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Results for “Minerals and the Environment”

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At least 253 records · Page 14Linked to original sources

USGS1977

Late diagenetic indicators of buried oil and gas

At least three hydrocarbon seepage mechanisms are interpreted to operate over oil and gas fields. These are: (1) effusion ofh ydrocarbons through inadequate caprocks and along faults and fractures, (2) low-molecular-weight hydrocarbons dissolved in water moving vertically through capping shales as a result of a hydrodynamic or chemical potential drive, and (3) diffusion of gases dissolved in water. Combinations of these mechanisms may also occur. Seeping hydrocarbons are oxidized near the earth's surface, and the resulting carbon dioxide reacts with water producing bicarbonate ions, which combine with calcium and magnesium dissolved in ground waters to yield isotopically distinctive pore-filling carbonate cements and surface rocks. The passage of hydrocarbons and associated compounds such as hydrogen sulfide through surface rocks causes a reducing environment and consequent reduction, mobilization, and loss of iron from iron-bearing minerals commonly resulting in a discoloration. Other metals such as manganese are also mobilized and redistributed. These changes in the physical and chemical properties of surface rocks correlate with the subsurface distribution of petroleum, and potentially can be detected from both airborne and spaceborne platforms.

Open-File Report↗

USGS1982

Geochemical and geostatistical evaluation, Arkansas Canyon Planning Unit, Fremont and Custer Counties, Colorado

A mineral assessment of the Arkansas Canyon Planning Unit was undertaken by Barringer Resources Inc., under the terms of contract YA-553-CTO-100 with the Bureau of Land Management, Colorado State Office. The study was based on a geochemical-geostatistical survey in which 700 stream sediment samples were collected and analyzed for 25 elements. Geochemical results were interpreted by statistical processing which included factor, discriminant, multiple regression and characteristic analysis. The major deposit types evaluated were massive sulfide-base metal, sedimentary and magmatic uranium, thorium vein, magmatic segregation, and carbonatite related deposits. Results of the single element data and multivariate geostatistical analysis indicate that limited potential exists for base metal mineralization near the Horseshoe, El Plomo, and Green Mountain Mines. Thirty areas are considered to be anomalous with regard to one or more of the geochemical parameters evaluated during this study. The evaluation of carbonatite related mineralization was restricted due to the lack of geochemical data specific to this environment.

Colorado↗

USGS1975

Depositional environments and paleocurrent directions in the Precambrian Moeda Formation, Minas Gerais, Brazil

The middle Precambrian Moeda Formation of Minas Gerais, Brazil, contains uranium and other minerals believed to be of detrital origin. Two areas of anomalously high concentrations of uranium have been discovered in conglomeratic zones that are interpreted as paleochannels. Because the distribution of uranium is believed to be controlled at least in part by sedimentation, a reconnaissance study was undertaken to assess the depositional environment and sediment dispersal pattern of the Moeda Formation.

Minas Gerais↗

USGS2024

A multidisciplinary approach that considers occurrence, geochemistry, bioavailability, and toxicity to prioritize critical minerals for environmental research

Critical minerals (or critical elements) are minerals or elements that are essential to global security and development and have supply chains vulnerable to disruption. In general, knowledge of the environmental behavior and health effects of critical elements is needed to support the development of safe and environmentally responsible supplies. This knowledge includes identifying potential consequences of increased critical element production and use, alternative critical element sources such as mine wastes, and adverse effects of critical elements on ecosystem condition and organismal health. Here we identify significant data gaps in the understanding of critical elements in surficial and aquatic environments, and the need, given the large number of commodities (50) identified on the 2022 critical minerals list for the United States, for an approach to prioritize them for study of their environmental fate and effects. We propose a multidisciplinary approach for this prioritization, considering measures of occurrence, geochemistry, bioavailability, and toxicity. We describe relatively easy-to-obtain metrics for each of these topic areas and demonstrate the utility of this integrated prioritization approach using indium and zinc as examples. This approach facilitates prioritizing research with a focus on those critical elements that are most mobile in the environment, bioavailable, toxic, or simply lacking data in these categories.

Environmental Science & Technology↗

USGS1997

Anaerobic degradation of benzene in diverse anoxic environments

Benzene has often been observed to be resistant to microbial degradation under anoxic conditions. A number of recent studies, however, have demonstrated that anaerobic benzene utilization can occur. This study extends the previous reports of anaerobic benzene degradation to sediments that varied with respect to contamination input, predominant redox condition, and salinity. In spite of differences in methodology, microbial degradation of benzene was noted in slurries constructed with sediments from various geographical locations and range from aquifer sands to fine-grained estuarine muds, under methanogenic, sulfate-reducing, and iron-reducing conditions. In aquifer sediments under methanogenic conditions, benzene loss was concomitant with methane production, and microbial utilization of [ 14 C]benzene yielded 14 CO 2 and 14 CH 4 . In slurries with estuarine and aquifer sediments under sulfate-reducing conditions, the loss of sulfate in amounts consistent with the stoichiometric degradation of benzene or the conversion of [ 14 C]benzene to 14 CO 2 indicates that benzene was mineralized. Benzene loss also occurred in the presence of Fe(III) in sediments from freshwater environments. Microbial benzene utilization, however, was not observed under denitrifying conditions. These results indicate that the potential for the anaerobic degradation of benzene, which was once thought to be resistant to non-oxygenase attack, exists in a variety of aquatic sediments from widely distributed locations.

Environmental Science & Technology↗

USGS1953

Results of reconnaissance for radioactive minerals in parts of the Alma district, Park County, Colorado

Pitchblende was discovered in July 1951 in the Alma mining district, Park County, Colo., by the U. S. Geological Survey acting on behalf of the U. S. Atomic Energy Commission. The pitchblende is associated with Tertiary veins of three different geologic environments: (1) veins in pre-Cambrian rocks, (2) the London vein system in the footwall block of the London fault, and (3) veins in a mineralized area east of the Cooper Gulch fault. Pitchblende is probably not associated with silver-lead replacement deposits in dolomite. Secondary uranium minerals, as yet undetermined, are associated with pitchblende on two London vein system mine dumps and occur in oxidized vein material from dumps of mines in the other environments. Although none of the known occurrences is of commercial importance, the Alma district is considered a moderately favorable area in which to prospect for uranium ore because 24 of the 43 localities examined show anomalous radioactivity; samples from anomalously radioactive localities, which include mine dumps and some underground workings, have uranium contents ranging from 0.001 to 1.66 percent.

Circular↗

USGS1961

Geologic control of mineral composition of stream waters of the eastern slope of the Southern Coast Ranges, California

Chemical analyses of waters of streams that drain the semiarid eastern slope of the southern Coast Ranges in California demonstrate that differences in the anion composition, especially in the ratio of bicarbonate to sulfate, are related chiefly to the lithologic character of the rocks exposed in the tributary drainage area. Where more than hall the drainage area of a typical eastern-slope stream is underlain by clastic marine sedimentary rocks of Jurassic and Cretaceous age, bicarbonate generally predominates over sulfate; the ratio of bicarbonate to sullate, both expressed in equivalents per million, in samples of the streams at low-flow stage ranges from 0.8 to 6. Conversely, where more than hall the drainage area is underlain by marine and continental deposits of Tertiary age and continental deposits of Quaternary age, sulfate predominates over bicarbonate, and the ratio of bicarbonate to sulfate in samples taken during the low-flow stage ranges from 0.02 to 0.7. Organic siliceous marine shale of Tertiary age deposited in a reducing environment is probably the primary source of sullate in the region. Secondary deposits of sulfate minerals, chiefly gypsum, which are abundant in the continental deposits of late Tertiary and Quaternary age, also contribute sullate to the stream waters.

Water Supply Paper↗

USGS2022

Mineral sources and transport pathways for arsenic release in a coastal watershed, USA

Metasedimentary bedrock of coastal Maine contains a diverse suite of As-bearing minerals that act as significant sources of elements found in ground and surface waters in the region. Arsenic sources in the Penobscot Formation include, in order of decreasing As content by weight: löllingite and realgar ( c. 70%), arsenopyrite, cobaltite, glaucodot, and gersdorffite (in the range of 34–45%), arsenian pyrite (<4%), and pyrrhotite (<0.15%). In the Penobscot Formation, the relative stability of primary As-bearing minerals follows a pattern where the most commonly observed highly altered minerals are pyrrhotite, realgar, niccolite, löllingite > glaucodot, arsenopyrite-cobaltian > arsenopyrite, cobaltite, gersdorffite, fine-grained pyrite, Ni-pyrite > coarse-grained pyrite. Reactions illustrate that oxidation of Fe-As disulphide group and As-sulphide minerals is the primary release process for As. Liberation of As by carbonation of realgar and orpiment in contact with high-pH groundwaters may contribute locally to elevated contents of As in groundwater, especially where As is decoupled from Fe. Released metals are sequestered in secondary minerals by sorption or by incorporation in crystal structures. Secondary minerals acting as intermediate As reservoirs include claudetite ( c. 75%), orpiment (61%), scorodite ( c. 45%), secondary arsenopyrite ( c. 46%), goethite (<4490 ppm), natrojarosite (<42 ppm), rosenite, melanterite, ferrihydrite, and Mn-hydroxide coatings. Some soils also contain Fe-Co-Ni-arsenate, Ca-arsenate, and carbonate minerals. Reductive dissolution of Fe-oxide minerals may govern the ultimate release of iron and arsenic – especially As(V) – to groundwater; however, dissolution of claudetite (arsenic trioxide) may directly contribute As(III). Processes thought to explain the release of As from minerals in bedrock include oxidation of arsenian pyrite or arsenopyrite, or carbonation of As-sulphides, and most models based on these generally rely on discrete minerals or on a fairly limited series of minerals. In contrast, in the Penobscot Formation and other metasedimentary rocks of coastal Maine, oxidation of As-bearing Fe-cobalt-nickel-sulphide minerals, dissolution (by reduction) of As-bearing secondary As and Fe hydroxide and sulphate minerals, carbonation and/or oxidation of As-sulphide minerals, and desorption of As from Fe-hydroxide mineral surfaces are all thought to be involved. All of these processes contribute to the occurrence of As in groundwaters in coastal Maine, as a result of variability in composition and in stability of the As source minerals. Arsenic contents of soils and groundwater thus reflect the predominant influence and integration of a spectrum of primary mineral reservoirs (instead of single or unique mineral reservoirs). Cycling of As through metasedimentary bedrock aquifers may therefore depend on consecutive stages of carbonation, oxidation and reductive dissolution of primary and secondary As host minerals.

Maine↗

USGS1975

Mineral deposits in western Saudi Arabia; a preliminary report

Mineral deposits in Saudi Arabia include a variety of deposits which were formed in many geologic environments. These include magmatic and late magmatic deposits in igneous masses, contact metamorphic deposits along the margins of igneous bodies, and stratiform sulfide deposits and veins. Notable deposits of sedimentary origin include deposits of iron oxides and phosphate. Strata-bound massive sulfide deposits containing copper, zinc, and nickel sulfides associated with pyrite and pyrrhotite in complexly deformed volcanic rocks in Saudi Arabia have been the subject of controversy. They are considered by some geologists to be of syngenetic or volcanogenic origin, and by others to be epigenetic. The principal mineral deposits in western Saudi Arabia are localized in mineral belts within tectonic zones that trend northerly, northeasterly, and northwesterly. These belts contain the exploration target areas most promising for future exploration. Noteworthy among these are: 1) the northerly-trending Bidah copper-zinc belt; 2) the Sayid copper-zinc zone; 3) the northwest-trending Nuqrah copper zinc-silver belt; and 4) the north-northwesterly-trending Al Amar belt. Gold and silver deposits are mainly localized in north-trending structural features of the Hijaz geotectonic cycle and northwest Najd trends. Saudi Arabian metal deposits known thus far contain reserves in the 2 billion dollar range. Further exploration should result in discoveries that could significantly increase this amount; Saudi Arabia may well have workable metallic and nonmetallic mineral resources for industrial developments in many parts of the Kingdom. In order to effectively carry on a search for new mineral deposits, the belts should be mapped in detail, with emphasis on the delineation of stratigraphic and structural features that control metallization. In addition, geochemical and geophysical studies should be made of promising areas to outline exploration targets. These targets could then be systematically explored.

Open-File Report↗

USGS1985

Culturing Selenastrum capricornutum (Chlorophyta) in a synthetic algal nutrient medium with defined mineral particulates

Algal nutrient studies in chemically-defined media typically employ a synthetic chelator to prevent iron hydroxide precipitation. Micronutrient-particulate interactions may, however, significantly affect chemical speciation and hence biovailability of these nutrients in natural waters. A technique is described by which Selenastrum capricornutum Printz (Chlorophyta) may be cultured in a medium where trace metal speciation (except iron) is controlled, not by organic chelation, but by sorption onto titanium dioxide. Application of this culturing protocol in conjunction with results from sorption studies of nutrient ions on mineral particles provides a means of studying biological impacts of sorptive processes in aquatic environments.

Hydrobiologia↗

USGS2008

Integrated Fe- and S-isotope study of seafloor hydrothermal vents at East Pacific Rise 9-10°N

In this study, we report on coupled Fe- and S-isotope systematics of hydrothermal fluids and sulfide deposits from the East Pacific Rise at 9–10°N to better constrain processes affecting Fe-isotope fractionation in hydrothermal environments. We aim to address three fundamental questions: (1) Is there significant Fe-isotope fractionation during sulfide precipitation? (2) Is there significant variability of Fe-isotope composition of the hydrothermal fluids reflecting sulfide precipitation in subsurface environments? (3) Are there any systematics between Fe- and S-isotopes in sulfide minerals? The results show that chalcopyrite, precipitating in the interior wall of a hydrothermal chimney displays a limited range of δ 56 Fe values and δ 34 S values, between − 0.11 to − 0.33‰ and 2.2 to 2.6‰ respectively. The δ 56 Fe values are, on average, slightly higher by 0.14‰ relative to coeval vent fluid composition while δ 34 S values suggest significant S-isotope fractionation (− 0.6 ± 0.2‰) during chalcopyrite precipitation. In contrast, systematically lower δ 56 Fe and δ 34 S values relative to hydrothermal fluids, by up to 0.91‰ and 2.0‰ respectively, are observed in pyrite and marcasite precipitating in the interior of active chimneys. These results suggest isotope disequilibrium in both Fe- and S-isotopes due to S-isotopic exchange between hydrothermal H 2 S and seawater SO 4 2− followed by rapid formation of pyrite from FeS precursors, thus preserving the effects of a strong kinetic Fe-isotope fractionation during FeS precipitation. In contrast, δ 56 Fe and δ 34 S values of pyrite from inactive massive sulfides, which show evidence of extensive late-stage reworking, are essentially similar to the hydrothermal fluids. Multiple stages of remineralization of ancient chimney deposits at the seafloor appear to produce minimal Fe-isotope fractionation. Similar affects are indicated during subsurface sulfide precipitation as demonstrated by the lack of systematic differences between δ 56 Fe values in both high-temperature, Fe-rich black smokers and lower-temperature, Fe-depleted vents.

Chemical Geology↗

USGS2016

The conjunction of factors that lead to formation of giant gold provinces and deposits in non-arc settings

It is quite evident that it is not anomalous metal transport, nor unique depositional conditions, nor any single factor at the deposit scale, that dictates whether a mineral deposit becomes a giant or not. A hierarchical approach thus is required to progressively examine controlling parameters at successively decreasing scales in the total mineral system to understand the location of giant gold deposits in non-arc environments. For giant orogenic, intrusion-related gold systems (IRGS) and Carlin-type gold deposits and iron oxide-copper-gold (IOCG) deposits, there are common factors among all of these at the lithospheric to crustal scale. All are sited in giant gold provinces controlled by complex fundamental fault or shear zones that follow craton margins or, in the case of most Phanerozoic orogenic giants, define the primary suture zones between tectonic terranes. Giant provinces of IRGS, IOCG, and Carlin-type deposits require melting of metasomatized lithosphere beneath craton margins with ascent of hybrid lamprophyric to granitic magmas and associated heat flux to generate the giant province. The IRGS and IOCG deposits require direct exsolution of volatile-rich magmatic-hydrothermal fluids, whereas the association of such melts with Carlin-type ores is more indirect and enigmatic. Giant orogenic gold provinces show no direct relationship to such magmatism, forming from metamorphic fluids, but show an indirect relationship to lamprophyres that reflect the mantle connectivity of controlling first-order structures. In contrast to their province scale similarities, the different giant gold deposit styles show contrasting critical controls at the district to deposit scale. For orogenic gold deposits, the giants appear to have formed by conjunction of a greater number of parameters to those that control smaller deposits, with resultant geometrical and lithostratigraphic complexity as a guide to their location. There are few giant IRGS due to their inferior fluid-flux systems relative to orogenic gold deposits, and those few giants are essentially preservational exceptions. Many Carlin-type deposits are giants due to the exceptional conjunction of both structural and lithological parameters that caused reactive and permeable rocks, enriched in syngenetic gold, to be located below an impermeable cap along antiformal “trends”. Hydrocarbons probably played an important role in concentrating metal. The supergiant Post-Betze deposit has additional ore zones in strain heterogeneities surrounding the pre-gold Goldstrike stock. All unequivocal IOCG deposits are giant or near-giant deposits in terms of gold-equivalent resources, partly due to economic factors for this relatively poorly understood, low Cu-Au grade deposit type. The supergiant Olympic Dam deposit, the most shallowly formed deposit among the larger IOCGs, probably owes its origin to eruption of volatile-rich hybrid magma at surface, with formation of a large maar and intense and widespread brecciation, alteration and Cu-Au-U deposition in a huge rock volume.

Geoscience Frontiers↗

USGS2004

Tectonics and metallogenesis of Proterozoic rocks of the Reading Prong

Detailed geologic mapping, petrography, and major and trace-element analyses of Proterozoic rocks from the Greenwood Lake Quadrangle, New York are compared with chemical analyses and stratigraphic information compiled for the entire Reading Prong. A persistent regional stratigraphy is evident in the mapped area whose geochemistry indicates protoliths consistent with a back-arc marginal basin sequence. The proposed marginal basin may have been floored by an older sialic basement and overlain by a basin-fill sequence consisting of a basal tholeiitic basalt, basic to intermediate volcanic or volcaniclastic rocks and carbonate sediments, a bimodal calc-alkaline volcanic sequence, and finally volcaniclastic, marine, and continental sediments. The presence of high-chlorine biotite and scapolite may indicate circulation of brine fluids or the presence of evaporite layers in the sequence. Abundant, stratabound magnetite deposits with a geologic setting very unlike that of cratonic, Proterozoic banded-iron formations are found throughout the proposed basin sequence. Associated with many of the magnetite deposits is unusual uranium and rare-earth element mineralization. It is proposed here that these deposits formed in an exhalative, volcanogenic, depositional environment within an extensional back-arc marginal basin. Such a tectonic setting is consistent with interpretations of protoliths in other portions of the Reading Prong, the Central Metasedimentary Belt of the Canadian Grenville Province, and recent interpretation of the origin of the Franklin lead-zinc deposits, suggesting a more cohesive evolving arc/back-arc tectonic model for the entire Proterozoic margin of the north-eastern portion of the North American craton. Published by Elsevier Ltd.

Journal of Geodynamics↗

USGS2001

In situ spectroscopic and solution analyses of the reductive dissolution of Mn02 by Fe(II)

The reductive dissolution of MnO 2 by Fe(II) under conditions simulating acid mine drainage (pH 3, 100 mM SO 4 2 - ) was investigated by utilizing a flow-through reaction cell and synchrotron X-ray absorption spectroscopy. This configuration allows collection of in situ, real-time X-ray absorption near-edge structure (XANES) spectra and bulk solution samples. Analysis of the solution chemistry suggests that the reaction mechanism changed (decreased reaction rate) as MnO 2 was reduced and Fe(III) precipitated, primarily as ferrihydrite. Simultaneously, we observed an additional phase, with the local structure of jacobsite (MnFe 2 O 4 ), in the Mn XANES spectra of reactants and products. The X-ray absorbance of this intermediate phase increased during the experiment, implying an increase in concentration. The presence of this phase, which probably formed as a surface coating, helps to explain the reduced rate of dissolution of manganese(IV) oxide. In natural environments affected by acid mine drainage, the formation of complex intermediate solid phases on mineral surfaces undergoing reductive dissolution may likewise influence the rate of release of metals to solution.

Environmental Science & Technology↗

USGS1987

Increased solubility of quartz in water due to complexing by organic compounds

Quartz is the most stable natural solid phase of silica. It weathers extremely slowly at the Earth's surface 1 , and often resists weathering even after all other silicate minerals have been degraded. However, there is ample evidence from both ancient and modern environments indicating enhanced dissolution and mobility of silica under conditions that cannot easily be explained by the inorganic controls of quartz solubility 2 . Increased solubility of quartz has been observed particularly in soils rich in organic material; however, no direct link between dissolved organic carbon and dissolved silica has been identified 3 . Here we present evidence for an increase in the solubility of quartz in a natural water brought about by dissolved organic compounds. These compounds were produced by the biodegradation of petroleum, and consist largely of a complex mixture of organic acids. We propose that silica is being complexed and mobilized by these organic acids in waters having close to neutral p H.

Nature↗

USGS1981

Reconnaissance investigation of brine in the eastern Rub al Khali, Kingdom of Saudi Arabia

Al Uruq al Mu'taridah-Umm as Samim area is located in a large topographic depression in the eastern Rub al Khali desert where playas several thousand square kilometers in area are exposedo A crust of eolian sand cemented with gypsum and halite has formed on many playa surfaces. Anhydrite nodules are common in the sampled area, where the depth to ground water generally exceeds 172 Cmo The chemistry of the three ground-water samples collected near the water well Ramallah-1 (lat 22?10'20'' N., long 54?20'37'' E.) is similar to that of sabkhah-related brines on the coast of the United Arab Emirates. Although there is no indication of economic quantities of evaporite minerals in the sampled area, the extent of the depression and its unique geologic environment recommend it for resource-evaluation studies.

Open-File Report↗

USGS1973

Dolomitization model for Upper Cambrian and Lower Ordovician carbonate rocks in the eastern United States

Existing models for dolomitization emphasize that penecontemporaneous dolomitization can occur in both subtidal and supratidal environments if the necessary chemical and physical factors favorable for the development of magnesium-rich hypersaline waters exist. Holocene shallow-water hypersaline environments that have the potential to produce dolomite without deposition of more soluble evaporite minerals are found in Shark Bay, Australia, and on the Great Bahama Bank. These hypersalinity systems are characterized by near-vertical isosalinity layers of increasing concentration landward from the open ocean and show little or no relationship to bottom topography. I suggest that a similar but larger scale epicontinentalsalinity system covering the Late Cambrian and Early Ordovician carbonate continental shelf produced a broad wedge of subtidally deposited dolomite in the eastern half of the United States from Mexico to Canada. The distribution of limestone and dolomite in this region is closely keyed to the salinity gradient and accounts for the natural progression from a normal marine limestone facies through a transition zone to a highly saline dolomite facies phase. Algal stromatolite mats and domes occupied low-energy niches in both the limestone and dolomite facies, whereas stratiform algal stromatolites were confined to the areas of moderate energy within the dolomite facies.

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

USGS1974

Equilibria of cinnabar, stibnite, and saturated solutions in the system HgS-Sb2S3-Na2S-H2O from 150° to 250°C at 100 bars, with implications concerning ore genesis

The common occurrence of cinnabar and stibnite in well-defined districts in the same epithermal environments suggests that similar physiochemical processes are responsible for the genesis of the two minerals; however, cinnabar and stibnite tend to be segregated within these districts and also within individual deposits that contain both minerals. Where cinnabar and stibnite occur in contact, textural evidence indicates that cinnabar is generally younger, although some textures suggest overlap of deposition. To better understand the physicochemical processes involved in the formation of cinnabar and stibnite deposits, we investigated the solubilities of cinnabar and stibnite in aqueous Na 2 S solutions that were simultaneously saturated with both cinnabar and stibnite at concentrations from 0.384 percent (0.0492 mol/kg) to 1.772 percent(0.227 mol/kg)Na 2 S at temperatures from 150° to 250°C, at 100 bars pressure. The ratio of dissolved Sb 2 S 3 to HgS under most conditions is larger than 25:1 moles per mole. We conclude that alkaline sulfide solutions could not transport geologically appreciable amounts of HgS while they are saturated with stibnite; major amounts of HgS could only be transported in solutions that are undersaturated with stibnite. Solubility behavior of HgS and Sb 2 S 3 is thus a possible mechanism for the segregation of cinnabar and stibnite, especially when the conduit system is modified during the episode of mineralization. The deposition of stibnite before that of cinnabar in most places but with minor overlapping deposition in some places is in accord with deductions made from the solubility studies.

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