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At least 1,657 records · Page 92Linked to original sources
USGS2000

The effects of calcium magnesium acetate (CMA) deicing material on the water quality of Bear Creek, Clackamas County, Oregon, 1999

This report presents the results of a study by the U.S. Geological Survey, done in cooperation with the Oregon Department of Transportation (ODOT), to evaluate the effects of the highway deicing material, calcium magnesium acetate (CMA), on the water quality of Bear Creek, in the Cascade Range of Oregon. ODOT began using CMA (an alternative deicer that has fewer adverse environmental effects than road salt) in the mid-1990s and began this study with the USGS to ensure that there were no unexpected effects on the water quality of Bear Creek. Streamflow, precipitation, dissolved oxygen, pH, specific conductance, and water temperature were measured continuously through the 1998?99 winter. There was no measurable effect of the application of CMA to Highway 26 on the biochemical oxygen demand (BOD), calcium concentration, or magnesium concentration of Bear Creek and its tributaries. BOD was small in all of the water samples, some of which were collected before CMA application, and some of which were collected after application. Five-day BOD values ranged from 0.1 milligrams per liter to 1.5 milligrams per liter, and 20-day BOD values ranged from 0.2 milligrams per liter to 2.0 milligrams per liter. Dissolved copper concentrations in a small tributary ditch on the north side of Highway 26 exceeded the U.S. Environmental Protection Agency aquatic life criteria on three occasions. These exceedances were probably not caused by the application of CMA because (1) one of the samples was a background sample (no recent CMA application), and (2) dissolved copper was not detected in Bear Creek water samples to which CMA was added during laboratory experiments.

Oregon↗
USGS2000

Two months of flooding in eastern North Carolina, September-October 1999: Hydrologic, water-quality, and geologic effects of hurricanes Dennis, Floyd, and Irene

The combined effects of Hurricanes Dennis, Floyd, and Irene in September and October 1999 resulted in 2 months of flooding throughout most of eastern North Carolina. Hurricane Dennis battered the Outer Banks for almost a week in early September, resulting in severe shore- line erosion in some locations near Buxton and Rodanthe. Upon making landfall less than 2 weeks before Hurricane Floyd, Hurricane Dennis delivered 4 to 8 inches of rain to much of the Tar and Neuse River Basins, breaking a drought and saturating soils. Hurricane Floyd will likely be the second or third most costly hurricane to strike the United States in the 20th century, resulting in more fatalities than any hurricane to strike the United States since 1972. Rainfall amounts recorded during Hurricane Floyd (September 14-17, 1999) and accumulated during the months of September and October were unprecedented for many parts of eastern North Carolina during more than 80 years of precipitation records. Most recording stations in eastern North Carolina received at least half the average annual rainfall during the 2 months. Flooding was at record levels, and 500-year or greater floods occurred in all of the State's river basins east of Raleigh. More than half of the average annual nitrogen and phosphorus loads were transported in the Neuse and Tar Rivers by floodwaters during the 1-month period between mid-September and mid-October. Shoreline erosion from the passage of Hurricane Floyd was particularly severe along Oak and Topsail Islands; the effects of Hurricane Floyd on shoreline erosion and dune retreat were greater than the effects of Hurricane Bonnie in 1998. Fortunately, Hurricane Irene in mid-October did not make landfall in North Carolina, but rainfall from the storm did help ensure that several rivers in eastern North Carolina remained above flood stage for almost 2 months.

North Carolina↗
USGS2000

Application of nonlinear least-squares regression to ground-water flow modeling, west-central Florida

A nonlinear least-squares regression technique for estimation of ground-water flow model parameters was applied to an existing model of the regional aquifer system underlying west-central Florida. The regression technique minimizes the differences between measured and simulated water levels. Regression statistics, including parameter sensitivities and correlations, were calculated for reported parameter values in the existing model. Optimal parameter values for selected hydrologic variables of interest are estimated by nonlinear regression. Optimal estimates of parameter values are about 140 times greater than and about 0.01 times less than reported values. Independently estimating all parameters by nonlinear regression was impossible, given the existing zonation structure and number of observations, because of parameter insensitivity and correlation. Although the model yields parameter values similar to those estimated by other methods and reproduces the measured water levels reasonably accurately, a simpler parameter structure should be considered. Some possible ways of improving model calibration are to: (1) modify the defined parameter-zonation structure by omitting and/or combining parameters to be estimated; (2) carefully eliminate observation data based on evidence that they are likely to be biased; (3) collect additional water-level data; (4) assign values to insensitive parameters, and (5) estimate the most sensitive parameters first, then, using the optimized values for these parameters, estimate the entire data set.

Water-Resources Investigations Report↗
USGS2000

Characterization and simulation of ground-water flow in the Kansas River Valley at Fort Riley, Kansas, 1990-98

Hydrologic data and a ground-water flow model were used to characterize ground-water flow in the Kansas River alluvial aquifer at Fort Riley in northeast Kansas. The ground-water flow model was developed as a tool to project ground-water flow and potential contaminant-transport paths in the alluvial aquifer on the basis of past hydrologic conditions. The model also was used to estimate historical and hypothetical ground-water flow paths with respect to a private- and several public-supply wells. The ground-water flow model area extends from the Smoky Hill and Republican Rivers downstream to about 2.5 miles downstream from the city of Ogden. The Kansas River Valley has low relief and, except for the area within the Fort Riley Military Reservation, is used primarily for crop production. Sedimentary deposits in the Kansas River Valley, formed after the ancestral Kansas River eroded into bedrock, primarily are alluvial sediment deposited by the river during Quaternary time. The alluvial sediment consists of as much as about 75 feet of poorly sorted, coarse-to-fine sand, silt, and clay, 55 feet of which can be saturated with ground water. The alluvial aquifer is unconfined and is bounded on the sides and bottom by Permian-age shale and limestone bedrock. Hydrologic data indicate that ground water in the Kansas River Valley generally flows in a downstream direction, but flow direction can be quite variable near the Kansas River due to changes in river stage. Ground-water-level changes caused by infiltration of precipitation are difficult to detect because they are masked by larger changes caused by fluctuation in Kansas River stage. Ratios of strontium isotopes Sr87 and Sr86 in water collected from wells in the Camp Funston Area indicate that the ground water along the northern valley wall originates, in part, from upland areas north of the river valley. Water from Threemile Creek, which flows out of the uplands north of the river valley, had Sr87:Sr86 ratios similar to those in ground water from wells in the northern Camp Funston Area. In addition, comparison of observed water levels from wells CF90-06, CF97-101, and CF97-401 in the Camp Funston Area and ground-water levels simulated for these wells using floodwave-response analysis indicates that ground-water inflow from bedrock is a hydraulic stress that, in addition to the changing stage in the Kansas River, acts on the aquifer. This hydraulic stress seems to be located near the northern valley wall because the effect of this stress is greater for well CF97-101, which is the well closest to the valley wall. Ground-water flow was simulated using a modular, three-dimensional, finite-difference ground-water flow model (MODFLOW). Particle tracking, used to visualize ground-water flow paths in the alluvial aquifer, was accomplished using MODPATH. Forward-in-time particle tracking indicated that, in general, particles released near the Kansas River followed much more variable paths than particles released near the valley wall. Although particle tracking does not simulate solute transport, this increased path variability indicates that, near the river, ground-water contaminants could follow many possible paths towards the river, whereas more distant from the river, ground-water contaminants likely would follow a narrower corridor. Particle tracks in the Camp Funston Area indicate that, for the 1990-98 simulation period, contaminants from the ground-water study sites in the Camp Funston Area would be unlikely to move into the vicinity of Ogden's supply wells. Backward-in-time particle tracking indicated that the flow-path and recharge areas for model cells corresponding to Ogden's supply wells lie near the northern valley wall and extend into the northern Camp Funston Area. The flow-path and recharge areas for model cells corresponding to Morris County Rural Water District wells lie within Clarks Creek Valley and probably extend outside the model area. Three hypothetical simulations, i

Water-Resources Investigations Report↗
USGS2000

Analysis of water-quality trends at two discharge stations — One within Big Cypress National Preserve and one near Biscayne Bay — Southern Florida, 1966-94

An analysis of water-quality trends was made at two U.S. Geological Survey daily discharge stations in southern Florida. The ESTREND computer program was the principal tool used for the determination of water-quality trends at the Miami Canal station west of Biscayne Bay in Miami and the Tamiami Canal station along U.S. Highway 41 in the Big Cypress National Preserve in Collier County. Variability in water quality caused by both seasonality and streamflow was compensated for by applying the nonparametric Seasonal Kendall trend test to unadjusted concentrations or flow-adjusted concentrations (residuals) determined from linear regression analysis. Concentrations of selected major inorganic constituents and physical characteristics; pH and dissolved oxygen; suspended sediment; nitrogen, phosphorus, and carbon species; trace metals; and bacteriological and biological characteristics were determined at the Miami and Tamiami Canal stations. Median and maximum concentrations of selected constituents were compared to the Florida Class III freshwater standards for recreation, propagation, and maintenance of a healthy, well-balanced population of fish and wildlife. The median concentrations of the water-quality constituents and characteristics generally were higher at the Miami Canal station than at the Tamiami Canal station. The maximum value for specific conductance at the Miami Canal station exceeded the State standard. The median and maximum concentrations for ammonia at the Miami and Tamiami Canal stations exceeded the State standard, whereas median dissolved-oxygen concentrations at both stations were below the State standard. Trend results were indicative of either improvement or deterioration in water quality with time. Improvement in water quality at the Miami Canal station was reflected by downward trends in suspended sediment (1987-94), turbidity, (1970-78), total ammonia (1971-94), total phosphorus (1987-94), barium (1978-94), iron (1969-94), and fecal coliform (1976-94). Deterioration in water quality at the same station was indicated by upward trends in specific conductance (1966-94), dissolved solids (1966-94, 1976-94, and 1987-94), chloride (1966-94), potassium (1966-94), magnesium (1966-94), sodium (1966-94), sulfate (1966-94), silica (1966-94), suspended sediment (1974-94), total organic carbon (1970-81), and fecal streptococcus (1987-94). The downward trend in pH (1966-94) was indicative of deterioration in water quality at the Miami Canal station. Improvement in water quality at the Tamiami Canal station was reflected by downward trends in fluoride (1967-93), total ammonia (1970-92), total nitrite plus nitrate (1975-85), and barium (1978-93). Deterioration in water quality at the same station was statistically significant by upward trends in specific conductance (1967-93), dissolved solids (1967-93), chloride (1967-93), sodium (1967-93), potassium (1967-93), magnesium (1967-93), strontium (1967-93), and suspended sediment (1976-93). The downward trend in dissolved oxygen (1970-93) was indicative of deterioration in water quality.

Florida↗
USGS2000

Sensitivity of ground water to contamination in Lawrence County, South Dakota

Ground-water supplies in Lawrence County, South Dakota, can be contaminated by agricultural, urban, suburban, commercial, and industrial land uses. To address this issue, the U.S. Geological Survey in cooperation with Lawrence County and the City of Spearfish mapped the sensitivity of ground water to contamination in Lawrence County. Sensitivity of ground water to contamination was determined by delineating hydrogeologic settings with common hydrogeologic characteristics as described in the DRASTIC method, developed by the U.S. Environmental Protection Agency and the National Water Well Association. Within the framework of 11 hydrogeologic settings, sensitivity to contamination was ranked for six intrinsic hydrogeologic characteristics: (1) aquifer media, (2) unsaturated media (3) hydraulic conductivity, (4) recharge rate, (5) depth to water, and (6) land-surface slope. The rating conventions of DRASTIC were modified to provide a relative ranking of hydrogeologic characteristics without assignment of a combined numerical score. Soil characteristics were not included as a map layer because detailed digital data were not available; however, the general distribution of two soil characteristics were shown. A total of 956 polygons were delineated and assigned a sensitivity-unit code that represented unique groups of sensitivity rank for the six intrinsic hydrogeologic characteristics. The polygons were created by overlaying and intersecting maps that describe the geology, precipitation, land-surface elevation, and depth to water using a geographic information system. Thirty drainage areas upstream from potential streamflow-loss zones were delineated to describe an additional mechanism of transport of potential contamination. The sensitivity of ground water to contamination was presented on a 1:100,000-scale map with code and label explanations. Limitations of the sensitivity map are described to facilitate appropriate use of the map as a screening tool to compare sensitivity to contamination.

Water-Resources Investigations Report↗
USGS2000

Quality-assurance design applied to an assessment of agricultural pesticides in ground water from carbonate bedrock aquifers in the Great Valley of eastern Pennsylvania

Assessments to determine whether agricultural pesticides are present in ground water are performed by the Commonwealth of Pennsylvania under the aquifer monitoring provisions of the State Pesticides and Ground Water Strategy. Pennsylvania's Department of Agriculture conducts the monitoring and collects samples; the Department of Environmental Protection (PaDEP) Laboratory analyzes the samples to measure pesticide concentration. To evaluate the quality of the measurements of pesticide concentration for a groundwater assessment, a quality-assurance design was developed and applied to a selected assessment area in Pennsylvania. This report describes the quality-assurance design, describes how and where the design was applied, describes procedures used to collect and analyze samples and to evaluate the results, and summarizes the quality assurance results along with the assessment results. The design was applied in an agricultural area of the Delaware River Basin in Berks, Lebanon, Lehigh, and Northampton Counties to evaluate the bias and variability in laboratory results for pesticides. The design—with random spatial and temporal components—included four data-quality objectives for bias and variability. The spatial design was primary and represented an area comprising 30 sampling cells. A quality-assurance sampling frequency of 20 percent of cells was selected to ensure a sample number of five or more for analysis. Quality-control samples included blanks, spikes, and replicates of laboratory water and spikes, replicates, and 2-lab splits of groundwater. Two analytical laboratories, the PaDEP Laboratory and a U.S. Geological Survey Laboratory, were part of the design. Bias and variability were evaluated by use of data collected from October 1997 through January 1998 for alachlor, atrazine, cyanazine, metolachlor, simazine, pendimethalin, metribuzin, and chlorpyrifos. Results of analyses of field blanks indicate that collection, processing, transport, and laboratory analysis procedures did not contaminate the samples; there were no false-positive results. Pesticides were detected in water when pesticides were spiked into (added to) samples. There were no false negatives for the eight pesticides in all spiked samples. Negative bias was characteristic of analytical results for the eight pesticides, and bias was generally in excess of 10 percent from the ‘true’ or expected concentration (34 of 39 analyses, or 87 percent of the ground-water results) for pesticide concentrations ranging from 0.31 to 0.51 mg/L (micrograms per liter). The magnitude of the negative bias for the eight pesticides, with the exception of cyanazine, would result in reported concentrations commonly 75-80 percent of the expected concentration in the water sample. The bias for cyanazine was negative and within 10 percent of the expected concentration. A comparison of spiked pesticide-concentration recoveries in laboratory water and ground water indicated no effect of the ground-water matrix, and matrix interference was not a source of the negative bias. Results for the laboratory-water spikes submitted in triplicate showed large variability for recoveries of atrazine, cyanazine, and pendimethalin. The relative standard deviation (RSD) was used as a measure of method variability over the course of the study for laboratory waters at a concentration of 0.4 mg/L. An RSD of about 11 percent (or about ?0.05 mg/L)characterizes the method results for alachlor, chlorpyrifos, metolachlor, metribuzin, and simazine. Atrazine and pendimethalin have RSD values of about 17 and 23 percent, respectively. Cyanazine showed the largest RSD at nearly 51 percent. The pesticides with low variability in laboratory-water spikes also had low variability in ground water. The assessment results showed that atrazinewas the most commonly detected pesticide in ground water in the assessment area. Atrazine was detected in water from 22 of the 28 wells sampled, and recovery results for atrazine were some of the worst (largest negative bias). Concentrations of the eight pesticides in ground water from wells were generally less than 0.3 µg/L. Only six individual measurements of the concentrations in water from six of the wells were at or above 0.3 µg/L, five for atrazine and one for metolachlor. There were eight additional detections of metolachlor and simazine at concentrations less than 0.1 µg/L. No well water contained more than one pesticide at concentra-tions at or above 0.3 µg/L. Evidence exists, how-ever, for a pattern of co-occurrence of metolachlor and simazine at low concentrations with higher concentrations of atrazine. Large variability in replicate samples and negative bias for pesticide recovery from spiked samples indicate the need to use data for pesticide recovery in the interpretation of measured pesti-cide concentrations in ground water. Data from samples spiked with known amounts of pesticides were a critical component of a quality-assurance design for the monitoring component of the Pesti-cides and Ground Water Strategy. Trigger concentrations, the concentrations that require action under the Pesticides and Ground Water Strategy, should be considered maximums for action. This consideration is needed because of the magnitude of negative bias.

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↗
USGS2000

Ground-water quality in alluvial aquifers in the eastern Iowa basins, Iowa and Minnesota

The quality of shallow alluvial ground water that is used for domestic supplies in the Wapsipinicon, Cedar, Iowa, and Skunk River Basins (Eastern Iowa Basins) is described. Water samples from 32 domestic-supply wells were collected from June through July 1998. This study of ground-water quality in alluvial aquifers in the Eastern Iowa Basins is part of the U.S. Geological Survey's National Water-Quality Assessment Program. Calcium and bicarbonate were the dominant ions in solution, likely derived from the dissolution of carbonate minerals in the alluvial aquifer material. Concentrations of iron exceeded the U.S. Environmental Protection Agency Secondary Maximum Contaminant Level (300 micrograms per liter) for drinking water in 53 percent of the samples, and 50 percent of the samples exceeded the Secondary Maximum Contaminant Level for manganese (50 micrograms per liter). pH and alkalinity increased and sulfate concentrations decreased with increasing well depth. Nitrite plus nitrate nitrogen was detected in 53 percent of the samples and exceeded the U.S. Environmental Protection Agency Maximum Contaminant Level of 10 milligrams per liter for drinking water in 13 percent of the samples. Nitrite plus nitrate nitrogen concentrations were negatively correlated with well depth and positively correlated with percentage of oxygen saturation. Ammonia plus organic nitrogen concentrations were positively correlated with well depth, and ratios of nitrite plus nitrate to ammonia were positively correlated with percentage of oxygen saturation. The majority of samples, 72 percent, contained water recharged since the early 1950's. The recharge date of water was earlier in deeper wells. Nitrite plus nitrate and total pesticide concentrations were greater in more recently recharged water. Eight pesticides and eight pesticide metabolites were detected in ground-water samples. Atrazine was the most commonly detected pesticide, and metolachlor ethanesulfonic acid was the most commonly detected metabolite. No pesticide detections exceeded U.S. Environmental Protection Agency drinking-water Maximum Contaminant Levels. The effects of land use on ground-water quality also were examined. There was a positive correlation between percentage of land used for soybean production and concentrations of metolachlor, metolachlor ethanesulfonic acid, and metolachlor oxanilic acid in ground-water samples. Data from this study and from previous studies in the Eastern Iowa Basins were compared statistically by well type (domestic, municipal, and monitoring wells). Well depths were significantly greater in domestic and municipal wells than in monitoring wells. pH, calcium, sulfate, chloride, and atrazine concentrations were significantly higher in municipal-well samples than in domestic-well samples. pH and sulfate concentrations were significantly higher in municipal-well samples than in monitoring-well samples. Ammonia was significantly higher in domestic-well samples than in monitoring-well samples, chloride was significantly higher in monitoring-well samples than in domestic-well samples, and fluoride was significantly higher in domestic-well samples than in municipal-well samples.

Iowa, Minnesota↗
USGS2000

Field tests of polyethylene-membrane diffusion samplers for characterizing volatile organic compounds in stream-bottom sediments, Nyanza Chemical Waste Dump Superfund site, Ashland, Massachusetts

A plume of volatile organic compounds (VOCs) in ground water extends from the Nyanza Chemical Waste Dump Superfund site in Ashland, Massachusetts, northward toward a mill pond on the Sudbury River and eastward toward the Sudbury River and former mill raceway downstream from the mill pond. Polyethylene-membrane water-to-vapor (vapor) and water-to-water (water) diffusion samplers were installed January 1999 in bottom sediments along the Sudbury River and former mill raceway in a pilot study to determine if vapor samplers would be useful in this setting for delineating a plume of contaminants in ground water near the river and raceway, to evaluate equilibration time for vapor-diffusion samplers, and to determine if diffusion samplers might be an alternative to seepage meters (inverted steel drums) and sediment sampling for evaluating concentrations of VOCs in bottom sediments. Of five tested compounds (benzene, trichloroethene, toluene, tetrachloroethene, and chlorobenzene), chlorobenzene and trichloroethene were most frequently detected in vapor from vapor-diffusion samplers. The distribution of VOCs was generally consistent with a previously mapped plume of contaminants in ground water. The field evaluation of equilibration times for vapor-diffusion samplers was inconclusive because of changing hydrologic conditions that may have affected concentrations of VOCs, possible variations in concentrations ofVOCs over short distances, and imprecise sampling and analytical methods. The limited data, however, indicated that equilibration may require 3 weeks or more in some settings. VOCs detected in samples from water-diffusion samplers and their concentrations were comparable to results from seepage meters, and VOCs detected in vapor-diffusion samplers correlated with VOCs detected in water-diffusion samplers. These results indicate that either vapor-or water-diffusion samplers would serve as an economical alternative to seepage meters for sampling of VOCs in pore water from stream-bottom sediments. Results from diffusion samplers correlated poorly with results from sediment samples, partly because of high quantitation limits for chemical analyses of sediments. In general, results from the diffusion samplers better represented the distribution of VOCs than the results from the sediment samples. This pilot study indicates that diffusion samplers are an economical means of identifying 'hotspots' for contaminants in bottom sediments and can provide insights on transport pathways for contaminants near surface-water bodies. After establishing equilibration times for a particular site, diffusion samplers also may be useful for studying variations in concentrations of VOCs over short distances, variations with time and changing hydrologic conditions, and processes such as chemical transformations by biodegradation and exchanges between surface water and ground water in the hyporheic zone.

Water-Resources Investigations Report↗
USGS2000

Effect of Georgetown Lake on the water quality of Clear Creek, Georgetown, Colorado, 1997-98

Georgetown Lake is a recreational reservoir located in the upper Clear Creek Basin, a designated Superfund site because of extensive metal mining in the past. Metals concentrations in Clear Creek increase as the stream receives runoff from mining-affected areas. In 1997, the U.S. Geological Survey, in cooperation with the U.S. Environmental Protection Agency, began a study to determine the effect of the reservoir on the transport of metals in Clear Creek. A bathymetric survey determined the capacity of the reservoir to be about 440 acre-feet of water, which remained constant during the study. Average water residence time in the reservoir is about 1-3 days during high flow. During low flow (10 cubic feet per second), average residence is about 22 days without ice cover and about 15 days with a 3-foot-thick ice cover. Sediment samples collected from the bottom of Georgetown Lake contained substantial concentrations of iron (average 25,500 milligrams per kilogram), aluminum (average 12,300 milligrams per kilogram), zinc (2,830 milligrams per kilogram), lead (618 milligrams per kilogram), manganese (548 milligrams per kilogram), and sulfide minerals (average 602 milligrams per kilogram as S). Sediment also contained abundant sulfate-reducing bacteria, indicating anoxic conditions. Algae and diatoms common to cold-water lakes were identified in sediment samples; one genus of algae is known to adapt to low-light conditions such as exist beneath ice cover. Vertical profiles of temperature, specific conductance, pH, and dissolved-oxygen concentrations were measured in the reservoir on July 28, 1997, when inflow to the reservoir was about 170 cubic feet per second and average residence time of water was about 1.3 days, and on February 13, 1998, when the reservoir was covered with about 3 feet of ice, inflow was about 15 cubic feet per second, and average residence time was about 12 days. The measurements on July 28, 1997, showed that the reservoir water was well mixed, although pH and dissolved-oxygen concentrations were increased by photosynthesis near the bottom of the reservoir. Measurements on February 13, 1998, indicated thermal and chemical stratification with warmer water (about 4 degrees Celsius) beneath colder water and increases in pH and dissolved-oxygen concentrations generally occurring near the top of the warmer layer. Concentrations of dissolved oxygen were saturated to over-saturated throughout the water column on both dates, although the concentrations were greater on February 13, 1998, because of colder temperature and photosynthesis. Median pH was about 0.5 unit higher on February 13, 1998, than on July 28, 1997, largely because the longer residence time on February 13, 1998, allowed greater cumulative effects of photosynthesis. Samples of inflow and outflow water were collected from August 1997 to August 1998. Dissolved cadmium and dissolved lead in inflow and outflow samples exceeded acute and chronic water-quality standards during some of the sampling period, whereas dissolved zinc exceeded both standards in inflow and outflow samples during the entire sampling period. Chromium, nickel, and silver were detected in a few samples at small concentrations. Arsenic, selenium, and thallium were not reported in any water samples. Georgetown Lake removes some metals from inflow water and releases others to outflow water. From August 1997 to August 1998, Georgetown Lake estimated outflow loads were about 21 percent less than the inflow load of cadmium and about 11 percent less than the inflow load of zinc. Estimated inflow loads were about 18 percent less than the outflow load of copper, about 13 percent less than the outflow load of iron, and about 27 percent less than the outflow load of manganese. Inflow and outflow loads of lead were essentially balanced. The outflow load of nitrite plus nitrate was about 14 percent less than the inflow load, probably because of plant uptake.

Colorado↗
USGS2000

Estimating the probability of elevated nitrate (NO2+NO3-N) concentrations in ground water in the Columbia Basin Ground Water Management Area, Washington

Logistic regression was used to relate anthropogenic (man-made) and natural factors to the occurrence of elevated concentrations of nitrite plus nitrate as nitrogen in ground water in the Columbia Basin Ground Water Management Area, eastern Washington. Variables that were analyzed included well depth, depth of well casing, ground-water recharge rates, presence of canals, fertilizer application amounts, soils, surficial geology, and land-use types. The variables that best explain the occurrence of nitrate concentrations above 3 milligrams per liter in wells were the amount of fertilizer applied annually within a 2-kilometer radius of a well and the depth of the well casing; the variables that best explain the occurrence of nitrate above 10 milligrams per liter included the amount of fertilizer applied annually within a 3-kilometer radius of a well, the depth of the well casing, and the mean soil hydrologic group, which is a measure of soil infiltration rate. Based on the relations between these variables and elevated nitrate concentrations, models were developed using logistic regression that predict the probability that ground water will exceed a nitrate concentration of either 3 milligrams per liter or 10 milligrams per liter. Maps were produced that illustrate the predicted probability that ground-water nitrate concentrations will exceed 3 milligrams per liter or 10 milligrams per liter for wells cased to 78 feet below land surface (median casing depth) and the predicted depth to which wells would need to be cased in order to have an 80-percent probability of drawing water with a nitrate concentration below either 3 milligrams per liter or 10 milligrams per liter. Maps showing the predicted probability for the occurrence of elevated nitrate concentrations indicate that the irrigated agricultural regions are most at risk. The predicted depths to which wells need to be cased in order to have an 80-percent chance of obtaining low nitrate ground water exceed 600 feet in the irrigated agricultural regions, whereas wells in dryland agricultural areas generally need a casing in excess of 400 feet. The predicted depth to which wells need to be cased to have at least an 80-percent chance to draw water with a nitrate concentration less than 10 milligrams per liter generally did not exceed 800 feet, with a 200-foot casing depth typical of the majority of the area.

Washington↗
USGS2000

Estimated flow-duration curves for selected ungaged sites in the Cimarron and lower Arkansas River basins in Kansas

Flow-duration curves for 1968-98 were estimated for 16 ungaged sites in the Cimarron and lower Arkansas River Basins in south-central Kansas. The method of estimation used six unique factors of flow duration: (1) mean streamflow and percentage duration of mean streamflow, (2) ratio of 1-percent-duration streamflow to mean streamflow, (3) ratio of 0.1-percent-duration streamflow to 1-percent-duration streamflow, (4) ratio of 50-percent-duration streamflow to mean streamflow, (5) percentage duration of appreciable streamflow (0.10 cubic foot per second), and (6) average slope of the flow-duration curve. These factors were previously developed from a regionalized study of flow-duration curves using streamflow data for 1921-76. The method was tested on a currently measured, continuous-record streamflow-gaging station on the Little Arkansas River at Valley Center, Kansas, and was found to adequately estimate the computed flow-duration curve for the station. The low-flow parts of the estimated flow-duration curves were improved substantially using low- to medium-flow discharge measurements made concurrently with discharge measurements and flow-duration analyses performed at nearby, long-term, continuous-record, streamflow-gaging stations. The estimated flow-duration curves at the ungaged sites can be used for projecting future flow frequencies for assessment of total maximum daily loads (TMDL's) or other water-quality constituents and for water-availability studies.

Kansas↗