DIET AND FORAGING BEHAVIOR OF SEA OTTERS IN SOUTHEAST ALASKA

Abstract: Direct observations of feeding sea otters ( Enhydra lutris ) at 11 sites in southeast Alaska showed infaunal clams to be the primary prey utilized by otters throughout the region. Foraging dive times associated with clam and sea urchin prey were significantly longer than those for more easily captured prey (crabs and mussels). Dive times and surface intervals were also generally correlated with water depth or apparent difficulty in obtaining buried prey. Male otters, which fed more extensively on clams than females, made significantly longer foraging dives than females. Foraging success remained high, even at sites where prey numbers were found to be very low during a related study. The very deeply burrowing geoduck clam ( Panope abrupta ), while common at several otter feeding sites, was rarely captured by otters. These results, combined with those of a companion study on prey numbers, indicate that butter clams ( Saxidomus giganteus ) account for the majority of the sea otter diet in southeast Alaska, and that sea urchins may represent relatively short-term prey in comparison to infaunal bivalves in regions where both prey types co-exist. Furthermore, the importance of butter clams in the sea otter diet and the tendency for this bivalve to retain chronically high levels of paralytic shellfish poisoning toxins in southeast Alaska increases the probability that toxic phytoplankton blooms influence sea otter distribution in this region.     

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.     

Life history plasticity and population regulation in sea otters

We contrasted body condition, and age‐specific reproduction and mortality between a growing population of sea otters (Enhydralutris) at Kodiak Island and a high‐density near‐equilibrium population at Amchitka Island, Alaska. We obtained data from marked individuals, population surveys, and collections of beach‐cast carcasses. Mass:length ratios indicated that females (but not males) captured in 1992 at Amchitka were in poorer condition than those captured at Kodiak in 1986–1987. In 1993, the condition of females at Amchitka improved in apparent response to two factors: (1) an episodic influx of Pacific smooth lumpsuckers, Aptocyclus ventricocus, from the epi‐pelagic zone, which otters consumed; and (2) an increase in the otters’ benthic invertebrate prey resulting from declining otter numbers. Reproductive rates varied with age (0.37 [CI=0.21 to 0.53] births female^?1 yr^?1 for 2–3‐yr‐olds, and 0.83 [CI=0.69 to 0.90] for females ≥4 yr old), and were similar at both areas. Weaning success (pups surviving to ≥120 d), in contrast, was almost 50% lower at Amchitka than at Kodiak and for females ≥4 yr of age was 0.52 (CI=0.38 to 0.66) vs 0.94 (CI=0.75 to 0.99), respectively. Sixty‐two percent of the preweaning pup losses at Amchitka occurred within a month of parturition and 79% within two months. Postweaning survival was also low at Amchitka as only 18% of instrumented pups were known to be alive one year after mother‐pup separation. Adult survival rates appeared similar at Amchitka and Kodiak. Factors affecting survival early in life thus are a primary demographic mechanism of population regulation in sea otters. By maintaining uniformly high reproductive rates over time and limiting investment in any particular reproductive event, sea otters can take advantage of unpredictable environmental changes favorable to pup survival. This strategy is consistent with predictions of “bet‐hedging” life history models.     

FORAGING DEPTHS OF SEA OTTERS AND IMPLICATIONS TO COASTAL MARINE COMMUNITIES

We visually observed 1,251 dives, of 14 sea otters instrumented with TDRs in southeast Alaska, and used attribute values from observed dives to classify 180,848 recorded dives as foraging (0.64), or traveling (0.36). Foraging dives were significantly deeper, with longer durations, bottom times, and postdive surface intervals, and greater descent and ascent rates, compared to traveling dives. Most foraging occurred in depths between 2 and 30 m (0.84), although 0.16 of all foraging was between 30 and 100 m. Nine animals, including all five males, demonstrated bimodal patterns in foraging depths, with peaks between 5 and 15 m and 30 and 60 m, whereas five of nine females foraged at an average depth of 10 m. Mean shallow foraging depth was 8 m, and mean deep foraging depth was 44 m. Maximum foraging depths averaged 61 m (54 and 82 for females and males, respectively) and ranged from 35 to 100 m. Female sea otters dove to depths ≤20 m on 0.85 of their foraging dives while male sea otters dove to depths ≥45 m on 0.50 of their foraging dives. Less than 0.02 of all foraging dives were >55 m, suggesting that effects of sea otter foraging on nearshore marine communities should diminish at greater depths. However, recolonization of vacant habitat by high densities of adult male sea otters may result in initial reductions of some prey species at depths >55 m.     

Mustelid herpesvirus-2, a novel herpes infection in northern sea otters (Enhydra lutris kenyoni)

Oral ulcerations and plaques with epithelial eosinophilic intranuclear inclusions were observed in northern sea otters (Enhydra lutris kenyoni) that died or were admitted for rehabilitation after the 1989 Exxon Valdez oil spill (EVOS) in Alaska, USA. Transmission electron microscopy demonstrated the presence of herpesviral virions. Additionally, a serologic study from 2004 to 2005 found a high prevalence of exposure to a herpesvirus in live-captured otters. Tissues from 29 otters after the EVOS and nasal swabs from 83 live-captured otters in the Kodiak Archipelago were tested for herpesviral DNA. Analysis identified a novel herpesvirus in the gamma subfamily, most closely related to Mustelid herpesvirus-1 from badgers. Results indicated that this herpesvirus is associated with ulcerative lesions but is also commonly found in secretions of healthy northern sea otters.     

Preliminary Findings of Fecal Gonadal Hormone Concentrations in Six Captive Sea Otters (Enhydra lutris) after Deslorelin Implantation

The sea otter (Enhydra lutris) is a popular exhibit animal in many zoos and aquariums worldwide. Captive sea otters from these populations are owned by the United States Fish and Wildlife Service (USFWS). The USFWS has requested that these sea otters be prevented from breeding in order to save captive space for wild rescued animals. Sea otters are often housed in mixed sex groups, therefore a chemical contraceptive method or surgical removal of gonads must be used to prevent potential pregnancy. The contraceptive, Suprelorin® or deslorelin, has been used in many different species to effectively suppress reproduction but duration of effect may vary not only between species but also individuals. Here, we report the effects of one to several consecutive deslorelin implants on gonadal reproductive hormones found in fecal samples from six captive sea otters (two males and four females) compared to two control otters (one male and one female) housed at three zoological institutions. We documented the longitudinal hormone signatures of many stages of the contraceptive cycle including pretreatment (PT), stimulatory phase (S), effective contraception (EC), and hormone reversal (HR) that was characterized by a return to normal hormone levels. Deslorelin was found to be an effective contraceptive in sea otters and was found to be reversible documented by a live birth following treatment, however the duration of suppression in females was much longer than expected with a 6‐month and a 1‐year implant lasting between 3 and 4 years in females. Zoo Biol. 32:307–315, 2013. © 2012 Wiley Periodicals, Inc.     

Patterns of growth and body condition in sea otters from the Aleutian archipelago before and after the recent population decline

1. Growth models for body mass and length were fitted to data collected from 1842 sea otters Enhydra lutris shot or live-captured throughout south-west Alaska between 1967 and 2004. Growth curves were constructed for each of two main year groups: 1967-71 when the population was at or near carrying capacity and 1992-97 when the population was in steep decline. Analyses of data collected from animals caught during 2004, when the population density was very low, were precluded by a small sample size and consequently only examined incidentally to the main growth curves. 2. Growth curves demonstrated a significant increase in body mass and body length at age in the 1990s. Asymptotic values of body mass were 12-18% higher in the 1990s than in the 1960s/70s, and asymptotic values for body length were 10-11% higher between the same periods. Data collected in 2004 suggest a continued increase in body size, with nearly all data points for mass and length falling significantly above the 1990s growth curves. 3. In addition to larger asymptotic values for mass and length, the rate of growth towards asymptotic values was more rapid in the 1990s than in the 1960s/70s: sea otters reached 95% of asymptotic body mass and body length 1-2 years earlier in the 1990s. 4. Body condition (as measured by the log mass/log length ratio) was significantly greater in males than in females. There was also an increasing trend from the 1960s/70s through 2004 despite much year-to-year variation. 5. Population age structures differed significantly between the 1960s/70s and the 1990s with the latter distribution skewed toward younger age classes (indicating an altered lx function) suggesting almost complete relaxation of age-dependent mortality patterns (i.e. those typical of food-limited populations). 6. This study spanned a period of time over which the population status of sea otters in the Aleutian archipelago declined precipitously from levels at or near equilibrium densities at some islands in the 1960s/70s to < 5% of estimated carrying capacity by the late 1990s. The results of this study indicate an improved overall health of sea otters over the period of decline and suggest that limited nutritional resources were not the cause of the observed reduced population abundance. Our findings are consistent with the hypothesis that the decline was caused by increased killer whale predation.     

Estimating Carrying Capacity for Sea Otters in British Columbia

ABSTRACT We estimated carrying capacity for sea otters (Enhydra lutris) in the coastal waters of British Columbia, Canada, by characterizing habitat according to the complexity of nearshore intertidal and sub-tidal contours. We modeled the total area of complex habitat on the west coast of Vancouver Island by first calculating the complexity of the Checleset Bay-Kyuquot Sound (CB-KS) region, where sea otters have been at equilibrium since the mid-1990s. We then identified similarly complex areas on the west coast of Vancouver Island (WCVI model), and adapted the model to identify areas of similar complexity along the entire British Columbia coast (BC model). Using survey data from the CB-KS region, we calculated otter densities for the habitat predicted by the 2 models. The density estimates for CB-KS were 3.93 otters/km² and 2.53 otters/km² for the WCVI and BC models, respectively, and the resulting 2 estimates of west coast of Vancouver Island complex habitat carrying capacity were not significantly different (WCVI model: 5,123, 95% CI = 3,337–7,104; BC model: 4,883, 95% CI = 3,223–6,832). The BC model identified the region presently occupied by otters on the central British Columbia coast, but the amount of coast-wide habitat it predicted (5,862 km²) was relatively small, and the associated carrying capacity estimate (14,831, 95% CI = 9,790–20,751) was low compared to historical accounts. We suggest that our model captured a type of high-quality or optimum habitat prevalent on the west coast of Vancouver Island, typified by the CB-KS region, and that suitable sea otter habitat elsewhere on the coast must include other habitat characteristics. We therefore calculated a linear, coast-wide carrying capacity of 52,459 sea otters (95% CI = 34,264–73,489)—a more realistic upper limit to sea otters in British Columbia. Our carrying capacity estimates are helping set population recovery targets for sea otters in Canada, and our habitat predictions represent a first step in Critical Habitat identification. This habitat-based approach to estimating carrying capacity is likely suitable for other nonmigratory, density-dependent species.     

A new metric for measuring condition in large predatory sharks

A simple metric (span condition analysis; SCA) is presented for quantifying the condition of sharks based on four measurements of body girth relative to body length. Data on 104 live sharks from four species that vary in body form, behaviour and habitat use (Carcharhinus leucas, Carcharhinus limbatus, Ginglymostoma cirratum and Galeocerdo cuvier) are given. Condition shows similar levels of variability among individuals within each species. Carcharhinus leucas showed a positive relationship between condition and body size, whereas the other three species showed no relationship. There was little evidence for strong differences in condition between males and females, although more male sharks are needed for some species (e.g. G. cuvier) to verify this finding. SCA is potentially viable for other large marine or terrestrial animals that are captured live and then released.     

REPRODUCTION, SURVIVAL AND TAG LOSS IN CALIFORNIA SEA OTTERS

We observed 40 California sea otters, Enhydra lutris , that were instrumented with implanted radio transmitters and flipper-tagged, and obtained additional data on the reproduction of tagged female otters from the California Department of Fish and Game.
The proportion of instrumented females accompanied by a pup peaked in the spring, with a secondary peak in the fall. Two methods of estimating the annual reproductive rate gave comparable values of 0.90 and 0.94. The average inter-birth interval was 389 d. Two methods of estimating pup survival to weaning gave values of 0.46 and 0.58. Pups either remained with a female less than 80 or more than 120 d. Early mortality of dependent pups appears to be more frequent in California than in Prince William Sound, Alaska.
Two methods of estimation indicated that adult females had the highest survival rates and adult males the lowest. Juvenile females had lower survival rates than adult females but juvenile males had higher survival rates than adult males. The survival rate of juvenile females was lower than that of juvenile males.
The estimated annual loss rate for flipper-tags, based on the instrumented individuals, was 0.26. More individuals lost two tags than would be expected by chance. It is unlikely that accurate estimates of sea otter survival rates can be derived from observations of tagged individuals.     

Highly asymmetric fine-scale genetic structure between sexes of African striped mice and indication for condition dependent alternative male dispersal tactics

Sex-biased dispersal is observed in many taxa, but few studies have compared sex-biased dispersal among and within populations. We addressed the magnitude and habitat dependency of sex-biased dispersal in social African striped mice by separating group-related from population-related genetic variance to understand the contribution of each sex to deme structure. As dispersal over unoccupied habitat is likely to be more costly than dispersal within a population, we predicted that individuals leaving the natal population have a lower body condition, being inferior to heavier territorial individuals. Fine-scale genetic structure was detected in both sexes. Female relatedness decreased continuously from R = 0.21 at 25 m to zero at 500 m. Maximum male relatedness R = 0.05 was constant at distances between 25 and 75 m, becoming zero at 100 m. Genetic variance (F(ST) ) among seven locations was significantly higher in females than in males, while inbreeding estimates (F(IS) ) were significantly higher in males than in females. Assignment tests estimated significantly more migrants among males, while Bayesian clustering estimated only a single genetic unit cluster for males among the seven locations. The mean body mass of migrant males (44 g) was significantly lower than for males that remained resident and thus dispersed within their sub-population (48 g). Combined, the results showed habitat-independent male-biased dispersal and high female philopatry, and suggested that body condition was more important than kinship in male dispersal decisions. We suggest that locally inferior males are important for gene flow between sub-populations. Thus, males might follow alternative dispersal tactics.     

Pregnancy of adult caribou (Rangifer tarandus): evidence for lactational infertility

To examine the relations between pregnancy, body condition, and lactation, 106 adult female caribou Rangifer tarandus granti ) of the Porcupine Herd were captured, weighed, measured, and scored for body condition in November 1990–1992. Blood samples were drawn for determination of pregnancy, and body fat content (kg) was estimated from the product of body weight and the body-condition score. Pregnant females were significantly fatter and heavier than non-pregnant females, and non- lactating females were significantly fatter, but no heavier, than lactating caribou. Probability of pregnancy was positively correlated with body weight and fat content, but prediction of pregnancy was improved when multiple independent variables, including skeletal dimensions and lactation status, were included in logistic models. Non-lactating females were more fertile than lactating females at a particular body weight and metatarsus length; but, at the same fatness, they were not more fertile than females that had lactated through the summer and were ceasing lactation in November. However, females that were extending lactation in November were least fertile, and this reduction of fertility was not explained by differences in body condition or skeletal dimensions. We suggest that the extended lactation group is exhibiting lactational infertility. Finally, unexplained differences in the relation between pregnancy rate and body condition exist among years, suggesting that interannual patterns in the nutrition and ecology of caribou affect the physiological relation between pregnancy and body condition.     

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.     

Variation in the response of an Arctic top predator experiencing habitat loss: feeding and reproductive ecology of two polar bear populations

Polar bears (Ursus maritimus) have experienced substantial changes in the seasonal availability of sea ice habitat in parts of their range, including the Beaufort, Chukchi, and Bering Seas. In this study, we compared the body size, condition, and recruitment of polar bears captured in the Chukchi and Bering Seas (CS) between two periods (1986–1994 and 2008–2011) when declines in sea ice habitat occurred. In addition, we compared metrics for the CS population 2008–2011 with those of the adjacent southern Beaufort Sea (SB) population where loss in sea ice habitat has been associated with declines in body condition, size, recruitment, and survival. We evaluated how variation in body condition and recruitment were related to feeding ecology. Comparing habitat conditions between populations, there were twice as many reduced ice days over continental shelf waters per year during 2008–2011 in the SB than in the CS. CS polar bears were larger and in better condition, and appeared to have higher reproduction than SB bears. Although SB and CS bears had similar diets, twice as many bears were fasting in spring in the SB than in the CS. Between 1986–1994 and 2008–2011, body size, condition, and recruitment indices in the CS were not reduced despite a 44‐day increase in the number of reduced ice days. Bears in the CS exhibited large body size, good body condition, and high indices of recruitment compared to most other populations measured to date. Higher biological productivity and prey availability in the CS relative to the SB, and a shorter recent history of reduced sea ice habitat, may explain the maintenance of condition and recruitment of CS bears. Geographic differences in the response of polar bears to climate change are relevant to range‐wide forecasts for this and other ice‐dependent species.     

Reproductive performance of otters Lutra lutra (Linnaeus, 1758) in Eastern Germany: low reproduction in a long-term strategy

The reproductive status of female otters ( Lutra lutra ) was determined from an examination of 518 carcasses collected from Eastern Germany between 1950 and 2001. In Germany otters mate throughout the year. Significant seasonal differences are evident with a distinct peak in summer. Females were in breeding condition between the ages of three and 15 years, with the majority between six and nine years. The mean litter size at birth was 2.36, which was the lowest when compared with other inland populations. There were no significant differences in litter size for regions, seasons or age. Prenatal losses account for 26.31%. The mortality between birth and first appearance of cubs following their mother is about 29%. An effective reproduction rate of 78.4% was deduced from the known age structure of the sample and the proportion of breeding females. Reproductively active females show a significantly higher body condition than non-reproductive females. Following these investigations into breeding status, suggestions on reproductive output and the life history of the otter are discussed.  © 2002 The Linnean Society of London, Biological Journal of the Linnean Society , 2002, 77 , 329–340.     

Growth Rates and Body Condition in Norops polylepis (Polychrotidae) Vary with Respect to Sex but not Mite Load1

Norops polylepis is a common anoline lizard that occupies both forest and pasture habitats at various elevations in southern Costa Rica. Previous studies have documented significant spatial variation in mite loads (Eutrombicula chiggers) on N. polylepis. My objective was to investigate whether mite load has a negative impact on growth rates and body condition. Growth rates were estimated in three sites using mark‐recapture with three intensive sampling periods over 12 mo. Nine hundred and forty lizards were captured and 200 individuals were recaptured across sampling periods. Mite load was significantly higher in forests than in pastures, and varied significantly among study sites. Males grew faster than females, and females and juveniles had higher body condition than males. I was unable, however, to detect any influence of mite load on growth rates or body condition. I conclude that Eutrombicula chiggers are either largely benign for N. polylepis or, if they do exert a negative effect on fitness, it is mediated through a trait other than growth or body condition.     

Activity Budgets Derived From Time-Depth Recorders in a Diving Mammal

Abstract: We describe a method to convert continuously collected time-depth data from archival time-depth recorders (TDRs) into activity budgets for a benthic-foraging marine mammal. We used data from 14 TDRs to estimate activity-specific time budgets in sea otters (Enhydra lutris) residing near Cross Sound, southeast Alaska, USA. From the TDRs we constructed a continuous record of behavior for each individual over 39-46 days during summer of 1999. Behaviors were classified as foraging (diving to the bottom), other diving (traveling, grooming, interacting), and nondiving (assumed resting). The overall average activity budget (proportion of 24-hr/d) was 0.37 foraging (8.9 hr/d), 0.11 in other diving (2.6 hr/d), and 0.52 nondiving time (12.5 hr/d). We detected significant differences in activity budgets among individuals and between groups within our sample. Historically, the sea otter population in our study area had been expanding and sequentially reoccupying vacant habitat since their reintroduction to the area in the 1960s, and our study animals resided in 2 adjacent yet distinct locations. Males (n = 5) and individuals residing in recently occupied habitat (n = 4) spent 0.28-0.30 of their time foraging (6.7-7.2 hr/d), 0.17-0.18 of their time in other diving behaviors (4.1-4.3 hr/d), and 0.53-0.54 of their time resting (12.7-13.0 hr/d). In contrast, females (n = 9) and individuals residing in longer occupied habitat (n = 10) spent 0.40 of their time foraging (9.6 hr/d), 0.08-0.09 of their time in other diving behaviors (1.9-2.2 hr/d), and 0.51-0.52 of their time resting (12.2-12.5 hr/d). Consistent with these differences, sea otters residing in more recently occupied habitat captured more and larger clams (Saxidomus spp., Protothaca spp., Macoma spp., Mya spp., Clinocardium spp.) and other prey, and intertidal clams were more abundant and larger in this area. We found that TDRs provided data useful for measuring activity time budgets and behavior patterns in a diving mammal over long and continuous time periods. Fortuitous contrasts in time budgets between areas where our study animals resided suggest that activity time budgets estimated from TDRs may be a sensitive indicator of population status, particularly in relation to prey availability.     

Reductions in the dietary niche of southern sea otters (Enhydra lutris nereis) from the Holocene to the Anthropocene

The sea otter (Enhydra lutris) is a marine mammal hunted to near extinction during the 1800s. Despite their well‐known modern importance as a keystone species, we know little about historical sea otter ecology. Here, we characterize the ecological niche of ancient southern sea otters (E. lutris nereis) using δ¹³C analysis and δ¹⁵N analysis of bones recovered from archaeological sites spanning ~7,000 to 350 years before present (N = 112 individuals) at five regions along the coast of California. These data are compared with previously published data on modern animals (N = 165) and potential modern prey items. In addition, we analyze the δ¹⁵N of individual amino acids for 23 individuals to test for differences in sea otter trophic ecology through time. After correcting for tissue‐specific and temporal isotopic effects, we employ nonparametric statistics and Bayesian niche models to quantify differences among ancient and modern animals. We find ancient otters occupied a larger isotopic niche than nearly all modern localities; likely reflecting broader habitat and prey use in prefur trade populations. In addition, ancient sea otters at the most southerly sites occupied an isotopic niche that was more than twice as large as ancient otters from northerly regions. This likely reflects greater invertebrate prey diversity in southern California relative to northern California. Thus, we suggest the potential dietary niche of sea otters in southern California could be larger than in central and northern California. At two sites, Año Nuevo and Monterey Bay, ancient otters had significantly higher δ¹⁵N values than modern populations. Amino acid δ¹⁵N data indicated this resulted from shifting baseline isotope values, rather than a change in sea otter trophic ecology. Our results help in better understanding the contemporary ecological role of sea otters and exemplify the strength of combing zooarchaeological and biological information to provide baseline data for conservation efforts.     

Patterns of mortality in southern sea otters (Enhydra lutris nereis) from 1998-2001

Detailed postmortem examination of southern sea otters (Enhydra lutris nereis) found along the California (USA) coast has provided an exceptional opportunity to understand factors influencing survival in this threatened marine mammal species. In order to evaluate recent trends in causes of mortality, the demographic and geographic distribution of causes of death in freshly deceased beachcast sea otters necropsied from 1998-2001 were evaluated. Protozoal encephalitis, acanthocephalan-related disease, shark attack, and cardiac disease were identified as common causes of death in sea otters examined. While infection with acanthocephalan parasites was more likely to cause death in juvenile otters, Toxoplasma gondii encephalitis, shark attack, and cardiac disease were more common in prime-aged adult otters. Cardiac disease is a newly recognized cause of mortality in sea otters and T. gondii encephalitis was significantly associated with this condition. Otters with fatal shark bites were over three times more likely to have pre-existing T. gondii encephalitis suggesting that shark attack, which is a long-recognized source of mortality in otters, may be coupled with a recently recognized disease in otters. Spatial clusters of cause-specific mortality were detected for T. gondii encephalitis (in Estero Bay), acanthocephalan peritonitis (in southern Monterey Bay), and shark attack (from Santa Cruz to Point A?o Nuevo). Diseases caused by parasites, bacteria, or fungi and diseases without a specified etiology were the primary cause of death in 63.8% of otters examined. Parasitic disease alone caused death in 38.1% of otters examined. This pattern of mortality, observed predominantly in juvenile and prime-aged adult southern sea otters, has negative implications for the overall health and recovery of this population.     

Diet and body condition of cave‐dwelling dwarf crocodiles (Osteolaemus tetraspis,Cope 1861) in Gabon

We present the first ever observations of dwarf crocodiles (Osteolaemus tetraspis) selectively utilizing a cave ecosystem. We analysed crocodile diet to preliminarily assess the degree of ecological isolation of cave‐dwelling crocodiles from their forest‐dwelling conspecifics despite their physical proximity. We additionally conducted the first study of body condition of dwarf crocodiles and compared cave‐dwelling individuals to surface‐dwelling individuals from a variety of alternative habitats and sites as a means to better understand the implications of a semihypogean life on this species. Crocodiles captured in the caves appeared to forage exclusively in the caves and ate mostly cave crickets and bats, whereas crocodiles captured in the surrounding forest habitat consumed primarily freshwater crustaceans and insects and were not found to consume cave‐dwelling prey. Juvenile cave crocodiles had significantly higher body condition compared to juvenile forest crocodiles, which did not vary amongst forest locations. The difference in body condition between adult cave and forest crocodiles was not statistically significant despite also being higher; we suspect this is an artefact of the low sample size rather than a real nondifference. Forest adult crocodiles generally had significantly higher body condition than juveniles, but did not vary by site or habitat. This lack of variation suggests that habitat type is not the most important factor influencing dwarf crocodile body condition. Our results provide a unique insight into facultative cave use by a principally surface‐dwelling species and reinforce the necessity for further research into this unique system to better understand the evolutionary‐scale implications of cave habitat use by dwarf crocodiles.