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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.

The extent of ice, thickness and dynamics of the Last Glacial Maximum (LGM) ice sheets in the Antarctic Peninsula region, as well as the pattern of subsequent deglaciation and climate development, are not well constrained in time and space. During the LGM, ice thickened considerably and expanded towards the middle–outer submarine shelves around the Antarctic Peninsula. Deglaciation was slow, occurring mainly between >14 Ky BP (14C kilo years before present) and ca. 6 Ky BP, when interglacial climate was established in the region. After a climate optimum, peaking ca. 4 - 3 Ky BP, a cooling trend started, with expanding glaciers and ice shelves. Rapid warming during the past 50 years may be causing instability to some Antarctic Peninsula ice shelves.

To investigate recent variability in accumulation and δ18O, we synthesize data from five snow cores, covering the period 1932–96, from the sector 16˚38’ W–4˚48’ E in coastal Dronning Maud Land (DML), Antarctica. the δ18O records from the different sites are remarkably similar and suggest a common stable moisture source for this coastal section of DML. While the accumulation pattern is local, and specific features restricted to the individual sites, the overall accumulation pattern is related to the temperature variability as indicated by coastal instrumental records. Accumulation and δ18O correlate between 1955 and 1985 but deviate thereafter, with the proxy-temperature record showing a positive trend while accumulation decreased. This occurs at the same time as an increase in sea-ice extent in the area, which may have resulted in circulation changes and more northerly storm paths. Both stacked accumulation and δ18O records show that large-scale atmospheric signals, as well as some pronounced individual events, are recorded in DML coastal ice cores.

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

Further details regarding the landing made by Klarius Mikkelsen in the Tryne Islands, Vestfold Hills, East Antarctica, are given, being derived mainly from newspaper accounts made by Leif Sørsdal. All involved in the landing on 20 February 1935 have been identified, details of material left in the depot under the raised flag are given, and more extended information relating to the voyage to and from the site and the area generally are presented. Some comparison is made between Sørsdal's accounts and others. While the national importance of the landing was commented on, only Sørsdal apparently realised (but did not state) the insular nature of the site. Recent observations at the site suggest that its location is 68°22′38.22″S, 78°24′50.10″E, rather than that previously stated; bracing of the flagpole itself has been modified at some stage since its erection. Finally, some discussion is made regarding on-going questions relating to the accepted time on board ship, and possible consequences of errors.

ABSTRACT: Hydrography, chlorophyll <i>a</i>, phytoplankton and zooplankton dynamics and the vertical flux of particulate organic carbon (POC) and pigments in the upper 200 m were investigated for 12 consecutive days during a drogue study conducted in the open waters of the ice-edge zone of the Lazarev Sea during the austral summer (December/January) 1994/95. Results of the study indicate that during the experiment, primary production, although variable, increased from ~300 to ~800 mgC m^-2d^-1. This increase could likely be related to development of a shallow pycnocline. Analysis of sediment trap data showed that the vertical carbon flux resulting from sedimentation and grazing activity was greatest in the upper water column (<80 m). The importance of grazers to total POC flux was highest at the beginning and the end of the investigation and accounted for up to 15% of total carbon flux. The contribution of grazers to vertical flux was negligible (<2%) during the intermediate part of the Southern Ocean Drogue study. Lower contribution of grazers to sedimentation of POC at depth can likely be related to community composition of zooplankton. Sedimentation of phytoplankton cells from the upper water column increased during the study. Here, downward POC flux resulting from sedimentation of microphytoplankton was equivalent to 15-75% of the total. Increase in sedimentation of phytoplankton during the study can be related to an increase in the average size of phytoplankton cells. Transport of POC from surface waters to deeper depths resulting from sedimentation or grazing activity was equivalent to <48% of total daily primary production, measured at 50 m, while the same value for phytoplankton flux did not exceed 27% of the total. Zooplankton density was insufficient to exert either a positive (via faecal pellets) or negative (via reducing suspended phytoplankton concentration) effect on particulate carbon sedimentation. This resulted in algal sink being the most important mechanism in downward POC flux during the onset of the phytoplankton bloom period in the Marginal Ice Zone, even in the presence of pelagic tunicates.

Much evidence suggests that life originated in hydrothermal habitats, and for much of the time since the origin of cyanobacteria (at least 2·5 Ga ago) and of eukaryotic algae (at least 2·1 Ga ago) the average sea surface and land surface temperatures were higher than they are today. However, there have been at least four significant glacial episodes prior to the Pleistocene glaciations. Two of these (approx. 2·1 and 0·7 Ga ago) may have involved a ‘Snowball Earth’ with a very great impact on the algae (sensu lato) of the time (cyanobacteria, Chlorophyta and Rhodophyta) and especially those that were adapted to warm habitats. By contrast, it is possible that heterokont, dinophyte and haptophyte phototrophs only evolved after the Carboniferous–Permian ice age (approx. 250 Ma ago) and so did not encounter low (≤5 °C) sea surface temperatures until the Antarctic cooled some 15 Ma ago. Despite this, many of the dominant macroalgae in cooler seas today are (heterokont) brown algae, and many laminarians cannot reproduce at temperatures above 18–25 °C. By contrast to plants in the aerial environment, photosynthetic structures in water are at essentially the same temperature as the fluid medium. The impact of low temperatures on photosynthesis by marine macrophytes is predicted to favour diffusive CO2 entry rather than a CO2‐concentrating mechanism. Some evidence favours this suggestion, but more data are needed.

Ground-based zenith sky UV–visible measurements of stratospheric bromine monoxide (BrO) slant column densities are compared with simulations from the SLIMCAT three-dimensional chemical transport model. The observations have been obtained from a network of 11 sites, covering high and midlatitudes of both hemispheres. This data set gives for the first time a near-global picture of the distribution of stratospheric BrO from ground-based observations and is used to test our current understanding of stratospheric bromine chemistry. In order to allow a direct comparison between observations and model calculations, a radiative transfer model has been coupled to the chemical model to calculate simulated slant column densities. The model reproduces the observations in general very well. The absolute amount of the BrO slant columns is consistent with a total stratospheric bromine loading of 20 ± 4 ppt for the period 1998–2000, in agreement with previous estimates. The seasonal and latitudinal variations of BrO are well reproduced by the model. In particular, the good agreement between the observed and modeled diurnal variation provides strong evidence that the BrO-related bromine chemistry is correctly modeled. A discrepancy between observed and modeled BrO at high latitudes during events of chlorine activation can be resolved by increasing the rate constant for the reaction BrO + ClO → BrCl + O2 to the upper limit of current recommendations. However, other possible causes of the discrepancy at high latitudes cannot be ruled out.

In Procellariiformes, parents guard the chick for some time after it has attained homeothermy. Such a strategy may have evolved to protect the chick from predation or inclement weather, but it is costly because only one parent can forage at a time. Therefore, the decision to leave the chick seems to be a trade-off between the chick's ability to care for itself, body condition of the parent present at the nest, and ability of the bird out foraging to return to the nest before its mate's body condition has degraded. We studied chick growth and survival together with number of days Snow Petrel (Pagodroma nivea) chicks were guarded before being left alone for the first time in relation to the parents body condition and ability to return to the nest in time. Parents in good body condition were more likely to produce a chick that survived the guard stage. They also guarded their chick for a longer period (range 2–8 days, x̄ = 4.5) and finally left it alone with a higher body mass than those in poor body condition. However, whether the foraging bird was able to return to the nest in time to relieve its mate was also strongly related to number of days the chick was guarded and its body mass. The chicks' survival from when they were left alone and until day 10 posthatch was positively related both to number of days they were guarded and their body condition (body mass corrected for age).

Protease-producing psychrotolerant bacteria were isolated from Antarctic biotopes on casein agar plates using different incubation temperatures. Most of the isolates were non-spore-forming Gram-negative motile rods with catalase activity, 30% were pigmented and none of them were glucose fermenters. All the strains were grown in liquid cultures at 20°C and protease secretion was tested using the azocasein method. Despite their capacity for production of a clear zone of hydrolysis in agar plates, some strains did not produce detectable levels of proteolytic activity in liquid cultures. The lowest apparent optimum temperature for protease activity found in culture supernatants was 40°C. Almost all the strains showed activation energy values about 10-20 kJ-mol?1 lower than that observed for a mesophilic Subtilisin. Most of the proteases showed optimal activity at neutral or alkaline pH values and developed a multiple-band profile on gelatine-SDS-PAGE. It was observed that the lower the strain isolation temperature was, the more stongly cold-adapted–in terms of optimal temperature and activation energy–were the proteases produced by them. This dependence of the characteristics of the proteases on the isolation temperature is an important factor to take into account in the design of screening programmes directed towards the isolation of psychrotolerant bacteria able to produce proteases strongly or weakly adapted to work in the cold. The Antarctic area explored proved to be a promising source of proteolytic bacteria with potential use in industrial processes to be carried out at low or moderate temperatures.

We present evidence for the absence of the George VI Ice Shelf during a brief period in the mid-Holocene and during one or more earlier interstadials or interglacials. Barnacle Bathylasma corolliforme shells sampled from ice shelf moraines at Two Step Cliffs on Alexander Island have been dated to c, 5750–6000 14C yr BP(c. 6550–6850 cal yr BP) and imply seasonally open water in the George VI Sound during this period. Other shells are beyond the range of radiocarbon dating and imply open water during one or more previous interglacial or interstadial period, prior to 40 000 14C yr BP. Our results show that the ongoing collapse of some Antarctic Peninsula ice shelves is not unprecedented.

Stegosoladidus simplex (K. H. Barnard, 1930) and S. ingens (Chevreux, 1906) are both figured and redescribed. Three new species (Stegosoladidus antarcticus, S. complex and S. debroyeri) are described. The terminology used for classification of both setae and different setae arrangements is discussed, and the main types of setae are figured.