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USGS2014

Succession of Laramide magmatic and magmatic-hydrothermal events in the Patagonia Mountains, Santa Cruz County, Arizona

This investigation of the space-time progression of magmatism and hydrothermal activity in the Patagonia Mountains of southern Arizona is based on field and paragenetic relationships, and on U-Pb and 40 Ar/ 39 Ar geochronology of igneous and hydrothermal minerals. The Patagonia Mountains consist of Precambrian, Paleozoic, and Mesozoic sedimentary, granitic, and volcanic rocks, Laramide volcanic rocks, and a core of Laramide intrusions that comprise the Patagonia Mountains batholith. Laramide igneous rocks and adjacent Paleozoic and Mesozoic rocks contain significant porphyry Cu-Mo deposits, Mo-Cu breccia pipes, Ag replacement deposits, and numerous other Cu-Pb-Zn-Ag replacement and vein deposits. Ages of igneous and hydrothermal minerals from 20 U-Pb and 52 40 Ar/ 39 Ar determinations define four magmatic and magmatic-hydrothermal events that formed the batholith and altered parts of it and adjacent rocks; cumulatively the events span at least 16 m.y., from ~74 to 58 Ma. The oldest event of this succession includes the 74 Ma Washington Camp stock and spatially associated Cu-Pb-Zn-Ag replacement deposits in Paleozoic carbonate rocks of the Washington Camp-Duquesne district. Eruption of 73 to 68 Ma volcanic rocks in the northern part of the range was the next youngest event, which coincides temporally with replacement and vein deposits in Paleozoic carbonate rocks at the Flux mine (~71 Ma). An event at 65 to 62 Ma is marked by emplacement of small-volume quartz monzonite, granodiorite, and diorite intrusions, formation of the Ventura breccia deposit in Jurassic granite at 65 to 64 Ma, and formation of other Pb-Zn-Ag-Cu replacement and vein deposits (~62 Ma; Blue Nose and Morning Glory). The Red Mountain porphyry Cu-Mo system is hosted by ~62 Ma granodiorite and Laramide volcanic rocks (73–68 Ma) at the northern end of the batholith. It includes a deep, chalcopyrite-bornite resource (~60 Ma) that is associated with potassic and sericitic alteration and a near-surface chalcocite-enargite resource (60 Ma) that is associated with advanced, supergene-enriched argillic alteration. The youngest event includes the Sunnyside porphyry Cu-Mo system and a Cu-Mo breccia deposit at Red Hill (Four Metals mine), both of which formed in large-volume quartz monzonite, granodiorite, quartz monzonite porphyry, and quartz feldspar porphyry (~61–59 Ma). Similar to the Red Mountain system, the Sunnyside system consists of a deep chalcopyrite resource that occurs in ~60 to 59 Ma quartz feldspar porphyry, and a near-surface, slightly younger (~59–58 Ma) enargite-chalcocite-tennantite resource that occurs in quartz feldspar porphyry, quartz monzonite porphyry, and Mesozoic rocks. The Red Hill Cu-Mo breccia deposit is hosted by large-volume quartz monzonite, granodiorite, and quartz monzonite porphyry (~61–59 Ma). Discrepancies between field and paragenetic relationships and some analytic ages at Sunnyside and Red Hill preclude precise dating of mineralization stages, and may reflect disturbance of isotope systems by multiple, co-spatial to juxtaposed intrusive and hydrothermal events, and/or by unrecognized intrusions. Numerous vein and replacement deposits at the northern end of the batholith, including the Hardshell Ag resource and the Three R supergene chalcocite resource, are distal deposits of the Sunnyside and Red Mountain systems. Small, ~61 to 59 Ma Cu-Mo deposits in large-volume intrusions in the southern part of the batholith consist of hydrothermal quartz, biotite, K-feldspar, muscovite, chalcopyrite, and molybdenite. The age span of magmatic and magmatic-hydrothermal events in the Patagonia Mountains, minimally 16 m.y., is comparable to that of certain other magmatic-hydrothermal successions that contain porphyry Cu-Mo systems. Magmatic-hydrothermal events of the Wasatch-Oquirrh igneous trend, Utah, and the Boulder batholith, Montana, both span ~17 m.y. and include the Bingham and Butte porphyry Cu-Mo, vein and replacement deposits, respectively. Plutons and mineral deposits in the Pima district, Arizona, which includes the porphyry Cu-Mo deposits at Sierrita-Esperanza, Mission-Pima-San Xavier North, and Twin Buttes, formed over an interval of ~14 m.y. The diversity of igneous and hydrothermal products likely reflects evolutionary processes occurring at multiple sites in the lithosphere and at different time scales from >10 m.y. to less than the geochronologic precision currently achievable.

Arizona↗

USGS2022

Perspectives on premetamorphic stratabound tourmalinites

Stratabound tourmalinites are metallogenically important rocks that locally show a close spatial association with diverse types of mineralization, especially volcanogenic massive sulfides (VMS) and clastic-dominated (CD) Zn-Pb deposits. These tourmalinite occurrences pan the geologic record from Eoarchean to Jurassic. Host lithologies are dominated by clastic metasedimentary rocks but in some areas include metavolcanic rocks, marble, or metaevaporites. Stratabound and stratiform (conformable) tourmalinites commonly display sedimentary structures such as graded beds, cross-beds, and rip-up clasts. In most cases, field and microtextural relationships are consistent with a synsedimentary to the early diagenetic introduction of boron as a precursor to tourmaline formation. Whole-rock geochemical data for major, trace, and rare earth elements (REE) provide valuable insights into tourmalinite origins. Al-normalized values relative to those for least-altered host metasedimentary rocks suggest that tourmalinites in proximal settings at or near hydrothermal vent sites characterized by high fluid/rock regimes (e.g., Sullivan Pb-Zn-Ag deposit, Canada) have very different signatures than those in low fluid/rock, distal settings (e.g., Broken Hill Pb-Zn-Ag deposit, Australia). The high fluid/rock regimes at Sullivan show large mass changes of +60 % for Mg and +180 % for Mn, as well as large variations in abundances of light and middle REE. In contrast, tourmalinite formation in low fluid/rock regimes yields minimal Al-normalized changes in major elements, trace elements, and REE. Boron isotope values of tourmalinite-hosted tourmaline vary widely from -26.1 to +27.5 ‰, and are attributed mainly to boron sources (e.g., sediments, evaporites) with generally minor influence from processes such as formational temperature, fluid/rock ratio, and secular variation in seawater δ 11 B values. Laterally extensive stratiform tourmalinites formed mainly by syngenetic or early diagenetic processes on or beneath the seafloor. The syngenetic process is attributed to the interaction of vented B-rich brines with aluminous minerals in sediments, whereas the diagenetic process involves the selective replacement of aluminous sediments by B-rich fluids. Modern examples of tourmalinites, as yet undiscovered, may exist in metalliferous sediments of the Red Sea and the eastern Pacific Ocean, in altered volcaniclastic sediments within active seafloor-hydrothermal systems of the South Pacific, and in hydrothermal mounds and vents associated with mafic sill complexes in extensional basins as in the North Sea and South China Sea. Stratabound tourmalinites that contain base-metal sulfides, high Mn concentrations (>1 wt. % MnO), or positive Eu anomalies can be valuable exploration guides for base-metal sulfide deposits in sedimentary and volcanic terranes.

Journal of Geosciences↗

USGS1999

Determination of chemical-constituent loads during base-flow and storm-runoff conditions near historical mines in Prospect Gulch, upper Animas River watershed, southwestern Colorado

Prospect Gulch is a major source of iron, aluminum, zinc, and other metals to Cement Creek. Information is needed to prioritize remediation and develop strategies for cleanup of historical abandoned mine sites in Prospect Gulch. Chemical-constituent loads were determined in Prospect Gulch, a high-elevation alpine stream in southwestern Colorado that is affected by natural acid drainage from weathering of hydro-thermally altered igneous rock and acidic metal-laden discharge from historical abandoned mines. The objective of the study was to identify metal sources to Prospect Gulch. A tracer solution was injected into Prospect Gulch during water-quality sampling so that loading of geochemical constituents could be calculated throughout the study reach. A thunderstorm occurred during the tracer study, hence, metal loads were measured for storm-runoff as well as for base flow. Data from different parts of the study reach represents different flow conditions. The beginning of the reach represents background conditions during base flow immediately upstream from the Lark and Henrietta mines (samples PG5 to PG45). Other samples were collected during storm runoff conditions (PG100 to PG291); during the first flush of metal runoff following the onset of rainfall (PG303 to PG504), and samples PG542 to PG700 were collected during low-flow conditions. During base-flow conditions, the percentage increase in loads for major constituents and trace metals was more than an order of magnitude greater than the corresponding 36 % increase in stream discharge. Within the study reach, the highest percentage increases for dissolved loads were 740 % for iron (Fe), 465 % for aluminum (Al), 500 % for lead (Pb), 380 % for copper (Cu), 100 % for sulfate (SO4), and 50 % for zinc (Zn). Downstream loads near the mouth of Prospect Gulch often greatly exceeded the loads generated within the study reach but varied by metal species. For example, the study reach accounts for about 6 % of the dissolved-Fe load, 13 % of the dissolved-Al load, and 18 % of the dissolved-Zn load; but probably contributes virtually all of the dissolved Cu and Pb. The greatest downstream gains in dissolved trace-metal loads occurred near waste-rock dumps for the historical mines. The major sources of trace metals to the study reach were related to mining. The major source of trace metals in the reach near the mouth is unknown, however is probably related to weathering of highly altered igneous rocks, although an unknown component of trace metals could be derived from mining sources The late-summer storm dramatically increased the loads of most dissolved and total constituents. The effects of the storm were divided into two distinct periods; (1) a first flush of higher metal concentrations that occurred soon after rainfall began and (2) the peak discharge of the storm runoff. The first flush contained the highest loads of dissolved Fe, total and dissolved Zn, Cu, and Cd. The larger concentrations of Fe and sulfate in the first flush were likely derived from iron hydroxide minerals such as jarosite and schwertmanite, which are common on mine dumps in the Prospect Gulch drainage basin. Peak storm runoff contained the highest measured loads of total Fe, and of total and dissolved calcium, magnesium, silica and Al, which were probably derived from weathering of igneous rocks and clay minerals in the drainage basin.

Colorado↗

USGS2011

Ages and sources of components of Zn-Pb, Cu, precious metal, and platinum group element deposits in the goodsprings district, Clark County, Nevada

The Goodsprings district, Clark County, Nevada, includes zinc-dominant carbonate replacement deposits of probable late Paleozoic age, and lead-dominant carbonate replacement deposits, copper ± precious metal-platinum group element (PGE) deposits, and gold ± silver deposits that are spatially associated with Late Triassic porphyritic intrusions. The district encompasses ~500 km 2 although the distribution of all deposits has been laterally condensed by late Mesozoic crustal contraction. Zinc, Pb, and Cu production from about 90 deposits was ~160,000 metric tons (t) (Zn > Pb >> Cu), 2.1 million ounces (Moz) Ag, 0.09 Moz Au, and small amounts of PGEs—Co, V, Hg, Sb, Ni, Mo, Mn, Ir, and U—were also recovered. Zinc-dominant carbonate replacement deposits (Zn > Pb; Ag ± Cu) resemble Mississippi Valley Type (MVT) Zn-Pb deposits in that they occur in karst and fault breccias in Mississippian limestone where the southern margin of the regional late Paleozoic foreland basin adjoins Proterozoic crystalline rocks of the craton. They consist of calcite, dolomite, sphalerite, and galena with variably positive S isotope compositions ( δ 34 S values range from 2.5–13‰), and highly radiogenic Pb isotope compositions ( 206 Pb/ 204 Pb >19), typical of MVT deposits above crystalline Precambrian basement. These deposits may have formed when southward flow of saline fluids, derived from basinal and older sedimentary rocks, encountered thinner strata and pinch-outs against the craton, forcing fluid mixing and mineral precipitation in karst and fault breccias. Lead-dominant carbonate replacement deposits (Pb > Zn, Ag ± Cu ± Au) occur among other deposit types, often near porphyritic intrusions. They generally contain higher concentrations of precious metals than zinc-dominant deposits and relatively abundant iron oxides after pyrite. They share characteristics with copper ± precious metal-PGE and gold ± silver deposits including fine-grained quartz replacement of carbonate minerals in ore breccias and relatively low S and Pb isotope values ( δ 34 S values vary from 0–~4‰; 206 Pb/ 204 Pb <18.5). Copper ± precious metal-PGE deposits (Cu, Co, Ag, Au, Pd, and Pt) consist of Cu carbonate minerals (after chalcocite and chalcopyrite) and fine-grained quartz that have replaced breccia clasts and margins of fissures in Paleozoic limestones and dolomites near porphyritic intrusions. Gold ± silver deposits occur along contacts and within small-volume stocks and dikes of feldspar porphyry, one textural variety of porphyritic intrusions. Lead isotope compositions of copper ± precious metal-PGE, gold ± silver, and lead-dominant carbonate replacement deposits are similar to those of Mojave crust plutons, indicating derivation of Pb from 1.7 Ga crystalline basement or from Late Proterozoic siliciclastic sedimentary rocks derived from 1.7 Ga crystalline basement. Four texturally and modally distinctive porphyritic intrusions are exposed largely in the central part of the district: feldspar quartz porphyry, plagioclase quartz porphyry, feldspar biotite quartz porphyry, and feldspar porphyry. Intrusions consist of 64 to 70 percent SiO 2 and variable K 2 O/Na 2 O (0.14–5.33) that reflect proportions of K-feldspar and albite phenocrysts and megacrysts as well as partial alteration to K-mica; quartz and biotite phenocrysts are present in several subtypes. Albite may have formed during emplacement of magma in brine-saturated basinal strata, whereas hydrothermal alteration of matrix, phenocrystic, and megacrystic feldspar and biotite to K-mica, pyrite, and other hydrothermal minerals occurred during and after intrusion emplacement. Small volumes of garnet-diopside-quartz and retrograde epidote-mica-amphibole skarn have replaced carbonate rocks adjacent to one intrusion subtype (feldspar-quartz porphyry), but alteration of carbonate rocks at intrusion contacts elsewhere is inconspicuous. Uranium-lead ages of igneous zircons vary inconsistently from ~ 180 to 230 Ma and are too imprecise to distinguish age differences among intrusion subtypes; most ages are 210 to 225 Ma, yielding a mean of 217 ± 1 Ma. K-Ar and 40 Ar/ 39 Ar ages of magmatic (plagioclase, biotite) and hydrothermal (K-mica) minerals span a similar range (183–227 Ma), demonstrating broadly contemporaneous intrusion emplacement and hydrothermal alteration but allowing for multiple Late Triassic magmatic-hydrothermal events. Imprecision and range of isotopic ages may have resulted from burial beneath Mesozoic and Tertiary strata and multiple intrusion of magmas, causing thermal disturbance to Ar systems and Pb loss from zircons in intrusions. Separate late Paleozoic (zinc-dominant carbonate replacement deposits) and Late Triassic (all other deposits) mineralizing events are supported by form, distribution, and host rocks of metal deposits, by hydrothermal mineral assemblages, isotope compositions, metal abundances, and metal diversity, and by small intrusion volumes. These characteristics collectively distinguish the Goodsprings district from larger intrusion related carbonate replacement districts in the western United States. They can be used to evaluate proximity to unexposed porphyritic intrusions associated with PGE and gold ± silver mineralization.

Nevada↗

USGS1979

Detection and mapping of hydrothermally altered rocks in the vicinity of the Comstock Lode, Virginia Range, Nevada, using enhanced Landsat images

The Virginia Range, immediately southeast of Reno, Nev., consists mainly of flows, breccias, and turfs of Miocene age. Most of these volcanic rocks are of intermediate composition; rhyodacite is the most common rock type. Basalt, rhyolite and rhyolite tuff, and tuffaceous sedimentary rocks of Miocene and Pliocene age also cover substantial areas in the range. Pre-Tertiary metasedimentary, metavolcanic, and granitic rocks are exposed in scattered inliers, mostly along the southern and eastern margins of the range. Several large areas and many small areas within the volcanic pile were subjected to hydrothermal alteration during and after the period of intermediate volcanic activity. Economic precious metal mineralization is spatially and temporally associated with the hydrothermal alteration in several areas. The most important deposit is the Comstock Lode, which produced 192 million troy ounces of silver and 8.3 million troy ounces of gold from epithermal veins (Bonham, 1969). The hydrothermally altered rocks include silicified, advanced argillic, montmorillonite-bearing argillic, and propylitic types. The first three types typically contain pyrite, and some propylitic rocks contain pyrite as well. Supergene oxidation of these pyritic rocks produces limonitic bleached rocks. The term 'limonite,' as used here, refers to any combination of the minerals hematite, goethite, and Jarosite. Where vegetation cover is sparse to moderate, these limonitic rocks are readily identified on Landsat images enhanced by the color-ratio composite technique developed by Rowan and others (1974), so the altered areas can be mapped. About 30 percent tree cover (here mainly pinyon pine) is sufficient to change the spectral signature of individual picture elements (pixels) enough so that limonitic materials can no longer be uniquely identified. As in all other areas where this technique has been applied, limonitic unaltered rocks with intermediate to high albedos have the same appearance on the color-ratio composite as limonitic altered rocks. This problem represents the most important limitation to the use of enhanced Landsat images for detection and mapping of hydrothermally altered rocks. Reflectance spectra of altered and unaltered rocks taken in the field in the Virginia Range show that most altered rocks have a conspicuous absorption band near 2.2 ?m produced by clay minerals or alunite, whereas unaltered rocks have no features in this spectral region. Thus spectral information for selected bands in the 1.1-2.5 ?m region may allow discrimination between limonitic altered and limonitic unaltered rocks (Rowan and others, 1977; Abrams and others, 1977; Rowan and Abrams, 1978). Another potential limitation is loss of spectral information on slopes with low effective sun angle. Although a minor problem in the Virginia Range, loss of information sufficient to preclude identification of limonitic altered rocks occurs with effective sun angle lower than 20-25 degrees. Thus, even at moderate latitudes substantial parts of areas with high topographic relief may be lost to observation.

Open-File Report↗

USGS2021

Hydrothermal alteration can result in pore pressurization and volcano instability

The collapse of a volcanic flank can be destructive and deadly. Hydrothermal alteration is common to volcanoes worldwide and is thought to promote volcano instability by decreasing rock strength. However, some laboratory studies have shown that not all alteration reduces rock strength. Our new laboratory data for altered rhyodacites from Chaos Crags (Lassen volcanic center, California, USA) show that pore- and crack-filling mineral precipitation can reduce porosity and permeability and increase strength, Young's modulus, and cohesion. A significant reduction in permeability, by as much as four orders of magnitude, will inhibit fluid circulation and create zones of high pore fluid pressure. We explored the consequences of pore fluid pressurization on volcano stability using large-scale numerical modeling. Upscaled physical and mechanical properties for hydrothermally altered rocks were used as input parameters in our modeling. Results show that a high-pore-pressure zone within a volcano increases volcano deformation and that increasing the size of this zone increases the observed deformation. Hydrothermal alteration associated with mineral precipitation, and increases to rock strength, can therefore promote pore pressurization and volcano deformation, increasing the likelihood of volcano spreading, flank collapses, and phreatic/phreatomagmatic explosions. We conclude that porosity-decreasing alteration, explored here, and porosity-increasing alteration can both promote volcano instability and collapse, but by different mechanisms. Hydrothermal alteration should therefore be monitored at volcanoes worldwide and incorporated into hazard assessments.

Geology↗

USGS2012

Sequestration of non-pure carbon dioxide streams in iron oxyhydroxide-containing saline repositories

Iron oxyhydroxide, goethite (α-FeOOH), was evaluated as a potential formation mineral reactant for trapping CO 2 in a mineral phase such as siderite (FeCO 3 ), when a mixture of CO 2 -SO 2 flue gas is injected into a saline aquifer. Two thermodynamic simulations were conducted, equilibrating a CO 2 -SO 2 fluid mixture with a NaCl-brine and Fe-rich rocks at 150 °C and 300 bar. The modeling studies evaluated mineral and fluid composition at equilibrium and the influence of pH buffering in the system. Results show siderite precipitates both in the buffered and unbuffered system; however, the presence of an alkaline pH buffer enhances the stability of the carbonate. Based on the model, an experiment was designed to compare with thermodynamic predictions. A CO 2 -SO 2 gas mixture was reacted in 150 ml of NaCl-NaOH brine containing 10 g of goethite at 150 °C and 300 bar for 24 days. Mineralogical and brine chemistry confirmed siderite as the predominant reaction product in the system. Seventy-six mg of CO 2 are sequestered in siderite per 10 g of goethite.

International Journal of Greenhouse Gas Control↗

USGS2017

Controls on pore types and pore-size distribution in the Upper Triassic Yanchang Formation, Ordos Basin, China: Implications for pore-evolution models of lacustrine mudrocks

Our main objectives are to (1) learn if pore-evolution models developed from marine mudrocks can be directly applied to lacustrine mudrocks, (2) investigate what controls the different pore types and sizes of Chang 7 organic matter (OM)-rich argillaceous mudstones of the Upper Triassic Yanchang Formation, and (3) describe the texture, fabric, mineralogy, and thermal maturity variation in the Chang 7 mudstones. Lacustrine mudstones from nine cored wells along a depositional dip in the southeastern Ordos Basin, China, were investigated. Helium porosimetry, nitrogen adsorption, and field-emission scanning electron microscopy of Ar-ion milled samples were applied. Measured average total porosity of samples from a proximal to distal transect ( ϕ = 5.0 % "> ϕ = 5.0 % ) is higher than those from the two adjacent cored wells ( ϕ = 2.3 % "> ϕ = 2.3 % ). This difference in porosity partly caused by differences in the clay mineral content implies that in the fluvial-deltaic-lacustrine depositional environment, reservoir quality can vary significantly in a short distance. Owing to the uneven distribution of the sample set from proximal to distal area, we mainly evaluate variations in the proximal setting. Results from nitrogen-gas adsorption experiments show that there are four distinct patterns of pore-size distribution within the Chang 7 member of the Yanchang Formation with no particular correlation with mineralogical composition and thermal maturity. The pore network within Chang 7 mudstones is dominated by OM-hosted pores, with a lesser abundance of interparticle and intraparticle pores. The size distribution of mineral-hosted pores within these mudstones is found to be closely related to the rock texture (sorting and grain size) and fabric. Mudstones with well-sorted grains and a higher percentage of coarser grains have more abundant mineral pores. The sizes of OM-hosted pores in these compaction-dominated lacustrine mudstones were one to two orders of magnitude smaller than those in the marine mudstones that display abundant early cementation.

Ordos basin↗

USGS2015

Association of anatase (TiO2) and microbes: unusual fossilization effect or a potential biosignature?

We combined microbial paleontology and molecular biology methods to study the Eyreville B drill core from the 35.3-Ma-old Chesapeake Bay impact structure,Virginia, USA. The investigated sample is a pyrite vein collected from the 1353.81-1353.89 m depth interval, located within a section of biotite granite. The granite is a pre-impact rock that was disrupted by the impact event. A search for inorganic (mineral) biosignatures revealed the presence of micron-size rod morphologies of anatase (TiO2) embedded in chlorite coatings on pyrite grains. Neither the Acridine Orange microbial probe nor deoxyribonucleic acid (DNA) extraction followed by polymerase chain reaction (PCR) amplifi cation showed the presence of DNA or ribonucleic acid (RNA) at the location of anatase rods, implying the absence of viable cells in the investigated area. A Nile Red microbial probe revealed the presence of lipids in the rods. Because most of the lipids are resistant over geologic time spans, they are good biomarkers, and they are an indicator of biogenicity for these possibly 35-Ma-old microbial fossils. The mineral assemblage suggests that rod morphologies are associated with low-temperature (<100 °C) hydrothermal alteration that involved aqueous fl uids. The temporal constraints on the anatase fossils are still uncertain because pre-impact alteration of the granite and postimpact heating may have provided identical conditions for anatase precipitation and microbial preservation.

Geological Society of America Bulletin↗

USGS2009

Geochemistry and geochronology of carbonate-hosted base metal deposits in the southern Brooks Range, Alaska: Temporal association with VMS deposits and metallogenic implications

The Brooks Range contains enormous accumulations of zinc and copper, either as VMS or sediment-hosted deposits. The Ruby Creek and Omar deposits are Cu-Co stratabound deposits associated with dolomitic breccias. Numerous volcanogenic Cu-Zn (+/-Ag, Au) deposits are situated ~20 km north of the Ruby Creek deposit. The carbonate-hosted deposits consist of chalcopyrite and bornite that fill open spaces, replace the matrix of the breccias, and occur in later cross-cutting veins. Cobaltiferous pyrite, chalcocite, minor tennantite-tetrahedrite, galena, and sphalerite are also present. At Ruby Creek, phases such as carrollite, renierite, and germanite occur rarely. The deposits have undergone post-depositional metamorphism (Ruby Creek, low greenschist facies; Omar, blueschist facies). The unusual geochemical signature includes Cu-Co +/- Ag, As, Au, Bi, Ge, Hg, Sb, and U with sporadic high Re concentrations (up to 2.7 ppm). New Re-Os data were obtained for chalcopyrite, bornite, and pyrite from the Ruby Creek deposit (analyses of sulfides from Omar are in progress). The data show extremely high Re abundances (hundreds of ppb, low ppm) and contain essentially no common Os. The Re-Os data provide the first absolute ages of ore formation for the Ruby Creek deposit and demonstrate that the Re-Os systematics of pyrite, chalcopyrite, and bornite are unaffected by greenschist metamorphism. The Re-Os data show that the main phase of Cu mineralization occurred at 384 +/-4.2 Ma, which coincides with zircon U-Pb ages from igneous rocks that are spatially and genetically associated with VMS deposits. This suggests a temporal link between regional magmatism and hydrothermal mineralization.

Alaska↗

USGS1989

Mineralogical studies of the nitrate deposits of Chile: VI. Hectorfloresite, Na9(IO3)(SO4)4, a new saline mineral

The new mineral hectorfloresite, known to occur in only one locality in the nitrate fields of northern Chile, consists of tiny prismatic crystals, generally less than 1 mm long and 0.2 mm in diameter, in cavities in dense nitrate ore consisting of saline-cemented silt, sand, and small rock fragments. The physical, optical and crystallographic properties of the new mineral are described. -from Authors

American Mineralogist↗

USGS1989

Diagenesis of hydrocarbon-bearing rocks in the Middle Ordovician Simpson Group, southeastern Anadarko Basin, Oklahoma

Quartzarenites and subarkoses in the Middle Ordovician Simpson Group in the Gulf Costello No. 1 and Sunray-DX Parker No. 1 Mazur wells, southeastern Anadarko basin, have undergone a complex diagenetic and petroleum-migration history. During early burial, petroleum migrated locally through sandstones; patches of bitumen in calcite and bitumen-lined quartz overgrowths containing oil-bearing inclusions reflect the introduction of petroleum-bearing fluids at shallow depths. Stable-isotope data reveal that early calcite precipitated at near-surface temperatures from fluids dominated by marine carbon. At moderate to deep burial, calcite dissolution, followed by ferroan-dolomite and clay-mineral precipitation, occurred at about the same time as the rocks reached levels of thermal maturity sufficient for the generation of hydrocarbons. Maximum paleotemperatures during deep burial are estimated from maturation models to have reached 250°F in the Costello well and 300°F in the Mazur well. Maturation-derived temperatures in the Costello well are consistent with preliminary homogenization temperatures (210-250°F) for oil inclusions along microscopic healed fractures that formed during deep burial, thus supporting an Early to Middle Pennsylvanian timing for the generation and migration of late-stage hydrocarbons. The early petroleum phase, emplaced while the rocks were at shallow burial depths, migrated from mature source rocks deeper in the basin.

Oklahoma↗

USGS2025

Reduction of red bed sedimentary rocks in connection with energy metal ore formation: A case study from the Sinbad seep, Mesa County, Colorado

The Paradox Basin’s Sinbad seep is a modern analog for ancient bleaching of red bed sediments by introduced alkaline, reducing brines. This bleaching, involving reductive alteration of former red beds, is essential ground preparation that enables the altered rocks to trap Cu, U, and V from later oxidized fluids, forming ore deposits. Study of Sinbad thus offers insights into these metallic mineralization processes in the Paradox and other sedimentary basins. The Sinbad seep occurs where shallow groundwater interacts with organic-rich petroleum source rocks, flows up a fault, and discharges into Salt Creek. Ratios of Na/Cl, Na/Br, and Cl/Br, plus high sulfate concentrations, indicate that the salinity of the seep water originated from dissolution of halite and gypsum during topographically driven flow of meteoric water across a diapir of the Pennsylvanian Paradox Formation, rather than from deep basinal brines. In contact with the organic-rich shales of the Paradox, these SO 4 -rich waters become reduced through bacterial reduction, producing H 2 S. The waters react with red beds of the Permian Cutler Formation, causing pervasive bleaching. The bleaching at Sinbad is characterized by iron-conservative reduction of ferric iron in diagenetic hematite and detrital ilmenite and magnetite to Fe sulfides. The ferrous iron is retained in these sulfides likely as sorbed Fe. Associated alteration includes precipitation of quartz and feldspar overgrowths, partial dissolution of detrital quartz and feldspar caused by pressure solution, formation of clay and authigenic rutile, and precipitation of carbonate and gypsum. The Fe sulfides rapidly degenerate to a mixture of jarosite and iron oxides on weathering at the surface. Among the major-oxide elements and most trace elements, there is no statistical difference between unbleached and bleached samples. The exceptions are uranium and sulfur, which are somewhat greater in bleached samples. Fission track radiography illuminates that uranium is preferentially concentrated in iron oxide cements, iron sorbed into detrital clasts, and finely disseminated iron oxide in illite cement in bleached samples. A leaching experiment suggests that uranium may be more easily available for mobilization from rocks that have undergone bleaching alteration, making them potential U sources. In addition, bleached rocks form effective traps for U, V, and some Cu mineralization.

Colorado↗

USGS2014

Composition of dust deposited to snow cover in the Wasatch Range (Utah, USA): Controls on radiative properties of snow cover and comparison to some dust-source sediments

Dust layers deposited to snow cover of the Wasatch Range (northern Utah) in 2009 and 2010 provide rare samples to determine the relations between their compositions and radiative properties. These studies are required to comprehend and model how such dust-on-snow (DOS) layers affect rates of snow melt through changes in the albedo of snow surfaces. We evaluated several constituents as potential contributors to the absorption of solar radiation indicated by values of absolute reflectance determined from bi-conical reflectance spectroscopy. Ferric oxide minerals and carbonaceous matter appear to be the primary influences on lowering snow-cover albedo. Techniques of reflectance and Mössbauer spectroscopy as well as rock magnetism provide information about the types, amounts, and grain sizes of ferric oxide minerals. Relatively high amounts of ferric oxide, indicated by hard isothermal remanent magnetization (HIRM), are associated with relatively low average reflectance (<0.25) across the visible wavelengths of the electromagnetic spectrum. Mössbauer spectroscopy indicates roughly equal amounts of hematite and goethite, representing about 35% of the total Fe-bearing phases. Nevertheless, goethite (α-FeOOH) is the dominant ferric oxide found by reflectance spectroscopy and thus appears to be the main iron oxide control on absorption of solar radiation. At least some goethite occurs as nano-phase grain coatings less than about 50 nm thick. Relatively high amounts of organic carbon, indicating as much as about 10% organic matter, are also associated with lower reflectance values. The organic matter, although not fully characterized by type, correlates strongly with metals (e.g., Cu, Pb, As, Cd, Mo, Zn) derived from distal urban and industrial settings, probably including mining and smelting sites. This relation suggests anthropogenic sources for at least some of the carbonaceous matter, such as emissions from transportation and industrial activities. The composition of the DOS samples can be compared with sediments in a likely dust-source setting at the Milford Flat Fire (MFF) area about 225 km southwest of Salt Lake City. The MFF area represents geologically and physiographically similar and widespread dust sources west-southwest of the Wasatch Range and heavily populated Wasatch Front. The DOS layers and MFF sediments are similar in some textural, chemical, and magnetic properties, as well as in the common presence of goethite, hematite, magnetite-bearing basalt fragments, quartz, plagioclase, illite, and kaolinite. Textural and some chemical differences among these deposits can be explained by atmospheric sorting as well as by inputs from other settings, such as salt-crusted playas and contaminant sources.

Utah↗

USGS2002

Influence of rock composition on the geochemistry of stream and spring waters from mountainous watersheds in the Gunnison, Uncompahgre, and Grand Mesa National Forests, Colorado

The ranges of geochemical baselines for stream and spring waters were determined and maps were constructed showing acid-neutralizing capacity and potential release of total dissolved solids for streams and spring waters for watersheds underlain by each of ten different rock composition types in the Gunnison, Uncompahgre, and Grand Mesa National Forests, Colorado (GMUG). Water samples were collected in mountainous headwater watersheds that have comparatively high precipitation and low evapotranspiration rates and that generally lack extensive ground-water reservoirs. Mountainous headwaters react quickly to changes in input of water from rain and melting snow and they are vulnerable to anthropogenic impact. Processes responsible for the control and mobility of elements in the watersheds were investigated. The geochemistry of water from the sampled watersheds in the GMUG, which are underlain by rocks that are relatively unmineralized, is compared to the geochemistry of water from the mineralized Redcloud Peak area. The water with the highest potential for release of total dissolved solids is from watersheds that are underlain by Paleozoic sedimentary rocks; that high potential is caused primarily by gypsum in those rocks. Water that has the highest acid-neutralizing capacity is from watersheds that are underlain by Paleozoic sedimentary rocks. The water from watersheds underlain by the Mancos Shale has the next highest acid-neutralizing capacity. Water that has the lowest acid-neutralizing capacity is from watersheds that are underlain by Tertiary ash-flow tuff. Tertiary sedimentary rocks containing oil shale, the Mesavede Formation containing coal, and the Mancos Shale all contain pyrite with elevated metal contents. In these mountainous head-water areas, water from watersheds underlain by these rock types is only slightly impacted by oxidation of pyrite, and over-all it is of good chemical quality. These geochemical baselines demonstrate the importance of rock composition in determining the types of waters that are in the headwater areas. The comparison of these geochemical baselines to later geochemical base-lines will allow recognition of any significant changes in water quality that may occur in the future.

Colorado↗

USGS1996

Origin and significance of high nickel and chromium concentrations in pliocene lignite of the Kosovo Basin, Serbia

Trace element data from 59 Pliocene lignite cores from the lignite field in the Kosovo Basin, southern Serbia, show localized enrichment of Ni and Cr (33-304 ppm and 8-176 ppm, respectively, whole-coal basis). Concentrations of both elements decrease from the western and southern boundaries of the lignite field. Low-temperature ash and polished coal pellets of selected bench and whole-coal samples were analyzed by X-ray diffraction and scanning electron microscopy with energy-dispersive X-ray analyses. These analyses show that most of the Ni and Cr are incorporated in detrital and, to a lesser degree, in authigenic minerals. The Ni- and Cr-bearing detrital minerals include oxides, chromites, serpentine-group minerals and rare mixed-layer clays. Possible authigenic minerals include Ni-Fe sulfates and sulfides. Analyses of three lignite samples by a supercritical fluid extraction technique indicate that some (1-11%) of the Ni is organically bound. Ni- and Cr-bearing oxides, mixed-layer clays, chromites and serpentine-group minerals were also identified in weathered and fresh samples of laterite developed on serpentinized Paleozoic peridotite at the nearby Glavica and C??ikatovo Ni mines. These mines are located along the western and northwestern rim, respectively, of the Kosovo Basin, where Ni contents are highest. The detrital Ni- and Cr-bearing minerals identified in lignite samples from the western part of the Kosovo Basin may have been transported into the paleoswamp by rivers that drained the two Paleocene laterites. Some Ni may have been transported directly into the paleoswamp in solution or, alternatively, Ni may have been leached from detrital minerals by acidic peat water and adsorbed onto organic matter and included into authigenic mineral phases. No minable source of Ni and Cr is known in the southern part of the lignite field; however, the mineral and chemical data from the lignite and associated rocks suggest that such a source area may exist.

International Journal of Coal Geology↗

USGS1989

Soil geochemistry of Mother Lode-type gold deposits in the Hodson mining district, central California, U.S.A.

The Hodson mining district is in the westernmost foothills of the Sierra Nevada in California, about 17 km west of the town of Angels Camp. This district is part of the West Gold Belt, which lies about 12-16 km west of, and generally parallel to, the better known Mother Lode Gold Belt in central California. The district produced several million dollars worth of Au between about 1890 and 1940. The geologic setting and mineral deposits in the West Gold Belt are generally similar to those in the Mother Lode Gold Belt. Rocks in the study area are of Jurassic age and consist of a mixture of (1) fine-grained, generally thin-bedded, clastic sedimentary rocks that have been metamorphosed to slates, schists, and phyllites, and (2) massive volcanic flows and welded tuffs that have been metamorphosed to metabasalts and metatuffs. All rocks were intensely faulted and folded during the Late Cretaceous Nevadan orogeny; northnorthwest- and northwest-trending faults dominate. Mining in the area was of low-grade gold-pyrite ores occurring principally in the carbonatized wall rocks adjacent to the major northwest-trending Hodson fault and its splays. Minor amounts of other sulfide minerals (principally chalcopyrite, arsenopyrite, sphalerite, and galena) are locally associated with the Au deposits.

California↗

USGS2011

Vadose zone controls on weathering intensity and depth: Observations from grussic saprolites

An investigation of vadose zone weathering processes has been undertaken on grussic saprolites developed on Californian granitoids. Preliminary results indicate strong climatic control, through infiltration, on the depth and intensity of weathering. At sites with higher infiltration, the vadose zone is comprehensively altered to grussic saprolite and saprock. Conversely, lower infiltration sites display only thin grussic saprolites, strongly influenced by rock texture. Both vadose zone and weathering depth appear to be governed by local base level, and vadose zone hydrology exerts a fundamental control on the effective operation and relative dominance of the key weathering reactions. In zones of matrix permeability, oxidation of biotite comprehensively disaggregates the rock but results in little mass loss and clay mineral formation. Conversely, the higher transient flow rates that characterize zones of fracture permeability result in plagioclase hydrolysis, significant mass losses and accompanying clay mineral formation. A variable hydrological regime may also contribute to high partial pressures of O 2 in vadose zone pore waters and pore spaces, thereby enhancing the oxidative environment and further predisposing grussic saprolite formation.

Applied Geochemistry↗