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Eight crabeater seals (Lobodon carcinophagus) (three females, five males), ranging in body mass between 125 and 220 kg, were captured off Queen Maud Land (70-72 degrees S, 7-16 degrees W) during the last week of February, just after moulting, and tagged with Argos satellite-linked dive recorders to provide data on location and diving depth and duration. During the first few weeks of March the seals were moving in the pack ice along the continental shelf edge, close to the coast of Queen Maud Land. In April and May, when the pack ice extended northwards, most of the seals moved north, one reaching 63 degrees S in late May. In the first half of June the two remaining seals turned south and moved back deep into the pack ice. The seals made about 150 dives per day each throughout the study period. Ninety percent of these were made to depths of less than 52 m. Individual maximum diving depths varied between 288 and 528 m. In March the seals were most active at night, when the dive depth was shallower than during the day. In April and May the seals were more active during day-time, with an absence of any diurnal change in diving depth. These results support the notion that crabeater seals predominantly feed on krill in Antarctic pack ice, even when winter returns to the waters off Queen Maud Land.

Levels of polychlorinated dibenzo-p-dioxins (PCDD) and dibenzofurans (PCDF) as well as of coplanar (non-ortho substituted) polychlorinated biphenyls (CB-77, CB-126 and CB-169) have been determined in 11 fur-seal blubber samples from female Antarctic fur seals. Measurable PCDD/PCDF concentrations averaging 2 ppt TEQ (Nordic model) were found. This is considerably less than in Arctic seals. In addition, the PCDD/PCDF congener patterns differed between Antarctic and Arctic seals. The levels of CB-77, CB-126 and CB-169 (8.5-41 pg g-1 for single congeners in average) in Antarctic fur seals were also much lower than in Arctic ringed and harp seals. A possible explanation of these differences is the overall lower environmental pollution of the Southern Hemisphere, though an influence of different age and sex distributions cannot be excluded. The data passed all quality assurance criteria that had been established for such low levels.

Survival at low temperatures was studied in three species of Tardigrada from Muhlig-Hofmannfjella, Dronning Maud Land, Antarctica. Both hydrated and dehydrated specimens of Echiniscus jenningsi, Macrobiotus furciger and Diphascon chilenense had high survival rates following exposure to -22 degrees C for ca. 600 days, and dehydrated specimens following 3040 days at this temperature. In hydrated E. jenningsi, mortality increased with the duration of exposure from 7 to 150 days at -80 degrees C, while mortalities of the two other species did not change. Hydrated specimens of all species were rapidly killed at -180 degrees C, but all species exhibited good survivorship in the dehydrated state after 14 days at -180 degrees C. In conclusion, hydrated tardigrades are able to survive extended periods at low temperatures, and dehydrated specimens are even better adapted to survive overwintering on Antarctic nunataks.

An integrated plume model is used to describe large scale gravity currents in the ocean. The model describes competing effects of (negative) buoyancy, friction, entrainment and Cariolis farce, as well as a pressure term due to variable plume thickness, on the flux, speed and flow direction of the plume. Equations for conservation of salt and internal energy (temperature) and a full equation of state far seawater is included in the model. The entrainment of ambient water is parameterized with support in empirical data, and a drag coefficient consistent with the entrainment is introduced. The model is tested against the overflow through the Denmark Strait, the flow down the Weddell Sea continental slope, and the outflow of saline water through the Gibraltar Strait and from the Spencer Gulf, Australia. The farmer gain an extra driving mechanism due to the thermobaric effect, while in the two latter cases the initial density difference is so large that this effect is not essential. Order of magnitude fit with measurements requires drag coefficient between 0.01 and 0.1. Conditions susceptible to meander behaviour and a singularity arising from the pressure dependency on the current thickness variations are briefly discussed.

A new araphid diatom genus, Synedropsis Hasle, Medlin et Syvertsen, is described from sea ice. The generitype, Synedropsis hyperborea (Grunow) Hasle, Medlin et Syvertsen from the Arctic, was first described as a species of Synedra, as was the antarctic Synedropsis fragilis (Manguin) Hasle, Syvertsen et Medlin. A second antarctic species of Synedropsis is a new combination of Cymatosira laevis Heiden in Heiden & Kolbe. In addition four new taxa, S. hyperboreoides Hasle, Syvertsen et Medlin, S. recta Hasle, Medlin et Syvertsen, S. lata Hasle, Medlin et Syvertsen and S. lata var. angustata Hasle, Medlin et Syvertsen are described from the Antarctic. The valve wall is laminar with uniseriate, often poorly developed striae and a wide sternum. Each valve possesses apical fields composed of slits. A labiate process is positioned near one apical slit field. The valve outline for most species exhibits considerable stadial variation. The girdle has several bands, most with one row of poroids close to the pars interior. Thus Synedropsis is closely related to the marine Fragilaria striatula Lyngbye except in the structure of the apical fields and the number of bands. Species observed in uncleaned material appeared in stellate or, more seldom, ribbon-shaped colonies. Synedropsis hyperborea is a common epiphyte on the ice-associated Melosira arctica Dickie in the Arctic. The antarctic species were found mainly in the bottom ice community, S. fragilis as an epiphyte on other diatoms.

During the Swedish Antarctic Expedition to Dronning Maud Land, Antarctica, 1988–89 the net accumulation was estimated for an area from the coast to about 400 km inland. Stake measurements were used to obtain the spatial variability and firn cores were used for the temporal variability. The mean annual accumulation for the period 1976–88 is about 0.4mw.e. for Riiser-Larsenisen and about 0.3mw.e. for the area above the grounding line. The accumulation rate at higher altitudes, > 2500 m a.s.1., is about 0.1 m w.e. for 1955–88. One record from the ice shelf covers the period 1957–88, and suggests an increase in accumulation of about 12%. Between 1976 and 1988, the accumulation has decreased by about 50%, most likely due to lower temperatures as suggested by the temperature record from Halley.

We present data on sexual dimorphism in some morphological measurements (wing length, head length, bill depth and bill length) in the Antarctic Petrel Thalassoica antarctica. Males were on average larger than females for all measurements. Sexual dimorphism was on average largest for bill depths whereas wing lengths discriminated least between the sexes. A discriminant function including bill depth, head length and wing length correctly sexed 92% of the sample. Due to between-measurer variation it is recommended that morphometric measurements obtained by others on sexed birds are compared with ours before proceeding with the use of the discriminant function on unsexed individuals.

A simple analytical model has been developed to study the formation of Ice Shelf Water (ISW). ISW is assumed to flow as a buoyancy-driven layer underneath the ice shelf. A relation between potential temperature and salinity in the ISW layer is calculated from the mass and energy balance. This temperature-salinity relation is shown to depend only on the temperature and the salinity of the source water mass and to be practically independent of entrainment and melt rates. The model results are obtained without making any assumptions about entrainment and melt rates. The model is in good agreement with observations under the Ronne Ice Shelf, and it indicates that ISW in the Filchner Depression is formed from Western Shelf Water (WSW) with salinity higher than 34.75 practical salinity units. Such high-salinity water is only observed in the Ronne Depression in the western part of the continental shelf. This implies a circulation of WSW, under the Filchner-Ronne Ice Shelf, from the Ronne Depression into the Filchner Depression. Similarly, the model shows that the ISW observed under J9 at the Ross Ice Shelf has been formed from Low Salinity Shelf Water (LSSW) from the eastern parts of the Ross Sea continental shelf. LSSW must therefore circulate under the eastern parts of the Ross Ice Shelf.

Eleven fish species from the Weddell Sea (Antarctic) were examined for infestation with anisakid nematodes. Two species of the genus Contracaecum and the sealworm Pseudoterranova decipiens were isolated from the liver and the body cavity of fish affected. Only two specimens of P. decipiens (1.4%) partly invaded the belly flaps. The following fish species were infested by P. decipiens at the given prevalences: Cygnodraco mawsoni (74.4%), Trematomus scotti (23.2%), Pagetopsis maculatus (10.0%), Cryodraco antarcticus (7.1%), Trematomus lepidorhinus (3.0%), and Dolloidraco longedorsalis (2.7%). All of these, except Trematomus scotti, are new host records. Chaenodraco wilsoni, Chionodraco myersi, Gerlachea australis, Racovitzia glacialis and T. eulepidotus were not infested. The reasons for low prevalence and intensity of infestation are seen in the difficulties of P. decipiens in completing its benthic life cycle in the Weddell Sea environment, in the absence of shallow coastal waters due to the floating shelf-ice. Cygnodraco mawsoni is a crucial intermediate host, without which completion of the parasite life cycle might not be possible. In order to clarify the taxonomical position of Antarctic Pseudoterranova, morphological comparisons with specimens of P. decipiens from the German and Norwegian coast were made using scanning electron microscopy. Results revealed no differences; hence, all specimens studied belong to the same species P. decipiens.

The bipolar foliose lichen Solorina spongiosa (Sm.) Anzi is reported from James Ross Island, Antarctica, where it grows on moss. This is only the third known occurrence of this lichen from the Southern Hemisphere, the other localities being in Tierra del Fuego and New Zealand. Its morphology resembles that of the New Zealand population and arctic-alpine populations from the Northern Hemisphere, although there are some differences in apothecial and spore size. As elsewhere, it occupies base-rich habitats colonized by predominantly calcicolous mosses and lichens.