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USGS1994

Physical, chemical, and biological characteristics of Pueblo Reservoir, Colorado, 1985-89

Physical, chemical, and biological characteristics of Pueblo Reservoir are described on the basis of data collected from spring 1985 through fall 1989. Also included are discussions of water quality of the upper Arkansas River Basin and the reservoir as they relate to reservoir operations. Pueblo Reservoir is a multipurpose, main-stem reservoir on the Arkansas River about 6 miles west of Pueblo, Colorado. At the top of its conservation pool, the reservoir is more than 9 miles long and ranges in depth from a few feet at the inflow to about 155 feet at the dam. Pueblo Reservoir derives most of its contents from the Arkansas River, which comprises native and transmountain flow. With respect to water temperature, the reservoir typically was well mixed to weakly stratified during the early spring and gradually became strongly stratified by May. The strong thermal stratification and underflow of the Arkansas River generally persisted into August, at which time the reservoir surface began to cool and the reservoir subsequently underwent fall turnover. Following fall turnover, the reservoir was stratified to some degree in the shallow upstream part and well mixed in the deeper middle and downstream parts. Reservoir residence times were affected by the extent of stratification present. When the reservoir was well mixed, residence times were as long as several months. During the summer when the reservoir was strongly stratified, reservoir releases were large, and when underflow was the prevalent flow pattern of the Arkansas River, reservoir residence times were as short as 30 days. Most particulate matter settled from the water column between the inflow and a distance of about 5 miles downstream. On occasions of large streamflows and sediment loads from the Arkansas River, particulate matter was transported completely through the reservoir. Water transparency, as measured with a Secchi disk, increased in a downstream direction from the reservoir inflow. The increase probably was a result of sediment settling from the water column in the upstream part of the reservoir. Secchi-disk depths in December through April were larger than those in May through November. Secchi-disk depths were small between May through August as inflow sediment loads and reservoir biomass increased. In the fall, Secchi-disk depths remained small possibly as the result of resuspension of sediment and detritus within the water column. Dissolved-oxygen concentrations generally were near supersaturation near the reservoir surface. Dissolved-oxygen concentrations decreased with increasing depth. On several occasions during the summer, dissolved oxygen became completely depleted in the hypolimnion of the downstream part of the reservoir. The most extensive period of anoxia that was measured was in August 1988; the bottom 12 to 30 feet of the downstream end of the reservoir was anoxic. Fall turnover typically resulted in well-oxygenated conditions throughout the water column from September or October through the spring. Values of pH ranged from 7.5 to 9.0 and typically were largest near the surface and decreased with depth. Dissolved-solids concentrations in the reservoir primarily are affected by dissolved solids in the inflow from the Arkansas River. Concentrations are largest during periods of decreased streamflows, September through April, and decrease with increasing streamflows in May through August. The median dissolved-solids concentration increased from 224 milligrams per liter at the inflow to 262 milligrams per liter at the outflow. However, a statistical analysis of dissolved solids indicated the apparent increase in dissolved-solids concentrations between the inflow and outflow was not significant. Calcium, sulfate, and bicarbonate are the major dissolved ions in Pueblo Reservoir. Concentrations of the major nutrients, nitrogen and phosphorus, varied within the reservoir because of settling of particulate matter, uptake by phytoplankton near the reservoir surface, and releases from the reservoir bottom sediments. Phosphorus was indicated to be a potentially growth-limiting nutrient in the reservoir because of its relatively small concentrations. During 1986 and 1987, the reservoir retained about 35 percent (359 tons) of the total nitrogen load and about 83 percent (203 tons) of the total phosphorus load. Settling of particulate matter from the water column and uptake by phytoplankton are the major nutrient sinks in the reservoir. Barium, iron, manganese, and zinc were the major trace elements in Pueblo Reservoir. Traceelement concentrations in the reservoir varied because of seasonality of trace-element concentrations in the Arkansas River, settling of particulate matter, and flux of trace elements from the bottom sediments. The aquatic-life standard in Pueblo Reservoir for total-recoverable iron (1,000 micrograms per liter) and the public water-supply standard for dissolved manganese (50 micrograms per liter) were exceeded on several occasions during the summer. Elevated concentrations of totalrecoverable iron and dissolved manganese in the Arkansas River during summer runoff contributed to exceedances in the upper part of the reservoir. Flux of manganese from the reservoir bottom sediments during periods of low or depleted dissolved-oxygen concentrations contributed to exceedances in the deeper, downstream parts of the reservoir. Concentrations of lead, mercury, and zinc were elevated in the reservoir bottom sediments and may be the result of metal-mine drainage in the upper Arkansas River Basin. Median concentrations of total organic carbon ranged from 3.1 to 4.5 milligrams per liter in May through September and from 2.5 to 3.5 milligrams per liter in October through April. Totalorganic-carbon concentrations in the reservoir were largest in the summer when streamflows and total-organic-carbon concentrations are largest in the Arkansas River. Total-organic-carbon concentrations in the reservoir decrease downstream from the reservoir inflow because of settling of particulate organic carbon. Levels of gross-alpha and gross-beta radioactivity generally were relatively low. In 7 of 31 samples collected, dissolved gross-alpha radioactivity, as natural uranium, exceeded 5 picocuries per liter, the level at which additional radiochemical analyses are recommended for drinking-water supplies. Potential sources of uranium in Pueblo Reservoir include weathering of exposed uranium ore deposits in the upper Arkansas River Basin and a uranium milling operation near Canon City. Phytoplankton densities and biovolumes measured during the winter, spring, and fall generally were indicative of a small to moderate algal biomass. Phytoplankton production tended to be largest during the summer. During the summer, phytoplankton densities and biovolumes generally were indicative of a moderate to large algal biomass. However, excessive algal production and biomass periodically occurred during the spring, summer, and fall. Three species of phytoplankton that are specifically associated with taste-and-odor problems in drinking water were identified on several occasions in water samples collected from Pueblo Reservoir. Reservoir operations and hydrodynamics can substantially affect processes that affect reservoir water quality. Stratification, underflow, and hypolimnetic withdrawals affect concentrations of dissolved solids, availability of nutrients, and concentrations of metals in the reservoir. Stratification impedes the mixing of epilimnetic and hypolimnetic waters, and the prevalent underflow that occurs during the summer results in a decrease in the potential dilution of inflowing river water with reservoir water. The underflow also decreases the maximum available nutrient load to the euphotic zone, which can, in turn, offset the maximum algal growth potential. Increased dissolved-solids, nutrient, and metal concentrations that occur in the hypolimnion during the summer are partially offset by hypolimnetic withdrawals.

Colorado↗

USGS2024

Suspended sediment and trace element transport in the Big River downstream from the Old Lead Belt in southeastern Missouri, 2018–21

Lead Belt, an area of major lead mining from the 1860s until 1972 where more than 8.5 million tons of lead were mined. After active mining ceased, the effects of mining activities persisted in the Big River system because of large mine waste pile erosion, and floodplain sediment and streambank contamination along several tributaries and the main stem of the Big River. Lead-contaminated streambed and floodplain sediments extend more than 90 miles from the Old Lead Belt to the confluence of the Big River with the Meramec River. The waste piles and mine-waste contaminated streambed and floodplain sediments have been sources of high concentrations of several trace elements, primarily cadmium, lead, and zinc. The U.S. Environmental Protection Agency Region 7 has made several efforts to prevent further erosion of contaminated sediments into the Big River including the capping of major mine waste piles, reclaiming sediment deposits along the floodplains, and monitoring soil conditions of croplands and residential properties. A cooperative effort began in 2011 between the U.S. Geological Survey and the U.S. Environmental Protection Agency Region 7 to characterize suspended sediment quantity and quality in the Big River downstream from the Old Lead Belt as reclamation activities in the drainage basin progressed. The study was completed in two phases, and each phase included continuous stage, turbidity, and water temperature monitoring at the Big River below Bonne Terre, Missouri, streamgage and sampling station. Periodic suspended sediment samples also were collected manually (discrete samples) during base flow and selected stormflow events. Continuous streamflow, turbidity, and discrete suspended sediment data were used to develop regression models to compute daily suspended sediment concentrations and loads. During both phases, the discrete stormflow event samples were also evaluated to determine particle size distribution and concentrations of select trace elements. Phase one was completed from October 2011 through September 2013, and phase two, which is the primary focus of this report, was completed from October 2018 through September 2021. Phase two also included time-integrated suspended sediment samples collected using passive samplers. Discrete samples (collected during stormflow events) and passive samples were analyzed for concentrations of barium, cadmium, lead, and zinc in two sediment size fractions (when possible) to estimate trace element loads. Suspended sediment concentrations and loads and select trace element concentration results computed during phase one were compared to those computed during phase two to identify trends in the Big River Basin during the full study period. The concentrations of cadmium, lead, and zinc in nearly all discrete stormflow event suspended sediment samples and passive suspended sediment samples exceeded the threshold effect concentrations and the probable effect concentrations, which are two sediment quality guidelines. Most samples also exceeded the toxic effect threshold, the level at which sediment is considered to be heavily contaminated and problematic for sediment-dwelling organisms. Bulk cadmium concentrations (median of 7.90 milligrams per kilogram [mg/kg]) exceeded the toxic effect threshold (3.0 mg/kg) in 17 discrete stormflow event samples, and bulk lead concentrations (median of 1,070 mg/kg) exceeded the toxic effect threshold (170 mg/kg) in all 18 discrete stormflow event samples. Bulk zinc concentrations (median of 500 mg/kg) exceeded the toxic effect threshold (540 mg/kg) in eight discrete stormflow event samples. Bulk concentrations of these trace elements in passive suspended sediment samples were slightly greater, with concentrations of cadmium (median of 14.0 mg/kg) and lead (median of 1,860 mg/kg) exceeding the toxic effect threshold in all 18 samples. Bulk concentrations of zinc (median of 733 mg/kg) exceeded the toxic effect threshold in 15 passive samples. Compared to phase one (water years 2012–13), phase two (water years 2019–21) concentrations of lead and cadmium in the fine fraction of discrete suspended sediment samples collected at Big River below Bonne Terre were statistically similar; concentrations of barium and zinc were statistically smaller in samples collected during phase two (water years 2018–21). Sediment quality data from passive samples and daily mean suspended sediment loads from the regression model were used to calculate annual oads of barium, cadmium, lead, and zinc at the Bonne Terre streamgage. Water year 2019 had the largest loads of barium, cadmium, lead, and zinc (58.6, 1.43, 194, and 76.5 tons, respectively). The total loads of barium, cadmium, lead, and zinc for phase two (water years 2019–21) were 149, 4.00, 520, and 213 tons, respectively. Less than 5 percent of the total lead load calculated for the study period was transported when daily mean streamflow was less than 455 cubic feet per second, which is the approximate flow at which the passive samplers were inundated and began sampling. This highlights that most of the lead load is transported during stormflow events and the effectiveness of using passive samplers for ongoing monitoring of the Big River. Annual suspended sediment loads at the Bonne Terre streamgage computed using the regression model were 113,000 tons in water year 2019, 83,400 tons in water year 2020, and 96,500 tons in water year 2021. The event-based suspended sediment loads for the eight sampled stormflow events ranged from 45.3 to 32,500 tons. Although only a portion of all stormflow events during phase two were sampled, the loads accounted for during these eight stormflow events represented approximately 30.9 percent of the total suspended sediment load calculated for the study period, confirming that a large part of suspended sediments continue to be transported in the Big River during stormflow events. Event-based loads of barium, cadmium, lead, and zinc were greatest during the stormflow events sampled in January 2020 (event 4) and March 2021 (event 8). Event-based loads calculated for event 4 for barium, cadmium, lead, and zinc were 17.1, 0.206, 27.2, and 14.5 tons, respectively. During event 8, an estimated 15.6 tons of barium, 0.239 tons of cadmium, 34.0 tons of lead, and 13.6 tons of zinc were transported in suspended sediments. The continued high concentrations of lead in suspended sediments in the Big River, despite reclamation activities, is likely because of the continual transport from streambed and stream banks of lead-enriched sediment, which remain in the system from historical mining activities.

Missouri↗

USGS1993

1993 Annual Report: San Francisco estuary regional monitoring program for trace substances

This first annual report of the San Francisco Estuary Regional Monitoring Program contains the results of monitoring measurements made in 1993. Measurements of conventional water quality parameters and trace contaminant concentrations were made at 16 stations throughout the Estuary three times during the year: the wet period (March), during declining Delta outflow (May), and during the dry period (September). Water toxicity tests were conducted at 8 of those stations. Measurements of sediment quality and contaminant concentrations were made at the same 16 stations during the wet and dry sampling periods. Sediment toxicity was measured at 8 of those stations. Transplanted, bagged bivalve bioaccumulation and condition was measured at 11 stations during the wet and dry sampling periods. Water Monitoring. Total or near-total (dissolved + particulate, see text) arsenic, cadmium, selenium, and dissolved (0.45 µm filtered) arsenic, cadmium, copper, nickel, silver, and zinc in water were highest in the South Bay. In general, dissolved metals in water were usually lowest in the Central Bay due to ocean influences. Near-total nickel and total mercury in water were highest in the northern estuary (San Pablo and Suisun Bays). Dissolved chromium and lead were highest at the Sacramento and San Joaquin River confluence stations. Six of the ten dissolved trace metals were highest in March during high runoff. Dissolved and total arsenic, selenium, and near-total cadmium were highest in September. Concentrations of trace organic contaminants are reported for the March sampling period. Total PAHs and PCBs were highest in the South Bay, but PCBs were also high in the Napa River. Dissolved PAHs were highest in the Central Bay, and dissolved PCBs were highest in the Napa River. Total and dissolved pesticides were highest in the Sacramento River and in the Extreme South Bay. Concentrations of trace elements in water (except selenium) were usually closely related with other environmental parameters. Total or near-total metals concentrations in water were most often associated with the amount of particulate material (TSS) in the water. Dissolved concentrations were usually associated with salinity or dissolved organic carbon (DOC) content. Dissolved PAHs were well correlated with TSS, but dissolved and total trace organic contaminants were poorly correlated with other water parameters. Based on deviations from conservative mixing of fresh and salt water, three different patterns of possible sources of metals were identified in 1993. For dissolved chromium and lead, rivers and local runoff appeared to be important sources. For dissolved arsenic, cadmium, copper, and nickel year-round inputs from the South Bay appeared to be important sources. Dissolved mercury, selenium, and zinc were associated with local runoff in the South Bay during the wet period. Dissolved silver did not fit any of these patterns. Although most contaminant concentrations were below water quality objectives, several trace contaminants were above the objectives at some stations. Comparisons to water quality objectives are used as a guide for evaluation of contaminant concentrations, but there are some differences in the way the RMP data are measured and that prescribed for regulatory purposes (see text). Concentrations of 5 metals in water were above EPA or Regional Basin Plan water quality objectives at six stations (see Table 30). Most of these elevated levels occurred at the northern estuary stations. Total PCB concentrations were above EPA human health objectives at all RMP stations. The pesticides chlordane, dieldrin, and DDTs were above the EPA objectives at several RMP stations, particularly at the northern-most, and river confluence stations. Although some of the contaminant concentrations were above water quality objectives, water toxicity tests (96 hour algal growth and 48 hour bivalve larval development tests) did not indicate toxicity (sometimes inconclusive) associated with the water samples collected at any of the RMP stations in 1993. Exposure to Bay San Francisco Estuary Regional Monitoring Program Regional Monitoring Program 1993 Report ii water actually enhanced algal growth at most stations. In addition to the Estuary-wide sampling, the Sacramento and San Joaquin Rivers were sampled upstream from their confluence. Stations in each river were sampled six times over a 6 week period of high flows. In the Sacramento River, seven of the ten dissolved metals measured had concentrations lower than those measured at the river confluence stations. Some metals concentrations in the San Joaquin River were higher, and some were lower than concentrations from the river confluence station. Metals concentrations in the Sacramento River were poorly related to river flow because the station at Rio Vista is under considerable tidal influence. In the San Joaquin River, flows were inversely related to 7 of 10 total metals concentrations. Sediment Monitoring. Concentrations of silver, mercury, and lead in sediment were highest in the South Bay. However, concentrations of most trace metals in sediments were highest in the northern estuary at stations with the finest (silt, clay) sediments. The northern estuary stations with the coarsest (sand, shell) sediments generally had the lowest metals concentrations. There were differences in concentrations of cadmium, lead, and selenium in sediments between the sampling periods, but no consistent trend as to which sampling period had higher values. In September, PAHs and PCBs in sediments were highest in the Central Bay, but pesticides in sediments were highest in the northern estuary and Extreme South Bay. NOAA’s Median Effects Ranges (ERM) for sediments were used as a guide for evaluation of sediment contaminant concentrations. Nickel was the only trace contaminant in sediment above the ERM guidelines, and it was high at all RMP stations. These high levels are probably due to natural, geologic sources. Although sediment contaminant concentrations were below ERMs, sediment toxicity tests (10 day amphipod mortality, and 48 hour bivalve larval development in elutriates) indicated toxicity at all stations tested. Sediment factors that could have caused the toxicity were not investigated. Bivalve Bioaccumulation. Mussels, oysters, and freshwater clams were transplanted to the RMP stations to evaluate bioaccumulation of trace substances. Trace metals were bioaccumulated at nearly all RMP stations. However, arsenic, lead, and mercury did not appear to bioaccumulate. There was generally more bioaccumulation during the dry season than during the wet season. In September, PAHs, PCBs, and pesticides accumulated in all samples. Bioaccumulation of PAHs and pesticides was generally highest at the river confluence stations, and the Napa River. PCBs accumulated most at Redwood Creek. There were substantial differences in the degree of bioaccumulation among the species. Oysters appeared to accumulate higher concentrations of trace metals than the other species, especially copper, which may be a natural phenomenon. There are no established tissue contaminant standards for trace metal and organic contaminants. Therefore, comparisons to Median International Standards (MIS) for human consumption, or U.S. Food and Drug Administration (USFDA) action levels for trace organics are used to evaluate the bioaccumulation results. Concentrations of selenium were higher than MIS guidelines at all stations during the wet season. Other trace metal concentrations were higher than MIS guidelines at various stations during one or the other sampling period. However, none of the bivalves contained concentrations above the USFDA or National Academy of Sciences (NAS) guidelines for trace organic contaminants. The transplanted bivalves survived well at all stations except in the Napa River where less than 35% survived during both sampling seasons. Measures of bivalve condition (dry weight, shell volume) indicated that bivalves deployed in the Central Bay grew significantly, but those at most other stations actually lost weight. Whether these differences were due to natural causes such as salinity or food supply, or to contamination, was not determined. Pilot Studies. Two pilot monitoring studies were conducted in 1993. A pilot study of Estuary hydrography and phytoplankton was conducted by scientists from the U.S. Summary Geological Survey in Menlo Park and U.C. Davis. Water column profiles at up to 37 stations were monitored along a transect of the Estuary run monthly between the South Bay and the Delta. The primary objective of this study was to define physical (salinity, temperature, suspended particulate matter, and light penetration), chemical (dissolved oxygen) and biological (chlorophyll a) characteristics of Estuary water that may influence other chemical and biological reactions. A second objective was to investigate planktonic indicators of ecosystem structure and function. The data collected in 1993 showed the extent and duration of the spring phytoplankton bloom in the South Bay, other localized blooms in the northern estuary, the stratification and mixing associated with the entrapment zone in the northern estuary, and mixing in the Estuary resulting from the high rainfall in 1993. Knowledge of the duration and extent of these natural features of the Estuary provide context for interpretation of the RMP contaminant data collected only 3 times per year. Another pilot study of suspended sediment transport processes was conducted by the USGS in Sacramento. This study used continuous recording sensors at Point San Pablo and the Bay Bridge to measure the amount of suspended sediment in the water at mid-depth and near the bottom, as well as tide height. The objectives of this study were to estimate which factors determine suspended solids concentrations in the Central Bay and to collect time series of suspended solids that are appropriate for continuous monitoring of suspended solids and for calibration and validation of numerical models. The investigators determined that spring tides accounted for most of the variation in suspended solids concentrations at the stations monitored, not runoff from the Sacramento or San Joaquin Rivers, or semidiurnal and diurnal tides. Comparisons were also made between measurements made by the continuous recordings and the RMP samples collected during the regular monitoring cruises. The different ways of measuring TSS were generally comparable, however only 3 measurements per year as made by the RMP could not provide the information of TSS variation actually occurring in the Estuary. This information is important because as shown by the RMP data, total contaminant concentrations in Estuary water is largely dependent on the TSS in the water. This implies that the RMP measurements alone cannot determine accurately the range of contaminant concentrations without better characterizing the dynamics of TSS. The RMP Pilot Studies are important to the developing RMP because they will help put RMP measurements into the perspective of Estuary processes and mechanisms at other time scales. The studies can relate those processes to the RMP measurements and will facilitate revision of sampling design and interpretation. Summaries of other monitoring activities pertinent to regional monitoring are also included in the Report: a description of the Regional Board’s Bay Protection Studies, the Sacramento Coordinated Monitoring Program, and a wetlands monitoring plan are included.

California↗

USGS2018

Assessment of dissolved-selenium concentrations and loads in the lower Gunnison River Basin, Colorado, as part of the Selenium Management Program, from 2011 to 2016

The Gunnison Basin Selenium Management Program implemented a water-quality monitoring network in 2011 in the lower Gunnison River Basin in Colorado. Selenium is a trace element that bioaccumulates in aquatic food chains and can cause reproductive failure, deformities, and other harmful effects. This report presents the percentile values of selenium because regulatory agencies in Colorado make decisions based on the U.S. Environmental Protection Agency (EPA) Clean Water Act Section 303(d) that uses percentile values of concentration. Also presented are dissolved-selenium loads at 18 sites in the lower Gunnison River Basin for water years (WYs) 2011–2016 (October 1, 2010, through September 30, 2016). Annual dissolved-selenium loads were calculated for five sites with continuous U.S. Geological Survey (USGS) streamflow-gaging stations. Annual dissolved-selenium loads for WY 2011 through WY 2016 ranged from 179 and 391 pounds (lb) at Uncompahgre River at Colona to 11,100 and 17,300 lb at Gunnison River near Grand Junction (herein called Whitewater), respectively. Instantaneous loads were calculated for five sites with continuous U.S. Geological Survey (USGS) streamflow-gaging stations and 13 ancillary sites where discrete water-quality sampling also took place, using discrete water-quality samples and the associated discharge measurements collected during the period. Median instantaneous loads ranged from 0.01 pound per day (lb/d) at Smith Fork near Lazear to 33.0 lb/d at Whitewater. Mean instantaneous loads ranged from 0.06 lb/d at Smith Fork near Lazear to 36.2 lb/d at Whitewater. Most tributary sites in the basin had a median instantaneous dissolved-selenium load of less than 20.0 lb/day. In general, dissolved-selenium loads at Gunnison River main-stem sites showed an increase from upstream to downstream. The State of Colorado water-quality standard for dissolved selenium of 4.6 micrograms per liter (µg/L) was compared to the 85th percentiles for dissolved selenium at selected sites. Annual 85th percentiles for dissolved selenium were calculated for the five core sites having USGS streamflow-gaging stations using estimated dissolved-selenium concentrations from linear regression models. The 85th-percentile concentrations for WYs 2011–2016 based on this method ranged from 0.62 µg/L and 1.1µg/L at Uncompahgre River at Colona to 12.1 µg/L and 18.7 µg/L at Uncompahgre River at Delta. The 85th percentiles for dissolved selenium also were calculated for sites with sufficient data using water-quality samples collected during WYs 2011–2016. The annual 85th-percentile concentrations based on the discrete samples ranged from 0.16 µg/L and 0.17 µg/L at Gunnison River below Gunnison Tunnel to 62.2 µg/L and 170 µg/L at Loutzenhizer Arroyo at North River Road. A trend analysis was completed for Whitewater to determine if dissolved-selenium loads are increasing or decreasing. The trend analysis indicates a decrease of 9,100 lb from WY 1986 to WY 2016, a 40.8 percent reduction during the time period. The trend analysis for the annual dissolved-selenium load for WY 1994 to WY 2016 indicates a decrease of 6,300 lb per year, or 33.3 percent.

Colorado↗

USGS2011

Distribution of trace metals at Hopewell Furnace National Historic Site, Berks and Chester Counties, Pennsylvania

Hopewell Furnace, located approximately 50 miles northwest of Philadelphia, was a cold-blast, charcoal iron furnace that operated for 113 years (1771 to 1883). The purpose of this study by the U.S. Geological Survey, in cooperation with the National Park Service, was to determine the distribution of trace metals released to the environment from an historical iron smelter at Hopewell Furnace National Historic Site (NHS). Hopewell Furnace used iron ore from local mines that contained abundant magnetite and accessory sulfide minerals enriched in arsenic, cobalt, copper, and other metals. Ore, slag, cast iron furnace products, soil, groundwater, stream base flow, streambed sediment, and benthic macroinvertebrates were sampled for this study. Soil samples analyzed in the laboratory had concentrations of trace metals low enough to meet Pennsylvania Department of Environmental Protection standards for non-residential use. Groundwater samples from the supply well met U.S. Environmental Protection Agency drinking-water regulations. Concentrations of metals in surface-water base flow at the five stream sampling sites were below continuous concentration criteria for protection of aquatic organisms. Concentrations of metals in sediment at the five stream sites were below probable effects level guidelines for protection of aquatic organisms except for copper at site HF-3. Arsenic, copper, lead, zinc, and possibly cobalt were incorporated into the cast iron produced by Hopewell Furnace. Manganese was concentrated in slag along with iron, nickel, and zinc. The soil near the furnace has elevated concentrations of chromium, copper, iron, lead, and zinc compared to background soil concentrations. Concentrations of toxic elements were not present at concentrations of concern in water, soil, or stream sediments, despite being elevated in ore, slag, and cast iron furnace products. The base-flow surface-water samples indicated good overall quality. The five sampled sites generally had low concentrations of nutrients and major ions but had elevated concentrations of iron, manganese, and strontium when compared to sites sampled in adjacent watersheds. The background site on Baptism Creek generally had the lowest concentrations and yields of constituents. Low concentrations of nutrients and major ions at all five sites indicate that measured concentrations can be attributed to general land use and geology and not to point sources. Streambed-sediment sampling results indicated higher concentrations of all metals except nickel at sites on French Creek compared to the background site on Baptism Creek. Concentrations of aluminum, cadmium, and nickel were highest in sediment from the sampling site upstream from Hopewell Furnace. The highest concentrations of arsenic, boron, cobalt, copper, iron, lead, manganese, mercury, and zinc were detected at the site just below Hopewell Furnace, which indicates that the source of these metals may be in Hopewell Furnace NHS. The invertebrate community at the background site on Baptism Creek was dominated by pollution sensitive taxa indicating a healthy, diverse benthic-macroinvertebrate community. Benthic-macroinvertebrate communities at sampling sites on French Creek indicated disturbed communities when compared to the background site on Baptism Creek and that the overall stream quality immediately above and below Hopewell Furnace NHS is degraded. The benthic-macroinvertebrate communities were dominated by pollution-tolerant taxa, and taxa were less diverse than at the background site. Habitat conditions at the upstream site on French Creek were good but were degraded at downstream sites on French Creek. The major habitat issues at these sites were related to a lack of stable substrate, erosion, and deposition. Water quality and streambed-sediment quality do not indicate that the degraded benthic-macroinvertebrate communities are the result of poor water quality. Habitat conditions (erosion and sedimentation) and physical alterations (water temperature) from the outfall of Hopewell Lake are the most likely causes of the impaired communities.

Pennsylvania↗

USGS2016

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 2007–9 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 “Joint Base site”) 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 2012–14. 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 (μg/kg). When detected, the concentrations of total PCBs in the stream-sediment samples collected from Leon Creek during 2012–14 ranged from an estimated 0.2 to 8.7 μg/kg. Sediment samples collected from Leon Creek by the USGS during 2007–9 and 2012–14 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↗

USGS2014

Groundwater-quality data in the Santa Cruz, San Gabriel, and Peninsular Ranges Hard Rock Aquifers study unit, 2011-2012: results from the California GAMA program

Groundwater quality in the 2,400-square-mile Santa Cruz, San Gabriel, and Peninsular Ranges Hard Rock Aquifers (Hard Rock) study unit was investigated by the U.S. Geological Survey (USGS) from March 2011 through March 2012, as part of the California State Water Resources Control Board (SWRCB) Groundwater Ambient Monitoring and Assessment (GAMA) Program’s Priority Basin Project (PBP). The GAMA-PBP was developed in response to the California Groundwater Quality Monitoring Act of 2001 and is being conducted in collaboration with the SWRCB and Lawrence Livermore National Laboratory (LLNL). The Hard Rock study unit was the 35th study unit to be sampled as part of the GAMA-PBP. The GAMA Hard Rock study was designed to provide a spatially unbiased assessment of untreated-groundwater quality in the primary aquifer system and to facilitate statistically consistent comparisons of untreated-groundwater quality throughout California. The primary aquifer system is defined as those parts of the aquifers corresponding to the perforation intervals of wells listed in the California Department of Public Health (CDPH) water-quality-monitoring database for the Hard Rock study unit. Groundwater quality in the primary aquifer system may differ from the quality in the shallower or deeper water-bearing zones; shallow groundwater may be more vulnerable to surficial contamination. In the Hard Rock study unit, groundwater samples were collected from 112 wells and springs in 3 study areas (the Santa Cruz, the San Gabriel, and the Peninsular Ranges) in San Mateo, Santa Clara, Santa Cruz, San Benito, Los Angeles, Orange, Riverside, San Bernardino, and San Diego Counties. Eighty-three wells and 11 springs were selected by using a spatially distributed, randomized grid-based method to provide statistical representation of the study unit (grid wells), and 15 wells and 3 springs were selected to aid in evaluation of water-quality issues (understanding wells). The groundwater samples were analyzed for field water-quality indicators; organic constituents; one constituent of special interest (perchlorate); naturally occurring inorganic constituents; and radioactive constituents. Naturally occurring isotopes and dissolved noble gases were also measured to help identify the sources and ages of the sampled groundwater. In total, 209 constituents and water-quality indicators were measured. Three types of quality-control samples (blanks, replicates, and matrix spikes) were collected at approximately 10 percent of the wells in the Hard Rock study unit, and the results for these samples were used to evaluate the quality of the data for the groundwater samples. Blanks rarely contained detectable concentrations of any constituent, suggesting that contamination from sample collection procedures was not a significant source of bias in the data for the groundwater samples. Replicate samples generally were within the limits of acceptable analytical reproducibility. Median matrix-spike recoveries were within the acceptable range (70 to 130 percent) for approximately 92 percent of the compounds. This study did not attempt to evaluate the quality of water delivered to consumers; after withdrawal from the ground, untreated groundwater typically is treated, disinfected, and (or) blended with other waters to maintain water quality. Regulatory benchmarks apply to water that is served to the consumer, not to untreated groundwater. However, to provide some context for the results, concentrations of constituents measured in the untreated groundwater were compared with regulatory and nonregulatory health-based benchmarks established by the U.S. Environmental Protection Agency (USEPA) and CDPH, and to nonregulatory benchmarks established for aesthetic concerns by the CDPH. Comparisons between data collected for this study and benchmarks for drinking water are for illustrative purposes only and are not indicative of compliance or non-compliance with those benchmarks. All organic constituents and most inorganic constituents that were detected in groundwater samples from the 112 wells in the Hard Rock study unit were detected at concentrations less than drinking-water benchmarks. Of the 149 organic and special-interest constituents, 34 were detected in groundwater samples; concentrations of all detected constituents were less than regulatory and nonregulatory health-based benchmarks. In total, VOCs were detected in 44 percent of the 94 grid wells sampled, pesticides and pesticide degradates were detected in 18 percent, and perchlorate was detected in 48 percent. Trace elements, nutrients, major and minor ions, and radioactive constituents were sampled for at 94 grid wells; most detected concentrations were less than health-based benchmarks. Exceptions in the Hard Rock study unit grid wells include 3 detections of arsenic greater than the USEPA maximum contaminant level (MCL-US) of 10 micrograms per liter (μg/L), 3 detections of boron greater than the CDPH notification level (NL-CA) of 1,000 μg/L, 2 detections of molybdenum greater than the USEPA lifetime health advisory level (HAL-US) of 40 μg/L, 2 detections of nitrite plus nitrate (as nitrogen) greater than the MCL-US of 10 milligrams per liter (mg/L), 3 detections of fluoride greater than the CDPH maximum contaminant level (MCL-CA) of 2 mg/L, 5 detections of radon-222 greater than the proposed MCL-US of 4,000 picocuries per liter (pCi/L), and 11 detections of unadjusted gross alpha radioactivity greater than the MCL-US of 15 pCi/L. Seven of the 11 samples having unadjusted gross alpha activity greater than the MCL-US also had total uranium concentrations greater than the MCL-US of 30 μg/L and (or) uranium activities greater than the MCL-CA of 20 pCi/L. Results for constituents with nonregulatory benchmarks set for aesthetic concerns showed that iron concentrations greater than the CDPH secondary maximum contaminant level (SMCL-CA) of 300 μg/L were detected in samples from 19 grid wells. Manganese concentrations greater than the SMCL-CA of 50 μg/L were detected in 27 grid wells. Chloride was detected at a concentration greater than the SMCL-CA upper benchmark of 500 mg/L in one grid well. TDS concentrations in three grid wells were greater than the SMCL-CA upper benchmark of 1,000 mg/L.

California↗

USGS2005

Radiochemical sampling and analysis of shallow ground water and sediment at the BOMARC Missile Facility, east-central New Jersey, 1999-2000

A field sampling experiment was designed using low-flow purging with a portable pump and sample-collection equipment for the collection of water and sediment samples from observation wells screened in the Kirkwood-Cohansey aquifer system to determine radionuclide or trace-element concentrations for various size fractions. Selected chemical and physical characteristics were determined for water samples from observation wells that had not been purged for years. The sampling was designed to define any particulate, colloidal, and solution-phase associations of radionuclides or trace elements in ground water by means of filtration and ultrafiltration techniques. Turbidity was monitored and allowed to stabilize before samples were collected by means of the low-flow purging technique rather than by the traditional method of purging a fixed volume of water at high-flow rates from the observation well. A minimum of four water samples was collected from each observation well. The samples of water from each well were collected in the following sequence. (1) A raw unfiltered sample was collected within the first minutes of pumping. (2) A raw unfiltered sample was collected after at least three casing volumes of water were removed and turbidity stabilized. (3) A sample was collected after the water was filtered with a 0.45-micron filter. (4) A sample was collected after the water passed through a 0.45-micron filter and a 0.003-micron tangential-flow ultrafilter in sequence. In some cases, a fifth sample was collected after the water passed through a 0.45-micron filter and a 0.05-micron filter in sequence to test for colloids of 0.003 microns to 0.05 microns in size. The samples were analyzed for the concentration of manmade radionuclides plutonium-238 and -239 plus -240, and americium-241. The samples also were analyzed for concentrations of uranium-234, -235, and -238 to determine whether uranium-234 isotope enrichment (resulting from industrial processing) is present. A subset of samples was analyzed for concentrations of thorium-232, -230, and -228 to determine if thorium-228 isotope enrichment, also likely to result from industrial processing, is present. Concentrations of plutonium isotopes and americium-241 in the water samples were less than 0.1 picocurie per liter, the laboratory reporting level for these manmade radionuclides, with the exception of one americium-241 concentration from a filtered sample. A sequential split sample from the same well did not contain a detectable concentration of americium-241, however. Other filtered and unfiltered samples of water from the same well did not contain quantities of americium-241 nearly as high as 0.1 pCi/L. Therefore, the presence of americium-241 in a quantifiable concentration in water samples from this well could not be confirmed. Neither plutonium nor americium was detected in samples of settled sediment collected from the bottom of the wells. Concentrations of uranium isotopes (maximum of 0.05 and 0.08 picocuries per liter of uranium-238 and uranium-234, respectively) were measurable in unfiltered samples of turbid water from one well and in the settled bottom sediment from 6 wells (maximum concentrations of 0.25 and 0.20 picocuries per gram of uranium-238 and uranium-234, respectively). The uranium-234/uranium-238 isotopic ratio was near 1:1, which indicates natural uranium. The analytical results, therefore, indicate that no manmade radionuclide contamination is present in any of the well-bottom sediments, or unfiltered or filtered water samples from any of the sampled wells. No evidence of manmade radionuclide contamination was observed in the aquifer as settled or suspended particulates, colloids, or in the dissolved phase.

New Jersey↗

USGS2005

Occurrence of radium-224, radium-226, and radium-228 in water of the unconfined Kirkwood-Cohansey aquifer system, southern New Jersey

Water in the unconfined Kirkwood-Cohansey aquifer system in the New Jersey Coastal Plain contains elevated concentrations (above 3 pCi/L (picocuries per liter)) of the alpha-particle-emitting radionuclide radium-224. Previously, water from the aquifer system had been found to contain radium-226 and radium-228. This observation is of concern because the previously undetected presence of radium-224 may pose an additional, quantifiable health risk that currently is not accounted for by the Maximum Contaminant Level (MCL) of 5 pCi/L for combined radium (the sum of radium-226 plus radium-228 is termed 'combined radium') in drinking water. Water samples were collected from a regional network of 88 wells for determination of concentrations of radium-224, radium-226, and radium-228; gross alpha-particle activity; and concentrations of major ions and selected trace elements. Both gamma and alpha spectroscopic techniques were used to determine concentrations of radium-224, which ranged from <0.5 to 16.8 pCi/L (median 2.1 pCi/L, interquartile range 1.2-3.7 pCi/L). Concentrations of radium-226 and radium-228 in the same samples ranged from <0.5 to 17.4 pCi/L (median 1.7 pCi/L, interquartile range 0.9-2.9 pCi/L) and <0.5 to 12.8 pCi/L (median 1.6 pCi/L, interquartile range, 0.9-2.6 pCi/L), respectively. Concentrations of radium-224 typically were greater than those of the other two radium radionuclides, as evidenced by the highest median, third quartile, and maximum concentrations, as well as the highest concentration among the three radium radioisotopes in 52 (59 percent) of the 88 samples. Concentrations of 5.0 to 5.5 pCi/L of radium-224 result in a gross alpha-particle activity of about 15 pCi/L (the MCL) 36 to 48 hours, respectively, after sample collection when ingrowth of radium-224 progeny radionuclides is considered, even with the unlikely assumption that no other alpha-particle-emitting radionuclide is present in the water. Concentrations of 3.4 to 3.7 pCi/L radium-224 result in a gross alpha-particle activity of 10 pCi/L 36 to 48 hours, respectively, after sample collection when ingrowth of Ra-224 progeny radionuclides is considered. In this latter case, it is possible that the summed alpha-particle activity from radium-226 present at a concentration less than or equal to 5 pCi/L (the MCL for combined radium) and from radium-224 present at a concentration about 3.4 pCi/L or greater may exceed the 15-pCi/L MCL for gross alpha-particle activity. In this study, gross alpha-particle activities were measured within 48 hours after sample collection and were found to exceed the MCL of 15 pCi/L in nearly half (43) of the 88 samples collected. The concentration of radium-224 exceeded that of radium-226 in 55 (62.5 percent) of the 88 samples. Concentrations of radium-224 correlate strongly with those of both radium-226 and radium-228 (Spearman correlation coefficients r=0.74 and 0.91, respectively). Concentrations of radium-224, radium-226, and radium-228 were greatest in the most acidic ground water. Concentrations of radium-224 and combined radium-226 and radium-228 in samples of ground water with pH less than 4.7 exceeded 5 pCi/L in 33 and 67 percent of the samples, respectively. Concentrations of radium-224, radium-226, and radium-228 (measured separately) were greatest in water from the southern part of the aquifer outcrop area. In water from the northern part of the aquifer system outcrop area, radium-224 concentrations were as high as 3.6 pCi/L, and concentrations of combined radium and gross alpha-particle activity in some samples exceeded their respective MCLs. The presence of gross alpha-particle activities greater than 15 pCi/L and combined radium-226 and radium-228 concentrations greater than 5 pCi/L in the southwestern part of the aquifer system outcrop area is common and had been documented before 1997. Results of this study confirm these earlier findings.

New Jersey↗

USGS2001

Water-quality conditions during low flow in the lower Youghiogheny River basin, Pennsylvania, October 5-7, 1998

In October 1998, a chemical synoptic survey was conducted by the U.S. Geological Survey, in cooperation with the U.S. Department of Energy, National Energy Technology Laboratory, in the Lower Youghiogheny River Basin in Pennsylvania to give a snapshot of present (1998) water quality during low-flow conditions. Water samples from 38 sites—12 mainstem sites, 22 tributaries, and 4 mine discharges that discharge directly to the Youghiogheny River—were used to identify sources of contaminants from mining operations. Specific conductance, water temperature, pH, and dissolved oxygen were measured in the field at each site and concentrations of major ions and trace elements were measured in the laboratory.z Unaccounted for gains and losses in streamflow were measured during the study. Unaccounted for losses in streamflow might be attributed to water loss through streambed fractures. Extensive mine tunnels are present in the basin and loss of water to these tunnels seems likely. Unaccounted for gains in streamflow may be from unmeasured tributaries or surface seeps, but most of the gains are suspected to come from artesian flow through fractures in the streambed from underground mine pools. Influent flows of rust-colored water were noted in some river sections. The pH values for all the samples collected during this survey were above 5.8, and most (33 of 38 samples) were above 7.0. Samples from the four mine-discharge sites also had pH values between 6.3 and 6.7. The lowest pH (5.8) was in a tributary, Galley Run. All 38 sampling sites had net alkalinity. The alkalinity load in the Youghiogheny River increased between Connellsville and McKeesport from 35 to 79 tons per day. Above Smithton, the measured alkalinity load in the Lower Youghiogheny River agreed well with the estimated alkalinity load. Below Smithton, measured alkalinity loads in the Lower Youghiogheny River are greater than calculated loads, resulting in unaccounted for gains in alkalinity. These gains are believed to be from seeps in the streambed. Approximately one-third of the load of total alkalinity in the Youghiogheny River at McKeesport is attributed to Sewickley Creek, which contributes 14 tons per day. Sulfate concentrations in the Youghiogheny River steadily increase from 33 milligrams per liter at Connellsville to 77 milligrams per liter near McKeesport. The measured concentrations of sulfate exceeded Pennsylvania water-quality standards at four tributary sites (Galley Run, Hickman Run, Sewickley Creek, and Gillespie Run) and all four mine-discharge sites but not at any main-stem sites. A large increase in sulfate load between West Newton and Sutersville can be attributed almost entirely to the contribution from Sewickley Creek (49 tons per day). Approximately 25 percent of the load measured between Connellsville and McKeesport is unaccounted for. These gains are believed to be from seeps in the streambed from underground mine pools. Similar patterns also were observed for loads of sodium, calcium, and magnesium. Unmeasured inputs from mine drainage are believed to be the source of these loads. Elevated concentrations (above background levels) of chemicals associated with drainage from coal-mining operations were measured in samples from tributaries, especially from Galley Run, Gillespie Run, and Sewickley Creek, and from the mine-discharge sites. The synoptic survey conducted for this study was successful in identifying generalized reaches of the Youghiogheny River where unaccounted for loads of constituents associated with mining activities are entering the river. However, the survey was not able to pinpoint the location of these loads. Remote-sensing techniques, such as thermal infrared imaging by the National Energy Technology Laboratory, could be useful for determining the precise locations of these inputs.

Water-Resources Investigations Report↗

USGS2003

Hydrology and water-quality characteristics of Muddy Creek and Wolford Mountain Reservoir near Kremmling, Colorado, 1990 through 2001

A water-quality monitoring program was begun in March 1985 on Muddy Creek in anticipation of the construction of a reservoir water-storage project. Wolford Mountain Reservoir was constructed by the Colorado River Water Conservation District during 1992-94. The reservoir began to be filled in 1995. Water quality generally was good in Muddy Creek and Wolford Mountain Reservoir throughout the period of record (collectively, 1990 through 2001), with low concentrations of nutrients (median total nitrogen less than 0.6 and median total phosphorus less than 0.05 milligrams per liter) and trace elements (median dissolved copper less than 2, median dissolved lead less than 1, and median dissolved zinc less than 20 micrograms per liter). Specific conductance ranged from 99 to 1,720 microsiemens per centimeter. Cation compositions at Muddy Creek sites were mixed calcium-magnesium-sodium. Anion compositions were primarily bicarbonate and sulfate. Suspended-sediment concentrations ranged from less than 50 milligrams per liter during low-flow periods to hundreds of milligrams per liter during snowmelt. Turbidity in prereservoir Muddy Creek generally was measured at less than 10 nephelometric turbidity units during low-flow periods and ranged to more than 360 nephelometric turbidity units during snowmelt. Compared to prereservoir conditions, turbidity in Muddy Creek downstream from the reservoir was substantially reduced because the reservoir acted as a sediment trap. During most years, peak flows were slightly reduced by the reservoir or similar to peaks upstream from the reservoir. The upper first to fifteenth percentiles of flows were decreased by operation of the reservoir compared to prereservoir flows. Generally, the fifteenth to one-hundredth percentiles of flow were increased by operation of the reservoir outflow compared to prereservoir flows. Nutrient transport in the inflow is proportional to the amount of inflow-water discharge in a given year. Some nitrogen was stored in the water column and gain/loss patterns for total nitrogen were somewhat related to reservoir storage. Nitrogen tended to move through the reservoir, whereas phosphorus was mostly trapped within the reservoir in bottom sediments. The reservoir gained phosphorus every year (1996- 2001) and, as a percentage, more phosphorus was retained than nitrogen in years when both were retained in the reservoir due to stronger phosphorus tendencies for adsorption, coprecipitation, and settling. Only small amounts of phosphorus were available in the water column at the outflow, and reservoir water-column storage did not influence phosphorus outflowloading patterns as much as settling further upstream in the reservoir. From 1990 to 2001, upstream from the reservoir, concentrations and values of dissolved solids, turbidity, some major ions, and dissolved iron increased (p-value less than 0.10), and acid-neutralizing capacity decreased. From 1990 to 2001, there were no significant (p-value less than 0.10) trends in nutrient concentrations upstream from the reservoir. From 1990 to 2001, downstream from the reservoir, trends in concentrations and values of dissolved solids, turbidity, major ions, total ammonia plus organic nitrogen, dissolved and total-recoverable iron, and total-recoverable manganese were downward. Upstream and downstream water-quality constituents for the prereservoir (1990 to 1995) period were compared. Concentrations and values of dissolved solids, major ions, turbidity, and manganese were greater (p-value less than 0.10) at the downstream site. From 1995 to 2001 (postconstruction), upstream and downstream water-quality constituents also were compared. Concentrations of specific conductance and major ions increased at the downstream site when compared to the upstream site (p-value less than 0.10), except for acid-neutralizing capacity and silica, which decreased. Turbidity, concentrations of total-recoverable and dissolved manganese, and

Water-Resources Investigations Report↗

USGS2003

Hydrology and water quality of Elkhead Creek and Elkhead Reservoir near Craig, Colorado, July 1995–September 2001

The U.S. Geological Survey, in cooperation with the Colorado River Water Conservation District, collected and analyzed baseline streamflow and water-quality information for Elkhead Creek and water-quality and trophic-state information for Elkhead Reservoir from July 1995 through September 2001. In the study area, Elkhead Creek is a meandering, alluvial stream dominated by snowmelt in mountainous headwaters that produces most of the annual discharge volume and discharge peaks during late spring and early summer. During most of water year 1996 (a typical year), daily mean discharge at station 09246400 (downstream from the reservoir) was similar to daily mean discharge at station 09246200 (upstream from the reservoir). Flow-duration curves for stations 09246200 and 09246400 were nearly identical, except for discharges less than about 10 cubic feet per second. Specific conductance generally had an inverse relation to discharge in Elkhead Creek. During late fall and winter when discharge was small and derived mostly from ground water, specific conductance was high, whereas during spring and early summer, when discharge was large and derived mostly from snowmelt, specific conductance was low. Water temperatures in Elkhead Creek were smallest during winter, about 0.0 degrees Celsius ( o C), and largest during summer, about 20–25 o C. Concentrations of major ions, nutrients, trace elements, organic carbon, and suspended sediment in Elkhead Creek indicated no substantial within-year variability and no substantial differences in variability from one year to the next. A seasonal pattern in the concentration data was evident for most constituents. The seasonal concentration pattern for most of the dissolved constituents followed the seasonal pattern of specific conductance, whereas some nutrients, some trace elements, and suspended sediment followed the seasonal pattern of discharge. Statistical differences between station 09246200 (upstream from the reservoir) and station 09246400 (downstream from the reservoir) were indicated for specific conductance, dissolved calcium, magnesium, sodium, and sulfate, acid-neutralizing capacity, and dissolved solids. Trend analysis indicated upward temporal trends for pH, dissolved ammonia plus organic nitrogen, total nitrogen, and total phosphorus at station 09246200; upward temporal trends for dissolved and total ammonia plus organic nitrogen, total nitrogen, and total phosphorus were indicated at station 09246400. No downward trends were indicated for any constituents. Annual loads for dissolved constituents during water years 1996–2001 were consistently larger at station 09246400 than at station 09246200, except for silica and sulfate. Mean monthly loads for dissolved constituents followed the seasonal pattern of discharge, indicating that most of the annual loads were transported during March–June. Annual dissolved nutrient loads at stations 09246400 and 09246200 were not substantially different, except for total phosphorus and total nitrogen loads, which were smaller at the downstream station than at the upstream station, most likely due to biological uptake and settling in the reservoir. Mean annual suspended-sediment load during water years 1996–2001 was about 87-percent smaller at the downstream station than at the upstream station. Temperature in Elkhead Reservoir varied seasonally, from about 0 o C during winter when ice develops on the reservoir to about 20 o C during summer. Specific conductance varied from minimums of 138 to 169 microsiemens per centimeter at 25 o C (µS/cm) during snowmelt inflow to maximums of 424 to 610 µS/cm during early spring low flow (April). Median pH in the reservoir ranged from 7.2 to 8.0 at all sites near the surface. Median dissolved oxygen ranged from 7.1 to 7.2 milligrams per liter (mg/L) in near-surface samples and from 4.8 to 5.6 mg/L in near-bottom samples. During reservoir stratification, specific conductance generally was largest in the epilimnion, resulting from warm and relatively concentrated water from Elkhead Creek that was routed through the reservoir in the relatively warm epilimnion. The pH in the epilimnion generally increased from May to September, probably a result of algal productivity. In the hypolimnion, pH decreased slightly with depth in the July and September, probably a result of biomass decay processes and a lack of circulation during stratification. Concentrations of nutrients in both near-surface and near-bottom samples from Elkhead Reservoir were highest during snowmelt inflow (April–May). Total phosphorus concentrations in near-surface samples generally were largest during runoff, whereas total phosphorus concentrations in near-bottom samples generally were largest during July or September. Concentrations of nitrite plus nitrate in near-surface samples were substantially depleted by biological uptake during July, September, and October, compared to near-bottom samples. Variations in concentration of chlorophyll- a in near-surface samples were large during the growing season with peak seasonal concentrations during runoff or late summer and fall. Trophic state for Elkhead reservoir ranged from oligotrophic to eutrophic.

Colorado↗

USGS2003

Survival, transport, and sources of fecal bacteria in streams and survival in land-applied poultry litter in the upper Shoal Creek basin, southwestern Missouri, 2001–2002

Densities of fecal coliform bacteria along a 5.7-mi (mile) reach of Shoal Creek extending upstream from State Highway 97 (site 3) to State Highway W (site 2) and in two tributaries along this reach exceeded the Missouri Department of Natural Resources (MDNR) standard of 200 col/100 mL (colonies per 100 milliliters) for whole-body contact recreation. A combination of techniques was used in this report to provide information on the source, transport, and survival of fecal bacteria along this reach of Shoal Creek. Results of water-quality samples collected during dye-trace and seepage studies indicated that at summer low base-flow conditions, pastured cattle likely were a substantial source of fecal bacteria in Shoal Creek at the MDNR monitoring site (site 3) at State Highway 97. Using repeat element Polymerase Chain Reaction (rep-PCR), cattle were the presumptive source of about 50 percent of the Escherichia coli ( E. coli ) isolates in water samples from site 3. Cattle, horses, and humans were the most common presumptive source of E. coli isolates at sites further upstream. Poultry was identified by rep-PCR as a major source of E. coli in Pogue Creek, a tributary in the upper part of the study area. Results of the rep-PCR were in general agreement with the detection and distribution of trace concentrations of organic compounds commonly associated with human wastewater, such as caffeine, the antimicrobial agent triclosan, and the pharmaceutical compounds acetaminophen and thiabendazole (a common cattle anthelmintic). Significant inputs of fecal bacteria to Shoal Creek occurred along a 1.6-mi reach of Shoal Creek immediately upstream from site 3. During a 36-hour period in July 2001, average densities of fecal coliform and E. coli bacteria increased from less than or equal to 500 col/100 mL upstream from this stream reach (sample site 2c) to 2,100 and 1,400 col/100 mL, respectively, at the MDNR sampling site. Fecal bacteria densities exhibited diurnal variability at all five sampling sites along the 5.7-mi study reach of Shoal Creek, but the trends at successive downstream sites were out of phase and could not be explained by simple advection and dispersion. At base-flow conditions, the travel time of bacteria in Shoal Creek along the 5.7-mi reach between State Highway W (site 2) and the MDNR sampling site (site 3) was about 26 hours. Substantial dispersion and dilution occurs along the upper 4.1 mi of this reach because of inflows from a number of springs and tributaries and the presence of several long pools and channel meanders. Minimal dispersion and dilution occurs along the 1.6-mi reach immediately upstream from the MDNR sampling site. Measurements of fecal bacteria decay in Shoal Creek during July 2001 indicated that about 8 percent of fecal coliform and E. coli bacteria decay each hour with an average first-order decay constant of 0.084 h -1 (per hour). Results of field test plots indicated that substantial numbers of fecal bacteria present in poul try litter can survive in fields for as much as 8 weeks after the application of the litter to the land surface. Median densities of fecal coliform and E. coli in slurry-water samples collected from fields increased from less than 60 col/100 mL before the application of turkey and broiler litter, to as large as 420,000 and 290,000 col/100 mL after the application of litter. Bacteria densities in the test plots generally decreased in a exponential manner over time with decay rates ranging from 0.085 to 0.185 d -1 (per day) for fecal coliform to between 0.100 and 0.250 d -1 for E. coli . The apparent survival of significant numbers of fecal bacteria on fields where poultry litter has been applied indicates that runoff from these fields is a potential source of fecal bacteria to vicinity streams for many weeks following litter application.

Water-Resources Investigations Report↗

USGS2022

Characterization of ambient groundwater quality within a statewide, fixed-station monitoring network in Pennsylvania, 2015–19

Pennsylvania leads the Nation in the number of individuals that use groundwater for private domestic water supply; more than 3 million rural and suburban Pennsylvania residents rely on private domestic supplies for drinking water. These supplies are not regulated nor routinely monitored; thus relevant groundwater-quality information is not widely available. The U.S. Geological Survey (USGS), in cooperation with the Pennsylvania Department of Environmental Protection (PaDEP) Safe Drinking Water Bureau, established a statewide, fixed-station ambient groundwater quality network in 2015. The goals for the Pennsylvania Groundwater Monitoring Network (GWMN) include characterizing ambient groundwater quality conditions in rural areas of the State and documenting potential changes in conditions over time. Seventeen wells were selected for monitoring at 6-month intervals beginning in 2015. Since then, several wells have been added to the GWMN, bringing the total number of wells sampled in the fall of 2019 to 28. Routinely monitored constituents included physical characteristics and chemical concentrations in filtered and unfiltered samples (major and trace elements, nutrients, and organic compounds). Samples for volatile organic compounds (VOCs), radionuclides, and dissolved hydrocarbon gases were collected during the first sampling event at each well. To offer insights on the quality of groundwater used for domestic supply in Pennsylvania, summary statistics for the 221 GWMN samples collected during 2015–19 are compared to U.S. Environmental Protection Agency (EPA) drinking-water standards, which are applicable to public water supplies. Results show that samples across the GWMN generally meet drinking-water standards for inorganic and organic constituents; however, a percentage of samples had concentrations that exceeded maximum contaminant level (MCL) thresholds for nitrate (3 percent) and secondary maximum contaminant level (SMCL) thresholds for iron (32 percent), manganese (36 percent), and aluminum (5 percent). Radon-222 activities, which were sampled only during the initial visit to a well, exceeded the lower proposed drinking water standard of 300 picocuries per liter (pCi/L) in 64 percent of wells in the GWMN; additionally, 7 percent of wells exceeded the higher proposed standard of 4,000 pCi/L. There were no exceedances for VOCs, but one well had a tribromomethane detection. Three wells had detectable concentrations of methane, with one sample exceeding the Pennsylvania action level of 7 milligrams per liter (mg/L). The pH and dissolved oxygen concentrations varied widely across the GWMN and were correlated with dissolved metal concentrations and other chemical characteristics of groundwater samples. Considering all samples collected for the study, the pH ranged from 4.2 to 8.3; 42 percent of pH values were either above or below the SMCL range of 6.5–8.5. The highest pH values resulted from contamination of loose grout used in the construction of one well and decreased to levels consistent with other wells in the vicinity after repeated sampling rounds. Dissolved oxygen (DO), which ranged from 0 to 13.9 mg/L, influences the mobility and prevalence of constituents with variable oxidation state, including iron, manganese, and nitrogen species. Samples with acidic pH (less than 6.5) and (or) low DO had the highest concentrations of manganese and iron, whereas those with neutral to alkaline pH values had the highest concentrations of calcium, magnesium, sodium, and other major ions. Analysis of major ions indicates that calcium/bicarbonate water types are the most common, with a few characterized as calcium/chloride or sodium/chloride, and most others as mixed water types including calcium-magnesium/bicarbonate, sodium-magnesium/bicarbonate, and sodium/bicarbonate-chloride. Nonparametric statistical methods were used to evaluate the data for spatial and temporal trends. A principal components analysis (PCA) model developed with ranked data values for the entire network resulted in three components, (1) dissolved solids, (2) redox, and (3) sodium-chloride, which explained 74.5 percent of variance in the dataset. On the basis of individual contributions to the PCA, certain wells were identified through hierarchical cluster analysis that shared relevant water-quality characteristics. The spatial distribution of sampling locations and the temporal trends of constituent concentrations indicate that hydrogeologic setting and topographic position as defined in the PCA model are important factors affecting the spatial and temporal patterns of groundwater quality in the GWMN.

Pennsylvania↗

USGS2004

Vertical gradients in water chemistry and age in the southern High Plains Aquifer, Texas, 2002

The southern High Plains aquifer is the primary source of water used for domestic, industrial, and irrigation purposes in parts of New Mexico and Texas. Despite the aquifer's importance to the overall economy of the southern High Plains, fundamental ground-water characteristics, such as vertical gradients in water chemistry and age, remain poorly defined. As part of the U.S. Geological Survey's National Water-Quality Assessment Program, water samples from nested, short-screen monitoring wells installed in the southern High Plains aquifer at two locations (Castro and Hale Counties, Texas) were analyzed for field parameters, major ions, nutrients, trace elements, dissolved organic carbon, pesticides, stable and radioactive isotopes, and dissolved gases to evaluate vertical gradients in water chemistry and age in the aquifer. Tritium measurements indicate that recent (post-1953) recharge was present near the water table and that deeper water was recharged before 1953. Concentrations of dissolved oxygen were largest (2.6 to 5.6 milligrams per liter) at the water table and decreased with depth below the water table. The smallest concentrations were less than 0.5 milligram per liter. The largest major-ion concentrations generally were detected at the water table because of the effects of overlying agricultural activities, as indicated by postbomb tritium concentrations and elevated nitrate and pesticide concentrations at the water table. Below the zone of agricultural influence, major-ion concentrations exhibited small increases with depth and distance along flow paths because of rock/water interactions and mixing with water from the underlying aquifer in rocks of Cretaceous age. The concentration increases primarily were accounted for by dissolved sodium, bicarbonate, chloride, and sulfate. Nitrite plus nitrate concentrations at the water table were 2.0 to 6.1 milligrams per liter as nitrogen, and concentrations substantially decreased with depth in the aquifer to a maximum concentration of 0.55 milligram per liter as nitrogen. Dissolved-gas and nitrogen-isotope data from the deep wells in Castro County indicate that denitrification occurred in the aquifer, removing 74 to more than 97 percent of the nitrate originally present in recharge. There was no evidence of denitrification in the deep part of the aquifer in Hale County. After correcting for denitrification effects, the background concentration of nitrate in water recharged before 1953 ranged from 0.4 to 3.2 milligrams per liter as nitrogen, with an average of 1.6 milligrams per liter as nitrogen. The d15N composition of background nitrate at the time of recharge was estimated to range from 9.6 to 12.3 per mil. Mass-balance models indicate that the decreases in dissolved oxygen and nitrate concentrations and small increases in major-ion concentrations along flow paths can be accounted for by small amounts of silicate-mineral and calcite dissolution; SiO2, goethite, and clay-mineral precipitation; organic-carbon and pyrite oxidation; denitrification; and cation exchange. Mass-balance models for some wells also required mixing with water from the underlying aquifer in rocks of Cretaceous age to achieve mole and isotope balances. Carbon mass transfers identified in the models were used to adjust radiocarbon ages of water samples recharged before 1953. Adjusted radiocarbon ages ranged from less than 1,000 to 9,000 carbon-14 years before present. Radiocarbon ages were more sensitive to uncertainties in the carbon-14 content of recharge than uncertainties in carbon mass transfers, leading to 1-sigma uncertainties of about ?2,000 years in the adjusted ages. Despite these relatively large uncertainties in adjusted radiocarbon ages, it appears that deep water in the aquifer was considerably older (at least 1,000 years) than water near the water table. There was essentially no change in ground-water age with depth in deeper parts of the aquifer, indicating that water in that

Texas↗

USGS2011

Contributing recharge areas, groundwater travel time, and groundwater quality of the Missouri River alluvial aquifer near the Independence, Missouri, well field, 1997-2008

The City of Independence, Missouri, operates a well field in the Missouri River alluvial aquifer. Contributing recharge areas (CRA) were last determined for the well field in 1996. Since that time, eight supply wells have been installed in the area north of the Missouri River and well pumpage has changed for the older supply wells. The change in pumping has altered groundwater flow and substantially changed the character of the CRA and groundwater travel times to the supply wells. The U.S Geological Survey, in a cooperative study with the City of Independence, Missouri, simulated steady-state groundwater flow for 2007 well pumpage, average annual river stage, and average annual recharge. Particle-tracking analysis was used to determine the CRA for supply wells and monitoring wells, and the travel time from recharge areas to supply wells, recharge areas to monitoring wells, and monitoring wells to supply wells. The simulated CRA for the well field is elongated in the upstream direction and extends to both sides of the Missouri River. Groundwater flow paths and recharge areas estimated for monitoring wells indicate the origin of water to each monitoring well, the travel time of that water from the recharge area, the flow path from the vicinity of each monitoring well to a supply well, and the travel time from the monitoring well to the supply well. Monitoring wells 14a and 14b have the shortest groundwater travel time from their contributing recharge area of 0.30 years and monitoring well 29a has the longest maximum groundwater travel time from its contributing recharge area of 1,701 years. Monitoring well 22a has the shortest groundwater travel time of 0.5 day to supply well 44 and monitoring well 3b has the longest maximum travel time of 31.91 years to supply well 10. Water-quality samples from the Independence groundwater monitoring well network were collected from 1997 to 2008 by USGS personnel during ongoing annual sampling within the 10-year contributing recharge area (CRA) of the Independence well field. Statistical summaries and the spatial and temporal variability of water quality in the Missouri River alluvial aquifer near the Independence well field were characterized from analyses of 598 water samples. Water-quality constituent groups include dissolved oxygen and physical properties, nutrients, major ions and trace elements, wastewater indicator compounds, fuel compounds, and total benzene, toluene, ethylbenzene, and xylene (BTEX), alachlor, and atrazine. The Missouri Secondary Maximum Contaminant Level (SMCL) for iron was exceeded in almost all monitoring wells. The Missouri Maximum Contaminant Level (MCL) for arsenic was exceeded 32 times in samples from monitoring wells. The MCL for barium was exceeded five times in samples from one monitoring well. The SMCL for manganese was exceeded 160 times in samples from all monitoring wells and the combined well-field sample. The most frequently detected wastewater indicator compounds were N,N-diethyl-meta-toluamide (DEET), phenol, caffeine, and metolachlor. The most frequently detected fuel compounds were toluene and benzene. Alachlor was detected in 22 samples and atrazine was detected in 37 samples and the combined well-field sample. The MCL for atrazine was exceeded in one sample from one monitoring well. Samples from monitoring wells with median concentrations of total inorganic nitrogen larger than 1 milligram per liter (mg/L) are located near agricultural land and may indicate that agricultural land practices are the source of nitrogen to groundwater. Largest median values of specific conductance; total inorganic nitrogen; dissolved calcium, magnesium, sodium, iron, arsenic, manganese, bicarbonate, and sulfate and detections of wastewater indicator compounds generally were in water samples from monitoring wells with CRAs that intersect the south bank of the Missouri River. Zones of higher specific conductance were located just upstream from the Independence well field at south-bank outfalls from wastewater treatment plants, the Blue River, and the south bank of the Missouri River near the closed oil refinery. The long-term presence of these south-bank outfalls and the large specific conductance indicate that the surface water at the south bank of the Missouri River near the Independence well field may have consistently higher dissolved solids and nutrients that can be induced into the aquifer by pumping. Large median concentrations of sodium and chloride from samples from monitoring wells may be the result of road salt use on State Highway 291 or from Mill Creek, which drains the uplands south of the Independence well field. Large median concentrations of arsenic in samples from some monitoring well nests are most likely associated with dissolution of iron and sulfide minerals and fluctuation between oxidizing and reducing conditions. Largest median concentrations for arsenic are in the shallow depth interval where fluctuations between oxidizing and reducing conditions occur. Median concentrations of iron are large in all monitoring wells and are most likely caused by the interaction between fluctuating oxidizing and reducing conditions and siderite and ferric hydroxide. Spatial and temporal trends are not evident from the fuel compounds or total BTEX sample results. Alachlor and atrazine were detected in most monitoring wells and atrazine was detected more often than alachlor. The source of alachlor and atrazine in groundwater near the Independence well field is most likely from nearby agricultural land management practices and (or) the Missouri River. Many of the samples from monitoring wells with alachlor or atrazine detections greater than 10 percent have contributing recharge areas that intersect either agricultural land or the Missouri River bed.

Missouri↗

USGS2011

Assessment of surface-water quantity and quality, Eagle River watershed, Colorado, 1947-2007

From the early mining days to the current tourism-based economy, the Eagle River watershed (ERW) in central Colorado has undergone a sequence of land-use changes that has affected the hydrology, habitat, and water quality of the area. In 2000, the USGS, in cooperation with the Colorado River Water Conservation District, Eagle County, Eagle River Water and Sanitation District, Upper Eagle Regional Water Authority, Colorado Department of Transportation, City of Aurora, Town of Eagle, Town of Gypsum, Town of Minturn, Town of Vail, Vail Resorts, City of Colorado Springs, Colorado Springs Utilities, and Denver Water, initiated a retrospective analysis of surface-water quantity and quality in the ERW. Surface-water quantity data and surface-water quality data were obtained from local, State, and Federal agencies to assist in the analysis of surface-water conditions in the ERW 1947-2007. Surface-water-quality data from 293 sites and 12 different source agencies were compiled into 192 unique sites located on streams and rivers in the ERW. Approximately 39 percent of the unique sites had fewer than 5 samples; while 23 percent of the sites had more than 100 samples. Physical properties were the most abundant type of samples collected, with major ions, nutrients, and trace elements also commonly collected. For selected water-quality properties and constituents in the watershed, this report: (1) characterizes available water quantity and water-quality data, (2) identifies spatial and seasonal variability in water quantity and water quality, (3) provides comparisons to Federal and State water-quality standards or recommendations, (4) characterizes temporal changes in water quality, and (5) where possible, identifies potential causes of these changes. This report provides reconnaissance-level statistical summaries and comparisons of water-quality conditions and characteristics using available data within the ERW. The report also includes streamflow statistics such as: mean annual runoff totals, peak-flood-frequency recurrence intervals, and minimum 7-day mean streamflows for selected sites within the watershed. The spatial patterns for concentrations of trace metals (aluminum, cadmium, copper, iron, manganese, and zinc) indicate an increase in dissolved concentrations of these metals near historical mining areas in the Eagle River and several tributaries near Belden. In general, concentrations decrease downstream from mining areas. Concentrations typically are near or below reporting limits in Gore Creek and other tributaries within the watershed. Concentrations for trace elements (arsenic, selenium, and uranium) in the watershed usually are below the reporting limit, and no prevailing spatial patterns were observed in the data. Step-trend analysis and temporal-trend analysis provide evidence that remediation of historical mining areas in the upper Eagle River have led to observed decreases in metals concentrations in many surface-waters. Comparison of pre- and post-remediation concentrations for many metals indicates significant decreases in metals concentrations for cadmium, manganese, and zinc at sites downstream from the Eagle Mine Superfund Site. Some sites show order of magnitude reductions in median concentrations between these two periods. Evaluation of monotonic trends for dissolved metals concentrations show downward trends at numerous sites in, and downstream from, historic mining areas. The spatial pattern of nutrients shows lower concentrations on many tributaries and on the Eagle River upstream from Red Cliff with increases in nutrients downstream of major urban areas. Seasonal variations show that for many nutrient species, concentrations tend to be lowest May-June and highest January-March. The gradual changes in concentrations between seasons may be related to dilution effects from increases and decreases in streamflow. Upward trends in nutrients between the towns of Gypsum and Avon were detected for nitrate, orthophosphate, and total phosphorus. An upward trend in nitrite was detected in Gore Creek. No trends were detected in un-ionized ammonia within the ERW. Exceedances of State water-quality standards (nitrite, nitrate, and un-ionized ammonia) and levels higher than U.S. Environmental Protection Agency recommendations (total phosphorus) occur in several areas within the ERW. The majority of the exceedances are from comparisons to the U.S. Environmental Protection Agency total phosphorus recommendations. A positive correlation was observed between suspended sediment and total phosphorus. An upward trend in total dissolved solids in Gore Creek may be the result of increases in chloride salts. Highly significant trends were detected in sodium, potassium, and chloride with a significant upward trend in magnesium and a weakly significant upward trend in calcium. A quantitative analysis of the relative abundance of calcium, magnesium, sodium, and potassium to the available anions suggests that chloride salts likely are the source for the detected upward trends because chloride is the only commonly occurring anion with a trend in Gore Greek. A potential source for the observed chloride salts may be the chemical anti-icing and deicing products used during winter road maintenance in municipal areas and on Interstate-70. A downward trend in dissolved solids in the Eagle River between Gypsum and Avon may be contributing to the detected trend on the Eagle River at Gypsum. Significant downward trends were detected in specific ions such as calcium, magnesium, sulfate, and silica. Measures of total dissolved solids as well as comparisons to specific ions show that in water-quality samples within the ERW concentrations generally are lower in the headwaters, with increases downstream from Wolcott. Differences in concentrations likely result from increased abundance of salt-bearing geologic units downstream from Avon. Few sites had measured concentrations that exceeded the State standards for chloride.

Scientific Investigations Report↗

USGS2000

Hydrogeology of the regional aquifer near Flagstaff, Arizona, 1994-97

Sandstones, siltstones, and limestones that are Pennsylvanian to Permian in age underlie the southern part of the Colorado Plateau near Flagstaff, Arizona, and contain a complex regional aquifer that has become increasingly important as a source of water for domestic, municipal, and recreational uses. Ground-water flow in the regional aquifer is poorly understood in this area because (1) depth of the aquifer limits exploratory drilling and testing and (2) the geologic structure increases the complexity of the aquifer characteristics and the ground-water flow system. Four methods were used to improve the understanding of the hydrogeology of the regional aquifer near Flagstaff. • Remote-sensing techniques and geologic mapping provided data to identify many structural features that indicate a more complex structural environment and history than previously realized. • Data from surface-geophysical techniques that included ground-penetrating radar, seismic reflection and seismic refraction, and square-array resistivity, verified that some of the geologic structures expressed at land surface propagate deep into the subsurface and through the principal water-bearing zones of the regional aquifer at near-vertical angles. • A well and spring inventory, borehole-geophysical methods, and well and aquifer tests provided additional information relating aquifer and ground-water flow characteristics to geologic structure. • Water-chemistry data, which included major ion, nutrient, trace-element, and radioactive and stable-isotope analyses, provided an independent means of verifying the hydrogeologic characteristics of the aquifer and were used to determine recharge and discharge areas, groundwater movement, and ground-water age. Ground-water recharge occurs throughout the area but is greatest at higher altitudes where precipitation is greater and in areas where heavily fractured rock units of the aquifer are exposed. The estimated annual average recharge to the regional aquifer in the study area is about 290,000 acre-feet. Ground water flows laterally and vertically through pore spaces in the rock and along faults and other fractures from high-altitude areas in the southern part of the study area to regional drains north of the study area along the Little Colorado and Colorado Rivers, and to drains south of the study area along Oak Creek and the Verde Valley. Ground-water discharge in these areas—about 400,000 acre-feet per year—exceeds the annual recharge to the aquifer in the Flagstaff area, but ground water from areas outside the study area contributes to this discharge as well. The saturated thickness of the regional aquifer averages about 1,200 feet, and the amount of water in storage could be as much as 4,800,000 acrefeet, or about 10 percent of the total volume of the aquifer. The quality of water in the regional aquifer in terms of dissolved-solids concentrations is good for most uses throughout the area. Dissolvedsolids concentrations generally are less than 500 milligrams per liter. Water in the regional aquifer is primarily a calcium magnesium bicarbonate type. In some areas near the Rio de Flag, the water has significant nitrate and chloride components, which indicate direct recharge in these areas from the Rio de Flag. Oxygen and deuterium data indicate a common recharge source for water in the aquifer and that some sites receive recharge from surface waters where evaporation has occurred. Estimated carbon-14 ages and tritium activities indicate ground-water ages from less than 200 years in the Lake Mary area to more than 5,000 years in the Wupatki area. The regional aquifer is heterogeneous and anisotrophic and has a complex ground-water flow system. The most productive water-bearing material tends to be fine- to medium-grained sandstones, and ground-water flow and potential well yields are related to geologic structure. Fracturing associated with structural deformation increases recharge locally and also increases the potential for high well yields. Surface-geophysical techniques provided information on the orientation of high-angle, deep-seated structure in the saturated zone. Borehole-geophysical data identified horizontal to near-horizontal fractures as significant components of the fracture-flow system not apparent in the surface-geophysical data. Structural features that strike northwest appear to be areas that have the greatest potential for high well yields. A north-northeastward-striking structure may be just as promising, but additional data are needed to verify this relation.

Arizona↗