Locomotor activity by diving marine mammals is accomplished while breath-holding and often exceeds predicted aerobic capacities. Video sequences of freely diving seals and whales wearing submersible cameras reveal a behavioral strategy that improves energetic efficiency in these animals. Prolonged gliding (greater than 78% descent duration) occurred during dives exceeding 80 meters in depth. Gliding was attributed to buoyancy changes with lung compression at depth. By modifying locomotor patterns to take advantage of these physical changes, Weddell seals realized a 9.2 to 59.6% reduction in diving energetic costs. This energy-conserving strategy allows marine mammals to increase aerobic dive duration and achieve remarkable depths despite limited oxygen availability when submerged.

The hunting behavior of a marine mammal was studied beneath the Antarctic fast ice with an animal-borne video system and data recorder. Weddell seals stalked large Antarctic cod and the smaller subice fish Pagothenia borchgrevinki , often with the under-ice surface for backlighting, which implies that vision is important for hunting. They approached to within centimeters of cod without startling the fish. Seals flushed P. borchgrevinki by blowing air into subice crevices or pursued them into the platelet ice. These observations highlight the broad range of insights that are possible with simultaneous recordings of video, audio, three-dimensional dive paths, and locomotor effort.

SUMMARY Foraging by mammals is a complex suite of behaviors that can entail high energetic costs associated with supporting basal metabolism, locomotion and the digestion of prey. To determine the contribution of these various costs in a free-ranging marine mammal, we measured the post-dive oxygen consumption of adult Weddell seals (N=9) performing foraging and non-foraging dives from an isolated ice hole in McMurdo Sound, Antarctica. Dives were classified according to behavior as monitored by an attached video-data logging system (recording activity, time, depth, velocity and stroking). We found that recovery oxygen consumption showed a biphasic relationship with dive duration that corresponded to the onset of plasma lactate accumulation at approximately 23 min. Locomotor costs for diving Weddell seals increased linearly with the number of strokes taken according to the relationship: locomotor cost =– 3.78+0.04 × stroke number (r²=0.74, N=90 dives), where locomotor cost is in ml O₂ kg^–1. Foraging dives in which seals ingested Pleuragramma antarcticum resulted in a 44.7% increase in recovery oxygen consumption compared to non-foraging dives, which we attributed to the digestion and warming of prey. The results show that the energy expended in digestion for a free-ranging marine mammal are additive to locomotor and basal costs. By accounting for each of these costs and monitoring stroking mechanics, it is possible to estimate the aerobic cost of diving in free-ranging seals where cryptic behavior and remote locations prevent direct energetic measurements.

We studied the ontogeny of diving behaviour in the Galápagos fur seal (Arctocephalus galapagoensis, Heller 1904). Six-month-old seals spent less than 12% of observation time at sea and were entirely dependent on maternal milk for nutrition. Maximum dive depths for this age group averaged 5.6 m, maximum durations 50 s (N = 12). Modal swim speeds averaged 0.55 m/s; maximum observed swim speeds ranged from 0.9-2 m/s (N = 5). Six-month-old seals swam distances of 2.9 km/24 hrs on average (N = 5). No diel patterns were apparent in their diving behaviour. One-year-old fur seals were the youngest age group to show substantial diving activity, reaching maximum depths of 47.5 m and durations of 2.4 min on average (N = 21). Modal swim speeds averaged 0.9 m/s, maximum speeds ranged from 1.4-2.3 m/s (N = 6). Total distances traveled averaged 15.4 km/trip to sea. Yearlings spent 23.9% of observation time at sea, the majority (> 95%) of that at night. This corresponds to the activity pattern of adult females who dive exclusively at night. Yearlings were the youngest age group to contribute to their own nutrition through independent foraging, but were still dependent on their mothers: no yearlings were successfully weaned in this study. 18-month-old seals were better divers, spending 27.6% of observation time at sea, mostly during the night. Maximum dive depths for this age group averaged 61.1 m; durations 3.1 min (N = 11). Modal swim speeds averaged 1.4 m/s (N = 4), and were comparable to modal speeds of two adult females of 1.2 and 1.6 m/s. Maximum speeds for these juveniles ranged from 2.2-2.7 m/s (N = 4); the two adult females reached 2.8 and 4 m/s respectively. Total travel distances averaged 42 km/trip to sea (N = 4 juveniles). These distances corresponded to those covered by two adult females, 43 and 45 km/trip. Two-year-old fur seals included the youngest that were successfully weaned in this study. They spent 35% of observation time at sea, primarily at night. Maximum dive depths averaged 69.7 m, durations 3.4 min (N = 20). Adult females were the best divers in this study, spending 49.5% of observation time at sea, almost exclusively at night. Maximum dive depths averaged 106.5 m, durations 4.5 min (N = 32). During ontogeny, age was the best predictor of time spent at sea. For animals older than six months, body mass was the best predictor for maximum dive depth as well as maximum and median durations. The physiological maturation process precludes weaning before the age of one year. After that, the diving capacity of young fur seals takes a central role in the weaning process, in conjunction with the temporal patterns of relative prey accessibility.