Platinum-group element, Gold, Silver and Base Metal distribution in compositionally zoned sulfide droplets from the Medvezky Creek Mine, Noril’sk, Russia

Concentrations of Ag, Au, Cd, Co, Re, Zn and Platinum-group elements (PGE) have been determined in sulfide minerals from zoned sulfide droplets of the Noril’sk 1 Medvezky Creek Mine. The aims of the study were; to establish whether these elements are located in the major sulfide minerals (pentlandite, pyrrhotite, chalcopyrite and cubanite), to establish whether the elements show a preference for a particular sulfide mineral and to investigate the model, which suggests that the zonation in the droplets is caused by the crystal fractionation of monosulfide solid solution (mss). Nickel, Cu, Ag, Re, Os, Ir, Ru, Rh and Pd, were found to be largely located in the major sulfide minerals. In contrast, less than 25% of the Au, Cd, Pt and Zn in the rock was found to be present in these sulfides. Osmium, Ir, Ru, Rh and Re were found to be concentrated in pyrrhotite and pentlandite. Palladium and Co was found to be concentrated in pentlandite. Silver, Cd and Zn concentrations are highest in chalcopyrite and cubanite. Gold and platinum showed no preference for any of the major sulfide minerals. The enrichment of Os, Ir, Ru, Rh and Re in pyrrhotite and pentlandite (exsolution products of mss) and the low levels of these elements in the cubanite and chalcopyrite (exsolution products of intermediate solid solution, iss) support the mss crystal fractionation model, because Os, Ir, Ru, Rh and Re are compatible with mss. The enrichment of Ag, Cd and Zn in chalcopyrite and cubanite also supports the mss fractionation model these minerals are derived from the fractionated liquid and these elements are incompatible with mss and thus should be enriched in the fractionated liquid. Gold and Pt do not partition into either iss or mss and become sufficiently enriched in the final fractionated liquid to crystallize among the iss and mss grains as tellurides, bismithides and alloys. During pentlandite exsolution Pd appears to have diffused from the Cu-rich portion of the droplet into pentlandite.     

A lead isotopic study of the Stillwater Complex,Montana: constraints on crustal contamination and source regions

Analyses of the Pb isotopic compositions of plagioclase from 23 samples covering the stratigraphic thickness of the Stillwater Complex indicate a narrow range of apparent initial isotopic compositions (²⁰⁶Pb/ ²⁰⁴Pb=13.95; ²⁰⁷Pb/²⁰⁴Pb=14.95–15.01; ²⁰⁸Pb/²⁰⁴Pb=33.6). The uniformity of our data is in contrast to, but not necessarily contradictory to, other recent investigations which give indications that the complex formed by repeated injection of magmas with at least two distinct compositions that were presumably derived from different source regions. Samples from the Basal series of the complex have consistently higher ²⁰⁷Pb/²⁰⁴Pb ratios, suggesting either minor contamination from adjacent country rocks or a slight distinction between parental magmas. Apparent initial Pb isotopic compositions of the complex are very radiogenic compared to Late Archean model-mantle values, but are nearly identical to initial Pb isotopic compositions found for the the adjacent, slightly older (2.73–2.79 Ga), Late Archean crustal suite in the Beartooth Mountains. Contamination of magmas parental to the Stillwater Complex by the Late Archean crustal suite is rejected for two reasons: (1) Th and U concentrations in Stillwater rocks and plagioclase are very low (about 0.08 and 0.02 ppm respectively), yet Th/U ratios are uniform at about 4, in contrast to the highly variable (2–26) but often high Th/U ratios found for the Late Archean crustal complex; (2) it seems improbable that any contamination process would have adjusted the isotopic compositions of the diverse magmas entering the Stillwater chamber to near-identical values. The preferred hypothesis to explain the Pb isotopic data for the Stillwater Complex and the associated Late Archean crustal suite involves a major Late Archean crust-forming event that resulted in a compositionally complex crust/mantle system with relatively homogeneous and unusual Pb isotopic compositions. The parental magmas of the Stillwater Complex were generated at different levels within this crust/mantle system, before isotopic contrasts could develop by radioactive decay within compositionally discrete reservoirs. This situation limits the utility of all isotopic tracer systems in discriminating among the various mantle and crustal reservoirs that may have affected the final isotopic character of the Stillwater magmas. The late Archean crustal complex and the Stillwater Complex melts were ultimately derived from the same distinct mantle without obvious direct interaction with the Middle to Early Archean crust present in the region.     

Magnetism in aluminous goethite

Magnetism in fine particles of goethite which contain 5, 11, 18 and 30 mole % aluminium has been investigated. Mössbauer spectroscopy was used, with the samples at 4.2 K and in applied magnetic fields of 0–8 T. Analysis was via a mean field model, in which the spectra from each sample were simultaneously least-squares fitted. The presence of aluminium increases the effective anisotropy, introduces a range of anisotropy fields, and induces ferrimagnetism. Quantitative measurements of these effects are presented. It is surmised that the anisotropy is principally determined by the local environment of ferric ions, and that the distribution of anisotropy fields is the result of a variety of atomic neighbour configurations. Ferrimagnetism is understood to arise from a strong preference, with 100% success at intermediate concentrations, for aluminium ions to crystallise on the same sublattice. Simulations of the net magnetic moment in small particle systems are presented, and it is shown that statistical fluctuations and the effects of surfaces are unimportant in the particles studied.     

Preliminary Cellular-Automata Forecast of Permit Activity from 1998 to 2010, Idaho and Western Montana

For public land management in Idaho and western Montana, the U.S. Forest Service (USFS) has requested that the U.S. Geological Survey (USGS) predict where mineral-related activity will occur in the next decade. Cellular automata provide an approach to simulation of this human activity. Cellular automata (CA) are defined by an array of cells, which evolve by a simple transition rule, the automaton. Based on exploration trends, we assume that future exploration will focus in areas of past exploration. Spatial-temporal information about mineral-related activity, that is permits issued by USFS and Bureau of Land Management (BLM) in the last decade, and spatial information about undiscovered resources, provide a basis to calibrate a CA. The CA implemented is a modified annealed voting rule that simulates mineral-related activity with spatial and temporal resolution of 1 mi² and 1 year based on activity from 1989 to 1998. For this CA, the state of the economy and exploration technology is assumed constant for the next decade. The calibrated CA reproduces the 1989–1998-permit activity with an agreement of 94%, which increases to 98% within one year. Analysis of the confusion matrix and kappa correlation statistics indicates that the CA underestimates high activity and overestimates low activity. Spatially, the major differences between the actual and calculated activity are that the calculated activity occurs in a slightly larger number of small patches and is slightly more uneven than the actual activity. Using the calibrated CA in a Monte Carlo simulation projecting from 1998 to 2010, an estimate of the probability of mineral activity shows high levels of activity in Boise, Caribou, Elmore, Lincoln, and western Valley counties in Idaho and Beaverhead, Madison, and Stillwater counties in Montana, and generally low activity elsewhere.     

Mineral chemistry and zoning in eclogite inclusions from Colorado Plateau diatremes

Eclogite inclusions from kimberlitic diatremes on the Colorado Plateau contain intricately zoned garnet and pyroxene and unusual textures. Detailed electron microprobe traverses for a clinopyroxene-garnet-phengite-lawsonite-rutile assemblage show garnet zoning from Alm₆₉Gr₂₁Py₁₀ (core) to Alm₆₁Gr₁₃Py₂₆ (rim) and pyroxene zoning from Jd₅₀ (core) through Jd₇₇ to Jd₅₅ (rim). Pyroxene cores are Cr-rich in another rock. Sharp compositional discontinuities and zoning reversals are preserved in garnet and pyroxene. Oscillatory zoning occurs in both phases on a 10–20 m scale, with variations of up to 6% Py in garnet and 15% Jd in pyroxene. Phengite is unzoned and contains 74% celadonite endmember.Skeletal, pyroxene-filled garnet crystals are common in some rocks, and garnets in other rocks clearly began growth as shell-like crystals. Some rocks contain domains of coarse, prismatic pyroxene with very fine-grained, interstitial magnesium silicates. The texture appears to have resulted from crystallization in the presence of a fluid phase, and water pressure is inferred to have equalled total pressure during crystallization. Eclogite formation at high water pressure may reflect subcrustal crystallization.An analysis of error propagation shows that ferrous iron calculations from electron probe data are not meaningful for these jadeitic pyroxenes, and temperature differences between core and rim crystallization cannot be documented. The garnet textures and oscillatory zoning are unusual for metamorphic rocks, and they suggest disequilibrium crystallization after overstepping of reaction boundaries. All data fit a model of eclogite formation during cooling and metasomatism of basaltic dikes intruded into a cool upper mantle, but the results here do not preclude other origins, such as subduction zone metamorphism.