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At least 1,153 records · Page 64Linked to original sources

Limited hydrologic response to Pleistocene climate change in deep vadose zones - Yucca Mountain, Nevada

Understanding the movement of water through thick vadose zones, especially on time scales encompassing long-term climate change, is increasingly important as societies utilize semi-arid environments for both water resources and sites viewed as favorable for long-term disposal or storage of hazardous waste. Hydrologic responses to Pleistocene climate change within a deep vadose zone in the eastern Mojave Desert at Yucca Mountain, Nevada, were evaluated by uranium-series dating of finely layered hyalitic opal using secondary ion mass spectrometry. Opal is present within cm-thick secondary hydrogenic mineral crusts coating floors of lithophysal cavities in fractured volcanic rocks at depths of 200 to 300 m below land surface. Uranium concentrations in opal fluctuate systematically between 5 and 550 μg/g. Age-calibrated profiles of uranium concentration correlate with regional climate records over the last 300,000 years and produce time-series spectral peaks that have distinct periodicities of 100- and 41-ka, consistent with planetary orbital parameters. These results indicate that the chemical compositions of percolating solutions varied in response to near-surface, climate-driven processes. However, slow (micrometers per thousand years), relatively uniform growth rates of secondary opal and calcite deposition spanning several glacial–interglacial climate cycles imply that water fluxes in the deep vadose zone remained low and generally buffered from the large fluctuations in available surface moisture during different climates.

Nevada↗

Modern U-Pb chronometry of meteorites: advancing to higher time resolution reveals new problems

In this paper, we evaluate the factors that influence the accuracy of lead (Pb)-isotopic ages of meteorites, and may possibly be responsible for inconsistencies between Pb-isotopic and extinct nuclide timescales of the early Solar System: instrumental mass fractionation and other possible analytical sources of error, presence of more than one component of non-radiogenic Pb, migration of ancient radiogenic Pb by diffusion and other mechanisms, possible heterogeneity of the isotopic composition of uranium (U), uncertainties in the decay constants of uranium isotopes, possible presence of "freshly synthesized" actinides with short half-life (e.g. 234 U) in the early Solar System, possible initial disequilibrium in the uranium decay chains, and potential fractionation of radiogenic Pb isotopes and U isotopes caused by alpha-recoil and subsequent laboratory treatment. We review the use of 232 Th/ 238 U values to assist in making accurate interpretations of the U-Pb ages of meteorite components. We discuss recently published U-Pb dates of calcium-aluminum-rich inclusions (CAIs), and their apparent disagreement with the extinct nuclide dates, in the context of capability and common pitfalls in modern meteorite chronology. Finally, we discuss the requirements of meteorites that are intended to be used as the reference points in building a consistent time scale of the early Solar System, based on the combined use of the U-Pb system and extinct nuclide chronometers.

Geochimica et Cosmochimica Acta↗

Selected trace-elements in alluvium and rocks, western Mojave Desert, southern California

Concentrations of twenty-seven elements, including naturally-occurring water-quality contaminants arsenic, chromium, and uranium, were measured in 217 samples of alluvium and rock from the western Mojave Desert, southern California, using portable (pXRF) and laboratory (LXRF) X-ray fluorescence. Comparison of measurements with NIST-traceable standards was good, although pXRF overestimated iron compared to LXRF. Results suggest pXRF survey data are sufficiently accurate to assess regional geochemical differences in geologic-source terrains. Principal component analysis showed rubidium and potassium were associated with alluvium eroded from felsic terrain, while iron, copper, chromium, and to a lesser extent titanium, manganese, and nickel were associated with alluvium eroded from mafic terrain. Zinc, vanadium, and arsenic were associated with alluvium eroded from hydrothermal terrain. Elemental assemblages associated with different source terrains were traced spatially to identify the source and composition of alluvium composing aquifers pumped for water supply. Changes in geologic source terrain to the Mojave River, associated with movement along the San Andreas Fault over the past one to five million years, reduced the mafic fraction and increased the felsic fraction of alluvium deposited to the regionally important floodplain aquifer along the Mojave River—lowering chromium concentrations in alluvium through geologic time. Comparison of pXRF and sequential extraction data from 40 samples showed arsenic and uranium were more abundant on the surfaces of mineral grains, while chromium and vanadium remained mostly within unweathered mineral grains—suggesting arsenic and uranium may be more readily mobilized into groundwater with changes in pH, redox, or ionic strength than chromium or vanadium.

California↗

Consequences of slow growth for 230Th/U dating of Quaternary opals, Yucca Mountain, NV, USA

Thermal ionization mass-spectrometry 234U/238U and 230Th/238U data are reported for uranium-rich opals coating fractures and cavities within the silicic tuffs forming Yucca Mountain, NV, the potential site of a high-level radioactive waste repository. High uranium concentrations (up to 207 ppm) and extremely high 230Th/232Th activity ratios (up to about 106) make microsamples of these opals suitable for precise 230Th/U dating. Conventional 230Th/U ages range from 40 to greater than 600 ka, and initial 234U/238U activity ratios between 1.03 and 8.2. Isotopic evidence indicates that the opals have not experienced uranium mobility; however, wide variations in apparent ages and initial 234U/238U ratios for separate subsamples of the same outermost mineral surfaces, positive correlation between ages and sample weights, and negative correlation between 230Th/U ages and calculated initial 234U/238U are inconsistent with the assumption that all minerals in a given subsample was deposited instantaneously. The data are more consistent with a conceptual model of continuous deposition where secondary mineral growth has occurred at a constant, slow rate up to the present. This model assumes that individual subsamples represent mixtures of older and younger material, and that calculations using the resulting isotope ratios reflect an average age. Ages calculated using the continuous-deposition model for opals imply average mineral growth rates of less than 5 mm/m.y. The model of continuous deposition also predicts discordance between ages obtained using different radiometric methods for the same subsample. Differences in half-lives will result in younger apparent ages for the shorter-lived isotope due to the greater influence of younger materials continuously added to mineral surfaces. Discordant 14C, 230Th/U and U-Pb ages obtained from outermost mineral surfaces at Yucca Mountain support this model. (C) 2000 Elsevier Science B.V. All rights reserved.

Chemical Geology↗

Oxidative dissolution of biogenic uraninite in groundwater at Old Rifle, CO

Reductive bioremediation is currently being explored as a possible strategy for uranium-contaminated aquifers such as the Old Rifle site (Colorado). The stability of U(IV) phases under oxidizing conditions is key to the performance of this procedure. An in situ method was developed to study oxidative dissolution of biogenic uraninite (UO 2 ), a desirable U(VI) bioreduction product, in the Old Rifle, CO, aquifer under different variable oxygen conditions. Overall uranium loss rates were 50–100 times slower than laboratory rates. After accounting for molecular diffusion through the sample holders, a reactive transport model using laboratory dissolution rates was able to predict overall uranium loss. The presence of biomass further retarded diffusion and oxidation rates. These results confirm the importance of diffusion in controlling in-aquifer U(IV) oxidation rates. Upon retrieval, uraninite was found to be free of U(VI), indicating dissolution occurred via oxidation and removal of surface atoms. Interaction of groundwater solutes such as Ca 2+ or silicate with uraninite surfaces also may retard in-aquifer U loss rates. These results indicate that the prolonged stability of U(IV) species in aquifers is strongly influenced by permeability, the presence of bacterial cells and cell exudates, and groundwater geochemistry.

Colorado↗

Temporal changes in water quality at a childhood leukemia cluster

Since 1997, 15 cases of acute lymphocytic leukemia and one case of acute myelocytic leukemia have been diagnosed in children and teenagers who live, or have lived, in an area centered on the town of Fallon, Nevada. The expected rate for the population is about one case every five years. In 2001, 99 domestic and municipal wells and one industrial well were sampled in the Fallon area. Twenty-nine of these wells had been sampled previously in 1989. Statistical comparison of concentrations of major ions and trace elements in those 29 wells between 1989 and 2001 using the nonparametric Wilcoxon signed-rank test indicate water quality did not substantially change over that period; however, short-term changes may have occurred that were not detected. Volatile organic compounds were seldom detected in ground water samples and those that are regulated were consistently found at concentrations less than the maximum contaminant level (MCL). The MCL for gross-alpha radioactivity and arsenic, radon, and uranium concentrations were commonly exceeded, and sometimes were greatly exceeded. Statistical comparisons using the nonparametric Wilcoxon rank-sum test indicate gross-alpha and -beta radioactivity, arsenic, uranium, and radon concentrations in wells used by families having a child with leukemia did not statistically differ from the remainder of the domestic wells sampled during this investigation. Isotopic measurements indicate the uranium was natural and not the result of a 1963 underground nuclear bomb test near Fallon. In arid and semiarid areas where trace-element concentrations can greatly exceed the MCL, household reverse-osmosis units may not reduce their concentrations to safe levels. In parts of the world where radon concentrations are high, water consumed first thing in the morning may be appreciably more radioactive than water consumed a few minutes later after the pressure tank has been emptied because secular equilibrium between radon and its immediate daughter progeny is attained in pressure tanks overnight.

Ground Water↗

Time differences in the formation of meteorites as determined from the ratio of lead-207 to lead-206

Measurements of the lead isotopic composition and the uranium, thorium, and lead concentrations in meteorites were made in order to obtain more precise radiometric ages of these members of the solar system. The newly determined value of the lead isotopic composition of Canyon Diablo troilite is as follows: 206 Pb/ 204 Pb = 9.307, 207 Pb/ 2O4 Pb = 10.294, and 208 Pb/ 204 Pb = 29.476. The leads of Angra dos Reis, Sioux County, and Nuevo Laredo achondrites are very radiogenic, the 206 Pb/ 204 Pb values are about 200, and the uranium-thorium-lead systems are nearly concordant. The ages of the meteorites as calculated from a single-stage 207 Pb/ 206 Pb isochron based on the newly determined primordial lead value and the newly reported 235 U and 838 U decay constants, are 4.528 x 10 9 years for Sioux County and Nuevo Laredo and 4.555 x 10 9 years for Angra dos Reis. When calculated with the uranium decay constants used by Patterson, these ages are 4.593 x 10 9 years and 4.620 x 10 9 years, respectively, and are therefore 40 to 70 x 10 6 years older than the 4.55 x 10 9 years age Patterson reported. The age difference of 27 x 10 6 years between Angra dos Reis and the other two meteorites is compatible with the difference between the initial 87 Sr/ 86 Sr ratio of Angra dos Reis and that of seven basaltic achondrites observed by Papanastassiou and Wasserburg. The time difference is also comparable to that determined by 129 1- 129 Xe chronology. The ages of ordinary chondrites (H5 and L6) range from 4.52 to 4.57 x 10 9 years, and, here too, time differences in the formation of the parent bodies or later metamorphic events are indicated. Carbonaceous chondrites(C2 and C3) appear to contain younger lead components.

Science↗

Boulder Creek batholith, Colorado part I: Allanite and its bearing upon age patterns

Allanite is abundant and commonly attains unusually large size as a late-replacement mineral in: (1) the comagnatic rocks of the Precambrian Boulder Creek batholith; (2) associated amphibolite xenoliths and related hybrid rocks; and (3) distinctly younger intrusions of Silver Plume Granite that cut the complex. Allanite porphyroblasts develop by replacement of biotite, probably in the presence of emanations from the rare earth-rich and thorium-rich Silver Plume Granite. The largest allanite crystals are made up of nearly isotropic (metamict) cores and birefringent (recrystallized) rims. Smaller crystals are made up exclusively of birefringent material. The maximum birefringence is shown to be that expectable in allanite of Late Cretaceous to early Tertiary age. As plotted on maps, the birefringence increases, and the thorium and uranium contents of the allanite decrease toward a Laramide stock. The variation in birefringence is, therefore, largely relatable to variations in the post-Laramide radiation dosage brought about by differences in the amounts of uranium and thorium lost during recrystallization. The recrystallized allanite is itself partly replaced by epidote which characteristically occurs as a border between allanite and biotite. Total rare-earth oxides for the eight samples of allanite analyzed range from 17.5 to 21.3 percent by weight. In 13 samples, thorium ranged from 0.50 to 1.14 percent by weight, and uranium from 54 to 158 parts pparts per million. Ranges in optical measurements for 20 samples using the spindle stage are: Nα = 1.719–1.759, Nβ = 1.731-1.774, N γ = 1.741–1.784, birefringence = 0.020–0.032, 2V X (calc.) 70°–84°. Ranges for unit-cell data obtained on 8 samples are: a = 8.948–8.985Å, b = 5.721-5.763Å, c = 10.184–10.240Å, β = 115°7.50′–115°25.89′ and volume = 473.02–478.43Å 3 . The average value for the ratio a:b:c = 1.561:1:1.778.

Colorado↗

Middle Proterozoic age for the Montpelier Anorthosite, Goochland terrane, eastern Piedmont, Virginia

Uranium-lead dating of zircons from the Montpelier Anorthosite confirms previous interpretations, based on equivocal evidence, that the Goochland terrane in the eastern Piedmont of Virginia contains Grenvillian basement rocks of Middle Proterozoic age. A very few prismatic, elongate, euhedral zircons, which contain 12–29 ppm uranium, are interpreted to be igneous in origin. The vast majority of zircons are more equant, subangular to anhedral, contain 38–52 ppm uranium, and are interpreted to be metamorphic in origin. One fraction of elongate zircon, and four fragments of a very large zircon (occurring in a nelsonite segregation) yield an upper intercept age of 1045 ± 10 Ma, interpreted as the time of anorthosite crystallization. Irregularly shaped metamorphic zircons are dated at 1011 ± 2 Ma (weighted average of the 207 Pb/ 206 Pb ages). The U-Pb isotopic systematics of metamorphic titanite were reset during the Alleghanian orogeny at 297 ± 5 Ma. These data provide a minimum age for gneisses of the Goochland terrane that are intruded by the anorthosite. Middle Proterozoic basement rocks of the Goochland terrane may be correlative with those in the Shenandoah massif of the Blue Ridge tectonic province, as suggested by similarities between the Montpelier Anorthosite and the Roseland anorthosite. Although the areal extent of Middle Proterozoic basement and basement-cover relations in the eastern Piedmont remain unresolved, results of this investigation indicate that the Goochland terrane is an internal massif of Laurentian crust rather than an exotic accreted terrane.

Geological Society of America Bulletin↗

New perspectives on a 140-year legacy of mining and abandoned mine cleanup in the San Juan Mountains, Colorado

The Gold King mine water release that occurred on 5 August 2015 near the historical mining community of Silverton, Colorado, highlights the environmental legacy that abandoned mines have on the environment. During reclamation efforts, a breach of collapsed workings at the Gold King mine sent 3 million gallons of acidic and metal-rich mine water into the upper Animas River, a tributary to the Colorado River basin. The Gold King mine is located in the scenic, western San Juan Mountains, a region renowned for its volcano-tectonic and gold-silver-base metal mineralization history. Prior to mining, acidic drainage from hydrothermally altered areas was a major source of metals and acidity to streams, and it continues to be so. In addition to abandoned hard rock metal mines, uranium mine waste poses a long-term storage and immobilization challenge in this area. Uranium resources are mined in the Colorado Plateau, which borders the San Juan Mountains on the west. Uranium processing and repository sites along the Animas River near Durango, Colorado, are a prime example of how the legacy of mining must be managed for the health and well-being of future generations. The San Juan Mountains are part of a geoenvironmental nexus where geology, mining, agriculture, recreation, and community issues converge. This trip will explore the geology, mining, and mine cleanup history in which a community-driven, watershed-based stakeholder process is an integral part. Research tools and historical data useful for understanding complex watersheds impacted by natural sources of metals and acidity overprinted by mining will also be discussed.

Colorado↗

Concentrations of trace elements in Great Lakes fishes

The concentration of 15 trace elements was determined by activation analysis of samples of whole fish and fish livers from three of the Great Lakes: Michigan, Superior, and Erie. The average concentrations of 7 elements in 19 whole fish from 3 species were as follows: uranium, 3ppb (parts per billion); thorium, 6ppb; cobalt, 28ppb; cadmium, 94ppb; arsenic, 16ppb; chromium, 1ppm; and copper, 1.3ppm. The average concentrations of 8 elements in 40 liver samples from 10 species of fish were as follows: uranium, 2ppb; thorium, 2ppb; cobalt, 40ppb; copper, 9ppm; zinc, 30ppm; bromine, 0.4ppm; arsenic, 30ppb; and cadmium, 0.4ppm. Other elements observed in most of the samples were: antimony, 5100ppb; gold, 25ppb; lanthanum, 120ppb; rhenium, 0.55ppb; rubidium, 0.064ppm; and selenium, 0.12ppb.Trace element concentrations varied with species and lake. Uranium and thorium varied with species, but not for the same species from different lakes. The levels of copper, cobalt, zinc, and bromine varied little between species and lakes. The concentration of cadmium, arsenic, and chromium varied between species and with species between lakes.

Great Lakes↗

Mineralization of breccia pipes in northern Arizona

The Paleozoic sedimentary rocks on the Colorado Plateau of northern Arizona are host to hundreds ofbreccia pipes. The uranium and copper deposits in these breccia pipes transgress formation boundaries from the Mississippian Redwall Limestone to the Triassic Chinle Formation. They are not classic breccia pipes in that there is no volcanic rock associated with them in time or space. They are the result of solution-collapse within the Redwall Limestone and stoping of the overlying strata. The karst development in the Redwall Limestone began in the Mississippian and apparently either continued to the Triassic or was at least once again active during that time. The mineralization apparently occurred shortly thereafter, sometime during the Mesozoic. Mining activity in breccia pipes of the Grand Canyon region began during the nineteenth century and continues today with the operation of the Hack I, II, and III mines, although the exploited commodity has changed from Cu to U. Although small in size, these pipes contain samples with up to 55 percent U 3 O 8 and can yield ore averaging between 0.30 and 0.60 percent U 3 O 8 .Mineralization at the surface commonly occurs within nodules and concretions associated with pyrite and goethite and along fractures, while the primary ore of the unoxidized zones is commonly within a comminuted sandstone matrix surrounding breccia fragments of overlying formations. The ore mineral is uraninite, although associated with it are sphalerite, galena, chalcopyrite, tennantite, millerite, siegenite, and/molybdenite. Some of the surface nodules are encrusted with malachite and are exceptionally enriched in Ag. Pyrite is abundant, and the organic carbon content of some rocks is high enough to suggest that it, along with the pyrite, may be a reductant for uranium. In contrast, it is possible, if uranium were transported as a bicarbonate or carbonate complex, that only a conduit of brecciated rock was necessary to release CO 2 , thus disrupting the equilibrium and allowing uraninite to precipitate. An extensive suite of elements is significantly enriched in the mineralized rock: Ag, As, Ba, Cd, Co, Cr, Cs, Cu, Hg, Mo, Ni, Pb, Sb, Se, Sr, U, V, Zn, and the rare earth elements. Of these, Cu, Pb, Zn, Ag, and particularly As appear to be the best geochemical indicators of mineralized pipes. At present the origin of the mineralizing fluids is not known. The lack of extensive silification within the breccia, along with the 80 degrees to 173 degrees C fluid inclusion-filling temperatures on sphalerite, dolomite, quartz, and calcite, suggests relatively low-temperature mineralizing fluids, although heated in excess of what would be expected from the normal geothermal gradient on the Colorado Plateau. With the exception of the U-mineralized rock, the mineral assemblage and geochemistry is similar to Mississippi Valley-type deposits.

Economic Geology↗

Finchite, Sr(UO2)2(V2O8)·5H2O, a new uranyl sorovanadate with the francevillite anion topology

Finchite (IMA2017-052), Sr(UO 2 ) 2 (V 2 O 8 )·5H 2 O, is the first uranium mineral known to contain essential Sr. The new mineral occurs as yellow-green blades up to ~10 µm in length in surface outcrops of the calcrete-type uranium deposit at Sulfur Springs Draw, Martin County, Texas, U.S.A. Crystals of finchite were subsequently discovered underground in the Pandora mine, La Sal, San Juan County, Utah, U.S.A., as diamond-shaped golden-yellow crystals reaching up to 1 mm. The crystal structure of finchite from both localities was determined using single-crystal X-ray diffraction and is orthorhombic, Pcan, with a = 10.363(6) Å, b = 8.498(5) Å, c = 16.250(9) Å, V = 1431.0(13) Å 3 , Z = 4 (R 1 = 0.0555) from Sulfur Springs Draw; and a = 10.3898(16), b = 8.5326(14), c = 16.3765(3) Å, V = 1451.8(4) Å 3 , Z = 4 (R 1 = 0.0600) from the Pandora mine. Electron-probe microanalysis provided the empirical formula (Sr 0.88 K 0.17 Ca 0.10 Mg 0.07 Al 0.03 Fe 0.02 ) Σ1.20 (UO 2 ) 2 (V 2.08 O 8 )·5H 2 O for crystals from Sulfur Springs Draw, and (Sr 0.50 Ca 0.28 Ba 0.22 K 0.05 ) Σ0.94 (U 0.99 O 2 ) 2 (V 2.01 O 8 )·5H 2 O for crystals from the Pandora mine, based on 17 O atoms per formula unit. The structure of finchite contains uranyl vanadate sheets based upon the francevillite topology. Finchite is a possible immobilization species for both uranium and the dangerous radionuclide 90 Sr because of the relative insolubility of uranyl vanadate minerals in water.

American Mineralogist↗

Radioactive deposits of Nevada

Thirty-five occurrences of radioactive rocks had been reported from Nevada prior to 1952. Twenty-five of these had been investigated by personnel of the U. S. Geological Surveyor of the U. S. Atomic Energy Commission. Of those investigated, uranium minerals were identified at 13 sites; two sites contained a thorium mineral (monazite); the source of radioactivity on nine properties was not ascertained, and one showed no abnormal radioactivity. Of the other reported occurrences, one is said to contain uraniferous hydrocarbons and nine are placers containing thorian monazite. Pitchblende occurs at two localities, the East Walker River area, and the Stalin's Present prospect, where it is sparsely disseminated in tabular bodies cutting granitic rocks. Other uranium minerals found in the state include: carnotite, tyuyamunite, autunite, torbernite, gummite, uranophane, kasolite, and an unidentified mineral which may be dumontite. Monazite is the only thorium mineral of possible economic importance that has been reported. From an economic standpoint, only four of the properties examined showed reserves of uranium ore in 1952; these are: the Green Monster mine, which shipped 5 tons of ore to Marysvale, Utah, during 1951; the Majuba Hill mine; the Stalin's Present prospect; and the West Willys claim in the Washington district. No estimate has been made of thorium reserves and no commercial deposits of thorium are known.

Bulletin↗

Results of reconnaissance for radioactive minerals in parts of the Alma district, Park County, Colorado

Pitchblende was discovered in July 1951 in the Alma mining district, Park County, Colo., by the U. S. Geological Survey acting on behalf of the U. S. Atomic Energy Commission. The pitchblende is associated with Tertiary veins of three different geologic environments: (1) veins in pre-Cambrian rocks, (2) the London vein system in the footwall block of the London fault, and (3) veins in a mineralized area east of the Cooper Gulch fault. Pitchblende is probably not associated with silver-lead replacement deposits in dolomite. Secondary uranium minerals, as yet undetermined, are associated with pitchblende on two London vein system mine dumps and occur in oxidized vein material from dumps of mines in the other environments. Although none of the known occurrences is of commercial importance, the Alma district is considered a moderately favorable area in which to prospect for uranium ore because 24 of the 43 localities examined show anomalous radioactivity; samples from anomalously radioactive localities, which include mine dumps and some underground workings, have uranium contents ranging from 0.001 to 1.66 percent.

Circular↗

Reconnaissance for radioactive deposits in the Darby Mountains, Seward Peninsula, Alaska, 1948

Radioactivity in the southern and eastern parts of the Darby Mountains, Seward Peninsula, Alaska, appears to be directly related to the occurrence of granite. Concentrates from placers derived from areas containing granite are more radioactive than concentrates from placers not derived from the granite and, generally, contain from 0.01 to 0.05 percent equivalent uranium. The radioactivity of these concentrates is largely due to radioactive elements in common accessory minerals in granite, such as sphene, allanite, zircon, and, locally, monazite. Locally, in the Clear Creek-Vulcan Creek rea, the headwaters of the Kwiniuk River, and on Golovnin Bay near McKinley Creek, concentrates from placers derived from granitic terrain contain as much as 0.1 percent equivalent uranium. The higher radioactivity of the concentrates from the Clear Creek area and on Golovnin Bay is due chiefly to an unidentified uranium-titanium niobate, whereas the higher radioactivity at the headwaters of the Kwiniuk River is due to thorianite.

Circular↗

The Alaska Mineral Resource Assessment Program: Background information to accompany folio of geologic and mineral resource maps of the Circle quadrangle, Alaska

The geology, geochemistry, geophysics, and Landsat imagery of the Circle quadrangle were investigated by an interdisciplinary research team for the purpose of assessing the mineral potential of the area. The quadrangle covers approximately 15,765 km 2 in east-central Alaska; most of it is included in the mountainous Yukon-Tanana Upland physiographic division, but the northernmost part is in the low-lying Yukon Flats section. The Circle mining district, in the east-central part of the quadrangle, has been a major producing area of placer gold since its discovery in 1893. For descriptive purposes, the Circle quadrangle is divided into three areas: the northwest Circle quadrangle, the area north of the Tintina fault zone, and the area south of the Tintina fault zone. The Tintina fault zone extends northwesterly through the northern part of the quadrangle. The northwest Circle quadrangle contains mostly folded and faulted, slightly metamorphosed sedimentary rocks that are intruded by Tertiary granitic plutons. In the northern part of the area north of the Tintina fault zone (Little Crazy Mountains and northern east Crazy Mountains), the rocks consist primarily of the gabbro and basalt of the Circle Volcanics and minor associated chert, graywacke, and limestone. Elsewhere in this area (south of the Circle Volcanics and in the western Crazy Mountains), the rocks are mostly slightly metamorphosed Paleozoic sedimentary rocks that have been folded and faulted. Rocks in the largest part of the quadrangle, the area south of the Tintina fault zone, consist largely of pelitic rocks that are regionally metamorphosed to greenschist and amphibolite facies. Felsic plutons, mostly Tertiary in age, occur throughout the area. The metamorphic rocks are separated from sedimentary rocks on the northwest by thrust faulting. The aeromagnetic and gravity data show clear differences between the areas north and south of the Tintina fault zone. The metamorphic terrane to the south has low overall gravity and local gravity lows over exposed granitic plutons. It is hypothesized that magnetic chlorite schist infolded with nonmagnetic quartzite and schist account for east-northeast-trending magnetic highs that approximately parallel the regional strike of the most prominent foliation in the metamorphic rocks. North of the Tintina fault zone, the Circle Volcanics are characterized by high gravity and east-west-trending magnetic highs. The Tintina fault zone has an intense magnetic high near the western margin of the Circle quadrangle overlying the magnetic granodiorite of the Victoria Mountain pluton. A magnetic high near Circle Hot Springs is less intense, but broader, and could reflect a buried magnetic pluton similar to that of the Victoria Mountain pluton. Computer-enhanced Landsat images of the Circle quadrangle show trends and patterns of concentrations of linear features. Features trending northeast-southwest predominate throughout the quadrangle; northwest-southeast-trending linear features are found mostly south of the Tintina fault zone. High concentrations of linear features were not found to correspond to areas of known mineralization in any consistent or significant way that could presently be used in locating areas of mineralization. Geochemical and mineralogical studies of stream sediment and heavy-mineral concentrates from the Circle quadrangle identify areas of anomalous concentrations of metallic elements, including gold, silver, tin, tungsten, lead, antimony, zinc, thorium, uranium, and beryllium. The data delineate areas of known mineral occurrences and areas that may contain undiscovered mineral resources. To date, placer gold has been the only significant metallic mineral resource from the Circle quadrangle, but the general geologic setting, especially the presence of post-orogenic plutons, is similar to that of regions that contain tin greisen deposits, tungsten skarn deposits, lode gold deposits in metasedimentary rocks, and uranium vein deposits. Six areas or tracts were identified in which such deposits might occur, and two more tracts were delineated as possible for the occurrence of shale-hosted Lead-zinc deposits. The discovery of two diamonds in the gravels of Cooked Creek point to the slight possibility of finding placer or lode diamond deposits. Although most of the past and present gold mining has taken place in four areas in the quadrangle, a sedimentary basin near the town of Central was identified as possibly containing buried placer gold deposits or sedimentary uranium deposits.

Alaska↗

Profiles of gamma-ray and magnetic data for aerial surveys over parts of the Western United States from longitude 108 to 126 degrees W. and from latitude 34 to 49 degrees N.

This CD-ROM contains images generated from geophysical data, software for displaying and analyzing the images and software for displaying and examining profile data from aerial surveys flown as part of the National Uranium Resource Evaluation (NURE) Program of the U.S. Department of Energy. The images included are of gamma-ray data (uranium, thorium, and potassium channels), Bouguer gravity data, isostatic residual gravity data, aeromagnetic anomalies, topography, and topography with bathymetry. This publication contains image data for the conterminous United States and profile data for the conterminous United States within the area longitude 108 to 126 degrees W. and latitude 34 to 49 degrees N. The profile data include apparent surface concentrations of potassium, uranium, and thorium, the residual magnetic field, and the height above the ground. The images on this CD-ROM include graytone and color images of each data set, color shaded-relief images of the potential-field and topographic data, and color composite images of the gamma-ray data. The image display and analysis software can register images with geographic and geologic overlays. The profile display software permits the user to view the profiles as well as obtain data listings and export ASCII versions of data for selected flight lines.

Data Series↗