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Rare earth mineral potential in the southeastern U.S. Coastal Plain from integrated geophysical, geochemical, and geological approaches

We combined geophysical, geochemical, mineralogical, and geological data to evaluate the regional presence of rare earth element (REE)−bearing minerals in heavy mineral sand deposits of the southeastern U.S. Coastal Plain. We also analyzed regional differences in these data to determine probable sedimentary provenance. Analyses of heavy mineral separates covering the region show strong correlations between thorium, monazite, and xenotime, suggesting that radiometric equivalent thorium (eTh) can be used as a geophysical proxy for those REE-bearing minerals. Airborne radiometric data collected during the National Uranium Resource Evaluation (NURE) program cover the southeastern United States with line spacing varying from ∼2 to 10 km. These data show eTh highs over Cretaceous and Tertiary Coastal Plain sediments from the Cape Fear arch in North Carolina to eastern Alabama; these highs decrease with distance from the Piedmont. Quaternary sediments along the modern coasts show weaker eTh anomalies, except near coast-parallel ridges from South Carolina to northern Florida. Prominent eTh anomalies are also observed over large riverbeds and their floodplains, even north of the Cape Fear arch where surrounding areas are relatively low. These variations were verified using ground geophysical measurements and sample analyses, indicating that radiometric methods are a useful exploration tool at varying scales. Further analyses of heavy mineral separates showed regional differences, not only in concentrations of monazite, but also of rutile and staurolite, and in magnetic susceptibility. The combined properties suggest the presence of subregions where heavy mineral sediments are primarily sourced from high-grade metamorphic, low-grade metamorphic, or igneous terrains, or where they represent a mixing of these sources. Comparisons between interpreted sources of heavy mineral sands near the Fall Line and igneous and metamorphic Piedmont and Blue Ridge units showed a strong correspondence with rocks closest to the Fall Line and poor correspondence with rocks farther inland. This strongly suggests that the primary source of those heavy minerals, especially monazite, is the rocks that formed the rocky coast that was present during opening of the Atlantic Ocean, which in turn indicates the importance of coastal processes in forming heavy mineral sand concentrations. Furthermore, narrow radiometric eTh and K anomalies are associated with major rivers, indicating limited spatial influence of fluvial processes. Later coastal plain sediment deposition appears to have involved reworking of sediments, providing an “inheritance” of the rocky coast composition that persists for some distance from the Fall Line. However, this inheritance is reduced with distance, and sediments within ∼100 km of the coast in Georgia and Florida exhibit properties indicative of mixing from multiple sources.

GSA Bulletin↗

Geophysical interpretation of U, Th, and rare earth element mineralization of the Bokan Mountain peralkaline granite complex, Prince of Wales Island, southeast Alaska

A prospectivity map for rare earth element (REE) mineralization at the Bokan Mountain peralkaline granite complex, Prince of Wales Island, southeastern Alaska, was calculated from high-resolution airborne gamma-ray data. The map displays areas with similar radioelement concentrations as those over the Dotson REE-vein-dike system, which is characterized by moderately high %K, eU, and eTh (%K, percent potassium; eU, equivalent parts per million uranium; and eTh, equivalent parts per million thorium). Gamma-ray concentrations of rocks that share a similar range as those over the Dotson zone are inferred to locate high concentrations of REE-bearing minerals. An approximately 1300-m-long prospective tract corresponds to shallowly exposed locations of the Dotson zone. Prospective areas of REE mineralization also occur in continuous swaths along the outer edge of the pluton, over known but undeveloped REE occurrences, and within discrete regions in the older Paleozoic country rocks. Detailed mineralogical examinations of samples from the Dotson zone provide a means to understand the possible causes of the airborne Th and U anomalies and their relation to REE minerals. Thorium is sited primarily in thorite. Uranium also occurs in thorite and in a complex suite of ± Ti ± Nb ± Y oxide minerals, which include fergusonite, polycrase, and aeschynite. These oxides, along with Y-silicates, are the chief heavy REE (HREE)-bearing minerals. Hence, the eU anomalies, in particular, may indicate other occurrences of similar HREE-enrichment. Uranium and Th chemistry along the Dotson zone showed elevated U and total REEs east of the Camp Creek fault, which suggested the potential for increased HREEs based on their association with U-oxide minerals. A uranium prospectivity map, based on signatures present over the Ross-Adams mine area, was characterized by extremely high radioelement values. Known uranium deposits were identified in the U-prospectivity map, but the largest tract occurs over a radioelement-rich granite phase within the pluton that is likely not related to mineralization. Neither mineralization type displays a well-defined airborne magnetic signature.

Alaska↗

Pathology and mineralogy demonstrate respirable crystalline silica is a major cause of severe pneumoconiosis in US coal miners

Rationale: The reasons for resurgent coal workers’ pneumoconiosis and its most severe forms, rapidly progressive pneumoconiosis and progressive massive fibrosis (PMF), in the United States (US) are not yet fully understood. Objective: To compare the pathologic and mineralogic features of contemporary coal miners suffering severe pneumoconiosis to their historical counterparts. Methods: Lung pathology specimens from 85 coal miners with PMF were included for evaluation and analysis. We compared the proportion of cases with pathologic and mineralogic findings in miners born between 1910 and 1930 (historical) to those born in or after 1930 (contemporary). Results: We found a significantly higher proportion of silica-type PMF (57% vs. 18%, p<0.001) among contemporary miners compared to their historical counterparts. Mineral dust alveolar proteinosis (MDAP) was also more common in contemporary miners compared to their historical counterparts (70% vs. 37%, p<0.01). In situ mineralogic analysis showed the percentage (26.1% vs. 17.8%, p<0.01) and concentration (47.3 x 108 vs. 25.8 X 108 particles/cm3, p=0.036) of silica particles was significantly greater in specimens from contemporary miners compared to their historical counterparts. The concentration of silica particles was significantly greater when silica-type PMF, MDAP, silicotic nodules, or immature silicotic nodules were present (p<0.05). Conclusions: Exposure to respirable crystalline silica appears causal in the unexpected surge in severe disease in contemporary miners. Our findings underscore the importance of controlling workplace silica exposure in order to prevent the disabling and untreatable adverse health effects afflicting US coal miners. Primary Source of Funding: Alpha Foundation for the Improvement of Mine Safety and Health, Inc.

Annals of the American Thoracic Society↗

Concealed basalt-matrix diatremes with Cu-Au-Ag-(Mo)-mineralized xenoliths, Santa Cruz Porphyry Cu-(Mo) System, Pinal County, Arizona

The Santa Cruz porphyry Cu-(Mo) system near Casa Grande, Arizona, includes the Sacaton mine deposits and at least five other concealed, mineralized fault blocks with an estimated minimum resource of 1.5 Gt @ 0.6% Cu. The Late Cretaceous-Paleocene system has been dismembered and rotated by Tertiary extension, partially eroded, and covered by Tertiary-Quaternary basin-fill deposits. The mine and mineralized fault blocks, which form an 11 km (~7 miles) by 1.6 km (~1 mile) NE-SW–trending alignment, represent either pieces of one large deposit, several deposits, or pieces of several deposits. The southwestern part of the known system is penetrated by three or more diatremes that consist of heterolithic breccia pipes with basalt and clastic matrices, and subannular tuff ring and maar-fill sedimentary deposits associated with vents. The tephra and maar-fill deposits, which are covered by ~485 to 910 m (~1,600–3,000 ft) of basin fill, lie on a mid-Tertiary erosion surface of Middle Proterozoic granite and Late Cretaceous porphyry, which compose most xenoliths in pipes and are the host rocks of the system. Some igneous xenoliths in the pipes contain bornite-chalcopyrite-covellite assemblages with hypogene grades >1 wt % Cu, 0.01 ounces per ton (oz/t) Au, 0.5 oz/t Ag, and small amounts of Mo (<0.01 wt %). These xenoliths were derived from mineralized rocks that have not been encountered in drill holes, and attest to additional, possibly higher-grade deposits within or subjacent to the known system. The geometry, stratigraphy, and temporal relationships of pipes and tephras, interpreted from drill hole spacing and intercepts, multigenerational breccias and matrices, reequilibrated and partially decomposed sulfide-oxide mineral assemblages, melted xenoliths, and breccia matrix compositions show that the diatremes formed in repeated stages. Initial pulses of basalt magma fractured granite, porphyry, and other crustal rocks during intrusion, transported multi-sized fragments of these rocks upward, and partially melted small fragments. Rapid decompression of magma induced catastrophic devolatilization that ruptured overlying rocks to the surface, and generated fragment-volatile suspensions that abraded conduits into near-vertical cylindrical structures. Fragments entrained in suspensions were milled and sorted, and ejected as basal surge, pyroclastic deposits, and airfall tephra that built tuff rings around vents and filled vent depressions. Comminuted m- to mm-sized fragments of wall rocks in magma and suspensions that remained in conduits solidified as heterolithic breccias. Subsequent pulses of basalt magma ascended through the same conduits, brecciated older heterolithic breccias, devolatilized, and quenched, leaving two or more generations of nested and mingled heterolithic breccias and internal zones of fluidized fragments. Tephra and maar-fill deposits from later eruptions are composed of more hydrous and oxidized minerals than earlier tephras, reflecting a higher proportion of water in transport fluid which, based on fluid inclusion populations in mineralized xenoliths, was saline water and CO 2 . The large vertical extent (~600 m; ~2,000 ft) of basalt matrix in pipes, near-paleosurface matrix vesiculation, and plastically deformed basalt lapilli indicates that diatreme eruptions were predominantly phreatic. Diatreme xenoliths represent crustal stratigraphy and, as in the Santa Cruz system, provide evidence of concealed mineral resources that can guide exploration drilling through cover. Vectors to the source of bornite-dominant xenoliths containing >1% Cu and significant Au and Ag could be determined by refinement of breccia pipe geometries, by reassembly of mineralized fault blocks using modal, chemical, and temporal characteristics of hydrothermal mineral assemblages and fluid inclusions, and by paleodrainage analysis.

Arizona↗

Mineralization of breccia pipes in northern Arizona

The Paleozoic sedimentary rocks on the Colorado Plateau of northern Arizona are host to hundreds ofbreccia pipes. The uranium and copper deposits in these breccia pipes transgress formation boundaries from the Mississippian Redwall Limestone to the Triassic Chinle Formation. They are not classic breccia pipes in that there is no volcanic rock associated with them in time or space. They are the result of solution-collapse within the Redwall Limestone and stoping of the overlying strata. The karst development in the Redwall Limestone began in the Mississippian and apparently either continued to the Triassic or was at least once again active during that time. The mineralization apparently occurred shortly thereafter, sometime during the Mesozoic. Mining activity in breccia pipes of the Grand Canyon region began during the nineteenth century and continues today with the operation of the Hack I, II, and III mines, although the exploited commodity has changed from Cu to U. Although small in size, these pipes contain samples with up to 55 percent U 3 O 8 and can yield ore averaging between 0.30 and 0.60 percent U 3 O 8 .Mineralization at the surface commonly occurs within nodules and concretions associated with pyrite and goethite and along fractures, while the primary ore of the unoxidized zones is commonly within a comminuted sandstone matrix surrounding breccia fragments of overlying formations. The ore mineral is uraninite, although associated with it are sphalerite, galena, chalcopyrite, tennantite, millerite, siegenite, and/molybdenite. Some of the surface nodules are encrusted with malachite and are exceptionally enriched in Ag. Pyrite is abundant, and the organic carbon content of some rocks is high enough to suggest that it, along with the pyrite, may be a reductant for uranium. In contrast, it is possible, if uranium were transported as a bicarbonate or carbonate complex, that only a conduit of brecciated rock was necessary to release CO 2 , thus disrupting the equilibrium and allowing uraninite to precipitate. An extensive suite of elements is significantly enriched in the mineralized rock: Ag, As, Ba, Cd, Co, Cr, Cs, Cu, Hg, Mo, Ni, Pb, Sb, Se, Sr, U, V, Zn, and the rare earth elements. Of these, Cu, Pb, Zn, Ag, and particularly As appear to be the best geochemical indicators of mineralized pipes. At present the origin of the mineralizing fluids is not known. The lack of extensive silification within the breccia, along with the 80 degrees to 173 degrees C fluid inclusion-filling temperatures on sphalerite, dolomite, quartz, and calcite, suggests relatively low-temperature mineralizing fluids, although heated in excess of what would be expected from the normal geothermal gradient on the Colorado Plateau. With the exception of the U-mineralized rock, the mineral assemblage and geochemistry is similar to Mississippi Valley-type deposits.

Economic Geology↗

Lead isotope compositions of Late Cretaceous and early Tertiary igneous rocks and sulfide minerals in Arizona: Implications for the sources of plutons and metals in porphyry copper deposits

Porphyry copper deposits in Arizona are genetically associated with Late Cretaceous and early Tertiary igneous complexes that consist of older intermediate volcanic rocks and younger intermediate to felsic intrusions. The igneous complexes and their associated porphyry copper deposits were emplaced into an Early Proterozoic basement characterized by different rocks, geologic histories, and isotopic compositions. Lead isotope compositions of the Proterozoic basement rocks define, from northwest to southeast, the Mojave, central Arizona, and southeastern Arizona provinces. Porphyry copper deposits are present in each Pb isotope province. Lead isotope compositions of Late Cretaceous and early Tertiary plutons, together with those of sulfide minerals in porphyry copper deposits and of Proterozoic country rocks, place important constraints on genesis of the magmatic suites and the porphyry copper deposits themselves. The range of age-corrected Pb isotope compositions of plutons in 12 Late Cretaceous and early Tertiary igneous complexes is 206 Pb/ 204 Pb = 17.34 to 22.66, 207 Pb/ 204 Pb = 15.43 to 15.96, and 208 Pb/ 204 Pb = 37.19 to 40.33. These Pb isotope compositions and calculated model Th/U are similar to those of the Proterozoic rocks in which the plutons were emplaced, thereby indicating that Pb in the younger rocks and ore deposits was inherited from the basement rocks and their sources. No Pb isotope differences distinguish Late Cretaceous and early Tertiary igneous complexes that contain large economic porphyry copper deposits from less rich or smaller deposits that have not been considered economic for mining. Lead isotope compositions of Late Cretaceous and early Tertiary plutons and sulfide minerals from 30 metallic mineral districts, furthermore, require that the southeastern Arizona Pb province be divided into two subprovinces. The northern subprovince has generally lower 206 Pb/ 204 Pb and higher model Th/U, and the southern subprovince has higher 206 Pb/ 204 Pb and lower model Th/U. These Pb isotope differences are inferred to result from differences in their respective post-1.7 Ga magmatic histories. Throughout Arizona, Pb isotope compositions of Late Cretaceous and early Tertiary plutons and associated sulfide minerals are distinct from those of Jurassic plutons and also middle Tertiary igneous rocks and sulfide minerals. These differences most likely reflect changes in tectonic setting and magmatic sources. Within Late Cretaceous and early Tertiary igneous complexes that host economic porphyry copper deposits, there is commonly a decrease in Pb isotope composition from older to younger plutons. This decrease in Pb isotope values with time suggests an increasing involvement of crust with lower U/Pb than average crust in the source(s) of Late Cretaceous and early Tertiary magmas. Lead isotope compositions of the youngest porphyries in the igneous complexes are similar to those in most sulfide minerals within the associated porphyry copper deposit. This Pb isotope similarity argues for a genetic link between them. However, not all Pb in the sulfide minerals in porphyry copper deposits is magmatically derived. Some sulfide minerals, particularly those that are late stage, or distal to the main orebody, or in Proterozoic or Paleozoic rocks, have elevated Pb isotope compositions displaced toward the gross average Pb isotope composition of the local country rocks. The more radiogenic isotopic compositions argue for a contribution of Pb from those rocks at the site of ore deposition. Combining the Pb isotope data with available geochemical, isotopic, and petrologic data suggests derivation of the young porphyry copper-related plutons, most of their Pb, and other metals from a hybridized lower continental crustal source. Because of the likely involvement of subduction-related mantle-derived basaltic magma in the hybridized lower crustal source, an indiscernible mantle contribution is probable in the porphyry magmas. Clearly, in addition, Pb was contributed from the local country rocks. This is most evident in sulfide minerals in veins that are late stage, hosted in Proterozoic gneiss, and/or peripheral to the porphyry copper deposit.

Economic Geology↗

Effect of sulfate and carbonate minerals on particle-size distributions in arid soils

Arid soils pose unique problems during measurement and interpretation of particle-size distributions (PSDs) because they often contain high concentrations of water-soluble salts. This study investigates the effects of sulfate and carbonate minerals on grain-size analysis by comparing analyses in water, in which the minerals dissolve, and isopropanol (IPA), in which they do not. The presence of gypsum, in particular, substantially affects particle-size analysis once the concentration of gypsum in the sample exceeds the mineral’s solubility threshold. For smaller concentrations particle-size results are unaffected. This is because at concentrations above the solubility threshold fine particles cement together or bind to coarser particles or aggregates already present in the sample, or soluble mineral coatings enlarge grains. Formation of discrete crystallites exacerbates the problem. When soluble minerals are dissolved the original, insoluble grains will become partly or entirely liberated. Thus, removing soluble minerals will result in an increase in measured fine particles. Distortion of particle-size analysis is larger for sulfate minerals than for carbonate minerals because of the much higher solubility in water of the former. When possible, arid soils should be analyzed using a liquid in which the mineral grains do not dissolve, such as IPA, because the results will more accurately reflect the PSD under most arid soil field conditions. This is especially important when interpreting soil and environmental processes affected by particle size.

Soil Science Society of America Journal↗

Environmental characteristics of clays and clay mineral deposits

Clays and clay minerals have been mined since the Stone Age; today they are among the most important minerals used by manufacturing and environmental industries. The U.S. Geological Survey (USGS) supports studies of the properties of clays, the mechanisms of clay formation, and the behavior of clays during weathering. These studies can tell us how and where these minerals form and provide industry and land-planning agencies with the information necessary to decide how and where clay and clay mineral deposits (fig. 1) can be developed safely with minimal effects on the environment. The term "clay" is applied both to materials having a particle size of less than 2 micrometers (25,400 micrometers = 1 inch) and to the family of minerals that has similar chemical compositions and common crystal structural characteristics (Velde, 1995) described in the next section. Clay minerals have a wide range of particle sizes from 10's of angstroms to millimeters. (An angstrom ( ) is a unit of measure at the scale of atoms.) Thus, clays may be composed of mixtures of finer grained clay minerals and clay-sized crystals of other minerals such as quartz, carbonate, and metal oxides. Clays and clay minerals are found mainly on or near the surface of the Earth.

Information Handout↗

Rare earth element mineral deposits in the United States

Because of their unique special chemical properties, many of the metals in the group of rare earth elements (REEs) have essential applications in 21st century technologies. Examples of products that use REEs are cell phones, computers, fluorescent and light-emitting-diode lights, flat-screen television and computer monitors, and in high-strength magnets used by clean energy technologies such as the generators of wind turbines and batteries of hybrid and electric vehicles. REEs are used in many defense applications, such as in components of jet engines, missile guidance systems, antimissile defense systems, satellites, and communication systems. The rare earth elements have become vital to manufacturing numerous high-tech products, which has been accompanied by a large increase in their demand. At the same time, there has been concern by the United States and many other Nations about the near-monopoly of mining, processing, and supply of REEs from one Nation, China. Between 2011 and 2017, China produced approximately 84 percent of the world’s REEs, and during this time the United States only produced REEs between 2012 and 2015. The U.S. production came entirely from the Mountain Pass mine in California, providing only about 4 percent of the world REE supply. Because REEs are essential for technological applications and are primarily supplied by one Nation, there has been an increased concern in identifying new sources of REEs, including economic REE deposits. In response to these concerns, since 2009, the U.S. Geological Survey (USGS) has conducted numerous studies focused on the distribution, geology, and potential resources for the REE-bearing mineral deposits in the United States. The basic characteristics of mineral deposit types that host REE enrichments in the United Sates are summarized in this report, with selected examples. Several types of REE-enriched mineral deposits are reviewed, including deposits in carbonatites, alkaline igneous rocks, sedimentary phosphate-rich rocks (phosphorite), regions containing REE-rich veins, iron oxide deposits containing REE-bearing apatite, monazite-xenotime-bearing placer deposits (heavy-mineral sands), and ion-adsorption clay deposits (REE in granite-derived regolith). A better understanding of these mineral deposits will assist in identifying domestic resources to help alleviate the dependence on imported REEs. The economic development of REE mineral deposits is affected by many factors beyond mining, such as commodity prices and mineral processing costs. Most of the REEs are hosted by minerals that have complex chemical formulas; this presents more challenges to process and extract the REEs. Continued advancements and refinements in mineral processing techniques may allow REE deposits with complex mineralogy to be economically developed in the future.

Circular↗

Petroleum and mineral resources of Antarctica

No known petroleum or mineral resources occur in Antarctica. The data on these subjects have been collected, mainly since the IGY (International Geophysical Year), 1957-58, as a part of other research carried out by geologists and geophysicists from a number of countries. Specific resource-related studies have not been made. Wright and Williams (1974) summarized what was known of Antarctic mineral resources a decade ago. The U.S. Geological Survey has been actively pursuing various investigations in Antarctica since 194 7. In the course of this work and that of our colleagues elsewhere in the United States and in other countries, much information relevant to petroleum and mineral resources has been obtained. Since 1976, modern state-of-the-art multichannel seismic reflection and aeromagnetic surveys by several countries over the continental margin of Antarctica have indicated thick sedimentary basins. However, no offshore drilling beneath the continental shelf has taken place since the DSDP (Deep Sea Drilling Project) holes in the Ross Sea in 1973. Geologic field investigations begun at the turn of the twentieth century have been intensified in the past two decades; most rock outcrops have been visited and samples collected. Technology to exploit resources, particularly in the Arctic, has been developing at a rapid rate, and much of it could be applied to Antarctica. As a result of the petroleum price increases of the past decade, the attention of a number of countries has turned to Antarctica, but under the policy of "voluntary restraint" adopted by the Antarctic Treaty nations, no active petroleum or mineral exploration is taking place. The Antarctic treaty countries are in the process of negotiating an Antarctic mineral resources regime that is anticipated to be completed within the next several years. Therefore it seemed timely to us to readdress the question of petroleum and mineral resources. These reports review and summarize the available information. The first report summarizes the information relevant to petroleum resources. Although uneconomic at present, petroleum is generally considered more likely to be exploited (if supergiant fields were ever found) in the next few decades than hard minerals. The second report reviews the reported occurrences of minerals in Antarctica and discusses their significance. The final report discusses the Dufek layered mafic intrusion, second only to the Bushveld Complex in size in the world; the Dufek intrusion might be considered as a potential target for mineral exploration.

Circular↗

The Ebola virus disease outbreak and the mineral sectors of Guinea, Liberia, and Sierra Leone

The mineral sector plays a key role in the economies of Guinea, Liberia, and Sierra Leone. The onset of the Ebola virus disease (EVD) outbreak in early 2014, together with changes in mineral market conditions, raised questions regarding the status of mining operations and of mineral development and exploration projects in all three countries. Mineral projects were the underpinnings of World Bank short-term forecasts of increases in gross domestic product (GDP) for all three countries and were expected to be the basis of future economic growth. The significant delay or cancellation of these projects could result in a major economic setback for all three countries. In response to the uncertainty surrounding the status of mineral projects in Guinea, Liberia, and Sierra Leone, the National Minerals Information Center compiled information on the distribution of mines, mineral facilities, and mineral projects under development in the three countries. This fact sheet provides information on the role that the mineral sector plays in their respective economies, on the operating status of mining projects through yearend 2014, and on the coordinated actions by mining companies to support governments and international relief organizations in their efforts to contain the EVD outbreak.

Fact Sheet↗

International geoscience collaboration to support critical mineral discovery

The importance of critical minerals and the need to expand and diversify critical mineral supply chains has been endorsed by the Federal governments of Australia, Canada, and the United States. The geoscience organizations of Geoscience Australia, the Geological Survey of Canada and the U.S. Geological Survey have created the Critical Minerals Mapping Initiative to build a diversified critical minerals industry in Australia, Canada, and the United States by developing a better understanding of known critical mineral resources, determining geologic controls on critical mineral distribution for deposits currently producing byproducts, identifying new sources of supply through critical mineral potential mapping and quantitative mineral assessments, and promoting critical mineral discovery in all three countries.

Fact Sheet↗

National map of focus areas for potential critical mineral resources in the United States

Introduction The U.S. Geological Survey (USGS) launched the Earth Mapping Resources Initiative (Earth MRI) to modernize the surface and subsurface geologic mapping of the United States, with a focus on identifying areas that may have the potential to contain critical mineral resources. EarthMRI can inform strategies to ensure secure and reliable domestic critical mineral supplies for the United States as mandated by Executive Order 13817 and the Infrastructure and Jobs Act of 2021 (Public Law 117–58, 135 Stat. 529). Earth MRI is a collaborative effort between the USGS and the State geological surveys as represented by the Association of American State Geologists to identify, prioritize, and acquire new geoscience data for geographic areas, or focus areas, across the Nation that have potential to host critical mineral resources. Mapping of focus areas was based on a framework of mineral systems and their associated mineral deposit types that could possibly host critical minerals. Using readily available geologic, geophysical, geochemical, and mineral deposit data, teams of USGS scientists worked with representatives of State geological surveys in a series of workshops to outline focus areas that contain evidence of key features for one or more mineral systems. These areas can be used to guide future efforts to collect new geologic, geophysical, geochemical, and topographic data that focus on critical minerals through Earth MRI.

Fact Sheet↗

Critical minerals in mine waste

Introduction Critical minerals are commodities with vulnerable supply chains that play a vital role in supporting the United States’ economy, national defense and security, emerging technologies, and energy independence. The prosperity of our Nation depends on generating a resilient supply of domestic critical minerals; mine waste may be an untapped source of these commodities. Mine waste from centuries of legacy mining persist on the landscape and may contain critical minerals and other valuable commodities previously deemed uneconomic to recover. At modern mines, the financial viability of recovering byproduct critical minerals, which are not the primary target, may be marginal and can ultimately destine them to mine waste. Further, mine waste can be a liability for the mining company or, at legacy mines, the taxpayer because of its effect on the landscape. The U.S. Geological Survey (USGS) has several initiatives to evaluate critical mineral resources in various types of waste. This factsheet highlights studies of mine waste carried out by USGS scientists at the Geology, Energy & Minerals Science Center in collaboration with other science centers funded through the USGS Mineral Resources Program. Recovery of critical minerals from mine waste can aid in remediation efforts and increase domestic supply of vital mineral resources.

Fact Sheet↗

Maps showing mineralogical data for nonmagnetic heavy-mineral concentrates in the Talkeetna Quadrangle, Alaska

Reconnaissance geochemical and mineralogical sampling was done in the Talkeetna Quadrangle during 1975 and 1976 as part of the Alaska Mineral Resource Assessment Program (AMRAP). These maps show the distribution of gold, scheelite, chalcopyrite, arsenopyrite, galena, fluorite, cinnabar, and malachite in the nonmagnetic fraction of heavy-mineral concentrates. Heavy-mineral concentrate samples were collected at 812 sites from active stream channels. The heavy-mineral concentrates were obtained by panning stream sediment in the field to remove most of the light minerals. The panned samples were then sieved through a 20-mesh (0.8 mm) sieve in the laboratory, and the minus-20-mesh fraction was further separated with bromoform (specific gravity, 2.86) to remove any remaining light-mineral grains. Magnetite and other strongly magnetic heavy minerals were removed from the heavy-mineral fraction by use of a hand magnet. The remaining sample was passed through a Frantz Isodynamic Separator and a nonmagnetic fraction was examined for its mineralogical content with the aid of a binocular microscope and an x-ray diffractometer. The nonmagnetic concentrates primarily contain phyllite fragments, muscovite, sphene, zircon, apatite, tourmaline, rutile, and anatase. Most ore and ore-related minerals also occur in this fraction.

Alaska↗

Mineralogical map showing the distribution and abundance of gold, scheelite, chalcopyrite, arsenopyrite, minium, and sapphire corundum in heavy-mineral concentrates in the Seward and Blying Sound quadrangles, Alaska

Reconnaissance geochemical and mineralogical sampling was done in the Seward and Blying Sound quadrangles during 1975 and 1976 as part of the Alaska Mineral Resources Assessment Program (AMRAP). These maps show the distribution and abundance of gold, scheelite, chalcopyrite, arsenopyrite, minium and sapphire corundum in heavy-mineral concentrates. Heavy-mineral concentrate samples were collected at 525 sites from active channels and, locally, from the interface of streambeds with intermediate- to low-tide beaches. The heavy-mineral concentrates were obtained by panning stream sediments in the field to remove most of the light minerals. The panned samples were sieved though a 20-mesh (0.8 mm) screen in the laboratory, and the minus-20 mesh fraction was further separated with bromoform (specific gravity: 2.86) to remove any remaining light-mineral grains. Magnetite and other strongly magnetic heavy minerals were removed from the heavy-mineral fraction by using a hand magnet. The remaining sample was passed through a Frantz Isodynamic Separator 1 and a nonmagnetic fraction was obtained at a setting of 0.6 amperes. A split of this nonmagnetic fraction was examined for its mineralogic content using a binocular microscope and X-ray diffraction. The nonmagnetic concentrates primarily contain muscovite, sphene, zircon, apatite, rutile, and anatase. Small amounts of other minerals such as gold, scheelite, minium, sapphire corundum, and most sulfides will also be found in this fraction. 1 The use of trade names is for descriptive purposes only and does not constitute endorsement of those products by the U.S. Geological Survey.

Alaska↗

User's Guide to Handlens - A Computer Program that Calculates the Chemistry of Minerals in Mixtures

HandLens is a computer program, written in Excel macro language, that calculates the chemistry of minerals in mineral mixtures (for example, in rocks, soils and sediments) for related samples from inputs of quantitative mineralogy and chemistry. For best results, the related samples should contain minerals having the same chemical compositions; that is, the samples should differ only in the proportions of minerals present. This manual describes how to use the program, discusses the theory behind its operation, and presents test results of the program's accuracy. Required input for HandLens includes quantitative mineralogical data, obtained, for example, by RockJock analysis of X-ray diffraction (XRD) patterns, and quantitative chemical data, obtained, for example, by X-ray florescence (XRF) analysis of the same samples. Other quantitative data, such as sample depth, temperature, surface area, also can be entered. The minerals present in the samples are selected from a list, and the program is started. The results of the calculation include: (1) a table of linear coefficients of determination (r2's) which relate pairs of input data (for example, Si versus quartz weight percents); (2) a utility for plotting all input data, either as pairs of variables, or as sums of up to eight variables; (3) a table that presents the calculated chemical formulae for minerals in the samples; (4) a table that lists the calculated concentrations of major, minor, and trace elements in the various minerals; and (5) a table that presents chemical formulae for the minerals that have been corrected for possible systematic errors in the mineralogical and/or chemical analyses. In addition, the program contains a method for testing the assumption of constant chemistry of the minerals within a sample set.

Open-File Report↗

Lineament analysis of mineral areas of interest in Afghanistan

During a preliminary mineral resource assessment of Afghanistan (Peters and others, 2007), 24 mineralized areas of interest (AOIs) were highlighted as the focus for future economic development throughout various parts of the country. In addition to located mineral resources of value, development of a viable mining industry in Afghanistan will require the location of suitable groundwater resources for drinking, processing of mineral ores for use or for export, and for agriculture and food production in areas surrounding and supporting future mining enterprises. This report and accompanying GIS datasets describe the results of both automated and manual mapping of lineaments throughout the 24 mineral occurrence AOIs described in detail by Peters and others (2007; 2011). For this study, we define lineaments as "mappable linear or curvilinear features of a surface whose parts align in a straight or slightly curving relationship that may be the expression of a fault or other linear zones of weakness" as derived from remote sensing sources such as optical imagery, radar imagery or digital elevation models (DEMs) (Sabins, 2007). Water wells in bedrock aquifers are generally more productive where boreholes intersect fractures or fracture zones. Lineament identification and analysis have long been used as a reconnaissance tool to identify such favorable conditions for groundwater resources in carbonate bedrock environments (Lattman and Parizek, 1964; Siddiqui and Parizek, 1971). More recently, lineament analysis has been used to identify areas of greater well yields in other bedrock settings, such as crystalline bedrock (Mabee and other, 1994; Moore and others, 2002). Lineaments provide an indication of bedrock areas that warrant further investigation for optimal water well placement. They may also indicate areas of preferential flow and storage of groundwater, and, thus, areas with a greater density of lineaments may indicate greater secondary porosity. Lineaments may indicate structurally trending mineralized areas (for example, Mars and Rowan, 2007), or locations of near-surface water resources, especially when surface vegetation growth coincides with lineaments. The purpose of this report and accompanying GIS data is to provide lineament maps that give one indication of areas that warrant further investigation for optimal bedrock water-well placement within 24 target areas for mineral resources (Peters and others, 2011). These data may also support the identification of faults related to modern seismic hazards (for example, Wheeler and others, 2005; Ruleman and others, 2007), as well as support studies attempting to understand the relationship between tectonic and structural controls on hydrothermal fluid flow, subsequent mineralization, and water-quality issues near mined and unmined mineral deposits (for example, Eppinger and others, 2007).

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