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The spleens of several seals from both the Arctic and the Antarctic were isolated and weighed when contracted. Spleens of the crabeater, leopard, and Weddell seals formed 0.23%, 0.39%, and 0.86% of the seals' body weights; those of the hooded and harp seals formed 0.56% and 0.35% of the seals' body weights. In these 5 phocids, a contracted spleen relates to the seal's body weight according to the equation (in which weights are in kilograms; n=26; r2=0.65): contracted spleen=0.006 (body weight)-0.11. Further, using the criterion reported in the literature that contracted spleens of hooded seal and harp seals weigh 80% less than when dilated, the sizes of dilated spleens were estimated for the 5 phocids of the study, plus that of the southern elephant seal. Dilated spleens ranged from 1 to 4% of the seal's body weight, which is in agreement with determinations of dilated spleens reported in the literature (harbor, 0.8–3.0%; harp, 1.5%; hooded, 2.2–4.0%). The general correlation among dilated spleens and the 6 phocids' body weights is: dilated spleen=0.026 (body weight)-0.39(where weights are in kilograms; n=31; r2=0.70). The size of the spleen (either contracted or dilated) from the different species of seals in this study appeared to be correlated with the diving capacity of the phocids, as given in the literature. The phocids with greater diving capacities are the ones with the larger spleens.

Southern elephant seals were counted and classified into subjective sex-age classes on a weekly basis during expeditions to Bouvet Island in the austral summers of 1996/1997 and 1998/1999. The expeditions coincided with the moulting period of elephant seals aged one year and older. The presence of weaned pups at the principal haulout site, Nyrøysa/Westwindstranda, during the latter expedition, indicates that breeding took place here during 1998. Elephant seal counts from previous expeditions are summarised.

During the austral summer of 1996/1997 we studied south polar skuas at Svarthamaren, Dronning Maud Land, Antarctica, where the world's largest known colony of Antarctic petrels is found. Our censuses suggested approximately 250 full-grown skuas and 140,000 breeding pairs of petrels were present. During their breeding season, skuas did not visit the open sea at least 200 km from the site; they relied entirely on prey caught and scavenged from the petrel colony. Because the site is so isolated, we asked whether the prey (petrels) had swamped the predators (skuas), or whether there was evidence that predator numbers were limited by the size of the prey population. Particularly at the end of the petrel incubation period, we found a close correspondence between the energy required by adult skuas and their chicks, ascertained from time budget studies, and the rate at which petrel eggs disappeared from the colony. This suggests that, in this closed system, the predator population was limited by the prey population, and that predator swamping was not an advantage that petrels gained by nesting in this remote location.

In the near coastal regions of Dronning Maud Land, Antarctica, below-surface ice-melt in blue-ice areas has been observed. The low scattering coefficients of the large-grained blue-ice allow penetration of solar radiation, thus providing an energy source below the ice surface. The sub-surface meltwater is significant enough to show up on remote-sensing imagery in the form of ice-covered lakes. Adjacent snow-accumulation areas have much higher scattering coefficients and consequently limit solar radiation penetration in these regions. These snow and ice surfaces are generally below freezing, and little surface melting occurs. To assess the response of these melt features to changes in atmospheric forcings such as cloudiness, air temperature, and snow accumulation, a physically-based model of the coupled atmosphere, radiation, snow, and blue-ice system has been developed. The model consists of a heat transfer equation with a spectrally-dependent solar-radiation source term. The penetration of radiation into the snow and blue-ice depends on the surface albedo, and the snow and blue-ice grain size and density. Model simulations show that ice melt occurring in this area is sensitive to potential variations in atmospheric forcing. Under certain conditions more traditional surface melting occurs and, under other conditions, the existing melt processes can be shut down completely. In light of the sensitivity of this system to variations in atmospheric forcing, and the ability to view melt-related features using remote sensing, a tool exists to efficiently monitor variations in Antarctic coastal climate.

1. Two hypotheses may explain how long-lived seabirds regulate the food provisioning to their chick. The fixed level of investment hypothesis states that the parents provide food for their chick according to an intrinsic rhythm, independent of their chick's need. The flexible investment hypothesis states that the parents adjust their food provisioning both according to their chick's and their own need. 2. We tested how the Antarctic petrels adjust the food-provisioning according to their own body condition or to their chick's need. First, we selected parents in poor and good body condition. Then we gave all parents randomly a chick of different body mass, but of the same age. We then measured the chicks daily until they were fed for the first time after swapping. 3. Parents in good body condition at hatching were more likely to produce a chick that was still alive 9 days after hatching than parents in poor body condition. Chick body mass at day 9 and at the end of the guarding period was positively related to the mean body condition of the parents at hatching. 4. The meal size provided by parents in good body condition was larger than that provided by parents in poor body condition. Parents in good body condition delivered more food to small than to large chicks, whereas no such relationship was found among parents in poor body condition. 5. Our results suggest that the Antarctic petrel parents adjust the amount of food delivered to their chick according to both the chick's need and their own body condition, and that the ability to respond to the chick's need is dependent upon their own body condition.

In Procellariiformes, the parents guard the chick after it has attained homeothermy. This strategy may reduce the probability that a small chick is taken by predators, but is costly as only one parent can forage at a time. The decision to leave the chick may therefore be a compromise between the chick's vulnerability to predators, the body condition of the parent on the nest and whether the foraging parent returns in time. We studied how the number of days that parents guarded the chick was related to the body mass of the parent at the nest and the time the foraging parent spent at sea in the Antarctic petrel Thalassoica antarctica. We also examined how the body mass of the parent on the nest and the duration of the foraging trips influenced the chicks' body condition at the end of the guarding period. When the foraging parent did not return to the nest in time to relieve its mate, the number of days the parent on the nest kept guarding the chick was positively related to its body mass on arrival in the colony. The number of days the foraging parent spent at sea was positively related to the body mass of its mate, but those that returned in time had a shorter stay at sea relative to their mate's body mass than those that did not return before their mate had left. Apparently, both the body mass of the parent at the nest and the ability of the foraging parent to adjust its stay at sea to the mate's body mass is important for the number of days the parents guard the chick and also the chick's body condition at this point. The inability to return to the nest before the mate has left may be the result of needing a minimum amount of time at sea to find food, or because some parents having low foraging success and therefore prolong their stay at sea.