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At least 973 records · Page 54Linked to original sources
USGS2026

Revisiting the utility of regional-scale, high-quality geophysical data in mineral exploration - A case study featuring the Mammoth Magnetic Anomaly, Pinal County, Arizona

Regional aeromagnetic surveys passively measure the total magnetic intensity (TMI) and are a foundational tool used in mineral exploration (Airo, 2015). With the increased global demand and the number of critical mineral resources required for manufacturing high-tech devices, developing high-quality, regional-scale geophysical surveys could aid critical mineral exploration efforts and geologic mapping. In 2019, the U. S. Geological Survey launched the Earth Mapping Resources Initiative (Earth MRI) to modernize the geologic and geophysical mapping of regions that have the potential to contain critical mineral resources within the United States. In support of planning Earth MRI geophysical surveys, Drenth and Grauch (2019) defined five aeromagnetic data quality rankings (rank 1 through rank 5) applying them to the airborne geophysical survey inventory of the United States (Johnson et al., 2021). Rank 1 aeromagnetic surveys are of the highest quality, meeting modern standards and allowing best practices for qualitative and quantitative interpretation; whereas rank 5 aeromagnetic surveys are of the lowest quality, being useful only for qualitative interpretation of broad features. Through the Earth MRI effort, 48 high-quality, regional-scale rank 1 and 2 airborne magnetic and radiometric geophysical surveys have been planned, collected, or publicly release through May 2025 (U. S. Geological Survey, 2025). Here, a portion of a rank 1 Earth MRI aeromagnetic survey in southeast Arizona is presented and compared to a legacy rank 5 aeromagnetic survey over the Mammoth Magnetic Anomaly (MMA), demonstrating how modern, high-quality aeromagnetic data improves our view of crustal geology, aiding mineral exploration.

Arizona↗
USGS2025

Understanding market sensitivity: Estimation of supply and demand elasticities for non-fuel minerals

In today’s rapidly changing economic landscape, understanding market responsiveness to price changes and the factors influencing commodity prices has become increasingly relevant. Price elasticities serve as indicators of how variations in market conditions affect supply and demand, providing insights into the sensitivity of commodity markets to price fluctuations. This paper presents a comprehensive analysis of price elasticities of supply and demand for 74 non-fuel mineral commodities including precious metals, base metals, minor metals, and industrial minerals that are utilized across various industries. We employ various econometric techniques, including fixed effects models for panel data and two-stage dynamic ordinary least squares (2S-DOLS) alongside autoregressive distributed lag (ARDL) models for time series analysis, to derive robust estimates of price elasticities. Our findings reveal variability in elasticities among different commodities and indicate that all studied mineral commodities exhibit price inelastic supply and demand in the short run, which we define as one year for the purposes of our analysis, given that the data is all annual. This research provides original estimates of price responsiveness for a wide range of commodities that have not been previously addressed in the literature, thereby enhancing the understanding of market dynamics in the mineral sector. Given that price elasticities can be influenced by factors such as market structure, technological advancements, mining costs, and industry-specific demand drivers, we use variables that serve as proxies for these factors.

Mineral Economics↗
USGS2026

Indirect mineral import reliance and provenance

Mineral commodity supply chain analyses rely on international trade data reported by individual countries as quantities of a mineral commodity form imported from (or exported to) a partner. However, export quantities frequently exceed a country’s domestic production, or occur when no production data are reported, suggesting that the trade partner is merely an intermediary in a transshipment. These discrepancies can result in misleading conclusions regarding supply chain vulnerabilities and dependencies. We present a two-stage methodology to reconcile gaps between reported material sources and actual producers. First, we construct trade networks for specific mineral forms, treating production as a type of import to distinguish producing nations from entrepôts. By tracing flows through these networks, we attribute a target country’s imports to original producers via both direct (in a single trade link) and indirect (transferring through intermediaries) pathways. Second, these production-attributed flows are incorporated into multi-stage supply chains to determine the upstream provenance of feedstock for domestic refining and processing. This approach provides a more representative picture of trade reliance. For example, while the United States (U.S.) Geological Survey reports no imports of unwrought antimony metal from Russia in 2022 (U.S. Geological Survey (2025). Mineral Commodity Summaries 2025. 10.3133/mcs2025), our analysis reveals that over 16% of U.S. imports can be traced back to Russian mining through intermediate processing in countries such as China, India, and Vietnam. Additionally, our analysis of the aluminum supply chain shows that while the U.S. is reported as 52% net import reliant on aluminum materials in 2022, it is 100% reliant on foreign bauxite, 7% of which arrived indirectly. This unreported reliance, which is predominantly tied to bauxite mined in Brazil (43%) and Jamaica (28%), highlights our methods ability to capture the supply chain’s dependence on foreign feedstock that may be missing in single-stage trade data.

Mineral Economics↗
USGS2020

Mineral commodity summaries 2020

Each chapter of the 2020 edition of the U.S. Geological Survey (USGS) Mineral Commodity Summaries (MCS) includes information on events, trends, and issues for each mineral commodity as well as discussions and tabular presentations on domestic industry structure, Government programs, tariffs, 5-year salient statistics, and world production and resources. The MCS is the earliest comprehensive source of 2019 mineral production data for the world. More than 90 individual minerals and materials are covered by two-page synopses.

Mineral Commodity Summaries↗
USGS2024

New occurrences of the rare, REE minerals daqingshanite, törnebohmite, biraite, sahamalite, and ferriperbøeite from the Sheep Creek area, Montana, USA

Over 30 small, discontinuous, tabular carbonatite bodies are located in the Sheep Creek area, Ravalli County, southwest Montana. The age and origin of these REE-Nb-rich deposits are currently being investigated. The purpose of this paper is to document the occurrence of several rare minerals, including daqingshanite, törnebohmite, biraite, sahamalite, and ferriperbøeite, in two of the carbonatite bodies. These minerals are found in association with monazite, hydroxylbastnäsite, ferriallanite, calcite, dolomite, baryte, quartz, actinolite, apatite, celsian, and Sr-rich aragonite. Automated SEM-EDS was used to target the areas of interest in polished specimens for more detailed spot SEM-EDS and electron probe microanalysis. Raman spectra were also acquired for each of the rare minerals. The complex mineralogy of the Sheep Creek carbonatites is most likely due to several overlapping thermal events, including primary magmatic, overprinting hydrothermal, and supergene weathering stages. The rare minerals described in this study are believed to be hydrothermal and/or carbothermal in origin, although no estimates of temperature are available at this time.

Montana↗
USGS2026

Niobium-bearing minerals from the Sheep Creek carbonatite-related deposits of southwest Montana, USA

The Sheep Creek area in southwest Montana contains a number of small, tabular, carbonatite-related deposits that are rich in Nb and REE minerals. Nb-rich minerals from Sheep Creek and nearby Woods Creek are herein described in detail. The carbonatite veins contain a mix of calcite and Fe-bearing dolomite, with locally abundant apatite, baryte, celsian, actinolite, phlogopite, monazite-(Ce), and allanite-(Ce). Nb-bearing minerals include columbite-(Fe), aeschynite-(Ce), baotite, niobobaotite, chevkinite, fergusonite-(Nd), and two varieties of Ti-Nb-Fe-oxide. An early oxide with Ti/Nb (atomic) near unity later broke down to a fine-grained mixture of columbite + rutile with distinctly lower Nb content. The earlier oxide is tentatively identified as a rare variety of Nb-rich brookite. In both oxide phases, pentavalent Nb entered the TiO 2 structure in coupled substitution with a mixture of Fe 3+ and Fe 2+ . A single zircon crystal intergrown with the Nb-REE minerals was dated by in situ U-Pb methods to 111.6 ± 2 Ma. This age is in agreement with previous dating of monazite (Th-Pb) and molybdenite (Re-Os), and supports the idea that the Sheep Creek deposits are Cretaceous in age.

Montana↗
USGS2006

Influence of mineral weathering reactions on the chemical composition of soil water, springs, and ground water, Catoctin Mountains, Maryland

During 1983 and 1984, wet precipitation was primarily a solution of dilute sulphuric acid, whereas calcium and bicarbonate were the major ions in springs and ground water in two small watersheds with a deciduous forest cover in central Maryland. Dominant ions in soil water were calcium, magnesium, and sulphate. The relative importance of mineral weathering reactions on the chemical composition of these subsurface waters was compared to the contribution from wet precipitation, biological processes, and road deicing salts. Mineral reaction models, developed from geochemical mass-balance relationships, involved reactions of primary and secondary minerals in metabasalt and metarhyolite with hydrogen ion. Geochemical weathering reactions account for the majority of total ion equivalents in soil water (46 per cent), springs (51 per cent), and ground water (68 to 77 per cent). The net contribution of total ion equivalents from biological processes was 20 and 16 per cent for soil water and springs, respectively, but less than 10 per cent for ground water. The contribution of total ion equivalents from deicing salts (10 to 20 per cent) was related to proximity to roads. Strong acids in precipitation contributed 44 per cent of the total amount of hydrogen ions involved in mineral-weathering reactions for ground water in contact with metarhyolite compared to 25 per cent for ground water in contact with metabasalt, a less resistant rock type to weathering.

Hydrological Processes↗
USGS1982

Geologic factors that control mineral matter in coal

Elements other than organically derived and bound C, H, N, O, and S constitute mineral matter in coal. Mineral matter may consist of discrete minerals such as calcite, quartz, clays, and pyrite, and/or organic compounds that contain organically bonded elements such as Ca and CI. Processes that may affect the association and content of mineral matter are operable from the initial peat-forming stage to the time of utilization of the coal. However, the objective of this paper is to discuss some of the various geologic processes that may influence content and associations in unmined coal.

Book chapter↗
USGS1996

Silt heavy-mineral distributions off the Southeastern United States

Until recently heavy-mineral studies of marine sediments were largely restricted to sand fractions. New techniques permitting analysis of decalcified silt fractions have been applied to sediments off the southeastern United States. Our data, which confirm predictions from the basic relationship among grain size, specific gravity, and equivalent hydraulic transport behavior, show that concentrations and average diameters of the silt heavy minerals progressively decrease seaward. Heavy minerals always constitute a substantially greater weight percent of the silt than of the sand fraction. Despite corroded surface textures suggestive of extensive weathering and dissolution, spatial trends in the detrital heavy-mineral populations are predominantly controlled by source and hydraulic factors.

Geo-Marine Letters↗
USGS2003

Mercury from mineral deposits and potential environmental impact

Mercury deposits are globally distributed in 26 mercury mineral belts. Three types of mercury deposits occur in these belts: silica-carbonate, hot-spring, and Almaden. Mercury is also produced as a by-product from several types of gold-silver and massive sulfide deposits, which account for 5% of the world's production. Other types of mineral deposits can be enriched in mercury and mercury phases present are dependent on deposit type. During processing of mercury ores, secondary mercury phases form and accumulate in mine wastes. These phases are more soluble than cinnabar, the primary ore mineral, and cause mercury deposits to impact the environment more so than other types of ore deposits enriched in mercury. Release and transport of mercury from mine wastes occur primarily as mercury-enriched particles and colloids. Production from mercury deposits has decreased because of environmental concerns, but by-product production from other mercury-enriched mineral deposits remains important.

Environmental Geology↗
USGS2004

A Complex Systems Model Approach to Quantified Mineral Resource Appraisal

For federal and state land management agencies, mineral resource appraisal has evolved from value-based to outcome-based procedures wherein the consequences of resource development are compared with those of other management options. Complex systems modeling is proposed as a general framework in which to build models that can evaluate outcomes. Three frequently used methods of mineral resource appraisal (subjective probabilistic estimates, weights of evidence modeling, and fuzzy logic modeling) are discussed to obtain insight into methods of incorporating complexity into mineral resource appraisal models. Fuzzy logic and weights of evidence are most easily utilized in complex systems models. A fundamental product of new appraisals is the production of reusable, accessible databases and methodologies so that appraisals can easily be repeated with new or refined data. The data are representations of complex systems and must be so regarded if all of their information content is to be utilized. The proposed generalized model framework is applicable to mineral assessment and other geoscience problems. We begin with a (fuzzy) cognitive map using (+1,0,-1) values for the links and evaluate the map for various scenarios to obtain a ranking of the importance of various links. Fieldwork and modeling studies identify important links and help identify unanticipated links. Next, the links are given membership functions in accordance with the data. Finally, processes are associated with the links; ideally, the controlling physical and chemical events and equations are found for each link. After calibration and testing, this complex systems model is used for predictions under various scenarios.

Environmental Management↗
USGS2012

Mineralogical, chemical, and crystallographic properties of supergene jarosite-group minerals from the Xitieshan Pb-Zn sulfide deposit, northern Tibetan Plateau, China

Supergene jarosite-group minerals are widespread in weathering profiles overlying Pb-Zn sulfide ores at Xitieshan, northern Tibetan Plateau, China. They consist predominantly of K-deficient natrojarosite, with lesser amounts of K-rich natrojarosite and plumbojarosite. Electron microprobe (EMP) analyses, scanning electron microcopy (SEM) investigation, and X-ray mapping reveal that the jarosite-group minerals are characterized by spectacular oscillatory zoning composed of alternating growth bands of K-deficient and K-bearing natrojarosite (K 2 O >1 wt.%). Plumbojarosite, whenever present, occurs as an overgrowth in the outermost bands, and its composition can be best represented by K 0.29 Na 0.19 Pb 0.31 Fe 2.66 Al 0.22 (SO 4 ) 1.65 (PO 4 ) 0.31 (AsO 4 ) 0.04 (OH) 7.37 . The substitution of monovalent for divalent cations at the A site of plumbojarosite is charge balanced by the substitution of five-valent for six-valent anions in XO, 4/sub> at the X site. Thermogravimetric analysis (TGA) of representative samples reveal mass losses of 11.46 wt.% at 446.6 °C and 21.42 wt.% at 683.4 °C due to dehydroxylation and desulfidation, respectively. TGA data also indicate that the natrojarosite structure collapses at 446.6 °C, resulting in the formation of NaFe(SO 4 ) 2 and minor hematite. The decomposition products of NaFe(SO 4 ) are hematite and Na, 2 SO 4 . Powder X-ray diffraction (XRD) analyses show that the jarosite-group minerals have mean unit-cell parameters of a =7.315 ä and c =016.598 ä. XRD and EMP data support the view that substitutions of Na for K in the A site and full Fe occupancy in the B site can considerably decrease the unit-cell parameter c , but only slightly increase a . The results from this study suggest that the observed oscillatory zoning of jarosite-group minerals at Xitieshan resulted mainly from substitutions of K for Na at the A site and P for S at the X site.

Tibetan Plateau↗
USGS2012

The effect of increasing salinity and forest mortality on soil nitrogen and phosphorus mineralization in tidal freshwater forested wetlands

Tidal freshwater wetlands are sensitive to sea level rise and increased salinity, although little information is known about the impact of salinification on nutrient biogeochemistry in tidal freshwater forested wetlands. We quantified soil nitrogen (N) and phosphorus (P) mineralization using seasonal in situ incubations of modified resin cores along spatial gradients of chronic salinification (from continuously freshwater tidal forest to salt impacted tidal forest to oligohaline marsh) and in hummocks and hollows of the continuously freshwater tidal forest along the blackwater Waccamaw River and alluvial Savannah River. Salinification increased rates of net N and P mineralization fluxes and turnover in tidal freshwater forested wetland soils, most likely through tree stress and senescence (for N) and conversion to oligohaline marsh (for P). Stimulation of N and P mineralization by chronic salinification was apparently unrelated to inputs of sulfate (for N and P) or direct effects of increased soil conductivity (for N). In addition, the tidal wetland soils of the alluvial river mineralized more P relative to N than the blackwater river. Finally, hummocks had much greater nitrification fluxes than hollows at the continuously freshwater tidal forested wetland sites. These findings add to knowledge of the responses of tidal freshwater ecosystems to sea level rise and salinification that is necessary to predict the consequences of state changes in coastal ecosystem structure and function due to global change, including potential impacts on estuarine eutrophication.

Biogeochemistry↗
USGS1992

Gold deposition by sulfidation of ferrous Fe in the lacustrine sediments of the Pueblo Viejo district (Dominican Republic): The effect of Fe-C-S diagenesis on later hydrothermal mineralization in a Maar-Diatreme complex

The Pueblo Viejo district, located in the Cordillera Central of the Dominican Republic, contains large Au-Ag deposits associated with acid-sulfate alteration within spilites, conglomerates and carbonaceous sedimentary rocks that were deposited in a maar-diatreme complex. Much of the Au mineralization occurs in pyritic, carbonaceous siltstones of the Pueblo Viejo Maar-Diatreme Member of the Cretaceous Los Ranchos Formation. Pyrite is the only Fe-bearing phase in mineralized rock, whereas siderite is the dominant Fe-bearing phase in siltstones distal to mineralization. Disseminated pyrite occurs as framboids, cubes, pyritohedra, concretions and cement. Early framboids occur throughout the district. Au occurs as inclusions in later non-framboid disseminated pyrite (NFDP); an occurrence that is interpreted to be indicative of contemporaneous deposition. Pyrite framboids exhibit a wide range of ??34Scdt-values (-17.5 to +4.8???) and are interpreted to have formed during biogenic reduction of pore-water sulfate. The NFDP yield restricted ??34Scdt-values ( x ?? = -5.2???, s = ??2.4???, n = 43) similar to those obtained from later vein pyrite ( x ?? = -6.4???, s = ??1.5???, n = 12). Alunite and barite have ??34S-values ranging from +18.8 to +21.6???. The interpretation that the NFDP, vein pyrite, alunite and barite, and possibly even the framboidal pyrite share a common source of igneous sulfur is supported by the ??34S data. Siderite occurs as concretions and cement, contains abundant Mg (Fe0.75Mg0.19Mn0.03Ca0.02CO3) and has ??13Cpdb- and ??18Osmow-values ranging from -2.5 to +1.1%. and +14.6 to +19.5???, respectively. These data are consistent with the interpretation that the siderite formed in lacustrine sediments and that the carbonate in the siderite is probably methanogenic, although contributions from oxidation of organic matter during biogenic sulfate reduction, thermal decarboxylation of organic matter, or magmatic vapor cannot be ruled out. Disseminated Au mineralization in the sedimentary rocks formed when a hydrothermal fluid encountered reactive Fe2+ in diagenetic siderite. The ensuing pyrite deposition consumed H2S and destabilized the Au (HS)-2 complex, leading to precipitation of Au. The capacity of the sedimentary rocks to consume H2S and precipitate Au was controlled by the amount of non-pyrite Fe present as siderite. The abundance of siderite was controlled by the extent of pyrite formation during diagenesis. ?? 1992.

Chemical Geology↗
USGS1993

Epigenetic sulfide mineralization associated with Pennsylvanian paleokarst in eastern Iowa, U.S.A.

Paleokarst-associated, sulfide-bearing mineral deposits are wide-spread in the Paleozoic carbonate rocks of eastern Iowa. Minerals occur in nodules enclosed in karst-filling mudstones, as sandstone cements, and as surface coatings on, and fracture fillings in, foundered carbonate rock clasts. Mineralogy and paragenetic sequence vary among the occurrences. Sulfur isotopic compositions exhibit wide variations within and among deposits (??34S = -33.8 to + 35.1???). Oxygen isotopic compositions of fracture-filling calcite spars (??18O = -8.41 to + 3.60???) are similar to the isotopic compositions of their carbonate rock hosts. Calcite spars are somewhat depleted in ??13C relative to host rock [??13C (spars) = - 5.66 to + 0.24??? vs. -1.54 to + 1.21??? (host rock)]. Results of mineralogic, paragenetic and isotopic investigations suggest that: (1) minerals are products of multiple events operating on a local, rather than a regional scale; (2) spatially-disjunct fracture-filling mineral deposits exposed in the same quarries are probably not cogenetic with paleokarst-associated deposits; (3) paleokarst-filling calcite spars formed at near-surface temperatures; and (4) paleokarst-associated deposits are probably not cogenetic with Upper Mississippi Valley ZnPb pitch-flat deposits. ?? 1993.

Chemical Geology↗
USGS1967

Borate mineral assemblages in the system Na2O-CaO-MgO-B2O3-H2O

The significant known hydrated borate mineral assemblages (principally of the western United States) in the system Na 2 O-CaO-MgO-B 2 O 3- H 2 O are expressible in three ternary composition diagrams. Phase rule interpretation of the diagrams is consistent with observation, if the activity of H 2 O is generally considered to be determined by the geologic environment. The absence of conflicting tie-lines on a diagram indicates that the several mineral assemblages of the diagram were formed under relatively narrow ranges of temperature and pressure. The known structural as well as empirical formulas for the minerals are listed, and the more recent (since 1960) crystal structure findings are discussed briefly. Schematic Gibbs free energy-composition diagrams based on known solubility-temperature relations in the systems Na 2 B 4 O 7 -H 2 O and Na 2 B 4 O 7 -NaCl-H 2 O, are highly useful in the interpretation and prediction of the stability relations in these systems; in particular these diagrams indicate clearly that tincalconite, although geologically important, is everywhere a metastable phase. Crystal-chemical considerations indicate that the same thermodynamic and kinetic behavior observed in the Na 2 B 4 O 7 -H 2 O system will hold in the Ca 2 B 6 O 11 -H 2 O system. This conclusion is confirmed by the petrologic evidence. The chemical relations among the mineral assemblages of a ternary diagram are expressed by a schematic “activity-activity” diagram. These activity-activity diagrams permit the tracing-out of the paragenetic sequences as a function of changing cation and H 2 O activities.

Geochimica et Cosmochimica Acta↗
USGS1987

Studies of Quaternary saline lakes-III. Mineral, chemical, and isotopic evidence of salt solution and crystallization processes in Owens Lake, California, 1969-1971

As a consequence of the 1969–1970 flooding of normally dry Owens Lake, a 2.4-m-deep lake formed and 20% of the 2-m-thick salt bed dissolved in it. Its desiccation began August 1969, and salts started crystallizing September 1970, ending August 1971. Mineralogic, brine-composition, and stable-isotope data plus field observations showed that while the evolving brine composition established the general crystallization timetable and range of primary and secondary mineral assemblages, it was the daily, monthly, and seasonal temperature changes that controlled the details of timing and mineralogy during this depositional process. Deuterium analyses of lake brine, interstitial brine, and hydrated saline phases helped confirm the sequence of mineral crystallizations and transformations, and they documented the sources and temperatures of waters involved in the reactions. Salts first crystallized as floating rafts on the lake surface. Natron and mirabilite, salts whose solubilities decrease greatly with lowering temperatures, crystallized late at night in winter, when surface-water temperatures reached their minima; trona, nahcolite, burkeite, and halite, salts with solubilities less sensitive to temperature, crystallized during the afternoon in summer, when surface salinities reached their maxima. However, different temperatures were generally associated with crystallization (at the surface) and accumulation (on the lake floor) because short-term temperature changes were transmitted to surface and bottom waters at different rates. Consequently, even when solubilities were exceeded at the surface, salts were preserved or not as a function of bottom-water temperatures. Halite, a nearly temperature-insensitive salt, was always preserved. Monitoring the lake-brine chemistry and mineralogy of the accumulating salts shows: (1) An estimated 0.9 × 10 6 tons of CO 2 was released to the atmosphere or consumed by the lake's biomass prior to most salt crystallization. (2) After deposition, some salts reacted in situ to form other minerals in less than one month, and all salts (except halite) decomposed or recrystallized at least once in response to seasons. (3) Warming in early 1971 caused solution of all the mirabilite and some of the natron deposited a few months earlier, a deepening of the lake (though the lake-surface lowered), and an increase in dissolved solids. (4) Phase and solubility-index data suggest that at the close of desiccation, Na 2 CO 3 ·7H 2 O, never reported as a mineral, could have been the next phase to crystallize.

Geochimica et Cosmochimica Acta↗
USGS1971

A general evaluation of the frequency distribution of clay and associated minerals in the alluvial soils of Ceylon

Clay mineral analyses were made of several alluvial clay materials from Ceylon. These studies show that the soil materials can be divided into 3 clay mineral provinces on the basis of the frequency distribution of clay and associated minerals. The provinces closely follow the climatic divisions. The characteristic feature of this classification is the progressive development of gibbsite from Dry to Wet Zone areas. Gibbsite has been used as a reliable indicator mineral.

Geoderma↗