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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 991 records · Page 55Linked to original sources

Mass-balance-consistent geological stock accounting: A new approach toward sustainable management of mineral resources

Global resource extraction raises concerns about environmental pressures and the security of mineral supply. Strategies to address these concerns depend on robust information on natural resource endowments, and on suitable methods to monitor and model their changes over time. However, current mineral resources and reserves reporting and accounting workflows are poorly suited for addressing mineral depletion or answering questions about the long-term sustainable supply. Our integrative review finds that the lack of a robust theoretical concept and framework for mass-balance (MB)-consistent geological stock accounting hinders systematic industry-government data integration, resource governance, and strategy development. We evaluate the existing literature on geological stock accounting, identify shortcomings of current monitoring of mine production, and outline a conceptual framework for MB-consistent system integration based on material flow analysis (MFA). Our synthesis shows that recent developments in Earth observation, geoinformation management, and sustainability reporting act as catalysts that make MB-consistent geological stock accounting increasingly feasible. We propose first steps for its implementation and anticipate that our perspective as “resource realists” will facilitate the integration of geological and anthropogenic material systems, help secure future mineral supply, and support the global sustainability transition.

Environmental Science and Technology↗

A reconnaissance method for delineation of tracts for regional-scale mineral-resource assessment based on geologic-map data

The U.S. Geological Survey (USGS) is proposing to conduct a global mineral-resource assessment using geologic maps, significant deposits, and exploration history as minimal data requirements. Using a geologic map and locations of significant pluton-related deposits, the pluton-related-deposit tract maps from the USGS national mineral-resource assessment have been reproduced with GIS-based analysis and modeling techniques. Agreement, kappa, and Jaccard's C correlation statistics between the expert USGS and calculated tract maps of 87%, 40%, and 28%, respectively, have been achieved using a combination of weights-of-evidence and weighted logistic regression methods. Between the experts' and calculated maps, the ranking of states measured by total permissive area correlates at 84%. The disagreement between the experts and calculated results can be explained primarily by tracts defined by geophysical evidence not considered in the calculations, generalization of tracts by the experts, differences in map scales, and the experts' inclusion of large tracts that are arguably not permissive. This analysis shows that tracts for regional mineral-resource assessment approximating those delineated by USGS experts can be calculated using weights of evidence and weighted logistic regression, a geologic map, and the location of significant deposits. Weights of evidence and weighted logistic regression applied to a global geologic map could provide quickly a useful reconnaissance definition of tracts for mineral assessment that is tied to the data and is reproducible.

Natural Resources Research↗

Understanding key mineral supply chain dynamics using economics-informed material flow analysis and Bayesian optimization

The low-carbon energy transition requires significant increases in production for many mineral commodities. Understanding demand, technological requirements, and prices associated with this production increase requires understanding the supply chain dynamics of many minerals simultaneously, and via a consistent framework. A generalized economics-informed material flow method, global materials modeling using Bayesian optimization, captures the market dynamics of key mineral commodities. The method relies only on a limited set of widely available historical data as input, enabling quantification of economic relationships (elasticities) for supply chain components where data are sparse, and relationships cannot be obtained via traditional statistical approaches. Building upon established material flow analysis (MFA) and economic modeling techniques, Bayesian optimization was applied to fit an economics-informed MFA model to global historical demand, supply, and price for aluminum, copper, gold, lead, nickel, silver, iron, tin, and zinc. This approach enables estimates for the evolution of ore grades, mine costs, refining charges, sector-specific demand, and scrap collection for each commodity. Economic relationships were quantified and compared with a database compiled from the literature, including 1333 values from 213 analyses across 65 publications. Discrepancies in methods and limited coverage make use of these parameters in modeling efforts difficult. This work provides a single, homogeneous, probabilistic approach to identifying economic relationships across mineral supply chains, with uncertainty quantification, a literature database for comparison, and a modeling framework in which to use them. This article met the requirements for a Gold-Gold JIE data openness badge described at http://jie.click/badges .

Journal of Industrial Ecology↗

Paleomagnetic and mineral magnetic constraints on Zn-Pb ore genesis in the Pend Oreille Mine, Metaline district, Washington, USA

Zinc-lead mineralization in the Metaline mining district of northeastern Washington, USA, is hosted by the Cambrian Metaline Formation and is classified into Yellowhead-type (YO) and Josephine-type (JO) ore based on texture and mineralogy. Paleomagnetic results are reported for four Cambrian Metaline Formation sites, one Ordovician Ledbetter slate site, 12 YO and 13 JO (including two breccia sites) mineralization sites in the Pend Oreille Mine, and eight sites from the nearby Cretaceous Kaniksu granite batholith. Thermal and alternating field step demagnetization, saturation isothermal remanence analysis, and synthetic specimen tests show that the remanence in the host carbonates and Zn-Pb mineralization is carried mostly by pseudosingle (PSD) to single domain (SD) pyrrhotite and mostly by PSD to SD magnetite in the Kaniksu granite. Based on thermomagnetic measurements, sphalerite and galena concentrates and tailings from the mine's mill contain hexagonal and monoclimc pyrrhotite. The postfolding characteristic remanent magnetization (ChRM), known thermal data, and paleoarc method of dating suggest that the Zn-Pb mineralization carries a primary chemical remanent magnetization (CRM), and Metaline Formation carbonates a secondary CRM that were acquired during the Middle Jurassic (166 ??6 Ma) during the waning stages of the Nevadan orogeny. A paleomagnetic breccia test favours a solution-collapse origin for the Josephine breccia. Finally, the Kaniksu paleopole is concordant with the North American Cretaceous reference paleopole, suggesting the Kootenay terrane has not been rotated since emplacement of the batholith at ???94 Ma. ?? 2007 NRC Canada.

Canadian Journal of Earth Sciences↗

Natural calcium isotonic composition of urine as a marker of bone mineral balance

Background: We investigated whether changes in the natural isotopic composition of calcium in human urine track changes in net bone mineral balance, as predicted by a model of calcium isotopic behavior in vertebrates. If so, isotopic analysis of natural urine or blood calcium could be used to monitor short-term changes in bone mineral balance that cannot be detected with other techniques. Methods: Calcium isotopic compositions are expressed as ??44Ca, or the difference in parts per thousand between the 44Ca/40Ca of a sample and the 44Ca/ 40Ca of a standard reference material. ??44Ca was measured in urine samples from 10 persons who participated in a study of the effectiveness of countermeasures to bone loss in spaceflight, in which 17 weeks of bed rest was used to induce bone loss. Study participants were assigned to 1 of 3 treatment groups: controls received no treatment, one treatment group received alendronate, and another group performed resistive exercise. Measurements were made on urine samples collected before, at 2 or 3 points during, and after bed rest. Results: Urine ??44Ca values during bed rest were lower in controls than in individuals treated with alendronate (P <0.05, ANOVA) or exercise (P <0.05), and lower than the control group baseline (P <0.05, Mest). Results were consistent with the model and with biochemical and bone mineral density data. Conclusion: Results confirm the predicted relationship between bone mineral balance and calcium isotopes, suggesting that calcium isotopic analysis of urine might be refined into a clinical and research tool. ?? 2007 American Association for Clinical Chemistry.

Clinical Chemistry↗

Nevadaite, (Cu2+, Al, V3+)6 [Al8 (PO4)8 F8] (OH 2 (H2O)22, a new phosphate mineral species from the Gold Quarry mine, Carlin, Eureka County, Nevada: Description and crystal structure

Nevadaite, (Cu 2+ , □, Al, V 3+ ) 6 (PO 4 ) 8 F 8 (OH) 2 (H 2 O) 22 , is a new supergene mineral species from the Gold Quarry mine, near Carlin, Eureka County, Nevada, U.S.A. Nevadaite forms radiating clusters to 1 mm of prismatic crystals, locally covering surfaces more that 2 cm across; individual crystals are elongate on [001] with a length:width ratio of > 10:1 and a maximum diameter of ~30 μm . It also occurs as spherules and druses associated with colorless to purple-black fluellite, colorless wavellite, strengitevariscite, acicular maroon-to-red hewettite, and rare anatase, kazakhstanite, tinticite, leucophosphite, torbernite and tyuyamunite. Nevadaite is pale green to turquoise blue with a pale powder-blue streak and a vitreous luster; it does not fluoresce under ultra-violet light. It has no cleavage, a Mohs hardness of ~3, is brittle with a conchoidal fracture, and has measured and calculated densities of 2.54 and 2.55 g/cm 3 , respectively. Nevadaite is biaxial negative, with 1.540, β 1.548, γ 1.553, 2 V (obs.) = 76°, 2 V (calc.) = 76° , pleochroic with X pale greenish blue, Y very pale greenish blue, Z blue, and with absorption Z ≫ X > Y and orientation X = c, Y = a, Z = b. Nevadaite is orthorhombic, space group P 2 1 mn , a 12.123(2), b 18.999(2), c 4.961(1) Å, V 1142.8(2) Å 3 , Z = 1, a:b:c = 0.6391:1:0.2611 . The strongest seven lines in the X-ray powder-diffraction pattern [ d in Å(I)( hkl )] are: 6.077(10)(200), 5.618(9)(130), 9.535(8)(020), 2.983(6)(241), 3.430(4)(041), 2.661(4)(061), and 1.844(4)(352). A chemical analysis with an electron microprobe gave P 2 O 5 32.54, Al 2 O 3 27.07, V 2 O 3 4.24, Fe 2 O 3 0.07, CuO 9.24, ZnO 0.11, F 9.22, H 2 O (calc.) 23.48, OH ≡ F–3.88, sum 102.09 wt.% ; the valence states of V and Fe, and the amount of H 2 O , were determined by crystal-structure analysis. The resulting empirical formula on the basis of 63.65 anions ( including 21.65 H 2 O pfu ) is ( (Cu 2.00 2+ Zn 0.02 V 0.98 3+ Fe 0.01 3+ Al 1.15 ) ∑ 4.16 Al 8 P 7.90 O 32 [F 8.37 (OH) 1.63 ] ∑10 (H 2 O) 21.65 . The crystal structure of nevadaite was solved by direct methods and refined to an R index of 4.0% based on 1307 observed reflections collected on a four-circle diffractometer with Mo K α X-radiation . The structure consists of ordered layers of vertex-sharing octahedra and tetrahedra alternating with layers of disordered vertex-sharing and face-sharing octahedra in the b direction. [Alϕ 5 ] chains of octahedra are decorated by (PO 4 ) tetrahedra that share vertices with octahedra adjacent in the chain . These chains link in the c direction by sharing vertices between octahedra and tetrahedra to form an ordered layer of the form [Al 8 (PO 4 ) 8 F 8 (H 2 O) 8 ] . In the disordered layer, octahedra containing positionally disordered Cu 2+ , V 3+ , Al and □ (vacancy) share trans faces to form columns that link by sharing octahedron vertices to form ribbons extending in the c direction; the resulting layer has the form {(Cu 2 2+ □ 2 V 3+ ,Al) ∑6 (H 2 O) 12 (OH) 2 (H 2 O) x }, x ≈ 2 . The layers link in the b direction by sharing vertices between octahedra and tetrahedra. Although decorated chains topologically equivalent to that in nevadaite are common in many oxysalt minerals, its chain is geometrically distinct from those topologically equivalent chains. The M – M linkage along the [ M ϕ 5 ] chains in most minerals take place through trans vertices of the octahedra, with one example of linkage through cis vertices; in nevadaite, the M – M linkage involves both trans and cis vertices, as does the chain in slavíkite . In most of these decorated chains, alternate tetrahedra along the chain occur either in a trans or a cis arrangement. In nevadaite and slavíkite, the tetrahedra are arranged in both trans and cis arrangements; the arrangements in these two minerals are geometrically distinct, however.

Nevada↗

The manganese oxide minerals, a preliminary report

This paper summarizes the results obtained thus far in an intensive study of the manganese oxide minerals. X-ray powder photographs, supplemented by chemical tests, have proved to be the best means for identifying these minerals. Formulas are suggested. Physical properties and X-ray data are listed for the commoner minerals and those for which new data have been obtained. Rules of nomenclature for these minerals are suggested.

Economic Geology↗

The Schwarzwalder uranium deposit, III: Alteration, vein mineralization, light stable isotopes, and genesis of the deposit

The Schwartzwalder uranium deposit formed at 69.3 + or - 1.1 m.y. in a complex fracture system during the inception of Laramide uplift of the Front Range in Colorado. Geologic and isotopic evidence demonstrates that the ore-forming fluids were in chemical equilibrium with the Proterozoic metavolcanic and metasedimentary host-rock terrane at depth and that the metals, sulfur, and carbonate deposited in the fractures were derived from the metamorphic rocks. The data are not consistent with chemical contributions from an unrecognized magma or from the overlying Phanerozoic sedimentary rocks. The protoliths for the metamorphic rocks were submarine volcanic rocks and related volcanogenic exhalative iron-formations and chert. Water trapped along the basement faults and in the regolith between the basement and the overlying Paleozoic sedimentary rocks interacted with the metavolcanic rocks to produce isotopically heavy fluids containing high concentrations of dissolved metals and carbonate. Calculated delta 18 O values for this fluid range from 4.3 to 8.2 per mil, indicating a low water/rock ratio in the source terrane.Two stages of alteration and three stages of vein mineralization are recorded in the Schwartzwalder deposit. At the onset of Laramide faulting, fluids migrated along the fracture systems to zones of low hydraulic potential. These fluids contained CO 2 and had a metastably large K/Na ratio; they altered the gneissic wall rocks to a carbonate-sericite assemblage, adding K (super +) and CO 2 and removing SiO 2 with little or no change in volume. As the fractures continued to open, CO 2 was evolved from the fluids, increasing the pH and superimposing a hematite-adularia alteration assemblage on the earlier alteration.The veins record three stages of mineralization, the second of which generated the high-grade uranium veins. Evidence for the stage I sulfide-carbonate mineralization is poorly preserved, but isotopic and temperature data from this stage are consistent with a trend in fluid composition culminating in stage II pitchblende deposition. Sudden, large movements along the faults caused episodic evolution of CO 2 from the fluid. This loss of CO 2 decreased the solubilities of carbonates and adularia and the stabilities of sulfur species in solution. Uranyl carbonate complexes dissociated and sulfur species in solution likely reduced the uranyl ions to produce stage II pitchblende. Carbonate, adularia, and sulfides dominated the vein mineralogy after deposition of pitchblende. Progressively lower delta 18 O values in vein carbonates suggest the mixing of cooler, less evolved, perhaps meteoric, waters during the later stages of mineralization. However, the fluid pressure remained high, as indicated by explosion breccias and inward collapse features which formed as fault movements produced sudden decreases in the confining pressure. Only the stage III carbonate-iron disulfide assemblage in the major postore segment of the Illinois fault may be the product of meteoric water alone.

Economic Geology↗

Geophysical and isotopic constraints on crustal structure related to mineral trends in north-central Nevada and implications for tectonic history

We combined information from Sr and Pb isotope data and magnetotelluric models to develop a new magnetic and gravity interpretation of the crustal structure of north - central Nevada to better understand the origin of mineral trends . The new interpretation suggests a crustal structure that is composed of Precambrian continental crust, transitional crust, and primarily oceanic crust that are separated by northwest- and northeast-striking fault zones. The magnetic expression of the buried Precambrian continental crust is recognized for the first time. Low magnetic values primarily reflect magnetite-poor crystalline crust rather than elevated temperatures at depth. Northwest- and northeast-striking crustal boundaries are defined by isotopic data and abrupt gradients in gravity and magnetic data. The Carlin and Battle Mountain-Eureka mineral trends are associated with two of three northwest-striking boundaries. The Carlin boundary is primarily defined by a change in density and isotopic character of the lower to middle crust. The Battle Mountain-Eureka boundary coincides with a density contrast in the upper crust and a change in isotopic character in the lower to middle crust. Magnetotelluric models suggest that the Battle Mountain-Eureka boundary represents a crustal fault zone for most of its extent, but that deep-rooted faulting is more complex near and northwest of Battle Mountain. Crustal fault zones inferred from the magnetotelluric models near the Carlin trend are oblique to it, suggesting that they may not have been controlled by the deep boundary seen in the gravity and isotopic data. The third northwest-trending boundary is related to the western edge of the buried Precambrian continent in west- central Nevada , but lacks an associated mineral trend . A northeast-striking boundary forms the northern limit of Precambrian continental and transitional crust. The boundaries may have originated as rift or transform faults during Precambrian breakup of Rodinia or as faults accommodating lateral movements or accretion during later Paleozoic tectonic events. Comparing the crustal structure to tectonic elements produced by successively younger events shows that it had a profound influence on subsequent sedimentation, deformation, magmatism, extension, and most important, mineralization.

Nevada↗

Wangyanite, PdNi8S8, a new Pd end-member mineral of the pentlandite group from the J-M reef, Stillwater Complex, Montana, USA

Wangyanite (IMA2024-008a), ideally PdNi 8 S 8 , is a Pd end-member mineral of the pentlandite group that was discovered in the J-M reef of the Stillwater Complex, Montana, USA. Wangyanite occurs as anhedral-subhedral granular crystals 200–400 µm in size, associated with isoferroplatinum, braggite, pentlandite, and chalcopyrite interstitial to plagioclase grains within anorthosite. Wangyanite exhibits a yellowish brown color with a black streak and a metallic luster. It is brittle with uneven fractures, and has a calculated density of 5.14 g/cm 3 . The mineral does not show discernible pleochroism, bireflectance, or anisotropy. It has an average composition of 9.95 wt.% Pd, 31.95 wt.% Ni, 25.02 wt.% Fe, 0.57 wt.% Co, 31.74 wt.% S, totaling 99.23 wt.%. The empirical formula, based on eight sulfur atoms per formula unit, is (Pd 0.76 Co 0.08 ) Σ0.84 (Ni 4.39 Fe 3.60 ) Σ7.99 S 8 . Wangyanite has a cubic cell with a space group of Fm -3 m (#225), having lattice parameters of a = 10.1167(12) Å, V = 1035.4(4) Å 3 , and Z = 4. Its crystal structure has been solved by single-crystal three-dimensional electron diffraction study. The strongest X-ray diffraction lines of wangyanite are claculated at [ d in Å ( I %)( hkl )]: 5.841(14.03)(111), 3.050(100)(311), 1.947(29.16)(115,333), 1.264(11.66)(800), 3.577(8.79)(220), 2.920(20.82)(222), and 2.321(9.34)(331). Wangyanite shares the same crystal structure as pentlandite, but the octahedrally coordinated site is mainly occupied by Pd in wangyanite. Based on the textural features and previous experimental Pd-Fe-Ni-S phase system, wangyanite could form by peritectic reaction between braggite, pentlandite and sulfide liquid. These mineral associations are stable in a Ni-Pd-rich sulfide melt system at about 550 °C or even lower temperature. Therefore, wangyanite can potentially serve as an indicator of the presence of Pd-rich residual melts. The mineral is named in honor of Prof. Christina Yan Wang, a well-known researcher on platinum-group element (PGE) occurrences and enrichment mechanisms in mafic-ultramafic intrusions, notably those deposits related to the Emeishan large igneous province in China.

Montana↗

Occurrence and origin of minerals in a chamosite-bearing coal of Late Permian age, Zhaotong, Yunnan, China

The minerals found in the no.5 coal (Late Permian) from the Zhaotong Coalfield, Yunnan Province, southwestern China, have been examined and found to consist mainly of kaolinite, pyrite, chamosite, quartz, and calcite, with trace amounts of illite and mixed-layer illite-smectite. The proportion of chamosite in clay minerals ranges from 32 to 56 wt%, with an average of 46 wt%. Chamosite is distributed not only in collodetrinite, but also occurs as cell fillings in fusinite, semifusinite, and telinite. The high content and mode of occurrence of chamosite in this mine indicate its formation by interaction of kaolinite with Fe-Mg-rich fluids during early diagenesis. Except for a minor amount of terfigenous quartz, most quartz is of authigenic origin and formed from kaolinite desilication. The calcite content of the no. 5 coal is 1.4-6.3% (with an average of 3%) and is distributed in collodetrinite and as cell fillings of coal-forming plants. Calcite originated from seawater invasion during peat accumulation. Pyrite occurs in several ways: as massive, framboidal, isolated enhedral/ anhedral, and euhedral forms. In addition, the presence of a large amount of pyritized red algae provides strong evidence of seawater invasion during peat accumulation. The red algae may have played an important role in the enrichment of sulfur in the coal. The characteristic assemblage of minerals in this mine resulted from a unique basinal environment in which the mineral matter was derived from a basaltic source region, volcanic activity, and seawater transgression during coal formation.

American Mineralogist↗

Biomineralization associated with microbial reduction of Fe 3+ and oxidation of Fe 2+ in solid minerals

Iron-reducing and oxidizing microorganisms gain energy through reduction or oxidation of iron, and by doing so play an important role in the geochemical cycling of iron. This study was undertaken to investigate mineral transformations associated with microbial reduction of Fe 3+ and oxidation of Fe 2+ in solid minerals. A fluid sample from the 2450 m depth of the Chinese Continental Scientific Drilling project was collected, and Fe 3+ -reducing and Fe 2+ -oxidizing microorganisms were enriched. The enrichment cultures displayed reduction of Fe 3+ in nontronite and ferric citrate, and oxidation of Fe 2+ in vivianite, siderite, and monosulfide (FeS). Additional experiments verified that the iron reduction and oxidation was biological. Oxidation of FeS resulted in the formation of goethite, lepidocrocite, and ferrihydrite as products. Although our molecular microbiological analyses detected Thermoan-aerobacter ethanolicus as a predominant organism in the enrichment culture, Fe 3+ reduction and Fe 2+ oxidation may be accomplished by a consortia of organisms. Our results have important environmental and ecological implications for iron redox cycling in solid minerals in natural environments, where iron mineral transformations may be related to the mobility and solubility of inorganic and organic contaminants.

American Mineralogist↗

Mineral resources of Colombia (other than petroleum)

The following report summarizes data acquired during 1942-45, in Colombia, by geologists and engineers of the Foreign Economic Administration, with whom the United States Geological Survey cooperated. Twenty-nine mineral commodities are considered, but the data for five of them are scant because they were of no interest to FEA personnel. Petroleum is not considered. Preliminary to a review of individual mineral commodities, resumes are given of the general geography and geology of Colombia and of the country's mining laws. The principal mineral commodities, besides petroleum, produced in Colombia are (1) emeralds, gold, platinum, and silver, mainly for export, and (2) barite, cement, clay, coal, gypsum, salt, sand and gravel, silica, and stone, mainly for the domestic market. A large number of other mineral commodities are known in "raw" prospects, some of which may eventually become productive. Their distribution and apparent potentialities, as of 1945, are given. Factors unfavorable to mining are the ruggedness of the terrain, the scarcity of outcrops, and the very high transportation costs.

Bulletin↗

Separation and identification of the silt-sized heavy-mineral fraction in sediments

The separation of silt-sized minerals by specific gravity is made possible by using a nontoxic, heavy liquid medium of sodium polytungstate and water. Once separated, the silt-sized heavy-mineral fraction is prepared for analysis with a scanning electron microscope equipped with an automatic image analyzer and energy-dispersive spectrometer. Particles within each sample are sized and sorted according to their chemistry, and the data are tabulated in histograms and tables. Where possible, the user can define the chemical categories to simulate distinct mineral groups. Polymorphs and minerals that have overlapping compositions are combined into a group and differentiated by X-ray diffraction. Hundreds of particles can be rapidly sized and classified by chemistry. The technique can be employed on sediments from any environment.

Circular↗

International Strategic Minerals Inventory summary report; manganese

Major world resources of manganese, a strategic mineral commodity, are described in this summary report of information in the International Strategic Minerals Inventory {ISMI). ISMI is a cooperative data-collection effort of earth-science and mineral-resource agencies in Australia, Canada, the Federal Republic of Germany, the Republic of South Africa, and the United States of America. This report, designed to be of benefit to policy analysts, contains two parts. Part I presents an overview of the resources and potential supply of manganese on the basis of inventory information. Part II contains tables of some of the geologic information and mineral-resource and production data that were collected by ISMI participants.

Circular↗

Selected Geochemical Data for Modeling Near-Surface Processes in Mineral Systems

The database herein was initiated, designed, and populated to collect and integrate geochemical, geologic, and mineral deposit data in an organized manner to facilitate geoenvironmental mineral deposit modeling. The Microsoft Access database contains data on a variety of mineral deposit types that have variable environmental effects when exposed at the ground surface by mining or natural processes. The data tables describe quantitative and qualitative geochemical analyses determined by 134 analytical laboratory and field methods for over 11,000 heavy-mineral concentrate, rock, sediment, soil, vegetation, and water samples. The database also provides geographic information on geology, climate, ecoregion, and site contamination levels for over 3,000 field sites in North America.

Data Series↗

Alaska Geochemical Database (AGDB)-Geochemical data for rock, sediment, soil, mineral, and concentrate sample media

The Alaska Geochemical Database (AGDB) was created and designed to compile and integrate geochemical data from Alaska in order to facilitate geologic mapping, petrologic studies, mineral resource assessments, definition of geochemical baseline values and statistics, environmental impact assessments, and studies in medical geology. This Microsoft Access database serves as a data archive in support of present and future Alaskan geologic and geochemical projects, and contains data tables describing historical and new quantitative and qualitative geochemical analyses. The analytical results were determined by 85 laboratory and field analytical methods on 264,095 rock, sediment, soil, mineral and heavy-mineral concentrate samples. Most samples were collected by U.S. Geological Survey (USGS) personnel and analyzed in USGS laboratories or, under contracts, in commercial analytical laboratories. These data represent analyses of samples collected as part of various USGS programs and projects from 1962 to 2009. In addition, mineralogical data from 18,138 nonmagnetic heavy mineral concentrate samples are included in this database. The AGDB includes historical geochemical data originally archived in the USGS Rock Analysis Storage System (RASS) database, used from the mid-1960s through the late 1980s and the USGS PLUTO database used from the mid-1970s through the mid-1990s. All of these data are currently maintained in the Oracle-based National Geochemical Database (NGDB). Retrievals from the NGDB were used to generate most of the AGDB data set. These data were checked for accuracy regarding sample location, sample media type, and analytical methods used. This arduous process of reviewing, verifying and, where necessary, editing all USGS geochemical data resulted in a significantly improved Alaska geochemical dataset. USGS data that were not previously in the NGDB because the data predate the earliest USGS geochemical databases, or were once excluded for programmatic reasons, are included here in the AGDB and will be added to the NGDB. The AGDB data provided here are the most accurate and complete to date, and should be useful for a wide variety of geochemical studies. The AGDB data provided in the linked database may be updated or changed periodically. The data on the DVD and in the data downloads provided with this report are current as of date of publication.

Data Series↗

Mineral resource potential of the Granite Chief Wilderness Study Area, Placer County, California

A mineral resource survey of the Granite Chief Wilderness Study Area in the Tahoe National Forest and Lake Tahoe Management Area was conducted between 1979 and 1981. The mineral resource potential of the area was evaluated from geologic and geochemical studies by the U.S. Geological Survey, and from the examination of existing published and unpublished records of mining prospects and field examination of prospects, mineralized rocks, and placer deposits by the U.S. Bureau of Mines. These investigations indicate that the study area has a low potential for mineral resources. Analyses of samples taken from prospect pits, altered outcrops, and stream-sediment samples indicate no minable quantities of precious or base metals. Placer deposits are too small and too low in grade to be considered a resource. Substantial deposits of sand, gravel, and glacial till suitable for construction materials occur within the area, but their inaccessibility and remoteness from major markets preclude their being classified as a resource. No potential for oil, gas, coal, or geothermal resources was identified.

California↗