Geochemical exploration for platinum-group elements in the Bushveld Complex, South Africa   总被引：2，自引：0，他引：2  

H. J. Wilhelm  H. Zhang  F. L. Chen  J. H. Elsenbroek  M. Lombard  D. de Bruin 《Mineralium Deposita》1997,32(4):349-361

Analyses of stream sediment and soil samples from the Bushveld Complex, South Africa have revealed enhanced precious metal concentrations, which can be related both to mining activities and the presence of hidden concentrations of platinum-group elements (PGEs) and gold. The economically important PGE deposits hosted by the Upper Critical Zone of the Rustenburg Layered Suite are revealed by a high PGE and Au content in the overlying soils. A second zone of elevated precious metal concentrations straddles the boundary between the Main and Upper Zones and has to date been traced for more than 100 km. This zone follows the igneous layering of the Rustenburg Layered Suite and is offset by the Brits Graben. It is therefore thought to be the reflection of a magmatic PGE-Au mineralisation. Received: 31 May 1996 / Accepted: 7 January 1997  相似文献   

The replacement of anthophyllite by jimthompsonite: a model for hydration reactions in biopyriboles     

Bernard Henry Grobéty 《Contributions to Mineralogy and Petrology》1997,127(3):237-247

Anthophyllite crystals found in ultramafic lenses of the Lepontine Alps (Switzerland) contain coherent, submicroscopic intergrowths of ordered and disordered biopyribole polysomes. The chain width distributions of disordered polysomes were analyzed using high resolution transmission electron microscopy (HRTEM). Chains wider than triple were interpreted as intermediate products in the transformation of anthophyllite to the triple chain silicate jimthompsonite. The concentration of individual chain types is strongly correlated with the reaction progress. Based on observed zipper terminations and the transformation rules given by Veblen and Buseck (1980) a scheme of possible reaction paths leading from anthophyllite to jimthomp sonite is proposed. The reaction scheme and a simple kinetic model for elementary reactions allow modeling of the observed chain width distributions. The model suggests that the complex reaction paths involving steps with increasing and decreasing chain width are more important in the formation of jimthompsonite than the direct transformation from anthophyllite. The wide chains (>triple) occurring as intermediate products of the multi-step paths are structurally closer to talc than jimthompsonite. The back-transformation of these wide chains to triple chains is, therefore, a strong argument that jimthompsonite is a stable phase and not only a metastable intermediate product in the transformation of anthophyllite to talc. Received: 8 July 1996 / Accepted: 13 December 1996  相似文献   

Quantitative methods in the earth sciences     

A. F?rster  D. F. Merriam 《Mathematical Geology》1997,29(2):315

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Multi-phase water-rhyolite interaction and ore fluid generation at Aljustrel, Portugal     

F. J. A. S. Barriga  W. S. Fyfe 《Mineralium Deposita》1997,33(1-2):188-207

Detailed study of the Aljustrel volcanic rocks, through petrography, mineral chemistry, whole-rock geochemistry, and previously published stable isotope data, show that the rocks experienced extreme metasomatism. The metasomatic phenomena presented are explained accurately by a sea-water convective model. The evolution of the sea-water-derived fluid as it progresses downwards through the rocks is evident, from cold, oxidising, Mg-bearing, to hot, reducing, Mg-free, and enriched in Si, Fe, Cu, Zn. Several lines of evidence (feldspar mineralogy, paragenetic relations between regional and ore-zone alteration, and stable isotope data) show that the temperature of the hydrothermal circulation increased through time, and that the water-to-rock ratio evolved from very high to low values. According to our data, about 30 ppm Cu and some 100 ppm Zn were removed from the Aljustrel Volcanics. This implies, for both metals, the same amount of leached rock to produce the 2 Mt Cu and 6 Mt Zn contained in the massive sulphide deposits of the Aljustrel area. With regard to Fe, about 1% was on average removed from the rocks, producing enough metal to account for all the Fe in the MS deposits and overlying chemical sediments. This study documents semi-quantitatively the provenance of the main metals in major massive sulphide deposits via sea water leaching of the immediate host rocks.

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Resumen (translated by E. Pascual) Un estudio detallado de las rocas volcánicas de Aljustrel, mediante petrografia, química mineral, geoquímica de roca total y datos de isótopos estables previamente publicados muestra que estas rocas han sufrido metasomatismo en grado extremo. Los fenómenos metasomáticos presentados se explican con precisión mediante un modelo convectivo con agua de mar. Es evidente la evolución del fluido derivado del agua de mar conforme progresa en profundidad a través de las rocas, desde un fluido frío, oxidante y con magnesio a otro reductor, sin magnesio y enriquecido en Si, Fe, Cu y Zn. Varias líneas de evidencia (mineralogía de los feldespatos, relaciones paragenéticas entre la alteración regional y de las zonas mineralizadas, isótopos estables) muestran que la temperatura y la circulación hidrotermal se incrementaron con el tiempo y que la relación agua-roca evolucionó de valores muy altos a bajos. De acuerdo con nuestros datos, de las rocas volcánicas de Aljustrel se han extraído unas 30 ppm de Cu y unas 100 ppm de Zn. Esto implica, para ambos metales, que la misma roca lixiviada ha producido los 2 Mt de Cu y los 6 Mt de Zn contenidos en los depósitos de sulfuros masivos del área de Aljustrel. En cuanto al Fe, una media de alrededor de 1% fue extraída de las rocas, produciendo metal suficiente para explicar todo el Fe de los depósitos de sulfuros masivos y de los sedimentos químicos suprayacentes. Este estudio documenta de forma semicuantitativa la procedencia de los principales metales en depósitos mayores de sulfuros masivos, mediante lixiviado por agua de mar de sus rocas huéspedes inmediatas.

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Received: 1 February 1997 / Accepted: 30 July 1997  相似文献   

Parental melts of melilitolite and origin of alkaline carbonatite: evidence from crystallised melt inclusions, Gardiner complex     

T. F. D. Nielsen  I. P. Solovova  I. V. Veksler 《Contributions to Mineralogy and Petrology》1997,126(4):331-344

Perovskite and melilite crystals from melilitolites of the ultramafic alkaline Gardiner complex (East Greenland) contain crystallised melt inclusions derived from: (1) melilitite; (2) low-alkali carbonatite; (3) natrocarbonatite. The melilitite inclusion (1) homogenisation temperature of 1060 °C is similar to liquidus temperatures of experimentally investigated natural melilitites. The compositions are peralkaline, low in MgO (ca.␣5 wt%), Ni and Cr, and they are low-pressure fractionates of more magnesian larnite-normative ultramafic lamprophyre-type melts of primary mantle origin. Low-alkali carbonatite compositions (2) homogenise at 1060–1030 °C and are compositionally similar to immiscible calcite carbonatite dykes derived from the melilitolite magma. Natrocarbonatite inclusions (3) homogenise between 1030 and 900 °C and are compositionally similar to natrocarbonatite lava from Oldoinyo Lengai. Nephelinitic to phonolitic dykes which are related to the calcite carbonatite dykes, are very Zr-rich and agpaitic (molecular Na₂O + K₂O/Al₂O₃ > 1.2) and resemble nephelinites of Oldoinyo Lengai. The petrographic, geochemical and temporal relationships indicate unmixing of carbonatite compositions (ca. 10% alkalies) from evolving melilitite melt and continued fractionation of melilitite to nephelinite. It is suggested that the natrocarbonatite compositions represent degassed supercritical high temperature fluid formed in a cooling body of strongly larnite-normative nephelinite or evolved melilitite. The Gardiner complex and similar melilitolite and carbonatite-bearing ultramafic alkaline complexes are believed to represent subvolcanic complexes formed beneath volcanoes comparable to Oldoinyo Lengai and that the suggested origin of natrocarbonatite may be applied to natrocarbonatites of Oldoinyo Lengai. Received: 18 January 1996 / Accepted: 2 September 1996  相似文献   

Harmonic Analysis of Sedimentary Cyclic Sequences in Kansas, Midcontinent, USA     

Daniel F. Merriam  Joseph E. Robinson 《Mathematical Geology》1997,29(8):953-962

Several stratigraphic sequences in the Upper Carboniferous (Pennsylvanian) in Kansas (Midcontinent, USA) were analyzed quantitatively for periodic repetitions. The sequences were coded by lithologic type into strings of datasets. The strings then were analyzed by an adaptation of a one-dimensional Fourier transform analysis and examined for evidence of periodicity. The method was tested using different states in coding to determine the robustness of the method and data. The most persistent response is in multiples of 8–10 ft (2.5–3.0 m) and probably is dependent on the depositional thickness of the original lithologic units. Other cyclicities occurred in multiples of the basic frequency of 8–10 with persistent ones at 22 and 30 feet (6.5–9.0 m) and large ones at 80 and 160 feet (25–50 m). These levels of thickness relate well to the basic cyclothem and megacyclothem as measured on outcrop. We propose that this approach is a suitable one for analyzing cyclic events in the stratigraphic record.  相似文献   

Seismic Ground Motion Expected for the Eastern District of Naples     

C. Nunziata  F. Vaccari  G.F. Panza  G. Luongo  D. FÄH 《Natural Hazards》1997,15(2-3):183-197

The seismic ground motion of a test area in the eastern district of Naples is computed with a hybrid technique based on the mode summation and the finite difference methods. This technique allows us the realistic modelling of source and propagation effects, including local soil conditions. In the modelling, we consider the 1980 Irpinia earthquake, a good example of strong shaking for the area of Naples, which is located about 90 km from the epicenter.The detailed geological setting is reconstructed from a large number of drillings. The sub-soil is mainly formed by alluvial (ash, stratified sand and peat) and pyroclastic materials overlying a pyroclastic rock (yellow neapolitan tuff), representing the neapolitan bedrock. The detailed information available on mechanical properties of the sub-soil and its geometry warrants the application of the sophisticated hybrid technique.As expected, the sedimentary cover causes an increase of the signal's amplitudes and duration. If thin peat layers are present, the amplification effects are reduced, and the peak ground accelerations are similar to those observed for the bedrock model. This can be explained by the backscattering of wave energy at such layers, that tend to seismically decouple the upper from the lower part of the structure.For SH-waves, the influence of the variations of the S-wave velocities on the spectral amplification is studied, by considering locally measured velocities and values determined from near-by down-hole measurements. The comparison between the computed spectral amplifications confirms the key role of an accurate determination of the seismic velocities of the different layers.The comparison performed between a realistic 2-D seismic response and a standard 1-D response, based on the vertical propagation of waves in a plane layered structure, shows considerable difference, from which it is evident that serious caution must be taken in the modelling of expected ground motion at a specific site.  相似文献   

Argillite debris converted to bauxite during karst weathering: evidence from immobile element geochemistry at the Olmedo Deposit, Sardinia     

W. H. MacLean  F. F. Bonavia  G. Sanna 《Mineralium Deposita》1997,32(6):607-616

The Olmedo bauxite deposit occurs in the Nurra district of northwest Sardinia. It forms a stratiform horizon in Cretaceous limestone and marl. Uplift in mid-Cretaceous had exposed recently deposited limestone to karst weathering, and a layer of argillaceous debris accumulated on its surface and was partly converted to bauxite. Intermediate products were desiccated marl, bauxitic argillite and argillaceous bauxite. Subsidence followed, and the bauxite was preserved by the deposition of late Cretaceous limestone and other sediments. Uplift in Oligocene-Miocene time, with ensuing erosion, exposed the bauxite horizon to its present configuration. Concentrations of normative minerals illustrate chemical processes and the build-up of Al in the bauxite horizon. Plots of chemical data and correlation coefficients show that Al, Ti, Zr, Nb, Th, Cr and V were immobile during the bauxitization process. Mass changes point to large net removal of Si, Mg and K from the system, although some of this material and slightly mobile Al were reprecipitated in the underlying argillite and altered marl. Immobile element ratios trace the source of the bauxite to the underlying argillaceous limestone. Al in the bauxite was accumulated from the degradation of 25 to 50 m of the argillaceous limestone. Received: 10 June 1996 / Accepted: 15 April 1997  相似文献   

Attenuation differences in layer 2A in intermediate- and slow-spreading oceanic crust     

D. Goldberg  Y.F. Sun 《Earth and Planetary Science Letters》1997,150(3-4):221-231

In situ seismic attenuationQ⁻¹logs are derived from borehole velocity profiles and reveal sharp boundaries between morphologies of the extrusive volcanic layers in intermediate- and slow-spreading oceanic crust.Q⁻¹logs are calculated from the scattering attenuation associated with vertical velocity heterogeneity in Ocean Drilling Program Holes 504B and 896A and in Hole 395A, located in 5.9–7.3 Ma crust on the Pacific and Atlantic plates, respectively. Our results strongly tie crustal properties to seismic measurables and observed geological structures: we find that the scattering attenuation can be used to identify the extrusive volcanic sequence because it is closely related to changes in the degree of vertical heterogeneity. We interpret a distinct decrease in the Q⁻¹log at the transition below the extrusive volcanic layer to correspond with the seismic layer 2A/2B boundary. The boundary is located at 465 m depth below the sea floor in both Hole 395A and 504B, although this is likely to be a coincidence of the sediment thickness at these sites. Layer 2A is estimated to be approximately 150 m thick in Hole 504B and > 300 m thick in Hole 395A. Cyclic sequences of high-porosity pillows and low-porosity massive units in the uppermost 100 m of volcanics in Hole 395A result in large velocity heterogeneities which cause > 5 times more attenuation in this layer than in Hole 504B. In Hole 896A, by contrast, fewer pillows, more massive flows, and a greater volume of carbonate veins decrease the velocity heterogeneity and attenuation significantly over only 1 km distance from Hole 504B. We conclude that the attenuation in the extrusive volcanics of the ocean crust is largely controlled by variation in local heterogeneity and morphology as well as by subsequent hydrothermal alteration. The observed differences inQ⁻¹profiles and layer 2A thickness at these sites may be attributed to variations in the volume and duration of volcanic activity at mid-ocean spreading centers for these Pacific and Atlantic ridge segments.  相似文献   

Estimation of groundwater evaporation and salt flux from Owens Lake, California, USA   总被引：3，自引：0，他引：3  

S. W. Tyler  S. Kranz  M. B. Parlange  J. Albertson  G. G. Katul  G. F. Cochran  B. A. Lyles  G. Holder 《Journal of Hydrology》1997,200(1-4):110-135

Groundwater evaporation and subsequent precipitation of soluble salts at Owens Lake in eastern California have created one of the single largest sources of airborne dust in the USA, yet the evaporation and salt flux have not been fully quantified. In this study, we compare eddy correlation, microlysimeters and solute profiling methods to determine their validity and sensitivity in playa environments. These techniques are often used to estimate evaporative losses, yet have not been critically compared at one field site to judge their relative effectiveness and accuracy. Results suggest that eddy correlation methods are the most widely applicable for the variety of conditions found on large playa lakes. Chloride profiling is shown to be highly sensitive to thermal and density-driven fluxes in the near surface and, as a result, appears to underestimate yearly groundwater evaporation. Yearly mean groundwater evaporation from the playa surface estimated from the three study areas was found to range from 88 to 104 mm year⁻¹, whereas mean evaporation from the brine-covered areas was 872 mm year⁻¹. Uncertainties on these mean rates were estimated to be ±25%, based on comparisons between eddy correlation and lysimeter estimates. On a yearly basis, evaporation accounts for approximately 47 × 10⁶ m³ of water loss from the playa surface and open-water areas of the lake. Over the playa area, as much as 7.5 × 10⁸ kg (7.5 × 10⁵ t) of salt are annually concentrated by evaporation at or near the playa surface, much of which appears to be lost during dust storms in area.  相似文献