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J. Thomas Nash

Publications and source records attributed to J. Thomas Nash.

At least 55 records · Page 3Linked to original sources
USGS1979

Uranium and thorium in granitic rocks of northeastern Washington and northern Idaho, with comments on uranium resource potential

Northeastern Washington and northern Idaho is a uranium province in which many Cretaceous and Tertiary granitic plutons contain abnormal amounts of uranium. Mean uranium content of 108 samples of granitic rock is 8.8 parts per million (ppm), more than twice normal for rocks of this composition. The mean thorium content, 20.3 ppm, and mean Th/U, 3.19, are normal. The most uraniferous and fertile rocks are the peraluminous two-mica granitic suite, although not all two-mica plutons are enriched in uranium. The muscovite-bearing suite has mean uranium content of 22.3 ppm, mean thorium content of 22.8 ppm, and mean Th/U of 2.82. Porphyritic quartz monzonite of the Midnite mine, which I interpret to be a two-mica granitic rock, is especially radioactive with mean U of 14.7 ppm, mean Th of 32.1 ppm, and mean Th/U of 2.72. Mean uranium and thorium contents of the two-mica granitic plutons are significantly different from those of the calcalkaline hornblende granitic suite, which are mean U, 5.0 ppm; mean Th, 17.6; and mean Th/U, 3.78. Biotite granitic rocks containing no hornblende or muscovite appear to be an intermediate suite in terms of U and Th, or possibly are variants of both hornblende and muscovite type; mean U is 3.88 ppm, mean Th is 14.4 ppm, and mean Th/U is 3.03 as calculated from the more abundant data of Castor and others (1978). occurrence of uranium and thorium in the muscovite and hornblende suites is systematically different. Many muscovite-bearing rocks are much more enriched in uranium (>15 ppm) than they are in thorium, and have a relatively low Th:U correlation coefficient of +0.409. Many of the uraniferous muscovite-bearing rocks contain less than 20 ppm Th, probably a consequence of forming by anatexis of thorium deficient sedimentary rocks. Uranium and thorium variation is much more regular in the hornblende suite, which has a Th:U correlation coefficient of +0.780. Uranium in the muscovite suite is held primarily in magnetite and biotite, and possibly as minute uraninite grains, whereas in the hornblende suite uranium resides primarily in sphene, zircon, and allanite. Many muscovite-bearing plutons are considered fertile by the following two criteria: high uranium content, and uranium residence in labile phases. The hornblende-bearing granitic plutons are not considered fertile, regardless of uranium content, because uranium resides in refractory phases. Twenty-one sample localities in four plutons are considered highly anomalous according to one or more of the following attributes: (1) Uranium content =115.8 ppm (total population mean plus 1 d). (2) Thorium content =30.3 ppm (mean plus 1 d) and uranium =8.8 ppm (mean). (3) Th/U lower than 1.68 (mean minus 1 d) and uranium content -18.8 ppm. The four identified highly anomalous plutons are, from southwest to northeast, (1) Cretaceous porphyritic quartz monzonite of the Midnite mine; (2) Cretaceous muscovite quartz monzonite east of Deer Lake; (3) Cretaceous quartz monzonite of Hungry Mountain, and (4) Cretaceous quartz monzonite of Granite Pass. The study area is favorable for at least five types of uranium deposits including: intragranitic hydrothermal veins as in the Massif Central, France; intragranitic supergene veins, as at the Daybreak mine; contact zone deposits, as at the Midnite mine; and basal-type sandstone deposits, as at the Sherwood mine. The fifth type is Rossing-type deposits for which the high-grade metamorphic terrane of the Kettle River Range, Ferry County, seems favorable, if sufficient volume of low-tenor rock can be located. The first four deposit types seem most likely in or adjacent to uraniferous plutons, as no other uranium source rocks have been identified in the area. Contact zone deposits and intragranitic hydrothermal veins, both possibly supergene-enriched, and basal-type deposits in Tertiary sandstone and conglomerate, seem most likely to be of economic importance. Exploration and discovery of potential uranium depositions

Open-File Report↗
USGS1977

Biogeochemical prospecting for uranium with conifers: results from the Midnite Mine area, Washington

The ash of needles, cones, and duff from Ponderosa pine (Pinus ponderosa Laws) growing near uranium deposits of the Midnite mine, Stevens County, Wash., contain as much as 200 parts per million (ppm) uranium. Needle samples containing more than 10 ppm uranium define zones that correlate well with known uranium deposits or dumps. Dispersion is as much as 300 m but generally is less. Background is about 1 ppm. Tree roots are judged to be sampling ore, low-grade uranium halo, or ground water to a depth of about 15 m. Uptake of uranium by Douglas fir (Pseudotsuga menziesii (Mirb.) Franco) needles appears to be about the same as by Ponderosa pine needles. Cones and duff are generally enriched in uranium relate to needles. Needles, cones, and duff are recommended as easily collected, uncomplicated sample media for geochemical surveys. Samples can be analyzed by standard methods and total cost per sample kept to about $6.

Open-File Report↗
USGS1977

Geology of the Midnite uranium mine area, Washington — Maps, description, and interpretation

Bedrock geology of about 12 km 2 near the Midnite mine has been mapped at the surface, in mine exposures, and from drilling, at scales from 1:600 to 1:12,000 and is presented here at 1:12,000 to provide description of the setting of uranium deposits. Oldest rocks in the area are metapelitic and metacarbonate rocks of the Precambrian (Y) Togo Formation. The chief host for uranium deposits is graphitic and pyritic mica phyllite and muscovite schist. Ore also occurs in calc-silicate hornfels and marble at the western edge of a calcareous section about 1,150 m thick. Calcareous rocks of the Togo are probably older than the pelitic as they are interpreted to be near the axis of a broad anticline. The composition and structural position of the calcareous unit suggests correlation with less metamorphosed carbonate-bearing rocks of the Lower Wallace Formation, Belt Supergroup, about 200 km to the east. Basic sills intrusive into the Togo have been metamorphosed to amphibolite. Unmetamorphosed rocks in the mine area are Cretaceous(?) and Eocene igneous rocks. Porphyritic quartz monzonite of Cretaceous age, part of the Loon Lake batholith, is exposed over one third of the mine area. It underlies the roof pendant of Precambrian rocks in which the Midnite mine occurs at depths of generally less than 300 m. The pluton is a two-mica granite and exhibits pegmatitic and aplitic textural features indicative of water saturation and pressure quenching. Eocene intrusive and extrusive rocks in the area provide evidence that the Eocene surface was only a short distance above the present uranium deposits. Speculative hypotheses are presented for penesyngenetic, hydrothermal, and supergene modes of uranium emplacement. The Precambrian Stratigraphy, similar in age and pre-metamorphic lithology to that of rocks hosting large uranium deposits in Saskatchewan and Northern Territory, Australia, suggests the possibility of uranium accumulation along with diagenetic pyrite in carbonaceous muds in a marine shelf environment. This hypothesis is not favored by the author because there is no evidence for stratabound uranium such as high regional radioactivity in the Togo. A hydrothermal mode of uranium emplacement is supported by the close apparent ages of mineralization and plutonism, and by petrology of the pluton. I speculate that uranium may have become enriched in postmagmatic fluids at the top of the pluton, possibly by hydrothermal leaching of soluble uranium associated with magnetite, and diffused outward into metasedimentary wall rocks to create an aureole about 100 m thick containing about 100 ppm uranium. Chemistry of the hydrothermal process is not understood, but uranium does not appear to have been transported by an oxidizing fluid, and the fluid did not produce veining and alteration comparable to that of base-metal sulfide deposits. Uranium in the low-grade protore is believed to have been redistributed into permeable zones in the Tertiary to create ore grades. Geologic and isotopic ages of uranium mineralization, and the small volume of porphyritic quartz monzonite available for leaching, are not supportive of supergene emplacement of uranium.

Washington↗
USGS1977

Uranium in Precambrian granitic rocks of the St. Francois Mountains, southeastern Missouri, with comments on uranium resource potential

Red granites of the St. Francois Mountains are highly radioactive and contain 4 to 34 parts per million (ppm) uranium. The most radioactive is the Graniteville Granite which contains an average of 16.9 ppm U and 42.6 ppm Th. The Butler Hill and Breadtray Granites also contain anomalous amounts, averaging 6.2 and 5.6 ppm U and 23.5 and 20.5 ppm Th respectively. Other Precambrian granitic rocks have normal concentrations of- U and Th. Fission track 'maps' indicate that high concentrations of uranium are associated with magnetite in the red granites; this uranium is presumed to be readily leachable by hydrothermal or supergene solutions. No uranium minerals or ore grade concentrations of uranium were observed in or near the granites, but there-are conceptual reasons for the possible existence of uranium deposits in intragranitic veins and onlapping Cambrian-Ordovician sedimentary rocks. Although the red granites constitute a good potential source of uranium, there is not much evidence for uranium having been mobilized. Identification of features such as lamprophyre dikes and 'episyenite' alteration, or sedimentary rocks containing reductants, would be of value for exploration and would permit more favorable resource appraisal.

Missouri↗
USGS1976

Fluid inclusions as a guide to porphyry copper deposits

Fluid-inclusion studies of 36 porphyry copper deposits, mainly in theUnited States, demonstrate that all but 3 evolved through a hydrothermal stage characterized by very high salinities, generally in excess of about 35 weight percent NaC1 equivalent, and boiling temperatures of these fluids ranged from about 250° to 700° C for various stages and deposits. Highsalinities, shown by halite-bearing inclusions, and boiling, suggested by coexisting gas and liquid-rich inclusions, are considered diagnostic of epizonal intrusions which are the most favorable parents for porphyry copper mineralization. Depth of emplacement of many copper-bearing stocks is deduced from fluid inclusions to have been about 6,000 to 10,000 feet (1,800 to 3,000 metres); fluid pressures during mineralization are interpreted generally to be less than 500 bars. Moderate-salinity (less than about 12 percent) and-moderate-temperature (<350°C) fluids are noted in all porphyry copper deposits and were responsible for the deposition of most copper and molybdenum in deposits such as Bagdad, Esperanza, Mineral Park, Morenci, Ray, Sierrita, in the southwestern United States and several in southern British Columbia. However, with only three exceptions, highly saline fluids apparently were present at an early stage and also deposited metals. The relative amounts and economic importance of copper and molybdenum deposited from high and moderate salinity fluids varies within the porphyry deposit class. There is compelling geologic and geochemical evidence that chloride ions are important for transport of metals in hydrothermal solutions, but the porphyry coppers stand out as a class associated with fluids of especially high salinity during at least one stage of their formation. Halite cubes in fluid inclusions are an effective although rough indicator of those salinities and can be conveniently monitored during petrographic study of thin sections. It is suggested that fluid inclusions be used to characterize favorable intrusions, metal anomalies, and cap rocks as an additional method of detecting possible disseminated porphyry copper-type metallization. The presence of halite-bearing inclusions, especially coexisting with gas-rich inclusions, is considered a favorable geochemical anomaly in the search for porphyry ore.

Open-File Report↗
USGS1976

Fluid-Inclusion Petrology - Data from Porphyry Copper Deposits and Applications to Exploration

Fluid-inclusion studies of 37 porphyry copper deposits, mainly in the United States, demonstrate that all but 3 evolved through a hydrothermal stage characterized by very high salinities, generally in excess of about 35 weight percent NaCI equivalent. Temperatures of these fluids ranged from about 250 deg to 700 deg C for various stages and deposits. Most systems boiled. High salinities, shown by halite-bearing inclusions, and boiling, suggested by coexisting gas and liquid-rich inclusions, are considered to be diagnostic of epizonal intrusions which are the most favorable parents for porphyry copper mineralization. Depth of emplacement of many copper-bearing stocks is deduced from fluid inclusions to have been about 6,000 to 10,000 feet (1,800 to 3,000 metres); fluid pressures during mineralization are interpreted generally to be less than 500 bars. Moderate-salinity (less than about 12 percent) and moderate-temperature <350 deg C) fluids are noted in all porphyry copper deposits and were responsible for the deposition of most copper and molybdenum in deposits, such as Bagdad, Esperanza, Mineral Park, Morenci, Ray, Sierrita, in the Southwestern United States and several in southern British Columbia. However, with only three exceptions, highly saline fluids apparently were present at an early stage and also deposited metals. The relative amounts and economic importance of copper and molybdenum deposited from high- and moderate-salinity fluids varies within the porphyry deposit class. There is compelling geologic and geochemical evidence that chloride is important for transport of metals, but the porphyry coppers stand out as a class associated with fluids of especially high salinity during at least one stage of their formation. Halite cubes in fluid inclusions are an effective, although rough, indicator of those salinities and can be conveniently monitored during petrographic study of thin sections. Thus, fluid inclusions can be used to characterize favorable intrusions, metal anomalies, and caprocks as an additional method of detecting possible disseminated porphyry copper metallization. The presence of halite-bearing inclusions, especially coexisting with gas-rich inclusions, is considered to be a favorable fluid anomaly in the search for porphyry ore.

Professional Paper↗
USGS1975

Fluid inclusion studies of vein, pipe, and replacement deposits, northwestern San Juan Mountains, Colorado

Base and precious metal ores valued in excess of $300 million have been mined from vein, pipe, and replacement deposits located on the northwest side of, and structurally related to, the middle Tertiary Silverton caldera. A belt of normal faults radial to the caldera contains veins which have been mined for as much as 15,000 feet (4,600 m) along strike and 3,700 feet (1,100 m) downdip. Structural relations, metal distributions, and fluid inclusion data suggest that many of the veins were open at the same general time and received the same mineralization. Fluid inclusions in quartz and sphalerite of the main ore stage of the Argentine and adjoining veins have filling temperatures ranging from 315 degrees to 249 degrees C and salinities from 7.9 to 0.1 wt percent NaCl equivalent. However, the majority of inclusions from base metal and gold stages are in a relatively narrow range near 280 degrees to 290 degrees C and salinities are unusually low (less than 2 wt %). Filling temperatures in postsulfide quartz and fluorite are as low as 153 degrees C and salinities are generally less than 0.5 wt percent. A pressure correction of about +25 degrees C should be added to the filling temperatures. Ore fluids were physically homogeneous liquids over the 3,700-foot (1,100 m) vertical and 11,200-foot (3,400 m) lateral range studied and no systematic variations in filling temperatures or salinity in this space are noted, but significant fluctuations are evident locally. Recently developed base metal replacement deposits occur in the Eocene Telluride Conglomerate adjacent to many metal-bearing veins. Calc-silicate alteration of the conglomerate host was probably by moderately saline fluids that ranged in temperature from 320 degrees to about 400 degrees C. Quartz-bearing clasts in altered zones contain secondary halitebearing inclusions with filling temperatures of about 250 degrees C and salinities about 34 wt percent; such inclusions are not known from the base metal stage and are interpreted to have been preore. Hydrothermal quartz, sphalerite, and calcite from replacement pods contain inclusions with filling temperatures ranging from 204 degrees to 309 degrees C and salinities from 11.2 to 0.2 wt percent. That the replacement zones and throughgoing veins are genetically related is suggested by the similarity of filling temperatures and compositions of base metal-stage fluid inclusions and by structural evidence. Small high-grade pipe deposits of base and precious metals occur along the ring-fault zone of the Silverton caldera. Filling temperatures for inclusions in quartz, sphalerite, and barite of the main ore stage of these deposits range from 216 degrees to 308 degrees C and salinities range from 1.6 to 0.2 wt percent NaCl. Quartz in altered wall rocks and silicified capping contains moderately saline secondary inclusions with relatively uniform liquid: vapor ratios that suggest filling temperatures of about 225 degrees to 300 degrees C. From the available samples there is no fluid inclusion evidence for boiling. Throttling, which had been hypothesized to explain the telescoped nature of the pipe ores, is neither substantiated nor discredited by the inclusion data.

Colorado↗
USGS1975

Geochemical studies in the Park City district; II, Sulfide mineralogy and minor-element chemistry, Mayflower mine

Fissure-filling and replacement Pb-Zn-Cu-Au-Ag ores of the Mayflower mine occur in calcareous sedimentary and intrusive wall rocks over a vertical interval of 3,000 feet. The ores are exceptional in the district for their chalcopyrite and gold content and for the unusual associated gangue minerals anhydrite, chlorite, and hematite. High oxygen fugacities are indicated for many stages of mineralization. Sphalerite compositions are highly variable in the range 0.09 to 5.9 weight percent Fe, an indication of large fluctuations in sulfur fugacity. Silver is carried in tetrahedrite-tennantite (0.2 to 16 wt %), enargite (0.5 to 0.8 wt %), in coupled substitution with Bi + Sb in galena (0.02 to 2.9 wt %), and in the minerals argentite, matildite, chalcocite, and bornite. Content of As, Se, Te, and other minor elements is small. Fractionation of Cd between sphalerite and coexisting galena is relatively consistent whereas the fractionation of Mn between sphalerite and galena is variable; calculated temperatures of formation are high and unreliable.

Economic Geology↗
USGS1975

Geology of the Midnite uranium mine, Stevens County, Washington; a preliminary report

The Midnite mine is one of only two mines in the United States currently producing uranium from discordant deposits in crystalline host rocks. Ore bodies are in metamorphosed steeply dipping Precambrian pelitic and calcareous rocks of a roof pendant adjacent to a Cretaceous(?) porphyritic quartz monzonite pluton. Production during 14 years, of operation has been about 8 million pounds of U3O8 from oxidized and reduced ores averaging 0.23 percent U3O8. Uranium deposits are generally tabular in form and dimensions range up to 380 m long, 210 m wide, and 50 m thick. Deposits are bounded on at least one side by unmineralized intrusive ribs of granitic rock, and thickest mineralized zones invariably occur at depressions in the intrusive contact. Upper limits of some deposits are nearly horizontal, and upper elevations of adjacent mineralized zones separated by ribs of granite are similar. Near surface ore is predominantly autunite, but ore at depth consists of pitchblende and coffinite with abundant pyrite and marcasite. Uranium minerals occur as .disseminations along foliation, replacements, and stockwork fracture-fillings. No stratigraphic controls on ore deposition are recognized. Rather, mineralized zones cut across lithologic boundaries if permeability is adequate. Most ore is in muscovite schist and mica phyllite, but important deposits occur in calc-silicate hornfels. Amphibolite sills and mid-Tertiary dacite dikes locally, carry ore where intensely fractured. High content of iron and sulfur, contained chiefly in FeS2, appear to be an important feature of favorable host rocks. Geometry of deposits, structural, and geochemical features suggest that uranium minerals were deposited over a span of time from late Cretaceous to late Tertiary. Ore occurs in but is not offset by a shear zone that displaces mid-Tertiary rocks.. Economic zones of uranium are interpreted to have been secondarily enriched in late Tertiary time by downward and lateral migration of uranium into permeable zones where deposition was influenced by ground water controls and minerals that could reduce or neutralize uranium-bearing solutions.

Open-File Report↗
USGS1975

Geology, geochemistry, and fluid-inclusion petrography of the Sapo Alegre porphyry copper prospect and its metavolcanic wallrocks, west-central Puerto Rico

The Sapo Alegre prospect, a small porphyry copper-molybdenum occurrence in west-central Puerto Rico, is characterized by distinct zones of alteration and mineralization of quartz diorite porphyry. A biotite-chlorite zone in the porphyry near its contact with surrounding metavolcanic rocks contains copper, molybdenum, gold, silver, selenium, and tellurium. A quartz-sericite-pyrite zone within the porphyry contains abundant sulfur and traces of selenium, but metals of the biotite-chlorite zone are nearly absent and zinc, manganese, nickel, sodium, calcium, and magnesium contents are very low. Quartz grains in the biotite-chlorite zone contain abundant fluid inclusions in which halite crystals are common, whereas in the quartz-sericite-pyrite zone inclusions are less abundant and rarely contain halite inclusions. Metavolcanic rocks northwest of the mineralized porphyry are altered to amphibolitic hornfels near the contact. Biotitic alteration is strong outward from the hornfels and grades into chlorite alteration. The hornfels has very low sulfide content, and the biotite zone has moderate amounts of copper and sulfur, decreasing outward. The chlorite zone is characterized by an abrupt increase in zinc and manganese content. Fluid-inclusion data suggest temperatures between 300° and 400°C for hydrothermal fluids in the biotite-chlorite zone of the porphyry and 250° to 300°C for fluids in the quartz-sericite-pyrite zone. Pressures equivalent to about 1.5 km of burial are indicated.

Río Víví district↗
USGS1974

Fluid inclusion and light stable isotope study of the climax molybdenum deposits, Colorado

The Climax mine contains three molybdenite ore bodies and widespread late quartz-pyrite-sericite barren mineralization, each related to separate intrusive phases of the Climax stock. Alteration zones spatially related to each molybdenite ore body include a silica zone below, a potassium-silicate zone that approximately coincides with ore, and overlying quartz-sericite-pyrite-topaz, argillic, and propylite zones . Delta 18 O values of quartz range from +8.4 to 10.9 per mil; delta 18 O values of muscovite and sericite range from --0.8 to +7.5 per mil. Eight of ten sericite values are between +5.8 and +7.5. All of the quartz and most of the sericite is in isotopic equilibrium with a calculated water at 350 degrees C with delta 18 O values of +3.0 to 5.5 per mil. Delta 18 O values of K-feldspars range from --4.5 to +7.5 per mil. This wide range indicates partial reequilibration of the feldspar with later, isotopically light, waters. Two muscovites have delta D values of --146 and --91 per mil; sericite ranges from --168 to --116 per mil. The calculated delta D values of water at 275 degrees C in equilibrium with sericite are --144 to --92. This range is the same as that of fluid inclusions in ore samples.Kaolinite in the argillic zone has delta 18 O values of --0.9 to --2.2 and delta D values of --162 per mil. Calculated water at 250 degrees C in equilibrium with kaolinite delta 18 O values of --4.7 to -6 and delta D of about -130 per mil. The isotopic and fluid inclusion data best fit a model whereby the Climax ore bodies were formed from a hydrothermal fluid that originated by mixing light and heavy waters. The light water is isotopically similar to present-day meteoric water; the heavy water has the isotopic composition postulated for magmatic water, although it could be meteoric water that was heavier than present-day meteoric water.

Colorado↗
USGS1974

Alteration and fluid inclusion studies of the porphyry copper ore body at Bingham, Utah

Distribution patterns for biotitic alteration, sericitic alteration, and distinctive fluid-inclusion types in igneous host rocks of the porphyry copper ore body at Bingham, Utah, have been determined by petrographic examination of about 300 samples. These patterns are related to differences in original rock composition, variations in physical-chemical conditions during periods of intrusion and mineralization, and spatial position within the ore body. The distribution of biotitic (potassium-silicate) alteration assemblages and high-salinity fluid inclusions generally follows the crudely triangular form of the disseminated copper ore zone. Variations in abundance of hydrothermal biotite are attributed to differences in original mafic mineral content of the igneous host rocks. Biotitic alteration and initial copper mineralization were accomplished by high-salinity fluids concentrated during final crystallization of the monzonitic parent magma; genetic continuity between magmatic and hydrothermal stages is indicated . Pervasive sericitic alteration of plagioclase is confined to rocks in the northern one-third of the Bingham stock; a subzone of argillic alteration in the north-central part of the ore body occurs within the broader area of sericitic alteration. Fluids responsible for sericitic and argillic alteration were channeled by a broad zone of northeast-trending fractures. Hydrothermal minerals and high-salinity fluid inclusions occur within a large volume of shattered rock. Boiling of fluids during crystallization of the aplitic porphyry may account for the shattering. Sericitic (and argillic) alteration were apparently super-imposed on the earlier biotitic assemblage as the hydrothermal system cooled. Cooling and hydrolytic alteration were promoted by progressive introduction of meteoric waters. The many generations of inclusions trapped from boiling fluids in the temperature range 400 degrees to 600 degrees C suggest that the system was recharged repeatedly during the period of mineralization. Estimated fluid pressures of about 800 bars in the early stages of mineralization correspond to a lithostatic load of about 3 km; pressures were even lower (less than 200 bars) in the later stages and were probably controlled by hydrostatic conditions. Distribution patterns for biotitic alteration, sericitic alteration, and distinctive fluid-inclusion types in igneous host rocks of the porphyry copper ore body at Bingham, Utah, have been determined by petrographic examination of about 300 samples. These patterns are related to differences in original rock composition, variations in physical-chemical conditions during periods of intrusion and mineralization, and spatial position within the ore body.The distribution of biotitic (potassium-silicate) alteration assemblages and high-salinity fluid inclusions generally follows the crudely triangular form of the disseminated copper ore zone. Variations in abundance of hydrothermal biotite are attributed to differences in original mafic mineral content of the igneous host rocks. Biotitic alteration and initial copper mineralization were accomplished by high-salinity fluids concentrated during final crystallization of the monzonitic parent magma; genetic continuity between magmatic and hydrothermal stages is indicated.Pervasive sericitic alteration of plagioclase is confined to rocks in the northern one-third of the Bingham stock; a subzone of argillic alteration in the north-central part of the ore body occurs within the broader area of sericitic alteration. Fluids responsible for sericitic and argillic alteration were channeled by a broad zone of northeast-trending fractures.Hydrothermal minerals and high-salinity fluid inclusions occur within a large volume of shattered rock. Boiling of fluids during crystallization of the aplitic porphyry may account for the shattering. Sericitic (and argillic) alteration were apparently super-imposed on the earlier biotitic assemblage as the hydrothermal system cooled. Cooling and hydrolytic alteration were promoted by progressive introduction of meteoric waters. The many generations of inclusions trapped from boiling fluids in the temperature range 400 degrees to 600 degrees C suggest that the system was recharged repeatedly during the period of mineralization. Estimated fluid pressures of about 800 bars in the early stages of mineralization correspond to a lithostatic load of about 3 km; pressures were even lower (less than 200 bars) in the later stages and were probably controlled by hydrostatic conditions.

Utah↗
USGS1973

Fluid-inclusion studies of the fluorspar and gold deposits, Jamestown district, Colorado

The Jamestown district, Boulder County, Colorado, is a major producer of fluorspar; prior to 1940, gold, gold-telluride, and lead-silver ores were mined. Fluorite occurs as a primary mineral in phases of the composite sodic granite stock at Jamestown and in breccia zones, stockworks, and pipe-shaped bodies in and adjacent to the stock. Gold and telluride mineralization occurs with and without fluorite in veins peripheral to the stock. A great variety of fluid-inclusion types is present in the district, reflecting chemically and physically diverse fluids. Fluid inclusions in early-stage quartz from the fluorspar deposits have filling temperatures of 250 degrees to 375 degrees C, salinities of 20 to 30%, and boiling is indicated at many locations. Most inclusions associated with the main fluorite stage have salinities of at least 26% to more than 50% and filling temperatures in the range of 250 degrees to 350 degrees C. Probable cognate fluorite on the inclusion walls and as many as ten daughter minerals precipitated from some primary inclusions in fluorite attest to the presence of salt and CaF 2 -rich polycomponent fluorspar-depositing fluids. Carbon dioxide-rich liquids and vapors were present during and after the main period of fluorspar deposition. Gold-bearing veins contain fluid inclusions indicating that two fundamentally different types of fluids were present. Inclusions in pregold quartz and fluorite have filling temperatures which range up to 375 degrees C, and most have very high salinities comparable to those from the fluorspar deposits, suggesting that early quartz and fluorite of the gold-bearing veins was roughly contemporaneous with the main period of fluorspar deposition. Fluid inclusion and other thermometric data (Kelly and Goddard, 1969) suggest that gold and telluride deposition occurred at temperatures below 300 degrees C. Fluid inclusions most directly associated with gold deposition have filling temperatures in the range 205 degrees to 270 degrees C and have about 4% salinity. These data suggest that the gold-bearing fluids either evolved from the fluorite-bearing fluids or were later unrelated hydrothermal pulses introduced on reopened structures. Boiling occurred at many locations that were at relatively high elevations or adjacent to the sodic granite stock. From the interpretation that boiling occurred and from the heterogeneity of CO 2 contents, we deduce that fluid pressures were low and variable, commonly near 150 bars, but ranging to as much as approximately 500 bars when CO 2 pressures were high; these determinations are compatible with the depth of cover estimated from geomorphic reconstruction using the Flattop peneplain. The absence of strong thermal or salinity zonation of fluids relative to the outcropping stock suggests that fluids were emanating from a larger intrusive body at depth.

Colorado↗
USGS1973

Geochemical studies in the Park City district; I, ore fluids in the Mayflower mine

Ore bodies in the Mayflower mine, Park City district, Utah, are localized along a normal fault zone which cuts Mississippian sedimentary and Tertiary intrusive rocks. Fissure filling and replacement Pb-Zn-Cu-Ag-Au mineralization occurs in both sedimentary and intrusive host rocks over a known vertical distance of 3,000 feet. The paragenesis of three major recognized veins in the mine is nearly the same, consisting of early quartz, anhydrite, hematite, and pyrite + or - chalcopyrite, followed by sphalerite and galena, grading into pyrite + chalcopyrite + hematite, in turn followed by quartz + carbonate and minor anhydrite, followed by sphalerite and chalcopyrite. Deep, early veins outside of the Mayflower ore zone are characterized by quartz, K-feldspar, biotite, pyrite, and anhydrite, and some also contain magnetite, amphibole or chalcopyrite; these veins contain halite-bearing and gas-rich inclusions which are not known from the ore zone. The deep, early fluids had 34 to 44% salinity, homogenization temperatures of 315 degrees to 430 degrees C, and at times were boiling. Fluid inclusions in samples from the three ore-bearing veins, which contain only simple two-phase inclusions with consistent phase proportions, indicate a marked change in the fluids prior to ore deposition. Homogenization temperatures range from 220 degrees to 300 degrees C, and probably require a pressure correction of approximately + 10 degrees C. Freezing tests indicate salinities in the range 0.3 to 11 wt %NaCl equivalent; no CO 2 -bearing phases were detected at reduced temperatures. Near-surface veins, presumably contemporaneous with the Mayflower ore zone, show evidence for boiling and suggest that there was approximately 90 bars pressure at the present Mayflower vein outcrop. The distribution of fluid densities, temperatures, boiling, and key minerals in time and space indicates a dramatic change from very hot dense post-magmatic fluids to cooler, relatively low salinity fluids at the onset of economic basemetal deposition, probably concurrent with normal faulting. The changes in the physical properties of the hydrothermal fluids are believed to reflect the structural and magmatic evolution of the area.

Utah↗
USGS1973

Microprobe analyses of sericite, chlorite, and epidote from Jerome, Arizona

Volcanic rocks in the vicinity of the massive sulfide deposits at the United Verde mine, Jerome, Ariz., have been modified in several periods of hydrothermal alteration and greenschist metamorphism. Chlorite, 2M, mica (sericite), and epidote are characteristic alteration products. Microprobe analyses for sericite, chlorite, and epidote are recalculated to structural formulas by the method employing oxygen anion equivalents. The sericite has the general composition of muscovite, but is moderately phengitic, and two samples have 6-12 percent paragonite in solid solution. Most of the chlorite is ripidolite with approximately one-third of the tetrahedral sites filled by aluminum; octahedral aluminum slightly exceeds tetrahedral. Fe:Fe+Mg+Mn ratios range from 0.34 to 0.66; low values are associated with sulfide minerals; higher values occur in a sample peripheral to the massive sulfide deposit. The epidote is a solid solution of 70 percent epidote, 30 percent clinozoisite.

Arizona↗