Geology topics

Thomas C. Shirley

Publications and source records attributed to Thomas C. Shirley.

7 recordsLinked to original sources

USGS2007

Spatial distribution of juvenile and adult female Tanner crabs (Chionoecetes bairdi) in a glacial fjord ecosystem: Implications for recruitment processes

A systematic pot survey in Glacier Bay, Alaska, was conducted to characterize the spatial distribution of juvenile and adult female Tanner crabs, and their association with depth and temperature. The information was used to infer important recruitment processes for Tanner crabs in glaciated ecosystems. High-catch areas for juvenile and adult female Tanner crabs were identified using local autocorrelation statistics. Spatial segregation by size class corresponded to features in the glacial landscape: high-catch areas for juveniles were located at the distal ends of two narrow glacial fjords, and high-catch areas for adults were located in the open waters of the central Bay. Juvenile female Tanner crabs were found at nearly all sampled depths (15–439 m) and temperatures (4–8°C), but the biggest catches were at depths <150 m where adults were scarce. Because adults may prey on or compete with juveniles, the distribution of juveniles could be influenced by the distribution of adults. Areas where adults or predators are scarce, such as glacially influenced fjords, could serve as refuges for juvenile Tanner crabs.

ICES Journal of Marine Science↗

USGS2007

North to Alaska: Evidence for conveyor belt transport of Dungeness crab larvae along the west coast of the United States and Canada

We propose and evaluate the hypothesis that Dungeness crab ( Cancer magister ) larvae from the northwestern coast of the United States and Canada can be transported northward to southeastern Alaska. Larvae collected in southeastern Alaska during May and June 1997–2004 had abundances and stages that varied seasonally, interannually, and spatially. An unexpected presence of late-stage larvae in spring raises a question regarding their origin, and the most plausible explanation is that they hatched off the northern Washington and British Columbia coasts and were transported to southeastern Alaska. Buoy drift tracks support the hypothesis that larvae released off the northern Washington and British Columbia coasts during the peak hatching season can be physically transported to southeastern Alaska, arriving as late-stage larvae in May and June, when local larvae are only beginning to hatch. A northward spring progression of monthly mean 7°C SST isotherms and phytoplankton blooms provide further evidence that environmental conditions are conducive for larval growth and metabolism during the transport period. The proposed larval transport suggests possible unidirectional gene flow between southern and northern populations of Dungeness crabs in southeastern Alaska.

Limnology and Oceanography↗

USGS2003

Dungeness crab, Cancer magister , do not extrude eggs annually in southeastern Alaska: An in situ study

The reproductive biology of female Dungeness crabs was studied with crab-pot and dive-transect sampling in five bays within or near Glacier Bay National Park and Preserve, southeastern Alaska, in April and September yearly from 1992 to 1998. A large percentage of nonovigerous, mature females was found in April, a time when females were expected to be brooding eggs that hatch in May and June. Our study examined differences between ovigerous and nonovigerous females collected in April and September samples to corroborate our previous laboratory study in which we found nonannual egg extrusion among Dungeness crabs. Seasonal differences in the catches of ovigerous and nonovigerous females, crab sizes, shell condition, and appendage injury were examined. Additionally, all crabs collected from two bays were tagged beginning in the fall of 1995; tagging was conducted twice annually. Our pot and dive data indicate that females, particularly larger ones, do not extrude eggs annually. Larger females have lower molting probabilities, which limits mating potential and increases reliance on stored sperm. The tagging study confirmed that at least some females do not extrude eggs in one year and then extrude eggs at a later time without molting, thus skipping at least one reproductive season. A reproductive cycle of Dungeness crabs in Alaska is introduced which includes earlier egg extrusion by larger females and nonannual egg extrusion.

Journal of Crustacean Biology↗

USGS2001

Critical habitat for ovigerous Dungeness crabs

The Dungeness crab, Cancer magister , supports an important fishery in the northeastern Pacific Ocean, yet there is limited knowledge of ovigerous female brooding locations and brooding behavior. Our earlier research suggests that ovigerous crabs aggregate at the same brooding locations for many years. Within these locations, ovigerous females occur in high densities, with the majority of the aggregation buried within the sediment. These locations often have similar water depths and sediment types and appear to be critical for this life history stage. Our study was designed to examine the bathymetric distribution of Dungeness crabs in bays with and without sea otters at eight locations within the Glacier Bay area by conducting transects with a video-equipped manned submersible. Two of the bays investigated contained large aggregations of ovigerous females. At both sites the substrate was composed primarily of sand. However, only a small percentage of the 33 km of transects were classified as sand. These data suggest that sand substrate may be a limiting resource. Since crab brooding aggregations represent a large portion of the crab population within a small area, and because they are a critical component of Dungeness life history, areas with these characteristics need to be investigated, mapped, and protected from development or exploitation. The areas requiring protection from the impact of anthropogenic wastes, fishing, and logging activities could be quite small, thus limiting conflict with alternative users.

Conference Paper↗

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↗

USGS1995

Nearshore distribution and abundance of Dungeness crabs in Glacier Bay National Park, Alaska

As part of an ongoing, multi-agency study to determine the effects of closure of the commercial fishery for Dungeness crabs, Cancer magister , on crab population structure we examined patterns of distribution and abundance of crabs in nearshore habitats at five locations in and near Glacier Bay National Park. Sampling was conducted in April and September 1992 and April 1993 prior to the anticipated closure of the fishery in the park. Divers censused crabs by sex and reproductive state (ovigerous/nonovigerous females) along belt transects (2m x 100m) laid perpendicular to shore in the depth range 0 m (mean lower low water) to 18 m. Preliminary results from the first three sampling periods revealed that the average densities of Dungeness crabs at the five locations ranged from 78 to 2012 crabs/ha. Crab densities differed between populations depending on sex, reproductive state of females and sampling period. Male crabs showed reduced densities at Gustavus Flats in April 1992 (P<0.01) and 1993 (P<0.001). Ovigerous females had greater density at Bartlett Cove in April 1993 (P<0.001). Sex ratios were frequently skewed toward females. At Bartlett Cove and Gustavus Flats females outnumbered males in April 1992 and 1993 (P<0.001). Most of the females at Bartlett Cove and Gustavus Flats in April 1992 and 1993 were ovigerous (P-0.001). Males tended to occupy greater depths than females in April 1992 (P<0.05) but not April 1993 (P-005). The mean depth of males shifted from deeper to shallower water between April and September 1992 (P<0.001). The depth distribution of ovigerous crabs did not differ from that of nonovigerous female crabs. Future research prior to the anticipated closure of the commercial Dungeness crab fishery in Glacier Bay will include a tagging study to determine the extent of crab movement and further study of the temporal as well as the spatial variability observed in the structure of these populations.

Alaska↗