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At least 793 records · Page 44Linked to original sources
USGS2006

Spectroscopic mapping of the white horse alunite deposit, Marysvale volcanic field, Utah: Evidence of a magmatic component

Previous studies have demonstrated that the replacement alunite deposits just north of the town of Marysvale, Utah, USA, were formed primarily by low-temperature (100??-170?? C), steam-heated processes near the early Miocene paleoground surface, immediately above convecting hydrothermal plumes. Pyrite-bearing propylitically altered rocks occur mainly beneath the steam-heated alunite and represent the sulfidized feeder zone of the H2S-dominated hydrothermal fluids, the oxidation of which at higher levels led to the formation of the alunite. Maps of surface mineralogy at the White Horse deposit generated from Airborne Visible/Infrared Imaging Spectrometer (AVIRIS) data were used in conjunction with X-ray diffraction studies of field samples to test the accuracy and precision of AVIRIS-based mineral mapping of altered rocks and demonstrate the utility of spectroscopic mapping for ore deposit characterization. The mineral maps identified multiple core zones of alunite that grade laterally outward to kaolinite. Surrounding the core zones are dominantly propylitically altered rocks containing illite, montmorillonite, and chlorite, with minor pyrite, kaolinite, gypsum, and remnant potassium feldspar from the parent rhyodacitic ash-flow tuff. The AVIRIS mapping also identified fracture zones expressed by ridge-forming selvages of quartz + dickite + kaolinite that form a crude ring around the advanced argillic core zones. Laboratory analyses identified the aluminum phosphate-sulfate (APS) minerals woodhouseite and svanbergite in one sample from these dickite-bearing argillic selvages. Reflectance spectroscopy determined that the outer edges of the selvages contain more dickite than do the medial regions. The quartz + dickite ?? kaolinite ?? APS-mineral selvages demonstrate that fracture control of replacement processes is more prevalent away from the advanced argillic core zones. Although not exposed at the White Horse deposit, pyrophyllite ?? ordered illite was identified using AVIRIS in localized, superimposed conduits within propylitically altered rocks in nearby alteration systems of similar age and genesis that have been eroded to deeper levels. The fracture zones bearing pyrophyllite, illite, dickite, natroalunite, and/or APS minerals indicate a magmatic component in the dominantly steam-heated system. ?? 2006 Society of Economic Geologists, Inc.

Economic Geology↗
USGS2006

Overview of the Microscopic Imager Investigation during Spirit's first 450 sols in Gusev crater

The Microscopic Imager (MI) on the Mars Exploration Rover Spirit has returned images of Mars with higher resolution than any previous camera system, allowing detailed petrographic and sedimentological studies of the rocks and soils at the Gusev landing site. Designed to simulate a geologist's hand lens, the MI is mounted on Spirit's instrument arm and can resolve objects 0.1 mm in size or larger. This paper provides an overview of MI operations, data calibration, processing, and analysis of MI data returned during the first 450 sols (Mars days) of the Spirit landed mission. The primary goal of this paper is to facilitate further analyses of MI data by summarizing the methods used to acquire and process the data, the radiometric and geometric accuracy of MI data products, and the availability of archival products. In addition, scientific results of the MI investigation are summarized. MI observations show that poorly sorted soils are common in Gusev crater, although aeolian bedforms have well‐sorted coarse sand grains on their surfaces. Abraded surfaces of plains rocks show igneous textures, light‐toned veins or fracture‐filling minerals, and discrete coatings. The rocks in the Columbia Hills have a wide variety of granular textures, consistent with volcaniclastic or impact origins. Case hardening and submillimeter veins observed in the rocks as well as soil crusts and cemented clods imply episodic subsurface aqueous fluid movement, which has altered multiple geologic units in the Columbia Hills. The MI also monitored Spirit's solar panels and the magnets on the rover's deck.

Journal of Geophysical Research E: Planets↗
USGS1982

Geology of areas marked by geophysical anomalies (B-35 and B-34), Wadi Bidah District, Kingdom of Saudi Arabia

Geophysical surveys in the Wadi Bidah district, in the southwestern part of the Kingdom of Saudi Arabia, have revealed anomalies of the type that may be caused by deposits of massive sulfides. Accordingly, a study was undertaken to investigate the geologic environment associated with the geophysical anomalies and to determine whether mineral exploration of the anomalous areas might be warranted. An extensive geochemical sampling program did not disclose any evidence of ore mineral concentrations in the rocks. Detailed geologic mapping shows the anomalous areas to be underlain by Precambrian carbonaceous graywacke, the outcrop patterns of which closely fit the anomaly patterns. Field evidence and petrologic studies indicate that carbonaceous material in the rocks is the cause of the geophysical anomalies. Nothing was found in the anomalous areas that suggests the presence of mineral deposits of commercial grade, and further mineral investigations or exploration in the areas is not recommended.

Open-File Report↗
USGS1982

Uranium-lead isochron age and preliminary sulfur isotope systematics of the Felder uranium deposit, south Texas

Uranium-lead isotope systematics of roll-front ores in Miocene sandstone at the Felder and McLean uranium deposits (south Texas coastal plain) give a well-defined 207 Pb/ 204 Pb- 235 U/ 204 Pb isochron age of 5.07 + or - 0.15 m.y. The relatively slight degree of scatter of the points defining the isochron is probably due to initial Pb isotope inhomogeneity, and the resulting inferred persistence of closed system behavior for U and Pb is probably the result of the long-term presence of U- and Pb-immobilizing H 2 S. 206 Pb/ 238 U systematics are badly scattered owing to long-term migration of radioactive daughters of 238 U. Beta- and gamma-activity systematics of the ores consistently identify those with grossly anomalous Pb isotope systematics, however, and proved highly useful in identifying ores that have gained gross amounts of uranium daughters.FeS 2 minerals in the altered tongue of the host sandstone are characterized by abundant postore pyrite and heavy delta 34 S values, whereas FeS 2 minerals in mineralized and unaltered, barren rock are characterized by abundant ore-stage marcasite and by light delta 34 S values. The delta 34 S values of FeS 2 minerals in the altered tongue are similar to those defined for sour gas from the underlying Edwards Limestone of Cretaceous age, indicating the probable source for the sulfur of an inferred resulfidization event. The 5.07-m.y. isochron age probably reflects the end of roll-front development; we believe that the end was due to the resulfidization and does not preclude significant earlier periods of mineralization. Modern ground water in the area is also sulfide bearing (thus helping preserve the deposit), but with delta 34 S values distinct from those of sulfides in the resulfidized zone of the host rock.

Texas↗
USGS1953

Reconnaissance geology of placer deposits containing radioactive minerals in the Bear Valley district, Valley County, Idaho

A reconnaissance of the Bear Valley district was undertaken to provide a geologic interpretation of placer deposits drilled by the U.S. Bureau of Mines. The placer minerals are monazite and a group of uranium bearing rare earth columbates and tantalates here referred to loosely as radioactive blacks. The monazite is an accessory mineral in the granitic country rock; the radioactive blacks occur in pegmatite dikes. The supply of these minerals to the placers was controlled (1) by the geography of their occurrence in the parent rock, and (2) by the distribution of alpine glaciers during two late Pleistocene glacial stages. By reason of a favorable combination of these factors, the richest placer deposits of the district are in Big Meadow, a valley fill formed as a result of the blocking of Bear Creek by a glacier from a tributary valley during the Illinoian (?) stage. The Big Meadow fill consists of intertonguing depositional units formed by Bear Creek and its tributaries, including both normal alluvium and glacial outwash, and ranging from rich to barren. The richest phase that has been blocked out by drilling was derived from the drainage basin of Casner Creek, an east tributary of Bear Creek. The geologic relations suggest that a neighboring stream, Howard Creek, should have supplied equally rich material, but the part of the valley fill formed by Howard Creek has not been tested. The Howard Creek deposits and shallow alluvium in the upper valleys of Casner and Howard Creeks may considerably increase the reserves of the district.

Open-File Report↗
USGS1968

Hypogene veins of gibbsite, pyrolusite, and lithiophorite in Nye County, Nevada

Gibbsite, lithiophorite, pyrolusite, and goethite, plus discrete mixtures of gibbsite and lithiophorite and of gibbsite and iron oxide, occur as replacement veins in limestone. Minor accessories are barite, alunite, opal. Minerals of wall-rock alteration are garnet, idocrase, K-feldspar, prehnite, sericite, and quartz. These silicates formed at higher temperature than the vein minerals, but the whole sequence is considered to be a product of the same solutions, of deep-seated origin, deposited over a long period of time.

Nevada↗
USGS1989

Geochemistry of intrusive rocks associated with the Latir volcanic field, New Mexico, and contrasts between evolution of plutonic and volcanic rocks

Plutonic rocks associated with the Latir volcanic field comprise three groups: 1) ???25 Ma high-level resurgent plutons composed of monzogranite and silicic metaluminous and peralkaline granite, 2) 23-25 Ma syenogranite, and alkali-feldspar granite intrusions emplaced along the southern caldera margin, and 3) 19-23 Ma granodiorite and granite plutons emplaced south of the caldera. Major-element compositions of both extrusive and intrusive suites in the Latir field are broadly similar; both suites include high-SiO2 rocks with low Ba and Sr, and high Rb, Nb, Th, and U contents. Moreover, both intermediateto siliciccomposition volcanic and plutonic rocks contain abundant accessory sphene and apatite, rich in rare-earth elements (REE), as well as phases in which REE's are essential components. Strong depletion in Y and REE contents, with increasing SiO2 content, in the plutonic rocks indicate a major role for accessory mineral fractionation that is not observed in volcanic rocks of equivalent composition. Considerations of the rheology of granitic magma suggest that accessory-mineral fractionation may occur primarily by filter-pressing evolved magmas from crystal-rich melts. More limited accessory-mineral crystallization and fractionation during evolution of the volcanic magmas may have resulted from markedly lower diffusivities of essential trace elements than major elements. Accessory-mineral fractionation probably becomes most significant at high crystallinities. The contrast in crystallization environments postulated for the extrusive and intrusive rocks may be common to other magmatic systems; the effects are particularly pronounced in highly evolved rocks of the Latir field. High-SiO2 peralkaline porphyry emplaced during resurgence of the Questa caldera represents non-erupted portions of the magma that produced the Amalia Tuff during caldera-forming eruption. The peralkaline porphyry continues compositional and mineralogical trends found in the tuff. Amphibole, mica, and sphene compositions suggest that the peralkaline magma evolved from metaluminous magma. Extensive feldspar fractionation occurred during evolution of the peralkaline magmas, but additional alkali and iron enrichment was likely a result of high halogen fluxes from crystallizing plutons and basaltic magmas at depth. ?? 1989 Springer-Verlag.

Contributions to Mineralogy and Petrology↗
USGS2008

Evolving magma storage conditions beneath Mount St. Helens inferred from chemical variations in melt inclusions from the 1980-1986 and current (2004-2006) eruptions

Major element, trace element, and volatile concentrations in 187 glassy melt inclusions and 25 groundmass glasses from the 1980-86 eruption of Mount St. Helens are presented, together with 103 analyses of touching FE-Ti oxide pairs from the same samples. These data are used to evaluate the temporal evolution of the magmatic plumbing system beneath the volcano during 1980-86 and so provide a framework in which to interpret analyses of melt inclusions from the current (2004-2006) eruption. Major and trace element concentrations of all melt inclusions lie at the high SiO 2 end of the data array defined by eruptive products of the late Quaternary age from Mount St. Helens. For several major and trace elements, the glasses define a trend that is oblique to the whole-rock trend, indicating that different mineral assemblages were responsible for the two trends. The whole-rock trend can be ascribed to differentiation of hydrous basaltic parents in a deep-seated magma reservoir, probably at depths great enough to stabilize garnet. In contrast, the glass trends were generated by closed-system crystallization of the phenocryst and microlite mineral assemblages at low pressures. The dissolved H 2 O content of the melt inclusions from 1980-86, as measured by the ion microprobe, ranges from 0 to 6.7 wt. percent, with the highest values obtained from the plinian phase of May 18, 1980. Water contents decrease with increasing SiO 2 , consistent with decompression-driven crystallization. Preliminary data for dissolved CO 2 in melt inclusions from the May 18 plinian phase from August 7, 1980, indicate that X H 2 O in a vapor phase was approximately constant at 0.80, irrespective of H 2 O content, suggestive of closed-system degassing with a high bubble fraction or gas streaming through the subvolcanic system. Temperature and f O 2 estimates for touching Fe-Ti oxides show evidence for heating during crystallization owing to release of latent heat. Consequently, magmas with the highest microlite crystallinities record the highest temperatures. Magmas also become progressively reduced during ascent and degassing, probably as a result of redox equilibria between exsolving S-bearing gases and magmas. The lowest temperature oxides have f O 2 ≈ NNO, similar to high-temperature fumarole gases from the volcano. The temperature and f O 2 of the magma tapped by the plinian phase of May 18, 1980, are 870-875°C and NNO+0.8, respectively. The dissolved volatile contents of the melt inclusions have been used to calculate sealing pressures; that is, the pressure at which chemical exchange between inclusion and matrix melt ceased. These are greatest for the May 18 plinian magma (120 to 320 MPa); lower pressures are recorded by samples of the preplinian cryptodome and by all post-May 18 magmas. Magma crystallinity, calculated from melt-inclusion Rb contents, is negatively correlated with sealing pressure, consistent with decompression crystallization. Elevated contents of Li in melt inclusions from the cryptodome and post-May 18 samples are consistent with transfer of Li in a magmatic vapor phase from deeper parts of the magma system to magma stored at shallower levels. The Li enrichment attains its maximum extent at ~150 MPa, which is ascribed to separation of a single vapor phase into H 2 O-rich gas and dense Li-rich brine at the top of the magma column. There are striking correlations between melt-inclusion chemistry and monitoring data for the 1980-86 eruption. Dissolved SO 2 contents of melt inclusions from any given event, multiplied by the mass of magma erupted during that event, correlate with the measured flux of SO 2 at the surface, suggesting that magma degassing and melt-inclusion sealing are closely related in time and space. Textural and chemical evidence indicates that melt inclusions became effectively sealed (physically or kinetically) shortly before eruption. Thus by converting pressure to depth using a density model and edifice-loading algorithm for the volcano, changing depths of magma extraction with time can be tracked and compared to the seismic record. The plinian eruption of May 18, 1980, involved magma stored 5-11 km below sea level; this is inferred to be the subvolcanic magma chamber. The preceding eruptions, including the May 18, 1980, blast, involved magma withdrawal from the cryptodome and conduit down to 5 km below sea level. Subsequent 1980 eruptions tapped magma down to depths of ≤10 km below sea level. Tapping of magma stored deeper than 2 km below sea level stopped abruptly at the end of 1980, coincident with the onset of extensive shallow seismicity and a change from explosive to effusive eruption style from 1981 to 1986. Overall, the 1980-86 eruption is consistent with the evisceration of a thin, vertically extensive body of magma extending from 5 to at least 11 km below sea level and connected to the surface by a thin conduit. In the absence of sustained high magma-supply rates from depth, decompression crystallization of magma ascending through the system leads eventually to plugging of the conduit. The current eruption of Mount St. Helens shares some similarities with the 1981-86 dome-building phase of the previous eruption, in that there is extensive shallow seismicity and extrusion of highly crystalline material in the form of a sequence of flows and spines. Melt inclusions from the current eruption have low H 2 O contents, consistent with magma extraction from shallow depths. Highly enriched Li in melt inclusions suggests that vapor transport of Li is a characteristic feature of Mount St. Helens. Melt inclusions from the current eruption have subtly different trace-element chemistry from all but one of the 1980-86 melt inclusions, with steeper rareearth-element (REE) patterns and low U, Th, and high-fieldstrength elements (HFSE), indicating addition of a new melt component to the magma system. It is anticipated that increasing involvement of the new melt component will be evident as the current eruption proceeds.

Washington↗
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↗
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↗