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Rapidly-formed ferromanganese deposit from the eastern Pacific Hess Deep

A thick ferromanganese deposit encrusting fresh basaltic glass has been dredged from the Hess Deep in the eastern Pacific. Contiguous layers within the Fe-Mn crust have been analysed for uranium-series isotopes and metal contents. The rate of accumulation of the deposit, based on the decline of uranium-unsupported 230Th, is calculated to be approximately 50 mm per 106 yr. Based on hydration-rind dating of the underlying glass and an 'exposure age' calculation, this rate is concluded to be too slow, and an accretion rate on the order of 1 mm per 103 yr is more consistent with our data. ?? 1977 Nature Publishing Group.

Nature↗

Radiometric dating of sediments using fission tracks in conodonts

Conodonts are microfossils which are commonly found in marine rocks of Cambrian to Triassic age. Although their biological affinities are difficult to assess, conodonts are valuable stratigraphical indices for much of their geological range1. Recent work has also established that conodont colour alteration indices (CAI) are useful guides to diagenetic temperatures and hence burial depth2. Fission tracks3 in conodonts allow measurement of uranium concentrations and estimates of 'age' to be made using isotopic methods4. We report here that fission tracks counted in irradiated, thermally unaltered (as indicated by CAI) middle Palaeozoic conodonts indicate typical uranium concentrations of ???1 part in 10 9, with some samples higher. A single specimen of Siphonodella from the Lower Mississippian yielded an age estimate of 380??140 Myr consistent with conventional interpolations. This method may also allow the unroofing of deeply buried sediments to be dated. ?? 1980 Nature Publishing Group.

Nature↗

Arsenic and other geogenic contaminants in global groundwater

Geogenic groundwater contaminants (GGCs) affect drinking-water availability and safety, with up to 60% of groundwater sources in some regions contaminated by more than recommended concentrations. As a result, an estimated 300–500 million people are at risk of severe health impacts and premature mortality. In this Review, we discuss the sources, occurrences and cycling of arsenic, fluoride, selenium and uranium, which are GGCs with widespread distribution and/or high toxicity. The global distribution of GGCs is controlled by basin geology and tectonics, with GGC enrichment in both orogenic systems and cratonic basement rocks. This regional distribution is broadly influenced by climate, geomorphology and hydrogeochemical evolution along groundwater flow paths. GGC distribution is locally heterogeneous and affected by in situ lithology, groundwater flow and water–rock interactions. Local biogeochemical cycling also determines GGC concentrations, as arsenic, selenium and uranium mobilizations are strongly redox-dependent. Increasing groundwater extraction and land-use changes are likely to modify GGC distribution and extent, potentially exacerbating human exposure to GGCs, but the net impact of these activities is unknown. Integration of science, policy, community involvement programmes and technological interventions is needed to manage GGC-enriched groundwater and ensure equitable access to clean water.

Nature Reviews Earth & Environment↗

Antiferromagnetism of UO2⋅2H2O

Magnetic susceptibility measurements have been made on UO 2 · x H 2 O for x =1.78 to x =2.13, and from 77° to 375°K. As the value of x decreased the susceptibility increased. Both these data and structural arguments imply that the formula of this compound is U(OH) 4 rather than the dihydrate form. Based on this concept the data have been corrected for diamagnetism and also small amounts of UO 2 and H 2 O which were present. The molar susceptibility of U 4+ in U(OH) 4 is nearly an order of magnitude less than in other uranium compounds, and it is suggested that this is probably due to superexchange between adjacent uranium atoms through intervening oxygen atoms.

Journal of Chemical Physics↗

Igneous rocks of the East Pacific Rise

The apical parts of large volcanoes along the East Pacific Rise (islands and seamounts) are encrusted with rocks of the alkali volcanic suite (alkali basalt, andesine- and oligoclase-andesite, and trachyte). In contrast, the more submerged parts of the Rise are largely composed of a tholeiitic basalt which has low concentrations of K, P, U, Th, Pb, and Ti. This tholeiitic basalt is either the predominant or the only magma generated in the earth's mantle under oceanic ridges and rises. It is at least 1000-fold more abundant than the alkali suite, which is probably derived from tholeiitic basalt by magmatic differentiation in and immediately below the larger volcanoes. Distinction of oceanic tholeiites from almost all continental tholeiites is possible on the simple basis of total potassium content, with the discontinuity at 0.3 to 0.5 percent K 2 O by weight. Oceanic tholeiites also are readily distinguished from some 19 out of 20 basalts of oceanic islands and seamount cappings by having less than 0.3 percent K 2 O by weight and more than 48 percent SiO 2 . Deep drilling into oceanic volcanoes should, however, core basalts transitional between the oceanic tholeiites and the presumed derivative alkali basalts. The composition of the oceanic tholeiites suggests that the mantle under the East Pacific Rise contains less than 0.10 percent potassium oxide by weight; 0.1 part per million of uranium and 0.4 part of thorium; a potassium: rubidium ratio of about 1200 and a potassium: uranium ratio of about 10 4 .

Science↗

Conditions and processes affecting radionuclide transport

Characteristics of host rocks, secondary minerals, and fluids would affect the transport of radionuclides from a previously proposed repository at Yucca Mountain, Nevada. Minerals in the Yucca Mountain tuffs that are important for retarding radionuclides include clinoptilolite and mordenite (zeolites), clay minerals, and iron and manganese oxides and hydroxides. Water compositions along flow paths beneath Yucca Mountain are controlled by dissolution reactions, silica and calcite precipitation, and ion-exchange reactions. Radionuclide concentrations along flow paths from a repository could be limited by (1) low waste-form dissolution rates, (2) low radionuclide solubility, and (3) radionuclide sorption onto geological media. The chief sources of radioactivity in spent nuclear fuel are americium, plutonium, and neptunium. Therefore, studies have concentrated on their geochemical mobility. Uranium-233, uranium-234, iodine-129, technetium-99, and other radionuclides also have been included in some experiments. Solubilities were determined experimentally in representative Yucca Mountain waters. Sorption coefficients were determined using water, rock, and pure mineral samples from Yucca Mountain. Batch experiments were performed at several pH levels and oxidizing conditions. Dynamic transport-column experiments, diffusion experiments, and solid-rock beaker experiments also were conducted. The batch tests gave slightly lower retardation factors than those derived from column-breakthrough experiments. This finding indicates that using batch-sorption coefficients to predict radionuclide transport will yield conservative results in a performance assessment. Understanding of unsaturated-zone transport is based on laboratory and field-scale experiments. Fractures provide advective transport pathways. Sorption and matrix diffusion may contribute to retardation of radionuclides. Conversely, sorption onto mobile colloids may enhance radionuclide transport.

GSA Memoirs↗

Pleistocene lakes and paleohydrologic environments of the Tecopa basin, California: Constraints on the drainage integration of the Amargosa River

The Tecopa basin in eastern California was a terminal basin that episodically held lakes during most of the Quaternary until the basin and its modern stream, the Amargosa River, became tributary to Death Valley. Although long studied for its sedimentology, diagenesis, and paleomagnetism, the basin’s lacustrine and paleoclimate history has not been well understood, and conflicting interpretations exist concerning the relations of Tecopa basin to the Amargosa River and to pluvial Lake Manly in Death Valley. Previous studies also did not recognize basinwide tectonic effects on lake-level history. In this study, we focused on: (1) establishing a chronology of shoreline deposits, as the primary indicator of lake-level history, utilizing well-known ash beds and new uranium-series and luminescence dating; (2) using ostracodes as indicators of water chemistry and water source(s); and (3) correlating lake transgressions to well-preserved fluvial-deltaic sequences. During the early Pleistocene, the Tecopa basin hosted small shallow lakes primarily fed by low-alkalinity water sourced mainly from runoff and (or) a groundwater source chemically unlike the modern springs. The first lake that filled the basin occurred just prior and up to the eruption of the 765 ka Bishop ash during marine isotope stage (MIS) 19; this lake heralded the arrival of the Amargosa River, delivering high-alkalinity water. Two subsequent lake cycles, coeval with MIS 16 (leading up to eruption of 631 ka Lava Creek B ash) and MIS 14 and (or) MIS 12, are marked by prominent accumulations of nearshore and beach deposits. The timing of the youngest of these three lakes, the High lake, is constrained by a uranium-series age of ca. 580 ± 120 ka on tufa-cemented beach gravel and by estimates from sedimentation rates. Highstand deposits of the Lava Creek and High lakes at the north end of the basin are stratigraphically tied to distinct sequences of fluvial-deltaic deposits fed by alkaline waters of the Amargosa River. The High lake reached the highest level achieved in the Tecopa basin, and it may have briefly discharged southward but did not significantly erode its threshold. The High lake was followed by a long hiatus of as much as 300 k.y., during which there is evidence for alluvial, eolian, and groundwater-discharge deposition, but no lakes. We attribute this hiatus, as have others, to blockage of the Amargosa River by an alluvial fan upstream near Eagle Mountain. A final lake, the Terminal lake, formed when the river once again flowed south into Tecopa basin, but it was likely short-lived due to rapid incision of the former threshold south of Tecopa. Deposits of the Terminal lake are inset below, and are locally unconformable on, deposits of the High lake and the nonlacustrine deposits of the hiatus. The Terminal lake reached its highstand at ca. 185 ± 21 ka, as dated by infrared-stimulated luminescence on feldspar in beach sand, a time coincident with perennial lake mud and alkaline-tolerant ostracodes in the Badwater core of Lake Manly during MIS 6. A period of stillstand occurred as the Terminal lake drained when the incising river encountered resistant Stirling Quartzite near the head of present-day Amargosa Canyon. Our studies significantly revise the lacustrine and drainage history of the Tecopa basin, show that the MIS 6 highstand was not the largest lake in the basin as previously published (with implications for potential nuclear waste storage at Yucca Mountain, Nevada), and provide evidence from shoreline elevations for ∼20 m of tectonic uplift in the northern part of the basin across an ENE-trending monoclinal flexure.

California↗

A theoretical model for the flux of radon from rock to ground water

A model is derived to predict the abundance of 222 Rn in ground water in contact with a rock of known uranium content. The model assumes that secular equilibrium is attained in the rock-water system as a whole, but is independent of any microscopic geometric properties of the system. The key variables in the model are bulk properties such as porosity, uranium content of the rock, emanating efficiency, and rock density, all of which are measurable. Thus, the model is simplified by the averaging effects of a macroscopic view of the system. Although less rigorous than other models presented in the literature, it is more generally applicable to natural systems because it does not rely on microscopic properties of the system, which are impossible to quantify. Application of the model to crystalline aquifers in the eastern United States shows that bulk emanation rates of radon are generally less than about 30%.

GSA Special Papers↗

Natural thorium resources and recovery: Options and impacts

This paper reviews the front end of the thorium fuel cycle, including the extent and variety of thorium deposits, the potential sources of thorium production, and the physical and chemical technologies required to isolate and purify thorium. Thorium is frequently found within rare earth element–bearing minerals that exist in diverse types of mineral deposits, often in conjunction with other minerals mined for their commercial value. It may be possible to recover substantial quantities of thorium as a by-product from active titanium, uranium, tin, iron, and rare earth mines. Incremental physical and chemical processing is required to obtain a purified thorium product from thorium minerals, but documented experience with these processes is extensive, and incorporating thorium recovery should not be overly challenging. The anticipated environmental impacts of by-product thorium recovery are small relative to those of uranium recovery since existing mining infrastructure utilization avoids the opening and operation of new mines and thorium recovery removes radionuclides from the mining tailings.

Nuclear Technology↗

Occurrence of selenium in sulfides from some sedimentary rocks of the western United States

Investigations of the minor- and trace-element content of sulfides associated with uranium ore deposits from sandstone-type deposits have shown that selenium commonly substitutes for sulfur. The Morrison formation and Entrada sandstone of Jurassic age and the Wind River formation of Eocene age seem to be seleniferous stratigraphic zones; sulfides deposited within these formations generally contain abnormal amounts of selenium. The selenium content of the pyrite, marcasite, and chalcocite is much greater than that reported in previously published data.Under the prevailing temperatures and pressures of formation of the Colorado Plateau uranium deposits the maximum amount of Se substituting for S in the pyrite structure was found to be 3 percent by weight. Ferroselite, the iron selenide (FeSe 2 ), was found in two deposits on the Colorado Plateau and it was also established that galena (PbS) forms an isomorphous series with clausthalite (PbSe) in nature.During oxidation of the selenium-bearing sulfides and selenides from the Colorado Plateau and Wyoming, the selenium forms pinkish crusts of either monoclinic or hexagonal native selenium intergrown with soluble sulfates, suggesting that under "normal" oxidizing conditions native selenium is more stable than selenites or selenates. The above-normal selenium content of these sulfides from sedimentary rocks of Mesozoic and Tertiary age is significant. The high selenium in these sulfides is related to periods of volcanic and intrusive activity penecontemporaneous with the formation of the containing sediments.

Arizona, Colorado, New Mexico, Utah, Wyoming↗

Detrital-appearing uraninite grains in the shinarump member of the chinle formation in northern Arizona

A sample of uranium-bearing conglomerate from the Shinarump member of the Chinle formation in northern Arizona was disaggregated in an ultrasonic separator. The sample, weighing 187 grams, contained about 60 grains of uraninite (from 0.1 to 1 mm diameter) which have the sphericity and polish suggestive of detrital grains . The detrital-appearing grains are associated with abundant interstitial uraninite , sphalerite, and pyrite, which presents conflicting evidence as to the origin of the uranium deposit. No definite conclusions are presented for the occurrence of these grains . However, the evidence strongly suggests that they are probably not detrital in origin, but are uraninite replacements of detrital grains ; the original mineral may have been quartz.

Arizona↗

The data of lead isotope geology related to problems of Ore Genesis

Searching questions about the origins of ore deposits have been asked for many years. Where do ore fluids originate-within the crust, or deeper? Can specific sources of ore metals be identified? When were ores deposited? How long did mineralization continue? What was the rate and paragenesis of deposition? Which deposits are cogenetic, and what metallogenetic provinces do they define? Isotope analyses of lead from rocks and ores provide a new tool for attacking such problems of ore genesis . About two thousand such analyses now available from more than 20 laboratories have been compiled and studied for this purpose. The data now available suggest partial answers to some questions and serve to define other, new problems , not previously recognized. Their greatest import, however, is to illustrate the potential future significance of lead - isotope studies. Ore - lead , as shown two decades ago, ranges widely in isotopic composition. Recent studies show that traces of lead in ordinary rocks of the earth's crust exhibit apparently similar variations. All these variations are attributable primarily to mixing of old lead with accumulations of new radiogenic lead from decay of radioactive uranium and thorium. Each sample of lead preserves in its isotopic composition a record of its own mixing history: a composite record of the time this lead was in different environments, its past associations with uranium and thorium, and the geochemical processes that moved it from place to place. Integrated study of all these variables will throw light on many difficult problems of ore genesis when adequate techniques are developed. Progress will be slow, however, until more accurate lead - isotope analyses can be made at lower cost and more objective criteria developed for interpreting measured isotopic compositions in terms of geologic history.

Economic Geology↗

The synthesis of ferroselite from an aqueous solution at low temperature

Ferroselite , FeSe 2 , is commonly associated with sandstone-type uranium deposits. Although it has been previously synthesized, the conditions of synthesis were not applicable to the natural system, and the literature did not provide any information on the formation of natural ferroselite . The U. S. Geological Survey's Ambrosia Lake study, however, was concerned with the formation of ferroselite under more natural conditions. Thus, in this work, the synthesis of ferroselite was restricted to conditions more nearly approaching the conditions of the formation of sandstone-type uranium deposits-a low temperature and an aqueous environment. A solution of sodium seleno-sulfate, Na 2 SSeO 3 , stood in contact with freshly precipitated iron sulfide, FeS, for 10 days under an inert atmosphere at 80° C. The final product was identified by its diffraction pattern and consisted of FeSe 2 mixed with about 10 percent FeS.

Economic Geology↗

Origin of a South Texas roll-type deposit; II, Sulfide petrology and sulfur isotope studies

Petrologic and sulfur isotopic studies have been carried out on drill core samples from a roll-type uranium deposit in the mid-Tertiary Catahoula Tuff, Webb County, south Texas. Epigenetic iron disulfide minerals formed in two distinct stages. The first stage involved sulfidization of the host rock by sulfide (H 2 S, HS-)-bearing solutions that emanated from a fault about 1.5 km downdip from and subparallel to the orebody. Pyrite was the dominant iron disulfide mineral formed from this fault sulfide. The isotopic composition (delta 34 S) of first-stage iron disulfide is quite heavy (>0 per mil), in part because the fault-derived H 2 S was isotopically heavy. The development of the second-stage sulfides was related to processes that formed the uranium roll. Iron disulfide minerals produced during this second stage commonly occur as rims around the first-stage sulfides. The rims are exclusively marcasite in and adjacent to ore, but the pyrite content in these rims increases with increasing distance from ore. The sulfur of the second-stage sulfides in the vicinity of the roll front is isotopically light (--25 to --40 per mil). The virtual absence of organic carbon in the host sand precludes a bacterial origin for the ore-stage iron disulfide minerals and, therefore, eliminates bacterial metabolism as the mechanism for isotopic fractionation. Instead, the sulfur source for ore-stage sulfides was preore (first stage) sulfides, remobilized via partial oxidation to soluble metastable sulfur oxyanions.

Texas↗

Decadal trends in the quality of groundwater used for public drinking-water supply in California, 2004–2023, California groundwater ambient monitoring and assessment program, priority basin project

This study provides a comprehensive assessment of decadal changes in the quality of groundwater used for public drinking-water supply at 444 monitoring sites across California during 2004–2023. We assessed decadal step trends in groundwater quality for 145 water-quality constituents and geochemical indicators statewide and across geographic and land-use based network groups. We evaluated the statistical significance of directional changes (predominant increase or decrease of constituent concentrations) and the magnitude of those changes across all network groups. Uranium showed the most widespread directional and high-magnitude increases of all constituents with regulatory benchmarks statewide, particularly in the agriculture-dominated Central Valley as well as urban- and desert-dominated regions of Southern California. Fluoride and perchlorate showed the most widespread directional and high-magnitude decreases of all constituents with regulatory benchmarks statewide, which were also most pronounced in Southern California. Although arsenic and nitrate did not often register significant directional changes across network groups, they showed widespread, high-magnitude changes in both directions (increase and decrease) at levels often exceeding 10 percent of respective regulatory benchmarks statewide. Triazine herbicides (atrazine and simazine) and the gasoline oxygenate methyl tert-butyl ether (MTBE) showed significant directional decreases statewide, but not at levels considered to be of high magnitude compared to respective regulatory benchmarks. We observed significant directional and high-magnitude increases of total dissolved solids (TDS) statewide, which were most pronounced in agricultural areas. Analysis of explanatory geochemical indicators indicated that prevalent statewide increases of alkalinity and calcium were the predominant components of the observed statewide increases in TDS by mass. Widespread increases in groundwater alkalinity and calcium across agricultural and urban areas may be related, in part, to warm-season irrigation and other anthropogenic factors that have shifted soil weathering dynamics over the long term. Increasing alkalinity concentrations were related to increasing uranium concentrations, particularly in areas with aquifer materials derived from granitic rocks. Conversely, increasing calcium concentrations were related to decreasing fluoride concentrations, particularly in areas where fluoride occurred naturally at elevated concentrations. Decrease of perchlorate, triazine herbicides, and MTBE are likely related to decreased anthropogenic source inputs over time and natural attenuation in aquifers.

EarthArXiv↗

Mineral resources of the Mount Tipton Wilderness Study Area, Mohave County, Arizona

The Mount Tipton Wilderness Study Area (AZ-020-012/ 042) comprises 33,950 acres in Mohave County, Ariz. At the request of the U.S. Bureau of Land Management, this area was evaluated for identified mineral resources (known) and mineral resource potential (undiscovered). This work was carried out by the U.S. Bureau of Mines and the U.S. Geological Survey in 1984-87. In this report, the area studied is referred to as the "wilderness study area" or simply "the study area." There are no identified mineral resources in the study area. The southernmost part of the study area is adjacent to the Wallapai (Chloride) mining district and has low mineral resource potential for gold, silver, copper, lead, zinc, and molybdenum in hydrothermal veins. This area also has a low mineral resource potential for tungsten in vein deposits and for uranium in vein deposits or pegmatites. In the central part of the wilderness study area, one small area has low mineral resource potential for uranium in vein deposits or pegmatites and another small area has low resource potential for thorium in vein deposits. The entire study area has low resource potential for geothermal energy but no potential for oil or gas resources.

Arizona↗

Airborne radioactivity surveys for phosphate in Florida

Airborne radioactivity surveys totaling 5, 600 traverse miles were made in 10 areas in Florida, which were thought to be geologically favorable for deposits of uraniferous phosphate. Abnormal radioactivity was recorded in 8 of the 10 areas surveyed. The anomalies are located in Bradford, Clay, Columbia, DeSoto, Dixie, Lake, Marion, Orange, Sumter, Taylor, and Union Counties. Two of the anomalies were investigated briefly on the ground. One resulted from a deposit of river-pebble phosphate in the Peace River valley; the river-pebble samples contain an average of 0.013 percent equivalent uranium. The other anomaly resulted from outcrops of leached phosphatic rock containing as much as 0. 016 percent equivalent uranium. Several anomalies in other areas were recorded at or near localities where phosphate deposits have been reported.

Florida↗

An occurrence of autunite, Lawrence County, South Dakota

In July 1952 an occurrence of autunite was found in the northern part of the Black Hills, South Dakota, during a reconnaissance for radioactive deposits. The autunite occurs as fracture coatings and disseminations in siltstone of the Deadwood formation of Cambrian age and is concentrated mainly in the lower 2 feet of the siltstone at the contact with an intrusive rhyolite porphyry; the radioactive zone is exposed in two old workings, which are 90 feet apart. An 18-inch vertical channel sample of the autanite-bearing siltstene contained 0. 048 percent uranium. The gangue minerals are fluorite and limonite. The uranium is believed to have been introduced into the siltstone by solutions of magmatic origin that migrated along the lower contact of the siltstone after or during emplacement of the porphyry'

South Dakota↗