CI 1293–8670) Kittlitz’s Murrelets Brachyramphus brevirostris resided in Glacier Bay during the month of June, together with 12 195 (5607–18 783) Marbled Murrelets B. marmoratus . When counts were prorated to assign unidentified Brachyramphus murrelets to species, population estimates increased to 5641 Kittlitz’s Murrelets and 13 810 Marbled Murrelets. Our surveys of bird numbers in Glacier Bay between 1991 and 2008 revealed that Kittlitz’s Murrelet declined by ≥85% during this period. Trend analysis suggested a rate of decline between -10.7% and -14.4% per year. No direct human impacts (e.g., bycatch, oil pollution, vessel disturbance) in our study area could fully account for a decline of this magnitude. Widespread declines of Brachyramphus murrelets and Harbor Seals Phoca vitulina in the Gulf of Alaska during the 1980s-1990s suggest large-scale influences on these marine predators, perhaps related to climate-mediated cycles in food supply. Other natural factors that may impact Glacier Bay populations include predation by avian and terrestrial predators, widespread glacial retreat and its effect on nesting and foraging habitats, and competition for food with marine predators whose abundance in Glacier Bay has increased markedly in recent years (Humpback Whales Megaptera novaeangliae and Steller Sea Lions Eumetopias jubatus ).

Alaska↗
USGS2007

Distribution of ground-nesting marine birds along shorelines in Glacier Bay, southeastern Alaska: An assessment related to potential disturbance by back-country users

With the exception of a few large colonies, the distribution of ground-nesting marine birds in Glacier Bay National Park in southeastern Alaska is largely unknown. As visitor use increases in back-country areas of the park, there is growing concern over the potential impact of human activities on breeding birds. During the 2003–05 breeding seasons, the shoreline of Glacier Bay was surveyed to locate ground-nesting marine birds and their nesting areas, including wildlife closures and historical sites for egg collection by Alaska Native peoples. The nesting distribution of four common ground-nesting marine bird species was determined: Arctic Tern ( Sterna paradisaea ), Black Oystercatcher ( Haematopus bachmani ), Mew Gull ( Larus canus ), and Glaucous-winged Gull ( Larus glaucescens ). Observations of less abundant species also were recorded, including Herring Gull ( Larus argentatus ), Red-throated Loon ( Gavia stellata ), Canada Goose ( Branta canadensis ), Willow Ptarmigan ( Lagopus lagopus ), Semipalmated Plover ( Charadrius semipalmatus ), Spotted Sandpiper ( Actitis macularia ), Least Sandpiper ( Calidris minutilla ), Parasitic Jaeger ( Stercorarius parasiticus ), and Aleutian Tern ( Sterna aleutica ). Nesting distribution for Arctic Terns was largely restricted to the upper arms of the bay and a few treeless islets in the lower bay, whereas Black Oystercatchers were more widely distributed along shorelines in the park. Mew Gulls nested throughout the upper bay in Geikie Inlet and in Fingers and Berg Bays, and most Glaucous-winged Gull nests were found at wildlife closures in the central and lower bays. Several areas were identified where human disturbance could affect breeding birds. This study comprises the first bay-wide survey for the breeding distribution of ground-nesting marine birds in Glacier Bay National Park, providing a minimum estimate of their numbers and distribution within the park. This information can be used to assess future human disturbance and track natural changes in nesting bird distribution over time.

Alaska↗
USGS2005

Monitoring of oceanographic properties of Glacier Bay, Alaska 2004

Glacier Bay is a recently (300 years ago) deglaciated fjord estuarine system that has multiple sills, very deep basins, tidewater glaciers, and many streams. Glacier Bay experiences a large amount of runoff, high sedimentation, and large tidal variations. High freshwater discharge due to snow and ice melt and the presence of the tidewater glaciers makes the bay extremely cold. There are many small- and large-scale mixing and upwelling zones at sills, glacial faces, and streams. The complex topography and strong currents lead to highly variable salinity, temperature, sediment, primary productivity, light penetration, stratification levels, and current patterns within a small area. The oceanographic patterns within Glacier Bay drive a large portion of the spatial and temporal variability of the ecosystem. It has been widely recognized by scientists and resource managers in Glacier Bay that a program to monitor oceanographic patterns is essential for understanding the marine ecosystem and to differentiate between anthropogenic disturbance and natural variation. This year’s sampling marks the 12th continuous year of monitoring the oceanographic conditions at 23 stations along the primary axes within Glacier Bay, AK, making this a very unique and valuable data set in terms of its spatial and temporal coverage.

Alaska↗
USGS2003

Living on the edge: Distribution of Dungeness crab Cancer magister in a recently deglaciated fjord

Glacier Bay, Alaska, has supported a productive Dungeness crab fishery, although the area where the fishery occurred was small relative to the remainder of the Bay. We hypothesized that 1 or more abiotic limiting factors prevented crabs from surviving in the upper Bay. We tested this hypothesis by systematically sampling for relative abundance of Dungeness crabs from the mouth to the head of the Bay. We measured salinity, temperature and turbidity at each of the sampling sites and at permanent stations to characterize the habitat within and among years. We expected to find a completely truncated spatial distribution. Instead, we found that adult Dungeness crabs can survive in habitats heavily influenced by tidewater glaciers. There were significantly fewer crabs in the upper Bay and a sharp decrease in abundance around 40 km from the mouth of the Bay. The region of the Bay beyond 40 km from the mouth had a very low density of predominately adult male crabs. The narrow size frequency distribution and the lack of small crabs is consistent with poor survival in one of the pre-adult life stages in the upper Bay.

Alaska↗
USGS2003

Sea otter studies in Glacier Bay National Park and Preserve: annual report 2002

Since 1995, the number of sea otters in Glacier Bay proper has increased from around 5 to more than 1200. Sea otter distribution is mostly limited to the Lower Bay, south of Sandy Cove, and is not continuous within that area. Concentrations occur in the vicinity of Sita Reef and Boulder Island and between Pt. Carolus and Rush Pt. on the west side of the Bay, although there have been occasional sightings north of Sandy Cove (Figure 1). Large portions of the Bay remain unoccupied by sea otters, but recolonization is occurring rapidly. Most prey recovered by sea otters in Glacier Bay are ecologically, commercially, or socially important species. In 2002 sea otter diet consisted of 35% clam, 26% mussel, 3% crab, 3.0% snail, 2% starfish, 11% urchins, 2% other, and 20% unidentified. Dominant clam species include the butter clam, Saxidomus gigantea , the Greenland cockle, Serripes groenlandicus , and the littleneck clam, Protothaca staminea . Urchins are primarily green urchins, Strongylocentrotus droebachiensis , and the mussel is Modiolus modiolus . Crabs observed in 2002 include the Dungeness, Cancer magister , the kelp crab Pugettia gracilis , and the helmet crab, Telmessus cherigonus . Although we characterize diet at broad geographic scales, we have previously found diet to vary between sites separated by as little as several hundred meters. Dietary variation among and within sites can reflect differences in prey availability as well as individual specialization. We estimated species composition, density, biomass, and sizes of subtidal clams, urchins, and mussels at 13 sites in Glacier Bay and 5 sites in nearby Port Althorp, where sea otters have been present for at least 20 years. All sites were selected based on the presence of abundant clam siphons and the absence of sea otters (Glacier Bay) or abundant shell litter and the presence of sea otters (Port Althorp). Glacier Bay sites were selected to achieve a broad geographic sample of dense subtidal clam beds within Glacier Bay prior to occupation and foraging by sea otters. Port Althorp sites were chosen to achieve a representative sample of subtidal clam beds already under prolonged foraging pressure by sea otters. There was no direct evidence of otter foraging at any of our Glacier Bay sampling sites. In Glacier Bay, we sampled 15,338 bivalves (average of 1,180/site) representing 14 species of clam, 2 species of mussel, and a single scallop and we sampled 6,917 urchins (average of 513/site). In Port Althorp, we sampled 1,034 bivalves (average of 207/site) representing 14 species of clam. We found only 5 urchins, all S. droebachiensis . Mean densities and biomass of all subtidal clams were significantly greater in Glacier Bay (59.2 and 99/0.25m 2 compared to Port Althorp (10.3 and 5.8/0.25m 2 (p<0.002 for both). Our contrasts of subtidal clam populations between Glacier Bay and Port Althorp suggest that clam densities will likely decline by about a factor of six and that clam biomass estimates will decline by more than a factor of ten. Numerically dominant species of clams, P. staminea , S. gigantea , Macoma sp. and Mya sp. were all significantly greater in density and biomass in Glacier Bay, while C. nutalli density was low but significantly higher in Port Althorp. Subtidal clam species diversity was significantly greater in Port Althorp compared to Glacier Bay, although this may simply reflect habitat differences. Sea urchin densities were high in Glacier Bay, while in Port Althorp urchins were virtually absent. Sea otters are now well established in limited areas of the lower portions of Glacier Bay. It is likely that distribution and numbers of sea otters will continue to increase in Glacier Bay in the near future. Glacier Bay supports large and diverse populations of clams that are largely unexploited by sea otters at present. It is predictable that the density and sizes of clam populations will decline in response to otter predation. This will result in fewer opportunities for human harvest, but will also trigger ecosystem level changes, as prey for other predators, such as octopus, sea stars, fishes, birds and mammals are modified. Sea otters will also modify benthic habitats through excavation of sediments required to extract burrowing infauna such as clams. Effects of sediment disturbance by foraging sea otters are not understood. Glacier Bay also supports large populations of other preferred sea otter prey, such as king ( Paralithodes sp. ), tanner ( Chionoecetes sp. ) and dungeness ( Cancer magister ) crabs and green sea urchins ( S. droebachiensis ). As the colonization of Park waters by sea otters continues, it is also likely that dramatic changes will occur in the species composition, abundance, and size class distribution of many components of the nearshore marine ecosystem. Many of the changes will occur as a direct result of predation by sea otters. Others will result from indirect or cascading effects of sea otter foraging, such as increased kelp production and modified prey availability for other nearshore predators. Without recognizing and quantifying the extent of change initiated by the colonization of Glacier Bay by sea otters, management of nearshore resources will be severely constrained for many decades.

Alaska↗
USGS2002

Multibeam bathymetry and selected perspective views of main part of Glacier Bay, Alaska

Glacier Bay is a diverse fjord ecosystem with multiple tidewater glaciers and complex biological, geological, and oceanographic patterns that vary greatly along its length. The bay was completely glaciated prior to the 1700's, and subsequently experienced the fastest glacial retreat recorded in historical times. As a result, some of the highest rates of glacial sedimentation and uplift are observed here. Glacier Bay is the deepest silled fjord in Alaska, with depths of over 450 meters. The variety of physical processes and depths creates many diverse habitats within a relatively small area. Mapping benthic (seafloor) habitats is thus crucial to understanding and managing Glacier Bay's complex marine ecosystem and the marine species therein. High-resolution multibeam mapping of the bay, funded jointly by USGS and the National Park System, provides an unprecedented new baseline for resource and habitat assessment. Full integration of the new data set will require additional ground-truthing data (sampling) and analysis. The USGS goal is to develop integrated geological and oceanographic habitat models for the marine benthos in Glacier Bay, as a step toward determining the habitat relationships of critical species and resources within the Park.

Alaska↗
USGS1998

Physical characteristics of dungeness crab and halibut habitats in Glacier Bay

In Glacier Bay National Park, Alaska there are ongoing studies of Dungeness Crab (Cancer magister) and Pacific Halibut (Hippoglosus stenolepis). Scientists of the United States Geological Survey (USGS) are attempting to ascertain life history, distribution, and abundance, and to determine the effects of commercial fishing in the park (Carlson et al., 1998). Statistical sampling studies suggest that seafloor characteristics and bathymetry affect the distribution, abundance and behavior of benthic species. Examples include the distribution of Dungeness crab which varies from 78 to 2012 crabs/ha in nearshore areas to depths of 18 m (O'Clair et al., 1995), and changes in halibut foraging behavior according to bottom type (Chilton et al., 1995). This report discusses geophysical data collected in six areas within the park in 1998. The geophysical surveying done in this and previous studies will be combined with existing population and sonic-tracking data sets as well as future sediment sampling, scuba, submersible, and bottom video camera observations to better understand Dungeness crab and Pacific halibut habitat relationships.

Alaska↗
USGS1996

Dispersion of adult Cancer magister at Glacier Bay, Alaska: Variation with spatial scale, sex, and reproductive status

Patterns of micro- to mesoscale distribution of Dungeness crabs ( Cancer magister ) in nearshore habitats at five locations in and near Glacier Bay National Park were revealed using subtidal transects. Sampling was conducted in April and September 1992 and 1993 and April 1994. Divers censused crabs by sex and reproductive status (ovigerous/nonovigerous females) along belt transects (2 m x 100 m) perpendicular to shore in the depth range 0 m (mean lower low water) to 18 m. A sample estimator of Morisita's index ( Î * Δ ) was used to quantify crab dispersion at 10 scales of measurement ranging from 20 m 2 to 200 m 2 at each location during each sampling period. Values of Î * Δ in ovigerous female C. magister deviated significantly (P < 0.05) from 1.0 (random distribution) toward contagion more frequently than did Î * Δ for nonovigerous female and male crabs. Ovigerous crabs also usually had higher Î * Δ than did nonovigerous female and male crabs, especially at smaller measurement scales (20-80 m 2 ). Morisita's index for all three groups of crabs decreased more frequently than it increased with an increase in measurement scale. We observed no relationship between t and crab density in nonovigerous female and male crabs, whereas Î * Δ was positively correlated with the density of ovigerous crabs. A total of 13 dense aggregations of ovigerous C. magister were observed nearshore (depth range 0-10 m) at the five study locations. About half of these were repeatedly observed at the same microsite over the course of this study. Ovigerous Dungeness crabs at Glacier Bay were usually aggregated, often forming dense aggregations with high site fidelity. These dense aggregations may concentrate a significant proportion of the brood stock of this species in a limited number of patches of optimal brooding habitat at Glacier Bay.

Alaska↗
USGS1996

Sea otter predation on Dungeness crabs in Glacier Bay, Alaska

Sea otter ( Enhydra lutris ) populations are increasing and expanding into areas of Southeast Alaska where Dungeness crabs ( Cancer magister ) are commercially harvested. Although sea otters are known to feed on Dungeness crabs, their effects upon crab demography have not been quantified. We censused Dungeness crabs in adjacent areas within Glacier Bay National Park and Preserve with and without sea otters in April 1993, 1994, and 1995 to investigate the effects of sea otter predation. Two different crab survey techniques were used. Commercial crab pots with sealed escape rings and baited similarly were soaked for 24 hours to measure CPUE in 0-25 m depths. A minimum of 50 pots was used for each site; 25 additional pots were used in 1994 and 1995 to sample crabs to 95 m depths. Divers censused crabs along belt transects (2 m x 100 m) laid perpendicular to shore from 0 m depth to 18 m; 15 transects were surveyed at each site on each date. Sea otter numbers were estimated from aerial surveys and boat observers. Prey types and feeding rates of sea otters were made from telescopic observations. In Outer Dundas Bay, where 46, 39, and 40 sea otters were present in 1993, 1994, and 1995 respectively, CPUE of Dungeness crabs in pots was 0.04, 0.04, and 0.2 crabs per day, respectively, at depths to 25 m, but was higher (4.0 crabs per day) at deeper depths (95 m). Only two Dungeness crabs were observed in 45 diver transects surveyed during three years in Outer Dundas Bay, however Dungeness crabs were a common prey item (15%) of sea otters. Approximately 16 km N in Inner Dundas Bay, where no sea otters were observed any year, CPUE of Dungeness in pots was 2.7, 1.8, and 2.5 crabs per day for 1993, 1994, and 1995, respectively. Adult crab density estimated from diver transects was 236, 78, and 50 crabs/ha in 1993, 1994, and 1995, respectively. Significantly lower crab densities and CPUE occurred in the site occupied by sea otters. Our data imply that sea otter predation decreases Dungeness crab abundance and may induce movement of crabs to greater depths. A depth refuge for crabs from sea otter predation may vary with local bathymetry.

Alaska↗
USGS1970

Observations of iceberg rafting in Glacier Bay, Alaska, and the identification of ancient ice-rafted deposits

Observations of icebergs in a modern glacial marine environment indicate that ancient rocks that received iceberg-rafted material should contain: (1) local concentrations of stones that originated when icebergs overturned, and (2) small pellets of till that were originally sediment filling the spaces between clear ice crystals. The till pellets are especially significant in identifying an ancient glacial setting because they originate through a process unique to glaciers—the flow-and recrystallization-induced segregation of originally disseminated fine sediment. Thus when freed by melting and deposited by iceberg rafting, the pellets would reliably indicate the presence of glacial ice in an ancient environment. In the Gowganda Formation, a Precambrian glacial deposit, strata that contain outsized, presumably iceberg-rafted stones also contain abundant small flattened clasts of unsorted graywacke interpreted as the lithified counterparts of the till pellets observed on modern icebergs.

Alaska↗
USGS1938

Some mineral deposits of Glacier Bay and vicinity, Alaska

Prospecting in the Glacier Bay National Monument has been confined so far to granitic rocks near contacts with Paleozoic sediments, which they intrude.Near Reid Glacier thin veins, a few of which are traceable for about 300 feet both horizontaliy and vertically, trend northerly and carry sphalerite, galena, and pyrite. Gold was panned from some of the better looking material.Near Sandy Cove, 30 miles away, more irregular, but locally thicker, veins appear to carry only pyrite. Here pyrite also occurs along the contact between the granitic rocks and the intruded limestone.Sparse ore minerals have been seen at other places in and near the monument. As yet, no large mineral deposits have been found there, but many miles of igneous contacts have not been prospected. In southeastern Alaska, as elsewhere, such contacts are considered favorable places in which to search for mineral deposits.

Alaska↗