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Analytical data, sample localities, and basic statistical data for stream-sediment, heavy-mineral-concentrate, magnetite, and rock samples collected from the Goshute Indian Reservation, Nevada and Utah
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Analytical data, sample localities, and basic statistical data for stream-sediment, heavy-mineral-concentrate, magnetite, and rock samples collected from the Goshute Indian Reservation, Nevada and Utah
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Stratiform zinc-lead mineralization in Nasina assemblage rocks of the Yukon-Tanana Upland in east-central Alaska
The Yukon-Tanana Upland of east-central Alaska and Yukon comprises thrust sheets of ductilely deformed metasedimentary and metaigneous rocks of uncertain age and origin that are overlain by klippen of weakly metamorphosed oceanic rocks of the Seventymile-Slide Mountain terrane, and intruded by post-kinematic Early Jurassic, Cretaceous and Tertiary granitoids. Metamorphosed continental margin strata in the Yukon-Tanana Upland of east-central Alaska are thought to be correlative, on the basis of stratigraphic similarities and sparse Mississippian U-Pb zircon and fossil ages (Mortensen, 1992), with middle Paleozoic metasedimentary and metavolcanic rocks in the eastern Alaska Range and in western and southeastern Yukon. Furthermore, rocks in the northern Yukon-Tanana Upland may correlate across the Tintina fault with unmetamorphosed counterparts in the Selwyn Basin (Murphy and Abbott, 1995). Volcanic-hosted (VMS) and sedimentary exhalative (sedex) massive sulfide occurrences are widely reported for these other areas (green-colored unit of fig. 1) but, as yet, have not been documented in the Alaskan part of the Yukon-Tanana Upland. Recent discoveries of VMS deposits in Devono-Mississippian metavolcanic rocks in the Finlayson Lake area of southeastern Yukon (Hunt, 1997) have increased the potential for finding VMS deposits in rocks of similar lithology and age in the Yukon-Tanana Upland of Alaska. Restoration of 450 km of early Tertiary dextral movement along the Tintina fault juxtaposes these two areas.
Geochemical data for stream-sediment, lagoon-sediment, heavy-mineral-concentrate, water, and rock samples collected in the western part of the Teller 2 x 3 degree quadrangle, Alaska
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Physical stratigraphy and mineral resources of Permian rocks in western Wyoming
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Mineral resources in Permian rocks of southwest Montana
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Ages of minerals from metamorphic and igneous rocks near Iron Mountain, Michigan
More than 100 independent isotopic ages have been determined for minerals from an area in northern Michigan about 35 miles square. Granites, pegmatites, and metamorphosed sedimentary and volcanic rocks have yielded Rb-Sr ages for feldspar, muscovite, and biotite, K-Ar ages for hornblende, muscovite, biotite, and feldspar, and U-Pb and Th-Pb ages for zircon. It was anticipated that we would learn from the measurements both the intrusive and metamorphic history of the area and would be able to place limits on the age of the Precambrian sediments in this area. The conclusions may be summarized as follows: (1) Granites and pegmatites with approximate ages of 2,700 and 1,900 m.y. have been found. (2) The major mineral -forming metamorphic event occurred between 1,800 and 2,000 m.y. ago. (3) The Precambrian sedimentary rocks called Animikie are older than 1, 900 m.y. and younger than 2,700 m.y. (4) Biotite Rb-Sr and K-Ar ages and muscovite K-Ar ages were strongly modified by the equivalent of a rise in temperature approximately 1,350 m.y. ago, although no mineral -forming event in this interval has been observed. (5) The K-Ar system was further affected by a thermal rise at about 1,100 m.y. This later event is probably recorded geologically by a few diabase dikes.The resistance to post-formation thermal events shown by the various minerals and decay systems tested may be classified as follows (lowest to highest): feldspar K-Ar, biotite K-Ar, muscovite K-Ar, biotite Rb-Sr, zircon U 238 -Pb 206 , zircon Th-Pb 208 , zircon U 235 -Pb 207 , muscovite Rb-Sr, feldspar Rb-Sr. The few hornblende K-Ar measurements indicate that the resistance of this system is about comparable to that of muscovite and feldspar Rb-Sr. The Pb 207 -Pb 206 age derived from the two U-Pb ages is somewhat more resistant to change than the feldspar Rb-Sr ages .
Contributions to Industrial-Minerals Research
Contributions to Industrial-Minerals Research, an ongoing series of U.S. Geological Survey (USGS) Bulletin chapters, presents research strategies, results, and updates of investigations of industrial minerals by USGS scientists and cooperators. Industrial minerals are defined as valuable nonmetallic, nonfuel geologic materials, generally rocks or minerals, used in a wide range of construction and industrial applications-for example, sand, gravel, and crushed rock used as aggregate for construction; limestone used for cement; phosphate for fertilizers and insecticides; and diatomite used for filtration, fillers, and abrasives. The term also comprises some processed materials, such as cement and metallic compounds with major utilization in nonmetallic forms. For example, titanium is commonly grouped with industrial minerals because more than 90 percent of it is sold and utilized in the form of the oxide (TiO2) rather than as Ti metal. Other metals and metallic compounds commonly grouped with industrial minerals include Mn, Cr, Fe oxides, and rare-earth elements (REEs).
Beyond the obvious limits of ore deposits: The use of mineralogical, geochemical, and biological features for the remote detection of mineralization
Far field features of ore deposits include mineralogical, geochemical, or biological attributes that can be recognized beyond the obvious limits of the deposits. They can be primary, if formed in association with mineralization or alteration processes, or secondary, if formed from the interaction of ore deposits with the hydrosphere and biosphere. This paper examines a variety of far field features of different ore deposit types and considers novel applications to exploration and discovery. Primary far field features include mineral and rock chemistry, isotopic or element halos, fluid pathways and thermal anomalies in host-rock sequences. Examples include the use of apatite chemistry to distinguish intrusive rocks permissive for iron oxide copper gold (IOCG) and porphyry deposits; resistate mineral (e.g., rutile, tourmaline) chemistry in exploration for volcanogenic massive sulfide (VMS), orogenic gold, and porphyry deposits; and pyrite chemistry to vector toward sedimentary exhalative (sedex) deposits. Distinctive whole-rock geochemical signatures also can be recognized as a far field feature of porphyry deposits. For example, unique Sr/Y ratios in whole-rock samples, used to distinguish barren versus fertile magmas for Cu mineralization, result from the differentiation of oxidized hydrous melts. Anomalous concentrations of halogen elements (Cl, Br, and I) have been found for distances of up to 200 m away from some mineralized centers. Variations in isotopic composition between ore-bearing and barren intrusions and/or systematic vertical and lateral zonation in sulfur, carbon, or oxygen isotope values have been documented for some deposit types. Owing to the thermal aureole that extends beyond the area of mineralization for some deposits, detection of paleothermal effects through methods such as conodont alteration indices, vitrinite or bitumen reflectance, illite crystallinity, and apatite or zircon thermochronology studies also can be valuable, particularly for deposits with a low-temperature thermal history. A number of newly investigated secondary far field features include the development of reduced columns by electrochemical processes in transported overburden, geochemical dispersion related to the expulsion of groundwater from tectonic and seismic compression, dispersion of vapor above ore deposits, and geochemical dispersion related to biological processes. Redox gradients have been found between underlying reduced and overlying oxidized environments associated with sulfide bodies, which result in mass transfer through electro-chemical dispersion. Recent studies have characterized the pH, oxidation-reduction potential (ORP), and self potential (SP) in overburden overlying sulfide-hosted gold and VMS deposits. Lateral migration of metals in groundwater is well understood from normal groundwater flow, but the processes responsible for vertical mass transfer of groundwater and its dissolved components have been recognized only recently. One process, termed cyclical dilatancy pumping, expels groundwater during and after earthquake events, which can cause the redistribution of metals around deposits in some environments. Soil gases are of interest owing to their high degree of mobility through the vadose zone in transported overburden. Numerous soil gas species (CO2, O2, Hg, Rn, He, sulfur compounds, and light hydrocarbons) have been measured and interpreted as diagnostic of some buried mineral deposits, and some evidence suggests a possible link between vapor dispersion and metal enrichment in soil. Geochemical enrichment in plant material and soils through successive growth-death cycles is well established, but the important role of microorganisms is now increasingly evident. Microorganisms significantly enhance the kinetics of sulfide oxidation and influence the distribution of metals around ore deposits. The presence of metal-resistant bacteria and enhanced concentrations of sulfate-reducing bacteria in exotic overburd
Metamorphism of Precambrian granitic xenoliths in a mica peridotite at Rose Dome, Woodson County, Kansas: Part 2, petrologic and mineralogic studies
Field, drill-core, petrographic, and mineralogic studies show that the Precambrian granitic rocks exposed on Rose Dome, Woodson County, Kansas, were emplaced as inclusions of basement rock in a mica peridotite magma that intruded the Pennsylvanian section of Rose Dome during Late Cretaceous time. High temperatures of the alkaline ultramafic magma (probably greater than 800° C) led to metamorphism of the granitic inclusions and the formation of high sanidine and high albite from original microcline and albite. Contact metamorphic effects on country rock include the development of buchite-like sanidine-magnesian biotite hornfels from Weston Shale (Pennsylvanian) that was intruded by the mica peridotite. The high temperatures of the peridotite magma also led to partial melting of the granitic rocks; a quartzofeldspathic matrix shows volcanic textures and binds mineral and rock fragments together to produce the varied range of textures and structures of the granitic xenoliths. Partial melting of the granitic rocks accounts for those features that led earlier workers to conclude that the “granite” on Rose Dome had intruded the Pennsylvanian section. Those features included xenoliths of hornfels enclosed by granitic material and apparently intrusive relationships between the granitic rocks and metamorphosed shale. The lack of concordance in the Rb-Sr ages of the granitic rocks (Part 1) may stem partly from melting of the “granite” and exchange of ions with the mica peridotite magma, from the “sampling” of different levels of granitic crust by the upwelling peridotite magma, or from weathering.
Value of domestic production of minerals from various classes of rocks
Fluids and sedimentary rocks accounted for 48 and 36 percent, respectively, of the total value of the 1946 domestic mineral production. The epigenetic (vein and replacement) and metamorphic deposits each contributed 6 percent of the total, and residual and igneous deposits accounted for 3 and 1 percent, respectively. Fuels were the most valuable of all the minerals produced--77 percent of the total. Petroleum, natural gas, and similar fluid fuels accounted for 47 percent of the total production and 98 percent of that from fluids; bituminous coal made up 24 percent of the total production and 67 percent of that from sedimentary rocks; anthracite coal was valued at 6 percent of the total production and 92 percent of that from metamorphic rocks. Exclusive of fuels, the bulk of the production of nonmetallics, and of the total mineral production too, was from sedimentary rocks (74 and 50 percent, respectively) and from veins and replacements (8 and 28 percent, respectively). Most of the production of metals, however, was from veins, etc. (62 percent) and residuum (29 percent).
Geophysical, geochemical, mineralogical, and enivronmental data for rock samples collected in a mineralized volcanic environment, upper Animas River watershed, Colorado
This report provides analyses of 90 rock samples collected in the upper Animas River watershed near Silverton, Colo., from 2001 to 2007. The samples are analyzed for geophysical, geochemical, mineralogical, and environmental rock properties of acid neutralizing capacity and net acid production. The database is derived from both published (n=68) and unpublished (n=32) data. New for all samples are geophysical measurements of electrical resistivity, density, and porosity. Rock samples were acquired from 12 geologic units that include key Tertiary volcanic and plutonic lithologies, all with varying degrees of alteration. The purpose of this study is to * provide a comprehensive and complete record of U.S. Geological Survey rock samples collected and similarly analyzed in the upper Animas River watershed for various physical, chemical, and geoenvironmental properties; * provide measurements of geophysical rock properties of lithologic units to establish ground truth with respect to watershed-scale airborne magnetic and electrical survey data; * use the data to interpret the airborne geophysical anomalies to characterize rocks in terms of acid neutralizing capacity or net acid production; and * provide measurements to study the geochemical, mineralogical, and geophysical characteristics of rocks having weak to extreme degrees of alteration and to develop an understanding of how these characteristics change with alteration type. Data are provided in two digital formats: an Arc/Info geodatabase and a Microsoft Excel spreadsheet.
Niobium and tantalum
Niobium and tantalum are transition metals that are almost always found together in nature because they have very similar physical and chemical properties. Their properties of hardness, conductivity, and resistance to corrosion largely determine their primary uses today. The leading use of niobium (about 75 percent) is in the production of high-strength steel alloys used in pipelines, transportation infrastructure, and structural applications. Electronic capacitors are the leading use of tantalum for high-end applications, including cell phones, computer hard drives, and such implantable medical devices as pacemakers. Niobium and tantalum are considered critical and strategic metals based on the potential risks to their supply (because current production is restricted to only a few countries) and the significant effects that a restriction in supply would have on the defense, energy, high-tech industrial, and medical sectors. The average abundance of niobium and tantalum in bulk continental crust is relatively low—8.0 parts per million (ppm) niobium and 0.7 ppm tantalum. Their chemical characteristics, such as small ionic size and high electronic field strength, significantly reduce the potential for these elements to substitute for more common elements in rock-forming minerals and make niobium and tantalum essentially immobile in most aqueous solutions. Niobium and tantalum do not occur naturally as pure metals but are concentrated in a variety of relatively rare oxide and hydroxide minerals, as well as in a few rare silicate minerals. Niobium is primarily derived from the complex oxide minerals of the pyrochlore group ((Na,Ca,Ce) 2 (Nb,Ti,Ta) 2 (O,OH,F) 7 ), which are found in some alkaline granite-syenite complexes (that is, igneous rocks containing sodium- or potassium-rich minerals and little or no quartz) and carbonatites (that is, igneous rocks that are more than 50 percent composed of primary carbonate minerals, by volume). Tantalum is derived mostly from the mineral tantalite ((Fe,Mn)(Ta,Nb) 2 O 6 ), which is found as an accessory mineral in rare-metal granites and pegmatites that are also enriched in lithium and cesium (termed lithium-cesium-tantalum (LCT)-type pegmatites). Brazil and Canada are the leading nations that produce niobium mineral concentrates, but Brazil is by far the leading producer, accounting for about 90 percent of production, which comes mostly from weathered material derived from carbonatites. Brazil and Canada also have the largest identified niobium resources; additional resources, although they are less well reported, occur in Angola, Australia, China, Greenland, Malawi, Russia, and South Africa. Australia and Brazil have been the leading producers of tantalum mineral concentrates, although recently Ethiopia and Mozambique have also been significant suppliers of tantalum. Artisanal mining of columbite-tantalite (also called coltan) is practiced in many countries, particularly Burundi, the Democratic Republic of the Congo (Congo [Kinshasa]), Nigeria, Rwanda, and Uganda. Brazil has about 40 percent of the identified tantalum resources; other countries and regions with identified tantalum resources include, in decreasing order of resources, Australia, Asia, Russia and the Middle East, Africa, North America, and Europe. Identified niobium and tantalum resources in the United States are small, low grade, and difficult to recover and process, and are thus not commercially recoverable at current prices. Consequently, the United States meets its current and expected future needs for niobium and tantalum through imports of primary mineral concentrates and alloys and through recovery from foreign and domestic alloy scrap that contain the metals. Environmentally, the main issues related to niobium and tantalum mining are land disruptions, the volume of waste materials and their disposal, and the radioactivity of some tailings and waste materials that contain thorium and uranium. Because of the relative biological inertness of niobium and tantalum, human and ecological health concerns are generally minimal under most natural conditions. Demand for both niobium and tantalum is expected to increase as the world economy continues to recover from the downturn that began in 2008. Increased demand for niobium is linked to increased consumption of microalloyed steel, which is used in the manufacture of cars, buildings, ships, and refinery equipment. Demand for these steels will likely increase with continued economic development in such countries as Brazil, China, and India. In addition, increased global demand for cars, cell phones, computers, superconducting magnets, and other high-tech devices will likely spur increased demand for both niobium and tantalum. The estimated global reserves and resources of niobium and tantalum are large and appear more than sufficient to meet global demand for the foreseeable future, possibly the next 500 years. The sale of “conflict coltan” attributed to rebel forces waging a civil war in Congo (Kinshasa) has been of recent concern and has highlighted the need for a transparent and traceable global supply chain that can exclude illegal columbite-tantalite from the conventional market while discerning legitimate artisanal mine production in central Africa.
A recently discovered trachyte-hosted rare earth element-niobium-zirconium occurrence in northern Maine, USA
Reported here are geological, geophysical, mineralogical, and geochemical data on a previously unknown trachyte-hosted rare earth element (REE)-Nb-Zr occurrence at Pennington Mountain in northern Maine, USA. This occurrence was newly discovered by a regional multiparameter, airborne radiometric survey that revealed anomalously high equivalent Th (eTh) and U (eU), confirmed by a detailed ground radiometric survey and by portable X-Ray fluorescence (pXRF) and whole-rock analyses of representative rock samples. The mineralized area occurs within an elongate trachyte body (~1.2 km 2 ) that intrudes Ordovician volcanic rocks. Geologic constraints suggest that the trachyte is also Ordovician in age. The eastern lobe (~900 × ~400 m) of the trachyte is pervasively brecciated with a matrix containing seams, lenses, and veinlets composed mainly of potassium feldspar, albite, and fine-grained zircon and monazite. Barite is locally abundant. Minor minerals within the matrix include columbite, bastnäsite, euxenite, chlorite, pyrite, sphalerite, and magnetite. The pXRF analyses of 22 samples (App. Table A1) collected from the eastern lobe demonstrate that this entire part of the trachyte is highly mineralized. Whole-rock geochemical analyses for samples from the eastern lobe document high average contents of Zr (1.17 wt %), Nb (1,656 ppm), Ba (3,132 ppm), Y (1,140 ppm), Hf (324 ppm), Ta (122 ppm), Th (124 ppm), U (36.5 ppm), Zn (689 ppm), and Sn (106 ppm). Among light REE, the highest average concentrations are shown by La (763 ppm) and Ce (1,479 ppm). For heavy REE (HREE), Dy and Er are the most abundant on average (167 and 114 ppm, respectively). No HREE-rich minerals such as xenotime have been identified; the HREE may reside chiefly in monazite and bastnäsite, and within the fine-grained zircon. Very strong positive correlations (R 2 ) of 0.92 to 0.98 exist between Th and Zr, Nb, Y, Ce, Yb, and Sn, indicating that the radiometric data for eTh are valid proxies for concentrations of these metals in the mineralized rocks.
Use of airborne imaging spectrometer data to map minerals associated with hydrothermally altered rocks in the northern Grapevine Mountains, Nevada, and California
Three flightlines of Airborne Imaging Spectrometer (AIS) data, acquired over the northern Grapevine Mountains, Nevada, and California, were used to map minerals associated with hydrothermally altered rocks. The data were processed to remove vertical striping, normalized using an equal area normalization, and reduced to reflectance relative to an average spectrum derived from the data. An algorithm was developed to automatically calculate the absorption band parameters band position, band depth, and band width for the strongest absorption feature in each pixel. These parameters were mapped into an intensity, hue, saturation (IHS) color system to produce a single color image that summarized the absorption band information, This image was used to map areas of potential alteration based upon the predicted relationships between the color image and mineral absorption band. Individual AIS spectra for these areas were then examined to identify specific minerals. Two types of alteration were mapped with the AIS data. Areas of quartz-sericite-pyrite alteration were identified based upon a strong absorption feature near 2.21 μm, a weak shoulder near 2.25 μm, and a weak absorption band near 2.35 μm caused by sericite (fine-grained muscovite). Areas of argillic alteration were defined based on the presence of montmorillonite, identified by a weak to moderate absorption feature near 2.21 μm and the absence of the 2.35 μm band. Montmorillonite could not be identified in mineral mixtures. Calcite and dolomite were identified based on sharp absorption features near 2.34 and 2.32 μm, respectively. Areas of alteration identified using the AIS data corresponded well with areas mapped using field mapping, field reflectance spectra, and laboratory spectral measurements.