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

At least 775 records · Page 43Linked to original sources

Zirconium-bearing accessory minerals in UK Paleogene granites: Textural, compositional, and paragenetic relationships

The mineral occurrences, parageneses, textures, and compositions of Zr-bearing accessory minerals in a suite of UK Paleogene granites from Scotland and Northern Ireland are described. Baddeleyite, zirconolite, and zircon, in that sequence, formed in hornblende + biotite granites (type 1) and hedenbergite–fayalite granites (type 2). The peralkaline microgranite (type 3) of Ailsa Craig contains zircon, dalyite, a eudialyte-group mineral, a fibrous phase which is possibly lemoynite, and Zr-bearing aegirine. Hydrothermal zircon is also present in all three granite types and documents the transition from a silicate-melt environment to an incompatible element-rich aqueous-dominated fluid. No textures indicative of inherited zircon were observed. The minerals crystallized in stages from magmatic through late-magmatic to hydrothermal. The zirconolite and eudialyte-group mineral are notably Y + REE-rich (REE signifies rare earth element). The crystallization sequence of the minerals may have been related to the activities of Si and Ca, to melt peralkalinity, and to local disequilibrium.

European Journal of Mineralogy↗

In situ lung dust analysis by automated Field Emission Scanning Electron Microscopy with Energy Dispersive X-ray Spectroscopy: A method for assessing inorganic particles in tissue from coal miners

Context.— Overexposure to respirable coal mine dust can cause severe lung disease including progressive massive fibrosis (PMF). Field emission scanning electron microscopy with energy dispersive x-ray spectroscopy (FESEM-EDS) has been used for in situ lung dust particle analysis for evaluation of disease etiology. Automating such work can reduce time, costs, and user bias. Objective.— To develop and test an automated FESEM-EDS method for in situ analysis of inorganic particles in coal miner lung tissue. Design.— We programmed an automated FESEM-EDS procedure to collect particle size and elemental data, using lung tissue from 10 underground coal miners with PMF and 4 control cases. A statistical clustering approach was used to establish classification criteria based on particle chemistry. Data were correlated to PMF/non-PMF areas of the tissue, using corresponding brightfield microscopy images. Results for each miner case were compared with a separate corresponding analysis of particles recovered following tissue digestion. Results.— In situ analysis of miner tissues showed higher particle number densities than controls and densities were generally higher in PMF than non-PMF areas. Particle counts were typically dominated by aluminum silicates with varying percentages of silica. Compared to digestion results for the miner tissues, in situ results indicated lower density of particles (number per tissue volume), larger size, and a lower ratio of silica to total silicates—probably due to frequent particle clustering in situ. Conclusions.— Automated FESEM-EDS analysis of lung dust is feasible in situ and could be applied to a larger set of mineral dust–exposed lung tissues to investigate specific histologic features of PMF and other dust-related occupational diseases.

Archives of Pathology↗

Scale-dependent associations of Band-tailed Pigeon counts at mineral sites

The abundance of Band-tailed Pigeons ( Patagioenas fasciata monilis ) has declined substantially from historic numbers along the Pacific Coast. Identification of patterns and causative factors of this decline are hampered because habitat use data are limited, and temporal and spatial variability patterns associated with population indices are not known. Furthermore, counts are influenced not only by pigeon abundance but also by rate of visitation to mineral sites, which may not be consistent. To address these issues, we conducted mineral site counts during 2001 and 2002 at 20 locations from 4 regions in the Pacific Northwest, including central Oregon and western Washington, USA, and British Columbia, Canada. We developed inference models that consisted of environmental factors and spatial characteristics at multiple spatial scales. Based on information theory, we compared models within a final set that included variables measured at 3 spatial scales (0.03 ha, 3.14 ha, and 7850 ha). Pigeon counts increased from central Oregon through northern Oregon and decreased into British Columbia. After accounting for this spatial pattern, we found that pigeon counts increased 12% ± 2.7 with a 10% increase in the amount of deciduous forested area within 100 m from a mineral site. Also, distance from the mineral site of interest to the nearest known mineral site was positively related to pigeon counts. These findings provide direction for future research focusing on understanding the relationships between indices of relative abundance and complete counts (censuses) of pigeon populations by identifying habitat characteristics that might influence visitation rates. Furthermore, our results suggest that spatial arrangement of mineral sites influences Band-tailed Pigeon counts and the populations which those counts represent.

Pacific Northwest↗

Minerals produced during cooling and hydrothermal alteration of ash flow tuff from Yellowstone drill hole Y-5

A rhyolitic ash-flow tuff in a hydrothermally active area within the Yellowstone caldera was drilled in 1967, and cores were studied to determine the nature and distribution of primary and secondary mineral phases. The rocks have undergone a complex history of crystallization and hydrothermal alteration since their emplacement 600,000 years ago. During cooling from magmatic temperatures, the glassy groundmass underwent either devitrification to alkali feldspar + ??-cristobalite ?? tridymite or granophyric crystallization to alkali feldspar + quartz. Associated with the zones of granophyric crystallization are prismatic quartz crystals in cavities similar to those termed miarolitic in plutonic rocks. Vapor-phase alkali feldspar, tridymite, magnetite, and sporadic ??-cristobalite were deposited in cavities and in void spaces of pumice fragments. Subsequently, some of the vapor-phase alkali feldspar crystals were replaced by microcrystalline quartz, and the vapor-phase minerals were frosted by a coating of saccharoidal quartz. Hydrothermal minerals occur primarily as linings and fillings of cavities and fractures and as altered mafic phenocrysts. Chalcedony is the dominant mineral related to the present hydrothermal regime and occurs as microcrystalline material mixed with various amounts of hematite and goethite. The chalcedony displays intricate layering and was apparently deposited as opal from silica-rich water. Hematite and goethite also replace both mafic phenocrysts and vapor-phase magnetite. Other conspicuous hydrothermal minerals include montmorillonite, pyrite, mordenite, calcite, and fluorite. Clinoptilolite, erionite, illite, kaolinite, and manganese oxides are sporadic. The hydrothermal minerals show little correlation with temperature, but bladed calcite is restricted to a zone of boiling in the tuff and clearly was deposited when CO2 was lost during boiling. Fractures and breccias filled with chalcedony are common throughout Y-5 and may have been produced by rapid disruption of rock caused by sudden decrease of fluid pressure in fractures, most likely a result of fracturing during resurgent doming in this part of the Yellowstone caldera. The chalcedony probably was deposited as opal or ??-cristobalite from a pre-existing silica floc that moved rapidly into the fractures and breccias immediately after the sudden pressure drop. ?? 1978.

Journal of Volcanology and Geothermal Research↗

Biogenic iron mineralization at Iron Mountain, CA with implications for detection with the Mars Curiosity rover

(Introduction) Microbe-mineral interactions and biosignature preservation in oxidized sulfidic ore bodies (gossans) are prime candidates for astrobiological study. Such oxidized iron systems have been proposed as analogs for some Martian environments. Recent studies identified microbial fossils preserved as mineral-coated filaments. This study documents microbially-mediated mineral biosignatures in hydrous ferric oxide (HFO) and ferric oxyhydroxysulfates (FOHS) in three environments at Iron Mountain, CA. We investigated microbial community preservation via HFO and FOHS precipitation and the formation of filamentous mineral biosignatures. These environments included 1) actively precipitating (1000's yrs), naturally weathered HFO from in situ gossan, and 3) remobilized iron deposits, which contained lithified clastics and zones of HFO precipitate. We used published biogenicity criteria as guidelines to characterize the biogenicity of mineral filaments. These criteria included A) an actively precipitating environment where microbes are known to be coated in minerals, B) presence of extant microbial communities with carbon signatures, C) structures observable as a part of the host rock, and D) biological morphology, including cellular lumina, multiple member population, numerous taxa, variable and 3-D preservation, biological size ranges, uniform diameter, and evidence of flexibility. This study explores the relevance and detection of these biosignatures to possible Martian biosignatures. Similar filamentous biosignatures are resolvable by the Mars Hand Lens Imager (MAHLI) onboard the Mars Science Laboratory (MSL) rover, Curiosity, and may be identifiable as biogenic if present on Mars.

California↗

Global nonfuel mineral exploration trends 2001-2015

The mission of the U.S. Geological Survey (USGS) National Minerals Information Center (NMIC) is to collect, analyze and disseminate information on the domestic and international supply of and demand for minerals and mineral materials essential to the U.S. economy and national security. Understanding mineral exploration activities and trends assists government policy makers, minerals industry decision makers and research entities in identifying where future sources of mineral supply are likely to be discovered, the amount and type of these resources and factors that may affect exploration and development.

Mining Engineering↗

A review of silver-rich mineral deposits and their metallogeny

Mineral deposits with large inventories or high grades of silver are found in four genetic groups: (1) volcanogenic massive sulfide (VMS), (2) sedimentary exhalative (SEDEX), (3) lithogene, and, (4) magmatichydrothermal. Principal differences between the four groups relate to source rocks and regions, metal associations, process and timing of mineralization, and tectonic setting. These four groups may be subdivided into specific metal associations on ternary diagrams based on relative metal contents. The VMS deposits rarely contain more than 15,600 t Ag (500 Moz). Grades average 33 g/t Ag. Variable Ag- Pb-Zn-Cu-Au ± Sn concentrations are interpreted as having been derived both from shallow plutons and by leaching of the volcanic rock pile in regions of thin or no continental crust and the mineralization is syngenetic. Higher silver grades are associated with areas of abundant felsic volcanic rocks. The SEDEX deposits rarely contain more than 15,600 t Ag (500 Moz). Grades average 46 g/t Ag. Silver, lead, and zinc in relatively consistent proportions are leached from sedimentary rocks filling rift-related basins, where the continental crust is thin, and deposited as syngenetic to diagenetic massive sulfides. Pre-mineral volcanic rocks and their detritus may occur deep within the basin and gold is typically absent. Lithogene silver-rich deposits are epigenetic products of varying combinations of compaction, dewatering, meteoric water recharge, and metamorphism of rift basin-related clastic sedimentary and interbedded volcanic rocks. Individual deposits may contain more than 15,600 t Ag (500 Moz) at high grades. Ores are characterized by four well-defined metal associations, including Ag, Ag-Pb-Zn, Ag-Cu, and Ag-Co-Ni-U. Leaching, transport, and deposition of metals may occur both in specific sedimentary strata and other rock types adjacent to the rift. Multiple mineralizing events lasting 10 to 15 m.y., separated by as much as 1 b.y., may occur in a single basin. Gold is absent at economic levels. The magmatic-hydrothermal silver-rich deposits are epigenetic and related to cordilleran igneous and volcanic suites. Six magmatic-hydrothermal districts each contain more than 31,000 t Ag (1,000 Moz) with grades of veins >600 g/t Ag. Mineralization occurs as veins, massive sulfides in carbonate rocks, and disseminated deposits including porphyry silver deposits, a proposed exploration model. Most deposits are epithermal with low-sulfidation alteration assemblages. Deposits are often telescoped and well-zoned. All large and high-grade magmatic-hydrothermal deposits appear confined to regions of relatively thick continental crust above Cenozoic consuming plate margins on the eastern side of the Pacific Rim. Silver in these deposits may be partly derived by hydrothermal leaching of rocks under or adjacent to the deposits. Specific metal associations in SEDEX and lithogene deposits may reflect confinement of fluid flow to and derivation of metals from specific source rock types. Variable metal associations in VMS and magmatichydrothermal deposits may reflect derivation of metals from a more diverse suite of rocks by convecting hydrothermal systems and processes related to the generation of magma. The discovery rate for silver-rich deposits has accelerated during the past decade, with new deposit types, metal associations, and exploration models being identified that provide numerous exploration and research opportunities.

Book chapter↗

New high resolution airborne geophysical surveys in Nevada And California for geothermal and mineral resource studies

The U.S. Geological Survey (USGS) and the Department of Energy (DOE) are collaborating to acquire high-resolution airborne magnetic and radiometric data to support geologic and geophysical mapping and modeling that will assist geothermal and critical mineral studies. Coordinated with these efforts are programs supporting geologic mapping and airborne LiDAR (light detection and ranging) surveys that yield detailed surface topographic models of the terrain over the same regions spanned by the geophysical surveys. The collaboration leverages resources from the USGS and DOE to acquire large regional datasets that will provide fundamental data necessary to map surface and subsurface geology and structure to benefit mineral and resource program objectives of both agencies. Such regionally uniform datasets are important for geothermal research to assist in identifying geologically favorable settings and as invaluable inputs in predictive models targeting undiscovered resources that use knowledge-driven (e.g., play fairway analysis) or data-driven approaches (e.g., machine-learning methods) to reduce risk associated with resource exploration. These data will also serve a wide range of other related activities from hazard (earthquake, volcano, landslide, environmental) and resource (water, mineral, energy) studies, to mapping and land management. Surveys were conducted in two areas that were selected because they host substantial geothermal and mineral potential in California and Nevada. The data will aid several ongoing USGS and DOE projects aimed at characterizing geothermal and mineral systems, understanding the factors controlling their occurrence, and improving future national resource assessments. The first of these surveys (referred to as GeoDAWN) was collected over northern and western Nevada and eastern California and spans areas of major resource potential associated with the Walker Lane and western Great Basin. This includes Clayton Valley, which hosts substantial lithium brine and clay resources, and the Humboldt Mafic Complex, which constitutes a potentially important resource of critical minerals (including cobalt, rare earth elements, platinum group elements, iron, chromium, nickel, and copper). The second survey area (referred to as GeoFlight) is focused over the Salton Trough in southern California that contains some of the largest and hottest known hydrothermal systems in the world, as well as a substantial lithium brine resource that could potentially meet the nation’s lithium demand for electric vehicles. Data from both surveys will be made publicly available through USGS publications and online data repositories. Future efforts under this collaboration are presently being evaluated and may involve acquisition of other data sets such as airborne gravity, electromagnetic or hyperspectral data to address research targets.

Conference Paper↗

Seamless Geologic Map Database for the Intermountain West, United States: A foundational dataset for mineral systems analysis

The Intermountain West has a complex geologic history, resulting in the formation of a diverse array of mineral deposits. Effective mineral exploration requires understanding the spatial and temporal relationships among geologic processes and events, a key focus of the mineral systems approach to exploration. This paper presents the Intermountain West Seamless Geologic Map Database, a unified dataset designed to support mineral exploration. Integrating geologic provinces, structural settings, and hydrothermal alteration, the database leverages the Seamless Integrated Geologic Mapping (SIGMa) extension to the USGS Geologic Map Schema (GeMS) to standardize geologic data from varied sources. SIGMa's hierarchical stratigraphic organization and feature-level metadata enhance data interoperability and reusability, enabling seamless query, analysis, and visualization of lithology, structural features, mineral deposits, geochronology, hydrothermal alteration. volcanic activity, and By providing a regionally consistent and dynamically evolving geologic map, this database provides a foundational framework for mineral exploration and geologic research. It also allows for an efficient workflow that expedites the publication of integrated geologic map databases.

Conference Paper↗

40Ar/39Ar geochronology supporting mineral resources research at USGS Denver

The 40 Ar/ 39 Ar geochronology method is used to date potassium-bearing rocks and minerals, based on the decay of 40 K to 40 Ar, which provides important temporal constraints for geological events. The USGS Denver Argon Geochronology Laboratory dates samples from a variety of projects, mainly in the USGS Mineral Resource Program and the National Cooperative Geologic Mapping Program, facilitating in-depth research into the timing of geological events and processes. Recent applications of this method include geochronological studies in the Yellow Pine district, revealing mineralization ages that range from 51 to 70 Ma, and investigations into the Bear Lodge alkaline complex, providing insights into the timing of REE carbonatite formation. Additionally, studies at Alunite Ridge highlight the method's potential for understanding concealed mineral deposits. Ongoing projects continue to leverage 40 Ar/ 39 Ar data to enhance understanding of geologic frameworks and mineral resources, underpinning its importance in modern geochronology and mineral resource assessment.

Conference Paper↗

Reactivity of clay minerals with acids and alkalies

One-g samples of a montmorillonite, a metabentonite, an illite, two kaolinites, and three halloysites were treated with 50 ml of hydrochloric acid (6⋅45 N, 1:1), acetic acid (4⋅5 N, 1:3), sodium hydroxide (2⋅8 N), sodium chloride solution (pH 6⋅10; Na = 35‰; Cl = 21⋅5‰), and natural sea water (pH 7⋅85; Na = 35⋅5‰; Cl = 21⋅ 5‰) for a 10-day period in stoppered plastic vials. The supernatant solutions were removed from the clay minerals and analyzed for SiO 2 , Al 2 O 3 , CaO, MgO, Na 2 O, and K 2 O. All the solutions removed some SiO 2 , Al 2 O 3 , and Fe 2 O 3 from the samples, but the quantities were small. Sodium hydroxide attacked the kaolin group minerals more strongly than it did montmorillonite, metabentonite, or illite. Halloysite was more strongly attacked by hydrochloric acid than was any of the other experimental minerals. Hydrochloric acid removed iron oxide coatings from soil clay minerals, but acetic acid did not remove them completely. The samples most strongly attacked by HCl and NaOH were examined by X-ray diffraction. Acid treatment did not destroy the structure of the clays, but the halloysite structure was partially destroyed. Sodium hydroxide attacked the halloysite structure, as shown by chemical analysis and X-ray diffraction. These experiments show that treatment in dilute acids has no harmful effect in the preparation of clays for X-ray diffraction. Acetic acid is preferred to hydrochloric acid for this purpose. Hydrochloric acid cleans clay minerals by removing free iron oxide from the surface; acetic acid is less effective.

Clays and Clay Minerals↗

Problem of the thermodynamic status of the mixed-layer minerals

Minerals that show mixed layering, particularly with the component layers in random sequence, pose problems because they may behave thermodynamically as single phases or as polyphase aggregates. Two operational criteria are proposed for their distinction. The first scheme requires two samples of mixed-layer material which differ only in the proportions of the layers. If each of these two samples are allowed to equilibrate with the same suitably chosen monitoring solution, then the intensive parameters of the solution will be invariant if the mixed-layer sample is a polyphase aggregate, but not otherwise. The second scheme makes use of the fact that portions of many titration curves of clay minerals show constancy of the chemical activities of the components in the equilibrating solutions, suggesting phase separation. If such phase separation occurs for a mixed-layer material, then, knowing the number of independent components in the system, it should be possible to decide on the number of phases the mixed-layer material represents. Knowledge of the phase status of mixed-layer material is essential to the study of the equilibrium relations of mineral assemblages involving such material, because a given mixed-layer mineral will be plotted and treated differently on a phase diagram, depending on whether it is a single phase or a polyphase aggregate. Extension of the titration technique to minerals other than the mixed-layer type is possible. In particular, this method may be used to determine if cryptoperthites and peristerites are polyphase aggregates. In general, for any high-order phase separation, the method may be used to decide just at what point in this continuous process the system must be regarded operationally as a polyphase aggregate.

Geochimica et Cosmochimica Acta↗

Tungsten skarn potential of the Yukon-Tanana Upland, eastern Alaska, USA—A mineral resource assessment

Tungsten (W) is used in a variety of industrial and technological applications and has been identified as a critical mineral for the United States, India, the European Union, and other countries. These countries rely on W imports mostly from China, which leaves them vulnerable to supply disruption. Consequently, the U.S. government has a current initiative to understand domestic resource potential. The eastern Alaska portion of the Yukon-Tanana Upland (YTU), is prospective for W skarn deposits, the major source of global W supply. The regional geology consists of juxtaposed Paleozoic lithotectonic packages that were reaccreted to North America in the Mesozoic . Multiple subsequent episodes of arc-related magmatism intruded the lithotectonic packages, accompanied by W skarn formation mostly associated with 100–90 Ma intrusions; major W skarn deposits in Canada are part of the same metallogenic event (e.g., Mactung, Cantung). In this paper, we present an assessment for undiscovered W skarn resources for parts of the lesser-explored western (Alaskan) portion of the YTU. We used GIS proximity analysis to map the intersection of pluton and carbonate-bearing rocks to define three permissive tracts for W skarn deposits. The permissive tracts were qualitatively assessed by mineral potential mapping using region-wide sediment geochemistry and mineral concentrate datasets. This analysis showed that much of the western YTU has high potential for undiscovered W skarn deposits, whereas the eastern and southern YTU had only isolated areas of medium to high potential. Historical production and the quality of the geochemistry data of the western YTU tract (ca. 9200 km 2 ) permitted a quantitative assessment of undiscovered W resources. Probabilistic estimates by a panel of 20 experts predicted a 70% chance of one to three undiscovered W skarn deposits in the western YTU tract. The rationale for favorability employed by the expert panel included favorable lithology, previous production, clustering of previously mined deposits, W placers in the area, lack of recent exploration, pan concentrates containing W minerals, and W geochemical anomalies. Estimates were combined with a global grade and tonnage model for W skarns in a Monte Carlo simulation and provided a median estimate of undiscovered resources of 94 kt WO 3 . If the undiscovered W skarn deposits are located close to infrastructure (e.g., near Fairbanks, or close to roads and/or power grid), application of an economic filter indicates that the median total economically recoverable WO 3 is 63 kt with a net present value (NPV) of $330 million USD (2008 dollars). Whereas if deposits are far from infrastructure, median recoverable WO 3 is only 30 kt and the NPV is $44 million. Our models for contained WO 3 resources and NPV estimates for the western YTU tract are considerably lower than the known resources in skarns in adjacent areas in Canada. Estimates for the western YTU are also lower than preliminary estimates for undiscovered W skarn deposits in areas of the western conterminous United States. We speculate that lower permeability and continuity of favorable carbonate rock horizons in the relatively higher-grade metamorphic country rocks in the Alaska portion of the YTU may explain some of the differences in prospectivity. More detailed geologic mapping, modern geochemistry, and geophysical surveys are needed to refine the resource potential of the whole YTU. Regardless, quantitative mineral resource assessment provides a useful tool for making first-order regional estimates of undiscovered resources, identifying target areas for new data acquisition, and guiding research on the fundamental controls of district-scale metallogenic endowments.

Alaska↗

Distribution and composition of sulfide minerals at Balmat, New York

In the Balmat area in northern New York , tabular deposits of sulfide minerals parallel the layering in folded, siliceous magnesian marbles of a metamorphic complex commonly referred to as the Precambrian Granville Series. Sphalerite, pyrite, and, locally, pyrrhotite and galena have replaced the carbonate minerals in parts of the marble units. The contacts between ore and marble are, in general, ill-defined; scattered grains of sulfides are present from several inches to hundreds of feet from the massive portions of ore. Access to the ore is provided through the Balmat No. 2 and No. 3 mines. The isotopic composition of lead from primary galena is uniform within an individual mine. The model age of this lead agrees with the age of the mineralization determined by other means - about a billion years. The isotopic composition of the leads in the marble is not uniform today, and calculations indicate that it was probably not uniform a billion years ago. Unless the lead in the ores is a uniform mixture of lead isotopes from an isotopically poorly mixed source, it is doubtful that the lead in the ores was derived from the surrounding marbles. Cobalt and nickel concentrations in pyrite from grains disseminated in the metasedimentary rocks away from the ore bodies are each greater than 200 ppm. Most samples of pyrite from the ore bodies at the No. 2 and No. 3 mines contain less than 50 ppm each of cobalt and nickel. Therefore the author believes it unlikely that the pyrite of the ores is genetically related to the pyrite in the metasedimentary rocks. Textural relationships suggest that pyrrhotite formed after most of the sphalerite, which in turn formed after most of the pyrite in the ore bodies. By use of the experimentally determined systems FeS-ZnS and FeS-FeS 2 , it is inferred from the amounts of iron in sphalerite and sulfur in pyrrhotite that the bulk of the sulfide minerals in the No. 2 mine formed above 320° C. The absolute temperature of formation of pyrrhotite indicated by the FeS-ZnS system is about 150° higher than that indicated by the FeS-FeS 2 system. The former system probably gives the more reliable estimate. The concentrations of individual minor elements in sphalerite and pyrite range considerably among specimens of the same sulfide mineral from the same level and ore body. An exception is cadmium in sphalerite which has a narrow concentration range around 1400 ppm in both the No. 2 and No. 3 mines. The ratio of the concentrations of minor elements between sphalerite-pyrite pairs varies considerably also. This variation probably indicates that exchange of minor elements between pyrite and sphalerite durin g the formation of the ores was very slow and incomplete.

New York↗

Mineral resource assessment of mafic and ultramafic rocks in the Greenville 1° x 2° quadrangle, South Carolina, Georgia, and North Carolina

Mineral resources of the Greenville 1° x 2° quadrangle, South Carolina, Georgia, and North Carolina, were assessed between 1984 and 1990 under the Conterminuous United States Mineral Assessment Program (CUSMAP) of the U.S. Geological Survey (USGS). The mineral resource assessments were made on the basis of geologic, geochemical, and geophysical investigations and on the distribution of mines, prospects and mineral occurrences reported in the literature. This report is an assessment of the mineral resources associated with mafic and ultramafic rocks in the Greenville quadrangle. It is based on the geology as mapped by Nelson and others (1987, 1989), on geochemistry of rock samples collected for this and other studies, on data available for known mines and prospects, and on the published geologic literature.

Georgia;North Carolina;South Carolina↗

Mineral resource inventory of North Dakota

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

North Dakota↗

Mineral resource of the month: vermiculite

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

Earth↗

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

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

Alaska↗