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 400 m 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

Movement of Southern Elephant Seals (Mirounga leonina L.) from Elephant Is. South Shetlands, Antarctica

In 1999, at-sea activity of two young southern elephant seal males (Mirounga leonina) from Elephant Is.(61°13’S,55°23’W), Antarctica, was monitored and tracked for 9 months. The individuals were randomly selected, captured,sedated (Zoletil 50®- 1mg/kg), weighed, measured, bled, paint-marked and fitted with satellite tags (STDR - ST- 6PPT, Telonics®, USA). Deployment of the STDR took about 45 min since each animal had a lower incisor tooth extracted for age determination. The seals exhibited individual behaviors. Seal “V”-23842 (BM ~ 801kg) moved from Elephant Is. (61.2ºS 55.3ºW) in Jan. 1999 to King George Is. (62.2ºS 58.1ºW) in Feb. 1999 when the tag stopped signaling. Seal “T”-23843 (BM ~ 656 kg) was restricted to the area around Elephant Is. (61.2ºS 54.4ºW -61.6ºS 55.4ºW) from January to May 1999, when it started to move south-eastwards. Although the age of these individuals was not yet determined it was likely to explain the difference in the two patterns of movement reported here. The temporal and spatial association of these movements with areas of high productivity is being investigated to assess whether the observed distribution reflects foraging activity

Sex differences in ageing in natural populations of vertebrates

In many long-lived vertebrates (including humans), adult males have shorter lifespans than adult females, partly as a result of higher annual rates of mortality in males and partly owing to sex differences in the rate of ageing. A probable explanation of the evolution of sex differences in ageing is that, in polygynous species, intense intrasexual competition between males restricts the number of seasons for which individual males are able to breed successfully, weakening selection pressures favouring adult longevity in males relative to females. If this is the case, sex differences in adult longevity and in the onset and rate of senescence should be greater in polygynous species than in monogamous ones and their magnitude should be related to the duration of effective breeding males compared with females. Here, we use data from longitudinal studies of vertebrates to show that reduced longevity in adult males (relative to females) is commonly associated with a more rapid decline in male than female survival with increasing age and is largely confined to polygynous species. The magnitude of sex differences in adult longevity in different species is consistently related to the magnitude of sex differences in the duration of effective breeding, calculated across surviving adults. Our results are consistent with the suggestion that sex differences in senescence in polygynous species are a consequence of weaker selection for longevity in males than females