SEARCH · Search USGS

Results for “Minerals and the Environment”

Search indexed USGS publications on groundwater, aquifers, geologic maps, mineral resources and earthquakes. Explore source records by subject and place.

SourceResearch connectionFrom yearThrough year

Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.

At least 145 records · Page 8Linked to original sources

USGS2003

Preliminary Mineralogic and Stable Isotope Studies of Altered Summit and Flank Rocks and Osceola Mudflow Deposits on Mount Rainier, Washington

About 5600 years ago part of Mount Rainier?s edifice collapsed with the resultant Osceola Mudflow traveling more than 120 km and covering an area of at least 505 km2. Mineralogic and stable isotope studies were conducted on altered rocks from outcrops near the summit and east flank of the volcano and samples of clasts and matrix from the Osceola Mudflow. Results of these analyses are used to constrain processes responsible for pre-collapse alteration and provide insight into the role of alteration in edifice instability prior to the Osceola collapse event. Jarosite, pyrite, alunite, and kaolinite occur in hydrothermally altered rock exposed in summit scarps formed by edifice collapse events and in altered rock within the east-west structural zone (EWSZ) of the volcano?s east flank. Deposits of the Osceola Mudflow contain clasts of variably altered and unaltered andesite within a clay-rich matrix. Minerals detected in samples from the edifice are also present in many of the clasts. The matrix includes abundant smectite, kaolinite and variably abundant jarosite. Hydrothermal fluid compositions calculated from hydrogen and oxygen isotope data of alunite, and smectite on Mount Rainier reflect mixing of magmatic and meteoric waters. The range in the dD values of modern meteoric water on the volcano (-85 to 155?) reflect the influence of elevation on the dD of precipitation. The d34S and d18OSO4 values of alunite, gypsum and jarosite are distinct but together range from 1.7 to 17.6? and -12.3 to 15.0?, respectively; both parameters increase from jarosite to gypsum to alunite. The variations in sulfur isotope composition are attributed to the varying contributions of disproportionation of magmatic SO2, the supergene oxidation of hydrothermal pyrite and possible oxidation of H2S to the parent aqueous sulfate. The 18OSO4 values of jarosite are the lowest recorded for the mineral, consistent with a supergene origin. The mineralogy and isotope composition of alteration minerals define two and possibly three environments of alteration. At deeper levels magmatic vapor, H2S, SO2 and other gases from venting magmas migrated upward and condensed into the meteoric water. Disproportionation of SO2 into aqueous sulfate and H2S resulted in acid-sulfate (alunite + kaolinite + pyrite) and related argillic and propylitic alteration envelopes in a magmatic hydrothermal environment. At shallow levels H2S reacted with andesite to form pyrite that is associated with smectite along fractures on both the flanks and upper edifice. It is not clear to what extent H2S was oxidized by atmospheric O2 to form aqueous sulfate in a steam-heated environment. Near the ground surface, pyrite is oxidized by atmospheric oxygen resulting in soluble iron-and aluminum-hydroxysulfates. These supergene hydroxysulfates, which may also form around fumaroles from the oxidation of H2S, are subject to continuous solution and redeposition.

Open-File Report↗

USGS2016

What do we really know about the role of microorganisms in iron sulfide mineral formation?

Iron sulfide mineralization in low-temperature systems is a result of biotic and abiotic processes, though the delineation between these two modes of formation is not always straightforward. Here we review the role of microorganisms in the precipitation of extracellular iron sulfide minerals. We summarize the evidence that links sulfur-metabolizing microorganisms and sulfide minerals in nature and we present a critical overview of laboratory-based studies of the nucleation and growth of iron sulfide minerals in microbial cultures. We discuss whether biologically derived minerals are distinguishable from abiotic minerals, possessing attributes that are uniquely diagnostic of biomineralization. These inquiries have revealed the need for additional thorough, mechanistic and high-resolution studies to understand microbially mediated formation of a variety of sulfide minerals across a range of natural environments.

Frontiers in Earth Science↗

USGS1999

Seismic tomography as a tool for measuring stress in mines

Spokane Research Center personnel have been investigating the use of seismic tomography to monitor the behavior of a rock mass, detect hazardous ground conditions and assess the mechanical integrity of a rock mass affected by mining. Seismic tomography can be a valuable tool for determining relative stress in deep, >1,220-m (>4,000-ft), underground pillars. If high-stress areas are detected, they can be destressed prior to development or they can be avoided. High-stress areas can be monitored with successive seismic surveys to determine if stress decreases to a level where development can be initiated safely. There are several benefits to using seismic tomography to identify high stress in deep underground pillars. The technique is reliable, cost-effective, efficient and noninvasive. Also, investigators can monitor large rock masses, as well as monitor pillars during the mining cycle. By identifying areas of high stress, engineers will be able to assure that miners are working in a safer environment.Spokane Research Center personnel have been investigating the use of seismic tomography to monitor the behavior of a rock mass, detect hazardous ground conditions and assess the mechanical integrity of a rock mass affected by mining. Seismic tomography can be a valuable tool for determining relative stress in deep, >1,200-m (>4,000-ft), underground pillars. If high-stress areas are detected, they can be destressed prior to development or they can be avoided. High-stress areas can be monitored with successive seismic surveys to determine if stress decreases to a level where development can be initiated safely. There are several benefits to using seismic tomography to identify high stress in deep underground pillars. The technique is reliable, cost-effective, efficient and noninvasive. Also, investigators can monitor large rock masses, as well as monitor pillars during the mining cycle. By identifying areas of high stress. engineers will be able to assure that miners are working in a safer environment.

Mining Engineering↗

USGS1975

Heavy-mineral trends in the Beaufort Sea

Sediments of the Beaufort Sea, off the North Slope of Alaska contain a great variety of heavy minerals. These include garnet, chrome spinel, augite, pigeonite, diopside, hornblende, enstatite, hypersthene, epidote, clinozoisite, zoisite, apatite, tourmaline, chloritoid, sphene, zircon, and opaque minerals. Much rarer constituents are glaucophane, lamprobolite, rutile, kyanite, staurolite, and riebeckite. The heavy-mineral fractions that were not treated with hydrochloric acid contain "iron-stained aggregates", grains of unidentifiable material encrusted with limonite. Samples containing relatively high percentages of iron-stained aggregates and altered opaque minerals occur in depths less than 10 m and within 16 km from shore. Garnet increases in abundance from east to west, which corresponds to a similar increase in garnet abundance in coastal outcrops of the Gubik Formation sands. Only garnet and iron-stained aggregates appear to have source-related distribution patterns. The other heavy minerals lack distinct distributive provinces, reflecting an environment dominated by intense mixing by ice-gouging and bioturbation and a homogenous source area. Waves and currents are not strong enough to sort sediments at depths greater than 10 m except during summer storms. The source of the Beaufort Sea heavy minerals is dominated by contributions from the Alaskan North Slope deposits of Tertiary and younger age. The Colville River, largest in the region, is probably the most influential in transporting sediments, but because of wave and current—mixing of sediments on the shelf, exact contributions from each river drainage cannot be ascertained. Coastal erosion of the Gubik Formation is probably at least as important as the Colville River in supplying heavy minerals to the Beaufort Sea.

Alaska↗

USGS1975

Lithium in sediments and brines--how, why and where to search

The possibility of using lithium in batteries to power electric vehicles and as fuel for thermonuclear power has focused attention on the limited resources of lithium other than in pegmatite minerals. The Clayton Valley, Nev., subsurface lithium brine has been the major source of lithium carbonate since about 1967, but the life of this brine field is probably limited to several more decades at the present rate of production. Lithium is so highly soluble during weathering and in sedimentary environments that no lithium-rich sedimentary minerals other than clays have been identified to date. The known deposits of lithium, such as the clay mineral hectorite and the lithium-rich brines, occur in closed desert basins of the Southwest in association with nonmarine evaporites. However, the ultimate source for the lithium in these deposits may be from hydrothermal solutions. The search for previously unreported deposits of nonpegmatitic lithium should consider its probable association, not only with nonmarine evaporite minerals, but also with recent volcanic and tectonic activity, as well as with deposits of boron, beryllium, fluorine, manganese, and possibly phosphate.

Journal of Research of the U.S. Geological Survey↗

USGS1966

Stratified deposits of the oxides and carbonates of manganese

Compared with the stratified deposits of iron minerals, those of manganese minerals have received little attention until recent years. Before 1930, students of the stratified deposits of manganese minerals have generally concluded that the contained manganese was derived from the decomposition of the rocks that formed the borders of the basins. Only in a few places have geologists recognized that if these rocks were the principal source of the contained manganese the basins should contain also enormous quantities of iron minerals, whereas most of the large deposits of manganese contain little iron. Even though more than 100 years ago some geologists proposed that the iron contained in some deposits of stratified iron minerals was probably derived from hydrothermal waters related to centers of volcanism, not until about 1930 was this source of manganese in similar deposits seriously proposed. This mode of origin was given the name "volcanogene sedimentaire" by French geologists working in Morocco. Since then, other names, such as "exhalative sedimentaire," have been used by geologists working in several European districts. Because of the development of new techniques for the study of the chemical and physical features of the minerals, and because close attention to the lithologic environments of the beds is being given more and more during recent years, it has seemed advisable to review the features of stratified deposits of the manganese minerals in many parts of the world and over a wide range in age. This study indicates that at least three sources may have contributed the manganese in the large deposits of iron-free oxides and carbonates : (1) the rocks that form the borders of the basins, either marine or continental; (2) the nearby underlying sediments, largely of igneous origin, decomposed by warm waters largely derived from depth; and (3) waters of hydrothermal origin derived from great depths during epochs of volcanism from which iron minerals with little manganese are deposited in deep zones, then minerals with much iron and more manganese at intermediate depths, and, finally, manganese minerals with little iron near the surface. As the hot waters of many thermal springs contain more manganese than iron, such waters could yield the pure manganese oxides and carbonates found in stratified deposits . Several kinds of evidence indicate that most of the manganese in the large stratified deposits of the oxides and carbonates of manganese in many parts of the world has been derived from hydrothermal waters from depth related to centers of volcanism. Obviously, manganese derived from decay of the rocks on the lands adjacent to large basins-marine and continental -may have been added to that derived from centers of volcanism to form the sedimentary deposits found in the basins.

Economic Geology↗

USGS2005

Chemical openness and potential for misinterpretation of the solute environment of coastal sabkhat

Sabkha deposits in the geologic record are commonly used to interpret the environmental conditions of deposition. Implicit in this use is the assumption that the solute system is chemically closed, that is, the authigenic minerals represent the composition of the fluids in their environment of origin. Thermodynamic and mass-balance calculations based on measurements of water and solute flux of contemporary Abu Dhabi coastal sabkha system, however, demonstrate that the system is open for sodium and chloride, where nearly half of the input is lost, but closed for sulfur, where nearly 100% is retained. Sulfur and chloride isotopes were consistent with this observation. If these sabkha deposits were preserved in the geologic record, they would suggest a solute environment rich in sulfate and poor in chloride; yet the reverse is true. In most coastal-sabkha environments, capillary forces bring solutes and water to the surface, where the water evaporates and halite, carnallite, sylvite, and other soluble minerals are precipitated. Retrograde minerals, such as anhydrite, calcite, dolomite, and gypsum, however, precipitate and accumulate in the capillary zone beneath the surface of the coastal sabkha. Because they possess relatively low solubility and are below the surface, these retrograde minerals are protected from dissolution and physical erosion occurring from infrequent but intense rainfall events. Thus, they are more likely to be preserved in the geological record than highly soluble minerals formed on the surface. ?? 2004 Elsevier B.V. All rights reserved.

Chemical Geology↗

USGS1978

Pressure gradients and boiling as mechanisms for localizing ore in porphyry systems

Fluid inclusions in ore zones of porphyry systems indicate that extensive boiling of hydrothermal fluids accompanies deposition of ore and gangue minerals. The boiling commonly accompanied a change from a lithostatic to a hydrostatic environment during evolution of an epizonal stock. Pressure gradients near the margin of the stock can determine whether ore or only a diffuse zone of mineralization is formed. A sharp drop in pressure in an epizonal environment is more likely to cause extensive boiling than a comparable change in a deeper environment, as the slope of the boiling curve steepens with an increase 'in pressure. The drop in pressure causes the hydrothermal fluids to boil and creates a crackle (stockwork) breccia, which hosts the veinlets of gangue quartz and ore minerals. The boiling selectively partitions CO 2 , H 2 S, and HCl into the vapor phase, changing the pH, composition, ionic strength, and thus the solubility product of metal complexes in the remaining liquid and causing the ore and gangue to come out of solution. Fluid inclusions trapped from boiling solutions can exhibit several forms, depending on the physical and chemical conditions of the hydrothermal fluid from which they were trapped. In one case, inclusions when heated can homogenize to either liquid or vapor at the same temperature, which is the true boiling temperature. In another case, homogenization of various inclusions can occur through a range of temperatures. The latter case results from the trapping of mixture of liquid and vapor. Variations in salinity can result from boiling of the hydrothermal fluid, or intermittent incorporation of high-salinity fluids from the magma, or trapping of fluids of varying densities at pressure-temperature conditions above the critical point of the fluid. In places, paleopressure-temperature transition zones can be recognized by fluid-inclusion homogenization temperatures and phase relationships and by the presence of anhydrite daughter minerals. Boiling of a hydrothermal fluid in the porphyry environment affects light stable isotopes. Hydrogen is preferentially fractionated into the vapor phase from water boiling below 223°C; above this temperature deuterium is selectively enriched in the vapor phase. In certain environments boiling creates a vapor-dominated system in which the condensate is swept away by meteoric waters and the H/D in the residual fluids is progressively increased through time.

Utah↗

USGS1982

Hydrogeochemical prospecting for porphyry copper deposits in the tropical-marine climate of Puerto Rico

A hydrogeochemical survey utilizing waters from streams and springs was conducted in the area of two known porphyry copper deposits in the tropical-marine climate of westcentral Puerto Rico. The most important pathfinder for regional hydrogeochemical surveys is sulfate which reflects the associated pyrite mineralization. Because of increased mobility due to intense chemical weathering and the low pH environment, dissolved copper can also be used as a pathfinder for regional surveys and has the advantage of distinguishing barren pyrite from pyrite associated with copper mineralization. For follow-up surveys, the most important pathfinders are copper, sulfate, pH, zinc, and fluoride. High concentrations of dissolved copper and moderate concentrations of sulfate is a diagnostic indication of nearby sources of copper minerals. An understanding of the geochemical processes taking place in the streambeds and the weathering environment, such as the precipitation of secondary copper minerals, contributes to the interpretation of the geochemical data and the selection of the most favorable areas for further exploration.

Puerto Rico↗

USGS2024

Deep resistivity geophysics of the San Juan–Silverton caldera complex, San Juan County, Colorado (USA)

Magnetotelluric (MT) and audiomagnetotelluric (AMT) data are used to better understand the subsurface geology and mineral resources in the San Juan–Silverton caldera complex located near Silverton, Colorado, western United States, as part of the extensive southern Rocky Mountains volcanic field that covers much of southwestern Colorado and northern New Mexico. Seven MT and AMT profiles of varying lengths image resistivity structure to depths of ~5 km. The AMT inversion models characterize geophysical responses of near-surface lithologies, structures, and mineralized systems and also help corroborate airborne electromagnetic data at shallow levels. The MT inversion models extend our depth of investigation from near the surface to great depths (~5 km) and help to form hypotheses about roots of the hydrothermal plumbing that fed shallower mineralized systems. Subsurface high resistivities occur beneath intermediate-composition lava flows and Proterozoic units. Subsurface moderate- to low-resistivity values may reflect hydrothermal plumbing that served as flow paths for mineralizing fluids and metallic ore formation. The model interpretations presented in this study could be utilized in remediation planning or mineral resource applications. The methods used could be applied to other watersheds with similar volcanic environments containing acid-generating historical mines or hydrothermally altered and mineralized source rocks.

Colorado↗

USGS1991

Facies development in the Lower Freeport coal bed, west-central Pennsylvania, U.S.A.

The Lower Freeport coal bed in west-central Pennsylvania is interpreted to have formed within a lacustrine-mire environment. Conditions of peat formation, caused by the changing chemical and physical environments, produced five coal facies and two mineral-rich parting facies within the coal bed. The coal bed facies are compositionally unique, having developed under varying conditions, and are manifested by megascopic, petrographic, palynologic and quality characteristics. The initial environment of the Lower Freeport peat resulted in a coal facies that is relatively high in ash yield and contains large amounts of lycopod miospores and moderate abundances of cryptotelinite, crypto-gelocollinite, inertinite and tree fern miospores. This initial Lower Freeport peat is interpreted to have been a topogenous body that was low lying, relatively nutrient rich (mesotrophic to eutrophic), and susceptible to ground water and to sediment influx from surface water. The next facies to form was a ubiquitous, clay-rich durain parting which is attributed to a general rise in the water table accompanied by widespread flooding. Following formation of the parting, peat accumulation resumed within an environment that inhibited clastic input. Development of doming in this facies restricted deposition of the upper shale parting to the margins of the mire and allowed low-ash peat to form in the interior of the mire. Because this environment was conducive to preservation of cellular tissue, this coal facies also contains large amounts of crypto-telinite. This facies development is interpreted to have been a transitional phase from topogenous, planar peat formation to slightly domed, oligotrophic (nutrient-poor) peat formation. As domed peat formation continued, fluctuations in the water table enabled oxidation of the peat surface and produced high inertinite concentrations toward the top of the coal bed. Tree ferns became an increasingly important peat contributor in the e upper facies, based on the palynoflora. This floral change is interpreted to have resulted from the peat surface becoming less wet or better drained, a condition that inhibited proliferation of lycopod trees. Accumulation of the peat continued until rising water levels formed a freshwater lake within which clays and silts were deposited. The development of the Lower Freeport peat from a planar mire through transitional phases toward domed peat formation may be an example of the type of peat formation of other upper Middle and Upper Pennsylvanian coal beds.

International Journal of Coal Geology↗

USGS2011

Reduction of structural Fe(III) in nontronite by methanogen Methanosarcina barkeri

Clay minerals and methanogens are ubiquitous and co-exist in anoxic environments, yet it is unclear whether methanogens are able to reduce structural Fe(III) in clay minerals. In this study, the ability of methanogen Methanosarcina barkeri to reduce structural Fe(III) in iron-rich smectite (nontronite NAu-2) and the relationship between iron reduction and methanogenesis were investigated. Bioreduction experiments were conducted in growth medium using three types of substrate: H 2 /CO 2 , methanol, and acetate. Time course methane production and hydrogen consumption were measured by gas chromatography. M. barkeri was able to reduce structural Fe(III) in NAu-2 with H 2 /CO 2 and methanol as substrate, but not with acetate. The extent of bioreduction, as measured by the 1,10-phenanthroline method, was 7–13% with H 2 /CO 2 as substrate, depending on nontronite concentration (5–10 g/L). The extent was higher when methanol was used as a substrate, reaching 25–33%. Methanogenesis was inhibited by Fe(III) reduction in the H 2 /CO 2 culture, but enhanced when methanol was used. High charge smectite and biogenic silica formed as a result of bioreduction. Our results suggest that methanogens may play an important role in biogeochemical cycling of iron in clay minerals and may have important implications for the global methane budget.

Geochimica et Cosmochimica Acta↗

USGS2018

Quartz-pebble-conglomerate gold deposits

Quartz-pebble-conglomerate gold deposits represent the largest repository of gold on Earth, largely due to the deposits of the Witwatersrand Basin, which account for nearly 40 percent of the total gold produced throughout Earth’s history. This deposit type has had a controversial history in regards to genetic models. However, most researchers conclude that they are paleoplacer deposits that have been modified by metamorphism and hydrothermal fluid flow subsequent to initial sedimentation. The deposits are found exclusively within fault-bounded depositional basins. The periphery of these basins commonly consists of granite-greenstone terranes, classic hosts for lode gold that source the detrital material infilling the basin. The gold reefs are typically located along unconformities or, less commonly, at the top of sedimentary beds. Large quartz pebbles and heavy-mineral concentrates are found associated with the gold. Deposits that formed prior to the Great Oxidation Event (circa 2.4 giga-annum [Ga]) contain pyrite, whereas younger deposits contain iron oxides. Uranium minerals and hydrocarbons are also notable features of some deposits. Much of the gold in these types of deposits forms crystalline features that are the product of local remobilization. However, some gold grains preserve textures that are undoubtedly of detrital origin. Other heavy minerals, such as pyrite, contain growth banding that is truncated along broken margins, which indicates that they were transported into place as opposed to forming by in situ growth in a hydrothermal setting. The ore tailings associated with these deposits commonly contain uranium-rich minerals and sulfides. Oxidation of the sulfides releases sulfuric acid and mobilizes various metals into the environment. The neutralizing potential of the tailings is minimal, since carbonate minerals are rare. The continuity of the tabular ore bodies, such as those of the Witwatersrand Basin, has allowed these mines to be the deepest in the world. The extreme depths create engineering complications and safety issues for the miners, such as rock bursts as a result of pressure release. The richness of these deposits makes them a desirable exploration target. However, the likelihood of future discoveries is minimal. Small deposits found in the United States include those found at Nemo in the Black Hills of South Dakota and Deep Lake in the Sierra Madre of Wyoming.

Scientific Investigations Report↗

USGS2009

Identification of hydrated silicate minerals on Mars using MRO-CRISM: Geologic context near Nili Fossae and implications for aqueous alteration

[1] The Noachian terrain west of the Isidis basin hosts a diverse collection of alteration minerals in rocks comprising varied geomorphic units within a 100,000 km 2 region in and near the Nili Fossae. Prior investigations in this region by the Observatoire pour l'Minéralogie, l'Eau, les Glaces, et l'Activité (OMEGA) instrument on Mars Express revealed large exposures of both mafic minerals and iron magnesium phyllosilicates in stratigraphic context. Expanding on the discoveries of OMEGA, the Compact Reconnaissance Imaging Spectrometer for Mars (CRISM) aboard the Mars Reconnaissance Orbiter (MRO) has found more spatially widespread and mineralogically diverse alteration minerals than previously realized, which represent multiple aqueous environments. Using CRISM near-infrared spectral data, we detail the basis for identification of iron and magnesium smectites (including both nontronite and more Mg-rich varieties), chlorite, prehnite, serpentine, kaolinite, potassium mica (illite or muscovite), hydrated (opaline) silica, the sodium zeolite analcime, and magnesium carbonate. The detection of serpentine and analcime on Mars is reported here for the first time. We detail the geomorphic context of these minerals using data from high-resolution imagers onboard MRO in conjunction with CRISM. We find that the distribution of alteration minerals is not homogeneous; rather, they occur in provinces with distinctive assemblages of alteration minerals. Key findings are (1) a distinctive stratigraphy, in and around the Nili Fossae, of kaolinite and magnesium carbonate in bedrock units always overlying Fe/Mg smectites and (2) evidence for mineral phases and assemblages indicative of low-grade metamorphic or hydrothermal aqueous alteration in cratered terrains. The alteration minerals around the Nili Fossae are more typical of those resulting from neutral to alkaline conditions rather than acidic conditions, which appear to have dominated much of Mars. Moreover, the mineralogic diversity and geologic context of alteration minerals found in the region around the Nili Fossae indicates several episodes of aqueous activity in multiple distinct environments.

Journal of Geophysical Research E: Planets↗

USGS1995

Alteration of basalt hyaloclastite at the off-axis Sea Cliff hydrothermal field, Gorda Ridge

The Sea Cliff hydrothermal field on the northern segment of the Gorda Ridge is situated along a rift-bounding normal fault about 2.6 km east of the neovolcanic zone and approximately 300 m above the spreading axis. The structural setting of this hydrothermal field differs from that of most other active seafloor hydrothermal sites investigated to date, which are typically situated in the neovolcanic zone. Mineralization occurs in basaltic talus covering a large normal-fault scarp. Hydrothermal crusts cover much of the seafloor in the area of the active hydrothermal field. These crusts form by extensive alteration of basaltic hyaloclastite in a zone of mixing between ascending hydrothermal fluid and entrained seawater. The initial stage of alteration is magnesian metasomatism of both crystalline basalt and basaltic glass, converting the rock to Mg-rich smectite and smectite/chlorite. Further alteration removes nearly all cations and ultimately leads to silicification. Preservation of basaltic texture in the silicified rocks provides evidence that even such sparingly soluble elements as A1 and Ti have been removed. Oxygen-isotopic ratios of the altered rocks constrain initial alteration to temperatures near 220°C, close to the maximum measured vent temperatures of 247°C. Silicification proceeded to much lower temperatures, and most amorphous silica deposition occurred at temperatures below 100°C. Sulfur-, strontium-, and lead-isotopic data all indicate a predominantly basaltic source, with important contributions from seawater but no significant contribution from sedimentary sources. Comparison with ophiolite-hosted massive sulfide deposits shows that the structural setting, alteration sequence, and depositional environment are all similar and suggests that mineralization and replacement of basaltic breccia in the Sea Cliff hydrothermal field likely occur in the subsurface beneath a capping layer of silicified hyaloclastite.

California, Oregon↗

USGS2003

Mercury from mineral deposits and potential environmental impact

Mercury deposits are globally distributed in 26 mercury mineral belts. Three types of mercury deposits occur in these belts: silica-carbonate, hot-spring, and Almaden. Mercury is also produced as a by-product from several types of gold-silver and massive sulfide deposits, which account for 5% of the world's production. Other types of mineral deposits can be enriched in mercury and mercury phases present are dependent on deposit type. During processing of mercury ores, secondary mercury phases form and accumulate in mine wastes. These phases are more soluble than cinnabar, the primary ore mineral, and cause mercury deposits to impact the environment more so than other types of ore deposits enriched in mercury. Release and transport of mercury from mine wastes occur primarily as mercury-enriched particles and colloids. Production from mercury deposits has decreased because of environmental concerns, but by-product production from other mercury-enriched mineral deposits remains important.

Environmental Geology↗

USGS2009

Pathogenic prion protein is degraded by a manganese oxide mineral found in soils

Prions, the aetiological agents of transmissible spongiform encephalopathies, exhibit extreme resistance to degradation. Soil can retain prion infectivity in the environment for years. Reactive soil components may, however, contribute to the inactivation of prions in soil. Members of the birnessite family of manganese oxides (MnO 2 ) rank among the strongest natural oxidants in soils. Here, we report the abiotic degradation of pathogenic prion protein (PrP TSE ) by a synthetic analogue of naturally occurring birnessite minerals. Aqueous MnO 2 suspensions degraded the PrP TSE as evidenced by decreased immunoreactivity and diminished ability to seed protein misfolding cyclic amplification reactions. Birnessite-mediated PrP TSE degradation increased as a solution's pH decreased, consistent with the pH-dependence of the redox potential of MnO 2 . Exposure to 5.6 mg MnO2 ml -1 (PrP TSE :MnO 2 =1 : 110) decreased PrPTSE levels by ???4 orders of magnitude. Manganese oxides may contribute to prion degradation in soil environments rich in these minerals. ?? 2009 SGM.

Journal of General Virology↗

USGS2011

Arsenic in sediments, groundwater, and streamwater of a glauconitic Coastal Plain terrain, New Jersey, USA-Chemical " fingerprints" for geogenic and anthropogenic sources

Glauconite-bearing deposits are found worldwide, but As levels have been determined for relatively few. The As content of glauconites in sediments of the Inner Coastal Plain of New Jersey can exceed 100 mg/kg, and total As concentrations (up to 5.95 μg/L) found historically and recently in streamwaters exceed the State standard. In a major watershed of the Inner Coastal Plain, chemical “fingerprints” were developed for streambed sediments and groundwater to identify contributions of As to the watershed from geologic and anthropogenic sources. The fingerprint for streambed sediments, which included Be, Cr, Fe and V, indicated that As was predominantly of geologic origin. High concentrations of dissolved organic C, nutrients (and Cl − ) in shallow groundwater indicated anthropogenic inputs that provided an environment where microbial activity released As from minerals to groundwater discharging to the stream. Particulates in streamwater during high flow constituted most of the As load; the chemical patterns for these particulates resembled the geologic fingerprint of the streambed sediments. The As/Cr ratio of these suspended particles likely indicates they derived not only from runoff, but from groundwater inputs, because As contributed by groundwater is sequestered on streambed sediments. Agricultural inputs of As were not clearly identified, although chemical characteristics of some sediments indicated vehicle-related inputs of metals. Sediment sampling during dry and wet years showed that, under differing hydrologic conditions, local anthropogenic fingerprints could be obscured but the geologic fingerprint, indicating glauconitic sediments as an As source, was robust.

New Jersey↗