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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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At least 595 records · Page 33Linked to original sources

USGS1997

Beryllium geochemistry in soils: Evaluation of 10Be/9Be ratios in authigenic minerals as a basis for age models

Soils contain a diverse and complex set of chemicals and minerals. Being an 'open system', both in the chemical and nuclear sense, soils have defied quantitative nuclear dating. However, based on the published studies of the cosmogenic atmospheric 10Be in soils, its relatively long half-life (1.5 Ma), and the fact that 10Be gets quickly incorporated in most soil minerals, this radionuclide appears to be potentially the most useful for soil dating. We therefore studied the natural variations in the specific activities of 10Be with respect to the isotope 9Be in mineral phases in eight profiles of diverse soils from temperate to tropical climatic regimes and evaluated the implications of the data for determining the time of formation of soil minerals, following an earlier suggestion [Lal et al., 1991. Development of cosmogenic nuclear methods for the study of soil erosion and formation rates. Current Sci. 61, 636-639.]. We find that the 10Be/9Be ratios in both bulk soils and in the authigenic mineral phases are confined within a narrower range than in 10Be concentrations. Also, the highest 10Be/9Be ratios in authigenic minerals are observed at the soil-rock interface as predicted by the model. We present model 10Be/9Be ages of the B-horizon and the corresponding soil formation rates for several soil profiles. The present study demonstrates that the 10Be/9Be ratios in the authigenic phases, e.g. clay and Fe-hydroxides, can indeed be used for obtaining useful model ages for soils younger than 10-15 Ma. However, the present work has to be pushed considerably further, to take into account more realistic age models in which, for instance, downward transport of 10Be and clays, and in-situ dissolution of clay minerals at depths, altering the 10Be/9Be ratios of the acidic solutions, are included. We show that in the case of younger soils (< 1 Ma) studied here, their 10Be inventories and 10Be/9Be ratios have been significantly disturbed possibly by mixing with transported soils. ?? 1997 Elsevier Science B.V.

Chemical Geology↗

USGS2002

Trace element abundances in major minerals of Late Permian coals from southwestern Guizhou province, China

Fourteen samples of minerals were separated by handpicking from Late Permian coals in southwestern Guizhou province, China. These 14 minerals were nodular pyrite, massive recrystallized pyrite, pyrite deposited from low-temperature hydrothermal fluid and from ground water; clay minerals; and calcite deposited from low-temperature hydrothermal fluid and from ground water. The mineralogy, elemental composition, and distribution of 33 elements in these samples were studied by optical microscopy, scanning electron microscope equipped with energy-dispersive X-ray spectrometer (SEM-EDX), X-ray diffraction (XRD), cold-vapor atomic absorption spectrometry (CV-AAS), atomic fluorescence spectrometry (AFS), inductively coupled-plasma mass spectrometry (ICP-MS), and ion-selective electrode (ISE). The results show that various minerals in coal contain variable amounts of trace elements. Clay minerals have high concentrations of Ba, Be, Cs, F, Ga, Nb, Rb, Th, U, and Zr. Quartz has little contribution to the concentration of trace elements in bulk coal. Arsenic, Mn, and Sr are in high concentrations in calcite. Pyrite has high concentrations of As, Cd, Hg, Mo, Sb, Se, Tl, and Zn. Different genetic types of calcite in coal can accumulate different trace elements; for example Ba, Co, Cr, Hg, Ni, Rb, Sn, Sr, and Zn are in higher concentrations in calcite deposited from low-temperature hydrothermal fluid than in that deposited from ground water. Furthermore, the concentrations of some trace elements are quite variable in pyrite; different genetic types of pyrites (Py-A, B, C, D) have different concentrations of trace elements, and the concentrations of trace elements are also different in pyrite of low-temperature hydrothermal origin collected from different locations. The study shows that elemental concentration is rather uniform in a pyrite vein. There are many micron and submicron mosaic pyrites in a pyrite vein, which is enriched in some trace elements, such as As and Mo. The content of trace element in pyrite vein depends upon the content of mosaic pyrite and of trace elements in it. Many environmentally sensitive trace elements are mainly contained in the minerals in coal, and hence the physical coal cleaning techniques can remove minerals from coal and decrease the emissions of potentially hazardous trace elements. ?? 2002 Elsevier Science B.V. All rights reserved.

International Journal of Coal Geology↗

USGS1996

Selected elements in major minerals from bituminous coal as determined by INAA: Implications for removing environmentally sensitive elements from coal

The four most abundant minerals generally found in Euramerican bituminous coals are quartz, kaolinite, illite and pyrite. These four minerals were isolated by density separation and handpicking from bituminous coal samples collected in the Ruhr Basin, Germany and the Appalachian basin, U.S.A. Trace-element concentrations of relatively pure (??? 99+%) separates of major minerals from these coals were determined directly by using instrumental neutron activation analysis (INAA). As expected, quartz contributes little to the trace-element mass balance. Illite generally has higher trace-element concentrations than kaolinite, but, for the concentrates analyzed in this study, Hf, Ta, W, Th and U are in lower concentrations in illite than in kaolinite. Pyrite has higher concentrations of chalcophile elements (e.g., As and Se) and is considerably lower in lithophile elements as compared to kaolinite and illite. Our study provides a direct and sensitive method of determining trace-element relationships with minerals in coal. Mass-balance calculations suggest that the trace-element content of coal can be explained mainly by three major minerals: pyrite, kaolinite and illite. This conclusion indicates that the size and textural relationships of these major coal minerals may be a more important consideration as to whether coal cleaning can effectively remove the most environmentally sensitive trace elements in coal than what trace minerals are present.

International Journal of Coal Geology↗

USGS2001

Lithodiversity and its spatial association with metallic mineral sites, Great Basin of Nevada

Geographical information system (GIS) techniques were used to investigate the spatial association between metallic mineral sites and lithodiversity in Nevada. Mineral site data sets include various size and type subsets of about 5,500 metal-bearing occurrences and deposits. Lithodiversity was calculated by counting the number of unique geological map units within four sizes of square-shaped sample neighborhoods (2.5-by-2.5, 5-by-5, 10-by-10, and 20-by-20 km) on three different scales of geological maps (national, 1:2,500,000; state, 1:500,000; county, 1:250,000). The spatial association between mineral sites and lithodiversity was observed to increase with increasing lithodiversity. This relationship is consistent for (1) both basin-range and range-only regions, (2) four sizes of sample neighborhoods, (3) various mineral site subsets, (4) the three scales of geological maps, and (5) areas not covered by large-scale maps. A map scale of 1:500,000 and lithodiversity sampling neighborhood of 5-by-5 km was determined to best describe the association. Positive associations occurred for areas having >3 geological map units per neighborhood, with the strongest observed at approximately >7 units. Areas in Nevada with more than three geological map units per 5-by-5 km neighborhood contain more mineral sites than would be expected resulting from chance. High lithodiversity likely reflects the occurrence of complex structural, stratigraphic, and intrusive relationships that are thought to control, focus, localize, or expose mineralization. The application of lithodiversity measurements to areas that are not well explored may help delineate regional-scale exploration targets and provide GIS-supported mineral resource assessment and exploration activity another method that makes use of widely available geological map data.

Nevada↗

USGS2012

Visible and near-infrared (0.4-2.5 μm) reflectance spectra of playa evaporite minerals

Visible and near-infrared (VNIR; 0.4–2.4 μm) reflectance spectra were recorded for 35 saline minerals that represent the wide range of mineral and brine chemical compositions found in playa evaporite settings. The spectra show that many of the saline minerals exhibit diagnostic near-infrared absorption bands, chiefly attributable to vibrations of hydrogen-bonded structural water molecules. VNIR reflectance spectra can be used to detect minor hydrate phases present in mixtures dominated by anhydrous halite or thenardite, and therefore will be useful in combination with X ray diffraction data for characterizing natural saline mineral assemblages. In addition, VNIR reflectance spectra are sensitive to differences in sample hydration state and should facilitate in situ studies of minerals that occur as fragile, transitory dehydration products in natural salt crusts. The use of spectral reflectance measurements in playa studies should aid in mapping evaporite mineral distributions and may provide insight into the geochemical and hydrological controls on playa mineral and brine development.

Journal of Geophysical Research↗

USGS1982

Clay mineralogy of weathering rinds and possible implications concerning the sources of clay minerals in soils

Weathering rinds on volcanic clasts in Quaternary deposits in the western United States contain only very fine grained and poorly crystalline clay minerals. Rinds were sampled from soils containing well-developed argillic B horizons in deposits about 10 5 yr old or more. The clay-size fraction of the rinds is dominated by allophane and iron hydroxy-oxides, whereas the B horizons contain abundant, well-crystallized clay minerals. The contrast between the clay mineralogy of the weathering rinds, in which weathering is isolated from other soil processes, and that of the associated soil matrices suggests a need to reassess assumptions concerning the rates at which clay minerals form and the sources of clay minerals in argillic B horizons. This study suggests that crystalline clay minerals form more slowly in weathering rinds than is generally assumed for soil environments and that the weathering of primary minerals may not be the dominant source of crystalline clay minerals in middle to late Pleistocene soils.

Geology↗

USGS2011

Porphyry Cu indicator minerals in till as an exploration tool: Example from the giant Pebble porphyry Cu-Au-Mo deposit, Alaska, USA

Porphyry Cu indicator minerals are mineral species in clastic sediments that indicate the presence of mineralization and hydrothermal alteration associated with porphyry Cu and associated skarn deposits. Porphyry Cu indicator minerals recovered from shallow till samples near the giant Pebble Cu-Au-Mo porphyry deposit in SW Alaska, USA, include apatite, andradite garnet, Mn-epidote, visible gold, jarosite, pyrite, and cinnabar. Sulphide minerals other than pyrite are absent from till, most likely due to the oxidation of the till. The distribution of till samples with abundant apatite and cinnabar suggest sources other than the Pebble deposit. With three exceptions, all till samples up-ice of the Pebble deposit contain <10 grains/10kg of garnet (0.25-0.5 mm). Samples in the immediate vicinity of the Pebble deposit contain 10-20 grains, whereas samples with the most grains (>40grains/10kg) are in close proximity to smaller porphyry and skarn occurrences in the region. The distribution of Mn-epidote closely mimics the distribution of garnet in the till samples and further supports the interpretation that these minerals most likely reflect skarns associated with the porphyry deposits. All but two till samples, including those up-ice from the deposit, contain some gold grains. However, tills immediately west and down-ice of Pebble contain more abundant gold grains, and the overall number of grains decreases in the down-ice direction. Furthermore, all samples in the immediate vicinity of Pebble contain more than 65% pristine and modified grains compared to mostly re-shaped grains in distal samples. The pristine gold in till reflects short transport distances and/or liberation of gold during in-situ weathering of transported chalcopyrite grains. Jarosite is also abundant (1-2 500 grains/10kg) in samples adjacent to and up to 7 km down-ice from the deposit. Most jarosite grains are rounded and preliminary Ar/Ar dates suggest the jarosite formed prior to glaciation and it implies that a supergene cap existed over Pebble West. Assuming this interpretation is accurate, it suggests a shallow level of erosion of the Pebble deposit by glacial processes. Overall the results of this study indicate that porphyry Cu indicator minerals in till samples may be useful in the exploration for porphyry deposits in SW Alaska.

Alaska↗

USGS1986

Quantitative estimation of undiscovered mineral resources: A case study of US Forest Service Wilderness tracts in the Pacific Mountain system

The need by land managers and planners for more quantitative measures of mineral values has prompted scientists at the U.S. Geological Survey to test a probabilistic method of mineral resource assessment on a portion of the wilderness lands that have been studied by the Survey during the past 20 years. A quantitative estimate of undiscovered mineral resources is made by linking the techniques of subjective estimation, geologic mineral deposit models, and Monte Carlo simulation. The study, which uses grade-tonnage and occurrence models for 21 geologic deposit types, considers 91 U.S. Forest Service wilderness tracts in California, Nevada, Oregon, and Washington. Estimates of the amounts of the 11 metals contained in undiscovered mineral deposits of the types studied range from negligible to several years of U.S. consumption. Although these estimates are limited to metals contained in undiscovered deposits of a small number of metallic mineral deposit types, the assessment procedure can be expanded by the use of additional deposit models and by using information about identified mineral resources. This will allow models of economic processes such as exploration, development, and production to be applied.

Economic Geology↗

USGS1987

Source of lead and mineralizing brines for rossie-type Pb-Zn veins in the Frontenac axis area, New York ( USA).

Veins composed mainly of calcite and some galena, sphalerite, fluorite, and other minerals are widespread in the Frontenac axis area of New York and Ontario. In New York, the veins (Fig. 1) occur mainly west and northwest of Gouverneur (Brown, 1983). The veins, mined in the 1800s for lead, were first described by Emmons (1838). Smyth (1903) called these the "Rossie lead veins," a name now used locally for all veins of this type. Similar veins in southeastern Ontario were described by Uglow (1916) and Sangster (1970). The steeply dipping veins are aligned along extensional fractures in metamorphic rocks of the Grenville Complex and in Paleozoic sedimentary rocks, including the Potsdam Sandstone of Late Cambrian age, and limestones as young as Middle Ordovician. However, the age of emplacement of Rossie veins is unknown. The veins are mineralogically simple, consisting of calcite (~95%) with minor and approximately equal amounts of sphalerite and galena, and sparse fluorite, barite, celestite, and chalcopyrite (Brown, 1983). Paragenetically early minerals are crushed and granulated; later undeformed minerals fill open spaces (Fig. 2). Sandstone dikes that originated from either the overlying Potsdam Sandstone or stratigraphically higher arenaceous rocks cut into the Rossie veins and occupy all available space. Their unstratified nature suggests that sand was intruded under high hydraulic pressure during tectonic events that reopened the veins. Most veins are vertical and narrow (1-3 cm wide) and those that were mined are as much as 1.7 m wide. The veins trend mainly northwest-southeast but have a local east-west orientation. The fractures and veins show evidence of strike-slip faulting with a right-lateral offset due to late reactivation of north-east-trending faults that originally formed during the Proterozoic Grenville orogeny. Relatively rare inclined veins, termed gash veins (Brown, 1983), occur in proximity to some of the regional northeast-trending faults. These veins contain open spaces lined with large, undeformed crystals of calcite (~90%) and green fluorite (~5%). The minerals of the northeast-trending gash veins, which dip to the northwest, are believed to be paragenetically late results of the same mineralization and tectonic event that produced the Rossie veins. For example, the green fluorite in the gash veins is similar in color and occurrence to small fluorite crystals in vugs in the vertical Rossie veins. Associated with the fluorite in both occurrences is coarse crystalline calcite containing tiny tetrahedra of chalcopyrite aligned along crystallographic planes. The present study of fluid inclusions and lead isotopes was done to understand better the nature and possible source of the mineralizing solutions for both vertical and gash veins and the possible origin of the lead and zinc mineralization. Large deposits of essentially syngenetic sphalerite with minor to trace galena occur in the Proterozoic rocks of this region (e.g., Balmat-Edwards, New York). Although none of these deposits are known in the immediate vicinity of Rossie veins, the possibility that Rossie veins contain remobilized metals from these older deposits was considered.

New York↗

USGS1988

Mineral and whole-rock compositions of seawater-dominated hydrothermal alteration at the Arctic volcanogenic massive sulfide prospect, Alaska

The Arctic volcanogenic massive sulfide prospect, located in the Ambler mineral district of northwestern Alaska, includes three types of hydrothermally altered rocks overlying, underlying, and interlayered with semimassive sulfide mineralization. Hydrothermal alteration of wall rocks and deposition of sulfide and gangue minerals were contemporaneous with Late Devonian or Early Mississippian basalt-rhyolite volcanism. Whole-rock analyses of altered rocks surrounding the prospect indicate that strong chemical gradients exist in major and minor oxides and volatiles. These were not homogenized or overprinted by Late Jurassic (?) to Middle Cretaceous greenschist to glaucophane-schist facies metamorphism. Very low alkali contents and moderate to very high contents of Ba, F, and Mg are the major chemical characteristics of the pervasively altered rocks. The strong Mg metasomatism, high Ba contents, and limited extent of altered rocks suggest a rapid influx of relatively cold seawater into a hot hydrothermal vent system. Alteration developed asymmetrically around a linear fissure, suggesting fracture control of ore fluids rather than a point source. Micro-probe analyses of phyllosilicates from the Arctic area indicate two discrete mineral populations. Magnesian chlorite, barian white mica, and barian fiuorphlogopite in hydrothermally altered rocks have compositions distinct from similar minerals (chlorite, phengite, biotite) developed during high-pressure metamorphism in metapelitic and metavolcanic lithologies. These differences in mineral chemistry are the result of differences in protolith composition caused by hydrothermal alteration-metasomatism. Without mineral composition data, the contacts between some alteration assemblages and relatively unaltered metavolcanic and metasedimentary rocks with similar mineralogy cannot be determined.

Economic Geology↗

USGS2005

Geology of the Vienna Mineralized Area, Blaine and Camas Counties, Idaho

The Vienna mineralized area of south-central Idaho was an important silver-lead-producing district in the late 1800s and has intermittently produced lead, silver, zinc, copper, and gold since that time. The district is underlain by biotite granodiorite of the Cretaceous Idaho batholith, and all mineral deposits are hosted by the biotite granodiorite. The granodiorite intrudes Paleozoic sedimentary rocks of the Sun Valley Group, is overlain by rocks of the Eocene Challis Volcanic Group, and is cut by numerous northeast-trending Eocene faults and dikes. Two mineralogically and texturally distinct vein types are present in a northwest- and east-trending conjugate shear-zone system. The shear zones postdate granodiorite emplacement and joint formation, but predate Eocene fault and dike formation. Ribbon veins consist of alternating bands of massive vein quartz and silver-sulfide (proustite and pyrargyrite) mineral stringers. The ribbon veins were sheared and brecciated during multiple phases of injection of mineralizing fluids. A quartz-sericite-pyrite-galena vein system was subsequently emplaced in the brecciated shear zones. Both vein systems are believed to be the product of mesothermal, multiphase mineralization. K-Ar dating of shear-zone sericite indicates that sericitization occurred at 80.7?2.8 Ma; thus mineralization in the Vienna mineralized area probably is Late Cretaceous in age.

Bulletin↗

USGS1992

Mineral resource assessment of the Dillon 1° x 2° quadrangle, Idaho and Montana

The Dillon 1 ° x2° quadrangle in southwestern Montana and east-central Idaho was investigated as part of the U.S. Geological Survey's Conterminous United States Mineral Assessment Program (CUSMAP) to determine its mineral resource potential. An interdisciplinary study was made of geology, geochemistry, geophysics (gravity and aeromagnetics), remote sensing, and mineral deposits. The results of those studies, as well as mineral resource assessment of numerous mineraldeposit types, are published separately as a folio of maps. This report summarizes the studies, provides background information on them, and presents a selected bibliography relevant to the geology and mineral resources of the quadrangle. The quadrangle contains large resources of gold and substantial resources of talc and chlorite, all of which were being mined in the 1980's and early 1990's. Submarginal resources of molybdenum, copper, tungsten, and iron range from moderately large to large. Other commodities that may be present in significant amounts are chromite, lead, zinc, silver, barite, zeolite minerals, and various nonmetallic metamorphic minerals.

Idaho, Montana↗

USGS1995

1995 annual report on Alaska's mineral resources

Section 1011 of the Alaska National Interest Lands Conservation Act (ANILCA) of 1980, as amended, requires that "On or before October 1, 1982, and annually thereafter, the President shall transmit to the Congress all pertinent public information relating to minerals in Alaska gathered by the United States Geological Surveys, United States Bureau of Mines, and any other Federal agency." This report has been prepared in response to that requirement. This circular is the fourteenth in the series of annual mineral reports mandated by the ANILCA. The report provides information about current Alaskan mineral projects and events during 1994; the emphasis is on Federal activity. The report addresses both onshore and offshore areas of Alaska. The U.S. Geological Survey (USGS), U.S. Bureau of Mines (USBM), and Minerals Management Service (MMS) are the principal Federal agencies that publish information about energy and mineral resources in Alaska. Their reports and data form the basis for decisions by other Federal agencies regarding land use, access, environmental impacts, and mining claim evaluation. The time required for sample analysis, data synthesis, and publication is lengthy; as a result, scientific reports are generally issued a year or more after initial sample and data collection. Other sources of information for this report include additional Federal and State publications, trade and professional journals, presentations at public meetings and hearings, and press releases. Information is provided for two broad categories of minerals: energy resources and nonfuel-mineral resources.

Circular↗

USGS2001

USGS Mineral Resources Program; national maps and datasets for research and land planning

The U.S. Geological Survey, the Nation’s leader in producing and maintaining earth science data, serves as an advisor to Congress, the Department of the Interior, and many other Federal and State agencies. Nationwide datasets that are easily available and of high quality are critical for addressing a wide range of land-planning, resource, and environmental issues. Four types of digital databases (geological, geophysical, geochemical, and mineral occurrence) are being compiled and upgraded by the Mineral Resources Program on regional and national scales to meet these needs. Where existing data are incomplete, new data are being collected to ensure national coverage. Maps and analyses produced from these databases provide basic information essential for mineral resource assessments and environmental studies, as well as fundamental information for regional and national land-use studies. Maps and analyses produced from the databases are instrumental to ongoing basic research, such as the identification of mineral deposit origins, determination of regional background values of chemical elements with known environmental impact, and study of the relationships between toxic elements or mining practices to human health. As datasets are completed or revised, the information is made available through a variety of media, including the Internet. Much of the available information is the result of cooperative activities with State and other Federal agencies. The upgraded Mineral Resources Program datasets make geologic, geophysical, geochemical, and mineral occurrence information at the state, regional, and national scales available to members of Congress, State and Federal government agencies, researchers in academia, and the general public. The status of the Mineral Resources Program datasets is outlined below.

Fact Sheet↗

USGS2011

Understanding processes affecting mineral deposits in humid environments

Recent interdisciplinary studies by the U.S. Geological Survey have resulted in substantial progress toward understanding the influence that climate and hydrology have on the geochemical signatures of mineral deposits and the resulting mine wastes in the eastern United States. Specific areas of focus include the release, transport, and fate of acid, metals, and associated elements from inactive mines in temperate coastal areas and of metals from unmined mineral deposits in tropical to subtropical areas; the influence of climate, geology, and hydrology on remediation options for abandoned mines; and the application of radiogenic isotopes to uniquely apportion source contributions that distinguish natural from mining sources and extent of metal transport. The environmental effects of abandoned mines and unmined mineral deposits result from a complex interaction of a variety of chemical and physical factors. These include the geology of the mineral deposit, the hydrologic setting of the mineral deposit and associated mine wastes, the chemistry of waters interacting with the deposit and associated waste material, the engineering of a mine as it relates to the reactivity of mine wastes, and climate, which affects such factors as temperature and the amounts of precipitation and evapotranspiration; these factors, in turn, influence the environmental behavior of mineral deposits. The role of climate is becoming increasingly important in environmental investigations of mineral deposits because of the growing concerns about climate change.

Fact Sheet↗

USGS2016

A world of minerals in your mobile device

Mobile phones and other high-technology communications devices could not exist without mineral commodities. More than one-half of all components in a mobile device—including its electronics, display, battery, speakers, and more—are made from mined and semiprocessed materials (mineral commodities). Some mineral commodities can be recovered as byproducts during the production and processing of other commodities. As an example, bauxite is mined for its aluminum content, but gallium is recovered during the aluminum production process. The images show the ore minerals (sources) of some mineral commodities that are used to make components of a mobile device. On the reverse side, the map and table depict the major source countries producing these mineral commodities along with how these commodities are used in mobile devices. For more information on minerals, visit http://minerals.usgs.gov .

General Information Product↗

USGS1992

Maps showing mineral resource assessment for vein and replacement deposits of base and precious metals, barite, and fluorspar, Dillon 1° x 2° quadrangle, Idaho and Montana

This report is one of several that assess the mineral resources in the Dillon quadrangle. For the purpose of the assessment, the deposits that are known in the quadrangle, or suspected to be present from a knowledge of the geologic setting, have been grouped into 30 deposit types on the basis of the mineralogy or commodity in the ore and the structural or depositional setting of the deposit. The emphasis in these assessment reports is on metallic minerals, but some important nonmetallic minerals are also considered. Fossil fuels are beyond the scope of this investigation, phosphate and uranium have been investigated previously (Swanson, 1970; Wodzicki and Krason, 1981 ), and certain nonmetallic minerals, including bulk commodities such as sand and gravel, are in large supply and thus are not considered. The mineral resource assessment discussed in this report concentrates on a single deposit type (of the total of 30 types) that we call "vein and replacement deposits of base and precious metals." Base and precious metals produced from such deposits are copper, lead, zinc, gold, and silver. Vein deposits of barite and fluorspar are also discussed, but because they seem to be of minor importance, they are treated briefly. Vein and replacement deposits of base and precious metals are classified as a single deposit type rather than as numerous possible subordinate types that might be distinguished on the basis of mineralogy, metal content, or other factors, because the characteristics of the ore, the ore bodies, and the structural setting are not sufficiently well known to yield a consistent detailed classification for the entire quadrangle. Furthermore, the criteria used here to explain the localization of deposits are too general to allow discrimination among subordinate types at a scale of 1 :250,000 or smaller. In assessing mineral resources, we have adopted a general philosophy similar to that of Harrison and others ( 1986). We attempt to identify parts of the quadrangle that are favorable for the occurrence of mineral resources, and we make an assignment of the relative resource potential of all parts of the quadrangle. We do not attempt to locate specific exploration targets nor to determine the quantity of reserves or resources present.

Idaho, Montana↗

USGS1981

Map showing mineral-resource potential of the King Range and Chemise Mountain Instant Study Areas, Humboldt and Mendocino counties, California

The potential for economic development of energy-related or metallic mineral resources in the King Range and Chemise Mountain Instant Study Areas is low to moderate as indicated by geologic, geophysical, and geochemical investigations. No oil or gas seeps or coal seams were detected within the King Range or Chemise Mountain Study Area. The low porosity and permeability of the Franciscan sandstones that underlie these areas indicate a very low potential for oil or gas. The geothermal resource potential of these areas also is low. Minor manganese resources occur adjacent to the southeast corner of the King Range Instant Study Area near Queen Peak. The manganese forms small stratabound deposits associated with radiolarian chert and pillow basalt. The known deposits are too small and the manganese too low in concentration for further economic exploitation. Similar manganese mineralization may be within the belt of melange in the southeast corner of the King Range area and within the Chemise Mountain Instant Study Area, but economic deposits are unlikely. Although there has been historical base- and precious-metal exploration activity north of the King Range in the Mattole River drainage, our geologic and geochemical field data indicate almost no gold potential and low potentials for lead, zinc, copper, and silver. During this investigation, one high-grade vein and several minor veins containing lead, zinc, copper, and silver were discovered at Point Delgada immediately south of the King Range Instant Study Area. The vein mineralization is Miocene and cuts Cretaceous basalt flows, dikes, flow breccia, and younger overlying sedimentary rocks of the King Range. The vein mineralization at Point Delgada could be remobilized from more extensive unexposed stratabound base-metal mineralization at depth. Traces of lead and zinc detected within the King Range Instant Study Area may have similar stratabound or vein origins, but no resource potential is indicated. Minor copper mineralization with associated lead, zinc, and manganese anomalies within the Chemise Mountain Instant Study Area is of low economic potential because of the shearing, isolation, and lenticularity of the basaltic and cherty rocks within the melange mineralization.

California↗