DISPERSAL, ROOKERY FIDELITY, AND METAPOPULATION STRUCTURE OF STELLER SEA LIONS (EUMETOPIAS JUBATUS) IN AN INCREASING AND A DECREASING POPULATION IN ALASKA

Over the past 24 yr, 8,596 Steller sea lion ( Eumetopias jubatus ) pups were branded on their natal rookeries throughout Alaska with the objectives of determining survival rates, recruitment, movements, and site fidelity. Our objectives here were to examine the extent of dispersal of Steller sea lions away from their natal rookeries, movements between stocks, and degree of natal rookery fidelity. Pups (<1 yr old) usually remained within 500 km of their natal rookery. Branded juveniles dispersed widely and were resighted at distances up to 1,785 km from their natal rookeries. Adults generally remained within 500 km of their natal rookeries. No interchange of breeding animals between the ES (eastern stock) and WS (western stock) was observed. Although natal rookery fidelity was prevalent, 33% of the 12 observations of females branded in the WS during 1987–1988 and 19% of the 29 observations of females branded in the ES during 1994–1995 were observed with newly born pups at sites other than their natal rookeries. Steller sea lions generally conformed to the metapopulation concept as depicted by Hanski and Simberloff (1997), with local breeding populations (rookeries) and movements among these local populations having the potential of affecting local dynamics.     

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.     

No Evidence of Metabolic Depression in Western Alaskan Juvenile Steller Sea Lions (Eumetopias jubatus)

Steller sea lion (Eumetopias jubatus) populations have undergone precipitous declines through their western Alaskan range over the last four decades with the leading hypothesis to explain this decline centering around changing prey quality, quantity, or availability for this species (i.e., nutritional stress hypothesis). Under chronic conditions of reduced food intake sea lions would conserve energy by limiting energy expenditures through lowering of metabolic rate known as metabolic depression. To examine the potential for nutritional stress, resting metabolic rate (RMR) and body composition were measured in free-ranging juvenile Steller sea lions (N = 91) at three distinct geographical locations (Southeast Alaska, Prince William Sound, Central Aleutian Islands) using open-flow respirometry and deuterium isotope dilution, respectively. Average sea lion RMR ranged from 6.7 to 36.2 MJ d⁻¹ and was influenced by body mass, total body lipid, and to a lesser extent, ambient air temperature and age. Sea lion pups captured in the Aleutian Islands (region of decline) had significantly greater body mass and total body lipid stores when compared to pups from Prince William Sound (region of decline) and Southeast Alaska (stable region). Along with evidence of robust body condition in Aleutian Island pups, no definitive differences were detected in RMR between sea lions sampled between eastern and western populations that could not be accounted for by higher percent total body lipid content, suggesting that that at the time of this study, Steller sea lions were not experiencing metabolic depression in the locations studied.     

Inter-Population Movements of Steller Sea Lions in Alaska with Implications for Population Separation

Genetic studies and differing population trends support the separation of Steller sea lions (Eumetopias jubatus) into a western distinct population segment (WDPS) and an eastern DPS (EDPS) with the dividing line between populations at 144° W. Despite little exchange for thousands of years, the gap between the breeding ranges narrowed during the past 15–30 years with the formation of new rookeries near the DPS boundary. We analyzed >22,000 sightings of 4,172 sea lions branded as pups in each DPS from 2000–2010 to estimate probabilities of a sea lion born in one DPS being seen within the range of the other DPS (either ‘West’ or ‘East’). Males from both populations regularly traveled across the DPS boundary; probabilities were highest at ages 2–5 and for males born in Prince William Sound and southern Southeast Alaska. The probability of WDPS females being in the East at age 5 was 0.067 but 0 for EDPS females which rarely traveled to the West. Prince William Sound-born females had high probabilities of being in the East during breeding and non-breeding seasons. We present strong evidence that WDPS females have permanently emigrated to the East, reproducing at two ‘mixing zone’ rookeries. We documented breeding bulls that traveled >6,500 km round trip from their natal rookery in southern Alaska to the northern Bering Sea and central Aleutian Islands and back within one year. WDPS animals began moving East in the 1990s, following steep population declines in the central Gulf of Alaska. Results of our study, and others documenting high survival and rapid population growth in northern Southeast Alaska suggest that conditions in this mixing zone region have been optimal for sea lions. It is unclear whether eastward movement across the DPS boundary is due to less-optimal conditions in the West or a reflection of favorable conditions in the East.     

The Effects of Birth Weight and Maternal Care on Survival of Juvenile Steller Sea Lions (Eumetopias jubatus)

Steller sea lions were listed as endangered following a collapse of the western distinct population beginning in the late 1970s. Low juvenile survival has been implicated as a factor in the decline. I conducted a multistate mark-recapture analysis to estimate juvenile survival in an area of the western population where sea lions are showing signs of recovery. Survival for males and females was 80% between 3 weeks and 1 year of age. Approximately 20% of juveniles continued to be nursed by their mothers between ages 1 and 2 and 10% between ages 2 and 3. Survival for juveniles that suckled beyond 1 year was 88.2% and 89.9% to ages 2 and 3, respectively. In contrast, survival for individuals weaned by age 1 was 40.6% for males and 64.2% for females between ages 1 and 2. Birth mass positively influenced survival for juveniles weaned at age 1 but had little effect on individuals continuing to suckle. Cumulative survival to age 4 was double that estimated during the population decline in this region. Evidence suggests that western Steller sea lions utilize a somewhat different maternal strategy than those in the eastern distinct population. Western adult females generally invest more in their pups during the first year but wean offspring by age 1 more often. This results in better survival to age 1, but greater mortality between ages 1 and 3 compared to the eastern population. Different maternal strategies may reflect density dependent pressures of populations at opposite levels of abundance.     

Alloparenting in Steller sea lions (<Emphasis Type="Italic">Eumetopias jubatus</Emphasis>): correlations with misdirected care and other observations

Alloparental care is rarely observed in Steller sea lions (Eumetopias jubatus) where maternal care is extended to a single pup for up to 1 year or more. However, we observed 28 allonursing events and one case of adoption at a small breeding rookery in the western Gulf of Alaska between the years 2001 and 2005. Multiparous and primiparous females were observed nursing nonfilial individuals with equal frequency, but primiparous females spent significantly more time nursing nonfilial individuals. Multiparous females allowed allonursing only while sleeping and unaware while most primiparous females were aware that they were allonursing. These results are consistent with the misdirected-care hypothesis suggesting that primiparous (presumably younger) females nurse nonfilial pups due to inexperience, whereas multiparous (presumably older) females are victims of milk stealing during times of inattentiveness. Nonfilial pups were aggressively tossed most often during the pupping season and only by multiparous females, while allonursing events occurred more frequently after the pupping season. Starveling pups were not cared for by any female, but two were attended by a single bull during separate autumn seasons.     

Effects of research disturbance on the behavior and abundance of Steller sea lions (Eumetopias jubatus) at two rookeries in Alaska

We examined the effects of research disturbance on the behavior and abundance of Steller sea lions (Eumetopias jubatus) at rookeries on Marmot and Ugamak Islands in Alaska. During 3 of 6 yr, researchers intentionally drove all adult and juvenile sea lions off at least part of the beach in order to permanently mark and measure sea lion pups. The research disturbance occurred after the majority of females had bred and when most pups were 1 mo old. We used generalized linear models to determine the relationship between research disturbance and sea lion behavior or abundance. Research disturbance was related to changes in the proportion of sea lions exhibiting two to three of nine behavior metrics: agonistic and resting females and active males at Marmot, and active and resting males and females at Ugamak. Model results indicated that changes lasted between 3 and 20 d depending on the sex, behavior, and rookery. Inclusion of research disturbance into Marmot abundance models did not improve the fit to the data, if variability between years was permitted. Optimally timed, low‐frequency research disturbance did not appear to have long‐term effects on sea lion behavior or abundance and was largely associated with changes that were similar to natural variation.     

STELLER SEA LION STATUS AND TREND IN SOUTHEAST ALASKA: 1979–1997

Steller sea lion (Eumetopias jubatus) numbers in the United States declined by about 75% over the past 20+ yr. They are classified, under the U. S. Endangered Species Act, as “threatened” in the eastern portion of their range and as “endangered” in the western portion. We analyzed trends in numbers of pup and non-pup Steller sea lions counted in Southeast Alaska between 1979 and 1997. Sea lion numbers, based on counts of pups on rookeries, increased by an average of 5.9% per year between 1979 and 1997. However, numbers of pups increased at a much slower rate (+ 1.7% per year) between 1989 and 1997. For counts of non-pup Steller sea lions we used models that controlled for the effects of date, time, and tide at the time of the survey to analyze trends. This technique reduced bias and increased precision of the resulting trend estimates. Numbers of sea lions were stable (+0.5%) between 1989 and 1996, based on counts of non-pups. We estimated the Southeast Alaska breeding population of Steller sea lions at about 19,000 animals of all ages in 1997, a level that is probably near the highest in recorded history.     

Neonatal mortality in New Zealand sea lions (Phocarctos hookeri) at Sandy Bay, Enderby Island, Auckland Islands from 1998 to 2005

As part of a health survey of New Zealand sea lions (Phocarctos hookeri) on Enderby Island, Auckland Islands (50 degrees 30'S, 166 degrees 17'E), neonatal mortality was closely monitored at the Sandy Bay colony for seven consecutive years. Throughout the breeding seasons 1998-99 to 2004-05, more than 400 postmortem examinations were performed on pups found dead at this site. The primary causes of death were categorized as trauma (35%), bacterial infections (24%), hookworm infection (13%), starvation (13%), and stillbirth (4%). For most pups, more than one diagnosis was recorded. Every year, two distinct peaks of trauma were observed: the first associated with mature bulls fighting within the harem and the second with subadult males abducting pups. In 2001-02 and 2002-03, epidemics caused by Klebsiella pneumoniae increased mortality by three times the mean in nonepidemic years (10.2%). The increased mortality was attributed directly to acute suppurative infection due to the bacterium and also to an increase in traumatic deaths of debilitated pups. Parasitic infection with the hookworm Uncinaria spp. was a common finding in all pups older than three weeks of age and debilitation by the parasite may have contributed to increased susceptibility to other pathogens such as Klebsiella sp. or Salmonella sp. This study provides valuable quantitative data on the natural causes of neonatal mortality in New Zealand sea lions that can be used in demographic models for management of threatened species.     

Age Specific Survival Rates of Steller Sea Lions at Rookeries with Divergent Population Trends in the Russian Far East

After a dramatic population decline, Steller sea lions have begun to recover throughout most of their range. However, Steller sea lions in the Western Aleutians and Commander Islands are continuing to decline. Comparing survival rates between regions with different population trends may provide insights into the factors driving the dynamics, but published data on vital rates have been extremely scarce, especially in regions where the populations are still declining. Fortunately, an unprecedented dataset of marked Steller sea lions at rookeries in the Russian Far East is available, allowing us to determine age and sex specific survival in sea lions up to 22 years old. We focused on survival rates in three areas in the Russian range with differing population trends: the Commander Islands (Medny Island rookery), Eastern Kamchatka (Kozlov Cape rookery) and the Kuril Islands (four rookeries). Survival rates differed between these three regions, though not necessarily as predicted by population trends. Pup survival was higher where the populations were declining (Medny Island) or not recovering (Kozlov Cape) than in all Kuril Island rookeries. The lowest adult (> 3 years old) female survival was found on Medny Island and this may be responsible for the continued population decline there. However, the highest adult survival was found at Kozlov Cape, not in the Kuril Islands where the population is increasing, so we suggest that differences in birth rates might be an important driver of these divergent population trends. High pup survival on the Commander Islands and Kamchatka Coast may be a consequence of less frequent (e.g. biennial) reproduction there, which may permit females that skip birth years to invest more in their offspring, leading to higher pup survival, but this hypothesis awaits measurement of birth rates in these areas.     

Health status of young Alaska Steller sea lion pups (Eumetopias jubatus) as indicated by blood chemistry and hematology

Blood chemistry and hematology were examined in 238 Steller sea lion pups (Eumetopias jubatus) to assess the health status of pups <1 month of age. Failure of juvenile recruitment (possibly due to nutritionally or physiologically compromised pups) into breeding populations has been proposed as a cause of recent declines of this endangered species in Alaska. To identify potential correlations with areas of high population decline, blood chemistry data were considered for three areas: eastern Aleutian Islands (low rates of population decline to stable populations), Gulf of Alaska (high rates of decline), and Southeast Alaska (stable to increasing population). Southeast Alaska pups showed elevated ketone body concentrations (beta-hydroxybutyrate,(beta-HBA)) and depressed glucose levels than pups in the Gulf of Alaska. Over 40% of the pups from Southeast Alaska had elevated beta-HBA concentrations suggesting they underwent longer periods of fasting than seen in pups from other areas. Hematocrit (Hct), hemoglobin concentration (Hb) and water content of the blood exhibited typical mammalian relationships. In summary, blood chemistry and hematology data showed no indication that Steller sea lion pups <1 month old from areas of population decline were nutritionally compromised.     

DEVELOPMENT OF DISPERSAL, MOVEMENT PATTERNS, AND HAUL-OUT USE BY PUP AND JUVENILE STELLER SEA LIONS (EUMETOPIAS JUBATUS) IN ALASKA

Population declines of Steller sea lions ( Eumetopias juhatus ) in western Alaska (west of 144°W) may be a result of reduced juvenile survival. We used satellite telemetry to study the at-sea distribution and movement patterns of pup (1.6–11.9 mo) and juvenile (12.0–35.1 mo) Steller sea lions. We studied trip distance, duration, and interhaul-out movements of sea lions in relation to age, sex, and month of year in the decreasing western population (WP; Prince William Sound, Kodiak, Aleutian Islands, Alaska) and the increasing eastern population (EP; Southeast Alaska). We deployed 103 satellite transmitters (29 WP; 74 EP) on sea lions between 1998 and 2001. Round trip distance and duration increased with age, trip distance was greater in the WP than the EP, trip duration was greater for females than males, and haul-out use was clustered. Changes in round trip distance and duration occurred from April to June for all age classes studied indicating that the annual timing of weaning may be less variable than the age of weaning. Overall, 90% of round trips were ≤ 15 km from haul-outs and 84% were <20 h, indicating nearshore areas adjacent to haulouts are critical to the developing juvenile.     

Adult Steller sea lion mortality on rookeries in the Russian Far East, 2002–2010

We used visual observations during nine field seasons to determine the causes and death rate of Steller sea lions older than 1 year on eight rookeries in the Russian Far East. The average annual death rate was 0.48% of the total recorded Steller sea lions on shore and varied among rookeriesy. The mortality did not exceed 0.29% in six rookeries, but reached 0.80–1.19% in two rookeries. Individuals of all age and sex groups were recorded among dead animals. Bulls died as a result of territorial conflicts, and cows and young lions were crushed or suffocated by bulls during copulation. The death of nearly half of the females was attributed to 11 bulls.     

Health status of young Alaska Steller sea lion pups (Eumetopias jubatus) as indicated by blood chemistry and hematology

Blood chemistry and hematology were examined in 238 Steller sea lion pups (Eumetopias jubatus) to assess the health status of pups <1 month of age. Failure of juvenile recruitment (possibly due to nutritionally or physiologically compromised pups) into breeding populations has been proposed as a cause of recent declines of this endangered species in Alaska. To identify potential correlations with areas of high population decline, blood chemistry data were considered for three areas: eastern Aleutian Islands (low rates of population decline to stable populations), Gulf of Alaska (high rates of decline), and Southeast Alaska (stable to increasing population). Southeast Alaska pups showed elevated ketone body concentrations (β-hydroxybutyrate, (β-HBA)) and depressed glucose levels when compared with animals from the Aleutian Islands and lower blood urea nitrogen (BUN) and glucose levels than pups in the Gulf of Alaska. Over 40% of the pups from Southeast Alaska had elevated β-HBA concentrations suggesting they underwent longer periods of fasting than seen in pups from other areas. Hematocrit (Hct), hemoglobin concentration (Hb) and water content of the blood exhibited typical mammalian relationships. In summary, blood chemistry and hematology data showed no indication that Steller sea lion pups <1 month old from areas of population decline were nutritionally compromised.     

A bald encounter: hairless southern sea lion at the Falkland Islands

A hairless adult male southern sea lion (Otaria flavescens) was sighted at Sea Lion Island, Falkland Islands, on the 14th of August 2009. The sea lion was observed on several further occasions and was defending a small harem consisting of four females. To our knowledge, this is the first report of an apparently healthy sea lion being entirely hairless with the exception of vibrissae on the muzzle.     

Population growth and colonization of Steller sea lions in the Glacier Bay region of southeastern Alaska: 1970s–2009

We estimated trends in numbers of Steller sea lions in the Glacier Bay region of the eastern population from the 1970s to 2009. We documented the colonization of several new haul‐outs and the transition of one haul‐out (Graves Rocks) to a rookery, assessed seasonal patterns in distribution, and compared counts from different observation platforms. Sea lions increased in the region by 8.2%/yr (95%CI = 6.4%–10.0%), with the most growth at South Marble Island in Glacier Bay (16.6%/yr, 1991–2009) and rapid growth in Cross Sound. Seasonal patterns in the distribution of sea lions were likely influenced by new breeding opportunities and the seasonal availability of prey. Factors that likely contributed to the exceptional growth include availability of new habitat following deglaciation, immigration, redistribution, decreases in mortality, and ecosystem‐level changes. The rapid increase in sea lion numbers in this region is of particular interest in light of dramatic declines in the western population and evidence that Steller sea lions from both the eastern and western populations colonized the Graves Rocks rookery. The colonization and rookery development in this dynamic area may signal the reversal of the reproductive isolation of the two populations.     

Short‐term survival of Steller sea lion (Eumetopias jubatus) pups: Investigating the effect of health status on survival

We estimated survival probabilities for Steller sea lion (Eumetopias jubatus) pups from 3 wk to 6 wk old and from 6 wk to 1 yr at three rookeries in southeastern Alaska. We also investigated the effect of mass, body condition, health variables, and the genetic origin on 3–6 wk survival. Survival differed substantially among rookeries and between sexes, with survival lowest at Hazy Islands, intermediate at White Sisters, and highest at Graves Rocks and survival lower for males than females. Body mass, body condition, and hematocrit were positively related to survival and blood %H₂O and haptoglobin level (for females; no relationship for males) were negatively related to survival. Taking predictor variables collectively, sea lion pups at Hazy Islands, which had the lowest survival probability, had the lowest mass, hematocrit, and hemoglobin, and had high levels of blood %H₂O, and hookworm infection. Values from Graves Rocks, which had the highest survival, were the opposite of those from Hazy Island (e.g., high mass, body condition, hematocrit, and hemoglobin), while those from White Sisters (intermediate survival) had varying means (e.g., high hematocrit and hemoglobin and low hookworms, but also low body condition); these patterns suggest that physiological factors potentially underlie rookery differences in survival.     

Hookworm enteritis with bacteremia in California sea lion pups on San Miguel Island

Large breeding populations of California sea lions (Zalophus californianus) are located on San Miguel and San Nicolas Islands in the Southern California Bight. In 2001, there was a substantial increase in pup mortality in late summer and fall. From June 2002 to January 2003, 208 freshly dead pups were examined on San Miguel Island, the most western of the Channel Islands off the coast of southern California. Tissues from 186 of these pups were examined histologically. The primary lesions in 133 (72%) of the pups were an enteritis associated with hookworms and infections in major organs. Emaciation/starvation in 43 pups (26%) was the second most important cause of death.     

BEHAVIORAL AND PHYSIOLOGICAL MEASUREMENTS OF MATERNAL INVESTMENT IN THE STELLER SEA LION, EUMETOPIAS JUBATUS

The onshore and at-sea cycles of females, suckling behavior of pups and their milk intake were studied in Steller sea lions ( Eumetopias jubatus ) during 1983 at Año Nuevo Island, California. Females averaged approximately 21 h ashore and 36 h at sea. The trips to sea lengthened as pups aged, resulting in an overall decline in female time ashore to 30% by the sixth week following parturition. Activity budgets of pups showed no significant differences among suckling time, age and sex. Milk intake, estimated using labeled water studies, revealed that heavier pups consumed more milk than lighter ones (milk ingestion in ml/d = 4.26 + 0.0687 [Pup Mass in kg]). Mean milk intake was 1.78 ± 0.33 liters/d. Mean pup growth rate was 0.38 ± 0.1 kg/d. The results suggest that female attendance patterns are shaped by the increasing nutritional demands of growing pups and their increasing efficiency at suckling.     

Population structure and social organization of Southern Elephant Seals, Mirounga leonina (L.)

The population structure and social organization of the Southern Elephant Seal, Mirounga leonina , were studied at South Georgia principally by extensive field census work and determination of age and reproductive history from sections of teeth taken from samples of bulls and cows.
The adult males of the South Georgia population were exploited from 1910 to 1964, mainly at the maximum sustainable yield for this population.
The present data are compared with similar information obtained from studies at South Georgia in 1951 during the exploitation phase and at Macquarie Island in the 1950's where sealing ended in 1919 and the population had stabilized.
Changes have been noted in the time of bull haul out, number of bulls ashore, cow: bull ratio, harem size and the age of harem bulls. These changes can all be attributed to the ending of exploitation. In contrast, the structure of the cow herd has not changed appreciably in the same period.
In addition, differences in growth, body size and population structure still persist between the South Georgia and Macquarie Island populations and it is likely that most of them may reflect differences in food availability at the two locations.