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At least 1,423 records · Page 79Linked to original sources
USGS1991

Geohydrologic, geochemical, and geologic controls on the occurrence of radon in ground water near Conifer, Colorado, USA

Integrated studies of geohydrology, geochemistry, and geology of crystalline rocks in the vicinity of Conifer, Colorado, reveal that radon concentrations do not correlate with variations in concentrations of other dissolved species. Concentrations of major ions show systematic variations along selected groundwater flowpaths, whereas radon concentrations are dependent on local geochemical and geologic phenomena (such as localized uranium concentration in the rock or the presence of faults or folds). When radon enters the flow system, concentrations do not increase along flowpaths because its decay rate is fast relative to groundwater flow rates. Radon-222 is not in secular equilibrium with 238 U and 226 Ra in the water. Therefore, most of the 238 U and 226 Ra necessary to support the waterborne 222 Rn must be present locally in the rock. High concentrations of dissolved radon are not found in zones of high transmissivity, and transmissivity is not correlated with rock type in the study area. A higher transmissivity can be indicative of higher water-volume to rock-surface-area ratios, which could effectively dilute 222 Rn entering the water and/or may indicate that emanated radon is carried away more rapidly. Water samples collected from individual wells over periods of several months showed significant fluctuations in the dissolved 222 Rn content. This fluctuation may be controlled by changes in the contributions of water-producing zones within the well resulting from seasonal fluctuations of the water table and/or pumping stresses.

Colorado↗
USGS1961

Mineralogy and geochemistry of vanadium in the Colorado Plateau

The chief domestic source of vanadium is uraniferous sandstone in the Colorado Plateau. Vanadium is 3-, 4-, or 5-valent in nature and, as oxides or combined with other elements, it forms more than 40 minerals in the Plateau ores. These ores have been studied with regard to the relative amounts of vanadium silicates and oxide-vanadates, uranium-vanadium ratios, the progressive oxidation of black low-valent ores to high-valent carnotite-type ores, and theories of origin.

Arizona, Colorado, New Mexico, Utah↗
USGS1982

Age determination of late Pleistocene marine transgression in western Alaska

Dating molluscs from sediments representing the Kotzebuan marine transgression in Alaska yields an average uranium-series age of 104,000 ± 22,000 yrs B.P. This and other selected Pleistocene marine deposits of western Alaska are tentatively correlated with radiometrically dated units of eastern Baffin Island, Arctic Canada.

Alaska↗
USGS1991

Dating lacustrine episodes in the eastern Sahara by the epimerization of isoleucine in ostrich eggshells

The eggshell of the African ostrich, Struthio camelus , closely approximates a closed system for the retention of indigenous proteinaceous residues. Epimerization of the protein amino acid isoleucine follows linear first-order kinetics in laboratory simulations nearly to racemic equilibrium, and the variation in D/L ratio within a single fragment, or between fragments of the same age, is significantly less than in other carbonate systems. These observations suggest that the extent of isoleucine epimerization (aIle/Ile ratio) in ostrich eggshell offers the potential for high-resolution geochronology of Quaternary deposits. From the simulation experiments, and dated early Holocene samples for which we have in situ mean annual sediment temperature measurements, Arrhenius parameters have been calculated; the activation energy is 30.33 kcal mol −1 , similar to that of other carbonate systems. We have measured the aIle/Ile ratio in ostrich eggshell associated with lacustrine episodes at Bir Tarfawi and Bir Sahara East, two depressions in what is currently the hyperarid eastern Sahara. The ratios can be used directly to indicate qualitatively the time represented by each series of lake sediment, and to correlate disjunct lacustrine deposits within and between the basins. Uranium-series disequilibrium dating of algal mats contained within some of the lake beds indicate that a major wet interval occurred about 130 ka ago. Using the U-series date for calibration, the amino acid ratios are used to date the most recent lacustrine interval to about 100 ka B.P., and two older intervals, one about 200 ± 25 ka B.P., and an older interval that occurred prior to 250 ka ago.

Palaeogeography, Palaeoclimatology, Palaeoecology↗
USGS2017

Geologic evidence for age of deposits at Hueyatlaco archeological site, Vasequillo, Mexico

Direct tracing of beds during excavation in May 1973, confirmed that the artifact-bearing layers at Hueyatlaco underlie 10 m of fine-grained, water-laid deposits that constitute part of the wide-spread Valsequillo gravels. Dissection of these deposits by the adjacent Río Atoyac has reached a depth of 50 m. The stratigraphic section at Hueyatlaco includes four distinctive tephra units. The oldest one occupies a small channel in a series of cut-and-fill stream deposits that have yielded bifacial tools. It lies more than a meter above flat-lying, fine-grained beds from which edge-retouched tools have been recovered. The three other tephra units occur higher in the section. Fission-track ages on zircon phenocrysts from two of the younger tephra layers (370,000 ± 200,000 and 600,000 ± 340,000 yr, 2σ) agree with concordant uranium-series dates for a camel pelvis that was found associated with bifacial tools at Hueyatlaco (245,000 ± 40,000 yr by 230 Th and > 180,000 yr by 231 Pa). These dates are compatible with the depth of burial and subsequent dissection of the Hueyatlaco deposits, as well as with the degree of hydration of volcanic glass shards and with the extent of etching of heavy-mineral phenocrysts from within the tephra layers. These findings suggest to us that further search for archaeological remains in deposits as old as those at Hueyatlaco would be warranted.

Vasequillo Reservoir↗
USGS2017

Ages of subsurface stratigraphic intervals in the Quaternary of Enewetak Atoll, Marshall Islands

Drill cores of Enewetak Atoll, Marshall Islands, reveal six stratigraphic intervals, numbered in downward sequence, which represent vertical coral growth during Quaternary interglaciations. Radiocarbon dates indicate that the Holocene sea transgressed the emergent reef platform by about 8000 yr B.P. The reef grew rapidly upward (about 5 to 10 mm/yr) until about 6500 yr B.P. Afterward vertical growth slowed to about 0.5 mm/yr, then lateral development became dominant during the last several thousand years. The second interval is dated at 131,000 ?? 3000 yr B.P. by uranium series. This unit correlates with oxygen-isotope substage 5e and with terrace VIIa of Huon Peninsula, New Guinea, and of Main Reef-2 terrace at Atauro Island. The third interval is not dated because corals were recrystallized and it is tentatively correlated with either oxygen-isotope stages 7 or 9. The age of the fourth interval is estimated at 454,000 ?? 100,000 yr B.P. from measured 234U 238U activity ratios. This unit is correlated with either oxygen-isotope stage 9, 11, or 13. ?? 1985.

Quaternary Research↗
USGS2017

Ages of travertine deposits in eastern Grand Canyon National Park, Arizona

Travertine deposits in eastern Grand Canyon National Park, Arizona, are inferred to have formed under conditions of effective wetness that were greater than present. Uranium-series dating of 17 samples indicates that the deposits formed at about 15,000, 71,000, 111,000, 171,000, and 338,000 yr B.P. Intervals of travertine deposition are essentially contemporaneous with dated high paleolake levels, montane glacial maxima, and high paleowater-table levels from several Great Basin localities. ?? 1990.

Quaternary Research↗
USGS1988

Paleolimnology of Lake Tubutulik, an iron-meromictic Eocene Lake, eastern Seward Peninsula, Alaska

Sideritic lacustrine mudstone was found in drill core from a uranium deposit in the Death Valley area in the eastern part of the Seward Peninsula, Alaska. The precursor sediments for this rock were deposited in an unusual “iron-meromictic” Eocene lake, herein named Lake Tubutulik, which occupied part of the Boulder Creek basin, a structural graben that is probably a southern extension of the larger Death Valley basin. The Boulder Creek basin is bounded on the west by granite of the Late Cretaceous Darby Pluton, on the east by Precambrian to Paleozoic metasedimentary rocks. The lake basin was formed by basaltic flows that dammed the river valley of the ancestral Tubutulik River in early Eocene time. Lake Tubutulik contained a nearshore facies of fine-grained organic mud and an offshore facies of laminated sideritic mud. The offshore (profundal) laminated mudstone consists of alternating layers of authigenic siderite and detrital layers containing mostly quartz and clay minerals. Both lacustrine facies contain turbidities. The lacustrine sediments graded laterally into an onshore facies of colluvial and fluvial sandstone, paludal mudstone, and coal. The ancient lake apparently occupied a small deep basin in a tectonically active area of high relief. Meromixus was probably stabilized by reduced iron and bicarbonate dissolved in the monimolimnion. The intensity of meromixus decreased as the lake became shallower from sediment filling. The source of the iron, abundant in the monimolimnion of Lake Tubutulik, was probably the Eocene basalt. Based on carbon isotope analysis of the siderite, the dissolved bicarbonate in the profundal facies was largely inorganic. Sideritic carbon in one sample from the onshore paludal facies has an isotopic signature ( δ 13 C = +16.9) consistent with residual carbon formed during methanogenic fermentation.

Alaska↗
USGS1983

Accumulation of fossil fuels and metallic minerals in active and ancient rift lakes

A study of active and ancient rift systems around the world suggests that accumulations of fossil fuels and metallic minerals are related to the interactions of processes that form rift valleys with those that take place in and around rift lakes. The deposition of the precursors of petroleum, gas, oil shale, coal, phosphate, barite, Cu-Pb-Zn sulfides, and uranium begins with erosion of uplifted areas, and the consequent input of abundant nutrients and solute loads into swamps and tectonic lakes. Hot springs and volcanism add other nutrients and solutes. The resulting high biological productivity creates oxidized/reduced interfaces, and anoxic and H 2 S-rich bottom waters which preserves metal-bearing organic tissues and horizons. In the depositional phases, the fine-grained lake deposits are in contact with coarse-grained beach, delta, river, talus, and alluvial fan deposits. Earthquake-induced turbidites also are common coarse-grained deposits of rift lakes. Postdepositional processes in rifts include high heat flow and a resulting concentration of the organic and metallic components that were dispersed throughout the lakebeds. Postdepositional faulting brings organic- and metal-rich sourcebeds in contact with coarse-grained host and reservoir rocks. A suite of potentially economic deposits is therefore a characteristic of rift valleys.

Tectonophysics↗
USGS1987

Provenance studies by fission-track dating of zircon-etching and counting procedures

In sedimentary rocks that have not been heated to high enough temperatures to anneal fission tracks in zircon (greater than ≈ 160°C), fission-track ages of individual detrital zircon grains provide valuable information about the source rocks eroded to form the sediments. The success of such studies depends, however, on the degree to which the ages determined from the detrital suite accurately portray the range of grain ages that are present in the suite. This in turn depends to a large extent on using counting and, in particular, etching procedures that permit proper sampling of grains with a wide range of age and uranium concentrations. Results are reported here of an experimental study of a ‘detrital’ zircon suite manufactured from several zircon populations of known age. This study suggests that multiple etches are required when a complete spectrum of ages in a zircon suite is desired.

International Journal of Radiation Applications an↗
USGS2015

The role of water in unconventional in situ energy resource extraction technologies

Global trends toward developing new energy resources from lower grade, larger tonnage deposits that are not generally accessible using “conventional” extraction methods involve variations of subsurface in situ extraction techniques including in situ oil shale retorting , hydraulic fracturing of petroleum reservoirs, and in situ recovery of uranium. Although these methods are economically feasible and perhaps result in a smaller above-ground land-use footprint, there remain uncertainties regarding potential subsurface impacts to groundwater. This chapter provides an overview of the role of water in these technologies and the opportunities and challenges for water reuse and recycling.

Book chapter↗
USGS1992

Ground water chemistry and geochemical modeling of water-rock interactions at the Osamu Utsumi mine and the Morro do Ferro analogue study sites, Poços de Caldas, Minas Gerais, Brazil

Surface and ground waters, collected over a period of three years from the Osamu Utsumi uranium mine and the Morro do Ferro thorium/rare-earth element (Th/REE) deposits, were analyzed and interpreted to identify the major hydrogeochemical processes. These results provided information on the current geochemical evolution of ground waters for two study sites within the Poços de Caldas Natural Analogue Project. The ground waters are a K–Fe–SO 4 –F type, a highly unusual composition related to intense weathering of a hydrothermally altered and mineralized complex of phonolites. Tritium and stable isotope data indicate that ground waters are of meteoric origin and are not affected significantly by evaporation or water–rock interactions. Recharging ground waters at both study sites demonstrate water of less than about 35 years in age, whereas deeper, more evolved ground waters are below 1 TU but still contain in most cases detectable tritium. These deeper ground waters may be interpreted as being of 35 to 60 or more years in age, resulting mainly from an admixture of younger with older ground waters and/or indicating the influence of subsurface produced tritium. Geochemical processes involving water–rock–gas interactions have been modeled using ground water compositions, mineralogic data, ion plots and computations of speciation, non-thermodynamic mass balance and thermodynamic mass transfer. The geochemical reaction models can reproduce the water chemistry and mineral occurrences and they were validated by comparing the results of thermodynamic mass transfer calculations (using the PHREEQE program, Parkhurst et al., 1980). The results from the geochemical reaction models reveal that the dominant processes are production of CO 2 in the soil zone through aerobic decay of organic matter, dissolution of fluorite, calcite, K-feldspar, albite, chlorite and manganese oxides, oxidation of pyrite and sphalerite, and precipitation of ferric oxides, silica and kaolinite. Gibbsite precipitation can be modeled for the shallow (recharge) water chemistry at Morro do Ferro, consistent with known mineralogy. Recharge waters are undersaturated with respect to barite and discharging waters and deeper ground waters are saturated to supersaturated with respect to barite demonstrating a strong solubility control. Strontium isotope data demonstrate that sources other than calcium-bearing minerals are required to account for the dissolved strontium in the ground waters. These may include K-feldspar, smectite–chlorite mixed-layer clays and goyazite [SrAl 3 (PO 4 ) 2 (OH) 5 • H 2 O]. 1992.

Journal of Geochemical Exploration↗
USGS2011

The delicate balance between soil production and erosion, and its role on landscape evolution

The diversity in landscapes at the Earth’s surface is the result, amongst other things, of the balance (or imbalance) between soil production and erosion. While erosion rates are well constrained, it is only recently that we have been able to quantify rates of soil production. Uranium-series isotopes have been useful to provide such estimates independently of erosion rates. In this study, new U-series isotope are presented data from weathering profiles developed over andesitic parent rock in Puerto Rico, and granitic bedrock in southeastern Australia. The site in Australia is located on a highland plateau, neighbouring a retreating escarpment where soil production rates between 10 and 50 mm/kyr have been determined. The results show that production rates are invariant in these two regions of Australia with values between 15 and 25 mm/kyr for the new site. Andesitic soils show much faster rates, about 200 mm/kyr. Overall, soil production rates determined with U-series isotopes range between 10 and 200 mm/kyr. This is comparable to erosion rates in soil-mantled landscapes, but faster than erosion in cratonic areas and slower than in alpine regions and cultivated areas. This suggests that soil-mantled landscapes maintain soil because they can: there is a balance between production and erosion. Similarly, thick weathering profiles develop in cratonic areas because, despite slow erosion rates, soil production is still significant. Bare landscapes in Alpine regions are probably the result of the inability of soil production to catch up with fast erosion rates, although this needs testing by U-series isotope studies of these regions. Finally, the range of production rates is up to several orders of magnitude lower than erosion rates in cultivated areas, demonstrating quantitatively the fast depletion of soil resources with common agricultural practices.

Applied Geochemistry↗
USGS2015

Modeling and management of pit lake water chemistry 1: Theory

Pit lakes are permanent hydrologic/landscape features that can result from open pit mining for metals, coal, uranium, diamonds, oil sands, and aggregates. Risks associated with pit lakes include local and regional impacts to water quality and related impacts to aquatic and terrestrial ecosystems. Stakeholders rely on predictive models of water chemistry to prepare for and manage these risks. This paper is the first of a two part series on the modeling and management of pit lakes. Herein, we review approaches that have been used to quantify wall-rock runoff geochemistry, wall-rock leachate geochemistry, pit lake water balance, pit lake limnology (i.e. extent of vertical mixing), and pit lake water quality, and conclude with guidance on the application of models within the mine life cycle. The purpose of this paper is to better prepare stakeholders, including future modelers, mine managers, consultants, permitting agencies, land management agencies, regulators, research scientists, academics, and other interested parties, for the challenges of predicting and managing future pit lakes in un-mined areas.

Applied Geochemistry↗
USGS2015

Cr(VI) occurrence and geochemistry in water from public-supply wells in California

Hexavalent chromium, Cr(VI), in 918 wells sampled throughout California between 2004 and 2012 by the Groundwater Ambient Monitoring and Assessment-Priority Basin Project (GAMA-PBP) ranged from less than the study reporting limit of 1 microgram per liter (μg/L) to 32 μg/L. Statewide, Cr(VI) was reported in 31 percent of wells and equaled or exceeded the recently established (2014) California Maximum Contaminant Level (MCL) for Cr(VI) of 10 μg/L in 4 percent of wells. Cr(VI) data collected for regulatory purposes overestimated Cr(VI) occurrence compared to spatially-distributed GAMA-PBP data. Ninety percent of chromium was present as Cr(VI), which was detected more frequently and at higher concentrations in alkaline (pH ≥ 8), oxic water; and more frequently in agricultural and urban land uses compared to native land uses. Chemical, isotopic (tritium and carbon-14), and noble-gas data show high Cr(VI) in water from wells in alluvial aquifers in the southern California deserts result from long groundwater-residence times and geochemical reactions such as silicate weathering that increase pH, while oxic conditions persist. High Cr(VI) in water from wells in alluvial aquifers along the west-side of the Central Valley results from high-chromium in source rock eroded to form those aquifers, and areal recharge processes (including irrigation return) that can mobilize chromium from the unsaturated zone. Cr(VI) co-occurred with oxyanions having similar chemistry, including vanadium, selenium, and uranium. Cr(VI) was positively correlated with nitrate, consistent with increased concentrations in areas of agricultural land use and mobilization of chromium from the unsaturated zone by irrigation return.

California↗
USGS2016

Use of mineral/solution equilibrium calculations to assess the potential for carnotite precipitation from groundwater in the Texas Panhandle, USA

This study investigated the potential for the uranium mineral carnotite (K 2 (UO 2 ) 2 (VO 4 ) 2 ·3H 2 O) to precipitate from evaporating groundwater in the Texas Panhandle region of the United States. The evolution of groundwater chemistry during evaporation was modeled with the USGS geochemical code PHREEQC using water-quality data from 100 groundwater wells downloaded from the USGS National Water Information System (NWIS) database. While most modeled groundwater compositions precipitated calcite upon evaporation, not all groundwater became saturated with respect to carnotite with the system open to CO 2 . Thus, the formation of calcite is not a necessary condition for carnotite to form. Rather, the determining factor in achieving carnotite saturation was the evolution of groundwater chemistry during evaporation following calcite precipitation. Modeling in this study showed that if the initial major-ion groundwater composition was dominated by calcium-magnesium-sulfate (>70 precent Ca + Mg and >50 percent SO 4 + Cl) or calcium-magnesium-bicarbonate (>70 percent Ca + Mg and <70 percent HCO 3 + CO 3 ) and following the precipitation of calcite, the concentration of calcium was greater than the carbonate alkalinity (2 m Ca +2 > m HCO 3 − + 2 m CO 3 −2 ) carnotite saturation was achieved. If, however, the initial major-ion groundwater composition is sodium-bicarbonate (varying amounts of Na, 40–100 percent Na), calcium-sodium-sulfate, or calcium-magnesium-bicarbonate composition (>70 percent HCO 3 + CO 3 ) and following the precipitation of calcite, the concentration of calcium was less than the carbonate alkalinity (2 m Ca +2 < m HCO 3 - + 2 m CO 3 −2 ) carnotite saturation was not achieved. In systems open to CO 2, carnotite saturation occurred in most samples in evaporation amounts ranging from 95 percent to 99 percent with the partial pressure of CO 2 ranging from 10 −3.5 to 10 −2.5 atm. Carnotite saturation occurred in a few samples in evaporation amounts ranging from 98 percent to 99 percent with the partial pressure of CO 2 equal to 10 −2.0 atm. Carnotite saturation did not occur in any groundwater with the system closed to CO 2 .

Texas↗
USGS2022

Occurrence and sources of lead in private wells, Sturbridge, Massachusetts

Lead (Pb) occurrence and sources and aqueous geochemistry were assessed in private wellhead and tap water at a targeted area of concern for possible exceedances and at a control area in the same geologic formation, and in wells at a nearby landfill in south-central Massachusetts (MA). Total Pb concentrations were below the U.S. Environmental Protection Agency (USEPA) Action Level of 15 μg/L in all samples, and about 6% of unfiltered samples contained Pb concentrations that exceeded 1.0 μg/L. Pb concentrations were higher under conditions that are acidic and oxic (pH ≤ 6.5 and dissolved oxygen [DO] ≥ 2 mg/L), in which minerals that could sequester lead or manganese typically are undersaturated, and adsorption by hydrous ferric oxide is limited. Under more neutral to alkaline conditions, the precipitation of Pb in solid solution series minerals such as (Ca,Pb)CO 3 and (Ba,Pb)SO 4 −2 , and adsorption by amorphous ferric hydroxides, could limit Pb solubility in the bedrock aquifer or in the plumbing. The low Pb concentrations and the absence of distinctive Pb and strontium (Sr) isotope ratio patterns in samples indicate that a nearby landfill is not likely a significant Pb source. Dissolved concentrations of Pb, copper (Cu), and zinc (Zn) in tap samples were significantly greater than those in wellhead samples, indicating that some Pb is derived from plumbing. Wellhead or tap samples with the highest Pb concentrations also had the greatest corrosivity potential based on the calcite saturation index and the PPGC (Potential to Promote Galvanic Corrosion) and supports the premise that Pb concentrations in tap samples were derived partly from corrosion of plumbing. Concentrations of other constituents, including arsenic (As), uranium (U), Sr, boron (B), and lithium (Li) were not statistically different between the tap and wellhead samples but, apart from Sr, all were statistically higher in the control area than in the target area. This variation in constituent concentrations suggests geochemical variation within the host Paxton Formation, possibly related to faulting and contact with the Ayer granite east of the control area.

Massachusetts↗
USGS2022

Isotopic analysis of radium geochemistry at discrete intervals in the Midwestern Cambrian-Ordovician aquifer system

Radium (Ra) is a geogenic radioactive contaminant that frequently occurs at elevated levels in the Midwestern Cambrian-Ordovician aquifer system (MCOAS). Geochemical indicators (e.g., redox conditions or total dissolved solids) can broadly characterize conditions associated with elevated Ra levels in groundwater, but do not consistently correlate to elevated Ra within specific stratigraphic horizons. A coupled geochemical and isotopic study of groundwater and aquifer solids for major and trace elements, Ra, and uranium (U) at discrete intervals in the MCOAS was used to elucidate processes that may be responsible for this disconnect, via analysis of groundwater as well as extracted and digested solid aquifer samples. We find that the potential for Ra mobilization varies by stratigraphic unit, as observed by whole-rock 226 Ra/ 238 U (dis)equilibrium. Overall, the examined aqueous geochemical characteristics (e.g., redox conditions, total dissolved solids) do not explain Ra concentrations within the system, suggesting that alternative factors, like solid-phase associations or the extent of alpha recoil damage, may be more important. A relation between aqueous 87 Sr/ 86 Sr and 226 Ra suggests that minerals with radiogenic 87 Sr/ 86 Sr are more likely to release 226 Ra to the aqueous system. Overall, the release of U and Ra due to water-rock interaction varies with discrete stratigraphy, depending on aqueous geochemistry and available mineral associations. Due to complex Ra-rock interactions and the heterogeneous geology of the MCOAS, aqueous geochemistry does not fully predict the mobilization and concentration of Ra in groundwater. As sources and sinks of Ra within the MCOAS vary across stratigraphy, knowledge of aqueous geochemistry, available solid-phase associations, and nuclide leachability all are important to consider for understanding elevated Ra occurrence in aquifer systems.

Wisconsin↗