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Minerals & deposits

Find USGS publications on mineral resources and deposits. Search commodities and geographic names, then check source reports for geology and assessment methods.

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USGS2023

Mineral commodity summaries 2023

Each mineral commodity chapter of the 2023 edition of the U.S. Geological Survey (USGS) Mineral Commodity Summaries (MCS) includes information on events, trends, and issues for each mineral commodity as well as discussions and tabular presentations on domestic industry structure, Government programs, tariffs, 5-year salient statistics, and world production, reserves, and resources. The MCS is the earliest comprehensive source of 2022 mineral production data for the world. More than 90 individual minerals and materials are covered by 2-page synopses. For mineral commodities for which there is a Government stockpile, detailed information concerning the stockpile status is included in the 2-page synopsis. Abbreviations and units of measure and definitions of selected terms used in the report are in Appendix A and Appendix B, respectively. Reserves and resources information is in Appendix C, which includes “Part A—Resource and Reserve Classification for Minerals” and “Part B—Sources of Reserves Data.” A directory of USGS minerals information country specialists and their responsibilities is in Appendix D. The USGS continually strives to improve the value of its publications to users. Constructive comments and suggestions by readers of the MCS 2023 are welcomed.

Mineral Commodity Summaries↗

USGS2011

Mineral Commodity Summaries 2011

Each chapter of the 2011 edition of the U.S. Geological Survey (USGS) Mineral Commodity Summaries (MCS) includes information on events, trends, and issues for each mineral commodity as well as discussions and tabular presentations on domestic industry structure, Government programs, tariffs, 5-year salient statistics, and world production and resources. The MCS is the earliest comprehensive source of 2010 mineral production data for the world. More than 90 individual minerals and materials are covered by two-page synopses. For mineral commodities for which there is a Government stockpile, detailed information concerning the stockpile status is included in the two-page synopsis. Mineral Commodity Summaries 2011 contains new chapters on iron oxide pigments, wollastonite, and zeolites. The chapters on mica (natural), scrap and flake and mica (natural), sheet have been combined into a single chapter - mica (natural). Abbreviations and units of measure, and definitions of selected terms used in the report, are in Appendix A and Appendix B, respectively. "Appendix C - Reserves and Resources" has been divided into "Part A - Resource/Reserve Classification for Minerals" and "Part B - Sources of Reserves Data," including some information that was previously in this introduction. A directory of USGS minerals information country specialists and their responsibilities is Appendix D. The USGS continually strives to improve the value of its publications to users. Constructive comments and suggestions by readers of the MCS 2011 are welcomed.

Mineral Commodity Summaries↗

USGS1998

Microbial mineralization of VC and DCE under different terminal electron accepting conditions

Production of 14CO2 from [1,2-14C] dichloroethene (DCE) or [1,2-14C] vinyl chloride (VC) was quantified in aquifer and stream-bed sediment microcosms to evaluate the potential for microbial mineralization as a pathway for DCE and VC biodegradation under aerobic, Fe(III)-reducing, SO4-reducing, and methanogenic conditions. Mineralization of [1,2-14C] DCE and [1,2-14C] VC to 14CO2 decreased under increasingly reducing conditions, but significant mineralization was observed for both sediments even under anaerobic conditions. VC mineralization decreased in the order of aerobic > Fe(III)-reducing > SO4-reducing > methanogenic conditions. For both sediments, VC mineralization was greater than DCE mineralization under all electron-accepting conditions examined. For both sediments, DCE mineralization was at least two times greater under aerobic conditions than under anaerobic conditions. Although significant microbial mineralization of DCE was observed under anaerobic conditions, recovery of 14CO2 did not differ substantially between anaerobic treatments.

Anaerobe↗

USGS1987

Residence of silver in mineral deposits of the Thunder Mountain caldera complex, Central Idaho, U.S.A.

Silver is an accessory element in gold, antimony, and tungsten deposits of the caldera complex. Most of the deposits are economically of low grade and genetically of xenothermal or epithermal character. Their gold- and silver-bearing minerals are usually disseminated, fine grained, and difficult to study. Sparsely disseminated pyrite and arsenoprite are common associates. Identified silver minerals are: native silver and electrum; the sulfides acanthite, argentite (the latter always inverted to acanthite), and members of the Silberkies group; the sulfosalts matildite, miargyrite, pyrargyrite, argentian tetrahedrite, and unnamed Ag-Sb-S and Ag-Fe-Sb-S minerals; the telluride hessite and the selenide naumannite; halides of the cerargyrite group; and the antimonate stetefeldtite. Suspected silver minerals include the sulfide uytenbogaardtite and the sulfosalts andorite, diaphorite, and polybasite. Electrum, acanthite, and argentian tetrahedrite are common, though nowhere abundant. The other silver minerals are rare. Silver is present as a minor element in the structure of some varieties of other minerals. These include arsenopyrite, chalcopyrite, chalcostibite, covelline, digenite, galena, sphalerite, and stibnite. The search for adventitious Ag in most of these minerals has been cursory. The results merely indicate that elemental silver is not confined to discrete silver minerals and is, therefore, an additional complication for the recovery of silver-bearing material from some deposits. Silver occurs cryptically in some plants of the region. At Red Mountain, for example, the ashed sapwood of Douglas-fir (Pseudotsuga menziesii) contains 2 to 300 ppm Ag. Silver in the ashed wood is roughly 100 times as abundant as it is in soil. The phenomenon, useful in biogeochemical exploration, deserves the attention of mineralogists. ?? 1987 Springer-Verlag.

Mineralogy and Petrology↗

USGS2012

Development and application of a soil organic matter-based soil quality index in mineralized terrane of the Western US

Soil quality indices provide a means of distilling large amounts of data into a single metric that evaluates the soil’s ability to carry out key ecosystem functions. Primarily developed in agroecosytems, then forested ecosystems, an index using the relation between soil organic matter and other key soil properties in more semi-arid systems of the Western US impacted by different geologic mineralization was developed. Three different sites in two different mineralization types, acid sulfate and Cu/Mo porphyry in California and Nevada, were studied. Soil samples were collected from undisturbed soils in both mineralized and nearby unmineralized terrane as well as waste rock and tailings. Eight different microbial parameters (carbon substrate utilization, microbial biomass-C, mineralized-C, mineralized-N and enzyme activities of acid phosphatase, alkaline phosphatase, arylsulfatase, and fluorescein diacetate) along with a number of physicochemical parameters were measured. Multiple linear regression models between these parameters and both total organic carbon and total nitrogen were developed, using the ratio of predicted to measured values as the soil quality index. In most instances, pooling unmineralized and mineralized soil data within a given study site resulted in lower model correlations. Enzyme activity was a consistent explanatory variable in the models across the study sites. Though similar indicators were significant in models across different mineralization types, pooling data across sites inhibited model differentiation of undisturbed and disturbed sites. This procedure could be used to monitor recovery of disturbed systems in mineralized terrane and help link scientific and management disciplines.

Environmental Earth Sciences↗

USGS1978

Identification and significance of accessory minerals from a bituminous coal

A scanning electron microscope (SEM) has been used to study the in situ accessory minerals in polished blocks and pellets of petrographically analysed samples of the Waynesburg coal (hvb). Individual grains from the low-temperature ash (LTA) of the same coal were also studied. The visual resolution of the SEM permitted the detection of submicron mineral grains, which could then be analysed by the attached energy-dispersive system. Emphasis was placed on the highly reflective grains in the carbominerite bands. Among the most abundant accessory minerals observed were rutile, zircon, and rare-earth-bearing minerals. Small (1–5 μm) particles of what may be authigenic iron-rich chromite and a nickel silicate form rims on quartz grains. The SEM also permits the observation of grain morphology and mineral intergrowths. These data are useful in determining authigenicity and diagenic alteration. Substances in density splits of LTA include authigenic, detrital, extraterrestrial magnetite, tourmaline, and evaporite (?) minerals, and a fluorine-bearing amphibole. This analytical approach allows the determination of specific sites for many of the trace elements in coals. In the Waynesburg coal, most of the chromium is in the iron-chromium rims, the fluorine is in the amphibole, and the rare-earth elements are in rare-earth-bearing minerals. The ability to relate trace-element data to specific minerals will aid in predicting the behaviour of elements in coal during combustion, liquefaction, gasification, weathering, and leaching processes. This ability also permits insight into the degree of mobility of these elements in coal and provides clues to sedimentological and diagenetic conditions.

Pennsylvania↗

USGS2009

Delineation of Magnesium-rich Ultramafic Rocks Available for Mineral Carbon Sequestration in the United States

The 2005 Intergovernmental Panel on Climate Change report on Carbon Dioxide Capture and Storage suggested that a major gap in mineral carbon sequestration is locating the magnesium-silicate bedrock available to sequester CO2. It is generally known that silicate minerals with high concentrations of magnesium are suitable for mineral carbonation. However, no assessment has been made covering the entire United States detailing their geographical distribution and extent, or evaluating their potential for use in mineral carbonation. Researchers at Columbia University and the U.S. Geological Survey have developed a digital geologic database of ultramafic rocks in the continental United States. Data were compiled from varied-scale geologic maps of magnesium-silicate ultramafic rocks. These rock types are potentially suitable as source material for mineral carbon-dioxide sequestration. The focus of the national-scale map is entirely on suitable ultramafic rock types, which typically consist primarily of olivine and serpentine minerals. By combining the map with digital datasets that show non-mineable lands (such as urban areas and National Parks), estimates on potential depth of a surface mine, and the predicted reactivities of the mineral deposits, one can begin to estimate the capacity for CO2 mineral sequestration within the United States. ?? 2009 Elsevier Ltd. All rights reserved.

Conference Paper↗

USGS2013

Quantifying mineral abundances of complex mixtures by coupling spectral deconvolution of SWIR spectra (2.1-2.4 μm) and regression tree analysis

This paper presents a methodology for assessing mineral abundances of mixtures having more than two constituents using absorption features in the 2.1-2.4 μm wavelength region. In the first step, the absorption behaviour of mineral mixtures is parameterised by exponential Gaussian optimisation. Next, mineral abundances are predicted by regression tree analysis using these parameters as inputs. The approach is demonstrated on a range of prepared samples with known abundances of kaolinite, dioctahedral mica, smectite, calcite and quartz and on a set of field samples from Morocco. The latter contained varying quantities of other minerals, some of which did not have diagnostic absorption features in the 2.1-2.4 μm region. Cross validation showed that the prepared samples of kaolinite, dioctahedral mica, smectite and calcite were predicted with a root mean square error (RMSE) less than 9 wt.%. For the field samples, the RMSE was less than 8 wt.% for calcite, dioctahedral mica and kaolinite abundances. Smectite could not be well predicted, which was attributed to spectral variation of the cations within the dioctahedral layered smectites. Substitution of part of the quartz by chlorite at the prediction phase hardly affected the accuracy of the predicted mineral content; this suggests that the method is robust in handling the omission of minerals during the training phase. The degree of expression of absorption components was different between the field sample and the laboratory mixtures. This demonstrates that the method should be calibrated and trained on local samples. Our method allows the simultaneous quantification of more than two minerals within a complex mixture and thereby enhances the perspectives of spectral analysis for mineral abundances.

Geoderma↗

USGS2013

Effect of organic matter properties, clay mineral type and thermal maturity on gas adsorption in organic-rich shale systems

A series of CH 4 adsorption experiments on natural organic-rich shales, isolated kerogen, clay-rich rocks, and artificially matured Woodford Shale samples were conducted under dry conditions. Our results indicate that physisorption is a dominant process for CH 4 sorption, both on organic-rich shales and clay minerals. The Brunauer–Emmett–Teller (BET) surface area of the investigated samples is linearly correlated with the CH 4 sorption capacity in both organic-rich shales and clay-rich rocks. The presence of organic matter is a primary control on gas adsorption in shale-gas systems, and the gas-sorption capacity is determined by total organic carbon (TOC) content, organic-matter type, and thermal maturity. A large number of nanopores, in the 2–50 nm size range, were created during organic-matter thermal decomposition, and they significantly contributed to the surface area. Consequently, methane-sorption capacity increases with increasing thermal maturity due to the presence of nanopores produced during organic-matter decomposition. Furthermore, CH 4 sorption on clay minerals is mainly controlled by the type of clay mineral present. In terms of relative CH 4 sorption capacity: montmorillonite ≫ illite – smectite mixed layer > kaolinite > chlorite > illite. The effect of rock properties (organic matter content, type, maturity, and clay minerals) on CH 4 adsorption can be quantified with the heat of adsorption and the standard entropy, which are determined from adsorption isotherms at different temperatures. For clay-mineral rich rocks, the heat of adsorption (q) ranges from 9.4 to 16.6 kJ/mol. These values are considerably smaller than those for CH 4 adsorption on kerogen (21.9–28 kJ/mol) and organic-rich shales (15.1–18.4 kJ/mol). The standard entropy (Δs°) ranges from -64.8 to -79.5 J/mol/K for clay minerals, -68.1 to -111.3 J/mol/K for kerogen, and -76.0 to -84.6 J/mol/K for organic-rich shales. The affinity of CH 4 molecules for sorption on organic matter is stronger than for most common clay minerals. Thus, it is expected that CH 4 molecules may preferentially occupy surface sites on organic matter. However, active sites on clay mineral surfaces are easily blocked by water. As a consequence, organic-rich shales possess a larger CH 4 -sorption capacity than clay-rich rocks lacking organic matter. The thermodynamic parameters obtained in this study can be incorporated into model predictions of the maximum Langmuir pressure and CH 4 - sorption capacity of shales under reservoir temperature and pressure conditions.

Conference Paper↗

USGS2007

From Projectile Points to Microprocessors - The Influence of Some Industrial Minerals

In the language of economic geology, Earth materials are classified as metallic ores, fuel minerals, gemstones, and industrial minerals. Most people know that metallic ores yield shiny, conductive, ductile elements such as copper, iron, or gold. Most understand that energy-producing coals constitute a fuel mineral. Likewise, dazzling rubies and rare sapphires are universally recognized as gemstones. The fourth group, industrial minerals, is largely unknown to the general public, even though industrial minerals are as essential to daily life as metals and fuel minerals. This report examines the occurrence and practical uses of nine important industrial minerals - constituting just a few of the more than 50 industrial minerals that shape human culture.

Circular↗

USGS2016

Historical files from Federal Government mineral exploration-assistance programs, 1950 to 1974

The Defense Minerals Administration (DMA), Defense Minerals Exploration Administration (DMEA), and Office of Minerals Exploration (OME) mineral exploration programs were active over the period 1950–1974. Under these programs, the Federal Government contributed financial assistance in the exploration for certain strategic and critical minerals. The information about a mining property that was collected under these programs was placed in files called dockets. A docket is a collection of material (application, contract, correspondence, maps, reports, results) about a property for which an individual applied for exploration assistance from the Federal Government. Information found in dockets describe where mineral deposits were examined, what was found, and whether it was mined. As such, they provide very useful information to private industry regarding potential and non-potential prospect areas, provide the U.S. Geological Survey with useful information on mineral occurrences that are used in national assessments for particular mineral deposits, and provide other U.S. Federal agencies (Bureau of Indian Affairs, Bureau of Land Management, and Environmental Protection Agency) information relevant to land management, permitting, and leasing.

Data Series↗

USGS1992

Maps showing mineral resource assessment for copper and molybdenum in porphyry and stockwork deposits and for tungsten, iron, gold, copper, and silver in skarn deposits, Dillon 1° x 2° quadrangle, Idaho and Montana

This report is one of several in the series that assess the mineral resources of the Dillon quadrangle. For the purpose of the assessment, mineral deposits· in the quadrangle that are either known or suspected from a knowledge of the geologic setting have been grou~d into 30 deposit types on the basis of mineralogy, commodity, or structural or depositional setting. The emphasis in these assessment reports is on metallic minerals, but some important nonmetallic minerals will also be assessed. Fossil fuels are beyond the scope of this investigation; phosphate and uranium have been investigated previously (Swanson, 1970; Wodzicki andKrason, 1981); and certain nonmetallic. minerals, including bulk commodities such as sand and gravel, are in large supply and thus not considered. The ·mineral resource assessment discussed in this report considers two deposit types: (1) porphyry or stockwork deposits of copper. and molybdenum (referred to generally in this report as porphyry deposits) and (2) skarn deposits of tungsten, iron, gold, copper, and silver. Combining copper and molybenum porphyry deposits into a single deposit type is believed necessary for this purpose· mainly because the two metals are found together in most .deposits in the quadrangle, a geochemical signature unique to each has not been determined, and the significant petrologic characteristics of many associated plutons are not well known, especially characterist~cs of subsurface plutons whose presence is .inferred from geophysical data. In assessing mineral resources,· we have adopted a general philosophy similar to that of Harrison and others (19S6). We attempt to identify those parts of the quadrangle that are favorable for the occurrence of mineral resources. We do not attempt to locate specific exploration targets nor to determine the quantity of reserves or resources present.

Idaho, Montana↗

USGS2002

Mapped minerals at Questa, New Mexico, using airborne visible-infrared imaging spectrometer (AVIRIS) data – Preliminary report for: First quarterly report of the U.S. Geological Survey investigation of baseline and pre-mining ground-water quality in the Red River Valley Basin, New Mexico, November 13, 2001

This preliminary study for the First Quarterly Report has spectrally mapped hydrothermally altered minerals useful in assisting in assessment of water quality of the Red River. Airborne Visible-Infrared Imaging Spectrometer (AVIRIS) data was analyzed to characterize mined and unmined ground at Questa, New Mexico. AVIRIS data covers the Red River drainage north of the river, from between the town of Questa on the west, to east of the town of Red River. The data was calibrated and analyzed using U.S. Geological Survey custom software and spectral mineral library. AVIRIS data was tested for spectral features that matched similar features in the spectral mineral library. Goodness-of-fit and band-depth were calculated for each comparison of spectral features and used to identify surface mineralogy. Mineral distribution, mineral associations, and AVIRIS pixel spectra were examined. Mineral maps show the distribution of iron hydroxides, iron sulfates, clays, micas, carbonates, and other minerals. Initial results show a system of alteration suites that overprint each other. Quartz-sericite-pyrite (QSP) alteration grading out to propylitic alteration (epidote and calcite) was identified at the Questa Mine (molybdenum porphyry) and a similar alteration pattern was mapped at the landslide ("scar") areas. Supergene weathering overprints the altered rock, as shown by jarosite, kaolinite, and gypsum. In the spectral analysis, hydrothermally altered ground appears to be more extensive at the unmined Goat Hill Gulch and the mined ground, than the ?scars? to the east. Though the "scars" have similar overall altered mineral suites, there are differences between the "scars" in sericite, kaolinite, jarosite, gypsum, and calcite abundance. Fieldwork has verified the results at the central unmined "scar" areas.

New Mexico↗

USGS2009

Geology and Nonfuel Mineral Deposits of Africa and the Middle East

A nation's endowment of nonfuel mineral resources, relative to the world's endowment, is a fundamental consideration in decisions related to a nation's economic and environmental well being and security. Knowledge of the worldwide abundance, distribution, and general geologic setting of mineral commodities provides a framework within which a nation can make decisions about economic development of its own resources, and the economic and environmental consequences of those decisions, in a global perspective. The information in this report is part of a U.S. Geological Survey (USGS) endeavor to evaluate the global endowment of both identified and undiscovered nonfuel mineral resources. The results will delineate areas of the world that are geologically permissive for the occurrence of undiscovered selected nonfuel mineral resources together with estimates of the quantity and quality of the resources. The results will be published as a series of regional reports; this one provides basic data on the identified resources and geologic setting, together with a brief appraisal of the potential for undiscovered mineral resources in Africa and the Middle East. Additional information, such as production statistics, economic factors that affect the mineral industries of the region, and historical information, is available in U.S. Geological Survey publications such as the Minerals Yearbook and the annual Mineral Commodity Summaries (available at http://minerals.usgs.gov/minerals).

Open-File Report↗

USGS2008

The Global Flows of Metals and Minerals

This paper provides a preliminary review of the trends in worldwide metals and industrial minerals production and consumption based on newly developed global metals and minerals Material Flow Accounts (MFA). The MFA developed encompass data on extraction and consumption for 25 metal and mineral commodities, on a country-by-country and year-by-year basis, for the period 1970 to 2004. The data-base, jointly developed by the authors, resides with the U.S. Geological Survey (USGS) as individual commodity Excel workbooks and within a Filemaker data management system for use in analysis. Numerous national MFA have been developed to provide information on the industrial metabolism of individual countries. These MFA include material flows associated with the four commodity categories of goods that are inputs to a country's economy, agriculture, forestry, metals and minerals, and nonrenewable organic material. In some cases, the material flows associated with the creation and maintenance of the built infrastructure (such as houses, buildings, roads, airports, dams, and so forth) were also examined. The creation of global metals and industrial minerals flows is viewed as a first step in the creation of comprehensive global MFA documenting the historical and current flows of all of the four categories of physical goods that support world economies. Metals and minerals represent a major category of nonrenewable resources that humans extract from and return to the natural ecosystem. As human populations and economies have increased, metals and industrial minerals use has increased concomitantly. This dramatic growth in metals and minerals use has serious implications for both the availability of future resources and the health of the environment, which is affected by the outputs associated with their use. This paper provides an overview of a number of the trends observed by examining the database and suggests areas for future study.

Open-File Report↗

USGS2021

Methodology and technical input for the 2021 review and revision of the U.S. Critical Minerals List

Pursuant to Section 7002 (“Mineral Security”) of Title VII (“Critical Minerals”) of the Energy Act of 2020 (Public Law 116–260, December 27, 2020, 116th Cong.), the Secretary of the Interior, acting through the Director of the U.S. Geological Survey, is tasked with reviewing and revising the methodology used to evaluate mineral criticality and the U.S. Critical Minerals List no less than every 3 years. The initial Critical Minerals List was published in the Federal Register on May 18, 2018, in response to Executive Order No. 13817, A Federal Strategy to Ensure Secure and Reliable Supplies of Critical Minerals (3 CFR, 2017 Comp, p. 397–399). This report documents the updated evaluation methodology and the resultant updated draft list of minerals recommended for inclusion in the Critical Minerals List.

Open-File Report↗

USGS1978

Mineral resources of the Rincon wilderness study area, Pima County, Arizona

The Rincon wilderness study area comprises about 254 km 2 (98 mi 2 ) of the Rincon Mountains 15-30 km (10-20 mi) east of Tucson, Arizona. The area lies within the Coronado National Forest and forms a belt around the north, east, and south sides of the Saguaro National Monument (fig. 1). A mineral resource survey was made of the area in 1977 by the U.S. Geological Survey and the U.S. Bureau of Mines. This study indicates that the potential for finding metallic or nonmetallic mineral deposits, petroleum or coal or geothermal energy in the study area is low. This appraisal is based on geologic and geochemical investigations and on examination of all mineralized prospects. A geologic map was made of the area and its immediate surrounding. Chemical and spectrographic analyses were made of 1.30 stream-sediment samples and of 143 rock samples. The locations of mining claims were compiled and samples from most of the claims were assayed. There has been no recorded mineral production from within the study area. The geology of the Rincon Mountains is structurally complex. The core of the Rincon Mountains, lying mainly within the Saguaro National Monument, is underlain by igneous and metamorphic rocks chiefly of Precambrian and Tertiary ages. The study area lies on the flanks of the mountains in a terrain of sedimentary, metamorphic, and igneous rocks mainly of Precambrian through mid-Tertiary age. The rocks of this area are cut by many faults, with low-angle or bedding-parallel faults abundant. the distribution of these faulted rocks around the flanks of the Rincon Mountains is the result of a doming in the core area, the sliding of rock masses from the high part of the dome down its flanks, and to the effects of erosion. The potential for economic metallic mineral deposits is considered low because the known areas of anomalous concentrations of metals are small and the concentration of metals weak and erratic. The surface signs of mineralization are largely restricted to 4 locales in which some prospects exist (fig. 1): (1) east of Colossal Cave, southwest or the Rincon Mountains, (2) north of Happy Valley, east of the mountains, (3) between Roble and Youtcy Canyons, northeast of the mountains, and (4) near Italian Trap north of the mountains. Very little primary sulfide mineralization is present and signs of alteration are restricted to narrow zones along faults and fractures. The geochemical anomalies are weak. The sites at which anomalous values of copper, molybdenum, or silver were obtained are mainly controlled by faults. Nonmetallic mineral resources occur in deposits that are too small and too remote to be economically attractive. Sand and gravel deposits in the main drainages are similar to larger deposits that occur closer to nearby highways and cities. Limestone and marble present in some of the metamorphic rocks are too impure and too broken for use as dimension stone. Use of this marble as decorative rock is limited by remote markets. Limestone suitable for making cement is not likely to be found in large quantities within the Rincon wilderness study area. Closely spaced fractures in the granitic rocks makes them of little value for building stone.

Arizona↗

USGS1978

Comparison of the Wilfley concentration table and hand panning for concentration of heavy minerals prior to geochemical analysis

Chemical analysis of heavy—mineral concentrates of stream sediments is a common geochemical exploration technique used by the U.S. Geological Survey. Generally these concentrates are prepared by hand panning at streamside or in a washtub and then further concentrated using heavy—liquid (bromoform) techniques in a laboratory. Concentration using heavy liquids is slow, tedious, and expensive for large surveys such as mineral evaluation of wilderness areas. In addition the cost of bromoform is expected to increase greatly because most if not all chemical companies in the United States have ceased production of the compound due to problems in meeting the safety standards of the U.S. Environmental Protection Agency (E.P.A.). Preliminary studies by the E.P.A. suggest a severe health hazard may be incurred by inhaling vapors of or contacting the skin with chemicals like bromoform. Heavy—liquid concentration of thousands of heavy— mineral samples carries an unavoidable risk of exposure to bromoform. The risk, expense, and time required by routine heavy—liquid concentration of heavy minerals should be eliminated by finding other methods to satisfactorily concentrate minerals whenever it is possible. Heavy—mineral concentrates can be used in several ways in geochemical exploration and each way has certain standards for the nature and quality of the mineral concentration required. The nature of the concentration refers to whether the heavy minerals are analyzed in bulk or whether they are split into magnetic fractions using a hand magnet and possibly a Frantz Isodynamic Magnetic Separator.

Open-File Report↗