Petrological Characteristics and Genesis of the Central Indian Ocean Basin Basalts

The Central Indian Ocean Basin (CIOB) basalts are plagioclase-rich, while olivine and pyroxene are very few. The analyses of 41 samples reveal high FeOT (~10–18 wt%) and TiO2 (~1.4–2.7 wt%) indicating a ferrobasaltic composition. The basalts have high incompatible elements (Zr 63–228 ppm; Nb ~1–5 ppm; Ba ~15–78 ppm; La ~3–16 ppm), a similar U/Pb (0.02–0.4) ratio as the normal mid-oceanic basalt (0.16±0.07) but the Ba/Nb (12.5–53) ratio is much larger than that of the normal mid-oceanic ridge basalt (~5.7) and Primitive Mantle (9.56). Interestingly almost all of the basalts have a significant negative Eu anomaly (Eu/Eu*=0.78–1.00) that may have been a result of the removal of feldspar and pyroxene during crystal fractionation. These compositional variations suggest that the basalts were derived through fractional crystallization together with low partial melting of a shallow seated magma.     

Geological Characterization of the Miocene–Pliocene Succession in the Semliki Basin,Uganda: Implications for Hydrocarbon Exploration and Drilling in the East African Rift System

Natural Resources Research - The Albertine Graben, an active sedimentary petroliferous basin, has gained global attention as the unexplored areas are recently being targeted for hydrocarbon...     

Uranium Content of Thirty-Three Rock Reference Samples Determined by the Delayed Fission Neutron Counting Method

The delayed fission neutron counting method has been used for the analysis of thirty-three international geochemical reference samples for their uranium contents in the range of 0.2 to 1500 ppm. These include three from the Canada Centre for Mineral and Energy Technology, three from Atomic Energy Commission, USA, New Brunswick Laboratory, two from Bhabha Atomic Research Centre, India, fourteen from Centre de Recherches Pétrographiques et Géochimiques and eleven from US Geological Survey. The experimental set up has a detection limit of 0.08 μg and a determination limit of 0.15 μg U. At the lower limit the precision of determination is about 20 percent while at concentrations higher than 1 ppm it is better than 10 percent.     

THE DETERMINATION OF FILTER COEFFICIENTS FOR THE COMPUTATION OF STANDARD CURVES FOR DIPOLE RESISTIVITY SOUNDING OVER LAYERED EARTH BY LINEAR DIGITAL FILTERING *

The technique of linear digital filtering developed for the computation of standard curves for conventional resistivity and electromagnetic depth soundings is applied to the determination of filter coefficients for the computation of dipole curves from the resistivity transform function by convolution. In designing the filter function from which the coefficients are derived, a sampling interval shorter than the one used in the earlier work on resistivity sounding is found to be necessary. The performance of the filter sets is tested and found to be highly accurate. The method is also simple and very fast in application.     

Geometric Means as Probable Values For Compiled Data on Geochemical Reference Samples

Trace element data compiled on, geoshemical reference samples present invariably skewed distributions. It is proposed to treat such data as lognormally distributed and to compute geometric means (X_gm) as probable values. As examples, the X_gm values derived for some trace elements in some rock reference samples are compared with the "recommended" values and with the "gamma" values of Christie.     

THEORY FOR THE BIPOLE-DIPOLE METHOD OF RESISTIVITY SOUNDING*

A theory for the bipole-dipole method of resistivity sounding is developed. Bipole-dipole apparent resistivities are related to Schlumberger apparent resistivities at two spacings. The theory can also be used to compute exact dipole-dipole apparent resistivity curves providing an improvement over the existing techniques which involve far field approximations. A comparison of bipole-dipole and dipole-dipole systems reveals the similarity between the two. However, the resolution of the bipole-dipole system depends on the azimuth angle. The flexibility of the theoretical expressions lead to a generalized field scheme independent of the bipolar or dipolar nature of the current source.     

Tectonochemistry and p-t Conditions of Ramgarh and Almora Gneisses from Askot Klippe,Kumaun Lesser Himalaya

The chemical and petrological correlation of metamorphic nappes and klippes overlying the Proterozoic sedimentary units in the Kumaun Himalaya is still debated. The Ramgarh and Almora gneisses, not previously distinguished in the Askot Klippe, show distinct field, petrological and chemical signatures markedly similar to the tectonostratigraphic disposition of the Almora Nappe. A negative Eu anomaly in the Ramgarh granitic gneisses indicates lesser plagioclase fractionation while the Eu anomaly in the Almora pelitic gneisses is likely to have been controlled by feldspar crystallization in restites. During the anatexis at 776°C temperature and 6.6 kbar pressure, the melt moved slightly away to its crystallization sites. The Rb/Sr ratio ?0.54 and Nb ?10 ppm is consistent with the granodioritic composition. The negative Sr anomaly in the underlying Ramgarh granitic gneisses indicates a distinct mantle derived source/plagioclase fractionation with a notable correspondence to other late orogenic granites, particularly the basement Ulleri gneisses from the Nepal Himalaya. Ramgarh gneisses plot in the late-and post-COLG field. The Askot ensemble is likely to be the tectonometamorphically reworked basement, viz. the Ramgarh Group along with its metapelitic cover o f the Almora Group, together comprising southward thrust remnants of the leading edge of the Indian Plate that collided with Tibet during the Tertiary Himalayan orogeny.