BREEDING BIOLOGY OF SOUTHERN ELEPHANT SEALS IN PATAGONIA

Abstract: Elephant seals breed in Patagonia (Península Valdés, Argentina) from late August to early November, reaching peak numbers during the first week in October. Observations of this population over the past ten years yielded similar results. Eighty percent of the pups were born by 2 October. Most (96%) of 663 females marked during three breeding seasons gave birth to a pup. Females stayed on land a mean of 28 d, gave birth 6 d after arrival, nursed their pups for 22 d, and copulated a mean of 2.5 times 20 d after parturition and 2 d before departure. Copulations peaked during the third week in October. Males spent 57–80 d on land fasting and defending harems of up to 134 females (median 11–13 females, depending on year). Most (96%) marked females that gave birth ( n = 636) also weaned their pups successfully. Pup sex ratio was unity. Harems were smaller and breeding occurred about three weeks earlier in Patagonia than in other colonies. Thermal conditions, day length and food availability may explain clines in the timing of breeding events between populations, Other parameters of the breeding season for the expanding Patagonia colony are similar to those for declining southern elephant seal populations elsewhere.     

Locomotion in diving elephant seals: physical and physiological constraints

To better understand how elephant seals (Mirounga angustirostris) use negative buoyancy to reduce energy metabolism and prolong dive duration, we modelled the energetic cost of transit and deep foraging dives in an elephant seal. A numerical integration technique was used to model the effects of swim speed, descent and ascent angles, and modes of locomotion (i.e. stroking and gliding) on diving metabolic rate, aerobic dive limit, vertical displacement (maximum dive depth) and horizontal displacement (maximum horizontal distance along a straight line between the beginning and end locations of the dive) for aerobic transit and foraging dives. Realistic values of the various parameters were taken from previous experimental data. Our results indicate that there is little energetic advantage to transit dives with gliding descent compared with horizontal swimming beneath the surface. Other factors such as feeding and predator avoidance may favour diving to depth during migration. Gliding descent showed variable energy savings for foraging dives. Deep mid-water foraging dives showed the greatest energy savings (approx. 18%) as a result of gliding during descent. In contrast, flat-bottom foraging dives with horizontal swimming at a depth of 400m showed less of an energetic advantage with gliding descent, primarily because more of the dive involved stroking. Additional data are needed before the advantages of gliding descent can be fully understood for male and female elephant seals of different age and body composition. This type of data will require animal-borne instruments that can record the behaviour, three-dimensional movements and locomotory performance of free-ranging animals at depth.     

A COMPARISON OF SOME CYCLOHEXAMINE BASED DRUG COMBINATIONS FOR CHEMICAL RESTRAINT OF SOUTHERN ELEPHANT SEALS (MIROUNGA LEONINA)

This study compared the effects of drug combinations commonly used for chemical restraint of southern elephant seals. The combinations were: ketamine and diazepam, ketamine and midazolam, ketamine and xylazine, and tiletamine and zolazepam. The main aims were to gather basic information regarding the response of the animals to the different combinations, and to determine which were most useful for routine chemical restraint. All drug combinations could be used safely although apnea and whole-body shaking occurred with each. There were significant differences in several of the responses measured. Poor muscle relaxation and prolonged apnea were associated with ketamine and diazepam use. Animals given ketamine and xylatine were more depressed, took longer to recover, had a higher incidence of thermoregulatory problems, and lower heart rate than after other combinations. Ketamine and midazolam and tiletamine and zolazepam produced fewer complications than the other drug combinations, and tiletamine and zolazepam showed greater predictability of response and ease of use, making it preferable for use by people with little experience in anesthesia of elephant seals.     

BODY TEMPERATURE IN THE NEWBORN SOUTHERN ELEPHANT SEAL, MIROUNGA LEONINA, AT MACQUARIE ISLAND

Newborn southern elephant seal pups were reported by Laws (1953) to be "to some extent poikilothermic at birth." Rectal temperatures of known age southern elephant seal pups were recorded during the 1985 pupping season at Macquarie Island. The mean pup rectal temperature was found to be 381°C ± 0.1°C SEM ( n = 131, range = 36.5°-39.1°C). Pups at two hours, six hours, and one day after birth had significantly higher rectal temperatures than pups two, three, or four days of age. Rectal temperatures of neonatal southern elephant seals were within the range observed for other pinnipeds, (but never as low as the 31°C previously observed for southern elephant seals at Signy Island in 1953). A significant though weak positive correlation was found between pup temperature and body weight. However, no correlation between pup temperature and age or any environmental factor was found. These observations demonstrated that southern elephant seal pups at Macquarie Island are homeothermic, rather than heterothermic from birth.     

AGING LIVE ANTARCTIC FUR SEALS AND SOUTHERN ELEPHANT SEALS

This study describes a method for extracting post-canine or incisor teeth from live antarctic fur seals ( Arctocephalus gazella ) and southern elephant seals ( Mirounga leonina ) respectively and their use to determine age in a field situation. Dental elevators were used to loosen the teeth from the alveolus and periodental ligament. Most teeth were removed within l-2 min and a total of 214 and 81 teeth were collected by this method from antarctic fur seals and southern elephant seals respectively. No seal recaptured at intervals up to a year after a tooth was extracted showed signs of infection or distress related to removal of the tooth. Teeth were thin-sectioned for the purpose of aging. In both species cementum growth layer groups were a more satisfactory indicator of age than dentinal growth layer groups. Estimates of age from cementum growth layers were confirmed for Antarctic fur seals using seals which had been tagged as pups up to 16 yr before sampling.     

DIVING PATTERNS OF NORTHERN ELEPHANT SEAL BULLS

We used small microprocessor-based, time-depth recorders to document the diving patterns of six adult male northern elephant seals ( Mirounga angustirostris ) from San Miguel Island, California. The recorders stored measurements of hydrostatic pressure every 30 or 60 set while the seals were at sea for 107 to 145 d in spring and early summer; collectively, over 36,000 dives were recorded. Seals dove continually while at sea, most often to depths of 350–450 m although two seals had secondary modes at about 700–800 m; maximum depths for two seals of 1,333 m and 1,529 m are the deepest yet measured for air-breathing vertebrates. Seals were submerged about 86% of the time they were at sea, rarely spending more than 5 min at the surface between dives; 99% of all post-dive surface intervals were shorter than 10 min. Dives averaged 21–24 min, the longest was 77 min. The uninterrupted patterns of long dives punctuated by brief surface periods suggest that most if not all dives were well within these seals'aerobic limits. Dives of bulls were, on average, about 18% longer than those published earlier for cows, evidently because of the substantially greater body mass of bulls and allometric scaling of dive endurance. Dive depths and dive durations varied seasonally; depths were greatest in spring, durations greatest in early summer. During each season dives were deepest during the day and shallowest at night except for the sixth seal whose consistently shallow dives (50–150 m) in spring were independent of time of day. Prey remains recovered by lavage from seals'stomachs were primarily of vertically migrating, epi- and meso-pelagic squid. The die1 patterns in dive depths suggest that five seals dove to and foraged in the offshore mesopelagic zone, pursuing those vertically migrating prey. The sixth seal behaved similarly in early spring and early summer but may have foraged in nearshore epibenthic habitats in spring.     

ESTIMATION OF BODY MASS IN THE SOUTHERN ELEPHANT SEAL, MIROUNGA LEONINA, BY PHOTOGRAMMETRY AND MORPHOMETRICS

A simple photographic technique was developed to indirectly estimate body mass data for southern elephant seal ( Mirounga leonina ) cows (postlactation), yearlings, and immature males and females. Regressions of mass on both photographic and morphometric variables (together and separately) yielded useful, predictable models. Using such variables, the best estimation of the actual mass was for postlactation cows, with a 95% confidence interval of ± 2.66% of the predicted body mass. Although combining photographic and morphometric variables produced the most reliable models specifically for cows and yearlings, the most practical model contained only the morphometric variables length and girth squared. Side area was the best correlated single photographic variable and this corresponded with other studies. Photogrammetry could be useful when animals cannot be sedated and are located on a flat surface, but it does require animals to be motionless when approached. Thus, the procedure may be more suited to bulls rather than other age classes and could have a role in studies where large numbers of mass estimations are rapidly required. If sedation is utilized in smaller animals, then the use of body length and girth is the most suitable indirect mass estimation technique to avoid the use of heavy weighing equipment.