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At least 883 records · Page 49Linked to original sources

USGS1978

Water resources inventory of Connecticut Part 8: Quinnipiac River basin

The Quinnipiac River basin area in southcentral Connecticut covers 363 square miles, and includes all drainage basins that enter Long Island Sound from the Branford to the Wepawaug Rivers. Its population in 1970 was estimated at 535,000. Precipitation averages 47 inches per year and provides an abundant supply of water. Twenty-one inches returns to the atmosphere as evapotranspiration; the remainder flows directly to streams or percolates to the water table and discharges to Long Island Sound. Small amounts of water are exported from the basin by the New Britain Water Department, and small amounts are imported to the basin by the New Haven Water Company. The amount of water that can be developed at a given place depends upon precipitation, variability of streamflow, hydraulic properties and areal extent of the aquifers, and hydraulic connection between the aquifers and major streams. The quality of the water is determined by the physical environment and the effects of man. Stratified drift is the only aquifer capable of large sustained yields of water to individual wells. Yields of 64 screened wells tapping stratified drift range from 17 to 2,000 gpm (gallons per minute); their median yield is 500 gpm. Till is widespread and generally provides only small amounts of water. Wells in till normally yield only a few hundred gallons of water daily and commonly are inadequate during dry periods. Till is generally used only as an emergency or secondary source of water. Bedrock aquifers underlie the entire report area and include sedimentary, igneous, and metamorphic rock types. These aquifers supply small but reliable quantities of water to wells throughout the basin and are the chief source for many nonurban homes and farms. About 90 percent of the wells tapping bedrock yield at least 2 pgm, and much larger yields are occasionally reported. Maximum well yields of 305 gpm for sedimentary, 75 gpm for igneous, and 200 gpm for metamorphic bedrock have been reported. Water potentially available from stratified drift was estimated on the basis of hydraulic characteristics of the aquifers and evaluation of natural and induced recharge. Long-term yields estimated for 14 favorable areas of stratified drift range from 0.8 to 16.1 mgd (million gallons per day), but detailed verification studies are needed before development. The natural quality of water in the report area is good. The water is generally low in dissolved solid and is soft to moderately hard. Surface water is less mineralized than ground water, especially during high flow when it is primarily surface runoff. A median dissolved-solids concentration of 117 mg/l (milligrams per liter) and a median hardness of 58 mg/l was determined for water samples collected at 20 sites on 16 streams during high flow. A median dissolved-solids concentration of 146 mg/l and a median hardness of 82 mg/l was determined for samples collected at the same sites during low flow. In contrast water from 130 wells had a median dissolved-solids concentration of 188 mg/l and a median hardness of 110 mg/l. Iron and manganese occur in objectionable concentrations in parts of the report area, particularly in water from streams draining swamps and in water from aquifers rich in iron- and manganese-bearing minerals. Concentrations of iron in excess of 0.3 mg/l were found in 40 percent of the high-streamflow samples, 59 percent of the low-streamflow samples and 20 percent of the ground-water samples. Human activities have modified the quality of water in much of the basin. Wide and erratic fluctuations in concentration of dissolved solids in streams, high bacterial content of the Quinnipiac River, and locally high nitrate and chloride concentrations in ground water are evidence of man's influence. Streams, wetlands, and some aquifers along the southern boundary of the basin contain salty water. Overpumping has caused extensive saltwater intrusion in aquifers in the southern and eastern parts of New Haven. The total amount of fresh water used in the area during 1970 is estimated at 35,710 million gallons, or 183 gallons per day per capita. Public water-supply systems met the domestic requirements of about 90 percent of the population; all the systems supplied water that met the drinking water standards of the Connecticut Department of Health.

Connecticut↗

USGS2024

On-orbit calibration and performance of the EMIT imaging spectrometer

The Earth surface Mineral dust source InvesTigation (EMIT) is a remote visible to shortwave infrared (VSWIR) imaging spectrometer that has been operating onboard the International Space Station since July 2022. This article describes EMIT's on-orbit spectroradiometric calibration and validation. Accurate spectroscopy is vital to achieve consistent mapping results with orbital imaging spectrometers. EMIT takes a unique approach to this challenge, with just six optical elements, no shutter, and no onboard calibration systems. Its simple design focuses on uniformity and stability to enable vicarious spectroradiometric calibration. Our experiments demonstrate that this approach is successful, approaching the fidelity of manual field spectroscopy in some cases, and enabling new and more accurate products across diverse Earth science disciplines. EMIT achieves several notable firsts for an instrument of its class. It demonstrates successful on-orbit adjustments of Focal Plane Array (FPA) alignment with sub-micron precision. It offers spectral uniformity better than 98%. Optical artifacts in the measurement channels are at least three orders of magnitude below the primary solar-reflected surface signals. Its noise performance enables percent-level discrimination in the depths of mineral absorption features. In these aspects, EMIT satisfies the stringent performance needs for the next generation of VSWIR imaging spectrometers to observe the Earth's ecosystems, geology , and water resources.

Remote Sensing of Environment↗

USGS1973

An empirical NaKCa geothermometer for natural waters

An empirical method of estimating the last temperature of water-rock interaction has been devised. It is based upon molar Na, K and Ca concentrations in natural waters from temperature environments ranging from 4 to 340°C. The data for most geothermal waters cluster near a straight line when plotted as the function log ( Na K ) + β log [ √ (Ca) Na ] "> log (NaK) + β log [ √(Ca)Na] vs reciprocal of absolute temperature, where β is either 1 3 "> 13 or 4 3 "> 43 depending upon whether the water equilibrated above or below 100°C. For most waters tested, the method gives better results than the Na K "> NaK methods suggested by other workers. The ratio Na K "> NaK should not be used to estimate temperature if √ ( M Ca ) M Na "> √ (MCa)MNa is greater than 1. The Na K "> NaK values of such waters generally yield calculated temperatures much higher than the actual temperature at which water interacted with the rock. A comparison of the composition of boiling hot-spring water with that obtained from a nearby well (170°C) in Yellowstone Park shows that continued water-rock reactions may occur during ascent of water even though that ascent is so rapid that little or no heat is lost to the country rock, i.e. the water cools adiabatically. As a result of such continued reaction, waters which dissolve additional Ca as they ascend from the aquifer to the surface will yield estimated aquifer temperatures that are too low. On the other hand, waters initially having enough Ca to deposit calcium carbonate during ascent may yield estimated aquifer temperatures that are too high if aqueous Na and K are prevented from further reaction with country rock owing to armoring by calcite or silica minerals. The Na-K-Ca geothermometer is of particular interest to those prospecting for geothermal energy. The method also may be of use in interpreting compositions of fluid inclusions.

Wyoming↗

USGS2014

A radiogenic isotope tracer study of transatlantic dust transport from Africa to the Caribbean

Many studies have suggested that long-range transport of African desert dusts across the Atlantic Ocean occurs, delivering key nutrients and contributing to fertilization of the Amazon rainforest. Here we utilize radiogenic isotope tracers – Sr, Nd and Pb – to derive the provenance, local or remote, and pathways of dust transport from Africa to the Caribbean. Atmospheric total suspended particulate (TSP) matter was collected in 2008 on quartz fibre filters, from both sides of the Atlantic Ocean at three different locations: in Mali (12.6°N, 8.0°W; 555 m a.s.l.), Tobago (11.3°N, 60.5°W; 329 m a.s.l.) and the U.S. Virgin Islands (17.7°N, 64.6°W; 27 m a.s.l.). Both the labile phase, representative of the anthropogenic signal, and the refractory detrital silicate fraction were analysed. Dust deposits and soils from around the sampling sites were measured as well to assess the potential contribution from local sources to the mineral dust collected. The contribution from anthropogenic sources of Pb was predominant in the labile, leachate phase. The overall similarity in Pb isotope signatures found in the leachates is attributed to a common African source of anthropogenic Pb, with minor inputs from other sources, such as from Central and South America. The Pb, Sr and Nd isotopic compositions in the silicate fraction were found to be systematically more radiogenic than those in the corresponding labile phases. In contrast, Nd and Sr isotopic compositions from Mali, Tobago, and the Virgin Islands are virtually identical in both leachates and residues. Comparison with existing literature data on Saharan and Sahelian sources constrains the origin of summer dust transported to the Caribbean to mainly originate from the Sahel region, with some contribution from northern Saharan sources. The source regions derived from the isotope data are consistent with 7-day back-trajectory analyses, demonstrating the usefulness of radiogenic isotopes in tracing dust provenance and atmospheric transport.

Africa;Atlantic Ocean;Caribbean;Sahara;Sahel↗

USGS2014

Distribution of metals in water and bed sediment in a mineral-rich watershed, Montana, USA

We sampled the Blackfoot River (Montana) and its major tributaries from the headwaters of the basin to near its confluence with the Clark Fork River over the course of 5 days in August 1998. We measured streamflow, collected fine-grained (<63 μm) streambed sediment, and sampled the dissolved (operationally defined as < 0.2 μm) phase of the surface water using clean techniques. Water and sediment collected from near the historic Heddleston mining district contained the highest concentrations of most trace elements in the basin. Many solute trace metals were at their highest several kilometers downstream from the mining district, where the river flows through an unremediated marsh system that has collected mine wastes in the past. Downstream on the headwaters area, water and bed sediment metal concentrations declined sharply. Comparison of sediment samples with those collected by other workers in August 1989 and August 1995 do not show evidence of basin-scale long term changes, despite the onset of remediation efforts in 1993. The area of the proposed McDonald gold deposit near the confluence of the Landers Fork with the Blackfoot River was not contributing anomalous concentrations of naturally-occurring dissolved and bed-sediment metals into the basin.

Montana↗

USGS2009

Structural characterization of terrestrial microbial Mn oxides from Pinal Creek, AZ

The microbial catalysis of Mn(II) oxidation is believed to be a dominant source of abundant sorption- and redox-active Mn oxides in marine, freshwater, and subsurface aquatic environments. In spite of their importance, environmental oxides of known biogenic origin have generally not been characterized in detail from a structural perspective. Hyporheic zone Mn oxide grain coatings at Pinal Creek, Arizona, a metals-contaminated stream, have been identified as being dominantly microbial in origin and are well studied from bulk chemistry and contaminant hydrology perspectives. This site thus presents an excellent opportunity to study the structures of terrestrial microbial Mn oxides in detail. XRD and EXAFS measurements performed in this study indicate that the hydrated Pinal Creek Mn oxide grain coatings are layer-type Mn oxides with dominantly hexagonal or pseudo-hexagonal layer symmetry. XRD and TEM measurements suggest the oxides to be nanoparticulate plates with average dimensions on the order of 11 nm thick × 35 nm diameter, but with individual particles exhibiting thickness as small as a single layer and sheets as wide as 500 nm. The hydrated oxides exhibit a 10-Å basal-plane spacing and turbostratic disorder. EXAFS analyses suggest the oxides contain layer Mn(IV) site vacancy defects, and layer Mn(III) is inferred to be present, as deduced from Jahn–Teller distortion of the local structure. The physical geometry and structural details of the coatings suggest formation within microbial biofilms. The biogenic Mn oxides are stable with respect to transformation into thermodynamically more stable phases over a time scale of at least 5 months. The nanoparticulate layered structural motif, also observed in pure culture laboratory studies, appears to be characteristic of biogenic Mn oxides and may explain the common occurrence of this mineral habit in soils and sediments.

Geochimica et Cosmochimica Acta↗

USGS2016

Increasing aeolian dust deposition to snowpacks in the Rocky Mountains inferred from snowpack, wet deposition, and aerosol chemistry

Mountain snowpacks are a vital natural resource for ∼1.5 billion people in the northern Hemisphere, helping to meet human and ecological demand for water in excess of that provided by summer rain. Springtime warming and aeolian dust deposition accelerate snowmelt, increasing the risk of water shortages during late summer, when demand is greatest. While climate networks provide data that can be used to evaluate the effect of warming on snowpack resources, there are no established regional networks for monitoring aeolian dust deposition to snow. In this study, we test the hypothesis that chemistry of snow, wet deposition, and aerosols can be used as a surrogate for dust deposition to snow. We then analyze spatial patterns and temporal trends in inferred springtime dust deposition to snow across the Rocky Mountains, USA, for 1993–2014. Geochemical evidence, including strong correlations (r 2 ≥ 0.94) between Ca 2+ , alkalinity, and dust concentrations in snow deposited during dust events, indicate that carbonate minerals in dust impart a strong chemical signature that can be used to track dust deposition to snow. Spatial patterns in chemistry of snow, wet deposition, and aerosols indicate that dust deposition increases from north to south in the Rocky Mountains, and temporal trends indicate that winter/spring dust deposition increased by 81% in the southern Rockies during 1993–2014. Using a multivariate modeling approach, we determined that increases in dust deposition and decreases in springtime snowfall combined to accelerate snowmelt timing in the southern Rockies by approximately 7–18 days between 1993 and 2014. Previous studies have shown that aeolian dust emissions may have doubled globally during the 20th century, possibly due to drought and land-use change. Climate projections for increased aridity in the southwestern U.S., northern Africa, and other mid-latitude regions of the northern Hemisphere suggest that aeolian dust emissions may continue to increase, compounding the risk that climate warming poses to snowpack water resources in arid/semi-arid regions of the world.

Atmospheric Environment↗

USGS2019

Water quality and hydrology of the Yellow Dog and Salmon Trout Watersheds, Marquette County, Michigan 2013–16

In 2013, the U.S. Geological Survey, in cooperation with the Keweenaw Bay Indian Community, began monitoring the water quality of springs and seeps within the Yellow Dog and Salmon Trout watersheds in Marquette County, Michigan. The objectives of this study were to (1) monitor streamflow and analyze the hydrology of the watersheds and (2) characterize the water quality in the watersheds prior to development of mineral resources within the watershed. Three continuous-record streamgages (U.S. Geological Survey stations 04043238, 04043244, and 04043275) were examined to identify runoff and baseflow components of streamflow and the relative magnitudes of those components. Streamflow at each station was dominated by groundwater discharge with about 70 to 80 percent of the annual streamflow being groundwater-derived baseflow. From May 2013 to October 2016, 239 water-quality samples were collected at 15 stations within the Yellow Dog and Salmon Trout watersheds. Of the 15 stations sampled, 8 of the stations were springs and 7 of the stations were streams. Samples were analyzed for nutrient, trace metal, and major-ion species at all stations with additional suspended-sediment samples collected at the 7 stream stations. Where applicable, water-quality results were compared to aquatic health guidelines used by the Michigan Department of Environmental Quality. Copper concentrations exceeded the final chronic value five times and the aquatic maximum value once, whereas silver concentrations exceeded the final chronic value twice and the aquatic maximum value once. Results indicate that chloride concentrations may be increasing at some stations, but values are generally low with a median concentration of 0.25 milligram per liter. Bed-sediment chemistry was evaluated twice for each stream sampling station. Samples were collected in the first and last year of the study and analyzed for trace metals. Sediment chemistry results were compared to consensus-based sediment quality guidelines. None of the metal constituents analyzed exceeded the threshold effect concentration or probable effect concentration thresholds, indicating a healthy aquatic environment in relation to bed-sediment quality.

Michigan↗

USGS1997

Long-term tillage and crop rotation effects on residual nitrate in the crop root zone and nitrate accumulation in the intermediate vadose zone

Tillage influences the physical and biological environment of soil. Rotation of crops with a legume affects the soil N status. A furrow irrigated site was investigated for long-term tillage and crop rotation effects on leaching of nitrate from the root zone and accumulation in the intermediate vadose zone (IVZ). The investigated tillage systems were disk-plant (DP), ridge-till (RT) and slot-plant (SP). These tillage treatments have been maintained on the Hastings silt loam (Udic Argiustoll) and Crete silt loam (Pachic Argiustoll) soils since 1976. Continuous corn (CC) and corn soybean (CS) rotations were the subtreatments. Since 1984, soybeans have been grown in CS plots in even calendar years. All tillage treatments received the same N rate. The N rate varied annually depending on the root zone residual N. Soybeans were not fertilized with N-fertilizer. Samples for residual nitrate in the root zone were taken in 8 of the 15 year study while the IVZ was only sampled at the end of the study. In seven of eight years, root zone residual soil nitrate-N levels were greater with DP than RT and SP. Residual nitrate-N amounts were similar in RT and SP in all years. Despite high residual nitrate-N with DP and the same N application rate, crop yields were higher in RT and SP except when DP had an extremely high root zone nitrate level. By applying the same N rates on all tillage treatments, DP may have been fertilized in excess of crop need. Higher residual nitrate-N in DP was most likely due to a combination of increased mineralization with tillage and lower yield compared to RT and SP. Because of higher nitrate availability with DP, the potential for nitrate leaching from the root zone was greater with DP as compared to the RT and SP tillage systems. Spring residual nitrate-N contents of DP were larger than RT and SP in both crop rotations. Ridge till and SP systems had greater nitrate-N with CS than CC rotations. Nitrate accumulation in IVZ at the upstream end of the field was twice as high with DP compared to RT and SP. At the downstream end, it was 2.4 and 1.6 times greater with DP than RT and SP, respectively. Nitrate concentration was greater in the IVZ of DP compared to RT and SP tillage systems. Nitrate accumulations in IVZ of RT and SP were not different. Continuous corn had slightly higher nitrate levels in IVZ than CS. The depth of nitrate penetration at the upstream end was greater than that of the downstream end. Estimated rates of nitrate movement ranged from 0.87 to 0.92 m yr-1 at the upstream end and 0.73 to 0.78 m yr-1 at the downstream end.

Transactions of the American Society of Agricultur↗

USGS2019

Isotopic ratios of Saturn's rings and satellites: Implications for the origin of water and Phoebe

Isotopic ratios have long been used to learn about physical processes acting over a wide range of geological environments, and in constraining the origin and/or evolution of planetary bodies. We report the spectroscopic detection of deuterium in Saturn's rings and satellites, and use these measurements to determine the (D/H) ratios in their near-surface regions. Saturn's moons, Phoebe and Iapetus, show a strong signature of CO2 and the 13C component of this molecule is detected and quantified. Large averages of spectra obtained by the Cassini Visual and Infrared Mapping Spectrometer, VIMS, were computed for the rings and icy satellites. The observed intensities of the infrared absorptions in H2O and CO2 and their isotopes were calibrated using laboratory data and radiative transfer models to derive the D/H and 13C/12C ratios. We find that the D/H in Saturn's rings and satellites is close to the Vienna Standard Mean Ocean Water (VSMOW) and bulk Earth (4% lower than VSMOW) value except for Phoebe, which is 8.3 times the VSMOW value. This is the highest value for any Solar-System surface yet measured, and suggests that Phoebe formed from material with a different D/H ratio than the other satellites in the Saturn system. Phoebe’s 13C/12C ratio is also unusual: 4.7 times greater than terrestrial, and greater than values measured for the interstellar medium and the galactic center. The high 13C abundance in the CO2 suggests that Phoebe was never warm enough for the large D/H ratio in its surface to have originated by evaporative fractionation of its waterice (e.g., from heating in the inner Solar System before its eventual capture by Saturn). We also report the detection of a probable O-D stretch absorption due to OD in minerals on Phoebe at 3.62 μm. This absorption is not detected on other Saturnian satellites. Stronger signatures of bound water absorptions are found in the dark material of Iapetus and we report a new detection of bound water at 1.9 μm. The position of this absorption matches that seen in spectra of hydrated iron oxides but does not match absorptions seen in spectra of tholins. Despite the strong bound water signature in the Iapetus dark material, no 3.62-μm OD absorption is seen in the spectra, further indicating the high deuterium level on Phoebe is unusual. As such, it is likely that Phoebe originated in a colder part of the outer Solar System, relative to the prevailing temperatures at Saturn’s distance from the Sun.

Icarus↗

USGS2021

Organic petrographic evaluation of carbonaceous material in sediments of the Kinnickinnic River, Milwaukee, WI, U.S.A.

This study examines the use of organic petrology techniques to quantify the amount of coal and carbonaceous combustion by-products (i.e., coke, coal tar/pitch, cenospheres) in sediments taken from the Kinnickinnic River adjacent to the former site of the Milwaukee Solvay Coke and Gas Company. These materials are of concern as contaminants like polycyclic aromatic hydrocarbons (PAHs) are known to readily adsorb to coal and combustion byproducts. Kinnickinnic River sediment samples (n = 36) ranging in depth (1–11 ft.) were collected from eight core locations to quantify and characterize carbonaceous material in the sediments. To determine the amount (vol%) of organic particulates, U.S. Geological Survey (USGS) modified the existing ASTM D2799 using the following categories: coal, coke, coal tar/pitch, inertinite organics, plant material, cenospheres, and mineral matter. Coal fragments were subdivided by rank using vitrinite reflectance (R o , %) and organic components were further subdivided into the size fractions of coarse (250–1000 μm), fine (63–250 μm), and very fine (<63 μm). Of the 36 samples analyzed, concentrations of coal, coke, and coal tar/pitch ranged from 0 to 18.2 vol%, 0 to 32.0 vol%, and 0 to 2.6 vol%, respectively, with the highest concentrations occurring near point sources (e.g. discharge pipe and coal unloading operations). Samples that were furthest upstream and downstream from the Solvay site exhibited a marked decrease in particulate organics, with exception of one upstream location which had 19.8 vol% coke. Overall, the modified ASTM method provided a means to quantify the abundance of carbonaceous material present in the sediments. Petrography and total PAH concentrations did not provide a clear correlation to organic matter type or size fraction but the samples with the highest vol% organic matter in each core generally corresponded to the sample with the highest bulk PAH content.

Wisconsin↗

USGS2020

Degradation of RDX (Hexahydro-1,3,5-trinitro-1,3,5-triazine) in contrasting coastal marine habitats: Subtidal non-vegetated (sand), subtidal vegetated (silt/eel grass), and intertidal marsh

Hundreds of explosive-contaminated marine sites exist globally, many of which contain the common munitions constituent hexahydro-1,3,5-trinitro-1,3,5-triazine (RDX). Quantitative information about RDX transformation in coastal ecosystems is essential for management of many of these sites. Isotopically labelled RDX containing 15 N in all 3 nitro groups was used to track the fate of RDX in three coastal ecosystem types. Flow-through mesocosms representing subtidal vegetated (silt/eel grass), subtidal non-vegetated (sand) and intertidal marsh ecosystems were continuously loaded with isotopically labelled RDX for 16–17 days. Sediment, pore-water and overlying surface water were analyzed to determine the distribution of RDX, nitroso-triazine transformation products (NXs) and nitrogen containing complete mineralization products, including ammonium, nitrate+nitrite, nitrous oxide and nitrogen gas. The marsh, silt, and sand ecotypes transformed 94%, 90% and 76% of supplied RDX, respectively. Total dissolved NXs accounted for 2%–4% of the transformed 15 N-RDX. The majority of RDX transformation in the water column was by mineralization to inorganic N (dissolved and evaded; 64%–78% of transformed 15 N-RDX). RDX was mineralized primarily to N 2 O (62–74% of transformed 15 N-RDX) and secondarily to N 2 (1–2% of transformed 15 N-RDX) which exchanged with the atmosphere. Transformation of RDX was favored in carbon-rich lower redox potential sediments of the silt and marsh mesocosms where anaerobic processes of iron and sulfate reduction were most prevalent. RDX was most persistent in the carbon-poor sand mesocosm. Partitioning of 15 N derived from RDX onto sediment and suspended particulates was negligible in the overall mass balance of RDX transformation (2%–3% of transformed 15 N-RDX). The fraction of 15 N derived from RDX that was sorbed or assimilated in sediment was largest in the marsh mesocosm (most organic carbon), and smallest in the sand mesocosm (largest grain size and least organic carbon). Sediment redox conditions and available organic carbon stores affect the fate of RDX in different coastal marine habitats.

Connecticut, New York↗

USGS2014

Geologic sources and concentrations of selenium in the West-Central Denver Basin, including the Toll Gate Creek watershed, Aurora, Colorado, 2003-2007

Toll Gate Creek, in the west-central part of the Denver Basin, is a perennial stream in which concentrations of dissolved selenium have consistently exceeded the Colorado aquatic-life standard of 4.6 micrograms per liter. Recent studies of selenium in Toll Gate Creek identified the Denver lignite zone of the non-marine Cretaceous to Tertiary-aged (Paleocene) Denver Formation underlying the watershed as the geologic source of dissolved selenium to shallow ground-water and surface water. Previous work led to this study by the U.S. Geological Survey, in cooperation with the City of Aurora Utilities Department, which investigated geologic sources of selenium and selenium concentrations in the watershed. This report documents the occurrence of selenium-bearing rocks and groundwater within the Cretaceous- to Tertiary-aged Denver Formation in the west-central part of the Denver Basin, including the Toll Gate Creek watershed. The report presents background information on geochemical processes controlling selenium concentrations in the aquatic environment and possible geologic sources of selenium; the hydrogeologic setting of the watershed; selenium results from groundwater-sampling programs; and chemical analyses of solids samples as evidence that weathering of the Denver Formation is a geologic source of selenium to groundwater and surface water in the west-central part of the Denver Basin, including Toll Gate Creek. Analyses of water samples collected from 61 water-table wells in 2003 and from 19 water-table wells in 2007 indicate dissolved selenium concentrations in groundwater in the west-central Denver Basin frequently exceeded the Colorado aquatic-life standard and in some locations exceeded the primary drinking-water standard of 50 micrograms per liter. The greatest selenium concentrations were associated with oxidized groundwater samples from wells completed in bedrock materials. Selenium analysis of geologic core samples indicates that total selenium concentrations were greatest in samples containing indications of reducing conditions and organic matter (dark gray to black claystones and lignite horizons). The Toll Gate Creek watershed is situated in a unique hydrogeologic setting in the west-central part of the Denver Basin such that weathering of Cretaceous- to Tertiary-aged, non-marine, selenium-bearing rocks releases selenium to groundwater and surface water under present-day semi-arid environmental conditions. The Denver Formation contains several known and suspected geologic sources of selenium including: (1) lignite deposits; (2) tonstein partings; (3) organic-rich bentonite claystones; (4) salts formed as secondary weathering products; and possibly (5) the Cretaceous-Tertiary boundary. Organically complexed selenium and/or selenium-bearing pyrite in the enclosing claystones are likely the primary mineral sources of selenium in the Denver Formation, and correlations between concentration of dissolved selenium and dissolved organic carbon in groundwater indicate weathering and dissolution of organically complexed selenium from organic-rich claystone is a primary process mobilizing selenium. Secondary salts accumulated along fractures and bedding planes in the weathered zone are another potential geologic source of selenium, although their composition was not specifically addressed by the solids analyses. Results from this and previous work indicate that shallow groundwater and streams similarly positioned over Denver Formation claystone units at other locations in the Denver Basin also may contain concentrations of dissolved selenium greater than the Colorado aquatic-life standard or the drinking- water standard.

Colorado↗

USGS2014

Quantity and quality of groundwater discharge in a hypersaline lake environment

Geophysical and geochemical surveys were conducted to understand groundwater discharge to Great Salt Lake (GSL) and assess the potential significance of groundwater discharge as a source of selenium (Se). Continuous resistivity profiling (CRP) focusing below the sediment/water interface and fiber-optic distributed temperature sensing (FO-DTS) surveys were conducted along the south shore of GSL. FO-DTS surveys identified persistent cold-water temperature anomalies at 10 separate locations. Seepage measurements were conducted at 17 sites (mean seepage rate = 0.8 cm/day). High resistivity anomalies identified by the CRP survey were likely a mirabilite (Na 2 SO 4 ·10H 2 O) salt layer acting as a semi-confining layer for the shallow groundwater below the south shore of the lake. Positive seepage rates measured along the near-shore areas of GSL indicate that a ∼1-m thick oolitic sand overlying the mirabilite layer is likely acting as a shallow, unconfined aquifer. Using the average seepage rate of 0.8 cm/day over an area of 1.6 km 2 , an annual Se mass loading to GSL of 23.5 kg was estimated. Determination of R/Ra values (calculated 3 He/ 4 He ratio over the present-day atmospheric 3 He/ 4 He ratio) <1 and tritium activities of 1.2–2.0 tritium units in groundwater within and below the mirabilite layer indicates a convergence of regional and local groundwater flow paths discharging into GSL. Groundwater within and below the mirabilite layer obtains its high sulfate salinity from the dissolution of mirabilite. The δ 34 S and δ 18 O isotopic values in samples of dissolved sulfate from the shallow groundwater below the mirabilite are almost identical to the isotopic signature of the mirabilite core material. The saturation index calculated for groundwater samples using PHREEQC indicates the water is at equilibrium with mirabilite. Water samples collected from GSL immediately off shore contained Se concentrations that were 3–4 times higher than other sampling sites >25 km offshore from the study site and may be originating from less saline groundwater seeps mixing with the more saline water from GSL. Additional evidence for mixing with near shore seeps is found in the δD and δ 18 O isotopic values and Br:Cl ratios. Geochemical modeling for a water sample collected in the vicinity of the study area indicates that under chemically reducing conditions, arsenic- (As) bearing minerals could dissolve while Se-bearing minerals will likely precipitate out of solution, possibly explaining why the shallow groundwater below and within the mirabilite salt layer contains low concentrations of Se (0.9–2.3 μg/L).

Utah↗

USGS2006

Gravity investigations of the Chickasaw National Recreation Area, south-central Oklahoma

The geological configuration of the Arbuckle Uplift in the vicinity of Chickasaw National Recreation Area in south-central Oklahoma plays a governing role in the distribution of fresh and mineral springs within the park and in the existence of artesian wells in and around the park. A confining layer of well-cemented conglomerate lies immediately below the surface of the recreation area, and groundwater migrates from an area of meteoric recharge where rocks of the Arbuckle-Simpson Aquifer crop out as close as two kilometers to the east of the park. Prominent, Pennsylvanian-aged faults are exposed in the aquifer outcrop, and two of the fault traces project beneath the conglomerate cover toward two groups of springs within the northern section of the park. We conducted gravity fieldwork and analysis to investigate the subsurface extensions of these major faults beneath Chickasaw National Recreation Area. By defining gravity signatures of the faults where they are exposed, we infer that the Sulphur and Mill Creek Faults bend to the south-west where they are buried. The South Sulphur Fault may project westward linearly if it juxtaposes rocks that have a density contrast opposite that of that fault's density configuration in the Sulphur Syncline area. The Sulphur Syncline, whose eastern extent is exposed in the outcrop area of the Arbuckle-Simpson Aquifer, does not appear to extend beneath Chickasaw National Recreation Area nor the adjacent City of Sulphur. The South Sulphur Fault dips steeply northward, and its normal sense of offset suggests that the Sulphur Syncline is part of a graben. The Mill Creek Fault dips vertically, and the Reagan Fault dips southward, consistent with its being mapped as a thrust fault. The Sulphur and Mill Creek Synclines may have formed as pull-apart basins in a left-lateral, left-stepping strike-slip environment. The character of the gravity field of Chickasaw National Recreation Area is different from the lineated gravity field in the area of Arbuckle-Simpson Aquifer outcrop. This change in character is not due to the presence of the overlying conglomerate layer, which is quite thin (<100 m) in the area of the park with the springs. The presence of relatively high-density Precambrian basement rocks in a broader region suggests that significant gravity anomalies may arise from variations in basement topography. Understanding of the geological configuration of Chickasaw National Recreation Area can be improved by expanding the study area and by investigating complementary geophysical and borehole constraints of the subsurface.

Open-File Report↗

USGS2014

Flow and sorption controls of groundwater arsenic in individual boreholes from bedrock aquifers in central Maine, USA

To understand the hydrogeochemical processes regulating well water arsenic (As) evolution in fractured bedrock aquifers, three domestic wells with [As] up to 478 μg/L are investigated in central Maine. Geophysical logging reveals that fractures near the borehole bottom contribute 70-100% of flow. Borehole and fracture water samples from various depths show significant proportions of As (up to 69%) and Fe (93-99%) in particulates (>0.45 μm). These particulates and those settled after a 16-day batch experiment contain 560-13,000 g/kg of As and 14-35% weight/weight of Fe. As/Fe ratios (2.5-20 mmol/mol) and As partitioning ratios (adsorbed/dissolved [As], 20,000-100,000 L/kg) suggest that As is sorbed onto amorphous hydrous ferric oxides. Newly drilled cores also show enrichment of As (up to 1300 mg/kg) sorbed onto secondary iron minerals on the fracture surfaces. Pumping at high flow rates induces large decreases in particulate As and Fe, a moderate increase in dissolved [As] and As(III)/As ratio, while little change in major ion chemistry. The δD and δ 18 O are similar for the borehole and fracture waters, suggesting a same source of recharge from atmospheric precipitation. Results support a conceptual model invoking flow and sorption controls on groundwater [As] in fractured bedrock aquifers whereby oxygen infiltration promotes the oxidation of As-bearing sulfides at shallower depths in the oxic portion of the flow path releasing As and Fe; followed by Fe oxidation to form Fe oxyhydroxide particulates, which are transported in fractures and sorb As along the flow path until intercepted by boreholes. In the anoxic portions of the flow path, reductive dissolution of As-sorbed iron particulates could re-mobilize As. For exposure assessment, we recommend sampling of groundwater without filtration to obtain total As concentration in groundwater.

Maine↗

USGS2012

Data resources for the Wyoming Landscape Conservation Initiative (WLCI) Integrated Assessment (IA)

The data contained in this report were compiled, modified, and analyzed for the Wyoming Landscape Conservation Initiative (WLCI) Integrated Assessment (IA). The WLCI is a long-term science based effort to assess and enhance aquatic and terrestrial habitats at a landscape scale in southwest Wyoming while facilitating responsible energy development through local collaboration and partnerships. The IA is an integrated synthesis and analysis of WLCI resource values based on best available data and information collected from multiple agencies and organizations. It is a support tool for landscape-scale conservation planning and evaluation, and a data and analysis resource that can be used for addressing specific management questions. The IA analysis was conducted using a Geographic Information System in a raster (that is, a grid) environment using a cell size of 30 meters. To facilitate the interpretation of the data in a regional context, mean values were summarized and displayed at the subwatershed unit (WLCI subwatersheds were subset from the National Hydrography Dataset, Hydrologic Unit Code 12/Level 6). A dynamic mapping platform, accessed via the WLCI webpage at http://www.wlci.gov is used to display the mapped information, and to access underlying resource values that were combined to produce the final mapped results. The raster data used in the IA are provided here for use by interested parties to conduct additional analyses and can be accessed via the WLCI webpage. This series contains 74 spatial data sets: WLCI subwatersheds (vector) and 73 geotiffs (raster) that are segregated into the major categories of Multicriteria Index (including Resource Index and Condition), Change Agents, and Future Change. The Total Multicriteria Index is composed of the Aquatic Multicriteria Index and the Terrestrial Multicriteria Index. The Aquatic Multicriteria Index is composed of the Aquatic Resource Index and the Aquatic Condition. The Aquatic Resource Index is composed of the following components: Groundwater, Special Management Areas, and Priority Areas. The Aquatic Condition is composed of the following components: Focal Species, Species of Concern, Focal Ecosystems, and Proper Functioning Condition. The Terrestrial Multicriteria Index is composed of the Terrestrial Resource Index and the Terrestrial Condition. The Terrestrial Resource Index is composed of the following components: Special Management Areas, Agriculture, and Priority Areas. The Terrestrial Condition is composed of the following components: Focal Species, Big Game, Species of Concern, Rare Plants, and Focal Ecosystems. The Change Agents are composed the following components: Roads, Energy, Mines, and Urban. The Future Change is composed of the following components: Oil-Gas-Coal, Wind, Minerals, Climate-Temperature, Invasive Species, and Urban.

Wyoming↗

USGS2000

Water-quality characteristics for selected streams in Lawrence County, South Dakota, 1988-92

During the 1980’s, significant economic development and population growth began to occur in Lawrence County in the northern part of the Black Hills of western South Dakota. Rising gold prices and heap-leach extraction methods allowed the economic recovery of marginal gold ore deposits, resulting in development of several large-scale, open-pit gold mines in Lawrence County. There was increasing local concern regarding potential impacts on the hydrologic system, especially relating to the quantity and quality of water in the numerous streams and springs of Lawrence County. In order to characterize the water quality of selected streams within Lawrence County, samples were collected from 1988 through 1992 at different times of the year and under variable hydrologic conditions. During the time of this study, the Black Hills area was experiencing a drought; thus, most samples were collected during low-flow conditions. Streamflow and water-quality characteristics in Lawrence County are affected by both geologic conditions and precipitation patterns. Most streams that cross outcrops of the Madison Limestone and Minnelusa Formation lose all or large part of their streamflow to aquifer recharge. Streams that are predominantly spring fed have relatively stable streamflow, varying slightly with dry and wet precipitation cycles. Most streams in Lawrence County generally have calcium magnesium bicarbonate type waters. The sites from the mineralized area of central Lawrence County vary slightly from other streams in Lawrence County by having higher concentrations of sodium, less bicarbonate, and more sulfate. False Bottom Creek near Central City has more sulfate than bicarbonate. Nitrogen, phosphorous, and cyanide concentrations were at or near the laboratory reporting limits for most sites and did not exceed any of the water-quality standards. Nitrite plus nitrate concentrations at Annie Creek near Lead, Whitetail Creek at Lead, Squaw Creek near Spearfish, and Spearfish Creek below Robison Gulch were somewhat higher than at other sites. Mining activity, agricultural activity, and domestic development are possible sources of nitrogen to the streams. Increased mining activities were identified as the probable cause of increased nitrogen concentrations in Annie Creek. In the mineralized area of the northern Black Hills, detectable concentrations of trace elements are common in stream water, occasionally exceeding beneficial-use and aquatic-life criteria. In addition, many basins have been disturbed by both historical and recent mining operations and cleanup activities. The maximum dissolved arsenic concentration at Annie Creek near Lead (48 micrograms per liter) approached the current arsenic drinking-water standard. Concentrations at or greater than 5 micrograms per liter were found in samples from Annie Creek near Lead, Spearfish Creek above Spearfish, Whitetail Creek at Lead, and False Bottom Creek near Spearfish. Bear Butte Creek near Deadwood had one sample with a dissolved copper concentration that exceeded acute and chronic aquatic-life criteria. Bear Butte Creek near Deadwood had several manganese concentrations that exceeded the secondary maximum contaminant level of 50 micrograms per liter. Bed-sediment and water-quality data from selected sites in small drainage basins were used to determine if factors such as pH, arsenic concentrations in bed sediments, and calcite saturation control dissolved arsenic concentrations. Arsenic solubility is controlled by adsorption, mainly on ferrihydrite. In addition, adsorption/desorption of arsenic is controlled by the pH of the stream, with high arsenic concentrations appearing only at higher pH conditions (above 8). There are significant arsenic sources available to almost all the small streams of the northern Black Hills mining area, but arsenic is less mobile in streams that are not influenced to the higher pH values by calcite. Streams where arsenic is more mobile have lower iron concentrations in their bed sediments, and they have relatively high concentrations of calcite Additional water-quality data have been collected as part of other studies or monitoring programs by the South Dakota Department of Environment and Natural Resources, U.S. Environmental Protection Agency, U.S. Forest Service, and the U.S. Geological Survey. Summaries of selected data from these other sources are included as additional information.

South Dakota↗