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At least 1,153 records · Page 64Linked to original sources
USGS2004

Water quality in Big Cypress National Preserve and Everglades National Park — Trends and spatial characteristics of selected constituents

Seasonal changes in water levels and flows in Big Cypress National Preserve (BICY) and Everglades National Park (EVER) affect water quality. As water levels and flows decline during the dry season, physical, geochemical and biological processes increase the breakdown of organic materials and the build-up of organic waste, nutrients, and other constituents in the remaining surface water. For example, concentrations of total phosphorus in the marsh are less than 0.01 milligram per liter (mg/L) during much of the year. Concentrations can rise briefly above this value during the dry season and occasionally exceed 0.1 mg/L under drought conditions. Long-term changes in water levels, flows, water management, and upstream land use also affect water quality in BICY and EVER, based on analysis of available data (1959-2000). During the 1980's and early 1990's, specific conductance and concentrations of chloride increased in the Taylor Slough and Shark River Slough. Chloride concentrations more than doubled from 1960 to 1990, primarily due to greater canal transport of high dissolved solids into the sloughs. Some apparent long-term trends in sulfate and total phosphorus were likely attributable, at least in part, to high percentages of less-than and zero values and to changes in reporting levels over the period of record. High values in nutrient concentrations were evident during dry periods of the 1980's and were attributable either to increased canal inflows of nutrient-rich water, increased nutrient releases from breakdown of organic bottom sediment, or increased build-up of nutrient waste from concentrations of aquatic biota and wildlife in remaining ponds. Long-term changes in water quality over the period of record are less pronounced in the western Everglades and the Big Cypress Swamp; however, short-term seasonal and drought-related changes are evident. Water quality varies spatially across the region because of natural variations in geology, hydrology, and vegetation and because of differences in water management and land use. Nutrient concentrations are relatively low in BICY and EVER compared with concentrations in parts of the northern Everglades that are near agricultural and urban lands. Concentrations of total phosphorus generally are higher in BICY (median values, 1991-2000, were mostly greater than 0.015 mg/L) than in EVER (median values, 1991-2000, less than 0.01 mg/L), probably because of higher phosphorus in natural sources such as shallow soils, rocks, and ground water in the Big Cypress region than in the Everglades region. Conversely, concentrations of chloride and sulfate are higher in EVER (median values in Shark River Slough, 1991-2000, mostly greater than 2 mg/L sulfate and 50 mg/L chloride) than in BICY (median values, 1991-2000, less than 1 mg/L sulfate and at most sites less than 20 mg/L chloride), probably because of the canal transport system, which conveys more water from an agricultural source into EVER than into BICY. Trace elements and contaminants such as pesticides and other toxic organic compounds are in relatively low concentrations in BICY and EVER compared with concentrations in parts of the northern Everglades near agricultural and urban sources. Concentrations rarely exceeded aquatic life criteria in BICY and EVER. Atrazine was the only pesticide found in water that exceeded the criteria (in 2 out of 304 samples). The pesticides heptachlor expoxide, lindane, and p,p?-DDE exceeded criteria in canal bed sediments in 1, 2, and 16 percent of the samples, respectively.

Florida↗
USGS1984

Reconnaissance of toxic substances in the Jordan River, Salt Lake County, Utah

A reconnaissance of toxic substances in the Jordan River, Salt Lake County, Utah, was made during July, 1980 to October, 1982 as part of a larger study of the river that included studies of sanitary quality, dissolved oxygen, and turbidity. Samples for toxic substances were collected at five sites on the Jordan River, at three major tributaries, and at six storm drains. The toxic substance that most frequently exceeded State standards was total mercury. About 78 percent of the 138 samples for total mercury exceeded the State standard of 0.05 microgram per liter. Other toxic substances that exceeded State standards were: Ammonia-18 percent of the samples analyzed, cadmium--9 percent, copper-9 percent, zinc--6 percent, and lead--2 percent. One sample for cyanide and one for iron also exceeded State standards. The diversity of toxic substances with concentrations large enough to cause them to be problems increased from the upstream sampling site at the Jordan Narrows to the next two downstream sites at 9000 South and 5800 South Streets. Concentrations of trace elements in stream-bottom materials also increased in a downstream direction. Substantial increases first were observed at 5800 South Street, and they were sustained throughout the downstream study area. Iron is transported in the greatest quantity of all the trace elements studied, with a mean load of 110 pounds per day. Notable loads of barium, boron, lead , and zinc also are transported by the river. DDD, DDE, DDT, dieldrin, heptachlor, methoxychlor, PCB, and 2,4-D were detected in bottom materials; and DDE, Silvex, and 2,4-D were detected in water samples. Of 112 organic compounds in the Environmental Protection Agency 's priority pollutant list, only chloroform was detected in the storm drains that empty into the Joran River. Several metals and phenol also were detected in the samples for priority pollutants. (USGS)

Water-Resources Investigations Report↗
USGS1976

Backflushing Filters for Field Processing of Water Samples Prior to Trace-Element Analyses

A portable unit is described for filtering water samples at field sites in such a manner that the filtrate is suitable for analysis not only of major constituents but also of trace elments at the mocrogram-per-liter level. A battery-operated peristaltic pump forces the water sample through medical-grade silicone tubing into and through an all-plastic in-line filter which can be backflushed when sediment clogs the filter membrane. Initial filtration rate exceeds 500 milliliter/minute and, because of the backflushing feature, a total time for filtering high-sediment-bearing waster samples is greatly reduced. (Woodard-USGS)

Water-Resources Investigations Report↗
USGS1999

Baseline water quality and preliminary effects of artificial recharge on ground water, south-central Kansas, 1995–98

To investigate the feasbility of artificial recharge as a method of meeting future water-supply needs and to protect the Equus Beds aquifer from saltwater intrusion from natural and anthropogenic sources to the west, the Equus Beds Ground-Water Recharge from Demonstration Project was begun in 1995. The project is a cooperative effort between the city of Wichita and the Bureau of Reclamation, U.S. Department of the Interior. During the project, high flows from the Little Arkansas River are captured and recharged into the Equus Beds aquifer through recharge basins, a trench, or a recharge well, located at two recharge sites near Halstead and Sedgwick, Kansas. To document baseline concentrations and compatibility of stream (recharge) and aquifer water, the U.S. Geological Survey collected water samples from February 1995 through August 1998. These samples were analyzed for dissolved solids, total and dissolved inorganic constituents, nutrients, organic and volatile organic compounds, radionuclides, and bacteria. Results of baseline sampling indicated that the primary constituents of concern for recharge were sodium, chloride, nitrite plus nitrate, iron and manganese, total coliform bacteria, and atrazine. Chloride and atrazine were of particular concern because concentrations of these constituents in water from the Little Arkansas River frequently exceeded regulatory criteria. The Little Arkansas River is used as the source water for recharge. The U.S. Environmental Protection Agency Secondary Maximum Contaminant Level for chloride is 250 mg/L (milligrams per liter), and the Maximum Contaminant Level for atrazine is 3.0 μg/L (micrograms per liter) as an annual mean. Baseline concentrations of chloride in surface water ranged from 8.0 to 400 μg/L. Baseline concentrations of atrazine in surface water ranged from less than 0.10 to 46 μg/L. Concentrations of chloride and atrazine have increased in water from some of the wells at both the Halstead and Sedgwick recharge sites after recharge began, although concentrations remained within the range of baseline values in the Equus Beds aquifer and are considerably less than U.S. Environmental Protection Agency drinking-water criteria. However, a substantial quantity of water has not been recharged at the Sedgwick site to determine the overall effects of artificial recharge on aquifer quality. Continued monitoring is necessary to determine long-term effects at both sites. Major ion and trace element concentrations in source water and receiving water were analyzed to determine the compatibility of recharge and receiving ground water for artificial recharge. Stiff diagrams of major ions were used to show the similarity or differences between source surface water and receiving ground water. The water from both sources, for the most part, was chemically compatible to the receiving aquifer water at both recharge sites. It may be possible to decrease the monitoring frequency at the Halstead recharge site because water-quality changes in receiving water at this site are very gradual. However, real-time water-quality monitoring of surrogates needs to be site specific for the determination of chloride and atrazine. Real-time water-quality monitoring potentially can be used to more effectively manage the artificial recharge process, enabling project officials to respond more rapidly to changes in water quality.

Water-Resources Investigations Report↗
USGS2012

Altitude, age, and quality of groundwater, Papio-Missouri River Natural Resources District, eastern Nebraska, 1992 to 2009

The U.S. Geological Survey, in cooperation with the Papio-Missouri River Natural Resources District (PMRNRD), conducted this study to map the water-level altitude of 2009 within the Elkhorn River Valley, Missouri River Valley, and Platte River Valley alluvial aquifers; to present the predevelopment potentiometric-surface altitude within the Dakota aquifer; and to describe the age and quality of groundwater in the five principal aquifers of the PMRNRD in eastern Nebraska using data collected from 1992 to 2009. In addition, implications of alternatives to the current PMRNRD groundwater-quality monitoring approach are discussed. In the PMRNRD, groundwater altitude, relative to National Geodetic Vertical Datum of 1929, ranged from about 1,080 feet (ft) to 1,180 ft in the Elkhorn River Valley alluvial aquifer and from about 960 ft to 1,080 ft in the Missouri River Valley and Platte River Valley alluvial aquifers. In the PMRNRD, the estimated altitude of the potentiometric surface of the Dakota aquifer, predevelopment, ranged from about 1,100 ft to 1,200 ft. To assess groundwater age and quality, groundwater samples were collected from a total of 217 wells from 1992 to 2009 for analysis of various analytes. Groundwater samples collected in the PMRNRD from 1992 to 2009 and interpreted in this report were analyzed for age-dating analytes (chlorofluorocarbons), dissolved gases, major ions, trace elements, nutrients, stable isotope ratios, pesticides and pesticide degradates, volatile organic compounds, explosives, and 222radon. Apparent groundwater age was estimated from concentrations of chlorofluorocarbons measured in samples collected in 2000. Apparent groundwater-recharge dates ranged from older than 1940 in samples from wells screened in the Missouri River Valley alluvial aquifer to the early 1980s in samples from wells screened in the Dakota aquifer. Concentrations of major ions in the most recent sample per well collected from 1992 to 2009 indicate that the predominant water type was calcium bicarbonate. Samples from 4 wells exceeded the U.S. Environmental Protection Agency (USEPA) Secondary Drinking Water Regulation (SDWR) for sulfate [250 milligrams per liter (mg/L)], and samples from 4 wells exceeded the USEPA Drinking Water Advisory Table for sodium (30-60 mg/L). Eighteen of the 21 trace elements analyzed in samples from PMRNRD wells have USEPA drinking-water standards. Sixteen of the trace elements with USEPA standards were detected in the selected samples. In the samples selected for trace-element analysis, the only trace-element concentration that exceeded an enforceable USEPA drinking-water standard, the Maximum Contaminant Level (MCL), was for arsenic; arsenic concentration exceeded the USEPA MCL of 10 micrograms per liter (μg/L) in 4 percent of the samples. Trace-element concentrations that exceeded the USEPA SDWR or Lifetime Health Advisory level were iron (46 percent of the samples were greater than USEPA SDWR of 300 μg/L), manganese (70 percent of the samples were greater than USEPA SDWR of 50 μg/L), and strontium (4 percent of the samples were greater than USEPA Lifetime Health Advisory level of 4,000 μ/L). The concentration of nitrate plus nitrite as nitrogen (nitrate-N) in the most recent nutrient samples collected from the network wells and from one randomly selected well in the well nests from 1992 to 2009 for most wells (80 percent) ranged from less than 0.06 to 8.55 mg/L, with a median value of 0.12 mg/L. Concentrations of nitrate-N in 13 (7 percent) nutrient samples, 1992 to 2009, were greater than or equal to the USEPA MCL and Nebraska Title-118 standard of 10 mg/L, and concentrations of nitrate-N in 35 (18 percent) nutrient samples, 1992 to 2009, were greater than or equal to 5 mg/L, which is the PMRNRD action level for possible management implementation to reduce nitrate concentrations in groundwater. Of the 61 pesticides or pesticide degradates analyzed from 2007 to 2009, 21 were detected. Three of the 21 pesticides detected (alachlor, atrazine, and metolachlor) have established health-based criteria; all detections of these compounds were at concentrations less than their USEPA standards. From 2007 to 2009, 1 or more pesticide compounds were detected in 16 of the 82 network wells and in 18 of the 26 wells in well nests. From 2007 to 2009, the individual pesticide compounds that were detected most frequently were alachlor ethane sulfonic acid, a degradate of alachlor; deethylcyanazine acid, a degradate of cyanazine; and atrazine. Analytes with concentrations that exceeded 30 percent of the applicable Nebraska Title-118 standard were identified so that the PMRNRD can plan to monitor groundwater in the area and consider possible actions should the analyte concentrations continue to rise. The analytical results from the most recent samples collected in the network wells and all the wells in well nests from 1992 to 2009 indicate that, in at least 1 sample, there was a concentration that exceeded 30 percent of the Nebraska Title-118 standard for at least 1 of 3 major ions (chloride, fluoride, and sulfate), 1 nutrient (nitrate-N), 1 pesticide (atrazine), or 3 trace elements (arsenic, iron, and manganese). In addition, 30 percent of the USEPA MCL or Nebraska Title-118 standard for gross alpha activity likely was exceeded in samples from three wells screened in the Dakota aquifer. Study findings indicate that some alternatives to the current PMRNRD groundwater-sampling approach that could be considered are to collect fewer samples for nutrient analysis and to collect samples periodically for determining concentrations of additional analytes, particularly the analytes with concentrations that were at least 30 percent or more than the Nebraska Title-118 standard.

Nebraska↗
USGS2020

Water Quality of groundwater used for public supply in principal aquifers of the western United States

Groundwater provides nearly half of the Nation’s drinking water. As the Nation’s population grows, the importance of (and need for) high-quality drinking-water supplies increases. As part of a national-scale effort to assess groundwater quality in principal aquifers (PAs) that supply most of the groundwater used for public supply, the U.S. Geological Survey National Water-Quality Assessment (NAWQA) Project staff sampled six principal aquifers in the western United States between 2013 and 2017: (1) the Basin and Range carbonate-rock aquifers, (2) Basin and Range basin-fill aquifers, (3) Rio Grande aquifer system, (4) High Plains aquifer, (5) Colorado Plateaus aquifers, and (6) Columbia Plateau basaltic-rock aquifers. These six PAs supply a large part of the Nation’s drinking water and cover a large geographic extent of the western conterminous United States. Groundwater samples were analyzed for a large suite of water-quality constituents including major ions, nutrients, trace elements, volatile organic compounds (VOCs), pesticide compounds, radioactive constituents, age tracers, and, in selected PAs, perchlorate. Two types of assessments were made: (1) a status assessment that describes the quality of the groundwater resource at time of collection and (2) an understanding assessment that evaluates relations between groundwater quality and potential explanatory factors that represent characteristics of the aquifer system. The assessments characterize untreated groundwater quality, which might be different than the quality of drinking water delivered to consumers. The assessments are based on water-quality data collected from 352 wells and 6 springs using an equal-area grid sampling design. This sampling approach allows for the estimation of the proportion of high, moderate, or low concentrations relative to federal water-quality benchmarks of selected constituents in the area of each PA. Results were compared to established benchmarks for drinking-water quality to provide context for evaluating the quality of untreated groundwater: Federal regulatory benchmarks for protecting human health, non-regulatory human-health benchmarks, and non-regulatory benchmarks for nuisance chemicals. Not all constituents that were analyzed have benchmarks and thus were not considered for assessments. Concentrations are characterized as high if they are greater than their benchmark. Concentrations are considered moderate if they are greater than one-half their benchmark (for inorganic constituents), or greater than one-tenth their benchmark (for organic constituents). Concentrations are considered low if they are less than moderate or the constituent was not detected. Status assessment results indicated that inorganic constituents more commonly occurred at high and moderate concentrations in the six PAs than organic constituents, and organic constituents predominately occurred at low concentrations. Inorganic constituents that exceeded health-based benchmarks (high concentrations) were present in all six PAs; aquifer-scale proportion were 30 percent in the Rio Grande aquifer system, 22 percent in the Basin and Range basin-fill aquifers, 20 percent in the Basin and Range carbonate-rock aquifers, 19 percent in the High Plains aquifer, 16 percent in the Colorado Plateaus aquifers, and 8 percent in the Columbia Plateau basaltic-rock aquifers. Arsenic, fluoride, manganese, and total dissolved solids were the constituents most commonly present at high concentrations. Organic constituents with human-health benchmarks (pesticide compounds and VOCs) did not occur at high concentrations and moderate concentrations were infrequent; aquifer-scale proportions ranged from 0 to 5 percent. Detections of organic compounds at low concentrations, however, occurred in all six PAs, with detection frequencies ranging from 10 to 26 percent for pesticide compounds and from 10 to 46 percent for VOCs. Specific organic constituents with detection frequencies greater than 10 percent were four herbicides (atrazine, didealkylatrazine, bromoform, and propazine), one insecticide (propoxur), and two VOCs (the trihalomethanes chloroform and bromodichloromethane). Where collected—in the Rio Grande aquifer system and High Plains aquifer—perchlorate did not occur at high concentrations; moderate aquifer-scale proportions were 3 and 11 percent, respectively. The understanding assessment included statistical tests to evaluate relations between constituent concentrations and potential explanatory factors to identify natural and human factors that affect groundwater quality. Potential explanatory factors included depth to bottom of well perforation, groundwater age category, land use, aquifer lithology, hydrologic conditions, and geochemical conditions. Higher concentrations of trace elements, radioactive constituents, and constituents with non-health-based benchmarks generally were associated with unconsolidated sand and gravel aquifer lithologies, premodern groundwater age, greater aridity, and more alkaline pH. Organic constituents with detection frequencies greater than 10 percent generally were associated with urban land use, shallower well depths, and higher total dissolved solids concentrations. The results for the six western PAs provide important insights into the quality of groundwater that is used for drinking water in the western United States, as well as natural and human factors that affect groundwater quality in this region.

Arizona, California, Colorado, Idaho, Kansas, Mont↗
USGS2014

Water-chemistry data collected in and near Kaloko-Honokohau National Historical Park, Hawaii, 2012–2014

Kaloko-Honokōhau National Historical Park (KAHO) on western Hawaiʻi was established in 1978 to preserve, interpret, and perpetuate traditional Native Hawaiian culture and activities, including the preservation of a variety of culturally and ecologically significant water resources that are vital to this mission. KAHO water bodies provide habitat for 1 threatened, 11 endangered, and 3 candidate threatened or endangered species. These habitats are sustained by, and in the case of ʻAimakapā Fishpond and the anchialine pools, entirely dependent on, groundwater from the Keauhou aquifer system. Development of inland impounded groundwater in the Keauhou aquifer system may affect the coastal freshwater-lens system on which KAHO depends, if the inland impounded-groundwater and coastal freshwater-lens systems are hydrologically connected. This report documents water-chemistry results from a U.S. Geological Survey study that collected and analyzed water samples from 2012 to 2014 from 25 sites in and near KAHO to investigate potential geochemical indicators in water that might indicate the presence or absence of a hydrologic connection between the inland impounded-groundwater and coastal freshwater-lens systems in the area. Samples were collected under high-tide and low-tide conditions for KAHO sites, and in dry-season and wet-season conditions for all sites. Samples were collected from two ocean sites, two fishponds, three anchialine pools, and three monitoring wells within KAHO. Two additional nearshore wells were sampled on property adjacent to and north of KAHO. Additional samples from the freshwater-lens system were collected from six inland wells located upslope from KAHO, including three production wells. Seven production wells in the inland impounded-groundwater system also were sampled. Water samples were analyzed for major ions, selected trace elements, rare-earth elements, strontium-isotope ratio, and stable isotopes of water. Precipitation samples from five sites were collected roughly along a transect upslope from KAHO. All precipitation samples were analyzed for stable isotopes of water and some precipitation samples were analyzed for rare-earth and selected trace elements.

Hawai'i↗
USGS2005

Hydrogeologic framework and water quality of the Vermont Army National Guard Ethan Allen Firing Range, northern Vermont, October 2002 through December 2003

The Ethan Allen Firing Range of the Vermont Army National Guard is a weapons-testing and training facility in a mountainous region of Vermont that has been in operation for about 80 years. The hydrologic framework and water quality of the facility were assessed between October 2002 and December 2003. As part of the study, streamflow was continuously measured in the Lee River and 24 observation wells were installed at 19 locations in the stratified drift and bedrock aquifers to examine the hydrogeology. Chemical analyses of surface water, ground water, streambed sediment, and fish tissue were collected to assess major ions, trace elements, nutrients, and volatile and semivolatile compounds. Sampling included 5 surface-water sites sampled during moderate and low-flow conditions; streambed-sediment samples collected at the 5 surface-water sites; fish-tissue samples collected at 3 of the 5 surface-water sites; macroinvertebrates collected at 4 of the 5 surface-water sites; and ground-water samples collected from 10 observation wells, and samples collected at all surface- and ground-water sites. The hydrogeologic framework at the Ethan Allen Firing Range is dominated by the upland mountain and valley setting of the site. Bedrock wells yield low to moderate amounts of water (0 to 23 liters per minute). In the narrow river valleys, layered stratified-drift deposits of sand and gravel of up to 18 meters thick fill the Lee River and Mill Brook Valleys. In these deposits, the water table is generally within 3 meters below the land surface and overall ground-water flow is from east to west. Streamflow in the Lee River averaged 0.72 cubic meters per second (25.4 cubic feet per second) between December 2002 and December 2003. Streams are highly responsive to precipitation events in this mountainous environment and a comparison with other nearby watersheds shows that Lee River maintains relatively high streamflow during dry periods. Concentrations of trace elements and nutrients in surface-water samples are well below freshwater-quality guidelines for the protection of aquatic life. Brook-trout samples collected in 1992 and 2003 show trace-metal concentrations have decreased over the past 11 years. concentrations in water samples are well below levels that restrict swimming at all five stream sites at moderate and low-flow conditions and in all observation wells. Comparisons among surface-water, streambed-sediment, and biological samples collected in 2003 to earlier studies at the Ethan Allen Firing Range indicate water-quality conditions are similar or have improved over the past 15 years. Ground water in the stratified-drift aquifers at the facility is well buffered with relatively high alkalinities and pH greater than 6. Concentrations of arsenic, cadmium, chromium, lead, nickel, uranium, and zinc were below detection levels in ground-water samples. Barium, cobalt, copper, iron, manganese, molybdenum, and strontium were the only trace elements detected in ground-water samples. Cobalt and iron were detected at low levels in two wells near Mill Brook, and copper was detected at the detection limit in one of these wells. These same two wells had concentrations of barium and manganese 2 to 10 times greater than other ground-water samples. Concentrations of nutrients are at or below detection levels in most ground-water samples. Volatile organic compounds and semivolatile organic compounds were not detected in any water samples from the Ethan Allen Firing Range.

Scientific Investigations Report↗
USGS2014

Stream-water and groundwater quality in and near the Citizen Potawatomi Nation Tribal Jurisdictional Area, Pottawatomie County, Oklahoma, 2012-13

The Citizen Potawatomi Nation needs to characterize their existing surface-water and groundwater resources in and near their tribal jurisdictional area to complete a water-resource management plan. Water resources in this area include surface water from the North Canadian and Little Rivers and groundwater from the terrace and alluvial aquifers and underlying bedrock aquifers. To assist in this effort, the U.S. Geological Survey (USGS), in cooperation with the Citizen Potawatomi Nation, collected water-quality samples at 4 sites on 3 streams and from 30 wells during 2012 and 2013 in and near the Citizen Potawatomi Nation Tribal Jurisdictional Area in central Oklahoma. Stream samples were collected eight times on the North Canadian River at the upstream USGS streamflow-gaging station North Canadian River near Harrah, Okla. (07241550); at the downstream USGS streamflow-gaging station North Canadian River at Shawnee, Okla. (07241800); and on the Little River at the USGS streamflow-gaging station Little River near Tecumseh, Okla., (07230500). Stream samples also were collected three times at an ungaged site, Deer Creek near McLoud, Okla. (07241590). Water properties were measured, and water samples were analyzed for concentrations of major ions, nutrients, trace elements, counts of fecal-indicator bacteria, and 69 organic compounds. The highest concentrations of dissolved solids and chlorides were measured in stream-water samples collected at the Little River near Tecumseh station. The Secondary Maximum Contaminant Level (SMCL) for dissolved solids in drinking water of 500 milligrams per liter (mg/L) was exceeded in 7 of 8 stream-water samples, with a median concentration of 844 mg/L at that station. The 250-mg/L SMCL for chloride was exceeded in 5 of the 8 stream-water samples collected at that station. Median concentrations of total dissolved nitrogen were about an order of magnitude higher in stream-water samples collected at the two stations on the North Canadian River than concentrations in stream-water samples collected at the Little River near Tecumseh station and the Deer Creek site. Median concentrations of total dissolved nitrogen were 4.36 and 2.89 mg/L in stream-water samples collected at the two North Canadian River stations, 0.35 mg/L in stream-water samples collected at the Little River near Tecumseh station, and 0.76 mg/L in stream-water samples collected at the Deer Creek site. Similar to nitrogen, median concentrations of total dissolved phosphorus were higher by about two orders of magnitude in stream-water samples collected at the two stations on the North Canadian River than concentrations in stream-water samples collected at the Little River near Tecumseh station and the Deer Creek site. Median concentrations of total dissolved phosphorus were 1.05 and 0.805 mg/L in stream-water samples collected at the two North Canadian River stations, 0.007 mg/L in stream-water samples collected at the Little River near Tecumseh station, and 0.032 mg/L from the Deer Creek site. Dissolved concentrations of total nitrogen, nitrate-nitrogen, orthophosphorus, and total phosphorus were highest in stream-water samples collected at the two North Canadian River stations at low streamflows, indicating that wastewater effluent may have been a notable source of these nutrients. Concentrations of most trace elements increased with increasing streamflow in stream-water samples collected at the two North Canadian River stations, indicating that most trace elements are washed into the river by runoff from the land surface or resuspended from streambed sediments. In general, most trace-element concentrations were below respective Maximum Contaminant Levels (MCLs) for public drinking-water supplies, except for one stream-water sample with an arsenic concentration of 10.1 micrograms per liter (µg/L) collected from the North Canadian River and one stream-water sample with a barium concentration of 2,690 µg/L collected from the Little River. At least one stream-water sample from each of the four stream sites sampled in this study contained a lead concentration exceeding the SMCL of 15 µg/L. All of these samples were collected during high streamflows. A greater number of organic compounds were detected in stream-water samples collected at the two stations on the North Canadian River than in stream-water samples collected at the Tecumseh station and Deer Creek site. In the 8 stream-water samples collected at the upstream Harrah station, 213 detections of organic compounds were measured, whereas in 8 samples collected at the downstream Shawnee station, 203 detections of organic compounds were measured. In contrast, 59 detections of organic compounds were measured in the 8 stream-water samples collected at the Tecumseh station, and 25 detections of organic compounds were measured in the 3 stream-water samples collected at the Deer Creek site; however, the 8 detections of 7 organic compounds in the 2 equipment-blank samples is problematic for evaluating these data, especially for the Deer Creek and Little River samples because of the comparatively low detection frequency and should be taken into consideration when evaluating these results. Groundwater samples also were collected once from 30 wells producing water from the Garber-Wellington aquifer; Admire, Chase, and Council Grove Groups; the Vanoss Formation; and the terrace and alluvial aquifers along the North Canadian River. Water properties were measured, and samples were analyzed for concentrations of major ions, nutrients, trace elements, and selected radionuclides in groundwater. Of 30 wells sampled for this study, 26 were completed in bedrock aquifers, and 4 were completed in terrace and alluvial aquifers. In general, groundwater in the study area is very hard, with a median concentration of 180 mg/L as calcium carbonate in water samples collected from the 30 wells. Concentrations of sulfate exceeded the 250-mg/L SMCL in two groundwater samples, and dissolved solids concentrations exceeded the 500-mg/L SMCL in nine groundwater samples. Trace-element concentrations did not exceed respective MCLs in the 30 groundwater samples collected for this study. Concentrations of the radionuclide uranium ranged from 0.03 to 79.5 µg/L, with a median concentration of 1.9 µg/L in the 30 groundwater samples collected. Two of the groundwater samples collected for this study had uranium concentrations exceeding the MCL of 30 µg/L, with concentrations of 79.5 and 31.1 µg/L. Generally, uranium concentrations were highest in water samples collected from wells completed in the Wellington Formation and the Chase, Council Grove, and Admire Groups in the southern and eastern parts of the study area.

Oklahoma↗
USGS2014

Water quality of the Ogallala Formation, central High Plains aquifer within the North Plains Groundwater Conservation District, Texas Panhandle, 2012-13

In cooperation with the North Plains Groundwater Conservation District (NPGCD), the U.S. Geological Survey collected and analyzed water-quality samples at 30 groundwater monitor wells in the NPGCD in the Texas Panhandle. All of the wells were completed in the Ogallala Formation of the central High Plains aquifer. Samples from each well were collected during February–March 2012 and in March 2013. Depth to groundwater in feet below land surface was measured at each well before sampling to determine the water-quality sampling depths. Water-quality samples were analyzed for physical properties, major ions, nutrients, and trace metals, and 6 of the 30 samples were analyzed for pesticides. There was a strong relation between specific conductance and dissolved solids as evidenced by a coefficient of determination ( R 2 ) value of 0.98. The dissolved-solids concentration in water from five wells exceeded the secondary drinking-water standard of 500 milligrams per liter set by the U.S. Environmental Protection Agency. Water from 3 of these 5 wells was near the north central part of the NPGCD. Nitrate values exceeded the U.S. Environmental Protection Agency maximum contaminant level of 10 milligrams per liter in 2 of the 30 wells. A sodium-adsorption ratio of 23.4 was measured in the sample collected from well Da-3589 in Dallam County, with the next largest sodium-adsorption ratio measured in the sample collected from well Da-3588 (12.5), also in Dallum County. The sodium-adsorption ratios measured in all other samples were less than 10. The groundwater was generally a mixed cation-bicarbonate plus carbonate type. Twenty-three trace elements were analyzed, and no concentrations exceeded the secondary drinking-water standard or maximum contaminant level set by the U.S. Environmental Protection Agency for water supplies. In 2012, 6 of the 30 wells were sampled for commonly used pesticides. Atrazine and its degradate 2-Chloro-4-isopropylamino-6-amino-s-triazine were detected in two samples. Tebuthiuron was detected in one sample at a detection level below the reporting level but above the long-term method detection level. There were no detections of the glyphosate, aminomethylphosphonic acid (AMPA), or glufosinate.

Texas↗
USGS2001

Effects of urbanization on benthic macroinvertebrate communities in streams, Anchorage, Alaska

The effect of urbanization on stream macroinvertebrate communities was examined by using data gathered during a 1999 reconnaissance of 14 sites in the Municipality of Anchorage, Alaska. Data collected included macroinvertebrate abundance, water chemistry, and trace elements in bed sediments. Macroinvertebrate relative-abundance data were edited and used in metric and index calculations. Population density was used as a surrogate for urbanization. Cluster analysis (unweighted-paired-grouping method) using arithmetic means of macroinvertebrate presence-absence data showed a well-defined separation between urbanized and nonurbanized sites as well as extracted sites that did not cleanly fall into either category. Water quality in Anchorage generally declined with increasing urbanization (population density). Of 59 variables examined, 31 correlated with urbanization. Local regression analysis extracted 11 variables that showed a significant impairment threshold response and 6 that showed a significant linear response. Significant biological variables for determining the impairment threshold in this study were the Margalef diversity index, Ephemeroptera-Plecoptera-Trichoptera taxa richness, and total taxa richness. Significant thresholds were observed in the water-chemistry variables conductivity, dissolved organic carbon, potassium, and total dissolved solids. Significant thresholds in trace elements in bed sediments included arsenic, iron, manganese, and lead. Results suggest that sites in Anchorage that have ratios of population density to road density greater than 70, storm-drain densities greater than 0.45 miles per square mile, road densities greater than 4 miles per square mile, or population densities greater than 125-150 persons per square mile may require further monitoring to determine if the stream has become impaired. This population density is far less than the 1,000 persons per square mile used by the U.S. Census Bureau to define an urban area.

Water-Resources Investigations Report↗
USGS1982

Water-quality characteristics of Everglades National Park, 1959-77, with reference to the effects of water management

The U.S. Geological Survey has collected water-quality data in the Everglades National Park since 1959. Major ions, macronutrients, trace elements, and pesticides are the primary chemical groups analyzed. The period of record and frequency of sampling vary for each chemical group, with the longest record for the major ions and the shortest for the macronutrients. Within the park there are three major drainageways: Big Cypress Swamp, Shark River Slough, and Taylor Slough. Each drainageway exhibits unique hydrologic conditions, yet there is a high degree of homogeneity in water-quality characteristics among these areas. Seasonal changes in major-ion, trace-element, and macronutrient concentrations are marked in the shallow marsh. Concentrations generally increase in the dry season due to evapotranspiration, changes in chemical equilibria, and precipitation. Water-management practices in south Florida have changed the water quality in the Shark River Slough. Most major-ion, dissolved-solid, and iron concentrations and color levels have steadily increased since 1963. The water quality in the other two drainageways has not changed since sampling began. Chlorinated-hydrocarbon insecticide residues in bottom material were found in low concentration at every sampling station in the park. (USGS)

Florida↗
USGS2012

Near-field receiving water monitoring of trace metals and a benthic community near the Palo Alto Regional Water Quality Control Plant in south San Francisco Bay, California: 2011

Trace-metal concentrations in sediment and in the clam Macoma petalum (formerly reported as Macoma balthica), clam reproductive activity, and benthic macroinvertebrate community structure were investigated in a mudflat 1 kilometer south of the discharge of the Palo Alto Regional Water Quality Control Plant (PARWQCP) in South San Francisco Bay, Calif. This report includes the data collected by U.S. Geological Survey (USGS) scientists for the period January 2011 to December 2011. These data serve as the basis for the City of Palo Alto's Near-Field Receiving Water Monitoring Program, initiated in 1994. Following significant reductions in the late 1980s, silver (Ag) and copper (Cu) concentrations in sediment and M. petalum appear to have stabilized. Data for other metals, including chromium, mercury, nickel, selenium, and zinc, have been collected since 1994. Over this period, concentrations of these elements have remained relatively constant, aside from seasonal variation that is common to all elements. In 2011, concentrations of Ag and Cu in M. petalum varied seasonally in response to a combination of site-specific metal exposures and annual growth and reproduction, as reported previously. Seasonal patterns for other elements, including Cr, Hg, Ni, Se, and Zn, were generally similar in timing and magnitude as those for Ag and Cu. In 2011, metal concentrations in both sediments and clam tissue were among the lowest concentrations on record. This record suggests that regional-scale factors now largely control sedimentary and bioavailable concentrations of Ag and Cu, as well as other elements of regulatory interest, at the Palo Alto site. Analyses of the benthic community structure of a mudflat in South San Francisco Bay over a 38-year period show that changes in the community have occurred concurrent with reduced concentrations of metals in the sediment and in the tissues of the biosentinel clam, M. petalum, from the same area. Analysis of the M. petalum community shows increases in reproductive activity concurrent with the decline in metal concentrations in the tissues of this organism. Reproductive activity is presently stable (2011), with almost all animals initiating reproduction in the fall and spawning the following spring. The community has shifted from being dominated by several opportunistic species to a community where the species are more similar in abundance, a pattern that indicates a more stable community that is subjected to fewer stressors. In addition, two of the opportunistic species (Ampelisca abdita and Streblospio benedicti) that brood their young and live on the surface of the sediment in tubes have shown a continual decline in dominance coincident with the decline in metals; both species had short-lived rebounds in abundance in 2008, 2009, and 2010. Heteromastus filiformis (a subsurface polychaete worm that lives in the sediment, consumes sediment and organic particles residing in the sediment, and reproduces by laying its eggs on or in the sediment) showed a concurrent increase in dominance and, in the last several years before 2008, showed a stable population. H. filiformis abundance increased slightly in 2011. An unidentified disturbance occurred on the mudflat in early 2008 that resulted in the loss of the benthic animals, except for those deep-dwelling animals like Macoma petalum. Animals immediately returned to the mudflat in 2008, which was the first indication that the disturbance was not due to a persistent toxin or to anoxia. The reproductive mode of most species present in 2011 is reflective of the species that were available either as pelagic larvae or as mobile adults. Although egg layers were lower in number in this group, the authors hypothesize that these species will return slowly as more species move back into the area. The use of functional ecology was highlighted in the 2011 benthic community data, which show that the animals that have now returned to the mudflat are those that can respond successfully to a physical, nontoxic disturbance. Today, community data show a mix of animals that consume the sediment, filter feed, have pelagic larvae that must survive landing on the sediment, and brood their young. USGS scientists continue to observe the community's response to the 2008 defaunation event because it allows them to examine the response of the community to a natural disturbance (possible causes include sediment accretion or freshwater inundation) and compare this recovery to the long-term recovery observed in the 1970s when the decline in sediment pollutants was the dominating factor.

California↗
USGS2003

Selenium contamination and remediation at Stewart Lake Waterfowl Management Area and Ashley Creek, middle Green River basin, Utah

Selenium is an element required in trace amounts for human and animal health, but it can cause health problems for livestock, wildlife, and humans when ingested in higher-than-required concentrations. Incidences of mortality, birth defects, and reproductive failure in waterfowl were discovered at Kesterson National Wildlife Refuge, San Joaquin Valley, California, by the U.S. Fish and Wildlife Service (USFWS) in 1983 (Presser, 1994). These problems were attributed to elevated concentrations of selenium in irrigation drainage that discharged to the refuge. Because of concern about possible adverse effects from irrigation drainage on Department of the Interior (DOI) projects elsewhere in the United States, the DOI organized scientists from the U.S. Geological Survey (USGS), USFWS, Bureau of Reclamation (BOR), and Bureau of Indian Affairs (BIA) to form the National Irrigation Water-Quality Program (NIWQP). The objectives of the program are to investigate DOI-managed lands for potential contamination related to irrigation drainage, conduct studies to identify the problems, investigate methodologies to remediate those problems, and implement remediation plans (U.S. Department of the Interior, 2002).

Utah↗
USGS2007

Occurrence of radium-224, radium-226 and radium-228 in water from the Vincentown and Wenonah-Mount Laurel aquifers, the Englishtown aquifer system, and the Hornerstown and Red Bank Sands, southwestern and south-central New Jersey

This investigation is the first regionally focused study of the presence of natural radioactivity in water from the Vincentown and Wenonah-Mount Laurel aquifers, Englishtown aquifer system, and the Hornerstown and Red Bank Sands. Geologic materials composing the Vincentown and Wenonah-Mount Laurel aquifers and the Hornerstown and Red Bank Sands previously have been reported to contain radioactive (uranium-enriched) phosphatic strata, which is common in deposits from some moderate-depth coastal marine environments. The decay of uranium and thorium gives rise to natural radioactivity and numerous radioactive progeny, including isotopes of radium. Naturally occurring radioactive isotopes, especially those of radium, are of concern because radium is a known human carcinogen and ingestion (especially in water used for drinking) can present appreciable health risks. A regional network in southwestern and south-central New Jersey of 39 wells completed in the Vincentown and Wenonah-Mount Laurel aquifers, the Englishtown aquifer system, and the Hornerstown and Red Bank Sands was sampled for determination of gross alpha-particle activity; concentrations of radium radionuclides, major ions, and selected trace elements; and physical properties. Concentrations of radium-224, radium-226, and radium-228 were determined for water from 28 of the 39 wells, whereas gross alpha-particle activity was determined for all 39. The alpha spectroscopic technique was used to determine concentrations of radium-224, which ranged from less than 0.5 to 2.7 pCi/L with a median concentration of less than 0.5pCi/L, and of radium-226, which ranged from less than 0.5 to 3.2 pCi/L with a median concentration of less than 0.5 pCi/L. The beta-counting technique was used to determine concentrations of radium-228. The concentration of radium-228 ranged from less than 0.5 to 4.3 pCi/L with a median of less than 0.5. Radium-228, when quantifiable, had the greatest concentration of the three radium radioisotopes in 9 of the 12 samples (75 percent). The concentration of radium-224 exceeded that of radium-226 in five of the six (83 percent) samples when both were quantifiable. The radium concentration distribution differed by aquifer, with the highest Ra-228 concentrations present in the Englishtown aquifer system and the highest Ra-226 concentrations present in the Wenonah-Mount Laurel aquifer. Radium-224 generally contributed a considerable amount of gross alpha-particle activity to water produced from all the sampled aquifers, but was not the dominant radionuclide as it is in water from the Kirkwood-Cohansey aquifer system, nor were concentrations greater than 1 pCi/L of radium-224 widespread. Gross alpha-particle activity was found to exceed the U.S Environmental Protection Agency (USEPA) Maximum Contaminant Level (MCL) of 15 pCi/L in one sample (16 pCi/L) from the Vincentown aquifer. A greater part of the gross alpha-particle activity in water from the Wenonah-Mount Laurel aquifer resulted from the decay of Ra-226 than did the gross alpha-particle activity in the other sampled aquifers; this relation is consistent with the concentration distribution of the Ra-226 itself. Concentrations of radium-224 correlate strongly with those of both radium-226 and radium-228 (Spearman correlation coefficients, r, +0.86 and +0.66, respectively). The greatest concentrations of radium-224, radium-226, and radium-228 were present in the most acidic ground water. All radium-224, radium-226, and radium-228 concentrations greater than 2.5 pCi/L were present in ground-water samples with a pH less than 5.0. The presence of combined radium-226 and radium-228 concentrations greater than 5 pCi/L in samples from the Vincentown and Wenonah-Mount Laurel aquifers and the Englishtown aquifer system was not nearly as common as in samples from the Kirkwood-Cohansey aquifer system, likely because of the slightly higher pH of water from these aquifers relative to that of Kirkwood-Cohansey aqu

New Jersey↗
USGS2015

The source, discharge, and chemical characteristics of selected springs, and the abundance and health of associated endemic anuran species in the Mojave network parks

Hydrological and biological investigations were done during 2005 and 2006 in cooperation with the U.S. National Park Service to investigate the source, discharge, and chemical characteristics of selected springs and the abundance and health of endemic anuran (frog and toad) species at Darwin Falls in Death Valley National Park, Piute Spring in Mojave National Preserve, and Fortynine Palms Oasis in Joshua Tree National Park. Discharge from the springs at these sites sustains isolated riparian habitats in the normally dry Mojave Desert. Data were collected on water quantity (discharge) and quality, air and water temperature, and abundance and health of endemic anuran species. In addition, a single survey of the abundance and health of endemic anuran species was completed at Rattlesnake Canyon in Joshua Tree National Park. Results from this study were compared to limited historical data, where they exist, and can provide a baseline for future hydrological and biological investigations to evaluate the health and sustainability of the resource and its response to changing climate and increasing human use. Radiocarbon dating of the water yielded estimated ages of about 7,000 years at Piute Spring and about 3,000 years at Darwin Spring, and tritium-helium-3 dating indicated an age of less than 2 years at Fortynine Palms Oasis. Stable hydrogen-isotope ratios were used to interpret an average altitude of recharge of 2,348 meters for Darwin Spring (about 1,415 meters higher than the altitude of Darwin Spring), 1,668 meters for Piute Spring (about 766 meters higher than the altitude of Piute Spring), and 1,400 meters for the Upper Pool at Fortynine Palms Oasis (about 543 meters higher than the altitude of the Upper Pool). Water-quality data collected for this study did not appear to be sensitive to trends in precipitation or seasonality in the Darwin Falls and Piute Spring study areas; however, it was sensitive to trends in Fortynine Palms Oasis where salinity increased by more than 10 percent during the 2 years of this study. Such a rapid response is consistent with the comparatively short travel time of less than 2 years from recharge to discharge at Fortynine Palms Oasis. Of the 14 trace elements analyzed, only concentrations of uranium at Fortynine Palms Oasis and arsenic at Darwin Spring were above drinking water standards; both constituents are derived from natural sources in the drainage basin and, therefore, are likely to have accumulated as a result of natural processes. Endemic anuran species were surveyed at Darwin Falls for the western toad ( Anaxyrus boreas ) and the red-spotted toad ( Anaxyrus punctatus ), at Piute Spring for the red-spotted toad, and at Fortynine Palms Oasis for the red-spotted toad and California treefrog ( Pseudacris cadaverina ). Historically, red-spotted toads were at the edge of their range at Darwin Falls, but they were not detected during this study and have not been detected since the early 1980s. The 2006 western toad population at Darwin Falls was estimated at 381 adults (95-percent confidence interval [CI] of 314–482). The population of red-spotted toads at Piute Spring was estimated at 1,153 adults (95-percent CI of 935–1,503). However, an elevated rate of abnormalities (approximately 5 percent) was recorded in red-spotted toads as well as the presence of the chytrid fungus, Bactrochochytrium dendrobatidis , at Piute Spring. In Joshua Tree National Park, the California treefrog now occupies only three of the seven historically occupied drainages. Populations of California treefrogs at Fortynine Palms Oasis have declined more than 50 percent from 288 in 1969–71 to 109 in 2006. A similar decline was observed in the populations of red-spotted toads at Fortynine Palms Oasis from 300 adults in 1969–71 to 155 adults (95-percent CI of 90–139) in 2006. The red-spotted toads at Fortynine Palms Oasis also exhibited the presence of Bactrochochytrium dendrobatidis .

California↗
USGS2012

Assessment of the geoavailability of trace elements from minerals in mine wastes: analytical techniques and assessment of selected copper minerals

In this study, four randomly selected copper-bearing minerals were examined—azurite, malachite, bornite, and chalcopyrite. The objectives were to examine and enumerate the crystalline and chemical properties of each of the minerals, to determine which, if any, of the Cu-bearing minerals might adversely affect systems biota, and to provide a multi-procedure reference. Laboratory work included use of computational software for quantifying crystalline and amorphous material and optical and electron imaging instruments to model and project crystalline structures. Chemical weathering, human fluid, and enzyme simulation studies were also conducted. The analyses were conducted systematically: X-ray diffraction and microanalytical studies followed by a series of chemical, bio-leaching, and toxicity experiments.

Scientific Investigations Report↗
USGS2000

Water-quality assessment of the Sacramento River Basin, California — Water quality of fixed sites, 1996-1998

Water-quality samples were collected from 12 sites in the Sacramento River Basin, Cali-fornia, from February 1996 through April 1998. Field measurements (dissolved oxygen, pH, specific conductance, alkalinity, and water tem-perature) were completed on all samples, and laboratory analyses were done for suspended sediments, nutrients, dissolved and particulate organic carbon, major ions, trace elements, and mercury species. Samples were collected at four types of locations on the Sacramento River?large tributaries to the Sacramento River, agricul-tural drainage canals, an urban stream, and a flood control channel. The samples were collected across a range of flow conditions representative of those sites during the timeframe of the study. The water samples from the Sacramento River indi-cate that specific conductance increases slightly downstream but that the water quality is indicative of dilute water. Water temperature of the Sacramento River increases below Shasta Lake during the spring and summer irrigation season owing to diversion of water out of the river and subsequent lower flow. All 12 sites had generally low concentrations of nutrients, but chlorophyll concentrations were not measured; therefore, the actual consequences of nutrient loading could not be adequately assessed. Concentrations of dis-solved organic carbon in samples from the Sacramento River and the major tributaries were generally low; the formation of trihalomethanes probably does not currently pose a problem when water from the Sacramento River and its major tributaries is chlorinated for drinking-water purposes. However, dissolved organic carbon concentrations were higher in the urban stream and in agricultural drainage canals, but were diluted upon mixing with the Sacramento River. The only trace element that currently poses a water-quality problem in the Sacramento River is mercury. A federal criterion for the protection of aquatic life was exceeded during this study, and floodwater concentrations of mercury were mostly higher than the criterion. Exceedances of water-quality standards happened most frequently during winter when suspended-sediment concen-trations also were elevated. Most mercury is found in association with suspended sediment. The greatest loading or transport of mercury out of the Sacramento River Basin to the San Francisco Bay occurs in the winter and principally follows storm events.

California↗