Population status and seasonal haulout patterns of the southern elephant seal (Mirounga leonina) at Heard Island

1999 ◽  
Vol 11 (1) ◽  
pp. 38-47 ◽  
Author(s):  
David J. Slip ◽  
Harry R. Burton
Keyword(s):  
Total Population ◽  
Elephant Seal ◽  
Southern Elephant Seal ◽  
Mirounga Leonina ◽  
Population Status ◽  
Elephant Seals ◽  
Adult Females ◽  
Seal Population ◽  
Heard Island ◽  
One Year

We surveyed the southern elephant seal population at Heard Island regularly from February 1992 to March 1993, and determined the haulout patterns of the major components of the population. While haulout patterns of moulting and immature seals may give broad indices of population trends, the breeding haulout of adult females was the only reliable haulout that could be used to determine annual pup production. During the breeding season 14 277 adult females were counted. Raw counts were corrected using two models, one purely mathematical and the other based on the haulout behaviour of adult female seals. The two models have slightly different assumptions, but both provided good fits to the observed haulout patterns and estimated total population with a coefficient of variation of less than 5%. Total pup production was estimated at between 17 000 and 18 000 for 1992. Previous counts of elephant seals from 1949–51, 1985 and 1987 were corrected using the same models. The two models gave estimates of the population that were within ± 2.5% for all but one year. The population declined by about 50% between 1949 and 1985 but there appears to have been little change from 1985–92. The previous decline may be related to changes in sea-ice.

Branding Elephant Seals for life-history studies

Polar Record ◽  
1967 ◽  
Vol 13 (85) ◽  
pp. 447-449 ◽  
Author(s):  
Susan E. Ingham
Keyword(s):  
Ecological Study ◽  
Individual Recognition ◽  
Elephant Seal ◽  
Southern Elephant Seal ◽  
Mirounga Leonina ◽  
Elephant Seals ◽  
Macquarie Island ◽  
Heard Island ◽  
Antarctic Research

In 1949 the Australian National Antarctic Research Expeditions (ANARE) began a long-term ecological study of the Southern Elephant Seal (Mirounga leonina) at HeardIsland. The biologists devised a method of branding seals for individual recognition (Chittleborough and Ealey, 1953) which has been modified only in detail since then (Carrick and Ingham, 1962a). At Heard Island, pups were branded every year until 1953, but the study here came to an end with the closing of the ANARE station in 1955. At Macquarie Island, pups have been branded every year from 1951 to 1965, giving a sample of individuals of known age and known history.

Dynamic age-distributions in a declining population of southern elephant seals

1999 ◽  
Vol 11 (4) ◽  
pp. 445-450 ◽  
Author(s):  
P.A. Pistorius ◽  
M.N. Bester ◽  
S.P. Kirkman
Keyword(s):  
Total Population ◽  
Conversion Factor ◽  
Elephant Seal ◽  
Southern Elephant Seal ◽  
Marion Island ◽  
Elephant Seals ◽  
Breeding Sites ◽  
Seal Population ◽  
Southern Elephant Seals ◽  
The Indian Ocean

Estimates of births and standing age-distributions were combined to estimate the size of the southern elephant seal population at Marion Island at various times during its decline. To estimate births each year from 1986 through 1997 we used the number of adult females hauled out on 15 October, which is the peak haulout date for breeding elephant seal females at all breeding sites in the Indian Ocean. A conversion factor (3.15) was derived from the standing age-distributions, and applied to estimates of annual births to yield total population size. The population at Marion Island declined 37.5% overall from 1986–97 at an annual rate of 4.3% from 1986–91 and c. 2.5% yr−1 afterwards.

The skin and hair of the southern elephant seal, Mirounga leonina (Linn.) I. The facial vibrissae

1966 ◽  
Vol 14 (5) ◽  
pp. 855 ◽  
Author(s):  
JK Ling
Keyword(s):  
Elephant Seal ◽  
Sensory Function ◽  
Southern Elephant Seal ◽  
Sweat Glands ◽  
Mirounga Leonina ◽  
Sebaceous Glands ◽  
Elephant Seals

The arrangement, number, and anatomy of the facial vibrissa follicles of the southern elephant seal, Mirounga leonina (Linn.), are described. There are three groups of vibrissae: mystacial, supraorbital, and rhinal, containing approximately 38, 7, and 1 follicles, respectively. These specialized hairs appear to be retained for at least 2 yr and are not shed with the pelage hairs at each annual moult. The histology of the vibrissa follicles and associated organs is described and discussed in relation to their sensory function. Vibrissa follicles of elephant seals are different in anatomy from those described in the mouse and rat: the ringwulst is relatively smaller and, in addition to the sebaceous glands, there are tubular glands of unidentified function but resembling apocrine sweat glands.

The skin and hair of the southern elephant seal, Mirounga leonina (Linn.). IV. Annual cycle of pelage follicle activity and moult

2012 ◽  
Vol 60 (4) ◽  
pp. 259 ◽  
Author(s):  
John K. Ling
Keyword(s):  
Hair Growth ◽  
Growth Cycle ◽  
Elephant Seal ◽  
Hair Follicles ◽  
Southern Elephant Seal ◽  
Growth Stages ◽  
Adult Males ◽  
Mirounga Leonina ◽  
Complete Replacement ◽  
Adult Females

Hair growth stages, anagen, catagen and telogen, were diagnosed histologically in skin samples taken at Macquarie Island from 103 southern elephant seals – 11 pups, 56 immatures, 23 adult females and 13 adult males – in order to correlate hair follicle activity with field observations of this species’ unusual type of moult. The duration of the hair growth cycle in fully developed follicles is ~12 weeks. Hair follicles are active for 2–3 months before, during and after the moult haul-out and are resting at other times of the year. A high proportion of adult females appear to commence hair growth between 4 January and 2 February. While implantation of the blastocyst may be triggered by some astral event, such as daylength, it does not depend on completion of the moult, as suggested by previous authors. The pelage cycle is possibly controlled by an endogenous rhythm established during follicle development and subsequent growth and shedding of the natal coat, but the timing and duration of the moult haul-out may depend on the nutritional status of seals within each particular age–sex class. In adult seals this will be governed by terrestrial activities that involve fasting during the breeding and moulting seasons, whereas immature seals haul out and fast, not only to moult but some also come ashore and rest during winter. There may also be metabolic demands for materials for the complete replacement of the pelage, and much of the stratum corneum.

Physiological implications of continuous, prolonged, and deep dives of the southern elephant seal (Mirounga leonina)

1992 ◽  
Vol 70 (2) ◽  
pp. 370-379 ◽  
Author(s):  
Mark A. Hindell ◽  
David J. Slip ◽  
Harry R. Burton ◽  
Michael M. Bryden
Keyword(s):  
Resting Metabolic Rate ◽  
Elephant Seal ◽  
Southern Elephant Seal ◽  
Adult Males ◽  
Mirounga Leonina ◽  
Physiological Mechanisms ◽  
Elephant Seals ◽  
Aerobic Dive Limit ◽  
Southern Elephant Seals ◽  
Extended Surface

The diving behaviour of 14 adult southern elephant seals was investigated using time depth recorders. Each of the seals performed some dives that were longer than its theoretical aerobic dive limit. Forty-four percent of all dives made by post-moult females exceeded the calculated limit compared with 7% of those made by postbreeding females and less than 1% of those made by adult males. The extended dives displayed characteristics that suggested that they were predominantly foraging dives, although some were apparently rest dives. Dives longer than the calculated aerobic limits often occurred in bouts; the longest consisted of 63 consecutive dives and lasted 2 days. Postmoult females performed longer bouts of extended dives than postbreeding females. Extended surface periods (longer than 30 min) were not related to the occurrence of extended dives or bouts of extended dives. The possible physiological mechanisms that permit such prolonged continuous dives are discussed. Southern elephant seals may increase the aerobic capacity of dives by lowering their metabolism to approximately 40% of the resting metabolic rate on long dives. There is substantial interseal variability in the methods used to cope with long dives. Some animals appear to use physiological strategies that allow them to prolong the time available to them at the bottom of a dive, while others use alternative strategies that may limit the time available at the bottom of their dives.

scholarly journals Movement responses to environment: fast inference of variation among southern elephant seals with a mixed effects model

2018 ◽  
Author(s):  
I. D. Jonsen ◽  
C. R. McMahon ◽  
T. A. Patterson ◽  
M. Auger-Méthé ◽  
R. Harcourt ◽  
...  
Keyword(s):  
Sea Ice ◽  
Movement Patterns ◽  
Elephant Seal ◽  
Mixed Effects ◽  
Foraging Strategies ◽  
Southern Elephant Seal ◽  
Mirounga Leonina ◽  
Movement Model ◽  
Elephant Seals ◽  
Southern Elephant Seals

AbstractLike many species, movement patterns of southern elephant seals (Mirounga leonina) are being influenced by long-term environmental change. These seals migrate up to 4000 km from their breeding colonies, foraging for months in a variety of Southern Ocean habitats. Understanding how movement patterns vary with environmental features and how these relationships differ among individuals employing different foraging strategies can provide insight into foraging performance at a population level. We apply new fast-estimation tools to fit mixed effects within a random walk movement model, rapidly inferring among-individual variability in southern elephant seal environment-movement relationships. We found that seals making foraging trips to the sea-ice on or near the Antarctic continental shelf consistently reduced speed and directionality (move persistence) with increasing sea ice coverage and had variable responses to chlorophyll a concentration, whereas seals that foraged pelagically reduced move persistence in regions where circumpolar deep water shoaled. Given future climate scenarios, pelagic foragers may encounter more productive habitat but sea-ice foragers may see reduced habitat availability. Our approach is scalable to large telemetry data sets and allows flexible combinations of mixed effects to be evaluated via model selection, thereby illuminating the ecological context of animal movements that underlie habitat use.

Temporal changes in the quality of hot-iron brands on elephant seal (Mirounga leonina L.) pups

2004 ◽  
Vol 31 (6) ◽  
pp. 619 ◽  
Author(s):  
John van den Hoff ◽  
Michael D. Sumner ◽  
Iain C. Field ◽  
Corey J. A. Bradshaw ◽  
Harry R. Burton ◽  
...  
Keyword(s):  
Elephant Seal ◽  
Poor Quality ◽  
Temporal Changes ◽  
Southern Elephant Seal ◽  
Mirounga Leonina ◽  
Skin Damage ◽  
Excessive Pressure ◽  
The Mean ◽  
One Year

Hot-iron brands were used to mark permanently 14 000 six-week-old southern elephant seal (Mirounga leonina L.) pups at Macquarie Island between 1993 and 2000. We assessed temporal changes in the quality of 4932 brands applied in 1998 and 1999 to determine the duration of the brand wound, and the relationships between brand healing, brand readability and the amount of skin and hair damage peripheral to the brand characters. Most (98%) brand wounds were healed within one year. Brand-mark healing, peripheral skin damage and brand readability were significantly (P < 0.05) correlated. The proportion of healed and readable brands increased in the population during the first annual moult, and thereafter these proportions remained high (>95%) for the marked population. The mean number of brand characters with peripheral skin damage decreased significantly over the same period. The seal’s annual hair and skin moult is the process that contributed most to the healing of brand wounds. We also assessed our branding technique to determine whether any of the features we measured contributed to a poor-quality brand. Excessive pressure used during brand-iron application is the most probable cause of unsightly peripheral skin damage, but this damage is short lived.

Cephalopod diet of the southern elephant seal, Mirounga leonina, at King George Island, South Shetland Islands

2000 ◽  
Vol 12 (1) ◽  
pp. 16-19 ◽  
Author(s):  
G.A. Daneri ◽  
A.R. Carlini ◽  
P.G.K. Rodhouse
Keyword(s):  
Stomach Contents ◽  
Elephant Seal ◽  
South Shetland Islands ◽  
Southern Elephant Seal ◽  
Mirounga Leonina ◽  
King George Island ◽  
Elephant Seals ◽  
Shetland Islands ◽  
Important Prey ◽  
Southern Elephant Seals

In the summer of 1995/96, 25 southern elephant seals, Mirounga leonina, were stomach lavaged at Stranger Point, King George Island, South Shetland Islands. Cephalopod remains were present in 72% of the individuals sampled (n = 18). Seven species of squid and three of octopus were identified. The squid Psychroteuthis glacialis was the most important prey in terms of numbers (77%), biomass (80.8%) and frequency of occurrence (94.4%). Next in importance in terms of mass was the squid Alluroteuthis antarcticus (7.8%) in the diet of females and the octopodid Pareledone ?charcoti in the diet of males (13.2%). Females preyed on a wider variety of squid taxa than males (7 vs 3) but octopodids occurred only in stomach contents from males. The predominance of P. glacialis in the prey of the South Shetland Islands elephant seals can be explained by the southerly location of the foraging areas of this population compared to South Georgia, Heard and Macquarie islands, where the diet of southern elephant seals has previously been analysed. Psychroteuthis glacialis is the predominant squid in waters close to the Antarctic continent.

Ultrasonic Measurement of Blubber Thickness of the Southern Elephant Seal, Mirounga-Leonina (Linn)

1987 ◽  
Vol 35 (3) ◽  
pp. 207 ◽  
Author(s):  
NJ Gales ◽  
HR Burton
Keyword(s):  
Subcutaneous Fat ◽  
Elephant Seal ◽  
Ultrasonic Measurement ◽  
Southern Elephant Seal ◽  
Future Research ◽  
Mirounga Leonina ◽  
Elephant Seals ◽  
Non Invasive ◽  
Fat Reserves ◽  
Southern Elephant Seals

Ultrasound measurements of subcutaneous fat at 18 body sites on each of 23 southern elephant seals Mirounga leonina (Linn.), together with circumference and length measurements, were used to estimate the total subcutaneous blubber weight on each animal. Twelve cows (including animals that were pregnant and others at early, mid-, late and post-lactation), 10 males and one male pup were anaesthetised for these measurements, made at Heard I. (53�01'S.,73�23'E.) on various dates in October and November 1985. Comparison of the estimates of blubber weight from cows at various stages of lactation allowed a mean blubber loss of 62.8 kg per cow per lactation to be calculated. It is suggested that measuring variations in the subcutaneous fat reserves of cows coming ashore to pup at Heard I. may be one relevant approach in any future research that attempts to explain the 60% drop in pup production at that island between 1949 and 1985. The use of ultrasound to estimate the subcutaneous fat reserves of seals was shown to be a safe, non-invasive and logistically practical technique.

Age in relation to Breeding to Status of the Male Southern Elephant Seal, Mirounga leonina (L.), at Macquarie Island

1981 ◽  
Vol 8 (2) ◽  
pp. 327 ◽  
Author(s):  
E Jones
Keyword(s):  
Elephant Seal ◽  
Progressive Increase ◽  
Southern Elephant Seal ◽  
Mirounga Leonina ◽  
Elephant Seals ◽  
Macquarie Island ◽  
Southern Elephant Seals ◽  
Definition Of ◽  
Breeding Seasons ◽  
Breeding Status

Records of the breeding status of known-age male southern elephant seals at Macquarie I. were kept during five breeding seasons between 1969 and 1976. The seven status categories used were: beachmaster, secure assistant, medium harem owner, insecure assistant, small harem owner, attending bachelor, avoiding bachelor. There was a progressive increase in breeding status with age; none younger than 10-y-old bred: 16% of 10-y-olds, 30% of 11-y-olds and 55% of 12-y-olds did so; none younger than 12-y-old attained secure assistant status. At the earliest, beachmaster status may be attained at 14 y old, but no beachmasters of known age were recorded. Due to mortality and competition, most males do not breed and few breed for more than two seasons. Problems associated with the precise definition of status categories are discussed.

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