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Minerals & deposits

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USGS2022

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↗

USGS2022

Late Jurassic-Early Cretaceous orogenic gold mineralization in the Klamath Mountains, California: Constraints from 40Ar/39Ar dating of hydrothermal muscovite

The Klamath Mountains gold province is the second most important historical producer in California, having produced more than 7 Moz of gold from both lode and placer sources. Hydrothermal muscovite grains from gold-bearing veins provide the first 40 Ar/ 39 Ar age constraints indicative of a protracted period of mineralization in the Klamath Mountains. The data indicate that the window for orogenic gold mineralization in the Klamath Mountains was from ∼160–140 Ma, coinciding in age with the oldest orogenic gold deposits in the Sierra Nevada foothills province to the south, although mineralization continued in the latter along the Mother Lode belt for another 20–30 million years. Despite the broad age overlap between hydrothermal activity and magmatism, the former relates to a regional thermal event, and there is no genetic link between the two. Instead, a correlation exists between the timing of lode gold formation and discrete tectonic events, changes in stress regime, and fault movement. The maximum age corresponds to a major plate reorganization in the Pacific basin and initial gold mineralization continuing into the Sierra Nevada foothills gold province to the south. The minimum age corresponds to the westerly lateral offset of the Klamath Mountains from the Sierra Nevada and the then-active arc, marking the termination of both magmatism and gold-producing hydrothermal activity in the Klamath Mountains. Lode gold mineralization in the Klamath Mountains is compatible with a crustal source of metals and fluids that were released during metamorphic devolatilization and focused via hydrothermal fluid flow along regional faults.

California↗

USGS2022

Petrogenesis and rare earth element mineralization of the Elk Creek carbonatite, Nebraska, USA

Although carbonatites are the primary source of the world’s rare earth elements (REEs), the processes responsible for ore-grade REE enrichment in carbonatites are still poorly understood. In this study, we present a petrologic, geochemical, and isotopic evaluation of the Elk Creek carbonatite in southeast Nebraska to constrain the origin of REE mineralization. The Elk Creek carbonatite is a multilithologic carbonatite comprised of an early apatite-dolomite carbonatite, a middle/heavy REE-enriched magnetite-dolomite carbonatite, and a late-stage light REE-enriched, barite-dolomite carbonatite, as well as a suite of breccias. Neodymium, strontium, and carbon isotopic data from the early apatite-dolomite carbonatite, ε Nd (T) = 2.3 to 3.4, 87 Sr/ 86 Sr (i) = 0.702704 to 0.702857, and δ 13 C = −3.3 to −3.4, indicate that the parental magma and REEs were derived from the mantle, and textural and chemical data suggest that hydrothermal processes played an important role in reaching ore-grade enrichment. Higher initial 87 Sr/ 86 Sr values (∼0.7041) of REE-mineralized lithologies are evidence that these fluids were derived, in part, from meteoric water that interacted with the country rock. Modeling of the C-O isotopic data reveals that some of the isotopic variation results from closed-system Rayleigh fractionation of an evolving carbonatitic magma between 300 and 500 °C, but an excursion to heavier δ 18 O is likely the result of interaction with H 2 O-CO 2 -fluids at temperatures from 400 to 100 °C. Hydrothermal dolomite has higher 87 Sr/ 86 Sr values than early-formed magmatic dolomite, consistent with metasomatism by fluids derived, in part, from a more radiogenic source such as the Precambrian-age wall rock. Rare earth element mineralization occurs primarily in fine-grained, cavity filling minerals including monazite, bastnäsite, parisite, and synchysite along with barite, dolomite, quartz, and iron oxides. We interpret the LREE enrichment at Elk Creek to be the product of hydrothermal fluids derived from the evolving carbonatite magma and fluids from the wall rock. The REEs likely became enriched in late-stage fluids from the evolving magma as well as being remobilization by the dissolution of earlier formed minerals. Middle/heavy REE-enrichment in the magnetite-dolomite carbonatite is hosted in hydrothermal dolomite and is attributed to variations in the composition of hydrothermal fluids.

Nebraska↗

USGS1997

Fe-Ca-phosphate, Fe-silicate, and Mn-oxide minerals in concretions from the Monterey Formation

Concentrically zoned phosphatic-enriched concretions were collected at three sites from the Monterey Formation. The following minerals were identified: vivianite, lipscombite, rockbridgeite, leucophosphite, mitridatite, carbonate fluorapatite, nontronite, todorokite, and barite. The mineralogy of the concretions was slightly different at each of the three collection sites. None of the concretions contains all of the minerals, but the spatial distribution of minerals in individual concretions, overlapping mineralogies between different concretions, and the geochemical properties of the separate minerals suggest a paragenesis represented by the above order. Eh increased from the precipitation of vivianite to that of rockbridgeite/lipscombite. The precipitation of leucophosphite, then mitridatite, carbonate fluorapatite and todorokite/Fe-oxide indicates increasing pH. Concretion growth culminated with the precipitation of todorokite, a Mn oxide, and minor amounts of barite along microfractures. Conspicuously absent are Fe-sulfide and Mn-phosphate minerals. The concretions are hosted by finely laminated diatomite. The laminations exhibit little to no deformation around the concretions, requiring that the concretions formed after compaction. We interpret this sediment feature and the paragenesis as recording the evolving pore-water chemistry as the formation was uplifted into the fresh-ground-water zone.

Chemical Geology↗

USGS2007

Chapter 7 Magmatic-hydrothermal fluid interaction and mineralization in alkali-syenite nodules from the Breccia Museo pyroclastic deposit, Naples, Italy

The Breccia Museo, a pyroclastic flow that crops out in the Campi Flegrei volcanic complex (Naples, Italy), contains alkali-syenite (trachyte) nodules with enrichment in Cl and incompatible elements (e.g., U, Zr, Th, and rare-earth elements). Zircon was dated at ≈52 ka, by U-Th isotope systematics using a SHRIMP. Scanning electron microscope and electron microprobe analysis of the constituent phases have documented the mineralogical and textural evolution of the nodules of feldspar and mafic accumulations on the magma chamber margins. Detailed electron microprobe data are given for alkali and plagioclase feldspar, salite to ferrosalite clinopyroxene, pargasite, ferrogargasite, magnesio-hastingsite hornblende amphibole, biotite mica, Cl-rich scapolite, and a member (probable davyne-type) of the cancrinite group. Detailed whole rock, major and minor element data are also presented for selected nodules. A wide variety of common and uncommon accessory minerals were identified such as zircon, baddeleyite, zirconolite, pollucite, sodalite, titanite, monazite, cheralite, apatite, titanomagnetite and its alteration products, scheelite, ferberite, uraninite/thorianite, uranpyrochlore, thorite, pyrite, chalcopyrite, and galena. Scanning electron microscope analysis of opened fluid inclusions identified halite, sylvite, anhydrite, tungstates, carbonates, silicates, sulfides, and phosphates; most are probably daughter minerals. Microthermometric determinations on secondary fluid inclusions hosted by alkali feldspar define a temperature regime dominated by hypersaline aqueous fluids. Fluid-inclusion temperature data and mineral-pair geothermometers for coexisting feldspars and hornblende and plagioclase were used to construct a pressure-temperature scenario for the development and evolution of the nodules. We have compared the environment of porphyry copper formation and the petrogenetic environment constructed for the studied nodules. The suite of ore minerals observed in the nodules supports a potential for mineralization, which is similar to that observed in the alkaline volcanic systems of southern Italy (Pantelleria, Pontine Archipelago, Mt. Somma-Vesuvius).

Campi Flegrei↗

USGS1997

Strontium 87/strontium 86 as a tracer of mineral weathering reactions and calcium sources in an alpine/subalpine watershed, Loch Vale, Colorado

Sr isotopic ratios of atmospheric deposition, surface and subsurface water, and geologic materials were measured in an alpine/subalpine watershed to characterize weathering reactions and identify sources of dissolved Ca in stream water. Previous studies have noted an excess of Ca in stream water above that expected from stoichiometric weathering of the dominant bedrock minerals. Mixing calculations based on 87 Sr/ 86 Sr indicate that on an annual basis, 26 ± 7% of Ca export in streams is atmospherically derived, 23 ± 1% is from weathering of plagioclase, and the remainder is from weathering of calcite present in trace amounts in the bedrock. A potential source of error when applying Sr isotopes in catchment studies is determination of the 87 Sr/ 86 Sr of Sr released by mineral weathering, which is complicated by the wide range of mineral isotopic compositions, particularly in older rocks, and the variable rates at which the minerals weather. In this study, base-flow stream chemistry was used to represent the 87 Sr/ 86 Sr of Sr derived from mineral weathering because it effectively integrates the potentially variable isotopic composition of Sr released by weathering in the alpine environment.

Colorado↗

USGS2004

A hydrogeologic model of stratiform copper mineralization in the Midcontinent Rift System, Northern Michigan, USA

This paper presents a suite of two-dimensional mathematical models of basin-scale groundwater flow and heat transfer for the middle Proterozoic Midcontinent Rift System. The models were used to assess the hydrodynamic driving mechanisms responsible for main-stage stratiform copper mineralization of the basal Nonesuch Formation during the post-volcanic/pre-compressional phase of basin evolution. Results suggest that compaction of the basal aquifer (Copper Harbor Formation), in response to mechanical loading during deposition of the overlying Freda Sandstone, generated a pulse of marginward-directed, compaction-driven discharge of cupriferous brines from within the basal aquifer. The timing of this pulse is consistent with the radiometric dates for the timing of mineralization. Thinning of the basal aquifer near White Pine, Michigan, enhanced stratiform copper mineralization. Focused upward leakage of copper-laden brines into the lowermost facies of the pyrite-rich Nonesuch Formation resulted in copper sulfide mineralization in response to a change in oxidation state. Economic-grade mineralization within the White Pine ore district is a consequence of intense focusing of compaction-driven discharge, and corresponding amplification of leakage into the basal Nonesuch Formation, where the basal aquifer thins dramatically atop the Porcupine Mountains volcanic structure. Equilibrium geochemical modeling and mass-balance calculations support this conclusion. We also assessed whether topography and density-driven flow systems could have caused ore genesis at White Pine. Topography-driven flow associated with the Ottawan orogeny was discounted because it post-dates main-stage ore genesis and because recent seismic interpretations of basin inversion indicates that basin geometry would not be conductive to ore genesis. Density-driven flow systems did not produce focused discharge in the vicinity of the White Pine ore district.

Michigan↗

USGS1962

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↗

USGS1965

Stratigraphy and heavy minerals of the bays formation, Bays Mountain synclinorium, northeast Tennessee

The Bays Mountain synclinorium is in the Valley and Ridge province in northeast Tennessee , southwest of Kingsport and west of Greeneville. The more clastic part of the Bays formation lies in the east section of the synclinorium . The thickness of the Bays decreases from about 870 feet on the east to about 600 feet on the west. Presumably, the red beds and primary features of the Bays formation formed under deltaic conditions. A Camarocladia Zone near its base indicates a time-transgression of the Bays . The Bays is older at the base to the east than at its base to the west. The heavy minerals of the Bays were compared with those of the Cambrian and Precambrian(?) sediments, volcanic rocks, and accessory minerals of the crystalline complex which now comprise the Blue Ridge. The minerals identified include nearly all those in the Cambrian and Precambrian(?) sediments as well as additional minerals not found in these older sediments but that are in the crystalline complex. Such minerals indicate that at least a part of the crystalline complex was above sea level during the Middle Ordovician.

Tennessee↗

USGS1984

U-Th-Pb, Rb-Sr, and Ar-Ar mineral and whole-rock isotopic systematics in a metamorphosed granitic terrane, southeastern California

Mesozoic structural domes are developed in an older Proterozoic crystalline basement of granitic to granodioritic foliate metaplutonic rocks in the Halloran Hills, southeastern California. Isotopic analyses of whole rocks and mineral separates from these rocks by U-Th-Pb, Rb-Sr, and Ar-Ar techniques yield a complex pattern of discordance that is the result of a fairly simple geologic history. Individual mineral isotopic systems have variably equilibrated with each other in response to Mesozoic regional metamorphism and locally to later heating during Mesozoic batholith emplacement. Discordant U-Th-Pb zircon data indicate that the granitic core rocks are 1,710 Ma and that one dioritic phase may be slightly older. Rb-Sr whole-rock model dates scatter about 1,700 Ma Rb-Sr amphibole–whole-rock and U-Th-Pb amphibole dates are also Proterozoic. Potassium feldspars retain a 207 Pb/ 206 Pb signature of their Proterozoic age. Ar-Ar amphibole spectra from the flank of the main dome reveal disturbed dates of 1,450 Ma to 1,100 Ma, and the dates become younger toward the structurally deeper core of the dome. All remaining isotopic determinations yield Mesozoic or younger dates for mineral–whole-rock systems. Rb-Sr whole-rock–apatite–feldspar–biotite analyses show nonequilibration of strontium isotopes, with resultant mineral pair dates from 4 foliate plutonic rocks ranging from 200 to 50 Ma. No single metamorphic age is indicated by the Rb-Sr data. Rb-Sr whole-rock–biotite dates are consistently younger than any other determinations and may be reduced by weathering or gain of nonradiogenic strontium from ground water. U-Pb sphene and apatite analyses from rocks that yield 1,710-Ma zircon dates are nearly concordant at 140 Ma. An amphibole from the structurally deepest rocks of the main dome that yield 140- to 150-Ma U-Pb sphene dates has an Ar-Ar plateau date of 144 Ma. The U-Pb sphene and Ar-Ar amphibole analyses are believed to be the best age estimate for the end of the highest-temperature phase of regional metamorphism. Th-Pb sphene and apatite dates and Ar-Ar biotite dates cluster at 90 ± 5 Ma as a consequence of regional cooling during Late Cretaceous time following extensive Mesozoic plutonism in the region at 97 to 90 Ma. We interpret the discordant mineral date patterns to have resulted from metamorphism of ∼1,700-Ma plutonic rocks during the Jurassic (≥ 140–50 Ma) and subsequent uplift and cooling to ∼200 °C at about 90 Ma. On the basis of this study, the isotope dating systems ranked in decreasing order of resistance to resetting are: U-Th-Pb zircon (concordia intercept) ≥ Rb-Sr whole rock ∼Rb-Sr amphibole ∼U-Th-Pb amphibole ∼Pb-Pb whole rock > Ar-Ar amphibole ≥ Rb-Sr sphene ≥ U-Pb sphene and apatite > Rb-Sr plagioclase-potassium feldspar-apatite > Th-Pb sphene and apatite ∼Ar-Ar biotite ∼U-Pb feldspars > Rb-Sr biotite.

California↗

USGS1998

Revising U.S. Geological Survey mineral-resource assessment methods

As a result of public controversy over recommendations related to the wilderness preservation system, the U.S. Geological Survey (USGS) conducted a series of reviews of its mineral-resource assessment methods. The first review panel recommended several short- and long-term modifications to improve future mineral-resource assessments (Harris and Rieber, 1993). Implementation of some of these recommendations requires the development of new tools to augment USGS assessment procedures. The second panel identified the need to improve the classification of known mineral deposits according to USGS deposit models and to improve the delineation of areas that are favorable for the occurrence of particular mineral-deposit types (Barton and others, 1995). The panels' major recommendations, however, were to develop two new tools as a first priority -- empirical rate-of-occurrence models for important mineral-deposit types (which aid in the subjective assessment of the number of undiscovered deposits in a given area) and economic cost filters.

Information Handout↗

USGS1993

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↗

USGS2013

Hyperspectral surface materials map of quadrangle 3260, Dasht-e-Chah-e-Mazar (419) and Anar Darah (420) quadrangles, Afghanistan, showing iron-bearing minerals and other materials

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

Open-File Report↗

USGS2013

Hyperspectral surface materials map of quadrangle 3770, Faizabad (217) and Parkhaw (218) quadrangles, Afghanistan, showing iron-bearing minerals and other materials

Open-File Report↗

USGS2015

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

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

Open-File Report↗

USGS2021

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↗

USGS1996

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

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

Canadian Mineralogist↗

USGS2005

Mineral resources and consumption in the twenty-first century

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

Book chapter↗