Rates of organic matter transformation within the production-destruction cycle of the White Sea

Rates of organic matter (OM) transformation within the production-destruction cycle of the White Sea were estimated on the basis of measured activity values of redox enzymes of the electron transport system and of hydrolytic enzymes (phosphatase and protease). It was found that OM oxidation processes were the most intensive in the Kandalaksha Bay, while minimum oxidation rates were characteristic of central parts of the Dvina and Onega bays. It was revealed that the highest rates of phosphate mineralization were characteristic of the central part of the sea and near-mouth areas of the Onega and Kandalaksha bays, with the lowest rates in the Dvina Bay. During the period of intense primary production when resources of inorganic phosphorus were practically depleted, high rates of phosphate regeneration were observed. It was shown that populations of micro- and zooplankton in the White Sea were characterized by low activation energies of the principal metabolism reactions (3-6 kcal/mol), which allowed these populations to provide exchange intensity comparable to that of inhabitants of warm waters during all the seasons.

Sr- and Nd-isotopic composition of bulk lithogenic sediments from the Eastern Mediterranean Sea (Table 1)

In order to characterize the provenance of lithogenic surface sediments from the Eastern Mediterranean Sea (EMS), residual (leached) fraction of 34 surface samples have been analysed for their 143Nd/144Nd and 87Sr/86Sr isotope ratios. The sample locations bracket all important entrances of riverine suspended matter into the EMS as well as all sub-basins of the EMS. The combined analyses of these two isotope ratios provide a precise characterization of the lithogenic fraction of surface sediments and record their dilution towards the central sub-basins. We reconstruct provenance and possible pathways of riverine dispersal and current redistribution, assuming more or less homogenous isotopic signatures and flux rates of the eolian fraction over the EMS. Lithogenic sediments entering the Ionian Sea from the Calabrian Arc and the Adriatic Sea are characterized by high 87Sr/86Sr isotope ratios and low epsilon-Nd(0) values (average 87Sr/86Sr=0.718005 and epsilon-Nd(0)=-11.06, n=5). Aegean Sea terrigenous sediments show an average ratio of 87Sr/86Sr=0.713089 (n=5) and values of epsilon-Nd(0)=-7.89 (n=5). The Aegean isotopic signature is traceable up to the southwest, south, and southeast of Crete. The sediment loads entering the EMS via the Aegean Sea are low and spread out mainly through the Strait of Casos (east of Crete). Surface sediments from the eastern Levantine Basin are marked by the highest epsilon-Nd(0) values (-3.3, n=6) and lowest 87Sr/86Sr isotope ratios (average 0.709541, n=6), reflecting the predominant input of the Nile sediment. The influence of the Nile sediment is traceable up to the NE-trending, eastern flank of the Mediterranean Ridge. The characterization of the modern riverine dispersal and eolian flux, based on isotope data, may serve as a tool to reconstruct climate-coupled variations of lithogenic sediment input into the EMS.

Composition of organic matter in bottom sediments from the Antarctic sector of the Atlantic Ocean

We identify geochemical features of sedimentary organic matter in various morphostructural zones of the Antarctic sector of the Atlantic. We present background geochemical organic parameters for shelf and deep-sea sediments from the Weddell and Scotia Seas and the Bransfield Strait. Geochemical organic parameters are good indicators of environmental and facial variations in sediments and could be used for environmental monitoring of the World Ocean.

Shell preservation of Limacina inflata in surface sediments of the Central and South Atlantic

Over 300 surface sediment samples from the Central and South Atlantic Ocean and the Caribbean Sea were investigated for the preservation state of the aragonitic test of Limacina inflata. Results are displayed in spatial distribution maps and are plotted against cross-sections of vertical water mass configurations, illustrating the relationship between preservation state, saturation state of the overlying waters, and overall water mass distribution. The microscopic investigation of L. inflata (adults) yielded the Limacina dissolution index (LDX), and revealed three regional dissolution patterns. In the western Atlantic Ocean, sedimentary preservation states correspond to saturation states in the overlying waters. Poor preservation is found within intermediate water masses of southern origin (i.e. Antarctic intermediate water (AAIW), upper circumpolar water (UCDW)), which are distinctly aragonite-corrosive, whereas good preservation is observed within the surface waters above and within the upper North Atlantic deep water (UNADW) beneath the AAIW. In the eastern Atlantic Ocean, in particular along the African continental margin, the LDX fails in most cases (i.e. less than 10 tests of L. inflata per sample were found). This is most probably due to extensive "metabolic" aragonite dissolution at the sediment-water interface combined with a reduced abundance of L. inflata in the surface waters. In the Caribbean Sea, a more complex preservation pattern is observed because of the interaction between different water masses, which invade the Caribbean basins through several channels, and varying input of bank-derived fine aragonite and magnesian calcite material. The solubility of aragonite increases with increasing pressure, but aragonite dissolution in the sediments does not simply increase with water depth. Worse preservation is found in intermediate water depths following an S-shaped curve. As a result, two aragonite lysoclines are observed, one above the other. In four depth transects, we show that the western Atlantic and Caribbean LDX records resemble surficial calcium carbonate data and delta13C and carbonate ion concentration profiles in the water column. Moreover, preservation of L. inflata within AAIW and UCDW improves significantly to the north, whereas carbonate corrosiveness diminishes due to increased mixing of AAIW and UNADW. The close relationship between LDX values and aragonite contents in the sediments shows much promise for the quantification of the aragonite loss under the influence of different water masses. LDX failure and uncertainties may be attributed to (1) aragonite dissolution due to bottom water corrosiveness, (2) aragonite dissolution due to additional CO2 release into the bottom water by the degradation of organic matter based on an enhanced supply of organic matter into the sediment, (3) variations in the distribution of L. inflata and hence a lack of supply into the sediment, (4) dilution of the sediments and hence a lack of tests of L. inflata, or (5) redeposition of sediment particles.

Stable carbon and nitrogen isotope composition of organic matter in sediments of the Oman Margin

Stable isotopic compositions of carbon and nitrogen and organic carbon content of sediments ranging from the Pliocene to the Pleistocene-Holocene in age from the Oman Margin (ODP Sites 724 and 725) are reported. In general, the organic carbon content is greater than 2% at Site 724. Prior to the Pleistocene-Holocene at this site, sediments with higher content of organic matter were deposited owing to favorable preservation conditions and/or higher productivity. In the Pleistocene, lower amounts of organic matter have been preserved; this material generally has more enriched nitrogen isotopic compositions. This may indicate intensification of the Oxygen Minimum Zone and denitrification with the onset of the Pleistocene. A correlation of carbon isotope content of these sediments with oxygen isotope stages at Site 724 indicates an enrichment in 13C during glacial events. Based on the stable isotope evidence of both carbon and nitrogen, there does not appear to be major input of terrigenous-derived allochthonous material in this marine environment. The timing and extent of monsoon winds on the productivity of this region are not evident, but require further studies for collaborative interpretation of small-scale features in the isotopic and carbon content of this environment.

Composition of bitumen in the organic matter of Black Sea sediments from DSDP Hole 42-379B

Bituminologic analysis of sediment cores from the Black Sea (water depth up to 2000 m, drilling depth up to 625 m) has revealed all components typical for fossilized rocks, viz. hydrocarbons, resins, asphaltenes, and insoluble matter. Proportions of these components, their composition and properties do not display any dependence on depth in hole and seem to be governed by composition of organic matter and conditions and degree of its transformation at early stages of lithogenesis.