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Evaluation of Approaches for Managing Nitrate Loading from On-Site Wastewater Systems near La Pine, Oregon

This report presents the results of a study by the U.S. Geological Survey, done in cooperation with the Oregon Department of Environmental Quality and Deschutes County, to develop a better understanding of the effects of nitrogen from on-site wastewater disposal systems on the quality of ground water near La Pine in southern Deschutes County and northern Klamath County, Oregon. Simulation models were used to test the conceptual understanding of the system and were coupled with optimization methods to develop the Nitrate Loading Management Model, a decision-support tool that can be used to efficiently evaluate alternative approaches for managing nitrate loading from on-site wastewater systems. The conceptual model of the system is based on geologic, hydrologic, and geochemical data collected for this study, as well as previous hydrogeologic and water quality studies and field testing of on-site wastewater systems in the area by other agencies. On-site wastewater systems are the only significant source of anthropogenic nitrogen to shallow ground water in the study area. Between 1960 and 2005 estimated nitrate loading from on-site wastewater systems increased from 3,900 to 91,000 pounds of nitrogen per year. When all remaining lots are developed (in 2019 at current building rates), nitrate loading is projected to reach nearly 150,000 pounds of nitrogen per year. Low recharge rates (2-3 inches per year) and ground-water flow velocities generally have limited the extent of nitrate occurrence to discrete plumes within 20-30 feet of the water table; however, hydraulic-gradient and age data indicate that, given sufficient time and additional loading, nitrate will migrate to depths where many domestic wells currently obtain water. In 2000, nitrate concentrations greater than 4 milligrams nitrogen per liter (mg N/L) were detected in 10 percent of domestic wells sampled by Oregon Department of Environmental Quality. Numerical simulation models were constructed at transect (2.4 square miles) and study-area (247 square miles) scales to test the conceptual model and evaluate processes controlling nitrate concentrations in ground water and potential ground-water discharge of nitrate to streams. Simulation of water-quality conditions for a projected future build-out (base) scenario in which all existing lots are developed using conventional on-site wastewater systems indicates that, at equilibrium, average nitrate concentrations near the water table will exceed 10 mg N/L over areas totaling 9,400 acres. Other scenarios were simulated where future nitrate loading was reduced using advanced treatment on-site systems and a development transfer program. Seven other scenarios were simulated with total nitrate loading reductions ranging from 15 to 94 percent; simulated reductions in the area where average nitrate concentrations near the water table exceed 10 mg N/L range from 22 to 99 percent at equilibrium. Simulations also show that the ground-water system responds slowly to changes in nitrate loading due to low recharge rates and ground-water flow velocity. Consequently, reductions in nitrate loading will not immediately reduce average nitrate concentrations and the average concentration in the aquifer will continue to increase for 25-50 years depending on the level and timing of loading reduction. The capacity of the ground-water system to receive on-site wastewater system effluent, which is related to the density of homes, presence of upgradient residential development, ground-water recharge rate, ground-water flow velocity, and thickness of the oxic part of the aquifer, varies within the study area. Optimization capability was added to the study-area simulation model and the combined simulation-optimization model was used to evaluate alternative approaches to management of nitrate loading from on-site wastewater systems to the shallow alluvial aquifer. The Nitrate Loading Management Model (NLMM) was formulated to find the minimum red

Scientific Investigations Report↗

Evaluation of hydrologic simulation models for fields with subsurface drainage to mitigated wetlands in Barnes, Dickey, and Sargent Counties, North Dakota

Proper identification of wetlands, along with a better understanding of the hydrology of mitigated wetlands, is needed to assist with conservation efforts aimed at maintaining the productivity and ecological function (wetland mitigation) of agricultural lands. The U.S. Geological Survey, in cooperation with the U.S. Department of Agriculture Natural Resources Conservation Service, completed a study to evaluate two models for simulating hydrologic conditions in fields with subsurface drainage to mitigated wetlands at several sites in North Dakota. These two models were evaluated as possible tools for water resource managers to use for designing wetland mitigation projects in the area in the future. The Soil-Plant-Atmosphere-Water (SPAW) model simulates the daily hydrologic water budgets of agricultural landscapes by two linked routines, one for farm fields (field hydrology) and one for impoundments such as wetlands and ponds (pond model). The DRAINMOD model was used in conjunction with the SPAW model because although the SPAW model can be used to simulate the hydrology of small drainage basins containing wetlands, the SPAW model does not contain routines to simulate drainage, either subsurface drainage or surface (drainage ditches), that can directly affect the wetland hydrology. The wetlands in the study areas in this report are all downstream from and adjacent to drained agricultural fields. SPAW and DRAINMOD models were developed and calibrated at three study areas (study areas B, D, and S) to evaluate how the models simulated field-scale hydrologic characteristics and the water balance in wetlands from January 1, 2003, through December 31, 2018. The SPAW model developed for study area B included five modeled fields in the field hydrology portion of SPAW that contributed inflow to one wetland simulated in the pond model portion of SPAW. Simulated wetland water depths were most similar to water depths measured at site BWET1, with an absolute mean error of 0.10 foot and a root mean square error of 0.14 foot. Site BWET2 had slightly larger errors, with an absolute mean error of 0.22 foot and a root mean square error of 0.28 foot. Simulated water depths were similar to the pattern of measured water depths at BWET1 and BWET2 from about mid-April 2018 through about mid-September 2018, but overpredicted water depths in the fall from about mid-September 2018 through about mid-October 2018. The SPAW model developed for study area D included six modeled fields in the field hydrology portion of SPAW that contributed inflow to five wetlands connected in series in the pond model portion of SPAW. Simulated water depths compared relatively well to water depths in the five wetlands, with the absolute mean error ranging from 0.17 foot (DWET1) to 0.39 foot (DWET2), and the root mean square error ranging from 0.28 foot (DWET1) to 0.56 foot (DWET5). The SPAW model developed for study area S included one modeled field in the field hydrology portion of SPAW that contributed inflow to one wetland in the pond model portion of SPAW. Among the SPAW models developed for the three study areas, the model for study area S had the best comparison between simulated and measured water depths, with an absolute mean error of 0.06 foot and a root mean square error of 0.10 foot. DRAINMOD models were developed and calibrated at the three study areas and provided inflow from subsurface drainage discharge to the SPAW models for simulating water levels in wetlands in the study areas. The calibrated DRAINMOD model for study area B showed the variability of hydrologic processes in the modeled field throughout the wide range of hydrologic conditions from January 1, 2003, through December 31, 2018. In general, the discharge through the modeled subsurface drainage system was in the spring and early summer (April through June) most years, with little to no discharge later in the year. Although the subsurface drainage system in study area D was the most complex among the three study areas and was simplified into a uniform system within DRAINMOD, simulated water table depths at study area D correlated better to measured water table depths compared to results from the model applications at the other two study areas. Simulated water table depths had an absolute mean error of 0.30 foot and root mean square error of 0.37 foot at site DGW1 and an absolute mean error of 0.29 foot and a root mean square error of 0.34 foot at site DGW2. Although the subsurface drainage system in study area S was the simplest and the modeled field was the smallest among the three study areas, simulated water table depths at study area S did not correlate as well to measured water table depths compared to results from the model applications at the other two study areas. The SPAW and DRAINMOD model applications at the three study areas in southeast North Dakota adequately simulated the hydrologic processes for fields with subsurface drainage that are connected to adjacent wetlands. However, more measured data would be needed to fully evaluate the models throughout the range of possible climatic conditions.

North Dakota↗

Estimated Loads of Suspended Sediment and Selected Trace Elements Transported through Milltown Reservoir in the Upper Clark Fork Basin, Montana, Water Years 2004-07

The purpose of this report is to present estimated daily and annual loads of suspended sediment and selected trace elements for water years 2004-07 at two sites upstream and one site downstream from Milltown Reservoir. Milltown Reservoir is a National Priorities List Superfund site in the upper Clark Fork basin of western Montana where sediments enriched in trace elements from historical mining and ore processing have been deposited since the construction of Milltown Dam in 1907. The estimated loads were used to quantify annual net gains and losses (mass balance) of suspended sediment and trace elements within Milltown Reservoir before and after June 1, 2006, which was the start of Stage 1 of a permanent drawdown of the reservoir in preparation for removal of Milltown Dam. This study was done in cooperation with the U.S. Environmental Protection Agency. Daily loads of suspended sediment were estimated for water years 2004-07 by using either high-frequency sampling as part of daily sediment monitoring or regression equations relating suspended-sediment discharge to streamflow. Daily loads of unfiltered-recoverable arsenic, cadmium, copper, iron, lead, manganese, and zinc were estimated by using regression equations relating trace-element discharge to suspended-sediment discharge. Regression equations were developed from data for eriodic water-quality samples collected during water years 2004-07. The equations were applied to daily records of either streamflow or suspended-sediment discharge to produce estimated daily loads. Variations in daily suspended-sediment and trace-element loads generally coincided with variations in streamflow. For most of the period before June 1, 2006, differences in daily loads transported to and from Milltown Reservoir were minor or indicated small amounts of deposition; however, losses of suspended sediment and trace elements from the reservoir occurred during temporary drawdowns in July-August 2004 and October-December 2005. After the start of Stage 1 of the permanent drawdown on June 1, 2006, losses of suspended sediment and trace elements from the reservoir persisted for all streamflow conditions during the entire interval of the Stage 1 drawdown (June 1, 2006-September 30, 2007) within the study period. Estimated daily loads of suspended sediment and trace elements were summed for each year to produce estimated annual loads used to determine the annual net gains (deposition) or losses (erosion) of each constituent within Milltown Reservoir during water years 2004-07. During water year 2004, there was an annual net gain of suspended sediment in the reservoir. The annual net gains and losses of trace elements were inconsistent in water year 2004, with gains occurring for arsenic ad iron, but losses occurring for cadmium, copper, lead, manganese, and zinc. In water year 2005, there were annual net gains of suspended sediment and all the trace elements within the reservoir. In water year 2006, there were annual net losses of all constituents from the reservoir, likely as the result of sediment erosion from the reservoir during both a temporary drawdown in October-December 2005 and Stage 1 of the permanent drawdown that continued after June 1, 2006. In water year 2007, when the Stage 1 drawdown was in effect for the entire year, there were large annual net losses of suspended sediment and trace elements from the reservoir. The annual net losses of constituents from Milltown Reservoir in water year 2007 were the largest of any year during the 2004-07 study period. In water year 2007, the annual net loss of suspended sediment from the reservoir was 130,000 tons, which was more than double (about 222 percent) the combined inflow to the reservoir. The largest annual net losses of trace elements in water year 2007, in percent of the combined inflow to the reservoir, occurred for cadmium, copper, lead, and zinc-about 190 percent for cadmium, 170 percent for copper, 150 percent for lead, and 238 p

Scientific Investigations Report↗

Estimated Loads of Suspended Sediment and Selected Trace Elements Transported through the Milltown Reservoir Project Area Before and After the Breaching of Milltown Dam in the Upper Clark Fork Basin, Montana, Water Year 2008

This report presents estimated daily and cumulative loads of suspended sediment and selected trace elements transported during water year 2008 at three streamflow-gaging stations that bracket the Milltown Reservoir project area in the upper Clark Fork basin of western Montana. Milltown Reservoir is a National Priorities List Superfund site where sediments enriched in trace elements from historical mining and ore processing have been deposited since the construction of Milltown Dam in 1907. Milltown Dam was breached on March 28, 2008, as part of Superfund remedial activities to remove the dam and contaminated sediment that had accumulated in Milltown Reservoir. The estimated loads transported through the project area during the periods before and after the breaching of Milltown Dam, and for the entire water year 2008, were used to quantify the net gain or loss (mass balance) of suspended sediment and trace elements within the project area during the transition from a reservoir environment to a free-flowing river. This study was done in cooperation with the U.S. Environmental Protection Agency. Streamflow during water year 2008 compared to long-term streamflow, as represented by the record for Clark Fork above Missoula (water years 1930-2008), generally was below normal (long-term median) from about October 2007 through April 2008. Sustained runoff started in mid-April, which increased flows to near normal by mid-May. After mid-May, flows sharply increased to above normal, reaching a maximum daily mean streamflow of 16,800 cubic feet per second (ft3/s) on May 21, which essentially equaled the long-term 10th-exceedance percentile for that date. Flows substantially above normal were sustained through June, then decreased through the summer and reached near-normal by August. Annual mean streamflow during water year 2008 (3,040 ft3/s) was 105 percent of the long-term mean annual streamflow (2,900 ft3/s). The annual peak flow (17,500 ft3/s) occurred on May 21 and was 112 percent of the long-term mean annual peak flow (15,600 ft3/s). About 81 percent of the annual flow volume was discharged during the post-breach period. Daily loads of suspended sediment were estimated directly by using high-frequency sampling of the daily sediment monitoring. Daily loads of unfiltered-recoverable arsenic, cadmium, copper, iron, lead, manganese, and zinc were estimated by using regression equations relating trace-element discharge to either streamflow or suspended-sediment discharge. Regression equations for estimating trace-element discharge in water year 2008 were developed from instantaneous streamflow and concentration data for periodic water-quality samples collected during all or part of water years 2004-08. The equations were applied to records of daily mean streamflow or daily suspended-sediment loads to produce estimated daily trace-element loads. Variations in daily suspended-sediment and trace-element loads generally coincided with variations in streamflow. Relatively small to moderately large daily net losses from the project area were common during the pre-breach period when low-flow conditions were prevalent. Outflow loads from the project area sharply increased immediately after the breaching of Milltown Dam and during the rising limb and peak flow of the annual hydrograph. Net losses of suspended sediment and trace elements from the project area decreased as streamflow decreased during the summer, eventually becoming small or reaching an approximate net balance between inflow and outflow. Estimated daily loads of suspended sediment and trace elements for all three stations were summed to determine cumulative inflow and outflow loads for the pre-breach and post-breach periods, as well as for the entire water year 2008. Overall, the mass balance between the combined inflow loads from two upstream source areas (upper Clark Fork and Blackfoot River basins) and the outflow loads at Clark Fork above Missoula indicates net losses

Scientific Investigations Report↗

Groundwater quality and the relation between pH values and occurrence of trace elements and radionuclides in water samples collected from private wells in part of the Kickapoo Tribe of Oklahoma Jurisdictional Area, central Oklahoma, 2011

From 1999 to 2007, the Indian Health Service reported that gross alpha-particle activities and concentrations of uranium exceeded the Maximum Contaminant Levels for public drinking-water supplies in water samples from six private wells and two test wells in a rural residential neighborhood in the Kickapoo Tribe of Oklahoma Jurisdictional Area, in central Oklahoma. Residents in this rural area use groundwater from Quaternary-aged terrace deposits and the Permian-aged Garber-Wellington aquifer for domestic purposes. Uranium and other trace elements, specifically arsenic, chromium, and selenium, occur naturally in rocks composing the Garber-Wellington aquifer and in low concentrations in groundwater throughout its extent. Previous studies have shown that pH values above 8.0 from cation-exchange processes in the aquifer cause selected metals such as arsenic, chromium, selenium, and uranium to desorb (if present) from mineral surfaces and become mobile in water. On the basis of this information, the U.S. Geological Survey, in cooperation with the Kickapoo Tribe of Oklahoma, conducted a study in 2011 to describe the occurrence of selected trace elements and radionuclides in groundwater and to determine if pH could be used as a surrogate for laboratory analysis to quickly and inexpensively identify wells that might contain high concentrations of uranium and other trace elements. The pH and specific conductance of groundwater from 59 private wells were measured in the field in an area of about 18 square miles in Lincoln and Pottawatomie Counties. Twenty of the 59 wells also were sampled for dissolved concentrations of major ions, trace elements, gross alpha-particle and gross beta-particle activities, uranium, radium-226, radium-228, and radon-222 gas. Arsenic concentrations exceeded the Maximum Contaminant Level of 10 micrograms per liter in one sample having a concentration of 24.7 micrograms per liter. Selenium concentrations exceeded the Maximum Contaminant Level of 50 micrograms per liter in one sample having a concentration of 147 micrograms per liter. Both samples had alkaline pH values, 8.0 and 8.4, respectively. Uranium concentrations ranged from 0.02 to 383 micrograms per liter with 5 of 20 samples exceeding the Maximum Contaminant Level of 30 micrograms per liter; the five wells with uranium concentrations exceeding 30 micrograms per liter had pH values ranging from 8.0 to 8.5. Concentrations of uranium and radon-222 and gross alpha-particle activity showed a positive relation to pH, with the highest concentrations and activity in samples having pH values of 8.0 or above. The groundwater samples contained dissolved oxygen and high concentrations of bicarbonate; these characteristics are also factors in increasing uranium solubility. Concentrations of radium-226 and radium-228 (combined) ranged from 0.03 to 1.7 picocuries per liter, with a median concentration of 0.45 picocuries per liter for all samples. Radon-222 concentrations ranged from 95 to 3,600 picocuries per liter with a median concentration of 261 picocuries per liter. Eight samples having pH values ranging from 8.0 to 8.7 exceeded the proposed Maximum Contaminant Level of 300 picocuries per liter for radon-222. Eight samples exceeded the 15 picocuries per liter Maximum Contaminant Level for gross alpha-particle activity at 72 hours (after sample collection) and at 30 days (after the initial count); those samples had pH values ranging from 8.0 to 8.5. Gross beta-particle activity increased in 15 of 21 samples during the interval from 72 hours to 30 days. The increase in gross beta-particle activity over time probably was caused by the ingrowth and decay of uranium daughter products that emit beta particles. Water-quality data collected for this study indicate that pH values above 8.0 are associated with potentially high concentrations of uranium and radon-222 and high gross alpha-particle activity in the study area. High pH values also are associated with potentially high concentrations of arsenic, chromium, and selenium in groundwater when these elements occur in the aquifer matrix along groundwater-flow paths.

Oklahoma↗

Groundwater flow conceptualization of the Pahute Mesa–Oasis Valley Groundwater Basin, Nevada—A synthesis of geologic, hydrologic, hydraulic-property, and tritium data

This report provides a groundwater-flow conceptualization that integrates geologic, hydrologic, hydraulic-property, and radionuclide data in the Pahute Mesa–Oasis Valley (PMOV) groundwater basin, southern Nevada. Groundwater flow in the PMOV basin is of interest because 82 underground nuclear tests were detonated, most near or below the water table. A potentiometric map and nine sets of hydrostratigraphic and hydrologic cross sections supplement the conceptualization. Potentiometric contours indicate that groundwater in the PMOV basin generally flows south-southwest and discharges at Oasis Valley. Groundwater encounters an alternating sequence of low- and high-transmissivity rocks, referred to as dams and pools, respectively, as it moves from east to west across eastern Pahute Mesa. Flow from all Pahute Mesa nuclear tests is to Oasis Valley and is well-constrained by water-level data. Flow converges along a corridor of high transmissivity between Pahute Mesa and Oasis Valley. The location of the lateral PMOV basin boundary is well defined, and this boundary, with a few minor exceptions, represents a no-flow boundary. Some boundary uncertainty exists in the northeastern part of the basin, but potential flow-rate estimates across the northeastern boundary resulting from this uncertainty are small relative to the basin groundwater budget. Recharge in the PMOV basin is derived from episodic pulses of modern water and the diffuse percolation of old water (greater than 1,000 years). Episodic recharge is a minor recharge component observed as a rise in groundwater levels that occurs 3 months to 1 year following a wet winter. Minor amounts of episodic recharge through an unsaturated zone in excess of 1,000 feet (ft) requires preferential flow through faults and fractures. The dominant recharge component is slow, steady, diffuse percolation of old water through the unsaturated zone. A large component of old water recharging the groundwater system is consistent with observations of isotopically light deuterium and oxygen 18 compositions in water from wells on Pahute Mesa and central Oasis Valley. About half the recharge in the PMOV basin is derived from the eastern Pahute Mesa area. The remaining recharge is derived primarily from other highland areas including Timber Mountain, Belted and Kawich Ranges, and Black Mountain. The PMOV groundwater system is nearly steady state, where recharge is balanced by the 5,900 acre-feet per year of natural discharge at Oasis Valley. This assumption is reasonable because the basin is dominated by steady-state conditions, where long-term changes in groundwater storage are minimal. Total groundwater withdrawals from 1963 to 2018 have amounted to less than 10 percent of annual groundwater discharge and less than 0.2 percent of the basin’s groundwater storage. Therefore, present-day (2020) conditions are considered representative of predevelopment (pre-1950) conditions in nearly all areas of the basin. The lower PMOV basin boundary is defined at 4,000 ft below the water table to encompass all underground nuclear tests and tritium plumes. This boundary defines the lower boundary of radionuclide migration. However, nearly all flow and tritium transport occur in the upper 1,600 ft of the saturated zone because a transmissivity-with-depth relation indicates that greater than 90 percent of the transmissivity contributing to groundwater flow occurs within 1,600 ft of the water table. Rocks at deeper depths have low transmissivity because argillic and mineralized alterations plug the fractures. Volcanic rocks form the primary aquifers and confining units in the PMOV basin. Volcanic hydrogeologic units (HGUs) and hydrostratigraphic units (HSUs) have transmissivity distributions that span up to eight orders of magnitude with considerable overlap between distributions. Despite the large overlap between units, mean transmissivities of aquifers are one-to-two orders of magnitude greater than the confining units. However, all volcanic-rock HGUs and HSUs are composite units, meaning that they can function spatially as either an aquifer or confining unit .

Nevada↗

Hydrogeology and simulation of source areas of water to production wells in a colluvium-mantled carbonate-bedrock aquifer near Shippensburg, Cumberland and Franklin Counties, Pennsylvania

This report presents the results of a study by the U.S. Geological Survey in cooperation with the Shippensburg Borough Authority to evaluate the source areas of water to production wells in a colluvium-mantled carbonate-bedrock aquifer in Cumberland and Franklin Counties, Pa. The areal extent of the zone of contribution was simulated for three production wells near Shippensburg, Pa. by use of a ground-water-flow model. A 111-square-mile area was selected as the model area and includes areas of the South Mountain Section and the Great Valley Section of the Valley and Ridge Physiographic Province. Within the model area, the geologic units in the South Mountain area are predominantly metamorphic rocks and the geologic units in the Great Valley are predominantly carbonate rocks. Hydrologic and geologic information were compiled to establish a conceptual model of ground-water flow. Characteristics of aquifer materials were determined, and streamflow and water levels were measured. Streamflow measurements in November 2003 showed all streams lost water as they flowed from South Mountain over the colluvium-mantled carbonate aquifer into the Great Valley. Some streams lost more than 1 cubic foot per second to the aquifer in this area. The Shippensburg Borough Authority owns three production wells in the model area. Two wells, Cu 969 and Fr 823, are currently (2004) used as production wells and produce 500,000 and 800,000 gallons per day, respectively. Well Cu 970 is intended to be brought on line as a production well in the future. Water levels were measured in 43 wells to use for model calibration. Water-level fluctuations and geophysical logs indicated confined conditions in well Cu 970. Ground-water flow was simulated with a model that consisted of two vertical layers, with five zones in each layer. The units were hydrostratigraphic units that initially were based on geologic formations, but boundaries were adjusted during model calibration. Model calibration resulted in a root mean square error of 9.8 feet. A parameter-estimation package was used during model calibration to estimate three parameters. The parameter estimation resulted in a value of 233 feet per day for horizontal hydraulic conductivity of the highly fractured carbonate rocks and sandy colluvium in layer 1; 3.97 feet per day for horizontal hydraulic conductivity of the ridge-forming unit in layer 1; and a value of 1.73 for horizontal anisotropy in both layers. The calibrated model was used to delineate the areal extent of the zone of contribution for wells Cu 969 and Fr 823. Although well Cu 970 is not currently (2004) being used, the areal extent of its zone of contribution also was simulated without additional model calibration. The shape of the areal extent of the zone of contribution was similar for each well and included an area that extended from the well southwest along the Tomstown Formation, and then extended southeast into the metamorphic rocks of South Mountain. The contributing areas from the watersheds of losing streams were also delineated because losing stream reaches bisect the areal extent of the zones of contribution. Spatial uncertainty of the areal extent of the zone of contribution was illustrated using a Monte-Carlo analysis. The model was run 1,000 times using randomly generated parameter sets that were normally distributed within the confidence interval around the optimal values for the three estimated parameters. The model converged and had a reasonable water budget for 980 of the model runs. For each of those 980 model runs, the recharge area was determined, and the results for all runs were compiled and contoured. The results of the Monte-Carlo analysis were compared to the results of the deterministic model, illustrating that the deterministic model has the greatest certainty in the area closest to each well in the Tomstown Formation. The areas farther from the well, upgradient, and in the metamorphic rocks have a higher degree

Pennsylvania↗

Occurrence of cyanobacteria, microcystin, and taste-and-odor compounds in Cheney Reservoir, Kansas, 2001-16

Cheney Reservoir, located in south-central Kansas, is one of the primary drinking-water supplies for the city of Wichita and an important recreational resource. Since 1990, cyanobacterial blooms have been present occasionally in Cheney Reservoir, resulting in increased treatment costs and decreased recreational use. Cyanobacteria, the cyanotoxin microcystin, and the taste-and-odor compounds geosmin and 2-methylisoborneol have been measured in Cheney Reservoir by the U.S. Geological Survey, in cooperation with the city of Wichita, for about 16 years. The purpose of this report is to describe the occurrence of cyanobacteria, microcystin, and taste-and-odor compounds in Cheney Reservoir during May 2001 through June 2016 and to update previously published logistic regression models that used continuous water-quality data to estimate the probability of microcystin and geosmin occurrence above relevant thresholds. Cyanobacteria, microcystin, and geosmin were detected in about 84, 52, and 31 percent of samples collected in Cheney Reservoir during May 2001 through June 2016, respectively. 2-methylisoborneol was less common, detected in only 3 percent of samples. Microcystin and geosmin concentrations exceeded advisory values of concern more frequently than cyanobacterial abundance; therefore, cyanobacteria are not a good indicator of the presence of these taste-and-odor compounds in Cheney Reservoir. Broad seasonal patterns in cyanobacteria and microcystin were evident, though abundance and concentration varied by orders of magnitude across years. Cyanobacterial abundances generally peaked in late summer or early fall (August through October), and smaller peaks were observed in winter (January through February). In a typical year, microcystin was first detected in June or July, increased to its seasonal maxima in the summer (July through September), and then decreased. Seasonal patterns in geosmin were less consistent than cyanobacteria and microcystin, but geosmin typically had a small peak during winter (January through March) during most years and a large peak during summer (July through September) during some years. Though the relation between cyanobacterial abundance and microcystin and geosmin concentrations was positive, overall correlations were weak, likely because production is strain-specific and cyanobacterial strain composition may vary substantially over time. Microcystin often was present without taste-and-odor compounds. By comparison, where taste-and-odor compounds were present, microcystin frequently was detected. Taste-and-odor compounds, therefore, may be used as indicators that microcystin may be present; however, microcystin was present without taste-and-odor compounds, so taste or odor alone does not provide sufficient warning to ensure human-health protection. Logistic regression models that estimate the probability of microcystin occurrence at concentrations greater than or equal to 0.1 micrograms per liter and geosmin occurrence at concentrations greater than or equal to 5 nanograms per liter were developed. Models were developed using the complete dataset (January 2003 through June 2016 for microcystin [14-year dataset]; May 2001 through June 2016 for geosmin [16-year dataset]) and an abbreviated 4-year dataset (January 2013 through June 2016 for microcystin and geosmin). Performance of the newly developed models was compared with previously published models that were developed using data collected during May 2001 through December 2009. A seasonal component and chlorophyll fluorescence (a surrogate for algal biomass) were the explanatory variables for microcystin occurrence at concentrations greater than or equal to 0.1 micrograms per liter in all models. All models were relatively robust, though the previously published and 14-year models performed better over time; however, as a tool to estimate microcystin occurrence at concentrations greater than or equal to 0.1 micrograms per liter in a real-time notification system near the Cheney Dam, the 4-year model is most representative of recent (2013 through 2016) conditions. All models for geosmin occurrence at concentrations greater than or equal to 5 nanograms per liter had different explanatory variables and model forms. The previously published and 16-year models were not robust over time, likely because of changing environmental conditions and seasonal patterns in geosmin occurrence. By comparison, the abbreviated 4-year model may be a useful tool to estimate geosmin occurrence at concentrations greater than or equal to 5 nanograms per liter in a real-time notification system near the Cheney Dam. The better performance of the abbreviated 4-year geosmin model during 2013 through 2016 relative to the previously published and 16-year models demonstrates the need for continuous reevaluation of models estimating the probability of occurrence.

Kansas↗

Hydrologic conditions and water-quality conditions following underground coal mining in the North Fork of the Right Fork of Miller Creek drainage basin, Carbon and Emery Counties, Utah, 2004-2005

In 2004 and 2005, the U.S. Geological Survey, in cooperation with the Bureau of Land Management, reassessed the hydrologic system in and around the drainage basin of the North Fork of the Right Fork (NFRF) of Miller Creek, in Carbon and Emery Counties, Utah. The reassessment occurred 13 years after cessation of underground coal mining that was performed beneath private land at shallow depths (30 to 880 feet) beneath the NFRF of Miller Creek. This study is a follow-up to a previous USGS study of the effects of underground coal mining on the hydrologic system in the area from 1988 to 1992. The previous study concluded that mining related subsidence had impacted the hydrologic system through the loss of streamflow over reaches of the perennial portion of the stream, and through a significant increase in dissolved solids in the stream. The previous study also reported that no substantial differences in spring-water quality resulted from longwall mining, and that no clear relationship between mining subsidence and spring discharge existed. During the summers of 2004 and 2005, the USGS measured discharge and collected water-quality samples from springs and surface water at various locations in the NFRF of Miller Creek drainage basin, and maintained a streamflow-gaging station in the NFRF of Miller Creek. This study also utilized data collected by Cyprus–Plateau Mining Corporation from 1992 through 2001. Of thirteen monitored springs, five have discharge levels that have not returned to those observed prior to August 1988, which is when longwall coal mining began beneath the NFRF of Miller Creek. Discharge at two of these five springs appears to fluctuate with wet and dry cycles and is currently low due to a drought that occurred from 1999–2004. Discharge at two other of the five springs did not increase with increased precipitation during the mid-1990s, as was observed at other monitored springs. This suggests that flowpaths to these springs may have been altered by land subsidence caused by underground coal mining. Analysis of possible impacts to the fifth spring were inconclusive due to a lack of data collected during the mid-1990s. Discharge at eight other monitored springs in the study area appears to be controlled mainly by climatic fluctuations and was generally near the value measured prior to 1988. Discharge at one of these eight springs is significantly greater than that measured during the longwall mining period. Concentrations of magnesium, calcium, sulfate, and dissolved solids at one undermined spring were elevated in relation to other springs in the study area. Dissolved solids concentration at this spring ranged from 539–709 milligrams per liter. Dissolved-solids concentration for all other springs in the study area ranged from 163 to 360 milligrams per liter and was near the median value measured prior to longwall mining beneath the NFRF of Miller Creek drainage basin. Baseflow measured at a streamflow-gaging station on the NFRF of Miller Creek located downstream of the mined area during the summer of 2004 was near 5 gallons per minute. Baseflow in 2005 increased to 7–8 gallons per minute, due to increased precipitation. This is slightly greater than the range of baseflow measured near the end of the longwall mining period which was approximately 3–5 gallons per minute. Seepage investigations carried out in the summer of 2004 and 2005 along the NFRF of Miller Creek showed a net loss of surface flow along the studied reach. Specific areas within the study reach had streamflow losses prior to longwall mining, however, the study reach as a whole was observed to gain in discharge when measured in 1986–1988, immediately before longwall mining began. The area where the greatest loss in discharge from the NFRF of Miller Creek occurred corresponds to an area where overburden (material overlying a deposit of useful geological materials or bedrock) is between 700 and 210 feet thick. Overburden thickness at the place where the streambed first dried up was approximately 600 feet thick. In 2004, approximately 1,600 ft of the streambed of the NFRF of Miller Creek was dry. Only 300 feet of the streambed was dry during the wetter year of 2005. Prior to longwall mining, no dry reaches were observed, though seepage loss was documented. Average discharge measured at a tributary to the NFRF of Miller Creek has increased from 1.6 gallons per minute measured during longwall mining to 7.2 gallons per minute measured in 2004–2005. During both years of this study, the lower reach of the stream regained flow from this tributary and from seepage gains. Water quality in the lower reach of the NFRF of Miller Creek downstream of the longwall-mined area, showed significantly higher concentrations of magnesium, calcium, sulfate, and strontium, in relation to water in the upper reach of the NFRF of Miller Creek and to the springs sampled in the area. Dissolved-solids concentration measured in the lower reach of the stream in 2004 and 2005 ranged from 1,880 to 2,220 milligrams per liter, while sulfate concentrations ranged from 1,090 to 1,320 mg/L. The maximum contaminant level for drinking water in the state of Utah for dissolved solids and sulfate is 2,000 and 1,000 mg/L respectively. Concentrations of these ions are slightly greater than those measured during and just following mining beneath the NFRF of Miller Creek drainage basin, but are significantly higher than those measured prior to mining. With the exception of strontium, dissolved metals concentrations in the NFRF of Miller Creek were similar to those measured in area springs. pH in the creek and at all spring sites was near neutral. Qualitative observations of the creek bottom suggest that mining-related activities have had little effect on vegetative growth.

Utah↗

Water-quality characteristics of the Red River of the North and tributaries in the Fargo-Moorhead metropolitan area, North Dakota, 2019–22

The Flood Risk Management Project was initiated in 2008 in the Fargo-Moorhead metropolitan area to reduce flood risk, flood damages, and flood protection costs in the Fargo-Moorhead metropolitan area. In cooperation with the U.S. Army Corps of Engineers, the U.S. Geological Survey initiated a water-quality monitoring study to describe the water-quality characteristics of the Red River of the North and its tributaries in the Fargo-Moorhead metropolitan area during the preconstruction period of the Flood Risk Management Project from October 1, 2019, to October 1, 2022. The monitoring study included the collection of discrete and continuous water-quality data and streamflow monitoring at selected sites that integrated and enhanced existing monitoring programs within the study area. Discrete samples collected at 10 sites in the Fargo-Moorhead metropolitan area were analyzed for major ions, trace elements, nutrients, suspended sediment, pesticides, and fecal indicator bacteria. In general, major ion concentrations were higher at sites on the tributaries (Wild Rice, Sheyenne, and Maple Rivers) compared to sites on the Red River of the North. In general, bicarbonate, calcium, magnesium, and sulfate represented most of the dissolved ions measured in samples collected at the 10 sites. Calcium, chloride, fluoride, potassium, silica, and sodium were also measured in samples, but they represented a smaller portion of the total dissolved ions. Sulfate was the most dominant dissolved ion that had the highest concentrations among the major ions measured in samples. A total of 18 trace elements were analyzed in discrete samples. Several of the trace elements had concentrations below the laboratory reporting level in all of the samples, including antimony, beryllium, cadmium, chromium, silver, and thallium. Sites on the Wild Rice River generally had the highest concentrations of arsenic, barium, boron, manganese, and nickel compared to the other sites. Nutrients analyzed in discrete samples included filtered and unfiltered concentrations of ammonia, nitrate plus nitrite, phosphorus, and organic carbon. The median filtered ammonia concentration at most sites was less than the laboratory reporting level of 0.03 milligram per liter as nitrogen except for the Sheyenne River at Harwood, North Dakota (U.S. Geological Survey [USGS] station 05060400), and Red River of the North near Georgetown, Minnesota (USGS station 05062130). The lowest median unfiltered nitrate plus nitrite concentration was measured at sites on the Red River of the North upstream from the Fargo-Moorhead metropolitan area and the highest median was at sites on the Red River of the North downstream from the Fargo-Moorhead metropolitan area compared to all other sites. The increase in nitrate plus nitrite concentrations could reflect the effect of the wastewater-treatment plant discharge that enters the Red River of the North upstream from the site located downstream from the Fargo-Moorhead metropolitan area and from urban runoff. Phosphorus (unfiltered) concentrations were generally higher at sites on the Maple and Sheyenne Rivers compared to the other sites and were higher at sites on the Red River of the North downstream from the Fargo-Moorhead metropolitan area compared to sites upstream on the Red River of the North. Suspended-sediment concentrations were generally highest at sites in the Sheyenne River and lowest in the upstream Red River of the North sites. Suspended-sediment concentration was highly variable in samples collected at the 10 sites, mostly influenced by the occurrence of snowmelt and rainfall-runoff events. The Sheyenne River near Kindred, N. Dak. (USGS station 05059000) had the largest range in sediment concentrations in samples collected at the 10 sites. For all sites other than the Sheyenne River near Kindred, N. Dak., 95 percent or more of the suspended sediment had particle diameter sizes less than 0.0625 millimeter in 50 percent of the samples (median). Of the 102 pesticides and pesticide degradates analyzed, 45 constituents had no detectable concentrations in any of the 17 samples collected at five sites. The remaining 57 pesticides had at least one detection in the samples collected at the five sites. The sites on the Wild Rice River (near Abercrombie, N. Dak., USGS station 05053000, and near St. Benedict, N. Dak., USGS station 05053500) and Sheyenne River near Kindred, N. Dak., had fewer pesticide detections compared to the Maple River below Mapleton, N.Dak. (USGS station 05060100) and the Red River of the North at Fargo, N. Dak (USGS station 05054000) and near Georgetown, Minn. Patterns in annual loads generally followed the same pattern as streamflow at the 10 sites for water years 2020–22. A water year is the 12-month period from October 1 to September 30 and is designated by the calendar year in which it ends. The greatest loads for all constituents were delivered at the two downstream sites on the Red River of the North; sites that also had the highest annual streamflows among the sites and the greatest loads were delivered in water year 2020 when the highest streamflows occurred at the sites. Likewise, the least loads for most constituents were at the Maple River and were least in 2021 compared to the other years because of low-streamflow conditions. Water-quality measurements continuously recorded at the Red River of the North at Hickson, N. Dak. (USGS station 05051522); Red River of the North at Fargo, N. Dak.; and Red River of the North near Georgetown, Minn. included water temperature, specific conductance, dissolved oxygen, pH, and turbidity. Specific conductance values were similar for the Red River of the North near Hickson, N. Dak., and Red River of the North at Fargo, N. Dak., when compared to the Red River of the North near Georgetown, Minn. that had higher values than the other two sites. Dissolved oxygen concentrations and pH were similar among the three sites on the Red River. The patterns in turbidity were mostly related to streamflow conditions and were similar among the three sites on the Red River of the North.

Minnesota, North Dakota↗

Spatial Distribution of Ground-Water Recharge Estimated with a Water-Budget Method for the Jordan Creek Watershed, Lehigh County, Pennsylvania

This report presents the results of a study by the U.S. Geological Survey, in cooperation with the Pennsylvania Geological Survey, to illustrate a water-budget method for mapping the spatial distribution of ground-water recharge for a 76-square-mile part of the Jordan Creek watershed, northwest of Allentown, in Lehigh County, Pennsylvania. Recharge was estimated by using the Hydrological Evaluation of Landfill Performance (HELP) water-budget model for 577 landscape units in Jordan Creek watershed, delineated on the basis of their soils, land use/land cover, and mean annual precipitation during 1951-2000. The water-budget model routes precipitation falling on each landscape unit to components of evapotranspiration, surface runoff, storage, and vertical percolation (recharge) for a five-layer soil column on a daily basis. The spatial distribution of mean annual recharge during 1951-2000 for each landscape unit was mapped by the use of a geographic information system. Recharge simulated by the water-budget model in Jordan Creek watershed during 1951-2000 averaged 12.3 inches per year and ranged by landscape unit from 0.11 to 17.05 inches per year. Mean annual recharge during 1951-2000 simulated by the water-budget model was most sensitive to changes to input values for precipitation and runoff-curve number. Mean annual recharge values for the crop, forest, pasture, and low-density urban land-use/land-cover classes were similar (11.2 to 12.2 inches per year) but were substantially less for high-density urban (6.8 inches per year), herbaceous wetlands (2.5 inches per year), and forested wetlands (1.3 inches per year). Recharge rates simulated for the crop, forest, pasture, and low-density urban land-cover classes were similar because those land-use/land-cover classes are represented in the model with parameter values that either did not significantly affect simulated recharge or tended to have offsetting effects on recharge. For example, for landscapes with forest land cover, values of runoff-curve number assigned to the model were smaller than for other land-use/land-cover classes (causing more recharge and less runoff), but the maximum depth of evapotranspiration was larger than for other land-use/ land-cover classes because of deeper root penetration in forests (causing more evapotranspiration and less recharge). The smaller simulated recharge for high-density urban and wetland land-use/land-cover classes was caused by the large values of runoff-curve number (greater than 90) assigned to those classes. The large runoff-curve number, however, certainly is not realistic for all wetlands; some wetlands act as areas of ground-water discharge and some as areas of recharge. Simulated mean annual recharge computed by the water-budget model for the 53-square-mile part of the watershed upstream from the streamflow-gaging station near Schnecksville was compared to estimates of recharge and base flow determined by analysis of streamflow records from 1967 to 2000. The mean annual recharge of 12.4 inches per year simulated by the water-budget method for 1967-2000 was less than estimates of mean annual recharge of 19.3 inches per year computed from the RORA computer program and base flow computed by the PART computer program (15.1 inches per year). In theory, the water-budget method provides a practical tool for estimating differences in recharge at local scales of interest, and the watershed- average recharge rate of 12.4 inches per year computed by the method is reasonable. However, the mean annual surface runoff of 4.5 inches per year simulated by the model is unrealistically small. The sum of surface runoff and recharge simulated by the water-budget model (16.9 inches per year) is 7 inches per year less than the streamflow measured at the gaging station near Schnecksville (23.9 inches per year) during 1967-2000, indicating that evapotranspiration is overestimated by the water-budget model by that amount. This discrepancy ca

Scientific Investigations Report↗

Water levels of the Ozark aquifer in northern Arkansas, 2013

The Ozark aquifer is the largest aquifer, both in area of outcrop and thickness, and the most important source of freshwater in the Ozark Plateaus physiographic province, supplying water to northern Arkansas, southeastern Kansas, southern Missouri, and northeastern Oklahoma. The study area includes 16 Arkansas counties lying completely or partially within the Ozark Plateaus of the Interior Highlands major physiographic division. The U.S. Geological Survey, in cooperation with the Arkansas Natural Resources Commission and the Arkansas Geological Survey, conducted a study of water levels in the Ozark aquifer within Arkansas. This report presents a potentiometric-surface map of the Ozark aquifer within the Ozark Plateaus of northern Arkansas, representing water-level conditions for the early spring of 2013 and selected water-level hydrographs. The Ozark aquifer in Arkansas is composed of dolomites, limestones, sandstones, and shales of Late Cambrian to Middle Devonian age and ranges in thickness from approximately 1,100 feet (ft) in northwestern Arkansas to more than 4,000 ft in the west-central part of Arkansas. Most wells completed in the aquifer yield between 50 and 100 gallons per minute (gal/min), although some wells may yield as much as 600 gal/min. Water-level measurements were made in wells completed in the Ozark aquifer from February to May 2013. Hydrographs were constructed for nine wells that have water-level measurements with a minimum 20-year period of record. Water-level altitudes in wells used to construct the potentiometric-surface map range from about 1,159 ft to 313 ft above National Geodetic Vertical Datum of 1929 (NGVD 29). The highest water-level altitudes occur in Carroll and Washington Counties while water-level altitudes of less than 400 ft above NGVD 29 are mapped along the eastern and southeastern part of the study area in Independence, Lawrence, Randolph, and Sharp Counties. The lowest water level of 313 ft above NGVD 29 was measured in southwestern Randolph County. The direction of groundwater flow generally is affected by local topography, flowing from high altitudes toward stream valleys. In southern Baxter, eastern Fulton, Independence, eastern Izard, Lawrence, Randolph, and Sharp Counties, the groundwater flow is generally to the south and southeast. In western Fulton and Izard Counties, the groundwater flow is generally to the southwest. In Boone, Marion, Newton, Searcy, and Stone Counties, the groundwater flow is generally to the east and northeast. In eastern Benton, Carroll, Madison, and eastern Washington Counties, the groundwater flow is generally to the north and northeast. In western Benton and western Washington Counties, the groundwater flow is generally to the west and northwest. The general level and shape of the potentiometric surface has changed little since predevelopment. A comparison of the predevelopment potentiometric surface and the 2007, 2010, and 2013 potentiometric surfaces indicate general agreement between the mapped surfaces with the exception of parts of Benton, Boone, Marion, and Washington Counties. In Boone and northern Marion Counties in 2013, water levels have declined when compared to the predevelopment potentiometric surface, although the direction of flow is still to the northeast and north. In southern Marion County, water levels have declined when compared to the predevelopment, 2007, and 2010 potentiometric surfaces, although the direction of flow is towards and along the stream valleys. In western Benton and northwestern Washington Counties, water levels are similar when compared to the predevelopment potentiometric surface, and the direction of flow is to the west and northwest, similar to the predevelopment direction of flow. The mapped 2007 and 2010 potentiometric surfaces are very different from the mapped 2013 potentiometric surface in western Benton and northwestern Washington Counties. The mapped 2013 potentiometric surface in western Benton and northwestern Washington Counties follows the contours of the top of the formation, similar to the predevelopment potentiometric surface. Since 1975, water use in the Ozark aquifer has declined 45 percent, while water levels in Benton, Boone, Marion, and Washington Counties continue to decline. Nine hydrographs were selected as representative of the water-level conditions in their respective counties. Wells in Fulton, Izard, and Newton Counties (station names 20N08W27ABD1, 18N09W15BCB1, and 16N21W34ABC1, respectively) have water levels that are within the usual range of values for their respective counties. Wells in Boone, Marion, and Washington Counties (station names 18N19W19BCC1, 19N15W20ACC1, and 16N32W09ABD1, respectively) have water levels that have recently declined or are declining for the period of record. Wells in Benton, Carroll, and Sharp Counties (station names 19N29W07DAA1, 21N26W17BCC1, and 15N05W06DDD1, respectively) have water levels that have been rising recently.

Arkansas↗

Effects of Historical Coal Mining and Drainage from Abandoned Mines on Streamflow and Water Quality in Newport and Nanticoke Creeks, Luzerne County, Pennsylvania, 1999-2000

This report characterizes the effects of historical mining and abandoned mine drainage (AMD) on streamflow and water quality and evaluates potential strategies for AMD abatement in the 14-square-mile Newport Creek Basin and 7.6-square-mile Nanticoke Creek Basin. Both basins are mostly within the Northern Anthracite Coal Field and drain to the Susquehanna River in central Luzerne County, Pa. The U.S. Geological Survey (USGS), in cooperation with the Earth Conservancy, conducted an assessment from April 1999 to September 2000 that included (1) continuous stage measurement at 7 sites; (2) synoptic water-quality and flow sampling at 21 sites on June 2-4, 1999, and at 24 sites on October 7-8, 1999; and (3) periodic measurement of flow and water quality at 26 additional sites not included in the synoptic sampling effort. Stream water and surface runoff from the unmined uplands drain northward to the valley, where most of the water is intercepted and diverted into abandoned underground mines. Water that infiltrates into the mine workings becomes loaded with acidity, metals, and sulfate and later discharges as AMD at topographically low points along lower reaches of Newport Creek, Nanticoke Creek, and their tributaries. Differences among streamflows in unmined and mined areas of the watersheds indicated that (1) intermediate stream reaches within the mined area but upgradient of AMD sites generally were either dry or losing reaches, (2) ground water flowing to AMD sites could cross beneath surface-drainage divides, and (3) AMD discharging to the lower stream reaches restored volumes lost in the upstream reaches. The synoptic data for June and October 1999, along with continuous stage data during the study period, indicated flows during synoptic surveys were comparable to average values. The headwaters upstream of the mined area generally were oxygenated (dissolved oxygen range was 4.7 to 11.0 mg/L [milligrams per liter]), near-neutral (pH range was 5.8 to 7.6), and net alkaline (net alkalinity range was 2.0 to 25.0 mg/L CaCO3), with relatively low concentrations of sulfate (6.40 to 24.0 mg/L) and dissolved metals (less than 500 ug/L [micrograms per liter] of iron, manganese, and aluminum). In contrast, the AMD discharges and downstream waters were characterized by elevated concentrations of sulfate and dissolved metals that exceeded Federal and State regulatory limits. The largest AMD sources were the Susquehanna Number 7 Mine discharge entering Newport Creek near its mouth (flow range was 4.7 to 19 ft3/s [cubic feet per second]), the Truesdale Mine Discharge (Dundee Outfall) entering Nanticoke Creek about 0.5 mile upstream of Loomis Park (flow range was 0.00 to 38 ft3/s), and a mine-pit overflow entering near the midpoint of Newport Creek (flow range was 4.0 to 6.9 ft3/s). The three large discharges were poorly oxygenated (dissolved oxygen concentration range was <0.05 to 6.4 mg/L) and had elevated concentrations of sulfate (range was 710 to 890 mg/L) and low concentrations of dissolved aluminum (less than 25 ug/L), but they had distinctive concentrations of net alkalinity and dissolved iron and manganese. Effluent from the Susquehanna Number 7 Mine was near-neutral (pH range was 5.9 to 6.6) and net alkaline (net alkalinity range was 12.0 to 42.0 mg/L CaCO3) with elevated concentrations of sulfate (718 to 1,170 mg/L), dissolved iron (52,500 to 77,400 ug/L), and manganese (5,200 to 5,300 ug/L). Effluent from the Truesdale Mine also was near-neutral (pH range was 5.9 to 6.3) but had variable net alkalinity (-19.0 to 57.0 mg/L CaCO3) with elevated concentrations of sulfate (571 to 740 mg/L), dissolved iron (30,500 to 43,000 ug/L), and manganese (3,600 to 5,200 ug/L). Effluent from the mine-pit overflow in Newport Creek Basin was acidic (pH range was 4.3 to 5.0; net alkalinity range was -42 to -38 mg/L CaCO3) with elevated concentrations of sulfate (800 to 840 mg/L), iron (13,000 to 16,000 ug/L), and manganese (6,800 to 7,000 ug

Scientific Investigations Report↗

Response of selenium concentrations in groundwater to seasonal canal leakage, lower Gunnison River Basin, Colorado, 2013

Selenium is a water-quality concern in the lower Gunnison River Basin because irrigation water interacting with seleniferous soils derived from the Mancos Shale Formation has mobilized selenium and increased its concentrations in surface water. Understanding the occurrence of elevated selenium concentrations in groundwater is necessary because groundwater discharge is an important source of selenium in surface water in the basin. In 2013, the U.S. Geological Survey, in cooperation with the Bureau of Reclamation and the Colorado Water Conservation Board, began a study to understand how changes in groundwater levels attributed to canal leakage affected the concentrations and speciation of dissolved selenium in groundwater. The purpose of this report is to characterize the groundwater adjacent to an unlined leaky canal. Two locations, near the East Canal (W-N1 and W-N2) and farther from the East Canal (W-M1 and W-M2), were selected for nested monitoring well installations. The pressure exerted by changes in canal stage was more readily transferred to the deep groundwater measured in the W-N1 near the canal than the shallow groundwater at the W-N2 well. No definitive relation could be made between canal water-level elevation and water-level elevations in monitoring wells farther from the canal (W-M1 and W-M2). Water flowing through the East Canal before the irrigation season had much higher selenium concentrations (140 micrograms per liter) than water in the canal during the irrigation season (3.02 micrograms per liter). Total selenium concentrations in the monitoring wells near the canal initially increased to 51.8 micrograms per liter in W-N1 and 1.66 micrograms per liter in W-N2. The initial increase in groundwater selenium concentrations presumably resulted from the dissolution of salts in the unsaturated zone by rising groundwater levels associated with canal leakage. The subsequent decrease in total selenium concentrations resulted from a combination of dilution by canal leakage and selenium reduction processes. Total selenium concentrations in monitoring wells located farther from the canal were not directly affected by canal leakage. Selenite/total selenium mass ratios in the East Canal samples ranged from about 0.02 to 0.13, indicating that about 2 to 13 percent of the total selenium in canal samples was composed of selenite. The increase in total selenium at W-N1 from before the irrigation season to the early irrigation season was accompanied by a decrease in the percentage of selenite from about 10 to 1 percent, indicating that selenate was added to the groundwater. A nitrate pulse occurred with the selenate pulse in W-N1 at the beginning of the irrigation season but apparently dissipated to a low enough concentration during the irrigation season to allow for selenate reduction to occur, as indicated by the relatively high percentages of selenite in W-N1 during the late irrigation season. W-N2 generally contained higher percentages of selenite than W-N1. Percentages of selenite in W-M1 did not change in response to filling the canal and generally composed less than 1 percent of the total selenium in that well. The predominance of selenate in W-M1, and apparent lack of selenate reduction, cannot be explained by a lack of anoxic conditions in the groundwater because all the available dissolved-oxygen data indicate that concentrations were less than 0.5 milligrams per liter. The most likely explanation for the lack of selenate reduction in W-M1 is that the exceptionally high concentrations of nitrate in the groundwater (about 340 to 390 milligrams per liter as nitrogen) inhibited selenate reduction. These high nitrate concentrations presumably come from the Mancos Shale and its weathering products because there was no evidence for a human source of nitrate at the lower Gunnison River Basin wetland. The high concentrations of selenate in W-M1 may persist and eventually discharge to surface water unless nitrate concentrations are reduced to low enough levels to permit substantial selenate reduction to occur. Well W-M2 contained relatively low concentrations of total selenium and high percentages of selenite before and at the onset of the irrigation season. An increase in total selenium concentration associated with a drying and wetting period later in the summer was accompanied by a decrease in the percentage of selenite to near 0 percent, indicating that selenate was added to the groundwater. This pattern is consistent with the examples of increasing concentrations of total selenium in the other wells and presumably resulted from the dissolution of selenate-bearing salts in the unsaturated zone by rising water levels in W-M2.

Colorado↗

Availability, sustainability, and suitability of ground water, Rogers Mesa, Delta County, Colorado: Types of analyses and data for use in subdivision water-supply reports

The population of Delta County, Colorado, like that in much of the Western United States, is forecast to increase substantially in the next few decades. A substantial portion of the increased population likely will reside in rural subdivisions and use residential wells for domestic water supplies. In Colorado, a subdivision developer is required to submit a water-supply plan through the county for approval by the Colorado Division of Water Resources. If the water supply is to be provided by wells, the water-supply plan must include a water-supply report. The water-supply report demonstrates the availability, sustainability, and suitability of the water supply for the proposed subdivision. During 2006, the U.S. Geological Survey, in cooperation with Delta County, Colorado, began a study to develop criteria that the Delta County Land Use Department can use to evaluate water-supply reports for proposed subdivisions. A table was prepared that lists the types of analyses and data that may be needed in a water-supply report for a water-supply plan that proposes the use of ground water. A preliminary analysis of the availability, sustainability, and suitability of the ground-water resources of Rogers Mesa, Delta County, Colorado, was prepared for a hypothetical subdivision to demonstrate hydrologic analyses and data that may be needed for water-supply reports for proposed subdivisions. Rogers Mesa is a 12-square-mile upland mesa located along the north side of the North Fork Gunnison River about 15 miles east of Delta, Colorado. The principal land use on Rogers Mesa is irrigated agriculture, with about 5,651 acres of irrigated cropland, grass pasture, and orchards. The principal source of irrigation water is surface water diverted from the North Fork Gunnison River and Leroux Creek. The estimated area of platted subdivisions on or partially on Rogers Mesa in 2007 was about 4,792 acres of which about 2,756 acres was irrigated land in 2000. The principal aquifer on Rogers Mesa consists of alluvial-fan deposits that overlie shale and, locally, sandstone. Maps of the base of the aquifer, the water table, and the saturated thickness of the aquifer were prepared from data from the well files of the Colorado Division of Water Resources. The base of the aquifer generally is topographically higher than the valleys of the North Fork Gunnison River and Leroux Creek, and direct hydraulic connection of the aquifer to North Fork Gunnison River and Leroux Creek is limited. The aquifer is recharged primarily by infiltration of surface water diverted for irrigation. Ground water discharges to seeps and springs and through slope deposits at the boundaries of the aquifer. Data from the well files also were used to estimate the specific capacity of wells and to estimate the transmissivity and hydraulic conductivity of the aquifer. A water budget was used to estimate recharge to and discharge from the aquifer. Although storage within the aquifer likely varies seasonally and from year to year, it was assumed that there were no long-term changes in ground-water storage. Estimated average annual recharge to and discharge from the aquifer during November 1998 through October 2006 were about 30,767 acre-feet per year. Although sufficient ground water is available on Rogers Mesa for additional domestic water supplies, conversion of irrigated land to residential land use likely would reduce recharge to the aquifer, affecting the sustainability of ground-water supplies on Rogers Mesa. Stream-depletion analyses indicate that the ground water in the aquifer likely would be considered tributary ground water and additional uses of ground water to supply new subdivisions likely would require implementation of augmentation plans. Although sufficient ground water is available on Rogers Mesa for additional domestic water supplies, conversion of irrigated land to residential land use likely would reduce recharge to the aquifer, affecting the sustainability of ground-water supplies on Rogers Mesa. Stream-depletion analyses indicate that the ground water in the aquifer likely would be considered tributary ground water and additional uses of ground water to supply new subdivisions likely would require implementation of augmentation plans. Although the dissolved solids and dissolved sulfate concentrations in ground water from Rogers Mesa aquifer commonly exceeded the U.S. Environmental Protection Agency Secondary Maximum Contaminant Levels for drinking-water supplies, the quality of ground water from the aquifer generally is suitable for residential use. Concentrations of total nitrogen (nitrite plus nitrate, as nitrogen) in ground water ranged from 0.38 to 3.2 milligrams per liter and were less than the State of Colorado maximum contaminant level of 10 milligrams per liter. Concentrations of selenium from seeps and springs at the boundaries of the aquifer commonly exceeded 50 micrograms per liter, the State of Colorado maximum contaminant level for drinking-water supplies. This preliminary evaluation of ground-water supplies on Rogers Mesa could be improved with the collection of additional data including: additional mapping of hydrogeologic features; more accurate locations and altitudes of wells; accurate estimates of water-budget components; measurements of ground-water levels; and collection and analyses of ground-water samples. The use of numerical models of ground-water flow could improve evaluations of the potential effects of changes in land and water use on the water budget, aquifer storage, stream depletion, and well interference.

Colorado↗

Evaluation of salinity and nutrient conditions in the Heart River Basin, North Dakota, 1970–2020

The Heart River Basin is predominantly an agricultural basin in western North Dakota and is approximately 3,350 square miles. The U.S. Geological Survey, in cooperation with the U.S. Department of Agriculture Natural Resources Conservation Service and the Grant County Soil Conservation District, completed a study to assess spatial and temporal patterns of water quality in the Heart River Basin. The purpose of this report is to describe the methods and results of a study to evaluate salinity and nutrients in the Heart River Basin in western North Dakota. Water-quality and streamflow data used in the study were compiled from 1970 to 2020 using the National Water Quality Monitoring Council Water Quality Portal and National Water Information System. Changes in streamflow characteristics were investigated at three sites from 1970 to 2020, and changes in water quality were investigated at four sites from 1974 to 2019. Streamflow analysis indicated decreasing streamflow from 1970 until the late 1990s followed by increasing streamflow through 2020, with the largest increase in the 7-day minimum streamflow or base flow. For the historical water-quality trend period (1974–2019), total dissolved solids, sulfate, sodium, chloride, and sodium adsorption ratio concentrations have increased since the mid-1970s through 2019. Potassium concentrations during the historical period remained mostly constant with some small fluctuations. Calcium and magnesium concentrations increased since the mid-1970s at all sites, except for a decrease at one site between 1974 and 1999. During the recent trend period (1999–2019), increasing concentrations in total dissolved solids, sulfate, sodium, chloride, calcium, magnesium, and sodium adsorption ratios were observed across the Heart River Basin. The magnitude of the increases was smaller at tributary sites compared to main-stem sites. During the recent period, potassium was mostly constant, although small (−0.9 milligram per liter or less) decreases on tributaries and minor (1.3 milligrams per liter) increases on the main-stem sites were detected. Unlike dissolved ion concentrations, significant increases in nutrient concentrations were not detected from 1999 to 2019, but nitrate plus nitrite concentrations most likely decreased upstream from Lake Tschida. Inverse modeling for period 1 (1974–99) in model zone 1 (Heart River reach from site 5 to site 6) had eight reasonable models that indicated the clay mineral-water interactions and dissolution of evaporites control the geochemistry. Results of the inverse modeling for period 2 (1999–2019) in model zone 1 also had eight reasonable models that indicated that the dissolution of evaporites was the major geochemical control. Results of the geochemical modeling for period 1 (1974–99) in model zone 2 (Heart River and Sweetbriar Creek reach from sites 20 and 21 to site 22) produced seven reasonable models, and the geochemical control of the system was the dissolution of sulfate evaporite minerals. Geochemical modeling results for period 2 (1999–2019) in model zone 2 produced 11 reasonable models and was also controlled by the dissolution of sulfate evaporite minerals. Differences between the two model zones indicated that geology controls some of the water-quality changes in the Heart River Basin. Loads were estimated for total dissolved solids, sulfate, sodium, and chloride and total phosphorus. Annual loads estimated for the Heart River from 2013 through 2020 at the Heart River site upstream from Lake Tschida (site 5) and near Mandan (site 22) were generally greatest in 2014 and least in 2016 for total dissolved solids, sulfate, sodium, and chloride. Most of the annual loads of total dissolved solids, sulfate, sodium, and chloride are delivered in March through July in the Heart River at these sites and are likely from snowmelt and spring and summer rains. The mean annual yields of total dissolved solids and sodium from 2013 to 2020 generally were largest in Big Muddy Creek (site 18), whereas yields of sulfate and chloride were largest at Sweetbriar Creek (site 21) compared to the other selected sites in the Heart River Basin. Larger yields of total dissolved solids, sulfate, sodium, and chloride at sites located on Big Muddy Creek and Sweet Briar Creek in the lower Heart River Basin were likely a result of differences in geology and soils upstream from the selected sites. A mass balance of total dissolved solids, sulfate, sodium, and chloride was estimated for the lower Heart River Basin, specifically the reach below Lake Tschida to Mandan (site 7 to site 22). Intervening flow was the largest contributor to the dissolved ion loads in the lower Heart River Basin and is an important part of understanding the transport of dissolved ions in the basin. The intervening load can include groundwater discharge, irrigation return flow, local runoff, and input from smaller ephemeral tributaries. Tributaries in the lower Heart River Basin contributed portions of the total dissolved solids, sulfate, sodium, and chloride loads at the Heart River near Mandan (site 22) that generally were proportional to the streamflow contributions. Annual loads for total phosphorus between 2013 and 2020 at the Heart River site upstream from Lake Tschida (site 5) and near Mandan (site 22) generally were largest in 2019 and smallest in 2016. Most of the total phosphorus loads for main-stem sites 5 and 22 were transported in March, April, and June, likely from snowmelt and early summer rains. The mean annual yields of total phosphorus for 2013–20 were largest on the main-stem site upstream from Lake Tschida (site 5) and Sweetbriar Creek (site 21), whereas the smallest yields were in Big Muddy Creek (site 18). Much of the phosphorus that enters Lake Tschida from the upper basin does not get transported downstream to the lower basin, and much of the phosphorus in the lower basin was attributed to intervening flow.

North Dakota↗

Hydrogeology, chemical characteristics, and water sources and pathways in the zone of contribution of a public-supply well in San Antonio, Texas

In 2001, the National Water-Quality Assessment (NAWQA) Program of the U.S. Geological Survey initiated a series of studies on the transport of anthropogenic and natural contaminants (TANC) to public-supply wells (PSWs). The main goal of the TANC project was to better understand the source, transport, and receptor factors that control contaminant movement to PSWs in representative aquifers of the United States. Regional- and local-scale study areas were selected from within existing NAWQA study units, including the south-central Texas Edwards aquifer. The local-scale TANC study area, nested within the regional-scale NAWQA study area, is representative of the regional Edwards aquifer. The PSW selected for study is within a well field of six production wells. Although a single PSW was initially selected, because of constraints of well-field operation, samples were collected from different wells within the well field for different components of the study. Data collected from all of the well-field wells were considered comparable because of similar well construction, hydrogeology, and geochemistry. An additional 38 PSWs (mostly completed in the confined part of the aquifer) were sampled throughout the regional aquifer to characterize water quality. Two monitoring well clusters, with wells completed at different depths, were installed to the east and west of the well field (the Zarzamora and Timberhill monitoring well clusters, respectively). One of the monitoring wells was completed in the overburden to evaluate potential hydrologic connectivity with the Edwards aquifer. Geophysical and flowmeter logs were collected from one of the well-field PSWs to determine zones of contribution to the wellbore. These contributing zones, associated with different hydrogeologic units, were used to select monitoring well completion depths and groundwater sample collection depths for depth-dependent sampling. Depth-dependent samples were collected from the PSW from three different depths and under three different pumping conditions. Additionally, selected monitoring wells and one of the well-field PSWs were sampled several times in response to a rainfall and recharge event to assess short-term (event-scale) temporal variations in water quality. For comparison purposes, groundwater samples were categorized as being from regional aquifer PSWs, from the well field (wellhead samples), from the monitoring wells (excluding the overburden well), from the overburden well, from the PSW depth-dependent sampling, and from temporal sampling. Groundwater samples were analyzed for inorganic, organic, isotopic, and age-dating tracers to characterize geochemical conditions in the aquifer and provide understanding of the mechanisms of mobilization and movement of selected constituents from source areas to a PSW. Sources, tracers, and conditions used to assess water quality and processes affecting the PSW and the aquifer system included (1) carbonate host rock composition; (2) physicochemical constituents; (3) major and trace element concentrations; (4) saturation indices with respect to minerals in aquifer rocks; (5) elemental ratios, such as magnesium to calcium ratios, that are indicative of water-rock interaction processes; (6) oxidation-reduction conditions; (7) nutrient concentrations, in particular nitrate concentrations; (8) the isotopic composition of nitrate, which can point to specific nitrate sources; (9) strontium isotopes; (10) stable isotopes of hydrogen and oxygen; (11) organic contaminant concentrations, including pesticides and volatile organic compounds; (12) age tracers, apparent-age distribution, and dissolved gas data used in age interpretations; (13) depth-dependent water chemistry collected from the PSW under different pumping conditions to assess zones of contribution; and (14) temporal variability in groundwater composition from the PSW and selected monitoring wells in response to an aquifer recharge event. Geochemical results indicate that the well-field and monitoring well samples were largely representative of groundwater in the regional confined aquifer. Constituents of concern in the Edwards aquifer for the long-term sustainability of the groundwater resource include the nutrient nitrate and anthropogenic organic contaminants. Nitrate concentrations (as nitrogen) for regional aquifer PSWs had a median value of 1.9 milligrams per liter, which is similar to previously reported values for the regional aquifer. Nitrate-isotope compositions for groundwater samples collected from the well-field PSWs and monitoring wells had a narrow range, with values indicative of natural soil organic values. A comparison with historical nitrate-isotope values, however, suggests that a component of nitrate in groundwater from biogenic sources might have increased over the last 30 years. Several organic contaminants (the pesticide atrazine, its degradate deethylatrazine, trichloromethane (chloroform; a drinking-water disinfection byproduct), and the solvent tetrachloroethene (PCE)) were widely distributed throughout the regional aquifer and in the local-scale TANC study area at low concentrations (less than 1 microgram per liter). Higher concentrations of PCE were detected in samples from the well-field PSWs and Zarzamora monitoring wells relative to the regional aquifer PSWs. The urban environment is a likely source of contaminants to the aquifer, and these results indicate that one or more local urban sources might be supplying PCE to the Zarzamora monitoring wells and the well-field wells. Samples from the well field also had high concentrations of chloroform relative to the monitoring wells and regional aquifer PSWs. For samples from the regional aquifer PSWs, the most frequently detected organic contaminants generally decreased in concentration with increasing well depth. Deeper wells might intercept longer regional flow paths with higher fractions of older water or water recharged in rural recharge areas in the western part of the aquifer that have been less affected by anthropogenic contaminants. A scenario of hypothetical contaminant loading was evaluated by using results from groundwater-flow-model particle tracking to assess the response of the aquifer to potential contamination. Results indicate that the aquifer responds quickly (less than 1 year to several years) to contaminant loading; however, it takes a relatively long time (decades) for concentrations to reach peak values. The aquifer also responds quickly (less than 1 year to several years) to the removal of contaminant loading; however, it also takes a relatively long time (decades) to reach near background concentrations. Interpretation of geochemical age tracers in this well-mixed karst system was complicated by contamination of a majority of measured tracers and complexities of extensive mixing. Age-tracer results generally indicated that groundwater samples were composed of young, recently recharged water with piston-flow model ages ranging from less than 1 to 41 years, with a median of 17 years. Although a piston-flow model is typically not valid for karst aquifers, the model ages provide a basis for comparing relative ages of different samples and a reference point for more complex hydrogeologic models for apparent-age interpretations. Young groundwater ages are consistent with particle-tracking results from hydrogeologic modeling for the local-scale TANC study area. Age-tracer results compared poorly with other geochemical indicators of groundwater residence time and anthropogenic effects on water quality, indicating that hydrogeologic conceptual models used in groundwater age interpretations might not adequately account for mixing in this karst system. Groundwater samples collected from the well field under a variety of pumping conditions were relatively homogeneous and well mixed for numerous geochemical constituents (with the notable exception of age tracers). Groundwater contributions to the PSW were dominated by well-mixed, relatively homogeneous groundwater, typical of the regional confined aquifer. Zones of preferential flow were determined for the PSW, but groundwater samples from different stratigraphic units were not geochemically distinct. Variations in chemical constituents in response to a rainfall and aquifer recharge event occurred but were relatively minor in the PSW and monitoring wells. This observation is consistent with the hypothesis that the response to individual recharge events in the confined aquifer, unless intersecting conduit flow paths, might be attenuated by mixing processes along regional flow paths. Results of this study are consistent with the existing conceptual understanding of aquifer processes in this karst system and are useful for water-resource development and management practices.

Texas↗

Occurrence and concentrations of selected trace elements and halogenated organic compounds in stream sediments and potential sources of polychlorinated biphenyls, Leon Creek, San Antonio, Texas, 2012–14

The Texas Department of State Health Services issued fish consumption advisories in 2003 and 2010 for Leon Creek in San Antonio, Texas, based on elevated concentrations of polychlorinated biphenyls (PCBs) in fish tissues. The U.S. Geological Survey (USGS) measured elevated PCB concentrations in stream-sediment samples collected during 2007&ndash;9 from Leon Creek at Lackland Air Force Base (now known as Joint Base San Antonio-Lackland; the sampling site at this base is hereinafter referred to as the &ldquo;Joint Base site&rdquo;) and sites on Leon Creek downstream from the base. This report describes the occurrence and concentrations of selected trace elements and halogenated organic compounds (pesticides, flame retardants, and PCBs) and potential sources of PCBs in stream-sediment samples collected from four sites on Leon Creek during 2012&ndash;14. In downstream order, sediment samples were collected from Leon Creek at northwest Interstate Highway 410 (Loop 410), Rodriguez Park, Morey Road, and Joint Base. The USGS periodically collected streambed-sediment samples during low flow and suspended-sediment samples during high flow. Trace element concentrations were low compared to the consensus-based sediment-quality guidelines (SQGs) for the threshold effect concentration (TEC) and probable effect concentration (PEC). Adverse effects to benthic biota are not expected at concentrations less than the TEC and are expected at concentrations greater than the PEC. No trace element concentrations were greater than the PEC in any of the samples. Trace element concentrations were greatest at the Morey Road and Joint Base sites and exceeded the TECs by 41 and 27 percent, respectively. Trace element concentrations were lowest at the Rodriguez Park and Loop 410 sites and exceeded the TECs by 18 and 14 percent, respectively. Pesticides that have been banned for several decades are commonly detected in Leon Creek stream sediments, particularly the chlordane compounds. Chlordane compounds were detected in 84 percent of the samples and at every sample collection site. The samples collected from the Rodriguez Park site had the most pesticide compounds detected. Only samples collected from the Joint Base site had dichlorodiphenyldichloroethane (DDD), dichlorodiphenyldichloroethylene (DDE), or dichlorodiphenyltrichloroethane (DDT) concentrations greater than the TEC, and a few were also greater than the PEC. Flame retardants were found at every site on Leon Creek where stream sediments were collected; however, a few compounds were frequently detected in the laboratory reagent blanks so their detections in the environmental samples may not be from local sources. Consensus-based SQGs were not available for flame retardants so samples were compared to Environment Canada Federal Environmental Quality Guidelines (FEQGs). The concentrations of flame retardants generally were greater in the suspended-sediment samples than the streambed-sediment samples and greater than the FEQGs in many cases. Eighteen PCB congeners were quantified in the sediment samples collected from Leon Creek. The samples collected from the Joint Base site had the most frequent PCB congener detections. Total PCB concentrations, computed as the sum of the 18 congeners by using the Kaplan-Meier method for left-censored environmental data, were much smaller than the TEC of 59.8 micrograms per kilogram (&mu;g/kg). When detected, the concentrations of total PCBs in the stream-sediment samples collected from Leon Creek during 2012&ndash;14 ranged from an estimated 0.2 to 8.7 &mu;g/kg. Sediment samples collected from Leon Creek by the USGS during 2007&ndash;9 and 2012&ndash;14 at a total of eight sites following identical field and laboratory methods were evaluated to determine if potential PCB sources could be identified. Total PCB concentrations in the sediment samples collected upstream from the Joint Base site were low or nondetections; while concentrations in the samples collected on and downstream from the Joint Base site were greater. Congeners 180 and 138 constituted the greatest proportion of the PCB mixture in samples collected upstream from, on, and downstream from the Joint Base site. Upstream from the Joint Base site, congeners 180 and 138 constituted 50 percent and 35 percent respectively of the PCBs congeners found in the samples. On and downstream from the Joint Base site, congeners 180 and 138 constituted 80 percent and 13 percent respectively of the PCBs congeners found in the samples. Chi-square (C2) tests also indicate that samples collected from the Loop 410 site were statistically different from samples collected from the Joint Base site and sites downstream. The PCB congener pattern in the Leon Creek samples is most like the congener mixture in Aroclor 1260, which is chemically similar to the PCBs detected in the fish samples that resulted in the 2003 fish consumption advisory.

Texas↗