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At least 937 records · Page 52Linked to original sources
USGS2005

U-Pb zircon geochronology of Mesoproterozoic postorogenic rocks and implications for post-Ottawan magmatism and metallogenesis, New Jersey Highlands and contiguous areas, USA

Postorogenic rocks are widespread in Grenville terranes of the north-central Appalachians where they form small, discordant, largely pegmatitic felsic intrusive bodies, veins, and dikes, and also metasomatic calcic skarns that are unfoliated and postdate the regional 1090 to 1030 Ma upper amphibolite- to granulite-facies metamorphism related to the Grenville (Ottawan) Orogeny. Zircons from magmatic and nonmagmatic rocks from northern New Jersey and southern New York were dated to provide information on the regional tectonomagmatic and metallogenic history following Ottawan orogenesis. We obtained U-Th-Pb zircon ages of 1004 ?? 3 Ma for pegmatite associated with the 1020 ?? 4 Ma Mount Eve Granite near Big Island, New York, 986 ?? 4 Ma for unfoliated, discordant pegmatite that intrudes supracrustal marble at the Buckwheat open cut, Franklin, New Jersey, ???990 Ma for a silicate-borate skarn layer in the Franklin Marble at Rudeville, New Jersey, and 940 ?? 2 Ma for a calc-silicate skarn layer at Lower Twin Lake, New York. This new data, together with previously published ages of 1020 ?? 4 to 965 ?? 10 Ma for postorogenic rocks from New Jersey and southern New York, provide evidence of magmatic activity that lasted for up to 60 Ma past the peak of high-grade metamorphism. Postorogenic magmatism was almost exclusively felsic and involved relatively small volumes of metaluminous to mildly peraluminous melt that fractionated from an A-type granite parent source. Field relationships suggest the melts were emplaced along lithosphere-scale fault zones in the Highlands that were undergoing extension and that emplacement followed orogenic collapse by least 30 Ma. Postorogenic felsic intrusions correspond to the niobium-yttrium-fluorine (NYF) class of pegmatites of C??erny?? (1992a). Geochronologic data provide a temporal constraint on late-stage hydrothermal activity and a metallogenic event in New Jersey at ???990 to 940 Ma that mineralized pegmatites with subeconomic to economic deposits of magnetite ?? U ?? Th ?? rare earth element (REE) and formed metasomatic calcic skarn bodies in marble and reactive carbonate rocks. Mineralization associated with this event overlaps the timing of pegmatite emplacement, suggesting a petrogenetic relationship. Coeval metallogeny at 975 to 950 Ma in the New York Hudson Highlands and 980 to 937 Ma in the Canadian Grenville Province implies that this event was widespread following the Ottawan phase of the Grenville Orogeny. ?? 2005 Elsevier B.V. All rights reserved.

Precambrian Research↗
USGS1984

Comparative geochronology in the reversely zoned plutons of the Bottle Lake Complex, Maine: U-Pb on zircons and Rb-Sr on whole rocks

The Bottle Lake Complex is a composite granitic batholith emplaced into Cambrian to Lower Devonian metasedimentary rocks. Both plutons (Whitney Cove and Passadumkeag River) are very coarse grained hornblende and biotite-bearing granites showing petrographic and geochemical reverse zonation. Two linear whole rock Rb/Sr isochrons on xenolith-free Whitney Cove and Passadumkeag River samples indicate ages of 379??5 m.y. and 381??4 m.y., respectively, in close agreement with published K-Ar ages for biotite from Whitney Cove of 377 m.y. and 379 m.y., and for hornblende 40Ar/39Ar determinations from Passadumkeag River which indicate an age of 378??4 m.y. The initial Sr isotopic ratio for Whitney Cove is 0.70553 and for Passadumkeag River is 0.70414. A whole-rock isochron on a suite of xenoliths from the Passadumkeag River granite indicates a whole rock Rb-Sr age of 496??14 m.y., with an initial Sr isotopic ratio of 0.70262. Two types of zircon exhibiting wide petrographic diversity are evident in variable proportions throughout the batholith. One of these types is preferentially found in a mafic xenolith and it is widely dispersed in the host granites forming discrete grains and probably as inclusions in the other type of zircon. U-Pb analyses of zircons give concordia intercept ages of 399??8 m.y. for Whitney Cove, 388??6 m.y. for Passadumkeag River, 415 m.y. for a mafic xenolith in Passadumkeag River, and 396??32 for combined Whitney Cove and Passadumkeag River granite. The zircons show a spread of up to 20 m.y. in the 207Pb/206Pb ages. Omitting the finest zircon fraction in the Passadumkeag River results in a concordia intercept age of 381??3 m.y., in better agreement with the whole-rock Rb-Sr and mineral K-Ar ages. For the Whitney Cove pluton, exclusion of the finest fraction does not bring the zircon age into agreement with the Rb-Sr data. Age estimates by the whole rock Rb-Sr, mineral K-Ar and Ar-Ar methods suggest that the crystallization age of the plutons is about 380 m.y., slightly younger than the U-Pb zircon intercept ages. A possible reason for this discrepancy is that the zircons contain inherited lead. Thus, zircon U-Pb ages might represent a mixture of newly developed zircon and older inherited zircon, whereas the Rb-Sr whole rock age (380 m.y.) reflects the time of crystallization, and the argon ages result from rapid cooling after emplacement. ?? 1984 Springer-Verlag.

Contributions to Mineralogy and Petrology↗
USGS1991

Vanadium accumulation in carbonaceous rocks: A review of geochemical controls during deposition and diagenesis

Published data relevant to the geochemistry of vanadium were used to evaluate processes and conditions that control vanadium accumulation in carbonaceous rocks. Reduction, adsorption, and complexation of dissolved vanadium favor addition of vanadium to sediments rich in organic carbon. Dissolved vanadate (V(V)) species predominate in oxic seawater and are reduced to vanadyl ion (V(IV)) by organic compounds or H2S. Vanadyl ion readily adsorbs to particle surfaces and is added to the sediment as the particles settle. The large vanadium concentrations of rocks deposited in marine as compared to lacustrine environments are the result of the relatively large amount of vanadium provided by circulating ocean water compared to terrestrial runoff. Vanadium-rich carbonaceous rocks typically have high contents of organically bound sulfur and are stratigraphically associated with phosphate-rich units. A correspondence between vanadium content and organically bound sulfur is consistent with high activities of H2S during sediment deposition. Excess H2S exited the sediment into bottom waters and favored reduction of dissolved V(V) to V(IV) or possibly V(III). The stratigraphic association of vanadiferous and phosphatic rocks reflects temporal and spatial shifts in bottom water chemistry from suboxic (phosphate concentrated) to more reducing (euxinic?) conditions that favor vanadium accumulation. During diagenesis some vanadium-organic complexes migrate with petroleum out of carbonaceous rocks, but significant amounts of vanadium are retained in refractory organic matter or clay minerals. As carbon in the rock evolves toward graphite during metamorphism, vanadium is incorporated into silicate minerals. ?? 1991.

Chemical Geology↗
USGS2025

Zircon as a pathfinder to REE mineralization

Carbonatites and alkaline silicate rocks are major primary sources of the rare earth elements (REE) and other critical metals, such as Nb. Despite the economic significance of these rocks, their formation and the processes of REE enrichment are poorly understood. Here, statistical analysis of a global dataset demonstrates that zircon geochemistry is a powerful recorder of REE metallogenesis and a potential pathfinder for REE deposits. Zircons from REE and Nb fertile intrusions lack Eu anomalies and have elevated Gd/Yb and Th/Yb, indicating they crystallised from magmas that originated from deep, oxidised and enriched mantle sources. Complexes with Nb enrichment have low U/Nb, reflecting an enriched mantle source, whereas high U/Nb in REE-only fertile intrusions suggest a subduction-metasomatised mantle source. Machine learning models demonstrate high accuracy in classifying zircon from barren and fertile deposits. Classification of detrital zircons shows that REE-enriched deposits correlate with supercontinent assembly, whereas Nb fertile complexes are associated with supercontinent breakup. This approach offers a new, mineral to global scale, petrologic and exploration tool that enhances understanding of REE metallogenesis.

Geochemical Perspectives Letters↗
USGS2014

Concealed basalt-matrix diatremes with Cu-Au-Ag-(Mo)-mineralized xenoliths, Santa Cruz Porphyry Cu-(Mo) System, Pinal County, Arizona

The Santa Cruz porphyry Cu-(Mo) system near Casa Grande, Arizona, includes the Sacaton mine deposits and at least five other concealed, mineralized fault blocks with an estimated minimum resource of 1.5 Gt @ 0.6% Cu. The Late Cretaceous-Paleocene system has been dismembered and rotated by Tertiary extension, partially eroded, and covered by Tertiary-Quaternary basin-fill deposits. The mine and mineralized fault blocks, which form an 11 km (~7 miles) by 1.6 km (~1 mile) NE-SW–trending alignment, represent either pieces of one large deposit, several deposits, or pieces of several deposits. The southwestern part of the known system is penetrated by three or more diatremes that consist of heterolithic breccia pipes with basalt and clastic matrices, and subannular tuff ring and maar-fill sedimentary deposits associated with vents. The tephra and maar-fill deposits, which are covered by ~485 to 910 m (~1,600–3,000 ft) of basin fill, lie on a mid-Tertiary erosion surface of Middle Proterozoic granite and Late Cretaceous porphyry, which compose most xenoliths in pipes and are the host rocks of the system. Some igneous xenoliths in the pipes contain bornite-chalcopyrite-covellite assemblages with hypogene grades >1 wt % Cu, 0.01 ounces per ton (oz/t) Au, 0.5 oz/t Ag, and small amounts of Mo (<0.01 wt %). These xenoliths were derived from mineralized rocks that have not been encountered in drill holes, and attest to additional, possibly higher-grade deposits within or subjacent to the known system. The geometry, stratigraphy, and temporal relationships of pipes and tephras, interpreted from drill hole spacing and intercepts, multigenerational breccias and matrices, reequilibrated and partially decomposed sulfide-oxide mineral assemblages, melted xenoliths, and breccia matrix compositions show that the diatremes formed in repeated stages. Initial pulses of basalt magma fractured granite, porphyry, and other crustal rocks during intrusion, transported multi-sized fragments of these rocks upward, and partially melted small fragments. Rapid decompression of magma induced catastrophic devolatilization that ruptured overlying rocks to the surface, and generated fragment-volatile suspensions that abraded conduits into near-vertical cylindrical structures. Fragments entrained in suspensions were milled and sorted, and ejected as basal surge, pyroclastic deposits, and airfall tephra that built tuff rings around vents and filled vent depressions. Comminuted m- to mm-sized fragments of wall rocks in magma and suspensions that remained in conduits solidified as heterolithic breccias. Subsequent pulses of basalt magma ascended through the same conduits, brecciated older heterolithic breccias, devolatilized, and quenched, leaving two or more generations of nested and mingled heterolithic breccias and internal zones of fluidized fragments. Tephra and maar-fill deposits from later eruptions are composed of more hydrous and oxidized minerals than earlier tephras, reflecting a higher proportion of water in transport fluid which, based on fluid inclusion populations in mineralized xenoliths, was saline water and CO 2 . The large vertical extent (~600 m; ~2,000 ft) of basalt matrix in pipes, near-paleosurface matrix vesiculation, and plastically deformed basalt lapilli indicates that diatreme eruptions were predominantly phreatic. Diatreme xenoliths represent crustal stratigraphy and, as in the Santa Cruz system, provide evidence of concealed mineral resources that can guide exploration drilling through cover. Vectors to the source of bornite-dominant xenoliths containing >1% Cu and significant Au and Ag could be determined by refinement of breccia pipe geometries, by reassembly of mineralized fault blocks using modal, chemical, and temporal characteristics of hydrothermal mineral assemblages and fluid inclusions, and by paleodrainage analysis.

Arizona↗
USGS1997

Strontium 87/strontium 86 as a tracer of mineral weathering reactions and calcium sources in an alpine/subalpine watershed, Loch Vale, Colorado

Sr isotopic ratios of atmospheric deposition, surface and subsurface water, and geologic materials were measured in an alpine/subalpine watershed to characterize weathering reactions and identify sources of dissolved Ca in stream water. Previous studies have noted an excess of Ca in stream water above that expected from stoichiometric weathering of the dominant bedrock minerals. Mixing calculations based on 87 Sr/ 86 Sr indicate that on an annual basis, 26 ± 7% of Ca export in streams is atmospherically derived, 23 ± 1% is from weathering of plagioclase, and the remainder is from weathering of calcite present in trace amounts in the bedrock. A potential source of error when applying Sr isotopes in catchment studies is determination of the 87 Sr/ 86 Sr of Sr released by mineral weathering, which is complicated by the wide range of mineral isotopic compositions, particularly in older rocks, and the variable rates at which the minerals weather. In this study, base-flow stream chemistry was used to represent the 87 Sr/ 86 Sr of Sr derived from mineral weathering because it effectively integrates the potentially variable isotopic composition of Sr released by weathering in the alpine environment.

Colorado↗
USGS2017

Platinum-group elements

The platinum-group elements (PGEs)—platinum, palladium, rhodium, ruthenium, iridium, and osmium—are metals that have similar physical and chemical properties and tend to occur together in nature. PGEs are indispensable to many industrial applications but are mined in only a few places. The availability and accessibility of PGEs could be disrupted by economic, environmental, political, and social events. The United States net import reliance as a percentage of apparent consumption is about 90 percent. PGEs have many industrial applications. They are used in catalytic converters to reduce carbon monoxide, hydrocarbon, and nitrous oxide emissions in automobile exhaust. The chemical industry requires platinum or platinum-rhodium alloys to manufacture nitric oxide, which is the raw material used to manufacture explosives, fertilizers, and nitric acid. In the petrochemical industry, platinum-supported catalysts are needed to refine crude oil and to produce aromatic compounds and high-octane gasoline. Alloys of PGEs are exceptionally hard and durable, making them the best known coating for industrial crucibles used in the manufacture of chemicals and synthetic materials. PGEs are used by the glass manufacturing industry in the production of fiberglass and flat-panel and liquid crystal displays. In the electronics industry, PGEs are used in computer hard disks, hybridized integrated circuits, and multilayer ceramic capacitors. Aside from their industrial applications, PGEs are used in such other fields as health, consumer goods, and finance. Platinum, for example, is used in medical implants, such as pacemakers, and PGEs are used in cancer-fighting drugs. Platinum alloys are an ideal choice for jewelry because of their white color, strength, and resistance to tarnish. Platinum, palladium, and rhodium in the form of coins and bars are also used as investment commodities, and various financial instruments based on the value of these PGEs are traded on major exchanges. PGEs are among the rarest metals; Earth’s upper crust contains only about 0.0005 part per million (ppm) platinum. Today, the average grade of PGEs in ores that are mined primarily for their PGE concentrations varies from 5 to 15 ppm, although the concentration of PGEs in hand-picked ore specimens may range from tens to hundreds of parts per million. More than 100 different minerals have one of the PGEs as an essential component. PGE minerals occur as native metals. They also occur as compounds with other transition metals (copper, iron, mercury, nickel, and silver), post-transition metals (bismuth, lead, and tin), metalloids (antimony, arsenic, and tellurium), and nonmetals (selenium and sulfur). From 1900 to 2011, approximately 14,200 metric tons of PGEs was produced, and roughly 95 percent of that production (13,500 metric tons) took place between 1960 and 2011. The breakdown of production by country shows that, since 1900, about 90 percent of the production came from South Africa and Russia. The secondary supply of platinum, palladium, and rhodium is obtained through the recycling of catalytic converters from end-of-life vehicles, jewelry, and electronic equipment. Recycled platinum, palladium, and rhodium provide a significant proportion of the world’s total supply; these secondary sources are sufficient to close the gap between world mine production and consumption. Exploration and mining companies report resources of about 104,000 metric tons of PGEs (including minor amounts of gold) in mineral deposits around the world that could be developed. For PGEs, almost all the reported production and identified resources are associated with deposits in three geologic features—the Bushveld Complex, which is a layered mafic-to-ultramafic intrusion in South Africa; the Great Dyke, which is a layered mafic-to-ultramafic intrusion in Zimbabwe; and sill-like intrusions associated with flood basalts in the Noril’sk-Talnakh area of Russia. The metallic forms of PGEs are generally considered to be inert. PGEs pose a risk to human health only in cases where individuals are occupationally exposed to synthetic PGE compounds, especially workers in precious-metal refineries. In the natural environment, background PGE concentrations are low in water, sediment, soil, and plants. Anthropogenic sources of PGEs in the environment include catalytic converters used in modern automobiles, platinum-based chemotherapy drugs, and smelter emissions. The abundance of sulfide minerals defines the environmental and geologic characteristics of PGE-enriched magmatic sulfide deposits; those deposits with the highest amount of sulfide minerals could have the highest environmental impact. Acid rock drainage from reef-type and contact-type deposits is unlikely because the ores and their host rocks contain low proportions of sulfide minerals. For some conduit-type orebodies with massive ores, mineral-processing techniques separate and produce concentrates of copper-, iron-, and nickel-bearing sulfide minerals; those with copper and nickel are processed to extract metal, but the iron-sulfide minerals, mainly pyrrhotite, are discarded as waste. This results in waste material with a high acid-generating potential. The most significant primary source of PGEs in the United States is a deposit in the Stillwater Complex, which is a layered igneous intrusion in Montana. Approximately 305 metric tons of platinum and palladium have been mined from the Stillwater Complex deposit since 1986. Exploration and development drilling indicate that another 2,200 metric tons are present. Mining has progressed to depths of 1,800 meters below the surface, but the bottom of the ore deposit has not been reached; geologic estimates suggest that another 1,000 to 6,200 metric tons of PGEs could be present at depth. In the future, PGEs may be mined from deposits found near the base of the Duluth Complex, which is a group of igneous intrusions in Minnesota.

Professional Paper↗
USGS1996

Feruvite from the Sullivan Pb-Zn-Ag deposit, British Columbia

Feruvite, an uncommon Ca- and Fe2+-rich tourmaline species, has been discovered in the footwall of the Sullivan Pb-Zn-Ag deposit (British Columbia) near gabbro sills and dikes. Its chemical composition varies according to occurrence: feruvite from the shallow footwall has lower Ca, higher Al, and higher X-site vacancies than that from the deep footwall. The major chemical substitution involved in the feruvite is the exchange vector CaMgO???-1Al-1(OH)-1. The most important factor controlling feruvite formation at Sullivan is likely the reaction of Fe-rich hydrothermal fluids with Ca-rich minerals in gabbro and host rocks. This reaction led to the breakdown of Ca-rich minerals (plagioclase and hornblende), with release of Ca to solution and its incorporation into feruvite. This process probably postdated the main stages of formation of fine-grained, intermediate schorl-dravite in the tourmalinite pipe in the footwall, and is attributed to postore intrusion of gabbro and associated albite-chlorite-pyrite alteration.

Canadian Mineralogist↗
USGS2018

Sulfur cycle in the Valles Caldera volcanic complex, New Mexico – Letter 1: Sulfate sources in aqueous system, and implications for S isotope record in Gale Crater on Mars

Initial in situ sulfur (S) isotope measurements of the Martian bedrock in Gale Crater have revealed an unexpectedly wide range of δ 34 S values (−47 to +28%). Generally, it is unclear what processes could have contributed to these large isotope fractionations. Therefore, we studied S sources and aqueous SO 2− 4 cycling in the Valles Caldera volcanic complex, New Mexico to better understand S isotope fractionations related to S degassing, hydrothermal activity, and low-temperature processes in aqueous environment. Overall, our study demonstrates that volcanic systems show large spatial heterogeneity in δ 34 S. Magmatic S sources are obvious in steam-dominated H 2 S degassing and precipitation of secondary minerals from hydrothermal fluids with low δ 34 S values of +0.9 ±3%. Locally, however, hydrothermal processes have resulted in more negative δ 34 S values in sulfide minerals (−18 to −4%) and more positive δ 34 S values in sulfate minerals (−1 to +3%). Major aqueous SO 2− 4 sources are oxidation of H 2 S from modern hydrothermal gas emission, and oxidation and dissolution of sulfide and sulfate minerals present in the hydrothermally altered bedrock and crater-lake sediments. The δ 34 S of aqueous SO 2− 4 in surface water and groundwater varies widely (−8 to +5%) and is similar to major S endmembers that undergo oxidation and/or dissolution by active hydrological system. Minor SO 2− 4 contributions with more positive δ 34 S values (+9 to +14%) come from deeply circulating geothermal fluids and negligible amounts from atmospheric deposition (+5 to +7% in snow). Elevated SO 2− 4 contents are mainly associated with modern and past H 2 S emissions and oxidations near the surface. On regional scale, however, most of the intracaldera bedrock is S-depleted, thus the SO 2− 4 contents are usually low in the surface aquatic system and younger sedimentary lake deposits formed at times of negligible near surface hydrothermal activity. In general, magmatic-hydrothermal processes apparently cause the largest δ 34 S variation in S-bearing minerals on volcanic terrains. Therefore, we infer that the measured wide range of δ 34 S values in the Gale sediments by the Curiosity rover on Mars can be explained by S isotope composition of magmatic-hydrothermal sulfide and sulfate minerals that were present in the initial igneous/volcanic rocks prior to crater formation. Later aqueous processes involved oxidation and dissolution of S minerals initially present in these rocks and led to subsequent formation of diagenetic fluids and alteration products enriched in SO 2− 4 with relatively large δ 34 S variation. Additionally, physical erosion, transport and deposition of detrital hydrothermal S minerals from igneous/volcanic rocks might be in part responsible for the measured wide range of δ 34 S in Gale Crater. These unique S isotope results, measured in situ on another planet for the first time, imply the importance of magmatic-hydrothermal fluids in S transport on early Mars and their subsequent alteration in low-temperature aqueous environments.

New Mexico↗
USGS1936

The Battle Branch gold mine, Auraria, Georgia

The Battle Branch mine, in north-central Georgia, is well known locally for its pockets of exceptionally rich gold ore. During the period from May 24, 1934, to May 20, 1935, 781.97 ounces of bullion, of an average fineness of about 850, was shipped to the mint. The deposit is of the lode type; it consists of many quartz stringers and lenses grouped in three zones in a schistose phase of the Carolina gneiss. Three stages of mineralization are recognized. An early high-temperature stage produced coarsely crystalline silicates, such as garnet, kyanite, tourmaline, biotite, and muscovite, which were probably formed by a recrystallization of the minerals in the country rock. During the intermediate stage ankerite, quartz, and pyrrhotite were formed. The last stage was marked by chlorite, galena, and gold. Throughout the period of mineralization minor amounts of movement in and across the lode occurred. The distribution of the ore shoots is dependent to a large extent upon the distribution of the cross fractures. The ore shoots are pod-shaped bodies, which pinch and swell abruptly. The gold in the rich shoots is contemporaneous with galena and is clearly of hypogene origin.

Georgia↗
USGS1974

The diorite at West Warren, south-central Massachusetts

Follated, syntectonic, concordant intrusive bodies of mostly diorite and meladiorite with less abundant quartz diorite and norite have been mapped in the West Warren area of south-central Massachusetts. The rocks of the pluton range from a medium colored phase of diorite and quartz diorite to a dark colored phase of meladiorite and norite. Major minerals In the dioritic rocks are calcic andesine, green hornblende, brown biotite, and hypersthene. Igneous textures are dominant, and retrograde or deuteric effects are generally minor. Silica and alumina contents of the dioritic rocks are somewhat higher than for average diorites; conversely, the oxides of iron, magnesium, and calcium are generally lower. Normative quartz, albite, and anorthite are higher and orthoclase is lower in the samples than In the average diorite. Sizeable plutons of diorite-norite are uncommon in central Massachusetts. The West Warren body, roughly 26 km2 (10 square miles) in area, bears little petrochemical relation to adjacent rock units. The pluton can be construed as belonging to a belt of intrusive mafic rocks which stretches from southeastern New York to coastal Maine.

Open-File Report↗
USGS1967

Sulfides associated with the Salton Sea geothermal brine

Concentrated saline brine tapped by a deep well drilled for geothermal power near the Salton Sea, California, deposited metal-rich siliceous scale at the rate of 2 to 3 tons per month. The iron-rich opaline scale contains an average of 20% Cu and up to 6% Ag present in bornite, digenite, chalcopyrite, a new dense polymorph of chalcocite, stromeyerite, and native silver.The brines are in equilibrium with an assemblage of sulfide minerals in the reservoir rocks. Sphalerite containing 16.6 mol % FeS is in equilibrium with the brine in which the activity of sulfur (a (sub s 2 ) ) is estimated at 10 (super -10.2) at 325 degrees C. This is in good agreement with the projected high-temperature data of Barton and Toulmin (2) for the system Fe-Zn-S. Other sulfides identified in the reservoir rocks are pyrite, pyrrhotite, chalcopyrite, and galena.The heavy metals in solution are apparently derived from the sediments of the brine reservoir, being released from the silicate minerals in which they occur in trace amounts, as metamorphism of the sediment proceeds. Although the total of the heavy metals in solution greatly exceeds the sulfur, on a molal basis, the brine is saturated with respect to sulfide components and addition of more sulfide ion would only cause precipitation of sulfides.

California↗
USGS1968

A lead isotope study of galenas and selected feldspars from mining Districts in Utah

The leads in feldspars from the main Tertiary intrusive bodies in each of three mining regions in Utah are isotopically similar to the lead deposits immediately associated with them. These deposits are the largest and also the least radiogenic in each region, whereas the smaller deposits are more radiogenic. Throughout each region the 'ore leads appear to be mixtures in various proportions of lead derived from the intrusive magma and a radiogenic lead component derived from the upper crustal rocks through which the mineralizing fluids passed. Linear relationships are exhibited between the lead isotope ratios within each mining region, and these enable the ages of the upper crustal basement rocks to be determined. A simple tvo-stage model theory for the development of the lead ores yields the folloving data: Oquirrh Mountains region, t 1,650 4-150 m.y., p-Cottonwood-Park City region, t = 2,415 4-30 m.y., p- = 8.87. Tintlc region, t 2,075 4-30 m.y., Milford region, t 1 765 4-70 m.y., p-T ( Us ) = , = 8.83. An alternative "mixing" model is also proposed which requires only 1,650-m.y. and 2,400-m.y. events in these regions. In either case these ages confirm and supplement our present geochronological knowledge of the basement rocks of Utah .

Utah↗
USGS2019

Geological and geophysical data for a three-dimensional view—Inside the San Juan and Silverton Calderas, Southern Rocky Mountains Volcanic Field, Silverton, Colorado

Introduction The San Juan-Silverton caldera complex located near Silverton, Colorado, in the Southern Rocky Mountains volcanic field is an ideal natural laboratory for furthering the understanding of shallow-to-deep volcanic-related mineral systems. Recent advances in geophysical data processing and three-dimensional (3D) model construction will help to characterize shallow properties important for understanding surface water and groundwater quality issues and will also improve knowledge of deep geological structures that may have been conduits for hydrothermal fluids that formed mineral deposits. The study has general applications to mineral resource assessments in other areas of the world and to identifying possible groundwater flow paths and associated geochemistry important in abandoned mine lands cleanup. Silverton, Colorado, is the site of a spectacular succession of igneous rocks that formed beginning about 35 million years ago (Ma). Base metals (copper, lead, and zinc) and precious metals (silver and gold) mined from the late 1870s to 1991 owe their existence to a 25-million-year cycle of igneous activity. The presence of economic, base, and precious metal deposits within a complex geological setting were largely responsible for stimulating studies by the U.S. Geological Survey (USGS) conducted during the early 20th century. The focus of investigations in the late 20th and 21st centuries have broadened in scope to include abandoned mine lands (AML) investigations. The legacy of hard rock mining in headwater catchment areas caused environmental challenges for local communities and downstream water resource users. The Gold King Mine, located a few kilometers north of Silverton, illustrates the potential environmental effects of abandoned mines. On August 5, 2015, during reclamation efforts at the Gold King Mine, a breach of collapsed workings sent approximately 3 million gallons of acidic and metal-rich mine water into the upper Animas River, a tributary to the Colorado River Basin. Mining-related sources of metals and acidity add to geological sources of metals in surface water and groundwater. Weathering processes of altered and mineralized rock have been a source of acid rock drainage that have been ongoing for millennia.

Colorado↗
USGS1999

Composition and origin of Early Cambrian Tiantaishan phosphorite-Mn carbonate ores, Shaanxi Province, China

The Tiantaishan phosphorite-Mn carbonate ores occur in the Early Cambrian Tananpo Formation in complexly folded and faulted rocks located in southern Shaanxi Province. About 65 x 106 tonnes of 17% P2O5 ore reserves exist and Mn-ore reserves are about 8.3 x 106 tonnes of +18% Mn. The stratigraphic sequence in ascending order consists of black phyllite, black to gray phosphorite ore, black phyllite, rhodochrostone ore, Mn mixed-carbonates, and dolostone. Data are presented from microprobe mineral chemistry, whole-rock chemistry, stable isotopes of carbonates, X-ray mineralogy, petrographic and SEM observations, and statistical analysis of chemical data. The dominant ore-forming minerals are hydroxy- and carbonate fluorapatite and Ca rhodochrosite, with Mg kutnahorite and dolomite comprising the Mn mixed-carbonate section. Pyrite occurs in all rock types and alabandite (MnS) occurs throughout the rhodochrostone section. The mean P2O5 content of phosphorite is 31% and argillaceous phosphorite is 16%, while the mean MnO content of rhodochrostone ore is 37%. Phosphorite ores are massive, spheroidal, laminated, and banded, while rhodochrostone ores have oolitic, spheroidal, and granular fabrics. The most distinguishing characteristics of the ores are high total organic carbon (TOC) contents (mean 8.4%) in the phosphorite and high P2O5 contents (mean 2.7%) in the rhodochrostone ore. The atypically high TOC contents in the Tiantaishan phosphorite probably result from very strong productivity leading to high sedimentation rates accompanied by weak reworking of sediments; poor utilization of the organic matter by bacteria; and/or partial replacement of bacterial or algal mats by the apatite. The depositional setting of the ores was the margin of an epicontinental seaway created as a direct consequence of global processes that included break-up of a supercontinent, formation of narrow seaways, creation of extensive continental shelves, overturn of stagnant, metal-rich deep-ocean waters, and marine transgression. Water depth increased from deposition of the black phyllite sequence through deposition of the Mn mixed-carbonate sequence, then shallowed again during deposition of the overlying dolostone sequence. Bottom waters were mostly dysoxic to suboxic, but fluctuated from oxic to anoxic. Productivity was high during deposition of the black phyllite sequence, increased during precipitation of phosphorite, and then decreased to moderate levels during precipitation of rhodochrostone ores. Biosilica contributions occur in each lithology, but are greatest in rhodochrostone. Changes in sedimentation were determined by changes in water depth, productivity, upwelling, sea-level change, and ventilation of the depositional basin. The source of the phosphorus was organic matter produced in great quantities during deposition of the black phyllite and phosphorite sequences in a zone of coastal upwelling. Organic matter accumulation was rapid. Globally, Mn was supplied by overturn of stagnant, metal-rich deep-ocean waters, which were redistributed to areas of coastal upwelling and seaways; that process may have been initiated by latest Proterozoic glaciations which would have promoted density stratification and accumulation and storage of metals. Regionally, Mn was supplied by terrigenous input into the shallow seaway and hydrothermal input into the deeper water parts of that seaway. Locally, Mn sources included leaching and transport of metals from the sediment column. Manganese was stored locally in low-oxygen (not anoxic) seawater prior to Mn-ore formation. The source of the carbon in the Mn carbonates and dolostones was predominantly seawater bicarbonate and secondarily CO2 derived from the oxidation of organic matter in the bacterially mediated diagenetic zone of sulfate reduction.

Ore Geology Reviews↗
USGS1982

Reconnaissance geology of the Wadi Dhahaban Quadrangle, sheet 18/41 D, Kingdom of Saudi Arabia

The Wadi Dhahaban quadrangle (sheet 18/41 D) lies between lat 18?00? and 18?30' N. and long 41?30' and 42?00' E. and encompasses an area of 2,937 km2 located along the Red Sea coast and includes part of the escarpment-mountains province. The geologic formations exposed in the quadrangle are comprised of Precambrian layered and intrusive rocks, Tertiary gabbro dikes, Quaternary basaltic lavas and pyroclastic rocks, and Quaternary surficial deposits. No economic mineral deposits have been found. The Precambrian rocks include layered sedimentary and volcanic rocks that have been assigned to the Baish, Bahah, and Ablah groups. They have been folded, metamorphosed, and invaded by three separate intrusions. The Precambrian rocks are cut by Miocene gabbro dikes that were intruded during the initial stages of the opening of the Red Sea rift. The Quaternary rocks include basalt, and coastal, pediment, and alluvial deposits of various kinds. The area is of special interest because of its unique display of the Tertiary and Quaternary basaltic volcanism that was associated with the opening of the Red Sea rift and that has continued in other parts of the Kingdom until historic times.

Open-File Report↗
USGS1950

Alteration and metallization in the Bagdad porphyry copper deposit, Arizona

The porphyritic to seriate-textured quartz monzonite host-rock at Bagdad was changed by hypogene alteration to a granular rock in which the plagioclase became albitic, orthoclase and quartz increased in amount, and hornblende and book-biotite were recrystallized to pale brown leafy biotite. Hypogene sulfides, pyrite and chalcopyrite, were added during the process of alteration, accompanied in part by sericite. Molybdenite is younger than the chalcopyrite. Locally, the host rock was altered to a quartz-orthoclase-sericite facies containing more quartz and orthoclase than is found in the main alteration facies. Chemical analyses indicate that alteration and mineralization of the host rock resulted in loss of iron, lime, and soda, and addition of sulfur, copper, and potash.Supergene changes include the formation of a chalcocite blanket in late Pliocene or early Pleistocene time. Chalcocite replaced chalcopyrite in preference to pyrite. The chalcocite blanket is truncated by the present erosion surface and its distribution can be recognized from the character of the iron oxide left in the leached cavities. Along some of the fractures and faults, supergene clay is present, consisting of kaolinite and a member of the saponite-montmorillonite group.

Arizona↗
USGS1986

RELATION BETWEEN SURFACE-WATER QUALITY AND THE COMPOSITION OF COAL IN PIKE COUNTY, KENTUCKY.

The quality of surface water in Pike County, Kentucky, seems to reflect the composition of coals in the county. Groundwater acquires mineral concentration characteristics of the rocks through which it moves. When groundwater is discharged to streams the mineral concentrations in streams, especially during low flow periods, are characteristic of several coal beds that are a part of the aquifier system contributing water to the streams. A regression analysis was also performed to develop statistical models to estimate the quality of surface water based on the composition of the coals. Twenty models consisting of 10 two-variable models and 10 three-variable models were developed for the maximum values.

Conference Paper↗