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At least 163 records · Page 9Linked to original sources

A reconnaissance Rb-Sr, Sm-Nd, U-Pb, and K-Ar study of some host rocks and ore minerals in the West Shasta Cu- Zn district, California

The Copley Greenstone, Balaklala Rhyolite, and Mule Mountain stock in the West Shasta Cu-Zn district, California, have Rb-Sr, Sm-Nd, U-Pb, and K-Ar systematics that indicate they are a cogenetic suite of ensimatic island-arc rocks about 400 m.y. Pervasive alteration and mineralization of these rocks, for the most part, was syngenetic and the major component of the mineralizing fluid was Devonian seawater. K-Ar ages of quartz-sericite concentrates from ore horizons and Rb-Sr systematics of a few rock and ore specimens record a later thermal and mineralizing event in the district of about 260 m.y. Contamination of some rocks with pelagic sediments is indicated by the Sm-Nd data.

Economic Geology

Method for determining the age of igneous rocks using the accessory minerals

The age of igneous rocks is determinable by a method based on the included accessory minerals . In the common igneous rocks , most of the lead is concentrated in the potassium minerals , and most of the radioactivity is in the zircon and other accessory minerals . The lead in the potassium minerals is believed to be mostly primary lead; that in zircon is probably chiefly radiogenic lead. By separating the zircon of fresh igneous rocks , determining the amount of lead with the spectrograph and the radioactivity by alpha counters, the age of Paleozoic and Precambrian rocks can be determined with an accuracy of approximately 90 per cent. Basalts and gabbros may contain too few accessory minerals for satisfactory age determination by this method . Zircon is the most satisfactory mineral for this kind of determination. Apatite and sphene give high results and therefore must contain primary lead. Sphene gives erratic results.

Geological Society of America Bulletin

Radioactive springs geochemical data related to uranium exploration

Radioactive mineral springs and wells at 33 localities in the States of Colorado, Utah, Arizona and New Mexico in the United States were sampled and studied to obtain geochemical data which might be used for U exploration. The major source of radioactivity at mineral spring sites is 226 Ra. Minor amounts of 228 Ra, 238 U and 232 Th are also present. Ra is presumed to have been selectively removed from possibly quite deep uranium-mineralized rock by hydrothermal solutions and is either precipitated at the surface or added to fresh surface water. In this way, the source rocks influence the geochemistry of the spring waters and precipitates. Characteristics of the spring waters at or near the surface are also affected by variations in total dissolved solids, alkalinity, temperature and co-precipitation. Spring precipitates, both hard and soft, consist of four major types: (1) calcite travertine; (2) iron- and arsenic-rich precipitates; (3) manganese- and barium-rich precipitates; and (4) barite, in some instances accompanied by S, Ra and U, if present in the spring water, are co-precipitated with the barite, Mn-Ba and Fe-As precipitates. Using parameters based on U and Ra concentrations in waters and precipitates springsite areas are tentatively rated for favourability as potential uraniferous areas.

Journal of Geochemical Exploration

Geochemical exploration for mineralized breccia pipes in northern Arizona, U.S.A.

Thousands of solution-collapse breccia pipe crop out in the canyons and on the plateaus of northern Arizona. Over 80 of these are known to contain U or Cu mineralized rock. The high-grade U ore associated with potentially economic concentrations of Ag, Pb, Zn, Cu, Co and Ni in some of these pipes has continued to stimulate mining and exploration activity in northern Arizona, despite periods of depressed U prices. Large expanses of northern Arizona are comprised of undissected high plateaus; recognition of pipes in these areas is particularly important because mining access to the plateaus is far better than to the canyons. The small size of the pipes, generally less than 600 ft (200 m) in diameter, and limited rock outcrop on the plateaus, compounds the recognition problem. Although the breccia pipes, which bottom in the Mississippian Redwall Limestone, are occasionally exposed on the plateaus as circular features, so are unmineralized near-surface collapse features that bottom in the Permian Kaibab and Toroweap Formations. The distinction between these two classes of circular features is critical during exploration for this unique type of U deposit.

Arizona

Geochemical soil sampling for deeply-buried mineralized breccia pipes, northwestern Arizona

Thousands of solution-collapse breccia pipes crop out in the canyons and on the plateaus of northwestern Arizona; some host high-grade uranium deposits. The mineralized pipes are enriched in Ag, As, Ba, Co, Cu, Mo, Ni, Pb, Sb, Se, V and Zn. These breccia pipes formed as sedimentary strata collapsed into solution caverns within the underlying Mississippian Redwall Limestone. A typical pipe is approximately 100 m (300 ft) in diameter and extends upward from the Redwall Limestone as much as 1000 m (3000 ft). Unmineralized gypsum and limestone collapses rooted in the Lower Permian Kaibab Limestone or Toroweap Formation also occur throughout this area. Hence, development of geochemical tools that can distinguish these unmineralized collapse structures, as well as unmineralized breccia pipes, from mineralized breccia pipes could significantly reduce drilling costs for these orebodies commonly buried 300–360 m (1000–1200 ft) below the plateau surface. Design and interpretation of soil sampling surveys over breccia pipes are plagued with several complications. (1) The plateau-capping Kaibab Limestone and Moenkopi Formation are made up of diverse lithologies. Thus, because different breccia pipes are capped by different lithologies, each pipe needs to be treated as a separate geochemical survey with its own background samples. (2) Ascertaining true background is difficult because of uncertainties in locations of poorly-exposed collapse cones and ring fracture zones that surround the pipes. Soil geochemical surveys were completed on 50 collapse structures, three of which are known mineralized breccia pipes. Each collapse structure was treated as an independent geochemical survey. Geochemical data from each collapse feature were plotted on single-element geochemical maps and processed by multivariate factor analysis. To contrast the results between geochemical surveys (collapse structures), a means of quantifying the anomalousness of elements at each site was developed. This degree of anomalousness, named the “correlation value”, was used to rank collapse features by their potential to overlie a deeply-buried mineralized breccia pipe. Soil geochemical results from the three mineralized breccia pipes (the only three of the 50 that had previously been drilled) show that: (1) Soils above the SBF pipe contain significant enrichment of Ag, Al, As, Ba, Ga, K, La, Mo, Nd, Ni, Pb, Sc, Th, U and Zn, and depletion in Ca, Mg and Sr, in contrast to soils outside the topographic and structural rim; (2) Soils over the inner treeless zone of the Canyon pipe show Mo and Pb enrichment anf As and Ga depletion, in contrast to soils from the surrounding forest; and (3) The soil survey of the Mohawk Canyon pipe was a failure because of the rocky terrane and lack of a B soil horizon, or because the pipe plunges. At least 11 of the 47 other collapse structures studied contain anomalous soil enrichments similar to the SBF uranium ore-bearing pipe, and thus have good potential as exploration targets for uranium. One of these 11, #1102, does contain surface mineralized rock. These surveys suggest that soil geochemical sampling is a useful tool for the recognition of many collapse structures with underlying ore-bearing breccia pipes.

Arizona

Isotopic variations of dissolved copper and zinc in stream waters affected by historical mining

Zinc and Cu play important roles in the biogeochemistry of natural systems, and it is likely that these interactions result in mass-dependent fractionations of their stable isotopes. In this study, we examine the relative abundances of dissolved Zn and Cu isotopes in a variety of stream waters draining six historical mining districts located in the United States and Europe. Our goals were to (1) determine whether streams from different geologic settings have unique or similar Zn and Cu isotopic signatures and (2) to determine whether Zn and Cu isotopic signatures change in response to changes in dissolved metal concentrations over well-defined diel (24-h) cycles. Average δ 66 Zn and δ 65 Cu values for streams varied from +0.02‰ to +0.46‰ and −0.7‰ to +1.4‰, respectively, demonstrating that Zn and Cu isotopes are heterogeneous among the measured streams. Zinc or Cu isotopic changes were not detected within the resolution of our measurements over diel cycles for most streams. However, diel changes in Zn isotopes were recorded in one stream where the fluctuations of dissolved Zn were the largest. We calculate an apparent separation factor of ∼0.3‰ ( 66/64 Zn) between the dissolved and solid Zn reservoirs in this stream with the solid taking up the lighter Zn isotope. The preference of the lighter isotope in the solid reservoir may reflect metabolic uptake of Zn by microorganisms. Additional field investigations must evaluate the contributions of soils, rocks, minerals, and anthropogenic components to Cu and Zn isotopic fluxes in natural waters. Moreover, rigorous experimental work is necessary to quantify fractionation factors for the biogeochemical reactions that are likely to impact Cu and Zn isotopes in hydrologic systems. This initial investigation of Cu and Zn isotopes in stream waters suggests that these isotopes may be powerful tools for probing biogeochemical processes in surface waters on a variety of temporal and spatial scales.

Geochimica et Cosmochimica Acta

Quantification of manganese for ChemCam Mars and laboratory spectra using a multivariate model

We report a new calibration model for manganese using the laser-induced breakdown spectroscopy instrument that is part of the ChemCam instrument suite onboard the NASA Curiosity rover. The model has been trained using an expanded set of 523 manganese-bearing rock, mineral, metal ore, and synthetic standards. The optimal calibration model uses the Partial Least Squares (PLS) and Least Absolute Shrinkage and Selection Operator (LASSO) multivariate techniques, with a novel “double blending” technique. We determined the detection limit for manganese is 82 ppm using a method blank procedure and is possibly as low as 27 ppm based on visual inspection of the spectra. Based on a representative test set consisting of measurements on 93 standards, the double blended multivariate model shows a Root Mean Squared Error of Prediction (RMSEP) accuracy of 1.39 wt% MnO for the full blended model. Employing a local RMSEP estimate where the model performance is evaluated based on nearby test samples, the accuracy is 0.03 wt% at the quantification limit (0.05 wt% MnO), 0.4 wt% accuracy at 1.0 wt% MnO, and 4.4 wt% accuracy at 100 wt% MnO. Precision is estimated using the standard deviation of the test set measurements, and is ±0.01 wt% MnO at the quantification limit, ±0.09 wt% MnO at 1.0 wt% MnO, and ± 2.1 wt% MnO at 100 wt% MnO (all 1 standard deviation). This new calibration is important for understanding the variation of manganese in the bedrock with the Curiosity rover on Mars, which provides insight into past redox conditions on Mars.

Spectrochimica Acta B

Weathering of slags

Weathering is a natural process causing the transformation of minerals, rocks, and related materials like glass under near-surface conditions. Although metallurgical slags are human-made materials, they also undergo natural weathering processes. As base metal slags weather, the released solutions may contain contaminants that could pose an environmental risk. On the other hand, weathering of ferrous slags is important because of the common reuse of the slags. This chapter summarizes factors that affect rates of slag weathering as well as defining and characterizing the two stages of weathering (incipient and advanced) as they are observed in a wide variety of individual phases and slags. We conclude that slags weather at different scales and rates depending on their chemistry and phase composition as well as the external conditions. Furthermore, weathering of slags is a process that is not perfectly reflected by natural processes because these materials are complex (in terms of texture, composition, and disequilibrium with surficial conditions) and not always analogous to rocks. Therefore, some information in this chapter on weathering is applicable to all slag types, some is relevant to only specific slag types, and some aspects require additional study.

Book chapter

Magmatic source of the opening phase of Kīlauea’s 2018 Lower East Rift Zone eruption

The 2018 eruption of Kīlauea volcano in its Lower East Rift Zone began with the discharge of evolved high-Ti basalt as weak lava fountains and short, slow-moving lava flows. The lavas were quickly geochemically recognized as being derived from magmas stored within the rift zone and remobilized by a new intrusion, a sequence that is common at Kīlauea. This initial phase of the 2018 eruption, referred to as phase 1a, lasted for 6 days and was followed by extrusion of mixed magma after a 3-day pause. Even though remobilization of older rift zone magmas is common within Kīlauea’s rift zones, it is difficult to determine which past intrusion(s) may have initially emplaced those stored magmas. This difficulty stems from the tendency for Kīlauea magmas to follow very similar differentiation paths without significant variations in major, minor, or even trace element chemistry. We investigate possible magma sources for the lavas erupted during phase 1a of the 2018 eruption using whole-rock, mineral, and glass major and trace element compositions from historical East Rift Zone eruptions with adjacent fissures. We consider two primary hypotheses for the phase 1a source: magmas associated with the 1955 Lower East Rift Zone eruption or the nine eruptions in the Middle and Upper East Rift Zone during the 1960s. Our results suggest that magma associated with the earliest phases of Kīlauea’s 1955 eruption was the most likely source of the 2018 phase 1a remobilized magma. We determine volatile saturation pressures from melt inclusion chemistry and find similar storage depths for the 2018 phase 1a and early 1955 magmas. The phase 1a and early 1955 lavas are nearly indistinguishable in all of the compositional criteria considered, implying that the leftover 1955 magma body barely cooled and differentiated in the 63 years between eruptions (cooling rates of ~0.1 °C/year). This study sheds light on the potential for protracted storage of eruptible magmas in rift zones at Kīlauea, and highlights some of the challenges and solutions to identifying genetic relationships between magmas at Kīlauea.

Hawaii

Lunar soil: Size distribution and mineralogical constituents

The lunar soil collected by Apollo 11 consists primarily of submillimeter material and is finer in grain size than soil previously recorded photographically by Surveyor experiments. The main constituents are fine-grained to glassy rocks of basaltic affinity and coherent breccia of undetermined origin. Dark glass, containing abundant nickel-iron spheres, coats many rocks, mineral, and breccia fragments. Several types of homogeneous glass occur as fragments and spheres. Colorless spheres, probably an exotic component, are abundant in the fraction finer than 20 microns.

Science

Analyses of rocks from the laboratory of the United States Geological Survey, 1880-1903

The present Geological Survey of the United States was organized in 1879. In 1880 a chemical laboratory was established at Denver, in connection with the Colorado work, in charge of Dr. W. F. Hillebrand, with whom were associated Mr. Antony Guyard and, later, Mr. L. G. Eakins. In 1882 Dr. W. H. Melville was placed in charge of a second laboratory at San Francisco, and in the autumn of 1883 the central laboratory was started in Washington, with myself as chief chemist. In November, 1885, Doctor Hillebrand was transferred to Washington; early in 1888 he was followed by Mr. Eakins, and the Denver laboratory was discontinued. In the spring of 1890 Doctor Melville also was transferred to Washington, and since then the chemical work of the Survey has been concentrated at headquarters. Up to January 1, 1904, over 5,300 analyses have been made in the laboratory at Washington. These represent rocks, minerals, ores, waters, sediments, coals, metals, and so on through all the range of substances with which geology has to do. There were also some hundreds of analyses made in the laboratories at Denver and San Francisco. A fair amount of research work upon mineralogical and analytical problems has also been done. In all of this work the following chemists have been employed: E. T. Allen, Charles Catlett, T. M. Chatard, F. W. Clarke, L. G. Eakins, F. A. Gooch, Antony Guyard, W. F. Hillebrand, W. H. Melville, R. B. Riggs, W. T. Schaller, E. A. Schneider, George Steiger, H. N. Stokes, E. C. Sullivan, William Valentine, and J. E. Whitfield. As many as eight of these have been at work simultaneously; at present only six are connected with the Survey. Other officers of the Survey have been occupied more or less with chemical questions; but the men named in this list were connected directly with the laboratory. Some work for the chemical division has also been done by chemists not regularly on the rolls of the Survey; but their analyses, with the exception of a single group to be noted later, do not fall within the scope of this paper.

Bulletin

Lithium use in batteries

Lithium has a number of uses but one of the most valuable is as a component of high energy-density rechargeable lithium-ion batteries. Because of concerns over carbon dioxide footprint and increasing hydrocarbon fuel cost (reduced supply), lithium may become even more important in large batteries for powering all-electric and hybrid vehicles. It would take 1.4 to 3.0 kilograms of lithium equivalent (7.5 to 16.0 kilograms of lithium carbonate) to support a 40-mile trip in an electric vehicle before requiring recharge. This could create a large demand for lithium. Estimates of future lithium demand vary, based on numerous variables. Some of those variables include the potential for recycling, widespread public acceptance of electric vehicles, or the possibility of incentives for converting to lithium-ion-powered engines. Increased electric usage could cause electricity prices to increase. Because of reduced demand, hydrocarbon fuel prices would likely decrease, making hydrocarbon fuel more desirable. In 2009, 13 percent of worldwide lithium reserves, expressed in terms of contained lithium, were reported to be within hard rock mineral deposits, and 87 percent, within brine deposits. Most of the lithium recovered from brine came from Chile, with smaller amounts from China, Argentina, and the United States. Chile also has lithium mineral reserves, as does Australia. Another source of lithium is from recycled batteries. When lithium-ion batteries begin to power vehicles, it is expected that battery recycling rates will increase because vehicle battery recycling systems can be used to produce new lithium-ion batteries.

Circular

Central Colorado Assessment Project - Application of integrated geologic, geochemical, biologic, and mineral resource studies

Central Colorado is one of the fastest-growing regions in the Western United States. Population along the Front Range increased more than 30 percent between 1990 and 2000 (http://www.demographia.com/db-metro3newworld.htm) with some counties within the study area, such as Park County, experiencing greater than 100-percent growth (http://www.censusscope.org/us/s8/rank_popl_growth.html). This growth has caused tremendous demand for natural resources and has created challenging land-management issues related to the interface between wilderness and urban expansion. Management of this wilderness/urban interface will benefit from current digital geoscience information collected by the U.S. Geological Survey (USGS) Central Colorado Assessment Project that began in 2003. Approximately 20,800 square miles (53,800 km2) of land divided almost equally between the public and private sectors were part of the assessment. The study area includes much of the Colorado Mineral Belt, a northeast-trending zone that contains 30 economically significant metal deposits. Historically, the area provided much of Colorado's metal production. The only active gold and molybdenum mines in Colorado lie within the study area. Recently, metal and uranium exploration activity has increased sharply in response to record prices for metals and uranium. This further underscores the need for up-to-date geoscience information presented in compatible GIS databases to facilitate rapid land-management decisions. Cooperative studies by USDA Forest Service, National Park Service supported by the USGS Mineral Resources Program (MRP), and National Cooperative Geologic Mapping Programs (NCGMP) contributed to the mineral-resource assessment and included regional geologic mapping at the scale 1:100,000, collection and geochemical studies of stream sediments, surface water, and bedrock samples, macroinvertebrate and biofilm studies in the riparian environment, remote-sensing studies, and geochronology. Geoscience information available as GIS layers has improved understanding of the distribution of metallic, industrial, and aggregate resources, location of areas that have potential for their discovery or development, helped to understand the relation of tectonics, magmatism, and paleohydrology to the genesis of the metal deposits in the region, and provided insight on the geochemical and environmental effects that historical mining and natural, mineralized rock exposures have on surface water, ground water, and aquatic life.

Fact Sheet

Ferricrete, manganocrete, and bog iron occurrences with selected sedge bogs and active iron bogs and springs in the upper Animas River watershed, San Juan County, Colorado

During 1996 to 2000, the Bureau of Land Management, National Park Service, Environmental Protection Agency, United States Department of Agriculture (USDA) Forest Service, and the U.S. Geological Survey (USGS) developed a coordinated strategy to (1) study the environmental effects of historical mining on Federal lands, and (2) remediate contaminated sites that have the greatest impact on water quality and ecosystem health. This dataset provides information that contributes to these overall objectives and is part of the USGS Abandoned Mine Lands Initiative. Data presented here represent ferricrete occurrences and selected iron bogs and springs in the upper Animas River watershed in San Juan County near Silverton, Colorado. Ferricretes (stratified iron and manganese oxyhydroxide-cemented sedimentary deposits) are one indicator of the geochemical baseline conditions as well as the effect that weathering of mineralized rocks had on water quality in the Animas River watershed prior to mining. Logs and wood fragments preserved in several ferricretes in the upper Animas River watershed, collected primarily along streams, yield radiocarbon ages of modern to 9,580 years B.P. (P.L. Verplanck, D.B. Yager, and S.E. Church, work in progress). The presence of ferricrete deposits along the current stream courses indicates that climate and physiography of the Animas River watershed have been relatively constant throughout the Holocene and that weathering processes have been ongoing for thousands of years prior to historical mining activities. Thus, by knowing where ferricrete is preserved in the watershed today, land-management agencies have an indication of (1) where metal precipitation from weathering of altered rocks has occurred in the past, and (2) where this process is ongoing and may confound remediation efforts. These data are included as two coverages-a ferricrete coverage and a bogs and springs coverage. The coverages are included in ArcInfo shapefile and ArcInfo interchange file format.

Colorado

USGS Digital Spectral Library splib05a

We have assembled a digital reflectance spectral library of spectra that covers wavelengths from the ultraviolet to near-infrared along with sample documentation. The library includes samples of minerals, rocks, soils, physically constructed as well as mathematically computed mixtures, vegetation, microorganisms, and man-made materials. The samples and spectra collected were assembled for the purpose of using spectral features for the remote detection of these and similar materials.

Open-File Report

Reconnaissance geochemical survey of the At Taif-Al Bahah region, southern Hijaz, Kingdom of Saudi Arabia

Pan concentrates were prepared from 265 wadi sediment samples collected during a geochemical reconnaissance conducted between At Taif and Al Bahah to further assess previously identified tungsten anomalies and to locate additional mineralized rock. The samples were analyzed by semiquantitative spectrographic methods for 30 elements, and tungsten was determined by colorimetry. All determinations in excess of two standard deviations greater than the population mean are considered anomalous, although any detectable amount of tin or tungsten (detection limits 10 and 50 parts per million, respectively) is defined as anomalous. An area south of At Taif containing significant tungsten was confirmed and found to be larger than initially determined. A possible porphyry copper pluton was discovered 50 km south-southeast of At Taif. Thirty kilometers south of At Taif, a low-grade tin anomaly associated with an S-type granite was identified. In addition, the sampling identified seven anomalous areas attributable to rock geochemically atypical of the study region. Finally, although samples from the A1 Lith-Hajrah area collected for an earlier study were found to contain anomalous concentrations of tungsten, samples collected there during this study do not support those findings.

Open-File Report

Reconnaissance geochemical survey of Al Jurdhawiyah and Wadi al Jarir quadrangles, sheets 25/42 D and 25/42 C, Kingdom of Saudia Arabia

A reconnaissance wadi-sediment geochemical survey was conducted in the Al Jurdhawiyah (sheet 28/42 D) and Wadi al Jarir (sheet 2G/42 C) quadrangles in order to identify anomalies potentially related to mineralized rock. Sieved bulk-sediment fractions and pan concentrates were created from the original samples collected from wadis in the two quadrangles. A semiquantitative 30-element spectrographic analysis was completed on both the sieved bulk-sediment fraction and the pan concentrate of each sample. The results were statistically analyzed in an attempt to identify anomalous regions. Anomaly threshold values were calculated for most elements; the threshold value of an element in a data set is defined as the geometric mean value plus two standard deviations. The Bald al Jimalah West tin-tungsten deposit (MODS 02661) in the southern part of the Al Jurdhawiyah quadrangle was identified by one pan-concentrate sample containing anomalous concentrations of tin and tungsten. Samples near the Bald al Jimalah East ancient lead-zinc-silver mines (MODS 00960) contain strongly anomalous concentrations of tin and lead and to a lesser extent of tungsten and copper. Both of these regions and other regions containing anomalous concentrations of certain elements are recommended for additional studies. A comparison of results obtained from sieved bulk-sediment fractions and pan concentrates indicates that the latter is the better medium for these geochemical investigations.

Open-File Report

Geochemistry of stream-sediment samples from the Santa Renia Fields and Beaver Peak quadrangles, northern Carlin Trend, Nevada

A broad west-to-east increase of many metal concentrations has been found in stream sediments during a reconnaissance investigation conducted in conjunction with geologic studies in the Santa Renia Fields and Beaver Peak 7–1/2 minute quadrangles near the northern end of the Carlin trend of gold deposits in the Tuscarora Mountains. This regional increase in metal concentrations coincides with a dramatic change in landform wherein high concentrations of metals in stream sediments appear to correlate directly with areas of high elevations and steep slopes in the Beaver Peak quadrangle. Robust erosion combined with high flow rates in streams from these higher elevations are envisaged to have contributed significantly to increased metal concentrations in the stream sediments by an enhanced presence of minerals with high specific gravities and a correspondingly diminished presence of minerals with low specific gravities. Minerals with low specific gravities probably have been preferentially flushed down stream because of high transporting capacities for sediment by streams in the Beaver Peak quadrangle. In addition, the Carlin trend, a generally northwest-alignment of gold deposits in the Santa Renia Fields quadrangle, is well outlined by arsenic concentrations that include a maximum of approximately 54 parts per million. Further, a weakly developed distal-to-proximal metal zonation towards these gold deposits appears to be defined respectively in plots showing distributions of thallium, arsenic, antimony, and zinc. A broad area of high metal concentrations—including sharply elevated abundances of Ag, As, Au, Cd, Co, Cu, Mn, Ni, P, Sb, Sc, Te, V, and especially Zn—near the southeast corner of the Beaver Peak quadrangle primarily could be the result of stratiform mineralized rocks in the Ordovician Vinini Formation or Devonian Slaven Chert, or the result of a subsequent Mesozoic or Tertiary epigenetic overprint.

Nevada