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USGS1964

Geology and hydrology of the West Milton area, Saratoga County, New York

This report describes the geology, ground-water conditions, streamflow characteristics, and quality of water in the West Milton area, Saratoga County, N.Y. The West Milton area is in the east-central part of New York in the hilly region that forms a transition zone between the Adirondack Mountains and the Hudson-Mohawk valley lowland. Bedrock underlying the area consists of crystalline rocks of Precambrian age and sandstone, dolomite, limestone, and shale formations of Cambrian and Ordovician age. The formations have been moderately folded and have been displaced as much as several hundred feet' along at least three northeast-trending normal faults. The bedrock is overlain in nearly all parts of the area by a layer of unconsolidated deposits which ranges in thickness from a few feet to more than 200 feet. The unconsolidated deposits are of Pleistocene age and consist of unstratified materials (till) laid down by glacial ice at stratified sediments deposited by glacial meltwaters. The topography of the bedrock surface differs greatly from the topography of the land surface. Although not evident in the present topography, at least two channels, cut in bedrock by preglacial streams, pass through the area. Ground-water supplies adequate to satisfy domestic requirements can be obtained from wells in any part of the area. Large ground-water supplies may be taken from coarse-grained stratified deposits comprising two aquifers in the valley of Kayaderosseras Creek. The Atomic Energy Commission has pumped as much as 1 mgd from a horizontal well drawing from the uppermost aquifer which is composed of flood-plain deposits. Part of the water yielded by this well during extended periods of pumping is induced flow from the creek. Three nearby vertical wells drilled by the Commission comprise a separate well field capable of yielding at least 2 mgd and possibly as much as 3 mgd from the deeper stratified deposits underlying the valley. A pumping test showed that at near the center of this well field the coefficient of transmissibility is about 125,000 gpd per ft and the coefficient of storage is about 0.0003. The water obtained from the sand and gravel has a hardness of about 125 ppm and contains about 150 ppm of dissolved solids. Most of the Government reservation is drained by Glowegee Creek, one of the larger tributaries of Kayaderosseras Creek. The average streamflow of Kayaderosseras Creek at West Milton is 141 cfs or about 1.5 cfs per sq. mi. The monthly mean discharge has ranged from a low of 21.7 cfs in September 1958 to a high of 866 cfs in March 1936, and the annual mean discharge has ranged from 94.5 cfs in 1941 to 198 cfs in 1952. The mean annual flood is 1,740 cfs and the 50-year flood is 5,300 cfs. Streamflow data have been collected on Glowegee Creek since 1948 at a station 0.5 mile south of West Milton. The average streamflow of Glowegee Creek at this station is 41 cfs or about 1.5 cfs per sq mi. The mean annual flood is 740 cfs and the 50-year flood is 2,250 cfs. The quality of the water in both Kayaderosseras Creek and Glowegee Creek is satisfactory for public supply and most industrial purposes. The mineral content of both streams is low--the dissolved-solids content averaging about 93 ppm in Kayaderosseras Creek and about 131 ppm in Glowegee Creek. The average hardness of water in Kayaderosseras Creek and Glowegee Creek is 68 ppm and 102 ppm, respectively. During periods of low flow, suspended sediment discharge in both streams is less than 10 tons per day, but during periods of high flow, the sediment discharge has been as great as 163 tons per day in Glowegee Creek and 437 tons per day in Kayaderosseras Creek.

Water Supply Paper↗

USGS1953

Airborne radioactivity survey of the Gulf of Mexico beach between Sanibel Island and Caladesi Island, Florida

The accompanying map shows the results of an airborne radioactivity survey along the Gulf of Mexico beach between Sanibel Island and Caladesi Island in Florida. This survey was made May 4, 1953, as part of a cooperative program with the U.S. Atomic Energy Commission. The survey was made with scintillation detection equipment mounted in a Douglas DC-3 aircraft and consisted of one flight line, at a 500-foot altitude , parallel to the beach. The vertical projection of the flight line coincided approximately with the landward limit of the modern beach. The width of the zone on the ground from which anomalous radiation is measured at the nominal 500 foot flight altitude varies with the areal extent and intensity of the radioactivity the width of the zone may be as much as 1400 feet. The accompanying map and index map show the approximate locations of the areas of greater-than-average radioactivity and the location of the traverse flown. The abnormal radioactivity is apparently caused by radioactive minerals associated with "black sand" deposits which occur locally along the beach in the region. The present technique of airborne radioactivity measurement does not permit distinguishing between activity due to thorium and that due to uranium. An anomaly, therefore, may represent radioactivity due entirely to one or to a combination of these elements. It is not possible to determine the extent or radioactive content of the materials responsible for the abnormal radioactivity. The information given in the accompanying map showing the localities of greater-than-average radioactivity therefore, suggests area in which uranium or thorium deposits are more likely to occur.

Florida↗

USGS2015

Barite: a case study of import reliance on an essential material for oil and gas exploration and development drilling

Global dependence on a limited number of countries for specific mineral commodities could lead to sudden supply disruptions for the United States, and barite is one such commodity. Analyses of barite supply amounts and sources for the United States are demonstrative of mineral commodities on which the country is import reliant. Mineral commodity trade flows can be analyzed more easily than import reliances for commodities in which U.S. domestic demand is primarily met by materials contained within manufactured products, as with the rare-earth elements in cellular phones and computers. Barite plays an essential role as a weighting material in drilling muds used in oil and gas drilling, primarily to prevent the explosive release of gas and oil during drilling. The Nation’s efforts to become more energy independent are based largely on the domestic oil and gas industry’s ability to explore and develop onshore and offshore fuel deposits. These activities include increased efforts by the United States to locate and recover oil and gas within unconventional deposits, such as those in the Bakken, Eagle Ford, and Marcellus Formations, using advanced drilling technologies. Domestic barite production was about 670,000 metric tons (t) in 2012, equivalent to about 20 percent of the domestic drilling industry’s barite demand. Mine production for the United States in 2012 was about one-third of what was produced in 1980. In 2012, barite imported from China was approximately 2.2 million t and comprised about 77 percent of total barite imports and about 70 percent of the barite used in domestic drilling. Barite from India (14 percent), Morocco (6 percent) and Mexico (2 percent) comprised the bulk of the remaining total import balance; drilling applications consumed nearly all barite imported from these three countries.

Scientific Investigations Report↗

USGS1982

Origin of the Mariano Lake uranium deposit, McKinley County, New Mexico

The Mariano Lake uranium deposit, hosted by the Brushy Basin Member of the Jurassic Morrison Formation, occurs in the trough of an east-west trending syncline at the western end of the Smith Lake-Mariano Lake group of uranium deposits near Crownpoint, New Mexico. The orebody, which contains abundant amorphous organic material, is situated on the reduced side of a regional reduction-oxidation (redox) interface. The presence of amorphous organic material suggests the orebody may represent a tabular (primary) deposit, whereas the close proximity of the orebody to the redox interface is suggestive that uranium was secondarily redistributed by oxidative processes from pre-existing tabular orebodies. Uranium contents correlate positively with both organic carbon and vanadium contents. Petrographic evidence and scanning electron microscope-energy dispersive analyses point to uranium residence in the epigentically introduced amorphous organic material, which coats detrital grains and fills voids. Uranium mineralization was preceded by the following diagenetic alterations: precipitation of pyrite (ẟ 34 S values ranging from-11.0 to-38.2 per mil); precipitation of mixed-layer smectite-illite clays; partial dissolution of some of the detrital feldspar population; and precipitation of quartz and adularia overgrowths. Alterations associated with uranium mineralization include emplacement of amorphous organic material (possibly uranium bearing); destruction of detrital iron-titanium oxide grains; coprecipitation of chlorite and microcrystalline quartz, and precipitation of pyrite and marcasite (ẟ 34 S values for these sulfides ranging from -29.4 to -41.6 per mil). After mineralization, calcite, dolomite, barite, and kaolinite precipitated, and authigenic iron disulfides were replaced by ferric oxides and hydroxides. Geochemical data (primarily the positive correlation of uranium content to both organic carbon and vanadium contents) and petrographic observations (epigentically introduced amorphous organic matter and uranium residence in this organic matter) indicate that the Mariano Lake orebody is a tabular-type uranium deposit. Oxidative processes have not noticeably redistributed and reconcentrated primary uranium in the immediate vicinity of the deposit nor have they greatly modified geochemical characteristics in the ore. Preservation of the Mariano Lake deposit may not only be related to its position along the synclinal trough, where oxidative destruction of the orebody has been inhibited by stagnation of oxidizing ground waters by the structure, but also due to the deflection of ground waters (resulting from low orebody porosity) around the orebody.

New Mexico↗

USGS1953

Airborne radioactivity survey of parts of the Atlantic Ocean beach, North and South Carolina

The accompanying map shows the results of an airborne radioactivity survey along the Atlantic Ocean beach between Edisto Island, South Carolina and Cape Fear, North Carolina. The survey was made May 20, 1953, as part of a cooperative program with the U.S. Atomic Energy Commission. The survey was made with scintillation detection equipment mounted in a Douglas DC-3 aircraft and consisted of one flight line, at a 500-foot altitude, parallel to the beach. The vertical projection of the flight line coincided approximately with the landward limit of the modern beach. The width of the zone on the ground from which anomalous radiation is measured at the nominal 500 foot flight altitude varies with areal extent and intensity of radioactivity of the source. For strong sources of radioactivity the width of the zone may be as much as 1400 feet. The accompanying maps show the approximate locations of the areas of greater-than-average radioactivity (at left) and the location of the traverse flown (at right). The abnormal radioactivity is apparently caused by radioactive minerals associated with "black sand" deposits which occur locally along the beach in this region. The present technique of airborne radioactivity measurement does not permit distinguishing between activity due to thorium and that due to uranium. An anomaly, therefore, may represent radioactivity due entirely to one or a combination of these elements. It is not possible to determine the extent or radioactive content of the materials responsible for the abnormal radioactivity. The information given in the accompanying map showing the localities of greater-than-average radioactivity therefore, suggests areas in which uranium and thorium deposits are more likely to occur.

North Carolina;South Carolina↗

USGS1999

Hydrated salt minerals on Europa's surface from the Galileo near-infrared mapping spectrometer (NIMS) investigation

We reported evidence of heavily hydrated salt minerals present over large areas of Europa's surface from analysis of reflectance spectra returned by the Galileo mission near infrared mapping spectrometer (NIMS) [ McCord et al. , 1997a, b, 1998a, b]. Here we elaborate on this earlier evidence, present spatial distributions of these minerals, examine alternate water-ice interpretations, expand on our hydrated-salts interpretation, consider salt mineral stability on Europa, and discuss the implications. Extensive well-defined areas on Europa show distinct, asymmetric water-related absorption bands in the 1 to 2.5-μm region. Radiative transfer modeling of water ice involving different particle sizes and layers at Europa temperatures does not reproduce the distinctive Europa water bands. However, ice near its melting temperature, such as in terrestrial environments, does have some characteristics of the Europa spectrum. Alternatively, some classes of heavily hydrated minerals do exhibit such water bands. Among plausible materials, heavily hydrated salt minerals, such as magnesium and sodium sulfates, sodium carbonate and their mixtures, are preferred. All Europa spectral features are present in some salt minerals and a very good match to the Europa spectrum can be achieved by mixing several salt spectra. However, no single or mix of salt mineral spectra from the limited library available has so far been found to perfectly match the Europa spectrum in every detail. The material is concentrated at the lineaments and in chaotic terrain, which are technically disrupted areas on the trailing side. Since the spectrum of the material on Europa is nearly the same everywhere so-far studied, the salt or salt-mixture composition may be nearly uniform. This suggests similar sources and processes over at least a near-hemispheric scale. This would suggest that an extensive subsurface ocean containing dissolved salts is the source, and several possible mechanisms for deposit emplacement are considered. The hydrogen bonds associated with hydration of these salts are similar or greater in strength and energy to those in pure water ice. Thus, once on the surface, the salt minerals should be as stable to disruption as water ice at the Europa temperatures, and mechanisms are suggested to enhance the stability of both materials. Spectra obtained of MgSO 4 ·6H 2 O at 77 K show only small differences from room temperature spectra. The main difference is the appearance of the individual absorptions composing the broad, composite water features and associated with the several different H 2 O sites in the salt hydrate molecule. This suggests that the Europa absorption bands are also composites. Thus higher spectral resolution may reveal these diagnostic features in Europa's spectrum. The specific salts present and their relative abundances would be indicators of the chemistry and conditions of an ocean environment, and areas of fresh, heavy concentration of these minerals should make ideal lander mission sampling sites.

Journal of Geophysical Research E: Planets↗

USGS1984

A workshop model simulating fate and effect of drilling muds and cuttings on benthic communities

Oil and gas exploration and production at marine sites has generated concern over potential environmental impacts resulting from the discharge of spent drilling muds and cuttings. This concern has led to a broad array of publicly and privately sponsored research. This report described a cooperative modeling effort designed to focus information resulting from this research through construction of explicit equations that simulate the potential impacts of discharge drilling fluids (muds) and cuttings on marine communities. The model is the result of collaboration among more than 30 scientists. The principal cooperating organizations were the E.S. Environmental Protection Agency, the U.S. Minerals Management Service, the Offshore Operators Committee, and the Alaska Oil and Gas Association. The overall simulation model can be conceptualized as three connected submodels: Discharge and Plume Fate, Sediment Redistribution, and Benthic Community Effects. On each day of simulation, these submodels are executed in sequence, with flows of information between submodels. The Benthic Community Effects submodel can be further divided into sections that calculate mortality due to burial, mortality due to toxicity, mortality due to resuspension disturbance, and growth of the community. The model represents a series of seven discrete 1-m 2 plots at specified distances along a transect in one direction away from a discharge point. It consists of coupled difference equations for which parameter values can easily be set to evaluate different conditions or to examine the sensitivity of output to various assumptions. Sets of parameter values were developed to represent four general cases or scenarios: (1) a shallow (5 m), cold environment with ice cover during a substantial fraction of the year, such as might be encountered in the Beaufort Sea, Alaska; (2) a shallow (20 m), temperate environment, such as might be encountered in the Gulf of Mexico; (3) a deeper (80 m), temperate environment, such as might be encountered in the Gulf of Mexico; and (4) a very deep (1,000 m) environment, such as might be encountered on the Atlantic slope. The focus of the modeling effort was on the connection of a reasonable representation of physical fate to the biological responses of populations, rather than on highly detailed representations of individual processes. For example, the calculations of physical fate are not as detailed as those in the recently published model of Brandsma et al. (1983). The value of the model described herein is in the broad scope of processes that are explicitly represented and linked together. The model cannot be considered to produce reliable predictions of the quantitative impacts of discharged drilling fluids and cuttings on biological populations at a particular site. Limitations of the model in predicting integrated fate and effects can be traced to three general areas: level of refinement of the algorithms used in the model; lack of understanding of the processes determining fate and effects; and parameter and data values. Despite the limitations, several qualitative conclusions concerning both potential impacts and the importance of various remaining data gaps can be drawn from the modeling effort. These include: (1) Simple, unequivocal conclusions about fate and effects across geographical regions and drilling operations are difficult, if not misleading, due to the large amount of variability in characteristics of discharged materials (e.g., oil content and toxicity), discharge conditions (e.g., duration of drilling operations), physical environments (e.g., water depth, current direction, and sediment disturbance regimes), and biological communities (e.g., intrinsic growth rates). Different combinations of these characteristics can result in substantial differences in simulated environmental fate and biological effects. For examples, simulated recovery in some high-energy environments occurs within months after the cessation of discharge operations, even at heavily impacted sites, whereas simulated recover in some low-energy environments takes years at heavily impacted sites. <2) Considerable difficulties remain in the reliable extrapolation of results from laboratory toxicity experiments to predictions of population effects in the field. (3) The volume of material discharged and duration of operations in the production drilling operations simulated by the model are sufficient to produce substantial simulated biological impacts at some plots, both in terms of differences from a control plot during the period of discharge operations, and in terms of the recovery period following the perturbations. Evaluation of the significance of potential effects involves the following factors: • Definition of a specific spatial and temporal reference frame (e.g., What is the natural variation? Is 1 year to be considered a "long" or "short" time? Is 50 m to be considered a "large" or "trivial" distance? • Consideration of rare or unique resources and particularly sensitive biotic assemblages. • Consideration of the potential for long term, cumulative effects. Some of these aspects are clearly beyond the scope of this modeling efforts (e.g., the model does not simulate the long term fate of resuspended material). The model does, however, contain an internal "reference frame" by comparison to simulated behavior at a control plot. The model, in general, simulates substantial "natural" variation at the reference or control plots, both over time, due to sediment disturbance events in medium to high energy environments, and over space, due to geographically varying conditions, such as water depth and current regime.

Report↗

USGS1953

Airborne radioactivity survey of parts of Atlantic Ocean beach, Virginia to Florida

The accompanying maps show the results of an airborne radioactivity survey along the Atlantic Ocean beach from Cape Henry, Virginia to Cape Fear, North Carolina and from Savannah Bach Georgia to Miami Beach, Florida. The survey was made March 23-24, 1953, as part of a cooperative program with the U.S. Atomic Energy Commission. The survey was made with scintillation detection equipment mounted in a Douglas DC-3 aircraft and consisted of one flight line, at a 500-foot altitude, parallel to the beach. The vertical projection of the flight line coincided approximately with the landward limit of the modern beach. The width of the zone on the ground from which anomalous radiation is measured at the normal 500 foot flight altitude varies with the areal extent radioactivity of the source. For strong sources of radioactivity the width of the zone would be as much as 1,400 feet. The location of the flight lines is shown on the index map below. No abnormal radioactivity was detected along the northern flight line between Cape Henry, Virginia and Cape Fear, North Carolina. Along the southern flight line fourteen areas of abnormal radioactivity were detected between Savannah Beach, Georgia and Anastasia Island, Florida as shown on the map on the left. The abnormal radioactivity is apparently due to radioactive minerals associated with "black sand" deposits with occur locally along the beach in this region. The present technique of airborne radioactivity measurement does not permit distinguishing between activity sue to thorium and that due to uranium. An anomaly, therefore, may represent radioactivity due entirely to one or to a combination of these elements. It is not possible to determine the extent or radioactive content of the materials responsible for the abnormal radioactivity. The information given on the accompanying map indicates only those localities of greater-than-average radioactivity and, therefore suggest areas in which uranium and thorium deposits are more likely to occur.

Florida;Georgia;North Carolina;South Carolina;Virg↗

USGS2019

Rare earth elements in coal and coal fly ash

The rare earth elements (REEs) are a group of 17 elements sharing similar chemical properties. They include yttrium (Y, atomic number 39), scandium (Sc, atomic number 21), and the 15 elements of the lanthanide series, atomic numbers 57 (lanthanum, La) to 71 (lutetium, Lu). Because promethium (Pm, atomic number 61) does not occur in the Earth’s crust and scandium typically has different geological occurrences from other REEs, they are not discussed further herein. REEs are, on average, more abundant than precious metals (for example, gold, silver, and platinum), but because of their unique geochemical properties, they do not commonly form economically viable ore deposits. Nevertheless, REEs are increasingly required for a range of modern applications in defense and renewable energy technologies and in commercial products, primarily as magnets, batteries, and catalysts. The United States currently (2018) produces REEs from a single mine in California, accounting for just 9 percent of global production, whereas 70 percent of global REE production comes from China. For these reasons, REEs are considered a critical resource, and the U.S. Geological Survey (USGS) has an interest in helping to identify new sources of REEs for domestic production. In 2017, coal use accounted for about 30 percent of the electric power generated in the United States. Fly ash, produced during the burning of coal, is a fine-grained solid derived from noncombustible constituents of coal, such as clay minerals and quartz. When coal is burned, REEs are retained and enriched in the fly ash and, as a result, fly ash has long been considered a potential resource for REEs. The United States has the world’s largest coal reserves and, even though gas-fired power generation has increased significantly in the last decade, the United States continues to produce vast quantities of fly ash, about half of which is beneficially reused, primarily in construction materials. The remainder is stored, mostly in landfills and impoundments. Thus, annual fly ash production, combined with fly ash already in storage, constitutes a large potential resource. Research into how to utilize coal and coal fly ash as sources of REEs is ongoing. Viable recovery of REEs from coal and coal ash requires identification of coals and ashes with the highest REE concentrations and development of workable methods for REE extraction and recovery. Understanding how REEs occur within fly ash, described in this fact sheet, is one of the keys to developing possible methods for their recovery.

Fact Sheet↗

USGS2026

The Great Lakes Geologic Mapping Coalition—Working collaboratively to understand the geology of the Great Lakes Region

Introduction The Great Lakes Geologic Mapping Coalition (GLGMC), commonly referred to as the “Coalition,” is a partnership between the U.S. Geological Survey (USGS), the U.S. States of Illinois, Indiana, Michigan, Minnesota, New York, Ohio, Pennsylvania, and Wisconsin and the Canadian province of Ontario. The member States receive funding for geologic mapping work from the USGS National Cooperative Geologic Mapping Program (NCGMP), whereas Ontario participates as a nonfunded partner. The mission of the GLGMC is to produce three-dimensional (3D) geologic maps that depict unconsolidated sediments and near-surface bedrock in the Great Lakes region of North America. Geologic maps are the basis of most earth science investigations and help support resource exploration (energy, minerals, groundwater), natural hazard mitigation, infrastructure development, and land-use planning, all of which can be used to advance economic development and strengthen national security in the Great Lakes region. During the last few million years, the Great Lakes region has experienced repeated glacial advances and retreats, leaving behind extensive sediments, abundant natural resources, and widespread effects on the underlying bedrock geology (Swezey and others, 2022). Linked by shared histories of past glaciations, industrial agriculture, and legacy automotive, coal, steel, and manufacturing industries, the GLGMC member States collaborate to improve the understanding of the 3D distribution of the sediments overlying the region’s bedrock (fig. 1). Developing a comprehensive subsurface 3D framework of this glaciated terrain can provide earth science data to policymakers at all levels. These insights facilitate informed decisions on the exploration, use, and protection of vital resources, such as critical minerals, industrial materials, and aquifers, thereby supporting economic prosperity and the well-being of the citizens of this region. Since its inception in 1998, the Coalition has completed more than 100 geologic mapping projects across the Great Lakes region. Each project aims to deliver geologic maps, 3D datasets, and other information that improves understanding of the geology of the Great Lakes region, with an emphasis on economic and water resources. Key deliverables include 3D geologic maps and models typically portraying sediment thickness, often derived from top-of-bedrock and borehole data. These products are developed through a combination of fieldwork, subsurface modeling, and the collection and analysis of rock and sediment cores. To support Coalition goals, member States collaborate with scientists working on related STATEMAP, EDMAP, and FEDMAP projects. Coalition scientists also engage with Tribal Nations in the Great Lakes region to ensure that Tribal interests pertaining to Coalition work are addressed. Through this collaboration, the Coalition unites the efforts of State, Federal, and Tribal Nation stakeholders to advance geologic data production and enhance understanding of the geologic resources of the Great Lakes region.

Illinois, Indiana, Michigan, Minnesota, New York, ↗

USGS2023

Sequestration and reoxidation of chromium in experimental microcosms

Groundwater containing hexavalent chromium, Cr(VI), downgradient from the Pacific Gas and Electric Company (PG&E) Hinkley compressor station in the Mojave Desert, 80 miles northeast of Los Angeles, California, is undergoing bioremediation using added ethanol as a reductant in a volume of the aquifer defined as the in situ reactive zone (IRZ). This treatment reduces Cr(VI) to trivalent chromium, Cr(III), which is rapidly sequestered by sorption to aquifer particle surfaces and by co-precipitation within iron (Fe) or manganese (Mn) bearing minerals forming in place as reduction proceeds. Successful mitigation of the Cr(VI) plume is projected to require 10–95 years, at which time bioremediation with ethanol will likely cease. This projection assumes that Cr(VI) removal is permanent and that no Cr(III) will oxidize back to Cr(VI) in the event of changing hydrologic conditions that may cause oxygen-rich water to re-enter the IRZ. Laboratory microcosm experiments were done to explore the process of reductive sequestration of Cr(VI) to Cr(III) and the potential for reoxidation of Cr(III) to Cr(VI). In reductive sequestration experiments, batch microcosms were prepared with aquifer materials collected from sites upgradient of the Cr(VI) regulatory plume. Control microcosms were prepared using Fe- and Mn-coated quartz sand. Unfiltered Mojave River groundwater containing an added tracer of isotopically labeled chromium-50 were reacted with microcosm materials for up to 2 years; during this time, bio-reduction was stimulated by repeated additions of diluted ethanol to maintain reduced conditions within appropriate ranges, avoiding sulfate reducing or methanogenic conditions as much as possible while mimicking field conditions. Analysis of chromium-50, Fe, and Mn obtained by sequential extraction from microcosms harvested (incubation terminated and microcosm contents analyzed) at various times showed that some aqueous chromium (Cr) was sorbed to particle surfaces within hours; reduction to Cr(III) and incorporation into amorphous and crystalline solid phases occurred during the next few months. Amorphous Cr-containing fractions included Fe and Mn hydroxides and organic matter. Ultimately, most of the chromium-50 tracer was present in the less reactive crystalline phase. However, Fe and Mn were broadly distributed at later stages of reduction, and both were spatially co-located with Cr on a micrometer (μm) scale. Solid-phase data collected using scanning electron microscopy with energy dispersive spectroscopy (SEM-EDS) and X-ray absorption spectroscopy (XAS) indicated that some Cr(III) was associated with mixed valence Fe oxides like magnetite and Fe-Mn oxides like jacobsite. Additionally, Cr(III) was observed within several μm of Fe and Mn embedded in clays and in mineral coatings. To evaluate the potential for reoxidation of Cr(III) to Cr(VI), additional batch microcosms of aquifer materials and mixtures of Fe- and Mn-coated sand were first reduced for more than 1 year and subsequently oxidized for almost 2 years. Hexavalent chromium was formed and was available for release to the aqueous phase during oxidation of all materials; however, the timing and amount of Cr(VI) formed and released varied among substrates. Artificial substrates containing more Mn produced more Cr(VI). Site material characteristic of recent Mojave River deposits contained within the IRZ produced the least Cr(VI) during oxidation, while site materials composed of older Mojave River aquifer material (containing more Mn) produced more Cr(VI). Site material collected from within the IRZ contained more Cr but produced an intermediate amount of Cr(VI) following oxidation. The combined results of microcosm chemistry and solid-phase analyses showed that the nature and locus of Cr(III) sequestration influenced its vulnerability to reoxidation to Cr(VI). It was concluded that co-location of Cr with Mn at later stages of reduction influenced the susceptibility of Cr(III) to reoxidation in microcosms. Reoxidation of Cr(III) to Cr(VI) was observed in experiments with previously reduced material after just 14 days exposure to oxygen. As much as 10 percent of added Cr was oxidized to Cr(VI) in microcosms prepared using recent Mojave River aquifer material, and as much as 20 percent of added Cr was oxidized to Cr(VI) in microcosms prepared using older Mojave River aquifer material. Less Cr(VI) (less than 3 percent of Cr added before reduction) was released to the aqueous phase, and this release occurred following longer oxygen exposure. Site managers may need to plan for long-term monitoring and the possibility of active maintenance of anoxic conditions within the IRZ to ensure permanent sequestration of Cr after bioremediation with ethanol ceases.

California↗

USGS2025

USGS—An Unparalleled Scientific Asset

The U.S. Geological Survey (USGS) delivers information critical to powering our economy, managing our natural resources, and keeping Americans safe and healthy. 1 Mapping the Nation $21B Geologic maps save users an estimated 15% in annual costs: a value of between $14B and $21B. $25.6B in annual value to users of imagery from Landsat satellites, which were codeveloped by NASA and the USGS and operated through their lifespans by the USGS. $13.5B in annual benefits is generated by the USGS's 3D Elevation Program. Securing America’s Energy Independence 44% USGS-identified undiscovered geothermal energy is equal to 44% of current U.S. electricity generation. 29.4B barrels of oil and 391.6 trillion cubic feet of gas in recoverable resources are available on U.S. public lands based on USGS assessments. Protecting Americans’ Health and Safety $424B in recent wildland fire damages highlight the need for USGS fire science, which supports efforts to protect communities and reduce risk. USGS earthquake, volcano, landslide, and coastal hazard monitoring and information save lives and minimize costs; for example, $2.8M can be saved because of USGS enhanced information about a Mauna Loa eruption. $4.5B is the estimated cost of annual flooding. Through a network of over 11,885 streamgages, the USGS supports public safety and enables forecasts, early warning systems, and management actions that protect lives and property. Supporting National Security $3.1B The USGS identified a $3.1B risk to the American economy if China restricts gallium imports. This is one example underscoring the importance of the USGS mapping critical minerals, investigating supply chains, and producing the Nation’s critical minerals list. Enhancing Our Lands and Waters $21B in estimated annual costs results from invasive species. The USGS’s invasive species research informs approaches used to reduce their effects on agriculture, water infrastructure, disease transmission, fisheries, and outdoor recreation. USGS innovations support early warnings for harmful algal blooms—over $2M in yearly benefits are provided to Kansas alone. $45B USGS science informs the management of big game (such as deer and elk). The big-game hunting industry contributes $45B to the U.S. economy. Fostering American Prosperity $4.1T Mineral commodities are necessary for the $4.1T in value added to the GDP by major industries that consume processed mineral materials and employ 1 million workers. Because of this, USGS data on mineral supply, demand, and trade are highly valued. 45,000 metric tons Rare earths power the growing technology economy, including cell phones, electric vehicles, and medical devices. For over 70 years, USGS work has supported the discovery of rare earth resources in California’s Mountain Pass area, which produced 45,000 metric tons of rare earth concentrates in 2024—over 11% of the global supply. Guarding American Food Security $70.2B USGS science informs early warning systems and management strategies to mitigate disease outbreaks in agriculture—critical research on highly pathogenic avian influenza, for example, helps safeguard the $70B value in poultry and egg production. $11.8B USGS groundwater tools are vital for agriculture; for example, in the Mississippi Alluvial Plain, 65% of farming relies on groundwater to support its $11.8B annual industry. 1 Values throughout are given in billions (B), millions (M), and trillions (T) of U.S. dollars. GDP is “Gross Domestic Product.” Percentages are shown as %.

General Information Product↗

USGS2019

Alaska Geochemical Database Version 3.0 (AGDB3)—Including “Best Value” Data Compilations for Rock, Sediment, Soil, Mineral, and Concentrate Sample Media

The Alaska Geochemical Database Version 3.0 (AGDB3) contains new geochemical data compilations in which each geologic material sample has one “best value” determination for each analyzed species, greatly improving speed and efficiency of use. Like the Alaska Geochemical Database Version 2.0 before it, the AGDB3 was created and designed to compile and integrate geochemical data from Alaska to facilitate geologic mapping, petrologic studies, mineral resource assessments, definition of geochemical baseline values and statistics, element concentrations and associations, environmental impact assessments, and studies in public health associated with geology. This relational database, created from data-bases and published datasets of the U.S. Geological Survey (USGS), Atomic Energy Commission National Uranium Resource Evaluation (NURE), Alaska Division of Geological & Geophysical Surveys (DGGS), U.S. Bureau of Mines, and U.S. Bureau of Land Management serves as a data archive in support of Alaskan geologic and geochemical projects and contains data tables in several different formats describing historical and new quantitative and qualitative geochemical analyses. The analytical results were determined by 112 laboratory and field analytical methods on 396,343 rock, sediment, soil, mineral, heavy-mineral concentrate, and oxalic acid leachate samples. Most samples were collected by personnel of these agencies and analyzed in agency laboratories or, under contracts, in commercial analytical laboratories. These data represent analyses of samples collected as part of various agency programs and projects from 1938 through 2017. In addition, mineralogical data from 18,138 nonmagnetic heavy-mineral concentrate samples are included in this database. The AGDB3 includes historical geochemical data archived in the USGS National Geochemical Database (NGDB) and NURE National Uranium Resource Evaluation-Hydrogeochemical and Stream Sediment Reconnaissance databases, and in the DGGS Geochemistry database. Retrievals from these data-bases were used to generate most of the AGDB data set. These data were checked for accuracy regarding sample location, sample media type, and analytical methods used. In other words, the data of AGDB3 supersedes data in the AGDB and the AGDB2, but the background about the data in these two earlier versions are needed by users of the current AGDB3 to understand what has been done to amend, clean up, correct and format this data. Corrections were entered, resulting in a significantly improved Alaska geochemical dataset, the AGDB3. Data that were not previously in these databases because the data predate the earliest agency geochemical data-bases, or were once excluded for programmatic reasons, are included here in the AGDB3 and will be added to the NGDB and Alaska Geochemistry. The AGDB3 data provided here are the most accurate and complete to date and should be useful for a wide variety of geochemical studies. The AGDB3 data provided in the online version of the database may be updated or changed periodically.

Alaska↗

USGS2005

Evaluation of argon ages and integrity of fluid-inclusion compositions: Stepwise noble gas heating experiments on 1.87 Ga alunite from Tapajós Province, Brazil

Quantitative analyses are reported for active (N 2 , CH 4 , CO, CO 2 , H 2 , O 2 , HF, HCl, H 2 S, SO 2 ) and noble (He, Ar, Ne) gases released by crushing and step heating of magmatic-hydrothermal alunite from the Tapajós gold province in Brazil. This is the oldest known alunite ( 40 Ar/ 39 Ar age of 1.87 Ga), and because it has undergone minimal postdepositional thermal or tectonic strain, it is excellent material to test the retention of gas species in fluid inclusions and within the crystal structure over geological time. The gas compositions of a single sample, in combination with Ar age-spectrum data derived from stepwise heating of 10 related samples, have been used to constrain the limits of modification of primary gas compositions in fluid inclusions and the possible extent of the loss of radiogenic Ar. The observed variations in the isotopic compositions of He, Ne, and Ar released by stepwise heating have been used to identify the residence sites and determine the diffusion coefficients of the gases in the mineral. The data suggest that the only modification to primary gas compositions after entrapment in fluid inclusions and formation of the mineral is due to radiogenic and nucleogenic processes which affect the noble gas isotopic compositions. Three gas retention sites are recognized in alunite: (1) primary fluid inclusions, (2) crystal structure OH sites, and (3) crystal structure sulfate sites. Alunite undergoes OH loss at <500°C, and K-SO 4 structural decomposition occurs at >600°C. Fluid inclusions generally are ≤1 μm in diameter and have variable but high vapor/liquid ratios. The gases in inclusion fluids are quantitatively released in vacuo by heating at 200°C for &sim;1 h. In the inclusion fluids, H 2 O is 32 mol% of total gas, H 2 S/SO 2 ranges from approximately 4 to 2, and N 2 /Ar from 0.3 to 96.3. The presence of large amounts of H 2 and CO indicates disequilibrium among the gas species in the fluids. Helium abundance is 214 ppm. Helium from fluid inclusions ( R /Ra=19.5) makes up about 4% of the total helium, whereas He ( R /Ra=0.2–2.0) from the crystal structure makes up about 65% of the total. Argon from fluid inclusions has 40 Ar/ 36 Ar=584–629 and that from crystal structure sites is >9.6×10 4 . Most gases are released from fluid inclusions at 200 °C, whereas most Ar (≥95%) is released between 525 and 725°C. Argon released from fluid inclusions at 200°C has 38 Ar/ 36 Ar=0.0–0.064. In contrast, Ar released from the matrix of the mineral at high temperature has 38 Ar/ 36 Ar=3.6–14.7. This difference suggests that, since the formation of the alunite at 1.87 Ga, traces of Cl in the mineral structure have undergone Cl ( n , γ ) and 41 K ( n , α ) in situ reactions with neutrons derived from U–Th. The amount of 36 Ar production from Cl nucleogenic reactions used in correcting for atmospheric 40 Ar typically increases the calculated age by 1–5 m.y., which is generally an insignificant component of the determined Ar age. Decay of U–Th over this time contributes 4 He ( α ) buildup in the crystal structure K-SO 4 sites. Atmospheric corrected excess 21 Ne/ 22 Ne=0.028–0.409 indicates that nucleogenic Ne was also produced via ( α , n ) reactions in matrix sites. Diffusion coefficients and activation energies for the diffusion of Ar and He, as determined using Arrhenius plots, indicate two distinct groups definable by their differences in activation energies. Argon log D o =2.45 and 15.33, with activation energies of 225 and 465 kJ mol −1 , respectively; the diffusion of He in alunite is quantified with log D o =−4.33 and E =106.8 kJ mol −1 . Model calculations of simplistic 1/ e -folding times and diffusion distance–time curves indicate that He should remain in alunite for millions of years at ≤100°C, whereas at <200–220°C, the alunite will retain Ar almost indefinitely. The data demonstrate why alunite is suitable for Ar geochronological applications and also show that, unless the alunite is subjected to metamorphic deformation, the inclusion fluids should retain their primary compositions.

Tapajós Province↗

USGS2012

Byproduct metals and rare-earth elements used in the production of light-emitting diodes—Overview of principal sources of supply and material requirements for selected markets

The use of light-emitting diodes (LEDs) is expanding because of environmental issues and the efficiency and cost savings achieved compared with use of traditional incandescent lighting. The longer life and reduced power consumption of some LEDs have led to annual energy savings, reduced maintenance costs, and lower emissions of carbon dioxide, sulfur dioxide, and nitrogen oxides from powerplants because of the resulting decrease in energy consumption required for lighting applications when LEDs are used to replace less-energy-efficient sources. Metals such as arsenic, gallium, indium, and the rare-earth elements (REEs) cerium, europium, gadolinium, lanthanum, terbium, and yttrium are important mineral materials used in LED semiconductor technology. Most of the world's supply of these materials is produced as byproducts from the production of aluminum, copper, lead, and zinc. Most of the rare earths required for LED production in 2011 came from China, and most LED production facilities were located in Asia. The LED manufacturing process is complex and is undergoing much change with the growth of the industry and the changes in demand patterns of associated commodities. In many respects, the continued growth of the LED industry, particularly in the general lighting sector, is tied to its ability to increase LED efficiency and color uniformity while decreasing the costs of producing, purchasing, and operating LEDs. Research is supported by governments of China, the European Union, Japan, the Republic of Korea, and the United States. Because of the volume of ongoing research in this sector, it is likely that the material requirements of future LEDs may be quite different than LEDs currently (2011) in use as industry attempts to cut costs by reducing material requirements of expensive heavy rare-earth phosphors and increasing the sizes of wafers for economies of scale. Improved LED performance will allow customers to reduce the number of LEDs in automotive, electronic, and lighting applications, which could reduce the overall demand for material components. Non-Chinese sources for rare earths are being developed, and some of these new sources are likely to be operational in time to meet increasing demand for rare earths from the LED sector. Because most LED component production and manufacturing occurs in Asia and many LED producers have established supply contracts with Chinese producers of rare earths, a significant amount of the metallic gallium, indium, and the rare earths used for LED production will likely continue to come from Chinese sources at least for the next 5 years; however, a greater amount of these materials are now being processed in Japan, the Republic of Korea, and Taiwan. As non-Chinese sources of rare earths come into production, these new mines are likely to be sources of light REEs, but China will likely remain the leading source of supply for the heavy REEs suitable for use as LED dopants and phosphors at least for the next few years. Increased research in the development of phosphors that use smaller amounts of or different REEs is intended to reduce dependence on rare earths from China. Supply disruption of rare earths and other specialty metals could take place if China's specialty metal exports are redirected to domestic markets. The cost of recovery is high and the lifespan for LEDs is comparatively long; thus, the LED waste volume was low in 2010, and few LEDs were recycled. The minute metal content of LEDs leads to a high cost for recovery, so recycling of LEDs outside of electronic waste is unlikely in the near term, although some LED producers are evaluating recycling options. Recycling of metals from LEDs in electronic waste is possible if the costs of recovering metals are justified by demand and metal prices.

Scientific Investigations Report↗

USGS1979

Analyses of surficial deposits, central Brooks Range, Alaska

Seventy-nine sediment samples from the central Brooks Range were analyzed for grain-size distribution, shape and composition of grains, and other physical properties. Four statistical measures (sorting, mean diameter, skewness, and kurtosis) were then computed for the sand-to-clay size fraction of all samples. Fan sediments resemble the other alluvial-gravel deposits in consisting of sand and gravel from which very fine sand and the smaller size fractions have been removed by running water. Sorting and rounding of particles is best at the distal ends of large fans. Modern alluvium is better sorted than most fan deposits, with more rounded clasts and generally higher ratios of sand to gravel. Other alluvial deposits from terraces and heavily dissected erosion remnants generally are comparable to modern alluvium. All classes of alluvial gravel are characterized by removal of fines and by decreasing values of mean 0, kurtosis, and skewness as sorting increases. Most samples also have high clay/silt ratios that probably were caused by deflation on windswept bars and floodplains. Lacustrine deposits have clay percentages ranging from about 85 to 35, with silt predominant in more than one-half of the samples. Several samples contain sand and gravel that presumably were ice rafted. Clay-sized particles are unweathered mineral grains, implying that glacial abrasion was their primary source. Flow-slide deposits are very poorly sorted mixtures of gravel, sand, and silt, with clay content averaging only about one percent. Clasts consist of angular fragments of local bedrock, usually schist and phyllite, and matrix materials usually are highly micaceous. Although related flow types, a mud-flow and a debris-flow in till, are generally similar to flow-slide deposits, the mudflow has been modified by running water and the debris flow reflects the composition of its parent till. Other colluvial deposits commonly have high silt and low clay contents, but one solifluction deposit has abundant clay derived from till. Several of the flow-slides and other colluvial deposits are polygenetic, having undergone several episodes of flow that incorporated different types of sediment. Sand deposits include silty floodplain and basin-fill deposits as well as five relatively pure and well sorted dunal and river-bar sands. The silt-rich deposits probably contain large amounts of loess that fell into late-Pleistocene basin fillings and muskegs and later was redeposited on Holocene floodplains. The five dunal and bar sands are dominantly medium to fine sand; relatively well sorted, symmetric to coarse skewed, and leptokurtic. The dunal sands can be distinguished by the presence of very fine sand: wind apparently is less effective than flowing water in removing the finest sand fraction. The glacial deposits consist of till, ice-content stratified drift, and outwash. Till is a poorly sorted mixed sediment that resembles many flow de-posits but typically contains more clay. Two clay-deficient tills resemble fan deposits, implying effective washing by meltwater during glacial transport or deposition of these deposits. The ice-contact stratified drift varies in character from fan-like gravel deposits to sand accumulations nearly as well sorted as those of river bars. Almost all samples reflect some restriction in washing of fines by meltwater, probably owing to irregular topography and resulting poor drainage on and around stagnating glaciers. Most outwash deposits have less fine sand than modern alluvium, probably reflecting the generally high energy of glacial meltwater streams and the absence of vegetation from their floodplains. Samples from the southern Brooks Range are better sorted than those from northern Brooks Range valleys, and their statistical values lie close to those of modern alluvium. Comparisons between the different classes of sediments are facilitated by combining them into (1) gravel, (2) sand, silt, and clay, and (3) mixed deposits. Deposits of unknown or uncertain origin may then be compared directly against sediments from modern streams, dunes, flow-slides and other known sources, and alternative origins of aberrant samples in each of the sediment classes can also be examined. Several samples that initially were classed as fan, lacustrine, or glacial proved to be mixed deposits created by frost-churning, frost-lifting of stones, flowage down faces of river bluffs, and other postdepositional processes. Sorting and mean ϕ of matrix materials were useful in distinguishing the different sediment classes, separating them into contrasting subgroups, and identifying atypical samples. Skewness and kurtosis were generally less useful in this study.

Alaska↗

USGS2003

Geochemistry of the Birch Creek Drainage Basin, Idaho

The U.S. Survey and Idaho State University, in cooperation with the U.S. Department of Energy, are conducting studies to describe the chemical character of ground water that moves as underflow from drainage basins into the eastern Snake River Plain aquifer (ESRPA) system at and near the Idaho National Engineering and Environmental Laboratory (INEEL) and the effects of these recharge waters on the geochemistry of the ESRPA system. Each of these recharge waters has a hydrochemical character related to geochemical processes, especially water-rock interactions, that occur during migration to the ESRPA. Results of these studies will benefit ongoing and planned geochemical modeling of the ESRPA at the INEEL by providing model input on the hydrochemical character of water from each drainage basin. During 2000, water samples were collected from five wells and one surface-water site in the Birch Creek drainage basin and analyzed for selected inorganic constituents, nutrients, dissolved organic carbon, tritium, measurements of gross alpha and beta radioactivity, and stable isotopes. Four duplicate samples also were collected for quality assurance. Results, which include analyses of samples previously collected from four other sites, in the basin, show that most water from the Birch Creek drainage basin has a calcium-magnesium bicarbonate character. The Birch Creek Valley can be divided roughly into three hydrologic areas. In the northern part, ground water is forced to the surface by a basalt barrier and the sampling sites were either surface water or shallow wells. Water chemistry in this area was characterized by simple evaporation models, simple calcite-carbon dioxide models, or complex models involving carbonate and silicate minerals. The central part of the valley is filled by sedimentary material and the sampling sites were wells that are deeper than those in the northern part. Water chemistry in this area was characterized by simple calcite-dolomite-carbon dioxide models. In the southern part, ground water enters the ESRPA. In this area, the sampling sites were wells with depths and water levels much deeper than those in the northern and central parts of the valley. The calcium and carbon water chemistry in this area was characterized by a simple calcite-carbon dioxide model, but complex calcite-silicate models more accurately accounted for mass transfer in these areas. Throughout the geochemical system, calcite precipitated if it was an active phase in the models. Carbon dioxide either precipitated (outgassed) or dissolved depending on the partial pressure of carbon dioxide in water from the modeled sites. Dolomite was an active phase only in models from the central part of the system. Generally the entire geochemical system could be modeled with either evaporative models, carbonate models, or carbonate-silicate models. In both of the latter types of models, a significant amount of calcite precipitated relative to the mass transfer to and from the other active phases. The amount of calcite precipitated in the more complex models was consistent with the amount of calcite precipitated in the simpler models. This consistency suggests that, although the simpler models can predict calcium and carbon concentrations in Birch Creek Valley ground and surface water, silicate-mineral-based models are required to account for the other constituents. The amount of mass transfer to and from the silicate mineral phases was generally small compared with that in the carbonate phases. It appears that the water chemistry of well USGS 126B represents the chemistry of water recharging the ESRPA by means of underflow from the Birch Creek Valley.

Idaho↗

USGS2015

Shift in Global Tantalum Mine Production, 2000–2014

Introduction Tantalum has a unique set of properties that make it useful in a number of diverse applications. The ability of the metal to store and release electrical energy makes it ideally suited for use in certain types of capacitors that are widely used in modern electronics. Approximately 60 percent of global tantalum consumption is in the electronics industry. The ductility and corrosion resistance of the metal lends itself to application in the chemical processing industry, and its high melting point and high strength retention at elevated temperatures make it an important component of super alloys used in aircraft engines. As a major industrialized nation, the United States is a leading consumer of tantalum and tantalum-containing products. Domestic deposits typically are of low grade, and no tantalum has been recovered from mining activities in the United States since 1959. Consequently, the United States is nearly completely reliant on imports to meet its domestic consumption of tantalum for economic and national security needs. The recovery of tantalum from mine production is economically viable in only a few countries. Although developed countries dominated tantalum mine production in the early 2000s, production today is dominated by countries in the Great Lakes Region of Africa. There is concern that the sales of minerals, including columbite-tantalite or “coltan,” a mineral from which tantalum is derived, have helped finance rebel groups accused of violating human rights as part of the continuing armed conflict in the Democratic Republic of the Congo (DRC) and neighboring countries. These accusations have prompted the passage of legislation in the United States to curb the procurement of these mineral commodities, referred to as “conflict minerals,” from the DRC. Specifically, section 1502 of the 2010 Dodd-Frank Wall Street Reform and Consumer Protection Act (Public Law 111–203, 124 Stat. 2213–2218) requires companies that source tantalum, tin, tungsten, and gold (3TG) to perform due diligence on their supply chains to determine if the materials they use originate from the DRC or adjoining countries (defined as sharing a border with the DRC). The DRC, Rwanda, and surrounding countries are not globally significant sources of tin, tungsten, or gold, accounting for only about 2 percent of the mined world supply for each of these elements. The region has, however, evolved to become the world’s largest producer of mined tantalum. A further complication of the production of tantalum stems from the opacity of the tantalum market. Unlike most base and precious metals, tantalum concentrates are not publicly traded through commodities exchanges but are bought and sold through networks of dealers and on contract between producers and consumers, some of whom may not provide accurate statistical data concerning the amounts, origins, and destination of the concentrates. Some price data can be found in trade journals or in other publications; however, there are no recognized official set exchange prices for either concentrate or tantalum metal. Because price is determined by negotiation between buyer and seller, published prices for concentrate are probably not representative of global prices paid for concentrate. The development of a mine-to-market supply-chain analysis is complicated and difficult because many of the industry participants that produce, trade, and consume tantalum do not publish statistical information, contracts are long term between miners and buyers, and much of the industry is vertically integrated. As a result of these and other considerations, tantalum is considered by many to be a “critical” commodity. This fact sheet identifies and addresses the major geographic shifts in the source of mine production of tantalum which have occurred over the past 15 years, some of the factors that drove this shift, and some of the related consequences. One of the activities of the U.S. Geological Survey National Minerals Information Center (USGS-NMIC) is to analyze global supply chains and characterize major components of mineral and material flows from ore extraction through processing to first tier products. These analyses support the core mission of the USGS-NMIC as the Federal entity responsible for the collection, analysis, and dissemination of objective, unbiased, factual information on minerals essential to the U.S. economy and national security.

Fact Sheet↗