Age models of ODP sites from the Barents Sea-Svalbard region

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.

Files of figures 2, 3 and table

Certain allelochemicals of the marine dinoflagellate Alexandrium tamarense cause lysis of a broad spectrum of target protist cells but the lytic mechanism is poorly defined. We first hypothesized that membrane sterols serve as molecular targets of these lytic compounds, and that differences in sterol composition among donor and target cells may cause insensitivity of Alexandrium and sensitivity of targets to lytic compounds. We investigated Ca2+ influx after application of lytic fractions to a model cell line PC12 derived from a pheochromocytoma of the rat adrenal medulla to establish how the lytic compounds affect ion flux associated with lysis of target membranes. The lytic compounds increased permeability of the cell membrane for Ca2+ ions even during blockade of Ca2+ channels with cadmium. Results of a liposome assay suggested that the lytic compounds did not lyse such target membranes non-specifically by means of detergent-like activity. Analysis of sterol composition of isolates of A. tamarense and of five target protistan species showed that both lytic and non-lytic A. tamarense strains contain cholesterol and dinosterol as major sterols, whereas none of the other tested species contain dinosterol. Adding sterols and phosphatidylcholine to a lysis bioassay with the cryptophyte Rhodomonas salina for evaluation of competitive binding indicated that the lytic compounds possessed apparent high affinity for free sterols and phosphatidylcholine. Lysis of protistan target cells was dose-dependently reduced by adding various sterols or phosphatidylcholine. For three tested sterols, the lytic compounds showed highest affinity towards cholesterol followed by ergosterol and brassicasterol. Cholesterol comprised a higher percentage of total sterols in plasma membrane fractions of A. tamarense than in corresponding whole cell fractions. We conclude therefore that although the molecular targets of the lytic compounds are likely to involve sterol components of membranes, A. tamarense must have a complex self-protective mechanism that still needs to be addressed.