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George A. Desborough

Publications and source records attributed to George A. Desborough.

32 records · Page 2Linked to original sources

BOWIEITE: A NEW RHODIUM-IRIDIUM-PLATINUM SULFIDE IN PLATINUM-ALLOY NUGGETS, GOODNEWS BAY, ALASKA.

Bowieite (Rh,Ir,Pt)//2S//3, a new mineral species, is found in three nuggets of platinum from Goodnews Bay, Alaska. In linearly polarized reflected light, and compared to the host, higher reflecting white platinum-iridium alloy, bowieite is pale gray to pale gray-brown; neither bireflectance nor reflectance pleochroism is apparent. With polars crossed, its anisotropic rotation tints vary from gray to dark brown. Luminance values (relative to the CIE illuminant C) for R//1 and R//2, computed from full spectral data for the most bireflectant grain, are 45. 8% and 48. 2% in air, and 30. 5% and 33. 0% in oil, respectively. VHN//1//0//0 1288 (858 to 1635). Bowieite is orthorhombic, space group Pnca, with a 8. 454(7) -8. 473(8), b 5. 995(1)-6. 002(7), c 6. 143(1)-6. 121(8) A, Z equals 4. Some grains that are 2. 6 to 3. 8 atomic % metal-deficient occur as an optically coherent rim on bowieite; the rim and the bowieite grain are not optically continuous.

Canadian Mineralogist

Quantitative analysis versus semiquantitative optical emission spectrographic analysis of chromium, nickel, zinc, vanadium, and molybdenum in organic-rich Paleozoic marine strata, Western United States

Comparison of analytical results between the quantitative method and the semiquantitative six-step optical-emission spectrographic method commonly shows significantly lower values for the semiquantitative method. The lower values are most obvious for splits from the same samples of fine-grained organic-rich rocks where the concentrations of the metals chromium, nickel, zinc, vanadium, and molybdenum are greater than about 200 ppm (parts per million). Samples compared are Paleozoic marine rocks from the Western United States; they include the Permian Phosphoria Formation (Idaho, Montana, Utah, Wyoming), Mississippian Chainman Shale (Nevada and Utah), Mississippian Heath Formation (Montana), Mississippian Doughnut Formation (Utah), Devonian Woodruff Formation (Nevada), and Ordovician Vinini Formation (Nevada). The semiquantitative method consistently underestimates the concentration of the five metals studied by a factor of 1.7 to 2.7 and, thus, cannot be considered reliable for determining the concentration of metals in these rocks if the reported semiquantitative values exceed about 100 ppm. It is noteworthy that the most comprehensive analytical and statistical studies of metal concentrations in black shales of the United States have used the semiquantitative six-step optical-emission method of analysis.

Idaho, Montana, Nevada, Utah, Wyoming

Metals in Devonian kerogenous marine strata at Gibellini and Bisoni properties in southern Fish Creek Range, Eureka County, Nevada

A kerogen-rich sequence of siliceous mudstone, siltstone, and chert as much as 60 m thick on ridge 7129 in the southern Fish Creek Range, referred to as Gibellini facies of the Woodruff Formation, has been evaluated on the surface and in drill holes principally for its potential resources of vanadium, zinc, selenium, molybdenum, and syncrude oil content. The strata are part of a strongly deformed allochthonous mass of eugeosynclinal Devonian marine rocks that overlie deformed allochthonous Mississippian siliceous rocks and relatively undeformed autochthonous Mississippian Antler flysch at this locality. The vanadium in fresh black rocks obtained from drill holes and fresh exposures in trenches and roadcuts occurs chiefly in organic matter. Concentrations of vanadium oxide (V2O5) in unoxidized samples range from 3,000 to 7,000 ppm. In oxidized and bleached rock that is prevalent at the surface, concentrations of vanadium oxide range from 6,000 to 8,000 ppm, suggesting a tendency toward enrichment due to surficial weathering and ground-water movement. Zinc occurs in sphalerite, and selenium occurs in organic matter; molybdenum appears to occur both in molybdenite and in organic matter. Concentrations of zinc in unoxidized rock range from 4,000 to 18,000 ppm, whereas in oxidized rock they range from 30 to 100 ppm, showing strong depletion due to weathering. Concentrations of selenium in unoxidized rock range from 30 to 200 ppm, whereas in oxidized rock they range from 200 to 400 ppm, indicating some enrichment upon weathering. Concentrations of molybdenum in unoxidized rock range from 70 to 960 ppm, whereas in oxidized rock they range from 30 to 80 ppm, indicating strong depletion upon weathering. Most fresh black rock is low-grade oil shale, and yields as much as 12 gallons/short ton of syncrude oil. Metahewettite is the principal vanadium mineral in the oxidized zone, but it also occurs sparsely as small nodules and fillings of microfractures in unweathered strata. In fresh rock, bluish-white opaline-like silica (chalcedonic quartz) fills microfractures, and is believed to have originated by diagenetic mobilization of opaline silica from radiolarian tests and sponge spicules. As revealed by microscopic study, the Gibellini facies originally consisted of siliceous muds, slimes, and oozes high in organic constituents. The organic matter is amorphous flaky and stringy sapropel, and probably includes remains of bacteria, phytoplankton, zooplankton, and minor higher plants. Recognizable organic remnants include radiolarian tests, sponge spicules, conodonts, brachiopod shells, algae, and humic debris. Diagnostic radiolarians indicate a Late Devonian age for the Gibellini facies of the Woodruff Formation. Some pyrite is disseminated through the rock and may be primary (syngenetic) but significant pyrite and marcasite occur in chalcedonic quartz veinlets and appear to be diagenetic. In fresh rock, black solid bitumen and liquid oil fill voids and microfractures. These early phase hydrocarbons probably were released during diagenesis from complex nonhydrocarbon molecular structures originating from living organisms, and formed without any major thermal degradation of the kerogen. Gas chromatographic analysis of the saturated hydrocarbon fraction indicates a very complex mixture dominated by branched and cyclic compounds. Conodont and palynomorph color alteration, vitrinite reflectance, and other organic geochemical data suggest that the organic matter in the rock is thermally immature and has not been subjected to temperatures greater than 60?C since deposition in Devonian time. All of these characteristics are consistent with the interpretation of a relatively low temperature and a shallow-burial history for the Gibellini facies on ridge 7129.

Open-File Report

Preliminary report on certain metals of potential economic interest in thin vanadium-rich zones in the Meade Park member of the Phosphoria Formation in western Wyoming and eastern Idaho

Electron microprobe, optical and chemical studies of fresh and weathered rocks permit preliminary conclusions concerning the concentration and mineralogical residence of certain elements of potential economic significance in thin, vanadium-rich zones in the Meade Peak Member of the Phosphoria Formation in western Wyoming and eastern Idaho. Elements of particular interest are V, Cr, Zn, Cd, Ag, Se, S, Ti, and Mo. Their principal mineralogical residence in fresh or unweathered rock has been established as follows: V is in, or associated with, organic material and minor amounts of V are in Ti-Fe oxysulfide and an unidentified Fe sulfide; Cr is in a 10 A mica. Zn and Cd are in sphalerite; Se is in pyrite; S is in pyrite, sphalerite and organic material; Ti is in TiO 2 and Ti 2 Fe(SO 3 ) 2 and Mo is in powellite. The principal minerals in fresh rocks are quartz, K-feldspar, albite, illite, calcite, and dolomite. Weathering or leaching by ground water removes pyrite, calcite, and dolomite. The leached rock sequences currently mined for phosphate may be amenable to extraction of the metals associated with the organic material.

Idaho, Wyoming

Energy dispersive spectrometry for quantitative mineralogical analyses: An ancillary system on an electron microphobe

Investigation of the Li-drifted Si-semiconductor X-ray detector for quantitative elemental analysis of some common rock-forming minerals shows that amounts of certain major elements having K spectra in the energy range of about 1.74 (Si) to 8.64 (Zn) kiloelectronvolts may be accurately determined, if spectral interferences are absent. Elements in major concentrations between 0.5 and 1.00 percent may be analyzed quantitatively without corrections of K spectra X-ray intensities when reference standards of similar composition are used and significant K spectra interferences between two adjacent elements are absent. Elemental concentrations less than about 0.5 weight percent cannot be precisely determined from raw X-ray intensity data owing to high and variable spectral background. Data show that spectral background corrections are feasible because spectral background is a linear function for the light-element oxides and silicates. Simultaneous quantitative elemental analysis, with both the energy dispersive spectrometer and the conventional wavelength dispersive spectrometers on the electron microprobe, is feasible.

Journal of Research of the U.S. Geological Survey

Annealing history limits for inhomogeneous, native gold grains as determined from Au-Ag diffusion rates

Quantitative study of intrinsic inhomogeneities in native gold grains from three deposits in the western United States has revealed concentration profiles that represent the integrated sum of natural diffusion plus original chemical heterogeneity. By assuming that measured natural concentration gradients result solely from diffusion, upper limits may be placed on the temperature-time annealing history of the gold nuggets. This assumption focuses on the end member case in which an initial step-discontinuity is assumed between measured extremes of concentration.Concentration changes of up to 30 weight percent Ag indicate probable deposition temperatures of less than 300 degrees C for electrum from Copper Basin, Arizona, and Alder Gulch, Montana. The gold in the Homestake, South Dakota, deposit probably was formed at temperatures well under 400 degrees C.In support of this study, new data for interdiffusion in the Au-Ag system were obtained from a series of annealing experiments followed by electron microprobe analysis. The interdiffusion coefficient, D, in the range 10 (super -10) to 10 (super -17) cm 2 sec (super -1) was determined from measured profiles across synthetic alloy pairs held at eight fixed temperatures from 297 degrees to 799 degrees C, for periods ranging from 32 hours to 730 days.

Arizona, Montana, South Dakota

Microprobe analysis of biotites - A method of correlating tuff beds in the Green River Formation, Colorado and Utah

Quantitative electron microprobe analyses of biotite grains for iron, magnesium, and titanium from tuff beds in the lacustrine Green River Formation (Eocene) of Colorado and Utah provide a tentative method of identification and a permissive stratigraphic correlation of tuffs. Tuff beds that have been identified and correlated by stratigraphic means were sampled at five localities in Colorado and Utah to determine if microprobe analyses of biotite could be used as a method of correlation. Although most of the original phenocrysts and glass shards of these pyroclastic beds have undergone extensive postdepositional alteration, biotite seems to have been unaffected. The iron, magnesium, and titanium contents of the biotite do not uniquely characterize individual tuff beds, but when the proportions of these elements are compared in a continuous stratigraphic sequence of beds, correlation of individual tuffs or groups of tuffs is possible over areas exceeding several hundred square miles. The method may be used for detailed correlation of pyroclastic beds where stratigraphic, faunal, and radiometric methods have been unsatisfactory.

Colorado, Utah

Distribution of silver and copper in placer gold derived from the northeastern part of the Colorado Mineral Belt

Placer gold grains from the modern streams originating in the Colorado Mineral Belt were examined for silver and copper content on a quantitative basis utilizing the electron microprobe. The variation among grains from a particular locality is large, but the mean silver content of the interior of the placer gold grains from each locality and (or) the variation in copper content may be of value in distinguishing lode sources and gold mining districts. Microprobe analysis of the interior of gold grains is independent of chemical actions that affect the border of placer gold grains during their transport history, and it is shown that distinct compositional groups of different lode sources may be identified even in a single sample--information that may aid in recognizing the existence of concealed lodes that once contributed to a placer environment.

Colorado