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At least 289 records · Page 16Linked to original sources

USGS2026

Recycling radiogenic osmium by crustal foundering in subduction zones: Evidence from pyroxenite xenoliths in the north Andean arc

Removal of mafic-ultramafic lower crust (e.g., via delamination) is fundamental to making andesitic continental crust, yet direct evidence of this process remains elusive. A unique suite of garnet clinopyroxenite and hornblendite (arclogite) xenoliths from the northern volcanic zone of the Andes, erupted to the surface in the mid-Pleistocene, have bulk-rock geochemistry and osmium (Os) isotopic compositions that demonstrate their crustal affinity, yet have equilibration pressures and temperatures below the arc Mohorovičić discontinuity (~53 km) and some as deep as within the sub-arc mantle wedge (~105 km). Garnet websterites from the same xenolith suite, sourced from depths approaching the Wadati-Benioff zone (~140 km), have elemental and isotopic compositions indicative of a mantle origin, likely formed as products of peridotite-liquid reactions above the subducting slab. Variability in bulk-rock 143 Nd/ 144 Nd values and garnet oxygen isotope ratios ( 𝛿 18 O) for these samples is attributed to minor assimilation of subducted components and/or older crustal material, but assimilation alone cannot account for the highly radiogenic Os isotopic compositions. These results provide direct petrologic evidence for modern arclogite formation and foundering in the Andean orogen, the archetypal active continental subduction system. Elevated 187 Os/ 188 Os values of Mercaderes arclogites imply that recycling of gravitationally unstable arc cumulates during continental crust formation introduces highly radiogenic Os into the convective mantle, which has implications for mass fluxes across the crust-mantle boundary as well as the sources and evolution of mantle heterogeneity as seen in orogenic peridotite massifs and in the sources of oceanic basalts

Earth and Planetary Science Letters↗

USGS2002

Geologic cross sections showing the concentrations of As, Cd, Co, Cu, Cr, Fe, Mo, Ni, Pb, and Zn in acid-insoluble residues of Paleozoic rocks within the Doniphan/Eleven Point Ranger District of the Mark Twain National Forest, Missouri, USA

This report is a product of a U.S. Geological Survey investigation that is focused on characterizing the potential environmental impacts of lead-zinc mining within the Doniphan/Eleven Point ranger district of the Mark Twain national forest. The elemental concentrations of iron (Fe), arsenic (As), cadmium (Cd), cobalt (Co), copper (Cu), chromium (Cr), nickel (Ni), lead (Pb), and zinc (Zn) in acidinsoluble residues are shown for boreholes along two geologic cross sections within Doniphan/Elevan Point ranger district (Figure 1). The purpose of this report is to characterize, in a general sense, the distribution of economically and environmentally important elements within the rocks and aquifers of the Doniphan/Eleven Point ranger district

Missouri↗

USGS1992

Metallogeny of the midcontinent rift system of North America

The 1.1 Ga Midcontinent rift system of North America is one of the world's major continental rifts and hosts a variety of mineral deposits. The rocks and mineral deposits of this 2000 km long rift are exposed only in the Lake Superior region. In the Lake Superior region, the rift cuts across Precambrian basement terranes ranging in age from ∼ 1850 Ma to more than 3500 Ma. Where exposed, the rift consists of widespread tholeiitic basalt flows with local interlayered rhyolite and clastic sedimentary rocks. Beneath the center of Lake Superior the volcanic and sedimentary rocks are more than 30 km deep as shown by recent seismic reflection profiles. This region hosts two major classes of mineral deposits, magmatic and hydrothermal. All important mineral production in this region has come from hydrothermal deposits. Rift-related hydrothermal deposits include four main types: (1) native copper deposits in basalts and interflow sediments; (2) sediment-hosted copper sulfide and native copper; (3) copper sulfide veins and lodes hosted by rift-related volcanic and sedimentary rocks; and (4) polymetallic (five-element) veins in the surrounding Archean country rocks. The scarcity of sulfur within the rift rocks resulted in the formation of very large deposits of native metals. Where hydrothermal sulfides occur (i.e., shale-hosted copper sulfides), the source of sulfur was local sedimentary rocks. Magmatic deposits have locally supported exploration and minor production, but most are subeconomic presently. These deposits occur in intrusions exposed near the margins of the rift and include CuNiPGE and TiFe (V) in the Duluth Complex, U-REE-Nb in small carbonatites, and breccia pipes resulting from local hydrothermal activity around small felsic intrusions. Mineralization associated with some magmatic bodies resulted from the concentration of incompatible elements during fractional crystallization. Most of the sulfide deposits in intrusions, however, contain sulfur derived from country rocks; the interaction between magma and country rocks was important in generation of the magmatic CuNi sulfide deposits. A mantle plume origin has been proposed for the formation of the Midcontinent rift. More than 1 million km 3 of mafic magma was erupted in the rift and a comparable volume of mafic intrusions are inferred beneath the rift, providing a ready and structurally confined supply of mafic source rocks that were available for leaching of metals by basinal brines. These brines were heated by a steep geothermal gradient that resulted from the melting and underplating of magma derived from the plume. Hydrothermal deposits were emplaced for at least 30–40 m.y. after rift magmatism and extension ceased. This time lag may reflect either the time required to heat deeply buried rocks and fluids within the rift, or may be due to the timing of post-rift compression that may have provided the driving mechanism for expulsion of hydrothermal fluids from deep portions of the rift.

Precambrian Research↗

USGS1960

Strategic graphite, a survey

Strategic graphite consists of certain grades of lump and flake graphite for which the United States is largely or entirely dependent on sources abroad. Lump graphite of high purity, necessary in the manufacture of carbon brushes, is imported from Ceylon, where it occurs in vein deposits. Flake graphite, obtained from deposits consisting of graphite disseminated in schists and other metamorphic rocks, is an essential ingredient of crucibles used in the nonferrous metal industries and in the manufacture of lubricants and packings. High-quality flake graphite for these uses has been obtained mostly from Madagascar since World War I. Some flake graphite of strategic grade has been produced, however, from deposits in Texas, Alabama, and Pennsylvania. The development of the carbon-bonded crucible, which does not require coarse flake, should lessen the competitive advantage of the Madagascar producers of crucible flake. Graphite of various grades has been produced intermittently in the United States since 1644. The principal domestic deposits of flake graphite are in Texas, Alabama, Pennsylvania, and New York. Reserves of flake graphite in these four States are very large, but production has been sporadic and on the whole unprofitable since World War I, owing principally to competition from producers in Madagascar. Deposits in Madagascar are large and relatively high in content of flake graphite. Production costs are low and the flake produced is of high quality. Coarseness of flake and uniformity of the graphite products marketed are cited as major advantages of Madagascar flake. In addition, the usability of Madagascar flake for various purposes has been thoroughly demonstrated, whereas the usability of domestic flake for strategic purposes is still in question. Domestic graphite deposits are of five kinds: deposits consisting of graphite disseminated in metamorphosed siliceous sediments, deposits consisting of graphite disseminated in marble, deposits formed by thermal or dynamothermal metamorphism of coal beds or other highly carbonaceous sediments, vein deposits, and contact metasomatic deposits in marble. Only the first kind comprises deposits sufficiently large and rich in flake graphite to be significant potential sources of strategic grades of graphite. Vein deposits in several localities are known, but none is known to contain substantial reserves of graphite of strategic quality. Large resources of flake graphite exist in central Texas, in northeastern Alabama, in eastern Pennsylvania, and in the eastern Adirondack Mountains of New York. Tonnages available, compared with the tonnages of flake graphite consumed annually in the United States, are very large. There have been indications that flake graphite from Texas, Alabama, and Pennsylvania can be used in clay-graphite crucibles as a substitute for Madagascar flake, and one producer has made progress in establishing markets for his flake products as ingredients of lubricants. The tonnages of various commercial grades of graphite recoverable from various domestic deposits, however, have not been established; hence, the adequacy of domestic resources of graphite in a time of emergency is not known. The only vein deposits from which significant quantities of lump graphite have been produced are those of the Crystal Graphite mine, Beaverhead County, Mont. The deposits are fracture fillings in Precambrian gneiss and pegmatite. Known reserves in the deposits are small. In Texas, numerous flake-graphite deposits occur in the Precambrian Packsaddle schist in Llano and Burnet Counties. Graphite disseminated in certain parts of this formation ranges from extremely fine to medium grained. The principal producer has been the mine of the Southwestern Graphite Co., west of the town of Burnet. Substantial reserves of medium-grained graphite are present in the deposit mined by the company. In northeastern Alabama, flake-graphite deposits occur in the Ashland mica schist in two belts that trend northeastward across Clay, Goosa, and Chilton Counties. The northeastern belt has been the most productive. About 40 mines have been operated at one time or another, but only a few have been active during or since World War I. The deposits consist of flake graphite disseminated in certain zones or "leads" consisting of quartz-mica-feldspar schists and mica quartzite. Most of past production has come from the weathered upper parts of the deposits, but unweathered rock has been mined at several localities. Reserves of weathered rock containing 3 to 5 percent graphite are very large, and reserves of unweathered rock are even greater. Flake graphite deposits in Chester County, Pa., have been worked intermittently since about 1890. The deposits consist of medium- to coarse-grained graphite disseminated in certain belts of the Pickering gneiss. The most promising deposit is one worked in the Benjamin Franklin and the Eynon Just mines. Reserves of weathered rock containing 1.5 percent graphite are of moderate size; reserves of unweathered rock are large. In the eastern Adirondack Mountains in New York there are two principal kinds of flake-graphite deposits: contact-metasomatic deposits and those consisting of flake graphite disseminated in quartz schist. The contact-metasomatic deposits are small, irregular, and very erratic in graphite content. The deposits in quartz schist are very large, persistent, and uniform in grade. There are large reserves of schist containing 3 to 5 percent graphite, but the graphite is relatively fine grained.

Bulletin↗

USGS2015

Temporal geochemical variations in above- and below-drainage coal mine discharge

Water quality data collected in 2012 for 10 above- and 14 below-drainage coal mine discharges (CMDs), classified by mining or excavation method, in the anthracite region of Pennsylvania, USA, are compared with data for 1975, 1991, and 1999 to evaluate long-term (37 year) changes in pH, SO 4 2− , and Fe concentrations related to geochemistry, hydrology, and natural attenuation processes. We hypothesized that CMD quality will improve over time because of diminishing quantities of unweathered pyrite, decreased access of O 2 to the subsurface after mine closure, decreased rates of acid production, and relatively constant influx of alkalinity from groundwater. Discharges from shafts, slopes, and boreholes, which are vertical or steeply sloping excavations, are classified as below-drainage; these receive groundwater inputs with low dissolved O 2 , resulting in limited pyrite oxidation, dilution, and gradual improvement of CMD water quality. In contrast, discharges from drifts and tunnels, which are nearly horizontal excavations into hillsides, are classified as above-drainage; these would exhibit less improvement in water quality over time because the rock surfaces continue to be exposed to air, which facilitates sustained pyrite oxidation, acid production, and alkalinity consumption. Nonparametric Wilcoxon matched-pair signed rank tests between 1975 and 2012 samples indicate decreases in Fe and SO 4 2− concentrations were highly significant ( p < 0.05) and increases in pH were marginally significant ( p < 0.1) for below-drainage discharges. For above-drainage discharges, changes in Fe and SO 4 2− concentrations were not significant, and increases in pH were highly significant between 1975 and 2012. Although a greater proportion of above-drainage discharges were net acidic in 2012 compared to below-drainage discharges, the increase in pH between 1975 and 2012 was greater for above- (median pH increase from 4.4 to 6.0) compared to below- (median pH increase from 5.6 to 6.1) drainage discharges. For cases where O 2 is limited, transformation of aqueous Fe II species to Fe III may be kinetically limited. In contrast, where O 2 is abundant, aqueous Fe concentrations may be limited by Fe III mineral precipitation; thus, trends in Fe may not follow those for SO 4 2− . In either case, when the supply of alkalinity is sufficient to buffer decreased acidity, the pH could increase by a step trend from strongly acidic (3–3.5) to near neutral (6–6.5) values. Modeled equilibrium with respect to Fe III precipitates varies with pH and Fe and SO 4 2− reconcentrations: increasing pH promotes the formation of ferrihydrite, while decreasing concentrations of Fe limit the formation of ferrihydrite, and decreasing Fe and SO 4 2− concentrations limit the precipitation of schwertmannite and favor formation of Fe III hydroxyl complexes and uncomplexed Fe 2+ and Fe 3+ . The analysis of the long-term geochemical changes in CMDs in the anthracite field and the effect of the hydrologic setting on water quality presented in this paper can help prioritize CMD remediation and facilitate selection and design of the most appropriate treatment systems.

Pennsylvania↗

USGS2004

Weathering of the meade peak phosphatic shale member, phosphoria formation: Observations based on uranium and its decay products

Variably weathered outcrop samples of the Meade Peak Phosphatic Shale Member of the Phosphoria Formation have 5-10% of the contained uranium (U) in a form readily extractable by 0.1 M sodium bicarbonate. Fission track radiography of outcrop samples and other less-weathered channel and core samples indicate that this mobile fraction of U is likely hosted by organic matter, secondary iron oxides and clay minerals, trace uraninite, and very fine-grained apatite cement. During weathering, this extractable U fraction is especially susceptible to redistribution, which produces small but measurable departures (1-15%) from radioactive (secular) equilibrium in the 238 U decay-series. The most weath- ered samples show the strongest isotopic evidence for redistribution of U during the last 350 ka, but sequestration of U by alteration products limits open-system losses of U at the whole-rock scale. In less-weathered samples, isotopic evidence for minor U loss (or gain) over longer time periods (1 Ma) is consistent with relatively non-aggressive attack of phosphatic rock during weathering. Comparative extractability of selenium (Se) suggests that a larger fraction of Se (19%) is readily available for mobilization during the earliest stages of weathering.

Book chapter↗

USGS2009

Climate-induced changes in high elevation stream nitrate dynamics

Mountain terrestrial and aquatic ecosystems are responsive to external drivers of change, especially climate change and atmospheric deposition of nitrogen (N). We explored the consequences of a temperature-warming trend on stream nitrate in an alpine and subalpine watershed in the Colorado Front Range that has long been the recipient of elevated atmospheric N deposition. Mean annual stream nitrate concentrations since 2000 are higher by 50% than an earlier monitoring period of 1991-1999. Mean annual N export increased by 28% from 2.03 kg N ha -1 yr -1 before 2000 to 2.84 kg N ha -1 yr -1 in Loch Vale watershed since 2000. The substantial increase in N export comes as a surprise, since mean wet atmospheric N deposition from 1991 to 2006 (3.06 kg N ha -1 yr -1 ) did not increase. There has been a period of below average precipitation from 2000 to 2006 and a steady increase in summer and fall temperatures of 0.12??C yr -1 in both seasons since 1991. Nitrate concentrations, as well as the weathering products calcium and sulfate, were higher for the period 2000-2006 in rock glacier meltwater at the top of the watershed above the influence of alpine and subalpine vegetation and soils. We conclude the observed recent N increases in Loch Vale are the result of warmer summer and fall mean temperatures that are melting ice in glaciers and rock glaciers. This, in turn, has exposed sediments from which N produced by nitrification can be flushed. We suggest a water quality threshold may have been crossed around 2000. The phenomenon observed in Loch Vale may be indicative of N release from ice features such as rock glaciers worldwide as mountain glaciers retreat. ?? 2009 Blackwell Publishing Ltd.

Global Change Biology↗

USGS1983

Eruption-triggered avalanche, flood, and lahar at Mount St. Helens - Effects of winter snowpack

An explosive eruption of Mount St. Helens on 19 March 1982 had substantial impact beyond the vent because hot eruption products interacted with a thick snowpack. A blast of hot pumice, dome rocks, and gas dislodged crater-wall snow that avalanched through the crater and down the north flank. Snow in the crater swiftly melted to form a transient lake, from which a destructive flood and lahar swept down the north flank and the North Fork Toutle River.

Washington↗

USGS2019

Variability in results from mineralogical and organic geochemical interlaboratory testing of U. S. Geological Survey shale reference materials

The expansion of unconventional petroleum resource exploration and production in the United States has led to an increase in source rock characterization efforts, particularly related to bulk organic and mineralogical properties. To support the analytical and research needs of industry and academia, as well as internal work, the U.S. Geological Survey (USGS) has collected and prepared shale geochemical reference materials (GRMs) from several major shale petroleum systems in the U.S. The sources of these materials are the Late Cretaceous Boquillas (lower Eagle Ford-equivalent) Formation (roadcut near Del Rio, TX), Late Cretaceous Mancos Shale (outcrop near Delta, CO), Devonian–Mississippian Woodford Shale (outcrop near Ardmore, OK), Late Cretaceous Niobrara Formation (quarry near Lyons, CO), Middle Devonian Marcellus Shale (creek bed in LeRoy, NY), and Eocene Mahogany zone oil shale of the Green River Formation (oil shale mine near Rifle, CO). Of particular interest in the development of these GRMs has been the examination of variability between laboratories and specific methods or instruments in commonly made measurements, including major- and trace-element concentrations, X-ray diffraction (XRD) mineralogy, total organic carbon (TOC) content, and programmed pyrolysis (PP) parameters. For the component concentrations and parameters we measured, the techniques and instrument types included: (1) elemental analysis by X-ray fluorescence, inductively coupled plasma mass spectrometry, and instrumental neutron activation analysis; (2) XRD mineralogy with various preparatory methods (spray drying or micronizing with or without internal standard); (3) TOC by combustion with infrared detection after carbonate removal or the PP approach; (4) PP by Rock-Eval 2 or more recently developed instruments (Rock-Eval 6, Source Rock Analyzer or SRA, and Hydrocarbon Analyzer With Kinetics or HAWK). Overall, the results showed that the selected shales cover a wide range of source rock organic and mineralogical properties. Major- and trace-element chemistry results showed low heterogeneity consistent with other USGS GRMs. Comparison of TOC results showed coefficients of variation (COV) of around 5% and the most consistent organic geochemical results between different laboratories and methods. Arguably the most relevant PP measurement, S2 or kerogen hydrocarbon-generating potential (mg-HC/g-rock), showed a somewhat wider range of variability than TOC (COV ~10%), but was consistent between the three modern instruments and the industry-standard Rock-Eval 2. Major phase mineralogy (mineral concentrations ≥10 wt. %, organic-free basis) were comparable between laboratories, but variability in minor phase identification and quantification was observed. Utilization of these shale GRMs as quality control samples and testing materials is expected to help support analytical and experimental efforts in the continued development of unconventional petroleum resources.

Colorado, Texas, Oklahoma↗

USGS1998

International strategic mineral issues summary report– Tungsten

Scheelite and wolframite are the principal minerals currently mined for tungsten. Both occur in hard-rock deposits; wolframite is also recovered from placer deposits. Most current mine production of tungsten is from vein/stockwork, skarn, porphyry, and strata-bound deposits. Minor amounts are produced from disseminated, pegmatite, breccia, and placer deposits. Most tungsten is used to make tungsten carbide and tungsten alloys for use in machine tools and drilling equipment. Other important applications are in lamp filaments and cathodes, high-speed steels, textile dyes, paints, and catalysts. The world is well endowed with tungsten resources. China and the former Soviet Union have 8 of the world's 10 largest deposits; these 8 contain about half of the world's resources of tungsten. If economic conditions are suitable, world tungsten resources in known deposits and their extensions (categories R1 and R2), including economic, marginal, and subeconomic resources, are sufficient to permit world production to continue at 1995 levels until well into the 21st century. World tungsten resources in identified deposits and districts that are currently economically exploitable (category R1E) appear to be sufficient to meet world demand at 1995 levels only until the year 2007. However, the figure for resources of this kind does not include or reflect resources whose economic parameters are unknown in major producing areas in the former Soviet Union, China, and other nonmarket-economy countries and thus severely underestimates future tungsten availability. In 1995, China and the former Soviet Union accounted for over three-fourths of the world's mine production of tungsten. China alone produced about two-thirds of world output. Given its vast resources, China will likely maintain its prominent role in world tungsten supply. By the year 2020, changes in supply patterns are likely to result from declining output from individual deposits in Australia, Austria, and Portugal and the opening of new mines in Canada, China, and the United Kingdom.

Circular↗

USGS2026

Spectral characteristics and mapping of lithium-rich playas in the Basin and Range Province, western United States

This report presents a comprehensive set of prospectivity maps for lithium in brines located within the playas of the Basin and Range Province of western United States. The prospectivity assessment is based on criteria established in the descriptive deposit model outlined in a previous U.S. Geological Survey report, with a focus on regional remote sensing methodologies. The playas within the study area have been systematically ranked according to several key factors, including size, the presence and abundance of source rocks, vegetation as an indicator of water availability, documented prospects, and data products derived from the Advanced Spaceborne Thermal Emission and Reflection Radiometer (ASTER) sensor. Notably, the deposits in the playa of Clayton Valley make it stand out as the sole lithium brine-producing playa in the United States. The ASTER sensor provides optimal regional coverage, characterized by a 60-kilometer swath width and unique multispectral capabilities that are not available with other remote sensing instruments. This report and the accompanying maps are intended to serve as resources for further multidisciplinary assessments of lithium or other elements or commodities where prospectivity can be inferred from the presence of proxies such as alteration minerals.

Arizona, Baja California, California, Chihuahua, I↗

USGS2002

PCR und ELISA - Alternativen zum Maustest für die Analyse des Botulismus-Neurotoxin-C1 Giftbildungspotentiales in Umweltproben? [PCR and ELISA - in vitro alternatives to the mouse-bioassay for assessing the botulinum-neurotoxin-C1 production potential in environmental samples?]

Botulism is one of the most important bird diseases world-wide and is caused by the intoxication with Botulinum-Neurotoxin-C1 (BoNt-C1), which is produced by toxigenic clostridia under appropriate conditions. Avian botulism leads regularly to large losses among the migrating bird populations breeding and resting at the saltwater pools of the Austrian national park Neusiedler See-Seewinkel. Despite of its ethical dubiousness and its high technical expense the mouse-bioassay is still used as the routine standard method for the detection of BoNt-C1. According to the 3R-concept, in vitro alternative methods for the qualitative detection of BoNt-C1 (immunostick-ELISA) and a corresponding BoNt-C1 gene fragment (nested-PCR) were established. In order to estimate the BoNt-C1 production potential the methods were tested with sediment samples from different saltwater pools subjected to cultivation conditions appropriate for in vitro BoNt-C1-production. With the mouse-bioassay, 52 out of 77 samples were found to have a positive toxin production potential. The immunostick-ELISA showed a similar sensitivity as the mouse-bioassay and exhibited a highly significant positive correlation (r=0.94; p<0.001) with the mouse-bioassay in detecting BoNt-C1. The nested-PCR approach revealed higher numbers of positive BoNt-C1 gene fragment detections as compared to the direct toxin analysis approaches. A weak correlation (r=0.21; p=0.07) with the mouse-bioassay was discernible, no correlation was found with the immunostick-ELISA (r=0.09; p=0.46). Obviously, the PCR approach detected the BoNt-C1 gene fragment in some of the samples where no toxin expression has occurred. Thus it is suggested that the qualitative immunostick-ELISA represents a potential in vitro alternative to the mouse-bioassay for assessing the BoNt-C1 production potential in environmental samples. In contrast, qualitative BoNt-C1 gene fragment detection via PCR led to an overestimation of the actual toxin production potential.

Neusiedler See-Seewinkel National Park↗

USGS2003

Lithologic mapping in the Mountain Pass, California area using Advanced Spaceborne Thermal Emission and Reflection Radiometer (ASTER) data

Evaluation of an Advanced Spaceborne Thermal Emission and Reflection Radiometer (ASTER) image of the Mountain Pass, California area indicates that several important lithologic groups can be mapped in areas with good exposure by using spectral-matching techniques. The three visible and six near-infrared bands, which have 15-m and 30-m resolution, respectively, were calibrated by using in situ measurements of spectral reflectance. Calcitic rocks were distinguished from dolomitic rocks by using matched-filter processing in which image spectra were used as references for selected spectral categories. Skarn deposits and associated bright coarse marble were mapped in contact metamorphic zones related to intrusion of Mesozoic and Tertiary granodioritic rocks. Fe-muscovite, which is common in these intrusive rocks, was distinguished from Al-muscovite present in granitic gneisses and Mesozoic granite. Quartzose rocks were readily discriminated, and carbonate rocks were mapped as a single broad unit through analysis of the 90-m resolution, five-band surface emissivity data, which is produced as a standard product at the EROS Data Center. Three additional classes resulting from spectral-angle mapper processing ranged from (1) a broad granitic rock class (2) to predominately granodioritic rocks and (3) a more mafic class consisting mainly of mafic gneiss, amphibolite and variable mixtures of carbonate rocks and silicate rocks. ?? 2002 Elsevier Science Inc. All rights reserved.

Remote Sensing of Environment↗

USGS2016

Linking silicate weathering to riverine geochemistry—A case study from a mountainous tropical setting in west-central Panama

Chemical analyses from 71 watersheds across an ∼450 km transect in west-central Panama provide insight into controls on weathering and rates of chemical denudation and CO 2 consumption across an igneous arc terrain in the tropics. Stream and river compositions across this region of Panama are generally dilute, having a total dissolved solute value = 118 ± 91 mg/L, with bicarbonate and silica being the predominant dissolved species. Solute, stable isotope, and radiogenic isotope compositions are consistent with dissolution of igneous rocks present in Panama by meteoric precipitation, with geochemical signatures of rivers largely acquired in their upstream regions. Comparison of a headwater basin with its entire watershed observed considerably more runoff production from the high-elevation upstream portion of the catchment than in its much more spatially extensive downstream region. Rock alteration profiles document that weathering proceeds primarily by dissolution of feldspar and pyroxene, with base cations effectively leached in the following sequence: Na > Ca > Mg > K. Control on water chemistry by bedrock lithology is indicated through a linking of elevated ([Na + K]/[Ca + Mg]) ratios in waters to a high proportion of catchment area silicic bedrock and low ratios to mafic bedrock. Sr-isotope ratios are dominated by basement-derived Sr, with only very minor, if any, contribution from other sources. Cation weathering of Ca sil + Mg sil + Na + K spans about an order in magnitude, from 3 to 32 tons/km 2 /yr. Strong positive correlations of chemical denudation and CO 2 consumption are observed with precipitation, mean watershed elevation, extent of land surface forest cover, and physical erosion rate.

Chagras and Pacora watersheds↗

USGS2010

Gas, oil, and water production from Grand Valley, Parachute, Rulison, and Mamm Creek fields in the Piceance Basin, Colorado

Gas, oil, and water production data for tight gas reservoirs were compiled from selected wells in western Colorado. These reservoir rocks—the relatively shallow Paleogene Wasatch G sandstone interval in the Parachute and Rulison fields and fluvial sandstones in the deeper Upper Cretaceous Mesaverde Group in the Grand Valley, Parachute, Rulison, and Mamm Creek fields—are characterized by low permeability, low porosity, and the presence of clay minerals in pore space. Production from each well is represented by two samples spaced five years apart, the first sample typically taken two years after production commenced, which was generally in the 1990s. For each producing interval, summary diagrams of oil-versus-gas and water-versus-gas production show fluid production rates, the change in rates during five years, the water-gas and oil-gas ratios, and the fluid type. These diagrams permit well-to-well and field-to-field comparisons. Fields producing water at low rates (water dissolved in gas in the reservoir) can be distinguished from fields producing water at moderate or high rates, and the water-gas ratios are quantified. Dry gas is produced from the Wasatch G interval and wet gas is produced from the Mesaverde Group. Production from the Wasatch G interval is also almost completely free of water, but water production commences with gas production in wells producing from the Mesaverde Group—all of these wells have water-gas ratios exceeding the amount that could exist dissolved in gas at reservoir temperature and pressure. The lack of produced water from the Wasatch G interval is attributed to expansion of the gas accumulation with uplift and erosion. The reported underpressure of the Wasatch G interval is here attributed to hydraulic connection to the atmosphere by outcrops in the Colorado River valley at an elevation lower than that of the gas fields. The amount of reduction of gas production over the five-year time span between the first and second samples is roughly one-half, with median values of second-sample to first-sample gas-production ratios ranging from 0.40 for Rulison-Mesaverde to 0.63 for Rulison-Wasatch G. Commencing with the first sample, the logarithm-of-production rate appears to decline linearly with time in many wells. However, water production is much more erratic as a function of time from an individual well and also from one well to the next within a field. Water production can either decrease or increase with time (from the first to the second sample). In this study, slightly more than half the wells producing from the Mesaverde Group show decreases in water production with time. Plots of water decline versus gas decline show little relation between the two, with only the wells in Rulison field displaying some tendency for water and gas to decline proportionately.

Colorado↗

USGS2015

Magmatism and Epithermal Gold-Silver Deposits of the Southern Ancestral Cascade Arc, Western Nevada and Eastern California

Many epithermal gold-silver deposits are temporally and spatially associated with late Oligocene to Pliocene magmatism of the southern ancestral Cascade arc in western Nevada and eastern California. These deposits, which include both quartz-adularia (low- and intermediate-sulfidation; Comstock Lode, Tonopah, Bodie) and quartz-alunite (high-sulfidation; Goldfield, Paradise Peak) types, were major producers of gold and silver. Ancestral Cascade arc magmatism preceded that of the modern High Cascades arc and reflects subduction of the Farallon plate beneath North America. Ancestral arc magmatism began about 45 Ma, continued until about 3 Ma, and extended from near the Canada-United States border in Washington southward to about 250 km southeast of Reno, Nevada. The ancestral arc was split into northern and southern segments across an inferred tear in the subducting slab between Mount Shasta and Lassen Peak in northern California. The southern segment extends between 42°N in northern California and 37°N in western Nevada and was active from about 30 to 3 Ma. It is bounded on the east by the northeast edge of the Walker Lane. Ancestral arc volcanism represents an abrupt change in composition and style of magmatism relative to that in central Nevada. Large volume, caldera-forming, silicic ignimbrites associated with the 37 to 19 Ma ignimbrite flareup are dominant in central Nevada, whereas volcanic centers of the ancestral arc in western Nevada consist of andesitic stratovolcanoes and dacitic to rhyolitic lava domes that mostly formed between 25 and 4 Ma. Both ancestral arc and ignimbrite flareup magmatism resulted from rollback of the shallowly dipping slab that began about 45 Ma in northeast Nevada and migrated south-southwest with time. Most southern segment ancestral arc rocks have oxidized, high potassium, calc-alkaline compositions with silica contents ranging continuously from about 55 to 77 wt%. Most lavas are porphyritic and contain coarse plagioclase ± hornblende, biotite, and pyroxene phenocrysts. Seven epithermal gold-silver deposits with >1 Moz gold production, several large elemental sulfur deposits, and many large areas (10s to >100 km2) of hydrothermally altered rocks are present in the southern ancestral arc, especially south of latitude 40°N. These deposits are principally hosted by intermediate to silicic lava dome complexes; only a few deposits are associated with mafic- to intermediate-composition stratovolcanoes. Large deposits are most abundant and well developed in volcanic fields whose evolution spanned millions of years. Most deposits are hundreds of thousands to several million years younger than their host rocks, although some quartz-alunite deposits are essentially coeval with their host rocks. Variable composition and thickness of crustal basement is the primary control on mineralization along the length of the southern ancestral arc; most deposits and large alteration zones are localized in basement rock terranes with a strong continental affinity, either along the edge of the North American craton (Goldfield, Tonopah) or in an accreted terrane with continental affinities (Walker Lake terrane; Aurora, Bodie, Comstock Lode, Paradise Peak). Epithermal deposits and quartz-alunite alteration zones are scarce to absent in the northern part of the ancestral arc above an accreted island arc (Black Rock terrane) or unknown basement rocks (Modoc Plateau). Walker Lane structures and areas that underwent large magnitude extension during the Late Cenozoic (areas with Oligocene-early Miocene volcanic rocks dipping >40°) do not provide regional control on mineralization. Instead, these features may have served as local-scale conduits for mineralizing fluids.

Eastern California and Western Nevada↗

USGS1990

Organic matter and thermochemical sulfate reduction in the Viburnum Trend, southeast Missouri

The role of organic matter in Mississippi Valley-type Pb-Zn deposits has been studied by systematically sampling and characterizing various types of organic matter in the Upper Cambrian Bonneterre formation in lead-zinc mines from the Viburnum Trend and from rocks as far as 20 km away from the Trend. Organic matter that is several kilometers from ore consists of insoluble disseminated kerogen in carbonates. Kerogen from brown dolostones yields mainly n-alkane pyrolysis products up to approximately n-C 20 H 42 , whereas gray and white carbonates that are poorer in organic carbon give much smaller quantities of pyrolysis products. Within meters to centimeters of ore in the Milliken mine, at the south end of the Viburnum Trend, organic matter occurs as solid, partly soluble tacky bitumen and insoluble hard blebs of millimeter to centimeter size. These hydrocarbon materials also yield n-alkane pyrolysis products up to C 20 . In contrast, the solid insoluble organic matter in intimate contact (intergrown) with ore (galena and chalcopyrite) is friable and brittle. Products from pyrolysis-gas chromatography-mass spectrometry of this material are quite different from the kerogen in rocks or the hydrocarbon blebs; they are substituted aromatic molecules such as toluene and methyl naphthalene, rather than n-alkanes.The sulfur content of solid organic matter from the Milliken mine varies and is lowest for tacky material away from ore, intermediate for blebs near ore, and highest for friable material in intimate contact with ore.Pyrolysis-gas chromatography of this sample suite documents the progression of kerogen (far from ore) through solid petroleumlike material (near ore) to degraded organic matter (in contact with ore). The change in the organic matter from n-alkane to a hydrogen poorer aromatic character with a higher sulfur content when associated with sulfide ores, suggests that chemical reactions such as nonbiological (thermochemical) sulfate reduction, which consume hydrogen and produce reactive sulfur, were responsible for organic degradation.

Economic Geology↗

USGS2006

Hydraulic and solute-transport properties and simulated advective transport of contaminated ground water in a fractured-rock aquifer at the Naval Air Warfare Center, West Trenton, New Jersey, 2003

Volatile organic compounds, predominantly trichloroethylene and its degradation products, have been detected in ground water at the Naval Air Warfare Center (NAWC), West Trenton, New Jersey. An air-stripping pump-and-treat system has been in operation at the NAWC since 1998. An existing ground-water-flow model was used to evaluate the effect of a change in the configuration of the network of recovery wells in the pump-and-treat system on flow paths of contaminated ground water. The NAWC is underlain by a fractured-rock aquifer composed of dipping layers of sedimentary rocks of the Lockatong and Stockton Formations. Hydraulic and solute-transport properties of the part of the aquifer composed of the Lockatong Formation were measured using aquifer tests and tracer tests. The heterogeneity of the rocks causes a wide range of values of each parameter measured. Transmissivity ranges from 95 to 1,300 feet squared per day; the storage coefficient ranges from 9 x 10-5 to 5 x 10-3; and the effective porosity ranges from 0.0003 to 0.002. The average linear velocity of contaminated ground water was determined for ambient conditions (when no wells at the site are pumped) using an existing ground-water-flow model, particle-tracking techniques, and the porosity values determined in this study. The average linear velocity of flow paths beginning at each contaminated well and ending at the streams where the flow paths terminate ranges from 0.08 to 130 feet per day. As a result of a change in the pump-and-treat system (adding a 165-foot-deep well pumped at 5 gallons per minute and reducing the pumping rate at a nearby 41-foot-deep well by the same amount), water in the vicinity of three 100- to 165-foot-deep wells flows to the deep well rather than the shallower well.

New Jersey↗