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At least 1,261 records · Page 70Linked to original sources
USGS1971

Origin and emplacement of the ultramafic rocks of the Emigrant Gap area, California

The ultramafic bodies of the Emigrant Gap area are part of a mafic complex within a large composite pluton of the northern Sierra Nevada. The pluton was magmatically emplaced and is surrounded by an aureole of hornblende-hornfels facies rocks. Inclusions of country rock in ultramafic rock are of pyroxene-hornfels facies and appear to have been partly melted. Gravity studies indicate that the ultramafic bodies have near-vertical contacts extending to depths of at least 1½ to 2½ km. The mafic complex shows rough concentric zoning of rock types: ultramafic bodies occur at the core; gabbro forms a discontinuous intermediate unit; and diorite, tonalite, and granodiorite occur at the margins. Within the ultramafic bodies, unserpentinized wehrlitic peridotite is dominant; dunite and olivine clinopyroxenite are present but greatly subordinate. The ultramafic rocks consist almost entirely of olivine (FO 80 ) and diopside (Ca 46 Mg 46 Fe 8 ); orthopyroxene, hornbolende, and plagioclase occur locally. The gabbro, diorite, tonalite, and granodiorite contain both ortho- and clinopyroxene. Both ultramafic and two-pyroxene-bearing rocks were emplaced nearly simultaneously, as partly crystallized magmas and magmatic crystal mushes that had similar temperature. In all the rocks the structures are dominantly magmatic and were produced by sorting and orientation of crystals by magmatic flow. Structures produced by post-consolidation deformation and replacement are minor and local. The structural and chemical relations within the mafic complex suggest that all the rocks are derived from a single gabbroic magma by crystal fractionation, with the ultramafic rocks formed by mechanical accumulation of early crystallized mafic minerals, and the two pyroxene-bearing granodiorite crystallized from a felsic differentiate. It is likely that flowage differentiation was the dominant process of crystal segregation. The Emigrant Gap mafic complex is similar in structure, rock texture, and mineralogy to zoned ultramafic complexes, such as those of south-eastern Alaska, and is very different from either stratiform or alpine-type bodies. Though unlike the Alaskan bodies in detail, it appears that this complex should be classed with the zoned complexes in any broad grouping of ultramafic occurrences.

California↗
USGS2013

Automated mapping of mineral groups and green vegetation from Landsat Thematic Mapper imagery with an example from the San Juan Mountains, Colorado

Multispectral satellite data acquired by the ASTER (Advanced Spaceborne Thermal Emission and Reflection Radiometer) and Landsat 7 Enhanced Thematic Mapper Plus (TM) sensors are being used to populate an online Geographic Information System (GIS) of the spatial occurrence of mineral groups and green vegetation across the western conterminous United States and Alaska. These geospatial data are supporting U.S. Geological Survey national-scale mineral deposit database development and other mineral resource and geoenvironmental research as a means of characterizing mineral exposures related to mined and unmined hydrothermally altered rocks and mine waste. This report introduces a new methodology for the automated analysis of Landsat TM data that has been applied to more than 180 scenes covering the western United States. A map of mineral groups and green vegetation produced using this new methodology that covers the western San Juan Mountains, Colorado, and the Four Corners Region is presented. The map is provided as a layered GeoPDF and in GIS-ready digital format. TM data analysis results from other well-studied and mineralogically characterized areas with strong hydrothermal alteration and (or) supergene weathering of near-surface sulfide minerals are also shown and compared with results derived from ASTER data analysis.

Colorado↗
USGS1998

Tectonic setting of synorogenic gold deposits of the Pacific Rim

More than 420 million oz of gold were concentrated in circum-Pacific synorogenic quartz loades mainly during two periods of continental growth, one along the Gondwanan margin in the Palaeozoic and the other in the northern Pacific basin between 170 and 50 Ma. These ores have many features in common and can be grouped into a single type of lode gold deposit widespread throughout clastic sedimentary-rock dominant terranes. The auriferous veins contain only a few percent sulphide minerals, have gold:silver ratios typically greater than 1:1, show a distinct association with medium grade metamorphic rocks, and may be associated with large-scale fault zone. Ore fluids are consistently of low salinity and are CO2-rich. In the early and middle Palaeozoic in the southern Pacific basin, a single immense turbidite sequence was added to the eastern margin of Gondwanaland. Deformation of these rocks in southeastern Australia was accompanied by deposition of at least 80 million oz of gold in the Victorian sector of the Lachlan fold belt mainly during the Middle and Late Devonian. Lesser Devonian gold accumulations characterized the more northerly parts of the Gondwanan margin within the Hodgkinson-Broken River and Thomson fold belts. Additional lodes were emplaced in this flyschoid sequence in Devonian or earlier Palaeozoic times in what is now the Buller Terrane, Westland, New Zealand. Minor post-Devonian growth of Gondwanaland included terrane collision and formation of gold-bearing veins in the Permian in Australia's New England fold belt and in the Jurassic-Early Cretaceous in New Zealand's Otago schists. Collision and accretion of dozens of terranes for a 100-m.y.-long period against the western margin of North America and eastern margin of Eurasia led to widespread, lattest Jurassic to Eocene gold veining in the northern Pacific basin. In the former location, Late Jurassic and Early Cretaceous veins and related placer deposits along the western margin of the Sierra Nevada batholith have yielded more than 100 million oz of gold. Additional significant ore-forming events during the development of North America's Cordilleran orogen included those in the Klamath Mountains region, California in the Late Jurassic and Early Cretaceous; the Klondike district, Yukon by the Early Cretaceous; the Nome and Fairbanks districts, Alaska, and the Bridge River district, British Columbia in the middle Cretaceous; and the Juneau gold belt, Alaska in the Eocene. Gold-bearing veins deposited during the Late Jurassic and Early Cretaceous terrane collision that formed the present-day Russian Far East have been the source for more than 130 million oz of placer gold. The abundance of gold-bearing quartz-carbonate veins throughout the Gondwanan, North American and Eurasian continental margins suggests the migration and concentration of large fluid volumes during continental growth. Such volumes could be released during orogenic heating of hydrous silicate mineral phases within accreted marine strata. The common temporal association between gold veining and magmatism around the Pacific Rim reflects these thermal episodes. Melting of the lower thickened crust during arc formation, slab rollback and extensional tectonism, and subduction of a slab window beneath the seaward part of the forearc region can all provide the required heat for initation of the ore-forming processes.

Ore Geology Reviews↗
USGS2025

Mappable criteria for Li-mineralized pegmatites in the Appalachian orogen (utilizing the mineral systems approach)

Li-mineralized pegmatites are found throughout the Appalachian orogenic belt. Available evidence layers (e.g. tectonic setting, structures, geochemistry, geochronology) are used to develop mappable criteria for mineral resource assessments of Li-mineralized pegmatites in the northern and southern U.S. Appalachians. These evidence layers are placed into a mineral systems anatomy and classification of tectonic settings approach. We find that triggers of Li-mineralized pegmatite petrogenesis are closely associated with terrane accretion, continental collision, and orogenic collapse, spanning the Acadian to Alleghanian orogenies. These include overthickened crust in the northern Appalachians (Acadian altiplano) and terrane accretion in the southern Appalachians. The energy drivers of the system are anatexis broadly plutonism and/or deformation-related melting processes. Metal sources are associated with magmatic fluids of highly differentiated granitoids (e.g. peraluminous, S-type) and Silurian- Devonian sedimentary rocks. In many instances permeability and pathways of these systems are structurally controlled along major fault systems and within highly deformed metasedimentary rocks in the north. Notably, there are Li-mineralized pegmatite gaps along the Appalachian orogen that include: 1) regions of exposure of unfavorable metamorphic grade rocks, 2) favorable areas deeply buried by sedimentary rocks, and 3) gaps of unknown causes. Exhumation and preservation of midcrustal rocks are favourable as hosts to lithiummineralized pegmatites.

southern Appalachian mineral resourse assessment a↗
USGS2014

Effects of smectite on the oil-expulsion efficiency of the Kreyenhagen Shale, San Joaquin Basin, California, based on hydrous-pyrolysis experiments

The amount of oil that maturing source rocks expel is expressed as their expulsion efficiency, which is usually stated in milligrams of expelled oil per gram of original total organic carbon (TOC O ). Oil-expulsion efficiency can be determined by heating thermally immature source rocks in the presence of liquid water (i.e., hydrous pyrolysis) at temperatures between 350°C and 365°C for 72 hr. This pyrolysis method generates oil that is compositionally similar to natural crude oil and expels it by processes operative in the subsurface. Consequently, hydrous pyrolysis provides a means to determine oil-expulsion efficiencies and the rock properties that influence them. Smectite in source rocks has previously been considered to promote oil generation and expulsion and is the focus of this hydrous-pyrolysis study involving a representative sample of smectite-rich source rock from the Eocene Kreyenhagen Shale in the San Joaquin Basin of California. Smectite is the major clay mineral (31 wt. %) in this thermally immature sample, which contains 9.4 wt. % total organic carbon (TOC) comprised of type II kerogen. Compared to other immature source rocks that lack smectite as their major clay mineral, the expulsion efficiency of the Kreyenhagen Shale was significantly lower. The expulsion efficiency of the Kreyenhagen whole rock was reduced 88% compared to that of its isolated kerogen. This significant reduction is attributed to bitumen impregnating the smectite interlayers in addition to the rock matrix. Within the interlayers, much of the bitumen is converted to pyrobitumen through crosslinking instead of oil through thermal cracking. As a result, smectite does not promote oil generation but inhibits it. Bitumen impregnation of the rock matrix and smectite interlayers results in the rock pore system changing from water wet to bitumen wet. This change prevents potassium ion (K + ) transfer and dissolution and precipitation reactions needed for the conversion of smectite to illite. As a result, illitization only reaches 35% to 40% at 310°C for 72 hr and remains unchanged to 365°C for 72 hr. Bitumen generation before or during early illitization in these experiments emphasizes the importance of knowing when and to what degree illitization occurs in natural maturation of a smectite-rich source rock to determine its expulsion efficiency. Complete illitization prior to bitumen generation is common for Paleozoic source rocks (e.g., Woodford Shale and Retort Phosphatic Shale Member of the Phosphoria Formation), and expulsion efficiencies can be determined on immature samples by hydrous pyrolysis. Conversely, smectite is more common in Cenozoic source rocks like the Kreyenhagen Shale, and expulsion efficiencies determined by hydrous pyrolysis need to be made on samples that reflect the level of illitization at or near bitumen generation in the subsurface.

California↗
USGS1956

Geology of the Ralston Buttes district, Jefferson County, Colorado: a preliminary report

The Ralston Buttes district in Jefferson County is one of the most significant new uranium districts located east of the Continental Divide in Colorado. The district is east of the Colorado Front Range mineral belt, along the east front of the range. From November 1953 through October 1956, about 10,000 tons of uranium ore, much of which was high-grade pitchblende-bearing vein material, was shipped from the district. The ore occurs in deposits that range in size from bodies containing less than 50 tons to ore shoots containing over 1,000 tons. The only other mining activity in the area has been a sporadic production of beryl, feldspar, and scrap mica from Precambrian pegmatites, and quarrying of dimension stone, limestone, and clay from sedimentary rocks. Most of the Ralston Buttes district consists of complexly folded Precambrian metamorphic and igneous rocks - gneiss, schist, quartzite, amphibolite, and granodiorite. Paleozoic and Mesozoic sedimentary rocks crop out in the northeastern part of the district. These rocks are cut by northwesterly-trending fault systems of Laramide age and by small bodies of intrusive rocks that are Tertiary in age. The typical uranium deposits in the district are hydrothermal veins occupying openings in Laramide fault breccias or related fractures that cut the Precambrian rocks. Pitchblende and lesser amounts of secondary uranium minerals are associated with sparse base-mental sulfides in a gangue of carbonate minerals, potash feldspar, and, more rarely, quartz. Less common types of deposits consist of pitchblende and secondary uranium minerals that occupy fractures cutting pegmatites and quartz veins. The uranium deposits are concentrated in two areas, the Ralston Creek area and the Golden Gate Canyon area. The deposits in the Ralston Creek area are located along the Rogers fault system, and the deposits in the Golden Gate Canyon area are along the Hurricane Hill fault system. Two geologic factors were important to the localization of the uranium deposits: (1) favorable structural environment and (2) favorable host rocks. The deposits in each of the two major areas are located where a northwesterly-trending Laramide fault system splits into a complex network of faults. Also, most of the deposits appear to be localized where the faults cut Precambrian rocks rich in hornblende, biotite, or garnet and biotite. The ore controls recognized in this relatively new uranium district may have wider application in areas of similar geology elsewhere in the Front Range.

Colorado↗
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↗
USGS1990

Fine-grained rutile in the Gulf of Maine: Diagenetic origin, source rocks, and sedimentary environment of deposition

The Gulf of Maine, an embayment of the New England margin, is floored by shallow, glacially scoured basins that are partly filled with late Pleistocene and Holocene silt and clay containing 0.7 to 1.0 wt percent TiO 2 , chiefly in the form of silt-size rutile. Eleven basins in the gulf are estimated to contain 479 X 10 6 metric tons of TiO 2 (to a depth of 10 m) in the U.S. exclusive economic zone and 168 X 10 6 in Canada, based on analyses of surface sediment and of cores 10 to 20 m long. The U.S. annually consumes approximately 1 X 10 6 metric tons of TiO 2 , of which 73 percent is imported. The inferred amount of fine-grained TiO 2 in the basins is large, and we interpret it to be predominantly rutile; but no attempt has been made yet to mine and beneficiate the fine-grained ore.Sedimentary rocks of Nova Scotia, New Brunswick, and northern Maine contain fine-grained rutile crystals and have been the major source of the fine-grained sediment in the Gulf of Maine basins during and after the Wisconsinan glaciation. We conclude that much of the rutile in the Gulf of Maine mud formed diagenetically in poorly cemented Carboniferous and Triassic coarse-grained sedimentary rocks of Nova Scotia and New Brunswick after the dissolution of titanium-rich detrital minerals (ilmenite, ilmenomagnetite). Another major source of rutile is the generally finer grained Paleozoic sedimentary rocks of northern Maine (and possibly northwestern New Brunswick) which contain recycled diagenetic rutile that most likely originated in sandstones. Additional Wisconsinan sources of fine-grained, diagenetic TiO 2 probably include sedimentary rocks of inferred Triassic age that underlie the Gulf of Maine.The diagenesis of rutlie in coarse sedimentary rocks (especially arkose and graywacke) followed by erosion, segregation, and deposition (and including recycling of fine-grained rutile from shales) can serve as a model for predicting and prospecting for unconsolidated deposits of fine-grained TiO 2 .Gulf of Maine mud is comparable in TiO 2 content to typical shale. A determination of whether the fine-grained TiO 2 in shales primarily occurs as detrital titanium minerals from metamorphic and igneous sources or as recycled, diagenetic titanium oxides from sedimentary sources may assist in interpreting shale provenance and environment of deposition.

Economic Geology↗
USGS1958

Minerals of the cassiterite-bearing veins at Irish Creek, Virginia, and their paragenetic relations

Major rock types of the Irish Creek district are gneisses and schists, intruded by granodiorite. All these rocks are believed to be Precambrian. The ore deposits are fissure veins consisting largely of quartz veins bordered by greisen, and enriched by recurrent deposition. From field and microscopic evidence six stages of mineral formation have been deduced: 1. Crystallization of the granodiorite with the formation of hypersthene, augite, hornblende, andesine, orthoclase, microcline, and quartz; and accessory apatite, rutile, ilmenite, titanomagnetite, and zircon. 2. Metamorphism of the granodiorite and gneiss with formation of uralitic actinolite, epidote, and sphene. 3. A period of fracturing and formation of quartz veins. 4. Greisenization of the host rock producing first: coarse muscovite, brown biotite, cassiterite, beryl, wolframite, and quartz; then producing a second group of minerals-fluorite, green biotite, chlorite, phenakite, siderite, ankerite, parisite, sphalerite, sulfides, including aikinite and galeno-bismutite, leucoxene, fine muscovite, and quartz. 5. Formation of late vein minerals, clinozoisite, calcite, nontronite, and montmorillonite. 6. Formation of surficial alteration products, kaolinite, vermiculite, hematite, limonite, and scorodite. The italicized mineral names indicate the minerals heretofore unreported from Irish Creek; parisite, aikinite, and galenobismutite are new minerals for Virginia. Included in the detailed descriptions of all the minerals is a chemical analysis of beryl.

Virginia↗
USGS1951

Metamorphic and igneous rocks of the merrimac area, Plumas National Forest, California

The pre-granitic rocks of an area in the northern Sierra Nevada consist of metamorphosed sedimentary and volcanic series ranging in age from Carboniferous to Jurassic. Synkinematic ultrabasic intrusives, now serpentines, cut these rocks concordantly and discordantly. Magmatic series ranging from basalt to dacite and soda-rhyolite occur together with the normal basalt-rhyolite series among the meta-volcanics. The younger intrusives (Sierra Nevada series), ranging from gabbros to granodiorites and granites, show great chemical similarity to the meta-volcanic series. Furthermore, soda-rich members are common among the pre-granitic intrusives and younger dike rocks. The pre-granitic rocks were folded and metamorphosed to green schist and epidote-amphibolite facies prior to emplacement of granodiorite and granite batholiths. The later contact metamorphism affected the areas next to the contacts of the batholitic intrusions, causing crystallization of such minerals as garnet, diopside, epidote, and andalusite. The plutonic rocks obtained the space needed partly by pushing the country rocks aside and partly by stoping and assimilation.

California↗
USGS1956

Geology and ore deposits of the Whitepine area, Tomichi mining district, Gunnison County, Colorado

The Tomichi mining district is on the western slope of the Continental Divide near the southern end of the Sawatch Range in southeastern Gunnison County, Colorado. The most productive part of the Tomichi district was the Whitepine area. It is estimated that since the discovery of ore in 1879 the area has produced approximately $7,000,000, principally in lead and zinc, with lesser amounts of silver, copper, and gold. Geologically, the Whitepine area is a faulted syncline of Paleozoic rocks that was intruded by Tertiary igneous rocks. The oldest rock of the area is the Silver Plume granite of pre-Cambrian age. Deposited upon this successively were the Sawatch quartzite (Late Cambrian), Manitou dolomite (Early Ordovician), Harding quartzite (Middle Ordovician), Fremont dolomite (Lade Ordovician), Chaffee formation (Late Devonian), Leadville limestone (Late Mississippian), and Beldon shale (Late Pennsylvanian); a total thickness of about 1,450 feet. During the Laramide Revolution, the sedimentary rocks were folded into a broad northward-plunging syncline, faulted, and intruded by a series of igneous rocks. The igneous rocks, in order of relative age from oldest to youngest, are: a rhyolite stock, the Princeton quartz monzonite batholith, quartz monzonite or quartz latite porphyry dikes, and rhyolite or pitchstone porphyry dikes. The ore deposits of the Whitepine area may be classified into replacement deposits, vein deposits, and contact metamorphic deposits. The replacement deposits may be further subdivided into deposits along faults and bedded deposits. Of the types of deposits, the most productive have been the replacement deposits along faults. The major replacement deposits along faults are those of the Akron, Morning Star, and Victor mines. The ore deposits of these mines are in the foot wall of the Star faults in the Akron mine in the Manitou dolomite and in the Morning Star and Victor mines in the Leadville limestone. The chief bedded replacement deposits are those of the Erie, North Star, and Tenderfoot mines. In the Erie mine the ore deposits are in the Leadville limestone at, or just below, its contact with the Belden shale. In the North Star and Tenderfoot mines the ore bodies are in the Manitou dolomite along the crest of an anticline and the trough of a syncline, respectively. The vein deposits occur in the Silver Plume granite, Princeton quartz monzonite, and Paleozoic sedimentary rocks. The only vein of commercial importance was that of the Spar Copper mine, which is in the Silver Plume granite. Contact metamorphic minerals are found chiefly in the top of the Leadville limestone in the vicinity of the Erie mine, and in the limestone of the Belden shale. Magnetite is the only ore mineral and it was produced only from the Iron King mine. The replacement deposits consist, in general, of sphalerite, galena, pyrite, and chalcopyrite in a gangue of siliclfied limestone or dolomite, quartz, and calcite. The veins, for the most part, consist of pyrite and quartz with only minor amounts of galena, sphalerite, and chalcopyrite. In both types of deposits gold is believed to be associated with the pyrite and sphalerite and silver with the galena. Oxidized ore was the chief product of the early mining. This ore consists of calamine, cerussite, smithsonite, or anglesite, or a combination of these minerals, in a gangue of siliceous limestone or silicified limestone or dolomite. Oxidation did not extend, in most cases, for more than 150 feetbelow the surface. The ore deposits are believed to be genetically related to the Princeton quartz monzonite batholith. Ore-bearing solutions derived from the cooling of magma are believed to have migrated upwards along the pre-existing faults replacing favorable zones in the sedimentary rocks, or depositing quartz and ore minerals in open fissures in the igneous rocks.

Open-File Report↗
USGS1966

Stratified deposits of the oxides and carbonates of manganese

Compared with the stratified deposits of iron minerals, those of manganese minerals have received little attention until recent years. Before 1930, students of the stratified deposits of manganese minerals have generally concluded that the contained manganese was derived from the decomposition of the rocks that formed the borders of the basins. Only in a few places have geologists recognized that if these rocks were the principal source of the contained manganese the basins should contain also enormous quantities of iron minerals, whereas most of the large deposits of manganese contain little iron. Even though more than 100 years ago some geologists proposed that the iron contained in some deposits of stratified iron minerals was probably derived from hydrothermal waters related to centers of volcanism, not until about 1930 was this source of manganese in similar deposits seriously proposed. This mode of origin was given the name "volcanogene sedimentaire" by French geologists working in Morocco. Since then, other names, such as "exhalative sedimentaire," have been used by geologists working in several European districts. Because of the development of new techniques for the study of the chemical and physical features of the minerals, and because close attention to the lithologic environments of the beds is being given more and more during recent years, it has seemed advisable to review the features of stratified deposits of the manganese minerals in many parts of the world and over a wide range in age. This study indicates that at least three sources may have contributed the manganese in the large deposits of iron-free oxides and carbonates : (1) the rocks that form the borders of the basins, either marine or continental; (2) the nearby underlying sediments, largely of igneous origin, decomposed by warm waters largely derived from depth; and (3) waters of hydrothermal origin derived from great depths during epochs of volcanism from which iron minerals with little manganese are deposited in deep zones, then minerals with much iron and more manganese at intermediate depths, and, finally, manganese minerals with little iron near the surface. As the hot waters of many thermal springs contain more manganese than iron, such waters could yield the pure manganese oxides and carbonates found in stratified deposits . Several kinds of evidence indicate that most of the manganese in the large stratified deposits of the oxides and carbonates of manganese in many parts of the world has been derived from hydrothermal waters from depth related to centers of volcanism. Obviously, manganese derived from decay of the rocks on the lands adjacent to large basins-marine and continental -may have been added to that derived from centers of volcanism to form the sedimentary deposits found in the basins.

Economic Geology↗
USGS2023

Fluorine-rich mafic lower crust in the southern Rocky Mountains: The role of pre-enrichment in generating fluorine-rich silicic magmas and porphyry Mo deposits

Fluorine-rich granites and rhyolites occur throughout the southern Rocky Mountains, but the origin of F-enrichment has remained unclear. We test if F-enrichment could be inherited from ancient mafic lower crust by: (1) measuring amphibole compositions, including F and Cl contents, of lower crustal mafic granulite xenoliths from northern Colorado to determine if they are unusually enriched in halogens; (2) analyzing whole-rock elemental and Sr, Nd, and Pb isotopic compositions for upper crustal Cretaceous to Oligocene igneous rocks in Colorado to evaluate their sources; and (3) comparing batch melting models of mafic lower crustal source rocks to melt F and Cl abundances derived from biotite data from the F-rich silicic Never Summer batholith. This approach allows us to better determine if the mafic lower crust was pre-enriched in F, if it is concentrated enough to generate F-rich anatectic melts, and if geochemical data support an ancient lower crustal origin for the F-rich rocks in the southern Rocky Mountains. Electron microprobe analyses of amphibole in lower crustal mafic granulite xenoliths show they contain 0.56–1.38 wt% F and 0.45–0.73 wt% Cl. Titanium in calcium amphibole thermometry indicates that the amphiboles equilibrated at high to ultrahigh temperature conditions (805 to 940 °C), and semiquantitative amphibole thermobarometry indicates the amphiboles equilibrated at 0.5 to 1.0 GPa prior to entrainment in magmas during the Devonian. Mass balance calculations, based on these new measurements, indicate parts of the mafic lower crust in Colorado are at least 3.5 times more enriched in F than average mafic lower crust. Intrusions coeval with the Laramide Orogeny (75 to 38 Ma) pre-date F-rich magmatism in Colorado and have Sr and Nd isotopic compositions consistent with mafic lower crust ± mantle sources, but many of these intrusions contain elevated Sr/Y ratios (>40) that suggest amphibole was a stable phase during magma generation. The F-rich igneous rocks from the Never Summer igneous complex and Colorado Mineral Belt also have Sr and Nd isotopic compositions that overlap with the lower crustal mafic granulite xenoliths, but they have lower Sr/Y, higher Nb and Y abundances, and distinctly less radiogenic 206 Pb/ 204 Pb i compositions than preceding Laramide magmatism. Batch melt modeling indicates low-degree partial melts derived from rocks similar to the mafic lower crustal xenoliths we analyzed can yield silicic melts with >2000 ppm F, similar to estimated F melt concentrations for silicic melts that are interpreted to be parental to evolved leucogranites. We suggest that F-rich silicic melts in the southern Rocky Mountains were sourced from garnet-free mafic lower crust, and that fluid-absent breakdown of amphibole in ultrahigh temperature metamorphic rocks was a key process in their generation. Based on the composition of high-F amphibole measured from lower crustal xenoliths, the temperature of amphibole breakdown and melt generation for these F-enriched source rocks is likely >100 °C higher than similar lower crust with low or average F abundances. As such, these source rocks only melted during periods of unusually high heat flow into the lower crust, such as during an influx of mantle-derived magmas related to rifting or the post-Laramide ignimbrite flare-up in the region. These data have direct implications for the genesis of porphyry Mo mineralization, because they indicate that pre-enrichment of F in the deep crust could be a necessary condition for later anatexis and generation of F-rich magmas.

Colorado, New Mexico↗
USGS2005

Arsenic in ground water of the United States: occurrence and geochemistry

Concentrations of naturally occurring arsenic in ground water vary regionally due to a combination of climate and geology. Although slightly less than half of 30,000 arsenic analyses of ground water in the United States were 1 μg/L, about 10% exceeded 10 μg/L. At a broad regional scale, arsenic concentrations exceeding 10 μg/L appear to be more frequently observed in the western United States than in the eastern half. Arsenic concentrations in ground water of the Appalachian Highlands and the Atlantic Plain generally are very low ( 1 μg/L). Concentrations are somewhat greater in the Interior Plains and the Rocky Mountain System. Investigations of ground water in New England, Michigan, Minnesota, South Dakota, Oklahoma, and Wisconsin within the last decade suggest that arsenic concentrations exceeding 10 μg/L are more widespread and common than previously recognized. Arsenic release from iron oxide appears to be the most common cause of widespread arsenic concentrations exceeding 10 μg/L in ground water. This can occur in response to different geochemical conditions, including release of arsenic to ground water through reaction of iron oxide with either natural or anthropogenic (i.e., petroleum products) organic carbon. Iron oxide also can release arsenic to alkaline ground water, such as that found in some felsic volcanic rocks and alkaline aquifers of the western United States. Sulfide minerals are both a source and sink for arsenic. Geothermal water and high evaporation rates also are associated with arsenic concentrations 10g/L in ground and surface water, particularly in the west. Arsenic release from iron oxide appears to be the most common cause of widespread arsenic concentrations exceeding 10 µg/L a ground water. This can occur in response to different geochemical conditions, including release of arsenic to ground water through reaction of iron oxide with either natural or anthropogenic (i.e., petroleum products) organic carbon. Iron oxide also can release arsenic to alkaline ground water, such as that found in some felsic volcanic rocks and alkaline aquifers of the Western United States. Sulfide minerals are both a source and sink for arsenic. Geothermal water and high evaporation rates also are associated with arsenic concentrations ≥ 10g/L in ground and surface water, particularly in the west.

Ground Water↗
USGS2017

Geologic map of the Dusar area, Herat Province, Afghanistan; Modified from the 1973 original map compilations of V.I. Tarasenko and others

The geologic maps and cross sections presented in this report are redrafted and modified versions of the Geologic map and map of useful minerals of the Dusar area (scale 1:50,000) and Geologic sketch map of the Dusar and Namak-sory ore occurrences (scale 1:10,000), located in the Herat Province, Afghanistan. The original maps and cross sections are contained in unpublished Soviet report no. 0290 (Tarasenko and others, 1973) prepared in cooperation with the Ministry of Mines and Industries of the Royal Government of Afghanistan, in Kabul during 1973 under contract no. 50728. The redrafted maps and cross sections (modified from Tarasenko and others, 1973) illustrate the geological structure and mineral occurrences of the Dusar copper-gold-silver-lead-zinc prospect area of western Afghanistan, located within the Dusar-Shaida copper and tin area of interest (AOI), Herat Province, Afghanistan. Mineralization in the Dusar area is hosted within Early Jurassic to Early Cretaceous stratified volcanic and sedimentary rocks associated with numerous diabase and gabbro-diabase intrusive bodies and is generally near a major northeast-trending system of faults and quartz veins. Host rocks consist of quartz keratophyre and quartz-feldspar porphyry, with layers of schist, phyllite, and quartz-chlorite and chlorite-sericite slate; and limestone and shale, with schist and carbonate-chlorite and chlorite slate. Known mineralization includes an extensive quartz vein system, shown on the map as the “northern occurrence,” as well as the Dusar and Namak-sory gossan zones, interpreted to have formed from remnant pyrite mineralization. The veins of the northern occurrence and their altered host rocks are known to contain anomalous to economic concentrations of precious and base metals, with concentrations locally in excess of 2 parts per million gold, 100 parts per million silver, 5 percent copper, and 1 percent lead. These veins occur in swarms, and are hosted along structures that are approximately concordant with the plane of the metamorphic fabric. The veins consist mostly of quartz, with minor carbonate and sulfide minerals, and display weak alteration halos along their margins. The gossans are locally anomalous in these metals, but their size and extent makes them attractive exploration targets for potential massive sulfide mineralization. The Dusar gossan zone is a massive, ochreous, and siliceous limonitic rock, approximately 2,200 meters long, 30 to 250 meters wide, and 2.0 to 7.2 meters thick. Drilling below the Dusar gossan intersected a siliceous, sericitic, and limonitic rock underlain by quartz keratophyre with abundant disseminated pyrite. Mineralized sections grade 0.06 weight percent copper and up to 0.05 weight percent zinc. The Namak-sory gossan zone contains a similar deposit with anomalous concentrations of copper, zinc, and gold. The redrafted maps and cross sections reproduce the topology of rock units, contacts, and faults of the original Soviet maps and cross sections, and include minor modifications based on examination of the originals and observations made during two brief field visits by USGS staff in August, 2010, and June, 2013.

Dusar Area, Herat Province↗
USGS1971

Geochemical, aeromagnetic, and generalized geologic maps showing distribution and abundance of lead and silver, Golconda and Iron Point quadrangles, Humboldt County, Nevada

Detailed geologic and geochemical studies of the four 7 1/2-minute quadrangles that make up the Edna Mountain 15-minute quadrangle in Humboldt County, Nevada, were begun during the 1969 summer field season. The objectives of the project are to map the geology of this struct urally complex area at 1:24·,000 scale and to determine the regional distribution and abundance of metals in rocks of the are\3. and the factors that control the distribution and abundance of those metals. Tungstenbearing hot-spring tufa, metalliferous black shale in Ordovician rocks, base-metal and barite deposits in Paleozoic sedimentary rocks, and copper-molybdenum in granodiorite plutons of Cretaceous age occur in the Edna Mountain area. None of these deposits have been of much economic significance, although tungsten was mined from the hot-spring deposits during World War II. The numerous occurrences of mineralized ground, however, along with the broad spectrum of types of mineralization, intensity of alteration, structural complexity, and abundance of intermediate to silicic igneous intrusive rocks suggest that concealed or heretofore unrecognized mineral deposits may exist in the area. Integrated geologic, geochemical, and geophysical studies on a district- wide scale might improve our un~erstanding of the factors that control the distribution, methods of emplacement, and spatial and genetic relationships (if any) of these different types of deposits. We hope that broad target areas or guidelines for mineral exploration in th.is area may be identified. This series of maps shows the distribu t ion and abundance of mercury, arsenic, antimony, tungsten, gold, copper, l ead, and s ilver related to a geologic and aeromagnetic base in the Golconda and Iron Point 7 1/2-minute quadrangles. All samples are rock samples; most are f rom shear or f ault zones, fractures, jasperoid, breccia reefs, and altered rocks . All the samples were prepared and analyzed in truck-mounted laboratories at Wi nnemucca, Nevada. Arsenic , tungs t en, copper, lead, and si lver were determined by semiquantitative spectrogr aph i c methods by D. F. Siems and E. F. Cooley . Mercury and gold were determined by atomi c absorption methods and antimony was determined by a colorimetric method by R. M. O'Leary, M. S. Erickson, and others.

Nevada↗
USGS1950

Preliminary examination of uranium deposits near Marysvale, Piute County, Utah

Autunite and other uranium minerals were discovered in 1948 by Pratt Seegmiller about 3 1/4 miles north of Marysvale, Piute County, Utah. Mining operations were begun in the summer of 1949 by the Vanadium Corporation of America on the Prospector and the Freedom claims, and by the Bullion Monarch Mining Company a the Bullion Monarch claims. These claims were examined briefly in December 1949 and January 1950 by the writers. The uranium deposits of the Marysvale district are in north-easterly striking fault zones in quartz monzonite that intrudes rocks of the "older" Tertiary volcanic sequence. Flows and tuffs of the "younger" Tertiary volcanic sequence uncomfortably overlie the earlier rocks. Autunite, tobernite, uranophane, schroeckingerite, and at least one unidentified secondary uranium mineral occur in the upper parts of the deposits. Pitchblende has been mined from the underground workings of the Prospector No. 1 mine. The uranium minerals are associated with dense quartz veins and intensely argillized wall rock. In the upper parts of the deposits pyrite is completely oxidized. The secondary uranium minerals probably were formed by the alteration of primary pitchblende by circulating meteoric waters.

Utah↗
USGS2025

Earth Mapping Resources Initiative protocols—Sampling hard-rock mine waste and perpetual mine water sources

Supporting the overarching goal to evaluate critical minerals nationwide, the mine waste characterization effort in the U.S. Geological Survey (USGS) Earth Mapping Resources Initiative has created a series of protocols to standardize sampling carried out under this effort by the participating State geological surveys and their cooperators. The protocols are based on published, reviewed methods that can be deployed in the field. The protocols include (1) collecting and processing composite samples of mine and mill waste, including tailings, waste rock, gangue, heap leach piles, ore stockpiles, slag, or other mineralized and processed materials and (2) collecting and preserving water samples from perpetual or long-term mine water sources. The protocols also specify information to document on field sheets and detail the collection of geospatial data. The analytical methods used by the USGS and USGS contract laboratories are described in this report, including the data delivery pathway for USGS-derived data.

Scientific Investigations Report↗