Tool use increases mechanical foraging success and tooth health in southern sea otters (Enhydra lutris nereis).

Although tool use may enhance resource utilization, its fitness benefits are difficult to measure. By examining longitudinal data from 196 radio-tagged southern sea otters (Enhydra lutris nereis), we found that tool-using individuals, particularly females, gained access to larger and/or harder-shelled prey. These mechanical advantages translated to reduced tooth damage during food processing. We also found that tool use diminishes trade-offs between access to different prey, tooth condition, and energy intake, all of which are dependent on the relative prey availability in the environment. Tool use allowed individuals to maintain energetic requirements through the processing of alternative prey that are typically inaccessible with biting alone, suggesting that this behavior is a necessity for the survival of some otters in environments where preferred prey are depleted.

Effects of ontogeny and oiling on the thermal function of southern sea otter (Enhydra lutris nereis) fur.

During the evolution of most marine mammals, fur as an insulator has been replaced with more buoyant, energy storing and streamlining blubber. By contrast, the sea otter (Enhydra lutris) relies on insulation from its dense, air-trapping pelage, which differs morphologically between natal and adult stages. In this study, we investigated the ontogenetic changes in thermal function of southern sea otter (Enhydra lutris nereis) pelts in air, in water, and when saturated with crude oil. Pelt thermal conductivity, thickness, and thermal resistance were measured for six age classes: neonate (<1 month), small pup (1-2 months), large pup (3-5 months), juvenile (6 months-1 year), subadult (1-3 years), and adult (4-9 years). Thermal conductivity was significantly higher for pelts in air than in water, with oiled pelts exhibiting the highest values (P < 0.001). Oiled pelts had the lowest thermal resistance, which suggests that regardless of age, all sea otters are vulnerable to the effects of oiling (P < 0.001). To scale up our laboratory findings, we used a volume-specific geometric model of conductive heat transfer for a simplified sea otter body, representing all tested age classes and treatments. Neonates, small pups, and large pups are more vulnerable to the effects of oiling compared with older age classes (P < 0.0001) due to a higher surface area-to-volume ratio. These results are consistent with the known thermal conductance values for adult sea otter pelts, yet this is the first time such thermal differences have been demonstrated in young otters. Overall, body size and age play a more important role in the thermal abilities of sea otters than previously thought.

Robust age estimation of southern sea otters from multiple morphometrics.

Reliable age estimation is an essential tool to assess the status of wildlife populations and inform successful management. Aging methods, however, are often limited by too few data, skewed demographic representation, and by single or uncertain morphometric relationships. In this study, we synthesize age estimates in southern sea otters Enhydra lutris nereis from 761 individuals across 34 years of study, using multiple noninvasive techniques and capturing all life stages from 0 to 17 years of age. From wild, stranded, and captive individuals, we describe tooth eruptions, tooth wear, body length, nose scarring, and pelage coloration across ontogeny and fit sex-based growth functions to the data. Dental eruption schedules provided reliable and identifiable metrics spanning 0.3-9 months. Tooth wear was the most reliable predictor of age of individuals aged 1-15 years, which when combined with total length, explained >93% of observed age. Beyond age estimation, dental attrition also indicated the maximum lifespan of adult teeth is 13‒17 years, corresponding with previous estimates of life expectancy. Von Bertalanffy growth function model simulations of length at age gave consistent estimates of asymptotic lengths (male Loo  = 126.0‒126.8 cm, female Loo  = 115.3‒115.7 cm), biologically realistic gestation periods (t 0 = 115 days, SD = 10.2), and somatic growth (male k = 1.8, SD = 0.1; female k = 2.1, SD = 0.1). Though exploratory, we describe how field radiographic imaging of epiphyseal plate development or fusions may improve aging of immature sea otters. Together, our results highlight the value of integrating information from multiple and diverse datasets to help resolve conservation problems.

Non-trophic impacts from white sharks complicate population recovery for sea otters.

Complex interactions between protected populations may challenge the recovery of whole ecosystems. In California, white sharks (Carcharodon carcharias) mistargeting southern sea otters (Enhydra lutris nereis) are an emergent impact to sea otter recovery, inhibiting the broader ecosystem restoration sea otters might provide. Here, we integrate and analyze tracking and stranding data to compare the phenology of interactions between white sharks and their targeted prey (elephant seals, Mirounga angustirostris) with those of mistargeted prey (sea otters, humans). Pronounced seasonal peaks in shark bites to otters and humans overlap in the late boreal summer, immediately before the annual adult white shark migration to elephant seal rookeries. From 1997 to 2017, the seasonal period when sharks bite otters expanded from 2 to 8 months of the year and occurred primarily in regions where kelp cover declined. Immature and male otters, demographics most associated with range expansion, were disproportionately impacted. While sea otters are understood to play a keystone role in kelp forests, recent ecosystem shifts are revealing unprecedented bottom-up and top-down interactions. Such shifts challenge ecosystem management programs that rely on static models of species interactions.