999 resultados para Barents Sea


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This study focused on the bacterial diversity associated with microbial mats of deep-sea cold seeps at the Norwegian continental margin. Study sites included the Storegga and Nyegga areas as well as the Håkon Mosby mud volcano, where the mats occurred at temperatures permanently close to the freezing point of seawater. Two visually different mat types, i.e. small gray mats and extensive white mats, were studied with the aim to determine the identity of the mat-forming sulfide oxidizers, and to investigate which environmental factors (e.g. sulfate reduction and methane oxidation rates) shown here could explain the observed diversity. Sequence data have been submitted to the EMBL database under accession No. FR847864-FR847887 (giant sulfur bacteria), No. FR827864 (Menez Gwen filament; see Supplementary Material) and No. FR875365-FR877509 (except FR875905; remaining partial sequences).

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The data show the survival data of Atlantic cod larvae from two different stocks, which were measured in two separate experiments in Kristineberg, Sweden in 2013 on the Western Baltic stock and in Tromsö, Norway in 2014 on the Barents Sea stock. Survival was measured as a response to ocean acidification, control tanks were kept at ambient CO2 concentrations. CO2 concentrations and feeding concentrations are also provided.

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In September-October 1998, during Cruise 14 of R/V Akademik Fedorov to the Barents Sea, in the region of 82° N between the Spitsbergen and Novaya Zemlya archipelagos samples of snow and ice were collected within four polygons. By means of atomic absorption with an electothermal atomizer (onboard the ship) in filtered (dissolved form) and unfiltered (sum of dissolved and particulate forms) samples of snow melt and ice melt concentrations of Fe, Mn, Cu, Cr, Ni, Co, Pb, and Cd were determined in order to estimate level of potential contamination of snow and ice with these metals. Excluding data on Ni, Cd (and probably Cu) in ice that were regarded to be unsatisfactory because of probable contamination of the ice samples during drilling concentrations of all the elements in snow and ice of the northern part of the Barents Sea appeared to be close to their background values or below. An attempt to identify the main sources of metal supply to snow from the atmosphere by comparison of ratios of metal particulate form to total content in snow of the Barents Sea and the same ratios in snow samples from clean regions of Finland and from contaminated areas of the Kola Peninsula showed that aerosols in the area of the expedition were supplied into the Barents Sea atmosphere from different sources, both natural and anthropogenic.

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Based on a revised chronostratigraphy, and compilation of borehole data from the Barents Sea continental margin, a coherent glaciation model is proposed for the Barents Sea ice sheet over the past 3.5 million years (Ma). Three phases of ice growth are suggested: (1) The initial build-up phase, covering mountainous regions and reaching the coastline/shelf edge in the northern Barents Sea during short-term glacial intensification, is concomitant with the onset of the Northern Hemisphere Glaciation (3.6-2.4 Ma). (2) A transitional growth phase (2.4-1.0 Ma), during which the ice sheet expanded towards the southern Barents Sea and reached the northwestern Kara Sea. This is inferred from step-wise decrease of Siberian river-supplied smectite-rich sediments, likely caused by ice sheet blockade and possibly reduced sea ice formation in the Kara Sea as well as glacigenic wedge growth along the northwestern Barents Sea margin hampering entrainment and transport of sea ice sediments to the Arctic-Atlantic gateway. (3) Finally, large-scale glaciation in the Barents Sea occurred after 1 Ma with repeated advances to the shelf edge. The timing is inferred from ice grounding on the Yermak Plateau at about 0.95 Ma, and higher frequencies of gravity-driven mass movements along the western Barents Sea margin associated with expansive glacial growth.

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Biogeochemical cycle of methane in the Barents Sea was studied using isotope geochemistry to determine rates of microbial methane oxidation. It was established that microbiological processes (glucose consumption, 14CO2 assimilation, sulfate reduction, and slow methane oxidation) in oxidized surface and weakly reduced sediments are marked by only insignificant change in SO4 concentration and absence of notable increase of total alkalinity and N/NH4 downward sediment cores. Microbial methane productivity was 0.111x10**6 mol/day. Taking into account volume of the water column, microbial methane consumption therein can be as much as 1.8x10**6 mol/day.