Basal dolomitic sediments ofthe Tyrrhenian Sea

Basal dolomitic sediments were recovered at three drill sites in the Tyrrhenian Sea during Ocean Drilling Program (ODP) Leg 107 (Sites 650, 651, and 655). These sediments overlie the basaltic basement complex and are enriched in iron, and in some instances, also in manganese. The manganese enrichments, together with a very slight enrichment in trace transition elements, strongly suggest that the basal sediments have an affinity to deep-sea metalliferous deposits of hydrothermal origin. At Sites 651 and 655, the dolostones contain variable amounts of authigenic palygorskite, a Mgrich clay mineral. At Site 651, the basal sediments are 40 m thick and contain nonstoichiometric dolomite, sometimes Ca rich, but primarily Mg rich. The occurrence of Mg-rich dolomite with excess Mg up to 4% is unusual for the deep-sea environment; it may be associated with a hydrothermally driven flux of altered sea water through the directly underlying basement complex, which comprises basalt, dolerite, and serpentinized peridotite. Low-temperature alteration of the basement complex could produce solutions enriched in Mg. Oxygen-isotope equilibrium temperatures indicate that all of the studied dolomites formed under low-temperature conditions (i.e., < 70?C). The carbon-isotope compositions, together with the strong isotopic covariance, suggest that the Mg-rich dolomite precipitated more rapidly than the Carich dolomite. We suggest that the low-temperature, hydrothermal convection of Mg-rich solutions through the basal sediments in this back-arc basin environment (1) overcame kinetic problems related to the formation of massive dolostones, and (2) provided a mass-transport mechanism for dolomitization.

Phosphorus in bottom sediments and micronodules from Core VITYAZ7414, Central Indian Ocean

Study of phosphorus distribution in grain size fractions of eupelagic clays showed high (up to 3%) content of P in Fe-Mn micronodules that can contain up to 20-30% of total P. Mineral P associated with Fe in ocean sediments is an analog of manganese in ocean sedimentogenesis. Sharp decrease of P contents in ocean Fe-Mn nodules compared to ones from seas results from decrease of Fe contents and partial neutralization of Fe activity by Mn.

Weather conditions and phosphorus speciation in waters of the Western Sargasso Sea in October-November 1977

Forms of phosphorus were determined for the first time in the area under study. Based on the ratio between organic and inorganic forms of phosphorus, it is concluded that sorption processes in the thin surface layer and photosynthetic processes in surface water are of the same intensity. Extremely high values of total phosphorus in the thin layer may be indicators of water pollution.

Porewater and solid-phase phosphorus geochemistry in surface sediments of sediment core GeoB9510-3, GeoB9518-4 and GeoB9519-6

Despite intensive research on the different domains of the marine phosphorus (P) cycle during the last decades, frequently discussed open questions still exist especially on controlling factors for the benthic behaviour of P and its general distribution in sediment-pore water systems. Steady state or the internal balance of all relevant physical and (bio)geochemical processes are amongst the key issues. In this study we present and discuss an extended data set from surface sediments recovered from three locations on the NW African continental slope. Pore water data and results from sequential sediment extractions give clear evidence to the well-known close relationship between the benthic cycles of P and iron. Accordingly, most of the dissolved phosphate must have been released by microbially catalyzed reductive dissolution of iron (oxhydr)oxides. However, rates of release and association of P and iron, respectively, are not directly represented in profiles of element specific sediment compositions. Results from steady-state based transport-reaction modelling suggest that particle mixing due to active bioturbation, or rather a physical net downward transport of P associated to iron (oxyhydr)oxides, is an essential process for the balance of the inspected benthic cycles. This study emphasizes the importance of balancing analytical data for a comprehensive understanding of all processes involved in biogeochemical cycles.