Geology topics

N.C. Sturchio

Publications and source records attributed to N.C. Sturchio.

10 recordsLinked to original sources

USGS2017

Uranium-Series Ages of Travertines and Timing of the Last Glaciation in the Northern Yellowstone Area, Wyoming-Montana

Uranium-series age determinations by mass spectrometric methods were done for travertines and associated carbonate veins related to clastic deposits of the last glaciation (Pinedale) in the northern Yellowstone area. Dramatic variations in the hydrologic head are inferred from variations in the elevation of travertine deposition with time and are consistent with the expected hydrologic effects of glaciation. We determine the following chronology of the Pinedale Glaciation, with the key assumption that travertine deposits (and associated carbonate veins) perched high above present thermal springs were deposited when glaciers filled the valley below these perched deposits: (1) the early Pinedale outlet glacier advanced well downvalley between 47,000 and 34,000 yr B.P.; (2) the outlet glacier receded to an interstadial position between 34,000 and 30,000 yr B.P.; (3) an extensive Pinedale ice advance occurred between 30,000 and 22,500 yr B.P.; (4) a major recession occurred between 22,500 and 19,500 yr B.P.; (5) a minor readvance (Deckard Flats) culminated after 19,500 yr B.P.; and (6) recession from the Deckard Flats position was completed before 15,500 yr B.P. This chronology is consistent with the general trend of climatic changes in the northern hemisphere as revealed by recent high-resolution ice-core records from the Greenland ice sheet.

Quaternary Research↗

USGS2009

Chlorine-36 as a tracer of perchlorate origin

Perchlorate (ClO 4 − ) is ubiquitous in the environment. It is produced naturally by atmospheric photochemical reactions, and also is synthesized in large quantities for military, aerospace, and industrial applications. Nitrate-enriched salt deposits of the Atacama Desert (Chile) contain high concentrations of natural ClO 4 − , and have been exported worldwide since the mid-1800s for use in agriculture. The widespread introduction of synthetic and agricultural ClO 4 − into the environment has contaminated numerous municipal water supplies. Stable isotope ratio measurements of Cl and O have been applied for discrimination of different ClO 4 − sources in the environment. This study explores the potential of 36 Cl measurements for further improving the discrimination of ClO 4 − sources. Groundwater and desert soil samples from the southwestern United States (U.S.) contain ClO 4 − having high 36 Cl abundances ( 36 Cl/Cl = 3100 × 10 −15 to 28,800 × 10 −15 ), compared with those from the Atacama Desert ( 36 Cl/Cl = 0.9 × 10 −15 to 590 × 10 −15 ) and synthetic ClO 4 − reagents and products ( 36 Cl/Cl = 0.0 × 10 −15 to 40 × 10 −15 ). In conjunction with stable Cl and O isotope ratios, 36 Cl data provide a clear distinction among three principal ClO 4 − source types in the environment of the southwestern U.S.

Environmental Science & Technology↗

USGS2009

Fractionation of stable isotopes in perchlorate and nitrate during in situ biodegradation in a sandy aquifer

An in situ experiment was performed in a shallow alluvial aquifer in Maryland to quantify the fractionation of stable isotopes in perchlorate (Cl and O) and nitrate (N and O) during biodegradation. An emulsified soybean oil substrate that was previously injected into this aquifer provided the electron donor necessary for biological perchlorate reduction and denitrification. During the field experiment, groundwater extracted from an upgradient well was pumped into an injection well located within the in situ oil barrier, and then groundwater samples were withdrawn for the next 30 h. After correction for dilution (using Br– as a conservative tracer of the injectate), perchlorate concentrations decreased by 78% and nitrate concentrations decreased by 82% during the initial 8.6 h after the injection. The observed ratio of fractionation effects of O and Cl isotopes in perchlorate (e18O/e37Cl) was 2.6, which is similar to that observed in the laboratory using pure cultures (2.5). Denitrification by indigenous bacteria fractionated O and N isotopes in nitrate at a ratio of ~0.8 (e18O/e15N), which is within the range of values reported previously for denitrification. However, the magnitudes of the individual apparent in situ isotope fractionation effects for perchlorate and nitrate were appreciably smaller than those reported in homogeneous closed systems (0.2 to 0.6 times), even after adjustment for dilution. These results indicate that (1) isotope fractionation factor ratios (e18O/e37Cl, e18O/e15N) derived from homogeneous laboratory systems (e.g. pure culture studies) can be used qualitatively to confirm the occurrence of in situ biodegradation of both perchlorate and nitrate, but (2) the magnitudes of the individual apparent e values cannot be used quantitatively to estimate the in situ extent of biodegradation of either anion.

Environmental Chemistry↗

USGS2005

Perchlorate isotope forensics

Perchlorate has been detected recently in a variety of soils, waters, plants, and food products at levels that may be detrimental to human health. These discoveries have generated considerable interest in perchlorate source identification. In this study, comprehensive stable isotope analyses ( 37 Cl/ 35 Cl and 18 O/ 17 O/ 16 O) of perchlorate from known synthetic and natural sources reveal systematic differences in isotopic characteristics that are related to the formation mechanisms. In addition, isotopic analyses of perchlorate extracted from groundwater and surface water demonstrate the feasibility of identifying perchlorate sources in contaminated environments on the basis of this technique. Both natural and synthetic sources of perchlorate have been identified in water samples from some perchlorate occurrences in the United States by the isotopic method.

Analytical Chemistry↗

USGS2004

Mars chronology: Assessing techniques for quantifying surficial processes

Currently, the absolute chronology of Martian rocks, deposits and events is based mainly on crater counting and remains highly imprecise with epoch boundary uncertainties in excess of 2 billion years. Answers to key questions concerning the comparative origin and evolution of Mars and Earth will not be forthcoming without a rigid Martian chronology, enabling the construction of a time scale comparable to Earth's. Priorities for exploration include calibration of the cratering rate, dating major volcanic and fluvial events and establishing chronology of the polar layered deposits. If extinct and/or extant life is discovered, the chronology of the biosphere will be of paramount importance. Many radiometric and cosmogenic techniques applicable on Earth and the Moon will apply to Mars after certain baselines (e.g. composition of the atmosphere, trace species, chemical and physical characteristics of Martian dust) are established. The high radiation regime may pose a problem for dosimetry-based techniques (e.g. luminescence). The unique isotopic composition of nitrogen in the Martian atmosphere may permit a Mars-specific chronometer for tracing the time-evolution of the atmosphere and of lithic phases with trapped atmospheric gases. Other Mars-specific chronometers include measurement of gas fluxes and accumulation of platinum group elements (PGE) in the regolith. Putting collected samples into geologic context is deemed essential, as is using multiple techniques on multiple samples. If in situ measurements are restricted to a single technique it must be shown to give consistent results on multiple samples, but in all cases, using two or more techniques (e.g. on the same lander) will reduce error. While there is no question that returned samples will yield the best ages, in situ techniques have the potential to be flown on multiple missions providing a larger data set and broader context in which to place the more accurate dates. ?? 2004 Elsevier B.V. All rights reserved.

Earth-Science Reviews↗

USGS1993

Radium isotope geochemistry of thermal waters, Yellowstone National Park, Wyoming, USA

Radium isotope activities ( 226 Ra, 228 Ra, and 224 Ra), chemical compositions, and sulfur isotope ratios in sulfate were determined for water samples from thermal areas in Yellowstone National Park, Wyoming. Activities of 226 Ra in these waters range from <0.2 to 37.9 dpm/kg. Activity ratios of 228 Ra 226 Ra "> 228Ra226Ra range from 0.26 to 14.2, and those of 224 Ra 228 Ra "> 224Ra228Ra range from 0.73 to 3.1. Radium concentrations are inversely correlated with aquifer equilibration temperatures (estimated from dissolved silica concentrations), while[ Ra Ba "> RaBa ] aq and 228 Ra 226 Ra "> 228Ra226Ra activity ratios depend upon U Ba "> UBa and Th U "> ThU ratios in aquifer rocks. Major controls on Ra concentration in Yellowstone thermal waters are inferred to be 1. (1) barite saturation (at Morris Geyser Basin, Mammoth Hot Springs, and other northern areas) and 2. (2) zeolitewater ion exchange (at Upper Geyser Basin). The data are consistent with a model in which 3. (1) radium and barium are supplied to water by bulk dissolution of aquifer rock, and 4. (2) chemical equilibration of water with rock is rapid relative to the 1602 year half-life of 226 Ra. The 228 Ra 226 Ra "> 228Ra226Ra activity ratios of the waters may in some cases reflect surface enrichments of 232 Th and/or may indicate that α-recoil input of 228 Ra is rapid relative to water-rock chemical equilibration. Activity ratios of 224 Ra 228 Ra "> 224Ra228Ra indicate a nearly ubiquitous 224 Ra excess that generally increases with decreasing pH. Near-surface (≤100 m) thermal water flow velocities at Mammoth Hot Springs are estimated from 224 Ra 228 Ra "> 224Ra228Ra variation to be ≥ 1 m h −1 .

Wyoming↗

USGS1991

New evidence on the hydrothermal system in Long Valley caldera, California, from wells, fluid sampling, electrical geophysics, and age determinations of hot-spring deposits

Data collected since 1985 from test drilling, fluid sampling, and geologic and geophysical investigations provide a clearer definition of the hydrothermal system in Long Valley caldera than was previously available. This information confirms the existence of high-temperature (> 200??C) reservoirs within the volcanic fill in parts of the west moat. These reservoirs contain fluids which are chemically similar to thermal fluids encountered in the central and eastern parts of the caldera. The roots of the present-day hydrothermal system (the source reservoir, principal zones of upflow, and the magmatic heat source) most likely occur within metamorphic basement rocks beneath the western part of the caldera. Geothermometer-temperature estimates for the source reservoir range from 214 to 248??C. Zones of upflow of hot water could exist beneath the plateau of moat rhyolite located west of the resurgent dome or beneath Mammoth Mountain. Lateral flow of thermal water away from such upflow zones through reservoirs in the Bishop Tuff and early rhyolite accounts for temperature reversals encountered in most existing wells. Dating of hot-spring deposits from active and inactive thermal areas confirms previous interpretations of the evolution of hydrothermal activity that suggest two periods of extensive hot-spring discharge, one peaking about 300 ka and another extending from about 40 ka to the present. The onset of hydrothermal activity around 40 ka coincides with the initiation of rhyolitic volcanism along the Mono-Inyo Craters volcanic chain that extends beneath the caldera's west moat. ?? 1991.

Journal of Volcanology and Geothermal Research↗

USGS1990

Geochemistry of reduced gas related to serpentinization of the Zambales ophiolite, Philippines

Methane-hydrogen gas seeps with mantle-like C and noble gas isotopic characteristics issue from partially serpentinized ultramafic rocks in the Zambales ophiolite, Philippines. New measurements of noble gas and 14 C isotope abundances, rock/mixed-volatile equilibrium calculations, and previous chemical and isotopic data suggest that these reduced gases are products of periodotite hydration. The gas seeps are produced in rock-dominated zones of serpentinization, and similar gases may be ubiquitous in ultramafic terranes undergoing serpentinization.

Applied Geochemistry↗

USGS1990

Geothermal systems within the Mammoth Corridor in Yellowstone National Park and the adjacent Corwin Springs KGRA

A study of potential impacts of geothermal development in the Corwin Springs KGRA north of Yellowstone Park on thermal springs within the Park is being conducted by the U.S. Geological Survey. Thermal waters in the KGRA and at Mammoth Hot Springs, located 13 km inside the Park boundary, are high in bicarbonate and sulfate and are actively depositing travertine. These similarities and the existence of numerous regional-scale structural and stratigraphic features that could provide conduits for fluid flow at depth indicate a possible cause for concern. The objectives of this study include delineations of any hydrologic connections between these thermal waters, the level of impact of geothermal development in the event of such connections, and mitigation measures to minimize or eliminate adverse impacts. The study involves a number of geochemical, geophysical, geologic, and hydrologic techniques, but does not include any test drilling. Preliminary results suggest that thermal waters at Bear Creek Springs may contain a component of water derived from Mammoth but that thermal waters at La Duke Hot Spring do not. The total rate of thermal water that discharges in the area proposed for geothermal development (near La Duke) has been determined; restricting the net production of thermal water to rates less than this total could provide a satisfactory margin of safety for development.

Conference Paper↗

USGS1990

Oxygen and carbon isotope ratios of hydrothermal minerals from Yellowstone drill cores

Oxygen and carbon isotope ratios were measured for hydrothermal minerals (silica, clay and calcite) from fractures and vugs in altered rhyolite, located between 28 and 129 m below surface (in situ temperatures ranging from 81 to 199??C) in Yellowstone drill holes. The purpose of this study was to investigate the mechanism of formation of these minerals. The ??18O values of the thirty-two analyzed silica samples (quartz, chalcedony, ??-cristobalite, and ??-cristobalite) range from -7.5 to +2.8???. About one third of the silica 7samples have ??18O values that are consistent with isotopic equilibrium with present thermal waters; most of the other silica samples appear to have precipitated from water enriched in 18O (up to 4.7???) relative to present thermal water, assuming precipitation at present in situ temperatures. Available data on fluid-inclusion homogenization temperatures in hydrothermal quartz indicate that silica precipitation occurred mostly at temperatures above those measured during drilling and imply that 15O enrichments in water during silica precipitation were generally larger than those estimated from present conditions. Similarly, clay minerals (celadonite and smectite) have ??18O values higher (by 3.5 to 7.9???) than equilibrium values under present conditions. In contrast, all eight analyzed calcite samples are close to isotopic equilibrium with present thermal waters. The frequent incidence of apparent 18O enrichment in thermal water from which the hydrothermal minerals precipitated may indicate that a higher proportion of strongly 18O-enriched deep hydrothermal fluid once circulated through shallow portions of the Yellowstone system, or that a recurring transient 18O-enrichment effect occurs at shallow depths and is caused either by sudden decompressional boiling or by isotopic exchange at low water/rock ratios in new fractures. The mineralogy and apparent 18O enrichments of hydrothermal fracture-filling minerals are consistent with deposition during transient boiling or rock-water exchange (fracturing) events. ?? 1990.

Journal of Volcanology and Geothermal Research↗