Pup mortality in southern elephant seals at Marion Island

Pre- and early post-weaning pup mortality of southern elephant seals (Mirounga leonina) at Marion Island from 1990 through 1999 ranged from 1.6% to 7.3% and averaged 3.8%. Mortality of pups after weaning before their first trip to sea accounted for only 12% of the total mortality. We found no relationship between population size and percentage pup mortality, indicating that pup survival is independent of seal density, at least at the densities of breeding seals that prevailed. Indeed, pup mortality was greatest in the smallest harems, apparently owing to a greater number of younger, less experienced mothers. Small harems were generally also found on less suitable beaches than larger harems and this could have contributed to pup injury as a cause of pup mortality on these beaches. Mother-pup separation and injury caused by beachmasters is likely to be responsible for pup mortality in the larger harems. The low rates of pup mortality observed in this study obviate it being a major population regulating agent at Marion Island.     

Leucistic southern elephant seal at Marion Island

We observed a light coloured female southern elephant seal juvenile (Mirounga leonina) twice at Marion Island in August 2008 and confirmed that it was leucistic rather than albinistic. Though there have been a few previous reports of light-coloured southern elephant seals, this is the first confirmed case of leucism in this species. Judged to be 1-year old, perhaps 2-years old at the most, and because we have not observed any leucistic pups at Marion Island during the past 2 years despite an extensive monitoring and tagging program, we think that this animal was born at nearby Prince Edward Island or perhaps further afield at Îles Crozet.     

Unmarked individuals in mark–recapture studies: Comparisons of marked and unmarked southern elephant seals at Marion Island

The presence of unmarked individuals is common in mark–recapture study populations; however, their origin and significance in terms of population dynamics remain poorly understood. At Marion Island, southern Indian Ocean, where virtually all southern elephant seal Mirounga leonina pups born annually (1983–2008) were marked in a long‐term mark–resight study, large numbers of unmarked seals occur. Unmarked seals originate either from marker (tag) loss or from immigration. We aimed to identify patterns in the occurrence of marked and unmarked individuals that will allude to the possible origin and significance of the untagged component of the population, predicting that tag loss will add untagged seals to mainly adult age categories whereas migrating untagged individuals will be mostly juveniles. We fitted a generalized linear model using the factors month, year and age‐class to explain the relative abundance of untagged seals (tag ratio) from 1997 to 2009. Site usage of untagged seals relative to tagged seals was assessed using a binomial test. Untagged seals, predominantly juveniles, were present in the highest proportions relative to tagged seals during the winter haulout (tagged seals/total seals less than 0.3) and the lowest proportion (approximately 0.5) during the female breeding haulout, increasing in relative abundance from 1997 to 2009. Untagged seals were distributed evenly across suitable haulout sites while tagged seals displayed high local site fidelity and occurred in greater numbers at or near large breeding beaches. Untagged seals are considered to be mostly migrant seals that disperse from other islands within the southern Indian Ocean and haul out at Marion Island during non‐breeding haulouts in particular. Some of these seals immigrate to the breeding population, which can be a key component of the local population dynamics. We emphasize the need for mark–recapture studies to evaluate the role of the unmarked component of a population, thereby inducing a more confident estimation of demographic parameters from the marked sample.     

Do southern elephant seals show density dependence in fecundity?

Here we provide an alternative interpretation to that of Pistorius et al. (2001), concerning density-dependent increases in fecundity resulting in population regulation of the southern elephant seal population at Marion Island. We do not contradict the findings of Pistorius et al. (2001), because it does appear: (1) that a change in fecundity has been observed, and (2) that some factor related to food supply is the most likely cause for an observed population decline and increase in reproductive performance. The main observation leading to the interpretation of density-dependent feedback in the population of southern elephant seals at Marion Island (one of the Prince Edward Islands) is that there has been a reduction in the population's rate of decline in recent years (reported by Pistorius et al. (1999b)), and that this could have resulted from a per capita increase in food availability. However, because rates of population change are rarely linearly constant, changes in population size should be expressed on a logarithmic, rather than a linear scale, as used by Pistorius et al. (1999b). Re-plotting the linear values of Pistorius et al. (1999b) on the natural logarithmic scale gave no clear change in the rate of population decline; therefore, we conclude that the rate of population change (decline) has remained constant from 1986 to 1997 (r=-0.0439). The Marion Island population is part of the larger Kerguelen population, and there might be considerable overlap in the foraging areas, and possibly prey, exploited by elephant seals from all sub-populations within this larger population. Changes in the number of intra-specific resource competitors at Marion Island are therefore unlikely to alter per capita food availability since the Marion population constitutes approximately 1% of the total Kerguelen population. We propose an alternative hypothesis that the present data support a mechanism driving the proposed increase in per capita food supply through changes in either: (1) inter-specific food competition, (2) rates of predation, (3) changes in weather pattern or (4) disease.     

Growth of female southern elephant seals Mirounga leonina at Macquarie Island

Body growth of 137 female southern elephant seals (Mirounga leonina) over 1 year of age was investigated at subantarctic Macquarie Island. An asymptotic straight line, snout–tail body length of 2.57±0.03 m was estimated to be attained at 9 years of age, using a three-parameter Gompertz equation. A significant increase of approximately 0.1 m (5%) in mean body length of females between 1 and 10 years of age was estimated to have occurred between the 1950–1960s and 1990s at Macquarie Island. This is consistent with a reduction in both the rate of population decline and the age of onset of sexual maturity. Age determination using dental cementum layers and the importance of standardised measurements in pinniped growth studies are discussed.     

Mass changes during their annual cycle in females of southern elephant seals at King George Island

Mass changes in female southern elephant seals, sampled sequentially at different points through their annual cycle, were measured at King George Island, South Shetland Islands, during the 1995/1996 and 1996/1997 field seasons. Females weighed after they had given birth showed an increase of 37 ± 36 kg (mean ± SD), which represented 6.2 ± 6.4% in relation to their mass in the first breeding season. During the first aquatic phase, between the end of lactation and the beginning of moult, females gained a mean of 128 ± 35 kg, (n = 18) (2.19 ± 0.65 kg day⁻¹), which represented between 27 and 83% of the mass they had lost during lactation. Nine females followed during moulting showed a mass loss rate of 5.0 ± 0.4 kg day⁻¹, which was half the rate during lactation. Total mass loss during moulting (129 ± 22 kg) was not significantly different from mass gain for the same females between lactation and moult (135 ± 37 kg). Furthermore, at the end of moulting, female mass was not significantly different from the mass at the end of lactation. These masses represented 65 ± 5% and 64 ± 5%, respectively, of their initial mass after parturition. During the second period at sea, from the end of the moult until females hauled out to give birth in the following breeding season, the estimated mass gain was 1.45 ± 0.24 kg day⁻¹ (n = 5), which was not significantly different to the rate of mass gain shown by the same females during the first period at sea (2.26 ± 0.70 kg day⁻¹). Total mass gain during the second aquatic phase (364 ± 63 kg) was not correlated with the mass at the end of moulting, but it was positively related to the mass loss experienced by females from parturition until the end of the moulting period in the first breeding season. Accepted: 5 September 1998     

Counts of southern elephant seals, Mirounga leonina, at Bouvet Island

Southern elephant seals were counted and classified into subjective sex-age classes on a weekly basis during expeditions to Bouvet Island in the austral summers of 1996/1997 and 1998/1999. The expeditions coincided with the moulting period of elephant seals aged one?year and older. The presence of weaned pups at the principal haulout site, Nyrøysa/Westwindstranda, during the latter expedition, indicates that breeding took place here during 1998. Elephant seal counts from previous expeditions are summarised.     

Lactation costs in southern elephant seals at King George Island,South Shetland Islands

Labelled-water methodology was used to quantify energy costs and energy transfer efficiency in 18 mother-pup pairs of southern elephant seals (Mirounga leonina) during lactation. During the lactation period, mothers lost a mean mass of 227±47 kg. Mass loss included 22% of the protein, 60% of the fat, and 51% of the energy in the mothers body upon arrival. Total body-energy reserves at parturition explained 69% of the variation in the total lactation costs and 50% of the variation in the pups body energy at weaning. On average, pups retained 48% of the mass, 49% of protein, 53% of fat and 51% of energy lost by their mothers. Greater, fatter females showed a decrease in the efficiency of energy and fat transfer and, at the same time, an increase in the efficiency of protein transfer. This may be due to an increased use of protein as metabolic fuel, as fat demands for milk production increase. There was no evidence that greater total lactation costs influence the ability of mothers to produce a pup in the next breeding season.     

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     

Changes in population sizes and distribution of fur seals at Marion Island

 Population censuses of the Antarctic fur seal (Arctocephalus gazella) and the sub-Antarctic fur seal (A. tropicalis) were conducted during the 1994/1995 breeding season at Marion Island. Pup numbers, determined from direct counts and a mark-recapture experiment, were used to estimate population sizes. Pup numbers of A. tropicalis showed a mean annual change of 2.0% over the previous 6 years, culminating in an estimated total population of 49, 523 for 1994/1995. The population appears to be entering the maturity phase of population growth and may therefore have recovered from the effects of uncontrolled sealing that ended in the early twentieth century. Numbers at the major colonies on Marion Island showed little change since 1989 and these sites may have reached carrying capacity. The extension of breeding to other parts of the island continues. Over the same period, A. gazella pup numbers showed a mean annual change of 17% and the total population numbered 1,205 in 1994/1995. This species has possibly entered the rapid recolonisation phase of population growth. A few hybrid seals were found. Received: 25 October 1995/Accepted: 14 April 1996     

Body mass loss of moulting female southern elephant seals,Mirounga leonina,at Macquarie Island

Thirteen female southern elephant seals moulting at Macquarie Island lost an average of 4.46±0.80 kg/day (10.01±1.20g/kg/day). There was no significant difference between this rate of body mass loss and that reported for moulting female southern elephant seals from South Georgia. Moulting female southern elephant seals however exhibited larger mass specific mass loss than either female northern elephant seals or male southern elephant seals, indicating a higher metabolic cost of moult in these animals.     

Decadal changes in habitat characteristics influence population trajectories of southern elephant seals

Understanding divergent biological responses to climate change is important for predicting ecosystem level consequences. We use species habitat models to predict the winter foraging habitats of female southern elephant seals and investigate how changes in environmental variables within these habitats may be related to observed decreases in the Macquarie Island population. There were three main groups of seals that specialized in different ocean realms (the sub‐Antarctic, the Ross Sea and the Victoria Land Coast). The physical and climate attributes (e.g. wind strength, sea surface height, ocean current strength) varied amongst the realms and also displayed different temporal trends over the last two to four decades. Most notably, sea ice extent increased on average in the Victoria Land realm while it decreased overall in the Ross Sea realm. Using a species distribution model relating mean residence times (time spent in each 50 × 50 km grid cell) to 9 climate and physical co‐variates, we developed spatial predictions of residence time to identify the core regions used by the seals across the Southern Ocean from 120°E to 120°W. Population size at Macquarie Island was negatively correlated with ice concentration within the core habitat of seals using the Victoria Land Coast and the Ross Sea. Sea ice extent and concentration is predicted to continue to change in the Southern Ocean, having unknown consequences for the biota of the region. The proportion of Macquarie Island females (40%) utilizing the relatively stable sub‐Antarctic region, may buffer this population against longer‐term regional changes in habitat quality, but the Macquarie Island population has persistently decreased (?1.45% per annum) over seven decades indicating that environmental changes in the Antarctic are acting on the remaining 60% of the population to impose a long‐term population decline in a top Southern Ocean predator.     

Extreme polygyny among southern elephant seals on Sea Lion Island, Falkland Islands

Elephant seals are known from long-term behavioral studies tobe highly polygynous and to show high variance in reproductivesuccess among males. However, genetic studies have determinedthat the level of polygyny varies between the closely relatednorthern and southern elephant seals. In the present study,we investigate paternal success at the Sea Lion Island southernelephant seal colony in the Falkland Islands by using both behavioralmeasures and genetic markers. We find that the average successof harem holding males at Sea Lion Island is significantly higherthan both the northern species and the nearby southern elephantseal population at Punta Delgada. We compare genetic paternitywith various behavioral indices of male mating success, andwe find that the behavioral measures provide a good estimateof the variance in male reproductive success. Only 28.2% ofmales achieved paternities, and among these, harem holders accountedfor 89.6%. We discuss the implications of our results in thecontext of the demographic and physical environment. Specifically,a comparatively high variance in resource holding potentialamong males, differences in male social behavior, and a smalltidal cycle limiting peripheral male access during female departurefrom the harem at this colony may be important factors leadingto the comparatively high variance in male reproductive successat Sea Lion Island.     

Electrophoretic transferrin variation in fur seals (Arctocephalus spp.) at Marion Island

1. Variation in transferrin types were investigated in sympatric populations of two fur seal species which are undergoing limited hybridization at Marion Island. 2. Vertical polyacrylamide gel electrophoresis of serum was performed to demonstrate the transferrin types. 3. The two species appear fixed for alternative alleles: A. tropicalis being homozygous for the fast allele, and A. gazella (with one exception) being homozygous for the slow allele, indicating low gene flow between these two species. The single hybrid tested was homozygous for the slow allele. 4. The use of electrophoretically determined transferrin variation holds promise for the investigation of these and other sympatric fur seal populations.     

Growth, age at sexual maturity and condition in bearded seals (Erignathus barbatus) from Svalbard, Norway

The aim of this study was to describe growth, determine age at sexual maturity and investigate the condition of bearded seals (Erignathus barbatus) collected in the fjords of Spitsbergen, Svalbard, Norway. Morphometric data, teeth and sex organs were collected from 110 animals. Age was determined by reading the cementum layers in hard longitudinal sections of canine teeth. Sexual maturity in males was determined according to the size of the testes and bacula. Females were defined as being sexually mature according to findings of mature follicles or corpora lutea/albicantia. Von Bertalanffy growth curves were applied to both standard length and body mass, and asymptotic values for males and females were 231.1 ± 11.4 cm and 269.9 ± 26.2 kg, and 233.1 ± 7.5 cm and 275.3 ± 47.8 kg, respectively. Maximum recorded lengths and masses were 254 cm and 313 kg in males and 242 cm and 358 kg in females. All males older than 6 years were found to have been sexually mature. Females were found to attain sexual maturity at about 90% of the asymptotic length, corresponding to an age of 5 years. In males a significant decrease in condition was observed from June to August, with a subsequent increase in September. In adult females, condition decreased from May to June and increased again from June to September. The conditional changes seen are likely to be due to the extra energetic cost and reduced food intake associated with reproduction, lactation and molt. Accepted: 28 July 1998     

Behavioural and morphometric measurements of parental investment in southern elephant seals at the Falkland Islands

Parental investment is a key variable in the study of breeding strategies and life-histories evolution. In Pinnipedia, parental investment is usually calculated from direct measurements of pup weight gain or energy transfer between the mother and the pup. These direct methods always involve handling and restraining procedures that pose practical, logistical and ethical problems. To evaluate if weighing can be substituted by indirect observational estimates of parental investment, we analysed the relationship among various behavioural measures of suckling and post-natal growth in the southern elephant seal population of Sea Lion Island (Falkland Islands). Behavioural measures were in all cases a poor predictor of true investment as estimated by weighing. We concluded that there are currently no effective alternatives to direct handling, and that the best way to reduce the potential adverse impact of investment studies is the improvement of the handling protocol, which should include an estimation of the long-term effects on the health of handled animals. Further research is needed to test the validity of non-behavioural indirect methods (e.g. 3D photogrammetry).     

Age-specific cost of first reproduction in female southern elephant seals

When to commence breeding is a crucial life-history decision that may be the most important determinant of an individual''s lifetime reproductive output and can have major consequences on population dynamics. The age at which individuals first reproduce is an important factor influencing the intensity of potential costs (e.g. reduced survival) involved in the first breeding event. However, quantifying age-related variation in the cost of first reproduction in wild animals remains challenging because of the difficulty in reliably recording the first breeding event. Here, using a multi-event capture–recapture model that accounts for both imperfect detection and uncertainty in the breeding status on an 18-year dataset involving 6637 individuals, we estimated age and state-specific survival of female elephant seals (Mirounga leonina) in the declining Macquarie Island population. We detected a clear cost of first reproduction on survival. This cost was higher for both younger first-time breeders and older first-time breeders compared with females recruiting at age four, the overall mean age at first reproduction. Neither earlier primiparity nor delaying primiparity appear to confer any evolutionary advantage, rather the optimal strategy seems to be to start breeding at a single age, 4 years.     

Equal investment in male and female offspring in southern elephant seals

Sex ratio theory predictions concerning differential parental investment in offspring by sex were tested on southern elephant seals, Mirounga leonina , breeding at Península Valdés, Argentina. Females invested equally in sons and daughters, as reflected by the similar mass at birth (mean ± 1 S.D.) of 14 males (44.1 ± 6.5 kg) and 14 females (43.4 ± 3.8 kg), and similar mass at weaning of 52 males (131.5 ± 22.4 kg) and 38 females (131.4 ± 18.3 kg). There were also no sex differences in the rate of mass gain during nursing (males = 4.0 ± 0.9 kg/day; females = 3.9 ± 0.8 kg/day), rate of mass loss during the first month of post-weaning fast (males = 0.85 ± 0.19 kg/day; females = 0.92 ± 0.15 kg/day), mean age at weaning (males = 22.3 ± 1.6 days; females = 22.7 ± 1.7 days), and female nursing behaviour. Mother's size accounted for most of the variation in mass of pups at weaning. Mothers ranked as small, medium and large, weaned pups with a mean mass of 102, 130 and 145 kg, respectively. The sex ratio of weanlings did not differ from unity. These data are consistent with Fisher's (1930) sex ratio theory.     

Ontogenetic niche partitioning in southern elephant seals from Argentine Patagonia

Elephant seals, Mirounga spp., are highly dimorphic, having different energetic requirements according to age and sex, and foraging in various ecological and oceanographic contexts. Resource partitioning has been shown for the sub-Antarctic populations of southern elephant seals, M. leonina, where colonies are surrounded by narrow shelves that deepen abruptly. In contrast, seals from Península Valdés (Argentina), in the northernmost extent of the breeding range, face an extended, shallow, temperate, and productive continental shelf. We integrated tracking data from 98 animals (juveniles and adults, males and females) gathered over more than two decades, and found that although all available habitats were used, individuals segregated by age and sex. Juvenile males favored shelf habitats, whereas subadult and adult males also used the shelf break. Juvenile females preferred the shelf and the more distant Argentine Basin used by postbreeding and postmolt adult females. Males showed the highest proportion of area-restricted search locations, suggesting more spatially concentrated feeding activity, and likely reflecting a preference for foraging habitat and prey. Our results are consistent with those from other populations, implying that elephant seals show remarkable similarities in habitat use by age and sex classes, despite broad differences in the offshore habitats between sub-Antarctic and temperate ecosystems.     

Population changes,movements of southern elephant seals on Crozet and Kerguelen Archipelagos in the last decades

Summary The elephant seal populations breeding on the Crozet and Kerguelen Archipelago were surveyed during the eighties. Elephant seals were observed moving between Kerguelen, Amsterdam, Heard Islands and Vestfold Hills and between Crozet and Prince-Edward Archipelagos. No exchanges were observed between Crozet and Kerguelen Archipelagos suggesting that the two populations are more isolated than previously stated. On the Crozet Archipelago, since 1966, the Possession Island population showed at 70% reduction in numbers of cows ashore and the population is still decreasing. On Kerguelen Island there has been a decline of 44% from 1956 to 1989 but the population appears to have stabilized since 1984. It is suggested that elephant seal populations in the Southern Indian Ocean may have been affected by a change at the trophic level over the last four decades. But the highest rate of decrease observed on the Crozet Archipelago and the fact that the population is still decreasing may be explained by additional factors, in particular by killer whale predation.