Status,trends, and equilibrium abundance estimates of the translocated sea otter population in Washington State

Sea otters (Enhydra lutris kenyoni) historically occurred in Washington State, USA, until their local extinction in the early 1900s as a result of the maritime fur trade. Following their extirpation, 59 sea otters were translocated from Amchitka Island, Alaska, USA, to the coast of Washington, with 29 released at Point Grenville in 1969 and 30 released at La Push in 1970. The Washington Department of Fish and Wildlife has outlined 2 main objectives for sea otter recovery: a target population level and a target geographic distribution. Recovery criteria are based on estimates of population abundance, equilibrium abundance (K), and geographic distribution; therefore, estimates of these parameters have important management implications. We compiled available survey data for sea otters in Washington State since their translocation (1977–2019) and fit a Bayesian state-space model to estimate past and current abundance, and equilibrium abundance at multiple spatial scales. We then used forward projections of population dynamics to explore potential scenarios of range recolonization and as the basis of a sensitivity analysis to evaluate the relative influence of movement behavior, frontal wave speed, intrinsic growth, and equilibrium density on future population recovery potential. Our model improves upon previous analyses of sea otter population dynamics in Washington by partitioning and quantifying sources of estimation error to estimate population dynamics, by providing robust estimates of K, and by simulating long-term population growth and range expansion under a range of realistic parameter values. Our model resulted in predictions of population abundance that closely matched observed counts. At the range-wide scale, the population size in our model increased from an average of 21 independent sea otters (95% CI = 13–29) in 1977 to 2,336 independent sea otters (95% CI = 1,467–3,359) in 2019. The average estimated annual growth rate was 12.42% and varied at a sub-regional scale from 6.42–14.92%. The overall estimated mean K density of sea otters in Washington was 1.71 ± 0.90 (SD) independent sea otters/km² of habitat (1.96 ± 1.04 sea otters/km², including pups), and estimated densities within the current range correspond on average to 87% of mean sub-regional equilibrium values (range = 66–111%). The projected value of K for all of Washington was 5,287 independent sea otters (95% CI = 2,488–8,086) and 6,080 sea otters including pups (95% CI = 2,861–9,300), assuming a similar range of equilibrium densities in currently un-occupied habitats. Sensitivity analysis of simulations of sea otter population growth and range expansion suggested that mean K density estimates in currently occupied sub-regions had the largest impact on predicted future population growth (r² = 0.52), followed by the rate of southward range expansion (r² = 0.26) and the mean K density estimate of currently unoccupied sub-regions to the south of the current range (r² = 0.04). Our estimates of abundance and sensitivity analysis of simulations of future population abundance and geographic range help determine population status in relation to population recovery targets and identify the most influential parameters affecting future population growth and range expansion for sea otters in Washington State.     

Survival estimates for the Australian sea lion: Negative correlation of sea surface temperature with cohort survival to weaning

The Australian sea lion (Neophoca cinerea) population at Seal Bay Conservation Park, South Australia, is estimated to be declining at a rate of 1.14% per breeding season. To better understand the potential causes of this decline, survival rates were examined to 14 yr of age for eight cohorts marked as pups (aged 0.17 yr) between 1991 and 2002. Apparent yearly survival rates (Φ) varied by cohort for pups from marking to weaning at 1.5 yr (Φ= 0.30–0.67). Postweaning juvenile survival (1.5–3 yr) was 0.89 and survival from 3 to 14 yr was constant (Φ female:male = 0.96:0.89). Φ of pup cohorts was negatively correlated to local sea surface temperature where the sea lions forage (SST) and was especially low for cohort 7 in 2000 (0.30). It is possible that periods of unusually warm oceanographic conditions may be limiting primary production and inhibiting maternal provisioning to pups. Pup survival to weaning is relatively low compared to other otariid species, is likely to limit recruitment, and may be contributing to the decline in pup abundance observed in the colony.     

Trend changes in sympatric Subantarctic and Antarctic fur seal pup populations at Marion Island,Southern Ocean

Recent pup population estimates of sympatric Subantarctic (Arctocephalus tropicalis) and Antarctic fur seals (A. gazella) at Marion Island are presented. Published pup population estimates of A. tropicalis (1995 and 2004) with an unpublished total island count in 2013, and annual counts on subsets of rookeries (2007–2015) were analyzed using a hierarchical Bayesian model. The pup population declined by 46% (95% credible interval CI: 43%–48%) between 2004 (mean = 15,260, CI: 14,447–16,169 pups) and 2013 (mean = 8,312, CI: 7,983–8,697), mirrored by a 58%–60% decline at rookeries counted annually (2007–2015). Population decline was highest at high‐density west and north coast rookeries, despite negligible change in female attendance patterns, pup mortality or median pupping date over the previous 25 yr. A better understanding of foraging behavior and its effects on reproductive success and survival in this A. tropicalis population is needed before we can attribute population decline to any external factors. In contrast, total island counts of A. gazella pups in 2007, 2010, and 2013, suggest that this population is still increasing although the annual intrinsic rate of population growth decreased from 17.0% (1995–2004, 744 pups) to 4.0% (2010–2013, 1,553 pups). The slowed growth of A. gazella is likely the result of saturation at the main rookery.     

SURVIVAL RATES OF SEA OTTER PUPS IN ALASKA AND CALIFORNIA

Adult female sea otters ( Enhydra lutris ) were instrumented with implanted radio-transmitters in Prince William Sound (PWS), Alaska, and survival rates were estimated for their dependent pups. Overall, 94 of 141 (67%) of the pups studied survived to a minimum age of 120 d and were assumed to have successfully weaned. Survival of pups in six cohorts ranged from 53% to 88%. The mean interval between successive visual observations was 12.5 d. For these calculations, the assumption was made that pups were successfully weaned if they accompanied mothers for at least 120 d. Estimated survival rates were different when this assumption was changed to either 90 d or 150 d (73% and 52%, respectively).
Females were palpated for pregnancy when instrumented. Of 19 believed to be pregnant, 17 were subsequently seen with young pups giving a detection rate for births of 89.5%. When the above observed survival rate of pups was adjusted for undetected births, the estimated overall survival rate for the study population was 60% (120 d minimum dependency).
Survival rates of pups in PWS and a population at Kodiak Archipelago (KOD) (Monson and DeGange 1995) were compared with that of pups in the population in California (CA, four studies). These data did not support the hypothesis that survival rates were lower in California (CA: 103/160, P_surv. 0.64; PWS: 94/141, P_surv. = 0.67; KOD: 19/23, P_surv. = 0.83; pairwise comparisons, X², P > 0.05). Comparison of pup survival rates among studies was hindered by small sample sizes, methodological differences, and lack of detail about assumptions underlying estimates.     

Postharvesting population dynamics of the South American sea lion (Otaria byronia) in the southwestern Atlantic

Many pinniped populations precipitously declined during the 19th and 20th centuries due to overharvesting. In Uruguay, the South American sea lion (SASL) was harvested until 1986. Birth rates in two nearby breeding colonies have had opposite trends for at least 20 yr. We assessed different mechanisms that could explain opposite trends in birth rates in the two SASL colonies. We compared feeding habits (δ¹⁵N and δ¹³C) of breeding females, birth mass, individual growth rate and early survival of pups and the social structure between colonies. Breeding females from the two colonies did not differ in their feeding habits. However, male and female pups grew faster but had a lower survival in the second month in the smallest colony. We found differences in the social structures, with a higher proportion of males in the smallest colony. The latter is important because peripheral SASL males may abduct and kill pups, which may explain the lower survival of pups in smaller colonies. We believe that the cumulative effects of population extractions have lowered the local SASL population size and disrupted its social structure to the point where Allee‐like effects could become important and hamper the recovery of the Uruguayan SASL population.     

Postbranding Survival of Steller Sea Lion Pups at Lowrie Island in Southeast Alaska

ABSTRACT Steller sea lion (Eumetopias jubatus) pups (n = 366) were hot-branded at Lowrie Island, Southeast Alaska, USA, in June 2001 and 2002 for vital-rates studies. To assess potential mortality following branding, we estimated weekly survival to 12 weeks postbranding using mark-recapture models. Survival estimates ranged from 0.984/week to 0.988/week, or 0.868 over the 12-week period; varied little with sex, year, and capture area; and were higher for larger than smaller male pups and unexpectedly lower for larger than smaller female pups. Inclusion of resights at 1–3 years of age prevented a −4.5% bias in cumulative survival to 12 weeks postbranding by accounting for pups that survived but permanently emigrated from Lowrie Island during the 12-week survey. Data from double-marked pups (i.e., branded and flipper-tagged) indicated the low brand-misreading probability of 3.1% did not bias survival estimates. Assuming survival differences between the first 2 weeks postbranding and later weeks were due entirely to the branding event, potential postbranding mortality of branded pups attributable to the branding event was 0.5–0.7%, or one pup for every 200 marked. Weekly survival of branded pups was nearly identical to estimates from a control group of undisturbed, unbranded pups born to 10–11-year-old branded adult females in 2005 (0.987–0.988/week) and similar to pup survival estimates from other otariid studies. Available data did not indicate substantial mortality to 12 weeks postbranding resulting from the branding disturbance, suggesting branding of Steller sea lion pups can be used effectively for investigations of population declines without significantly affecting population health or study goals.     

Mark‐recapture modeling accounting for state uncertainty provides concurrent estimates of survival and fecundity in a protected harbor seal population

Harbor seal breeding behavior and habitats constrain opportunities for individual‐based studies, and no current estimates of both survival and fecundity exist for any of the populations studied worldwide. As a result, the drivers underlying the variable trends in abundance exhibited by harbor seal populations around the world remain uncertain. We developed an individual‐based study of harbor seals in northeast Scotland, whereby data were collected during daily photo‐identification surveys throughout the pupping seasons between 2006 and 2011. However, a consequence of observing seals remotely meant that information on sex, maturity‐stage, or breeding status was not always available. To provide unbiased estimates of survival rates we conditioned initial release of individuals on the first time sex was known to estimate sex‐specific survival rates, while a robust design multistate model accounting for uncertainty in breeding status was used to estimate reproductive rate of multiparous and ≥3‐yr‐old females. Survival rates were estimated at 0.95 (95% CI = 0.91–0.97) for females and 0.92 (0.83–0.96) for males, while reproductive rate was estimated at 0.89 (0.75–0.95) for multiparous and 0.69 (0.64–0.74) for ≥3‐yr‐old females. Stage‐based population modeling indicated that this population should be recovering, even under the current shooting quotas implemented by the recent management plan.     

Growth and survival of New Zealand sea lions, <Emphasis Type="Italic">Phocarctos hookeri:</Emphasis> birth to 3 months

Offspring birth mass and growth rate represent important life history traits, which influence many vital population and individual characteristics, while offspring survival is a key factor in variation in female reproductive success. For a threatened population of pinnipeds, such as New Zealand sea lions, Phocarctos hookeri, (Grey, 1844, NZ sea lions), understanding individual life history parameters and population dynamics is vital for their management and conservation. This is the first study of the behaviour of females during parturition, pup birth mass and growth, and pre-weaning survival of NZ sea lions, Enderby Island, Auckland Islands during austral summer breeding seasons, 2001/2002 to 2003/2004. Pregnant females arrived ashore 2.1 ± 0.16 days prior to giving birth. After parturition, mothers suckled their pups for 8.6 ± 0.16 days before leaving on their first foraging trip. Male pups were born significantly heavier than female (males 10.6 ± 1.4 kg, females 9.7 ± 0.9 kg). Pups lost on average 48 ± 0.14 g per day mass during the early postpartum period (between birth and mothers first foraging trip). Pup mortality did not vary by pup sex, birth mass, date of birth or any maternal characteristics however it varied significantly between years due to a bacterial infection epidemic (Pup mortality at 60 days: 2001 32%; 2002 21%; 2003 12%). The absolute growth rate per day for pups was 151 g/day over all years. Pup growth rate measured as the slope of linear line fitted to pup mass by age was consistently higher for pups with heavier birth mass, male pups and during the 2002 season. High offspring mortality and slow growth rates coupled with maternal foraging behaviour at their physiological limits may reflect a threatened species which has limited ability for population growth in an environment which is at the extreme of their historical range and impacted upon by fisheries.     

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.     

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.     

The population decline of the New Zealand sea lion Phocarctos hookeri: a review of possible causes

• 1 The New Zealand (NZ) sea lion Phocarctos hookeri is NZ's only endemic pinniped and is listed as ‘nationally critical’. The species breeds in the NZ sub‐Antarctic: 71% of the population at the Auckland Islands (2010 pup production: 1814 ± 39) and the remaining 29% on Campbell Island (726 pups in 2010).
• 2 Pup production at the Auckland Islands has declined by 40% since 1998 (1998: 3021 pups produced): only 1501 pups were born in 2009. This decline is directly linked to philopatric females not returning to breeding areas. While the Auckland Island population has declined, the Campbell Island population appears to be increasing slowly.
• 3 Potential reasons for the decline in the Auckland Island population, but not in the Campbell Island population, include non‐anthropogenic factors: (i) disease epizootics, (ii) predation, (iii) permanent dispersal or migration, (iv) environmental change; and anthropogenic impacts: (v) population ‘overshoot’, (vi) genetic effects, (vii) effects of contaminants, (viii) indirect effects of fisheries (i.e. resource competition) and (ix) direct effects of fisheries (i.e. by‐catch deaths). Of the nine potential reasons examined here, six can be discounted (ii–vii). Bacterial epizootics (i) occur in the NZ sea lion population, but their impact has predominantly increased pup mortality, which is unlikely to cause the severe decline observed, as pup mortality throughout the species is naturally high and variable.
• 4 The most plausible hypotheses, based on available evidence, are that the observed decline, in particular, the decreasing number of breeding females in the Auckland Island population, is caused by (viii) fisheries‐induced resource competition and (ix) fisheries‐related by‐catch. By‐catch is the main known anthropogenic cause of mortality in the species. Competition with fisheries resulting in resource competition, nutrient stress and decreased reproductive ability in NZ sea lions should be a priority area for future research.

     

Age‐ and sex‐specific survival of California sea lions (Zalophus californianus) at San Miguel Island,California

We conducted a mark‐recapture study of California sea lions (Zalophus californianus) using pups branded on San Miguel Island, California, from 1987 to 2014, and annual resightings from 1990 to 2015. We used the Burnham model (Burnham 1993), an extension of the Cormack‐Jolly‐Seber mark‐recapture model, which includes recoveries of dead animals, to analyze age, sex, and annual patterns in survival. Generally, females had higher survival than males. For female pups, the average annual survival was 0.600 and for male pups it was 0.574. Yearling survival was 0.758 and 0.757 for females and males, respectively. Peak annual survival was at age 5 and was 0.952 for females and 0.931 for males. Pups with larger mass at branding had higher survival as pups and yearlings, but the effect was relative within each cohort because of large between‐cohort variability in survival. Annual variability in sea surface temperature (SST) affected survival. For each 1°C increase in SST, the odds of survival decreased by nearly 50% for pups and yearlings; negative SST anomalies yielded higher survival. Annual variation in male survival was partly explained by leptospirosis outbreaks. Our study provides a unique view of one demographic parameter that contributed to the successful recovery of the California sea lion population.     

Lifetime survival rates and senescence in northern elephant seals

The aim of this study was to extend 40 yr of prior demographic work on northern elephant seals (Mirounga angustirostris) at Año Nuevo, California, by including the oldest animals. We used a Bayesian mark‐recapture analysis to estimate lifelong survival and lifespan of a cohort of 372 weaned pups branded in 1985–1987 and resighted until 2008. Annual survival probability of females averaged 86.3%/yr at ages 5–16, then declined until age 21, the age of the oldest female. Male survival was lower, averaging 67.7%/yr from age 1 to age 15, the age of the oldest male. Northern elephant seal females in the expanding population at Año Nuevo live longer than southern elephant seal females (M. leonina) at colonies whose populations are declining. This comparison suggests that high survival of females is a key factor in population growth.     

HP1BP3 expression determines maternal behavior and offspring survival

Maternal care is an indispensable behavioral component necessary for survival and reproductive success in mammals, and postpartum maternal behavior is mediated by an incompletely understood complex interplay of signals including effects of epigenetic regulation. We approached this issue using our recently established mice with targeted deletion of heterochromatin protein 1 binding protein 3 (HP1BP3), which we found to be a novel epigenetic repressor with critical roles in postnatal growth. Here, we report a dramatic reduction in the survival of pups born to Hp1bp3^?/? deficient mouse dams, which could be rescued by co‐fostering with wild‐type dams. Hp1bp3^?/? females failed to retrieve both their own pups and foster pups in a pup retrieval test, and showed reduced anxiety‐like behavior in the open‐field and elevated‐plus‐maze tests. In contrast, Hp1bp3^?/? females showed no deficits in behaviors often associated with impaired maternal care, including social behavior, depression, motor coordination and olfactory capability; and maintained unchanged anxiety‐associated hallmarks such as cholinergic status and brain miRNA profiles. Collectively, our results suggest a novel role for HP1BP3 in regulating maternal and anxiety‐related behavior in mice and call for exploring ways to manipulate this epigenetic process.     

Nursing Behavior in Mexican Free-tailed Bat Maternity Colonies

The nursing behavior of Mexican free-tailed bats (Tadarida brasiliensis mexicana) was examined in two large maternity cave roosts during six nursing seasons. After depositing pups in large creches, adults return to these creches two or more times daily to nurse. Densities, movements, and roosting associations of pups in creches were documented, and a night-vision device and infrared-sensitive video system were used to observe female-pup reunions and nursing affiliations. Densities of young (< 15 d) pups in creches averaged 4000 pups/m². Pups moved independently of one another between milk meals. Stable roosting associations among pups were absent, and females evidently could not predict where a given pup would be relocated. Upon returning to the creche, females searched for and relocated pups using vocal and olfactory cues. Experiments with marked individuals demonstrated that females nursed the same pups on subsequent nights. These same experiments indicated that female/pup recognition was mutual and that the pup participated in reunions by moving toward its putative mother. However, pups also attempted to suckle from other females and 35 instances of apparently successful milk “theft” were observed. Observed milk theft was insufficient to account for the frequency of alloparental nursing that was estimated independently using genotype tests. The high densities of bats within roosts and the lack of stable roosting associations among individuals argue against selection for shared nursing via kin selection and/or reciprocity. Errors in pup recognition, milk-dumping by females, and adoption by mothers whose own pup had died may occur, but high pup survival to weaning suggests that adoption is rare. The estimate of alloparental nursing obtained from genotype tests may be inflated as a result of increased opportunities for milk theft caused by our disturbance of adults. Current evidence suggests that energetic costs to females of alloparental nursing and searching for pups are compensated by mutualistic benefits obtained from aggregative roosting.     

The Effects of Breeder Loss on Wolves

Abstract Managers of recovering wolf (Canis lupus) populations require knowledge regarding the potential impacts caused by the loss of territorial, breeding wolves when devising plans that aim to balance population goals with human concerns. Although ecologists have studied wolves extensively, we lack an understanding of this phenomenon as published records are sparse. Therefore, we pooled data (n = 134 cases) on 148 territorial breeding wolves (75 M and 73 F) from our research and published accounts to assess the impacts of breeder loss on wolf pup survival, reproduction, and territorial social groups. In 58 of 71 cases (84%), ≥1 pup survived, and the number or sex of remaining breeders (including multiple breeders) did not influence pup survival. Pups survived more frequently in groups of ≥6 wolves (90%) compared with smaller groups (68%). Auxiliary nonbreeders benefited pup survival, with pups surviving in 92% of cases where auxiliaries were present and 64% where they were absent. Logistic regression analysis indicated that the number of adult-sized wolves remaining after breeder loss, along with pup age, had the greatest influence on pup survival. Territorial wolves reproduced the following season in 47% of cases, and a greater proportion reproduced where one breeder had to be replaced (56%) versus cases where both breeders had to be replaced (9%). Group size was greater for wolves that reproduced the following season compared with those that did not reproduce. Large recolonizing (>75 wolves) and saturated wolf populations had similar times to breeder replacement and next reproduction, which was about half that for small recolonizing (≤75 wolves) populations. We found inverse relationships between recolonizing population size and time to breeder replacement (r= —0.37) and time to next reproduction (r= —0.36). Time to breeder replacement correlated strongly with time to next reproduction (r=0.97). Wolf social groups dissolved and abandoned their territories subsequent to breeder loss in 38% of cases. Where groups dissolved, wolves reestablished territories in 53% of cases, and neighboring wolves usurped territories in an additional 21% of cases. Fewer groups dissolved where breeders remained (26%) versus cases where breeders were absent (85%). Group size after breeder loss was smaller where groups dissolved versus cases where groups did not dissolve. To minimize negative impacts, we recommend that managers of recolonizing wolf populations limit lethal control to solitary individuals or territorial pairs where possible, because selective removal of pack members can be difficult. When reproductive packs are to be managed, we recommend that managers only remove wolves from reproductive packs when pups are ≥6 months old and packs contain ≥6 members (including ≥3 ad-sized wolves). Ideally, such packs should be close to neighboring packs and occur within larger (≥75 wolves) recolonizing populations.     

Lactation and resource limitation affect stress responses,thyroid hormones,immune function,and antioxidant capacity of sea otters (Enhydra lutris)

Lactation is the most energetically demanding stage of reproduction in female mammals. Increased energetic allocation toward current reproduction may result in fitness costs, although the mechanisms underlying these trade‐offs are not well understood. Trade‐offs during lactation may include reduced energetic allocation to cellular maintenance, immune response, and survival and may be influenced by resource limitation. As the smallest marine mammal, sea otters (Enhydra lutris) have the highest mass‐specific metabolic rate necessitating substantial energetic requirements for survival. To provide the increased energy needed for lactation, female sea otters significantly increase foraging effort, especially during late‐lactation. Caloric insufficiency during lactation is reflected in the high numbers of maternal deaths due to End‐Lactation Syndrome in the California subpopulation. We investigated the effects of lactation and resource limitation on maternal stress responses, metabolic regulation, immune function, and antioxidant capacity in two subspecies of wild sea otters (northern: E. l. nereis and southern: E. l. kenyoni) within the California, Washington, and Alaska subpopulations. Lactation and resource limitation were associated with reduced glucocorticoid responses to acute capture stress. Corticosterone release was lower in lactating otters. Cortisol release was lower under resource limitation and suppression during lactation was only evident under resource limitation. Lactation and resource limitation were associated with alterations in thyroid hormones. Immune responses and total antioxidant capacity were not reduced by lactation or resource limitation. Southern sea otters exhibited higher concentrations of antioxidants, immunoglobulins, and thyroid hormones than northern sea otters. These data provide evidence for allocation trade‐offs during reproduction and in response to nutrient limitation but suggest self‐maintenance of immune function and antioxidant defenses despite energetic constraints. Income‐breeding strategists may be especially vulnerable to the consequences of stress and modulation of thyroid function when food resources are insufficient to support successful reproduction and may come at a cost to survival, and thereby influence population trends.     

ATYPICAL PUP REARING STRATEGIES BY SEA OTTERS

Eight tagged sea otter (Enhydra lutris) pups in central Prince William Sound, Alaska, weighed 6–15 kg at the time of separation from their mother. Four pups weighing 15 kg were able to forage successfully on their own. Three pups weighing ≤9 kg had negligible chances of survival and apparently were abandoned by sick females. Abandonment of a pup may reduce the burden on a sick female, enabling recovery and subsequent reproduction. One of the three sick females that abandoned a pup in this study recovered and pupped again. Abandonment of pups should occur most often in populations where females are stressed by poor food resources. Reassociation with a previous offspring, as observed once in this study, also may occur most frequently in food-limited populations where reproductive failures are most common and pup survivorship is significantly increased by additional maternal assistance.     

Age‐specific recruitment and natality of California sea lions at San Miguel Island,California

We conducted a 15 yr mark‐resight study of branded California sea lions (Zalophus californianus) at San Miguel Island, California, to estimate age‐specific recruitment and natality of the population. We used the Schwarz and Stobo model to estimate sighting, survival, recruitment, timing of births, abundance, and age‐specific natality from sighting histories of 1,276 parous females. The advantage of this approach was that the reproductive status of females did not have to be known for all females of reproductive age. Probability of recruitment into the reproductive population began at age 3 or 4, peaked between ages 5 and 7, and slowly declined. Age‐specific natality was similar for ages 4–16 but declined after age 17, suggesting that reproductive senescence occurs in older females. The average annual natality for parous females 4–16 yr of age was 0.77 (SE = 0.03); natality declined to 0.56 (SE = 0.10) for parous females 17–21 yr of age. Natality for both age classes was reduced during El Niño conditions by 24% and 34%, respectively. In addition to reducing natality, El Niño events may result in a delay of recruitment if females experience El Niño conditions before they turn 4 yr of age.     

Direct Estimation of Early Survival and Movements in Eastern Wolf Pups

Abstract: Determining juvenile survival and recruitment rates is essential to assess status and viability of animal populations. Currently, the demographic attributes of juvenile carnivores, specifically wolves (Canis lycaon), are poorly known but of considerable conservation interest. We measured survival and dispersal rates for 51 juvenile (age 3.5–31 weeks) wolves in Algonquin Provincial Park, Canada, from 2004 to 2005, using implantable very high frequency transmitters. Monthly pup survival was high (0.970, 95% CI = 0.951–0.990) and constant from June to November, and most pup mortality was from natural causes. Pups dispersed as early as age 15 weeks, and monthly dispersal rates were high for young pups (min. = 0.008, 95% CI = 0.000–0.019; max. = 0.030, 95% CI = 0.010–0.050). We failed to detect any influence of pack or litter size on pup survival or probability of dispersal. Radiotelemetry offers an individual-based monitoring technique capable of providing direct assessment of wolf pup survival and movements, with rigorous estimation of survival and dispersal rates and quantification of cause-specific mortality.