Abundance and biomass of planktonic diatom Proboscia alata and associated species, chlorophyll a, organic carbon and nitrogen concentrations in waters over the Bering Sea middle shelf in August 2001

During most of the vegetation season from late May to early September large-sized diatom alga Proboscia alata forms local patches with high abundances and biomasses in different oceanographic domains of the eastern Bering Sea shelf. For 0-25 m layer average abundance and biomass of species in these patches are 700000 cells/l and 5 g/m**3 (wet weight), while corresponding estimates for the layer of maximal species concentrations are 40000000 cells/l and 38 g/m**3 (wet weight) or 1.6 g C/m**3. These levels of abundance and biomass are typical for the spring diatom bloom in the region. Outbursts of P. alata mass development are important for the carbon cycle in the pelagic zone of the shelf area in the summer season. The paradox of P. alata summertime blooms over the middle shelf lies in their occurrences against the background of the sharp seasonal pycnocline and deficiency in nutrients in the upper mixed layer. Duration of the outbursts in P. alata development is about two weeks and size of patches with high abundances can be as large as 200 km across. Degradation of the P. alata summertime outbursts may occur during 4-5 days. Rapid sinking of cells through the seasonal pycnocline results in intense transport of organic matter to bottom sediments. One of possible factors responsible for rapid degradation of the blooms is affect on the population by ectoparasitic flagellates. At terminal stages of the P. alata blooms percentage of infected cells can reach 70-99%.

Lithostatigraphy of the CESAR cores

Sixteen piston cores and twelve gravity cores were successfully recovered from northern and southern crests of the eastern Alpha Ridge andfrom the Alpha Ridge graben. All but one core contain late Cenozoic muds with variable amounts of sand- to pebble-sized clastic material that probably reflects transport by ice during the past 4-5 Ma. Sixteen Cenozoic-Holocene lithostratigraphic units have been delimited on the basis of sediment texture, structure, colour, detrital carbonate and authigenicferromanganese content. The composition of the upper 13 units in the CESAR cores is similar to the Fletcher's Ice Island cores; hence most units can be broadly correlated over most of the Central Arctic Ocean. Three new lithostratigraphic units (A1-A3) occur at the base of CESAR cores from the northern Alpha Ridge crest. Paleomagnetic and palynological data indicate a Late Miocene-Early Pliocene age for unit A3, which confirms previous reports of a slow sedimentation rate during the Cenozoic. CESAR core 6 was obtained from an erosional surface on top of a fault block at the north edge of the Alpha Ridge graben. This core contains ca. 2m of laminated diatom ooze of Campanian-Maastrichtian age and two ?Paleogene volcanic ash units below a brown mud unit which probably corresponds to units A2 and A3. The biosiliceous ooze contains no foraminifera or silicoflagellates and only few dinoflagellates. There is little difference in biogenic or clastic sediment content between light and dark laminae and the rhythmites do not appear to be annual varves produced in an upwelling environment. The microstructure and fluctuating mineral composition of the laminae most closely resemble those of lami- nated chert beds in the Triassic forearc basins of Japan.

210Pb dates, radiocarbon ages and sedimentation and accumulation rates of sediment cores JM99-1198 and MD99-2297

The magnitude of Late Holocene climatic variations are less significant than those that took place during ice ages and deglaciations. However, detailed knowledge about this period is vital in order to understand and model future climate scenarios both as a result of natural climate variation and the effects of global warming. Oceanic heat flux is important for the sensitive climate regime of northern Europe. Our aim is to connect hydrographical changes, reflected by the dinoflagellates cyst (dinocysts) assemblages in the sediments in the Malangen fjord, to local and regional climatic phases. Previous studies have shown that dinocyst assemblages are influenced by temperature, salinity, and the availability of nutrients (e.g. de Vernal et al. 2005, doi:10.1016/j.quascirev.2004.06.014; de Vernal et al. 2001, doi:10.1002/jqs.659; Grosfjeld et al. this volume; Rochon et al. 2008, doi:10.1016/j.marmicro.2008.04.001; Solignac et al. this volume). Dinoflagellates are mostly unicellular organisms that make up one of the main groups of phytoplankton. They are able to regulate their depth within the photic zone and to concentrate along oceanic fronts, which provide nutrient-enriched waters. The dinoflagellate cysts are the hypnozygotes of dinoflagellates naturally produced during the life cycle. Their wall is composed of a highly resistant organic material, which has a high potential to fossilize. Because dinocysts species are linked to particular abiotic and biotic parameters, the dinocyst assemblages provide information about past surface water conditions. Since each fjord has its own hydrographic setting, it is necessary to establish a firm link between the dinocyst composition of the sediment surface samples and the surface water conditions. Indeed the modern dinocyst distribution in subarctic fjords is little known. Thus, in addition to detailing dinocyst results from two shallow cores, several sediment surface samples located along a transect running from the head to the mouth of the fjord, and extending onto the shelf, are also presented.