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

USGS2025

Fish-assemblage and water-quality recovery with declining acidic deposition in Adirondack mountain streams, New York, USA

Long-term records of air-pollutant emissions and atmospheric deposition, as well as water quality in streams of the Adirondack Mountains of New York, USA, indicate that chemical recovery from acidic deposition is progressing. Although Brook Trout Salvelinus fontinalis (Mitchill, 1814) have recently repopulated several lakes, the degree to which fish assemblages and individual species populations have recovered in streams of the region is unknown. The United States Geological Survey sampled acid–base chemistry and fish assemblages at 42 Adirondack region streams (2014–2021), most of which were also sampled in 2 prior periods (primarily 1979–1984 and 1999), to determine the extent and degree of chemical and biological recovery and whether responses could be linked to regional declines in acidic deposition. Between 1990 and 2021, total annual emissions of SO 2 and NO x declined nationwide by 94% and 87%, respectively, and paralleled 88% and 70% decreases in SO 4 2− and NO 3 − concentrations, respectively, in wet deposition in the region. During this interval, mean acid neutralizing capacity increased by 19.9 µeq/L, pH increased by 0.33 units, and inorganic Al (Al i ) decreased by 6.0 µmol/L at one continuously monitored stream, whereas mean acid neutralizing capacity increased by 38.5 µeq/L and mean Al i concentration decreased by ∼3.0 µmol/L during springtime at all 42 Adirondack region streams. Between the 1 st and 3 rd periods, mean fish-assemblage richness, density, and biomass at 40 sites increased by 112%, 236%, and 66%, respectively. Although mean Brook Trout density and biomass did not meaningfully change among periods, their distribution expanded from 20 sites in the strongly impacted sampling period (1979–1984) to 33 sites in the recovery period (2014–2021). Trends in pollutant emissions and deposition, water quality, and fish-assemblage metrics indicate aquatic ecosystems in many Adirondack mountain streams improved markedly following implementation of the 1990 Clean Air Act Amendments and recent N and S allowance-trading and emissions regulations.

New York↗

USGS1976

The national coal-resources data system of the U.S. geological survey

The National Coal Resources Data System (NCRDS) was designed by the U.S. Geological Survey (USGS) to meet the increasing demands for rapid retrieval of information on coal location, quantity, quality, and accessibility. An interactive conversational query system devised by the USGS retrieves information from the data bank through a standard computer terminal. The system is being developed in two phases. Phase I, which currently is available on a limited basis, contains published areal resource and chemical data. The primary objective of this phase is to retrieve, calculate, and tabulate coal-resource data by area on a local, regional, or national scale. Factors available for retrieval include: state, county, quadrangle, township, coal field, coal bed, formation, geologic age, source and reliability of data, and coal-bed rank, thickness, overburden, and tonnage, or any combinations of variables. In addition, the chemical data items include individual values for proximate and ultimate analyses, BTU value, and several other physical and chemical tests. Information will be validated and deleted or updated as needed. Phase II is being developed to store, retrieve, and manipulate basic point source coal data (e.g., field observations, drill-hole logs), including geodetic location; bed thickness; depth of burial; moisture; ash; sulfur; major-, minor-, and trace-element content; heat value; and characteristics of overburden, roof rocks, and floor rocks. The computer system may be used to generate interactively structure-contour or isoline maps of the physical and chemical characteristics of a coal bed or to calculate coal resources. ?? 1976.

Computers & Geosciences↗

USGS2008

Environmental chemical data for perishable sediments and soils collected in New Orleans, Louisiana, and along the Louisiana Delta following Hurricanes Katrina and Rita, 2005

In October 2005, nearly one month after Hurricanes Katrina and Rita, a team of scientists from the U.S. Geological Survey and the Missouri University of Science and Technology deployed to southern Louisiana to collect perishable environmental data resulting from the impacts of these storms. Perishable samples collected for this investigation are subject to destruction or ruin by removal, mixing, or natural decay; therefore, collection is time-critical following the depositional event. A total of 238 samples of sediment, soil, and vegetation were collected to characterize chemical quality. For this analysis, 157 of the 238 samples were used to characterize trace element, iron, total organic carbon, pesticide, and polychlorinated biphenyl concentrations of deposited sediment and associated shallow soils. In decreasing order, the largest variability in trace element concentration was detected for lead, vanadium, chromium, copper, arsenic, cadmium, and mercury. Lead was determined to be the trace element of most concern because of the large concentrations present in the samples ranging from 4.50 to 551 milligrams per kilogram (mg/kg). Sequential extraction analysis of lead indicate that 39.1 percent of the total lead concentration in post-hurricane sediment is associated with the iron-manganese oxide fraction. This fraction is considered extremely mobile under reducing environmental conditions, thereby making lead a potential health hazard. The presence of lead in post-hurricane sediments likely is from redistribution of pre-hurricane contaminated soils and sediments from Lake Pontchartrain and the flood control canals of New Orleans. Arsenic concentrations ranged from 0.84 to 49.1 mg/kg. Although Arsenic concentrations generally were small and consistent with other research results, all samples exceeded the U.S. Environmental Protection Agency’s Human Health Medium-Specific Screening Level of 0.39 mg/kg. Mercury concentrations ranged from 0.02 to 1.30 mg/kg. Comparing the mean mercury concentration present in post-hurricane samples with regional background data from the U.S. Geological Survey National Geochemical Dataset, indicates that mercury concentrations in post-hurricane sediment generally are larger. Sequential extraction analysis of 51 samples for arsenic indicate that 54.5 percent of the total arsenic concentration is contained in the extremely mobile iron-manganese oxide fraction. Pesticide and polychlorinated biphenyl Arochlor concentrations in post-hurricane samples were small. Prometon was the most frequently detected pesticide with concentrations ranging from 2.4 to 193 micrograms per kilogram (µg/kg). Methoxychlor was present in 22 samples with a concentration ranging from 3.5 to 3,510 µg/kg. Although methoxychlor had the largest detected pesticide concentration, it was well below the U.S. Environmental Protection Agency’s High-Priority Screening Level for residential soils. Arochlor congeners were not detected for any sample above the minimum detection level of 7.9 µg/kg.

Louisiana↗

USGS1985

Selected test-well data from the MX-missile siting study, Tooele, Juab, Millard, Beaver, and Iron Counties, Utah

This report contains well data collected from 1979 to 1983 in a part of the Great Basin in western Utah (fig. 1). The area is characterized by a series of generally north-trending mountain ranges separated by alluviumfilled basins that are partially filled with sedimentary deposits eroded from the adjacent mountains and lacustrine sediments deposited by Lake Bonneville. Most of the intermountain basins are elongated in the northward direction, but some are almost equidimensional. This report was prepared as part of the Great Basin Regional AquiferSystem Analysis (RASA) program. The report is intended to make well data from the MX-missile siting study readily available to water-resource managers and the general public. It includes well data obtained in areas for which little or no such data have been published previously. Well-drilling and well-completion data were compiled by Ertec, Inc. (formerly Fugro National, Inc.) under contract with the U. S. Air Force. Those data along with aquifer test data, geophysical logs, and drillers1 or geologists1 logs were obtained from Ertec, Inc. under an agreement with the U.S. Air Force. The authors thank the officials of both Ertec, Inc. and the U.S. Air Force for their helpful cooperation. The U.S. Geological Survey obtained accurate locations of the test wells (pi. 1) and accurate water-level measurements in those wells (table 1). Chemical analyses of water samples collected from several of the test wells drilled in the Sevier Desert have been published in a report by Enright and Holmes (1982, table 5). Test drilling for the MX-missile siting study consisted of two parts, the verification phase and the water-resources phase. The verification jhase was designed to obtain information necessary for the design and construction of the MX-basing system. Numerous small diameter wells were bored with depths ranging from 92 to 205 feet. Two-inch diameter JVC casing with the bottom 20 feet perforated was installed in each borehole. The water-resources phase was designed to determine ground-water availibility and to estimate the effects of ground-water withdrawals required for the construction of the MX-basing system. Six large-diameter production test wells were drilled along with associated small-diameter observation wells. Depths ranged from 310 to 1,399 feet. Lithologic logs for selected production test wells or associated observation wells are listed in table 2. Geophysical logs and aquifer test data are available in the files of the U. S. Geological Survey, as indicated in table 1.

Utah↗

USGS1989

The U.S. Geological Survey Federal-State Cooperative Water- Resources Program: Fiscal Year 1988

The Federal-State Cooperative Program is a partnership between the U.S. Geological Survey and State and local agencies. It provides a balanced approach to the study and resolution of water-related problems and to acquiring hydrologic data. The principal program objectives are to: (1) collect, on a systematic basis, data needed for the continuing determination and evaluation of the quantity, quality, and use of the Nation's water resources, and (2) appraise the availability and the physical, chemical, and biological characteristics of surface and ground water through analytical and interpretive investigations. During fiscal year 1988, hydrologic data collection, interpretive investigations, and research were conducted by Geological Survey personnel in offices in every State, Puerto Rico, and several territories in cooperation with more than 1,000 local, State, and regional agencies. In fiscal year 1988, Federal funding of almost $60 million was matched by cooperating agencies, who also provided approximately $6 million unmatched for a total program of about $126 million. This amounted to more than 40 percent of the total funds for Geological Survey water-resources activities. This report presents examples of current (1988) investigations. It also lists about 250 water-resources investigations related to agricultural activities that the Geological Survey conducted from 1970 to 1988.

Open-File Report↗

USGS2009

Hydrochemical analysis of groundwater using multivariate statistical methods - The Volta region, Ghana

Q and R-mode multivariate statistical analyses were applied to groundwater chemical data from boreholes and wells in the northern section of the Volta region Ghana. The objective was to determine the processes that affect the hydrochemistry and the variation of these processes in space among the three main geological terrains: the Buem formation, Voltaian System and the Togo series that underlie the area. The analyses revealed three zones in the groundwater flow system: recharge, intermediate and discharge regions. All three zones are clearly different with respect to all the major chemical parameters, with concentrations increasing from the perceived recharge areas through the intermediate regions to the discharge areas. R-mode HCA and factor analysis (using varimax rotation and Kaiser Criterion) were then applied to determine the significant sources of variation in the hydrochemistry. This study finds that groundwater hydrochemistry in the area is controlled by the weathering of silicate and carbonate minerals, as well as the chemistry of infiltrating precipitation. This study finds that the ??D and ?? 18 O data from the area fall along the Global Meteoric Water Line (GMWL). An equation of regression derived for the relationship between ??D and ?? 18 O bears very close semblance to the equation which describes the GMWL. On the basis of this, groundwater in the study area is probably meteoric and fresh. The apparently low salinities and sodicities of the groundwater seem to support this interpretation. The suitability of groundwater for domestic and irrigation purposes is related to its source, which determines its constitution. A plot of the sodium adsorption ratio (SAR) and salinity (EC) data on a semilog axis, suggests that groundwater serves good irrigation quality in the area. Sixty percent (60%), 20% and 20% of the 67 data points used in this study fall within the medium salinity - low sodicity (C2-S1), low salinity -low sodicity (C1-S1) and high salinity - low sodicity (C3-S1) fields, which ascribe good irrigation quality to groundwater from this area. Salinities range from 28.1 to 1956 ??S/cm, whilst SAR values fall within the range 0-3. Extremely low sodicity waters of this kind, with salinities lower than 600 ??S/cm, have the tendency to affect the dispersive properties of irrigation soils when used for irrigation. About 50% of the groundwater in the study area fall within this category and need prior treatment before usage. ?? 2009 Korean Society of Civil Engineers and Springer-Verlag Berlin Heidelberg GmbH.

KSCE Journal of Civil Engineering↗

USGS2013

Streamflow and water-quality conditions including geologic sources and processes affecting selenium loading in the Toll Gate Creek watershed, Aurora, Arapahoe County, Colorado, 2007

Toll Gate Creek is a perennial stream draining a suburban area in Aurora, Colorado, where selenium concentrations have consistently exceeded the State of Colorado aquatic-life standard for selenium of 4.6 micrograms per liter since the early 2000s. In cooperation with the City of Aurora, Colorado, Utilities Department, a synoptic water-quality study was performed along an 18-kilometer reach of Toll Gate Creek extending from downstream from Quincy Reservoir to the confluence with Sand Creek to develop a detailed understanding of streamflow and concentrations and loads of selenium in Toll Gate Creek. Streamflow and surface-water quality were characterized for summer low-flow conditions (July–August 2007) using four spatially overlapping synoptic-sampling subreaches. Mass-balance methods were applied to the synoptic-sampling and tracer-injection results to estimate streamflow and develop spatial profiles of concentration and load for selenium and other chemical constituents in Toll Gate Creek surface water. Concurrent groundwater sampling determined concentrations of selenium and other chemical constituents in groundwater in areas surrounding the Toll Gate Creek study reaches. Multivariate principal-component analysis was used to group samples and to suggest common sources for dissolved selenium and major ions. Hydrogen and oxygen stable-isotope ratios, groundwater-age interpretations, and chemical analysis of water-soluble paste extractions from core samples are presented, and interpretation of the hydrologic and geochemical data support conclusions regarding geologic sources of selenium and the processes affecting selenium loading in the Toll Gate Creek watershed.

Colorado↗

USGS1995

A regional monitoring network to investigate the occurrence of agricultural chemicals in near-surface aquifers of the midcontinental USA

Previous state and national surveys conducted in the mid-continental USA have produced a wide range in results regarding the occurrence of agricultural chemicals in groundwater. At least some of these differences can be attributed to inconsistencies between the surveys, such as different analytical reporting limits. The US Geological Survey has designed a sampling network that is geographically and hydrogeologically representative of near-surface aquifers in the corn- and soybean-producing region of the midcontinental USA. More than 800 water quality samples have been collected from the network since 1991. Six of the seven most frequently detected compounds from this study were herbicide metabolites. A direct relation was determined between tritium content to herbicide and nitrate contamination. The unconsolidated aquifers sampled were found to be more susceptible to herbicide and nitrate contamination than the bedrock aquifers. Knowledge of the regional occurrence and distribution of agricultural chemicals acquired through the study of data collected at network sites will assist policy makers and planners with decisions regarding the protection of drinking-water supplies.

Conference Paper↗

USGS2019

Understanding organic matter heterogeneity and maturation rate by Raman spectroscopy

Solid organic matter (OM) in sedimentary rocks produces petroleum and solid bitumen when it undergoes thermal maturation. The solid OM is a ‘geomacromolecule’, usually representing a mixture of various organisms with distinct biogenic origins, and can have high heterogeneity in composition. Programmed pyrolysis is a common method to reveal bulk geochemical characteristics of the dominant OM, while detailed organic petrography is required to reveal information about the biogenic origin of contributing macerals. Despite the advantages of programmed pyrolysis, it cannot provide information about the heterogeneity of chemical compositions present in the individual OM types. Therefore, other analytical techniques such as Raman spectroscopy are necessary. In this study, we compared geochemical characteristics and Raman spectra of two sets of naturally and artificially matured Bakken source rock samples. A continuous Raman spectral map on solid bitumen particles was created from the artificially matured hydrous pyrolysis residues, in particular, to show the systematic chemical modifications in microscale. Spectroscopic data was plotted for both sets against thermal maturity to compare maturation rate/path for these two separate groups. The outcome showed that artificial maturation through hydrous pyrolysis does not follow the same trend as naturally-matured samples although having similar solid bitumen reflectance values (%SBRo). Furthermore, Raman spectroscopy of solid bitumen from artificially matured samples indicated the heterogeneity of OM decreases as maturity increases. This may represent an alteration in chemical structure towards more uniform compounds at higher maturity. This study may emphasize the necessity of using analytical methods such as Raman spectroscopy along with conventional geochemical methods to better reveal the underlying chemical structure of OM. Finally, observation by Raman spectroscopy of chemical alteration of OM during artificial maturation may assist in the proposal of improved pyrolysis protocols to better resemble natural geologic processes.

North Dakota↗

USGS2013

Geologic effects on groundwater salinity and discharge into an estuary

Submarine groundwater discharge (SGD) can be an important pathway for transport of nutrients and contaminants to estuaries. A better understanding of the geologic and hydrologic controls on these fluxes is critical for their estimation and management. We examined geologic features, porewater salinity, and SGD rates and patterns at an estuarine study site. Seismic data showed the existence of paleovalleys infilled with estuarine mud and peat that extend hundreds of meters offshore. A low-salinity groundwater plume beneath this low-permeability fill was mapped with continuous resistivity profiling. Extensive direct SGD measurements with seepage meters ( n = 551) showed fresh groundwater discharge patterns that correlated well with shallow porewater salinity and the hydrogeophysical framework. Small-scale variability in fresh and saline discharge indicates influence of meter-scale geologic heterogeneity, while site-scale discharge patterns are evidence of the influence of the paleovalley feature. Beneath the paleovalley fill, fresh groundwater flows offshore and mixes with saltwater before discharging along paleovalley flanks. On the adjacent drowned interfluve where low-permeability fill is absent, fresh groundwater discharge is focused at the shoreline. Shallow saltwater exchange was greatest across sandy sediments and where fresh SGD was low. The geologic control of groundwater flowpaths and discharge salinity demonstrated in this work are likely to affect geochemical reactions and the chemical loads delivered by SGD to coastal surface waters. Because similar processes are likely to exist in other estuaries where drowned paleovalleys commonly cross modern shorelines, the existence and implications of complex hydrogeology are important considerations for studies of groundwater fluxes and related management decisions.

Delaware↗

USGS1996

Preliminary assessment of the occurrence and possible sources of MTBE in groundwater in the United States, 1993-1994

The 1990 Clean Air Act Amendments require fuel oxygenates to be added to gasoline used in some metropolitan areas to reduce atmospheric concentrations of carbon monoxide or ozone. Methyl tert-butyl ether (MTBE) is the most commonly used fuel oxygenate and is a relatively new gasoline additive. Nevertheless, out of 60 volatile organic chemicals analyzed, MTBE was the second most frequently detected chemical in samples of shallow ambient groundwater from urban areas that were collected during 1993-1994 aspart of the U.S. Geological Survey's National Water-Quality Assessment program. Samples were collected from five drinking water wells, 12 springs, and 193 monitoring wells in urban areas. No MTBE was detected in drinking water wells. At a reporting level of 0.2 ??g/L, MTBE was detected most frequently in shallow groundwater from urban areas (27% of 210 wells and springs sampled in eight areas) as compared to shallow groundwater from agricultural areas (1.3% of 549 wells sampled in 21 areas) or deeper groundwater from major aquifers (1.0% of 412 wells sampled in nine areas). Only 3% of the shallow wells sampled in urban areas had concentrations of MTBE that exceed 20 ??g/L, which is the estimated lower limit of the United States Environmental Protection Agency draft drinking water health advisory. Because MTBE is persistent and mobile in groundwater, it can move from shallow to deeper aquifers with time. In shallow urban groundwater, MTBE generally was not found with benzene, toluene, ethylbenzene, or xylene (BTEX) compounds, which commonly are associated with gasoline spills. This disassociation causes uncertainty as to the source of MTBE. Possible sources of MTBE in groundwater include point sources, such as leaking storage tanks, and non-point sources, such as recharge of precipitation and stormwater runoff.

Environmental Science & Technology↗

USGS1990

Ostwald ripening of clays and metamorphic minerals

Analyses of particle size distributions indicate that clay minerals and other diagenetic and metamorphic minerals commonly undergo recrystallization by Ostwald ripening. The shapes of their particle size distributions can yield the rate law for this process. One consequence of Ostwald ripening is that a record of the recrystallization process is preserved in the various particle sizes. Therefore, one can determine the detailed geologic history of clays and other recrystallized minerals by separating, from a single sample, the various particle sizes for independent chemical, structural, and isotopic analyses.

Science↗

USGS2009

Rocky Mountain Snowpack Physical and Chemical Data for Selected Sites, 1993-2008

The Rocky Mountain Snowpack program established a network of snowpack-sampling sites in the Rocky Mountain region from New Mexico to Montana to monitor the chemical content of snow to help in the understanding of the effects of atmospheric deposition to this region. The U.S. Geological Survey, in cooperation with the National Park Service, the USDA Forest Service, Teton County in Wyoming, Rio Blanco County in Colorado, Pitkin County in Colorado, and others, collected and analyzed snowpack samples annually for 48 or more sites in the Rocky Mountain region during 1993-2008. Forty-eight of the 162 snow-sampling sites have been sampled annually since 1993. Data include acid-neutralization capacity, specific conductance, pH, hydrogen ion concentrations, dissolved concentrations of major constituents (calcium, magnesium, sodium, potassium, ammonium, chloride, sulfate, and nitrate), dissolved organic carbon concentrations, snow/ water equivalent, snow depth, stable sulfur isotope ratios, total mercury concentrations (beginning in 2001), and ionic charge balance. Quality-assurance data for field and laboratory blanks and field replicates for individual years (1993-2008) also are included.

Data Series↗

USGS2011

Rocky Mountain snowpack physical and chemical data for selected sites, 2010

The Rocky Mountain Snowpack program established a network of snowpack-sampling sites in the Rocky Mountain region, from New Mexico to Montana, to monitor the chemical content of snow and to understand the effects of regional atmospheric deposition on freshwater systems. Scientists with the U.S. Geological Survey, in cooperation with the National Park Service; the U.S. Department of Agriculture Forest Service; the Colorado Department of Public Health and Environment; Teton County, Wyoming; and others, annually collected and analyzed snow-pack samples at 48 or more sites in the Rocky Mountain region during 1993-2010. Sixty-three snowpack-sampling sites were each sampled once in 2010, and those data are presented in this report. Data include acid-neutralization capacity, specific conductance, pH, hydrogen ion concentrations, dissolved concentrations of major constituents (calcium, magnesium, sodium, potassium, ammonium, chloride, sulfate, and nitrate), dissolved organic carbon concentrations, snow-water equivalent, snow depth, total mercury concentrations, and ionic charge balance. Quality-assurance data for field and laboratory blanks and field replicates for 2010 also are included.

Rocky Mountains↗

USGS2008

Water Availability--The Connection Between Water Use and Quality

Water availability has become a high priority in the United States, in large part because competition for water is becoming more intense across the Nation. Population growth in many areas competes with demands for water to support irrigation and power production. Cities, farms, and power plants compete for water needed by aquatic ecosystems to support their minimum flow requirements. At the same time, naturally occurring and human-related contaminants from chemical use, land use, and wastewater and industrial discharge are introduced into our waters and diminish its quality. The fact that degraded quality limits the availability and suitability of water for critical uses is a well-known reality in many communities. What may be less understood, but equally true, is that our everyday use of water can significantly affect water quality, and thus its availability. Landscape features (such as geology, soils, and vegetation) along with water-use practices (such as ground-water withdrawals and irrigation) govern water availability because, together, they affect the movement of chemical compounds over the land and in the subsurface. Understanding the interactions of human activities with natural sources and the landscape is critical to effectively managing water and sustaining water availability in the future.

Fact Sheet↗

USGS2008

Comparison of two cell lysis procedures for recovery of microcystins in water samples from silver lake in Dover, Delaware, with microcystin producing cyanobacterial accumulations

A collaboration was developed between Abraxis, LLC, the State of Delaware Department of Natural Resources and Environmental Control Division of Water Resources Environmental Laboratory, the University of Delaware, and the United States Geological Survey to investigate the efficacy of the QuikLyse procedure developed by Abraxis, LLC as an alternative cell-lysis technique suitable for use with an existing liquid chromatography/tandem mass spectrometry research method developed at the United States Geological Survey Organic Geochemistry Research Laboratory to analyze cyanotoxins. A comparison of three sequential freeze/thaw cycles versus QuikLyse, a proprietary chemical lysis procedure was conducted on four water samples collected from Silver Lake in Dover, Delaware. Results from the Abraxis Microcystins-DM enzyme-linked immunosorbent assay and liquid chromatography/tandem mass spectrometry were tabulated as a function of the cell lysis technique. Stastical comparison of percent relative standard deviations showed no significant difference (alpha = 0.05) between both cell-lysis techniques when measured by enzyme-linked immunosorbent assay or liquid chromatography/tandem mass spectrometry for three of the four samples.

Delaware↗

USGS1989

Flow of ground water through fractured carbonate rocks in the Prairie du Chien-Jordan Aquifer, southeastern Minnesota

Contamination of groundwater from point and nonpoint sources (such as landfills, feedlots, agricultural chemicals applied to fields, and septic systems) is a recognized problem in the karst area of southeastern Minnesota. The US Geological Survey, in cooperation with the Minnesota Department of Natural Resources and the Legislative Commission on Minnesota Resources, Began a study in October 1987 to improve the understanding of local groundwater flow through karst terrain in southeastern Minnesota. The objectives of the study are to: (1) describe the orientations of systematic rock fractures and solution channels of the Prairie du Chien Group of Ordovician-age carbonate rocks in southeastern Minnesota, and, if possible, to define the principal and minor axes of these orientations; and (2) evaluate the effect of fractures and solution channels in the Prairie du Chien Group on the local flow of groundwater. Groundwater in the Upper Carbonate aquifer regionally flows toward the periphery of the aquifer and locally flows into streams and bedrock valleys. The hydraulic gradient in this aquifer generally is greatest near areas of groundwater seepage to streams. Regional groundwater flow in the Prairie du Chien-Jordan aquifer generally is to the south and east in much of Fillmore and Houston Counties and in the southern parts of Olmsted and Winona Counties. Groundwater seepage to selected streams was evaluated by current-meter measurements of downstream gains or losses of streamflow and by an experimental approach based on radon activity in streams. The activity of radon in groundwater ranges from two to four orders of magnitude greater than the activity in surface water; therefore, groundwater seepage to streams generally increases the in-stream radon activity.

Minnesota↗

USGS2003

Surface-water/ground-water interaction of the Spokane River and the Spokane Valley/Rathdrum Prairie aquifer, Idaho and Washington

Historical mining in the Coeur d’Alene River Basin of northern Idaho has resulted in elevated concentrations of some trace metals (particularly cadmium, lead, and zinc) in water and sediment of Coeur d’Alene Lake and downstream in the Spokane River in Idaho and Washington. These elevated trace-metal concentrations in the Spokane River have raised concerns about potential contamination of ground water in the underlying Spokane Valley/Rathdrum Prairie aquifer, the primary source of drinking water for the city of Spokane and surrounding areas. A study conducted as part of the U.S. Geological Survey’s National Water-Quality Assessment Program examined the interaction of the river and aquifer using hydrologic and chemical data along a losing reach of the Spokane River. The river and ground water were extensively monitored over a range of hydrologic conditions at a streamflow-gaging station and 25 monitoring wells situated from 40 to 3,500 feet from the river. River stage, ground-water levels, water temperature, and specific conductance were measured hourly to biweekly. Water samples were collected on nearly a monthly basis between 1999 and 2001 from the Spokane River and were collected up to nine times between June 2000 and August 2001 from the monitoring wells. Hydrologic and chemical data indicate that the Spokane River recharges the Spokane Valley/ Rathdrum Prairie aquifer along a 17-mile reach between Post Falls, Idaho, and Spokane, Washington. Ground-water levels in the near-river aquifer (less than 300 feet from the river) indicate variably saturated conditions below the river and a ground-water flow gradient away from the losing reach of the river. Calculated monthly mean losses, during water years 2000 and 2001 along a nearly 7-mile reach between two gages, ranged from near 69 to 810 cubic feet per second. Losses generally increased with increased streamflow. However, late summer warm water temperatures also appear to be a factor as losses increased due to lower viscosity as water temperatures increased. Chemical data indicated that river recharge may influence ground-water chemistry as far as 3,000 feet from the river, but ground water within a few hundred feet of the river is most affected. Major-ion concentrations, stable isotopes, and temperature of the river and ground water from near-river wells were similar and exhibited similar temporal trends, whereas ground water from wells located farther from the river generally had higher major-ion concentrations and more stable temperatures and chemistry. Although trace-element concentrations sometimes exceeded aquatic-life criteria in the water of the Spokane River and were elevated above national median values in the bed sediment, trace-element concentrations of all river and ground-water samples were at levels less than U.S. Environmental Protection Agency drinking-water standards. The Spokane River appears to be a source of cadmium, copper, zinc, and possibly lead in the near-river ground water. Dissolved cadmium, copper, and lead concentrations generally were less than 1 microgram per liter (µg/L) in the river water and ground water. During water year 2001, dissolved zinc concentrations were similar in water from near-river wells (17-71 µg/L) and the river water (22-66 µg/L), but were less than detection levels in wells farther from the river. Arsenic, found to be elevated in ground water in parts of the aquifer, does not appear to have a river source. Although the river does influence the ground-water chemistry in proximity to the river, it does not appear to adversely affect the ground-water quality to a level of human-health concern.

Idaho;Washington↗