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At least 1,441 records · Page 80Linked to original sources
USGS2007

Occurrence of Agricultural Chemicals in Shallow Ground Water and the Unsaturated Zone, Northeast Nebraska Glacial Till, 2002-04

Agricultural chemicals applied at the land surface in northeast Nebraska can move downward, past the crop root zone, to ground water. Because agricultural chemicals applied at the land surface are more likely to be observed in the shallowest part of an aquifer, an assessment of shallow ground-water and unsaturated zone quality in the northeast Nebraska glacial till was completed between 2002 and 2004. Ground-water samples were collected at the first occurrence of ground water or just below the water table at 32 sites located in areas likely affected by agriculture. Four of the 32 sites were situated along a ground-water flow path with its downgradient end next to Maple Creek. Twenty-eight sites were installed immediately adjacent to agricultural fields throughout the glacial-till area. In addition to those 32 sites, two sites were installed in pastures to represent ground-water conditions in a non-cropland setting. Ground-water samples were analyzed for physical properties and concentrations of nitrogen and phosphorus compounds, selected pesticides and pesticide degradates, dissolved solids, major ions, trace elements, and dissolved organic carbon. Chlorofluorocarbons (CFCs) or sulfur hexafluoride (SF6) concentrations were analyzed at about 70 percent of the monitoring wells to estimate the residence time of ground water. Borehole-core samples were collected from 28 of the well boreholes. Sediment in the unsaturated zone was analyzed for nitrate, chloride, and ammonia concentrations. Analytical results indicated that the agricultural chemicals most often detected during this study were nitrates and herbicides. Nitrate as nitrogen (nitrate-N) concentrations (2003 median 9.53 milligrams per liter) indicated that human activity has affected the water quality of recently recharged ground water in approximately two-thirds of the wells near corn and soybean fields. The principal pesticide compounds that were detected reflect the most-used pesticides in the area and included parent or degradate compounds of acetochlor, alachlor, atrazine, and metolachlor. Overall, pesticide concentrations in ground-water samples collected in 2003 and 2004 were small and did not exceed public drinking-water standards where established. On average, more pesticides were detected in the flow-path wells than in the glacial-till network wells. The presence of a perennial stream within 1,640 feet of a well was correlated to smaller nitrate-N concentrations in the well water, and the presence of a road ditch within 164 feet of the well was correlated to the presence of detectable pesticides in the well water. All other variables tested showed no significant correlations to nitrate-N concentrations or pesticide detections. Unsaturated zone soil cores collected in 2002 from well boreholes indicated that nitrogen in the forms of nitrate-N and ammonia as nitrogen (ammonia-N) was available in the unsaturated zone for transport to ground water. Concentrations of nitrate-N and ammonia-N in these soil cores were inversely correlated to depth, and nitrate-N concentrations were correlated to chloride concentrations.

Scientific Investigations Report↗
USGS2002

Water quality and aquatic communities of upland wetlands, Cumberland Island National Seashore, Georgia, April 1999 to July 2000

Cumberland Island is the southernmost and largest barrier island along the coast of Georgia. The island contains about 2,500 acres of freshwater wetlands that are located in a variety of physical settings, have a wide range of hydroperiods, and are influenced to varying degrees by surface and ground water, rainwater, and seawater. In 1999-2000, the U.S. Geological Survey, in cooperation with the National Park Service, conducted a water-quality study of Cumberland Island National Seashore to document and interpret the quality of a representative subset of surface- and ground-water resources for management of the seashore's natural resources. As part of this study, historical ground-water, surface-water, and ecological studies conducted on Cumberland Island also were summarized. Surface-water samples from six wetland areas located in the upland area of Cumberland Island were collected quarterly from April 1999 to March 2000 and analyzed for major ions, nutrients, trace elements, and field water-quality constituents including specific conductance, pH, temperature, dissolved oxygen, alkalinity, tannin and lignin, and turbidity. In addition, water temperature and specific conductance were recorded continuously from two wetland areas located near the mean high-tide mark on the Atlantic Ocean beaches from April 1999 to July 2000. Fish and invertebrate communities from six wetlands were sampled during April and December 1999. The microbial quality of the near-shore Atlantic Ocean was assessed in seawater samples collected for 5 consecutive days in April 1999 at five beaches near campgrounds where most recreational water contact occurs. Ground-water samples were collected from the Upper Floridan aquifer in April 1999 and from the surficial aquifer in April 2000 at 11 permanent wells and 4 temporary wells (drive points), and were analyzed for major ions, nutrients, trace elements, and field water-quality constituents (conductivity, pH, temperature, dissolved oxygen, and alkalinity). Fecal-coliform bacteria concentrations were measured, but not detected, in samples collected from two domestic water-supply wells. During the 12-month period from April 1999 to March 2000 when water-quality and aquatic-community samples were collected, rainfall was 12.93 inches below the 30-year average rainfall. Constituent concentrations were highly variable among the different wetlands during the study period. Rainfall and tidal surges associated with tropical storms and hurricanes substantially influenced water quantity and quality, particularly in wetland areas directly influenced by tidal surges. Although surface waters on Cumberland Island are not used as sources of drinking water, exceedances of U.S. Environmental Protection Agency primary and secondary standards for drinking water were noted for comparative purposes. A nitrate concentration of 12 milligrams per liter in one sample from Whitney outflow was the only exceedance of a maximum contaminant level. Secondary standards were exceeded in 26 surface-water samples for the following constituents: pH (10 exceedances), chloride (8), sulfate (5), total dissolved solids (4), iron (2), fluoride (1), and manganese (1). The total-dissolved-solids concentrations and the relative abundance of major ions in surface-water samples collected from wetlands on Cumberland Island provide some insight into potential sources of water and influences on water quality. Major-ion chemistries of water samples from Whitney Lake, Willow Pond, and South End Pond 3 were sodium-chloride dominated, indicating direct influence from rainwater, salt aerosol, or inundation of marine waters. The remaining wetlands sampled had low total-dissolved-solids concentrations and mixed major-ion chemistries--North Cut Pond 2A was magnesium-sodium-chloride-sulfate dominated and Lake Retta and the two beach outflows were sodium-calcium-bicarbonate-chloride dominated. The higher percent calcium and bicarbonate in some wetlands sugg

Georgia↗
USGS2012

Water-quality characteristics and trends for selected sites at and near the Idaho National Laboratory, Idaho, 1949-2009

The U.S. Geological Survey, in cooperation with the U.S. Department of Energy, analyzed water-quality data collected from 67 aquifer wells and 7 surface-water sites at the Idaho National Laboratory (INL) from 1949 through 2009. The data analyzed included major cations, anions, nutrients, trace elements, and total organic carbon. The analyses were performed to examine water-quality trends that might inform future management decisions about the number of wells to sample at the INL and the type of constituents to monitor. Water-quality trends were determined using (1) the nonparametric Kendall's tau correlation coefficient, p -value, Theil-Sen slope estimator, and summary statistics for uncensored data; and (2) the Kaplan-Meier method for calculating summary statistics, Kendall's tau correlation coefficient, p -value, and Akritas-Theil-Sen slope estimator for robust linear regression for censored data. Statistical analyses for chloride concentrations indicate that groundwater influenced by Big Lost River seepage has decreasing chloride trends or, in some cases, has variable chloride concentration changes that correlate with above-average and below-average periods of recharge. Analyses of trends for chloride in water samples from four sites located along the Big Lost River indicate a decreasing trend or no trend for chloride, and chloride concentrations generally are much lower at these four sites than those in the aquifer. Above-average and below-average periods of recharge also affect concentration trends for sodium, sulfate, nitrate, and a few trace elements in several wells. Analyses of trends for constituents in water from several of the wells that is mostly regionally derived groundwater generally indicate increasing trends for chloride, sodium, sulfate, and nitrate concentrations. These increases are attributed to agricultural or other anthropogenic influences on the aquifer upgradient of the INL. Statistical trends of chemical constituents from several wells near the Naval Reactors Facility may be influenced by wastewater disposal at the facility or by anthropogenic influence from the Little Lost River basin. Groundwater samples from three wells downgradient of the Power Burst Facility area show increasing trends for chloride, nitrate, sodium, and sulfate concentrations. The increases could be caused by wastewater disposal in the Power Burst Facility area. Some groundwater samples in the southwestern part of the INL and southwest of the INL show concentration trends for chloride and sodium that may be influenced by wastewater disposal. Some of the groundwater samples have decreasing trends that could be attributed to the decreasing concentrations in the wastewater from the late 1970s to 2009. The young fraction of groundwater in many of the wells is more than 20 years old, so samples collected in the early 1990s are more representative of groundwater discharged in the 1960s and 1970s, when concentrations in wastewater were much higher. Groundwater sampled in 2009 would be representative of the lower concentrations of chloride and sodium in wastewater discharged in the late 1980s. Analyses of trends for sodium in several groundwater samples from the central and southern part of the eastern Snake River aquifer show increasing trends. In most cases, however, the sodium concentrations are less than background concentrations measured in the aquifer. Many of the wells are open to larger mixed sections of the aquifer, and the increasing trends may indicate that the long history of wastewater disposal in the central part of the INL is increasing sodium concentrations in the groundwater.

Idaho↗
USGS2004

Quality of water on the Prairie Band Potawatomi Reservation, northeastern Kansas, May 2001 through August 2003

Water-quality samples were collected from 20 surface-water sites and 11 ground-water sites on the Prairie Band Potawatomi Reservation in northeastern Kansas in an effort to describe existing water-quality conditions on the reservation and to compare water-quality conditions to results from previous reports published as part of a multiyear cooperative study with the Prairie Band Potawatomi Nation. Water is a valuable resource to the Prairie Band Potawatomi Nation as tribal members use the streams draining the reservation, Soldier, Little Soldier, and South Cedar Creeks, to fulfill subsistence hunting and fishing needs and as the tribe develops an economic base on the reservation. Samples were collected once at 20 surface-water monitoring sites during June 2001, and quarterly samples were collected at 5 of the 20 monitoring sites from May 2001 through August 2003. Ground-water-quality samples were collected once from seven wells and twice from four wells during April through May 2003 and in August 2003. Surface-water-quality samples collected from May through August 2001 were analyzed for physical properties, nutrients, pesticides, fecal indicator bacteria, and total suspended solids. In November 2001, an additional analysis for dissolved solids, major ions, trace elements, and suspended-sediment concentration was added for surface-water samples. Ground-water samples were analyzed for physical properties, dissolved solids, major ions, nutrients, trace elements, pesticides, and fecal indicator bacteria. Chemical oxygen demand and volatile organic compounds were analyzed in a sample from one monitoring well located near a construction and demolition landfill on the reservation. Previous reports published as a part of this ongoing study identified total phosphorus, triazine herbicides, and fecal coliform bacteria as exceeding their respective water-quality criteria in surface water on the reservation. Previous ground-water assessments identified occasional sample concentrations of dissolved solids, sodium, sulfate, boron, iron, and manganese as exceeding their respective water-quality criteria. Forty percent of the 65 surface-water samples analyzed for total phosphorus exceeded the aquatic-life goal of 0.1 mg/L (milligrams per liter) established by the U.S. Environmental Protection Agency (USEPA). Concentrations of dissolved solids and sodium occasionally exceeded USEPA Secondary Drinking-Water Regulations and Drinking-Water Advisory Levels, respectively. One of the 20 samples analyzed for atrazine concentrations exceeded the Maximum Contaminant Level (MCL) of 3.0 ?g/L (micrograms per liter) as an annual average established for drinking water by USEPA. A triazine herbicide screen was used on 63 surface-water samples, and triazine compounds were frequently detected. Triazine herbicides and their degradates are listed on the USEPA Contaminant Candidate List. Nitrite plus nitrate concentrations in two ground-water samples from one monitoring well exceeded the MCL of 10 mg/L established by USEPA for drinking water. Arsenic concentrations in two samples from one monitoring well also exceeded the proposed MCL of 10 ?g/L established by the USEPA for drinking water. Concentrations of dissolved solids and sulfate in some ground-water samples exceeded their respective Secondary Drinking-Water Regulations, and concentrations exceeded the taste threshold of the USEPA?s Drinking-Water Advisory Level for sodium. Consequently, in the event that ground water on the reservation is to be used as a drinking-water source, additional treatment may be necessary to remove excess dissolved solids, sulfate, and sodium.

Scientific Investigations Report↗
USGS2021

Groundwater quality and age of secondary bedrock aquifers in the glaciated portion of eastern Nebraska, 2016–18

The Eastern Nebraska Water Resources Assessment (ENWRA) project was initiated in 2006 to assist water managers by developing a hydrogeologic framework and water budget for the glaciated portion of eastern Nebraska. Within the ENWRA area, the primary groundwater sources for municipal, domestic, and irrigation water needs are provided by withdrawals from alluvial, buried paleovalley, and the High Plains aquifer (where present). Generally, other bedrock aquifers are considered a secondary water source. However, in some areas, such as parts of Sarpy and Nemaha Counties, these secondary bedrock aquifers are the only source of water within glaciated upland areas. To improve the understanding of the quality, geochemistry, and age of groundwater from bedrock aquifers, the U.S. Geological Survey (USGS), in cooperation with the ENWRA group, which includes the Lewis and Clark, Lower Elkhorn, Lower Platte North, Lower Platte South, Nemaha, and Papio-Missouri River Natural Resources Districts, designed a study to sample 31 wells completed in the secondary bedrock aquifers and analyze samples for major ions, physical properties, nutrients, stable isotopes, and selected age tracers. Of the 31 samples collected for this report, 22 samples were collected from the Dakota aquifer contained in the Dakota Sandstone, 3 from the Niobrara aquifer contained in the Niobrara Formation of Colorado Group, and 6 from Paleozoic aquifers contained in undifferentiated Paleozoic-age units. The results of this study indicate that major ion data collected from the Dakota aquifer can be used for assessing the quality, recharge source, and age of groundwater. Calcium bicarbonate dominant samples were characterized as modern or mixed, indicating that, in these areas, groundwater is unconfined and is recharged by precipitation and (or) surface water. If groundwater extraction rates exceed recharge rates, total dissolved solid concentrations may increase as a result of upwelling of groundwater from deeper units or formations, which can adversely affect groundwater quality. Sampling results presented in this report indicate water quality is good, but that groundwater in the Dakota aquifer with calcium bicarbonate water type may be vulnerable to surface contamination. In contrast, groundwater sampled from the Dakota aquifer, having a dominant water type other than calcium bicarbonate, generally has low dissolved oxygen and nitrate concentrations, and higher concentrations of total dissolved solids and trace elements, including iron and strontium. The geochemical characteristics of noncalcium bicarbonate samples from the Dakota aquifer indicated confining conditions and limited groundwater recharge from local precipitation. Apparent groundwater ages estimated from radiocarbon (carbon-14) sampling of noncalcium bicarbonate samples from the Dakota aquifer indicated that the time of groundwater recharge to the Dakota aquifer occurred during Pleistocene time. Depleted stable isotopes results indicate recharge during a colder climate. Groundwater under confined conditions is not easily recharged from precipitation or surface water. Future groundwater-level monitoring in locations where the Dakota aquifer appears to be confined could provide information to evaluate whether groundwater supplies remain sufficient to meet future municipal, domestic, and irrigation needs. For the Niobrara aquifer and Paleozoic aquifers, the dominant water type was not a diagnostic indicator of recharge source, age, and groundwater quality as with the Dakota aquifer. Most likely this is because the host formation was dominated by calcium-carbonate-rich rocks; however, few samples were collected from these aquifers to be able to confirm this interpretation. Samples collected from wells completed in the Niobrara aquifer and Paleozoic aquifers and characterized as calcium sulfate water type have statistically significantly higher concentrations of total dissolved solids compared to other samples from the Niobrara aquifer and Paleozoic aquifers characterized as calcium bicarbonate. Given that six of the nine of samples collected from the Niobrara and Paleozoic aquifers indicated modern recharge, these secondary bedrock aquifers are reliant on precipitation to sustain groundwater levels and may be vulnerable to a multiyear drought. Well yields of the Niobrara and Paleozoic aquifers are dependent on the presence of secondary porosity and these units offer little storage. Samples collected from wells completed in Paleozoic aquifers were the most isotopically enriched and similar to modern precipitation and had the highest concentrations of nitrate, indicating that groundwater is affected by agricultural activities. Future groundwater sampling would be beneficial to characterize groundwater-quality changes within the Niobrara and Paleozoic aquifers over time.

Nebraska↗
USGS2001

Ground-water quality, Cook Inlet Basin, Alaska, 1999

As part of the U.S. Geological Survey?s National Water-Quality Assessment Program, ground-water samples were collected from 34 existing wells in the Cook Inlet Basin in south-central Alaska during 1999. All ground-water samples were from aquifers composed of glacial or alluvial sediments. The water samples were used to determine the occurrence and distribution of selected major ions, nutrients, trace elements, volatile organic compounds, pesticides, radioisotopes, and environmental isotopes. Of 34 samples, 29 were from wells chosen by using a grid-based random-selection process. Water samples from five major public-supply wells also were collected. Radon-222 and arsenic concentrations exceeded drinking-water standards proposed by the U.S. Environmental Protection Agency in 39 and 18 percent of sampled wells, respectively. The highest radon concentration measured during this study was 610 picocuries per liter; 12 of 31 samples exceeded the proposed maximum contaminant level of 300 picocuries per liter. The highest arsenic concentration was 29 micrograms per liter; 6 of 34 samples exceeded the proposed maximum contaminant level of 10 micrograms per liter. Human activities may be increasing the concen- tration of nitrate in ground water, but nitrate concentrations in all samples were less than the maximum contaminant level of 10 milligrams per liter as nitrogen. Concentrations of nitrate were highest in Anchorage and were as great as 4.8 milligrams per liter as nitrogen. Dissolved-solids concentrations ranged from 77 to 986 milligrams per liter; only 2 of 34 wells yielded water having greater than 500 milligrams per liter. Iron and manganese concentrations exceeded secondary maximum contaminant levels in 18 and 42 percent of samples, respectively. Concentrations of all pesticides and volatile organic compounds detected in ground-water samples were very low, less than 1 microgram per liter. No pesticide or volatile organic compounds were detected at concentrations exceeding drinking-water standards or guidelines. Water samples from one-half of the wells sampled had no detectable concentrations of pesticides or volatile organic carbons, at the parts-per-billion level. Concentrations of stable isotopes of hydrogen and oxygen in ground-water samples were similar to concentrations expected for modern precipitation and for water that has been affected by evaporation. Tritium activities and concentrations of chlorofluorocarbons indicated that the water samples collected from most wells were recharged less than 50 years ago.

Alaska↗
USGS2015

Feasibility and potential effects of the proposed Amargosa Creek Recharge Project, Palmdale, California

Historically, the city of Palmdale and vicinity have relied on groundwater as the primary source of water, owing, in large part, to the scarcity of surface water in the region. Despite recent importing of surface water, groundwater withdrawal for municipal, industrial, and agricultural use has resulted in groundwater-level declines near the city of Palmdale in excess of 200 feet since the early 1900s. To meet the growing water demand in the area, the city of Palmdale has proposed the Amargosa Creek Recharge Project (ACRP), which has a footprint of about 150 acres along the Amargosa Creek 2 miles west of Palmdale, California. The objective of this study was to evaluate the long-term feasibility of recharging the Antelope Valley aquifer system by using infiltration of imported surface water from the California State Water Project in percolation basins at the ACRP. Three monitoring sites were constructed, and geophysical surveys (gravity, seismic, and resistivity) were completed to define the thickness of valley-fill deposits, depth to water, and location of faults that could influence groundwater flow. Data collected at the monitoring sites, and results from the geophysical surveys, were used to identify three northwest-southeast trending faults in the vicinity of the proposed recharge facility; these faults are probably related to the nearby San Andreas fault zone. Water levels collected from wells at the monitoring sites showed water-level altitude differences as much as 230 feet between the upgradient and downgradient sides of the faults, indicating that these faults are barriers to groundwater flow. Lithologic and geophysical logs indicated the presence of a coarse gravel and sand unit extending from land surface to about 150 feet below land surface that did not appear to be disrupted by faulting. Water samples collected from the monitoring wells were analyzed for major ions, nutrients, trace elements, dissolved organic carbon, volatile organic compounds, stable isotopes of oxygen (oxygen-18) and hydrogen (hydrogen-2, or deuterium), and the radioactive isotopes of hydrogen (hydrogen-3, or tritium) and carbon (carbon-14, or 14 C) to determine the water quality of the aquifer system and to help determine the source and age of the groundwater. Results of the water-quality analysis indicated that the source of natural recharge is Amargosa Creek near the ACRP, but that the creek does not provide modern-day recharge downstream of the ACRP. Potential effects of artificial recharge at the ACRP were evaluated by using a local-scale model of groundwater flow. On the basis of geologic samples collected during drilling, the hydraulic conductivity of the sand and gravel unit in the upper 150 feet was assumed to range from 10 to 100 feet per day. To address the goal of minimizing the potential for liquefaction during an earthquake from water-table rise associated with groundwater recharge at the ACRP, simulated water levels were constrained to remain at least 50 feet below land surface, except beneath the proposed artificial-recharge facility. The hydraulic conductivities of faults were estimated on the basis of water-level data and an estimate of natural recharge along Amargosa Creek. With assumed horizontal hydraulic conductivities of 10 and 100 feet per day in the upper 150 feet, the simulated maximum artificial recharge rates to the regional flow system at the ACRP were 3,400 and 9,400 acre-feet per year, respectively. These maximum recharge rates were limited primarily by the horizontal hydraulic conductivity in the upper 150 feet and by the liquefaction constraint. Future monitoring of water-level and soil-water content changes during the proposed project would allow improved estimation of aquifer hydraulic properties, the effect of the faults on groundwater movement, and the overall recharge capacity of the ACRP.

California↗
USGS2000

Water-quality assessment of the Trinity River Basin, Texas— Ground-water quality of the Trinity, Carrizo-Wilcox, and Gulf Coast aquifers, February-August 1994

Ground-water samples were collected from wells in the outcrops of the Trinity, Carrizo-Wilcox, and Gulf Coast aquifers during February-August 1994 to determine the quality of ground water in the three major aquifers in the Trinity River Basin study unit, Texas. These samples were collected and analyzed for selected properties, nutrients, major inorganic constituents, trace elements, pesticides, dissolved organic carbon, total phenols, methylene blue active substances, and volatile organic compounds as part of the U.S. Geological Survey National Water-Quality Assessment Program. Quality-control practices included the collection and analysis of blank, duplicate, and spiked samples. Samples were collected from 12 shallow wells (150 feet or less) and from 12 deep wells (greater than 150 feet) in the Trinity aquifer, 11 shallow wells and 12 deep wells in the Carrizo-Wilcox aquifer, and 14 shallow wells and 10 deep wells in the Gulf Coast aquifer. The three aquifers had similar water chemistries-calcium was the dominant cation and bicarbonate the dominant anion. Statistical tests relating well depths to concentrations of nutrients and major inorganic constituents indicated correlations between well depth and concentrations of ammonia nitrogen, nitrite plus nitrate nitrogen, bicarbonate, sodium, and dissolved solids in the Carrizo-Wilcox aquifer and between well depth and concentrations of sulfate in the Gulf Coast aquifer. The tests indicated no significant correlations for the Trinity aquifer. Concentrations of dissolved solids were larger than the secondary maximum contaminant level of 500 milligrams per liter established for drinking water by the U.S. Environmental Protection Agency in 12 wells in the Trinity aquifer, 4 wells in the Carrizo-Wilcox aquifer, and 6 wells in the Gulf Coast aquifer. Iron concentrations were larger than the secondary maximum contaminant level of 300 micrograms per liter in at least 3 samples from each aquifer, and manganese concentrations were larger than the secondary maximum contaminant level of 50 micrograms per liter in at least 2 samples from each aquifer. The pesticides atrazine, deethylatrazine, and pp'-DDE were detected in at least one sample from each aquifer. Diazinon was detected in 11 Trinity aquifer samples and 4 Carrizo-Wilcox aquifer samples. Each aquifer had one detection of a volatile organic compound-benzene in the Trinity aquifer, trichlorofluoromethane in the Carrizo-Wilcox aquifer, and trichloromethane in the Gulf Coast aquifer.

Texas↗
USGS2004

Effects of flow modification on a cattail wetland at the mouth of Irondequoit Creek near Rochester, New York: Water levels, wetland biota, sediment, and water quality

An 11-year (1990-2001) study of the Ellison Park wetland, a 423-acre, predominantly cattail (Typha glauca) wetland at the mouth of Irondequoit Creek, was conducted to document the effects that flow modifications, including installation of a flow-control structure (FCS) in 1997 and increased diversion of stormflows to the backwater areas of the wetland, would have on the wetland's ability to decrease chemical loads transported by Irondequoit Creek into Irondequoit Bay on Lake Ontario. The FCS was designed to raise the water-surface elevation and thereby increase the dispersal and detention of stormflows in the upstream half of the wetland; this was expected to promote sedimentation and microbial utilization of nutrients, and thereby decrease the loads of certain constituents, primarily phosphorus, that would otherwise be carried into Irondequoit Bay. An ecological monitoring program was established to document changes in the wetland's water levels, biota, sedimentation rates, and chemical quality of water and sediment that might be attributable to the flow modifications. Water-level increases during storms were mostly confined to the wetland area, within about 5,000 ft upstream from the FCS. Backwater at a point of local concern, about 13,000 ft upstream, was due to local debris jams or constriction of flow by bridges and was not attributable to the FCS. Plant surveys documented species richness, concentrations of nutrients and metals in cattail tissues, and cattail productivity. Results indicated that observed differences among survey periods and between the areas upstream and downstream from the FCS were due to seasonal changes in water levels—either during the current year or at the end of the previous year's growing season—that reflected the water-surface elevation of Lake Ontario, rather than water-level control by the FCS. Results showed no adverse effects from the naturally high water levels that prevail annually during the spring and summer in the wetland, nor from the short-duration increases in water levels that result from FCS operation. Fish surveys documented the use of the wetland by 44 species, of which 25 to 29 species were found in any given year. Community composition was relatively consistent during the study, but seasonal and year-to-year variations in dominant resident and nonresident species were noted, and probably reflected natural or regional population patterns in Lake Ontario and Irondequoit Bay. The FCS allowed fish passage at all water levels and had no discernible adverse effect on the fish community. Bird surveys documented the use of the wetland by more than 90 species for breeding, feeding, and migration. Ground-nesting birds were unaffected by the FCS. Seasonally high water levels, rather than short-duration increases caused by the FCS, might have caused the scarcity or absence of certain wetland species by limiting the extent of breeding habitat for some species and the exposure of mud flats that attracted other species. Some noticeably scarce or absent species also were rare or absent elsewhere along the south-central shore of Lake Ontario. Benthic-macroinvertebrate studies were of minimal use for evaluating the effect of the FCS because no surveys were conducted after FCS installation. The precontrol results allowed assessment of the ecological quality of the wetland on the basis of biotic indices, and generally indicated moderately to severely impaired conditions. Differences between the macroinvertebrate communities in the southern part of the wetland and those in the northern part were attributed to habitat differences, such as substrate composition, water depth, and density of submerged aquatic vegetation. Sedimentation rates in the areas upstream and downstream from the FCS increased after the flow modifications, more in the area upstream from the FCS than in the downstream area. The concurrent downstream increase and the dynamic patterns of deposition and scour indicated that although the FCS and the other flow modifications undoubtedly were major factors in the postcontrol upstream increase in sedimentation rates, other factors, such as the magnitude, frequency, and the timing (season) of peak flows, might also have contributed. Periodic analyses of sediment samples from three longterm depositional sites in the wetland documented the concentrations of major and trace elements, polycyclic aromatic hydrocarbons, and organochlorine and organophosphate compounds. The concentrations of most constituents showed no substantial fluctuation or consistent upward or downward trend during the years sampled, nor did they identify any change after FCS installation. Comparison of the measured concentrations with sediment-quality guidelines that are used to assess the ecological quality of substrate environments indicated that the wetland was moderately to severely impaired—an assessment consistent with the benthic-macroinvertebrate biotic indices. During the precontrol period (1990–96), the wetland was a sink for particulate constituents (removal efficiencies for total phosphorus and total suspended solids were 28 and 47 percent, respectively), but had little effect on conservative constituents (chloride and sulfate). The wetland was a source of orthophosphate and ammonia (removal efficiencies were -38 and -84 percent, respectively). During the postcontrol period (1997–2001), the wetland continued to be a sink for particulate constituents (removal efficiencies for total phosphorus and total suspended solids were 45 and 52 percent, respectively); the exportation of orthophosphate by the wetland decreased (by 7 percent), whereas that of ammonia increased (by about 70 percent). The outflow loads of orthophosphate and ammonia represented about 15 and 2.3 percent of total phosphorus and total nitrogen loads, respectively. Changes in the loads of conservative constituents were negligible, and the overall removal efficiencies for other constituents during the precontrol period differed from those of the postcontrol period by no more than 5.4 percent. Statistical analyses of monthly inflow and outflow loads indicated significant differences between inflow and outflow loads of most constituents during the pre- and postcontrol periods. Load data were adjusted to remove the effects of dissimilar hydrologic conditions that prevailed during the pre- and postcontrol periods, and to isolate the water-quality-improvement effect that could be attributed solely to the FCS. Results indicated that the FCS contributed significantly to the decrease in total phosphorus loads, and slightly to a decrease in ammonia-plus-organic nitrogen loads, but had little or no significant effect on loads of other constituents.

New York↗
USGS2011

Water-quality characteristics of urban storm runoff at selected sites in East Baton Rouge Parish, Louisiana, February 2006 through November 2009

Water samples were collected at three watersheds in East Baton Rouge Parish, Louisiana, during February 2006 through November 2009 for continued evaluation of urban storm runoff. The watersheds represented land uses characterized predominantly as established commercial, industrial, and residential. The following water-quality data are reported: physical and chemical-related properties, fecal coliform, nutrients, trace elements, and organic compounds. Results of water-quality analyses enabled calculation of event-mean concentrations and estimated annual contaminant loads and yields of storm runoff from nonpoint sources for 12 water-quality properties and constituents. Lead met or exceeded the U.S. Environmental Protection Agency Maximum Contaminant Level of 15 micrograms per liter for drinking water standards in 4 of 14 samples. Low level concentrations of mercury were detected in all 14 samples, and half were two to four times above the reporting limit of 0.02 micrograms per liter. The average dissolved phosphorus concentrations from each land use were two to four times the U.S. Environmental Protection Agency criterion of 0.05 milligrams per liter. Diazinon was detected in one sample at a concentration of 0.2 micrograms per liter. In the residential watershed, the largest at 216 acres, contaminant loads for 5 of the 12 water-quality properties and constituents were highest, with 4 of these being nutrients. The industrial watershed, 97 acres, had the highest contaminant loads for 6 of the 12 water-quality properties and constituents with 3 of these being metals, which is indicative of the type of land use. Zinc had the highest metal load (155 pounds per year) in the industrial watershed, compared to 36 pounds per year in the residential watershed, and 32 pounds per year in the established commercial watershed. The industrial watershed had the highest yields for 8 of the 12 water-quality properties and constituents, whereas the established commercial watershed had the lowest yield for 5 of the 12. Lower yields from the established commercial and residential watersheds could be from Best Management Practices in place that help control increased runoff from impervious areas and land development. Metal yields from all the watersheds were less than 1 pound per acre per year, except for the zinc from the industrial watershed, which was 2 pounds per acre per year. Nutrient yields in the established commercial watershed were lowest for total nitrogen, ammonia plus organic nitrogen (Kjeldahl nitrogen), and dissolved phosphorus.

Louisiana↗
USGS2017

Hydrogeology and water quality of sand and gravel aquifers in McHenry County, Illinois, 2009–14, and comparison to conditions in 1979

Baseline conditions for the sand and gravel aquifers (groundwater) in McHenry County, Illinois, were assessed using data from a countywide network of 44 monitoring wells collecting continuous water-level data from 2009–14. In 2010, water-quality data were collected from 41 of the monitoring wells, along with five additional monitoring wells available from the U.S. Geological Survey National Water Quality Assessment Program. Periodic water-quality data were collected from 2010–14 from selected monitoring wells. The continuous water-level data were used to identify the natural and anthropogenic factors that influenced the water levels at each well. The water-level responses to natural influences such as precipitation, seasonal and annual variations, barometric pressure, and geology, and to anthropogenic influences such as pumping were used to determine (1) likely hydrogeologic setting (degree of aquifer confinement and interconnections) that, in part, are related to lithostratigraphy; and (2) areas of recharge and discharge related to vertical flow directions. Water-level trends generally were determined from the 6 years of data collection (2009–14) to infer effects of weather variability (drought) on recharge. Precipitation adds an estimated 2.4 inches per year of recharge to the aquifer. Some of this recharge is subsequently discharged to streams and some is discharged to supply wells. A few areas in the eastern half of the county had higher average recharge rates, indicating a need for adequate protection of these recharge areas. Downward vertical flow gradients in upland areas indicate that recharge to the confined aquifer units occurs near upland areas. Upward vertical flow gradients in lowland areas indicate discharge at locations of surface water and groundwater interaction (wetlands, ponds, and streams). Monitoring wells were sampled for major and minor ions, metals, and nutrients and a subset of wells was sampled for trace elements, dissolved gases, pesticides, and volatile organic compounds. The results were compared to health ‑ based and aesthetically based standards, which include the U.S. Environmental Protection Agency Maximum Contaminant Level (EPA MCL), and EPA Secondary Maximum Contaminant Levels (SMCL), as well as EPA Health-based Standards Drinking Water Advisories. Health‑based standards were exceeded for arsenic in 22 percent, sodium in 20 percent, and nitrates in 2 percent of the monitoring wells sampled. Aesthetically based standards were exceeded for total dissolved solids in 33 percent, chloride in 11 percent, iron in 85 percent, and manganese in 30 percent of the wells sampled. Many of these same constituents, such as arsenic, iron, and manganese, are naturally occurring but become elevated in areas that have anoxic, mixed, and suboxic conditions. Some areas of potential vulnerability to anthropogenic-sourced constituents in the sand and gravel aquifers were evidenced by trace amounts of volatile organic compounds and pesticides detected in water-quality samples from shallow wells (total depth less of than 46 feet below land surface) near urban settings, and by the detection of elevated major ions (chloride, sodium, magnesium, and calcium) associated, in part, with road-salt applications. Source analysis for chloride indicates mixtures of road salt, water softeners, and sewage. Continuously measured specific conductance values were used as a surrogate for continuously measured chloride concentrations in the groundwater. The estimated chloride concentrations generally were highest in spring and lowest in summer, and occasionally peak during spring melt. Overall, the range of concentrations varied depending on the local thickness and hydraulic conductivity of the aquifer. Water levels and water quality from the countywide groundwater monitoring network were compared to water levels and water-quality results in 1979 from a previous U.S. Geological Survey study. Potentiometric surface maps show areas with inferred decreases of water levels near the southern and southeastern areas of McHenry County. Significant increases were noted for total dissolved solids and specific conductance. Chloride concentrations increased as much as 521 percent in three of six wells resampled in 2015 from the previous study.

Illinois↗
USGS1978

Stream quality in the San Lorenzo River Basin, Santa Cruz County, California

Stream quality in the San Lorenzo River basin, Calif., was studied from November 1973 through June 1975 to determine areal and temporal variations in water quality, problem areas and times of water quality degradation, and compliance with State and local water-quality objectives. Sampling from November 1973 through July 1974 was done at five stations in the Zayante Creek drainage basin and at one station on the San Lorenzo River at Big Trees. Sampling from August 1974 through June 1975 was done at 15 stations in the San Lorenzo River basin, including one station in the Zayante Creek subbasin. Properties and constituents measured were water temperature, specific conductance, pH, alkalinity, dissolved oxygen, turbidity, fecal-coliform and fecal-streptococcal bacteria, major dissolved ions, nutrients (nitrogen and phosphorus), chemical and biochemical oxygen demand, and trace elements. Benthic invertebrates were collected during autumn 1974 and spring 1975 at two stations. Results show that the water in most streams in the basin can be classified as calcium bicarbonate, but based on the dissolved-ion concentrations the basin can be divided into three water-quality areas that correspond generally to three geologic areas. The most pronounced change in water quality occurs during storms when streamflow, turbidity, and total Kjeldahl-nitrogen, total-phosphorus, dissolved-potassium, and fecal-coliform concentrations increase, while concentrations of most dissolved ions decrease owing to dilution of the nonstorm part of the flow. Late winter and early spring nonstorm flows yield water of the best quality because the concentrations of most dissolved ions and fecal-coliform and fecal-streptococcal bacteria are relatively low, whereas turbidity values are the same as, or not appreciably greater than, during the summer low-flow period. Dissolved-ion concentrations exceeded objectives at stations on east-side streams north of the Zayante fault, probably because of lower-than-normal streamflows during water year 1975. Total-nitrogen and fecal-coliform concentrations exceeded objectives in the Zayante Creek and Branciforte Creek drainage basins, probably because of domestic sewage from improperly operating septic-tank systems. The high total-nitrogen and fecal-coliform concentrations in the Zayante Creek basin might also result from the primary-treated effluent discharged by the city of Scotts Valley into an old sand pit. Results of diel studies (intensive sampling for a 24-hour period) made at two stations on the San Lorenzo River indicate that residential areas between the stations do not contribute sufficient quantities of oxygen-demanding wastes to the river during low streamflow to cause appreciable dissolved-oxygen depletion. Greater streamflows and residential development seem to be responsible for unstable streambed substrates and reduced diversity of benthic invertebrates during the spring at a station downstream of most of the residential areas in the San Lorenzo River valley.

California↗
USGS2013

Water quality, streamflow conditions, and annual flow-duration curves for streams of the San Juan–Chama Project, southern Colorado and northern New Mexico, 1935-2010

The Albuquerque–Bernalillo County Water Utility Authority supplements the municipal water supply for the Albuquerque metropolitan area, in central New Mexico, with water diverted from the Rio Grande. Water diverted from the Rio Grande for municipal use is derived from the San Juan–Chama Project, which delivers water from streams in the southern San Juan Mountains in the Colorado River Basin in southern Colorado to the Rio Chama watershed and the Rio Grande Basin in northern New Mexico. The U.S. Geological Survey, in cooperation with Albuquerque–Bernalillo County Water Utility Authority, has compiled historical streamflow and water-quality data and collected new water-quality data to characterize the water quality and streamflow conditions and annual flow variability, as characterized by annual flow-duration curves, of streams of the San Juan–Chama Project. Nonparametric statistical methods were applied to calculate annual and monthly summary statistics of streamflow, trends in streamflow conditions were evaluated with the Mann–Kendall trend test, and annual variation in streamflow conditions was evaluated with annual flow-duration curves. The study area is located in northern New Mexico and southern Colorado and includes the Rio Blanco, Little Navajo River, and Navajo River, tributaries of the San Juan River in the Colorado River Basin located in the southern San Juan Mountains, and Willow Creek and Horse Lake Creek, tributaries of the Rio Chama in the Rio Grande Basin. The quality of water in the streams in the study area generally varied by watershed on the basis of the underlying geology and the volume and source of the streamflow. Water from the Rio Blanco and Little Navajo River watersheds, primarily underlain by volcanic deposits, volcaniclastic sediments and landslide deposits derived from these materials, was compositionally similar and had low specific-conductance values relative to the other streams in the study area. Water from the Navajo River, Horse Lake Creek, and Willow Creek watersheds, which are underlain mostly by Cretaceous-aged marine shale, was compositionally similar and had large concentrations of sulfate relative to the other streams in the study area, though the water from the Navajo River had lower specific-conductance values than did the water from Horse Lake Creek above Heron Reservoir and Willow Creek above Azotea Creek. Generally, surface-water quality varied with streamflow conditions throughout the year. Streamflow in spring and summer is generally a mixture of base flow (the component of streamflow derived from groundwater discharged to the stream channel) diluted with runoff from snowmelt and precipitation events, whereas streamflow in fall and winter is generally solely base flow. Major- and trace-element concentrations in the streams sampled were lower than U.S. Environmental Protection Agency primary and secondary drinking-water standards and New Mexico Environment Department surface-water standards for the streams. In general, years with increased annual discharge, compared to years with decreased annual discharge, had a smaller percentage of discharge in March, a larger percentage of discharge in June, an interval of discharge derived from snowmelt runoff that occurred later in the year, and a larger discharge in June. Additionally, years with increased annual discharge generally had a longer duration of runoff, and the streamflow indicators occurred at dates later in the year than the years with less snowmelt runoff. Additionally, the seasonal distribution of streamflow was more strongly controlled by the change in the amount of annual discharge than by changes in streamflow over time. The variation of streamflow conditions over time at one streamflow-gaging station in the study area, Navajo River at Banded Peak Ranch, was not significantly monotonic over the period of record with a Kendall’s tau of 0.0426 and with a p-value of 0.5938 for 1937 to 2009 (a trend was considered statistically significant at a p-value ≤ 0.05). There was a relation, however, such that annual discharge was generally lower than the median during a negative Pacific Decadal Oscillation interval and higher than the median during a positive Pacific Decadal Oscillation interval. Streamflow conditions at Navajo River at Banded Peak Ranch varied nonmonotonically over time and were likely a function of complex climate pattern interactions. Similarly, the monthly distribution of streamflow varied nonmonotonically over time and was likely a function of complex climate pattern interactions that cause variation over time. Study results indicated that the median of the sum of the streamflow available above the minimum monthly bypass requirement from Rio Blanco, Little Navajo River, and Navajo River was 126,240 acre-feet. The results also indicated that diversion of water for the San Juan–Chama Project has been possible for most months of most years.

Colorado;New Mexico↗
USGS2013

Geology, water-quality, hydrology, and geomechanics of the Cuyama Valley groundwater basin, California, 2008--12

To assess the water resources of the Cuyama Valley groundwater basin in Santa Barbara County, California, a series of cooperative studies were undertaken by the U.S. Geological Survey and the Santa Barbara County Water Agency. Between 2008 and 2012, geologic, water-quality, hydrologic and geomechanical data were collected from selected sites throughout the Cuyama Valley groundwater basin. Geologic data were collected from three multiple-well groundwater monitoring sites and included lithologic descriptions of the drill cuttings, borehole geophysical logs, temperature logs, as well as bulk density and sonic velocity measurements of whole-core samples. Generalized lithologic characterization from the monitoring sites indicated the water-bearing units in the subsurface consist of unconsolidated to partly consolidated sand, gravel, silt, clay, and occasional cobbles within alluvial fan and stream deposits. Analysis of geophysical logs indicated alternating layers of finer- and coarser-grained material that range from less than 1 foot to more than 20 feet thick. On the basis of the geologic data collected, the principal water-bearing units beneath the monitoring-well sites were found to be composed of younger alluvium of Holocene age, older alluvium of Pleistocene age, and the Tertiary-Quaternary Morales Formation. At all three sites, the contact between the recent fill and younger alluvium is approximately 20 feet below land surface. Water-quality samples were collected from 12 monitoring wells, 27 domestic and supply wells, 2 springs, and 4 surface-water sites and were analyzed for a variety of constituents that differed by site, but, in general, included trace elements; nutrients; dissolved organic carbon; major and minor ions; silica; total dissolved solids; alkalinity; total arsenic and iron; arsenic, chromium, and iron species; and isotopic tracers, including the stable isotopes of hydrogen and oxygen, activities of tritium, and carbon-14 abundance. Of the 39 wells sampled, concentrations of total dissolved solids and sulfate from 38 and 37 well samples, respectively, were greater than the U.S. Environmental Protection Agency’s secondary maximum contaminant levels. Concentrations greater than the maximum contaminant levels for nitrate were observed in five wells and were observed for arsenic in four wells. Differences in the stable-isotopic values of hydrogen and oxygen among groundwater samples indicated that water does not move freely between different formations or between different zones within the Cuyama Valley. Variations in isotopic composition indicated that recharge is derived from several different sources. The age of the groundwater, expressed as time since recharge, was between 600 and 38,000 years before present. Detectable concentrations of tritium indicated that younger water, recharged since the early 1950s, is present in parts of the groundwater basin. Hydrologic data were collected from 12 monitoring wells, 56 domestic and supply wells, 3 surface-water sites, and 4 rainfall-gaging stations. Rainfall in the valley averaged about 8 inches annually, whereas the mountains to the south received between 12 and 19 inches. Stream discharge records showed seasonal variability in surface-water flows ranging from no-flow to over 1,500 cubic feet per second. During periods when inflow to the valley exceeds outflow, there is potential recharge from stream losses to the groundwater system Water-level records included manual quarterly depth-to-water measurements collected from 68 wells, time-series data collected from 20 of those wells, and historic water levels from 16 wells. Hydrographs of the manual measurements showed declining water levels in 16 wells, mostly in the South-Main zone, and rising water levels in 14 wells, mostly in the Southern Ventucopa Uplands. Time-series hydrographs showed daily, seasonal, and longer-term effects associated with local pumping. Water-level data from the multiple-well monitoring sites indicated seasonal fluctuations as great as 80 feet and water-level differences between aquifers as great as 40 feet during peak pumping season. Hydrographs from the multiple-well groundwater monitoring sites showed vertical hydraulic gradients were upward during the winter months and downward during the irrigation season. Historic hydrographs showed water-level declines in the Southern-Main, Western Basin, Caliente Northern-Main, and Southern Sierra Madre zone ranging from 1 to 7 feet per year. Hydrographs of wells in the Southern Ventucopa Uplands zone showed several years with marked increases in water levels that corresponded to increased precipitation in the Cuyama Valley. Investigation of hydraulic properties included hydraulic conductivity and transmissivity estimated from aquifer tests performed on 63 wells. Estimates of horizontal hydraulic conductivity ranged from about 1.5 to 28 feet per day and decreased with depth. The median estimated hydraulic conductivity for the older alluvium was about five times that estimated for the Morales Formation. Estimates of transmissivity ranged from 560 to 163,400 gallons per day per foot and decreased with depth. The median estimated transmissivity for the younger alluvium was about three times that estimated for the older alluvium. Geomechanical analysis included land-surface elevation changes at five continuously operating global positioning systems (GPS) and land-subsidence detection at five interferometric synthetic aperture radar (InSAR) reference points. Analysis of data collected from continuously operating GPS stations showed the mountains to the south and west moved upward about 1 millimeter (mm) annually, whereas the station in the center of the Southern-Main zone moved downward more than 7 mm annually, indicating subsidence. It is likely that this subsidence is inelastic (permanent) deformation and indicates reduced storage capacity in the aquifer sediments. Analysis of InSAR data showed local and regional changes that appeared to be dependent, in part, on the time span of the interferogram, seasonal variations in pumping, and tectonic uplift. Long-term InSAR time series showed a total maximum detected subsidence rate of approximately 12 mm per year at one location and approximately 8 mm per year at a second location, while short-term InSAR time series showed maximum subsidence of about 15 mm at one location and localized maximum uplift of about 10 mm at another location.

California↗
USGS2009

Diel Sampling of Groundwater and Surface Water for Trace Elements and Select Water-Quality Constituents at a Former Zinc Smelter Site near Hegeler, Illinois, August 1-3, 2007

Surface water can exhibit substantial diel variations in the concentration of a number of constituents. Sampling regimens that do not characterize diel variations in water quality can result in an inaccurate understanding of site conditions and of the threat posed by the site to human health and the environment. Surface- and groundwater affected by acid drainage were sampled every 60 to 90 minutes over a 48-hour period at a former zinc smelter known as the Hegeler Zinc Superfund Site, in Hegeler, Ill. Groundwater-quality data from a well at the site indicate stable, low pH, weakly oxidizing geochemical conditions in the aquifer. With the exceptions of temperature and pH, no constituents exhibited diel variations in groundwater. Variations in temperature and pH likely were not representative of conditions in the aquifer. Surface water was sampled at a site on Grape Creek. Diel variations were observed in temperature, dissolved oxygen, pH, and specific conductance, and in the concentrations of nitrite, barium, iron, lead, vanadium, and possibly uranium. Concentrations during the diel cycles varied by about an order of magnitude for nitrite and varied by about a factor of two for barium, iron, lead, vanadium, and uranium. Temperature, dissolved oxygen, specific conductance, nitrite, barium, lead, and uranium generally reached maximum values during the afternoon and minimum values during the night. Iron, vanadium, and pH generally reached minimum values during the afternoon and maximum values during the night. These variations would need to be accounted for during sampling of surface-water quality in similar hydrologic settings. The temperature variations in surface water were affected by variations in air temperature. Concentrations of dissolved oxygen were affected by variations in the intensity of photosynthetic activity and respiration. Nitrite likely was formed by the oxidation of ammonium by dissolved oxygen and degraded by its anaerobic oxidation by ammonium or as part of the decomposition of organic matter. Variations in pH were affected by the photoreduction of Fe3+ to Fe2+ and the precipitation of iron oxyhydroxides. Diel variations in concentrations of iron and vanadium were likely caused by variations in the dissolution and precipitation of iron oxyhydroxides, oxyhydroxysulfates, and hydrous sulfates, which may have been affected by in the intensity of insolation, iron photoreduction, and the concentration of dissolved oxygen. The concentrations of lead, uranium, and perhaps barium in Grape Creek may have been affected by competition for sorption sites on iron oxyhydroxides. Competition for sorption sites was likely affected by variations in pH and the concentration of Fe2+. Constituent concentrations likely also were affected by precipitation and dissolution of minerals that are sensitive to changes in pH, temperature, oxidation-reduction conditions, and biologic activity. The chemical and biologic processes that resulted in the diel variations observed in Grape Creek occurred within the surface-water column or in the underlying sediments.

Scientific Investigations Report↗
USGS2007

Surface-Water Hydrology and Quality at the Pike Hill Superfund Site, Corinth, Vermont, October 2004 to December 2005

The hydrology and quality of surface water in and around the Pike Hill Brook watershed, in Corinth, Vermont, was studied from October 2004 to December 2005 by the U.S. Geological Survey in cooperation with the U.S. Environmental Protection Agency (USEPA). Pike Hill was mined intermittently for copper from 1847 to 1919 and the site is known to be contributing trace elements and acidity to Pike Hill Brook and an unnamed tributary to Cookville Brook. The site has been listed as a Superfund site since 2004. Streamflow, specific conductance, pH, and water temperature were measured continuously and monthly at three sites on Pike Hill Brook to determine the variation in these parameters over an annual cycle. Synoptic water-quality sampling was done at 10 stream sites in October 2004, April 2005, and June 2005 and at 13 stream sites in August 2005 to characterize the quality of surface water in the watershed on a seasonal and spatial basis, as well as to assess the effects of wetlands on water quality. Samples for analysis of benthic macroinvertebrate populations were collected at 11 stream sites in August 2005. Water samples were analyzed for 5 major ions and 32 trace elements. Concentrations of trace elements at sites in the Pike Hill Brook watershed exceeded USEPA National Recommended Water Quality Criteria acute and chronic toxicity standards for aluminum, iron, cadmium, copper, and zinc. Concentrations of copper exceeded the chronic criteria in an unnamed tributary to Cookville Brook in one sample. Concentrations of sulfate, calcium, aluminum, iron, cadmium, copper, and zinc decreased with distance from a site directly downstream from the mine (site 1), as a result of dilution and through sorption and precipitation of the trace elements. Maximum concentrations of aluminum, iron, cadmium, copper, and zinc were observed during spring snowmelt. Concentrations of sulfate, calcium, cadmium, copper, and zinc, and instantaneous loads of calcium and aluminum were statistically different (p<0.05) among the three continuously monitored sites (sites 1, 4, and 5). Instantaneous loads of aluminum, iron, and copper decreased by one to three orders of magnitude from site 1 to a site 1.1 mi downstream (site 4). Instantaneous loads of sulfate were similar between sites 1, 4, and at a site 3 mi downstream (site 5). Instantaneous loads of cadmium and zinc were similar between sites 1 and 4, and loads of iron and copper were similar between sites 4 and 5. Loads of chemical constituents were compared at site 1 (closest to the mine waste piles) and site 5 (near the mouth of Pike Hill Brook and below a majority of the wetlands). Annually, the loads of dissolved cadmium and zinc at site 1 were about five times greater than loads at site 5, and the load of dissolved copper at site 1 was about 17 times greater than at site 5. The ratio of loads for dissolved cadmium, copper, and zinc to total cadmium, copper, and zinc at site 1 was about 1. Samples collected in Pike Hill Brook upstream and downstream from the wetlands during low flows in August 2005 showed that oxidation of ferrous iron and precipitation of iron-hydroxides were probably not affecting trace metals in the wetlands through sorption; however, a significant portion of the iron entering the wetlands was in particulate form and may have transported sorbed copper and other trace metals. Thus, aerobic activity in the wetlands was probably not affecting metal cycling in the watershed. Concentrations and loads of sulfate may be unlikely to define unequivocally the role of the wetlands with regard to anaerobic bacterial sulfate reduction; however, bacterial sulfate removal may have affected loads of sulfate. Loads of copper increased downstream from the wetlands and may reflect the reductive dissolution of ferric hydroxide particulates in anaerobic parts of the wetlands.Concentrations of dissolved iron increased downstream from the wetlands. The most apparent effects on the macroinvertebr

Scientific Investigations Report↗
USGS2004

Water-quality characteristics and ground water quantity of the Fraser River watershed, Grand County, Colorado, 1998-2001

The U.S. Geological Survey, in cooperation with the Grand County Board of County Commissioners, conducted a 4-year study to assess ground- and surface-water-quality conditions and ground-water quantity in the 302-square-mile Fraser River watershed in north-central Colorado. The Fraser River flows north about 28 miles from the headwaters near the Continental Divide, through the towns of Winter Park, Fraser, Tabernash, and Granby, and is one of the major tributaries to the Upper Colorado River. Increasing urban development, as well as the seasonal influx of tourists, is placing more demands on the water resources in the Fraser River watershed. A ground-water sampling network of 11 wells was established to represent different aquifer systems (alluvial, Troublesome Formation, Precambrian granite), land uses (urban, nonurban), and areas with or without individual septic disposal system use. The well network was sampled for ground-water quality on a semiannual basis from August 1998 through September 2001. The sampling included field properties and the collection of water samples for analysis of major ions, trace elements, nutrients, dissolved organic carbon, bacteria, methylene blue active substances, and radon-222. One surface-water site, on the Fraser River just downstream from the town of Tabernash, Colorado, was sampled bimonthly from August 1998 through September 2001 to assess the cumulative effects of natural and human processes on water quality in the upper part of the Fraser River watershed. Surface-water-quality sampling included field properties and the collection of water-quality samples for analysis of major ions, trace elements, nutrients, organic carbon, and bacteria. Ground water was a calcium-bicarbonate type water and is suitable as a drinking-water, domestic, municipal, industrial, and irrigation source. In general, no widespread ground-water-quality problems were indicated. All pH values and concentrations of dissolved solids, chloride, fluoride, sulfate, nitrite, and nitrate in the ground-water samples met or were substantially less than U.S. Environmental Protection Agency drinking-water standards and health advisories or State of Colorado water-quality standards. Federal standards for turbidity and concentrations of iron, manganese, methylene blue active substances, and radon-222 were not met in water samples from at least one well. The only ground-water-quality concern assessed by this study is radon-222, which was detected in all radon- analyzed samples from 10 wells at levels exceeding the proposed U.S. Environmental Protection Agency drinking-water standard of 300 picocuries per liter. Concentrations of chloride, magnesium, and sulfate were statistically different (higher) in ground-water samples from wells completed in the alluvial aquifer, urbanized areas, and areas with individual septic disposal system use than those from wells completed in the Troublesome Formation, nonurban areas, and areas without individual septic disposal system use. Dissolved organic carbon concentrations were statistically higher in ground-water samples from wells completed in the alluvial aquifer and areas without individual septic disposal system use than those from wells completed in the Troublesome Formation and areas with individual septic disposal system use. Differences in dissolved organic-carbon concentrations between the latter category and areas without septic systems likely had no environmental significance. Surface water at the site Fraser River below Crooked Creek at Tabernash was a calcium-bicarbonate type water and is suitable as a drinking-water, residential, commercial, and irrigation resource. All pH values and concentrations of dissolved oxygen were within the State of Colorado instream water-quality standards, and all concentrations of chloride, sulfate, iron, manganese, un-ionized ammonia, nitrite, nitrate, and fecal coliform bacteria met State standards. Seasonal changes in the values or conc

Colorado↗
USGS2004

Quality of water in the Trinity and Edwards aquifers, south-central Texas, 1996-98

During 1996–98, the U.S. Geological Survey studied surface- and ground-water quality in south-central Texas. The ground-water components included the upper and middle zones (undifferentiated) of the Trinity aquifer in the Hill Country and the unconfined part (recharge zone) and confined part (artesian zone) of the Edwards aquifer in the Balcones fault zone of the San Antonio region. The study was supplemented by information compiled from four ground-water-quality studies done during 1996–98. Trinity aquifer waters are more mineralized and contain larger dissolved solids, sulfate, and chloride concentrations compared to Edwards aquifer waters. Greater variability in water chemistry in the Trinity aquifer likely reflects the more variable lithology of the host rock. Trace elements were widely detected, mostly at small concentrations. Median total nitrogen was larger in the Edwards aquifer than in the Trinity aquifer. Ammonia nitrogen was detected more frequently and at larger concentrations in the Trinity aquifer than in the Edwards aquifer. Although some nitrate nitrogen concentrations in the Edwards aquifer exceeded a U.S. Geological Survey national background threshold concentration, no concentrations exceeded the U.S. Environmental Protection Agency public drinking-water standard. Synthetic organic compounds, such as pesticides and volatile organic compounds, were detected in the Edwards aquifer and less frequently in the Trinity aquifer, mostly at very small concentrations (less than 1 microgram per liter). These compounds were detected most frequently in urban unconfined Edwards aquifer samples. Atrazine and its breakdown product deethylatrazine were the most frequently detected pesticides, and trihalomethanes were the most frequently detected volatile organic compounds. Widespread detections of these compounds, although at small concentrations, indicate that anthropogenic activities affect ground-water quality. Radon gas was detected throughout the Trinity aquifer but not throughout the Edwards aquifer. Fourteen samples from the Trinity aquifer and 10 samples from the Edwards aquifer exceeded a proposed U.S. Environmental Protection Agency public drinking-water standard. Sources of radon in the study area might be granitic sediments underlying the Trinity aquifer and igneous intrusions in and below the Edwards aquifer. The presence of tritium in nearly all Edwards aquifer samples indicates that some component of sampled water is young (less than about 50 years), even for long flow paths in the confined zone. About one-half of the Trinity aquifer samples contained tritium, indicating that only part of the aquifer contains young water. Hydrogen and oxygen isotopes of water provide indicators of recharge sources to the Trinity and Edwards aquifers. Most ground-water samples have a meteorological isotopic signature indicating recharge as direct infiltration of water with little residence time on the land surface. Isotopic data from some samples collected from the unconfined Edwards aquifer indicate the water has undergone evaporation. At the time that ground-water samples were collected (during a drought), nearby streams were the likely sources of recharge to these wells.

Texas↗