Chemical composition of ultrabasite and gabbro from the rift zones of the Arabian-Indian and Western Indian ridges

Results of petrographic studies of ultrabasite and gabbro from the rift zones of the Indian Ocean ridges are discussed using materials of R/V Vityaz Cruise 36. Rocks sampled from two sites 2700 km apart are close to each other in their composition. Petrographically ultrabasic rocks are divided into four subgroups: I - dunite; II - harzburgite, serpentinite; III - plagioclase lherzolite; and IV - metamorphically altered rocks. Petrographic description and chemical composition of basic rock varieties are presented as well as description of rock-forming minerals and their optical properties. Formation of pyroxene and plagioclase is shown to be related to autometasomatosis, which concludes the magmatic phase proper in rock mass formation accompanied by activity of residual intragranular liquid. Formation of ultrabasite in the rift zones is related to complicated processes.

Geochemical composition of olivine, spinel and amphibole in ODP Hole 209-1271B

Dunite and gabbroic materials recovered from Hole 1271B, Ocean Drilling Program (ODP) Leg 209, were examined for mineral chemistry to understand melt flow and melt-mantle reactions in the shallowest upper mantle of the Mid-Atlantic Ridge near the 15°20' Fracture Zone. Hole 1271B was drilled to 103.8 meters below seafloor on the inner corner high along the south wall of the 15°20' Fracture Zone. The total length of core collected was 15.9 m (recovery = ~15%). The dominant rock type in Hole 1271B is dunite, followed by brown amphibole gabbro, olivine gabbro, and troctolite, along with minor amounts of harzburgite and olivine gabbronorite. A large proportion of the dunite is associated with gabbroic rocks in Hole 1271B, similar to those observed in the Mohorovicic (Moho) transition zone of the Oman ophiolite, indicating significant magmatic activity in this region near the 15°20' Fracture Zone. Olivine Fo content varies from 89.2 to 91.2 in impregnated dunite and from 85.6 to 88.6 in troctolite, olivine gabbro, and olivine gabbronorite. Spinel Cr# (= 100 x Cr/[Cr + Al] molar ratio) ranges from 38.9 to 62.7 in dunite and from 46.3 to 57.6 in troctolites, olivine gabbro, and olivine gabbronorite. Compositional trends for spinel from dunite through troctolite toward olivine gabbro/gabbronorite are characterized by increases in TiO2, Cr#, and Fe3+#, very similar to those reported from Hess Deep Site 895. Olivine gabbro, olivine gabbronorite, and troctolite in Hole 1271B are considered to have formed as hybrid rocks between dunite and an evolved melt in the walls of a melt channel in the shallowest upper mantle that is tens of meters wide. The melt trapped in the wall rock crystallized plagioclase and clinopyroxene. On the other hand, dunite in the center of the melt channel became more refractory by melt-mantle reactions, increasing spinel Cr# to 62.5.

Chemical composition of rocks from the Eastern Indian Ocean

The monograph presents results of comprehensive geological and geophysical studies carried out in 1973 and 1976 during Cruises 54 and 58 of R/V "Vityaz" in the Eastern Indian Ocean. On the base of obtained data a description of topography, magnetic and gravity fields, structure of the sedimentary series and deep crustal structure of the East Indian Ridge, Central, West Australian and Cocos Basins, the Sunda Trench has been done. Materials on petrography, petrochemistry and geochemistry of igneous rocks in the region have been summarized. New geological and geophysical information has been compared with with DSDP materials. Tectonics and geological history of the Eastern Indian Ocean are under consideration.

Chemical composition of rocks and minerals from the Central Atlantic fracture zones

The monograph summarizes materials on geology and deep structure of the Central Atlantic fracture zones. These materials have been obtained during eight expeditions of R/V ''Akademik Nikolaj Strakhov''. The studies have been based on the integrated geological approach. As a result, many new tectonic, magmatic, metallogenic and historical-geological features of these phenomenal structures of the deep ocean have been revealed.

(Table 1) Elemental composition of benthic foraminifera from South Atlantic core top samples

The ocean plays a major role in the global carbon cycle, and attempts to reconstruct past changes in the marine carbonate system are increasing. The speciation of dissolved uranium is sensitive to variations in carbonate system parameters, and previous studies have shown that this is recorded in the uranium-to-calcium ratio (U/Ca) of the calcite shells of planktonic foraminifera. Here we test whether U/Ca ratios of deep-sea benthic foraminifera are equally suited as an indicator of the carbonate system. We compare U/Ca in two common benthic foraminifer species (Planulina wuellerstorfi and Cibicidoides mundulus) from South Atlantic core top samples with the calcite saturation state (Delta [CO3**2-] = [CO3**2-]in situ - [CO3**2-]sat) of the ambient seawater and find significant negative correlations for both species. Compared with planktonic foraminifera, the sensitivity of U/Ca in benthic foraminifera to changes in Delta [CO3**2-] is about 1 order of magnitude higher. Although Delta [CO3**2-] exerts the dominant control on the average foraminiferal U/Ca, the intertest and intratest variability indicates the presence of additional factors forcing U/Ca.

(Table 2) Concentrations and composition of aliphatic hydrocarbons in bottom sediments of the Sakhalin shelf

Aliphatic and polycyclic aromatic hydrocarbons were examined in the surface layer of bottom sediments from the eastern part of the Sakhalin Island shelf (materials were sampled in summer 2002). Concentrations of hydrocarbons were determined to know changed since beginning of development of oil fields (compared with earlier years). According to distribution of markers in hydrocarbon compositions, bottom sediments are dominated by allochthonous (terrigenous) hydrocarbons that are the most stable compounds. Occurrence of transformed anthropogenic oil alkanes that have never been found before may be indicative of increasing pollution in the region.

The influence of temperature and seawater carbonate saturation state on 13C-18O bond ordering in bivalve mollusks

The shells of marine mollusks are widely used archives of past climate and ocean chemistry. Whilst the measurement of mollusk delta 18O to develop records of past climate change is a commonly used approach, it has proven challenging to develop reliable independent paleothermometers that can be used to deconvolve the contributions of temperature and fluid composition on molluscan oxygen isotope compositions. Here we investigate the temperature dependence of 13C-18O bond abundance, denoted by the measured parameter Delta 47, in shell carbonates of bivalve mollusks and assess its potential to be a useful paleothermometer. We report measurements on cultured specimens spanning a range in water temperatures of 5 to 25 °C, and field collected specimens spanning a range of -1 to 29 °C. In addition we investigate the potential influence of carbonate saturation state on bivalve stable isotope compositions by making measurements on both calcitic and aragonitic specimens that have been cultured in seawater that is either supersaturated or undersaturated with respect to aragonite. We find a robust relationship between Delta 47 and growth temperature. We also find that the slope of a linear regression through all the Delta 47 data for bivalves plotted against seawater temperature is significantly shallower than previously published inorganic and biogenic carbonate calibration studies produced in our laboratory and go on to discuss the possible sources of this difference. We find that changing seawater saturation state does not have significant effect on the Delta 47 of bivalve shell carbonate in two taxa that we examined, and we do not observe significant differences between Delta 47-temperature relationships between calcitic and aragonitic taxa.

Influence of temperature and CO2 on the strontium and magnesium composition of coccolithophore calcite

Marine calcareous sediments provide a fundamental basis for palaeoceanographic studies aiming to reconstruct past oceanic conditions and understand key biogeochemical element cycles. Calcifying unicellular phytoplankton (coccolithophores) are a major contributor to both carbon and calcium cycling by photosynthesis and the production of calcite (coccoliths) in the euphotic zone, and the subsequent long-term deposition and burial into marine sediments. Here we present data from controlled laboratory experiments on four coccolithophore species and elucidate the relation between the divalent cation (Sr, Mg and Ca) partitioning in coccoliths and cellular physiology (growth, calcification and photosynthesis). Coccolithophores were cultured under different seawater temperature and carbonate chemistry conditions. The partition coefficient of strontium (DSr) was positively correlated with both carbon dioxide (pCO2) and temperature but displayed no coherent relation to particulate organic and inorganic carbon production rates. Furthermore, DSr correlated positively with cellular growth rates when driven by temperature but no correlation was present when changes in growth rates were pCO2-induced. Our results demonstrate the complex interaction between environmental forcing and physiological control on the strontium partitioning in coccolithophore calcite and challenge interpretations of the coccolith Sr / Ca ratio from high-pCO2 environments (e.g. Palaeocene-Eocene thermal maximum). The partition coefficient of magnesium (DMg) displayed species-specific differences and elevated values under nutrient limitation. No conclusive correlation between coccolith DMg and temperature was observed but pCO2 induced a rising trend in coccolith DMg. Interestingly, the best correlation was found between coccolith DMg and chlorophyll a production, suggesting that chlorophyll a and calcite associated Mg originate from the same intracellular pool. These and previous findings indicate that Mg is transported into the cell and to the site of calcification via different pathways than Ca and Sr. Consequently, the coccolith Mg / Ca ratio should be decoupled from the seawater Mg / Ca ratio. This study gives an extended insight into the driving factors influencing the coccolith Mg / Ca ratio and should be considered for future palaeoproxy calibrations.