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At least 55 records · Page 3Linked to original sources
USGS1976

The weathering of sulfide ores in Shasta County, California, and its relationship to pollution associated with acid mine drainage

The West Shasta Copper-Zinc District of Shasta County, California is presently acting as a source of acid mine drainage which is entering the Shasta Lake and the Keswick Reservoirs (Nordstrom et al., 1976). The purpose of the present investigation was to study in the field the weathering of these sulfide ores and their associated wastes to elucidate the processes involved in the formation of acid mine drainage. An understanding of these processes is essential to the design of abatement projects for the district. The area investigated is illustrated in Figure 1. The detailed geology of the mining district has been summarized by Kinkel et al. (1956), whose work served as the geologic framework for this investigation. The process of sulfide weathering was examined in two distinct environments, i.e. in-situ and in waste piles associated with mining operations. A suite of 59 solid samples and associated waters were collected from various examples of the two environments. The mineral samples were studied by X-ray diffraction, reflected light microscopy, and by selective chemical analysis. The waters were studied through field measurement of pH, eH, conductivity, detailed chemical analysis by atomic absorption (D. Kirk Nordstrom, analyst), and emission spectrographic analysis of evaporates (Chris Heropoulos, analyst).

California↗
USGS1978

Principal uranium deposits of the world

The geology of the principal world uranium deposits that have identified uranium reserves and production, as described in published literature, is summarized briefly, including such features as type of deposit, host rock and age of host roc, age of mineralization, depositional environment, and mineralogy. The deposits are located on four maps with the deposit grouped according to age of host rocks?Precambrian, Paleozoic, Mesozoic, and Cenozoic?and further subdivided into types of deposits and size categories. Types of deposits are penecordant sandstone, quartz-pebble conglomerate, vein and vein-type, marine black shale, phosphate deposits, coaly carbonaceous rocks, and pegmatic and alaskitic rocks. The economically most significant deposits of uranium known in 1975 are in quartz-pebble conglomerates and sandstones, which together represented about 75 percent of the world?s total production. The largest deposits occur in quartz-pebble conglomerate at the Elliot Lake-Blind River area, Canada (average grade 0.12 percent U3O8), and at the Witwatersrand basin area in the Republic of South Africa (average grade 0.025 percent U3O8), where uranium is produced principally as a byproduct or coproduct of gold mining; and in medium-grained sandstones in the Colorado Plateau, USA (average grade 0.2 percent U3O8). Other economically significant concentrations are vein, pegmatite or contact metamorphic types, containing smaller but relatively high-grade tonnages and representing about 20 percent of the world?s total production. At Vastergotland (Billingen) and Narke in Sweden, uranium has been recovered on a pilot-plant basis from black shale deposits having an uncommonly high grade for black shale of 0.03 percent U3O8. ?Recoverable reserves? in the near future (40 year period, lifetime of nuclear plants) is on the order of 50,000 metric tons U. Over 50 percent of the world?s total uranium reserves is located on or near the trend of the iron deposits in the Precambrian iron formation, referred to as the ?iron band?.

Open-File Report↗
USGS2007

Influence of the diversion of Bear River into Bear Lake (Utah and Idaho) on the environment of deposition of carbonate minerals

Bear River, the largest river in the Great Basin, had some of its flow diverted into Bear Lake through a series of canals constructed between 1911 and 1918, turning Bear Lake into a reservoir. The prediversion lake had an unusually high Mg2+ : Ca2+ ratio (38 by weight), which resulted in precipitation of CaCO3 as aragonite. The amount and mineralogy of the carbonate did not change immediately after the diversion, but during the middle of the 20th century, high-Mg calcite began to precipitate. In contrast, at the time of diversion there were very distinct changes in the isotopic composition of the carbonate that clearly define the time of diversion within the sediments. Sediment-trap studies show that the CaCO3 polymorph that precipitates in the epilimnion of the lake today is high-Mg calcite. Samples in sediment traps placed 2 m above the bottom of the lake in 45 m of water (bottom traps) contain predominantly aragonite and quartz, with lesser amounts of high-Mg and low-Mg calcite and dolomite. Isotopic evidence from the sediments shows that the aragonite that accumulated in the bottom sediment traps and that constitutes the bulk of postdiversion sediments is reworked and redistributed from shallow sites to deep sites. ?? 2007, by the American Society of Limnology and Oceanography, Inc.

Limnology and Oceanography↗
USGS1955

Relation of uranium to hypogene mineral zoning in the Front Range mineral belt, Colorado

Many of the mining districts of the Colorado Front Range mineral belt contain mesothermal sulfide ores that exhibit a zonal distribution. Present data indicate that in most of the zoned districts pitchblende and/or secondary uranium minerals are most abundant in a transition zone between central areas containing predominantly pyritic gold ores and peripheral areas containing dominantly lead-zinc-silver deposits. Copper in the form of chalcopyrite is also probably more abundant in the transition zone than in adjacent zones. Many mineralized areas in the Front Range mineral belt are roughly co-extensive with and probably related to groups of Tertiary intrusives. The solutions that deposited sulfide and pitchblende in these areas probably were derived from many different types of source magma, but some bostonite magmas were probably particularly important sources of uranium-bearing solutions. At most localities where the relative ages of pitchblende and associated sulfides are known, the pitchblende is early in the paragenetic sequence, and not of intermediate age as suggested by its zonal position. This discrepancy may be the result of overlapping zones of deposition related to adjacent centers of mineralization, to changing environments of deposition within zones during the period of mineralization, or to unknown factors. Uranium is also present in districts in which the dominant mineralization is markedly different from the common pyritic gold-base metal sulfide mineralization. In the Jamestown district uranium appears to be associated'.mainly with fluorspar;, in other districts that exhibit little or no systematic hypogene zoning) it is ubiquitous. If uranium is present in zoned districts, a large proportion of she deposits probably should be in the transition zones. The application of this concept may be a valuable guide in prospecting for uranium.

Arizona;Colorado↗
USGS2000

Stable isotope systematics of sulfate minerals

Stable isotope studies of sulfate minerals are especially useful for unraveling the geochemical history of geological systems. All sulfate minerals can yield sulfur and oxygen isotope data. Hydrous sulfate minerals, such as gypsum, also yield oxygen and hydrogen isotope data for the water of hydration, and more complex sulfate minerals, such as alunite and jarosite also yield oxygen and hydrogen isotope data from hydroxyl sites. Applications of stable isotope data can be divided into two broad categories: geothermometry and tracer studies. The equilibrium partitioning of stable isotopes between two substances, such as the isotopes of sulfur between barite and pyrite, is a function of temperature. Studies can also use stable isotopes as a tracer to fingerprint various sources of hydrogen, oxygen, and sulfur, and to identify physical and chemical processes such as evaporation of water, mixing of waters, and reduction of sulfate to sulfide. Studies of sulfate minerals range from low-temperature surficial processes associated with the evaporation of seawater to form evaporite deposits to high-temperature magmatic-hydrothermal processes associated with the formation of base-and precious-metal deposits. Studies have been conducted on scales from submicroscopic chemical processes associated with the weathering of pyrite to global processes affecting the sulfur budget of the oceans. Sulfate isotope studies provide important information to investigations of energy and mineral resources, environmental geochemistry, paleoclimates, oceanography (past and present), sedimentary, igneous, and metamorphic processes, Earth systems, geomicrobiology, and hydrology. One of the most important aspects of understanding and interpreting the stable isotope characteristics of sulfate minerals is the complex interplay between equilibrium and kinetic chemical and isotopic processes. With few exceptions, sulfate minerals are precipitated from water or have extensively interacted with water at some time in their history. Because of this nearly ubiquitous association with water, the kinetics of isotopic exchange reactions among dissolved species and solids are fundamental in dictating the isotopic composition of sulfate minerals. In general, the heavier isotope of sulfur is enriched in the higher oxidation state, such that under equilibrium conditions, sulfate minerals (e.g. barite, anhydrite) are expected to be enriched in the heavy isotope relative to disulfide minerals (e.g. pyrite, marcasite), which in turn are expected to be enriched relative to monosulfide minerals (e.g. pyrrhotite, sphalerite, galena) ( Sakai 1968 , Bachinski 1969 ). The kinetics of isotopic exchange among minerals with sulfur at the same oxidation state, such as sphalerite, and galena, are such that equilibrium is commonly observed. In contrast, isotopic equilibrium for exchange reactions between minerals of different oxidation states depends on factors such as the pH, time and temperature of reaction, the direction of reaction, fluid composition, and the presence or absence of catalysts ( Ohmoto and Lasaga 1982 ). The kinetics of oxygen isotope exchange between dissolved sulfate and water are extremely sluggish. Extrapolation of the high-temperature (100 to 300°C) isotopic exchange kinetic data of Chiba and Sakai (1985) to ambient temperatures suggests that it would take several billions of years for dissolved sulfate and seawater to reach oxygen isotopic equilibrium. In contrast, the residence time of sulfate in the oceans is only 7.9 million years ( Holland 1978 ). However, at higher temperatures (>200°C), oxygen isotopic exchange is sufficiently rapid to permit application of sulfate isotope geothermometry to geothermal systems and hydrothermal mineral deposits. In general, equilibrium prevails at low pH and high temperatures, whereas kinetic factors preclude equilibrium at low temperatures even at low pH. Thus, the sluggish kinetics of sulfur and oxygen isotope exchange reaction at low temperatures impair the use of these isotopes to understand the conditions of formation of sulfate minerals in these environments. However, because of these slow kinetics, the oxygen and sulfur isotopic compositions of sulfate minerals may preserve a record of the sources and processes that initially produced the dissolved sulfate, because the isotope ratios may not re-equilibrate during fluid transport and mineral precipitation. The first part of this chapter is designed to provide the reader with a basic understanding of the principles that form the foundations of stable isotope geochemistry. Next, an overview of analytical methods used to determine the stable isotope composition of sulfate minerals is presented. This overview is followed by a discussion of geochemical processes that determine the stable isotope characteristics of sulfate minerals and related compounds. The chapter then concludes with an examination of the stable isotope systematics of sulfate minerals in a variety of geochemical environments.

Reviews in Mineralogy and Geochemistry↗
USGS2005

Geochemistry of sulfate minerals in high- and low-temperature environments: A tribute to Robert O. Rye

This special issue is a tribute to Robert O. Rye, known as "Bob" to most, in light of his highly productive and ongoing career. Almost all of the papers in this issue are derived from topical sessions on sulfate minerals in hydrothermal and low-temperature environments. The sessions, held at the 2000 Geological Society of America meeting in Reno, NV, and sponsored jointly by the Mineralogical Society of America, the Society of Economic Geologists and the Geochemical Society, included 29 oral and 9 poster presentations. The sessions complemented a short course on the crystallography, geochemistry and environmental significance of sulfate minerals, sponsored by the Mineralogical Society of America and the Geochemical Society, which immediately preceded the meeting (Alpers et al., 2000). The 23 papers in this special issue typify the breadth of Bob Rye’s research in this important area of geochemistry.

Chemical Geology↗
USGS2011

Annotated bibliography of environmentally relevant investigations of uranium mining and milling in the Grants Mineral Belt, northwestern New Mexico

Studies of the natural environment in the Grants Mineral Belt in northwestern New Mexico have been conducted since the 1930s; however, few such investigations predate uranium mining and milling operations, which began in the early 1950s. This report provides an annotated bibliography of reports that describe the hydrology and geochemistry of groundwaters and surface waters and the geochemistry of soils and sediments in the Grants Mineral Belt and contiguous areas. The reports referenced and discussed provide a large volume of information about the environmental conditions in the area after mining started. Data presented in many of these studies, if evaluated carefully, may provide much basic information about the baseline conditions that existed over large parts of the Grants Mineral Belt prior to mining. Other data may provide information that can direct new work in efforts to discriminate between baseline conditions and the effects of the mining and milling on the natural environment.

New Mexico↗
USGS1959

Ion exchange in clays and other minerals

Ion exchange in clays and other minerals is dependent on the crystalline structure of the mineral and on the chemical composition of any solution in contact with the mineral. The structures of clay minerals and zeolites are briefly described to provide a background for the discussion of their ion-exchange reactions. Ion exchange in these minerals is a reversible chemical reaction that takes place between ions held near a mineral surface by unbalanced electrical charges within the mineral framework and ions in a solution in contact with the mineral. Generally the excess charge on the mineral is negative, and it attracts cations from the solution to neutralize this charge. The chemical reactions in ion exchange follow the law of mass action, but the reactions are restricted by the number of exchange sites on the mineral and by the strength of the bonding of the exchangeable cations to the mineral surface. Titration of H-clays with bases shows that montmorillonites and "illites" behave like a mixture of two or three different acids, whereas kaolinite, with an indefinite number of exchange sites, behaves like an indefinite number of acids. Ion-exchange capacity is measured in chemical equivalents of base adsorbed at pH 7. Each clay mineral has a range of exchange capacities because of differences in structure and in chemical composition. The ranges (in milliequivalents per 100 grams) are kaolinite, 3-15; halloysite (2H 2 O), 5-10; halloysite (4H 2 O), 40-50; montmorillonite, 70-100; "illite," 10-40; vermiculite, 100-150; glauconite, 11-20; attapulgite, 20-30; and allophane, 70. The common metallic cations found in exchange positions in clay minerals are Ca +2 , Mg +2 , Na + , and K + . At low pH values H + replaces other cations. The order of replaceability of the common cations has been found to be: Li + < Na + < K + < Rb + < Cs + and Mg +2 < Ca+2 < Sr +2 < Ba +2 Bivalent cations enter the exchange sites preferentially to univalent cations. The common exchangeable cation in most clay minerals in soils is Ca +2 . Other exchange phenomena discussed are anion exchange, fixation of cations and anions by clay minerals, effect of environment on cation exchange, and the exchange capacity of zeolites, of rocks, of other minerals, of organic matter and organic complexes, and of amorphous mineral material.

GSA Bulletin↗
USGS1982

Water resources inventory of Connecticut Part 10: Lower Connecticut River basin

The lower Connecticut River basin study area in south-central Connecticut includes 639 square miles and is drained principally by the Connecticut River and by seven smaller streams that flow directly to Long Island Sound between the West River on the west and the Connecticut River on the east. The population in 1979 was estimated to be 210,380. Much of the industrial development and population centers are in the Mattabesset River basin in the northwestern part, and the largest water use is also in the Mattabesset River basin. Precipitation averages 47 inches per year and provides an abundant supply of water. About 20 inches returns to the atmosphere as evapotranspiration, and the remainder either flows directly to streams or percolates to the water table, eventually discharging to Long Island Sound. Small quantities of water are exported from the basin by the New Haven and Meridan Water Departments, and small quantities are imported by the New Britain Water Department and Metropolitan Direct Commission. Precipitation during 1931-60 resulted in an average annual runoff of 302 billion gallons. In inflow from the Connecticut River is added to the average annual runoff, the 4,370 billion gallon s per year is potentially available for water ue. The domestic, institutional, commercial, and industrial (other than cooling water) water use for 1970 was 7 billion gallons, which is only 3 percent of the total water used, whereas 97 percent of the total is cooling water for power plants. Approximately 60 percent of the 7 billion gallons is treated before being discharged back to the streams. The total amount of fresh water used during 1970 was estimated to be 256,000 million gallons (Mgal), of which 247,000 Mgal was used for cooling water at stream electric-generating plants. The quantity for domestic, commercial, industrial, and agricultural used was 9,000 Mgal, which was approximately 120 gallons a day per person. Public water systems providing 70 percent of these requirement and all the systems supplying water met the drinking water standards of the Connecticut General Assembly (1975). Till is widespread and generally provides only small amounts of water. Wells in till normally yield only a few hundred gallons of water daily and may be inadequate during dry periods. The thickness of of till ranges from 0 to 15 feet; a median thickness of 26 feet is estimated from information provided in drillers' logs of 467 wells penetrating underlying bedrock. The till is generally used only as an emergency or secondary source of water. Bedrock aquifers underlie the entire area and include sedimentary and crystalline (igneous and metamorphic) rock types. These aquifers supply small and usually reliable quantities of water to wells and are the chief source of water for many rural homes and farms., About 90 percent of the wells tapping bedrock yield at least 2 gal/min. The median yields from wells tapping aquifers in sedimentary, igneous, and metamorphic rocks are 11, 8, and 6.5 gal/min, respectively. The quantity of water potentially available from stratified drift was estimated on the basis of hydraulic characteristics of the aquifers, mathematical modeling of the aquifer system, and evaluation of natural and induced recharge. Long-term yields estimated or ten areas underlain by significant thickness of stratified drift range from 0.4 to 4.4 million gallons per day (Mgal/d). A change in well spacing or numbering could increase the long-term yields, but detailed modeling verification studies are needed to confirm optimal well locations. The chemical and physical (turbidity, color, taste, and sediment load) quality of water is good. The water if generally low in dissolved solids and is classified as soft to hard. Surface water is less mineralized than ground water, especially during high flow, when it is primarily derived from surface runoff rather than groundwater runoff. A median dissolved-solids concentration of 42 milligrams per liter (mg/L) and median hardness of 18 mg/L were determined from water samples collected from 26 streams during the high-flow period. During the low-flow period, median dissolved-solids concentration of 61 mg/L and median hardness of 27 mg/L were determined from sample from the same streams. The quality of water in stratified-drift and crystalline-rock aquifers is generally better than that in the sedimentary-rock aquifers. Water from 32 wells tapping stratified drift had median dissolved-solids concentrations of 116 mg/L; and 33 wells tapping stratified drift and 42 tapping crystalline rock had median hardness of 73 mg/L and 68 mg/L, respectively. Water from 32 wells tapping sedimentary rock had median dissolved concentrations of 231 and 156 mg/L, respectively. Sedimentary rock generally yields the hardest water. Iron and manganese occur objectionable concentrations in places, particularly in water from streams draining swamps and in water from aquifers either rich in iron and manganese-nearing minerals or where the reducing environment for solution of these minerals is favorable. Concentrations of iron in excess of 0.3 mg/L were found in 35 percent of the high streamflow samples, and in 45 percent of the ground-water samples. Most of the high iron and manganese concentration in streams and aquifers are found east of the Connecticut River. Human activities and tidal influence along the coast have modified the quality of water in much f the study area. The greatest influence from human activities has been in the northwestern part, in the Mattabesset River basin. There, the quality of water has been affected by domestic and animal wastes, which cause high dissolved-solids concentrations, high nitrate and phosphate loads and high bacterial counts. In the entire area, high nitrate in groundwater occur only locally, and its presence in an individual water supply is chiefly a function of its proximity to sources of contamination, of well construction, and of thickness of overburden. Thirty public-supply wells did have water that had high sodium concentrations or objectionable iron and manganese concentrations, but these are not considered health hazards in the concentrations found in the water samples. Streams, wetlands, and some aquifers along the sough boundary of the basin contain salty water because of tidal movement or extensive ground-water withdrawals. High sediment concentrations also occur as a result of tidal influence in this area.

Connecticut↗
USGS2010

Fluorine, fluorite, and fluorspar in central Colorado

Fluorine (F) is a widespread element that was deposited in a variety of rocks, minerals, and geologic environments in central Colorado. It occurs as a trace element, as a major component of the mineral fluorite (CaFs), and as a major economic source of fluorine in fluorspar deposits, which are massive concentrations of fluorite. This study has compiled available geochemical analyses of rocks, both unmineralized and mineralized, to determine the distribution of fluorine in specific age-lithologic categories, ranging from 1.8-giga-annum (Ga) metamorphic rocks to modern soils, throughout central Colorado. It also draws upon field studies of fluorine-rich mineral deposits, including fluorspar deposits, to decipher the nearly two-billion-year-long geologic history of fluorine in the study area, with implications for mineral-resource evaluations and exploration. The resulting compilation provides an important inventory of the naturally occurring levels and sources of fluorine that ultimately weather, erode, and become part of surface waters that are used for domestic water supplies in densely populated areas along the Colorado Front Range. Most commonly, fluorine is a trace element in virtually all rocks in the region. In the 3,798 unmineralized rocks that were analyzed for fluorine in the study area, the average fluorine content was 1,550 parts per million (ppm). The median was 640 ppm, nearly identical to the average crustal abundance of 650 ppm, and some high-fluorine rocks in the Pikes Peak area skewed the average to a value much greater than the median. Most unmineralized age-lithologic rock suites, including Proterozoic metamorphic rocks, 1.7- and 1.4-Ga granitic batholiths, Cambrian igneous rocks, Phanerozoic sedimentary rocks, and Laramide and Tertiary igneous rocks, had median fluorine values of 400 to 740 ppm fluorine. In all suites, however, a small number of analyzed samples contained more than 1 percent (10,000 ppm) fluorine. The 1.1-Ga plutonic rocks related to the Pikes Peak batholith had a mean fluorine content of 1,700 ppm, and primary magmatic fluorite and fluorite-bearing pegmatites are common throughout that igneous mass. Fluorine was deposited in many types of economic mineral deposits in central Colorado, and it currently is a significant trace element in some thermal springs. In the fluorspar deposits, fluorine contents were as high as 37 percent. Some fluorine-rich porphyry systems, such as Jamestown, had fluorine values that ranged from 200 ppm to nearly 37 percent fluorine, and veins in other deposits contained hydrothermal fluorite, although it was not ubiquitous. For the 495 samples from non-fluorspar mining districts (and excluding Jamestown), however, the median fluorine content was 990 ppm. This is above the crustal average but still relatively modest compared to the fluorspar deposits, and it indicates that the majority of the mineralizing systems in central Colorado did not deposit large amounts of fluorine. Nevertheless, the fluorine- and fluorite-rich mineral deposits could be used as guides for the evaluation and discovery of related but concealed porphyry and epithermal base- and precious-metal deposits. The Cenozoic geologic history of central Colorado included multiple periods during which fluorine-bearing rocks and mineral deposits were exposed, weathered, and eroded. This protracted history has released fluorine into soils and regoliths, and modern rainfall and snowmelt interact with these substrates to add fluorine to the hydrosphere. This study did not evaluate the fluorine contents of water or make any predictions about what areas might be major sources for dissolved fluorine. However, the abundant data that are available on fluorine in surface water and ground water can be coupled with the results of this study to provide additional insight into natural sources of fluorine in domestic drinking water.

Scientific Investigations Report↗
USGS2005

Secondary sulfate minerals associated with acid drainage in the eastern US: Recycling of metals and acidity in surficial environments

Weathering of metal-sulfide minerals produces suites of variably soluble efflorescent sulfate salts at a number of localities in the eastern United States. The salts, which are present on mine wastes, tailings piles, and outcrops, include minerals that incorporate heavy metals in solid solution, primarily the highly soluble members of the melanterite, rozenite, epsomite, halotrichite, and copiapite groups. The minerals were identified by a combination of powder X-ray diffraction (XRD), scanning electron microscopy (SEM), and electron-microprobe. Base-metal salts are rare at these localities, and Cu, Zn, and Co are commonly sequestered as solid solutions within Fe- and Fe-Al sulfate minerals. Salt dissolution affects the surface-water chemistry at abandoned mines that exploited the massive sulfide deposits in the Vermont copper belt, the Mineral district of central Virginia, the Copper Basin (Ducktown) mining district of Tennessee, and where sulfide-bearing metamorphic rocks undisturbed by mining are exposed in Great Smoky Mountains National Park in North Carolina and Tennessee. Dissolution experiments on composite salt samples from three minesites and two outcrops of metamorphic rock showed that, in all cases, the pH of the leachates rapidly declined from 6.9 to <3.7, and specific conductance increased gradually over 24 h. Leachates analyzed after 24-h dissolution experiments indicated that all of the salts provided ready sources of dissolved Al (>30 mg L-1), Fe (>47 mg L-1), sulfate (>1000 mg L-1), and base metals (>1000 mg L-1 for minesites, and 2 mg L-1 for other sites). Geochemical modeling of surface waters, mine-waste leachates, and salt leachates using PHREEQC software predicted saturation in the observed ochre minerals, but significant concentration by evaporation would be needed to reach saturation in most of the sulfate salts. Periodic surface-water monitoring at Vermont minesites indicated peak annual metal loads during spring runoff. At the Virginia site, where no winter-long snowpack develops, metal loads were highest during summer months when salts were dissolved periodically by rainstorms following sustained evaporation during dry spells. Despite the relatively humid climate of the eastern United States, where precipitation typically exceeds evaporation, salts form intermittently in open areas, persist in protected areas when temperature and relative humidity are appropriate, and contribute to metal loadings and acidity in surface waters upon dissolution, thereby causing short-term perturbations in water quality.

Chemical Geology↗
USGS1978

Iron-titanium oxide minerals and associated alteration phases in some uranium-bearing sandstones

Detrital iron-titanium (Fe-Ti) oxide minerals of the ulvospinel-magnetite (titanomagnetite) and ilmenite-hematite (titanohematite) solid solution series are common in uranium-bearing sandstones. Alteration of Fe-Ti oxide minerals in oxidizing environments formed secondary products (primarily hematite) that are distinct from those produced under reducing conditions (iron disulfide minerals). Oxidation of sulfidized Fe-Ti oxide minerals, by the processes that formed uranium rolls, produced ferric oxide minerals (limonite) having textures that mimic those of the iron disulfides. Titanomagnetite and titanohematite have been severely depleted in the ore-bearing zones of some uranium deposits. The alteration of detrital Fe-Ti oxide minerals near uranium ore deposits may produce characteristic signatures in the magnetization of the sandstone. Knowledge of the distribution and magnetic properties of these minerals can aid in interpreting data from total magnetic-field and magnetic-susceptibility surveys of uranium deposits.

Colorado, New Mexico, Texas, Wyoming↗
USGS2004

Mineral stimulation of subsurface microorganisms: release of limiting nutrients from silicates

Microorganisms play an important role in the weathering of silicate minerals in many subsurface environments, but an unanswered question is whether the mineral plays an important role in the microbial ecology. Silicate minerals often contain nutrients necessary for microbial growth, but whether the microbial community benefits from their release during weathering is unclear. In this study, we used field and laboratory approaches to investigate microbial interactions with minerals and glasses containing beneficial nutrients and metals. Field experiments from a petroleum-contaminated aquifer, where silicate weathering is substantially accelerated in the contaminated zone, revealed that phosphorus (P) and iron (Fe)-bearing silicate glasses were preferentially colonized and weathered, while glasses without these elements were typically barren of colonizing microorganisms, corroborating previous studies using feldspars. In laboratory studies, we investigated microbial weathering of silicates and the release of nutrients using a model ligand-promoted pathway. A metal-chelating organic ligand 3,4 dihydroxybenzoic acid (3,4 DHBA) was used as a source of chelated ferric iron, and a carbon source, to investigate mineral weathering rate and microbial metabolism. In the investigated aquifer, we hypothesize that microbes produce organic ligands to chelate metals, particularly Fe, for metabolic processes and also form stable complexes with Al and occasionally with Si. Further, the concentration of these ligands is apparently sufficient near an attached microorganism to destroy the silicate framework while releasing the nutrient of interest. In microcosms containing silicates and glasses with trace phosphate mineral inclusions, microbial biomass increased, indicating that the microbial community can use silicate-bound phosphate inclusions. The addition of a native microbial consortium to microcosms containing silicates or glasses with iron oxide inclusions correlated to accelerated weathering and release of Si into solution as well as the accelerated degradation of the model substrate 3,4 DHBA. We propose that silicate-bound P and Fe inclusions are bioavailable, and microorganisms may use organic ligands to dissolve the silicate matrix and access these otherwise limiting nutrients.

Chemical Geology↗
USGS1961

Some aspects of the geochemistry of sphalerite, Central City District, Colorado

Detailed studies of sphalerite , as a part of a larger study of the Central City district , Colorado , have been undertaken to learn something of the physico-chemical environment of ore deposition. More than 90 samples have been analyzed by chemical and spectrochemical methods and these data are interpreted in the light of experimental information. Sphalerite is a widespread and moderately abundant constituent of the gold- and silver-rich veins of the district . It was deposited during one stage of mineralization, in all environments of the concentrically zoned district except in the core. On a district -wide basis it occurs in three mineral assemblages: sphalerite -pyrite- chalcopyrite-tennantite-galena, sphalerite -pyrite-tennantite-galena, and sphalerite -pyrite-enargite-tennan-tite-galena. Quartz and, locally, other gangues are present.The sphalerite samples contain from 12 to 0.05 weight percent iron and detectable amounts of a restricted suite of minor elements, principally manganese, cadmium, copper, and lead. Manganese correlates directly with iron content, but the other minor elements have random correlations.The iron content of Central City sphalerite is interpreted to be mainly a function of activity of sulfur and temperature. Total pressure and minor elements that may enter the structure of either sphalerite or coexisting pyrite are thought to have negligible effects on the amount of iron in the sphalerite .The iron content of the sphalerite and fluid inclusion studies indicate that mineralization occurred over a temperature range from at least 620° C to about 150° C. In general, the temperatures tended to decrease from the vicinity of the central zone outward toward the peripheral zone. The thermal pattern, however, was complex, and marked by local irregularities.The activity of sulfur decreased with temperature, but to an extent such that more sulfur-rich mineral assemblages could form toward the margins of the district .The minor-element content of the sphalerite is governed by the activities of the various components and by the ability of the host mineral to accomodate it. Manganese varies widely because (1) it is geochemically much more abundant than is zinc and (2) it can also enter other minerals on a large scale. Conversely, because the amount of cadmium is small relative to that of zinc and because it enters only sphalerite in quantitatively significant amounts in hydrothermal environments, the cadmium content of sphalerite is constant. The copper content of the sphalerites is low and in good agreement with recent experimental data of Priestley Toulmin 3d.

Colorado↗
USGS2007

Surface-water, ground-water, and sediment geochemistry of epizonal and shear-hosted mineral deposits in the Tintina Gold Province--Arsenic and antimony distribution and mobility

Epigenetic mineral deposits in the Tintina Gold Province are generally characterized by high concentrations of arsenic and antimony in their mineral assemblage. A total of 347 samples (ground water, surface water, and stream sediment) were collected to investigate the distribution and mobility of arsenic and antimony in the environment near known mineral deposits. Samples were collected from east to west at Keno Hill and Brewery Creek, Yukon, Canada; and Cleary Hill, True North, Scrafford Mine, Fairbanks, Ryan Lode, Stampede Creek, Slate Creek, and Donlin Creek, all in Alaska. Surface- and ground-water samples are all slightly acidic to near-neutral in pH (5-8), have a wide range in specific conductance (surface water 17-2,980 microsiemens per centimeter and ground water 170-2,940 microsiemens per centimeter), and show elevated dissolved arsenic and antimony concentrations (arsenic in surface water is less than 1 to 380 micrograms per liter and in ground water is less than 1 micrograms per liter to 1.5 milligrams per liter; antimony in surface water is less than 2 to 660 micrograms per liter and in ground water is less than 2 to 60 micrograms per liter). Stream sediments downstream from these deposits have high concentrations of arsenic and antimony (arsenic median is 1,670 parts per million, maximum is 10,000 parts per million; antimony median is 192 parts per million, maximum is 7,200 parts per million). The mobility of arsenic and antimony is controlled by the local redox environment, with arsenic being less mobile in oxidized surface waters relative to antimony, and arsenic more mobile in reduced ground water. These factors suggest that both antimony and arsenic may be useful pathfinder elements in water and sediment for targeting similar style deposits elsewhere in the Tintina Gold Province.

Alaska, Yukon↗
USGS2000

Regional Crustal Structures and Their Relationship to the Distribution of Ore Deposits in the Western United States, Based on Magnetic and Gravity Data

Upgraded gravity and magnetic databases and associated filtered-anomaly maps of western United States define regional crustal fractures or faults that may have guided the emplacement of plutonic rocks and large metallic ore deposits. Fractures, igneous intrusions, and hydrothermal circulation tend to be localized along boundaries of crustal blocks, with geophysical expressions that are enhanced here by wavelength filtering. In particular, we explore the utility of regional gravity and magnetic data to aid in understanding the distribution of large Mesozoic and Cenozoic ore deposits, primarily epithermal and porphyry precious and base metal deposits and sediment-hosted gold deposits in the western United States cordillera. On the broadest scale, most ore deposits lie within areas characterized by low magnetic properties. The Mesozoic Mother Lodge gold belt displays characteristic geophysical signatures (regional gravity high, regional low-to-moderate background magnetic field anomaly, and long curvilinear magnetic highs) that might serve as an exploration guide. Geophysical lineaments characterize the Idaho-Montana porphyry belt and the La Caridad-Mineral Park belt (from northern Mexico to western Arizona) and thus indicate a deep-seated control for these mineral belts. Large metal accumulations represented by the giant Bingham porphyry copper and the Butte polymetallic vein and porphyry copper systems lie at intersections of several geophysical lineaments. At a more local scale, geophysical data define deep-rooted faults and magmatic zones that correspond to patterns of epithermal precious metal deposits in western and northern Nevada. Of particular interest is an interpreted dense crustal block with a shape that resembles the elliptical deposit pattern partly formed by the Carlin trend and the Battle Mountain-Eureka mineral belt. We support previous studies, which on a local scale, conclude that structural elements work together to localize mineral deposits within regional zones or belts. This study of mineral deposits of the western United States demonstrates the ability of magnetic and gravity data to elucidate the regional geologic framework or structural setting and to contribute in locating favorable environments for hydrothermal mineralization.

Economic Geology↗
USGS2016

U.S. Geological Survey Mineral Resources Program—Mineral resource science supporting informed decisionmaking

The USGS Mineral Resources Program (MRP) delivers unbiased science and information to increase understanding of mineral resource potential, production, and consumption, and how mineral resources interact with the environment. The MRP is the Federal Government’s sole source for this mineral resource science and information. Program goals are to (1) increase understanding of mineral resource formation, (2) provide mineral resource inventories and assessments, (3) broaden knowledge of the effects of mineral resources on the environment and society, and (4) provide analysis on the availability and reliability of mineral supplies.

Fact Sheet↗
USGS2007

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↗