Kenneth W. Pitcher

Reproductive Biology of Steller Sea Lions in the Gulf of Alaska

Reproductive biology of Steller sea lions ( Eumetopias jubatus ) in the Gulf of Alaska was studied between 1975 and 1979 by examination of reproductive tracts, estimation of ages from dental annuli, and observations at rookeries and hauling areas. Timing of key reproductive events was: 1) birth, mid-May to mid-July; 2) breeding, late-May to mid- or late-July; and 3) implantation, late-September and October. The female-pup bond usually was 1 year, however, 1-, 2-, and 3-year-old animals occasionally were seen to suckle females. Some males became sexually mature by 3 years and all were sexually mature by 8 years. Mature males had seasonal spermatogenic activity with abundant epididymal spermatozoa from late April through July. Initial ovulations and pregnancies occurred between 2 and 8 years of age. The average age at first ovulation was 4.6 ±0.8 years (95% confidence limits) and first pregnancy 4.9 ± 1.2 years. Ovulation rates ranged from 26% at 3 years to 100% for animals ≤6 years. Incidence of pregnancy ranged from 20% at 3 years to 87% for females 8 to 20 years. Prenatal mortality between implantation and birth was estimated at 4.7% per month. The annual birth rate of full-term pups was estimated to be about 63% for sexually mature females.

SPATIAL AND TEMPORAL VARIATION IN THE TIMING OF BIRTHS OF STELLER SEA LIONS

Abstract Throughout the range of the Steller sea lion (Eumetopias jubatus), nearly all births of full-term pups observed from 1968 to 1998 occurred between 15 May and 15 July. We found significant differences in timing of births between rookeries with the earliest mean date of birth (4 June) at Forrester Island, Alaska, and the latest (21 June) at Año Nuevo Island, California. Mean date of birth becomes progressively later both north and south of Forrester Island. Births at individual rookeries were synchronous, with 90% of pups born within a 25-day period. We hypothesize that timing of births at rookeries is determined through selection for time periods when weather conditions are generally favorable for pup survival and when adequate prey items are predictably available near rookeries for lactating females. Temporal differences also were found in mean date of birth at 4 rookeries, with a maximum difference between earliest and latest mean date of birth of 10.2 days at Año Nuevo Island. The most likely explanation for temporal variability at individual rookeries is variable nutritional status of reproductive females.

Mercury concentrations in the fur of Steller sea lions and northern fur seals from Alaska

We compared total mercury (THg) concentrations in the fur of northern fur seals (Callorhinus ursinus) from the depleted Pribilof Islands population with those of both declining and thriving populations of Steller sea lions (Eumetopias jubatus) from Prince William Sound (PWS) and Southeast Alaska (SEA), respectively. Relatively low wet weight concentrations (ranges) of THg were detected in the fur of Steller sea lion (SSL) pups (0.90-3.14 microg/g) and juveniles (0.56-6.75 microg/g) from both areas in 1998 and 2000 compared to northern fur seal (NFS) pups (3.15-8.14 microg/g) in 2000. The mean concentration +/- SD for SSLs sampled were 1.46 +/- 0.64 microg/g for pups (n = 22) and 2.74 +/- 2.89 microg/g for juveniles (n = 6). Analyses indicated higher THg concentrations from SSL pups from PWS compared to the SEA. Mean +/- SD. THg in the NFS pups was 4.90 +/- 1.42 microg/g (n = 34) and for post-partum dams was 7.84 +/- 1.78 microg/g (n = 12).

Cohort effects and spatial variation in age-specific survival of Steller sea lions from southeastern Alaska

Information concerning mechanistic processes underlying changes in vital rates and ultimately population growth rate is required to monitor impacts of environmental change on wildlife. We estimated age-specific survival and examined factors influencing survival for a threatened population of Steller sea lions (Eumetopias jubatus) in southeastern Alaska. We used mark-recapture models and data from 1,995 individuals marked at approximately one month of age at four of five rookeries in southeastern Alaska, and resighted from Oregon to the Bering Sea. Average annual survival probability for females was 0.64 for pups and 0.77 for yearlings, and increased from 0.91 to 0.96 from age 3–7 yrs. Annual survival probability of males averaged 0.60 for pups and 0.88 by 7 yrs, resulting in probability of survival to age 7, 33% lower for males compared to females. Pups from northern southeastern Alaska (including an area of low summer population size but rapid growth) were twice as likely to survive to age 7 compared to pups from southern rookeries (including a large, historical, stable rookery). Effects of early conditions on future fitness were observed as (1) environmental conditions in the birth year equally affected first- and second-year survival, and (2) effects of body mass at approximately one month of age were still apparent at 7 yrs. Survival from 0–2 yrs varied among five cohorts by a maximum absolute difference of 0.12. We observed survival costs for long-distance dispersal for males, particularly as juveniles. However, survival was higher for non-pups that dispersed to northern southeastern Alaska, suggesting that moving to an area with greater productivity, greater safety, or lower population size may alleviate a poor start and provide a mechanism for spatial structure for sea lion populations.

Bacular size, growth, and allometry in the largest extant otariid, the Steller sea lion (Eumetopias jubatus)

Abstract Bacula are relatively small in terrestrially mating species of pinnipeds (otariids and elephant seals, Mirounga), perhaps reflecting adaptive size reduction to minimize bacular fracture. Fur seals and sea lions (Otariidae) are a good group with which to investigate this question, because most species copulate solely on land and body size varies interspecifically. We studied bacular size and relative growth in the largest extant otariid, the Steller sea lion (Eumetopias jubatus). Bacula roughly tripled in length and increased 30-fold in mass between 1 and 8 years of age. Allometric relationships changed over development; bacular length and mass changed from being initially positively allometric to body length to negatively allometric and isometric, respectively; bacular mass and thickness were positively allometric to body length throughout life, and apical growth was isometric then was positively allometric to bacular length. In adults (>7 years of age), bacula averaged 18.1 cm length (6.2% of body length), 36.7 g mass, and 2.02 g/cm density (mass : length). The baculum of Eumetopias is about the same length relative to body length as in other adult male otariids but is about twice the density, presumably to increase strength. Information on small or aquatically mating species of otariid are needed to extend our findings and interpretations.

Natal and breeding philopatry of female Steller sea lions in southeastern Alaska

Information on drivers of dispersal is critical for wildlife conservation but is rare for long-lived marine mammal species with large geographic ranges. We fit multi-state mark-recapture models to resighting data of 369 known-aged Steller sea lion (Eumetopias jubatus) females marked as pups on their natal rookeries in southeastern Alaska from 1994–2005 and monitored from 2001–15. We estimated probabilities of females being first observed parous at their natal site (natal philopatry), and of not moving breeding sites among years (breeding philopatry) at large (> 400 km, all five rookeries in southeastern Alaska) and small (< 4 km, all islands within the largest rookery, Forrester Island Complex, F) spatial scales. At the rookery scale, natal philopatry was moderately high (0.776–0.859) for most rookeries and breeding philopatry was nearly 1, with < 3% of females switching breeding rookeries between years. At more populous islands at F, natal philopatry was 0.500–0.684 versus 0.295–0.437 at less populous islands, and breeding philopatry was 0.919–0.926 versus 0.604–0.858. At both spatial scales, the probability of pupping at a non-natal site increased with population size of, and declined with distance from, the destination site. Natal philopatry of < 1 would increase gene flow, improve population resilience, and promote population recovery after decline in a heterogeneous environment. Very high breeding philopatry suggests that familiarity with neighboring females and knowledge of the breeding site (the topography of pupping sites and nearby foraging locations) may be a critical component to reproductive strategies of sea lions.

Organochlorine contaminant concentrations in multiple tissues of free-ranging Steller sea lions (Eumetopias jubatus) in Alaska.

The relationships of selected organochlorine (OC) contaminants between blubber, blood, feces, and milk of young, free-ranging Steller sea lions (Eumetopias jubatus) were examined. Both between and within each tissue there was considerable individual variation. In spite of the variation, similar patterns were observed across the tissues for most of the selected PCB congeners. In all four tissues, the major PCB congeners were PCB101, PCB118, PCB138, and PCB153. The most prominent congener, both as a weight (ng/g lipid) and as a percentage of summed PCBs (∑PCBs), was PCB 153. Comparisons between paired tissues showed that ∑DDTs in blubber samples were related to concentrations in blood, feces, and milk. The ∑PCBs in blubber were related to concentrations in milk and fecal samples, though the relationship with feces was weak. Our findings show milk samples, in particular, are useful for assessing OCs in young sea lions. Blubber concentrations of PCB101, PCB118, and PCB138 were an order of magnitude higher than those in milk, supporting the biomagnification of these PCB congeners in SSL tissues. The findings indicate alternative tissues may be used as indicators of relative contaminant exposure in lieu of surgical blubber biopsy.

Correction: Natal and breeding philopatry of female Steller sea lions in southeastern Alaska

[This corrects the article DOI: 10.1371/journal.pone.0176840.].