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

At least 1,153 records · Page 64Linked to original sources

Perched silica minerals on mordenite fiber

Ellipsoidal quartz grains and spherulitic chalcedony are perched on mordenite fibers in geodes from Chihuahua, Mexico. Examination of samples of fibrous mordenite from six additional localities indicated that most mordenites have perched quartz crystals. A linear relationship exists between the Si:Al ratios and the refractive indices of the mordenites. The pH of the mineralizing solutions appears to be the primary factor controlling the presence of perched silica minerals (the lower the pH, the higher the Si:Al ratios and the lower the probability of precipitating quartz). Other factors that may affect the presence of lurched silica minerals are (1) the compactness of the mordenite fibers, (2) the morphology of the fibers, and (3) the concentration of Al, Ca, Na, and K in the mineralizing solutions.

Journal of Research of the U.S. Geological Survey↗

Coastal deposits of heavy mineral sands; Global significance and US resources

Ancient and modern coastal deposits of heavy mineral sands (HMS) are the principal source of several heavy industrial minerals, with mining and processing operations on every continent except Antarctica. For example, HMS deposits are the main source of titanium feedstock for the titanium dioxide (TiO 2 ) pigments industry, obtained from the minerals ilmenite (Fe 2 +TiO 3 ), rutile (TiO 2 ) and leucoxene (an alteration product of ilmenite). HMS deposits are also the principal source of zircon (ZrSiO 4 ), from which zirconium dioxide (ZrO 2 ) is obtained for uses mostly in refractory products. Sometimes monazite [(Ce,La,Nd,Th)PO 4 ] is recovered as a byproduct mineral, sought for its rare earth elements and thorium (Ault and others, 2016; Sengupta and Van Gosen, 2016; Van Gosen and Tulsidas, 2016).

Mining Engineering↗

Magmatism, metasomatism, tectonism, and mineralization in the Humboldt Range, Pershing County, Nevada

Introduction The Humboldt Range, Pershing County, Nevada, predominantly consists of Mesozoic igneous and sedimentary rocks that were modified several times by magmatism, metasomatism, and tectonism, and contain a variety of metallic (Ag, Au, Pb, Zn, Sb, W, Hg) and non-metallic (dumortierite, pinite, fluorite) mineral deposits (Knopf, 1924; Kerr and Jenney, 1935; Kerr, 1938; Cameron, 1939; Campbell, 1939; Kerr, 1940; Page et al., 1940; Johnson, 1977; Vikre, 1978; 1981; Crosby, 2012). Early Triassic Koipato Group volcanic rocks, which are widely exposed in the range, have been altered to quartz, muscovite (sericite), chlorite, pyrite, and other minerals during emplacement of Mesozoic intrusions and by crustal thickening. Most hydrothermal alteration of volcanic rocks and formation of mineral deposits involved externally derived water and other volatiles, although some volcanic strata were apparently altered by pore or dehydration water. Cospatial hydrothermal mineral assemblages and associations, produced by events widely spaced in time, are difficult to separate because of common mineralogy (quartz, sericite, and pyrite), partial to complete recrystallization, thermally compromised Ar geochronology, and lack of comprehensive investigations of volatile sources and deformational fabric. Distinguishing between metasomatic and metamorphic processes that affected rocks in the Humboldt Range is not straightforward.

Nevada↗

Precious and base metal mineralization within the lower stratigraphy of the Stillwater Complex: New targets defined and old targets revisited

Group Ten Metals is exploring for base and precious metals within the Stillwater Complex, a 2.7 Ga layered mafic/ultramafic intrusion, host to the world-class Sibanye platinum group element (PGE) mines. Group Ten controls approximately 25 kilometers of strike length of prospective mafic and ultramafic rocks in the western portion of the Complex. The property includes multiple target types and individual prospects. Stillwater Complex magmatic stratigraphy is divided into three major series based on the proportions of cumulus minerals—Basal, Ultramafic and Banded. Group Ten explores primarily within the lower third of the intrusion, from the Basal Series at the footwall contact, upwards into the Ultramafic Series which is divided into a lower Peridotite Zone and an upper Bronzitite Zone. Rocks of the Peridotite Zone are repetitive, laterally continuous and layered sequences of olivine, chromite and pyroxene cumulates. This model was developed in the eastern portion of the Complex. Mapping in the western portion of the Complex indicates that the Peridotite Zone is thinner than to the east and with cyclic units not as regularly developed. Group Ten has reviewed data from over 50 years of historical exploration in light of different commodity focus, land positions, analytical menus, and petrogenetic models to define a series of exploration targets. A six hole, 1,600 meter diamond drilling program targeting the Iron Mountain sector was completed in 2019; results are discussed in more detail below. At Iron Mountain the primary targets are Ni-Cu-PGE magmatic sulfides located within the Basal Series and lower Peridotite Zone, near the basal contact of the Complex. Important objectives included establishing the PGE tenor of sulfide mineralization drilled by AMAX in the 1970’s and penetrating basement rock rafts known to conceal mineralized (but not previously analyzed) ultramafic rocks beneath. Drilling also tested the PGE-enriched A-B chromitite package which rests stratigraphically above the previously tested zones. At Chrome Mountain, magmatic layering was disturbed or destroyed over large areas along a WNW axis that may be an artifact of early magma chamber deformation or result from much later, Laramide tectonism. Correlation of marker units, for example chromitite seams, are problematic in the disturbed area; these rocks are termed the Hybrid Unit. In addition, normal igneous stratigraphy appears to be intruded by discordant dunite masses, pyroxenite pegmatoids and magmatic breccias. This unusual assemblage of rock types is accompanied by significant and previously underappreciated PGE mineralization related to chromite schlieren and minor but persistent base metal sulfides.

Conference Paper↗

Alteration of reactive mineral surfaces by ground water

Two different investigations of shallow sandy aquifers inform our thinking about the role of reactive iron minerals in hydrogeological systems. Ground water in a number of settings has been described as having elevated concentrations of dissolved iron in anoxic portions of contaminant plumes (e.g. Baedecker et al., 1993; Lyngkilde and Christensen, 1992), and the coupling of microbial reduction of Fe(III) to the degradation of organic compounds links the study of the biogeochemistry of iron to our desire to understand processes influencing contaminated aquifers. Questions about the transport and fate of reactive constituents in ground water are linked to the study of iron through recognition of the importance of sorption processes on sesquioxide mineral surfaces common in sedimentary aquifers limiting the migration of metals, anions, and bacteria. We have been grappling with questions related to the stability of iron mineral phases in contaminated aquifers and the role of Fe(III)- bearing minerals and grain coatings as sorption substrates

Conference Paper↗

The US Geological Survey’s Earth Mapping Resources Initiative (Earth MRI)—Providing framework geologic, geophysical, and elevation data to the nation’s critical mineral-bearing regions

New detailed mapping of the geologic resources of the Nation has the potential to significantly close the gap in the essential data needed to fuel a modern era of economic development and technological innovation, while at the same time dramatically enhancing our understanding of the fundamental way geology impacts everyday life, from the domestic critical mineral resources that are necessary for modern technology and the economy, to domestic energy and water resources, geologic hazards, agriculture, and other pressing needs. The U.S. Geological Survey established the Earth Resources Mapping Initiative (Earth MRI) to address the shortfall in geologic, geophysical, and elevation data with sufficient detail to support evaluation of regions in the United States that have potential to host critical mineral resources. The new effort is a collaboration with the Association of American State Geologists, who are providing new detailed geologic maps and making available online archived data and information related to critical mineral resources. The geophysical and lidar surveys are being contracted through industry specialists to assure that high-quality data are available to the public. This article provides an overview of the Earth MRI effort with discussions on the initial geophysical surveys funded for areas that have known potential for rare earth element resources. Subsequent projects are being designed to address areas that may host other critical mineral resources.

Fast Times↗

Sedex hydrothermal systems triggered upheavals to marine chemistry and mass extinctions: Applications for ore genesis research and mineral exploration

New USGS research reveals that the discharge of metal-rich brine that formed sedex deposits on ancient seafloors had profound effects on global ocean chemistry and biologic evolution. For example, brine expulsion caused short-duration positive excursions (“spikes”) in the global marine Sr isotope record. While these spikes are unexplained by conventional oceanic models, our chronostratigraphic correlations of major sedex events, combined with mass balance evidence and oceanographic modeling, confirm that the flux of radiogenic Sr from sedex brines during ore formation was sufficient to cause these once enigmatic 87Sr/86Sr spikes. Recognition that the timing of peak 87 Sr/ 86 Sr spikes correlates exactly with global δ 13 C (and δ 18 O) spikes, climate change, deposition of metal-rich black shales and ironstones, metal-induced malformation (teratology) of marine organisms, and mass extinctions, establishes a causal relationship between sedex deposits and these dramatic events in earth history. The relationships among these features are not fully understood. However, our new model demonstrates that the flux of key biolimiting nutrients and metals contained in sedex brines exceeds that of the total modern riverine flux to the ocean. Undoubtably, these immense nutrient fluxes spurred ocean eutrophication, which, ultimately, through a series of positive feedback mechanisms, may be a previously unrecognized trigger of global ocean anoxic events (OAEs) that produced these chemical and biological perturbations. A derivative result from this integrative research is the recognition that OAEs resulted in the formation of “bathtub rim” deposits at redox boundaries along continental margins that concentrated various redox sensitive critical minerals. For example, we have identified midcontinent phosphorite deposits that contains heavy REE grades and tonnages that rival any REE deposit in the world. The recognition that sedex-forming fluid expulsion events are recorded in the global marine isotopic, geologic, and biological records, defines a new approach to the study of and exploration for sedex deposits. Traditional ore genesis research, coupled with chronostratigraphic correlation and high-resolution 87 Sr/ 86 Sr isotope chemostratigraphy can be used to answer long-standing questions about geologic processes responsible for formation of these extraordinary deposits. This approach allows us to constrain, for the first time, the age, duration, and fluxes of fluids and metals vented into the ocean by these giant hydrothermal systems. Accordingly, the fact that large mineralizing events are recorded in the marine sedimentary record opens the tantalizing prospect that we have the ability to conduct effective resource assessments and define prospective basins anywhere in the world. This innovative approach allows for identification of favorable stratigraphic ages and basins and remote evaluation of the size (and, thus, the mineral potential) of undiscovered mineral deposits. This methodology could be applied on regional basin-wide assessments, to evaluate sedimentary basin prospectivity, resource favorability of specific horizons therein, and to the evaluation of the potential of early-stage prospects.

Geological Society of Nevada Newsletter↗

Recognition of oxidized sulfide minerals as an exploration guide for uranium

The difference in color between tan to red oxidized sandstone and gray reduced sandstone on either side of the reduction-oxidation (redox) interface, which is- the locus of uranium concentration in roll-type deposits, has been noted and used locally as an exploration guide within known uranium districts. Reduced sandstone is characterized in many deposits by the presence of iron sulflde minerals (particularly marcasite and pyrite) that occur as replacements of and overgrowths on iron-titanium oxide minerals and plant debris and as cement of detrital grains. Oxidation of the sulfldes by oxygenated ground water forms yellow to red ferric oxide and ferric hydroxide phases ("limonite") that replace the FeS 2 minerals. Processes other than the oxidation of sulfldes, however, can cause reddening of clastic sediments without the creation of a redox boundary, and so color alone is not a sufficient condition by which to judge the potential for uranium ore in frontier areas. Ferric oxides that form by the oxidation of iron sulflde minerals can be distinguished from other forms of ferric oxide by reflection microscopic examination of polished grain mounts- and polished thin sections'. Diagnostic features of oxidized sulfldes are limonite pseudomorphs of sulfldes and limonite containing internal textures that mimic characteristic textures of previously sulfldized detrital phases. Recognition of oxidized sulfides by reflection microscopy, then, can distinguish oxidized sandstones, which might have a redox boundary downdip and which would therefore be favorable hosts for uranium concentration, from those without such potential.

Journal of Research of the U.S. Geological Survey↗

Blue Ribbon Lineament, an east-trending structural zone within the Pioche mineral belt of southwestern Utah and eastern Nevada

The Blue Ribbon lineament is an east-west structural zone that is about 25 kilometers wide and passes through the Pioche mineral belt at about 38°10' N. It is best known in Utah, where it is at least 190 km long, and extends from the southern Sevier Plateau in the High Plateaus westward and across southern Mountain Home (Needle) Range in the Great Basin. It probably continues westward an additional 170 km into Nevada, where it connects with the eastern end of the 230-km Warm Springs lineament. The Blue Ribbon lineament is defined by range terminations and east-trending valleys, alinement of eruptive centers of middle Miocene (20 million years) to Pliocene(?) (5-1.8 m.y.) alkalic rhyolite, alinement of areas of middle Miocene to Pliocene mineralized rocks (mostly fluorine, uranium, tungsten) and hydrothermally altered rocks, east-trending magnetic highs and interruptions of magnetic anomalies, and east-striking basin-range faults of late Tertiary and Quaternary age. Mountains south of the lineament are topographically and structurally lower than those to the north. North-striking Quaternary basin-range faults, the Thermo hot springs area, several warm springs and former hot springs, and numerous dacitic to andesitic volcanic centers of early to middle Miocene age (26-20 m.y.) occur along the lineament. The Blue Ribbon lineament is believed to be a deep crustal fault zone dating from at least middle Miocene time and possibly much earlier. It thus developed generally coincident with northerly trending classical basin-range faults. Its fracture system was an important, long-lived conduit for mineralizing fluids, and it should be an attractive target for minerals exploration in the future. The lineament could be due to an east-trending warp in the subducting mantle plate, or it could be part of a past or present intracontinental transform fault that locally gets younger eastward and dies out eastward in the western Colorado Plateaus province.

Utah↗

USGS Critical Minerals Review: 2021

In 2021, the U.S. Geological Survey (USGS) continued to play a central role in understanding and anticipating potential supply chain disruptions by defining and quantitatively evaluating mineral criticality. In addition, the USGS continued to evaluate new sources of domestic critical minerals by conducting mineral resource assessments, mapping and surveying regions prospective for critical minerals, re-assessing mine waste, and pursuing fundamental research in support of responsible, sustainable mining.

Mining Engineering↗

Pleistocene rhyolite of the Mineral Mountains, Utah: Geothermal and archeological significance

Little-eroded rhyolitic tuffs, flows, and domes extend over about 25 km 2 along the western side of the Mineral Mountains, southwestern Utah, which is along the eastern edge of the Roosevelt KGBA (Known Geothermal Resource Area). Initial eruptions resulted in two low-viscosity lava flows of nonporphyritic rhyolite. These were followed by bedded pumice falls and nonwelded ash flows. The youngest activity produced at least nine viscous domes and small lava flows of rhyolite that contain 1-5 percent phenocrysts of quartz, plagioclase, sodic sanidine, and biotite; distinction between domes and eroded flow segments locally is difficult. Potassium-argon ages indicate that all the rhyolite of the Mineral Mountains was erupted between 0.8 and 0.5 m.y. ago. The rhyolite rests on dissected granite of the Mineral Mountains pluton, the largest intrusion in Utah, which has yielded published K-Ar ages of 9 and 15 m.y. A small older dissected rhyolite dome, about 8 m.y. old, occurs just west of the range front. Whether the young ages of the pluton represent time of intrusion or of later reheating, they, in conjunction with the Pleistocene rhyolite in the Mineral Mountains, do indicate a major late Cenozoic thermal anomaly, the size and age of which is significant to evaluation of the Roosevelt KGRA. The rhyolite is also the only known source of implement-grade obsidian in the southwest between eastern California and northern New Mexico.

Utah↗

Critical mineral inventory of select IOA-IOCG deposits, southwestern USA

Critical minerals are necessary for modern technology and strategic purposes. Their increasing importance requires finding new and nontraditional resources. Samples of ore, altered, and unaltered host rock were collected from 26 iron mines and prospects in California, Nevada, and Utah to assess the potential of these deposits to host economic quantities of different critical minerals. Geochemical analyses were conducted by 61 element ICP-OES-MS sodium peroxide fusion and major elements determined by WDXRF. These deposits concentrated many critical minerals beyond what is found in average upper crustal abundances, such as Sb, As, Bi, Co, Ga, Mg, Mn, Ni, Nb, Pd, REE, Sc, Te, Sn, Ti, W, V, and Zn. However, most of these are not concentrated enough in the ore to be considered as economic resources. Those critical minerals that are enriched enough in some of these deposits to possibly be considered as by-product commodities are Ni, REE, V, and potentially Co and Ga. These enrichments were not uniform, with REE more likely to be enriched in IOA deposits, whereas Co, Ga, Ni, and V could be found enriched in either IOA or IOCG deposits.

California, Nevada, Utah↗

Fluoride content of clay minerals and argillaceous earth materials

A reliable method, utilizing a fluoride ion-selective electrode, is described for the determination of fluoride in clays and shales. Interference by aluminum and iron is minimal. The reproducibility of the method is about ±5% at different levels of fluoride concentration. Data are presented for various clay minerals and for the <2-µm fractions of marine and nonmarine clays and shales. Fluoride values range from 44 ppm (0.0044%) for nontronite from Colfax, WA, to 51,800 ppm (5.18%) for hectorite from Hector, CA. In general, clays formed under hydrothermal conditions are relatively high in fluoride content, provided the hydrothermal waters are high in fluoride content. Besides hectorite, dickite from Ouray, CO, was found to contain more than 50 times as much fluoride (6700 ppm) as highly crystalline geode kaolinite (125 ppm). The clay stratum immediately overlying a fluorite mineralized zone in southern Illinois was found to have a higher fluoride content than the same stratum in a nonmineralized zone approximately 1 mile away. Nonmarine shales in contact with Australian coals were found to be lower in fluoride content than were marine shales in contact with Illinois coals. It is believed that, in certain instances, peak shifts on DTA curves of similar clay minerals are the result of significant differences in their fluoride content.

Clays and Clay Minerals↗

Porphyry copper: Revisiting mineral resource assessment predictions for the Andes

A mineral resource assessment of porphyry copper deposits in the Andes Mountains of South America was done in 2005 in cooperation with geological surveys in South America. The study identified 590 million metric tons (Mt) of copper in identified resources. Continued exploration and development in the region over a 15-year period provide an opportunity to compare the predicted assessment results with new discoveries and resource growth in previously known deposits. The 2005 assessment estimated that 145 undiscovered deposits could contain a mean of 750 Mt of copper. The actual number of deposits increased (2005 to 2020) from 69 to 120 and the amount of identified copper resources increased from 590 Mt to 1600 Mt. Although most of the new deposits and copper resources are concentrated in Miocene-Pliocene and Eocene-Oligocene mineral belts, new deposits have been discovered in Jurassic and Cretaceous mineral belts. Resource growth in porphyry copper deposits known in the Andes in 2005 (1100 Mt copper) exceeds copper resources in new discoveries since 2005 (490 Mt copper) by a factor of 2.

Andes Mountains↗

Compositional and mineralogic constraints on the genesis of ophiolite hosted nickel mineralization in the Pevkos area, Limassol Forest, Cyprus

Mineralization composed dominantly of primary troilite, maucherite, pentlandite, and chalcopyrite, and secondary valleriite occurs in serpentinized transition zone rocks of the Limasol Forest segment of the Troodos ophiolite complex, Cyprus. Whole-rock and electron microprobe analyses of this mineralization gives ranges of Cu/(Cu+Ni)=0.16 to 0.47, Pt/(Pt+Pd)=0.66 to 0.51, Ni/Co=6.33 to 13.4, and chondrite normalized plots with low concentrations of Rh, Pt, and Pd, but relatively high Au. Estimated distribution coefficients of nickel and iron between olivine and ore range from 0.5 to 7.4. Most of these data are unlike values from magmatic sulfide deposits and indicate either a complete alteration of a preexisting magmatic sulfide concentration or, more likely, a nonmagmatic origin for this mineralization. ?? 1985 Springer-Verlag.

Mineralium Deposita↗

Mineralized and unmineralized calderas in Spain; Part I, evolution of the Los Frailes Caldera

The Cabo de Gata volcanic field of southeastern Spain contains several recently-recognized calderas. Some of the calderas are mineralized with epithermal gold, alunite, and base metal deposits, and others are barren, and yet they formed under generally similar conditions. Comparison of the magmatic, geochemical, and physical evolution of the Los Frailes, Rodalquilar, and Lomilla calderas provides insight into the processes of caldera evolution that led to precious-metal mineralization. The Los Frailes caldera formed at 14.4 Ma and is the oldest caldera. It formed in response to multiple eruptions of hornblende dacite magma. Following each eruption, the area collapsed and the caldera was invaded by the sea. Dacite domes fill the lower part of the caldera. Pyroxene andesites were erupted through the solidified core of the caldera and were probably initially responsible for magma generation. The Los Frailes caldera did not evolve to rhyolites nor was it subjected to the amount of structural development that the younger, mineralized Rodalquilar and Lomilla calderas were. ?? 1990 Springer-Verlag.

Mineralium Deposita↗

Chromium in rocks and minerals from the southern California batholith

Chromium, determined by neutron-activation analysis in a suite of rocks and minerals from the southern California batholith, shows Cr concentrated in the mafic differentiates, decreasing as the more felsic rocks are approached. This trend is evident for samples of the Woodson Mountain Granodiorite from a single differentiated stock. The distribution of Cr in the minerals from the rocks of the southern California batholith shows that Cr was depleted in the magma during the course of crystallization. The data indicate that the minerals were in equilibrium with the magma during crystallization, and the distribution coefficient (Cr in biotite/Cr in hornblende) is correlated with differentiation indices, indicating either temperature or compositional dependence. The average distribution coefficient (Cr in biotite/Cr in hornblende) is 1.18, which compares favorably with the average values found by other investigators for other suites. ?? 1976.

Chemical Geology↗

Evidence for Late-Paleozoic brine migration in Cambrian carbonate rocks of the central and southern Appalachians: Implications for Mississippi Valley-type sulfide mineralization

Many Lower Paleozoic limestones and dolostones in the Valley and Ridge province of the central and southern Appalachians contain 10 to 25 weight percent authigenic potassium feldspar. This was considered to be a product of early diagenesis, however, 40 Ar 39 Ar "> 40 Ar 39 Ar analyses of overgrowths on detrital K-feldspar in Cambrian carbonate rocks from Pennsylvania, Maryland, Virginia, and Tennessee yield Late Carboniferous-Early Permian ages (278–322 Ma). Simple mass balance calculations suggest that the feldspar could not have formed isochemically, but required the flux of multiple pore volumes of fluid through the rocks, reflecting regional fluid migration events during the Late-Paleozoic Alleghanian orogeny. Microthermometric measurements of fluid inclusions in overgrowths on detrital K-feldspar and quartz grains from unmineralized rocks throughout the study area indicate homogenization temperatures from 100° to 200°C and freezing point depressions of −14° to −18.5°C (18–21 wt.% NaCl equiv). The apparent similarity of these fluids to fluid inclusions in ore and gangue minerals of nearby Mississippi Valley-type (MVT) deposits suggests that the regional occurrences of authigenic K-feldspar and MVT mineralization may be genetically related. This hypothesis is supported by the discovery of authigenic K-feldspar intergrown with sphalerite in several mines of the Mascot-Jefferson City District, E. Tennessee. Regional potassic alteration in unmineralized carbonate rocks and localized occurrences of MVT mineralization are both explainable by a gravity-driven flow model, in which deep brines migrate towards the basin margin under a hydraulic gradient established during the Alleghanian orogeny. The authigenic K-feldspar may reflect the loss of K during disequilibrium cooling of the ascending brines. MVT deposits are probably localized manifestations of the same migrating fluids, occurring where the necessary physical and chemical traps are present.

Geochimica et Cosmochimica Acta↗