Isotopic composition and major and trace element concentrations of mafic rocks obtained from western Dronning Maud Land

On the basis of new bulk major and trace element (including REE) as well as Sm-Nd and Rb-Sr isotope data, used in conjunction with available geochronological data, a post-tectonic mafic igneous province and four groups of pre- to syntectonic amphibolite are distinguished in the polymetamorphic Maud Belt of western Dronning Maud Land, East Antarctica. Protoliths of the Group 1 amphibolites are interpreted as volcanic arc mafic intrusions with Archaean to Palaeoproterozoic Nd model ages and depletion in Nb and Ta. Isotopic and lithogeochemical characteristics of this earliest group of amphibolite indicate that the Maud Belt was once an active continental volcanic arc. The most likely position of this arc, for which a late Mesoproterozoic age (c. 1140 Ma) is indicated by available U-Pb single-zircon age data, was on the southeastern margin of the Kaapvaal-Grunehogna Craton. The protoliths of Group 2 amphibolites are attributed to the 1110 Ma Borgmassivet-Umkondo thermal event on the basis of comparable Nd model ages and trace element distributions. Group 3 amphibolite protoliths are characterized by mid-ocean ridge basalt-type REE patterns and low Th/Yb ratios, and they are related to Neoproterozoic extension. Group 4 amphibolite protoliths are distinguished by high Dy/Yb ratios and are attributed to a phase of syntectonic Pan-African magmatism as indicated by Rb-Sr isotope data.

(Table 1) Zoobenthos from the gas-hydrate seep area near the Paramushir Island and its chemical composition

Distributions of Mn, Fe, Cu, Cd, Cr, Co and Ni in sea water are investigated (42 samples, dissolved and particulate forms) in the vicinity of the underwater gas vent field on the northwestern slope of the Paramushir Island. While regular background distributions of the elements occur in the shore zone, there is a column of elevated concentrations of particulate matter, particulate Mn, and dissolved Mn, Fe, Cu, Cd, Cr, Co and Ni that coincides with location of the gas plume. This column can be traced as high as 780 m above the bottom. High metal concentrations in water of the plume are attributable to physico-chemical concentration at the phase interface; the source of elevated mineral concentrations is obviously flux of dissolved minerals from interstitial waters, which extends to considerable distances in vertical direction.

Last Glacial Maximum carbon isotopic composition

We present Holocene and last glacial maximum (LGM) oxygen and carbon isotope measurements on Planulina wuellerstorfi in six southeast Pacific cores. Sedimentation rates are low in this part of the ocean, and measurements were made on individual foraminiferal shells in order to identify the Holocene and glacial individuals on the basis of their extreme d18O. The new d13C data were combined with previous P. wuellerstorfi data for interpretation of global thermohaline circulation. Data from the Southern Ocean were examined closely for regional coherency and a few anomalous d13C values suspected of having productivity overprint were removed. The resulting global d13C distributions and gradients indicate that the deep water circulation was similar during the Holocene and LGM. This interpretation brings d13C data to a better agreement with Cd/Ca data and marks a sharp contrast with a widely held view based on d13C measurements that the glacial Southern Ocean was the terminus of the thermohaline circulation. The proposed presence of glacial North Atlantic Deep Water does not necessarily contradict the postulated presence of Glacial North Atlantic Intermediate Water.

Bulk geochemistry and grain-size composition of surface sediments from the SW Atlantic

Surface sediments from the South American continental margin surrounding tbe Argentine Basin were studied with respect to bulk geochemistry (Caeo) and C ) and grain-size composition (sand/silt/clay relation and terrigenous silt grain-size distribution). The grain-size distributions of the terrigenous silt fraction were unmixed into three end members (EMs), using an end-member modelling algorithm. Three unimodal EMs appear to satisfactorily explain the variations in the data set of the grain-size distributions ofterrigenous silt. The EMs are related to sediment supply by rivers, downslope transport, winnowing, dispersal and re-deposition by currents. The bulk geochemical composition was used to trace the distribution of prominent water masses within the vertical profile. The sediments of the eastern South American continental margin are generally divided into a coarse-grained and carbonate-depleted southwestern part, and a finer-grained and carbonate-rich northeastern part. The transition of both environments is located at the position of the Brazil Malvinas Confluence (BMC). The sediments below the confluence mixing zone of the Malvinas and Brazil Currents and its extensions are characterised by high concentrations of organic carbon, low carbonate contents and high proportions of the intennediate grain-size end member. Tracing these properties, the BMC emerges as a distinct north-south striking feature centered at 52-54°W crossing the continental margin diagonally. Adjacent to this prominent feature in the southwest, the direct detrital sediment discharge of the Rio de la Plata is clearly recognised by a downslope tongue of sand and high proportions of the coarsest EM. A similar coarse grain-size composition extends further south along the continental slope. However, it displays bener sorting due to intense winnowing by the vigorous Malvinas Current. Fine-grained sedimentary deposition zones are located at the southwestern deeper part of the Rio Grande Rise and the southern abyssal Brazil Basin, both within the AABW domain. Less conspicuous winnowing/accumulation panerns are indicated north of the La Plata within the NADW level according to the continental margin topography. We demonstrate that combined bulk geochemical and grain-size properties of surface sediments, unmixed with an end-member algorithm, provide a powerful tool to reconstruct the complex interplay of sedimentology and oceanography along a time slice.

Sterol, n-alcohol and n-alkane composition of living fen plants

In groundwater-fed fen peatlands, the surface biomass decays rapidly and, as a result, highly humified peat is formed. A high degree of humification constrains palaeoecological studies because reliable identification of plant remains is hampered. Organic geochemistry techniques as a means of identifying historical plant communities have been successfully applied tobog peat. The method has also been applied to fen peat, but without reference to the composition of fen plants. We have applied selected organic geochemistry methods to determine the composition of the neutral lipid fractions from 12 living fen plants, to investigate the potential for the distributions to characterize and separate different fen plants and plant groups. Our results show correspondence with previous studies, e.g. C23 and C25n-alkanes dominating Sphagnum spp. and C27 to C31 alkanes dominating vascular plants. However, we also found similarities in n-alkane distributions between Sphagnum spp. and the below ground parts of some vascular plants. We tested the efficiency of different n-alkane ratios to separate species and plant groups. The ratios used for bog studies (e.g. n-C23/n-C25 and n-C23/n-C29) did not work as consistently for fen plants. Some differences in sterol distribution were found between vascular plants and mosses; in general vascular plants had a higher concentration of sterols. When distributions of n-alkanes, n-alkane ratios and sterols were all included as variables, redundancy analysis (RDA) separated different plant groups into their own clusters. Our results imply that the pattern for bog biomarkers cannot directly be applied to fen environments. Nevertheless, they encourage further testing to determine whether or not the identification of plant groups, plants or plant parts from highly humified peat is possible by applying fen species-specific biomarker proxies.

Carbonate and terrigenous content and chemical composition of sediments in the Central Equatorial Pacific

This study addresses changes in the absolute magnitude and spatial geometry of particle flux and export production in a meridional transect across the central equatorial Pacific Ocean's upwelling system during oxygen isotope Stage 11 and Stage 12 and compares these time periods to the current Holocene interglacial system. Temporal and spatial variability in several chemical proxies of export production, and in particular the distributions of Ba, scavenged Al, and P, are studied in a suite of sediment cores gathered along a cross-equator transect at 5°S, 2°S, 0°, 2°N, and 4°N. Because this latitudinal range preserves strong gradients in biogenic particle flux in the modern equatorial Pacific Ocean, we are able to assess variations in the relative magnitude of export production as well as the meridional width of the equatorial system through the late Quaternary glacial/interglacial cycles. During interglacial oxygen isotope Stage 11 the chemical proxies each indicate lower particle flux and export production than during Stage 12. These records are consistent throughout the transect during this time period, but geographic narrowing (during the interglacial) and widening (during the glacial) of the meridional gradient also occurs. Although carbonate concentration varies dramatically through glacial/interglacial cycles at all latitudes studied, the productivity proxies record only minimal glacial/interglacial change at 5°S and 4°N, indicating that the carbonate minima at these latitudes is controlled dominantly by dissolution rather than production. The chemical data indicate that although the spatial geometry of the system during Stages 11 and 12 indicates maximum productivity at the equator during both glacial and interglacial conditions, the absolute magnitude of export production integrated from 5°S to 4°N during Stage 11 was 25-50% less than during Stage 12, and also was 25-50% less than it is now.

(Table 2) Chemical composition of surface sediments from stations of Cruise 11A of R/V Akademik Mstislav Keldysh

Distributions of Mn, Fe, Cu, Cd, Cr, Co and Ni in sea water are investigated (42 samples, dissolved and particulate forms) in the vicinity of the underwater gas vent field on the northwestern slope of the Paramushir Island. While regular background distributions of the elements occur in the shore zone, there is a column of elevated concentrations of particulate matter, particulate Mn, and dissolved Mn, Fe, Cu, Cd, Cr, Co and Ni that coincides with location of the gas plume. This column can be traced as high as 780 m above the bottom. High metal concentrations in water of the plume are attributable to physico-chemical concentration at the phase interface; the source of elevated mineral concentrations is obviously flux of dissolved minerals from interstitial waters, which extends to considerable distances in vertical direction.

Total organic carbon content and maceral composition of sediment at DSDP Holes 72-515B and 72-516F

The amount, type, and thermal maturation of organic matter in sediments from two DSDP holes in the South Atlantic (Leg 72) were investigated. Isolated kerogens were studied by microscopy, and nonaromatic hydrocarbons were characterized by capillary gas chromatography. Organic carbon values are low in all samples and range between 0.05 and 0.21% in Hole 515B (Brazil Basin) and only between 0.02 and 0.10% in Hole 516F (Rio Grande Rise). The organic matter is predominantly terrigenous, mixed with some unicellular marine algae; it is severely oxidized in most samples. N-alkane distributions are usually dominated by long-chain wax alkanes with odd-over-even carbon number predominance; when the marine organic matter is relatively more abundant, however, significant amounts of n-alkanes are centered upon n-C17. The organic matter is not mature enough in any sample to generate appreciable amounts of hydrocarbons.