Geology topics
Roger P. Ashley
Publications and source records attributed to Roger P. Ashley.
Alteration mapping using multispectral images: Cuprite mining district, Esmeralda County, Nevada
No abstract available.
Spectra of altered rocks in the visible and near infrared
Visible and near-infrared (0.35 to 2.5 mu m) bidirectional reflection spectra were recorded for a suite of well-characterized hydrothermally altered rock samples. The spectra typically display well-defined bands caused by both electronic and vibrational processes in the individual mineral constituents.Electronic transitions in the iron-bearing constituent minerals produce diagnostic minima near 0.43, 0.65, 0.85, and 0.93 mu m. Vibrational transitions in clay and water-bearing mineral constituents typically produce characteristic single or multiple features over limited spectral ranges near 1.4, 1.75, 1.9, 2.2, and 2.35 mu m. The most abundant feature-producing minerals present in these rocks are hematite, goethite, and alunite, while others frequently present are jarosite, kaolinite, potassium micas, pyrophyllite, montmorillonite, diaspore, and gypsum.This study shows that visible-near infrared spectrometry is a reliable and rapid technique for detecting and identifying clay minerals and alunite in rocks. Because these minerals are important constituents of altered rocks, the feasibility of using the visible and near infrared for detecting altered rocks by remote-sensing techniques is indicated. The spectral region near 2.2 mu m is particularly important for this purpose.
Detection and mapping of hydrothermally altered rocks in the vicinity of the Comstock Lode, Virginia Range, Nevada, using enhanced Landsat images
The Virginia Range, immediately southeast of Reno, Nev., consists mainly of flows, breccias, and turfs of Miocene age. Most of these volcanic rocks are of intermediate composition; rhyodacite is the most common rock type. Basalt, rhyolite and rhyolite tuff, and tuffaceous sedimentary rocks of Miocene and Pliocene age also cover substantial areas in the range. Pre-Tertiary metasedimentary, metavolcanic, and granitic rocks are exposed in scattered inliers, mostly along the southern and eastern margins of the range. Several large areas and many small areas within the volcanic pile were subjected to hydrothermal alteration during and after the period of intermediate volcanic activity. Economic precious metal mineralization is spatially and temporally associated with the hydrothermal alteration in several areas. The most important deposit is the Comstock Lode, which produced 192 million troy ounces of silver and 8.3 million troy ounces of gold from epithermal veins (Bonham, 1969). The hydrothermally altered rocks include silicified, advanced argillic, montmorillonite-bearing argillic, and propylitic types. The first three types typically contain pyrite, and some propylitic rocks contain pyrite as well. Supergene oxidation of these pyritic rocks produces limonitic bleached rocks. The term 'limonite,' as used here, refers to any combination of the minerals hematite, goethite, and Jarosite. Where vegetation cover is sparse to moderate, these limonitic rocks are readily identified on Landsat images enhanced by the color-ratio composite technique developed by Rowan and others (1974), so the altered areas can be mapped. About 30 percent tree cover (here mainly pinyon pine) is sufficient to change the spectral signature of individual picture elements (pixels) enough so that limonitic materials can no longer be uniquely identified. As in all other areas where this technique has been applied, limonitic unaltered rocks with intermediate to high albedos have the same appearance on the color-ratio composite as limonitic altered rocks. This problem represents the most important limitation to the use of enhanced Landsat images for detection and mapping of hydrothermally altered rocks. Reflectance spectra of altered and unaltered rocks taken in the field in the Virginia Range show that most altered rocks have a conspicuous absorption band near 2.2 ?m produced by clay minerals or alunite, whereas unaltered rocks have no features in this spectral region. Thus spectral information for selected bands in the 1.1-2.5 ?m region may allow discrimination between limonitic altered and limonitic unaltered rocks (Rowan and others, 1977; Abrams and others, 1977; Rowan and Abrams, 1978). Another potential limitation is loss of spectral information on slopes with low effective sun angle. Although a minor problem in the Virginia Range, loss of information sufficient to preclude identification of limonitic altered rocks occurs with effective sun angle lower than 20-25 degrees. Thus, even at moderate latitudes substantial parts of areas with high topographic relief may be lost to observation.
Mapping of hydrothermal alteration in the Cuprite mining district, Nevada, using aircraft scanner images for the spectral region 0.46 to 2.36µm
Color composites of Landsat Multispectral Scanner ratio images that display variations in the intensity of ferric-iron absorption bands are highly effective for mapping limonitic altered rocks but are ineffective for mapping nonlimonitic altered rocks. Analysis of 0.45- to 2.5-µm field and laboratory spectra shows that iron-deficient opalized rocks in the Cuprite mining district, Nevada, have an intense OH-absorption band near 2.2 µm, owing to their content of clay minerals and alunite, and that this spectral feature is absent or weak in adjacent unaltered tuff and basalt. Altered rocks in the district can be discriminated from unaltered rocks with few ambiguities by use of color-ratio composite images derived from multispectral (0.46 to 2.36 µm) aircraft data. In addition, some effects of mineralogical zoning can be discriminated within the altered area. Only variations in amounts of limonite can be discerned in shorter wavelength aircraft data, Landsat Multispectral Scanner bands, and color aerial photographs.
Discrimination of hydrothermal altered and unaltered rocks in visible and near infrared multispectral images
Mineralogical differences between altered rocks and most unaltered rocks in south-central Nevada cause visible and near-infrared (0.45 to 2.4 mu m) spectral-reflectance differences which can be used to discriminate these broad categories of rocks in multispectral images. The most important mineralogical differences are the increased abundance of goethite, hematite, and jarosite, and the presence of alunite, montmorillonite, and kaolinite in the altered rocks. Analysis of reflectance spectra recorded in the field showed that the altered rock spectra are characterized by broad absorption bands in the 0.45-0.50 mu m and 0.85-0.95 mu m regions which are due to electronic processes in the iron ions, and a band near 2.2 mu m which is due to vibrational processes in the OH ions. These features are absent or weak in most of the unaltered rock spectra. Therefore, the shapes of the 0.45-2.4 mu m spectra for these altered and unaltered rocks are conspicuously different. However, because of the wavelength positions and widths of the Landsat Multispectral Scanner (MSS) bands, these spectral differences are not apparent in individual or color-infrared composite MSS images.The technique developed to enhance these subtle spectral differences combines rationing of the MSS bands and contrast stretching. The stretched ratio values are used to produce black-and-white images which depict materials according to spectral reflectance; ratioing minimizes the influence of topography and overall albedo on the grouping of spectrally similar materials. Color compositing of two or more stretched ratio images to form color-ratio composites provides additional enhancement. The most effective color-ratio composite for discriminating between the altered and unaltered areas, as well as among many of the unaltered rocks in south-central Nevada, was prepared using the following diazo color and stretched ratio image combinations: blue for MSS 4/5, yellow for MSS 5/6, and magenta for MSS 6/7. Altered areas appear green and brown in this combination.Field evaluation of this color-ratio composite shows that excluding alluvial areas, approximately 80 percent of the green and brown color patterns are related to hydrothermal alteration. The remaining 20 percent consists mainly of pink hematitic crystallized tuff, a result of vapor-phase crystallization, and of tan and red ferruginous shale and siltstone. Discrimination of this unaltered tuff from the altered rocks may be possible in the 2.2 mu m region because this absorption band is absent in the tuff spectra. However, because the shale and siltstone are mineralogically and spectrally similar to the altered rocks, there appears to be little prospect of distinguishing these rocks from altered rocks in visible and near-infrared multispectral images.
Middle Tertiary plutonism in the Santa Catalina and Tortolita mountains, Arizona
Recent reconnaissance geologic mapping in the Santa Catalina and Tortolita Mountains of southeastern Arizona, supplemented by new and published potassium-argon and fission-track ages, suggests that a large composite batholith of middle Tertiary (about 25 million years) age crops out extensively in both mountains. More than two-thirds of the batholith and contiguous wallrocks is gneissic, the gneissosity comprising strong cataclasis and mylonitization, penetrative planar and linear structures, and crystallization of muscovite and biotite in the foliation planes. New radiometric ages indicate that the deformation followed the crystallization of the batholith so closely that the K-Ar dating method cannot distinguish a difference, whereas previously published ages from the gneisses indicate a short time between the two events.
Direct dating of mineralization at Goldfield, Nevada, by potassium-argon and fission-track methods
Potassium-argon dating of hypogene alunite and K-mica from hydrothermally altered rocks at Goldfield, Nevada, yields mineralization ages of 20 to 21 m.y., in good agreement with a mineralization age established by potassium-argon dating of unaltered premineralization and postmineralization volcanic units. Premineralization volcanic units that are pervasively propylitized cannot be dated by the potassium-argon method but yield zircon fission-track ages, and in several cases yield concordant apatite fission-track ages. Two samples from premineralization units yield apatite ages concordant with the age of mineralization established by potassium-argon geochronometry, reflecting annealing of the apatite during the hydrothermal episode.Potassium-argon dating of supergene alunite samples yields imprecise ages in the range 9 to 12 m.y. that probably record the first exposure of their hydrothermally altered host rocks to oxidizing conditions. Potassium-argon dating of postmineralization basalts and silicic tuffs interbedded with conglomerates bearing altered rock clasts shows that the altered area was eroded nearly to present topographic levels by 11 m.y. ago, at which time it was covered by basalt flows now represented only by scattered remnants. Apatites from premineralization volcanic units give fission-track ages of 20 m.y. or more, indicating that no significant thermal event has affected altered rocks at Goldfield since mineralization took place.
Distribution of gold and other ore-related elements near ore bodies in the oxidized zone at Goldfield, Nevada
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Primary and secondary sulfates at Goldfield, Nevada
High S-34 values for primary alunites (formed during hydrothermal phase) replacing plagioclase and groundmass of altered volcanic rocks, secondary alunite veins (formed during supergene alteration) with S-34 values near zero permil
Preliminary geologic map of the Goldfield mining district, Esmeralda and Nye counties, Nevada
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Geochemical data for the Sixteen-to-one mine, near Silver Peak, Esmeralda County, Nevada
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Age of ore deposition at Goldfield, Nevada, from potassium-argon dating of alunite
No abstract available.
Evaluation of color and color infrared photography from the Goldfield mining district, Esmeralda and Nye Counties, Nevada
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