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At least 73 records · Page 4Linked to original sources
USGS1975

Hydrologic evaluation of the Haystack Butte area : with emphasis on possible discharge of class-I wastes, Edwards Air Force Base, California

The discharge of 3 acre-feet (4 x 10 -3 cubic hectometres) per year of Class-I wastes in the Haystack Butte area of Edwards Air Force Base, Calif., has been proposed by the Air Force. Evaporation in this arid basin exceeds the 4 inches (100 millimetres) of annual precipitation. Fifteen test holes, ranging in depth from 40 to 240 feet (12 to 73 metres) below land surface, indicate that ground water occurs mostly in Tertiary volcanic and sedimentary rocks overlying pre-Tertiary quartz monzonite. Depth to water averages about 100 feet (30 metres) below land surface. Hydraulic conductivity of cores of Tertiary rock taken from a test hole at depths of 9 to 88 feet (2.7 to 27 metres) below land surface suggests values of 6.9 x 10-5 to 4.9 x 10 -3 feet per day (2.1 x 10 -5 to 1.5 x 10 -3 metres per day). Petrographic analyses of these cores indicate a material consisting mostly of weathered volcanic rocks with a moderate concentration of montmorillonite clay. The water-level gradient averages about 4 feet per mile (0.76 metre per kilometre). Ground-water discharge through a narrow gap in the southeastern part of the basin is calculated to be 3.8 x 10 -4 acre-feet (4.7 x 10 -7 cubic hectometres) per year. After leaving the basin, the underflow becomes part of a regional flow system discharging into Harper Lake playa. An increase in the underflow from 3.8 x 10 -4 acre-feet (4.7 x 10 -7 cubic hectometres) per year to 3 acre-feet (4 x 10 -3 cubic hectometres) per year may result in an undesirable surface-water flow by increasing the saturated thickness of the aquifer near the narrow gap in the southeastern part of the basin. Also, the very low hydraulic-conductivity values suggest that some difficulties may exist in percolating 3 acre-feet (4 x 10 -3 cubic hectometres) per year of wastes resulting in possible saturation of the ground surface outside the boundaries of the potential Class-I site. Because the rate of evaporation is very high (116 inches or 294.6 millimetres per year) in the study area, many of the problems associated with the percolation of the waste water and the subsequent changes in ground-water movement could be minimized by evaporating the wastes to complete dryness. The quality of the ground water in the basin is generally unsuitable for domestic, industrial, and irrigation purposes. The concentration and type of chemical constituents in the ground water suggest slow circulation in a geologic environment with soluble minerals.

California↗
USGS1989

Chemical hydrogeology in natural and contaminated environments

Chemical hydrogeology, including organic and inorganic aspects, has contributed to an increased understanding of groundwater flow systems, geologic processes, and stressed environments. Most of the basic principles of inorganic-chemical hydrogeology were first established by investigations of organic-free, regional-scale systems for which simplifying assumptions could be made. The problems of groundwater contamination are causing a shift of emphasis to microscale systems that are dominated by organic-chemical reactions and that are providing an impetus for the study of naturally occurring and manmade organic material. Along with the decrease in scale, physical and chemical heterogeneity become major controls. Current investigations and those selected from the literature demonstrate that heterogeneity increases in importance as the study site decreases from regional-scale to macroscale to microscale. Increased understanding of regional-scale flow systems is demonstrated by selection of investigations of carbonate and volcanic aquifers to show how applications of present-day concepts and techniques can identify controlling chemical reactions and determine their rates; identify groundwater flow paths and determine flow velocity; and determine aquifer characteristics. The role of chemical hydrogeology in understanding geologic processes of macroscale systems is exemplified by selection of investigations in coastal aquifers. Phenomena associated with the mixing zone generated by encroaching sea water include an increase in heterogeneity of permeability, diagenesis of minerals, and formation of geomorphic features, such as caves, lagoons, and bays. Ore deposits of manganese and uranium, along with a simulation model of ore-forming fluids, demonstrate the influence of heterogeneity and of organic compounds on geochemical reactions associated with genesis of mineral deposits. In microscale environments, importance of heterogeneity and consequences of organic reactions in determining the distribution and concentrations cf. constituents are provided by several studies, including infiltration of sewage effluent and migration of creosote in coastal plain aquifers. These studies show that heterogeneity and the dominance of organically controlled reactions greatly increase the complexity of investigations.Current investigations and those selected from the literature demonstrate that heterogeneity increases in importance as the study site decreases from regional-scale to macroscale to microscale. Increased understanding of regional-scale flow systems is demonstrated by selection of investigations of carbonate and volcanic aquifers to show how application of present-day concepts and techniques can identify controlling chemical reactions and determine their rates; identify groundwater flow paths and determine flow velocity; and determine aquifer characteristics. The role of chemical hydrogeology in understanding geologic processes of macroscale systems is exemplified by selection of investigations in coastal aquifers. Ore deposits of manganese and uranium, along with a simulation model of ore-forming fluids, demonstrate the influence of heterogeneity and of organic compounds on geochemical reactions associated with genesis of mineral deposits. In microscale environments, importance of heterogeneity is illustrated by studies of infiltration of sewage effluent and migration of creosote in coastal plain aquifers.

Journal of Hydrology↗
USGS2012

Geologic and environmental characteristics of porphyry copper deposits with emphasis on potential future development in the Bristol Bay Watershed, Alaska (Appendix H)

This report is prepared in cooperation with the Bristol Bay Watershed Assessment being conducted by the U.S. Environmental Protection Agency. The goal of the assessment is to help understand how future large-scale development in this watershed may affect water quality and the salmon fishery. Mining has been identified as a potential source of future large scale development in the region, especially because of the advanced stage of activity at the Pebble prospect. The goal of this report is to summarize the geologic and environmental characteristics of porphyry copper deposits in general, largely on the basis of literature review. Data reported in the Pebble Project Environmental Baseline Document, released by the Pebble Limited Partnership in 2011, are used to enhance the relevance of this report to the Bristol Bay watershed. The geologic characteristics of mineral deposits are paramount to determining their geochemical signatures in the environment. The geologic characteristics of mineral deposits are reflected in the mineralogy of the mineralization and alteration assemblages; geochemical associations of elements, including the commodities being sought; the grade and tonnage of the deposit; the likely mining and ore-processing methods used; the environmental attributes of the deposit, such as acid-generating and acid-neutralizing potentials of geologic materials; and the susceptibility of the surrounding ecosystem to various stressors related to the deposit and its mining, among other features (Seal and Hammarstrom, 2003). Within the Bristol Bay watershed, or more specifically the Nushagak and Kvichak watersheds, the geologic setting is permissive for the occurrence of several mineral deposit types that are amenable for large-scale development. Of these deposit types, porphyry copper deposits (e.g., Pebble) and intrusion-related gold deposits (e.g., Shotgun) are the most important on the basis of the current maturity of exploration activities by the mining industry. The Pebble deposit sits astride the drainage divide between the Nushagak and Kvichak watersheds, whereas the Humble, Big Chunk, and Shotgun deposits are within the Nushagak watershed. The Humble and Big Chunk prospects are geophysical anomalies that exhibit some characteristics similar to those found at Pebble. Humble was drilled previously in 1958 and 1959 as an iron prospect on the basis of an airborne magnetic anomaly. Humble is approximately 85 miles (137 km) west of Pebble; Big Chunk is approximately 30 miles (48 km) north-northwest of Pebble; and Shotgun is approximately 110 miles (177 km) northwest of Pebble. The H and D Block prospects, west of Pebble, represent additional porphyry copper exploration targets in the watershed.

Alaska↗
USGS2026

Top-down targeted network analysis of critical mineral commodities applied to international geochemistry database

The global demand for critical mineral commodities is rapidly increasing, making domestic production an important factor in supporting the economy and national security. Large scale, publicly available geochemical databases allow for the application of data informatics methods to interrogate critical mineral commodities data for correlations in deposit formation and distribution, particularly for identifying enrichment of multiple critical mineral commodities at the same deposit. In this study, we applied network analysis to the Critical Minerals Mapping Initiative (CMMI) ore geochemistry (Critical Minerals in Ores, CMiO) database to identify the high concentration (defined as 10× bulk crustal abundance) co-occurrence of different critical mineral commodities across a mineral system hierarchy from deposit environments to individual deposits. Identifying patterns or unique outliers in enrichment in network communities will allow for the location of secondary critical mineral commodity resources from under-utilized deposits. We find trends in the enrichment of critical mineral commodities in network-communities between the elements praseodymium (Pr), neodymium (Nd), terbium (Tb), and dysprosium (Dy) across multiple CMiO database deposit environments and groups down to specific deposit types and sites. A separate trend in network community deposition is observed as well between iridium (Ir) and platinum (Pt) in deposit environments, groups, types, and sites. Network analysis focused on critical minerals in magmatic-hydrothermal deposits identified multiple deposit sites from different deposit types within the CMiO database with concentrations of Dy, Nd, Tb, Pr, Ir, and Pt that are at least ten times greater than the crustal average. This approach can be applied to any target element(s) or deposit(s) of interest, allowing broad investigation of co-enriched critical mineral commodities.

Journal of Geochemical Exploration↗
USGS2009

The geologic relationships of industrial mineral deposits and asbestos in the western united states

In recent years, U.S. regulatory agencies have placed emphasis on identifying and regulating asbestos dust exposures in the mining environment, with a particular focus upon industrial mineral deposits in which asbestos occurs as an accessory mineral. Because asbestos minerals form in specific geologic environments, only certain predictable types of industrial mineral deposits can potentially host asbestos mineralization. By applying a basic knowledge of asbestos geology, the costly and time consuming efforts of asbestos monitoring and analyses can be directed towards those mineral deposit types most likely to contain asbestos mineralogy, while saving efforts on the mineral deposits that are unlikely to contain asbestos. While the vast majority of industrial mineral deposits in the Western United States are asbestos-free, there are several types that can, in some instances, host asbestos mineralization, or be closely associated with it. These industrial mineral deposits include a few types of aggregate, dimension, and decorative stone, and some deposits of chromite-nickel, magnesite, nepheline syenite, olivine, rare earth elements, talc, vermiculite, and wollastonite.

Conference Paper↗
USGS1995

Sorption and coprecipitation of trace concentrations of thorium with various minerals under conditions simulating an acid uranium mill effluent environment

Sorption of thorium by pre-existing crystals of anglesite (PbSO 4 ), apatite (Ca 5 (PO 4 ) 3 (HO)), barite (BaSO 4 ), bentonite (Na 0.7 Al 3.3 Mg 0.7 Si 8 O 20 (OH) 4 ), celestite (SrSO 4 ), fluorite (CaF 2 ), galena (PbS), gypsum (CaSO 4 ·2H 2 O), hematite (Fe 2 O 3 ), jarosite (KFe 3 (SO 4 ) 2 (OH) 6 ), kaolinite (Al 2 O 3 ·2SiO 2 ·2H 2 O), quartz (SiO 2 ) and sodium feldspar (NaAlSi 3 O 8 ) was studied under conditions that simulate an acidic uranium mill effluent environment. Up to 100% removal of trace quantitiees of thorim (approx. 1.00 ppm in 0.01 N H 2 SO 4 ) from solution occurred within 3 h with fluorite and within 48 h in the case of bentonite. Quartz, jarosite, hematite, sodium feldspar, gypsum and galena removed less than 15% of the thorium from solution. In the coprecipitation studies, barite, anglesite, gypsum and celestite were formed in the presence of thorium (approx. 1.00 ppm). Approximately all of the thorium present in solution coprecipitated with barite and celestite; 95% coprecipitated with anglesite and less than 5% with gypsum under similar conditions. When jarosite was precipitated in the presence of thorium, a significant amount of thorium (78%) was incorporated in the precipitate.

Inorganica Chimica Acta↗
USGS2009

Sediment-hosted zinc-lead deposits of the world— Database and grade and tonnage models

This report provides information on sediment-hosted zinc-lead mineral deposits based on the geologic settings that are observed on regional geologic maps. The foundation of mineral-deposit models is information about known deposits. The purpose of this publication is to make this kind of information available in digital form for sediment-hosted zinc-lead deposits. Mineral-deposit models are important in exploration planning and quantitative resource assessments: Grades and tonnages among deposit types are significantly different, and many types occur in different geologic settings that can be identified from geologic maps. Mineral-deposit models are the keystone in combining the diverse geoscience information on geology, mineral occurrences, geophysics, and geochemistry used in resource assessments and mineral exploration. Too few thoroughly explored mineral deposits are available in most local areas for reliable identification of the important geoscience variables, or for robust estimation of undiscovered deposits - thus, we need mineral-deposit models. Globally based deposit models allow recognition of important features because the global models demonstrate how common different features are. Well-designed and -constructed deposit models allow geologists to know from observed geologic environments the possible mineral-deposit types that might exist, and allow economists to determine the possible economic viability of these resources in the region. Thus, mineral-deposit models play the central role in transforming geoscience information to a form useful to policy makers. This publication contains a computer file of information on sediment-hosted zinc-lead deposits from around the world. It also presents new grade and tonnage models for nine types of these deposits and a file allowing locations of all deposits to be plotted in Google Earth. The data are presented in FileMaker Pro, Excel and text files to make the information available to as many as possible. The value of this information and any derived analyses depends critically on the consistent manner of data gathering. For this reason, we first discuss the rules applied in this compilation. Next, the fields of the data file are considered. Finally, we provide new grade and tonnage models that are, for the most part, based on a classification of deposits using observable geologic units from regional-scaled maps.

Open-File Report↗
USGS1961

Distribution of uranium ore deposits in the elk ridge area, San Juan County, Utah

The Elk Ridge area of southeastern Utah contains uranium ore deposits in two lower members of the Chinle formation of Late Triassic age. Each member is mineralized in different parts of the area , and where both are present only the lower contains ore . Across the Elk Ridge area from southwest to northeast, successively younger beds lap onto the unconformity that separates the Chinle from the underlying Moenkopi formation of Triassic(?), Early and Middle(?) Triassic age. Important uranium deposits have been found only in sandstone beds of the Chinle that are in contact with the Moenkopi. Sandstone of the Chinle formation lies on the Moenkopi (or is separated from it by gray mudstone of the Chinle no thicker than the depths of most of the known paleostream channel scours) in two separate parts of the Elk Ridge area . These "favorable areas" contain all the mines and important prospects. The ore deposits are flat-lying tabular to lenticular bodies in fluvial sandstone beds of the Chinle with fine-grained black uranium minerals chiefly interstitial to sand grains and as replacement of carbonaceous material. Most of the ore -bearing sandstone beds are discontinuous lenses intertonguing with and overlain by relatively impermeable mudstone. Contact of the host sandstone with the underlying Moenkopi seems to be a prerequisite for ore as the ore bodies are generally within a few feet of such contact areas and sandstone lenses separated from the Moenkopi by gray mudstone are generally not ore bearing. The consistent association of ore deposits with the Chinle-Moenkopi contact suggests that mineralizing solutions were introduced into the host beds from their areas of contact with the Moenkopi formation. Impermeable barriers overlying ore -bearing parts of the host sandstones were probably an important control on the deposition of ore minerals from solution. Hypofiltration of metallic constituents from ascending ore solutions may have been important. It is also possible that the overlying barriers formed traps for H2S gas or fluid hydrocarbons and thus localized a reducing chemical environment in which ore minerals were later precipitated.

Utah↗
USGS1988

Heavy-Mineral Placer Potential Map of the U.S. Continental Shelf, Western and Northern Gulf of Mexico

The establishment of the Exclusive Economic Zone (EEZ) in 1983 by Presidential Proclamation opened for natural resource exploration a vast offshore frontier area contiguous to the United States and its territories. The EEZ extends from the seaward limit of state waters (3 nautical mi from shore) to 200 nautical mi offshore, and it includes the continental shelves. Within the context of the EEZ natural resource assessment effort, the purpose of this study is to delineate, on a regional basis, the potential for heavy-mineral placers on the U.S. Continental Shelf in the western and northern Gulf of Mexico from the United States-Mexico border to the Alabama-Florida state line. This map is intended to serve as a general guide for placer exploration. It shows favorable sea-floor areas for placer occurrence in water depths ranging from 0 to 100 fathoms (600 ft). The map can be used as a guide for focusing costly exploratory efforts, such as coring operations and geophysical surveys. The potential economic value of heavy-mineral placer concentrations on the U.S. Continental Shelf is a function of both geologic and economic variables. Geologic variables include the composition and concentration of the heavy-mineral assemblages and their environment of deposition. Economic variables include the current world market price of extracted metals, as well as the cost of mining, processing, and marketing the metals. These economic factors, in turn, are tempered by the nation1s socio-political climate, which determines its need for specific mineral resources at any given time.

Miscellaneous Field Studies Map↗
USGS1971

Coronadite — Modes of occurrence and origin

The lead manganate, "coronadite," was first recognized at the Coronado mine in the Morenci district, Arizona, by Lindgren in 1903. Several years later, the identity of the mineral was questioned and it was not until 1932 that Orcel recognized it in material from Morocco. Since 1955, the mineral has been recognized at numerous places; in the USSR, east of the Ural Mountains, in several districts in Morocco, England, Australia, and India. In recent years, coronadite had been identified at numerous localities in New Mexico, Arizona, Nevada, and California by the writer and others. At this time, it has been identified at 22 localities, and in the opinion of this writer, it will be found at many more places if it is sought for carefully. Author's review of the known occurrences of coronadite and interpretation of the modes of geologic environment show that the mineral is found in veins and hot spring aprons, where it seems to have been deposited by hydrothermal waters from depth and that it is one of the manganese oxide minerals deposited as sediments. Probably it is more widely found in assemblages of minerals of supergene origin.

Arizona, Asturias, California, Chihuahua, Durango,↗
USGS2005

Ground water to surface water: Chemistry of thermal outflows in Yellowstone National Park

Geothermal waters in the earth’s subsurface boil with steam separation and may mix with dilute ground waters (that may or may not contain sulfuric acid from sulfur oxidation), resulting in a wide range of compositions when they discharge and emerge at the surface. As they discharge onto the ground surface they undergo evaporative cooling, degassing, oxidation, and mineral precipitation. Within this aquatic environment of rapidly changing physical and chemical parameters, numerous microbial communities develop—some of which affect oxidation and mineral precipitation. Microbes are responsible for rapid oxidation of iron and arsenic in thermal outflows, and for catalyzing the production of sulfuric acid from the oxidation of elemental sulfur. The attractive visual display of colors observed in Yellowstone’s geothermal waters reflects this interplay of physical, chemical, and biological phenomena. Oxidation of dissolved sulfide to thiosulfate occurs abiotically, and thiosulfate can be found in many of Yellowstone’s thermal waters—at any pH, temperature, and composition. Polythionates, on the other hand, are rarely found in Yellowstone waters but are associated with sulfur hydrolysis in Cinder Pool. Oxidation rates of iron and arsenic in overflows have been estimated at 1-3 mM/h and 0.04-0.1 mM/h, respectively—orders of magnitude faster than the abiotic rate. The abiotic production of thiosulfate from oxidation of dissolved sulfi de at Angel Terrace and Ojo Caliente is about 3-30 µM/min, faster by 2-3 orders of magnitude than the laboratory rate at 25°C. The partitioning of dissolved sulfide between that volatilized to the air and that oxidized to thiosulfate has been estimated at Angel Terrace and at Ojo Caliente. For the pH range of 6-8 and the temperature range of 50-93°C, 67-86% of the dissolved sulfide is lost to the atmosphere and 10-33% is oxidized to thiosulfate. Only a very small percentage, if any, forms elemental sulfur under these conditions.

Wyoming↗
USGS2017

Tectonic Speleogenesis of Devils Hole, Nevada, and Implications for Hydrogeology and the Development of Long, Continuous Paleoenvironmental Records

Devils Hole, in southern Nevada, is a surface collapse into a deep, planar, steeply dipping fault-controlled fissure in Cambrian limestone and dolostone. The collapse intersects the water table about 15 m below land surface and the fissure extends at least 130 m deeper. Below water, most of the fissure is lined with a >30-cm-thick layer of dense maxillary calcite that precipitated continuously from groundwater for >500,000 yr. The thick mammillary calcite coat implies a long history of calcite-supersaturated groundwaters, which, combined with the absence of dissolutional morphologies, suggests that Devils Hole was not formed by karst processes. Devils Hole is located in a region of active extension; its tectonic origin is shown by evidence of spreading of its planar opening along a fault and by the orientation of its opening and others nearby, perpendicular to the northwest-southeast minimum principal stress direction of the region. Most Quaternary tectonic activity in the area, including seismicity and Quaternary faults and fractures, occurs on or parallel to northeast-striking structures. The hydrogeologic implications of this primarily structural origin are that fracture networks and caves opened by extensional tectonism can act as groundwater flowpaths functionally similar to those developed by karst processes and that, during active extension, transmissivity can be maintained despite infilling by mineral precipitation. Such extensional environments can provide conditions favorable for accumulation of deposits preserving long, continuous paleoenvironmental records. The precipitates in Devils Hole store chronologies of flow system water-level fluctuations, hydrochemistry, a half-million-yr proxy paleoclimate record, evidence of Devils Hole's tectonic origin, and probably atmospheric circulation.

Quaternary Research↗
USGS1967

Sulfide solubilities in alteration-controlled systems

Solubilities of sphalerite (ZnS) and galena (PbS) were determined at 300° to 500°C and 1000 bars total pressure in a chemical environment buffered by silicate mineral equilibria. Chloride solutions and muscovite-bearing assemblages characteristic of hydrothermal wall-rock alteration were used; weak acidities at temperature were therefore involved. The metal concentrations encountered tended to be higher than those observed in high bisulfide-H 2 S systems at neutral to weakly basic pH used in most previous experimentation; the chemical conditions of the work, although not completely satisfactory, are geologically more realistic than previous experimentation done in the basic-pH region.

Science↗
USGS2003

Chromium geochemistry of serpentinous sediment in the Willow core, Santa Clara County, California

A preliminary investigation of Cr geochemistry in serpentinous sediment completed for a multiple-aquifer ground-water monitoring well (Willow core of Santa Clara County, CA) determined sediment at depths >225 meters contains Cr concentrations ranging from 195 to 1155 mg/kg. Serpentinous sediment from this site is a potential source of non-anthropogenic Cr contamination. Chromium-bearing minerals such as Cr-spinel appear to be the main source of Cr in the sediment; however, Cr-bearing silicates and clay minerals are additional Cr sources. Aqueous Cr concentrations in the sediment are <4.6 mg/L; however, the valence of Cr was not identified in the solutions or in the sediment. Although there is no indication of Cr(VI) contamination derived from the serpentinous sediment, elevated Cr concentrations in the sediment, the observed ‘dissolution’ textures of the Cr-bearing minerals, the estimated redox environment, and water chemistry indicate the formation of Cr(VI) is potentially favorable.

California↗
USGS1983

Preliminary results of spectral induced polarization measurements, Wadi Bidah District, Kingdom of Saudi Arabia

Laboratory spectral induced polarization (SIP) measurements on 29 carbonaceous schist samples from the Wadi Bidah district show that most are associated with very long polarization decays or, equivalently, large time constants. In contrast, measurements on two massive sulfide samples indicate shorter polarization decays or smaller time constants. This difference in time constants for the polarization process results in two differences in the phase spectra in the frequency range of from 0.06 to 1Hz. First, phase values of carbonaceous rocks generally decrease as a function of increasing frequency. Second, phase values of massive sulfide-bearing rocks increase as a function of increasing frequency. These results from laboratory measurements agree well with those from other reported SIP measurements on graphites and massive sulfides from the Canadian Shield. Four SIP lines, measured by using a 50-m dipole-dipole array, were surveyed at the Rabathan 4 prospect to test how well the results of laboratory sample measurements can be applied to larger scale field measurements. Along one line, located entirely over carbonaceous schists, the phase values decreased as a function of increasing frequency. Along a second line, located over both massive sulfides and carbonaceous schists as defined by drilling, the phase values measured over carbonaceous schists decreased as a function of increasing frequency, whereas those measured over massive sulfides increased. In addition, parts of two lines were surveyed down the axes of the massive sulfide and carbonaceous units. The phase values along these lines showed similar differences between the carbonaceous schists and massive sulfides. To date, the SIP survey and the SIP laboratory measurements have produced the only geophysical data that indicate an electrical difference between the massive sulfide-bearing rocks and the surrounding carbonaceous rocks in the Wadi Bidah district. However, additional sample and field measurements in areas of known mineralization would fully evaluate the SIP method as applied to various geologic environments and styles of massive sulfide mineralization. Additionally, the efficiency of SIP surveys in delineating areas of sulfide mineralization might be improved by surveying lines down the axes of known electrical conductors. An evaluation of the applied research done on the SIP method to date suggests that this technique offers significant exploration applications to massive sulfide exploration in the Kingdom of Saudi Arabia.

Open-File Report↗
USGS2009

Systematic approaches to comprehensive analyses of natural organic matter

The more that is learned of the chemistry of aquatic natural organic matter (NOM) the greater is the scientific appreciation of the vast complexity of this subject. This complexity is due not only to a multiplicity of precursor molecules in any environment but to their associations with each other and with other components of local environments such as clays, mineral acids and dissolved metals. In addition, this complex system is subject to constant change owing to environmental variables and microbial action. Thus, there is a good argument that no two NOM samples are exactly the same even from the same source at nearly the same time. When ubiquity of occurrence, reaction with water treatment chemicals, and subsequent human exposure are added to the list of NOM issues, one can understand the appeal that this subject holds for a wide variety of environmental scientists.

Annals of Environmental Science↗
USGS1993

Impact-shocked zircons: Discovery of shock-induced textures reflecting increasing degrees of shock metamorphism

Textural effects specifically characteristic of shock metamorphism in zircons from impact environments have not been reported previously. However, planar deformation features (PDF) due to shock metamorphism are well documented in quartz and other mineral grains from these same environments. An etching technique was developed that allows SEM visualization of PDF and other probable shock-induced textural features, such as granular (polycrystalline) texture, in zircons from a variety of impact shock environments. These textural features in shocked zircons from K/T boundary distal ejecta form a series related to increasing degrees of shock that should correlate with proportionate resetting of the UPb isotopic system.

Earth and Planetary Science Letters↗
USGS2017

Antimony

Antimony is an important mineral commodity used widely in modern industrialized societies. The element imparts strength, hardness, and corrosion resistance to alloys that are used in many areas of industry, including in lead-acid storage batteries. Antimony’s leading use is as a fire retardant in safety equipment and in household goods, such as mattresses. The U.S. Government has considered antimony to be a critical mineral mainly because of its use in military applications. The great majority of the world’s antimony comes from China, and much of the remainder is shipped to China for smelting. Antimony resources are unevenly distributed around the world. China has the bulk of the world’s identified resources; other countries that have identified antimony resources include Bolivia, Canada, Mexico, Russia, South Africa, Tajikistan, and Turkey. Resources in the United States are located mainly in Alaska, Idaho, Montana, and Nevada. The most significant antimony mineral deposits occur in geologic environments with a thick sequence of siliciclastic sedimentary rocks in areas with significant fault and fracture systems. The most common antimony ore mineral is stibnite (Sb2 S3 ), but more than 100 other minerals also contain antimony. The presence of antimony in surface waters and groundwaters results primarily from rock weathering, soil runoff, and anthropogenic sources. Global emissions of antimony to the atmosphere average 6,100 metric tons per year. Empirical data suggest that the acid-generating potential of antimony mine waste is low.

Professional Paper↗