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Fluid infiltration into Proterozoic and Early Palaeozoic dry, orthopyroxene-bearing granitoids and gneisses in Dronning Maud Land, Antarctica, has caused changes to rock appearance, mineralogy, and rock chemistry. The main mineralogical changes are the replacement of orthopyroxene by hornblende and biotite, ilmenite by titanite, and various changes in feldspar structure and composition. Geochemically, these processes resulted in general gains of Si, mostly of Al, and marginally of K and Na but losses of Fe, Mg, Ti, Ca, and P. The isotopic oxygen composition (δ18OSMOW = 6.0‰–9.9‰) is in accordance with that of the magmatic precursor, both for the host rock and infiltrating fluid. U-Pb isotopes in zircon of the altered and unaltered syenite to quartz-monzonite indicate a primary crystallization age of 520.2 ± 1.0 Ma, while titanite defines alteration at 485.5 ± 1.4 Ma. Two sets of gneiss samples yield a Rb-Sr age of 517 ± 6 Ma and a Sm-Nd age of 536 ± 23 Ma. The initial Sr and Nd isotopic ratios suggest derivation of the gneisses from a relatively juvenile source but with a very strong metasomatic effect that introduced radiogenic Sr into the system. The granitoid data indicate instead a derivation from Mid-Proterozoic crust, probably with additions of mantle components.

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.

The main purpose of the present paper is to estimate the orthometric height of the Global Positioning System (GPS)-station at Troll, Dronning Maud Land, Antarctica. Located at approximately 1300 m above sea level Troll has been connected to the Geodetic Infrastructure forAntarctica (GIANT)-network, but it’s orthometric height remains undetermined. A local geoid has been determined based on gravity-, tidal- and GPS-observations and available gravity anomalies. Information about the ice-thickness has been included in the terrain model. Based on tidal measurements the mean sea level was determined in Jutulgryta, a rift zone in the Fimbulisen ice shelf. Several gravity- and GPS-stations were measured between the two points (Jutulgryta andTroll), a distance of approximately 100 km.

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.

In the Jutulgryta area of Dronning Maud Land, Antarctica, subsurface melting of the ice sheet has been observed. The melting takes place during the summer months in blue-ice areas under conditions of below-freezing air and surface temperatures. Adjacent snow-covered regions, having the same meteorological and climatic conditions, experience little or no subsurface melting. To help explain and understand the observed melt-rate differences in the blue-ice and snow-covered areas, a physically based numerical model of the coupled atmosphere, radiation, snow and blue-ice system has been developed. The model comprises a heat-transfer equation which includes a spectrally dependent solar-radiation source term. The penetration of radiation into the snow and blue ice depends on the solar-radiation spectrum, the surface albedo and the snow and blue-ice grain-sizes and densities. In addition, the model uses a complete surface energy balance to define the surface boundary conditions. It is run over the full annual cycle, simulating temperature profiles and melting and freezing quantities throughout the summer and winter seasons. The model is driven and validated using field observations collected during the Norwegian Antarctic Research Expedition (NARE) 1996–97. The simulations suggest that the observed differences between subsurface snow and blue-ice melting can be explained largely by radiative and heat-transfer interactions resulting from differences in albedo, grain-size and density between the two mediums.

Temperature, density and accumulation data were obtained from shallow firn cores, drilled during an overland traverse through a previously unknown part of Dronning Maud Land, East Antarctica. The traverse area is characterised by high mountains that obstruct the ice flow, resulting in a sudden transition from the polar plateau to the coastal region. The spatial variations of potential temperature, near-surface firn density and accumulation suggest that katabatic winds are active in this region. Proxy wind data derived from firn-density profiles confirm that annual mean wind speed is strongly related to the magnitude of the surface slope. The high elevation of the ice sheet south of the mountains makes for a dry, cold climate, in which mass loss owing to sublimation is small and erosion of snow by the wind has a potentially large impact on the surface mass balance. A simple katabatic-wind model is used to explain the variations of accumulation along the traverse line in terms of divergence/convergence of the local transport of drifting snow. The resulting wind- and snowdrift patterns are closely connected to the topography of the ice sheet: ridges are especially sensitive to erosion, while ice streams and other depressions act as collectors of drifting snow.

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.