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At least 415 records · Page 23Linked to original sources
USGS2006

Distribution patterns of individually identifiable West Indian manatees ( Trichechus manatus ) in Florida

Photographs of distinctively scarred manatees ( Trichechus manatus ) were taken at aggregation sites throughout Florida and assembled into a catalog for identifying individuals. Resightings of known manatees in different years or at different locations enabled us to document site fidelity and long-distance movements. Of the 891 individuals included in the catalog as of August 1986, 470 (53%) were resighted at least once. We documented 219 cases of seasonal returns to specific aggregation sites and 98 instances of movements between areas. Movements in excess of 820 km were documented for individuals on the east coast of Florida. Rapid movements south during early winter, as well as northerly spring movements, verify a seasonal migration pattern for many individuals along Florida's east coast. The wide-ranging migratory habits of manatees in Florida must be considered if meaningful management strategies are to be developed and implemented.

Florida↗
USGS2006

Reproductive characteristics of female sea otters

Several important aspects of reproduction in the female sea otter, such as gestation, pupping frequency, period of pup dependency, and annual pupping rate, were unclear when this study was begun. We present data from 75 tagged adult females that indicate gestation is variable, but on average is about 6 months, the length of pup dependency is 6 mo, thus the pupping interval is usually 12–13 mo. Most females breed for the first time in their fifth year of life. About 85–90% of adult females pup in a given year.

Alaska, California↗
USGS2006

Experimental recovery of sea otter carcasses at Kodiak Island, Alaska, following the Exxon Valdez oil spill

ound, Alaska, spilling approximately 11 million barrels of crude oil. Oil was deposited on beaches nearly 700 km from the spill site (Galt and Payton 1990, Piatt et al. 1990), affecting thousands of hectares of sea otter (Enhydra lutris) habitat. Two of the principal limitations in determining the initial effects of the Exxon Valdez oil spill on sea otter populations were a lack of recent population data, and a lack of information on the proportion of the total number of sea otters killed by the spill that were actually recovered. ound, Alaska, spilling approximately 11 million barrels of crude oil. Oil was deposited on beaches nearly 700 km from the spill site (Galt and Payton 1990, Piatt et al. 1990), affecting thousands of hectares of sea otter (Enhydra lutris) habitat. Two of the principal limitations in determining the initial effects of the Exxon Valdez oil spill on sea otter populations were a lack of recent population data, and a lack of information on the proportion of the total number of sea otters killed by the spill that were actually recovered. On 24 March 1989, the T/V Exxon Valdez ran aground in Prince William Sound, Alaska, spilling approximately 11 million barrels of crude oil. Oil was deposited on beaches nearly 700 km from the spill site (Galt and Payton 1990, Piatt et al . 1990), affecting thousands of hectares of sea otter ( Enhydra lutris ) habitat. Two of the principal limitations in determining the initial effects of the Exxon Valdez oil spill on sea otter populations were a lack of recent population data, and a lack of information on the proportion of the total number of sea otters killed by the spill that were actually recovered. In late April and early May oil spread to the Kodiak Archipelago. With the oil came wildlife rescue, beach cleanup, and other spill-response activities including searches for dead birds and mammals. We took this opportunity to assess experimentally the recovery of sea otter carcasses in the Kodiak Island area. Specifically, we were interested in the proportion of the total number of dead sea otters the recovered carcasses represented.

Alaska↗
USGS2006

Detection of sea otters in boat-based surveys of Prince William Sound, Alaska

Boat-based surveys have been commonly used to monitor sea otter populations, but there has been little quantitative work to evaluate detection biases that may affect these surveys. We used ground-based observers to investigate sea otter detection probabilities in a boat-based survey of Prince William Sound, Alaska. We estimated that 30% of the otters present on surveyed transects were not detected by boat crews. Approximately half (53%) of the undetected otters were missed because the otters left the transects, apparently in response to the approaching boat. Unbiased estimates of detection probabilities will be required for obtaining unbiased population estimates from boat-based surveys of sea otters. Therefore, boat-based surveys should include methods to estimate sea otter detection probabilities under the conditions specific to each survey. Unbiased estimation of detection probabilities with ground-based observers requires either that the ground crews detect all of the otters in observed subunits, or that there are no errors in determining which crews saw each detected otter. Ground-based observer methods may be appropriate in areas where nearly all of the sea otter habitat is potentially visible from ground-based vantage points.

Alaska↗
USGS2006

Investigating trophic relationships of pinnipeds in Alaska and Washington using stable isotope ratios of nitrogen and carbon

We measured stable-nitrogen (δ 15 N) and stable-carbon (δ 13 C) isotope ratios in muscle and hair from 7 northern fur seals ( Callorhinus ursinus ) from the Pribilof Islands, Alaska, and 27 Steller sea lions ( Eumetopias jubatus ), and 14 harbor seals ( Phoca vitulina ) from the Gulf of Alaska and coast of Washington State, in order to contrast dietary information derived from isotopic vs. available conventional dietary studies. Stable-nitrogen-isotope analysis of muscle revealed that harbor seals were enriched over sea lions (mean δ 15 N = 18.6‰ vs. 17.5‰) which were in turn enriched over northern fur seals (mean δ 15 N = 16.6‰). Trophic segregation among these species likely results primarily from differential reliance on herring ( Clupea harengus ), Atka mackerel ( Pleurogrammus monopterygius ), and large vs. small walleye pollock ( Theregra chalcogramma ). According to their δ 15 N values, adult male Steller sea lions showed a higher trophic position than adult females (mean δ 15 N: 18.0‰ vs. 17.2‰), whereas adult female northern fur seals were trophically higher than juvenile male fur seals (mean δ 15 N: 16.5‰ vs. 15.0‰). Each of these observed differences likely resulted from differential reliance on squid or differences in the size range of pollock consumed. Three northern fur seal pups showed higher δ 15 N enrichment over adults (mean 17.7‰ vs. 15.8‰) due to their reliance on their mother's milk. Stable-carbon isotope measurements of hair revealed a cline toward more negative values with latitude. Segregation in hair δ 13 C between Steller sea lions and harbor seals off the coast of Washington (mean δ 13 C: -13.6‰ vs. - 15.0‰) reflected the greater association of harbor seals with freshwater input from the Columbia River. Our study demonstrates the utility of the stable isotope approach to augment conventional dietary analyses of pinnipeds and other marine mammals.

Alaska, Washington↗
USGS2006

Status of sea otters (Enhydra lutris) in Mexico

Sea otters in North America historically were distributed from the Near Islands in the western Aleutian Archipelago to about Punta Morro Hermoso on the Pacific coast of Baja California (Kenyon 1969, Rodriguez-Jaramillo and Gendron 1996). During the 18th and 19th centuries they were so common that they formed the basis for a lucrative fur trade (Ogden 1941), but by the early 1900s they were exploited to extinction in Baja California (Kenyon 1369).

Marine Mammal Science↗
USGS2006

Sea otter mortality from the Exxon Valdez spill: Evaluation of an estimate from boat-based surveys

The Exxon Valadez oil spill killed large numbers of sea otters ( Enhydra lutris ) in Prince William Sound (PWS), Alaska, where the spill originated, as well as within the oil’s path along the coasts of the Kenai Peninsula and Kodiak Island. Sea otters attracted particular attention after the spill due to their public appeal (Batten 1990) and known vulnerability to oil (Costa and Kooyman 1982, Siniff et al. 1982, Davis et al. 1988, Williams et al. 1988). Extensive efforts were made to rescue and rehabilitate oiled otters at a resulting cost of ca. $80,000 per animal (Estes 1991). The argument that otters lost in the spill should be similarly valued made the estimate of mortality a matter of substantial concern to those involved in spill-related litigation or out-of-court settlements.

Alaska↗
USGS2006

Generic names of northern and southern fur seals (Mammalia: Otariidae)

We have resolved a nomenclatural problem discovered during research on the northern fur seal that concerns the correct generic name for this taxon and for fur seals of the Southern Hemisphere. The unfortunate practice by some 19th-century authors to use names in their Latinized form but to date them from their first appearance as French common names led to the use of Arctocepbalus for southern fur seals when the name correctly applies to the northern fur seal, known today as Callorbinus ursinus . However, Arctocepbalus and Callorbinus are antedated by Otoes G. Fischer, 1817, which is the earliest available generic name for the fur seal of the northern Pacific. The earliest available generic name for southern fur seals is Halarctus Gill, 1866. To avoid the confusion that would result from replacing the currently used generic names with those required by strict adherence to the Principle of Priority, we have petitioned the International Commission on Zoological Nomenclature to preserve Arctocepbalus and Callorbinus for the southern and northern fur seals, respectively.

Marine Mammal Science↗
USGS2006

Response of Pacific walruses to disturbances from capture and handling activities at a haul-out in Bristol Bay, Alaska

Observations were made on hems of the Pacific walrus (Odobenus rosmarus divergens) to study their response during the capturing and handling of adult males in summer 1995 at a haul-out at Cape Peirce in southwestern Alaska. Three behaviors (alertness, displacement, and dispersal) were quantified from 16 capture sessions. Herd sizes ranged from 622 to 5,289 walruses. Handling of an immobilized walrus consisted of attempts to attach telemetry devices to the tusks and collect various biological samples. Handling activities resulted in an average of about 10-fold or greater levels of behavior in alertness, displacement, and dispersal than during precapture and darting periods. High levels of behavior usually occurred within the first 45 min of handling. In 8 of 10 capture sessions, walruses returned to predisturbance levels of behavior within 40 min of cessation of the handling disturbance. Alertness and displacement were moderately and negatively correlated with herd size during the handling period, which may reflect an effect of a threshold distance from the point of disturbance to responding individuals. Observations of walruses tagged with VHF radio transmitters indicated that the activities from a given capture session did not preclude tagged walruses from using the haul-out over a subsequent 11-wk monitoring period. Moreover, non-tagged walruses continued to extensively use the haul-out during and after the period in which capture sessions were conducted.

Marine Mammal Science↗
USGS2006

Interactions between northern elephant seals and vehicles near Point Piedras Blancas, California

Northern elephant seals, Mirounga angustirostris , were nearly extirpated in the late 19th and early 20th centuries. However, they have recovered to the point where they are now locally abundant (Stewart e t al. 1994). Stimulated by the report of human/northern elephant seal interactions in Baja California Sur (Webster and Baird 1998), we report here on an unusual terrestrial example of the increasing conflict between the growing populations of these two species in central California.

California↗
USGS2006

Attendance patterns of California sea lion (Zalophus californianus) females and pups during the non-breeding season at San Miguel Island

The attendance patterns of California sea lions were studied during the non-breeding seasons from 1991 to 1994. Lactating females frequented the rookery to nurse their pups until weaning; most non-lactating females left the rookery for the season. Females spent over 70% of their time at sea except in 1993 when they spent 59% of their time at sea. The mean foraging trip length in the winter and spring ranged from 3.3 to 4.6 d; the mean nursing visit ranged from 1.2 to 1.4 d. The duration of foraging trips and nursing visits was variable over the season for individuals but no pattern of change was detected. Interannual and seasonal differences were not significant for time at sea, visits ashore, or foraging-trip duration before, during, or after the 1992-1993 El Nino event. Pups spent an average of 66.6% of their time ashore and up to three days away from the rookery during their mother's absence. Most females and pups stayed associated until April or May. The results suggest that seasonal movement of prey is more important in determining attendance patterns late in the lactation period than increasing energy demands of the pup.

California↗
USGS2006

Age- and sex-specific mortality and population structure in sea otters

We used 742 beach-cast carcasses to characterize age- and sex-specific sea otter mortality during the winter of 1990-1991 at Bering Island, Russia. We also examined 363 carcasses recovered after the 1989 grounding of the T/V Exxon Valdez , to characterize age and sex composition in the living western Prince William Sound (WPWS) sea otter population. At Bering Island, mortality was male-biased (81%), and 75% were adults. The WPWS population was female-biased (59%) and most animals were subadult (79% of the males and 45% of the females). In the decade prior to 1990-1991 we found increasing sea otter densities (particularly among males), declining prey resources, and declining weights in adult male sea otters at Bering Island. Our findings suggest the increased mortality at Bering Island in 1990-1991 was a density-dependent population response. We propose male-maintained breeding territories and exclusion of juvenile females by adult females, providing a mechanism for maintaining densities in female areas below densities in male areas and for potentially moderating the effects of prey reductions on the female population. Increased adult male mortality at Bering Island in 1990-1991 likely modified the sex and age class structure there toward that observed in Prince William Sound.

Marine Mammal Science↗
USGS2006

Comparison of methods used to estimate numbers of walruses on sea ice

The US and former USSR conducted joint surveys of Pacific walruses on sea ice and at land haul-outs in 1975, 1980, 1985, and 1990. One of the difficulties in interpreting results of these surveys has been that, except for the 1990 survey, the Americans and Soviets used different methods for estimating population size from their respective portions of the sea ice data. We used data exchanged between Soviet and American scientists to compare and evaluate the two estimation procedures and to derive a set of alternative estimates from the 1975, 1980, and 1985 surveys based on a single consistent procedure. Estimation method had only a small effect on total population estimates because most walruses were found at land haul-outs. However, the Soviet method is subject to bias that depends on the distribution of the population on the sea ice and this has important implications for interpreting the ice portions of previously reported surveys for walruses and other pinniped species. We recommend that the American method be used in future surveys. Future research on survey methods for walruses should focus on other potential sources of bias and variation.

Chukchi Sea↗
USGS2006

Summer diving behavior of male walruses in Bristol Bay, Alaska

Pacific walruses ( Odobenus rosmarus divergens ) make trips from ice or land haul-out sites to forage for benthic prey. We describe dive and trip characteristics from time-depth-recorder data collected over a one-month period during summer from four male Pacific walruses in Bristol Bay, Alaska. Dives were classified into four types. Shallow (4 m), short (2.7 min), square-shaped dives accounted for 11% of trip time, and many were probably associated with traveling. Shallow (2 m) and very short (0.5 min) dives composed only 1% of trip time. Deep (41 m), long (7.2 min), square-shaped dives accounted for 46% of trip time and were undoubtedly associated with benthic foraging. V-shaped dives ranged widely in depth, were of moderate duration (4.7 min), and composed 3% of trip time. These dives may have been associated with navigation or exploration of the seafloor for potential prey habitat. Surface intervals between dives were similar among dive types, and generally lasted 1–2 min. Total foraging time was strongly correlated with trip duration and there was no apparent diel pattern of diving in any dive type among animals. We found no correlation between dive duration and postdive surface interval within dive types, suggesting that diving occurred within aerobic dive limits. Trip duration varied considerably within and among walruses (0.3–9.4 d), and there was evidence that some of the very short trips were unrelated to foraging. Overall, walruses were in the water for 76.6% of the time, of which 60.3% was spent diving.

Alaska↗
USGS2006

An estimation of carrying capacity for sea otters along the California coast

Carrying capacity (K) for the California sea otter ( Enhydra lutris nereis ) was estimated as a product of the density of sea otters at equilibrium within a portion of their existing range and the total area of available habitat. Equilibrium densities were determined using the number of sea otters observed during spring surveys in 1994, 1995, and 1996 in each of three habitat types where sea otters currently exist. Potential sea otter habitat was defined as from the California coastline to the 40-m isobath and classified as rocky, sandy, or mixed habitat according to the amount of kelp and rocky substrate in the area. The amount of habitat available to sea otters in California was estimated using a Geographic Information Systems (GIS) program. The estimated mean number of sea otters that could be supported by the marine environment to a depth of 40 m in California was 15,941 (95% CI 13,538–18,577). The GIS-based approach incorporated detailed bathymetric contours, produced repeatable and accurate estimates, and served as an innovative method of measuring sea otter habitat. We believe the approach described in this paper represents the best available information on how a sea otter population at equilibrium would be distributed along the California coast.

California↗