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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.

The summer of 1997 was characterized by unusually large amounts of pack ice in the southeastern Weddell Sea, and less than 10% of the area that is commonly ice-free in summer was open. A modest phytoplankton bloom developed in the upper mixed layer in the northernmost area (72°S). The bloom peaked in mid-February with max chlorophyll concentrations of 1.5 μg l−1, and integrated stocks of 55–60 mg m−2. Autotrophic flagellates dominated the biomass (80–90% of the chlorophyll) at first, while diatoms increased relative to flagellates during the bloom. Nutrient deficits, however, indicated that a much larger biomass was produced than was observed. Freezing starting after mid-February probably terminated the bloom, resulting in a pelagic growth season limited in time (less than two months) and space. The sea ice had a distinct brown layer of algae, usually at 1–2 m depth, with average chlorophyll biomass of 10.3 mg m−2. The ice cover exhibited a substantial amount of ridges, with ice algae growing in cavities and other structures, but with lower biomass than in the bands. Ice algae were also found growing on the lower 2 m of the ice shelf (visible at low tide). The overall growth season in the ice lasted several months, and ice algal production may have exceeded pelagic production in the Weddell Sea during the growth season of 1997. Pennate diatoms, like Fragilariopsis curta and F. cylindrus, dominated both in ice and in open water above the pycnocline, while Phaeocystis antarctica dominated in deeper layers and in crack pools. Euphausiids, particularly young stages, were frequently observed grazing on ice algae in ridges and on all sides of the floes, (confirmed by the gut content). Ice algae would thus have served as an ample food supply for the krill in the summer of 1997.

We have investigated the intermediate water mass of the central Weddell Gyre using TCO2 and oxygen data of FS Polarstern cruises in 1992, 1996 and 1998. This water mass, designated as Central Intermediate Water (CIW), is enriched in CO2 and depleted in O-2 relative to its source water due to biological degradation. CO2 enrichment and O-2 depletion were quantified by calculating the difference between the concentrations in the CIW and those in the, more southern source water, the Circumpolar Deep Water, which derives from the Antarctic Circumpolar Current. Inventories of enrichment and depletion were determined over the whole depth range of CIW, i.e. about 200800 m. The O-2 depletion inventory was greater than that of TCO2 enrichment which is in line with a biological origin of the signal. Spatial and interannual variation appeared to be small. Because subsurface remineralization in the central Weddell Gyre is largely restricted to the CIW, the export production estimate from previous work has been applied to compute the renewal time of CIW from these inventories. A renewal time of only three years was found. TCO2- and O-2-based computations were consistent, the former showing larger variation, though. From renewal time and volume of the CIW, a transport velocity (renewal rate) of 6-7 Sv was obtained. Of this, about I Sv is upwelled into the surface layer. The remaining 5-6 Sv CIW must be exported to the north, which is opposite to previous views. Results of water mass age and transport rate have thus been obtained using a method based on biogeochemical parameters. As the CIW cannot be identified by temperature and salinity, nor with transient tracers because it is hardly ventilated, this is the only way to obtain such results. As part of the CIW export, a large amount of remineralized CO2 enters the abyssal oceans where it is sequestered for long periods of time. The CIW is a principal and highly efficient player in the biological pump mechanism of the Southern Ocean.

Nitrate, phosphate and silicate data are presented from 1992 austral winter and 1998 austral autumn cruises with “FS Polarstern” in the Weddell Gyre. Because in the Weddell Gyre, away from the boundary current, the surface layer is eventually formed from upwelled deep water, the difference in nutrient concentrations between these layers can be used to compute net nutrient consumptions (identical with the export production). This method renders a value for the export production that is based on observed annual changes. The results are consistent for two years and two regions within the central gyre. The calculated net nitrate and phosphate consumptions were scaled to net carbon consumptions using canonical Redfield ratios, yielding 16–17μmolCkg−1yr−1. This equals 21±4gCm−2yr−1 as a robust estimate for the marginal ice zone. The net annual silicate consumption in the surface layer, which equals the export of biogenic silica, amounts to 15–18μmolkg−1yr−1. There is a tendency for higher values in the eastern Weddell Gyre. The estimated silicate consumption of about 1.8molSim−2yr−1 is relatively high compared to earlier estimations of biogenic silica export. The silicate to carbon consumption ratio of about 1 is very high, and documents the dominance of diatoms in the export of organic material. Résumé Sont présentées les distributions verticales de nitrate, de phosphate et de silicate en Mer de Weddell, pour les périodes de l’hiver austral 1992 et de l’automne austral 1998. Les eaux de surface du tourbillon à grande échelle de la Mer de Weddell (temps de résidence égal à 2.9 ans) sont formées par l’upwelling des eaux profondes. La différence de concentrations des sels nutritifs entre les couches profondes et de surface permettent de calculer la consommation annuelle, équivalente à la production exportée de l’élément nutritif considéré vers les couches profondes. Les résultats sont comparables pour les deux scénarios annuels étudiés. La production exportée de carbone pour les eaux de surface de la zone marginale de la glace, calculée à partir des consommations annuelles en nitrates et phosphates après transformation grâce aux rapports de Redfield, est estimée à 16–17μmolCkg−1yr−1 soit en moyenne 21±4gCm−2yr−1. La consommation annuelle de silicate est estimée à 1.8mol Si m−2yr−1, relativement élevée en comparaison des estimations antérieures. Le rapport molaire Si/C, voisin de 1 dans le matériel exporté, traduit la dominance des diatomées dans l’export de matières organiques.

We present the first year-long current meter records ever obtained near the floating Filchner-Ronne Ice Shelf in the Weddell Sea. The currents are steered along the ice front, but in the lower layer where the bottom topography is descending toward the west the current has a component toward the ice front of about 3 cm s−1. During winter the temperature stayed near the surface freezing point, while the salinity increased, indicating that ice was formed and brine released. The seasonal variation in salinity was 0.15±0.05 psu, corresponding to the formation of 1–2 m of ice on a shelf depth of 400 m. The transport of High-Salinity Shelf Water (HSSW) into the ice shelf cavity was found to be of the order 0.5×106 m3 s−1. The production of this water due to oscillating tides and off shelf winds was found to be of the same order of magnitude. In contact with glacial ice at great depths, and because of the depression of the freezing point, the HSSW is transformed to Ice Shelf Water (ISW) by cooling and melting processes. The melting rate was estimated to 1×1011 ton yr−1. This corresponds to the melting of 0.2 m ice per year if the melting is evenly distributed over the Filchner-Ronne Ice Shelf. If the melting is concentrated along a path from the Berkner Shelf around the Berkner Island to the Filchner Depression, then melting rates up to 7 m yr−1 must be expected. A comparison of HSSW characteristics in the Ronne Depression, our winter observations on the Berkner Shelf, and the ISW flowing out of the Filchner Depression indicates that very little water passes through the cavity from the Ronne to the Filchner Depression. It appears that most of the ISW originating from processes on the Berkner Shelf escapes the cavity in the Filchner Depression. This leaves the Berkner Shelf as the important source of ISW and subsequently of the Weddell Sea Bottom Water formed from ISW.

In the northern Weddell Gyre at the prime meridian, Total TCO2 changes in the Weddell Sea Bottom Water (WSBW) have been investigated. Following a suggestion by [Poisson and Chen, 1987], the TCO2 difference at potential temperatures of 0.2°C and −0.8°C was determined using data from 1996 and 1998. No significant difference was found to similar differences for the years 1973 and 1981 reported by Poisson and Chen. Thus, over a period of 25 years an at most minor amount of anthropogenic CO2 has penetrated into the WSBW at this location. This suggests that this abyssal subpolar region is relatively unimportant for the storage of anthropogenic CO2. The same core of WSBW exhibited a marked increase of chlorofluorocarbon (CFC). For the Southern Ocean, therefore, CFCs are apparently of limited value as analogues of anthropogenic CO2, in contrast to some other ocean provinces.

A light, mining drill rig deployed from the stern of a research vessel has been used to carry out shallow drilling in 212 m water depth on the continental shelf in the eastern Weddell Sea. Penetration was 15 m below the seabed with 18% recovery in the 31 hours available for the experiment. The recovered glacigenic sediments are predominantly volcanic material of basaltic and andesitic composition with petrological characteristics and age similar to the continental flood basalts exposed in Vestfjella, about 130 km upstream from the drill site. The sediments include a reworked marine Miocene diatom flora. The material documents oscillations of the East Antarctic Ice Sheet over the past 30 ka. The lowermost diamicton probably represents a deformation till, and the grounding line retreated past the drill site 30 km from the shelf edge about 30 kyr BP. A readvance occurred during the Late Wisconsin Glacial Maximum. Assuming a reservoir correction of 1300 yr, marine conditions existed at the site between 10.1-7 kyr BP, and later at least between 2.8 and 2.5 kyr BP. The stratigraphy at the site has been disturbed by iceberg ploughing and/or contact between the ice shelf and the sea floor during local advances after 2.5 kyr BP.

A detailed survey of the continental margin in the eastern Weddell Sea demonstrates shelf progradation by material input from discrete glacial wedges that amalgamate to form the present near rectilinear shelf edge. Kvitkuven Ice Rise is located between two trough mouth fans and rests on a thick sediment substratum that predates the shelf sequences north of it. Shelf progradation, west of the ice rise, preceded the progradation east of it. In this way the seaward progression of a shelf edge may reflect the broad scale expansion of the East Antarctic Ice Sheet, but the timing of shelf progradation can be different in adjacent areas. The progradational glacial wedges on the continental shelf mapped by this survey are correlated stratigraphically to be within the post Late Miocene glacial sequence, drilled at ODP Site 693 on the middle continental slope 200 km to the northeast. Two submarine moraine ridge complexes on the shelf parallel the shelf edge. A radiocarbon age of 18:950 ^ 280 years BP from the front of the inner complex (water depth 319 m) suggests that grounded ice at most reached the present mid-shelf area in front of the ice rise during the Late Wisconsin Glacial Maximum, or had retreated to this position at that time.

For ease in discerning an Antarctic circumpolar wave in the perimeter of the ice pack, we construct a time series of the sea ice extents (essentially the area within the ice perimeter) in 1-degree longitudinal sectors for the period 1978-1996, as observed with the multichannel microwave imagers on board the NASA Nimbus 7 and the DOD (Dept. of Defense) DMSP (Defense Meteorological Satellite Program) F8, F11, and F13 satellites. After converting the time series into complex numbers by means of a Hilbert transform, we decompose the time series of the 360 sectors into its complex principal components (CPCs), effectively separating the spatial and temporal values. Then we decompose the real and imaginary parts of the temporal portions of the first three CPCs (complex principal compenents) by Empirical Mode Decomposition into their intrinsic modes, each representing a narrow frequency band, resulting in a collection of three CPCs for each intrinsic mode. Finally, we reconstruct the data in two different ways. First, we low-pass filter the data by combining all of the intrinsic modes of each CPC with periods longer than two years, which we designate as lowpass filtered. Next, we select the intrinsic mode of each CPC with periods of approximately four years, which we designate the quasiquadrennial (QQ) modes. The low-pass filtered time series shows eastward propagating azimuthal motion in the Ross and Weddell Seas, but no clearly circumpolar motion. The QQ time series, on the other hand, clearly shows eastward propagating circumpolar waves, but with occasional retrograde motion to the west.

An infiltration community was the dominating ice algal community in pack-ice off Queen Maud Land, Southern Ocean, in January 1993. The community was dominated by autotrophic processes, and the most common species were the prymnesiophyte Phaeocystis antarctica and the diatoms Chaetoceros neglectus and Fragilariopsis cylindrus. The concentration of chlorophyll a was 1.3–47.9 μg l−1, and the inner part of the community was nitrate depleted. Uptake rates of nitrate, nitrite, ammonium, urea and amino acids were measured using 15N. Nitrate was the major nitrogen source for ice algal growth (67 ± 6% nitrate uptake). It is suggested that % nitrate uptake in the infiltration community decreases during the growth season, from 92% during spring (literature data) to 67% during summer. Scalar irradiance in the infiltration community was high and variable. It reached ca. 2000 μmol m−2 s−1 at some locations, and nitrate uptake rate was potentially photoinhibited at irradiances >500 μmol m−2 s−1. Nitrate uptake rate in an average infiltration community (0.6 m of snow cover) was lowered by 13% over a 2-week period due to photoinhibition.

The efficiency of physical concentration mechanisms for enrichment of algae and bacteria in newly formed sea-ice was investigated under defined conditions in the laboratory. Sea-ice formation was simulated in a 3,000 l tank under different patterns of water movement. When ice formed in an artificially generated current pattern, algal cells were substantially enriched within the ice matrix. Enrichment factors for chlorophyll a calculated from the ratio between the concentrations in ice and underlying water reached values of up to 53. Repeated mixing of ice crystals into the water column, as well as flow of water through the new ice layer, contributed to the enrichment of algae in the ice. Wave action during ice formation revealed lower phytoplankton enrichment factors of up to 9. Mixing of floating ice crystals with underlying water and pumping of water into the ice matrix by periodical expansion and compression of the slush ice layer were responsible for the wave-induced enrichment of algal cells. Physical enrichment of bacteria within the ice was negligible. Bacterial biomass within new ice was enhanced only when the concentration of algae was high. At low algal biomass, bacteria experienced substantial losses in the ice, most likely due to brine drainage, which were not observed for the microalgae. Bacterial cells are therefore not scavenged by ice crystals and the observed enrichment and sustainment of bacterial biomass within newly formed ice depend on their attachment to cells or aggregates of algae. Division rates of bacteria changed only slightly during ice formation.