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.     

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.     

Past and present status of the southern elephant seal (Mirounga leonina) at Macquarie Island

The southern elephant seal population at Macquarie Island has undergone a serious decline since regular surveys were commenced in 1949. Approximately 2,900 cows and 250 bulls were counted in the isthmus study area during the 1985 breeding season. Comparisons with 20 other counts made in the same area between 1949 and 1984 showed that, although there was considerable fluctuation between the years, the number of seals ashore has dropped at an average rate of 2.1% per year, resulting in a net decrease of approximately 50% for both males and females. This is similar to the ratio of decline of elephant seal populations in the southern Indian Ocean. The census information from all major elephant seal populations was reviewed and it was concluded that there may be a common factor, or group of factors, acting to reduce the Macquarie Island and Indian Ocean populations, while the populations of the South Atlantic seem to be stable. Several potential explanations for these observations are advanced, but it is concluded that a greater knowledge of the ecology of the seals is needed if the declines are to be understood.     

The annual cycle of the epididymis of the elephant seal (Mirounga leonina) at Macquarie Island

The tubules of the head and body of the elephant seal epididymis undergo large increases in diameter and principal cell height for the duration of the breeding season, and regress at the conclusion of breeding. The tubules of the tail show a lesser development, and only towards the end of breeding. Spermatozoa, first produced in the testis in August, reach the tail of the epididymis in September, and are present in large numbers throughout the epididymis in October and November. In December, the first month of sexual quiescence following the breeding season, sperm are almost totally absent from the epididymis.     

The annual cycle of the testis of the elephant seal (Mirounga leonina) at Macquarie Island

The testis of the Southern elephant seal demonstrates seasonal changes in weight, with highest values early in the breeding season (September-November) and lowest values in mid-winter (May-June). Weight changes originate in the seminiferous tubules, there being little variation in the interstitial tissue.
Spermatogenesis begins in August, one month before the breeding season, and stops in November. Testicular testosterone concentration is significantly elevated in the months July-September. Plasma testosterone concentration is high only in September, the first month of breeding.     

Inter-population differences in diving behaviour of adult male southern elephant seals (Mirounga leonina)

Access to different environments may lead to inter-population behavioural changes within a species that allow populations to exploit their immediate environments. Elephant seals from Marion Island (MI) and King George Island (KGI) (Isla 25 de Mayo) forage in different oceanic environments and evidently employ different foraging strategies. This study elucidates some of the factors influencing the diving behaviour of male southern elephant seals from these populations tracked between 1999 and 2002. Mixed-effects models were used to determine the influence of bathymetry, population of origin, body length (as a proxy for size) and individual variation on the diving behaviour of adult male elephant seals from the two populations. Males from KGI and MI showed differences in all dive parameters. MI males dived deeper and longer (median: 652.0?m and 34.00?min) than KGI males (median: 359.1?m and 25.50?min). KGI males appeared to forage both benthically and pelagically while MI males in this study rarely reached depths close to the seafloor and appeared to forage pelagically. Model outputs indicate that males from the two populations showed substantial differences in their dive depths, even when foraging in areas of similar water depth. Whereas dive depths were not significantly influenced by the size of the animals, size played a significant role in dive durations, though this was also influenced by the population that elephant seals originated from. This study provides some support for inter-population differences in dive behaviour of male southern elephant seals.     

Minimum population size estimates demonstrate an increase in southern elephant seals (Mirounga leonina) on Livingston Island, maritime Antarctica

Southern elephant seals (Mirounga leonina) are apex predators of marine Antarctic food webs, and variations in their populations have been linked to environmental changes. Consequently, measuring and reporting the status of elephant seal populations provide insights into the environmental status of Antarctica. Here, we present new information on the size of the elephant seal subpopulation on Byers Peninsula (Livingston Island, South Shetland Islands, maritime Antarctica). Based on a total count of 1,510 pups, we estimated a total subpopulation size of 5,530 individuals by using a conversion factor of 3.5. This represents an increase of 150 % since the subpopulation was first counted 30 years ago. Based on this finding, we hypothesize that the overall South Georgia stock, to which the subpopulation we estimated on Byers Peninsula belongs, could be increasing instead of remaining stable as previously thought.     

Aggression and sexual activity of male Southern elephant seals, Mirounga leonina

The agonistic and sexual activity of individual male Southern elephant seals (Mirounga leonina) was studied during the breeding season at South Georgia. Harem bulls were older and larger than non-harem bulls and, although size and age are related, harem bulls were also larger than non-harem bulls of the same age. Large body size conferred advantages in fighting and the agonistic relationships of the bulls gave rise to a dominance hierarchy with access to harems and activity within harems, being determined by rank. Vocalizations were the most highly rank-related aggressive behaviours. The most common vocalization, the roar, probably functioned in both individual recognition and size assessment. Over 90% of encounters of high-ranked bulls were "walkovers" and only 4% of 4003 agonistic interactions nvolved physical contact.     

The dynamics of male harem dominance in southern elephant seals (Mirounga leonina) at the South Shetland Islands

Breeding chronology, harem structure and changes in male harem dominance were studied at Stranger Point, Isla 25 de Mayo/King George Island, principally by extensive field census work during the 2003 breeding season. Males were individually identified and their size estimated by using a photogrammetric method. Peak female haul out for the population occurred on 31 October, when a total of 276 females were observed along 7 km of coastline, distributed in ten harems with a median size of 16 females. Overall sex ratio and harem sex ratio for the breeding population were 1:6.7 and 1:10.6, respectively. A total of 33 males were identified associated with harems. Male size conferred an advantage in terms of dominance hierarchy, since dominant males (4.91±0.15 m) were significantly longer than subordinate males (4.63±0.19 m). Harems were dominated by an average of 4.5 (range 2–7) different males during the breeding season. Elephant seals at Stranger Point breed in very low density aggregations. The main breeding events in this population occurred later than at other breeding sites, which agrees with previous observations in the area. Male movement among harems suggests that differences in mating success among males could be achieved through their different behaviours.     

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     

Energy gain and loss during lactation and postweaning in southern elephant seal pups (Mirounga leonina) at King George Island

Deuterium-labeled water was used to measure changes in the proximate body composition during the lactation period and after weaning in southern elephant seal pups at King George Island, South Shetland Islands, Antarctica. During the lactation period (23.0 ± 1.4 days) pups gained a mean of 4.9 ± 0.5 kg/day (n=7). Of the total mass gain (112 ± 8 kg), 38% was water, 48% was fat, and 11% was protein. This represented an increase in total body gross energy of 2437 ± 145 MJ. The proportion of body mass represented by fat was less than 2% at birth, increasing to 35 ± 2% at weaning. We followed the pups during a mean period of 36 ± 3 days after weaning. During this period, pups had a mean loss of 1.21 ± 0.10 kg/day (n=7) comprising 39% water, 48% fat, and 12% protein. The energy cost over this period was 952 ± 168 MJ, which represented, on average, 39% of the total energy gained during the suckling period. Accepted: 3 January 2000     

Mass transfer from mothers to pups and mass recovery by mothers during the post-breeding foraging period in southern elephant seals (Mirounga leonina) at King George Island

Mass transfer from mother to pup during the lactation period, and mass recovery for the same females during the foraging period were measured in the southern elephant seal at King George Island, Antarctica. During the 19.2 ± 0.9-day lactation period measured (which represented 87% of the entire nursing), females lost a mean mass of 10.56 ± 1.76 kg/day (n = 27), while their pups gained a mean mass of 5.27 ± 1.1 kg/day. There was a correlation between daily body weight gain in pups and daily weight loss by their mothers. Pup weaning mass was positively related to maternal post-partum mass. Serial samples showed that weight losses by females and gains by their pups were not linear over lactation, but showed lower values at the beginning and at the end of lactation. During the 60.5 ± 6.2-day foraging phase between the end of lactation and molt, females gained 2.21 ± 0.65 kg/day (n = 12), or 54% of the mass lost during nursing. Growth rates reported here are higher than those reported in other breeding sites. However, the ratio of body mass loss by females to gain by their pups was similar, suggesting that higher growth rates and greater weaning mass at South Shetland are due to a higher mean weight of females on arrival at this breeding site. The foraging period was shorter and the mass gained greater than those measured at South Georgia; this could be related to relatively shorter distances to foraging areas. Received: 20 September 1996 / Accepted: 28 April 1997     

The chromosomes of the southern elephant seal, Mirounga leonina (Phocidae: Mammalia).

Chromosome analyses were carried out on bone marrow cells from three elephant seal pups (Mirounga leonina), a species characterized by a 2n = 34 chromosome number. Arm ratios for the different chromosomes were calculated to facilitate the classification of chromosomes into groups. The karyotype of the southern elephant seal differs from other reported 34-chromosome phocids in the morphology of the Y chromosome and in that of one of the autosomal chromosome pairs.     

You are what you eat: describing the foraging ecology of southern elephant seals (Mirounga leonina) using blubber fatty acids

Understanding the trophodynamics of marine ecosystems requires data on the temporal and spatial variation in predator diet but, particularly for wide-ranging species, these data are often unavailable. The southern elephant seal (Mirounga leonina) consumes large quantities of fish and squid prey in the Southern Ocean relative to other marine mammals; however, how diet varies relative to seasonal and spatial foraging behaviour is unknown. We used fatty acid (FA) signature analysis of 63 blubber cores from adult female M. leonina over three seasons (winter 1999, summer 2000 and winter 2001) to determine diet structure. We detected significant differences between seasons and between the main foraging regions (Antarctic continental shelf versus pelagic). We used the FA profiles from 53 fish, squid and krill species to construct a discriminant function that would classify each seal, from its blubber sample as having a fish- or squid-FA profile. We determined that a higher proportion of M. leonina had fish-dominated diets during the winter and when foraging around the Antarctic continental shelf, and the majority had more squid-dominated diets during the summer when foraging pelagically. Thus, we were able to measure the coarse-scale diet structure of a major marine predator using FA profiles, and estimate its associated seasonal and temporal variation.     

Rate of passage of digesta through the alimentary tract of southern elephant seals (Mirounga leonina) (Carnivora: Phocidae)

The inert markers chromium-EDTA (liquid phase marker) and ytterbium nitrate (solid phase marker) were added to the food of three southern elephant seals in Taronga Zoo, Sydney, in a series of nine trials. The enclosures were checked at 15 to 30 minute intervals for up to 60 hours after dosing, and all faeces voided on land were collected (91 samples). Marker concentrations in faecal dry matter were determined and mean retention times calculated from the concentration-time curves.
The faeces were soft to semiliquid, with mean water content of 58% (range 24–80%). The marker concentration curves indicated a rapid rate of food transit through the gastro-intestinal tract in elephant seals compared with other carnivores. The mean time between dosing and first recovery of marker (Initial Recovery Time) was nine hours. This was significantly longer than the figure of 4.8 hours for northern elephant seals reported previously, and possible reasons for the differences are discussed. Mean Retention Time, a better index of rate of passage of ingesta, was 13 hours for the three southern elephant seals. This compares with times of 22 hours for the dog, 15 hours for the raccoon, and 13 hours for the cat, all carnivores with much shorter gastrointestinal tracts, both absolutely and relative to body size, than the southern elephant seal.
It is suggested that the very long small intestine may be an adaptation to foraging at depth, combined with long periods of submergence and the need to ingest large amounts of food when the animal is at sea continuously for weeks or months.