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At least 451 records · Page 25Linked to original sources
USGS2024

Conventional rare earth element mineral deposits: The global landscape

Four conventional mineral deposit types—carbonatite, alkaline igneous, heavy mineral sand, and regolith-hosted ion-adsorption clay deposits—currently supply global markets with the rare earth elements (REEs) and rare earth oxides (REOs) necessary to meet the technological needs of global communities. The unique properties of REEs make them useful in a wide variety of applications, such as alloys, batteries, catalysts, magnets, phosphors, and polishing compounds. Rare earth element minerals are complex in both composition and structure. Carbonate, oxide, silicate, and phosphate-type minerals contain highly variable amounts of rare earths. Most rare earth-bearing minerals contain mainly lighter rare earths, a mixture of all the rare earths, or only the heavier rare earths. Diverse technological applications require the full range of light, middle, and heavy rare earths. The production of these elements, in particular the heavy rare earths, remains highly dependent on deposits from China. Diversification of rare earth supply chains is contingent on expanded knowledge of globally distributed resources and an understanding of the degree to which those resources have been explored and evaluated. The knowledge of tectonic setting, typical rock associations, deposit morphology, and deposit genesis has led to the discovery of many conventional-type rare earth deposit types. Recent developments are anticipated to result in further discoveries that have the potential to meet the ever-expanding applications of REEs and REOs to address modern societal needs.

Book chapter↗
USGS2017

Long-term flow-through column experiments and their relevance to natural granitoid weathering rates

Four pairs of fresh and partly-weathered granitoids, obtained from well-characterized watersheds—Merced River, CA, USA; Panola, GA, USA; Loch Vale, CO, USA, and Rio Icacos, Puerto Rico—were reacted in columns under ambient laboratory conditions for 13.8 yrs, the longest running experimental weathering study to date. Low total column mass losses (<1 wt. %), correlated with the absence of pitting or surface roughening of primary silicate grains. BET surface area (S BET ) increased, primarily due to Fe-oxyhydroxide precipitation. Surface areas returned to within factors of 2 to 3 of their original values after dithionite extraction. Miscible displacement experiments indicated homogeneous plug flow with negligible immobile water, commonly cited for column experiments. Fresh granitoid effluent solute concentrations initially declined rapidly, followed by much slower decreases over the next decade. Weathered granitoid effluent concentrations increased modestly over the same time period, indicating losses of natural Fe-oxide and/or clay coatings and the increased exposure of primary mineral surfaces. Corresponding (fresh and weathered) elemental effluent concentrations trended toward convergence during the last decade of reaction. NETPATH/PHREEQC code simulations indicated non-stoichiometric dissolution involving Ca release from disseminated calcite and excess K release from interlayer biotite. Effluent 87 Sr/ 85 Sr ratios reflected a progressive weathering sequence beginning and ending with 87 Sr/ 85 Sr values of plagioclase with an additional calcite input and a radiogenic biotite excursion proportional to the granitoid ages. Effluents became thermodynamically saturated with goethite and gibbsite, slightly under-saturated with kaolinite and strongly under-saturated with plagioclase, consistent with kinetically-limited weathering in which solutes such as Na varied with column flow rates. Effluent Na concentrations showed no clear trend with time during the last decade of reaction (fresh granitoids) or increased slowly with time (weathered granitoids). Analysis of cumulative Na release indicated that plagioclase dissolution achieved steady state in 3 of the 4 fresh granitoids during the last decade of reaction. Surface-area normalized plagioclase dissolution rates exhibited a narrow range (0.95 to 1.26 10 -13 moles m -2 s -1 ), in spite of significant stoichiometric differences (An 0.21 to An 0.50 ). Rates were an order of magnitude slower than previously reported in shorter duration experiments but generally 2 to 3 orders of magnitude faster than corresponding natural analogs. CrunchFlow simulations indicated that more than a hundredfold decrease in column flow rates would be required to produce near-saturation reaction affinities that would start to slow plagioclase weathering to real-world levels. Extending simulations to approximate long term weathering in naturally weathered profiles required additional decreases in the intrinsic plagioclase dissolution and kaolinite precipitation rates and relatively large decreases in the fluid flow rate, implying that exposure to reactive mineral surfaces is significantly limited in the natural environment compared to column experiments.

Geochimica et Cosmochimica Acta↗
USGS1996

Loess stratigraphy of the Lower Mississippi Valley

Loesses of the Lower Mississippi Valley (LMV) are world-famous. Sir Charles Lyell (1847), Hilgard (1860), Stafford (1869), Call (1891) and Mabry (1898), thought the LMV loess was a single water deposit although "double submergence" was noted by Call (1891) and Salisbury (1891). Shimek (1902) and Emerson (1918) recognized LMV loess as a wind deposit which came from the valley. Although wind-deposited loess gained wide acceptance, Russell (1944a) published his controversial theory of "loessification" which entailed weathering of backswamp deposits, downslope movement and recharge by carbonates to form loess. Wascher et al. (1947) identified three LMV loesses, mapped distributions and strongly supported eolian deposition. Leighton and Willman (1950), identified four loesses and supported eolian deposition as did Krinitzsky and Turnbull (1967) and Snowden and Priddy (1968), but Krinitzsky and Turnbull questioned the deepest loess. Daniels and Young (1968) and Touchet and Daniels (1970) studied the distribution of loesses in south-central Louisiana. West et al. (1980) and Rutledge et al. (1985) studied the source areas and wind directions which deposited the loesses on and adjoining Crowley's Ridge. B.J. Miller and co-workers (Miller et al., 1985, 1986, Miller and Alford, 1985) proposed that the Loveland Silt was Early Wisconsin rather than Illinoian age and advanced the name Sicily Island loess. They proposed the underlying loess was Illinoian and advanced the name Crowley's Ridge. We termed the loesses, from the surface downward, Peoria Loess, Roxana Silt, Loveland/Sicily Island loess, Crowley's Ridge Loess and Marianna loess. Researchers agree that the surfical Peoria Loess is Late Wisconsin and the Roxana Silt is Late to Middle Wisconsin, but little agreement exists on the age of the older loesses. Pye and Johnson (1988) proposed Early Wisconsin for the Loveland/Sicily Island. McKay and Follmer (1985) suggested this loess correlated with a loess under Illinoian till. Clark et al. (1989) agreed on Crowley's Ridge, but suggested the Loveland/Sicily Island loess on Sicily Island was older. Mirecki and Miller (1994) and Millard and Maat (1994) suggested an Illinoian age for the Loveland/Sicily Island loess. Miller and co-workers suggested, as did Pye and Johnson (1988), an Illinoian age for the Crowley's Ridge loess. McKay and Follmer (1985) suggested it correlated with a loess under "Kansan" till. Stratigraphy indicates the Marianna is the older of the five loesses. Researchers identified loess on both the east and west side of the LMV as well as on higher terraces within the valley. Many researchers assumed unaltered loesses were commonly yellowish brown, and silts or silt loams (West et al., 1980; Miller et al., 1986). The nonclay fraction of unweathered LMV loesses was dominated by quartz followed by carbonates, mainly dolomites, followed by feldspars, and micas. Clays were dominated by montmorillonite followed by micaceous minerals, kaolinite and vermiculite (Miller et al., 1986). Soils in the Crowley's Ridge loess are most developed, followed by the soils in the Loveland/Sicily Island which are more developed than the modern soils in the Peoria Loess. Soils in the Roxana and Marianna loesses are least developed and the Farmdale Soil of the Roxana is the weaker of the two (Miller et al., 1986). There is certainly overlapping range in the degree of soil development in the various loesses.

Engineering Geology↗
USGS1986

Geology of the Harrisonburg and Bridgewater quadrangles, Virginia

The Harrisonburg and Bridgewater quadrangles comprise an area of approximately 117 square miles in Rockingham County in northwestern Virginia.This area is in the western part of the Shenandoah Valley, a portion of the Valley and Ridge physiographic province, and contains parts of three major geologic structures-the Staunton and North Mountain thrust faults and the Massanutten synclinorium.The roeks within the two quadrangles are folded and faulted limestones, dolomites, shales, and sandstones of Paleozoic age. These rocks have been divided into groups, formations, and members that include the Elbrook and Conococheague formations (Cambrian), the Stonehenge Formation, the Beekmantown Group, the New Market Limestone, and the Lineolnshire, Edinburg, and Martinsburg formations (Ordovieian), the Massanutten Sandstone and the Bloomsburg Formation (Silurian), and probably Upper Silurian and Iower and Middle Devonian limestones and shales that are not exposed but are judged to be on Massanutten Mountain. Triassic diabase dikes and Eocene volcanic pipes intrude the Paleozoic sequence locally. Much of the sequenee is eovered by alluvium or talus of Quaternary age. Selected strata of the Cambrian and Ordovician carbonate roek sequence are sources for road aggregate, agricultural lime, concrete aggregate, dimension stone, tettazzo, portland cement, flux stone, and pellet lime. Some of the carbonate rocks may be potential sources of lead and zinc minerals. Ordovician shale formations have potential for structural clay products.

Virginia↗
USGS1989

A semiquantitative X-ray diffraction method to determine mineral composition in stream sediments with similar mineralogy

A semiquantitative X‐ray diffraction procedure has been developed that can be used to acquire reproducible mineralogic data from geographically unrelated stream‐sediment samples having similar mineralogy. Weight percentages for quartz, total‐feldspar, and total‐clay can be determined by direct comparison of intensities with standard‐mineral mixtures of known weight percent. Matrix effects and mass‐absorption differences are circumvented by taking the ratio of peak‐intensity, in counts per second, for quartz relative to that of other minerals being quantified. Mineral percentages generally are reproducible to within 10 percent.

Environmental Technology Letters↗
USGS1985

Crystalline gold in soil and the problem of supergene nugget formation: Freezing and exclusion as genetic mechanisms

Many of the world's richest gold placer deposits now occur in cold regions despite differences in their climatic history. It therefore seems possible that there may be some fundamental connection between freezing climates and the local chemical behavior of gold in the weathering cycle. This hypothesis, along with the problematical occurrence of gold as euhedral crystals in arctic gravel and soil placers, has led me to review low temperature phenomena that may bear on the geochemistry of gold. Several effects which may influence the weathering of natural gold-bearing rocks, the chemical complexation of gold, and its subsequent mobility and deposition appear to be strongly connected with freeze action. The exclusion of dissolved solutes, solute gases, and particles from ice, subjects rock and soil minerals to increased corrosion from thin, unfrozen, adsorbed water films which remain at particle surfaces throughout the freezing of rocks and soils. The preferential exclusion of cations (over anions) from growing ice crystals creates charge separations and measurable current flow across waterice phase boundaries in freezing soil — a phenomenon which leads to troublesome seasonal electrolytic corrosion of pipelines buried in soil; this phenomenon may also favor the dissolution of normally insoluble metals such as gold during geologic time periods. The ice-induced accumulation of clays, organic acids, bacteria, and other organic matter at mineral surfaces may also speed chemical attack by providing a nearby sink of alternate cation-binding sites and hence rapid removal of liberated cations from solution. The latter mechanism may be operative in both the dissolution and redeposition of gold. These physical, chemical, and electrical effects are favorable to the dissolution of rocks (in addition to frost shattering) and to the dissolution, mobilization, and redeposition of gold and other noble metals and must therefore contribute significantly to the behavior of gold at low temperatures. The occurrence of large numbers of gold placer deposits in northern Canada, Alaska, and Siberia may thus be due in part to the low temperatures common to these regions.

Precambrian Research↗
USGS2007

Type region of the Ione Formation (Eocene), central California: Stratigraphy, paleogeography, and relation to auriferous gravels

The middle Eocene Ione Formation extends over 200 miles (320 km) along the western edge of the Sierra Nevada. Our study was concentrated in the type region, 30 miles (48 km) along strike. There a bedrock ridge forms the seaward western side of the Ione depositional tract, defining a subbasin margin. The eastern limit of the type Ione is locally defined by high-angle faults. Ione sediments were spread over Upper Mesozoic metamorphic and plutonic bedrock, fed by gold-bearing streams dissecting the western slope of the ancestral Sierra Nevada. By middle Eocene time, a tropical or subtropical climate prevailed, leading to deep chemical weathering (including laterization) and a distinctively mature mineral assemblage was fed to and generated within Ione deposits. The Ione is noted for its abundant kaolinitic clay, some of it coarsely crystalline; the clay is present as both detrital grains and authigenic cement. Quartz is abundant, mostly as angular grains. Heavy mineral fractions are dominated by altered ilmenite and zircon. Distribution of feldspar is irregular, both stratigraphically and areally. Non-marine facies are most voluminous, and include conglomerates, especially at the base and along the eastern margins of the formation where they pass into Sierran auriferous gravels. Clays, grading into lignites, and gritty sands are also common facies. Both braided and meandering fluvial facies have been recognized. Shallow marine waters flooded the basin probably twice. Tongues of sediment exhibiting a variety of estuarine to marine indicators are underlain and overlain by fluvial deposits. Marine body fossils are found at only a few localities, but burrows identified as Ophiomorpha and cf. Thalassinoides are abundant in many places. Other clues to marginal marine deposition are the occurrence of glauconite in one bed, typical relations of lagoonal to beach (locally heavy-mineral-rich) lithofacies, closed-basin three-dimensional morphology of basinal facies, and high sulfur content of some marginal coals. The Ione has been said to be deltaic; however the two transgressional-regressional cycles we propose imply that only the regressional parts were deltaic. At other times, much of the type Ione would better be termed an intertidal estuary. Because the lower marine sequence was deposited against a paleobasin margin on the west, deltaic morphology was constrained, but apparently progradation was from north to south despite drainage into the basin from the east. Relations to the south are unclear due to the Stockton arch. The eastern margin of the type-Ione basin, and to some extent even its marine facies, are poorly constrained. A surface on Sierran bedrock to the east may have been stripped of some Ione basinal facies, leaving only coeval entrenched fluvial channel deposits.

California↗
USGS1991

Maps showing industrial mineral resources of the Joplin 1° x 2° quadrangle, Kansas and Missouri

This map is part of a folio of maps of the Joplin 1° X 2° quadrangle, Kansas and Missouri prepared under the Conterminuous United States Mineral Assessment Program (CUSMAP). Other publications in this folio to date include U.S. Geological Survey Miscellaneous Field Studies Map MF-2125-A (Erickson and others, 1990). Additional maps showing various geologic aspects of the Joplin quadrangle will be published as U.S. Geological Survey Miscellaneous Field Studies Maps bearing this same serial number with different letter suffixes (MF-2125-C, -D, and so on). The industrial mineral resources of the Joplin 1° X 2° quadrangle are crushed stone, dimension stone, clay and shale, construction sand and gravel (including chat, or chert-rich tailings from metal mines), and asphaltic sandstone. At present only crushed stone, clay and shale, and construction sand and gravel are of economic importance; the remainder are considered hypothetical resources. The value of industrial mineral production during 1987, the most recent year of complete data as supplied by the U.S. Bureau of Mines, was nearly $25,600,000. In terms of finished products such as cement and brick, the value is several times that amount. Figure 1 shows the annual value of industrial mineral production within the quadrangle from 1960 through 1987.

Kansas;Missouri↗
USGS2014

Local-area-enhanced, 2.5-meter resolution natural-color and color-infrared satellite-image mosaics of the Ghazni1 mineral district in Afghanistan

The U.S. Geological Survey (USGS), in cooperation with the U.S. Department of Defense Task Force for Business and Stability Operations, prepared databases for mineral-resource target areas in Afghanistan. The purpose of the databases is to (1) provide useful data to ground-survey crews for use in performing detailed assessments of the areas and (2) provide useful information to private investors who are considering investment in a particular area for development of its natural resources. The set of satellite-image mosaics provided in this Data Series (DS) is one such database. Although airborne digital color-infrared imagery was acquired for parts of Afghanistan in 2006, the image data have radiometric variations that preclude their use in creating a consistent image mosaic for geologic analysis. Consequently, image mosaics were created using ALOS (Advanced Land Observation Satellite; renamed Daichi) satellite images, whose radiometry has been well determined (Saunier, 2007a,b). This part of the DS consists of the locally enhanced ALOS image mosaics for the Ghazni1 mineral district, which has spectral reflectance anomalies indicative of clay, aluminum, gold, silver, mercury, and sulfur deposits. ALOS was launched on January 24, 2006, and provides multispectral images from the AVNIR (Advanced Visible and Near-Infrared Radiometer) sensor in blue (420-500 nanometer, nm), green (520-600 nm), red (610-690 nm), and near-infrared (760-890 nm) wavelength bands with an 8-bit dynamic range and a 10-meter (m) ground resolution. The satellite also provides a panchromatic band image from the PRISM (Panchromatic Remote-sensing Instrument for Stereo Mapping) sensor (520-770 nm) with the same dynamic range but a 2.5-m ground resolution. The image products in this DS incorporate copyrighted data provided by the Japan Aerospace Exploration Agency ((c)JAXA, 2008, 2009), but the image processing has altered the original pixel structure and all image values of the JAXA ALOS data, such that original image values cannot be recreated from this DS. As such, the DS products match JAXA criteria for value added products, which are not copyrighted, according to the ALOS end-user license agreement. The selection criteria for the satellite imagery used in our mosaics were images having (1) the highest solar-elevation angles (near summer solstice) and (2) the least cloud, cloud-shadow, and snow cover. The multispectral and panchromatic data were orthorectified with ALOS satellite ephemeris data, a process which is not as accurate as orthorectification using digital elevation models (DEMs); however, the ALOS processing center did not have a precise DEM. As a result, the multispectral and panchromatic image pairs were generally not well registered to the surface and not coregistered well enough to perform resolution enhancement on the multispectral data. Therefore, it was necessary to (1) register the 10-m AVNIR multispectral imagery to a well-controlled Landsat image base, (2) mosaic the individual multispectral images into a single image of the entire area of interest, (3) register each panchromatic image to the registered multispectral image base, and (4) mosaic the individual panchromatic images into a single image of the entire area of interest. The two image-registration steps were facilitated using an automated control-point algorithm developed by the USGS that allows image coregistration to within one picture element. Before rectification, the multispectral and panchromatic images were converted to radiance values and then to relative-reflectance values using the methods described in Davis (2006). Mosaicking the multispectral or panchromatic images started with the image with the highest sun-elevation angle and the least atmospheric scattering, which was treated as the standard image. The band-reflectance values of all other multispectral or panchromatic images within the area were sequentially adjusted to that of the standard image by determining band-reflectance correspondence between overlapping images using linear least-squares analysis. The resolution of the multispectral image mosaic was then increased to that of the panchromatic image mosaic using the SPARKLE logic, which is described in Davis (2006). Each of the four-band images within the resolution-enhanced image mosaic was individually subjected to a local-area histogram stretch algorithm (described in Davis, 2007), which stretches each band's picture element based on the digital values of all picture elements within a 500-m radius. The final databases, which are provided in this DS, are three-band, color-composite images of the local-area-enhanced, natural-color data (the blue, green, and red wavelength bands) and color-infrared data (the green, red, and near-infrared wavelength bands). All image data were initially projected and maintained in Universal Transverse Mercator (UTM) map projection using the target area's local zone (42 for Ghazni1) and the WGS84 datum. The images for the Ghazni1 area are provided as embedded geotiff images, which can be read and used by most geographic information system (GIS) and image-processing software. The tiff world files (tfw) are provided, even though they are generally not needed for most software to read an embedded geotiff image.

Ghazni1 Mineral District↗
USGS1985

Hydrogeologic appraisal of five selected aquifers in Erie County, New York

Hydrogeologic conditions and water quality at four stratified-drift aquifers and a bedrock (Onondaga Limestone) aquifer were investigated by the U.S. Geological Survey in cooperation with the Erie County Department of Environment and Planning. The Clarence-Lancaster-Newstead area includes two aquifers--one is a complex of morainal, beach, and outwash sand and gravel; the second is the underlying production aquifer in Onondage Limestone. Most wells tap the limestone aquifer. Water quality is suitable for most uses in both aquifers except for road-salt contamination at shallow wells near the New York State Thruway. A landfill on the aquifer has affected the water quality in some areas along its perimeter. The Sardinia and Springville areas each include an aquifer consisting of surficial outwash sand and gravel ranging in thickness from less than 10 feet to 95 feet. Several deeper water-bearing zones occur within till and lacustrine deposits 400 to 600 feet thick in the valleys. Ground water moves from the north and from the aquifer 's edges to the center of the valley and discharges into the main streams in the middle of the valley and to springs along the southern edge of the aquifers. Water quality is generally suitable for most uses. A landfill adjacent to the Sardinia aquifer has not significantly affected the aquifer. The Alden area includes an aquifer that consists of two sand and gravel zones separated by 10 to 20 feet of clay or till. The more productive lower zone has mineralized water derived from underlying shale.

New York↗
USGS1991

Assessing the solubilities and reaction kinetics of aluminous minerals in soils

The use of chemical thermodynamics and reaction kinetics is necessary to quantitatively model the transformation of aluminous minerals and their dissolved constituents in soils and other geochemical systems. Soils are thermodynamically open systems subject to atmospheric and biological forces and do not attain overall thermodynamic equilibrium with respect to either mass or time. However, local or partial equilibrium conditions may persist for particular minerals and their dissolved constituents. Igneous and metamorphic primary minerals break down chemically to yield disordered gels or colloids and constituent ions, which can then reorganize or precipitate to form more stable hydrous oxides, silicates, carbonates or other mineral species. Naturally-occurring iron and aluminum hydrous oxides and kaolin clays, abundant in highly weathered soils, are commonly believed to be the ultimate, stable end products of weathering reactions, but usually are thermodynamically metastable with respect to more perfectly ordered, synthetic specimens. Thermodynamic stability is no guaranty of mineral persistence; with sufficient time, even the most perfectly crystallized, stable mineral will yield to the solubilizing assault of undersaturated surface waters. All of the dissolution and precipitation reactions of soil minerals are driven by energy differences in the thermodynamic stabilities of reactants and products, and the velocities (or kinetics) of such reactions are regulated by variables of the hydrogeochemical environment.

Book chapter↗
USGS1998

Geological factors affecting the distribution of trace metals in glacial sediments of central Newfoundland

In central Newfoundland (NTS 12A/10, 15, 16, 2H/1), As, Pb, and Zn concentrations in the clay-sized (< 0.002 mm) and silt and clay-sized (< 0.063 mm) fractions of till reflect compositional differences among and within rock terranes at scales of kilometers to tens of kilometers. In those fractions, till derived from volcanic bedrock of Victoria Lake Group (Tulks Hill) is notably enriched in As (50- > 1000 ppm), exceeding levels commonly set for purposes of environmental protection. Near Pb-Zn mines at Buchans, geochemical variation with depth reflects the dispersal of detritus from mineralized bedrock, and differences in sediment type and provenance. There, surface sediments are rich in granitic debris derived from the Topsails igneous terrane 5 km north of Buchans and contain low concentrations of trace metals. These sediments are compositionally unrelated to either Buchans Group volcanic rock or an underlying, older till enriched in sulphide minerals and trace metals. Metal-rich till extending up to 10 km southwest of Buchans results from combined glacial and debris flow transport related to two distinct geological events. Trace metals are enriched (two- to fourfold) in the clay-sized fraction of till compared to the silt and clay-sized, and are associated with Al- and Mg-bearing minerals that preferentially concentrate in the clay fraction. The geochemistry of the silt and clay-sized fraction can approximate that of the < 2-mm fraction. Background variations in till illustrate the important role of a geological framework to the interpretation of geochemical surveys and the origins of trace metals in the environment.

Environmental Geology↗
USGS2005

Evolution of the magmatic-hydrothermal acid-sulfate system at Summitville, Colorado: Integration of geological, stable-isotope, and fluid-inclusion evidence

The Summitville Au-Ag-Cu deposit is a classic volcanic dome-hosted high-sulfidation deposit. It occurs in the Quartz Latite of South Mountain, a composite volcanic dome that was emplaced along the coincident margins of the Platoro and Summitville calderas at 22.5??0.5 Ma, penecontemporaneous with alteration and mineralization. A penecontemporaneous quartz monzonite porphyry intrusion underlies the district and is cut and overlain by pyrite-quartz stockwork veins with traces of chalcopyrite and molybdenite. Alteration and mineralization proceeded through three hypogene stages and a supergene stage, punctuated by at least three periods of hydrothermal brecciation. Intense acid leaching along fractures in the quartz latite produced irregular pipes and lenticular pods of vuggy silica enclosed sequentially by alteration zones of quartz-alunite, quartz-kaolinite, and clay. The acid-sulfate-altered rocks host subsequent covellite+enargite/luzonite+chalcopyrite mineralization accompanied by kaolinite, and later barite-base-metal veins, some containing high Au values and kaolinite. The presence of both liquid- and vapor-rich fluid inclusions indicates the episodic presence of a low-density fluid at all levels of the system. In the mineralized zone, liquid-rich fluid inclusions in healed fractures in quartz phenocrysts and in quartz associated with mineralization homogenize to temperatures between 160 and 390 ??C (90% between 190 and 310 ??C), consistent with the range (200-250 ??C) estimated from the fractionation of sulfur isotopes between coexisting alunite and pyrite. A deep alunite-pyrite pair yielded a sulfur-isotope temperature of 390 ??C, marking a transition from hydrostatic to lithostatic pressure at a depth of about 1.5 km. Two salinity populations dominate the liquid-rich fluid inclusions. One has salinities between 0 and 5 wt.% NaCl equivalent; the other has salinities of up to 43 wt.% NaCl equivalent. The occurrence of high-salinity fluid inclusions in vein quartz associated with mineralization, as well as in the deep stockwork veins, suggests that brines originating deep in the system transported the metals. The ??34S values of sulfides in magnetite (-2.3???) and of sulfate in apatite (5.4???) in unaltered quartz latite indicate that ??34S???S was near 0???. The ??34S values of coexisting alteration alunite and pyrite are 18.2??? to 24.5??? and -8.1??? to -2.2???, respectively. Deep in the system, most of the change in ??34S values occurs in the sulfates, indicating that the fluids were initially H2S-dominant, their redox state buffered at depth by equilibration with igneous rocks. However, in the main alteration zone, most of the change in ??34S values occurs in pyrite, indicating that the fluids moved off the rock buffer and became SO42- -dominant as pyrite precipitated and SO2 disproportionation produced the sulfuric acid requisite for acid leaching. The ??34S values of the late-stage barite and sulfides indicate that the system returned to high H2S/SO42- ratios typical of the original rock-buffered fluid. The ??DH2O of alunite parent fluids was near -45??? and their ??18O ranged from 7??? to -1???, depending on the degree of exchange in the alteration zone at low water-rock ratio, or mixing with unexchanged meteoric water. The low ??D values of some alunite samples are interpreted to result from postdepositional exchange with later ore fluids. Fluid exsolved fr om the magma at depth had ??DH2O and ??18OH2O values near -70??? and 10???, respectively. During and following migration to the top of the magma chamber, the fluid underwent isotopic exchange with the partially crystallized magma and its solid and cooler, but still plastic, carapace just below the transition from a lithostatic to hydrostatic pressure regime. These evolved magmatic fluids had ??DH2O and ??18OH2O values close to -40??? and 5???, respectively, prior to release into the superjacent hydrostatically pressured fracture zone, wherein the fluids separat

Chemical Geology↗
USGS2007

Ball clay

The article offers information on ball clay. Among the companies that mine ball clay in the U.S. are H.C. Spinks Clay, Kentucky-Tennessee Clay and Old Hickory Clay. In 2006, an estimated 1.2 million tons of the mineral was sold or used domestically and exported. Forty-percent of the total sales is accounted for ceramic floor and wall tile followed by sanitaryware and miscellaneous ceramics. Its average value was $ 45 per ton in 2006.

Mining Engineering↗
USGS1997

Epithermal mercury-antimony and gold-bearing vein lodes of southwestern Alaska

Epithermal mineral deposits and occurrences of southwestern Alaska consist of Hg-Sb and gold- and sulfide-bearing vein lodes. Numerous Hg-Sb lodes are located throughout a region measuring several tens of thousands of square kilometers in and surrounding the Kuskokwim River basin in southwestern Alaska. The Hg-Sb lodes are hosted in sedimentary rocks of the Cretaceous Kuskokwim Group, the Triassic to Cretaceous Gemuk Group, and the Paleozoic Holitna Group, as well as in Late Cretaceous and early Tertiary mafic to felsic intrusive rocks. Mineralized Hg-Sb vein and vein breccia lodes are found in the sedimentary or igneous rocks or at their contacts. The minerology of the Hg-Sb lodes is dominated by cinnabar and stibnite, with subordinate realgar, orpiment, and native mercury, pyrite, gold, and hematite, as well as solid and liquid hydrocarbons; quartz, carbonate, limonite, dickite, and sercite are alteration gangue minerals. The largest mercury mine in Alaska, Red Devil, produced about 36,000 flasks of mercury, but the Hg-Sb lodes of southwestern Alaska generally consist of small, discontinuous veins that rarely exceed a few meters in width and a few tens of meters in strike length. The Hg-Sb lodes generally contain about 1 to 5 percent Hg and less than 1 percent Sb and As but are generally poor in base emtals and precious metals. Anomalous concentrations of gold in some lodes, however, suggest that gold deposits may be present in higher temperature environments below some of the Hg-Sb lodes. The formation of the Hg-Sb lodes is closely correlated with igneous activity of a Late Cretaceous and early tertiary magmatic arc in southwestern Alaska. Geologic and geochemical characteristics of the Hg-Sb lodes suggest that ore fluids were generated in local sedimentary rocks as they were intruded by magmas. These intrusions provided the heat to initiate dehydration reactions and expel fluids from hydrous minerals and formational waters in the sedimentary rocks, causing thermal convection and hydrothermal fluid flow along fractures and faults. Isotopic data from sulfide and alteration minerals of the Hg-Sb lodes indicate multiple sources for the ore fluids; most fluids appear to have originated from local sedimentary rocks. Hydrothermal fluids with isotopically heavy oxygen but isotopically light hydrogen and sulfur compositions indicate derivation of these species from sedimentary rocks. Isotopically shifted, evolved meteoric water was a primary component in ore fluids from a few Hg-Sb lodes. Geochemical, isotopic, and fluid inclusion data also indicate that Hg, Co 2 , CH 4 , N2, and local hydrocarbons were derived from breakdown of organic matter in sedimentary rocks when they were heated by intrusions. Radiometric 40 Ar/ 39 Ar ages of 70 ± 3 Ma from hydrothermal sercites in the Hg-Sb lodes indicate a temporal association of igneous activity and mineralization, which is consistent with the geologic characteristics. Most epithermal gold-bearing vein lodes on the Alaska Peninsula and Aleutian Islands are located in Eocene to Pleistocene volcanic-arc rocks, commonly andesite and dacite. These vein and vein breccia lodes, such as the Alaska-Apollo and Shumagin deposits on Unga Island, tend to be aligned along regional, northeast-striking, steeply dipping faults and fractures. The Alaska-Apollo mine produced about 500,000 metric tons (t) of ore that yielded an estimated 3,500 kg (130,000 oz) of gold from veins that were as much as 12 m wide and extended for 1,500 m laterally and 420 m vertically. Ore minerals include gold, galena, sphalerite, chalcopyrite, pyrite, marcasite, arsenopyrite, and native copper; gangue minerals are quartz, sericite, calcite, and chlorite and locally, barsite, clay, rhodonite, and adularia. Ores generally have Au-Ag-Te-Pb-Zn-Mn-Cu geochemical signatures, with wide As-Hg aureoles around some veins. Geologic and mineralogical characteristics of these lodes are similar to adularia-sericite volcanic-hosted epithermal deposits. The gold-bearing vein lodes may be related to arc porphyry systems, but more data are required to verify this association.

Alaska↗
USGS1984

Interlaboratory comparison of mineral constituents in a sample from the Herrin (No. 6) coal bed from Illinois

Approximately 20 kg of the Herrin (No. 6) coal was collected from a strip mine in St. Clair County, Ill. A 10-kg portion was ground to -60 mesh, homogenized, and riffled into 128 splits of 70-80 g each. Homogeneity of these splits was confirmed by moisture, ash, and sulfur analyses of six randomly selected splits. Results of these analyses were within the ASTM (American Society for Testing and Materials) guidelines for interlaboratory precision. Splits of the Herrin (No. 6) coal were then transmitted to more than 30 laboratories for analysis. Low-temperature plasma oxidation was used to isolate inorganic matter for quantitative chemical and mineralogical analysis. Despite a wide variation in ashing conditions, only minor variations in ash yields were obtained; these variations were attributed to differences in operating temperature and moisture content. Mineralogical analyses of low-temperature ash (LTA) concentrates prepared by five different laboratories indicated variations within the limits of analytical error. The mean values, in weight percent, for the major minerals are as follows: calcite, 9; quartz, 20; pyrite, 23; kaolinite, 14; and illite+mixed-layer clays, 31. Normative mineralogical calculations and Fourier transform infrared analysis (FTIR) yielded results similar to those obtained from X-ray diffraction (XRD). Choosing appropriate mineral standards was found to be critical for the proper use of analytical techniques such as XRD and FTIR. Good interlaboratory agreement was obtained for most major, minor, and trace elements despite differences in analytical procedures and in the type of sample analyzed (coal, high-temperature ash, or LTA). Discrepancies between analyses for zinc, strontium, manganese, and iron may be attributed to sampling inhomogeneity problems. Mossbauer spectroscopy showed that approximately 44 percent of the pyritic sulfur was lost through weathering in the first year after preparation of the interlaboratory sample. Szomolnokite and possibly coquimbite and jarosite were also identified. Scanning electron microscopy studies indicated ubiquitous pyrite framboids and, less commonly, euhedral crystals, skeletal grains, irregularly shaped particles, and vein fillings. Minor accessory minerals such as rare-earth phosphates and possibly silicates, zircon, barium sulfate, titanium oxide, and sphalerite were also found. The textural evidence indicates that the minerals in the banded material are detrital whereas the minerals occurring as vein and pore fillings are authigenic. Magnetic measurements indicate that coal crushed in a steel pulverizer is contaminated by small quantities of abrasion fragments from the crusher, which seriously affect the measured magnetic properties of the coal.

Circular↗
USGS1950

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↗
USGS1986

Origin of the Mariano Lake uranium deposit, McKinley County, New Mexico

The Mariano Lake uranium deposit, hosted by the Brushy Basin Member of the Jurassic Morrison Formation, occurs in the Smith Lake district of the Grants uranium region, New Mexico. The orebody, contains abundant amorphous organic material, which suggests that it represents a primary-type deposit; however, the orebody is close to a regional reduction-oxidation interface, which suggests that uranium was secondarily redistributed by oxidative processes. Uranium contents correlate positively with organic carbon contents. Petrographic evidence points to uranium residence in amorphous organic material that was post- depositionally introduced in the diagenetic history of the host sandstone. Uranium mineralization was preceded by precipitation of pyrite (δ 34 S values of — 11.0 to — 38.2 per mil), mixed-layer smectite-illite clays, and quartz and potassium feldspar overgrowths; and also partial dissolution of some detrital feldspars. Alterations associated with uranium mineralization include precipitation of the organic material, microcrys- talline quartz, and pyrite and marcasite (δ 34 S values of -29.4 to -41.6 per mil), and the destruction of detrital Fe-Ti oxide grains. Following mineralization, calcite, dolomite, barite, and kaolinite were precipitated, and some iron disulfides were replaced by ferric oxides. Geochemical data and petrographic observations both indicate that the Mariano Lake orebody is a primary-type deposit. Oxidative processes have not noticeably redistributed uranium in the immediate vicinity of the deposit, nor have they greatly modified geochemical characteristics in the ore. Impedance of ground-water flow by local folds and the lower porosity characteristics of ore zones may have helped to preserve the deposit.

New Mexico↗