Description and chemical composition of manganese nodules during R/V "Tyro" cruise APNAP 1 to the Madeira Abyssal Plain in 1986

The porewater and sediment composition of two boxcores and of a small gravity core, taken on a manganese-nodule-covered hill and in the Madeira Abyssal Plain proper respectively, are compared. The pore-water study of the two boxcores indicates that oxic conditions prevail in both cores. In addition, it indicates that no detectable fluxes of Mn or Fe occur from the porewater to the ocean bottom water. Variations in the geochemical composition of the sediments can be explained by fluctuations in the amount of carbonate, which acts as a diluting agent. A clear carbonate minimum is observed at 20-22 cm depth in the two cores. This minimum is likely to be associated with the last glacial period (10-20 kyr B.P.). This association is supported by the sediment accumulation rate of 15 mm/kyr as found by extrapolation from the rate for pelagic sediments in the Madeira Abyssal Plain. The bulk composition of the manganese nodules recovered from the submarine hill is chemically almost identical to the average composition of Atlantic nodules. The trace metal and Rare Earth Elements composition indicate a hydrogenous origin for the manganese nodules of this study. On the basis of the chemical composition, and that of nodules relative to that of the adjacent sediments, an average nodule accretian rate of 2.8-3.3 mm/myr has been calculated. Although the analyses of the entire ferromanganese nodules that have been studied seem to indicate a homogenous composition, internal structures of the nodules reveal great inhomogeneity, both visually and chemically. These fluctuations may be related to variations in the fluxes of Mn and Fe, which in turn could be climate-related.

(Table 3) Contents of phosphorus, iron, and manganese in various zones of Fe-Mn nodules from the Pacific radiolarian belt

Phosphorus content in the surface layer of bottom sediments varies from 0.07% to 0.73%. Clayey radiolarian and radiolarian clayey oozes contain 0.12% P, miopelagic clays 0.21% P, and sediments with high iron and manganese concentrations 0.46% P (average contents). Phosphorus content of iron-manganese nodules varies from 0.14% to 0.39%, average 0.19%. Correlation between phosphorus contents in nodules and surrounding sediments is indicated indirectly by P/Fe ratio. Phosphorus is non-uniformly distributed in some nodules and sometimes correlates with iron. Accumulation of phosphorus in iron-manganese nodules is governed by a degree of manganese predominance in ore components.

Geochemistry of basalts from Serocki Volcano

Basalts collected during drilling and diving programs on Serocki Volcano mostly fall within a limited compositional range, and are moderately evolved, normal MORBs with distinctive high MgO contents (averaging 7.60 wt%) and high A1203 concentrations (averaging 16.14 wt% in whole rock samples). However, samples recovered from within the central crater have lower Ti02 and FeO*/MgO, and higher MgO and Al2O3 concentrations, and are most similar to glasses recovered at Site 649 about 45 km to the north. Comparison of the observed geochemical variations with low-pressure experimental work and other samples from the region suggests that the Serocki Volcano and Site 649 data are compatible with crystal-liquid fractionation involving both olivine and early-stage clinopyroxene, as well as plagioclase, and that the sources may be similar even though Sites 648 and 649 are located in different, but adjacent, spreading cells. Consideration of the stratigraphy and morphology of Serocki Volcano suggests that this feature is more properly described as a megatumulus or lava delta, associated with a steeper, conical peak to the southwest. The evolution of Serocki Volcano involved early construction of a marginal rampart of pillows, followed by doming of this feature and the formation of a perched lava pond. Draining of this pond resulted in collapse and the formation of the central crater.

Agricultural pesticide in sediment cores from the Lac de Saint-André, France

Agricultural pesticide use has increased worldwide during the last several decades, but the long-term fate, storage, and transfer dynamics of pesticides in a changing environment are poorly understood. Many pesticides have been progressively banned, but in numerous cases, these molecules are stable and may persist in soils, sediments, and ice. Many studies have addressed the question of their possible remobilization as a result of global change. In this article, we present a retro-observation approach based on lake sediment records to monitor micropollutants and to evaluate the long-term succession and diffuse transfer of herbicides, fungicides, and insecticide treatments in a vineyard catchment in France. The sediment allows for a reliable reconstruction of past pesticide use through time, validated by the historical introduction, use, and banning of these organic and inorganic pesticides in local vineyards. Our results also revealed how changes in these practices affect storage conditions and, consequently, the pesticides' transfer dynamics. For example, the use of postemergence herbicides (glyphosate), which induce an increase in soil erosion, led to a release of a banned remnant pesticide (dichlorodiphenyltrichloroethane, DDT), which had been previously stored in vineyard soil, back into the environment. Management strategies of ecotoxicological risk would be well served by recognition of the diversity of compounds stored in various environmental sinks, such as agriculture soil, and their capability to become sources when environmental conditions change.

Composition of rocks, minerals, water, and gases from uplift areas of the Central Atlantic

Original geological, geophysical, lithological, mineralogical data on uplifts of the Central Atlantic are given in the book based on materials of Cruise 1 of the R/V Akademik Nikolaj Strakhov. Geological and geophysical studies include description of the obtained material and analysis of structural and morphological elements of the ocean floor. Results of lithological, petrochemical and geochemical studies were extremely innovative and develop a conceptual model. The latter include studies of petrochemical evolution of tholeiitic alkaline plate volcanism, large-scale hydrothermal transformation of basement rocks - palygorskitization, phosphatization and ferromanganese mineralization. Showing imposition Superposition of hydrogenic alteration on hydrothermally altered rocks and its role in Cenozoic history of sedimentation is shown.

Isotopic and chemical compositions of lower crust rocks and minerals from ODP Hole 176-735B

The composition of gabbroic rocks from the drill core of Hole 735B (ODP Leg 176) at the 11 Ma Atlantis II bank close to the slow spreading Southwest Indian Ridge (SWIR) has been analyzed for major and trace elements and Sr, Nd and Pb isotopic composition. The samples are thought to represent much of the mineralogical and geochemical variation in a vertical 1-km section (500-1500 m below the sea floor) of the lower ocean crust. Primitive troctolitic gabbros, olivine gabbros and gabbros that have Mg#=84-70, Ca#>61 and low Na# (Na/(Na+Al)) (8-17) are intruded by patches or veins of more evolved FeTi-oxide rich gabbroic and dioritic rocks with Mg# to 20, Ca# to 32, Na#=14-23, TiO2<7 wt.% and FeOtotal<18 wt.%. All rocks are acdcumulates, and incompatible element concentrations are low, e.g. Pb=0.1-0.7 ppm and U

Geochemical analyses of ODP Leg 135 samples

Statistical analysis of X-ray fluorescence data acquired during Leg 135 indicates that this instrument produces data of comparable precision to good land-based laboratories. We also examined contamination of certain elements caused by crushing during the use of the tungsten carbide apparatus. Although the concentrations of most elements are not altered during crushing, the powders prepared on the ship should not be used in subsequent studies where key elements of the investigation include W, Co, Ta, Pb, and low levels of Nb.