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Shipboard hydrography and current profiles collected in 2003 and time series from moored current meters deployed in late 1990s are analyzed to study the variability of mixing in the southeastern Weddell Sea. Profiles of eddy diffusivity Kρ are inferred from fine-scale shear (vertical derivative of horizontal velocity) and strain (vertical derivative of isopycnal displacement) variance using parameterizations which relate the internal wave energy to the dissipation rate at small scales. The highest mixing rates are seen near the bottom where the eddy diffusivities are elevated by 1 order of magnitude from those in the interior and exceed 10−4 m2 s−1. The observations show latitudinal variability in Kρ, particularly near the bottom, where Kρ significantly increases near 74° 28′S, the critical latitude for lunar semidiurnal (M2) tides. In this region, the critical latitude coincides with near-critical topography on the upper continental slope, a situation which favors generation of M2 internal waves. Consistent with the results from fine-scale shear and strain parameterizations, which indicate highest bottom diffusivities near the critical latitude, independent analysis of current time series from moored instruments shows a thickening of the frictional bottom boundary layer near the critical latitude. Semidiurnal tidal dynamics at the upper continental slope together with the critical latitude effects lead to mixing that might significantly affect the regional heat budget and the circulation in the study area.

Polar regions are particularly sensitive to climate change, with the potential for significant feedbacks between ocean circulation, sea ice, and the ocean carbon cycle. However, the difficulty in obtaining in situ data means that our ability to detect and interpret change is very limited, especially in the Southern Ocean, where the ocean beneath the sea ice remains almost entirely unobserved and the rate of sea-ice formation is poorly known. Here, we show that southern elephant seals (Mirounga leonina) equipped with oceanographic sensors can measure ocean structure and water mass changes in regions and seasons rarely observed with traditional oceanographic platforms. In particular, seals provided a 30-fold increase in hydrographic profiles from the sea-ice zone, allowing the major fronts to be mapped south of 60°S and sea-ice formation rates to be inferred from changes in upper ocean salinity. Sea-ice production rates peaked in early winter (April?May) during the rapid northward expansion of the pack ice and declined by a factor of 2 to 3 between May and August, in agreement with a three-dimensional coupled ocean?sea-ice model. By measuring the high-latitude ocean during winter, elephant seals fill a ?blind spot? in our sampling coverage, enabling the establishment of a truly global ocean-observing system.

A distinctive halo of sea ice deformation was observed above the Maud Rise seamount in the eastern Weddell Sea in the winter of 2005. The deformation halo is coincident with a halo of low mean ice concentration that is often observed in the region. Monthly mean ice vorticity estimates for the months July through November reveal the deformation zone most clearly in an arc about 100 km northwest of the seamount where there is a strong gradient in the bathymetry at depths of 3000–5000 m. The deformation was computed from satellite-based ice motion vectors derived from Envisat Synthetic Aperture Radar backscatter images. The deformation halo is evidence of a Taylor cap circulation over the seamount, which has been described and analyzed with modeling studies and concurrent oceanographic observations obtained during an extensive field campaign.

Model simulations of circulation and melting beneath Fimbulisen, Antarctica, obtained using an isopycnic coordinate ocean model, are presented. Model results compare well with available observations of currents and hydrography in the open ocean to the north of Fimbulisen and suggest that Warm Deep Water exists above the level of a sub-ice-shelf bedrock sill, the principal pathway for warm waters to enter the sub-ice-shelf cavity. The model shows a southward inflow of Warm Deep Water over this sill and into the cavity, producing a mean cavity temperature close to −1.0°C. This leads to high levels of basal melting (>10 m/a) at the grounding line of Jutulstraumen and an average melting over the ice shelf base close to 1.9 m/a. The southward inflow is a compensating flow caused by the northward outflow of fresh, cold water produced by the basal melting. Results on inflow and melting are difficult to validate since no in situ measurements yet exist in the cavity. If such high melt rates are realistic, the mass balance of Fimbulisen must be significantly negative, and the ice shelves along Dronning Maud Land must contribute about 4.4 mSv of melt water to the Weddell Sea, about 15% of the total Antarctic meltwater input to the Southern Ocean.

This study explores the changes in the surface water fugacity of carbon dioxide (fCO2) and biological carbon uptake in two Southern Ocean iron fertilisation experiments with different hydrographic regimes. The Southern Ocean Iron Release Experiment (SOIREE) experiment was carried out south of the Antarctic Polar Front (APF) at 61°S, 141°E in February 1999 in a stable hydrographic setting. The EisenEx experiment was conducted in a cyclonic eddy north of the APF at 48°S, 21°E in November 2000 and was characterised by a rapid succession of low to storm-force wind speeds and dynamic hydrographic conditions. The iron additions promoted algal blooms in both studies. They alleviated algal iron limitation during the 13-day SOIREE experiment and probably during the first 12 days of EisenEx. The fCO2 in surface water decreased at a constant rate of 3.8μatmday−1 from 4 to 5 days onwards in SOIREE. The fCO2 reduction was 35μatm after 13 days. The evolution of surface water fCO2 in the iron-enriched waters (or ‘patch’) displayed a saw tooth pattern in EisenEx, in response to algal carbon uptake in calm conditions and deep mixing and horizontal dispersion during storms. The maximum fCO2 reduction was 18–20μatm after 12 and 21 days with lower values in between. The iron-enriched waters in EisenEx absorbed four times more atmospheric CO2 than in SOIREE between 5 and 12 days, as a result of stronger winds. The total biological uptake of inorganic carbon across the patch was 1389ton C (±10%) in SOIREE and 1433ton C (±27%) in EisenEx after 12 days (1ton=106g). This similarity probably reflects the comparable size of the iron additions, as well as algal growth at a similar near-maximum growth rate in these regions. The findings imply that the different mixing regimes had less effect on the overall biological carbon uptake across the iron-enriched waters than suggested by the evolution of fCO2 in surface water.

A suite of standard ocean hydrographic and circulation metrics are applied to the equilibrium physical solutions from 13 global carbon models participating in phase 2 of the Ocean Carbon-cycle Model Intercomparison Project (OCMIP-2). Model-data comparisons are presented for sea surface temperature and salinity, seasonal mixed layer depth, meridional heat and freshwater transport, 3-D hydrographic fields, and meridional overturning. Considerable variation exists among the OCMIP-2 simulations, with some of the solutions falling noticeably outside available observational constraints. For some cases, model-model and model-data differences can be related to variations in surface forcing, subgrid-scale parameterizations, and model architecture. These errors in the physical metrics point to significant problems in the underlying model representations of ocean transport and dynamics, problems that directly affect the OCMIP predicted ocean tracer and carbon cycle variables (e.g., air-sea CO2 flux, chlorofluorocarbon and anthropogenic CO2 uptake, and export production). A substantial fraction of the large model-model ranges in OCMIP-2 biogeochemical fields (±25–40%) represents the propagation of known errors in model physics. Therefore the model-model spread likely overstates the uncertainty in our current understanding of the ocean carbon system, particularly for transport-dominated fields such as the historical uptake of anthropogenic CO2. A full error assessment, however, would need to account for additional sources of uncertainty such as more complex biological-chemical-physical interactions, biases arising from poorly resolved or neglected physical processes, and climate change.

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.