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USGS2004

Water Resources Data North Dakota Water Year 2003, Volume 1. Surface Water

Water-resources data for the 2003 water year for North Dakota consists of records of discharge, stage, and water quality for streams; contents, stage, and water quality for lakes and reservoirs; and water levels and water quality for ground-water wells. Volume 1 contains records of water discharge for 108 streamflow-gaging stations; stage only for 24 river-stage stations; contents and/or stage for 14 lake or reservoir stations; annual maximum discharge for 32 crest-stage stations; and water-quality for 99 streamflow-gaging stations, 5 river-stage stations, 11 lake or reservoir stations, 8 miscellaneous sample sites on rivers, and 63 miscellaneous sample sites on lakes and wetlands. Data are included for 7 water-quality monitor sites on streams and 2 precipitation-chemistry stations. These data represent that part of the National Water Data System operated by the U.S. Geological Survey and cooperating Federal, State, and local agencies in North Dakota.

Water Data Report↗

USGS2005

Water resources data--North Dakota, water year 2004, volume 1. Surface water

Water-resources data for the 2004 water year for North Dakota consists of records of discharge, stage, and water quality for streams; contents, stage, and water quality for lakes and reservoirs; and water levels and water quality for ground-water wells. Volume 1 contains records of water discharge for 106 streamflow-gaging stations; stage only for 23 river-stage stations; contents and/or stage for 14 lake or reservoir stations; annual maximum discharge for 31 crest-stage stations; and water-quality for 92 streamflow-gaging stations, 6 river-stage stations, 15 lake or reservoir stations, 22 miscellaneous sample sites on rivers, and 67 miscellaneous sample sites on lakes and wetlands. Data are included for 5 water-quality monitor sites on streams and 2 precipitation-chemistry stations. These data represent that part of the National Water Data System operated by the U.S. Geological Survey and cooperating Federal, State, and local agencies in North Dakota.

Water Data Report↗

USGS2006

Water resources data--North Dakota water year 2005, Volume 1. Surface water

Water-resources data for the 2005 water year for North Dakota consists of records of discharge, stage, and water quality for streams; contents, stage, and water quality for lakes and reservoirs; and water levels and water quality for ground-water wells. Volume 1 contains records of water discharge for 107 streamflow-gaging stations; stage only for 22 river-stage stations; contents and/or stage for 13 lake or reservoir stations; annual maximum discharge for 31 crest-stage stations; and water quality for 93 streamflow-gaging stations, 6 river-stage stations, 15 lake or reservoir stations, and about 50 miscellaneous sample sites on lakes and wetlands. Data are included for 8 water-quality monitor sites on streams and 2 precipitation-chemistry stations. These data represent that part of the National Water Data System operated by the U.S. Geological Survey and cooperating Federal, State, and local agencies in North Dakota.

Water Data Report↗

USGS2020

Utica shale play oil and gas brines: Geochemistry and factors influencing wastewater management

The Utica and Marcellus Shale Plays in the Appalachian Basin are the fourth and first largest natural gas producing plays in the United States, respectively. Hydrocarbon production generates large volumes of brine (“produced water”) that must be disposed of, treated, or reused. Though Marcellus brines have been studied extensively, there are few studies from the Utica Shale Play. This study presents new brine chemical analyses from 16 Utica Shale Play wells in Ohio and Pennsylvania. Results from Na–Cl–Br systematics and stable and radiogenic isotopes suggest that the Utica Shale Play brines are likely residual pore water concentrated beyond halite saturation during the formation of the Ordovician Beekmantown evaporative sequence. The narrow range of chemistry for the Utica Shale Play produced waters (e.g., total dissolved solids = 214–283 g/L) over both time and space implies a consistent composition for disposal and reuse planning. The amount of salt produced annually from the Utica Shale Play is equivalent to 3.4% of the annual U.S. halite production. Utica Shale Play brines have radium activities 580 times the EPA maximum contaminant level and are supersaturated with respect to barite, indicating the potential for surface and aqueous radium hazards if not properly disposed of.

Kentucky, Maryland, New York, Ohio, Pennsylvania, ↗

USGS1998

Seasonal uranium distributions in the coastal waters off the Amazon and Mississippi Rivers

The chemical reactivity of uranium was investigated across estuarine gradients from two of the world’s largest river systems: the Amazon and Mississippi. Concentrations of dissolved (<0.45 μm) uranium (U) were measured in surface waters of the Amazon shelf during rising (March 1990), flood (June 1990) and low (November 1991) discharge regimes. The dissolved U content was also examined in surface waters collected across estuarine gradients of the Mississippi outflow region during April 1992, August 1993, and November (1993). All water samples were analyzed for U by isotope dilution inductively coupled plasma mass spectrometry (ICP-MS). In Amazon shelf surface waters uranium increased nonconservatively from about 0.01 μg I −1 at the river’s mouth to over 3 μg I −1 at the distal site, irrespective of river discharge stage. Observed large-scale U removal at salinities generally less than 15 implies a) that riverine dissolved U was extensively adsorbed by freshly-precipitated hydrous metal oxides (e.g., FeOOH, MnO 2 ) as a result of flocculation and aggregation, and b) that energetic resuspension and reworking of shelf sediments and fluid muds on the Amazon shelf released a chemically reactive particle/colloid to the water column which can further scavenge dissolved U across much of the estuarine gradient. In contrast, the estuarine chemistry of U is inconclusive within surface waters of the Mississippi shelf-break region. U behavior is most likely controlled less by traditional sorption and/or desorption reactions involving metal oxides or colloids than by the river’s variable discharge regime (e.g., water parcel residence time during estuarine mixing, nature of particulates, sediment storage and resuspension in, the confined lower river), and plume dispersal. Mixing of the thin freshwater lens into ambient seawater is largely defined by wind-driven rather than physical processes. As a consequence, in the Mississippi outflow region uranium predominantly displays conservative behavior; removal is evident only during anomalous river discharge regimes. ‘Products-approach’ mixing experiments conducted during the Flood of 1993 suggest the importance of small particles and/or colloids in defining a depleted U versus salinity distribution.

Louisiana↗

USGS1972

Interstitial water studies on small core samples, Leg 9

The chemistry of the pore fluids obtained on Leg 9 is remarkable primarily in its constancy. Excepting silicon and strontium, only at one site do the concentrations of the major and minor constituents deviate notably from sea water concentrations (see Tables 1 and 2). The trends, or lack of them, seen in these samples have been discussed previously and only references will be given here. The constancy of composition and similarity to sea water is particularly noteworthy, as the sediments at all of the 9 sites are thought to be intruded by the basal basalt. The pore fluid chemistry exhibits no evidence of intrusion except possibly at Site 84.

Initial reports of the Deep Sea Drilling Project↗

USGS2009

Elevated naturally occurring arsenic in a semiarid oxidizing system, Southern High Plains aquifer, Texas, USA

High groundwater As concentrations in oxidizing systems are generally associated with As adsorption onto hydrous metal (Al, Fe or Mn) oxides and mobilization with increased pH. The objective of this study was to evaluate the distribution, sources and mobilization mechanisms of As in the Southern High Plains (SHP) aquifer, Texas, relative to those in other semiarid, oxidizing systems. Elevated groundwater As levels are widespread in the southern part of the SHP (SHP-S) aquifer, with 47% of wells exceeding the current EPA maximum contaminant level (MCL) of 10 μg/L (range 0.3–164 μg/L), whereas As levels are much lower in the north (SHP-N: 9% ⩾ As MCL of 10 μg/L; range 0.2–43 μg/L). The sharp contrast in As levels between the north and south coincides with a change in total dissolved solids (TDS) from 395 mg/L (median north) to 885 mg/L (median south). Arsenic is present as arsenate (As V) in this oxidizing system and is correlated with groundwater TDS (Spearman’s ρ = 0.57). The most likely current source of As is sorbed As onto hydrous metal oxides based on correlations between As and other oxyanion-forming elements (V, ρ = 0.88; Se, ρ = 0.54; B, ρ = 0.51 and Mo, ρ = 0.46). This source is similar to that in other oxidizing systems and constitutes a secondary source; the most likely primary source being volcanic ashes in the SHP aquifer or original source rocks in the Rockies, based on co-occurrence of As and F ( ρ = 0.56), oxyanion-forming elements and SiO 2 ( ρ = 0.41), which are found in volcanic ashes. High groundwater As concentrations in some semiarid oxidizing systems are related to high evaporation. Although correlation of As with TDS in the SHP aquifer may suggest evaporative concentration, unenriched stable isotopes (δ 2 H: −65 to −27; δ 18 O: −9.1 to −4.2) in the SHP aquifer do not support evaporation. High TDS in the SHP aquifer is most likely related to upward movement of saline water from the underlying Triassic Dockum aquifer. Mobilization of As in other semiarid oxidizing systems is caused by increased pH; however, pH in the SHP aquifer is near neutral (10–90 percentiles, 7.0–7.6). Although many processes, such as competitive desorption with SiO 2 , VO 4 , or PO 4 , could be responsible for local mobilization of As in the SHP aquifer, the most plausible explanation for the regional As distribution and correlation with TDS is the counterion effect caused by a change from Ca- to Na-rich, water as shown by the high correlation between As and Na/(Ca) 0.5 ratios ( ρ = 0.57). This change in chemistry is related to mixing with saline water that moves upward from the underlying Dockum aquifer. This counterion effect may mobilize other anions and oxyanion-forming elements that are correlated with As (F, V, Se, B, Mo and SiO 2 ). Competition among the oxyanions for sorption sites may enhance As mobilization. The SHP case study has similar As sources to those of other semiarid, oxidizing systems (original volcanic ash source followed by sorption onto hydrous metal oxides) but contrasts with these systems by showing lack of evaporative concentration and pH mobilization of As but counterion mobilization of As instead in the SHP-S aquifer.

Texas↗

USGS1989

Effects of highway runoff on the quality of water and bed sediments of two wetlands in central Florida

Results of a study of the effects of highway runoff on the chemical quality of water and bed sediments of a cypress wetlands and a freshwater marsh in central Florida indicate that detention of the runoff prior to release into the wetland reduces concentrations of automobile-related chemicals in the water and bed sediments in the wetland. Detention of highway runoff for the cypress wetland occurs in a 68-ft by 139-ft detention pond, and in a 12-ft by 25 ft trash retainer for the freshwater marsh. The analysis of the chemical data for water and bed sediments indicates that many of the observed differences in chemistry are due to the difference in detention facilities. Water quality generally improved from the inlet to the outlet of both wetlands. Only inlet and outlet data were collected at the cypress wetland, and these showed a reduction in concentrations through the wetland. Spatial data collected at the freshwater marsh indicated that constituent concentrations in water generally decreased with distance from the inlet. Results of analysis of variance of grouped data for 40 water quality variables at the freshwater marsh inferred that 26 of the 40 variables tested were significantly different among five general locations within the wetland: inlet, outlet, near, intermediate, and far sites (with respect to the inlet). Results from this study indicate that detention structures, larger than the trash retainer at the freshwater marsh, may cause sufficient sorption and settling of substances contained in highway runoff to minimize the transport and deposition of some undesirable chemicals into wetlands. (USGS)

Water-Resources Investigations Report↗

USGS1999

Chemical composition and geologic history of saline waters in Aux Vases and Cypress Formations, Illinois Basin

Seventy-six samples of formation waters were collected from oil wells producing from the Aux Vases or Cypress Formations in the Illinois Basin. Forty core samples of the reservoir rocks were also collected from the two formations. Analyses of the samples indicated that the total dissolved solids content (TDS) of the waters ranged from 43,300 to 151,400 mg/L, far exceeding the 35,400 mg/mL of TDS found in typical seawater. Cl-Br relations suggested that high salinities in the Aux Vases and Cypress formation waters resulted from the evaporation of original seawater and subsequent mixing of the evaporated seawater with concentrated halite solutions. Mixing with the halite solutions increased Na and Cl concentrations and diluted the concentration of other ions in the formation waters. The elemental concentrations were influenced further by diagenetic reactions with silicate and carbonate minerals. Diagenetic signatures revealed by fluid chemistry and rock mineralogy delineated the water-rock interactions that took place in the Aux Vases and Cypress sandstones. Dissolution of K-feldspar released K into the solution, leading to the formation of authigenic illite and mixed-layered illite/smectite. Some Mg was removed from the solution by the formation of authigenic chlorite and dolomite. Dolomitization, calcite recrystallization, and contribution from clay minerals raised Sr levels significantly in the formation waters. The trend of increasing TDS of the saline formation waters with depth can be explained with density stratification. But, it is difficult to explain the combination of the increasing TDS and increasing Ca/Na ratio with depth without invoking the controversial 'ion filtration' mechanism.

Aquatic Geochemistry↗

USGS2021

Completion summary for boreholes USGS 148, 148A, and 149 at the Materials and Fuels Complex, Idaho National Laboratory, Idaho

In 2019, the U.S. Geological Survey (USGS), in cooperation with the U.S. Department of Energy, drilled and constructed boreholes USGS 148A and USGS 149 for stratigraphic framework analyses and long-term groundwater monitoring of the eastern Snake River Plain aquifer at the Idaho National Laboratory (INL) in southeastern Idaho. Initially, boreholes USGS 148A and USGS 149 were continuously cored to allow the USGS and INL subcontractor to collect select geophysical and seismic data and evaluate properties of recovered core material. The USGS geophysical data and descriptions of core material are described in this report; however, data collected by the INL contractor, including seismic data, are not included as part of the report. The unsaturated zone at both borehole locations is relatively thick, depth to water was measured at approximately 663.6 feet (ft) below land surface (BLS) in USGS 148A, and at approximately 654.1 ft BLS at USGS 149. On completion of coring and data collection, both boreholes (USGS 148A and USGS 149) were repurposed as monitoring wells. Well USGS 148A was constructed to a depth of 759 ft BLS and instrumented with a dedicated submersible pump and measurement line; well USGS 149 was constructed to a depth of 974 ft BLS and instrumented with a multilevel monitoring system (Westbay TM ). Geophysical data, collected by the USGS, were used to characterize the subsurface geology and aquifer conditions. Natural gamma log measurements were used to assess sediment-layer thickness and location. Neutron and gamma-gamma source logs were used to confirm fractured and vesicular basalt identified for aquifer testing and multilevel monitoring well zone testing. Acoustic televiewer logs, collected for well USGS 149, were used to identify fractures and assess groundwater movement when compared with neutron measurements. Furthermore, gyroscopic deviation measurements were used to measure horizontal and vertical displacement for the constructed boreholes USGS 148A and USGS 149. A single-well aquifer test was done in well USGS 148A during November 6–7, 2019, to provide estimates of transmissivity and hydraulic conductivity. Estimates for transmissivity and hydraulic conductivity were 6.34×10 3 feet squared per day and 3.17 feet per day, respectively. The aquifer test was run overnight (21.3 hours) and measured drawdown was relatively small (0.09 ft) at sustained pumping rates ranging from 15.7 to 16.1 gallons per minute. The transmissivity estimates for well USGS 148A were slightly lower than those determined from previous aquifer tests for wells near the Materials and Fuels Complex, but well within range of other aquifer tests done at the INL. Water-quality samples, collected from well USGS 148A and from four zones in well USGS 149, were analyzed for cations, anions, metals, nutrients, volatile organic compounds, stable isotopes, and radionuclides. Water samples for most of the inorganic constituents showed similar chemistry in USGS 148A and all four zones in USGS 149. Water samples for stable isotopes of oxygen and hydrogen indicated some possible influence of irrigation on the water quality. Nitrate plus nitrite concentrations indicated influence from anthropogenic sources. The volatile organic compound and radiochemical data indicated that wastewater disposal practices at the Materials and Fuels Complex or from drilling had no detectable influence on these wells.

Idaho↗

USGS1971

Distribution of copper, lead, zinc, mercury, and arsenic in the surface sediments off the coast of northwestern Alaska

Increasing interest in potentially harmful substances utilized and discarded by man has raised question about the normal distribution of chemical elements in the natural environment. This interest prompted a baseline study of a pristine region off the northern coast of Alaska. Information was gathered on currents, water clarity, nutrients, temperature and salinity, zooplakton, benthic communities, neritic fauna, bird and mammal population and pesticide residues, sediment composition and chemistry of the sediments and their interstitial waters. This information will provide a base for ascertaining and evaluating future changes and for assessment of the potential hazard in this region and ecosystems elsewhere.

Alaska↗

USGS2009

Geochemical investigation of the Arbuckle-Simpson Aquifer, South-Central Oklahoma, 2004-06

A geochemical reconnaissance investigation of the Arbuckle-Simpson aquifer in south-central Oklahoma was initiated in 2004 to characterize the ground-water quality at an aquifer scale, to describe the chemical evolution of ground water as it flows from recharge areas to discharge in wells and springs, and to determine the residence time of ground water in the aquifer. Thirty-six water samples were collected from 32 wells and springs distributed across the aquifer for chemical analysis of major ions, trace elements, isotopes of oxygen and hydrogen, dissolved gases, and age-dating tracers. In general, the waters from wells and springs in the Arbuckle-Simpson aquifer are chemically suitable for all regulated uses, such as public supplies. Dissolved solids concentrations are low, with a median of 347 milligrams per liter (mg/L). Two domestic wells produced water with nitrate concentrations that exceeded the U.S. Environmental Protection Agency's nitrate maximum contaminant level (MCL) of 10 mg/L. Samples from two wells in the confined part of the aquifer exceeded the secondary maximum contaminant level (SMCL) for chloride of 250 mg/L and the SMCL of 500 mg/L for dissolved solids. Water samples from these two wells are not representative of water samples from the other wells and springs completed in the unconfined part of the aquifer. No other water samples from the Arbuckle-Simpson geochemical reconnaissance exceeded MCLs or SMCLs, although not every chemical constituent for which the U.S. Environmental Protection Agency has established a MCL or SMCL was analyzed as part of the Arbuckle-Simpson geochemical investigation. The major ion chemistry of 34 of the 36 samples indicates the water is a calcium bicarbonate or calcium magnesium bicarbonate water type. Calcium bicarbonate water type is found in the western part of the aquifer, which is predominantly limestone. Calcium magnesium bicarbonate water is found in the eastern part of the aquifer, which is predominantly a dolomite. The major ion chemistry for these 34 samples is consistent with a set of water-rock interactions. Rainfall infiltrates the soil zone, where the host rock, limestone or dolomite, dissolves as a result of uptake of carbon dioxide gas. Some continued dissolution of dolomite and precipitation of calcite occur as the water flows through the saturated zone. The major ion chemistry of the two samples from wells completed in the confined part of the aquifer indicates the water is a sodium chloride type. Geochemical inverse modeling determined that mixing of calcite-saturated recharge water with brine and dissolving calcite, dolomite, and gypsum accounts for the water composition of these two samples. One of the two samples, collected at Vendome Well in Chickasaw National Recreation Area, had a mixing fraction of brine of about 1 percent. The brine component of the sample at Vendome Well is likely to account for the relatively large concentrations of many of the trace elements (potassium, fluoride, bromide, iodide, ammonia, arsenic, boron, lithium, selenium, and strontium) measured in the water sample. Carbon-14, helium-3/tritium, and chlorofluorocarbons were used to calculate ground-water ages, recharge temperatures, and mixtures of ground water in the Arbuckle-Simpson aquifer. Thirty four of 36 water samples recharged the aquifer after 1950, indicating that water is moving quickly from recharge areas to discharge at streams and springs. Two exceptions to this classification were noted in samples 6 and 15 (Vendome Well). Ground-water ages determined for these two samples by using carbon-14 are 34,000 years (site 6) and 10,500 years (site 15). Concentrations of dissolved argon, neon, and xenon in water samples were used to determine the temperature of the water when it recharged the aquifer. The mean annual air temperature at Ada, Oklahoma, is 16 degrees Celsius (C) and the median temperature of the 30 reconnaissance water samples was 18.1 C. The av

Oklahoma↗

USGS2011

Limnological and water-quality data from Wonder Lake, Chilchukabena Lake, and Lake Minchumina, Denali National Park and Preserve and surrounding area, Alaska, June 2006-August 2008

Growing visitor traffic and resource use, as well as natural and anthropogenic land and climatic changes, can place increasing stress on lake ecosystems in Denali National Park and Preserve. Baseline data required to substantiate impact assessment in this sub-arctic region is sparse to non-existent. The U.S. Geological Survey, in cooperation with the National Park Service, conducted a water-quality assessment of several large lakes in and around the Park from June 2006 to August 2008. Discrete water-quality samples, lake profiles of pH, specific conductivity, dissolved-oxygen concentration, water temperature, turbidity, and continuous-record temperature profile data were collected from Wonder Lake, Chilchukabena Lake, and Lake Minchumina. In addition, zooplankton, snow chemistry data, fecal coliform, and inflow/outflow water-quality samples also were collected from Wonder Lake.

Open-File Report↗

USGS2003

Geohydrologic Framework of Recharge and Seawater Intrusion in the Pajaro Valley, Santa Cruz and Monterey Counties, California

Pajaro Valley is a coastal watershed of 160 square miles located along Monterey Bay north of Elkhorn Slough and south of the city of Santa Cruz. The valley has been predominantly developed for agriculture since the late 1800s. In 1984 the Pajaro Valley Water Management Agency (PVWMA) was formed and was delegated with the responsibility of the management of the water resources within the Pajaro Valley by the State of California. About 84 percent of the water is used for agriculture and 16 percent is used for industrial and municipal water supply; almost all of the demand is supplied by ground water. Ground-water pumpage varies with seasonal and climatic periods. The alluvial aquifers are composed of Quaternary- and Tertiary-aged sediments that are layered marine and terrestrial coarse-grained deposits separated by extensive fine-grained deposits that potentially restrict vertical movement of ground water and seawater intrusion in the coastal subareas. The coarse-grained deposits, which persist over large areas, control pumpage and related seawater intrusion. The Aromas Sand crops out throughout the north and central parts of the PVWMA area and offshore on the continental shelf and in Monterey submarine canyon. Because many of the wells in the coastal and inland subregions are screened at depths of 200 to 400 feet below land surface, a direct avenue is provided for seawater intrusion through the coarse-grained deposits of the shallower alluvium and Aromas Sand. Geophysical logs from monitoring wells indicate discrete zones of saline water that are related to pumpage and seawater intrusion in the aquifers of the shallower alluvium and upper Aromas Sand in the upper-aquifer system and to deeper saline waters in the lower Aromas Sand within the lower-aquifer system. The precipitation data indicate that there were at least nine dry and nine wet periods that range from 2 to 19 years during the period of record, 1880?1997. The ground-water pumpage, runoff, streamflow and related water quality of streamflow also vary with seasonal and climatic periods. Recharge occurs from deep percolation of precipitation and from infiltration of streamflow. Streamflow originates from local runoff and from outside the valley as inflow from the Pajaro River. Although partly regulated, streamflow in the Pajaro River at Chittenden is less than 200 cubic feet per second 88 percent of the time and is less than 12 cubic feet per second 50 percent of the time. Streamflow water-quality data suggest that there may be several sources of poor-quality water that contribute to elevated chloride, sulfate, and nitrate concentrations in streamflow. The poor water quality occurring during lower streamflows indicates that low flows may be an additional source of salinity for ground-water recharge as streamflow infiltration along the Pajaro River. The geochemical data from this study indicate that the two main sources of recharge are deep percolation of local runoff and streamflow infiltration of Pajaro River water. The geophysical and geochemical data suggest that only the shallow alluvial aquifer and parts of the upper Aromas Sand that constitute the upper-aquifer system are being replenished by recent recharge in the coastal areas of Pajaro Valley and represent the renewable ground-water resources. These data also suggest that there is very little vertical flow through the layered aquifer systems in the coastal regions. The confining aquitards are laterally extensive but may be missing in places owing to fluvial erosion or offsetting by fault movement. Geochemical and geophysical data indicate that the ground water from some parts of the upper and lower Aromas Sand in the coastal regions was recharged thousands of years ago and may, in part, represent nonrenewable ground-water resources. The analysis of major-ion chemistry, in combination with isotope and trace-element/chloride ratios, indicates that the coastal ground-water and surface-water samples

Water-Resources Investigations Report↗

USGS2016

Geochemistry of formation waters from the Wolfcamp and “Cline” shales: Insights into brine origin, reservoir connectivity, and fluid flow in the Permian Basin, USA

Despite being one of the most important oil producing provinces in the United States, information on basinal hydrogeology and fluid flow in the Permian Basin of Texas and New Mexico is lacking. The source and geochemistry of brines from the basin were investigated (Ordovician- to Guadalupian-age reservoirs) by combining previously published data from conventional reservoirs with geochemical results for 39 new produced water samples, with a focus on those from shales. Salinity of the Ca–Cl-type brines in the basin generally increases with depth reaching a maximum in Devonian (median = 154 g/L) reservoirs, followed by decreases in salinity in the Silurian (median = 77 g/L) and Ordovician (median = 70 g/L) reservoirs. Isotopic data for B, O, H, and Sr and ion chemistry indicate three major types of water. Lower salinity fluids (<70 g/L) of meteoric origin in the middle and upper Permian hydrocarbon reservoirs (1.2–2.5 km depth; Guadalupian and Leonardian age) likely represent meteoric waters that infiltrated through and dissolved halite and anhydrite in the overlying evaporite layer. Saline (>100 g/L), isotopically heavy (O and H) water in Leonardian [Permian] to Pennsylvanian reservoirs (2–3.2 km depth) is evaporated, Late Permian seawater. Water from the Permian Wolfcamp and Pennsylvanian “Cline” shales, which are isotopically similar but lower in salinity and enriched in alkalis, appear to have developed their composition due to post-illitization diffusion into the shales. Samples from the “Cline” shale are further enriched with NH 4 , Br, I and isotopically light B, sourced from the breakdown of marine kerogen in the unit. Lower salinity waters (<100 g/L) in Devonian and deeper reservoirs (>3 km depth), which plot near the modern local meteoric water line, are distinct from the water in overlying reservoirs. We propose that these deep meteoric waters are part of a newly identified hydrogeologic unit: the Deep Basin Meteoric Aquifer System. Chemical, isotopic, and pressure data suggest that despite over-pressuring in the Wolfcamp shale, there is little potential for vertical fluid migration to the surface environment via natural conduits.

New Mexico, Texas↗

USGS2021

In vitro effects-based method and water quality screening model for use in pre- and post-distribution treated waters

Recent urban public water supply contamination events emphasize the importance of screening treated drinking water quality after distribution. In vitro bioassays, when run concurrently with analytical chemistry methods, are effective tools to evaluating the efficacy of water treatment processes and water quality. We tested 49 water samples representing the Chicago Department of Water Management service areas for estrogen, (anti)androgen, glucocorticoid receptor-activating contaminants and cytotoxicity. We present a tiered screening approach suitable to samples with anticipated low-level activity and initially tested all extracts for statistically identifiable endocrine activity; performing a secondary dilution-response analysis to determine sample EC 50 and biological equivalency values (BioEq). Estrogenic activity was detected in untreated Lake Michigan intake water samples using mammalian (5/49; median: 0.21 ng E2Eq/L) and yeast cell (5/49; 1.78 ng E2Eq/L) bioassays. A highly sensitive (anti)androgenic activity bioassay was applied for the first time to water quality screening and androgenic activity was detected in untreated intake and treated pre-distribution samples (4/49; 0.93 ng DHTEq/L). No activity was identified above method detection limits in the yeast androgenic, mammalian anti-androgenic, and both glucocorticoid bioassays. Known estrogen receptor agonists were detected using HPLC/MS-MS (estrone: 0.72-1.4 ng/L; 17α-estradiol: 1.3-1.5 ng/L; 17β-estradiol: 1.4 ng/L; equol: 8.8 ng/L), however occurrence did not correlate with estrogenic bioassay results. Many studies have applied bioassays to water quality monitoring using only relatively small samples sets often collected from surface and/or wastewater effluent. However, to realistically adapt these tools to treated water quality monitoring, water quality managers must have the capacity to screen potentially hundreds of samples in short timeframes. Therefore, we provided a tiered screening model that increased sample screening speed, without sacrificing statistical stringency, and detected estrogenic and androgenic activity only in pre-distribution Chicago area samples.

Illinois, Indiana↗

USGS2005

Delineating a recharge area for a spring using numerical modeling, Monte Carlo techniques, and geochemical investigation

Recharge areas of spring systems can be hard to identify, but they can be critically important for protection of a spring resource. A recharge area for a spring complex in southern Wisconsin was delineated using a variety of complementary techniques. A telescopic mesh refinement (TMR) model was constructed from an existing regional-scale ground water flow model. This TMR model was formally optimized using parameter estimation techniques; the optimized "best fit" to measured heads and fluxes was obtained by using a horizontal hydraulic conductivity 200% larger than the original regional model for the upper bedrock aquifer and 80% smaller for the lower bedrock aquifer. The uncertainty in hydraulic conductivity was formally considered using a stochastic Monte Carlo approach. Two-hundred model runs used uniformly distributed, randomly sampled, horizontal hydraulic conductivity values within the range given by the TMR optimized values and the previously constructed regional model. A probability distribution of particles captured by the spring, or a "probabilistic capture zone," was calculated from the realistic Monte Carlo results (136 runs of 200). In addition to portions of the local surface watershed, the capture zone encompassed areas outside of the watershed - demonstrating that the ground watershed and surface watershed do not coincide. Analysis of water collected from the site identified relatively large contrasts in chemistry, even for springs within 15 m of one another. The differences showed a distinct gradation from Ordovician-carbonate-dominated water in western spring vents to Cambrian-sandstone-influenced water in eastern spring vents. The difference in chemistry was attributed to distinctive bedrock geology as demonstrated by overlaying the capture zone derived from numerical modeling over a bedrock geology map for the area. This finding gives additional confidence to the capture zone calculated by modeling.

Ground Water↗

USGS1983

Evaluation of ground-water quality data from Kentucky

The report reviews and summarizes 10,578 chemical analyses, from 2,362 wells and springs in Kentucky. These water-quality data were collected prior to September 30, 1981, and are available in computer files of the U.S. Geological Survey. The principal water-bearing rocks in Kentucky were combined into 10 major groups to aid in data summary preparation and general description of the ground-water quality of the State. Ground water in Kentucky is generally fresh near the outcrop of the rocks comprising the aquifer. Slightly saline to briny water occurs at variable depths beneath the freshwater. Preparation of quadrilinear diagrams revealed three principal geochemical processes in the aquifers of Kentucky: (1) mixing of freshwater and saline water in an interface zone; (2) dedolomitization of the Devonian and Silurian and Lower Mississippian carbonate rocks; (3) sodium for calcium exchange in the freshwater sections of many of the sandstone-shale aquifers. A number of errors and deficiencies were found in the data base. The principal deficiencies were: (1) very few complete analyses which included important field measurements; (2) inadequate definition of the chemistry of the freshwater-saline water interface zone throughout much of the State; (3) no analyses of stable isotopes and dissolved gases; (4) fewer than 10 analyses of most trace metals, radionuclides, and man-made organic chemicals; and (5) no data on bacteria in ground water from any aquifer in the State. (USGS)

Kentucky↗