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In the Southern Ocean near the Antarctic Peninsula, Antarctic Circumpolar Current (ACC) fronts interact with shelf waters facilitating lateral transport of shelf-derived components such as iron into high-nutrient offshore regions. To trace these shelf-derived components and estimate lateral mixing rates of shelf water, we used naturally occurring radium isotopes. Short-lived radium isotopes were used to quantify the rates of shelf water entrainment while Fe/228Ra ratios were used to calculate the Fe flux. In the summer of 2006 we found rapid mixing and significant lateral iron export, namely, a dissolved iron flux of 1.1 × 105 mol d−1 and total acid leachable iron flux of 1.1 × 106 mol d−1 all of which is transported in the mixed layer from the shelf region offshore. This dissolved iron flux is significant, especially considering that the bloom observed in the offshore region (0.5–2 mg chl a m−3) had an iron demand of 1.1 to 4 × 105 mol Fe. Net vertical export fluxes of particulate Fe derived from 234Th/238U disequilibrium and Fe/234Th ratios accounted for only about 25% of the dissolved iron flux. On the other hand, vertical upward mixing of iron rich deeper waters provided only 7% of the lateral dissolved iron flux. We found that similarly to other studies in iron-fertilized regions of the Southern Ocean, lateral fluxes overwhelm vertical inputs and vertical export from the water column and support significant phytoplankton blooms in the offshore regions of the Drake Passage.

Species of the genus Pyramimonas (Prasinophyceae) are a common, widespread, but minor component of the Antarctic marine phytoplankton. They are often associated with the seasonal sea-ice environment. Pyramimonas gelidicola (McFadden, Moestrup & Wetherbee, 1982) was isolated from the water column of a saline Antarctic lake, and observations on the organism’s life history as it grew in unialgal cultures were made. The alga proved to be pleomorphic: capable of producing several morphologically distinct life stages. We recorded motile single-celled quadriflagellates that formed two statistically distinct size classes, a rare uniflagellate cell-type, and aggregations of quadriflagellate cells, multilobed forms and an encystment stage. Multilobed forms and cell aggregations, never before observed in an Antarctic Pyramimonas species, are presumed to be growth medium-induced morphotypes. Multilobed forms contained an equal number of nuclei and lobes, suggesting that they are the product of asexual reproduction. Some of the morphotypes we report here may never be observed under natural field conditions, but the potential for this alga to alternate between morphotypes is clearly demonstrated.

The vertical distribution (0–550 m) of zooplankton biomass, and indices of respiration (electron transfer system [ETS]) and structural growth (aminoacyltRNA synthetases activity [AARS]), were studied in waters off the Antarctic Peninsula during the austral summer of 2000. The dominant species were the copepod Metridia gerlachei and the euphausiid Euphausia superba. We observed a vertical krill/copepod substitution in the water column. The zooplankton biomass in the layer at a depth of 200–500 m was of the same magnitude as the biomass in the layer at a depth of 0–200 m, indicating that biomass in the mesopelagic zone is an important fraction of the total zooplankton in Antarctic waters. The metabolic rates of the zooplankton community were sustained by less than 0.5% of the primary production in the area, suggesting that microplankton or small copepods are the main food source. Neither food availability nor predation seemed to control mesozooplankton biomass. The wide time lag between the abundance peak of the dominant copepod (M. gerlachei) and the phytoplankton bloom is suggested to be the main explanation for the low summer zooplankton biomass observed in these waters.

Two sediment cores obtained from the continental shelf of the northern South Shetland Islands, West Antarctica, consist of: an upper unit of silty mud, bioturbated by a sluggish current, and a lower unit of well-sorted, laminated silty mud, attributed to an intensified Polar Slope Current. Geochemical and accelerator mass spectrometry 14C analyses yielded evidence for a late Holocene increase in sea-ice extent and a decrease in phytoplankton productivity, inferred from a reduction in the total organic carbon content and higher C : N ratios, at approximately 330 years B.P., corresponding to the Little Ice Age. Prior to this, the shelf experienced warmer marine conditions, with greater phytoplankton productivity, inferred from a higher organic carbon content and C : N ratios in the lower unit. The reduced abundance of Weddell Sea ice-edge bloom species (Chaetoceros resting spores, Fragilariopsis curta and Fragilariopsis cylindrus) and stratified cold-water species (Rhizosolenia antennata) in the upper unit was largely caused by the colder climate. During the cold period, the glacial restriction between the Weddell Sea and the shelf of the northern South Shetland Islands apparently hindered the influx of ice-edge bloom species from the Weddell Sea into the core site. The relative increases in the abundance of Actinocyclus actinochilus and Navicula glaciei, indigenous to the coastal zone of the South Shetland Islands, probably reflects a reduction in the dilution of native species, resulting from the diminished influx of the ice-edge species from the Weddell Sea. We also document the recent reduction of sea-ice cover in the study area in response to recent warming along the Antarctic Peninsula.

Investigations into Fe(II) cycling during two Southern Ocean mesoscale iron enrichment experiments, SOFeX and EIFeX, clearly show the importance of Fe(II) to iron speciation during these experiments. In both cases the added Fe(II) persisted significantly longer than its expected oxidation time indicating a significant Fe reduction process at work. During EIFeX diel studies showed a strong photochemically induced cycle in Fe(II) production in sunlit surface waters. Our results suggest that the photochemical cycling of iron may also be important in unfertilized waters of the Southern Ocean.

Diverse microbial communities survive within the sea ice matrix and are integral to the energy base of the Southern Ocean. Here we describe initial findings of a four season survey (between 1999–2004) of community structure and biomass of microalgae within the sea ice and in the underlying water column at Cape Evans and Cape Hallett, in the Ross Sea, Antarctica as part of the Latitudinal Gradient Project. At Cape Evans, bottom-ice chlorophyll a levels ranged from 4.4 to 173 mg Chl a m−2. Dominant species were Nitzschia stellata, N. lecointei, and Entomoneis kjellmanii, while the proportion of Berkeleya adeliensis increased steadily during spring. Despite being obtained later in the season, the Cape Hallett data show considerably lower standing stocks of chlorophyll ranging from 0.11 to 36.8 mg Chl a m−2. This difference was attributed to a strong current, which may have ablated much of the bottom ice biomass and provided biomass to the water below. This loss of algae from the bottom of the ice may explain why the ice community contributed only 2% of the standing stock in the total water column. Dominant species at Cape Hallett were Nitzschia stellata, Fragilariopsis curta and Cylindrotheca closterium. The low biomass at Cape Hallett and the prevalence of smaller-celled diatoms in the bottom ice community indicate that the ice here is more typical of pack ice than fast ice. Further data will allow us to quantify and model the extent to which ice-driven dynamics control the structure and function of the sea ice ecosystem and to assess its resilience to changing sea ice conditions.

The role of iron and light in controlling photosynthate production and allocation in phytoplankton populations of the Atlantic sector of the Southern Ocean was investigated in April–May 1999. The 14C incorporation into five biochemical pools (glucan, amino acids, proteins, lipids and polysaccharides) was measured during iron/light perturbation experiments. The diurnal Chl a-specific rates of carbon incorporation into these pools did not change in response to iron addition, yet were decreased at 20 μmol photons m−2 s−1, an irradiance comparable with the one at 20–45 m in situ depth. This suggests that the low phytoplankton biomass encountered (0.1–0.6 μg Chl a L−1) was mainly caused by light limitation in the deep wind mixed layer (>40 m). Regional differences in Chl a-specific carbon incorporation rates were not found in spite of differences in phytoplankton species composition: at the Antarctic Polar Front, biomass was dominated by a diatom population of Fragilariopsis kerguelensis, whereas smaller cells, including chrysophytes, were relatively more abundant in the Antarctic Circumpolar Current beyond the influence of frontal systems. Because mixing was often in excess of 100 m in the latter region, diatom cells may have been unable to fulfil their characteristically high Fe demand at low average light conditions, and thus became co-limited by both resources. Using a model that describes the 14C incorporation, the consistency was shown between the dynamics in the glucan pool in the field experiments and in laboratory experiments with an Antarctic diatom, Chaetoceros brevis. The glucan respiration rate was almost twice as high during the dark phase as during the light phase, which is consistent with the role of glucan as a reserve supplying energy and carbon skeletons for continued protein synthesis during the night.

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.

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.

Phytoplankton dynamics in the open waters of the ice-edge zone of the Lazarev Sea were investigated over 12 consecutive days during a drogue study conducted in austral summer (December/January) 1994/1995. Throughout the study, the upper water column (<30 m) was stratified with a well-defined pycnocline evident. Although a subsurface intrusion of colder, more saline water into the region was recorded on days 5–9 of the experiment, its effect on the water column structure was negligible. Total surface chlorophyll a biomass doubled between days 1 and 5 (from 0.82 to 1.62 mg m–3), and then showed a tendency to stabilise, while the depth-integrated chlorophyll a standing stock displayed an increasing trend during the entire experiment. All changes in biomass were associated with an increase in microphytoplankton. Flagellates and picoplankton dominated cell counts, while diatoms composed most of the phytoplankton biovolume. Results of the study indicate that, during the period of investigation, average cell abundance decreased. Coupled with this decrease was an increase in the biovolume and average size of the phytoplankton. Phytoplankton succession was observed in the ice edge during the drogue study. Typical ice-associated species of genera Haslea, Fragilariopsis and Chaetoceros, which dominated at the beginning of study, were replaced by open-water species of genera Corethron, Dactyliosolen and Rhizosolenia. The shift in phytoplankton species composition and size can likely be related to high light intensities and grazing by microzooplankton. The intrusion of colder, more saline water on day 5 appeared to modify the diatom succession, indicating extreme variability in phytoplankton dynamics in the near ice-edge zone of the Lazarev Sea.