Two diamond-bearing peridotite xenoliths from the finsch kimberlite,South Africa

Two diamond bearing xenoliths found at Finsch Mine are coarse garnet lherzolites, texturally and chemically similar to the dominant mantle xenoliths in that kimberlite. A total of 46 diamonds weighing 0.053 carats have been recovered from one and 53 diamonds weighing 0.332 carats from the other. The diamonds are less corroded than diamonds recovered from the kimberlite. Geothermobarometric calculations indicate that the xenoliths equilibrated at 1,130° C and pressures 50 kb which is within the diamond stability field; this corresponds to depths of 160 km and would place the rocks on a shield geotherm at slightly greater depths than most coarse garnet lherzolites from kimberlite. The primary minerals in the two rocks are very similar to each other but distinctly different to the majority of mineral inclusions in Finsch diamonds. This suggests a different origin for the diamonds in the kimberlite and the diamonds in the xenoliths although the equilibration conditions for both suites are approximately coincident and close to the wet peridotite solidus.     

Storm deposits and storm-generated coarse carbonate breccias on a pelagic outer shelf (South-East Basin, France)

Uppermost Jurassic limestones of the South‐East Basin (France) are organized into four facies associations that were deposited in four distinct zones: (1) peritidal lagoonal limestones; (2) bioclastic and reefal limestones; (3) pelagic lime mudstones; (4) lime mudstones/calcarenites/coarse breccias. Calcarenite deposits of zone 4 exhibit sedimentary structures that are diagnostic of deposition under wave‐induced combined flow. In subzone 4a, both vertical and lateral transitions from lime mudstone/calcarenite to breccia indicate in situ brecciation under wave‐cyclic loading. Breccias were produced by heterogeneous liquefaction of material previously deposited on the sea floor. Deposits in subzone 4a record relatively long periods (>400 kyr) of sedimentation below wave base, alternating with periods of deposition under wave‐induced currents and periods of in situ deformation. In this zone, storm waves were attenuated by wave–sediment interaction, and wave energy was absorbed by the deformation of soft sediment. With reference to present‐day wave attenuation, water depths in this zone ranged between 50 and 80 m. Landwards of the attenuation zone, in zone 3, storm waves were reduced to fair‐weather wave heights. Storm wave base was not horizontal and became shallower landwards. As a consequence, water depth and wave energy were not linearly related. On a small area of the seaward edge of subzone 4a, cobbles were removed by traction currents and redeposited in subzone 4b. There, they formed a 100‐m‐thick wedge, which prograded over 3 km and was built up by the stacking of 5‐ to 20‐m‐thick cross‐stratified sets of coarse breccia. This wedge records the transport and redeposition of cobbles by a high‐velocity unidirectional component of a combined flow. The increase in flow velocity in a restricted area is proposed to result from flow concentration in a channel‐like structure of the downwelling in the gulf formed by the basin. In more distal subzone 4c, the hydrodynamic effect of wave‐induced currents was quasi‐permanent, and brecciation by wave–sediment interaction occurred only episodically. This indicates that, seawards of the attenuation zone, hydrodynamic storm wave base was deeper than mechanical storm wave base. Uppermost Jurassic carbonates were deposited and soft‐sediment deformed on a hurricane‐dominated ramp of very gentle slope and characterized by a zone of storm wave degeneration, located seawards of a zone of sedimentation below wave base.     

The geology and geophysics of the ambrym caldera,New Hebrides

Ambrym Island has an unusually large, well-preserved basaltic caldera 13 km across. The caldera occurs in the central region of an early broad composite cone, which formed a north-south line with three smailer volcanoes. Alter the caldera was formed volcanism occurred within it and along fissure lines running nearly east-west. Two volcanic cones are active almost continuously and historic fissure cruptions have been recorded. The caldera formed by quiet subsidence, or by subsidence accompanied by eruption of scoria lappili similar to that erupted prior and subsequent to caldera formation. The collapse was at least 600 metres and radiocarbon dating suggests it took place less than 2000 years ago. The caldera is detined by gravity anomalies 10 to 14 milligals lower than those at its rim suggesting predominantly ash infilling. Aeromagnetic anomalies show a prominent. nearly east-west lineation, with normally magnetised bipole anomalies over the centre of the caldera and over fissure lines east of it. The source of the present volcanic activity is believed to be located along dyke fissures, with a perched magma chamber beneath the caldera. The geophysical evidence on Ambrym, together with that of regional east trending magnetic anomalies and recent bathymetric results, suggests that the volcanic activity is localised by the intersection of an east-west fracture zone with the axis of the New Hebrides island are.     

Equilibrium coexistence of three amphiboles

Electron probe and wet chemical analyses of amphibole pairs from the sillimanite zone of central Massachusetts and adjacent New Hampshire indicated that for a particular metamorphic grade there should be a restricted composition range in which three amphiboles can coexist stably. An unequivocal example of such an equilibrium three amphibole rock has been found in the sillimanite-orthoclase zone. It contains a colorless primitive clinoamphibole, space group P2₁/m, optically and chemically like cummingtonite with blue-green hornblende exsolution lamellae on (100) and (¯101) of the host; blue-green hornblende, space group C2/m, with primitive cummingtonite exsolution lamellae on (100) and (¯101) of the host; and pale pinkish tan anthophyllite, space group Pnma, that is free of visible exsolution lamellae but is a submicroscopic intergrowth of two orthorhombic amphiboles. Mutual contacts and coarse, oriented intergrowths of two and three host amphiboles indicate the three grew as an equilibrium assemblage prior to exsolution. Electron probe analyses at mutual three-amphibole contacts showed little variation in the composition of each amphibole. Analyses believed to represent most closely the primary amphibole compositions gave atomic proportions on the basis of 23 oxygens per formula unit as follows: for primitive cummingtonite (Na_0.02Ca_0.21 ^– Mn_0.06Fe²⁺ _2.28Mg_4.12Al_0.28) (Al_0.17Si_7.83), for hornblende (Na_0.35Ca_1.56Mn_0.02Fe_1.71Mg_2.85Al_0.92) (Al_1.37Si_6.63), and for anthophyllite (Na_0.10Ca_0.06Mn_0.06Fe_2.25Mg_4.11Al_0.47) (Al_0.47Si_7.53). The reflections violating C-symmetry, on X-ray single crystal photographs of the primitive cummingtonite, are weak and diffuse, and suggest a partial inversion from a C-centered to a primitive clinoamphibole. Single crystal photographs of the anthophyllite show split reflections indicating it is an intergrowth of about 80% anthophyllite and about 20% gedrite which differ in their b crystallographic dimensions. Split reflections are characteristic of all analyzed orthorhombic amphiboles so far examined from Massachusetts and New Hampshire except the most aluminous gedrites, and the relative intensity of the gedrite reflections is roughly proportional to the degree of Na and Al substitution. Thin sections of a few of these anthophyllite specimens show lamellae parallel to (010) that are just resolved with a high power objective.Publication approved by the Director, U.S. Geological Survey.     

Analysis of some aromatic hydrocarbons in a benzene-soluble bitumen from Green River shale

The hydrocarbon content of an aromatic fraction, isolated from the bitumen of Green River shale, was studied by mass spectrometry, infra-red spectrometry, gas chromatography and a dehydrogenation technique. The hydrocarbon types and their distribution in this aromatic fraction, as determined by mass spectrometry, include the following: C_nH_2n?6(10%), C_nH_{2n?8 (31 %)}, C_nH_2n?10(18%), C_nH_2n?12(12%), C_nH_2n?14(8%) and a series of alkenylbenzenes (20%). The carbon-number range, empirical formulae and quantity of each compound in the major types are reported. Mass spectra of several compounds and homologous mixtures of compounds isolated from the aromatic fraction are also given.     

Partitioning of manganese,iron, copper,zinc, lead,cobalt, and nickel in black coatings on stream boulders in the vicinity of the Magruder mine,Lincoln Co., Georgia

Sequential digestions of Fe-Mn oxide coated boulders collected upstream and downstream from the Magruder mine, Lincoln Co., Georgia, indicate probable partitioning relationships for Zn, Cu, Pb, Co, and Ni with respect to Mn and Fe. Initial digestion with 0.1M hydroxylamine hydrochloride (Hxl) in 0.01M HNO₃ selectively dissolyes Mn oxides, whereas subsequent digestion with 1:4 HCl dissolves remaining Fe oxides.The results indicate that partitioning is not constant, but varies systematically with respect to the location of metal-rich waters derived from sulfide mineralization. Upstream from the mineralized zone Zn and Ni are distinctly partitioned to the Fe oxide component and Co and Cu are partitioned to the Mn oxide component. Immediately downstream from the mineralized zone, Mn oxides become relatively more enriched in Zn, whereas Fe oxides are relatively more enriched in Cu, Co, and Ni. Analytical precision for Pb is poor, but available data suggests it is more closely associated with Fe oxides.For routine geochemical surveys utilizing coated surfaces, a one-step digestion method is probably adequate. Parameters useful for detecting sulfide mineralization are metal concentrations normalized to surface area or various ratios (e.g. Zn/(Mn + Fe), Cu/Mn, Pb/Fe). Ratios can be obtained much faster, and at lower analytical costs than conventional analysis of stream sediment.