Interannual assessment of territory quality for male sea otters (Enhydra lutris) in Simpson Bay, Prince William Sound, Alaska

2010 ◽  
Vol 88 (3) ◽  
pp. 289-298 ◽  
Author(s):  
Shannon E. Finerty ◽  
Heidi C. Pearson ◽  
Randall W. Davis

Territory quality and site fidelity were assessed for male sea otters ( Enhydra lutris (L., 1758)) in Simpson Bay, Prince William Sound, Alaska, during the summer months (May–August) from 2003 to 2006. Territory quality was coded with a score of 0–2 for four attributes: territory size, shoreline enclosure, territory accessibility, and number of females observed feeding in each territory. Total quality scores ranged from 0.14 to 1.96 (0.9 ± 0.61, mean ± SD), with the highest quality territories having large areas, moderate to little shoreline enclosure, high accessibility, and many foraging females. A total of 13.1 km2 (62.5%) of Simpson Bay was occupied at least once by a territorial male during the 4-year study, and 7.9 km2 (37.5%) was never occupied by a territorial male. There were 7 ± 2.4 (mean ± SD) territorial males in Simpson Bay each year. Five males maintained territories for two consecutive years, with their respective territories having a 16%–34% overlap between years, indicating that repeat territory holders returned to the same area. The number of territorial sea otters, the size of territories, and whether or not a sea otter was a repeat territory holder did not significantly influence the size or quality of male territories.

Oryx ◽  
2021 ◽  
pp. 1-6
Author(s):  
Igor Popov ◽  
Alexey Scopin

Abstract We describe the population of the Еndangered sea otter Enhydra lutris on Urup Island, one of the main wildlife refuges in the southern Kuril Islands of Russia. We reviewed historical and local reports of the sea otter, identified its habitat around the island, and surveyed the coastal waters of the island in 2019. Sea otters were numerous on Urup Island in the past but were hunted excessively and almost exterminated by the 1950s. Since then, sea otter populations have increased, and as the island is almost uninhabited we expected otters to be numerous. This was not the case, and we estimated the total population to be 363 ± SE 126 individuals. Our observation of two skinned carcasses on the shore suggests the low numbers are a result of poaching for the illegal fur trade. The case of Urup Island demonstrates that sea otters require active conservation, as even on a remote island they remain threatened. Establishment of protected areas would be an effective conservation measure for this species, although the suppression of demand for sea otter fur is of the greatest importance.


2020 ◽  
Vol 7 ◽  
Author(s):  
Melissa A. Miller ◽  
Megan E. Moriarty ◽  
Laird Henkel ◽  
Martin Tim Tinker ◽  
Tristan L. Burgess ◽  
...  

We compiled findings from 15 years (1998–2012) of southern sea otter (Enhydra lutris nereis) necropsies, incorporating data from 560 animals. Sensitive diagnostic tests were used to detect biotoxins, bacteria, parasites and fungi. Methods to classify primary and contributing causes of death (COD) and sequelae utilized an updated understanding of health risks affecting this population. Several interesting patterns emerged, including identification of coastal regions of high mortality risk for sea otter mortality due to shark bite, cardiomyopathy, toxoplasmosis, sarcocystosis, acanthocephalan peritonitis and coccidioidomycosis. We identified demographic attributes that enhanced the risk of disease in relation to age, sex, and reproductive stage. Death due to white shark (Carcharodon carcharias) bite increased dramatically during the study period and was the most common primary COD. However, when primary and contributing COD were combined, the most prevalent COD was infectious disease (affecting 63% of otters), especially fatal infections by acanthocephalans (Profilicollis spp.) and protozoa (e.g., Sarcocystis neurona and Toxoplasma gondii). Fatal bacterial infections were also extremely common as a primary process or a sequela, affecting 68% of examined otters. Substantial advances were made in identifying sea otters that died following exposure to the pervasive marine neurotoxin domoic acid (DA), and DA intoxication was conservatively estimated as a primary or contributing COD for 20% of otters. Cardiomyopathy was also highly prevalent as a primary or contributing COD (41%) and exhibited significant associations with DA intoxication and protozoal infection. For adult and aged adult females in late pup care through post-weaning at the time of death, 83% had end lactation syndrome (ELS) as a primary or contributing COD. This comprehensive longitudinal dataset is unique in its depth and scope. The large sample size and extensive time period provided an opportunity to investigate mortality patterns in a changing environment and identify spatial and temporal disease “hot spots” and emerging threats. Our findings will help improve estimates of population-level impacts of specific threats and optimize conservation and environmental mitigation efforts for this threatened species.


2020 ◽  
Vol 287 (1940) ◽  
pp. 20202343
Author(s):  
Hannah P. Wellman ◽  
Rita M. Austin ◽  
Nihan D. Dagtas ◽  
Madonna L. Moss ◽  
Torben C. Rick ◽  
...  

Genetic analyses are an important contribution to wildlife reintroductions, particularly in the modern context of extirpations and ecological destruction. To address the complex historical ecology of the sea otter ( Enhydra lutris ) and its failed 1970s reintroduction to coastal Oregon, we compared mitochondrial genomes of pre-extirpation Oregon sea otters to extant and historical populations across the range. We sequenced, to our knowledge, the first complete ancient mitogenomes from archaeological Oregon sea otter dentine and historical sea otter dental calculus. Archaeological Oregon sea otters ( n = 20) represent 10 haplotypes, which cluster with haplotypes from Alaska, Washington and British Columbia, and exhibit a clear division from California haplotypes. Our results suggest that extant northern populations are appropriate for future reintroduction efforts. This project demonstrates the feasibility of mitogenome capture and sequencing from non-human dental calculus and the diverse applications of ancient DNA analyses to pressing ecological and conservation topics and the management of at-risk/extirpated species.


2020 ◽  
Vol 138 ◽  
pp. 207-213
Author(s):  
AR Armwood ◽  
CE Anderson ◽  
T Clauss ◽  
AC Camus

Southern sea otters Enhydra lutris nereis, a threatened marine mammal species, face numerous environmental and infectious disease challenges in their native habitat of coastal California, USA. However, there are few published cases describing neoplasia in sea otters despite their relatively long life span when cared for in aquarium settings. An 18 yr old neutered male southern sea otter, born and raised in human care, presented with an acute onset of seizures and dull mentation. Magnetic resonance imaging of the head revealed a large, central brain lesion. After no improvement with treatment, euthanasia was elected due to a poor prognosis. Grossly, a poorly demarcated, granular, tan mass expanded the cranial meninges in the longitudinal fissure at the level of the cruciate sulcus and extended into the underlying gray matter and superficial white matter. Histologically, the mass was composed of spindle cells, forming haphazardly arranged interlacing bundles and herringbone patterns, with a high mitotic count, moderate cellular pleomorphism, and prominent vascularization. Neoplastic cells demonstrated positive immunoreactivity for vimentin and negative immunoreactivity for smooth muscle actin, factor VIII-related antigen, S100, melan-A, E-cadherin, desmin, glial fibrillary acidic protein, and cytokeratin AE1/AE3. Based on gross, histologic, and immunohistochemical findings, the mass was most consistent with a primary intracranial fibrosarcoma (PIF). PIFs are a rare neoplasm in both humans and other animals with few reports in the veterinary literature. This is the first recorded case of a PIF in a sea otter.


2016 ◽  
Vol 130 (2) ◽  
pp. 91 ◽  
Author(s):  
Erin Rechsteiner ◽  
Angeleen Olson

Foraging animals may risk association with potential predators to obtain otherwise inaccessible prey. We observed this strategy in wintering Harlequin Ducks (Histrionicus histrionicus) scavenging fragments of Red Sea Urchins (Mesocentrotus franciscanus) from foraging Sea Otters (Enhydra lutris) that were re-occupying an area from which they had been ecologically absent since about 1850. Harlequin Ducks, like other sea ducks, have not previously been reported scavenging from other birds or mammals. In British columbia, Red Sea Urchins have reached large sizes and densities since the removal of Sea Otter predators by the marine fur trade in the 18th and 19th centuries. Observations of Sea Otters and Harlequin Ducks were made in 4 areas, spanning a time gradient of Sea Otter occupation from 1 to 5 years. During 3 months of observations (December 2013 – February 2014), Harlequin Ducks were associated with foraging Sea Otters only at sites that were recently occupied by Sea Otters (≤ 2 months), where the proportion of urchins in Sea Otter diets was highest and where the ducks acquired urchin fragments from foraging Sea Otters. We suggest that Sea Otters re-occupying their historic range and consuming predominantly large Red Sea Urchins provide a temporarily available prey subsidy for Harlequin Ducks. Our observations document a novel effect of Sea Otters providing important prey supplementation to a marine bird when foraging in urchin-rich habitats, contributing to the overall role of Sea Otters as a keystone species.


2003 ◽  
Vol 81 (9) ◽  
pp. 1494-1510 ◽  
Author(s):  
B E Ballachey ◽  
J L Bodkin ◽  
S Howlin ◽  
A M Doroff ◽  
A H Rebar

We estimated survival of sea otters (Enhydra lutris) for 1 year post weaning during 1992–1993 in Prince William Sound (PWS), location of the 1989 Exxon Valdez oil spill. We sampled 38 pups in eastern PWS (EPWS), an unoiled area occupied by sea otters for <15 years, and 33 pups from oiled western PWS (WPWS), occupied for >25 years. We compared survival between areas, sexes, and condition groups. We also examined the relation of blood parameters to survival. Survival was estimated at 0.74 in EPWS and 0.52 in WPWS. Female survival was 0.86 in EPWS and 0.64 in WPWS, whereas male survival was lower, 0.61 in EPWS and 0.44 in WPWS. Sea otters from EPWS were in better condition (mass/length) than WPWS sea otters. Pups in better condition had higher survival in EPWS but not in WPWS. Foraging success was greater in EPWS than in WPWS, consistent with either an effect of length of occupation or the effects of oil on the prey base or a combination of these effects. Area differences in blood parameters suggested liver damage in WPWS sea otters, perhaps resulting from continued exposure to oil. Thus, both length of occupation and oiling history likely influenced juvenile survival in PWS.


1984 ◽  
Vol 62 (12) ◽  
pp. 2648-2658 ◽  
Author(s):  
David L. Garshelis ◽  
Ancel M. Johnson ◽  
Judith A. Garshelis

Sea otters in Prince William Sound. Alaska, were spatially segregated into predominantly (97%) male areas at the front of the expanding population and breeding areas with fewer (up to 33%) males. From 1975 to 1984 we captured and marked 267 otters with tags and (or) radio transmitters and investigated their reproductive strategies, social relationships, and patterns of sexual segregation. Mating occurred year-round, but peaked in September and October. Females first bred at 4 years of age and were capable of pupping annually; they generally separated from their pup before mating. Males established breeding territories that enabled prolonged precopulatory interactions that may have prompted female–pup separation and post-copulatory interactions that precluded females from mating with other males. Male mating success was related to age, weight, territory quality, and the length of time they maintained their territory. After the breeding season, territorial males returned to male areas where food was more abundant. Young, dispersing males also entered male areas and remained there until attaining breeding age. In male areas, otters commonly rested in groups of >50 individuals. Gregariousness promoted social interactions and likely enhanced food finding and (historically) predator protection. As food diminished, males moved into adjacent, unoccupied regions; females then occupied former male areas.


2004 ◽  
Vol 118 (2) ◽  
pp. 270
Author(s):  
Kimberly Raum-Suryan ◽  
Kenneth Pitcher ◽  
Richard Lamy

On 27 June 2001 we observed and photographed a Sea Otter (Enhydra lutris) adjacent to a Steller Sea Lion (Eumetopias jubatus) haulout near Sgang Gwaay (Anthony Island), Haida Gwaii / Queen Charlotte Islands. This is one of only eight documented sightings of Sea Otters in these waters during the past 30 years. These sightings may represent the beginning of the expansion of Sea Otters to their former range off Haida Gwaii.


2020 ◽  
Vol 8 (1) ◽  
Author(s):  
M J Murray ◽  
M A Young ◽  
R M Santymire

Abstract After nearly being hunted to extinction during the fur trade of the late 20th Century, sea otter (Enhydra lutris) populations have recovered to varying degrees of their historical range. While overall population numbers and range have increased, there are regions in which expansion has occurred at a slower rate and/or animal numbers have decreased, which may be a result of chronic stress from a variety of sources. Some have employed glucocorticoid analysis in their attempts to validate these explanations. Our goal was to conduct a controlled study using sea otters managed under human care to validate the use of serum glucocorticoid analysis to monitor stress physiology in the sea otter. We used a standard ACTH challenge test to compare cortisol and corticosterone responses, thereby identifying the primary glucocorticoid in the sea otter. Fourteen sea otters of both sexes (five males, nine females), including juveniles, sub-adults and adults, participated in the study. The results of the testing supported cortisol as the primary glucocorticoid in the sea otter. Sex and age did not affect how the individual responded to the ACTH or saline injection. Interestingly, the saline injection not only confirmed the effects of the ACTH on glucocorticoid release from the adrenal glands but also provided information on how long it takes the sea otter’s glucocorticoid levels to return to baseline after capture and sedation. The insight gained from this study will aid in future efforts to better understand the role of stress in free-ranging sea otter populations. Recognition of the primary glucocorticoid will facilitate evaluation of more stable biological material, such as fur or whiskers, which tend to be less affected by the diurnal cycling of glucocorticoids.


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