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Minerals & deposits

Find USGS publications on mineral resources and deposits. Search commodities and geographic names, then check source reports for geology and assessment methods.

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USGS2022

A model to assess industry vulnerability to disruptions in mineral commodity supplies

Mineral commodity supply disruptions have the potential to ripple through and impact the economy in many ways. Industrial vulnerability is a crucial component of mineral commodity criticality tools as it provides guidance on the economic importance of these commodities to regional criticality indices. Using an economic model that links mineral commodity end-use data to input-output tables and a linear optimization routine, reductions in economic output of individual industries and of the overall economy may be calculated. Such a model can also help to identify industries, be they direct or indirect consumers of the mineral commodities in question, that are most vulnerable to specific mineral commodity supply disruptions at different disruption magnitudes. In this assessment, 56 commodities’ end-use data for the year 2012 were paired with the United States’ detail-level Benchmark Input-Output accounts to build an industrial vulnerability model. The model does not evaluate the likelihood of specific supply disruptions but can be used to assess potential industry impacts for a range of scenarios. The model findings indicate that when the supplies of mineral commodities such as mica, lithium, and fluorspar were disrupted, large overall economic decline was paired with a large decline in many industries. On the other hand, gold, lead, and rhenium disruptions resulted in low declines and few disrupted industries.

Resources Policy↗

USGS2000

The effect of mineral bond strength and adsorbed water on fault gouge frictional strength

Recent studies suggest that the tendency of many fault gouge minerals to take on adsorbed or interlayer water may strongly influence their frictional strength. To test this hypothesis, triaxial sliding experiments were conducted on 15 different single-mineral gouges with various water-adsorbing affinities. Vacuum dried samples were sheared at 100 MPa, then saturated with water and sheared farther to compare dry and wet strengths. The coefficients of friction, μ, for the dry sheet-structure minerals (0.2-0.8), were related to mineral bond strength, and dropped 20-60% with the addition of water. For non-adsorbing minerals (μ = 0.6-0.8), the strength remained unchanged after saturation. These results confirm that the ability of minerals to adsorb various amounts of water is related to their relative frictional strengths, and may explain the anomalously low strength of certain natural fault gouges.

Geophysical Research Letters↗

USGS2004

Crystallographic controls on the frictional behavior of dry and water-saturated sheet structure minerals

We compare the frictional strengths of 17 sheet structure mineral powders, measured under dry and water-saturated conditions, to identify the factors that cause many of them to be relatively weak. The dry coefficient of friction μ ranges upward from 0.2 for graphite, leveling off at 0.8 for margarite, clintonite, gibbsite, kaolinite, and lizardite. The values of μ (dry) correlate directly with calculated (001) interlayer bond strengths of the minerals. This correlation occurs because shear becomes localized along boundary and Riedel shears and the platy minerals in them rotate into alignment with the shear planes. For those gouges with μ (dry) < 0.8, shear occurs by breaking the interlayer bonds to form new cleavage surfaces. Where μ (dry) = 0.8, consistent with Byerlee's law, the interlayer bonds are sufficiently strong that other frictional processes dominate. The transition in dry friction mechanisms corresponds to calculated surface energies of 2–3 J/m 2 . Adding water causes μ to decrease for every mineral tested except graphite. If the minerals are separated into groups with similar crystal structures, μ (wet) increases with increasing interlayer bond strength within each group. This relationship also holds for the swelling clay montmorillonite, whose water-saturated strength is consistent with the strengths of nonswelling clays of similar crystal structure. Water in the saturated gouges forms thin, structured films between the plate surfaces. The polar water molecules are bonded to the plate surfaces in proportion to the mineral's surface energy, and μ (wet) reflects the stresses required to shear through the water films.

Journal of Geophysical Research B: Solid Earth↗

USGS2021

Clays are not created equal: How clay mineral type affects soil parameterization

Clay minerals dominate the soil colloidal fraction and its specific surface area. Differences among clay mineral types significantly influence their effects on soil hydrological and mechanical behavior. Presently, the soil clay content is used to parameterize soil hydraulic and mechanical properties (SHMP) for land surface models while disregarding the type of clay mineral. This undifferentiated use of clay leads to inconsistent parameterization, particularly between tropical and temperate soils, as shown herein. We capitalize on recent global maps of clay minerals that exhibit strong climatic and spatial segregation of active and inactive clays to consider spatially resolved clay mineral types in SHMP estimation. Clay mineral-informed pedotransfer functions and machine learning algorithms trained with datasets including different clay types and soil structure formation processes improve SHMP representation regionally with broad implications for hydrological and geomechanical Earth surface processes.

Geophysical Research Letters↗

USGS2026

Hydrothermal manganese-oxide mineralization of a carbonate ooze, Samoan hotspot region, South Pacific Ocean

Low-temperature hydrothermal manganese oxides occur throughout the global oceans. However, the hydrothermal replacement of a carbonate ooze by manganese oxides is described here for the first time. The 24 samples dredged from three locations around the Territory of American Samoa in the South Pacific Ocean include six samples with remnant carbonate and volcaniclastic sediments, which we refer to as “low Mn,” and 18 samples in which the mineralization is pervasive and has replaced most original sediment, termed “high Mn.” The 18 high-Mn samples exhibit a mean Mn content of 51 wt.%. Higher Li and Mn contents and lower Fe contents in the high-Mn samples indicate a hydrothermal origin and distinguish these samples from hydrogenetic ferromanganese crusts. Mn-oxide layers are up to 90 mm thick, some with columns to 44 mm long and 10 mm wide, the magnitude of which has not been described previously. Samples are composed of birnessite and 10 Å phyllomanganate minerals. Textures of the thickest Mn layers indicate mineralization below the seabed from ascending fluids during multiple hydrothermal pulses. Mineralization took place by complete to partial replacement and cementation of foraminiferal sediments intermixed with volcaniclastic sediments in varying amounts. Our results highlight the production of carbonate sediment-hosted hydrothermal Mn oxides from multiple hydrothermal sources within the Samoan volcanic chain. The potential extensive distribution on the regional scale of this newly described mineralization process and unique element enrichments raise questions about its broader distribution globally and potential importance to hydrothermal processes, element mass balance, and seabed mineral resources.

Geochemistry, Geophysics, Geosystems↗

USGS2022

Lithospheric conductors reveal source regions of convergent margin mineral systems

The clean energy transition will require a vast increase in metal supply, yet new mineral deposit discoveries are declining, due in part to challenges associated with exploring under sedimentary and volcanic cover. Recently, several case studies have demonstrated links between lithospheric electrical conductors imaged using magnetotelluric (MT) data and mineral deposits, notably Iron Oxide Copper Gold (IOCG). Adoption of MT methods for exploration is therefore growing but the general applicability and relationship with many other deposit types remains untested. Here, we compile a global inventory of MT resistivity models from Australia, North and South America, and China and undertake the first quantitative assessment of the spatial association between conductors and three mineral deposit types commonly formed in convergent margin settings. We find that deposits formed early in an orogenic cycle such as volcanic hosted massive sulfide (VHMS) and copper porphyry deposits show weak to moderate correlations with conductors in the upper mantle. In contrast, deposits formed later in an orogenic cycle, such as orogenic gold, show strong correlations with mid-crustal conductors. These variations in resistivity response likely reflect mineralogical differences in the metal source regions of these mineral systems and suggest a metamorphic-fluid source for orogenic gold is significant. Our results indicate the resistivity structure of mineralized convergent margins strongly reflects late-stage processes and can be preserved for hundreds of millions of years. Discerning use of MT is therefore a powerful tool for mineral exploration.

North America, South America↗

USGS2011

Influence of changing water sources and mineral chemistry on the everglades ecosystem

Human influences during the previous century increased mineral inputs to the Florida Everglades by changing the sources and chemistry of surface inflows. Biogeochemical responses to this enrichment include changes in the availability of key limiting nutrients such as P, the potential for increased turnover of nutrient pools due to accelerated plant decomposition, and increased rates of mercury methylation associated with sulfate enrichment. Mineral enrichment has also been linked to the loss of sensitive macrophyte species, although dominant Everglades species appear tolerant of a broad range of mineral chemistry. Shifts in periphyton community composition and function provide an especially sensitive indicator of mineral enrichment. Understanding the influence of mineral chemistry on Everglades processes and biota may improve predictions of ecosystem responses to ongoing hydrologic restoration efforts and provide guidelines for protecting remaining mineral-poor areas of this peatland.

Florida↗

USGS2017

The application of microtextural and heavy mineral analysis to discriminate between storm and tsunami deposits

Recent work has applied microtextural and heavy mineral analyses to sandy storm and tsunami deposits from Portugal, Scotland, Indonesia and the USA. We looked at the interpretation of microtextural imagery (scanning electron microscopy) of quartz grains and heavy mineral compositions. We consider inundation events of different chronologies and sources (the AD 1755 Lisbon and 2004 Indian Ocean tsunamis, the Great Storm of 11 January 2005 in Scotland, and Hurricane Sandy in 2012) that affected contrasting coastal and hinterland settings with different regional oceanographic conditions. Storm and tsunami deposits were examined along with potential source sediments (alluvial, beach, dune and nearshore sediments) to determine provenance. Results suggest that tsunami deposits typically exhibit a significant spatial variation in grain sizes, microtextures and heavy minerals. Storm deposits show less variability, especially in vertical profiles. Tsunami and storm quartz grains had more percussion marks and fresh surfaces compared to potential source material. Moreover, in the studied cases, tsunami samples had fewer fresh surfaces than storm deposits. Heavy mineral assemblages are typically site-specific. The concentration of heavy minerals decreases upwards in tsunamigenic units, whereas storm sediments show cyclic concentrations of heavy minerals, reflected in the laminations observed macroscopically in the deposits.

Geological Society, London, Special Publications↗

USGS2022

Demonstration of a novel quantitative microscopy technique for automated characterization of in situ particulate matter in coal miners with progressive massive fibrosis

Rationale: Increasing exposure to respirable crystalline silica (RCS) linked to changes in mining production processes has been implicated in the resurgence of severe lung disease in U.S. coal miners. Lung mineralogy can provide insight into particle pathogenesis. However, standard approaches to characterizing in situ particulate matter (PM) by pulmonary pathologists have poor inter-rater comparability, and consensus agreement is time consuming. Scanning electron microscopy/energy-dispersive spectroscopy (SEM/EDX) is technically complex and labor intensive. We developed a method for quantitative in situ PM characterization using conventional polarized light microscopy (PLM) and explored PM features in lung tissue of coal miners with progressive massive fibrosis (PMF). Methods: With institutional review board approval, PLM images were obtained from 30 miners with PMF, classified by pathologists consensus based on PM profusion; 10 from each profusion group (mild/moderate/severe) were selected. Automated PM counting and characterization (including dimensions and grayscale intensity of PM > 0.3 m diameter) was performed on image samples using PLM with modified cell-counting software (BZ-X800 light microscope, Keyence Corporation, Osaka, Japan) (Figure 1). Quantitative PM density loge(PM count)/mm3 tissue was calculated for each sample and compared to pathologist PM profusion groups. PMF lesion type using consensus pathologist classification (13 coal-type, 9 mixed-type, and 8 silicotic-type) was compared to automated PM birefringence level (% particles with mean grayscale intensity <65, range 0-255). RCS particles are expected to be weakly birefringent (lower intensity) relative to other common minerals (e.g., silicates) contained in coal mine dust. PM features were analyzed in R 4.0.3 using one-way ANOVA for between-group comparisons. Results: Measured PM log-density increased significantly with higher qualitative profusion group (mild=10.480.98/mm3, moderate=11.460.81/mm3, severe=12.520.86/mm3, p<0.0001). Prevalence of weakly birefringent particles was significantly higher among silicotic-type PMF samples (31.57.9%) compared to either coal-type (21.510.1%, p=0.022) or mixed-type lesions (21.510.5%, p=0.025). Conclusion: This pilot study demonstrates the feasibility of a novel quantitative microscopy technique for counting and characterizing in situ lung PM in coal miners with PMF. Quantitative PM burden was comparable to pulmonary pathologists consensus profusion classification, but this method was substantially less time consuming and labor intensive and provided additional information about relevant PM features. The higher prevalence of weakly birefringent particles seen in silicotic-type PMF lesions may help inform mineralogic pathogenesis of RCS. Future efforts will expand the number of PMF cases analyzed, further validate our mineralogic findings using data from SEM/EDX and lung tissue digestate methods, and compare findings in historical versus contemporary coal miners with PMF.

Conference Paper↗

USGS2018

Proposed nomenclature for samarskite-group minerals: new data on ishikawaite and calciosamarskite

The current definition of samarskite-group minerals suggests that ishikawaite is a uranium rich variety of samarskite whereas calciosamarskite is a calcium rich variety of samarskite. Because these minerals are chemically complex, usually completely metamict, and pervasively altered, their crystal chemistry and structure are poorly understood. Warner and Ewing (1993) proposed that samarskite is an A 3+ B 5+ O 4 mineral with an atomic arrangement related to α-PbO 2 . X-ray diffraction analyses of the recrystallized type specimen of ishikawaite and the Ca-rich samarskite reveal that they have the same structure as samarskite-(Y) recrystallized at high temperatures. Electron microprobe analyses show that the only significant difference between samarskite-(Y), ishikawaite, and calciosamarskite lies in the occupancy of the A -site. The A -site of samarskite-(Y) is dominated by Y+ REE whereas the A -site of ishikawaite is dominantly U+Th and calciosamarskite is dominantly Ca. Additionally, a comparison of these data to those of Warner and Ewing (1993) show that in several cases Fe 2+ or Fe 3+ are dominant in the A -site. We propose that the name samarskite-( REE +Y) should be used when one of these elements is dominant and that the mineral be named with the most abundant of these elements as a suffix. The name ishikawaite should be used only when U+Th are dominant and the name calciosamarskite should only be used when Ca is the dominant cation at the A -site. Finally, because of the inability to quantify the valence state of iron in these minerals, the exact nature of the valence state of iron in these minerals could not be determined in this study.

Mineralogical Magazine↗

USGS2013

Integrated geophysical imaging of a concealed mineral deposit: a case study of the world-class Pebble porphyry deposit in southwestern Alaska

We combined aeromagnetic, induced polarization, magnetotelluric, and gravity surveys as well as drillhole geologic, alteration, magnetic susceptibility, and density data for exploration and characterization of the Cu-Au-Mo Pebble porphyry deposit. This undeveloped deposit is almost completely concealed by postmineralization sedimentary and volcanic rocks, presenting an exploration challenge. Individual geophysical methods primarily assist regional characterization. Positive chargeability and conductivity anomalies are observed over a broad region surrounding the deposit, likely representing sulfide minerals that accumulated during multiple stages of hydrothermal alteration. The mineralized area occupies only a small part of the chargeability anomaly because sulfide precipitation was not unique to the deposit, and mafic rocks also exhibit strong chargeability. Conductivity anomalies similarly reflect widespread sulfides as well as water-saturated glacial sediments. Mineralogical and magnetic susceptibility data indicate magnetite destruction primarily within the Cu-Au-Mo mineralized area. The magnetic field does not show a corresponding anomaly low but the analytic signal does in areas where the deposit is not covered by postmineralization igneous rocks. The analytic signal shows similar lows over sedimentary rocks outside of the mineralized area, however, and cannot uniquely distinguish the deposit. We find that the intersection of positive chargeability anomalies with analytic signal lows, indicating elevated sulfide concentrations but low magnetite at shallow depths, roughly delineates the deposit where it is covered only by glacial sediments. Neither chargeability highs nor analytic signal lows are present where the deposit is covered by several hundred meters of sedimentary and volcanic rocks, but a 3D resistivity model derived from magnetotelluric data shows a corresponding zone of higher conductivity. Gravity data highlight geologic features within the deposit, including shallow diorite sills that locally contain higher-grade mineralization. The results thus show ways in which an integrated survey approach might be used to distinguish zones of potentially economic mineralization.

Alaska↗

USGS2004

Changes in plant functional groups, litter quality, and soil carbon and nitrogen mineralization with sheep grazing in an Inner Mongolian Grassland

This study reports on changes in plant functional group composition, litter quality, and soil C and N mineralization dynamics from a 9-year sheep grazing study in Inner Mongolia. Addressed are these questions: 1) How does increasing grazing intensity affect plant community composition? 2) How does increasing grazing intensity alter soil C and N mineralization dynamics? 3) Do changes in soil C and N mineralization dynamics relate to changes in plant community composition via inputs of the quality or quantity of litter? Grazing plots were set up near the Inner Mongolia Grassland Ecosystem Research Station (IMGERS) with 5 grazing intensities: 1.3, 2.7, 4.0, 5.3, and 6.7 sheep ha −1 ·yr −1 . Plant cover was lower with increasing grazing intensity, which was primarily due to a dramatic decline in grasses, Carex duriuscula , and Artemisia frigida . Changes in litter mass and percentage organic C resulted in lower total C in the litter layer at 4.0 and 5.3 sheep ha −1 ·yr −1 compared with 2.7 sheep ha −1 ·yr −1 . Total litter N was lower at 5.3 sheep ha −1 ·yr −1 compared with 2.7 sheep ha −1 ·yr −1 . Litter C:N ratios, an index of litter quality, were significantly lower at 4.0 sheep ha −1 ·yr −1 relative to 1.3 and 5.3 sheep ha −1 ·yr −1 . Cumulative C mineralized after 16 days decreased with increasing grazing intensity. In contrast, net N mineralization ( NH 4 NO − 3 ) after a 12-day incubation increased with increasing grazing intensity. Changes in C and N mineralization resulted in a narrowing of CO 2 -C:net N min ratios with increasing grazing intensity. Grazing explained 31% of the variability in the ratio of CO 2 -C:net N min . The ratio of CO 2 -C:net N min was positively correlated with litter mass. Furthermore, there was a positive correlation between litter mass and A. frigida cover. Results suggest that as grazing intensity increases, microbes become more C limited resulting in decreased microbial growth and demand for N.

Journal of Range Management↗

USGS2012

Strata-bound Fe-Co-Cu-Au-Bi-Y-REE deposits of the Idaho Cobalt Belt: Multistage hydrothermal mineralization in a magmatic-related iron oxide copper-gold system

Mineralogical and geochemical studies of strata-bound Fe-Co-Cu-Au-Bi-Y-rare-earth element (REE) deposits of the Idaho cobalt belt in east-central Idaho provide evidence of multistage epigenetic mineralization by magmatic-hydrothermal processes in an iron oxide copper-gold (IOCG) system. Deposits of the Idaho cobalt belt comprise three types: (1) strata-bound sulfide lenses in the Blackbird district, which are cobaltite and, less commonly, chalcopyrite rich with locally abundant gold, native bismuth, bismuthinite, xenotime, allanite, monazite, and the Be-rich silicate gadolinite-(Y), with sparse uraninite, stannite, and Bi tellurides, in a gangue of quartz, chlorite, biotite, muscovite, garnet, tourmaline, chloritoid, and/or siderite, with locally abundant fluorapatite or magnetite; (2) discordant tourmalinized breccias in the Blackbird district that in places have concentrations of cobaltite, chalcopyrite, gold, and xenotime; and (3) strata-bound magnetite-rich lenses in the Iron Creek area, which contain cobaltiferous pyrite and locally sparse chalcopyrite or xenotime. Most sulfide-rich deposits in the Blackbird district are enclosed by strata-bound lenses composed mainly of Cl-rich Fe biotite; some deposits have quartz-rich envelopes. Whole-rock analyses of 48 Co- and/or Cu-rich samples show high concentrations of Au (up to 26.8 ppm), Bi (up to 9.16 wt %), Y (up to 0.83 wt %), ∑REEs (up to 2.56 wt %), Ni (up to 6,780 ppm), and Be (up to 1,180 ppm), with locally elevated U (up to 124 ppm) and Sn (up to 133 ppm); Zn and Pb contents are uniformly low (≤821 and ≤61 ppm, respectively). Varimax factor analysis of bulk compositions of these samples reveals geochemically distinct element groupings that reflect statistical associations of monazite, allanite, and xenotime; biotite and gold; detrital minerals; chalcopyrite and sparse stannite; quartz; and cobaltite with sparse selenides and tellurides. Significantly, Cu is statistically separate from Co and As, consistent with the general lack of abundant chalcopyrite in cobaltite-rich samples. Paragenetic relations determined by scanning electron microscopy indicate that the earliest Y-REE-Be mineralization preceded deposition of Co, Cu, Au, and Bi. Allanite, xenotime, and gadolinite-(Y) commonly occur as intergrowths with and inclusions in cobaltite; the opposite texture is rare. Monazite, in contrast, forms a poikiloblastic matrix to cobaltite and thin rims on allanite and xenotime, reflecting a later metamorphic paragenesis. Allanite and xenotime also show evidence of late dissolution and reprecipitation, forming discordant rims on older anhedral allanite and xenotime and separate euhedral crystals of each mineral. Textural data suggest extensive deformation of the deposits by folding and shearing, and by pervasive recrystallization, all during Cretaceous metamorphism. Sensitive high resolution ion microprobe U-Pb geochronology by Aleinikoff et al. (2012) supports these paragenetic interpretations, documenting contemporaneous Mesoproterozoic growth of early xenotime and crystallization of megacrystic A-type granite on the northern border of the district. These ages are used together with mineralogical and geochemical data from the present study to support an epigenetic, IOCG model for Fe-Co-Cu-Au-Bi-Y-REE deposits of the Idaho cobalt belt. A sulfide facies variant of IOCG deposits is proposed for the Blackbird district, in which reducing hydrothermal conditions favored deposition of sulfide minerals over iron oxides. This new model includes Mesoproterozoic vein mineralization and related Fe-Cl metasomatism that formed the biotite-rich lenses, a predominantly felsic magmatic source for metals in the deposits, given their local abundance of Y, REEs, and Be, and a major sedimentary component in the hydrothermal fluids based on independent sulfur isotope and boron isotope data for sulfides and ore-related tourmaline, respectively.

Economic Geology↗

USGS2013

Pb-Sr-Nd isotopes in surficial materials at the Pebble Porphyry Cu-Au-Mo Deposit, Southwestern Alaska: can the mineralizing fingerprint be detected through cover?

The Cretaceous Pebble porphyry Cu-Au-Mo deposit is covered by tundra and glacigenic sediments. Pb-Sr-Nd measurements were done on sediments and soils to establish baseline conditions prior to the onset of mining operations and contribute to the development of exploration methods for concealed base metal deposits of this type. Pebble rocks have a moderate range for 206 Pb/ 204 Pb = 18.574 to 18.874, 207 Pb/ 204 Pb = 15.484 to 15.526, and 208, Pb/ 204 Pb = 38.053 to 38.266. Mineralized granodiorite shows a modest spread in 87 Sr/ 86 Sr (0.704354–0.707621) and 143 Nd/ 144 Nd (0.512639–0.512750). Age-corrected (89 Ma) values for the granodiorite yield relatively unradiogenic Pb (e.g., 207 Pb/ 204 Pb <15.52), low values of 87 Sr/ 86 Sr, and positive values of ɛNd (1.00–4.52) that attest to a major contribution of mantle-derived source rocks. Pond sediments and soils have similar Pb isotope signatures and 87 Sr/ 86 Sr and 143 Nd/ 144 Nd values that resemble the mineralized granodiorites. Glacial events have obscured the recognition of isotope signatures of mineralized rocks in the sediments and soils. Baseline radiogenic isotope compositions, prior to the onset of mining operations, reflect natural erosion, transport and deposition of heterogeneous till sheets that included debris from barren rocks, mineralized granodiorite and sulfides from the Pebble deposit, and other country rocks that pre- and postdate the mineralization events. Isotopic variations suggest that natural weathering of the deposit is generally reflected in these surficial materials. The isotope data provide geochemical constraints to glimpse through the extensive cover and together with other geochemical observations provide a vector to concealed mineralized rocks genetically linked with the Pebble deposit.

Alaska↗

USGS2003

Geology of the Ivanhoe Hg-Au district, northern Nevada: Influence of Miocene volcanism, lakes, and active faulting on epithermal mineralization

The mercury-gold deposits of the Ivanhoe mining district in northern Nevada formed when middle Miocene rhyolitic volcanism and high-angle faulting disrupted a shallow lacustrine environment. Sinter and replacement mercury deposits formed at and near the paleosurface, and disseminated gold deposits and high-grade gold-silver veins formed beneath the hot spring deposits. The lacustrine environment provided abundant meteoric water; the rhyolites heated the water; and the faults, flow units, and lakebeds provided fluid pathways for the hydrothermal fluids. A shallow lake began to develop in the Ivanhoe area about 16.5 Ma. The lake progressively expanded and covered the entire area with fine-grained lacustrine sediments. Lacustrine sedimentation continued to at least 14.4 Ma, and periodic fluctuations in the size and extent of the lake may have been responses to both climate and nearby volcanism . The eruption of rhyolite and andesite flows and domes periodically disrupted the lacustrine environment and produced interfingered flows and lake sediments. The major pulse of rhyolitic volcanism took place between 15.16 ± 0.05 and 14.92 ± 0.05 Ma. High-angle faulting began in the basement about 15.2 Ma, penetrated to and disrupted the paleosurface after 15.10 ± 0.06 Ma, and largely ceased by 14.92 ± 0.05 Ma. Ground motion related to both faulting and volcanism created debris flows and soft-sediment deformation in the lakebeds. Mercury-gold mineralization was coeval with rhyolite volcanism and high-angle faulting , and it took place about 15.2 to 14.9 Ma. At and near the paleosurface, hydrothermal fluids migrated through tuffaceous sediments above relatively impermeable volcanic and Paleozoic units, creating chalcedonic, cinnabar-bearing replacement bodies and sinters. Disseminated gold was deposited in sedimentary and volcanic rocks beneath the mercury deposits, although the hydrologic path between the two ore types is unclear. Higher-grade gold-silver deposits formed in massive rhyolites and Paleozoic quartzites at deeper levels, and these mineralized zones possibly represent the feeder zones for the higher-level deposits. Fluctuations in the ground-water table locally produced hydrothermal oxidation of the near-surface mercury and disseminated gold deposits. The locus of mineralization shifted with time, moving south and east from its inception point in the west-central part of the district . Thus, although mineralization in the district took place during a span of 300,000 years, the duration of mineralization at any one place probably was much shorter. The low-sulfidation deposits of the Ivanhoe district formed at the same time and under similar conditions as those in the nearby Midas district , 15 km to the northwest, which includes the large, high-grade Ken Snyder gold-silver epithermal vein deposit. The exposures in the Ivanhoe district are interpreted to represent the near-surface example of the paleosurface that originally was present above the Midas mineralizing system. The resulting combined Ivanhoe -Midas model provides an exploration guide for epithermal deposits in similar geologic environments in northern Nevada .

Economic Geology↗

USGS1995

Characteristics of mineral licks used by white-tailed deer (Odocoileus virginianus)

Characteristics of mineral licks used by white-tailed deer ( Odocoileus virginianus ) were examined in the northern Black Hills of South Dakota in May 1992. Concentrations of sodium, nitrogen, phosphorus, potassium, calcium, chloride and magnesium, and soil texture, organic matter and pH for licks and nonlick soils were compared. Black Hills lick and nonlick samples also were compared to 67 other North American licks characterized by Jones and Hanson (1985). Degree of use (high or low), and vegetative and topographic characteristics also were determined. Use of mineral licks by deer was highest in spring and early summer; mineral licks were not used by deer in winter. Mostly adult females, and on a few occasions fawns visited licks. Soil texture was finer and organic matter was lower (P < 0.05) in lick than nonlick soils. Soil pH, soluble salts, sodium and nitrate nitrogen were higher (P < 0.05) in lick than in nonlick soils. Chloride was the only mineral that differed (P = 0.03) between high-use and low-use licks but was not considered important in lick selection. Sodium was the primary mineral sought by white-tailed deer using mineral licks.

American Midland Naturalist↗

USGS1990

Mineral Resources of the Mount Nutt Wilderness Study Area, Mohave County, Arizona

The Mount Nutt Wilderness Study Area (AZ-020-024) is located in the Black Mountains about 15 mi west of Kingman, Arizona. At the request of the U.S. Bureau of Land Management, approximately 27,210 acres of the wilderness study area was evaluated for mineral resources (known) and mineral resource potential (undiscovered). In this report, the area studied is referred to as the 'wilderness study area' or simply 'the study area'; any reference to the Mount Nutt Wilderness Study Area refers only to that part of the wilderness study area (27,210 acres) for which a mineral survey was requested. The U.S. Geological Survey and the U.S. Bureau of Mines conducted geological, geochemical, and geophysical surveys to assess the identified mineral resources and mineral resource potential of the study area. Fieldwork for this report was carried out in 1987 and 1988. A gold resource totaling at least 56,000 troy oz has been identified at two sites in Secret Pass Canyon, less than 0.5 mi north of the study area. No other metallic mineral resources were identified inside the study area. An area near the center of the study area contains fire agate, a gem stone. On the basis of tonnage, site accessibility, and current production methods, this area is considered an indicated subeconomic fire-agate resource for the foreseeable future. Sand and gravel are present in the study area. An area surrounding the Tincup mine and including a small portion of the extreme north-central part of the study area has high potential for gold and low potential for silver, lead, and mercury. Three areas in the extreme northwestern, north-central, and southwestern parts of the study area have moderate potential for gold and low potential for silver, lead, and mercury. A small area near the known fire-agate resource in the south-central part of the study area has low potential for fire agate. Large areas in the eastern and central parts of the study area have low potential for perlite and zeolite resources. The entire study area has no potential for oil and gas and no potential for geothermal resources.

Bulletin↗

USGS2003

Contributions to Industrial-Minerals Research

Contributions to Industrial-Minerals Research, an ongoing series of U.S. Geological Survey (USGS) Bulletin chapters, presents research strategies, results, and updates of investigations of industrial minerals by USGS scientists and cooperators. Industrial minerals are defined as valuable nonmetallic, nonfuel geologic materials, generally rocks or minerals, used in a wide range of construction and industrial applications-for example, sand, gravel, and crushed rock used as aggregate for construction; limestone used for cement; phosphate for fertilizers and insecticides; and diatomite used for filtration, fillers, and abrasives. The term also comprises some processed materials, such as cement and metallic compounds with major utilization in nonmetallic forms. For example, titanium is commonly grouped with industrial minerals because more than 90 percent of it is sold and utilized in the form of the oxide (TiO2) rather than as Ti metal. Other metals and metallic compounds commonly grouped with industrial minerals include Mn, Cr, Fe oxides, and rare-earth elements (REEs).

Bulletin↗