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Results for “Geochemical Transactions”

Search indexed USGS publications on groundwater, aquifers, geologic maps, mineral resources and earthquakes. Explore source records by subject and place.

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At least 19 recordsLinked to original sources
USGS2003

Sulfur geochemistry of hydrothermal waters in Yellowstone National Park, Wyoming, USA. III. An anion-exchange resin technique for sampling and preservation of sulfoxyanions in natural waters

A sampling protocol for the retention, extraction, and analysis of sulfoxyanions in hydrothermal waters has been developed in the laboratory and tested at Yellowstone National Park and Green Lake, NY. Initial laboratory testing of the anion-exchange resin Bio-Rad??? AG1-X8 indicated that the resin was well suited for the sampling, preservation, and extraction of sulfate and thiosulfate. Synthetic solutions containing sulfate and thiosulfate were passed through AG1-X8 resin columns and eluted with 1 and 3 M KCl, respectively. Recovery ranged from 89 to 100%. Comparison of results for water samples collected from five pools in Yellowstone National Park between on-site IC analysis (U.S. Geological Survey mobile lab) and IC analysis of resin-stored sample at SUNY-Stony Brook indicates 96 to 100% agreement for three pools (Cinder, Cistern, and an unnamed pool near Cistern) and 76 and 63% agreement for two pools (Sulfur Dust and Frying Pan). Attempts to extract polythionates from the AG1-X8 resin were made using HCl solutions, but were unsuccessful. Bio-Rad??? AG2-X8, an anion-exchange resin with weaker binding sites than the AG1-X8 resin, is better suited for polythionate extraction. Sulfate and thiosulfate extraction with this resin has been accomplished with KCl solutions of 0.1 and 0.5 M, respectively. Trithionate and tetrathionate can be extracted with 4 M KCl. Higher polythionates can be extracted with 9 M hydrochloric acid. Polythionate concentrations can then be determined directly using ion chromatographic methods, and laboratory results indicate recovery of up to 90% for synthetic polythionate solutions using AG2-X8 resin columns. ?? The Royal Society of Chemistry and the Division of Geochemistry of the American Chemical Society 2003.

Geochemical Transactions↗
USGS2011

A 50-year record of NOx and SO2 sources in precipitation in the Northern Rocky Mountains, USA

Ice-core samples from Upper Fremont Glacier (UFG), Wyoming, were used as proxy records for the chemical composition of atmospheric deposition. Results of analysis of the ice-core samples for stable isotopes of nitrogen (δ 15 N, ) and sulfur (δ 34 S, ), as well as and deposition rates from the late-1940s thru the early-1990s, were used to enhance and extend existing National Atmospheric Deposition Program/National Trends Network (NADP/NTN) data in western Wyoming. The most enriched δ 34 S value in the UFG ice-core samples coincided with snow deposited during the 1980 eruption of Mt. St. Helens, Washington. The remaining δ 34 S values were similar to the isotopic composition of coal from southern Wyoming. The δ 15 N values in ice-core samples representing a similar period of snow deposition were negative, ranging from -5.9 to -3.2 ‰ and all fall within the δ 15 N values expected from vehicle emissions. Ice-core nitrate and sulfate deposition data reflect the sharply increasing U.S. emissions data from 1950 to the mid-1970s.

Wyoming↗
USGS2012

How to overcome inter-electrode variability and instability to quantify dissolved oxygen, Fe(II), mn(II), and S(−II) in undisturbed soils and sediments using voltammetry

Background - Although uniquely capable of measuring multiple redox constituents nearly simultaneously with no or minimal sample pretreatment, voltammetry is currently underutilized in characterizing redox conditions in aquatic and terrestrial systems. Investigation of undisturbed media such as pore water requires a solid-state electrode, and such electrodes can be difficult to fabricate reproducibly. An approach to determine the concentrations of electroactive constituents using indirectly calibrated electrodes has been developed, but the protocol for and accuracy of this approach—the pilot ion method—has not been documented in detail. Results - A detailed procedure for testing electrode quality is provided, and the application and limitations of the pilot ion method have been documented. To quantify Fe(II) and Mn(II), subtraction of non-linear baseline functions from voltammetric signals produced better calibration curves than did linear baselines, enabled lower detection limits and reliable deconvolution of overlapping signals, and was successfully applied to sediment pore water signals. We observed that electrode sensitivities often vary by tens of percent, and that the sensitivity declines over time. The ratio of calibration slopes of Mn(II) to Fe(II) varied by no more than 11% from one Hg/Au electrode to another and Fe(II) concentrations predicted by the Mn(II) pilot ion were, on average, 13% different from their actual values. However, concentration predictions by the pilot ion method were worse for less than 15 μM Fe(II) (46% different on average). The ratio of calibration slopes of Mn(II) to S(−II) varied by almost 20% from one Hg/Au electrode to another, and S(−II) predicted concentrations were as much as 58% different from their actual values. These predictions of Fe(II) and S(−II) concentrations indicate that the accuracy of the pilot ion method depends on how independent calibration slope ratios are from the electrode used. At medium-to-high concentration for the ocean, naturally derived dissolved organic carbon did not significantly affect the baseline-corrected electrode response of Mn(II) and Fe(II), but did significantly affect the response of S(−II). Conclusions - Despite their intrinsic variability, Hg/Au electrodes fabricated by hand can be used to quantify O2, S(−II), Fe(II), and Mn(II) without calibrating every electrode for every constituent of interest. The pilot ion method can achieve accuracies to within 20% or less, provided that the underlying principle—the independence of slope ratios—is demonstrated for all voltammetric techniques used, and effects of the physicochemical properties of the system on voltammetric signals are addressed through baseline subtraction.

Geochemical Transactions↗
USGS2007

Microbial sulfate reduction and metal attenuation in pH 4 acid mine water

Sediments recovered from the flooded mine workings of the Penn Mine, a Cu-Zn mine abandoned since the early 1960s, were cultured for anaerobic bacteria over a range of pH (4.0 to 7.5). The molecular biology of sediments and cultures was studied to determine whether sulfate-reducing bacteria (SRB) were active in moderately acidic conditions present in the underground mine workings. Here we document multiple, independent analyses and show evidence that sulfate reduction and associated metal attenuation are occurring in the pH-4 mine environment. Water-chemistry analyses of the mine water reveal: (1) preferential complexation and precipitation by H2S of Cu and Cd, relative to Zn; (2) stable isotope ratios of 34S/32S and 18O/16O in dissolved SO4 that are 2-3 ??? heavier in the mine water, relative to those in surface waters; (3) reduction/oxidation conditions and dissolved gas concentrations consistent with conditions to support anaerobic processes such as sulfate reduction. Scanning electron microscope (SEM) analyses of sediment show 1.5-micrometer, spherical ZnS precipitates. Phospholipid fatty acid (PLFA) and denaturing gradient gel electrophoresis (DGGE) analyses of Penn Mine sediment show a high biomass level with a moderately diverse community structure composed primarily of iron- and sulfate-reducing bacteria. Cultures of sediment from the mine produced dissolved sulfide at pH values near 7 and near 4, forming precipitates of either iron sulfide or elemental sulfur. DGGE coupled with sequence and phylogenetic analysis of 16S rDNA gene segments showed populations of Desulfosporosinus and Desulfitobacterium in Penn Mine sediment and laboratory cultures. ?? 2007 Church et al; licensee BioMed Central Ltd.

Geochemical Transactions↗
USGS2011

The U.S. Geological Survey's gravity program in the Rocky Mountain and Basin Range areas

Most of the gravity surveys of the U.S. Geological Survey have been support programs in connection with regional geologic structural studies, ground-water investigations, and heavy-metals exploration. Many of the studies were undertaken in conjunction with geological mapping and mineral investigations by the Survey's project geologists. Gravity data often complement aeromagnetic surveys to identify the sources of potential-field anomalies; other gravity data have been used to supplement high-resolution seismic and electrical investigations [ Mattick , 1967]. Geochemical follow-up has been fruitful in western Montana [ Mudge et al, 1967].

Arizona, Colorado, Idaho, Montana, Nevada, New Mex↗
USGS2014

A graphic procedure in the geochemical interpretation of water‐analyses

This paper outlines certain fundamental principles in a graphic procedure which appears to be an effective tool in segregating analytical data for critical study with respect to sources of the dissolved constituents in waters, modifications in the character of a water as it passes through an area, and related geochemical problems. The procedure is based on a multiple‐trilinear diagram (Fig. 1) whose form has been evolved gradually and independently by the writer during the past several years through trial and modification of less comprehensive antecedent forms. Neither the diagram nor the procedure here described is a panacea for the easy solution of all geochemical problems. Many problems of interpretation can be answered only by intensive study of critical analytical data by other methods.

Eos, Transactions, American Geophysical Union↗
USGS2017

Geochemical and mineralogical characterization of the Eagle Ford Shale: Results from the USGS Gulf Coast #1 West Woodway core

The Eagle Ford shale is a major continuous oil and gas resource play in southcentral Texas and a source for other oil accumulations in the East Texas Basin. As part of the U.S. Geological Survey’s (USGS) petroleum system assessment and research efforts, a coring program to obtain several immature, shallow cores from near the outcrop belt in central Texas has been undertaken. The first of these cores, USGS Gulf Coast #1 West Woodway, was collected near Waco, Texas, in September 2015 and has undergone extensive geochemical and mineralogical characterization using routine methods to ascertain variations in the lithologies and chemofacies present in the Eagle Ford at this locale. Approximately 270 ft of core was examined for this study, focusing on the Eagle Ford Group interval between the overlying Austin Chalk and underlying Buda Limestone (~20 ft of each). Based on previous work to identify the stratigraphy of the Eagle Ford Group in the Waco area and elsewhere (Liro et al., 1994; Robison, 1997; Ratcliffe et al., 2012; Boling and Dworkin, 2015; Fairbanks et al., 2016, and references therein), several lithological units were expected to be present, including the Pepper Shale (or Woodbine), the Lake Waco Formation (or Lower Eagle Ford, including the Bluebonnet, Cloice, and Bouldin or Flaggy Cloice members), and the South Bosque Member (Upper Eagle Ford). The results presented here indicate that there are three major chemofacies present in the cored interval, which are generally consistent with previous descriptions of the Eagle Ford Group in this area. The relatively high-resolution sampling (every two ft above the Buda, 432.8 ft depth, and below the Austin Chalk, 163.5 ft depth) provides great detail in terms of geochemical and mineralogical properties supplementing previous work on immature Eagle Ford Shale near the outcrop belt.

Gulf Coast Association of Geological Societies Tra↗
USGS2011

New episodes of volcanism at Kilauea Volcano, Hawaii

Mid‐2007 was a time of intense activity at Kilauea Volcano, Hawaii (see Figure 1). In June, the long‐lived Pu'u 'Ō'ō—Kupaianaha eruption, a dual‐vent system along the east rift zone (ERZ) that has been erupting since 1983 [Heliker et al., 2003], paused due to the outbreak of a new vent farther up the rift (see Figure 2). The Pu'u 'Ō'ō vent collapsed following that activity, and the resulting reorganization of the magma plumbing system led to the formation of a second new eruptive vent 2 kilometers downrift of Pu'u 'Ō'ō. These events were well documented by geological, geophysical, and geochemical monitoring. This article summarizes results from these monitoring efforts and interprets the changes that have occurred at Kilauea since June 2007.

Hawaii↗
USGS2012

Mapping temperature and radiant geothermal heat flux anomalies in the Yellowstone geothermal system using ASTER thermal infrared data

The purpose of this work was to use satellite-based thermal infrared (TIR) remote sensing data to measure, map, and monitor geothermal activity within the Yellowstone geothermal area to help meet the missions of both the U.S. Geological Survey Yellowstone Volcano Observatory and the Yellowstone National Park Geology Program. Specifically, the goals were to: 1) address the challenges of remotely characterizing the spatially and temporally dynamic thermal features in Yellowstone by using nighttime TIR data from the Advanced Spaceborne Thermal Emission and Reflection Radiometer (ASTER) and 2) estimate the temperature, geothermal radiant emittance, and radiant geothermal heat flux (GHF) for Yellowstone’s thermal areas (both Park wide and for individual thermal areas). ASTER TIR data (90-m pixels) acquired at night during January and February, 2010, were used to estimate surface temperature, radiant emittance, and radiant GHF from all of Yellowstone’s thermal features, produce thermal anomaly maps, and update field-based maps of thermal areas. A background subtraction technique was used to isolate the geothermal component of TIR radiance from thermal radiance due to insolation. A lower limit for the Yellowstone’s total radiant GHF was established at ~2.0 GW, which is ~30-45% of the heat flux estimated through geochemical (Cl-flux) methods. Additionally, about 5 km 2 was added to the geodatabase of mapped thermal areas. This work provides a framework for future satellite-based thermal monitoring at Yellowstone as well as exploration of other volcanic / geothermal systems on a global scale.

Wyoming↗
USGS1970

Nuclear methods applied to uranium geochemistry

Stable and radioactive daughter products produced from nuclear disintegrations of uranium have proved useful in fundamental studies of the geochemistry of uranium in igneous rock and sedimentary environments and in ore deposits. Information gained from geochemical studies of uranium migration has been used to develop models for attempts to date archeological, geological, and oceanographic environments represented by samples of bone, wood, charcoal, continental and marine carbonates, marine sediments, and glacially derived soils. Recent improvements of nuclear instrumentation and techniques allowed accurate measurements of natural radioactive isotopes, and it is now believed that radioactive equilibrium between the long-lived isotopes of the two uranium decay series is more the exception than the rule in nature. It was assumed that the 234U and 238U isotopes were in equilibrium until Thurber confirmed that considerable separation between 234U daughter and 238U parent exists in nature. It now has been documented that the 234U content may range from 60% deficient to 500% in excess relative to 238U. An excess of 15% of 234U isotope in sea water is well documented. A summary of previous work has shown that geochemical fractionation of the radioactive nuclides in 238U and 235U decay series takes place in the hydrologic environment, resulting in depletion of 230Th and 231Pa with respect to their parents, 238U, 234U, and 235U, in water and a complementary enrichment of these daughter nuclides in some sediments. Subsequent assimilation of Uranium, essentially free of radioactive daughters, occurs in some specific types of deposits such as carbonates and phosphates.

IEEE Transactions on Nuclear Science↗
USGS2014

A study of salt‐water encroachment in the Galveston Area, Texas

A survey of the ground‐ water resources of the region in which Houston and Galveston are situated was started in December 1930 by the United States Geological Survey in cooperation with the Texas Board of Water Engineers. In connection with this survey a special study is being made of the geochemical relations of the ground‐waters of an area about 25 miles wide and 90 miles long, extending from Galveston northwestward through Houston. This study considers the influence on the ground‐waters of the age and degree of weathering of the outcrop formations, base‐exchange materials, salt ‐domes, and salt ‐ water encroachment . In this paper, however, attention is confined to salt ‐ water encroachment along the line from Galveston to Houston (Fig. 1).

Texas↗
USGS2005

Wilcox group coal-bed methane in north-central Louisiana

Significant coal-bed gas resources may exist in subsurface Wilcox Group (Paleocene-Eocene) coal beds that are found across much of north-central Louisiana. About a dozen wells recently completed in Wilcox Group coal zones in this area have an initial production that ranges from 7 to 229 thousand cubic feet (Mcf) of gas per day. Production of saline water from these wells ranges from 0 to 550 barrels (bbls) per day. Depth to the targeted Wilcox coal beds, which have a maximum thickness of about 20 ft, ranges from 1,500 to 5,000 ft. The thickest coal beds tend to be in the lower Wilcox coal zone. Cumulative Wilcox coal thickness can exceed 100 ft. Measured gas content of the coal beds ranges from less than 40 standard cubic ft per ton (scf/t, raw basis; or 65 scf/t dry, ash free basis, daf) at depths less than 1,600 ft, to greater than 158 scf/t (213 scf/t daf) in deeper (>2,700 ft) parts of the basin. Although geochemical and petrographic data from Wilcox Group coals from across the region show that the coal beds are lignite in rank at depths less than about 350 ft, they reach a rank of subbituminous B, or greater, at depths of approximately 2,500 ft. Preliminary gas isotope data indicate that Wilcox coal gas originated from the microbial reduction of CO 2 and that, in some places, these gases may be mixed with migrated thermal gases.

Louisiana↗
USGS1999

Compilation of gas geochemistry and isotopic analyses from The Geysers geothermal field: 1978-1991

We present 45 chemical and isotopic analyses from well discharges at The Geysers geothermal field and summarize the most notable geochemical trends. H 2 and H 2 S concentrations are highest in the Southeast Geysers, where steam samples have δD and δ 18 O values that reflect replenishment by meteoric water. In the Northwest Geysers, samples are enriched in gas/steam, CO 2 , CH 4 , and N 2 /Ar relative to the rest of the field, and contain steam that is elevated in δD and δ18O, most likely due to substantial contributions from Franciscan-derived fluids. The δ13C of CO 2 , trends in CH 4 vs. N 2 , and abundance of NH 3 indicate that the bulk of the non-condensable gases are derived from thermal breakdown of organic materials in Franciscan meta-sediments.

Geothermal Resources Council Transactions↗
USGS2020

Mariana serpentinite mud volcanism exhumes subducted seamount materials: Implications for the origin of life

The subduction of seamounts and ridge features at convergent plate boundaries plays an important role in the deformation of the overriding plate and influences geochemical cycling and associated biological processes. Active serpentinization of forearc mantle and serpentinite mud volcanism on the Mariana forearc (between the trench and active volcanic arc) provides windows on subduction processes. Here, we present (1) the first observation of an extensive exposure of an undeformed Cretaceous seamount currently being subducted at the Mariana Trench inner slope; (2) vertical deformation of the forearc region related to subduction of Pacific Plate seamounts and thickened crust; (3) recovered Ocean Drilling Program and International Ocean Discovery Program cores of serpentinite mudflows that confirm exhumation of various Pacific Plate lithologies, including subducted reef limestone; (4) petrologic, geochemical and paleontological data from the cores that show that Pacific Plate seamount exhumation covers greater spatial and temporal extents; (5) the inference that microbial communities associated with serpentinite mud volcanism may also be exhumed from the subducted plate seafloor and/or seamounts; and (6) the implications for effects of these processes with regard to evolution of life.

Philosophical Transactions of the Royal Society A:↗
USGS2011

Relationships between silicic plutonism and volcanism: Geochemical evidence

Field associations (voluminous ash flow deposits, rhyolitic stocks and dykes, ring complexes), evidence of repeated influxes of mafic magma, and thermal constraints indicate that many high-level silicic plutons (magma chambers) acted as open systems for considerable parts of their history. The long thermal lifetime, as well as other evidence from the volcanic record, suggests that some such systems reached a quasi-steady state in which magma input was balanced by magma output for times longer than those required for crystallisation. Reconstruction of the evolution of large, long-lived caldera-forming systems, such as that of the Jemez Mountains, New Mexico, indicates that many chambers have lost a highly fractionated silicic cap, in some cases cyclically. Crystallised plutons may contain no obvious record of this evolutionary phase. Geochemical data from silicic ash flow deposits can be used to reconstruct the volcanic stage of pluton development. Many silicic systems, especially of alkaline affinity, apparently pass from a stage in which melt evolution is dominated by crystal-liquid processes to one in which other processes may also contribute to differentiation. Apparently, the transition is most readily achieved in volatile-rich, alkaline silicic systems emplaced in complex, ancient sialic crust of the cratons. Once established, the preservation of highly fractionated caps on magma chambers requires a balance between thermal input and cooling-induced crystallisation. If heat enters the system too quickly, the cap may get stirred into the dominant magma volume by convection. If heat input is too slow, the magma body will crystallise inward from the margins, and the plutonic-consolidation stage will begin. © 1988, Royal Society of Edinburgh. All rights reserved.

Transactions of the Royal Society of Edinburgh, Ea↗
USGS2012

Preliminary evaluation of the shale gas prospectivity of the Lower Cretaceous Pearsall Formation in the onshore Gulf Coast region, United States

Recent work by the U.S. Geological Survey indicated that the Lower Cretaceous Pearsall Formation contains an estimated mean undiscovered, technically recoverable unconventional gas resource of 8.8 trillion cubic ft in the Maverick Basin, South Texas. Cumulative gas production from horizontal wells in the core area of the emerging play has exceeded 5 billion cubic ft since 2008. However, very little information is available to characterize the Pearsall Formation as an unconventional gas resource beyond the Maverick Basin in the greater Gulf Coast region. Therefore, this reconnaissance study examines spatial distribution, thickness, organic richness and thermal maturity of the Pearsall Formation in the onshore U.S. Gulf states using wireline logs and drill cuttings sample analysis. Spontaneous potential and resistivity curves of approximately forty wireline logs from wells in five Gulf Coast states were correlated to ascertain the thickness of the Pearsall Formation and delineate its three members: Pine Island Shale, James Limestone or Cow Creek Limestone, and Bexar Shale, in ascending stratigraphic order. In Florida and Alabama the Pearsall Formation is up to about 300 ft thick; in Mississippi, Louisiana, Arkansas, and East Texas, thickness is up to as much as 800 ft. Drill cuttings sampled from 11 wells at depths ranging from 4600 to 19,600 feet subsurface indicate increasingly oxygenated depositional environments (predominance of red shale) towards the eastern part of the basin. Cuttings vary widely in lithology but indicate interbedded clastics and limestones throughout the Pearsall Formation, consistent with previous regional studies. Organic petrographic and geochemical analyses of 17 cutting samples in the Pearsall Formation indicate a wide range in thermal maturity, from immature (0.43% Ro [vitrinite reflectance]) in paleo-high structural locations to the peak oil window (0.99% Ro) in the eastern portion of the Gulf Coast Basin. This is in contrast to dry gas thermal maturity throughout the Pearsall Formation in the South Texas Maverick Basin. Organic carbon content is low overall, even in immature samples, with a range of 0.17 to 1.08 wt.% by Leco in 22 Pearsall Formation samples. The pyrolysis output range was 0.23 to 2.33 mg hydrocarbon/g rock. The thermal maturity and Rock-Eval pyrolysis data and organic petrologic observations from this study will be used to better focus specific areas of investigation where the Pearsall Formation may be prospective as an unconventional hydrocarbon source and reservoir.

Alabama;Arkansas;Louisiana;Mississippi;Oklahoma;Te↗
USGS1979

Geochemical surveys in the United States in relation to health.

Geochemical surveys in relation to health may be classified as having one, two or three dimensions. One-dimensional surveys examine relations between concentrations of elements such as Pb in soils and other media and burdens of the same elements in humans, at a given time. The spatial distributions of element concentrations are not investigated. The primary objective of two-dimensional surveys is to map the distributions of element concentrations, commonly according to stratified random sampling designs based on either conceptual landscape units or artificial sampling strata, but systematic sampling intervals have also been used. Political units have defined sample areas that coincide with the units used to accumulate epidemiological data. Element concentrations affected by point sources have also been mapped. Background values, location of natural or technological anomalies and the geographic scale of variation for several elements often are determined. Three-dimensional surveys result when two-dimensional surveys are repeated to detect environmental changes. -Author

Philosophical Transactions of the Royal Society B:↗