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USGS2021

Hydraulic characterization of carbonate-rock and basin-fill aquifers near Long Canyon, Goshute Valley, northeastern Nevada

Understanding groundwater flow and pumping effects near pending mining operations requires accurate subsurface hydraulic characterization. To improve conceptual models of groundwater flow and development in the complex hydrogeologic system near Long Canyon Mine, in northwestern Goshute Valley, northeastern Nevada, the U.S. Geological Survey characterized the hydraulic properties of carbonate rocks and basin-fill aquifers using an integrated analysis of steady-state and stressed aquifer conditions informed by water chemistry and aquifer-test data. Hydraulic gradients and groundwater-age data in northern Goshute Valley indicate carbonate rocks in the Pequop Mountains just west and south of the Long Canyon Mine project area constitute a more permeable and active flow system than saturated rocks in the northern Pequop Mountains, western Toano Range, and basin fill. Permeable carbonate rocks in the northern Pequop Mountains, in part, discharge to the Johnson Springs wetland complex (JSWC), where mean groundwater ages range from 500 to 2,400 years and samples all contain a small fraction of modern waters, relative to mean ages of 8,600 to more than 22,000 years for most groundwater sampled to the north and east. Recharge to the JSWC occurs from a roughly 27-square-mile area in the upgradient Pequop Mountains to the west, composed mostly of permeable carbonate rock and fractured quartzite, and bounded by low-permeability shales and marbleized and siliclastic rocks. Single-well aquifer-test analyses provided transmissivity estimates at pumped wells. Transmissivity estimates ranged from 7,000 to 400,000 feet squared per day (ft 2 /d) in carbonate rocks and from 2,000 to 80,000 ft 2 /d in basin fill near the Long Canyon Mine. Water-level drawdown from multiple-well aquifer testing and rise from unintentional leakage into the overlying basin-fill aquifer were estimated and distinguished from natural fluctuations in 93 pumping and monitoring sites using analytical water-level models. Leakage of disposed aquifer-test pumpage occurred south of the aquifer test area through an unlined irrigation ditch. Drawdown was detected at distances of as much as 3 miles (mi) from pumping wells at all but one carbonate-rock site, at basin-fill sites on the alluvial fan immediately downgradient from pumping wells, and in Big Spring and spring NS-05. Similar drawdowns in carbonate rocks within the drawdown detection area suggest all wells penetrate a highly transmissive zone (HTZ) that is bounded by low-permeability rocks. Drawdown was not detected in carbonate rocks to the west of Canyon fault, in any basin-fill sites on the valley floor east of the Hardy fault, or at volcanic sites to the north, indicating that these major fault structures and (or) permeability contrasts between hydrogeologic units impeded groundwater flow or obscured pumping signals. Alternatively, unintentional leakage might have obscured drawdown at basin-fill sites on the valley floor, where water-level rise was detected at nine sites over 3 mi. Consistent hydraulic properties were estimated by simultaneously interpreting steady-state flow during predevelopment conditions and changes in groundwater levels and springflows from the 2016 carbonate-rock aquifer test with an integrated groundwater-flow model. Hydraulic properties were distributed across carbonate rocks, basin fill, volcanic rocks, and siliciclastic rocks with a hydrogeologic framework developed from geologic mapping and hydraulic testing. Estimated transmissivity distributions spanned at least three orders of magnitude in each rock unit. In the HTZ, simulated transmissivities ranged from 10,000 to 23,000,000 ft 2 /d, with the most transmissive areas occurring around Big Spring. Comparatively low carbonate-rock transmissivities of less than 10,000 ft 2 /d were estimated in the northern Pequop Mountains and poorly defined values of less than 1,000 ft 2 /d were estimated in the western Toano Range. Transmissivities in basin fill ranged from less than 10 to 80,000 ft 2 /d and were minimally constrained by the 2016 carbonate-rock aquifer test because poorly quantified leakage affected water levels more so than pumping. The most transmissive areas were informed by single-well aquifer tests along the eastern edge of the Pequop Mountains near Long Canyon Mine and could be indicative of a hydraulic connection between basin fill and more transmissive underlying carbonate rocks. Simulated transmissivities of volcanic and low-permeability rocks mostly are less than 1,000 ft 2 /d. The estimated hydraulic-property distributions and informed interpretation of hydraulic connections among hydrogeologic units improved the characterization and representation of groundwater flow near the Long Canyon Mine.

Nevada↗

USGS1983

Geohydrologic data for test well USW H-5, Yucca Mountain area, Nye County, Nevada

This report presents data on drilling operations, lithology, borehole geophysics, water-level monitoring, core analysis, ground-water chemistry, pumping tests, and packer-injection tests for test well USW H-5. The well is one of a series of test wells drilled in and near the southwestern part of the Nevada Test Site, Nye County, Nevada, in cooperation with the U.S. Department of Energy. These test wells are part of the Nevada Nuclear Waste Storage Investigations to identify suitable sites for storage of high-level radioactive wastes. Test well USW H-5 was drilled to a total depth of 1,219 meters through volcanic rocks consisting mostly of ash-flow tuff. Depth to water in the well ranged between 703.8 and 707.2 meters below land surface, at an approximate altitude of 704 meters above sea level. Drawdown in the well exceeded 6 meters after test pumping more than 3,000 minutes at a rate of 10 liters per second. Borehole-flow surveys showed that about 90 percent of the water in the well is contributed by the zone between 707 and about 820 meters below land surface. Two composite water samples collected after well completion contained 206 and 220 milligrams per liter of dissolved solids. Sodium and bicarbonate were the predominant dissolved anion and cation. The concentration of dissolved silica was 48 milligrams per liter in both samples, which is a relatively large concentration for most natural waters.

Nevada↗

USGS2016

Climatic drivers for multidecadal shifts in solute transport and methane production zones within a large peat basin

Northern peatlands are an important source for greenhouse gases, but their capacity to produce methane remains uncertain under changing climatic conditions. We therefore analyzed a 43 year time series of the pore-water chemistry to determine if long-term shifts in precipitation altered the vertical transport of solutes within a large peat basin in northern Minnesota. These data suggest that rates of methane production can be finely tuned to multidecadal shifts in precipitation that drive the vertical penetration of labile carbon substrates within the Glacial Lake Agassiz Peatlands. Tritium and cation profiles demonstrate that only the upper meter of these peat deposits was flushed by downwardly moving recharge from 1965 to 1983 during a Transitional Dry-to-Moist Period. However, a shift to a moister climate after 1984 drove surface waters much deeper, largely flushing the pore waters of all bogs and fens to depths of 2 m. Labile carbon compounds were transported downward from the rhizosphere to the basal peat at this time producing a substantial enrichment of methane in Δ 14 C with respect to the solid-phase peat from 1991 to 2008. These data indicate that labile carbon substrates can fuel deep production zones of methanogenesis that more than doubled in thickness across this large peat basin after 1984. Moreover, the entire peat profile apparently has the capacity to produce methane from labile carbon substrates depending on climate-driven modes of solute transport. Future changes in precipitation may therefore play a central role in determining the source strength of peatlands in the global methane cycle.

Minnesota↗

USGS2007

Relationship between annual runoff and watershed area for the eastern United States

As part of the U.S. Environmental Protection Agency's effort to determine the long-term effects of acidic deposition on surface water chemistry, annual runoff was estimated for about 1000 ungaged sites in the eastern U.S. using runoff contour maps. One concern in using contour maps was that a bias may be introduced in the runoff estimates due to the size of the 1000 ungaged sites relative to the size of the watersheds used in developing the maps. To determine if a bias was present the relationship between the annual runoff (expressed as depth) and the watershed area for the Northeast (NE) and Southern Blue Ridge Province (SBRP) was tested using five regional data bases. One short-term data base (1984 Water Year, n = 531) and two long-term data bases (1940–57, n = 134 and 1951–80, n = 342) were used in the NE. In the SBRP one short-term database (1984 Water Year, n = 531) and one long-term data base (1951–80, n = 60) were used. For the NE and the SBRP, runoff was not directly correlated with watershed area using the five regional databases. Also, runoff normalized by precipitation was not related to watershed area.

northeastern United States↗

USGS1983

Geohydrologic data for test well USW H-6 Yucca Mountain area, Nye County, Nevada

The following data are presented for test well USW H-6: drilling operations, lithology, availability of borehole geophysical logs , water levels, future availability of core analyses, water chemistry, pumping tests, and packer-injection tests. The well is one of a series of test wells drilled in and near Yucca Mountain adjacent to the Nevada Test Site, Nye County, Nevada, in cooperation with the U.S. Department of Energy. These investigations are part of the Nevada Nuclear Waste Storage Investigations to identify suitable sites for underground storage of high-level radioactive wastes. Test well USW H-6 was drilled to a total depth of 1,220 m. Rocks penetrated are predominantly ash-flow tuffs. Lava was encountered from 877 to 1 ,126 m. The composite static water level is approximately 526 m below land surface. The well was pumped during two periods. Maximum drawdown was about 18 m after pumping for 4,822 min at 28 L/sec, and 12 m after pumping for 2,226 min at 27 L/sec. A borehole flow survey showed that 91% of the water withdrawn from the well came from the depth intervals from 616 to 631 m, and from 777 to 788 m. (Author 's abstract)

Open-File Report↗

USGS1986

Geohydrology of the aquifers that may be affected by the surface mining of coal in the Fruitland Formation in the San Juan Basin, northwestern New Mexico

A monitoring network of 50 wells was installed from 1975 to 1979 in the surface-mineable coal area. The purpose of the network was to collect hydrologic data and to establish a data base. The hydrologic data consist of water level measurements, water chemistry, and selected aquifer characteristics. The four aquifers considered in this study are: (1) The Pictured Cliffs Sandstone; (2) coal seams and interbedded lithologic units of the Fruitland Formation; (3) overburden of the Kirtland Shale and Fruitland Formation; and (4) the alluvium along the Chaco River and its eastern and northeastern tributaries. Five sites were selected for study. Four of these sites, Western Coal Company 's lease near Fruitland, Bisti West, Kimbeto, and Ojo Encino, have surface-mineable coal. The Chaco River alluvium was selected because it is downstream from anticipated mining activity. The specific conductances of the representative water samples from selected wells in the 4 aquifers in the 5 study areas ranged from 800 to 23,000 microsiemens/cm at 25 C. The dominant cation in all samples was sodium. The water is brackish in the Pictured Cliffs Sandstone and in the coal seams and interbedded lithologic units of the Fruitland Formation. It is fresh to saline in the overburden of the Fruitland Shale and Fruitland Formation, and fresh to brackish in the Chaco River alluvium. (Author 's abstract)

Water-Resources Investigations Report↗

USGS1997

Transport and transformations of chlorinated-solvent contamination in a saprolite and fractured rock aquifer near a former wastewater-treatment plant, Greenville, South Carolina

The transport and fate of chlorinated-ethene contamination was investigated in a fractured-rock aquifer downgradient from a wastewater-treatment plant at a gas-turbine manufacturing facility in Greenville, South Carolina. A vapor-diffusion-sampler technique, developed for this investigation, located fracture zones that discharged contaminated ground water to surface water. The distribution of chlorinated compounds and sulfate, comparison of borehole geophysical data, driller's logs, and the aquifer response to pumpage allowed subsurface contaminant-transport pathways to be delineated.The probable contaminant-transport pathway from the former aeration lagoon was southward. The probable pathway of contaminant transport from the former sludge lagoon was southward to and beneath Little Rocky Creek. South of the creek, the major pathway of contaminant transport appeared to be at a depth of approximately 80 to 107 feet below land surface. The contaminant-transport pathway from the former industrial lagoon was not readily discernible from existing data. A laboratory investigation, as well as examination of ground- water-chemistry data collected during this investigation and concentrations of chlorinated compounds collected during previous investigations,indicates that higher chlorinated compounds are being degraded to lower-chlorinated compounds in the contaminated aquifer. The approaches used in this investigation, as well as the findings, have potential application to other fractured-rock aquifers contaminated by chlorinated ethenes.

South Carolina↗

USGS2021

Machine learning predictions of mean ages of shallow well samples in the Great Lakes Basin, USA

The travel time or “age” of groundwater affects catchment responses to hydrologic changes , geochemical reactions, and time lags between management actions and responses at down-gradient streams and wells. Use of atmospheric tracers has facilitated the characterization of groundwater ages, but most wells lack such measurements. This study applied machine learning to predict ages in wells across a large region around the Great Lakes Basin using well, chemistry, and landscape characteristics. For a dataset of age tracers in 961 samples, the travel time from the land surface to the sample location was estimated for each sample using parametric functions. The mean travel times were then modeled using a gradient boosting machine (GBM) algorithm with cross validation tuning of model metaparameters. The GBM approach was able to closely match estimated ages for the training data (RMSE = 0.26 natural-log scale years) and provided a reasonable match to testing data (RMSE = 0.84). Of the variables tested, well characteristics (e.g. depth), land use, hydrologic indicators (e.g. topographic wetness index), and water chemistry (e.g. nitrate, fluoride, and pH), substantially affected the predictions of age. GBM prediction was applied to 14,335 groundwater samples with median sample depth of 5.4 m, indicating for the Great Lakes Basin a broad distribution of ages among wells with a median of 32.9 years. Lag times of decades are likely for these wells to respond to changing solute fluxes near land surface. While depth variables most strongly affected predicted mean ages, chemical constituents exhibited smooth trends with age, consistent with prevailing conceptual models of evolving sources and geochemistry flowpaths. The results provide proof of concept for use of readily available variables of well, landscape, and chemical characteristics to improve groundwater age estimates across large regions.

Great Lakes basin↗

USGS2007

Mining-impacted sources of metal loading to an alpine stream based on a tracer-injection study, Clear Creek County, Colorado

Base flow water in Leavenworth Creek, a tributary to South Clear Creek in Clear Creek County, Colorado, contains copper and zinc at levels toxic to aquatic life. The metals are predominantly derived from the historical Waldorf mine, and sources include an adit, a mine-waste dump, and mill-tailings deposits. Tracer-injection and water-chemistry synoptic studies were conducted during low-flow conditions to quantify metal loads of mining-impacted inflows and their relative contributions to nearby Leavenworth Creek. During the 2-year investigation, the adit was rerouted in an attempt to reduce metal loading to the stream. During the first year, a lithium-bromide tracer was injected continuously into the stream to achieve steady-state conditions prior to synoptic sampling. Synoptic samples were collected from Leavenworth Creek and from discrete surface inflows. One year later, synoptic sampling was repeated at selected sites to evaluate whether rerouting of the adit flow had improved water quality. The largest sources of copper and zinc to the creek were from surface inflows from the adit, diffuse inflows from wetland areas, and leaching of dispersed mill tailings. Major instream processes included mixing between mining- and non-mining-impacted waters and the attenuation of iron, aluminum, manganese, and othermetals by precipitation or sorption. One year after the rerouting, the Zn and Cu loads in Leavenworth Creek from the adit discharge versus those from leaching of a large volume of dispersed mill tailings were approximately equal to, if not greater than, those before. The mine-waste dump does not appear to be a major source of metal loading. Any improvement that may have resulted from the elimination of adit flow across the dump was masked by higher adit discharge attributed to a larger snow pack. Although many mine remediation activities commonly proceed without prior scientific studies to identify the sources and pathways of metal transport, such strategies do not always translate to water-quality improvements in the stream. Assessment of sources and pathways to gain better understanding of the system is a necessary investment in the outcome of any successful remediation strategy.

Colorado↗

USGS1996

The Beaver Creek story

Beaver Creek watershed in West Tennessee includes about 95,000 acres of the Nation's most productive farmland and most highly erodible soils. In 1989 the U.S. Geological Survey, in cooperation with the Tennessee Department of Agriculture, began a study to evaluate the effect of agricultural activities on water quality in the watershed and for best management practices designed to reduce agricultural nonpoint-source pollution. Agrichemical monitoring included testing the soils, ground water, and streams at four farm sites ranging from 27 to 420 acres. Monitoring stations were operated downstream to gain a better understanding of the water chemistry as runoff moved from small ditches into larger streams to the outlet of the Beaver Creek watershed. Prior to the implementation of best management practices at one of the farm study sites, some storms produced an average suspended-sediment concentration of 70,000 milligrams per liter. After the implementation of BMP's, however, the average value never exceeded 7,000 milligrams per liter. No-till crop production was the most effective best management practice for conserving soil on the farm fields tested. A natural bottomland hardwood wetland and a constructed wetland were evaluated as instream resource-management systems. The wetlands improved water quality downstream by acting as a filter and removing a significant amount of nonpoint-source pollution from the agricultural runoff. The constructed wetland reduced the sediment, pesticide, and nutrient load by approximately 50 percent over a 4-month period. The results of the Beaver Creek watershed study have increased the understanding of the effects of agriculture on water resources. Study results also demonstrated that BMP's do protect and improve water quality.

Open-File Report↗

USGS2004

Geochemistry of shallow ground water in coastal plain environments in the southeastern United States: Implications for aquifer susceptibility

Ground-water chemistry data from coastal plain environments have been examined to determine the geochemical conditions and processes that occur in these areas and assess their implications for aquifer susceptibility. Two distinct geochemical environments were studied to represent a range of conditions: an inner coastal plain setting having more well-drained soils and lower organic carbon (C) content and an outer coastal plain environment that has more poorly drained soils and high organic C content. Higher concentrations of most major ions and dissolved inorganic and organic C in the outer coastal plain setting indicate a greater degree of mineral dissolution and organic matter oxidation. Accordingly, outer coastal plain waters are more reducing than inner coastal plain waters. Low dissolved oxygen (O2) and nitrate (NO 3-) concentrations and high iron (Fe) concentrations indicate that ferric iron (Fe (III)) is an important electron acceptor in this setting, while dissolved O2 is the most common terminal electron acceptor in the inner coastal plain setting. The presence of a wide range of redox conditions in the shallow aquifer system examined here underscores the importance of providing a detailed geochemical characterization of ground water when assessing the intrinsic susceptibility of coastal plain settings. The greater prevalence of aerobic conditions in the inner coastal plain setting makes this region more susceptible to contamination by constituents that are more stable under these conditions and is consistent with the significantly (p<0.05) higher concentrations of NO3- found in this setting. Herbicides and their transformation products were frequently detected (36% of wells sampled), however concentrations were typically low (<0.1 ??g/L). Shallow water table depths often found in coastal plain settings may result in an increased risk of the detection of pesticides (e.g., alachlor) that degrade rapidly in the unsaturated zone.

Applied Geochemistry↗

USGS1997

Mercury accumulation in Devils Lake, North Dakota effects of environmental variation in closed-basin lakes on mercury chronologies

Sediment cores were collected from lakes in the Devils Lake Basin in North Dakota to determine if mercury (Hg) accumulation chronologies from sediment-core data are good indicators of variations in Hg accumulation rates in saline lakes. Sediment cores from Creel Bay and Main Bay, Devils Lake were selected for detailed analysis and interpretation. The maximum Hg concentration in the Creel Bay core was 0.15 micrograms per gram at 8 to 9 centimeters. The maximum Hg concentration in the Main Bay core was 0.07 micrograms per gram at 5 to 7 centimeters. The general decreases in Hg concentrations with depth are attributed to historic variations in atmospheric Hg deposition rate. Hg stratigraphies combined with 210Pb and 137Cs dating analyses yield Hg chronologies that indicate a general increase in Hg accumulation rates in Devils Lake since the middle of the 19th century. Mean modern Hg accumulation rates in Creel Bay were 4.9 nanograms per square centimeter per year, and rates in Main Bay were 1.8 nanograms per square centimeter per year. Mean preindustrial Hg accumulation rates in Creel Bay were 1.2 nanograms per square centimeter per year, and rates in Main Bay were 1.6 nanograms per square centimeter per year. Relatively low Hg concentrations in recent sediments in the Devils Lake Basin, along with similarities in Hg accumulation rates between lakes in the Devils Lake Basin and other lakes in the northern interior of North America, indicate that local sources of Hg are not important sources of Hg. Results of the study indicate that accurate Hg chronologies are discernible in sediment cores collected from saline lakes. However, spatial and temporal variations in lake level and water chemistry common to saline lakes make interpretation of radioisotopic and geochemical chronologies difficult. Hg geochemistry in Devils Lake, and presumably in other saline lakes, is dynamic. The results of this study indicate that the absolute amount of sediment transported to Devils Lake, along with the associated Hg and total organic carbon, and the distribution of sedimentation patterns in Devils Lake may be affected by changing lake levels.

Water, Air, & Soil Pollution↗

USGS2013

Species and life-history affects the utility of otolith chemical composition to determine natal stream-of-origin in Pacific salmon

To test the utility of otolith chemical composition as a tool for determining the natal stream of origin for salmon, we examined water chemistry and otoliths of juvenile and adult Chum Salmon Oncorhynchus keta and Coho Salmon O. kisutch from three watersheds (five rivers) in the Norton Sound region of Alaska. The two species are characterized by different life histories: Coho Salmon rear in freshwater for up to 3 years, whereas Chum Salmon emigrate from freshwater shortly after emergence. We used laser ablation (LA) inductively coupled plasma (ICP) mass spectrometry (MS) to quantify element: Ca ratios for Mg, Mn, Zn, Sr, and Ba, and we used multicollector LA-ICP-MS to determine 87 Sr: 86 Sr ratios in otolith regions corresponding to the period of freshwater residence. Significant differences existed in both water and otolith elemental composition, suggesting that otolith composition could be used to discriminate the natal origin of Coho Salmon and Chum Salmon but only when 87 Sr: 86 Sr ratios were included in the discriminant function analyses. The best discriminant model included 87 Sr: 86 Sr ratios, and without 87 Sr: 86 Sr ratios it was difficult to discriminate among watersheds and rivers. Classification accuracy was 80% for Coho Salmon and 68% for Chum Salmon, indicating that this method does not provide sufficient sensitivity to estimate straying rates of Pacific salmon at the scale we studied.

Alaska↗

USGS1990

Effect of faults on fluid flow and chloride contamination in a carbonate aquifer system

A unified, multidiscipline hypothesis is proposed to explain the anomalous pattern by which chloride has been found in water of the Upper Floridan aquifer in Brunswick, Glynn County, Georgia. Analyses of geophysical, hydraulic, water chemistry, and aquifer test data using the equivalent porous medium (EPM) approach are used to support the hypothesis and to improve further the understanding of the fracture-flow system in this area. Using the data presented herein we show that: (1) four major northeast-southwest trending faults, capable of affecting the flow system of the Upper Floridan aquifer, can be inferred from structural analysis of geophysical data and from regional fault patterns; (2) the proposed faults account for the anomalous northeastward elongation of the potentiometric surface of the Upper Floridan aquifer; (3) the faults breach the nearly impermeable units that confine the Upper Floridan aquifer from below, allowing substantial quantities of water to leak vertically upward; as a result, aquifer transmissivity need not be excessively large (as previously reported) to sustain the heavy, long-term pumpage at Brunswick without developing a steep cone of depression in the potentiometric surface; (4) increased fracturing at the intersection of the faults enhances the development of conduits that allow the upward migration of high-chloride water in response to pumping from the Upper Floridan aquifer; and (5) the anomalous movement of the chloride plume is almost entirely controlled by the faults.

Georgia↗

USGS2007

Occurrence of Uranium and 222Radon in Glacial and Bedrock Aquifers in the Northern United States, 1993-2003

Water-quality data collected from 1,426 wells during 1993-2003 as part of the U.S. Geological Survey National Water-Quality Assessment (NAWQA) program were evaluated to characterize the water quality in glacial and bedrock aquifers of the northern United States. One of the goals of the NAWQA program is to synthesize data from individual studies across the United States to gain regional- and national-scale information about the behavior of contaminants. This study focused on the regional occurrence and distribution of uranium and 222radon in ground water in the glacial aquifer system of the United States as well as in the Cambrian-Ordovician and the New York and New England crystalline aquifer systems that underlie the glacial aquifer system. The occurrence of uranium and 222radon in ground water has long been a concern throughout the United States. In the glacial aquifers, as well as the Cambrian-Ordovician and the New York and New England crystalline aquifer systems of the United States, concentrations of uranium and 222radon were highly variable. High concentrations of uranium and 222radon affect ground water used for drinking water and for agriculture. A combination of information or data on (1) national-scale ground-water regions, (2) regional-scale glacial depositional models, (3) regional-scale geology, and (4) national-scale terrestrial gamma-ray emissions were used to confirm and(or) refine the regions used in the analysis of the water-chemistry data. Significant differences in the occurrence of uranium and 222radon, based primarily on geologic information were observed and used in this report. In general, uranium was highest in the Columbia Plateau glacial, West-Central glacial, and the New York and New England crystalline aquifer groups (75th percentile concentrations of 22.3, 7.7, and 2.9 micrograms per liter (ug/L), respectively). In the Columbia Plateau glacial and the West-Central glacial aquifer groups, more than 10 percent of wells sampled had concentrations of uranium that exceeded the U.S. Environmental Protection Agency (USEPA) Maximum Contaminant Level of 30 ug/L; in the New York and New England crystalline aquifer group, 4 percent exceeded 30 ug/L. Ground-water samples with high concentrations of uranium were commonly linked to geologic sources rich in uranium. In eight of nine aquifer groups defined for this study, concentrations of uranium correlated significantly with concentrations of sulfate in ground water (Spearman's rho = 0.20 to 0.56; p < 0.05). In the Columbia Plateau, glacial aquifers were derived in part from basaltic lava flows, some felsic volcanic rocks, and some paleo-lake bed materials that may be rich in uranium. In the Columbia Plateau and West-Central glacial aquifer groups, uranium correlated with total dissolved solids, bicarbonate, boron, lithium, selenium, and strontium. In the West-Central glacial aquifer group, rocks such as Cretaceous marine shales, which are abundant in uranium, probably contribute to the high concentrations in ground water; in the southern part of this group, which extends into Nebraska, the glacial or glacial-related sediment may be interbedded with uranium-rich materials that originated to the north and west and in the Rocky Mountains. In New England, crystalline bedrock that is granitic, such as two-mica granites, as well as other high-grade metamorphic rocks, has abundant uranium that is soluble in the predominantly oxic to sub-oxic geochemical conditions. This appears to contribute to high uranium concentrations in ground water. The highest 222radon concentrations were present in samples from wells completed in the New York and New England crystalline aquifer group; the median value (2,122 picocurries per liter (pCi/L)) was about 10 times the median values of all other aquifer groups. More than 25 percent of the samples from the New York and New England crystalline aquifer group wells had 222radon concentrations that exceeded the USEPA Alternative

Scientific Investigations Report↗

USGS2006

Impact of quaternary climate on seepage at Yucca Mountain, Nevada

Uranium-series ages, oxygen-isotopic compositions, and uranium contents were determined in outer growth layers of opal and calcitefrom 0.5- to 3-centimeter-thick mineral coatings hosted by lithophysal cavities in the unsaturated zone at Yucca Mountain, Nevada, the proposed site of a permanent repository for high-level radioactive waste. Micrometer-scale growth layering in the minerals was imaged using a cathodoluminescence detector on a scanning electron microscope. Determinations of the chemistry, ages, and delta oxygen-18 (??18O) values of the growth layers were conducted by electron microprobe analysis and secondary ion mass spectrometry techniques at spatial resolutions of 2 to about 20 micrometers (??m) and 25 to 40 ??m, respectively. Growth rates for the last 300 thousand years (k.y.) calculated from about 300 new high-resolution uranium-series ages range from approximately 0.5 to 1.5 ??m/k.y. for 1- to 3-centimeter-thick coatings, whereas coatings less than about 1-centimeter-thick have growth rates less than 0.5 ??m/k.y. At the depth of the proposed repository, correlations of uranium concentration and ??18O values with regional climate records indicate that unsaturated zone percolation and seepage water chemistries have responded to changes in climate during the last several hundred thousand years.

Conference Paper↗

USGS2007

Sensitivity of high-elevation streams in the Southern Blue Ridge Province to acidic deposition

The Southern Blue Ridge Province, which encompasses parts of northern Georgia, eastern Tennessee, and western North Carolina, has been predicted to be sensitive to impacts from acidic deposition, owing to the chemical composition of the bedrock geology and soils. This study confirms the predicted potential sensitivity, quantifies the level of total alkalinity and describes the chemical characteristics of 30 headwater streams of this area. Water chemistry was measured five times between April 1983 and June 1984 at first and third order reaches of each stream during baseflow conditions. Sensitivity based on total alkalinity and the Calcite Saturation Index indicates that the headwater streams of the Province are vulnerable to acidification. Total alkalinity and p11 were generally higher in third order reaches (mean, 72 ?eq/? and 6.7) than in first order reaches (64 ?eq/? and 6.4). Ionic concentrations were low, averaging 310 and 340 ?eq/? in first and third order reaches, respectively. A single sampling appears adequate for evaluating sensitivity based on total alkalinity, but large temporal variability requires multiple sampling for the detection of changes in pH and alkalinity over time. Monitoring of stream water should continue in order to detect any subtle effects of acidic deposition on these unique resource systems.

Journal of the American Water Resources Associatio↗

USGS2001

Progression of natural attenuation processes at a crude oil spill site: II. Controls on spatial distribution of microbial populations

A multidisciplinary study of a crude-oil contaminated aquifer shows that the distribution of microbial physiologic types is strongly controlled by the aquifer properties and crude oil location. The microbial populations of four physiologic types were analyzed together with permeability, pore-water chemistry, nonaqueous oil content, and extractable sediment iron. Microbial data from three vertical profiles through the anaerobic portion of the contaminated aquifer clearly show areas that have progressed from iron-reduction to methanogenesis. These locations contain lower numbers of iron reducers, and increased numbers of fermenters with detectable methanogens. Methanogenic conditions exist both in the area contaminated by nonaqueous oil and also below the oil where high hydrocarbon concentrations correspond to local increases in aquifer permeability. The results indicate that high contaminant flux either from local dissolution or by advective transport plays a key role in determining which areas first become methanogenic. Other factors besides flux that are important include the sediment Fe(II) content and proximity to the water table. In locations near a seasonally oscillating water table, methanogenic conditions exist only below the lowest typical water table elevation. During 20 years since the oil spill occurred, a laterally continuous methanogenic zone has developed along a narrow horizon extending from the source area to 50–60 m downgradient. A companion paper [J. Contam. Hydrol. 53, 369–386] documents how the growth of the methanogenic zone results in expansion of the aquifer volume contaminated with the highest concentrations of benzene, toluene, ethylbenzene, and xylenes.

Journal of Contaminant Hydrology↗