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At least 1,135 records · Page 63Linked to original sources
USGS2013

Porphyry copper assessment of Europe, exclusive of the Fennoscandian Shield: Chapter K in Global mineral resource assessment

The U.S. Geological Survey (USGS) collaborated with European geologists to assess resources in porphyry copper deposits in Europe, exclusive of Scandinavia (Sweden, Denmark, Norway, and Finland) and Russia. Porphyry copper deposits in Europe are Paleozoic and Late Cretaceous to Miocene in age. A number of the 31 known Phanerozoic deposits contain more than 1 million metric tons of contained copper, including the Majdanpek deposit, Serbia; Assarel, Bulgaria; Skouries, Greece; and Rosia Poeni, Romania. Five geographic areas were delineated as permissive tracts for post-Paleozoic porphyry copper deposits. Two additional tracts were delineated to show the extent of permissive igneous rocks associated with porphyry copper mineralization related to the Paleozoic Caledonian and Variscan orogenies. The tracts are based on mapped and inferred subsurface distributions of igneous rocks of specific age ranges that define areas where the occurrence of porphyry copper deposits within 1 kilometer of the Earth’s surface is possible. These tracts range in area from about 4,000 to 93,000 square kilometers. Although maps at a variety of different scales were used in the assessment, the final tract boundaries are intended for use at a scale of 1:1,000,000. The post-Paleozoic deposits in Europe all formed in conjunction with the tectonic evolution of southern Europe as the former Tethyan Ocean closed by convergence of the African and Arabian Plates with Europe, accompanied by accretion of microcontinents to the southern Eurasian Plate and development and demise of magmatic arcs and ocean basins. Many of the deposits formed in extensional or post-collisional settings; these tectonic environments are increasingly being recognized as environments where porphyry copper deposits occur. Probabilistic estimates of undiscovered porphyry copper deposits were made for four Phanerozoic permissive tracts; the other tracts are discussed qualitatively. Assessment participants estimated numbers of undiscovered deposits at different levels of confidence for the four tracts. These estimates were then combined with grade and tonnage models using Monte Carlo simulation to generate probabilistic estimates of amounts of in-place undiscovered resources. Additional resources that may be present in extensions of known deposits were not evaluated. Assessment results are reported in tables and graphs as expected amounts of metal and rock in undiscovered deposits at different quantile levels, as well as the arithmetic mean for each commodity for each tract. This assessment estimated a mean of 14 undiscovered porphyry copper deposits within the four permissive tracts for which estimates were made. On the basis of global grade and tonnage models, mean (arithmetic) estimated resources that could be associated with undiscovered deposits are about 46 million metric tons of copper and about 2,600 metric tons of gold, as well as byproduct molybdenum and silver. Reliable reported identified resources for the 27 deposits in the assessed areas total about 44 million metric tons of copper and about 2,300 metric tons of gold. Exploration for gold-rich porphyry systems is ongoing in some parts of historical copper mining districts in central Europe and in northwesternmost (European) Turkey. Political and social conflicts, environmental concerns associated with historical mining, and the global economic situation have had negative effects on exploration, development, and mining in Europe for many years. The assessment includes an overview with summary tables. Detailed descriptions of each tract, including the rationales for delineation and assessment, are given in appendixes A–G. Appendix H describes a geographic information system (GIS) that includes tract boundaries and point locations of known porphyry copper deposits and significant prospects.

Scientific Investigations Report↗
USGS2004

Chapter 21 Western phosphate field - Depositional and economic deposit models

The Western Phosphate Field (WPF), composed of Permian marine sedimentary strata that cover over 300,000 km 2 in the middle Rocky Mountains of Idaho, Montana, Utah, and Wyoming in the United States, contains vast resources of phosphate mined for fertilizer and a range of other industrial applications. The richest deposits of phosphate in the WPF occur in the Meade Peak Phosphatic Shale Member of the Phosphoria Formation in southeast Idaho. Phosphate is an essential and even limiting nutrient of algal production, which occurs at the bottom of the marine food web in the oceanic photic zone. The high concentrations of phosphate and trace elements in the Phosphoria Formation reflect a low accumulation rate of diluting phases, such as terrigenous siliciclastic debris and carbonate, rather than an unusually high level of primary productivity at the time of deposition. Indeed, the mean rate of accumulation of PO 4 3 required a continuous flux of PO 4 3 into the basin and the photic zone of the water column, but only at a moderate level. This flux was maintained by upwelling of nutrient-rich seawater, imported at depth from the open ocean. Although only a fraction of the organic matter that hosted the PO 4 3 and other nutrients (NO 3 , Cd, Cu, Mo, Ni, and Zn) actually escaped oxidation in the water column, their rate of accu- mulation on the sea floor defined the basin hydrography. Rates of accumulation of Cr, U, V, and rare-earth elements by precipitation and adsorp- tion reactions identify redox conditions in the bottom water as having been denitrifying, maintained by a balance between the rate of oxidation of organic matter settling through the water column and the flux of open-ocean seawater at depth. Atmospheric mixing maintained oxygen respiration in the uppermost several tens of meters of the water column. This hydrography and seawater chemistry are present in several sedimentary envi- ronments in the ocean today. In the WPF, there is an estimated surface mineable reserve base and subeconomic resource of 7.6 billion mt, at an average grade of 24% P 2 O 5 ; a subeconomic underground- mineable resource of 17 billion mt, at a grade of 28%; and 507 billion mt of subresource- grade phosphatic material that underlie the WPF at a depth greater than 305 m. The relationship between phosphate-ore specifications and weathering suggests that significant changes in processing, with associated cost increases, will be required to extend recovery of ore below the relatively strongly weathered zone near the surface. Four open pit mines currently extract phosphate from two moderately to steeply dipping ore zones that typically contain between 20% and 35% P 2 O 5 . Although the shales are enriched in trace elements, especially As, Cd, Cr, Cu, Mo, Se, U, V, Zn, and rare-earth elements, the relative concentration of organic carbon and selected major element oxides determines the suitability of phosphate-rich rock for feed to processing plants and its other applications. Selected specifications from the four operating mines include the following: minimum P 2 O 5 of 18-20% and average of 26-27%; maximum A1 2 O 3 of 1.6-5.0%; maximum MgO of 0.3-0.6%; a CaO/P 2 O 5 ratio of 1.5-1.6; and total carbon content of 4%-5%. Weathering to a depth of as much as 100 m significantly enhances ore quality by decreasing the proportions of calcite, dolomite, and organic matter relative to carbonate fluorapatite, the primary ore mineral

Colorado, Idaho, Montana, Nebraska, North Dakota, ↗
USGS2020

The nature and composition of the J-M Reef, Stillwater Complex, Montana, USA

In this contribution, we analyze 30 years of mine development data and quantitatively identify the processes that control the grade and tenor of the mineralized rock. An assay database of more than 60,000 samples was used to examine variations in ore grade and tenor of the sulfide mineralization in the J-M reef horizon of the Stillwater Complex along the strike and down the dip of the deposit in the area of the Stillwater mine. We compare these results with data from the East Boulder mine and whole-rock lithogeochemistry of samples collected along the entire strike length of the complex. We find significant variation in the composition of the reef sulfides in different spatial domains of the Stillwater mine area and between the Stillwater and East Boulder mines. Most of the variation in the grade and tenor can be explained by a variation in the mass of silicate magma with which the sulfide liquid equilibrated (i.e., R factor); however, geochemical and textural evidence suggests that parts of the reef may have experienced significant S loss following initial sulfide melt segregation. Some variability in the reef tenor and grade can be attributed to variable amounts of sulfur loss due to low-temperature hydrothermal fluids and the overestimation or underestimation of metal concentrations in reef assays due to the nugget effect. Furthermore, we address the Pd/Pt ratio of the reef samples and suggest that the lower solubility of Pt in the parental silicate melt may have caused the crystallization and removal of Pt alloys at some point before the melt reached sulfide saturation and Pt could partition into the sulfide liquid. This disparity between the prior evolution of Pt and Pd in the silicate melt resulted in the observed Pd/Pt ratio of ~3.65 across all areas of the reef—a value significantly larger than anticipated for primitive mantle-derived magmas.

Montana↗
USGS2003

Alligator ridge district, East-Central Nevada: Carlin-type gold mineralization at shallow depths

Carlin - type deposits in the Alligator Ridge mining district are present sporadically for 40 km along the north-striking Mooney Basin fault system but are restricted to a 250-m interval of Devonian to Mississippian strata. Their age is bracketed between silicified ca. 45 Ma sedimentary rocks and unaltered 36.5 to 34 Ma volcanic rocks. The silicification is linked to the deposits by its continuity with ore-grade silicification in Devonian-Mississippian strata and by its similar δ 18 O values (_e1∼17‰) and trace element signature (As, Sb, Tl, Hg). Eocene reconstruction indicates that the deposits formed at depths of ≤300 to 800 m. In comparison to most Carlin - type gold deposits, they have lower Au/Ag, Au grades, and contained Au, more abundant jasperoid, and textural evidence from deposition of an amorphous silica precursor in jasperoid. These differences most likely result from their shallow depth of formation. The peak fluid temperature (_e1∼230°C) and large δ 18 O H2O value shift from the meteroric water line (_e1∼20‰) suggest that ore fluids were derived from depths of 8 km or more. A magnetotelluric survey indicates that the Mooney Basin fault system penetrates to mid-crustal depths . Deep circulation of meteoric water along the Mooney Basin fault system may have been in response to initial uplift of the East Humboldt-Ruby Mountains metamorphic core complex; convection also may have been promoted by increased heat flow associated with large magnitude extension in the core complex and regional magmatism. Ore fluids ascended along the fault system until they encountered impermeable Devonian and Mississippian shales, at which point they moved laterally through permeable strata in the Devonian Guilmette Formation, Devonian-Mississippian Pilot Shale, Mississippian Joana Limestone, and Mississippian Chainman Shale toward erosional windows where they ascended into Eocene fluvial conglomerates and lake sediments. Most gold precipitated by sulfidation of host-rock Fe and mixing with local ground water in zones of lateral fluid flow in reactive strata, such as the Lower Devonian-Mississippian Pilot Shale.

Economic Geology↗
USGS2004

Structure of the Red Dog District, western Brooks Range, Alaska

The Red Dog district of the western Brooks Range of northern Alaska, which includes the sediment-hosted Zn-Pb-Ag ± Ba deposits at Red Dog, Su-Lik, and Anarraaq, contains one of the world's largest reserves of zinc. This paper presents a new model for the structural development of the area and shows that understanding the structure is crucial for future exploration efforts and new mineral discoveries in the district. In the Red Dog district, a telescoped Late Devonian through Jurassic continental passive margin is exposed in a series of subhorizontally stacked, internally imbricated, and regionally folded thrust sheets. These sheets were emplaced during the Middle Jurassic to Late Cretaceous Brookian orogeny and subsequently were uplifted by late tectonic activity in the Tertiary. The thrust sheet stack comprises seven tectonostratigraphically distinct allochthonous sheets, three of which have been subject to regional and detailed structural analysis. The lowermost of these is the Endicott Mountains allochthon, which is overlain by the structurally higher Picnic Creek and Kelly River allochthons. Each individual allochthon is itself internally imbricated into a series of tectonostratigraphically coherent and distinct thrust plates and subplates. This structural style gives rise to duplex development and imbrication at a range of scales, from a few meters to tens of kilometers. The variable mechanical properties of the lithologic units of the ancient passive margin resulted in changes in structural styles and scales of structures across allochthon boundaries. Structural mapping and analysis of the district indicate a dominant northwest to west-northwest direction of regional tectonic transport. Local north to north-northeast transport of thrust sheets is interpreted to reflect the influence of underlying lateral and/or oblique ramps, which may have been controlled by inherited basin margin structures. Some thrust-sheet stacking patterns suggest out-of-sequence thrusting. The west-northwest-east-southeast-trending Wrench Creek and Sivukat Mountain faults were previously interpreted to be strike-slip faults, but this study shows that they are Tertiary (Eocene?) late extensional faults with little or no lateral displacement.

Alaska↗
USGS2014

Mapping advanced argillic alteration at Cuprite, Nevada, using imaging spectroscopy

Mineral maps based on Airborne Visible/Infrared Imaging Spectrometer (AVIRIS) data were used to study late Miocene advanced argillic alteration at Cuprite, Nevada. Distributions of Fe-bearing minerals, clays, micas, sulfates, and carbonates were mapped using the Tetracorder spectral-shape matching system. The Al content of white micas increases toward altered areas and near intrusive rocks. Alunite composition varies from pure K to intimate mixtures of Na-K endmembers with subpixel occurrences of huangite, the Ca analogue of alunite. Intimately mixed Na-K alunite marks areas of relatively lower alteration temperature, whereas co-occurring Na-alunite and dickite may delineate relict hydrothermal conduits. The presence of dickite, halloysite, and well-ordered kaolinite, but absence of disordered kaolinite, is consistent with acidic conditions during hydrothermal alteration. Partial lichen cover on opal spectrally mimics chalcedony, limiting its detection to lichen-free areas. Pods of buddingtonite are remnants of initial quartz-adularia-smectite alteration. Thus, spectral maps provide a synoptic view of the surface mineralogy, and define a previously unrecognized early steam-heated hydrothermal event. Faulting and episodes of hydrothermal alteration at Cuprite were intimately linked to upper plate movements above the Silver Peak-Lone Mountain detachment and growth, collapse, and resurgence of the nearby Stonewall Mountain volcanic complex between 8 and 5 Ma. Isotopic dating indicates that hydrothermal activity started at least by 7.61 Ma and ended by about 6.2 Ma. Spectral and stable isotope data suggest that Cuprite is a late Miocene low-sulfidation adularia-sericite type hot spring deposit overprinted by late-stage, steam-heated advanced argillic alteration formed along the margin of the Stonewall Mountain caldera.

Nevada↗
USGS1960

Deposits of the manganese oxides

One of the problems of the wartime program of studies of domestic manganese deposits concerned the identification of, and modes of origin of the manganese oxide minerals. Of the hundreds of specimens of the oxides collected in the United States, the minerals of about 250 specimens were identified by X-ray analysis; complete chemical analyses were made of about 35 specimens and partial analyses of about 150 specimens. This report presents the conclusions that arise out of a review of the geologic environment under which the specimens were found. One conclusion of this review concerns the supergene vs. hypogene origin of the oxides. In order to reach conclusions concerning the supergene and hypogene origin of the 33 oxides of manganese recognized thus far, it was necessary to define the criteria that seemed usable.One group of oxides appears to be persistently supergene: groutite, hydrohausmannite, lithiophorite, rancieite, hetaerolite, hydrohetaerolite, chalcophanite, crednerite, woodruffite, and wad. Another group of oxides appears to have been formed only by hypogene processes: manganosite, hausmannite, pyrochroite, bixbyite, galaxite, jacobsite, franklinite, pyrophanite, and ilmenite. A third group of oxides appear to have been formed by supergene processes in some places and by hypogene processes in other places: manganite, pyrolusite, ramsdellite, cryptomelane, psilomelane, hollandite, braunite, and coronadite.Another conclusion concerns a genetic relation between: (1) veins of manganese oxides in the southwest, largely in Tertiary volcanic rocks, (2) bodies of oxides in travertine aprons near active hot springs, and inactive Pleistocene springs, and (3) stratified oxides, largely in late Tertiary sedimentary rocks in the southwest. From the features of these three groups of deposits of oxides and their geologic and geographic distribution, it appears that hot water from great depth rose on fractures in areas of volcanic activity, deposited oxides in the fractures, appeared at the surface as hot springs, deposited oxides in the aprons near the springs and continuing to local basins, deposited manganese oxides with local debris as persistent beds in sediments, partly or wholly of volcanic origin.

Economic Geology↗
USGS2020

Noble gases fingerprint the source and evolution of ore-forming fluids of Carlin-type gold deposits in the Golden Triangle, south China

Precise constraints on the source and evolution of ore-forming fluids of Carlin-type gold deposits in the Golden Triangle (south China) are of critical importance for a better understanding of the ore genesis and a refined genetic model for gold mineralization. However, constraints on the source of ore fluid components have long been a challenge due to the very fine grained nature of the ore and gangue minerals in the deposits. Here we present He, Ne, and Ar isotope data of fluid inclusion extracts from a variety of ore and gangue minerals (arsenian pyrite, realgar, quartz, calcite, and fluorite) representing the main and late ore stages of three well-characterized major gold deposits (Shuiyindong, Nibao, and Yata) to provide significant new insights into the source and evolution of ore-forming fluids of this important gold province. Measured He isotopes have R/R A ratios ranging from 0.01 to 0.4 that suggest a maximum of 5% mantle helium with an R/R A of 8. The Ne and Ar isotope compositions are broadly comparable to air-saturated water, with a few analyses indicating the presence of an external fluid containing nucleogenic 38 Ar and radiogenic 40 Ar. Plotted on the 20 Ne/ 4 He vs. helium R/R A and 3 He/ 20 Ne vs. 4 He/ 20 Ne diagrams, the results define two distinct arrays that emanate from a common sedimentary pore fluid or deeply sourced metamorphic fluid end-member containing crustal He. The main ore-stage fluids are interpreted as a mixture of magmatic fluid containing mantle He and sedimentary pore fluid or deeply sourced metamorphic fluid with predominantly crustal He, whereas the late ore-stage fluids are a mixture of sedimentary pore fluid or deeply sourced metamorphic fluid bearing crustal He and shallow meteoric groundwater containing atmospheric He. Results presented here, when combined with independent evidence, support a magmatic origin for the ore-forming fluids. The ascending magmatic fluid mixed with sedimentary pore fluid or deeply sourced metamorphic fluid in the ore stage and subsequently mixed with the meteoric groundwater in the late ore stage, eventually producing the Carlin-type gold deposits in the Golden Triangle.

Golden Triangle, south China↗
USGS1963

Studies of fluid inclusions; [Part] 2, Freezing data and their interpretation

Aqueous and non-aqueous inclusions in 84 samples of various minerals from a wide range of geologic environments were studied with the freezing stage in order to gain an insight into the range of concentrations and compositions of fluid inclusions . Inclusions in most Mississippi Valley-type ore minerals contain highly concentrated saline solutions, showing freezing temperatures between -23.4° and -10.5° C; minerals from ore deposits of more typically hydrothermal affiliations mainly show temperatures of -9.4° to nearly 0° C; and inclusions in quartz crystals from sedimentary, metamorphic, and igneous rock environments show a wide range of freezing temperatures. Inclusions in pegmatite minerals in particular vary over a wide range, from the most concentrated solutions found in any inclusion (> 40% salts) to fairly dilute solutions (< 5% salts). Most inclusions in quartz from Swiss Alpine-type veins, and from Brazilian quartz veins and pegmatites, show freezing temperatures in the range -8.5° to - 2 .5°, and considerable free C02. Other geologic environments sampled include Colombian emerald, pegmatitic topaz and fluorite, the Triassic traprock zeolite assemblage, and sedimentary halite beds. Not all the phenomena exhibited by inclusions at low temperature are completely understood at present but several crystalline hydrate phases, such as NaCl-2H,0 and CO,-5%H,0 (structural formula 8C02-46H20), are shown to be stable in inclusions of appropriate composition even at temperatures above 0° C, and probably exist in the inclusions in natural rocks in polar regions. More significantly, the formation and recognition of such phases aid in establishing the gross composition of individual inclusions far too small for chemical analysis. The data obtained are useful in a variety of ways, such as: discriminating among gas, liquid, and supercritical fluid , and among liquid water, liquid oil, and liquid C02 in inclusions ; improving precision of the pressure corrections applied to inclusion filling temperature determinations; proving the general lack of leakage into or out of inclusions ; estimating the minimum pressure at the time of deposition of certain samples; verifying the lack of extraneous solid crystallization nuclei in the inclusions and hence their formation from exceedingly quiet, clean solutions; determining the total equivalent NaCl concentrations and some information concerning the composition of the fluids from which ores have formed; and determining changes in the composition of the fluids bathing a single crystal during its growth, and at certain times throughout its history.

Economic Geology↗
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↗
USGS1995

Tilting history of the San Manuel-Kalamazoo porphyry system, southeastern Arizona

The Laramide San Manuel-Kalamazoo porphyry system of Arizona has been pivotal in concepts of both extensional tectonics and alteration-mineralization zoning. This paper reexamines the tilting history in light of new work in the region and reinterprets the geometry of the deposit. The porphyry mineralization occurs in and near an intrusion of Laramide San Manuel porphyry in Precambrian Oracle Granite. The area has an extremely complicated history of Tertiary crustal extension and fanglomerate deposition, but the blocks containing the two main fragments of the original orebody (separated by the San Manuel fault) were involved in only the later parts of this history and are less tilted than other nearby blocks. Originally horizontal features of mid-Tertiary age are tilted about 30 degrees , those of Laramide age about 35 degrees , and those of pre-Laramide age about 45 degrees to the northeast. Paleomagnetism of the porphyry intrusion itself suggests tilting of about 33 degrees . The data thus suggest that postemplacement tilt of the Laramide porphyry system was 30 degrees to 35 degrees and that virtually all of it was mid-Tertiary in age. An earlier interpretation of greater tilt magnitude was apparently based in part on correlation with adjacent areas showing greater tilt magnitude (as in the Tar Wash allochthon) and in part on a choice of cross section that gives the impression of a nearly recumbent attitude. However, Lowell's sections are oriented along the strike of both the orebodies and the productive porphyry intrusion, which are dipping tablo-cylindroidal bodies. Ore forms a hollow envelope whose inner margin has an aspect ratio of about >4.3 (length)/>2.5 (downdip height)/l (limb separation). The productive intrusion, around which ore is wrapped, has a similar aspect ratio in the same plane (strike N 58 degrees E, dip 47 degrees SE). Reconstruction of the original attitudes of intrusion and ore yields a common strike near N 75' E and a steep dip to the south. This is a common attitude for undisturbed productive porphyry dikes of Laramide age.

Arizona↗
USGS1958

Technique for the extraction and partial chemical analysis of fluid-filled inclusions from minerals

A method has been developed for the extraction and limited chemical analysis of the materials in solution in the fluid from the very minute fluid-filled inclusions such as commonly occur in whitish or milky quartz. The method may also be applied, with some reservations, to a variety of other minerals. As the amounts of substances in the fluid are small compared with possible contaminants, great care is needed in sample purification and cleaning; an electrolytic method has been found to be the only satisfactory final cleaning step. Following this, the inclusions are opened by ball milling of the cleaned sample, with deionized water, in an alumina ball mill using alumina grinding media. The ions present in the resultant slurry are separated from the ground quartz by electrodialysis and analyzed. Other methods, such as the decrepitation of a sample in an absorption train, are used to estimate the amount of H2O and CO2 in the inclusions. The most significant part of the analytical work has been to determine the ratios between the alkali metals. The materials in solution in the fluid-filled inclusions from 11 samples of quartz have been analyzed by the ball milling-electrodialysis method. Although there are large differences between samples, the average weights of the alkali metal ions found, for all samples, in milligrams per kilogram of quartz, are: Li+-0.92, Na+-99, K+-133, Rb+-0.45, Cs+-0.38 (atomic ratios, in the same sequence: 0.03/1.00/0.79/0.001/0.0007). In addition, 27 to 193 milligrams of CI", and 5 to 140 milligrams of SOr were found, per kilogram of quartz. H2O and COa were determined on only one sample. Six of the samples were from gold-quartz veins in the Grass Valley district, California. In these six the Na+/K+ ratios were all very similar, but the amounts of Li+, Rb+ and Cs+ found varied greatly. Although there are serious limitations to this and to all other techniques developed, it is felt that the results presented are sufficiently encouraging to warrant further study and possible application to specific geologic problems, such as the identification of epochs of quartz deposition

Economic Geology↗
USGS1958

The relation of phosphorites to ground water in Beaufort County, North Carolina

Recent ground-water studies undertaken by the U.S. Geological Survey in cooperation with the North Carolina Division of Mineral Resources have delineated phosphorite deposits, tentatively regarded as being of middle Miocene age, in Beaufort County. These deposits lie unconforma-bly on limestone of Eocene age and are unconformably overlain by late Miocene marl. The phosphorites, buried beneath strata ranging in thickness from 45 to 250 feet, underlie an area approximating 450 square miles. The total thickness of the phosphorite column throughout the area ranges from several feet to nearly 90 feet. The phosphorite column consists of phosphatic sands and intercalated shell limestones. The sands, composed of pellets of brown sand-size collophane (probably carbonate-fluorapatite) and sand-size, flat-sided angular quartz with some silt, clay, and organic material, have a median diameter between 0.50 and 0.25 mm. Chemical analyses of representative samples of the raw sand show a variation in PaOs content from 8 to 31 percent. The P2O5 content is apparently proportionate to the collophane content throughout the area. Reconstruction of the geologic history suggests that the phosphorites were deposited as chemical precipitates and as in situ replacements in a restricted marine basin where the pH of the water acted as the primary depositional control. Reconstruction of the hydrologic history of the phosphorites indicates that the deposits were preserved under artesian conditions; they were never subjected to alteration under water-table conditions. The absence of postpositional alteration makes this area a potentially classic one for studies of phosphorite genesis. Chemical analyses of artesian waters from the phosphorites and from limestones overlain by phosphorites reveal significantly greater concentrations of iodide and bromide in solution than are present in water from overlying sediments or from underlying limestones not overlain by phosphorites. Such anomalies, if present in other similar terranes, may indicate the presence of buried phosphorites. The depth and size distribution of the material suggest a recovery method utilizing wells constructed to "pump sand."

North Carolina↗
USGS1996

Cierco Pb-Zn-Ag vein deposits: Isotopic and fluid inclusion evidence for formation during the mesozoic extension in the pyrenees of Spain

The Cierco Pb-Zn-Ag vein deposits, located in the central Pyrenees of Spain, crosscut Paleozoic metasedimentary rocks and are in close proximity to Hercynian granodiorite dikes and plutons. Galena and sphalerite in the deposits have average delta 34 S values of - 4.3 and - 0.8 per mil (CDT), respectively. Coexisting mineral pairs give an isotopic equilibration temperature range of 89 degrees to 163 degrees C which overlaps with the 112 degrees to 198 degrees C range obtained from primary fluid inclusions. Coexisting quartz has a delta 18 O value of 19 + or - 1 per mil (VSMOW). The fluid which deposited these minerals is inferred to have had delta 18 O (sub H 2 ) O and delta 34 S (sub H 2 ) S values of 5 + or - 1 and -1 + or - 1 per mil, respectively. Chemical and microthermometric analyses of fluid inclusions in quartz and sphalerite indicate salinities of 3 to 29 wt percent NaCl equiv with Na (super +) and Ca (super 2+) as the dominant cations in solution. The Br/Cl and I/Cl ratios differ from those characteristic of magmatic waters and pristine seawater, but show some similarity to those observed in deep ground waters in crystalline terranes, basinal brines, and evaporated seawater. Barite, which postdates the sulfides, spans isotopic ranges of 13 to 21 per mil, 10 to 15 per mil, and 0.7109 to 0.7123 for delta 34 S, delta 18 O, and 87 Sr/ 86 Sr, respectively. The three parameters are correlated providing strong evidence that the barites are products of fluid mixing.We propose that the Cierco deposits formed along an extensional fault system at the margin of a marine basin during the breakup of Pangea at some time between the Early Triassic and Early Cretaceous. Sulfide deposition corresponded to an upwelling of hydrothermal fluid from the Paleozoic basement and was limited by the amount of metals carried by the fluid. Barite deposition corresponded to the waning of upward flow and the collapse of sulfate-rich surface waters onto the retreating hydrothermal plume. Calcite precipitated late in the paragenesis as meteoric or marine waters descended into the fault system, possibly during a regression in the overlying basin.There are other deposits resembling Cierco elsewhere in the Iberian peninsula. Taken as a group, they are evidence that hydrothermal circulation systems were widespread during Mesozoic extension. Differences among the deposits can be related to the fact that H 2 S and other solutes had local and variable sources.

Economic Geology↗
USGS2013

Geological analysis of aeromagnetic data from southwestern Alaska: Implications for exploration in the area of the Pebble porphyry Cu-Au-Mo deposit

Aeromagnetic data are used to better understand the geology and mineral resources near the Late Cretaceous Pebble porphyry Cu-Au-Mo deposit in southwestern Alaska. The reduced-to-pole (RTP) transformation of regional-scale aeromagnetic data shows that the Pebble deposit is within a cluster of magnetic anomaly highs. Similar to Pebble, the Iliamna, Kijik, and Neacola porphyry copper occurrences are in magnetic highs that trend northeast along the crustal-scale Lake Clark fault. A high-amplitude, short- to moderate-wavelength anomaly is centered over the Kemuk occurrence, an Alaska-type ultramafic complex. Similar anomalies are found west and north of Kemuk. A moderate-amplitude, moderate-wavelength magnetic low surrounded by a moderate-amplitude, short-wavelength magnetic high is associated with the gold-bearing Shotgun intrusive complex. The RTP transformation of the district-scale aeromagnetic data acquired over Pebble permits differentiation of a variety of Jurassic to Tertiary magmatic rock suites. Jurassic-Cretaceous basalt and gabbro units and Late Cretaceous biotite pyroxenite and granodiorite rocks produce magnetic highs. Tertiary basalt units also produce magnetic highs, but appear to be volumetrically minor. Eocene monzonite units have associated magnetic lows. The RTP data do not suggest a magnetite-rich hydrothermal system at the Pebble deposit. The 10-km upward continuation transformation of the regional-scale data shows a linear northeast trend of magnetic anomaly highs. These anomalies are spatially correlated with Late Cretaceous igneous rocks and in the Pebble district are centered over the granodiorite rocks genetically related to porphyry copper systems. The spacing of these anomalies is similar to patterns shown by the numerous porphyry copper deposits in northern Chile. These anomalies are interpreted to reflect a Late Cretaceous magmatic arc that is favorable for additional discoveries of Late Cretaceous porphyry copper systems in southwestern Alaska.

Alaska↗
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↗
USGS1986

Rb-Sr, K-Ar, and stable isotope evidence for the ages and sources of fluid components of gold-bearing quartz veins in the northern Sierra Nevada foothills metamorphic belt, California

Gold-bearing quartz veins occur in and near major fault zones in deformed oceanic and island-arc rocks west of the main outcrop of the Sierra Nevada composite batholith. Veins typically occupy minor reverse faults that crosscut blueschist to amphibolite-grade metamorphic rocks whose metamorphic ages range from early Paleozoic to Jurassic. Vein micas and carbonate-quartz-mica assemblages that formed by hydrothermal metasomatism of ultramafic wall rocks in the Alleghany, Grass Valley, Washington, and Mother Lode districts yield concordant K-Ar and Rb-Sr ages. The dated veins are significantly younger than prograde metamorphism, penetrative deformation, and accretion of their host rocks to the continental margin. New and previously published mineralization ages from 13 localities in the Sierra foothills range from about 140 to 110 m.y. ago, with mean and median between 120 and 115 m.y. The age relations suggest that mineralizing fluids were set in motion by deep magmatic activity related to the resumption of east-dipping subduction along the western margin of North America following the Late Jurassic Nevadan collision event.CO 2 -bearing fluids responsible for metasomatism and much of the vein mica, carbonate, albite, and quartz deposition in several northern mines were isotopically heavy (delta 18 O [asymp] 8-14ppm; delta D between about -10 and -50ppm) and do not resemble seawater, magmatic, or meteoric waters. Metasomatic and vein-filling mica, dolomite, magnesite, and quartz in altered ultramafic rocks generally formed from fluids with similar Sr and O isotope ratios at a given locality. Consistent quartz-mica delta 18 O fractionations (delta 18 O (sub Q-M) = 4.5-4.9ppm) from various localities imply uniform equilibration temperatures, probably between 300 degrees and 350 degrees C. On a local (mine) scale, fluids responsible for both carbonate alteration of mafic and ultramafic wall rocks and albitic alteration of felsic and pelitic rocks had similar Sr isotope ratios.Samples from three veins in the central Alleghany district fit a 115.7 + or - 3-m.y. Rb-Sr isochron with a ( 87 Sr/ 86 Sr) i value of approximately 0.7119. Inferred 87 Sr/ 86 Sr ratios of metasomatic fluids from mines in different parts of the foothills region vary considerably (0.704-0.718), suggesting that Sr was derived from sources ranging from "western assemblage" Mesozoic ophiolitic or arc volcanic rocks to early Paleozoic continent-derived clastic rocks of the Shoo Fly Complex. Systematic geographic variations in both Sr and O isotopes can be rationalized by assuming extensive fluid interaction with rocks similar to the ones that are exposed within a few kilometers of the veins, but the ultimate sources of the fluids, and of Au and other constituents, may be independent of these. Isotopically lighter (meteoric?) fluids deposited some late quartz overgrowths and occupied secondary fluid inclusions in earlier vein quartz.

Economic Geology↗
USGS2002

Age and origin of base and precious metal veins of the Coeur d'Alene mining district, Idaho

Ore-bearing quartz-carbonate veins of the Coeur d'Alene mining district yield 87Sr/86Sr ratios of 0.74 to >1.60 for low Rb/Sr, carbonate gangue minerals, similar to current ranges measured in Middle Proterozoic, high Rb/Sr rocks of the Belt Supergroup. Stable isotope and fluid inclusion studies establish a genetic relationship between vein formation and metamorphic-hydrothermal systems of the region. These extraordinary 87Sr/86Sr ratios require accumulation of radiogenic 87Sr in a high Rb/Sr system over an extended period prior to incorporation of Sr into the hydrothermal veins. Evaluation of the age and composition of potential sources of highly radiogenic Sr indicates that the ore-bearing veins of the Coeur d'Alene district formed during the Cretaceous from components scavenged from rocks of the Belt Supergroup, the primary host rocks of the district. Proterozoic Pb isotope ratios observed in galena from many Coeur d'Alene veins were established when Pb separated from uranium during deposition or diagenesis of the Belt Supergroup at 1400 to 1500 Ma, possibly as disseminated syngenetic deposits. K-Ar and Rb-Sr apparent ages and ??18O values of Belt Supergroup rocks decrease from the Coeur d'Alene district toward the Idaho and Kaniksu batholiths, approximately normal to the trends of metamorphic isograds, fold axes, foliation, and the major reverse faults of the district. Isoclinal folding, thrust faulting, high-temperature metamorphism, granitic plutonism, and regional-scale metamorphic-hydrothermal activity is documented in the region between 140 and 45 Ma, representing the only such combination of events in the Coeur d'Alene region subsequent to about 1300 Ma. The Sr and oxygen results and geologic evidence favor formation of the ore-bearing carbonate veins by fluids related to a complex metamorphic-hydrothermal system during the Cretaceous. Pb with Proterozoic isotopic compositions was probably mobilized and incorporated like other metals into the hydrothermal veins during this event. The ore-bearing veins were sheared and displaced during early Tertiary northwest-trending dextral strike-slip faulting along the Osburn fault and related structures of the Lewis and Clark line.

Economic Geology↗