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At least 1,297 records · Page 72Linked to original sources
USGS2002

A three-dimensional numerical model of predevelopment conditions in the Death Valley regional ground-water flow system, Nevada and California

In the early 1990's, two numerical models of the Death Valley regional ground-water flow system were developed by the U.S. Department of Energy. In general, the two models were based on the same basic hydrogeologic data set. In 1998, the U.S. Department of Energy requested that the U.S. Geological Survey develop and maintain a ground-water flow model of the Death Valley region in support of U.S. Department of Energy programs at the Nevada Test Site. The purpose of developing this 'second-generation' regional model was to enhance the knowledge an understanding of the ground-water flow system as new information and tools are developed. The U.S. Geological Survey also was encouraged by the U.S. Department of Energy to cooperate to the fullest extent with other Federal, State, and local entities in the region to take advantage of the benefits of their knowledge and expertise. The short-term objective of the Death Valley regional ground-water flow system project was to develop a steady-state representation of the predevelopment conditions of the ground-water flow system utilizing the two geologic interpretations used to develop the previous numerical models. The long-term objective of this project was to construct and calibrate a transient model that simulates the ground-water conditions of the study area over the historical record that utilizes a newly interpreted hydrogeologic conceptual model. This report describes the result of the predevelopment steady-state model construction and calibration. The Death Valley regional ground-water flow system is situated within the southern Great Basin, a subprovince of the Basin and Range physiographic province, bounded by latitudes 35 degrees north and 38 degrees 15 minutes north and by longitudes 115 and 118 degrees west. Hydrology in the region is a result of both the arid climatic conditions and the complex geology. Ground-water flow generally can be described as dominated by interbasinal flow and may be conceptualized as having two main components: a series of relatively shallow and localized flow paths that are superimposed on deeper regional flow paths. A significant component of the regional ground-water flow is through a thick Paleozoic carbonate rock sequence. Throughout the flow system, ground water flows through zones of high transmissivity that have resulted from regional faulting and fracturing. The conceptual model of the Death Valley regional ground-water flow system used for this study is adapted from the two previous ground-water modeling studies. The three-dimensional digital hydrogeologic framework model developed for the region also contains elements of both of the hydrogeologic framework models used in the previous investigations. As dictated by project scope, very little reinterpretation and refinement were made where these two framework models disagree; therefore, limitations in the hydrogeologic representation of the flow system exist. Despite limitations, the framework model provides the best representation to date of the hydrogeologic units and structures that control regional ground-water flow and serves as an important information source used to construct and calibrate the predevelopment, steady-state flow model. In addition to the hydrogeologic framework, a complex array of mechanisms accounts for flow into, through, and out of the regional ground-water flow system. Natural discharges from the regional ground-water flow system occur by evapotranspiration, springs, and subsurface outflow. In this study, evapotranspiration rates were adapted from a related investigation that developed maps of evapotranspiration areas and computed rates from micrometeorological data collected within the local area over a multiyear period. In some cases, historical spring flow records were used to derive ground-water discharge rates for isolated regional springs. For this investigation, a process-based, numerical model was developed to estimat

Water-Resources Investigations Report↗
USGS1994

Land use in, and water quality of, the Pea Hill Arm of Lake Gaston, Virginia and North Carolina, 1988-90

The City of Virginia Beach currently (1994) supplies water to about 400,000 people in southeastern Virginia. The city plans to withdraw water from the Pea Hill Arm of Lake Gaston to meet projected water needs of the population to the year 2030. The purpose of this report is to (1) describe the temporal and spatial distribution of selected water-quality constituents, (2) document current (1989) land use and land cover in the Pea Hill Arm drainage basin, and (3) discuss relations, if any, between the quality of water in the inlets within the Pea Hill Arm and land uses. The report focuses on water-quality problems in the basin, including changes in concentrations of major ions, nutrients, and algae associated with urban development adjacent to water bodies. The Pea Hill Arm was classified as mesotrophic on the basis of the range of concentrations of total phosphorus (0.001 to 0.61 milligrams per liter); the range of concentrations of total organic-plus-ammonia nitrogen (0.2 to 1.4 milligrams per liter); and the range of concentrations of chlorophyll a (1.4 to 56 micrograms per liter). These water-quality data were collected at 3 feet below the water surface during water years 1989-90. Thermal stratification in Pea Hill Arm generally began in April and ended in September. Water below a depth of about 25 feet generally became anoxic by June. Destratification generally began in late September and was completed by November. Lake Gaston followed the same general stratification and destratification pattern as Pea Hill Arm, except Lake Gaston was partially destratified during the summer when large amounts of water were released from John H. Kerr Reservoir and Lake Gaston Dams. During water year 1988, streamflows were 33 percent below the long-term mean-annual streamflows at one of the major streams to Lake Gaston. Low streamflows contributed to elevated specific conductances and concentrations of sodium, calcium, magnesium, and alkalinity from October 1988 to February 1989 at sampling stations in the Pea Hill Arm and Lake Gaston. About 75 percent of the land use in the Pea Hill Arm is forest land. The remaining 25 percent of the Pea Hill Arm drainage basin is 8 percent pasture/open land, 8 percent open water, 6 percent residential land, and 3 percent cropland. No statistical relations are present between water-quality constituents measured and developed land uses within 11 basins in the Pea Hill Arm Basin, except during periods of stormwater runoff. During a stormwater-runoff event, there was a relation between total nitrite plus nitrate and land use (Kendall's tau correlation coefficient of 0.69). The relation between the developed land use and total nitrite plus nitrate can also be related to the increased ground-water inputs during high base-flow periods. Spatial differences in water-quality constituents as determined by Wilcoxon (matched-pairs) signed-rank tests and cluster analyses were longitudinal and primarily grouped into riverine, transition, and lacustrine zones. These zones were grouped on the basis of flow characteristics and nutrient concentrations.

North Carolina, Virginia↗
USGS2000

Distribution, movement, and fate of nitrate in the surficial aquifer beneath citrus groves, Indian River, Martin, and St. Lucie Counties, Florida

The surficial aquifer system beneath citrus groves in Indian River, Martin, and St. Lucie Counties, Florida, was studied to determine the effects of citrus agriculture on ground-water quality. The surficial aquifer is the primary drinking-water source for Martin and St. Lucie Counties and furnishes about 33 percent of the drinking-water for Indian River County. Water-quality samples and water-level data were collected from December 1996 through October 1998. Nitrate concentrations in ground water exceeded 10 milligrams per liter (mg/L), the U.S. Environmental Protection Agency's maximum contaminant level for nitrate reported as nitrogen, in 5 percent of the samples from citrus groves. These exceedances occurred in samples from wells with depths of 10 feet or less at citrus groves, and mostly in samples collected during or immediately following fertilizer applications. Samples from wells with depths of 20-25 feet contained little or no nitrate. The decreased nitrate concentrations in ground water with depth was not consistent with chloride and dissolved-solids concentrations, two other common indicators of agricultural activity. Chloride and dissolved-solids concentrations remained elevated in ground-water samples from all depths at citrus groves; median chloride and dissolved-solids concentrations in samples from citrus sites were 125 and 779 mg/L, respectively. In comparison, samples from the reference site had maximum chloride and dissolved-solids concentrations of 61 and 366 mg/L, respectively. Based on the age of ground water at 20-25 foot depths (3-50 years, measured with tritium and helium-3 concentration ratios), nitrate concentrations also should have remained elevated with depth because fertilizers have been used for at least 20-30 years at these citrus groves. Nitrate concentrations decreased with depth as a result of denitrification. This could have occurred because favorable conditions for denitrification existed in the aquifer, including high concentrations of dissolved organic carbon and iron (median concentrations of 25.5 and 1.75 mg/L, respectively at citrus sites) and low concentrations of dissolved oxygen (median concentration of 0.9 mg/L at citrus sites), which indicates that reducing conditions were present. Evidence that denitrification occurred included the enrichment of ground water with depth in the heavier isotope of nitrogen, nitrogen-15 ( 15 N). Ground water from wells screened 10-15 feet below land surface had a median d 15 N value of 24.6 per mil, whereas ground water from wells screened 5-10 feet below land surface had a median d 15 N value of 9.4 per mil. Fertilizer samples had a median d 15 N value of 3.0 per mil. Increased d 15 N values coincident with decreased nitrate concentrations with depth indicates that fractionation occurred during denitrification reactions. Finally, excess nitrogen gas, a byproduct of denitrification reactions, was detected at concentrations ranging from 0-8 mg/L in samples from wells screened 10-25 feet below land surface.

Florida↗
USGS1994

Water quality of the Apalachicola-Chattahoochee-Flint and Ocmulgee River Basins related to flooding from Tropical Storm Alberto; pesticides in urban and agricultural watersheds; and nitrate and pesticides in ground water, Georgia, Alabama, and Florida

This report presents preliminary water-quality information from three studies that are part of the National Water-Quality Assessment (NAWQA) Program in the Apalachicola-Chattahoochee-Flint (ACF) River basin and the adjacent Ocmulgee River basin. During the period July 3-7, 1994, heavy rainfall from tropical storm Alberto caused record flooding on the Ocmulgee and Flint Rivers and several of their tributaries. Much of the nitrogen load transported during the flooding was as organic nitrogen generally derived from organic detritus, rather than nitrate derived from other sources, such as fertilizer. More than half the mean annual loads of total phosphorus and organic nitrogen were trans- ported in the Flint and Ocmulgee Rivers during the flood. Fourteen herbicides, five insecticides, and one fungicide were detected in floodwaters of the Ocmulgee, Flint, and Apalachicola Rivers. In a second study, water samples were collected at nearly weekly intervals from March 1993 through April 1994 from one urban and two agricultural watersheds in the ACF River basin, and analyzed for 84 commonly used pesticides. More pesticides were detected and at generally higher concentrations in water from the urban watershed than the agricultural water- sheds, and a greater number of pesticides were persistent throughout much of the year in the urban watershed. Simazine exceeded U.S. Environmental Protection Agency (EPA) drinking-water standards in one of 57 samples from the urban watershed. In a third study, 38 wells were installed in surficial aquifers adjacent to and downgradient of farm fields within agricultural areas in the southern ACF River basin. Even though regional aquifers are generally used for irrigation and domestic- and public-water supplies, degradation of water quality in the surficial aquifers serves as an early warning of potential contamination of regional aquifers. Nitrate concentrations were less than 3 mg/L as N (indicating minimal effect of human activities) in water from about two-thirds of the wells. Water from the remaining wells had elevated nitrate con- centrations, probably the result of human activity. Nitrate concentrations in two of these wells exceeded EPA drinking-water standards. Water samples from eight wells had pesticide concentrations above method detection limits. With the exception of two samples for shallow ground-water wells and one surface-water sample from the urban watershed, concentrations of nitrate nitrogen and detected pesticides were below EPA standards and guidelines for drinking water. However, concentrations of the insecticides chlorpyrifos, carbaryl, and diazinon in the surface-water samples approached or exceeded guidelines for protection of aquatic life.

Alabama, Florida, Georgia↗
USGS1998

Dissolved organic carbon concentrations and compositions, and trihalomethane formation potentials in waters from agricultural peat soils, Sacramento-San Joaquin Delta, California; implications for drinking-water quality

Water exported from the Sacramento-San Joaquin River delta (Delta) is an important drinking-water source for more than 20 million people in California. At times, this water contains elevated concentrations of dissolved organic carbon and bromide, and exceeds the U.S. Environmental Protection Agency's maximum contaminant level for trihalomethanes of 0.100 milligrams per liter if chlorinated for drinking water. About 20 to 50 percent of the trihalomethane precursors to Delta waters originates from drainage water from peat soils on Delta islands. This report elucidates some of the factors and processes controlling and affecting the concentration and quality of dissolved organic carbon released from peat soils and relates the propensity of dissolved organic carbon to form trihalomethanes to its chemical composition. Soil water was sampled from near-surface, oxidized, well-decomposed peat soil (upper soil zone) and deeper, reduced, fibrous peat soil (lower soil zone) from one agricultural field in the west central Delta over 1 year. Concentrations of dissolved organic carbon in the upper soil zone were highly variable, with median concentrations ranging from 46.4 to 83.2 milligrams per liter. Concentrations of dissolved organic carbon in samples from the lower soil zone were much less variable and generally slightly higher than samples from the upper soil zone, with median concentrations ranging from 49.3 to 82.3 milligrams per liter. The dissolved organic carbon from the lower soil zone had significantly higher aromaticity (as measured by specific ultraviolet absorbance) and contained significantly greater amounts of aromatic humic substances (as measured by XAD resin fractionation and carbon-13 nuclear magnetic resonance analysis of XAD isolates) than the dissolved organic carbon from the upper soil zone. These results support the conclusion that more aromatic forms of dissolved organic carbon are produced under anaerobic conditions compared to aerobic conditions. Dissolved organic carbon concentration, trihalomethane formation potential, and ultraviolet absorbance were all highly correlated, showing that trihalomethane precursors increased with increasing dissolved organic carbon and ultraviolet absorbance for whole water samples. Contrary to the generally accepted conceptual model for trihalomethane formation that assumes that aromatic forms of carbon are primary precursors to trihalomethanes, results from this study indicate that dissolved organic carbon aromaticity appears unrelated to trihalomethane formation on a carbon-normalized basis. Thus, dissolved organic carbon aromaticity alone cannot fully explain or predict trihalomethane precursor content, and further investigation of aromatic and nonaromatic forms of carbon will be needed to better identify trihalomethane precursors.

California↗
USGS2001

Saline contamination of soil and water on Pawnee tribal trust land, eastern Payne County, Oklahoma

The Bureau of Land Management reported evidence of saline contamination of soils and water in Payne County on Pawnee tribal trust land. Representatives of the Bureau of Land Management and U.S. Geological Survey inspected the site, in September 1997, and observed dead grass, small shrubs, and large trees near some abandoned oil production wells, a tank yard, an pit, and pipelines. Soil and bedrock slumps and large dead trees were observed near a repaired pipeline on the side of the steep slope dipping toward an unnamed tributary of Eagle Creek. The U.S. Geological Survey, in cooperation with the Bureau of Land Management, initiated an investigation in March 1998 to examine soil conductance and water quality on 160 acres of Pawnee tribal trust land where there was evidence of saline contamination and concern about saline contamination of the Ada Group, the shallowest freshwater aquifer in the area. The proximity of high specific conductance in streams to areas containing pipeline spill, abandoned oil wells, the tank yard, and the pit indicates that surface-water quality is affected by production brines. Specific conductances measured in Eagle Creek and Eagle Creek tributary ranged from 1,187 to 10,230 microsiemens per centimeter, with the greatest specific conductance measured downgradient of a pipeline spill. Specific conductance in an unnamed tributary of Salt Creek ranged from 961 to 11,500 microsiemens per centimeter. Specific conductance in three ponds ranged from 295 to 967 microsiemens per centimeter, with the greatest specific conductance measured in a pond located downhill from the tank yard and the abandoned oil well. Specific conductance in water from two brine storage pits ranged from 9,840 to 100,000 microsiemens per centimeter, with water from the pit near a tank yard having the greater specific conductance. Bartlesville brine samples from the oil well and injection well have the greatest specific conductance, chloride concentration, and dissolved solids concentrations, and plot the furthest from meteoric water on a graph of 8 deuterium and d 18oxygen. Waterflooding of the Bartlesville sand in the study area started in 1957 and continued until 1998. Waterflooding is the process of injecting brine water under pressure to drive the remaining oil to the production wells. The high dissolved solids concentration samples from observation wells 1, 3B, 5,7, and 8 could result from mixing of the Bartlesville brine from the waterfiood with meteoric water.

Water-Resources Investigations Report↗
USGS2003

Methodology for estimating times of remediation associated with monitored natural attenuation

Natural attenuation processes combine to disperse, immobilize, and biologically transform anthropogenic contaminants, such as petroleum hydrocarbons and chlorinated ethenes, in ground-water systems. The time required for these processes to lower contaminant concentrations to levels protective of human health and the environment, however, varies widely between different hydrologic systems, different chemical contaminants, and varying amounts of contaminants. This report outlines a method for estimating timeframes required for natural attenuation processes, such as dispersion, sorption, and biodegradation, to lower contaminant concentrations and mass to predetermined regulatory goals in groundwater systems. The time-of-remediation (TOR) problem described in this report is formulated as three interactive components: (1) estimating the length of a contaminant plume once it has achieved a steady-state configuration from a source area of constant contaminant concentration, (2) estimating the time required for a plume to shrink to a smaller, regulatoryacceptable configuration when source-area contaminant concentrations are lowered by engineered methods, and (3) estimating the time needed for nonaqueous phase liquid (NAPL) contaminants to dissolve, disperse, and biodegrade below predetermined levels in contaminant source areas. This conceptualization was used to develop Natural Attenuation Software (NAS), an interactive computer aquifers. NAS was designed as a screening tool and requires the input of detailed site information about hydrogeology, redox conditions, and the distribution of contaminants. Because NAS is based on numerous simplifications of hydrologic, microbial, and geochemical processes, the program may introduce unacceptable errors for highly heterogeneous hydrologic systems. In such cases, application of the TOR framework outlined in this report may require more detailed, site-specific digital modeling. The NAS software may be downloaded from the Web site http://www.cee.vt.edu/NAS/ Application of NAS illustrates several general characteristics shared by all TOR problems. First, the distance of stabilization of a contaminant plume is strongly dependent on the natural attenuation capacity of particular ground-water systems. The time that it takes a plume to reach a steady-state configuration, however, is independent of natural attenuation capacity. Rather, the time of stabilization is most strongly affected by the sorptive capacity of the aquifer, which is dependent on the organic matter content of the aquifer sediments, as well as the sorptive properties of individual contaminants. As a general rule, a high sorptive capacity retards a plume.s growth or shrinkage, and increases the time of stabilization. Finally, the time of NAPL dissolution depends largely on NAPL mass, composition, geometry, and hydrologic factors, such as ground-water flow rates. An example TOR analysis for petroleum hydrocarbon NAPL was performed for the Laurel Bay site in South Carolina. About 500 to 1,000 pounds of gasoline leaked into the aquifer at this site in 1991, and the NAS simulations suggested that TOR would be on the order of 10 years for soluble and poorly sorbed compounds, such as benzene and methyl tertiary-butyl ether (MTBE). Conversely, TOR would be on the order of 40 years for less soluble, more strongly sorbed compounds, such as toluene, ethylbenzene, and xylenes (TEX). These TOR estimates are roughly consistent with contaminant concentrations observed over 10 years of monitoring at this site where benzene and MTBE concentrations were observed to decrease rapidly and are approaching regulatory maximum concentration limits, whereas toluene, ethylbenzene, and xylene concentrations decreased at a slower rate and have remained relatively high. An example TOR analysis for petroleum hydrocarbon NAPL was performed for the Laurel Bay site in South Carolina.

South Carolina↗
USGS1999

Hydrogeology of, water withdrawal from, and water levels and chloride concentrations in the major Coastal Plain aquifers of Gloucester and Salem Counties, New Jersey

Eight aquifers underlying Gloucester and Salem Counties in the southwestern Coastal Plain of New Jersey provide nearly all the drinking water for the 295,000 people who live in the area. Ground-water withdrawals in the two-county area and adjoining counties have affected water levels in several of these aquifers. Ground-water withdrawals in the two-county area also have affected the quality of water, increasing the chloride concentration in several of the aquifers as a result of saltwater intrusion. This report contains hydrologic data from the two-county area, including geometry and extent of hydrogeologic units, thickness and altitude of each aquifer, withdrawals from and water levels in major aquifers, and chloride concentrations in water from each aquifer. Reported ground-water withdrawals in Gloucester and Salem Counties during 1975-95 averaged 7,800 Mgal/yr (million gallons per year) for public supply, 4,900 Mgal/yr for industrial use, 700 Mgal/yr for irrigation, 500 Mgal/yr for power plants, 50 Mgal/yr for commercial use, and about 40 Mgal/yr for mining. Withdrawals for domestic self-supply in 1994 are estimated to be about 2,600 Mgal/yr, but only about 20 percent (520 Mgal/yr) is thought to be consumptive use; the remainder is returned to the aquifer through septic systems. The most heavily used aquifer in Salem and Gloucester Counties is the Upper Potomac-Raritan-Magothy aquifer, followed by, in decreasing order of use, the Middle Potomac-Raritan-Magothy aquifer, the Lower Potomac-Raritan-Magothy aquifer, the Kirkwood-Cohansey aquifer system, and the Wenonah-Mount Laurel aquifer. Reported withdrawals from these aquifers during 1975-95 averaged 5,000, 3,700, 3,200, and 330 Mgal/yr, respectively. Withdrawals from the Wenonah-Mount Laurel aquifer in Gloucester County increased during 1993-96 because of New Jersey Department of Environmental Protection restrictions on new withdrawals from the deeper Potomac-Raritan-Magothy aquifer system. Because of the increased rate of withdrawal, water-level altitudes in the Wenonah-Mount Laurel aquifer in some parts of the two counties in 1996 were from 5 to 40 ft lower than water levels measured in 1993 and previous years, reaching a low of almost 40 ft below sea level in Washington Township, Gloucester County. Ground water in the Upper, Middle, and Lower Potomac-Raritan-Magothy aquifers in the study area is withdrawn from the outcrop areas near the Delaware River downdip to the Glassboro vicinity. Water-level altitudes in 1993 in the three aquifers were near sea level in the outcrop areas near the Delaware River, but were as low as 80 ft below sea level in parts of Gloucester County that were affected by withdrawals in Camden County and were 20 to 60 ft below sea level near major withdrawal centers in the study area. Chloride concentrations in water samples from selected wells in seven aquifers throughout Gloucester and Salem Counties have been monitored since 1949. These aquifers include the Kirkwood-Cohansey aquifer system, the Vincentown and Wenonah-Mount Laurel aquifers, the Englishtown aquifer system, and the Upper, Middle, and Lower Potomac-Raritan-Magothy aquifers. The results of chloride analyses of 4,221 samples from 496 wells indicate the extent and magnitude of saltwater intrusion in these aquifers, six of which have been affected to varying degrees by saltwater intrusion. The confined Piney Point aquifer and the unconfined Kirkwood-Cohansey aquifer system show no measurable effects of saltwater intrusion in the study area. Chloride concentrations in water from selected public-supply wells screened in the Upper, Middle, and Lower Potomac-Raritan-Magothy aquifers have increased over time in communities along the Delaware River and further inland in both Gloucester and Salem Counties. Elevated chloride concentrations in the Potomac-Raritan-Magothy aquifer system are widespread in this area but rarely exceed the drinking-water standard of 250 milligrams per liter.

Water-Resources Investigations Report↗
USGS2001

Hydrodynamic and suspended-solids concentration measurements in Suisun Bay, California, 1995

Sea level, current velocity, water temperature, salinity (computed from conductivity and temperature), and suspended-solids data collected in Suisun Bay, California, from May 30, 1995, through October 27, 1995, by the U.S. Geological Survey are documented in this report. Data were collected concurrently at 21 sites. Various parameters were measured at each site. Velocity-profile data were collected at 6 sites, single-point velocity measurements were made at 9 sites, salinity data were collected at 20 sites, and suspended-solids concentrations were measured at 10 sites. Sea-level and velocity data are presented in three forms; harmonic analysis results; time-series plots (sea level, current speed, and current direction versus time); and time-series plots of low-pass-filtered time series. Temperature, salinity, and suspended-solids data are presented as plots of raw and low-pass-filtered time series.The velocity and salinity data presented in this report document a period when the residual current patterns and salt field were transitioning from a freshwater-inflow-dominated condition towards a quasi steady-state summer condition when density-driven circulation and tidal nonlinearities became relatively more important as long-term transport mechanisms. Sacramento-San Joaquin River Delta outflow was high prior to and during this study, so the tidally averaged salinities were abnormally low for this time of year. For example, the tidally averaged salinities varied from 0-12 at Martinez, the western border of Suisun Bay, to a maximum of 2 at Mallard Island, the eastern border of Suisun Bay. Even though salinities increased overall in Suisun Bay during the study period, the near-bed residual currents primarily were directed seaward. Therefore, salinity intrusion through Suisun Bay towards the Delta primarily was accomplished in the absence of the tidally averaged, two-layer flow known as gravitational circulation where, by definition, the net currents are landward at the bed. The Folsom Dam spillway gate failure on July 17, 1995, was analyzed to determine the effect on the hydrodynamics of Suisun Bay. The peak flow of the American River reached roughly 1,000 cubic meters per second as a result of the failure, which is relatively small. This was roughly 15 percent of the approximate 7,000 cubic meters per second tidal flows that occur daily in Suisun Bay and was likely attenuated greatly. Based on analysis of tidally averaged near-bed salinity and depth-averaged currents after the failure, the effect was essentially nonexistent and is indistinguishable from the natural variability.

Water-Resources Investigations Report↗
USGS2002

Metal concentrations and sources in the Miller Creek watershed, Park County, Montana, August 2000

Miller Creek is a tributary of Soda Butte Creek in south-central Montana near the northeast corner of Yellowstone National Park. Surface-water and streambed-sediment samples were collected from streams and seeps throughout the Miller Creek watershed during low-flow conditions on August 28-31, 2000, to characterize metal concentrations and identify possible sources contributing metal to Miller Creek. Most water in Miller Creek appears to be unaffected by mining disturbances or natural weathering of mineralized rocks, although such effects are common elsewhere in the New World Mining District. Values for pH were near neutral to basic. Total-recoverable copper, lead, and zinc concentrations were low, relative to State of Montana water-quality standards, with many concentrations less than the analytical minimum reporting levels. Metal concentrations in Miller Creek during this study ranged from 1 to 6 micrograms per liter (?g/L) for total-recoverable copper, <1 to 5 ?g/L for total-recoverable lead, and <1 to 26 ?g/L for total-recoverable zinc. Concentrations of cadmium, copper, lead, and zinc in all samples from Miller Creek were less than the chronic aquatic-life criteria, except for one total-recoverable lead value (5 ?g/L) just downstream from the Black Warrior Mine inflow. Leachable lead and zinc concentrations in streambed-sediment samples collected during this study were highest at the Black Warrior Mine inflow. Leachable concentrations at this site were about 20 times greater for lead and 11 times greater for zinc than concentrations in the streambed-sediment sample collected from Miller Creek upstream from this inflow. However, these elevated concentrations had little effect on the leachable metal concentrations in the streambed-sediment sample collected downstream from the Black Warrior Mine inflow. Metal loading to Miller Creek during this low-flow study was relatively small. Three small left-bank inflows having elevated copper concentrations entered Miller Creek near the middle of the study reach and their combined total-recoverable copper load accounted for about 96 percent of the copper load in Miller Creek. Small loads of lead (about 2 micrograms per second) entered Miller Creek from the Black Warrior Mine inflow and a right bank inflow. None of the loads entering Miller Creek had an appreciable effect on mainstem metal concentrations. In addition, substantial differences between mining related areas and areas influenced by local geology could not be determined.

Montana↗
USGS2000

Environmental Setting and Effects on Water Quality in the Great and Little Miami River Basins, Ohio and Indiana

The Great and Little Miami River Basins drain approximately 7,354 square miles in southwestern Ohio and southeastern Indiana and are included in the more than 50 major river basins and aquifer systems selected for water-quality assessment as part of the U.S. Geological Survey's National Water-Quality Assessment Program. Principal streams include the Great and Little Miami Rivers in Ohio and the Whitewater River in Indiana. The Great and Little Miami River Basins are almost entirely within the Till Plains section of the Central Lowland physiographic province and have a humid continental climate, characterized by well-defined summer and winter seasons. With the exception of a few areas near the Ohio River, Pleistocene glacial deposits, which are predominantly till, overlie lower Paleozoic limestone, dolomite, and shale bedrock. The principal aquifer is a complex buried-valley system of sand and gravel aquifers capable of supporting sustained well yields exceeding 1,000 gallons per minute. Designated by the U.S. Environmental Protection Agency as a sole-source aquifer, the Buried-Valley Aquifer System is the principal source of drinking water for 1.6 million people in the basins and is the dominant source of water for southwestern Ohio. Water use in the Great and Little Miami River Basins averaged 745 million gallons per day in 1995. Of this amount, 48 percent was supplied by surface water (including the Ohio River) and 52 percent was supplied by ground water. Land-use and waste-management practices influence the quality of water found in streams and aquifers in the Great and Little Miami River Basins. Land use is approximately 79 percent agriculture, 13 percent urban (residential, industrial, and commercial), and 7 percent forest. An estimated 2.8 million people live in the Great and Little Miami River Basins; major urban areas include Cincinnati and Dayton, Ohio. Fertilizers and pesticides associated with agricultural activity, discharges from municipal and industrial wastewater-treatment and thermoelectric plants, urban runoff, and disposal of solid and hazardous wastes contribute contaminants to surface water and ground water throughout the study area. Surface water and ground water in the Great and Little Miami River Basins are classified as very hard, calcium-magnesiumbicarbonate waters. The major-ion composition and hardness of surface water and ground water reflect extensive contact with the carbonate-rich soils, glacial sediments, and limestone or dolomite bedrock. Dieldrin, endrin, endosulfan II, and lindane are the most commonly reported organochlorine pesticides in streams draining the Great and Little Miami River Basins. Peak concentrations of the herbicides atrazine and metolachlor in streams commonly are associated with post-application runoff events. Nitrate concentrations in surface water average 3 to 4 mg/L (milligrams per liter) in the larger streams and also show strong seasonal variations related to application periods and runoff events. Ambient iron concentrations in ground water pumped from aquifers in the Great and Little Miami River Basins often exceed the U.S. Environmental Protection Agency Secondary Maximum Contaminant Level (300 micrograms per liter). Chloride concentrations are below aesthetic drinking-water guidelines (250 mg/L), except in ground water pumped from low-yielding Ordovician shale; chloride concentrations in sodium-chloriderich ground water pumped from the shale bedrock can exceed 1,000 mg/L. Some of the highest average nitrate concentrations in ground water in Ohio and Indiana are found in wells completed in the buried-valley aquifer; these concentrations typically are found in those parts of the sand and gravel aquifer that are not overlain by clay-rich till. Atrazine was the most commonly detected herbicide in private wells. Concentrations of volatile organic compounds in ground water generally were below Federal drinking-water standards, except near areas of known or suspected contamination. Evaluation of fish and macroinvertebrate community performance in streams and rivers draining the Great and Little Miami River Basins indicates that most streams meet basic aquatic-life-use criteria set by the Ohio Environmental Protection Agency for warmwater habitat. Stream reaches whose biological community performance meet aquatic-lifeuse criteria defined for exceptional warmwater habitat are found in Twin Creek, the Upper Great Miami River, the Little Miami River, and the Whitewater River Basins. Other streams have exhibited significant improvements in biological community performance (and water quality)'that are attributed primarily to reduced pollutant loadings from wastewater-treatment plants upgraded since 1972. Four hydrogeomorphic regions were delineated in the Great and Little Miami River Basins based on distinct and relatively homogeneous natural characteristics. Primary features used to delineate the hydrogeomorphic regions include bedrock geology, surficial geology, physiography, hydrology, soil types, and vegetation. These four regions Till Plains, Drift Plains/Unglaciated, Interlobate, and Fluvial are used in the Great and Little Miami River Basins study to assess the influence of natural features of the environmental setting on surface- and ground-water quality.

Indiana, Ohio↗
USGS2001

Occurrence of selected radionuclides in ground water used for drinking water in the United States: A reconnaissance survey, 1998

The U.S. Geological Survey, in collaboration with the U.S. Environmental Protection Agency, the American Water Works Association, and the American Water Works Service Company, completed a targeted national reconnaissance survey of selected radionuclides in public ground-water supplies. Radionuclides analyzed included radium-224 (Ra-224), radium-226 (Ra-226), radium-228 (Ra-228), polonium-210 (Po-210) and lead-210 (Pb-210).This U.S. Geological Survey reconnaissance survey focused intentionally on areas with known or suspected elevated concentrations of radium in ground water to determine if Ra-224 was also present in the areas where other isotopes of radium had previously been detected and to determine the co-occurrence characteristics of the three radium isotopes (Ra-224, Ra-226, and Ra-228) in those areas. Ninety-nine raw-water samples (before water treatment) were collected once over a 6-month period in 1998 and 1999 from wells (94 of which are used for public drinking water) in 27 States and 8 physiographic provinces. Twenty-one of the 99 samples exceeded the current U.S. Environmental Protection Agency drinking-water maximum contaminant level of 5 picocuries per liter (pCi/L) for combined radium (Ra-226 + Ra-228). Concentrations of Ra-224 were reported to exceed 1 pCi/L in 30 percent of the samples collected, with a maximum concentration of 73.6 pCi/L measured in water from a nontransient, noncommunity, public-supply well in Maryland. Radium-224 concentrations generally were higher than those of the other isotopes of radium. About 5 percent of the samples contained concentrations of Ra-224 greater than 10 pCi/L, whereas only 2 percent exceeded 10 pCi/L for either Ra-226 or Ra-228. Concentrations of Ra-226 greater than 1 pCi/L were reported in 33 percent of the samples, with a maximum concentration of 16.9 pCi/L measured in water from a public-supply well in Iowa. Concentrations of Ra-228 greater than 1 pCi/L were reported in 22 samples, with a maximum concentration of 72.3 pCi/L measured in water from a non-transient, noncommunity, public-supply well in Maryland.Radium-224, which is a decay product of Ra-228 in the Th-232 decay series, was significantly correlated with Ra-228 (Spearman?s rank correlation coefficient ?r? equals 0.82) and to a lesser degree with Ra-226 (r equals 0.69), which is an isotope in the U-238 decay series. The rank correlation coefficient between Ra-226 and Ra-228 was 0.63. The high correlation between Ra-224 and Ra-228 concentrations and the corresponding isotopic ratios of the two (about 1:1 in 90 percent of the samples) indicates that the two radionuclides occur in approximately equal concentrations in most ground water sampled. Thus, Ra-228 can be considered as a reasonable proxy indicator for the occurrence of Ra-224 in ground water.The maximum concentration of Po-210 was 4.85 pCi/L and exceeded 1 pCi/L in only two samples. The maximum concentration of Pb-210 was 4.14 pCi/L, and about 10 percent of the samples exceeded 1 pCi/L. Areas with known, or suspected, elevated concentrations of polonium and lead were not targeted in this survey.Three major implications are drawn for future radionuclide monitoring on the basis of this information: (1) grossalpha particle analyses of ground water should be done within about 48-72 hours after collection to determine the presence of the short-lived, alpha-particle emitting isotopes, such as Ra-224, which was detected in elevated concentrations in many of the samples collected for this survey; (2) the isotope ratios of Ra-224 to Ra-228 in ground water are variable on a national scale, but the two radioisotopes generally occur in ratios near 1:1, therefore, the more commonly measured Ra-228 can be used as an indicator of Ra-224 occurrence for some general purposes other than compliance; and (3) the isotopic ratios of Ra-226 to Ra-228 were less than 3:2 in many samples. These ratios corroborate results of previous studies that have shown the presence of Ra-228.

Water-Resources Investigations Report↗
USGS2001

Documentation and verification of VST2D; a model for simulating transient, Variably Saturated, coupled water-heat-solute Transport in heterogeneous, anisotropic 2-Dimensional, ground-water systems with variable fluid density

This report describes a model for simulating transient, Variably Saturated, coupled water-heatsolute Transport in heterogeneous, anisotropic, 2-Dimensional, ground-water systems with variable fluid density (VST2D). VST2D was developed to help understand the effects of natural and anthropogenic factors on quantity and quality of variably saturated ground-water systems. The model solves simultaneously for one or more dependent variables (pressure, temperature, and concentration) at nodes in a horizontal or vertical mesh using a quasi-linearized general minimum residual method. This approach enhances computational speed beyond the speed of a sequential approach. Heterogeneous and anisotropic conditions are implemented locally using individual element property descriptions. This implementation allows local principal directions to differ among elements and from the global solution domain coordinates. Boundary conditions can include time-varying pressure head (or moisture content), heat, and/or concentration; fluxes distributed along domain boundaries and/or at internal node points; and/or convective moisture, heat, and solute fluxes along the domain boundaries; and/or unit hydraulic gradient along domain boundaries. Other model features include temperature and concentration dependent density (liquid and vapor) and viscosity, sorption and/or decay of a solute, and capability to determine moisture content beyond residual to zero. These features are described in the documentation together with development of the governing equations, application of the finite-element formulation (using the Galerkin approach), solution procedure, mass and energy balance considerations, input requirements, and output options. The VST2D model was verified, and results included solutions for problems of water transport under isohaline and isothermal conditions, heat transport under isobaric and isohaline conditions, solute transport under isobaric and isothermal conditions, and coupled water-heat-solute transport. The first three problems considered in model verification were compared to either analytical or numerical solutions, whereas the coupled problem was compared to measured laboratory results for which no known analytic solutions or numerical models are available. The test results indicate the model is accurate and applicable for a wide range of conditions, including when water (liquid and vapor), heat (sensible and latent), and solute are coupled in ground-water systems. The cumulative residual errors for the coupled problem tested was less than 10–8 cubic centimeter per cubic centimeter, 10-5 moles per kilogram, and 102 calories per cubic meter for liquid water content, solute concentration and heat content, respectively. This model should be useful to hydrologists, engineers, and researchers interested in studying coupled processes associated with variably saturated transport in ground-water systems.

Water-Resources Investigations Report↗
USGS1994

User's guide to revised method-of-characteristics solute-transport model (MOC--version 31)

The U.S. Geological Survey computer model to simulate two-dimensional solute transport and dispersion in ground water (Konikow and Bredehoeft, 1978; Goode and Konikow, 1989) has been modified to improve management of input and output data and to provide progressive run-time information. All opening and closing of files are now done automatically by the program. Names of input data files are entered either interactively or using a batch-mode script file. Names of output files, created automatically by the program, are based on the name of the input file. In the interactive mode, messages are written to the screen during execution to allow the user to monitor the status and progress of the simulation and to anticipate total running time. Information reported and updated during a simulation include the current pumping period and time step, number of particle moves, and percentage completion of the current time step. The batch mode enables a user to run a series of simulations consecutively, without additional control. A report of the model's activity in the batch mode is written to a separate output file, allowing later review. The user has several options for creating separate output files for different types of data. The formats are compatible with many commercially available applications, which facilitates graphical postprocessing of model results. Geohydrology and Evaluation of Stream-Aquifer Relations in the Apalachicola-Chattahoochee-Flint River Basin, Southeastern Alabama, Northwestern Florida, and Southwestern Georgia By Lynn J. Torak, Gary S. Davis, George A. Strain, and Jennifer G. Herndon Abstract The lower Apalachieola-Chattahoochec-Flint River Basin is underlain by Coastal Plain sediments of pre-Cretaceous to Quaternary age consisting of alternating units of sand, clay, sandstone, dolomite, and limestone that gradually thicken and dip gently to the southeast. The stream-aquifer system consism of carbonate (limestone and dolomite) and elastic sediments, which define the Upper Floridan aquifer and Intermediate system, in hydraulic connection with the principal rivers of the basin and other surface-water features, natural and man made. Separate digital models of the Upper Flori-dan aquifer and Intermediate system were constructed by using the U.S. Geological Survey's MODular Finite-Element model of two dimensional ground-water flow, based on concep- tualizations of the stream-aquifer system, and calibrated to drought conditions of October 1986. Sensitivity analyses performed on the models indicated that aquifer hydraulic conductivity, lateral and vertical boundary flows, and pumpage have a strong influence on groundwater levels. Simulated pumpage increases in the Upper Floridan aquifer, primarily in the Dougherty Plain physiographic district of Georgia,. caused significant reductions in aquifer discharge to streams that eventually flow to Lake Seminole and the Apalachicola River and Bay. Simulated pumpage increases greater than 3 times the October 1986 rates caused drying ofsome stream reaches and parts of the Upper Floridan aquifer in Georgia. Water budgets prepared from simulation results indicate that ground- water discharge to streams and recharge by horizontal and vertical flow are the principal mechanisms for moving water through the flow system. The potential for changes in ground-water quality is high in areas where chemical constituents can be mobilized by these mechanisms. Less than 2 percent of ground-water discharge to streams comes from the Intermediate system; thus, it plays a minor role in the hydrodynamics of the stream- aquifer system.

Water-Resources Investigations Report↗
USGS1987

Cenozoic stratigraphy and geologic history of the Tucson Basin, Pima County, Arizona

This report was prepared as part of a geohydrologic study of the Tucson basin conducted by the U.S. Geological Survey in cooperation with the city of Tucson. Geologic data from more than 500 water supply and test wells were analyzed to define characteristics of the basin sediments that may affect the potential for land subsidence induced by groundwater withdrawal. The Tucson basin is a structural depression within the Basin and Range physiographic province. The basin is 1,000 sq mi in units area and trends north to northwest. Three Cenozoic stratigraphic unit--the Pantano Formation of Oligocene age, the Tinaja beds (informal usage) of Miocene and Pliocene age, and the Fort Lowell Formation of Pleistocene age--fill the basin. The Tinaja beds include lower, middle, and upper unconformable units. A thin veneer of stream alluvium of late Quaternary age overlies the Fort Lowell Formation. The Pantano Formation and the lower Tinaja beds accumulated during a time of widespread continental sedimentation, volcanism, plutonism, uplift, and complex faulting and tilting of rock units that began during the Oligocene and continued until the middle Miocene. Overlying sediments of the middle and upper Tinaja beds were deposited in response to two subsequent episodes of post-12-million-year block faulting, the latter of which was accompanied by renewed uplift. The Fort Lowell Formation accumulated during the Quaternary development of modern through-flowing the maturation of the drainage. The composite Cenozoic stratigraphic section of the Tucson basin is at least 20,000 ft thick. The steeply tilted to flat-lying section is composed of indurated to unconsolidated clastic sediments, evaporites, and volcanic rocks that are lithologically and structurally complex. The lithology and structures of the section was greatly affected by the uplift and exhumation of adjacent metamorphic core-complex rocks. Similar Cenozoic geologic relations have been identified in other parts of southern Arizona. (Author 's abstract)

Water-Resources Investigations Report↗
USGS1995

Ground-water levels and directions of flow in Geauga County, Ohio, September 1994, and changes in ground-water levels, 1986-94

This report presents the results of a study by the U.S. Geological Survey, in cooperation with the Geauga County Planning Commission and Board of County Commissioners, to determine directions of ground-water flow and to assess differences from 1986 to 1994 in groundwater levels in the glacial deposits and Pottsville Formation, Cuyahoga Group, and the Berea Sandstone. Water levels were measured in 219 wells in Geauga County, Ohio, in September 1994. Water levels measured in January and February 1986 in 88 of the 219 wells were used for comparison. Water-level maps constructed from measurements made in September 1994 show that ground-water levels in the Pottsville Formation and the glacial deposits generally correspond to the land-surface configuration and that ground water flows from the uplands to adjacent streams and buried valleys. Ground-water flow in the Cuyahoga Group is generally downward from the Pottsville Formation to the Berea Sandstone. Directions of ground-water flow in the Berea Sandstone are toward outcrop areas at the north and east edges of Geauga County and toward subcrops beneath buried glacial valley deposits in Chardon, Chester, Munson, and Russell Townships and along the west edge of the county. A comparison of water level measurements in 1986 and 1994 indicates that water levels declined in 70 percent of the measured wells and increased in 30 percent. The change in water levels from 1986 to 1994 ranged from an increase of 13.58 feet to a decrease of 29.25 feet. Thirty percent of all water-level changes were less than 1 foot in magnitude. In nearly 80 percent of the wells, water-level changes were within the range of plus or minus 5 feet. Among the wells for which two or more historical measurements were available, the 1994 water levels in 54 percent were outside the range of water-levels observed in previous studies (only 24 percent were greater than 1 foot outside of the previously-observed range). Water-level declines of greater than 10 feet were primarily in the Cuyahoga Group and Berea Sandstone. Some factors considered in the analysis of the differences in water levels in 1986 and 1994 were changes in water use, population, and the amount of available recharge. Water level differences could not be correlated to population changes between the 1980 and 1990 censuses. A decrease in the available recharge from 1986 to 1994 may be part of the cause for the decrease in water levels observed in two-thirds of the wells in and adjacent to Geauga County. Effects of withdrawal rates due to population increase on water levels, if present, are overshadowed by the effects of annual variations in precipitation.

Ohio↗
USGS1998

Hydrogeology and simulation of ground-water flow in the Paluxy aquifer in the vicinity of Landfills 1 and 3, U.S. Air Force Plant 4, Fort Worth, Texas

Ground-water contamination of the surficial terrace alluvial aquifer has occurred at U.S. Air Force Plant 4, a government-owned, contractor-operated facility, northwest of Fort Worth, Texas. A poorly constructed monitoring well, P–22M, open to the underlying middle zone of the Paluxy aquifer was installed at landfill 3, October 1987, allowing leakage of contaminated ground water to reach the Paluxy aquifer. This well was plugged and abandoned in November 1995. Additionally, volatile organic compounds have been detected in fractures in the Goodland-Walnut confining unit, the hydrogeologic unit separating the terrace alluvial aquifer from the underlying Paluxy aquifer, beneath the western part of landfill 1. Volatile organic compounds in concentrations near the analytical detection limit were detected in the upper Paluxy prior to the drilling of well P–22M. The ground-water-flow simulation model described in this report was developed to examine the best logistically feasible location to install recovery wells to capture the low concentration (less than 100 micrograms per liter) trichloroethylene plume beneath landfills 1 and 3 (west Paluxy plume). Once the recovery wells were installed (1996), the simulation model was recalibrated with new data. This report documents the capture area of the installed recovery wells. Four geologic units are pertinent to this site-specific model. From oldest to youngest, these are the Glen Rose Formation, Paluxy Formation, Walnut Formation, and Goodland Limestone. The Glen Rose Formation is relatively impermeable in the study area and forms the confining unit underlying the Paluxy Formation. The Paluxy Formation forms the Paluxy aquifer, which is a public drinking water supply for the City of White Settlement. The Walnut Formation and Goodland Limestone form the Goodland-Walnut confining unit overlying the Paluxy aquifer. Near landfill 3, gamma-ray logs indicate three distinct zones of the Paluxy Formation; upper, middle, and lower. The formation is about 170-feet thick near landfill 3, and each zone is about 57-feet thick. Two steady-state simulations using the computer program MODFLOW were analyzed using the particle-tracking computer program, MODPATH. One simulation is the calibration simulation using Paluxy aquifer water-level data for May 1993. The second simulation includes the installed recovery wells. A variably spaced grid was designed for the model. The smallest grid cells, 25 by 25 feet, are in the vicinity of landfills 1 and 3. The largest cells, 4,864.5 by 1,441.5 feet, are at the northwestern corner of the model grid near the Parker-Tarrant County line. The modeling was accomplished with three layers representing the upper, middle, and lower zones of the Paluxy aquifer. Particles, which represent contaminant molecules moving in solution with the ground water, were tracked from well P–22M and an area below landfill 1, at the top of the upper zone of the Paluxy aquifer, for 9 years (forward tracking). The forward tracking estimates where contaminants might move by advection from 1987 to 1996. Analysis of backward tracking from the new recovery wells indicates that the simulated contributing area to the recovery wells intercepts the contaminant plume, minimizing off-site migration of the west Paluxy plume. To determine the effectiveness of the recovery wells, monitoring wells southeast of Building 14 have been installed (1996–97) for sampling.

Texas↗
USGS2000

Biodegradation of chlorinated ethenes at a karst site in middle Tennessee

This report presents results of field and laboratory investigations examining the biodegradation of chlorinated ethenes in a karst aquifer contaminated with trichloroethylene (TCE). The study site, located in Middle Tennessee, was selected because of the presence of TCE degradation byproducts in the karst aquifer and available site hydrologic and chlorinated-ethene information. Additional chemical, biological, and hydrologic data were gathered to evaluate whether the occurrence of TCE degradation byproducts in the karst aquifer was the result of biodegradation within the aquifer or simply transport into the aquifer. Geochemical analysis established that sulfate-reducing conditions, essential for reductive dechlorination of chlorinated solvents, existed in parts of the contaminated karst aquifer. Other areas of the aquifer fluctuated between anaerobic and aerobic conditions and contained compounds associated with cometabolism, such as ethane, methane, ammonia, and dissolved oxygen. A large, diverse bacteria population inhabits the contaminated aquifer. Bacteria known to biodegrade TCE and other chlorinated solvents, such as sulfate-reducers, methanotrophs, and ammonia-oxidizers, were identified from karst-aquifer water using the RNA-hybridization technique. Results from microcosms using raw karst-aquifer water found that aerobic cometabolism and anaerobic reductive-dechlorination degradation processes were possible when appropriate conditions were established in the microcosms. These chemical and biological results provide circumstantial evidence that several biodegradation processes are active in the aquifer. Additional site hydrologic information was developed to determine if appropriate conditions persist long enough in the karst aquifer for these biodegradation processes to be significant. Continuous monitoring devices placed in four wells during the spring of 1998 indicated that pH, specific conductance, dissolved oxygen, and oxidation-reduction potentials changed very little in areas isolated from active ground-water flow paths. These stable areas in the karst aquifer had geochemical conditions and bacteria conducive to reductive dechlorination of chlorinated ethenes. Other areas of the karst aquifer were associated with active ground-water flow paths and fluctuated between anaerobic and aerobic conditions in response to rain events. Associated with this dynamic environment were bacteria and geochemical conditions conducive to cometabolism. In summary, multiple lines of evidence developed from chemical, biological, and hydrologic data demonstrate that a variety of biodegradation processes are active in this karst aquifer.

Tennessee↗