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At least 1,207 records · Page 67Linked to original sources
USGS1996

Radon in ground water of the lower Susquehanna and Potomac River basins

Ground-water samples collected from 267 wells were analyzed for radon as part of a water-quality reconnaissance of subunits of the Lower Susquehanna and Potomac River Basins conducted by the United States Geological Survey (USGS) as part of the National Water-Quality Assessment (NAWQA) program. Radon is a product of the radioactive decay of uranium. Airborne radon has been cited by the Surgeon General of the United States as the second-leading cause of lung cancer and the United States Environmental Protection Agency (USEPA) has identified ground-water supplies as possible contributing sources of indoor radon. Eighty percent of ground-water samples collected for this study were found to contain radon at activities greater than 300 pCi/L (picocuries per liter), the USEPA's proposed Maximum Contaminant Level for radon in drinking water, and 31 percent of samples contained radon at activities greater than 1,000 pCi/L. The 10 subunits where samples were collected were grouped into three classes - median ground-water radon activity less than 300 pCi/L, between 300 pCi/L and 1,000 pCi/L, and greater than 1,000 pCi/L. Subunits underlain by igneous and metamorphic rocks of the Piedmont Physiographic Province typically have the highest median ground-water radon activities (greater than 1,000 pCi/L); although there is a large variation in radon activities within most of the subunits. Lower median radon activities (between 300 pCi/L and 1,000 pCi/L) were found in ground water in subunits underlain by limestone and dolomite. Of three subunits underlain by sandstone and shale, one fell into each of the three radon-activity classes. The large variability within these subunits may be attributed to the fact that the uranium content of sandstone and shale is related to the uranium content of the sediments from which they formed.

lower Susquehanna and Potomac River basins↗
USGS1997

Water-quality assessment of the Rio Grande Valley, Colorado, New Mexico and Texas: Ground-water quality in the Rio Grande flood plain, Cochiti Lake, New Mexico, to El Paso, Texas, 1995

From March to May of 1995, water samples were collected from 30 wells located in the flood plain of the Rio Grande between Cochiti Lake, New Mexico, and El Paso, Texas. These samples were analyzed for a broad host of constituents, including field parameters, major constituents, nutrients, dissolved organic carbon, trace elements, radiochemicals, pesticides, and volatile organic compounds. The main purpose of this study was to observe the quality of ground water in this part of the Rio Grande Valley study unit of the U.S. Geological Survey National Water-Quality Assessment program. The sampling effort was limited to the basin- fill aquifer beneath the above-defined reach of the Rio Grande flood plain because of the relative homogeneity of the hydrogeology, the large amount of ground-water use for public supply, and the potential for land-use activities to affect the quality of ground water. Most of the wells sampled for the study are used for domestic purposes, including drinking water. Depths to the tops of the sampling intervals in the 30 wells ranged from 10 to 345 feet below land surface, and the median was 161.5 feet; the sampling intervals in most of the wells spanned about 10 feet or less. Quality-control data were collected at three of the wells. A significant amount of variation was found in the chemical composition of ground water sampled throughout the study area, but the water generally was found to be of suitable chemical quality for use as drinking water, according to current enforceable standards established by the U.S. Environmental Protection Agency (EPA). Nutrients generally were measured at concentrations near or below their method reporting limits. The most dominant nutrient species was nitrite plus nitrate, at a maximum concentration of 1.9 milligrams per liter (as N). Only eight of the trace elements analyzed for had median concentrations greater than their respective minimum reporting levels. Water from one well exceeded the lifetime health advisory established by the EPA for molybdenum; water from a different well exceeded the proposed EPA maximum contaminant level for uranium. Gross alpha and gross beta particle activities generally appeared to strongly correlate with quantities of uranium and potassium, respectively, detected in ground water. However, water from one well exceeded the EPA maximum contaminant level for gross alpha particle activity and may exceed the EPA maximum contaminant level for beta particle and photon activity, although current data on gross beta particle activities are not conclusive on this point. Radon concentrations did not appear to directly correlate with uranium concentrations. The herbicide prometon was the only synthetic organic compound detected in ground water in the study area, and was detected in only one well, at a concentration of 0.038 microgram per liter. This well is shallow and is not used for drinking water. With the exception of the one detection of prometon, no strong evidence was found of effects on ground-water quality from human activities. Therefore, most of the water sampled probably recharged at the margins of the alluvial basins or recharged through the flood plain before human development began. With respect to major constituents, the concentrations of dissolved solids ranged from 209 to 3,380 milligrams per liter, and the median concentration was 409.5 milligrams per liter. There is evidence that the overall chemical composition of ground water in the study area may be affected by several processes, including cation exchange, feldspar weathering, calcite dissolution and precipitation, dissolution of volcanic glass, and microbial activity. Several chemical constituents in ground water showed relatively distinct spatial patterns that appear to be related to one or more of these processes.

Texas↗
USGS2022

Potential for critical mineral deposits in Maine, USA

An analysis of the potential for deposits of critical minerals and elements in Maine presented here includes data and discussions for antimony, beryllium, cesium, chromium, cobalt, graphite, lithium, manganese, niobium, platinum group elements, rhenium, rare earth elements, tin, tantalum, tellurium, titanium, uranium, vanadium, tungsten, and zirconium. Deposits are divided into two groups based on geological settings and common ore-deposit terminology. One group consists of known deposits (sediment-hosted manganese, volcanogenic massive sulphide, porphyry copper-molybdenum, mafic- and ultramafic-hosted nickel-copper [-cobalt-platinum group elements], pegmatitic lithium-cesium-tantalum) that are in most cases relatively large, well-documented, and have been explored extensively in the past. The second, and much larger group of different minerals and elements, comprises small deposits, prospects, and occurrences that are minimally explored or unexplored. The qualitative assessment used in this study relies on three key criteria: (1) the presence of known deposits, prospects, or mineral occurrences; (2) favourable geologic settings for having certain deposit types based on current ore deposit models; and (3) geochemical anomalies in rocks or stream sediments, including panned concentrates. Among 20 different deposit types considered herein, a high resource potential is assigned only to three: (1) sediment-hosted manganese, (2) mafic- and ultramafic-hosted nickel-copper(-cobalt-platinum group elements), and (3) pegmatitic lithium-cesium-tantalum. Moderate potential is assigned to 11 other deposit types, including: (1) porphyry copper-molybdenum (-rhenium, selenium, tellurium, bismuth, platinum group elements); (2) chromium in ophiolites; (3) platinum group elements in ophiolitic ultramafic rocks; (4) granite-hosted uranium-thorium; (5) tin in granitic plutons and veins; (6) niobium, tantalum, and rare earth elements in alkaline intrusions; (7) tungsten and bismuth in polymetallic veins; (8) vanadium in black shales; (9) antimony in orogenic veins and replacements; (10) tellurium in epithermal deposits; and (11) uranium in peat.

Maine↗
USGS2006

Testing the concept of drift shadow at Yucca Mountain, Nevada

If proven, the concept of drift shadow, a zone of reduced water content and slower ground-water travel time beneath openings in fractured rock of the unsaturated zone, may increase performance of a proposed geologic repository for high-level radioactive waste at Yucca Mountain, To test this concept under natural-flow conditions present in the proposed repository horizon, isotopes within the uranium-series decay chain (uranium-238, uranium-234, and thorium-230, or 238U-234U-230Th) have been analyzed in samples of rock from beneath four naturally occurring lithophysal cavities. All rock samples show 234U depletion relative to parent 238U indicating varying degrees of water-rock interaction over the past million years. Variations in 234U/238U activity ratios indicate that depletion of 234U relative to 238U can be either smaller or greater in rock beneath cavity floors relative to rock near cavity margins. These results are consistent with the concept of drift shadow and with numerical simulations of meter-scale spherical cavities in fractured tuff. Differences in distribution patterns of 234U/ 238U activity ratios in rock beneath the cavity floors are interpreted to reflect differences in the amount of past seepage into lithophysal cavities, as indicated by the abundance of secondary mineral deposits present on the cavity floors.

Conference Paper↗
USGS2015

In-situ arsenic removal during groundwater recharge through unsaturated alluvium

OBJECTIVES The purpose of this study was to determine the feasibility and sustainability of in-situ removal of arsenic from water infiltrated through unsaturated alluvium. BACKGROUND Arsenic is naturally present in aquifers throughout the southwestern United States and elsewhere. In January 2006, the U.S. Environmental Protection Agency (EPA) lowered the Maximum Contaminant Level (MCL) for arsenic from 50 to 10 micrograms per liter (g/L). This raised concerns about naturally-occurring arsenic in groundwater. Although commercially available systems using sorbent iron or aluminum oxide resins are available to treat high-arsenic water, these systems are expensive to build and operate, and may generate hazardous waste. Iron and aluminum oxides occur naturally on the surfaces of mineral grains that compose alluvial aquifers. In areas where alluvial deposits are unsaturated, these oxides may sorb arsenic in the same manner as commercial resins, potentially providing an effective low-cost alternative to commercially engineered treatment systems. APPROACH The Antelope Valley within the Mojave Desert of southern California contains a shallow water-table aquifer with arsenic concentrations of 5 g/L, and a deeper aquifer with arsenic concentrations of 30 g/L. Water was pumped from the deep aquifer into a pond and infiltrated through an 80 m-thick unsaturated zone as part of field-scale and laboratory experiments to treat high-arsenic groundwater and recharge the shallow water table aquifer at the site. The field-scale recharge experiment included the following steps: 1) construction of a recharge pond 2) test drilling for sample collection and instrument installation adjacent to the pond 3) monitoring downward migration of water infiltrated from the pond 4) monitoring changes in selected trace-element concentrations as water infiltrated through the unsaturated zone Data from instruments within the borehole adjacent to the pond were supplemented with borehole and surface geophysical data to evaluate the lateral spreading of water as it moved downward through the unsaturated zone. Three laboratory studies were undertaken. Sequential extraction was used to evaluate the abundance of iron, aluminum, and manganese oxides and selected trace elements on operationally defined sites on the surfaces of mineral grains collected before and after infiltration from the pond. Secondly, radio-labeled arsenic-73 microcosm experiments evaluated the potential for incorporation of arsenic sorbed to exchange sites on mineral grains into less reactive crystalline mineral structures with time. Finally, column studies evaluated arsenic sorption and the pH dependence of sorption for selected unsaturated zone materials. RESULTS/CONCLUSIONS Between December 2010 and July 2012, more than 120,000 cubic meters (m3 ) (about 97 acre-feet) of high-arsenic groundwater was pumped from the deep aquifer into a 0.11 hectare (about 0.27 acres) pond and infiltrated though an 80-meter (about 260 feet) thick unsaturated zone to recharge a water-table aquifer. Arsenic concentrations were lowered from 30 to 2 g/L as water infiltrated though the unsaturated zone at the site. Some uranium, possibly associated with past agricultural land use at the site, was mobilized to concentrations as high as 66 g/L within the unsaturated zone during the experiment. Uranium was resorbed and the high uranium concentrations did not reach the water table at the site. Concentrations of other trace elements, including antimony, chromium, vanadium, and selenium were low throughout the study. Infiltration rates from the pond were as high as 0.4 meters per day (1.1 feet per day, ft/d), and the wetting front moved downward about 25 centimeters per day (cm/d) (0.8 ft/d) to a depth of about 50 m (about 165 feet). Clay layers at that depth slowed the downward movement of the wetting front to about 5 cm/d (0.16 ft/d). Lateral movement of the wetting front was monitored using sequential direct-current (DC) surface and sequential electromagnetic (EM) and DC borehole resistivity. Most lateral movement occurred on a clay layer about 50 m (about 165 feet) below land surface. Infiltrated water reached the water table in January 2013. At the water table, the “wetted footprint” of water infiltrated from the pond, indicated by surface resistivity data, was about 13 hectares (about 32 acres). On the basis of data collected at the site, there is enough sorbent material to operate this pond and treat groundwater having an arsenic concentration of 30 g/L to 2 g/L for about 500 years. Toxicity Characteristic Leaching Procedure (TCLP) data showed arsenic concentrations to be below hazardous levels beneath the pond after the experiment. Pond maintenance may be required to keep infiltration rates high, and prevent accumulation of organic material on the pond bottom, although organic material on the pond bottom may increase removal of other trace elements in infiltrated water including chromium, selenium, and vanadium. Laboratory results are consistent with the field data and show sorption of arsenic in 10 cm (0.3 feet) columns to about 2 g/L over a pH range of 6 to 8, and at influent arsenic concentrations as high as 300 g/L, without breakthrough in 50 pore volumes. Column results suggest that the insitu treatment may remove arsenic in a range of hydrogeologic settings, and would not necessarily be restricted to alkaline alluvial aquifers common throughout the southwestern United States. Radiolabeled arsenic-73 experiments show that although arsenic is initially weakly sorbed (and potentially mobile), with time arsenic is incorporated into amorphous materials. One year after sorption onto surface exchange sites, most sorbed arsenic is incorporated into crystalline oxide minerals on the surfaces of primary mineral grains and is less mobile. Results of the study suggest that long-term land use restrictions on sites used for in-situ treatment of arsenic may not be needed to control water applied to surface materials. This minimizes some regulatory concerns about future land use at sites used for in-situ arsenic treatment. However, future land uses that may alter reduction-oxidation conditions in the subsurface should be avoided, such as infiltration of stormwater recharge or recharge with other water having high organic carbon concentrations (including unsewered residential land use, dairy or other confined animal operations).

Report↗
USGS1975

An occurrence of disseminated uraninite in Wheeler Basin, Grand County, Colorado

Disseminated uraninite occurs in Wheeler Basin, Grand County, Colo., about 5 mi (8 km) southeast of Monarch Lake, in Precambrian metamorphic rocks consisting of migmatized gneiss and mixed gneiss and pegmatite. An intrusion of Precambrian Y Silver Plume Granite lies within 400 ft (122 m) of the occurrence. The disseminated uraninite is confined to parts of the host rock that are rich in biotite; highest grade found was 0.73 percent uranium. The disseminated uraninite occurs as cubes and grains, generally from 0.1 to 0.3 mm across. Unit cell edge of the uraninite, ≈ 5.48 A, suggests its pegmatitic origin. The origin of the uraninite disseminations is attributed by us to remobilization and concentration of elements during metamorphism caused by the intrusion of Silver Plume Granite. Uranium and lead isotopic analyses by K. R. Ludwig of uraninite and monazite from biotite concentrations confirm an apparent age of 1,450±20 m.y. for these minerals. This age is equivalent to that reported for the Silver Plume Granite. Although the Wheeler Basin occurrence is small in size, it has many similarities to the Rossing uranium deposit in South-West Africa.

Colorado↗
USGS1977

Effect of initial radioactive-daughter disequilibrium on U-Pb isotope apparent ages of young minerals

Most calculations of U-Pb isotope apparent ages are made by use of equations that assume initial secular equilibrium of the uranium decay-chains. The possible error in calculated Pb/U isotope ratios arising from this assumption (especially for ores of sandstone uranium deposits) can be over 10 percent at 1 million years and exceed analytical error even at a 30 m.y. apparent age. Use of the more general equations (adapted from the Bateman equations) is desirable for calculation and interpretation of U-Pb isotope apparent ages of both open and closed systems in the range of 2 to 20 m.y. and is essential for apparent ages less than about 2 m^y. For very young sandstone uranium deposits, a significant uncertainty in the 208 Pb/ 238 U systematics may still persist owing to the uncertainty in the initial value of 234 U/ 238 U.

Journal of Research of the U.S. Geological Survey↗
USGS2015

Long-term anoxia and release of ancient, labile carbon upon thaw of Pleistocene permafrost

The fate of permafrost carbon upon thaw will drive feedbacks to climate warming. Here we consider the character and context of dissolved organic carbon (DOC) in yedoma permafrost cores from up to 20 m depth in central Alaska. We observed high DOC concentrations (4 to 129 mM) and consistent low molecular weight organic acid concentrations in three cores. We estimate a DOC production rate of 12 µmol DOC m −2 yr −1 based on model ages of up to ~200 kyr derived from uranium isotopes. Acetate C accounted for 24 ± 1% of DOC in all samples. This proportion suggests long-term anaerobiosis and is likely to influence thaw outcomes due to biolability of acetate upon release in many environments. The combination of uranium isotopes, ammonium concentrations, and calcium concentrations explained 86% of the variation in thaw water DOC concentrations, suggesting that DOC production may be related to both reducing conditions and mineral dissolution over time.

Geophysical Research Letters↗
USGS2006

Sea-cave temperature measurements and amino acid geochronology of British Late Pleistocene Sea stands

‘Calibrating’ amino acid ratios with uranium-series dates requires an accurate knowledge of current mean annual temperatures (CMATs) over the region studied. To measure these, test-tube sized ‘diffusion sensors’ were emplaced for 1 year (in 1984, 1985 and 1986), both outside and inside Minchin Hole sea-cave in South Wales and Belle Hougue sea-cave in Jersey, both of which have yielded Oxygen Isotope Substage 5e uranium-series ages on speleothems. Our outside temperatures agreed with meteorological ones. Our inside temperatures were over 1°C lower. To allow for this, a mean of ‘empirical’, ‘linear’ and ‘parabolic’ epimerisation calculations suggests that ratios from molluscs inside the caves should be multiplied by over 1.1 for comparison with outside ratios. This raises Bowen et al .'s ‘Pennard’ stage ratios from inside Minchin (and Bacon) Hole up towards the ‘Unnamed’ stage ratios outside, and suggests that the Unnamed sites are also from Oxygen Isotope Substage 5e, as proposed by Proctor and Smart. The same conclusion is reached more strongly by comparisons with the ratios and temperatures inside Belle Hougue to the south, and at Eemian (assumed 5e) sites in The Netherlands, Germany and Denmark to the east. The Pennard ratios from outside sites may provide further evidence for global sea stands close to the present level later in Oxygen Isotope Stage 5.

Journal of Quaternary Science↗
USGS1992

Sampling and analysis for radon-222 dissolved in ground water and surface water

Radon-222 is a naturally occurring radioactive gas in the uranium-238 decay series that has traditionally been called, simply, radon. The lung cancer risks associated with the inhalation of radon decay products have been well documented by epidemiological studies on populations of uranium miners. The realization that radon is a public health hazard has raised the need for sampling and analytical guidelines for field personnel. Several sampling and analytical methods are being used to document radon concentrations in ground water and surface water worldwide but no convenient, single set of guidelines is available. Three different sampling and analytical methods-bubbler, liquid scintillation, and field screening-are discussed in this paper. The bubbler and liquid scintillation methods have high accuracy and precision, and small analytical method detection limits of 0.2 and 10 pCi/l (picocuries per liter), respectively. The field screening method generally is used as a qualitative reconnaissance tool.

Environmental Monitoring and Assessment↗
USGS1994

An integrated data-directed numerical method for estimating the undiscovered mineral endowment in a region

An integrated data-directed numerical method has been developed to estimate the undiscovered mineral endowment within a given area. The method has been used to estimate the undiscovered uranium endowment in the San Juan Basin, New Mexico, U.S.A. The favorability of uranium concentration was evaluated in each of 2,068 cells defined within the Basin. Favorability was based on the correlated similarity of the geologic characteristics of each cell to the geologic characteristics of five area-related deposit models. Estimates of the undiscovered endowment for each cell were categorized according to deposit type, depth, and cutoff grade. The method can be applied to any mineral or energy commodity provided that the data collected reflect discovered endowment. ?? 1994 Oxford University Press.

Nonrenewable Resources↗
USGS2009

Unconventional energy resources: 2007-2008 review

This paper summarizes five 2007–2008 resource commodity committee reports prepared by the Energy Minerals Division (EMD) of the American Association of Petroleum Geologists. Current United States and global research and development activities related to gas hydrates, gas shales, geothermal resources, oil sands, and uranium resources are included in this review. These commodity reports were written to advise EMD leadership and membership of the current status of research and development of unconventional energy resources. Unconventional energy resources are defined as those resources other than conventional oil and natural gas that typically occur in sandstone and carbonate rocks. Gas hydrate resources are potentially enormous; however, production technologies are still under development. Gas shale, geothermal, oil sand, and uranium resources are now increasing targets of exploration and development, and are rapidly becoming important energy resources that will continue to be developed in the future.

Natural Resources Research↗
USGS2020

Sediment record of mining legacy and water quality from a drinking-water reservoir, Aztec, New Mexico, USA

The record of mining legacy and water quality was investigated in sediments collected in 2018 from four trenches in the Aztec, New Mexico, drinking-water reservoir #1. Bulk chemical analysis of sediments with depth in the reservoir revealed variable trace-element (uranium, vanadium, arsenic, copper, sulfur, silver, lead, and zinc) concentrations, which appear to coincide with historical mining and milling operations. Cesium-137 age dating, which identified the location of the 1963 radioactive fallout maximum, combined with the known age of the bottom and top of the sediment trenches, was used to estimate a polynomial sedimentation rate (average rate = 1.7 cm/yr). The clay size fraction (< 0.004 mm) was the dominant grain-size fraction of the sediments. Abundant fine-grained phyllosilicate (clay) minerals, predominantly montmorillonite and kaolinite, may explain sorption properties of trace elements. Scanning electron microscopy evaluation of sediments from two trenches showed copper and zinc associated with sulfur, and arsenic associated with iron and aluminum oxides. Results from laboratory batch experiments indicated that uranium, vanadium, and arsenic were released when sediments were reacted with a 150 mg/L sodium bicarbonate solution whereas copper was released when sediments were reacted with 2 mMol/L acetic acid. Observed concentrations from the two leach tests were below regulatory thresholds for delivery of solids to a landfill and were below drinking-water standards. Diatom relative abundance indicates that the water quality in the reservoir was not impaired by high metal concentrations.

Colorado, New Mexico↗
USGS1958

The next decade in geochemistry

The purpose, associations, functions; and activities of the Geochmical Society are reviewed briefly. Work on the Colorado Plateau uranium deposits is described as an example of what geochemical research, in conjunction with detailed field work, mineralogical studies, and related techniques can contribute to the understanding of a type of deposit. It is pointed out that not only have these studies given a great deal of information about the origin of the ores, but they have brought about directly a manifold increase in production and reserves of uranium in the United States. Indirectly, they aided the discovery of the tremendous deposits of the Blind River area in Ontario. It is suggested that similar broad cooperative attacks could not only yield comparable results with other types of mineral deposits, such as laterites and Mississippi Valley type lead-zinc deposits, but could also advance our knowledge and understanding of such diverse problems of geology and cosmology as the origin of granites, origin and geologic implications of meteorites (including tektites), origin and search for petroleum, and geochemical relations and interpretations of natural waters. For each of these problems methods of approach are outlined and for some of them, specific projects and correlative problems are mentioned. It is further suggested that the broad cooperative attack needed for most of these problems might be fostered most effectively by a programme comparable to that of the I.G.Y., even though for most types of geochemical research synoptic sampling and observations are not as important as they are for many projects in geophysics.

Geochimica et Cosmochimica Acta↗
USGS1959

New occurrences of ferroselite (FeSe2)

Iron selenide from the uranium-vanadium ores of the Colorado Plateau was under investigation when ferroselite was described as a new mineral in Russia by Bur'yanova and Komkov (1955). Association of ferroselite with selenian pyrite and marcasite within discrete areas of these uranium-vanadium deposits suggests an unusual environment of formation. Its association with apparent low temperature assemblages in the United States and Bussia indicates that its minimum temperature of formation is quite low. Chemical analyses of ferroselite agree well with the theoretical formula FeSe 2 ; material from the Virgin no. 3 mine, Montrose County, Colorado, gives the formula FeSe 2.07 and that from the A.E.C. no. 8 mine, Temple Mountain, Utah, gives the formula (Fe, Co)Se 2.08 . The similarity of hastite and ferroselite suggests that a complete series FeSe 2 -CoSe 2 may exist. In contrast to this, pyrite associated with ferroselite apparently will camouflage only 4 per cent (molecular) FeSe 2 within its structure. Ferroselite cannot be distinguished from rammelsbergite (FeAs 2 ) by X-ray or in polished section; therefore, the exact identification of these two minerals can be made only by specific tests for As or Se. As hastite (CoSe 2 ) and marcasite are in the same structure group as ferroselite and rammelsbergite, identification of these minerals should include qualitative chemical determinations.

Geochimica et Cosmochimica Acta↗
USGS1994

A precise 232Th-208Pb chronology of fine-grained monazite: Age of the Bayan Obo REE-Fe-Nb ore deposit, China

We have obtained precise Th-Pb internal isochron ages on monazite and bastnaesite for the world's largest known rare earth elements (REE)-Fe-Nb ore deposit, the Bayan Obo of Inner Mongolia, China. The monazite samples, collected from the carbonate-hosted ore zone, contain extremely small amounts of uranium (less than 10 ppm) but up to 0.7% ThO 2 . Previous estimates of the age of mineralization ranged from 1.8 to 0.255 Ga. Magnetic fractions of monazite and bastnaesite samples (<60-μm size) showed large ranges in 232 Th 204 Pb "> 232 Th 204 Pb values (900–400,000) and provided precise Th-Pb internal isochron ages for paragenetic monazite mineralization ranging from 555 to 398 Ma within a few percent error (0.8% for two samples). These results are the first indication that REE mineralization within the giant Bayan Obo ore deposit occurred over a long period of time. The initial lead isotopic compositions (low 206 Pb 204 Pb "> 206 Pb 204 Pb and high 208 Pb 204 Pb) "> 208 Pb 204 Pb) and large negative ϵ Nd values for Bayan Obo ore minerals indicate that the main source(s) for the ores was the lower crust which was depleted in uranium, but enriched in thorium and light rare earth elements for a long period of time. Zircon from a quartz monzonite, located 50 km south of the ore complex and thought to be related to Caledonian subduction, gave an age of 451 Ma, within the range of monazite ages. Textural relations together with the mineral ages favor an epigenetic rather than a syngenetic origin for the orebodies. REE mineralization started around 555 Ma (disseminated monazite in the West, the Main, and south of the East Orebody), but the main mineralization (banded ores) was related to the Caledonian subduction event ca. 474-400 Ma.

Bayan Obo, Kuanggou Fault↗
USGS1989

Chemical hydrogeology in natural and contaminated environments

Chemical hydrogeology, including organic and inorganic aspects, has contributed to an increased understanding of groundwater flow systems, geologic processes, and stressed environments. Most of the basic principles of inorganic-chemical hydrogeology were first established by investigations of organic-free, regional-scale systems for which simplifying assumptions could be made. The problems of groundwater contamination are causing a shift of emphasis to microscale systems that are dominated by organic-chemical reactions and that are providing an impetus for the study of naturally occurring and manmade organic material. Along with the decrease in scale, physical and chemical heterogeneity become major controls. Current investigations and those selected from the literature demonstrate that heterogeneity increases in importance as the study site decreases from regional-scale to macroscale to microscale. Increased understanding of regional-scale flow systems is demonstrated by selection of investigations of carbonate and volcanic aquifers to show how applications of present-day concepts and techniques can identify controlling chemical reactions and determine their rates; identify groundwater flow paths and determine flow velocity; and determine aquifer characteristics. The role of chemical hydrogeology in understanding geologic processes of macroscale systems is exemplified by selection of investigations in coastal aquifers. Phenomena associated with the mixing zone generated by encroaching sea water include an increase in heterogeneity of permeability, diagenesis of minerals, and formation of geomorphic features, such as caves, lagoons, and bays. Ore deposits of manganese and uranium, along with a simulation model of ore-forming fluids, demonstrate the influence of heterogeneity and of organic compounds on geochemical reactions associated with genesis of mineral deposits. In microscale environments, importance of heterogeneity and consequences of organic reactions in determining the distribution and concentrations cf. constituents are provided by several studies, including infiltration of sewage effluent and migration of creosote in coastal plain aquifers. These studies show that heterogeneity and the dominance of organically controlled reactions greatly increase the complexity of investigations.Current investigations and those selected from the literature demonstrate that heterogeneity increases in importance as the study site decreases from regional-scale to macroscale to microscale. Increased understanding of regional-scale flow systems is demonstrated by selection of investigations of carbonate and volcanic aquifers to show how application of present-day concepts and techniques can identify controlling chemical reactions and determine their rates; identify groundwater flow paths and determine flow velocity; and determine aquifer characteristics. The role of chemical hydrogeology in understanding geologic processes of macroscale systems is exemplified by selection of investigations in coastal aquifers. Ore deposits of manganese and uranium, along with a simulation model of ore-forming fluids, demonstrate the influence of heterogeneity and of organic compounds on geochemical reactions associated with genesis of mineral deposits. In microscale environments, importance of heterogeneity is illustrated by studies of infiltration of sewage effluent and migration of creosote in coastal plain aquifers.

Journal of Hydrology↗
USGS1991

Pliocene-Pleistocene coastal events and history along the western margin of Australia

Coastal deposits along the western coastal margin of Australia, a region of relative tectonic stability, record Plio-Pleistocene events and processes affecting the inner shelf and adjacent hinterland. Tectonic deformation of these deposits is more apparent in the Carnarvon Basin, and rather less so in the Perth Basin. The most complete record comes from the Perth Basin, where units of Pliocene and Pleistocene ages are well represented. In the Perth Basin, the predominantly siliciclastic Yoganup Formation, Ascot Formation and Bassendean Sand represent a complex of shoreline, inner shelf and regressive-dune facies equivalents, the deposition of which began at an undetermined stage of the Pliocene, through to the Early Pleistocene. The deposition of this sequence closed with a major regression and significant faunal extinction. Bioclastic carbonates characterize the Middle and Late Pleistocene of the Perth and Carnarvon basins. Fossil assemblages include a distinct subtropical element, unknown from the Ascot Formation and suggesting a strengthening of the Leeuwin Current. The estuarine arcoid bivalve Anadara trapezia characterizes assemblages of Oxygen Isotope Stages 5 and 7 in the Perth and Carnarvon basins, where it is now extinct. Deposits of Substage 5e (Perth Basin) also record a southerly expansion of warm-water corals and other fauna consistent with shelf temperatures warmer than present. New uranium-series ages on corals from marine sequences of the Tantabiddi Member, of the Bundera Calcarenite of the western Cape Range are consistent with the ‘double peak’ hypothesis for levels of Substage 5e but the evidence remains less than conclusive. Initial uranium-series dates from the Bibra and Dampier formations of Shark Bay indicate that both derive from the Late Pleistocene. These numerical ages contradict previous interpretations of relative ages obtained from field studies. The age relationship of the units requires further investigation.

Quaternary Science Reviews↗