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At least 523 records · Page 29Linked to original sources
USGS2022

Geochemical studies of the Green River Formation in the Piceance Basin, Colorado: I. Major, minor, and trace elements

The Eocene Green River Formation contains the largest oil shale deposits in the world and is a welldocumented example of a lacustrine depositional system. In addition, mineral resources associated with oil shale in the Piceance Basin nahcolite [NaHCO3] and dawsonite [NaAl(CO3)(OH)2)] are of current and potential economic value, respectively. Detailed geochemical analysis across the basin can aid in the understanding of the depositional environment, sedimentary processes, and water-chemistry evolution in this system. Quantitative geochemical data for Green River oil shale from the Piceance Basin of Colorado were collected by inductively coupled plasma optical emission spectroscopy and mass spectrometry as part of this study. The basin margin is represented by samples from exposures at Douglas Pass (Garfield County) and the basin center area is characterized by core samples from two drilled wells: the Shell 23X-2 and John Savage 24-1 (Rio Blanco County). Major elements and groups of elements are used as proxies for clastic influx (Si, Al, K, Ti), carbonate deposition (Ca, Mg), salinity (Na), paleo-productivity (P), and redox state (Fe, S), respectively. Minor and trace elements reinforce observations based on major elements, including Rb, Zr, Nb for clastic influx and Mn, Sr for carbonate. Trace elements are used to characterize redox conditions (As, Mo, U, V, Co, Ni, Cu, Zn) and salinity (Rb/K, B/Ga). Chemical distinctions between the basin margin and the basin center, in terms of these components and total organic carbon concentrations, support the model of a permanently stratified lake through most of the depositional interval. A primary purpose of the study was to conduct more extensive sampling to confirm conclusions of a previous reconnaissance study. Geochemical data from this study indicates elevated Na around the basin margin occurring earlier than in the deeper basin. Early in the history of Lake Uinta, the salinity may have been elevated first in the shallower marginal waters, due to increased evaporation, which then led to elevated salinity in the basin center through transport of saline density currents. Other indicators of salinity (Rb/K, B/Ga) do not track Na content in intervals where clay minerals are absent due to diagenetic alteration under hypersaline conditions but may be used to indicate the salinities at which authigenic Na-bearing minerals begin to form. Most Na-rich samples show high proportions of clastic constituents (Si, Al, K, Ti) compared to conventional carbonate constituents (Ca, Mg). Redox-sensitive period IV transition metal elements (V, Co, Ni, Cu, Zn) show only local occurrence of significant enrichment relative to average shale abundances. Analysis of Fe/Al ratios for this dataset suggests that the depletion of these elements may be related to source rocks depleted in mafic constituents, with apparent redox-related enrichments subdued by this effect. The basin margin samples reflect generally oxic bottom waters, with some intervals deposited under more reducing, possibly dysoxic to anoxic conditions. The basin center results indicate more reducing conditions, with Mo and U enrichment factors suggesting operation of a particulate shuttle mechanism that scavenged Mo on Fe/Mn-oxyhydroxides that redissolved at depth, with Mo precipitating along with sulfides and/or organic matter at or near the sediment/water interface.

Colorado↗
USGS1979

Preliminary report on Tertiary volcanism and uranium mineralization in the Thomas Range and northern Drum Mountains, Juab County, Utah

The Thomas Range and northern Drum Mountains have a history of volcanism, faulting, and mineralization that began about 42 m.y. ago. Volcanic activity and mineralization in the area can be divided into three stages according to the time-related occurrence of rock types, trace element associations, and chemical nature of mineralization. Volcanic activity switched abruptly from rhyodacite-quartz latite (42-39 m.y. ago) to rhyolite (38-32 m.y. ago) to alkali rhyolite stages (21 and 6-7 m.y. ago); these stages correspond to periods of chalcophile and siderophile metal mineralization, no mineralization, and lithophile metal mineralization, respectively. Angular unconformities record episodes of cauldron collapse and block faulting between the stages of volcanic activity and mineralization. The youngest angular unconformity formed between 21 and 7 m.y. ago during basin-and-range faulting. Early rhyodacite-quartz latite volcanism from composite volcanoes and fissures produced flows, breccias, and ash-flow tuff of the Drum Mountains Rhyodacite and Mt. Laird Tuff. Eruption of the Mt. Laird Tuff about 39 m.y. ago from an area north of Joy townsite was accompanied by collapse of the Thomas caldera. Part of the roof of the magma chamber did not collapse, or the magma was resurgent, as is indicated by porphyry dikes and plugs in the Drum Mountains. Chalcophile and siderophile metal mineralization, including copper, gold, and manganese, accompanied early volcanism. The middle stage of volcanic activity was characterized by explosive eruption of rhyolitic ash-flow tuffs and collapse of the Dugway Valley cauldron. Eruption of the Joy Tuff 38 m.y. ago was accompanied by subsidence of this cauldron and followed by collapse and sliding of Paleozoic rocks from the west wall of the cauldron. Landslides in The Dell were covered by the Dell Tuff, erupted 32 m.y. ago from an unknown source to the east. An ash-flow of the Needles Range Formation was erupted 30-31 m.y. ago, probably from a distant source outside the volcanic field. The rhyolitic stage of volcanism was barren of mineralization. The last stage of volcanism was contemporaneous with basin-and-range faulting and was characterized by explosive eruption of ash and pumice, forming stratified tuff, and by quiet eruption of alkali rhyolite as viscous flows and domes. The first episode of alkali rhyolite volcanism deposited the beryllium tuff and porphyritic rhyolite members of the Spor Mountain Formation 21 m.y. ago. After a period of block faulting, the stratified tuff and alkali rhyolite of the Topaz Mountain Rhyolite were erupted 6-7 m.y. ago along faults and fault intersections. Erosion of Spor Mountain may have provided abundant dolomite detritus to the beryllium tuff member. The alkali rhyolite of both formations is fluorine-rich, as is evident from abundant topaz, and contains anomalous amounts of lithophile metals. Alkali rhyolite volcanism was accompanied by lithophile metal mineralization which deposited fluorite, beryllium, and uranium. The structure of the area is dominated by the Thomas caldera, and the younger Dugway Valley cauldron, which is nested within the Thomas caldera; the Thomas caldera is surrounded by a rim of Paleozoic rocks at Spor Mountain and Paleozoic to Precambrian rocks in the Drum Mountains. The Joy fault and Dell fault system mark the ring fracture zone of the Thomas caldera. These structural features began to form about 39 m.y. ago during eruption of the Mt. Laird Tuff and cauldon subsidence. The Dugway Valley cauldron sank along a series of step-like normal faults southeast of Topaz Mountain in response to collapse of the magma chamber of the Joy Tuff. The caldera structure was modified by block faulting between 21 and 7 m.y. ago, the time of widespread extensional faulting in the basin-and-range province. Vents erupted alkali rhyolite 6-7 m.y. ago along basin-and-range faults. Uranium mineralization was associated with the stage of alkali rhyolite volcanism, extensional basin-and-range faulting, and lithophile metal mineralization; it occurred at least 11 m.y. after the end of the caldera cycle. Uranium, derived from alkali rhyolite magma, was concentrated in trace amounts by magmatic fluids and in potentially economic amounts by hydrothermal fluids and ground water. Hydrothermal fluids deposited uraniferous fluorite as pipes in carbonate rocks of Paleozoic age on Spor Mountain and uranium-bearing disseminated deposits of fluorite and beryllium in the beryllium tuff member of the Spor Mountain Formation. Uranium of hydrothermal origin is dispersed in fluorite and opal. Uranium in fluorite may be tetravalent(?) but that in opal is probably hexavalent; no primary minerals of tetravalent uranium are known to occur. Ground waters have concentrated significant ores of hexavalent uranium minerals in the beryllium tuff member of the Spor Mountain Formation at the Yellow Chief Mine, and are probably also responsible for widespread low concentrations (0.0X percent) of uranium that occur separately from beryllium ore in the beryllium tuff member. More deposits of the Yellow Chief type may occur in down-faulted sections of beryllium tuff beneath the Thomas Range. The ground water ores show no evidence of a reducing environment; instead, precipitation of hexavalent uranium minerals occurred by evaporation, decline in concentration of complexing ions such as carbonate, or some other mechanism. Reducing environments for hydrothermal deposits must be sought around rhyolite vents and in a hypothesized pluton of alkali rhyolite composition beneath Spor Mountain; for ground-water deposits, reducing environments may occur in basin fill such as that of the Dugway Valley cauldron.

Utah↗
USGS1919

Contributions to economic geology, 1918, Part I, Metals and nonmetals except fuel

The Survey's "Contributions to economic geology " have been published annually since 1902. In 1906 the increase in the number of papers coming under this (Classification made it necessary to divide the contributions into two parts, one including, papers on metals and nonmetals except fuels and the other including papers on mineral fuels. In 1915 the year included in the title was changed from the year in which the field work reported in these papers was done to the year of publication, and in consequence there was no volume entitled "Contributions to economic geology, 1914.” The subjoined table gives a summary of these bulletins. As the subtitle indicates, the papers included in these volumes are of two classes (1) short papers giving comparatively detailed descriptions of occurrences that have economic interest but are not of sufficient importance to warrant a more extended description; (2) preliminary reports on economic investigations the results of which are to be published later in more detailed form. These papers are such only as Have a direct economic bearing, all topics of purely scientific interest being excluded. Brief abstracts of the publications of the year are given in the annual report of the Director. The complete list of Survey publications affords, by means of finding lists of subjects and of authors, further aid in ascertaining the extent of the Survey's work in economic geology. The reports on work in Alaska have been printed in a separate series since 1904, the volumes so far issued being Bulletins 259, 284, 314, 345, 379, 442, 480, 520, 542, 592, 622, 642, and 662.

Bulletin↗
USGS1956

Non-pegmatitic resources of beryllium in United States

During the period from 1948 to 1950 the U.S. Geological Survey conducted a program of field and laboratory research w determine the mode of occurrence of beryllium in non-pegmatitic rocks and mineral deposits as part of the Beryllium Program of the Division of Raw Materials of the U.S. Atomic Energy Commission. Approximately 23 man months were spent in the field collecting samples from 146 localities in 15 states; a total of 680 samples were collected and analyzed for beryllium. Additional samples collected by the Geological Survey. U.S. Bureau of Mines, various state Geological Surveys and other institutions. and private companies were analyzed for beryllium. In total, the beryllium content of 1,238 samples from about 600 localities in the United States is compiled in the final report which is being prepared for publication by the U.S. Geological Survey. The main topics discussed are: uses and properties of beryllium; methods of analysis and mineralogy of beryllium; occurrence of beryllium in igneous, sedimentary and metamorphic rocks, pyrometasomatic and related deposits, vein deposits, and hot spring deposits; the genesis of beryllium deposits; and a description of the deposits examined. This abstract and table 1 summarize the more pertinent economic data. Beryllium is more abundant than arsenic, gold, silver, and molybdenum in the lithosphere, but its chemical and physical properties prohibit its concentration in minerals which are common w large commercial vein and replacement deposits. There are 29 minerals in which beryllium is an essential constituent but of these only beryl, mined from granite pegmatites, is an ore of beryllium., Beryl also occurs disseminated in granites and high-temperature veins. The other 28 minerals occur as rare constituents in syenite and granite pegmatites, granites, and pyrometasomatic deposits. Beryllium, as a trace constituent, has been detected in 49 minerals but recovery of the beryllium requires metallurgical methods as yet unknown.

Trace Elements Investigations↗
USGS1969

Experimental studies of pegmatite genesis: I. A model for the derivation and crystallization of granitic pegmatites

The genesis of granitic igneous pegmatites is here considered in terms of a model conceived from results of field and laboratory studies and subsequently tested by means of experimental investigations. This model emphasizes the roles of water (and/or other relatively volatile substances), both as a dissolved constituent in granitic magmas and as the dominant constituent of a separate fluid phase that is in the supercritical state under most conditions of pegmatite formation. Pegmatite magma, as distinguished by a content of dissolved water that is high relative to the limit of solubility under existing confining pressure, can be formed either through partial melting of crustal materials or as rest-liquid in a cooling igneous body yielding dominantly anhydrous crystalline phases. Such granitic magma can be expected to consolidate according to the following three-fold sequence: 1. Crystallization from hydrous silicate melt, yielding anhydrous solid phases with or without OH-bearing phases. The product is characterized by normal phaneritic textures that generafly are coarse grained. It has been termed pegmatite in some occurrences, and granite in others. 2. Crystallization concomitantly from silicate melt and from a coexisting exsolved aqueous fluid of considerably lower viscosity, yielding giant-textured pegmatite along with much finer-grained, even aplitic, mineral aggregates. Segregation of these products can vary enormously in scale and degree. Partitioning of constituents between melt and aqueous fluid, rapid diffusion of constituents through the aqueous phase, and gravitational rising of this fluid through the system contribute to formation of pods, zones, and other rock units of unusual composition and texture. 3. Crystallization in the absence of silicate melt, yielding a wide variety of late-stage products. These include so-called "pocket minerals" and numerous mineral aggregates formed through exchanges of material among aqueous fluid and earlier-formed crystal-line phases. Development of pegmatite bodies can begin with either Step 1 or Step 2, but it is suggested that the processes involved in Step 2 are essential to the formation of all true pegmatites of igneous origin. The appearance of a second fluid phase, in general a supercritical aqueous fluid derived from the crystallizing melt, is regarded as the decisive event; it is promptly followed by fundamental changes in distribution and texture of the solid phases being formed. The processes can operate effectively in a fully closed system, and they also can modify the surrounding rocks if the system is open at any stage. Step 1 can include reactions between magma and earlier-formed crystals, but far more rapid and extensive exchanges of materials are subsequently effected by processes included in Steps 2 and 3; indeed, such exchanges also can account satisfactorily for pegmatites of metamorphic origin. Crystallization of most granitic magmas in the absence of a separate aqueous phase probably would begin within the temperature range 1,300°-650 ° C, the specific liquidus temperature depending mainly upon the amounts of volatile constituents held in solution at the time. This compositional factor also would be important in controlling the stage of crystallization-late, intermediate, or early-at which a separate aqueous fluid would make its appearance. Depending upon confining pressure as dictated by geologic conditions for a given system, the stage in crystallization represented by the presence of both silicate melt and aqueous fluid could begin within about the same temperature range of 1.300°-650 ° C. Exhaustion of the melt could occur within range extending downward to temperatures of 600C or even somewhat lower. Textural and structural features appear to be the most reliable indicators of the stages and fundamental processes involved in crystallization of both natural and synthetic pegmatites. The contrasting processes of crystallization from one fluid and from more than one fluid can operate over such broad P-T-X ranges that simple genetic pegmatite classifications based largely upon "key minerals," presumed temperature or pressure intervals, or the presence or absence of supercritical conditions appear to be somewhat unrealistic. © 1969 Society of Economic Geologists, Inc.

Economic Geology↗
USGS1978

The United States Geological Survey in Alaska; organization and status of programs in 1978

United States Geological Survey projects in Alaska study a wide range of topics of economic and scientific interest. Work done in 1977 includes contributions to economic geology, regional geology, stratigraphy, engineering geology, hydrology, and marine geology. Many maps and reports covering various aspects of the geology and mineral and water resources of the State were published. In addition, the published 1:1,000,000-scale map of the State has been revised in two areas. A bibliography containing 263 reports on Alaska published in 1977 is included. (Woodard-USGS)

Circular↗
USGS1978

The United States Geological Survey in Alaska: Accomplishments during 1977

United States Geological Survey projects in Alaska study a wide range of topics of economic and scientific interest. Work done in 1977 includes contributions to economic geology, regional geology, stratigraphy, engineering geology, hydrology, and marine geology. Many maps and reports covering various aspects of the geology and mineral and water resources of the State were published. In addition, the published 1:1,000,000-scale map of the State has been revised in two areas. A bibliography containing 263 reports on Alaska published in 1977 is included.

Alaska↗
USGS1971

A lower paleozoic paleoaquifer; the Kingsport Formation and Mascot dolomite of Tennessee and southwest Virginia

The Kingsport Formation (Lower Ordovician) in one section may be composed of two dominant rock types--limestone and medium to coarsely crystalline dolomite--whereas in an adjacent section, most of the formation may be largely composed of breccia. The breccia bodies, which are interpreted to be solution-collapse features, range in width from 30 feet to several hundred feet, in thickness from a few feet to more than 200 feet, and are hundreds of feet long. Many of the complexities of the Kingsport can be directly related to the development of an unconformity at the top of the overlying Mascot Dolomite. Erosion associated with the unconformity produced a widespread karst topography with an attendant paleoaquifer system. Ground water, apparently reacting to differences in solubility between limestone of the Kingsport and dense dolomite of the Mascot, is thought to be a major contributing factor in regional dolomitization and localization of solution-thinning and collapse features at the contact of the Kingsport and Mascot. Later mineralizing solutions invaded the paleoaquifer, locally depositing commercial quantities of zinc ore.

Virginia, Tennessee↗
USGS1985

Mineralization of breccia pipes in northern Arizona

The Paleozoic sedimentary rocks on the Colorado Plateau of northern Arizona are host to hundreds ofbreccia pipes. The uranium and copper deposits in these breccia pipes transgress formation boundaries from the Mississippian Redwall Limestone to the Triassic Chinle Formation. They are not classic breccia pipes in that there is no volcanic rock associated with them in time or space. They are the result of solution-collapse within the Redwall Limestone and stoping of the overlying strata. The karst development in the Redwall Limestone began in the Mississippian and apparently either continued to the Triassic or was at least once again active during that time. The mineralization apparently occurred shortly thereafter, sometime during the Mesozoic. Mining activity in breccia pipes of the Grand Canyon region began during the nineteenth century and continues today with the operation of the Hack I, II, and III mines, although the exploited commodity has changed from Cu to U. Although small in size, these pipes contain samples with up to 55 percent U 3 O 8 and can yield ore averaging between 0.30 and 0.60 percent U 3 O 8 .Mineralization at the surface commonly occurs within nodules and concretions associated with pyrite and goethite and along fractures, while the primary ore of the unoxidized zones is commonly within a comminuted sandstone matrix surrounding breccia fragments of overlying formations. The ore mineral is uraninite, although associated with it are sphalerite, galena, chalcopyrite, tennantite, millerite, siegenite, and/molybdenite. Some of the surface nodules are encrusted with malachite and are exceptionally enriched in Ag. Pyrite is abundant, and the organic carbon content of some rocks is high enough to suggest that it, along with the pyrite, may be a reductant for uranium. In contrast, it is possible, if uranium were transported as a bicarbonate or carbonate complex, that only a conduit of brecciated rock was necessary to release CO 2 , thus disrupting the equilibrium and allowing uraninite to precipitate. An extensive suite of elements is significantly enriched in the mineralized rock: Ag, As, Ba, Cd, Co, Cr, Cs, Cu, Hg, Mo, Ni, Pb, Sb, Se, Sr, U, V, Zn, and the rare earth elements. Of these, Cu, Pb, Zn, Ag, and particularly As appear to be the best geochemical indicators of mineralized pipes. At present the origin of the mineralizing fluids is not known. The lack of extensive silification within the breccia, along with the 80 degrees to 173 degrees C fluid inclusion-filling temperatures on sphalerite, dolomite, quartz, and calcite, suggests relatively low-temperature mineralizing fluids, although heated in excess of what would be expected from the normal geothermal gradient on the Colorado Plateau. With the exception of the U-mineralized rock, the mineral assemblage and geochemistry is similar to Mississippi Valley-type deposits.

Economic Geology↗
USGS1986

Ages of igneous and hydrothermal events in the Round Mountain and Manhattan gold districts, Nye County, Nevada

About 60 new isotopic age determinations help clarify the geologic history of the Round Mountain and Manhattan gold districts, Nevada. Cretaceous granite of Shoshone Mountain, southeast of Round Mountain, was emplaced about 95 m.y. ago and was domed, metamorphosed, and mineralized with tungsten-bearing quartz veins 80 m.y. ago. The granite of Pipe Spring, south of Manhattan, was emplaced probably at about 80 m.y. ago. Mineralization associated with the Pipe Spring body occurred about 75 m.y. ago. A granodiorite stock and associated rhyolite and andesitc dikes intruded the granite southeast of Round Mountain 36 m.y. ago; apparently base and precious metals mineralization accompanied their intrusion, but mineralization has not been dated isotopically. Ash-flow tuff at Round Mountain was emplaced about 26 m.y. ago, the Manhattan caldera formed about 25 m.y. ago, and gold mineralization at Round Mountain occurred at about 25 m.y. ago. Gold mineralization at Manhattan took place 16 m.y. ago.The isotopic data allow interpretation of the cooling histories of some of the igneous rocks and suggest possible thermal events that reset mineral ages.

Economic Geology↗
USGS1990

The Ag-Mn-Pb-Zn vein, replacement, and skarn deposits of Uchucchacua, Peru; studies of structure, mineralogy, metal zoning, Sr isotopes, and fluid inclusions

Uchucchacua is an Ag-Mn-Pb-Zn vein, replacement, and skarn mineral district in the central Andes of Peru. Host rocks are massive Jumasha Formation shelf limestones of Turonian age that have been folded into an asymmetric northeast-verging anticline of Andean trend. Strata near the fold crest are cut by minor dacitic intrusions and have been displaced by a conjugate set of steep wrench faults that strike northwest-southeast and northeast-southwest. Most ore occurrences are restricted to host rocks that lie below marly limestone at the top of the middle Jumasha Formation. Vein ores located along the fracture system have formed by fissure infill and by replacement of limestone wall rocks. Larger sheetlike replacement orebodies are parallel and adjacent to a large fault. Replacement is in zones of brecciation adjacent to fault bends which were dilatent during sinistral slip of the master fracture. Such fracture belts may have been subject to paleokarst solution processes before mineralization.Four paragenetic stages have been identified. Fe, Mn, and Si were introduced at the exoskarn stage (I) as the anhydrous silicates ferroan tephroite, johannsenite, rhodonite, and bustamite. During the early main stage (II) ferroan tephroite was replaced by friedelite and magnetite under oxidizing conditions at a relatively low pH. Pb, Zn, Fe, Cu, and B were introduced; principal sulfides are pyrrhotite, Fe-rich sphalerite, Mn-rich wurtzite, alabandite, galena, chalcopyrite, and tetrahedrite. Pyrrhotite was replaced by other sulfides during later stage II. Main gangue minerals were calcite, kutnohorite, rhodochrosite, and quartz. Ag, As, and Sb were introduced during the late stage (III) in the form of sulfosalts, principally pyrargyrite. Redistribution of metals introduced at stage II resulted in the growth of Fe-poor sphalerite and alabandite accompanied by calcite gangue. Decreasing Fe contents of alabandite and sphalerite during late stage II and stage III, together with the appearance of pyrite, indicate an increase in sulfur fugacity and/or decrease in temperature over this period. The supergene stage (IV) affects the upper 30 to 150 m of most veins and involves the growth of Mn hydroxides, goethite, orpiment, marcasite, cerussite, and siderite.Distribution patterns of metal ratios and high metal values define ore bands, with a succession of antiforms and synforms. Ore-band locations are determined by vein width, itself a function of wall-rock reactivity, and fracture permeability. Metal ratio distributions in the Luz vein show symmetric dispersion of metals at right angles to the ore-band axis. Ag shows the least dispersion with progressively greater dispersion of Pb and Zn.Geologic considerations indicate mineralization at a minimum depth of 1,600 m. Most primary fluid inclusions in calcite of probable stage II origin were trapped over a temperature range of about 200 degrees to 337 degrees C (hydrostatic pressure) or about 225 degrees to 362 degrees C (lithostatic). Fluid inclusions from late stage II quartz were trapped at about 165 degrees to 205 degrees C (hydrostatic) or 190 degrees to 230 degrees C (lithostatic). Salinity ranged from 0.5 to 29.7 equiv wt percent NaCl-CaCl 2 with little relation to temperature. Calcite 87 Sr/ 86 Sr values of 0.70743 to 0.71122 extend well outside the range of values both determined for magmatic rocks of the region and estimated for the host limestones but are probably compatible with older sedimentary rocks of the mine district. Salinity levels and NaCl/CaCl 2 ratios are similar to basinal brines associated with Mississippi Valley-type deposits. It is concluded that basinal brine, expelled from the deforming Mesozoic sequence, was a significant component of the ore fluid. This fluid was probably heated by dacitic magmas or cooling dacitic intrusions; a polygenetic high-salinity magmatic-basinal fluid then rose along existing strike-slip fractures toward the mineralization site where it mixed with heated low-salinity ground water.

Uchucchacua↗
USGS1994

Mineralogy, paragenesis, and mineral zoning of the Bulldog Mountain vein system, Creede District, Colorado

The Bulldog Mountain vein system, Creede district, Colorado, is one of four major epithermal vein systems from which the bulk of the district's historical Ag-Pb-Zn-Cu production has come. Ores deposited along the vein system were discovered in 1965 and were mined from 1969 to 1985.Six temporally gradational mineralization stages have been identified along the Bulldog Mountain vein system, each with a characteristic suite of minerals deposited or leached and a characteristic distribution within the vein system; some of these stages are also strongly zoned within the vein system. Stage A was dominated by deposition of rhodochrosite along the lower levels of the Bulldog Mountain ore zone. Stage B in the northern parts of the ore zone is characterized by abundant fine-grained sphalerite and galena, with lesser tetrahedrite and minor chlorite and hematite. With increasing elevation to the south, stage B ores become progressively more barite and silver rich, with alternating barite and fine-grained sphalerite + galena generations; native silver + or - acanthite assemblages are also locally abundant within southern stage B barite sulfide ores, whereas chalcopyrite and other Cu and Ag sulfides and sulfosalts are present erratically in minor amounts. Stage C in the upper and northern portions of the ore zone is characterized by abundant quartz and fluorite, minor adularia, hematite, Mn siderite, sphalerite, and galena, and major leaching of earlier barite; to the south, some barite and sulfides may have been deposited. Stage D sphalerite and galena were deposited in the upper and northern portions of the ore zone; a barite- and silver-rich facies of this stage may also be present in the southern portions of the vein system. Late in stage D, mineralogically complex assemblages containing chalcopyrite, tetrahedrite, polybasite, bornite, pyrargyrite, and a variety of other sulfides and sulfosalts were deposited in modest amounts throughout the vein system. This complex assemblage marked the transition to stage E. During stage E, the final sulfide stage, abundant botryoidal pyrite and marcasite with lesser stibnite, sphalerite, and sulfosalts were deposited primarily along the top of the Bulldog Mountain ore zone. Stage F, the final mineralization stage along the vein system, is marked by wire silver and concurrent leaching of earlier sulfides and sulfosalts; this stage may reflect the transition to a supergene environment.The sequence of mineralization stages identified in this study along the Bulldog Mountain system can be correlated with corresponding stages identified by other researchers along the OH and P veins, and the southern Amethyst vein system. Mineral zoning patterns identified along the Bulldog Mountain vein system also parallel larger scale zoning patterns across the central and southern Creede district.The complex variations in mineral assemblages documented in time and space along the Bulldog Mountain vein system were produced by the combined effects of many processes. Large-scale changes in vein mineralogy over time produced discrete mineralization stages. Short-term mineralogical fluctuations produced complex interbanding of mineralogically distinct generations. Fluid chemistry evolution within the vein system produced large-scale lateral zoning patterns within certain stages. Hypogene leaching substantially modified the distributions of some minerals. Finally, structural activity, mineral deposition, and mineral leaching modified fluid flow pathways repeatedly during mineralization, and so added to the complex mineral distribution patterns within the vein system.

Colorado↗
USGS1997

Secondary precious metal enrichment by steam-heated fluids in the Crofoot-Lewis hot spring gold-silver deposit and relation to paleoclimate

The Crofoot-Lewis deposit is an adularia-sericite-type (low-sulfidation) epithermal Au-Ag deposit, whose well-preserved paleosurface includes abundant opaline sinters, widespread and intense silicification, bedded hydrothermal eruption breccias, and a large zone of acid sulfate alteration. Radiogenic isotope ages indicate that the system was relatively long-lived, with hydrothermal activity starting around 4 Ma and extending, at least intermittently, for the next 3 m.y.Field evidence indicates that the surficial zone of acid sulfate alteration formed in a steam-heated environment within an active geothermal system. A drop in the water table enabled descending acid sulfate waters to leach Au and Ag from zones of low-grade disseminated mineralization, resulting in the redistribution and concentration of Au and Ag into ore-grade concentrations. These zones of secondary Au-Ag enrichment are associated with opal + alunite + kaolinite + montmorillonite + or - hematite and were deposited in open space fractures at, and within a few tens of meters below, the paleowater table.The stable isotope systematics of alunite and kaolinite in the steam-heated environment are relatively complex, due to variations in the residence time of aqueous SO 4 that formed from the oxidation of H 2 S prior to precipitation of alunite, and the susceptibility of fine-grained kaolinites to hydrogen isotope exchange with later waters. Most of the alunites are enriched in 34 S relative to early sulfide minerals, reflecting partial S isotope exchange between aqueous SO 4 and H 2 S. About half of the alunites give reasonable calculated delta 18 O (sub SO 4 -OH) temperatures for a steam-heated environment indicating O isotope equilibrium between aqueous SO 4 and water. The delta D (sub H 2 O) values of the hydrothermal fluids varied by almost 60 per rail over the life of the meteoric water-dominated system, suggesting significant climate changes.Mineralization is believed to have resulted from large-scale convection of meteoric water controlled largely by basin and range fractures and a high geothermal gradient with H 2 S for Au complexing derived from organic matter in basin sediments. A wet climate resulted in the formation of a large inland lake which provided abundant recharge water for the hydrothermal system. A fluctuating water table controlled by changing climatic conditions enabled steam-heated acid sulfate fluids to overprint lower grade mineralization resulting in ore-grade precious metal enrichment.

Economic Geology↗
USGS1989

National assessment of undiscovered conventional oil and gas resources, USGS-MMS working paper

In 1981, the U.S. Geological Survey (USGS) published the results of a 1980 national assessment of undiscovered oil and natural gas resources for the United States, including the Outer Continental Shelf (OCS). The publication, USGS Circular 860, was entitled "Estimates of Undiscovered Recoverable Conventional Resources of Oil and Gas in the United States" (hereafter referred to as Circular 860). The assessment provided an update to the previous USGS estimates for the Nation (published in 1975 as Circular 725). In 1982, the Minerals Management Service (MMS) was formed from a portion of USGS and other Department of the Interior (DOI) organizations for resource management of Federal offshore areas and for management of revenues collected from onshore and offshore Federal mineral leases. The HMS published estimates of undiscovered oil and natural gas resources for the OCS in 1985 in a report entitled "Estimates of Undiscovered, Economically Recoverable Oil and Gas Resources for the Outer Continental Shelf as of July 1984" (OCS Report MMS 85-0012). The agencies, both part of DOI, agreed in 1985 to conduct a cooperative assessment of the entire United States to estimate undiscovered oil and natural gas based upon a common date. These working papers provide estimates for the onshore and offshore geologic provinces of the Nation and summarize the methodologies, assumptions, and data utilized in the development of those estimates. (Figs. 1.5 and 1.6 are index maps showing the geologic provinces.) The methodologies, assumptions, and data differ from those used in the previous assessments, thereby making direct comparisons between estimates of this and previous assessments difficult to interpret. Therefore, these working papers have been prepared as a means of eliciting comments from peer scientific, academic, and industry experts in the estimation of oil and natural gas resources.

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USGS1973

Geology and mineral resources of central Antioquia Department (Zone IIA), Colombia

This report summarizes the geology of an area of some 6000 square kilometers in the northern part of the Central Cordillera of the Colombian Andes. The area, in north-central Department of Antioquia, was mapped between 1964 and 1968 as part of the Inventario Minero Nacional (IMN) project. Mineral resources are summarized within a larger area, designated as subzone ILK of IMN Zone If, which comprises almost 22,000 sq. kin, including the area mapped geologically by IMN and additional areas mapped by other agencies. The oldest formation is a micaceous paragneiss of early Paleozoic or possibly late Precambrian age. A thick geosynclinal sedimentary series accumulated during the Paleozoic Era and became regionally metamorphosed to greenschist (locally amphibolite) facies during the Permian or early Triassic; these schists and gneisses are designated collectively as the Valdivia Group. The Permian(?) orogenic episode included intrusion of concordant syntectonic plutons, mostly of tonalitic composition. Rocks of unequivocal Triassic or Jurassic age are not recognized. The Cretaceous is well represented by both igneous and sedimentary assemblages. Eugeosynclinal alpine ophiolites comprising submarine basalt flows and numerous intrusions of gabbro and serpentinite are prominent in the Lower Cretaceous, together with flysch composed of marine shale and lesser sandstone and conglomerate. The Upper Cretaceous is represented along the west border of the mapped area by submarine basalt flows and pyroclastic rocks, locally Interbedded with fine-grained clastic sedimentary beds, and lenses of dark laminated chert, at least part of which is radiolarian. The Late Cretaceous was marked by an orogenic event that profoundly folded and faulted all rocks and in the Central Cordillera caused low-grade metamorphism, the overprint of which is hardly observable in pre-Cretaceous rocks elsewhere. The Late Cretaceous orogeny culminated with discordant intrusion of the epizonal tonalitic Antioquian batholith. Displacement along the great Romeral wrench fault may have begun in the Cretaceous. Plutonism continued into the Cenozoic, exemplified by the hornblende-diorite Sabanalarga pluton. Intermontane basins were filled with molasse derived from the erosion of adjacent highlands; Tertiary sedimentation in marshy areas included organic carboniferous matter subsequently converted to lignite or subbituminous coal. The Sabanalarga fault system originated in the Late Tertiary; intermittent displacement continued on the older wrench faults such as the Romeral. Epeirogenic uplift, which probably began in the Pliocene and continued through the Pleistocene and Holocene, brought on renewed erosion which has sculptured the mountains into their present form. Mineral resources in subzone IIA are varied but not of outstanding importance. Gold and silver mining, significant in past centuries, is minor today. Ferruginous laterite on serpentinite once considered as a potential source of iron ore is not economically exploitable. IMN has explored nickeliferous laterite at the extreme northwest corner of subzone IIA; this is a potential resource, exploitable only after exhaustion of the larger and richer nickel laterite deposit at Cerro Matoso, farther to the north and outside the boundaries of Zone If. Known deposits of mercury, chromium, manganese, and copper are small, with limited economic potential. Nonmetallic resources include raw materials for cement, including portland cement. Saprolite clay is widely used in making common red brick and tile, still a dominant construction material in all but the most modern multistory buildings. Aggregate materials are varied and abundant. Kaolin of good quality near La Union is important as a ceramic raw mineral filler. Tertiary subbituminous coal beds are an important energy resource in western subzone IIA, and have a good potential for greater development. Deposits of sodic feldspar, talc, decorative stone, and silica a

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