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Net energy payback and CO2 emissions from three midwestern wind farms: An update

This paper updates a life-cycle net energy analysis and carbon dioxide emissions analysis of three Midwestern utility-scale wind systems. Both the Energy Payback Ratio (EPR) and CO2 analysis results provide useful data for policy discussions regarding an efficient and low-carbon energy mix. The EPR is the amount of electrical energy produced for the lifetime of the power plant divided by the total amount of energy required to procure and transport the materials, build, operate, and decommission the power plants. The CO2 analysis for each power plant was calculated from the life-cycle energy input data. A previous study also analyzed coal and nuclear fission power plants. At the time of that study, two of the three wind systems had less than a full year of generation data to project the life-cycle energy production. This study updates the analysis of three wind systems with an additional four to eight years of operating data. The EPR for the utility-scale wind systems ranges from a low of 11 for a two-turbine system in Wisconsin to 28 for a 143-turbine system in southwestern Minnesota. The EPR is 11 for coal, 25 for fission with gas centrifuge enriched uranium and 7 for gaseous diffusion enriched uranium. The normalized CO2 emissions, in tonnes of CO2 per GW eh, ranges from 14 to 33 for the wind systems, 974 for coal, and 10 and 34 for nuclear fission using gas centrifuge and gaseous diffusion enriched uranium, respectively. ?? Springer Science+Business Media, LLC 2007.

Natural Resources Research↗

Reduction of red bed sedimentary rocks in connection with energy metal ore formation: A case study from the Sinbad seep, Mesa County, Colorado

The Paradox Basin’s Sinbad seep is a modern analog for ancient bleaching of red bed sediments by introduced alkaline, reducing brines. This bleaching, involving reductive alteration of former red beds, is essential ground preparation that enables the altered rocks to trap Cu, U, and V from later oxidized fluids, forming ore deposits. Study of Sinbad thus offers insights into these metallic mineralization processes in the Paradox and other sedimentary basins. The Sinbad seep occurs where shallow groundwater interacts with organic-rich petroleum source rocks, flows up a fault, and discharges into Salt Creek. Ratios of Na/Cl, Na/Br, and Cl/Br, plus high sulfate concentrations, indicate that the salinity of the seep water originated from dissolution of halite and gypsum during topographically driven flow of meteoric water across a diapir of the Pennsylvanian Paradox Formation, rather than from deep basinal brines. In contact with the organic-rich shales of the Paradox, these SO 4 -rich waters become reduced through bacterial reduction, producing H 2 S. The waters react with red beds of the Permian Cutler Formation, causing pervasive bleaching. The bleaching at Sinbad is characterized by iron-conservative reduction of ferric iron in diagenetic hematite and detrital ilmenite and magnetite to Fe sulfides. The ferrous iron is retained in these sulfides likely as sorbed Fe. Associated alteration includes precipitation of quartz and feldspar overgrowths, partial dissolution of detrital quartz and feldspar caused by pressure solution, formation of clay and authigenic rutile, and precipitation of carbonate and gypsum. The Fe sulfides rapidly degenerate to a mixture of jarosite and iron oxides on weathering at the surface. Among the major-oxide elements and most trace elements, there is no statistical difference between unbleached and bleached samples. The exceptions are uranium and sulfur, which are somewhat greater in bleached samples. Fission track radiography illuminates that uranium is preferentially concentrated in iron oxide cements, iron sorbed into detrital clasts, and finely disseminated iron oxide in illite cement in bleached samples. A leaching experiment suggests that uranium may be more easily available for mobilization from rocks that have undergone bleaching alteration, making them potential U sources. In addition, bleached rocks form effective traps for U, V, and some Cu mineralization.

Colorado↗

The geochronology of foraminiferal ooze deposits in the "Southern Ocean"

Many cores raised from the Drake Passage are characterized by alternating zones of foraminiferal ooze and sandysilt. Cores raised from the East Pacific Rise are foraminiferal ooze or alternating siliceous and carbonate ooze. The uranium and thorium concentrations and isotopic ratios in foraminifers separated from these cores were measured by alpha-spectroscopy. 230 Th in foraminiferal tests is found to be out of equilibrium with its parent ( 234 U), enabling the “excess 230 Th” method to be used in estimating sedimentation rates. The uranium concentration of the tests is constant, suggesting constant uranium concentrations in the sea and thus constant production of 230 Th during periods of foraminiferal production. 232 Th concentration is 2.1 ± 0.7 ppm in the Drake Passage and below the level of detection in tests from the East Pacific Rise. Within each core the 232 Th is constant, varying closely with distance from the source. Based on the degree of disequilibrium of 230 Th, correlations between cores can be made. Age estimates of the foraminiferal zones indicate deposition occurred between 8 000 and 120 000 and between 190 000 and 280 000 years before present. Reported dates of high stands of the sea fall between the ages estimated for the foraminiferal zones, suggesting these zones were deposited during northern hemisphere glacial maxima.

Earth and Planetary Science Letters↗

A theoretical study of alpha star populations in loaded nuclear emulsions

This theoretical study of the alpha star populations in loaded emulsions was undertaken in an effort to find a quantitative method for the analysis of less than microgram amounts of thorium in the presence of larger amounts of uranium. Analytical expressions for each type of star from each of the significantly contributing members of the uranium and thorium series as well as summation formulas for the whole series have been computed. The analysis for thorium may be made by determining the abundance of five-branched stars in a loaded nuclear emulsion and comparing of observed and predicted star populations. The comparison may also be used to check the half-lives of several members of the uranium and thorium series.

Geochimica et Cosmochimica Acta↗

Variation of Nb-Ta, Zr-Hf, Th-U and K-Cs in two diabase-granophyre suites

Concentrations of Nb, Ta, Zr, Hf, Th, U and Cs have been determined in samples of igneous rocks representing the diabase-granophyre suites from Dillsburg, Pennsylvania, and Great Lake, Tasmania. Niobium and tantalum have a three to fourfold increase with differentiation in each of the suites. The chilled margin of the Great Lake intrusion contains half the niobium and tantalum content (5.3 ppm and 0.4 ppm, respectively) of the chilled basalt from Dillsburg (10 ppm and 0.9 ppm, respectively). The twofold difference between the suites is correlated with differences in their titanium content. The average Nb Ta "> NbTa ratios for each suite are similar: 13.5 for the Great Lake suite, and 14.4 for the Dillsburg suite. The zirconium content of the two suites is essentially the same and increases from 50 to 60 ppm in the chilled margins to 240–300 ppm in the granophyres. Hafnium is low in the early formed rocks (0.5 –1.5 ppm and achieves a maximum in the granophyres (5–8 ppm). The Zr Hf "> ZrHf ratio decreases from 68 to 33 with progressive differentiation. In the Dillsburg suite thorium and uranium increase from 2.6 ppm and 0.6 ppm, respectively, in the chilled samples to 11.8 ppm and 3.1 ppm in the granophyres. The chilled margin of the Great Lake suite contains 3.2 ppm thorium and 9.8 ppm uranium; the granophyre contains 11.2 ppm thorium and 2.8 ppm uranium. The average Th U "> ThU ratios of the Dillsburg and Great Lake suites are nearly the same—4.1 and 4.4, respectively. Within each suite the Th U "> ThU ratio remains quite constant. Cesium and the K Cs "> KCs ratio do not vary systematically in the Dillsburg suite possibly because of redistribution or loss of cesium by complex geologic processes. Except for the chilled margin of the Great Lake suite, the variation of Cs and the K Cs "> KCs ratio are in accord with theoretical considerations. Cesium increases from about 0.6 ppm in the lower zone to 3.5 ppm in the granophyre; the K Cs "> KCs ratio varies from 10 × 10 3 in the lower zone to 6 × 10 3 in the granophyre. A comparison of the abundance of some of these elements is made with those reported on oceanic tholeiites from the Atlantic and Pacific oceans. Trace elements with large ionic radii (Th, U, Cs) are present in significantly greater concentrations in the two continental tholeiitic series than in the oceanic tholeiites. However, this does not seem to be true for lithophilic elements of smaller ionic radii (Zr and Nb). These trace element distribution patterns, when considered with other minor element and isotopic studies, indicate that 1. crustal contamination does not entirely account for differences between continental and oceanic tholeiites, and 2. the oceanic tholeiites do not necessarily delimit the geochemical characteristics of the mantle.

Geochimica et Cosmochimica Acta↗

Geochemical soil sampling for deeply-buried mineralized breccia pipes, northwestern Arizona

Thousands of solution-collapse breccia pipes crop out in the canyons and on the plateaus of northwestern Arizona; some host high-grade uranium deposits. The mineralized pipes are enriched in Ag, As, Ba, Co, Cu, Mo, Ni, Pb, Sb, Se, V and Zn. These breccia pipes formed as sedimentary strata collapsed into solution caverns within the underlying Mississippian Redwall Limestone. A typical pipe is approximately 100 m (300 ft) in diameter and extends upward from the Redwall Limestone as much as 1000 m (3000 ft). Unmineralized gypsum and limestone collapses rooted in the Lower Permian Kaibab Limestone or Toroweap Formation also occur throughout this area. Hence, development of geochemical tools that can distinguish these unmineralized collapse structures, as well as unmineralized breccia pipes, from mineralized breccia pipes could significantly reduce drilling costs for these orebodies commonly buried 300–360 m (1000–1200 ft) below the plateau surface. Design and interpretation of soil sampling surveys over breccia pipes are plagued with several complications. (1) The plateau-capping Kaibab Limestone and Moenkopi Formation are made up of diverse lithologies. Thus, because different breccia pipes are capped by different lithologies, each pipe needs to be treated as a separate geochemical survey with its own background samples. (2) Ascertaining true background is difficult because of uncertainties in locations of poorly-exposed collapse cones and ring fracture zones that surround the pipes. Soil geochemical surveys were completed on 50 collapse structures, three of which are known mineralized breccia pipes. Each collapse structure was treated as an independent geochemical survey. Geochemical data from each collapse feature were plotted on single-element geochemical maps and processed by multivariate factor analysis. To contrast the results between geochemical surveys (collapse structures), a means of quantifying the anomalousness of elements at each site was developed. This degree of anomalousness, named the “correlation value”, was used to rank collapse features by their potential to overlie a deeply-buried mineralized breccia pipe. Soil geochemical results from the three mineralized breccia pipes (the only three of the 50 that had previously been drilled) show that: (1) Soils above the SBF pipe contain significant enrichment of Ag, Al, As, Ba, Ga, K, La, Mo, Nd, Ni, Pb, Sc, Th, U and Zn, and depletion in Ca, Mg and Sr, in contrast to soils outside the topographic and structural rim; (2) Soils over the inner treeless zone of the Canyon pipe show Mo and Pb enrichment anf As and Ga depletion, in contrast to soils from the surrounding forest; and (3) The soil survey of the Mohawk Canyon pipe was a failure because of the rocky terrane and lack of a B soil horizon, or because the pipe plunges. At least 11 of the 47 other collapse structures studied contain anomalous soil enrichments similar to the SBF uranium ore-bearing pipe, and thus have good potential as exploration targets for uranium. One of these 11, #1102, does contain surface mineralized rock. These surveys suggest that soil geochemical sampling is a useful tool for the recognition of many collapse structures with underlying ore-bearing breccia pipes.

Arizona↗

Diel cycles in dissolved barium, lead, iron, vanadium, and nitrite in a stream draining a former zinc smelter site near Hegeler, Illinois

Diel variations in the concentrations of a number of constituents have the potential to substantially affect the appropriate sampling regimen in acidic streams. Samples taken once during the course of the day cannot adequately reflect diel variations in water quality and may result in an inaccurate understanding of biogeochemical processes, ecological conditions, and of the threat posed by the water to human health and the associated wildlife. Surface water and groundwater affected by acid drainage were sampled every 60 to 90 min over a 48-hour period at a former zinc smelter known as the Hegeler Zinc Superfund Site, near Hegeler, Illinois. Diel variations related to water quality in the aquifer were not observed in groundwater. Diel variations were observed in the temperature, pH, and concentration of dissolved oxygen, nitrite, barium, iron, lead, vanadium, and possibly uranium in surface water. Temperature, dissolved oxygen, nitrite, barium, lead, and uranium generally attained maximum values during the afternoon and minimum values during the night. Iron, vanadium, and pH generally attained minimum values during the afternoon and maximum values during the night. Concentrations of dissolved oxygen were affected by the intensity of photosynthetic activity and respiration, which are dependent upon insolation. Nitrite, an intermediary in many nitrogen reactions, may have been formed by the oxidation of ammonium by dissolved oxygen and converted to other nitrogen species as part of the decomposition of organic matter. The timing of the pH cycles was distinctly different from the cycles found in Midwestern alkaline streams and likely was the result of the photoreduction of Fe 3+ to Fe 2+ and variations in the intensity of precipitation of hydrous ferric oxide minerals. Diel cycles of iron and vanadium also were primarily the result of variations in the intensity of precipitation of hydrous ferric oxide minerals. The diel variation in the concentrations of lead, uranium, and barium may have been affected by competition with Fe + 2 for sorption sites on hydrous ferric oxide minerals.

Illinois↗

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↗