BACULAR AND TESTICULAR GROWTH AND ALLOMETRY IN THE CAPE FUR SEAL ARCTOCEPHALUS P. PUSILLUS (OTARIIDAE)

The baculum in Arctocephalus p. pusillus reaches up to 14.1 cm in length, 13.5 g in mass, and 1.3 g/cm in density (= mass/length). A pubertal growth spurt occurs between 2 and 3 yr of age, when bacular length increases by 28%, mass by 124%, and density by 77%; concurrently, body length increases by 14%. A second, weaker spurt occurs at social maturity (9-10 yr of age). Testes grow most rapidly between 1 and 2 yr of age, when testicular length increases by 29%. After 3 yr of age, growth in bacular and testicular length slows, and bacular mass continues to increase approximately linearly. Bacular and testicular lengths average 6.8% and 3.4% (respectively) of body length in adults, compared with 9.9% and 5.7% in the promiscuous harp seal ( Pagophilus groenlandicus ). Bacular length, mass, and density, and testicular length, are positively allometric to body length over growth; bacular length is isometric to testicular length. Among animals of the same age, bacular length and mass are positively allometric to body length in young animals, with negative allometry or isometry thereafter; testicular length is isometric to body length in young animals and negatively allometric thereafter. Patterns of early growth and allometry of the baculum and testes are interpreted as adaptations for mating opportunities, years before territoriality is possible. The baculum and testes of adult Cape fur seals and other otariids are small compared with those of most phocids, because sperm competition among male otariids is weak.     

SUCCESSFUL USE OF A TRANSLOCATION PROGRAM TO INVESTIGATE DIVING BEHAVIOR IN A MALE AUSTRALIAN FUR SEAL, ARCTOCEPHALUS PUSILLUS DORIFERUS

This study reports some of the first foraging behavior data collected for male fur seals. A nonbreeding male Australian fur seal, Arctocephalus pusillus doriferus , captured at a commercial salmon farm in southern Tasmania, Australia, was relocated 450 km from the site of capture. The animal was equipped with a geolocating time-depth recorder that recorded diving behavior and approximate location for the 14.4 d that it took the seal to travel down the east coast of Tasmania and be recaptured at the salmon farm. During its time at sea, the seal spent most of its time over the relatively shallow shelf waters. It spent 30% of its time ashore on a number of different haul-out sites. The deepest dive was 102 m and the maximum duration was 6.8 min. "Foraging" type dives made up 31.2% of the time at sea and had a median duration of 2.5 min and a median depth of 14 m. The seal performed these dives more commonly during the latter part of its time at sea, while it was on the east coast. Unlike other fur seal species studied to date, there was no evidence of a diurnal foraging pattern; it made dives at all times of the day and night.     

INVESTIGATING THE BIASES IN THE USE OF HARD PREY REMAINS TO IDENTIFY DIET COMPOSITION USING ANTARCTIC FUR SEALS (ARCTOCEPHALUS GAZELLA) IN CAPTIVE FEEDING TRIALS

The analysis of pinniped scats has been used to quantify their diet, using prey remains to identify species and to estimate the numbers and sizes of prey consumed. There are, however, potential biases involved with scat analysis and, for this method to be used successfully, these biases need to be quantified. Thirty-six Antarctic fur seals ( Arctocephalus gazella ) were fed meals of exclusively either fish, squid, or krill and their scats were collected and analyzed. The major sources of error in the analysis of prey remains from scats were the differential erosion and passage rate of items in relation to their size. However, using simple correction functions, such as those which model otolith erosion, it is possible to reduce these errors. Using plastic beads as dietary markers showed recovery rates were negatively related to their size. Larger squid beaks had lower recovery rates than smaller beaks, but there was no size-related bias in the recovery rates of krill carapaces. Only 33% of the squid beaks and 27% of the otoliths originally fed were recovered from the scats. Recovery rates were greater for squid (77%) and fish (50%) eye lenses and these structures gave a better estimate of numbers eaten. Differences found between experimentally derived and published regression equations (used to calculate prey sizes eaten from prey remains) highlights the need for regression equations based on local prey characteristics, if these are to be used with any success to describe the prey eaten.