Mathematical modeling of the variation in the survival of female northern fur seals, <Emphasis Type="Italic">Callorhinus ursinus</Emphasis> (Linnaeus, 1758), on Tyuleniy Island

The dynamics of the survival and number of female northern fur seals, Callorhinus ursinus, on Tyuleniy Island have been studied. The data on the age structure and physiological condition of females (obtained during observations in 1958–1988) were used to estimate the model parameters. The adequacy of the model estimates of female number was evaluated using the data on the number of newborn pups at the rookery in 1958–2013. It has been found that a reduction in the survival rate of individuals of younger age groups, a decrease in the proportion of females, as well as aging of the population occurred in the 1958–1988 period. The use of numerical simulation methods shows that the rate of survival of females among individuals under 3 years of age increased substantially after 1988, indicating a positive trend in the dynamics of their number.     

First-year survival of southern elephant seals,Mirounga leonina,at sub-Antarctic Macquarie Island

Juvenile seals branded on the isthmus of Macquarie Island as pups displayed a high degree of philopatry. They returned more often and in greater densities to the northern third of the island within 10 km of their birth sites. Juvenile seals were observed to haul out more frequently and in greater numbers on the east coast as opposed to the west. Juvenile seals typically hauled out on two occasions, once during the winter, and once to moult. The probability of recapturing (resighting) branded and tagged seals was greater during the mid-year haulout. First-year survival estimates were obtained from searches of all Macquarie Island beaches for marked (branded and tagged) seals. From a branded population of 2000 seals, 897 were known to be alive at age 1 year, and minimum first-year survival was calculated at 44.85%. To this minimum estimate was added the number of seals overlooked during systematic and standardised searches of the island, and a revised estimate of 65.60% was calculated. Survival rates calculated using a custom model and a conventional mark-recapture model (MARK) were compared and no differences detected. Actual survival data and probability of sighting estimates were included in the revised estimate of first-year survival of southern elephant seals at Macquarie Island. There were no differences in the number of surviving males and females. Accepted: 25 October 1998     

Vagrant Subantarctic fur seal at Cape Shirreff,Livingston Island,Antarctica

A vagrant adult male Subantarctic fur seal Arctocephalus tropicalis was observed among Antarctic fur seals A. gazella at Cape Shirreff, Livingston Island, Antarctica, which is located to ~4,190 and ~5,939 km from the nearest breeding colonies of Subantarctic fur seals. Although the colony of origin of this animal and the reason for its movement outside its distribution range are unknown, this sighting shows the high dispersal capacity of this species and provides an insight into possible changes in its distribution. Although this vagrant was not observed with females Antarctic fur seal, news sightings in the future could result in viable hybrid, and introgressive hybridization could represent a threat for Cape Shirreff population recovery, if still the population way to go to recover to presailing levels.     

SURVIVAL RATES FOR THE HAWAIIAN MONK SEAL (MONACHUS SCHAUINSLANDI)

Abstract: Endangered Hawaiian monk seal ( Monachs schauinslandi ) pups at all the major breeding islands in the Northwestern Hawaiian Islands have been tagged since the early 1980s. Pups were double flipper tagged as soon as possible post-weaning. With few exceptions, an extensive tag resighting effort was conducted annually at the same islands. These resighting data were used to estimate seal survival rates from the time of tagging to age one at all locations using the ratio of seals alive in the second year to number of pups tagged. These survival rates among the islands, from weaning to age one, averaged over the years of the study, ranged from 0.80 to 0.90. For young seals over age one, capture-recapture methods were used to calculate survival pooled through several years, and these rates ranged from 0.85 to 0.98. At French Frigate Shoals and Laysan Island, the higher numbers of tagged pups allowed separate estimates of male and female survival to be calculated. These rates suggested that survival of immature females was better than males. Beginning in 1989, survival of immature seals at French Frigate Shoals declined sharply.     

Survivorship of a declining population of southern elephant seals, Mirounga leonina, in relation to age, sex and cohort

This study quantified both the age- and sex-specific survival rates of juveniles and adults, and tested for interannual differences in age-specific survival rates of the southern elephant seal population at Marion Island. Pups were tagged on an annual basis from 1983 onwards at Marion Island, and a consistent recapture program yielded data that was analysed using the software package MARK to obtain maximum-likelihood estimates of survival and capture probability. On average, 1st-year survival was 0.58 and 0.62, and survival rate averaged over the first 3 years of life, 0.69 and 0.74 for males and females, respectively. From years 4 to 9, the average survival rate was 0.66 and 0.75 for males and females, respectively. Survival estimates for elephant seals in their 10th–13th year are also presented, although these are based on very small sample sizes. Averages of age-specific survival estimates from the earlier (mostly 1983–1987 cohorts) and later (mostly 1988–1992 cohorts) periods were compared and considerable reductions were observed in 4th- and 5th-year male survival, and 4th-year female survival. The comparatively low adult survival is suggested as the proximate cause, and food limitation as deduced from the decline in survival of elephant seals with comparatively high energetic demands as the ultimate cause behind the population decline at Marion Island. Although not tied in with the decline of the population, 1987, 1990 and 1993 were identified as high-mortality years. Received: 14 December 1998 / Accepted: 14 June 1999     

Prey selection of subadult male northern fur seals (Callorhinus ursinus) and evidence of dietary niche overlap with adult females during the breeding season

During the breeding season northern fur seals (Callorhinus ursinus) congregate on the Pribilof Islands in large numbers creating the potential for intraspecific competition. Due to the declining trend in the Pribilof Islands population of fur seals, it is important to understand how prey resources are partitioned among the population. Fur seals exhibit a high degree of sexual dimorphism resulting in energetic differences among age and sex classes. Therefore, we hypothesized that subadult male and adult female fur seals would differ in the type and size of prey consumed. We examined the diets of subadult male (age 2–8; mean mass 28–176 kg) and adult female (age ≥ 3 yr; mean mass 13–50 kg) seals on St. Paul Island from 1992 to 2000. Prey remains found in fecal samples were compared using niche overlap indices. There was nearly complete dietary niche overlap between subadult male and adult female fur seals. Walleye pollock (Theragra chalcogramma), Pacific salmon (Oncorhynchus spp.), Pacific herring (Clupeia pallasi), and cephalopods were common prey items found in the diets of both groups. We found differences in the size of pollock consumed and that geographic location of sample collection may be important in determining diet differences. Our results indicate high levels of dietary overlap among subadult male and adult female fur seals.     

The diet of Antarctic fur seals,Arctocephalus gazella,during the summer-autumn period at Mossman Peninsula,Laurie Island (South Orkneys)

Summary From mid January to April 1988 a total of 105 faecal samples of non breeding male fur seals, Arctocephalus gazella, was collected at Mossman Peninsula, Laurie Island. Examination of scats containing prey remains showed that fur seals fed mainly on krill, occurring in 100% of samples but fish were also a common food item (78.8%). Myctophids constituted more than 90% of fish taken by fur seals. Squid beaks occurred in 34.3% of scats, being more common in the autumn period.     

Population status and breeding season chronology of Heard Island fur seals

Fur seals were eliminated by sealers at Heard Island soon after its discovery in the 1850s. The first recorded breeding of Antarctic fur seals (Arctocephalus gazella) since sealing was reported in early 1963 (two pups). The most recent survey of the Heard Island fur-seal population was undertaken between November 2000 and March 2001, when 1,012 Antarctic fur-seal pups were born. This represents a fourfold increase since the last complete census in 1987/1988 (13 years), when 248 births were recorded. Pup estimates and counts available for eight breeding seasons since 1962/1963 suggest the population has been increasing at between 12 and 20% per year. Based on pup production, the breeding population is estimated to number approximately 4,100 seals. The number of fur seals on Heard Island peaked in late February/early March at 29,256 indicating that, in addition to the breeding population, a significant number of seals born elsewhere haul out on the island. Most of these are moulting sub-adult and adult males. As in 1987/1988, only one subantarctic fur-seal pup (A. tropicalis) was observed, suggesting this species is not colonising the island, as has been speculated.     

Fur seals at Macquarie Island: post-sealing colonisation,trends in abundance and hybridisation of three species

Commercial sealers exterminated the original fur seal population at Macquarie Island in the early 1800s. The first breeding record since the sealing era was not reported until March 1955. Three species of fur seal now occur at Macquarie Island, the Antarctic (Arctocephalus gazella), subantarctic (A. tropicalis) and New Zealand (A. forsteri) fur seal. Census data from 54 breeding seasons in the period 1954–2007 were used to estimate population status and growth for each species. Between the 1950s and 1970s, annual increases in pup production for the species aggregate were low. Between 1986 and 2007, pup production of Antarctic fur seals increased by about 8.8% per year and subantarctic fur seals by 6.8% per year. The New Zealand fur seal, although the most numerous fur seal species on Macquarie Island, has yet to establish a breeding population, due to the absence of reproductively mature females. Hybridisation among species is significant, but appears to be declining. The slow establishment and growth of fur seal populations on Macquarie Island appears to have been affected by its distance from major population centres and hence low immigration rates, asynchronous colonisation times of males and females of each species, and extensive hybridisation.     

TOOTH WEIGHTS OF JUVENILE MALE NORTHERN FUR SEALS, CALLORHINUS URSINUS

Tooth weight and body length of juvenile male northern fur seals, Callorhinus ursinus , collected on St. Paul Island, Alaska, from 1948 to 1984 were compared. The relationship between these variables was investigated for individual and combined age classes. A density-dependent increase in mean tooth weight occurred during a decline in fur seal abundance. Consistent, though poorly understood, differences in tooth weight were found among males associated with different rookeries (breeding grounds). Storing the teeth for long periods may affect the weights, but such effects, if any, are too small to account for the changes observed.     

Antarctic fur seal predation on cephalopods at Marion Island

We report two observations of adult male Antarctic fur seals, Arctocephalus gazella, preying on large octopods at subAntarctic Marion Island during July and August 2008. If Antarctic fur seals take cephalopods opportunistically, as previously suggested, our observations may be a rare event representing such opportunistic predation.     

DENSITY DEPENDENCE IN NORTHERN FUR SEALS (CALLORHINUS URSINUS)

This paper summarizes, updates, and interprets information on density-dependent dynamics of populations of the northern fur seal ( Callorhinus ursinus ). Density-dependent changes observed in these populations have involved various aspects of growth (body length, body weight, tooth weight, and size of other skeletal parts, especially the skull), survival, age at maturation, incidence of disease, and time spent foraging. For the population of northern fur seals on St. Paul Island of the Pribilof Islands, which was observed during a major increase and during two significant declines, density-dependent changes that occurred during the growth of the population were reversed during the declines. The Robben Island population in the western Pacific declined after 1965, and the decline was accompanied by changes similar to those observed during the declines on the Pribilof Islands. Although data are not available for all age and sex classes, it appears that most or all components of the populations exhibit similar changes. The overall implication of these changes is that current populations on Robben Island and the Pribilof Islands are reduced to levels below what could be supported by the resources available in their environments. Density dependence for this species is consistent with that of other large mammals, specifically in that vital rates for fur seals ate related to density in a nonlinear fashion.     

Vagrant Antarctic pinnipeds at Gough Island

Opportunistic sightings of Antarctic fur seals Arctocephalus gazella and a leopard seal Hydrurga leptonyx at Gough Island (40°20′S, 09°54′W) in the South Atlantic Ocean represent the northernmost island records for vagrant Antarctic fur seals, and only the second for a vagrant leopard seal at Gough Island. Some ten different individual Antarctic fur seals were sighted on a single day, up to seven on a single beach. An overall total of 18 individuals were recorded over a 7-week period in October/November 2005, before the onset of the breeding (pupping) season of the resident population of Subantarctic fur seals Arctocephalus tropicalis. Most were immature, male and mostly in good condition (n = 11, 61%); one mature male and six putative females were also present. All had departed after 23 November, although only a fraction of the available beaches was searched.     

Characterization of Australian fur seal vocalizations during the breeding season

The vocal repertoire, structure, and behavioral context of airborne vocalizations produced by Australian fur seals (Arctocephalus pusillus doriferus) are described using recordings made at a breeding colony on Kanowna Island, Bass Strait, Australia. The study identified six different call types: three produced by males (bark, guttural threat, and submissive call); five produced by females (bark, guttural threat, submissive call, growl, and pup attraction call) and the female attraction call produced by pups and yearlings. Vocalizations were compared according to age and sex classes. The overall structure and function of the pup attraction and female attraction call produced by females, yearlings, and pups, was similar. However, while similar in their overall appearance, certain call types have a lower fundamental frequency when compared with other fur seals. In addition, the male bark call alters in rate of production according to the context used, where calls are slower when males are stationary and advertising their territorial status and faster when males are involved in confrontations with other males or actively herding females. Further research is required to investigate changes in environmental conditions and their effects on shaping the call structure and communication in Australian fur seals.     

Vagrant Antarctic fur seals at Gough Island in 2009

The Antarctic fur seal Arctocephalus gazella at Gough Island (40°20′S, 09°54′W) in the South Atlantic Ocean, first seen in October/November 2005, was recorded again in September–October 2009. Up to three different individual Antarctic fur seals were sighted on a single day, on a particular beach. A total of seven different individuals were recorded over a 3-week period, well before the onset of the breeding (pupping) season of the resident population of Subantarctic fur seals A. tropicalis. Positively identified individuals were all male, mostly subadult and lean. Only a fraction (~20%) of the available beaches was searched, and it is unknown if the Antarctic fur seals were still present at Gough Island during the austral summer breeding season of southern fur seals.     

Foraging a new trail with northern fur seals (Callorhinus ursinus): Lactating seals from islands with contrasting population dynamics have different foraging strategies,and forage at scales previously unrecognized by GPS interpolated dive data

We reconstructed the foraging tracks of lactating northern fur seals (Callorhinus ursinus) from two eastern Bering Sea islands (St. Paul Island and Bogoslof Island) using linear interpolation between GPS locations recorded at a maximum of four times per hour and compared it to tri‐axial accelerometer and magnetometer data collected at 16 Hz to reconstruct pseudotracks between the GPS fixes. The high‐resolution data revealed distances swum per foraging trip were much greater than the distances calculated using linearly interpolated GPS tracks (1.5 times further for St. Paul fur seals and 1.9 times further for Bogoslof fur seals). First passage time metrics calculated from the high resolution data revealed that the optimal scale at which the seals searched for prey was 500 m (radius of circle searched) for fur seals from St. Paul Island that went off‐shelf, and 50 m for fur seals from Bogoslof Island and surprisingly, 50 m for fur seals from St. Paul that foraged on‐shelf. These area‐restricted search scales were significantly smaller than those calculated from GPS data alone (12 km for St. Paul and 6 km for Bogoslof) indicating that higher resolution movement data can reveal novel information about foraging behaviors that have important ecological implications.     

MAJOR DECLINE IN NUMBER OF HARBOR SEALS, PHOCA VITULINA RICHARDSI, ON TUGIDAK ISLAND, GULF OF ALASKA

Tugidak Island, located in the Gulf of Alaska, was once the site of one of largest local concentrations of harbor seals ( Phoca vitulina richardsi ) in the world. This population, which probably consisted of about 20,500 animals in the mid-1960s declined by about 85% between 1976 and 1988. The population appeared to decline more rapidly during the late 1970s than during the 1980s. Causes for the decline are not apparent. There appear to be both similarities and dissimilarities between this decline and recent declines in abundance of northern fur seals ( Callorhinus ursinus ) and Steller sea lions ( Eumetopias jubatus ) in the Bering Sea and Gulf of Alaska.     

New records of South American sea lion <Emphasis Type="Italic">Otaria flavescens</Emphasis> predation on southern rockhopper penguins <Emphasis Type="Italic">Eudyptes chrysocome</Emphasis> at Staten Island,Argentina

Predation by fur seals and sea lions has been identified, among others, as a potential cause of the declines in rockhopper penguin populations. Here, we report a multiple predation event of southern rockhopper penguins Eudyptes chrysocome by South American sub-adult male sea lions Otaria flavescens at Staten Island, Argentina. The sea lions attacked and preyed on penguins mostly using a wait and rush tactic at sea, but in some cases, penguins were also pursued on land. Although observations suggested that only a few sea lions are involved in predation, further research is necessary to elucidate the importance of this predation in the rate of population decline.     

Seasonal diving behaviour in lactating subantarctic fur seals on Amsterdam Island

Diving behaviour was investigated in female subantarctic fur seals (Arctocephalus tropicalis) breeding on Amsterdam Island, Indian Ocean. Data were collected using electronic Time Depth Recorders on 19 seals during their first foraging trip after parturition in December, foraging trips later in summer, and during winter. Subantarctic fur seals at Amsterdam Island are nocturnal, shallow divers. Ninety-nine percent of recorded dives occurred at night. The diel dive pattern and changes in dive parameters throughout the night suggest that fur seals follow the nycthemeral migrations of their main prey. Seasonal changes in diving behaviour amounted to the fur seals performing progressively deeper and longer dives from their first foraging trip through winter. Dive depth and dive duration increased from the first trip after parturition (16.6 ± 0.5 m and 62.1 ± 1.6 s respectively, n=1000) to summer (19.0 ± 0.4 m and 65 ± 1 s, respectively, n=2000) through winter (29.0 ± 1.0 m and 91.2 ± 2.2 s, respectively, n=800). In summer, subantarctic fur seals increased the proportion of time spent at the bottom during dives of between 10 and 20 m, apparently searching for prey when descending to these depths, which corresponded to the oceanic mixed layer. In winter, fur seals behaved similarly when diving between 20 and 50 m, suggesting that the most profitable depths for feeding moved down during the study period. Most of the dives did not exceed the physiological limits of individuals. Although dive frequency did not vary (10 dives/h of night), the vertical travel distance and the time spent diving increased throughout the study period, while the post-dive interval decreased, indicating that subantarctic fur seals showed a greater diving effort in winter, compared to earlier seasons. Accepted: 1 August 1999     

ESTIMATION OF AGE-SPECIFIC PROBABILITIES OF FIRST RETURN AND ANNUAL SURVIVAL RATES FOR THE MALE GRAY SEAL (HALICHOERUS GRYPUS) ON SABLE ISLAND FROM CAPTURE-RECAPTURE DATA

We used a longitudinal capture-recapture study to estimate the age-specific probabilities of first return to the breeding colony and annual survival rates for male gray seals ( Halichoerus grypus ), based on resightings of seals branded as young on Sable Island. We estimated that the average age of first returns for seals born in 1969–1970 to be 9.1 (SE 0.4) yr; for seals born in 1973–1974 it is estimated to be 9.8 (SE 0.2) yr. The estimated annual survival rate of these males was estimated to be 0.976 (SE 0.003).