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At least 1,459 records · Page 81Linked to original sources

USGS2012

Rapid runoff via shallow throughflow and deeper preferential flow in a boreal catchment underlain by frozen silt (Alaska, USA)

In high-latitude catchments where permafrost is present, runoff dynamics are complicated by seasonal active-layer thaw, which may cause a change in the dominant flowpaths as water increasingly contacts mineral soils of low hydraulic conductivity. A 2-year study, conducted in an upland catchment in Alaska (USA) underlain by frozen, well-sorted eolian silt, examined changes in infiltration and runoff with thaw. It was hypothesized that rapid runoff would be maintained by flow through shallow soils during the early summer and deeper preferential flow later in the summer. Seasonal changes in soil moisture, infiltration, and runoff magnitude, location, and chemistry suggest that transport is rapid, even when soils are thawed to their maximum extent. Between June and September, a shift occurred in the location of runoff, consistent with subsurface preferential flow in steep and wet areas. Uranium isotopes suggest that late summer runoff erodes permafrost, indicating that substantial rapid flow may occur along the frozen boundary. Together, throughflow and deep preferential flow may limit upland boreal catchment water and solute storage, and subsequently biogeochemical cycling on seasonal to annual timescales. Deep preferential flow may be important for stream incision, network drainage development, and the release of ancient carbon to ecosystems

Alaska↗

USGS2020

Geochemical characterization of groundwater evolution south of Grand Canyon, Arizona (USA)

Better characterization of the geochemical evolution of groundwater south of Grand Canyon, Arizona (USA), is needed to understand natural conditions and assess potential effects from breccia-pipe uranium mining in the region. Geochemical signatures of groundwater at 28 sampling locations were evaluated; baseline concentrations for select trace elements (As, B, Ba, Cr, Li, Mo, Rb, Se, Sr, Th, Tl, U, V) were established, and anomalous chemistry characteristics were identified. Concentrations at some groundwater sites exceeded the USEPA drinking water standard for As of 10 μg/L (Red Canyon, Miners, JT, Havasu, and Warm Springs) and U of 30 μg/L (Salt Creek Spring). Four springs from the study area (Blue, Havasu, Fern, and Warm Springs) had unique chemistry, which may indicate a deep flow path or potential contribution of fluids from lower in the crust. Other springs in the study area were distinguished by major anion water type: sulfate, bicarbonate, and a mixture of the two. Water type distinctions were somewhat spatially segregated, with sulfate type present on the western side of the study area, bicarbonate type on the eastern side, and a mixture of the two interspersed between the endmember sites. Sulfate-type water from this study area had low strontium isotopic ratio (87Sr/86Sr) values. The location of spring discharge within single drainages of the Grand Canyon may influence chemistry, as groundwater discharging from bedrock was altered after flowing through alluvial material. Geochemical analysis of groundwater in Grand Canyon indicates the importance of continued monitoring and better understanding of short-term chemical fluctuations.

Arizona↗

USGS2005

Indoor radon risk potential of Hawaii

A comprehensive evaluation of radon risk potential in the State of Hawaii indicates that the potential for Hawaii is low. Using a combination of factors including geology, soils, source-rock type, soil-gas radon concentrations, and indoor measurements throughout the state, a general model was developed that permits prediction for various regions in Hawaii. For the nearly 3,100 counties in the coterminous U.S., National Uranium Resource Evaluation (NURE) aerorad data was the primary input factor. However, NURE aerorad data was not collected in Hawaii, therefore, this study used geology and soil type as the primary and secondary components of potential prediction. Although the radon potential of some Hawaiian soils suggests moderate risk, most houses are built above ground level and the radon soil potential is effectively decoupled from the house. Only underground facilities or those with closed or recirculating ventilation systems might have elevated radon potential. ?? 2005 Akade??miai Kiado??.

Journal of Radioanalytical and Nuclear Chemistry↗

USGS1966

Disequilibrium of the 238U series in basalt

Radioisotope analyses of basalt samples from Hawaii, Japan, and Iwo Jima show that: (1) 234 U and 238 U are virtually in radioactive equilibrium, (2) 230 Th exceeds equilibrium values in all these samples, (3) 210 Pb concentrations range from 10–200% of the equilibrium values and average 30% deficient, and (4) 226 Ra is probably not in equilibrium with 234 U. The source regions of the basalts or magma forming processes are open systems, chemically. The enrichment of some of the uranium-daughter nuclides is insufficient to account for the excess 206 Pb in volcanic rocks. The isotopic composition of lead and specific activity of 210 Pb in sublimates from Showa-shinzan, Japan are also reported.

Hawaii↗

USGS1969

Lead isotopes in volcanic rocks and possible ocean-floor thrusting beneath island arcs

The isotopic composition of lead in the Japanese primary basalts gradually decreases in radiogenic character in a transverse from the Pacific Ocean side to the Japan Sea side, whereas the observed 238 U 204 Pb "> 238U204Pb and 232 Th 204 Pb "> 232Th204Pb ratios in the basalts increase in the same direction. The isotopic composition of lead suggests that tholeiite (Pacific side) is generated at a shallower depth than alkali basalt (Japan Sea side) as postulated by Kuno. The inverse correlation of the 238 U 204 Pb "> 238U204Pb with the 206 Pb 204 Pb "> 206Pb204Pb ratios could be due to preferential Pb extraction with respect to uranium at shallow depths. Alternatively, these geochemical results can be interpreted in terms of the Pacific oceanic rigid plate being underthurst beneath the island arc. The isotopic variation in basalts across the Japanese island arc would result from different proportions of the plate material and the upper mantle of continental side in the partial melt.

Earth and Planetary Science Letters↗

USGS1966

Chemical composition of phosphorites of the Phosphoria Formation

The chemical composition, both major and minor constituents, of 60 samples of phosphorite from the Phosphoria Formation was determined. Major constituents of the average phosphorite are, by weight per cent: SiO 2 , 11·9; Al 2 O 3 , 1·7; Fe 2 O 3 ,1·1; MgO, 0·3; CaO, 44·0; Na 2 O, 0·6; K 2 O, 0·5; total H 2 O, 2·2; H 2 O − , 0·6; TiO 2 , 0·1; P 2 O 5 , 30·5; CO 2 , 2·2; SO 3 , 1·8; F, 3·1; organic matter, 2·1; and oil, 0·2. Uranium averages 0·009 per cent. The phosphate mineral is basically apatite, Ca 5 (PO 4 ) 3 F, with small but significant and variable substitutions—Na, Sr, U and Th for Ca, and CO 3 and SO 4 for PO 4 . Rare metals not associated with apatite are associated principally with the organic-matter component of the rocks. This group includes As, Ag, Cd, Cr, Cu, Mo, Ni, Sb, Se, V and Zn. Chromium is the most abundant, having a modal abundance of 0·1 per cent and a maximum concentration of 0·3 per cent. The average phosphorite is composed of approximately 80 per cent apatite, 10 per cent quartz, 5 per cent muscovite-illite, 2 per cent organic matter, 1 per cent dolomite—calcite, 1 per cent iron oxide, and 1 per cent other components. It is texturally a medium-grained pellet phosphorite.

Geochimica et Cosmochimica Acta↗

USGS1969

The isotopic composition of lead in potassium feldspars from some 1.0-b.y. old North American igneous rocks

The isotopic composition of lead and the uranium, thorium and lead concentrations in potassium feldspars are determined for more than 30 1.0-b.y. old North American igneous rocks. Samples representing a broad spectrum in petrographic type and mode of occurrence were chosen; an effort was made to include only rocks having well-documented ages from 950 to 1140 m.y. and showing minimal evidence of subsequent metamorphism. Most samples, including those from extensive terranes of contemporaneous age, have limited lead isotope variations ( Pb 206 Pb 204 = 16.74–17.38 "> Pb206Pb204= 16.74–17.38 ; Pb 207 Pb 204 = 15.39–15.59 "> Pb207Pb204= 15.39–15.59 ; Pb 208 Pb 204 = 36.38–37.10 "> Pb208Pb204= 36.38–37.10 ), which yield model ages close to the radiometric ages. Granite, pegmatite, and rhyolite from within the Grenville province of Canada and age-equivalent rocks of New York, Virginia, Texas, and Colorado and granophyric units associated with the Duluth Gabbro Complex of Minnesota are among the materials yielding this main isotopic spectrum. Several samples were encountered which had isotopic compositions very different from the above group. Lead showing a marked deficiency in radiogenic isotopes was found in two granitic bodies associated with older Labrador Trough rocks from Quebec, in a rapakivi granite from southern Nevada, and in a small granite stock from Mellen, Wisconsin. These occurrences all involve small intrusions of granite which lie near considerably older areas of basement rock. Model ages calculated from the Pb 206 Pb 204 "> Pb206Pb204 ratio are older than the age of the intrusions and approach the age of the host basement rock. Several possible interpretations are offered to explain the isotopic behavior encountered in this study. In particular, a “vertically differentiated crust” model is proposed which will account for both the main spectrum and the anomalous lead. The significance of lead isotopic studies in understanding crustal structure in continental regions is discussed.

Geochimica et Cosmochimica Acta↗

USGS1970

A new technique for pumping hydrogen gas

A system for pumping hydrogen gas without isotopic fractionation has been developed. The pump contains uranium metal, which when heated to about 80°C reacts with hydrogen to form UH 3 . The UH 3 is heated to above 500°C to decompose the hydride and regenerate the hydrogen.

Geochimica et Cosmochimica Acta↗

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↗

USGS1984

Laboratory analysis and airborne detection of materials stimulated to luminesce by the sun

The Fraunhofer line discriminator (FLD) is an airborne electro-optical device used to image materials which have been stimulated to luminesce by the Sun. Such materials include uranium-bearing sandstone, sedimentary phosphate rock, marine oil seeps, and stressed vegetation. Prior to conducting an airborne survey, a fluorescence spectrometer may be used in the laboratory to determine the spectral region where samples of the target material exhibit maximum luminescence, and to select the optimum Fraunhofer line.

Journal of Luminescence↗

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↗