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At least 73 records · Page 4Linked to original sources
USGS2005

Porphyry copper deposits of the world: database, map, and grade and tonnage models

Mineral deposit models are important in exploration planning and quantitative resource assessments for two reasons: (1) grades and tonnages among deposit types are significantly different, and (2) 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. 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 porphyry copper deposits. This report is an update of an earlier publication about porphyry copper deposits. In this report we have added 84 new porphyry copper deposits and removed 12 deposits. In addition, some errors have been corrected and a number of deposits have had some information, such as grades, tonnages, locations, or ages revised. This publication contains a computer file of information on porphyry copper deposits from around the world. It also presents new grade and tonnage models for porphyry copper deposits and for three subtypes of porphyry copper deposits and a map showing the location of all deposits. 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 used in this compilation. Next, the fields of the data file are considered. Finally, we provide new grade and tonnage models.

Open-File Report↗
USGS2008

Porphyry copper deposits of the world: Database and grade and tonnage models, 2008

This report is an update of earlier publications about porphyry copper deposits (Singer, Berger, and Moring, 2002; Singer, D.A., Berger, V.I., and Moring, B.C., 2005). The update was necessary because of new information about substantial increases in resources in some deposits and because we revised locations of some deposits so that they are consistent with images in GoogleEarth. In this report we have added new porphyry copper deposits and removed a few incorrectly classed deposits. In addition, some errors have been corrected and a number of deposits have had some information, such as grades, tonnages, locations, or ages revised. Colleagues have helped identify places where improvements were needed. Mineral deposit models are important in exploration planning and quantitative resource assessments for a number of reasons including: (1) grades and tonnages among deposit types are significantly different, and (2) 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. 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 porphyry copper deposits. The consistently defined deposits in this file provide the foundation for grade and tonnage models included here and for mineral deposit density models (Singer and others, 2005: Singer, 2008).

Open-File Report↗
USGS2011

Hydrogeochemical processes governing the origin, transport and fate of major and trace elements from mine wastes and mineralized rock to surface waters

The formation of acid mine drainage from metals extraction or natural acid rock drainage and its mixing with surface waters is a complex process that depends on petrology and mineralogy, structural geology, geomorphology, surface-water hydrology, hydrogeology, climatology, microbiology, chemistry, and mining and mineral processing history. The concentrations of metals, metalloids, acidity, alkalinity, Cl - , F - and SO 4 2- found in receiving streams, rivers, and lakes are affected by all of these factors and their interactions. Remediation of mine sites is an engineering concern but to design a remediation plan without understanding the hydrogeochemical processes of contaminant mobilization can lead to ineffective and excessively costly remediation. Furthermore, remediation needs a goal commensurate with natural background conditions rather than water-quality standards that might bear little relation to conditions of a highly mineralized terrain. This paper reviews hydrogeochemical generalizations, primarily from US Geological Survey research, that enhance our understanding of the origin, transport, and fate of contaminants released from mined and mineralized areas. Mobility of potential or actual contaminants from mining and mineral processing activities depends on (1) occurrence : is the mineral source of the contaminant actually present? (2) abundance : is the mineral present in sufficient quantity to make a difference? (3) reactivity : what are the energetics, rates, and mechanisms of sorption and mineral dissolution and precipitation relative to the flow rate of the water? and (4) hydrology : what are the main flow paths for contaminated water? Estimates of relative proportions of minerals dissolved and precipitated can be made with mass-balance calculations if minerals and water compositions along a flow path are known. Combined with discharge, these mass-balance estimates quantify the actual weathering rate of pyrite mineralization in the environment and compare reasonably well with laboratory rates of pyrite oxidation except when large quantities of soluble salts and evaporated mine waters have accumulated underground. Quantitative mineralogy with trace-element compositions can substantially improve the identification of source minerals for specific trace elements through mass balances. Post-dissolution sorption and precipitation (attenuation) reactions depend on the chemical behavior of each element, solution composition and pH, aqueous speciation, temperature, and contact-time with mineral surfaces. For example, little metal attenuation occurs in waters of low pH (<3.5) and metals tend to maintain element ratios indicative of the main mineral or group of minerals from which they dissolved, except Fe, SiO 2 , and redox-sensitive oxyanions (As, Sb, Se, Mo, Cr, V). Once dissolved, metal and metalloid concentrations are strongly affected by redox conditions and pH. Iron is the most reactive because it is rapidly oxidized by bacteria and archaea and Fe(III) hydrolyzes and precipitates at low pH (1&ndash;3) which is related directly to its first hydrolysis constant, pK 1 = 2.2. Several insoluble sulfate minerals precipitate at low pH including anglesite, barite, jarosite, alunite and basaluminite. Aluminum hydrolyzes near pH 5 (pK 1 = 5.0) and provides buffering and removal of Al by mineral precipitation from pH 4&ndash;5.5. Dissolved sulfate behaves conservatively because the amount removed from solution by precipitation is usually too small relative to the high concentrations in the water column and relative to the flow rate of the water.

Applied Geochemistry↗
USGS2002

Porphyry copper deposits of the world: Database, maps, and preliminary analysis

Mineral deposit models are important in exploration planning and quantitative resource assessments for two reasons: (1) grades and tonnages among deposit types are significantly different, and (2) 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. Far 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, such as those presented here, 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. 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 a group of porphyry copper deposits. This publication contains a computer file of information on porphyry copper deposits around the world. It also presents new grade and tonnage models for three subtypes of porphyry copper deposits, maps showing locations and general ages of these deposits, and a preliminary analysis with a number of figures summarizing many of the properties of these porphyry-style deposits. These summaries can be considered a new, quantified, form of most parts of descriptive models such as those in Cox and Singer (1986). The value of this information and analyses depends critically on the consistent manner of data gathering. For this reason, we first discuss the rules used in this compilation. Next the fields of the data file are considered. Finally, we discuss some of the things that can be done with the data.

Open-File Report↗
USGS2016

Geochemistry of host rocks in the Howards Pass district, Yukon-Northwest Territories, Canada: implications for sedimentary environments of Zn-Pb and phosphate mineralization

Detailed lithogeochemical data are reported here on early Paleozoic sedimentary rocks that host the large Howards Pass stratiform Zn-Pb deposits in Yukon-Northwest Territories. Redox-sensitive trace elements (Mo, Re, V, U) and Ce anomalies in members of the Duo Lake Formation record significant environmental changes. During the deposition of lower footwall units (Pyritic siliceous and Calcareous mudstone members), bottom waters were anoxic and sulphidic, respectively; these members formed in a marginal basin that may have become increasingly restricted with time. Relative to lower members, a major environmental change is proposed for deposition of the overlying Lower cherty mudstone member, which contains phosphorite beds up to ∼0.8 m thick in the upper part, near the base of the Zn-Pb deposits. The presence of these beds, together with models for modern phosphorite formation, suggests P input from an upwelling system and phosphorite deposition in an upper slope or outer shelf setting. The overlying Active mudstone member contains stratabound to stratiform Zn-Pb deposits within black mudstone and gray calcareous mudstone. Data for unmineralized black mudstone in this member indicate deposition under diverse redox conditions from suboxic to sulphidic. Especially distinctive in this member are uniformly low ratios of light to heavy rare earth elements that are unique within the Duo Lake Formation, attributed here to the dissolution of sedimentary apatite by downward-percolating acidic metalliferous brines. Strata that overlie the Active member (Upper siliceous mudstone member) consist mainly of black mudstone with thin (0.5–1.5 cm) laminae of fine-grained apatite, recording continued deposition on an upper slope or outer shelf under predominantly suboxic bottom waters. Results of this study suggest that exploration for similar stratiform sediment-hosted Zn-Pb deposits should include the outer parts of ancient continental margins, especially at and near stratigraphic transitions from marginal basin facies to overlying slope or shelf facies.

Mineralium Deposita↗
USGS2022

Marine minerals in Alaska — A review of coastal and deep-ocean regions

Minerals occurring in marine environments span the globe and encompass a broad range of mineral categories, forming within varied geologic and oceanographic settings. They occur in coastal regions, either from the continuation or mechanical reworking of terrestrial mineralization, as well as in the deep ocean, from diagenetic, hydrogenetic, and hydrothermal processes. The oceans cover most of the Earth’s surface and as a result, any inventory of global resources is incomplete without the inclusion of marine minerals. This study by the U.S. Geological Survey reviews current knowledge regarding deep-ocean and coastal marine minerals within the marine areas surrounding Alaska, including the Alaska Outer Continental Shelf (OCS). For the purposes of this study, we have divided these areas in to eight regions: (1) Gulf of Alaska seamounts, (2) Chukchi Borderland, (3) Canada Basin, (4) Aleutian Arc, (5) Seward Peninsula, (6) Goodnews Bay, (7) Bristol Bay and Alaska Peninsula, and (8) southern and southeastern Alaska. The Alaska OCS encompasses several areas broadly conducive to marine mineral formation, including extensional basins resulting from an active subduction zone where massive sulfide deposits may form, deep abyssal plains with conditions that may lead to manganese nodule formation, seamounts that can provide substrate for the growth of ferromanganese crusts, and erosional settings and submerged continental crust where placer deposits are found. For deep-ocean hydrothermal minerals and manganese nodules, the Alaska OCS contains prospective regions, including the Canada Basin and the Aleutian Arc; however, no such minerals have yet been identified. We explore the probability that these minerals occur based on reviews of existing geologic and oceanographic data within the relevant sections. In regions far from shore data are limited. Deep-ocean ferromanganese crusts are known to occur in two regions: (1) the Gulf of Alaska seamounts and (2) the Chukchi Borderland in the Arctic Ocean. Limited sampling has occurred in both regions, and along the Chukchi Borderland the sampling was outside of the OCS and the U.S. Exclusive Economic Zone. Data relevant to coastal minerals is more extensive, and in some places fairly systematic sampling was conducted. Several nearshore placer deposits have been exploited for decades; however, the potential for nearshore extension of terrestrial ore deposits is less well considered. This contribution considers the state of knowledge regarding marine mineral occurrences within the Alaska regions and identifies the data gaps in order to help inform future marine mineral related research efforts around Alaska.

Alaska↗
USGS2011

Mineral transformations associated with goethite reduction by Methanosarcina barkeri

To investigate the interaction between methanogens and iron-containing minerals in anoxic environments, we conducted batch culture experiments with Methanosarcina barkeri in a phosphate-buffered basal medium (PBBM) to bioreduce structural Fe(III) in goethite with hydrogen as the sole substrate. Fe(II) and methane concentrations were monitored over the course of the bioreduction experiments with wet chemistry and gas chromatography, respectively. Subsequent mineralogical changes were characterized with X-ray diffraction (XRD) and scanning electron microscopy (SEM). In the presence of an electron shuttle anthraquinone-2,6-disulfonate (AQDS), 30% Fe(III) in goethite (weight basis) was reduced to Fe(II). In contrast, only 2% Fe(III) (weight basis) was bioreduced in the absence of AQDS. Most of the bioproduced Fe(II) was incorporated into secondary minerals including dufrénite and vivianite. Our data implied a dufrénite–vivianite transformation mechanism where a metastable dufrénite transformed to a more stable vivianite over extended time in anaerobic conditions. Methanogenesis was greatly inhibited by bioreduction of goethite Fe(III). These results have important implications for the methane flux associated with Fe(III) bioreduction and ferrous iron mineral precipitation in anaerobic soils and sediments.

Chemical Geology↗
USGS2021

Mapping critical minerals from the sky

Critical mineral resources titanium, zirconium, and rare earth elements occur in placer deposits over vast parts of the U.S. Atlantic Coastal Plain. Key questions regarding provenance, pathways of minerals to deposit sites, and relations to geologic features remain unexplained. As part of a national effort to collect data over regions prospective for critical minerals, the first public high-resolution aeroradiometric survey over the U.S. Atlantic Coastal Plain was conducted over Quaternary sediments in South Carolina. The new data provide an unprecedented view of potential deposits by imaging Th-bearing minerals in the heavy mineral assemblage. Sand ridges show the highest radiometric Th values with localized, linear anomalies, especially along the shoreface and in areas reworked by multiple processes and/or during multiple episodes. Estuarine areas with finer-grained sediments show lower, distributed Th anomalies. Th values averaged over geologic unit areas are similar for both environments, suggesting that heavy minerals are present but have not been locally concentrated in the lower-energy estuarine environments. Radiometric K highlights immature minerals such as mica and potassium feldspar. K is elevated within shallow sediments younger than ca. 130 ka, an attribute that persists in regional data from northern South Carolina to northern Florida. Both K and Th are elevated over the floodplains of the Santee River and other rivers with headwaters in the igneous and metamorphic Piedmont Terrane. The persistence of K anomalies for distances of more than 100 km from the Santee River floodplain suggests that heavy minerals are delivered from the Piedmont to offshore areas by major rivers, transported along the coast by the longshore current, and redeposited onshore by marine processes.

Florida, Georgia, South Carolina↗
USGS2002

Microbial transformation of elements: The case of arsenic and selenium

Microbial activity is responsible for the transformation of at least one third of the elements in the periodic table. These transformations are the result of assimilatory, dissimilatory, or detoxification processes and form the cornerstones of many biogeochemical cycles. Arsenic and selenium are two elements whose roles in microbial ecology have only recently been recognized. Known as "essential toxins", they are required in trace amounts for growth and metabolism but are toxic at elevated concentrations. Arsenic is used as an osmolite in some marine organisms while selenium is required as selenocysteine (i.e. the twenty-first amino acid) or as a ligand to metal in some enzymes (e.g. FeNiSe hydrogenase). Arsenic resistance involves a small-molecular-weight arsenate reductase (ArsC). The use of arsenic and selenium oxyanions for energy is widespread in prokaryotes with representative organisms from the Crenarchaeota, thermophilic bacteria, low and high G+C gram-positive bacteria, and Proteobacteria. Recent studies have shown that both elements are actively cycled and play a significant role in carbon mineralization in certain environments. The occurrence of multiple mechanisms involving different enzymes for arsenic and selenium transformation indicates several different evolutionary pathways (e.g. convergence and lateral gene transfer) and underscores the environmental significance and selective impact in microbial evolution of these two elements.

International Microbiology↗
USGS2002

Worldwide occurrences of arsenic in ground water

Numerous aquifers worldwide carry soluble arsenic at concentrations greater than the World Health Organization--and U.S. Environmental Protection Agency--recommended drinking water standard of 10 mg per liter. Sources include both natural (black shales, young sediments with low flushing rates, gold mineralization, and geothermal environments) and anthropogenic (mining activities, livestock feed additives, pesticides, and arsenic trioxide wastes and stockpiles). Increased solubility and mobility of arsenic is promoted by high pH (>8.5), competing oxyanions, and reducing conditions. In this Policy Forum, Nordstrom argues that human health risks from arsenic in ground water can be minimized by incorporating hydrogeochemical knowledge into water management decisions and by more careful monitoring for arsenic in geologically high-risk areas.

Science↗
USGS1985

Aeromagnetic maps of the Latir Peak and Wheeler Peak Wildernesses and the Columbine-Hondo Wilderness Study Area, Taos County, New Mexico

This report interprets data from a helicopter-borne magnetic survey to help delineate subsurface geology. Such data, acquired near the ground, reflect greater magnetic detail than do data acquired at higher altitude. Data from a high-altitude reconnaissance aeromagnetic survey (U.S. Geological Survey, 1976) are used selectively to assist in the interpretation of the helicopter data. Interpretations are chiefly empirical, wherein magnetic anomalies characterizing known geologic features in the region are used as interpretive criteria for identifying such features where they are concealed. Identifying geologic environments favorable for mineral deposits is a primary objective of this report. Geophysical interpretations of a broader and more general scope are made from other geophysical data by Cordell and Jones (in press).

New Mexico↗
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↗
USGS1958

The geology and ore deposits of Upper Mayflower Gulch, Summit County, Colorado

Upper Mayflower Gulch is on the highly glaciated western side of the Tenmile Range near Kokomo in central Colorado. Somewhat less than $500,000 in silver and gold has been produced from the area since the first mining in the 1880' s. In the mapped area high grade regional metamorphism has produced two varieties of gneiss and a granulite. Total thickness of the rocks is about 5,000 feet. Relict bedding is preserved in compositional banding which strikes north to N. 20 ? E. and dips 70 ? to 80 ? southeast. No significant folding was observed. Normal faulting has occurred since the Precambrian; two major sets of faults are recognizable: (1) a set striking N. 70 ? to 85 ? E. and dipping 75?-85 ? NW; and (2) a set striking N. 70?-50 ? W. and dipping 50?-60 ? SW. Tabular bodies of pegmatite and retrogressively metamorphosed schist along many faults indicate Precambrian movement. The Mayflower fault, a 90 to 300 foot wide zone of siltification and shattered rock, strikes about N. 40 ? W. It extends the entire length of the gulch and appears to form the northern terminus for the northeast trending Mosquito Fault. The Mayflower fault shows repeated movement since the Precambrian, totaling about 3,000 feet of apparent dip slip and 640 feet of apparent strike slip. Faulting during the Tertiary includes both additional movement along Precambrian faults and development of shears trending N. to N. 20 ? E. The shears served as channels for the intrusion of two varieties of quartz latite porphyry dikes. Specular hematite and base-metal sulfide mineralization followed intrusion of the porphyry dikes; the minerals were deposited in open fault zones by high temperature solutions in a low pressure environment. The principal metallic minerals in order of deposition are: hematite, pyrite, chalcopyrite, sphalerite, galena, and rarer argentite. The major mines are the Gold Crest, Payrock, Nova Scotia Boy, and Bird's Nest.

Open-File Report↗
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↗