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The distribution of calcareous dinoflagellates has been analysed for the Maastrichtian–Miocene interval of Ocean Drilling Project Hole 689B (Maud Rise, Weddell Sea). The investigation thus represents a primary evaluation of the long-term evolution in high-latitude calcareous dinoflagellate assemblages during the transition from a relatively warm Late Cretaceous to a cold Neogene climate. Major assemblage changes during this interval occurred in characteristic steps: (1) an increase in relative abundance of tangentially structured species – particularly Operculodinella operculata – at the Cretaceous/Tertiary boundary; (2) a diversity decrease and several first and last appearances across the Middle–Late Eocene boundary, possibly attributed to increased climate cooling; (3) a diversity decrease associated with the dominance of Calciodinellum levantinum in the late Early Oligocene; (4) the reappearance and dominance of Pirumella edgarii in the Early Miocene, probably reflecting a warming trend; (5) monogeneric assemblages dominated by Caracomia spp. denoting strong Middle Miocene cooling. The results not only extend the biogeographic ranges of many taxa into the Antarctic region, but also indicate that the evolution of high-latitude calcareous dinoflagellate assemblages parallels the changing environmental conditions in the course of the Cenozoic climate transition. Therefore, calcareous dinoflagellates contribute to our understanding of the biotic effects associated with palaeoenvironmental changes and might possess the potential for reconstructing past conditions. The flora in the core includes one new taxon: Caracomia arctica forma spinosa Hildebrand-Habel and Streng, forma nov. Additionally, two new combinations are proposed: Fuettererella deflandrei (Kamptner, 1956) Hildebrand-Habel and Streng, comb. nov. and Fuettererella flora (Fütterer, 1990) Hildebrand-Habel and Streng, comb. nov.

Sediment textural properties and total organic carbon (TOC) contents of three sediment cores from Maxwell Bay, King George Island, West Antarctica, record changes in Holocene glaciomarine sedimentary environments. The lower sedimentary unit is mostly composed of TOC-poor diamictons, indicating advanced coastal glacier margins and rapid iceberg discharge in proximal glaciomarine settings with limited productivity and meltwater supply. Fine-grained, TOC-rich sediments in the upper lithologic unit suggest more open water and warm conditions, leading to enhanced biological productivity due to increased nutrient-rich meltwater supply into the bay. The relationship between TOC and total sulfur (TS) indicates that the additional sulfur within the sediment has not originated from in situ pyrite formation under the reducing condition, but rather may be attributed to the detrital supply of sand-sized pyrite from the hydrothermal-origin, quartz-pyrite rocks widely distributed in King George Island. The evolution of bottom-water hydrography after deglaciation was recorded in the benthic foraminiferal stable-isotopic composition, corroborated by the TOC and lithologic changes. The Ø18O values indicate that bottom-water in Maxwell Bay was probably mixed gradually with intruding 18O-rich seawater from Bransfield Strait. In addition, the Ø13C values reflect a spatial variability in the carbon isotope distribution in Maxwell Bay, depending on marine productivity as well as terrestrial carbon fluxes by meltwater discharge. The distinct lithologic transition, dated to approximately 8000 yr BP (uncorrected) and characterized by textural and geochemical contrasts, highlights the postglacial environmental change by a major coastal glacier retreat in Maxwell Bay.

We use new data from the southern Weddell Sea continental shelf to describe water mass conversion processes in a formation region for cold and dense precursors of Antarctic Bottom Water. The cruises took place in early 1995, 1998, and 1999, and the time series obtained from moored instruments were up to 30 months in length, starting in 1995. We obtained new bathymetric data that greatly improve our definition of the Ronne Depression, which is now shown to be limited to the southwestern continental shelf and so cannot act as a conduit to northward flow from Ronne Ice Front. Large-scale intrusions of Modified Warm Deep Water (MWDW) onto the continental shelf occur along much of the shelf break, although there is only one location where the MWDW extends as far south as Ronne Ice Front. High-Salinity Shelf Water (HSSW) produced during the winter months dominates the continental shelf in the west. During summer, Ice Shelf Water (ISW) exits the subice cavity on the eastern side of the Ronne Depression, flows northwest along the ice front, and reenters the cavity at the ice front's western limit. During winter the ISW is not observed in the Ronne Depression north of the ice front. The flow of HSSW into the subice cavity via the Ronne Depression is estimated to be 0.9 ± 0.3 Sv. When combined with inflows along the remainder of Ronne Ice Front (reported elsewhere), sufficient heat is transported beneath the ice shelf to power an average basal melt rate of 0.34 ± 0.1 m yr−1.

Longlines that sink fast reduce the time available to seabirds to attack baited hooks and are important in efforts to minimise seabird by-catch in longline fisheries. We measured sink rates in still seawater of longlines commonly used in the world’s demersal fisheries. Lines with integrated weight (lead cores) sank two to three times faster (45–52cm/s) than conventional (unweighted) lines. Conventional 9mm diameter lines made from polyester sank at 23cm/s compared to 18cm/s for 9mm Silver lines (blend of polyester, polyethylene and polypropylene). Samples of lines set by hand in still water sank significantly faster than longlines set from a fishing vessel, presumably because of the effect of the sea swell and upwellings from the propeller on the line set from the vessel.

We present mid-Pliocene (4.3–2.6 Ma) benthic stable oxygen and carbon isotope data from Ocean Drilling Program Site 1092 (ODP Leg 177) drilled in the sub-Antarctic sector of the Southern Ocean. The results are compared with the stable isotope results from nearby Site 704 (ODP Leg 114). Oxygen isotope data show that minimum values are about 0.5‰ less than those of the Holocene, which is consistent with the results from Site 704, indicating only minor deglaciation of Antarctica during the studied interval. Oxygen isotope data from both Site 1092 and Site 704 are slightly higher relative to Pacific values during several intervals which could be related to the contribution of warm, saline North Atlantic Deep Water (NADW). Comparisons of benthic carbon isotope gradients between sites located in the North Atlantic, sub-Antarctic sector of the Southern Ocean, and Pacific indicate that at times, the gradient between the Southern Ocean and the Pacific evolved differently than the Atlantic–Pacific gradient. This suggests that variations in NADW strength alone might not be responsible for the observed carbon isotope values in the Southern Ocean.

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.

Marine soft sediments comprise one of the largest and oldest habitats in the world, yet remarkably little is known about patterns of species richness. Here I present a short review of patterns of species richness and possible factors that influence such patterns. Species richness in general is remarkably high in both shallow coastal areas and the deep sea. However, there are clear differences the deep-sea has higher number of species for a given number of individuals than the coast. This can be explained by the larger amounts of primary production that reach coastal compared with deep-sea sediments, leading to higher numbers of individuals per unit area. Species density (the number of species per unit area) is also higher in the deep-sea than in coastal areas, but it is not obvious why this is so. Most studies of the broad patterns of species richness have used samples taken at small scales only. The problem with such analyses is that unless a large number of samples are taken, the true underlying pattern (or lack of it) may be wrongly interpreted. Recent studies have analysed species richness at larger scales. In general there seems to be a cline of increasing species richness from the Arctic to the tropics, but this is not the case in the southern hemisphere, where Antarctic species richness is high. However, it is not known whether high species richness in the Antarctic occurs at all spatial scales. To what extent these patterns are determined by evolutionary factors remains to be determined by the application of molecular methods. The available evidence suggests that environmental factors such as productivity, temperature, and sediment grain-size diversity play dominant roles in determining patterns of regional-scale species richness and patterns in species turnover, and it is probably the regional scale that primarily determines local species richness. KEYWORDS: Diversity · Deep sea · Coasts · Patterns · Scales