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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 883 records · Page 49Linked to original sources

Hyperspectral surface materials map of quadrangles 2964, 2966, 3064, and 3066, Shah-Esmail (617), Reg-Alaqadari (618), Samandkhan-Karez (713), Laki-Bander (611), Jahangir-Naweran (612), and Sreh-Chena (707) quadrangles, Afghanistan, showing carbonates, phyllosilicates, sulfates, altered minerals, and other materials

This map shows the spatial distribution of selected carbonates, phyllosilicates, sulfates, altered minerals, and other materials derived from analysis of airborne HyMap™ imaging spectrometer (hyperspectral) data of Afghanistan collected in late 2007. The map is one in a series of U.S. Geological Survey/Afghanistan Geological Survey quadrangle maps covering Afghanistan. Flown at an altitude of 50,000 feet (15,240 meters (m)), the HyMap™ imaging spectrometer measured reflected sunlight in 128 channels, covering wavelengths between 0.4 and 2.5 μm. The data were georeferenced, atmospherically corrected and converted to apparent surface reflectance, empirically adjusted using ground-based reflectance measurements, and combined into a mosaic with 23-m pixel spacing. Variations in water vapor and dust content of the atmosphere, in solar angle, and in surface elevation complicated correction; therefore, some classification differences may be present between adjacent flight lines. The reflectance spectrum of each pixel of HyMap™ imaging spectrometer data was compared to the reference materials in a spectral library of minerals, vegetation, water, and other materials. Minerals occurring abundantly at the surface and those having unique spectral features were easily detected and discriminated, while minerals having slightly different compositions but similar spectral features were less easily discriminated; thus, some map classes consist of several minerals having similar spectra, such as “Epidote or chlorite.” A designation of “Not classified” was assigned to the pixel when there was no match with reference spectra.

Open-File Report↗

Mineral potential tracts for polymetallic Pb-Zn-Cu vein deposits (phase V, deliverable 71): Chapter I in Second projet de renforcement institutionnel du secteur minier de la République Islamique de Mauritanie (PRISM-II)

In Mauritania, mineral occurrences of the polymetallic Pb-Zn-Cu vein deposit type are found near the Florence-El Khdar shear zone in northeast Mauritania. The deposits visited were deemed representative of other similar occurrences and consist of quartz veins with trace sulfides. The low sulfide and Pb-Zn-Cu content in the quartz veins is unlike producing polymetallic Pb-Zn-Cu vein deposits, such that the veins are not considered to belong to this deposit type. Mineral potential tracts for polymetallic Pb-ZnCu veins are highly speculative considering the lack of known mineralization belonging to this deposit type. Mineral potential tracts for polymetallic Pb-Zn-Cu veins are associated with and surround major shear zones in the Rgueïbat Shield and zones of complex faulting in the southern Mauritanides, at the exclusion of the imbricated thrust faults that are not considered favorable for this deposit type. No skarn and replacement deposits have been documented in Mauritania and the low mineral potential is indicated by lack of causative Mesozoic and Cenozoic mafic to felsic stocks.

Open-File Report↗

A process for reducing rocks and concentrating heavy minerals

To obtain minerals suitable for age-dating and other analyses, it is necessary to first reduce the mineral-bearing rock to a fine, sand-like consistency. Reducing whole rock requires crushing, grinding, and sieving. Ideally, the reduced material should range in size from 80- to 270-mesh (an opening between wires in a sieve). The openings in an 80-mesh sieve are equal to 0.007 inches, 0.177 millimeters, or 177 micrometers. This size range ensures that compound grains are mostly disaggregated and that grains, in general, are dimensionally similar. This range also improves the segregation rate of conspicuous to extremely small individual heavy mineral grains. Once the rock is reduced to grains, it is necessary to separate the grains into paramagnetic and nonparamagnetic and heavy and light mineral fractions. In separating grains by property, those minerals chemically suited for radiometric dating are abundantly concentrated. Grams of mineralogical material can then be analyzed and characterized by multiple methods including trace element chemistry, laser ablation, and in particular, ion geochronology .

Open-File Report↗

Mineral resource inventory of North Dakota

Aside from construction aggregate materials, the value of nonfuel mineral commodities that have been produced in North Dakota is small, although there is potential for the existence of several mineral resource deposit types which are not economically viable at this time. In this report, we present a mineral resource inventory of the State of North Dakota, developed by the U.S. Geological Survey at the request the Bureau of Land Management. To set the stage for that inventory, we briefly outline the long and complex geologic history of North Dakota that extends back more than 3 billion years. Using several existing databases, we summarize the distribution of known mineral commodities and the results of commodity exploration over time. Using all available data, we discuss the potential for economic occurrences of 13 commodities in North Dakota, including some listed as Critical Minerals.

North Dakota↗

A geochemical evaluation of the Ash Sha'ib mineral prospect, Asir quadrangle, Kingdom of Saudi Arabia

The mineralized zone at the remotely located Ash Sha'ib ancient mine contains only a small tonnage of moderately low grade sulfide- bearing rock. Based on present data the gross value of the deposit, with a value of $25.00 or more per ton, is $20,000,000. A belt of metasedimentary rocks, intruded by gabbro to the south and granite to the north, was the host for fissure vein-replacement type mineralization. Most of the mineralization is in a siliceous dolomite transected by fissures. The main sulfide mineral is sphalerite, but minor amounts of chalcopyrlte and argentlferous galena contribute to the value of the mineralized sections.

Open-File Report↗

Geology and mineral deposits of the Jabal ash Shumta quadrangle, Kingdom of Saudi Arabia

Rocks, structures, and mineral deposits which are the result of both the older Halaban petro-tectonic cycle and the younker Najd Wrench Fault deformation are present in the Ash Shumta area. Northward-trending belts of granitic rocks and folded, layered metavolcanic and metasedimentary rocks of the Halaban Formation which they intrude represent the effects of the Halaban cycle. These older rocks are everywhere transected and deformed by northwestward- and northeastward-striking fractures and strike-slip faults and by eastward-striking fractures and fracture-controlled silicic dikes which belong to the Najd Wrench Fault deformation. Several kinds of epigenetic mineral deposits of hydrothermal origin are present throughout the Ash Shumta area. All occur in or ape closely associated with structures of the Najd Wrench Fault deformation. The mineralization which produced the deposits is thought to have taken place during the period of deformation which produced the Najd Wrench Fault structures. The hydrothermal deposits include many metalliferous quartz veins most of which occur in three mineralized areas: two major areas at Jabal Ash Shumta and Jabal El Khom in the northern half of the quadrangle and a minor area along Wadj al Boharah in the southeastern part of the quadrangle. The metalliferous lodes possess the only economic potential in the area of the Jabal Ash Shumta quadrangle. These lodes consist mainly of gold and base metal-bearing quartz veins, some of which were mined for gold in ancient times. The mineralized area at Jabal Ash Shumta has the best of these veins. Higher temperature veins with wolframite as a major constituent and beryl as a minor one occur in a granite cupola in the eastern part of the El Khom area. These veins have altered, gneissen-like wall rocks. Although the grade of the veins is low at the surface, the made could increase at depth. The tungsten-bearing veins and El Khom area possess the greatest economic promise in the Jabal Ash Shumta quadrangle. They deserve detailed surface investigation followed if needed by exploration at depth.

Open-File Report↗

A topology of mineralization and its meaning for prospecting

Epigenetic mineral deposits are universal members of an orderly spatial-temporal arrangement of igneous rocks, endomorphic rocks, and hydrothermally altered rocks. The association and sequence of these rocks is invariant whereas the metric relations and configurations of the properties of these rocks are unlimited in variety. This characterization satisfies the doctrines of topology. Metric relations are statistical, and their modes are among the better guides to optimal areas for exploration. Metric configurations are graphically irregular and unpredictable mathematical surfaces like mountain topography. Each mineral edifice must be mapped to locate its mineral deposits. All measurements and observations are only positive or neutral for the occurrence of a mineral deposit. Effective prospecting is based on an increasing density of positive data with proximity to the mineral deposit. This means sampling for maximal numbers of positive data, pragmatically the highest ore-element assays at each site, by selecting rock showing maximal development of lode attributes.

Open-File Report↗

An evaluation of the applicability of the telluric-electric and audio-magnetotelluric methods to mineral assessment on the Arabian Shield, Kingdom of Saudi Arabia

Feasibility studies of two electromagnetic methods were made in selected areas of the Jabal Hibshi (1:250,000) quadrangle, 26F, in the Kingdom of Saudi Arabia in March of 1983. The methods tested were the natural source-field telluricelectric and audio-magnetotelluric methods developed and extensively used in recent years by the U.S. Geological Survey in some of its domestic programs related to geothermal and mineral resource assessment. Results from limited studies in the Meshaheed district, the Jabal as Silsilah ring complex, and across a portion of the Raha fault zone clearly demonstrate the appropriateness of these sub-regional scale, reconnaissance-type studies to mineral resource assessment. The favorable results obtained are largely attributed to distinctive and large contrasts in the electrical resistivity of the major rock types encountered. It appears that the predominant controlling factor governing the rock resistivities is the amount of contained clay minerals. Accordingly, unaltered (specifically, non-argillic) igneous and metamorphic rocks have very high resistivities; metasedimentary rocks of the Murdama group that contain several percent clay minerals have intermediate values of resistivity; and highly altered rocks, containing abundant clay minerals, have very low values of resistivity. Water-filled fracture porosity may be a secondary, but important, factor in some settings. However, influences from variations in interstitial or intercrystalline, water-filled porosity are probably small because these types of porosity are generally low. It is reasonable to expect similar results in other areas within the Arabian Shield.

Open-File Report↗

Investigation of the potential for concealed base-metal mineralization at the Drenchwater Creek Zn-Pb-Ag occurrence, northern Alaska, using geology, reconnaissance geochemistry, and airborne electromagnetic geophysics

In 2005, the U.S. Geological Survey, Bureau of Land Management, and State of Alaska cooperated on an investigation of the mineral potential of a southern part of the National Petroleum Reserve in Alaska, Howard Pass quadrangle, to provide background information for future land-use decisions. The investigation incorporated an airborne electromagnetic (EM) survey covering 1,500 mi 2 (~3,900 km 2 ), including flight lines directly over the Drenchwater Creek sediment-hosted Zn-Pb-Ag occurrence, the largest known base-metal occurrence in the survey area. Samples from the mineralized outcrop and rubblecrop contain metal concentrations that can exceed 11 percent Zn+Pb, with appreciable amounts of Ag. Soil samples with anomalous Pb concentrations are distributed near the sulfide-bearing outcrops and along a >2.5 km zone comprising mudstone, shale, and volcanic rocks of the Kuna Formation. No drilling has taken place at the Drenchwater occurrence, so alternative data sources (for example, geophysics) are especially important in assessing possible indicators of mineralization. Data from the 2005 electromagnetic survey define the geophysical character of the rocks at Drenchwater and, in combination with geological and surface-geochemical data, can aid in assessing the possible shallow (up to about 50 m), subsurface lateral extent of base-metal sulfide accumulations at Drenchwater. A distinct >3-km-long electromagnetic conductive zone (observed in apparent resistivity maps) coincides with, and extends further westward than, mineralized shale outcrops and soils anomalously high in Pb concentrations within the Kuna Formation; this conductive zone may indicate sulfide-rich rock. Models of electrical resistivity with depth, generated from inversion of electromagnetic data, which provide alongflight-line conductivity-depth profiles to between 25 and 50 m below ground surface, show that the shallow subsurface conductive zone occurs in areas of known mineralized outcrops and thins to the east. Broader, more conductive rock along the western ~1 km of the geophysical anomaly does not reach ground surface. These data suggest that the Drenchwater deposit is more extensive than previously thought. The application of inversion modeling also was applied to another smaller geochemical anomaly in the Twistem Creek area. The results are inconclusive, but they suggest that there may be a local conductive zone, possibly due to sulfides.

Professional Paper↗

FEDERAL MINERAL LAND INFORMATION SYSTEM.

The ability of geographic information systems to combine point, line, and areal data has been widely documented, although the establishment of a particular data base presents its own unique problems. The U. S. Geological Survey is developing a geographic information system consisting of information on Federal surface ownership, Federal subsurface mineral rights, location of actual mineral occurrences and (or) known potential, and formal restrictions to mineral development. By utilizing information already compiled or soon to be collected by other agencies, the Federal Mineral Land Information System should be able to provide answers relating to mineral availability on public lands.

Conference Paper↗

COEXISTING GALENA, PbS//S//S AND SULFOSALTS: EVIDENCE FOR MULTIPLE EPISODES OF MINERALIZATION IN THE ROUND MOUNTAIN AND MANHATTAN GOLD DISTRICTS, NEVADA.

Studies of galena and Pb-Bi-Ag-Cu(Hg) sulfosalts of varied compositions in the Round Mountain and Manhattan gold districts of Nevada corroborate the occurrence of several distinct mineralized systems characterized by different mineral compositions and assemblages. The different episodes of mineralization are related to different Cretaceous and Tertiary magmatic-hydrothermal events, although the assignment of specific mineral compositions and associations with dated mineralized systems is still incomplete. At the Fairview mine, galena associated with Pb-Bi-Ag sulfosalts and simple sulfides occurs as intergrowths of discretely different composition controlled by silver and bismuth content. A galena-type phase (Pbs//s//s) with solid solution toward matildite, AgBiS//2(composition Gal//6//0Mat//4//0) was found. If silver and, to a lasser extent, bismuth are absent, the galena formed will be almost pure PbS. Some minor antimony may substitute for bismuth. This study confirms a linear relationship between a cell edge and Ag-Bi(Sb) content for galena containing less than about 15 wt. percent Ag and Bi(Sb).

Canadian Mineralogist↗

Oxygen and carbon isotope ratios of hydrothermal minerals from Yellowstone drill cores

Oxygen and carbon isotope ratios were measured for hydrothermal minerals (silica, clay and calcite) from fractures and vugs in altered rhyolite, located between 28 and 129 m below surface (in situ temperatures ranging from 81 to 199??C) in Yellowstone drill holes. The purpose of this study was to investigate the mechanism of formation of these minerals. The ??18O values of the thirty-two analyzed silica samples (quartz, chalcedony, ??-cristobalite, and ??-cristobalite) range from -7.5 to +2.8???. About one third of the silica 7samples have ??18O values that are consistent with isotopic equilibrium with present thermal waters; most of the other silica samples appear to have precipitated from water enriched in 18O (up to 4.7???) relative to present thermal water, assuming precipitation at present in situ temperatures. Available data on fluid-inclusion homogenization temperatures in hydrothermal quartz indicate that silica precipitation occurred mostly at temperatures above those measured during drilling and imply that 15O enrichments in water during silica precipitation were generally larger than those estimated from present conditions. Similarly, clay minerals (celadonite and smectite) have ??18O values higher (by 3.5 to 7.9???) than equilibrium values under present conditions. In contrast, all eight analyzed calcite samples are close to isotopic equilibrium with present thermal waters. The frequent incidence of apparent 18O enrichment in thermal water from which the hydrothermal minerals precipitated may indicate that a higher proportion of strongly 18O-enriched deep hydrothermal fluid once circulated through shallow portions of the Yellowstone system, or that a recurring transient 18O-enrichment effect occurs at shallow depths and is caused either by sudden decompressional boiling or by isotopic exchange at low water/rock ratios in new fractures. The mineralogy and apparent 18O enrichments of hydrothermal fracture-filling minerals are consistent with deposition during transient boiling or rock-water exchange (fracturing) events. ?? 1990.

Journal of Volcanology and Geothermal Research↗

Jensenite, Cu 3 Te (super 6+) O 6 .2H 2 O, a new mineral species from the Centennial Eureka Mine, Tintic District, Juab County, Utah

Jensenite, ideally Cu 3 Te (super 6+) O 6 .2H 2 O, is monoclinic, P2 1 /n (14), with unit-cell parameters refined from powder data: a 9.204(2), b 9.170(2), c 7.584(1) Aa, beta 102.32(3) degrees , V 625.3(3) Aa 3 , a:b:c 1.0037:1:0.8270, Z = 4. The strongest six reflections of the X-ray powder-diffraction pattern [d in Aa(I)(hkl)] are: 6.428(100)(101,110), 3.217(70)(202), 2.601(40)(202), 2.530(50)(230), 2.144(35)(331) and 1.750(35)(432). The mineral is found on the dumps of the Centennial Eureka mine, Juab County, Utah, where it occurs as isolated crystals or as groups of crystals on drusy white quartz. Associated minerals are mcalpineite, xocomecatlite and unnamed Cu(Mg,Cu,Fe,Zn) 2 Te (super 6+) O 6 .6H 2 O. Individual crystals of jensenite are subhedral to euhedral, and form simple rhombs that are nearly equant. Some crystals are slightly elongate [101], with a length-to-width ratio up to 2:1. The largest crystal is approximately 0.4 mm in size; the average size is between 0.1 and 0.2 mm. Cleavage {101} fair. Forms are: {101} major; {110} medium; {100} minor; {301}, {201}, {203}, {102}, {010} very small. The mineral is transparent, emerald green, with a less intense streak of the same color and an uneven fracture. Jensenite is adamantine, brittle and nonfluorescent; H (Mohs) 3-4; D (calc.) 4.78 for the idealized formula, 4.76 g/cm 3 for the empirical formula. In a polished section, jensenite is very weakly bireflectant and nonpleochroic. In reflected plane-polarized light in air, it is a nondescript grey, and in oil, it is a much darker grey in color with a brownish tint, with ubiquitous bright green internal reflections. Anisotropy is not detectable. Measured values of reflectance, in air and in oil, are tabulated. Electron-microprobe analyses yielded CuO 50.91, ZnO 0.31, TeO 3 38.91, H 2 O (calc.) [8.00], total [98.13] wt.%. The empirical formula, derived from crystal-structure analysis and electron-microprobe analyses, is (Cu (sub 2.92) Zn (sub 0.02) ) (sub Sigma 2.94) Te (super 6+) (sub 1.01) O (sub 5.97) .2.03H 2 O, based on O = 8. The mineral name honors Martin C. Jensen, Reno, Nevada, who discovered the mineral.

Canadian Mineralogist↗

Mineral resources and consumption in the twenty-first century

Modern societies are highly dependent upon energy and mineral resources to produce and deliver the material goods and even the services of everyday life. Although societies' dependence upon fossil fuels is evident and understood by much of the population, few people are as well informed about their dependence upon a wide variety of nonfuel minerals. This ignorance may result from two interrelated conditions. First, in contrast to fossil fuels, few people directly use nonfuel minerals in recognizable forms because most use is as part of manufactured products. Second, the value of raw ($38 billion) and even processed ($397 billion) nonfuel minerals in the United States in 2002 was small relative to the value the industries that consume these materials contribute to the economy ($1,700 billion). That is, although nonfuel mineral inputs are indispensable to construction and to the manufacture of durable and even nondurable goods (USGS 2003), their value is modest compared with the value of the final products.

Book chapter↗

Ocean minerals

Nearly 71 percent of the Earth is covered by ocean, yet during the entire history of societies, the mineral resources essential for nation building have been acquired solely from the continents. Deep-ocean minerals were discovered over a century ago during the Challenger expedition of 1873—1876, but only relatively recently did programs develop to determine their origin, distribution, and resource potential. Continental margin marine mineral deposits include aggregate, sand, placer minerals, and phosphorite. Aggregate, sand, and placers are detrital minerals that were transported and deposited on the shelf, whereas phosphorite is a chemical sedimentary deposit that formed in place from chemical reactions in the near-surface sediment. Seawater makes up 98.8 percent of the world's surface water and contains every element in the periodic table, mostly in trace concentrations. Fe-Mn crusts are found on rock surfaces of seamounts, ridges, and plateaus as pavements and coatings on talus in areas that remain sediment-free for millions of years.

Book chapter↗

Mineral resource of the month: vermiculite

Vermiculite comprises a group of hydrated, laminar magnesium-aluminum-iron silicate minerals resembling mica. They are secondary minerals, typically altered biotite, iron-rich phlogopite or other micas or clay-like minerals that are themselves sometimes alteration products of amphibole, chlorite, olivine and pyroxene. Vermiculite deposits are associated with volcanic ultramafic rocks rich in magnesium silicate minerals, and flakes of the mineral range in color from black to shades of brown and yellow. The crystal structure of vermiculite contains water molecules, a property that is critical to its processing for common uses. Using a process called exfoliation-in which vermiculite flakes are heated to 900 degrees Celsius or higher, causing water within the flakes to flash to steam and expand-crude vermiculite ore is processed into particles that are eight to 20 times larger. The resulting lightweight material is chemically inert and fire resistant, with low density and low thermal conductivity. It is also odorless, has high liquid absorption capacity and catalytic properties. Because it is lightweight and thermally insulating, vermiculite is used in general building plasters and concrete products, alone or combined with other lightweight aggregates such as perlite. Special plasters, in which vermiculite is combined with binders like gypsum or portland cement, fillers or other additives, provide fire protection and soundproofing. As insulation, exfoliated vermiculite, sometimes treated with a water repellent, is used to fill pores and cavities in masonry construction and hollow blockwork to enhance acoustic properties, fire rating and insulation performance. Exfoliated vermiculite can also be used to produce refractory and insulation concretes and mortars, and to make high-temperature binders for construction materials, gaskets, specialty papers, textiles and vehicle brake linings. Finer grades of exfoliated vermiculite can be used to produce various shapes of insulation pellets, high-temperature insulation, as a primary component in cementitious coatings, and as a filler in inks, paints, plastics and other materials. Vermiculite can absorb liquids such as fertilizers, herbicides and insecticides, which can then be transported as free-flowing solids. It is used in the fertilizer and pesticide markets because of its ability to act as a bulking agent, carrier and extender. In horticulture, exfoliated vermiculite improves soil aeration and moisture retention, and when mixed with peat or other composted materials, such as pine bark, vermiculite produces a good growing medium for plants. As a soil conditioner, exfoliated vermiculite improves aeration in clay-rich soils and water retention in sandy soils, while reducing the likelihood of compaction, cracking and crusting of the soil. For more information on the commercial use of vermiculite, visit minerals.usgs.gov/minerals/ .

Earth↗

Exploration case study using indicator minerals in till at the giant Pebble porphyry Cu-Au-Mo deposit, southwest Alaska, USA

The Pebble deposit in southwest Alaska (Fig. 1) contains one of the largest resources of copper and gold in the world. It includes a measured and indicated resource of 5,942 million tonnes (Mt) at 0.42% Cu, 0.35 g/t Au, and 250 ppm Mo (0.30% copper equivalent, CuEQ, cut off) and contains significant concentrations of Ag, Pd, and Re (Northern Dynasty Minerals 2011). The deposit remains open at depth. The Pebble West zone was discovered in 1989 by Cominco American. In 2005, Northern Dynasty Minerals Ltd. (NDM) discovered Pebble East, and in July 2007, NDM partnered with Anglo American to form the Pebble Limited Partnership (PLP). The U.S. Geological Survey began collaborative investigations with PLP in 2007 to identify techniques that will improve mineral exploration in covered terranes. The Pebble deposit is an ideal location for such a study because the deposit is undisturbed (except for drilling), is almost entirely concealed by post-mineral volcanic rocks and glacial deposits, and because its distribution is well constrained in the subsurface by PLP’s drill-hole geology and geochemistry. An exploration method developed by Averill (2007) that utilizes porphyry copper indicator minerals (PCIMR) in glacial till samples was applied at Pebble; samples were collected up- and down-ice (of former glaciers) from the deposit. The distribution of several PCIMs identifies the deposit, which suggests that PCIMs may be useful in exploration for other concealed porphyry deposits in the region. In this study, we compare the efficacy of PCIMs relative to that of pond and stream sediments also collected in the deposit area. The Pebble deposit is located 380 km southwest of Anchorage, in the Bristol Bay region of southwest Alaska. There is no road network and access to the study area is by helicopter. The deposit is situated in a broad glacially sculpted topographic low at the head of three drainages, Talarik Creek, North Fork Koktuli River, and the South Fork Koktuli River (Fig. 1). The study area is in a zone of discontinuous permafrost and is masked by lichen-rich tundra vegetation.

Alaska↗

Mineral resource of the month: Vermiculite

Vermiculite comprises a group of hydrated, laminar magnesium-aluminum-iron silicate minerals resembling mica. They are secondary minerals, typically altered biotite, iron-rich phlogopite or other micas or clay-like minerals that are themselves sometimes alteration products of amphibole, chlorite, olivine and pyroxene. Vermiculite deposits are associated with volcanic ultramafic rocks rich in magnesium silicate minerals, and flakes of the mineral range in color from black to shades of brown and yellow. The crystal structure of vermiculite contains water molecules, a property that is critical to its processing for common uses.

Earth↗