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USGS2005

Water-Quality Assessment of the Yellowstone River Basin, Montana and Wyoming-Water Quality of Fixed Sites, 1999-2001

The National Water-Quality Assessment Program of the U.S. Geological Survey initiated an assessment in 1997 of the quality of water resources in the Yellowstone River Basin. Water-quality samples regularly were collected during 1999-2001 at 10 fixed sites on streams representing the major environmental settings of the basin. Integrator sites, which are heterogeneous in land use and geology, were established on the mainstem of the Yellowstone River (4 sites) and on three major tributaries?Clarks Fork Yellowstone River (1 site), the Bighorn River (1 site), and the Powder River (1 site). Indicator sites, which are more homogeneous in land use and geology than the integrator sites, were located on minor tributaries with important environmental settings?Soda Butte Creek in a mineral resource area (1 site), the Tongue River in a forested area (1 site), and the Little Powder River in a rangeland area (1 site). Water-quality sampling frequency generally was at least monthly and included field measurements and laboratory analyses of fecal-indicator bacteria, major ions, dissolved solids, nutrients, trace elements, pesticides, and suspended sediment. Median concentrations of fecal coliform and Escherichia coli were largest for basins that were predominantly rangeland and smallest for basins that were predominantly forested. Concentrations of fecal coliform and Escherichia coli significantly varied by season (p-value <0.001); the smallest median concentrations were during January?March and the largest median concentrations were during April?June. Fecal-coliform concentrations exceeded the U.S. Environmental Protection Agency recommended limit for a single sample of 400 colonies per 100 milliliters in 2.6 percent of all samples. Escherichia coli concentrations exceeded the U.S. Environmental Protection Agency recommended limit for a single sample of 298 colonies per 100 milliliters for moderate use, full-body contact recreation in 7.6 percent of all samples. Variations in water type in the basin are reflective of the diverse geologic terrain in the Yellowstone River Basin. The water type of Soda Butte Creek and the Tongue River was calcium bicarbonate. These two sites are in forested and mountainous areas where igneous rocks and Paleozoic-era and Mesozoic-era sedimentary rocks are the dominant geologic groups. The water type of the Little Powder River was sodium sulfate. The Little Powder River originates in the plains, and geology of the basin is nearly homogenous with Tertiary-period sedimentary rocks. Water type of the Yellowstone River changed from a mixed-cation bicarbonate type upstream to a mixed-cation sulfate type downstream. Dissolved-solids concentrations ranged from fairly dilute in Soda Butte Creek, which had a median concentration of 118 milligrams per liter, to concentrated in the Little Powder River, which had a median concentration of 2,840 milligrams per liter. Nutrient concentrations generally were small and reflect the relatively undeveloped conditions in the basin; however, some correlations were made with anthropogenic factors. Median dissolved-nitrate concentrations in all samples from the fixed sites ranged from 0.04 milligram per liter to 0.54 milligram per liter. Flow-weighted mean dissolved-nitrate concentrations were positively correlated with increasing agricultural land use and rangeland on alluvial deposits upstream from the sites and negatively correlated with increasing forested land. Ammonia concentrations generally were largest in samples collected from the Yellowstone River at Corwin Springs, Montana, which is downstream from Yellowstone National Park and receives discharge from geothermal waters that are high in ammonia. Median total-phosphorus concentrations ranged from 0.007 to 0.18 milligram per liter. Median total-phosphorus concentrations exceeded the U.S. Environmental Protection Agency's recommended goal of 0.10 milligram per liter for preventing nuisance plant growth for samples collec

Scientific Investigations Report↗

USGS2009

Quality of Shallow Groundwater and Drinking Water in the Mississippi Embayment-Texas Coastal Uplands Aquifer System and the Mississippi River Valley Alluvial Aquifer, South-Central United States, 1994-2004

The Mississippi embayment-Texas coastal uplands aquifer system is an important source of drinking water, providing about 724 million gallons per day to about 8.9 million people in Texas, Louisiana, Mississippi, Arkansas, Missouri, Tennessee, Kentucky, Illinois, and Alabama. The Mississippi River Valley alluvial aquifer ranks third in the Nation for total withdrawals of which more than 98 percent is used for irrigation. From 1994 through 2004, water-quality samples were collected from 169 domestic, monitoring, irrigation, and public-supply wells in the Mississippi embayment-Texas coastal uplands aquifer system and the Mississippi River Valley alluvial aquifer in various land-use settings and of varying well capacities as part of the U.S. Geological Survey's National Water-Quality Assessment Program. Groundwater samples were analyzed for physical properties and about 200 water-quality constituents, including total dissolved solids, major inorganic ions, trace elements, radon, nutrients, dissolved organic carbon, pesticides, pesticide degradates, and volatile organic compounds. The occurrence of nutrients and pesticides differed among four groups of the 114 shallow wells (less than or equal to 200 feet deep) in the study area. Tritium concentrations in samples from the Holocene alluvium, Pleistocene valley trains, and shallow Tertiary wells indicated a smaller component of recent groundwater than samples from the Pleistocene terrace deposits. Although the amount of agricultural land overlying the Mississippi River Valley alluvial aquifer was considerably greater than areas overlying parts of the shallow Tertiary and Pleistocene terrace deposits wells, nitrate was rarely detected and the number of pesticides detected was lower than other shallow wells. Nearly all samples from the Holocene alluvium and Pleistocene valley trains were anoxic, and the reducing conditions in these aquifers likely result in denitrification of nitrate. In contrast, most samples from the Pleistocene terrace deposits in Memphis, Tennessee, were oxic, and the maximum nitrate concentration measured was 6.2 milligrams per liter. Additionally, soils overlying the Holocene alluvium and Pleistocene valley trains, generally in areas near the wells, had lower infiltration rates and higher percentages of clay than soils overlying the shallow Tertiary and Pleistocene terrace deposits wells. Differences in these soil properties were associated with differences in the occurrence of pesticides. Pesticides were most commonly detected in samples from wells in the Pleistocene terrace deposits, which generally had the highest infiltration rates and lowest clay content. Median dissolved phosphorus concentrations were 0.07, 0.11, and 0.65 milligram per liter in samples from the shallow Tertiary, Pleistocene valley trains, and Holocene alluvium, respectively. The widespread occurrence of dissolved phosphorus at concentrations greater than 0.02 milligram per liter suggests either a natural source in the soils or aquifer sediments, or nonpoint sources such as fertilizer and animal waste or a combination of natural and human sources. Although phosphorus concentrations in samples from the Holocene alluvium were weakly correlated to concentrations of several inorganic constituents, elevated concentrations of phosphorus could not be attributed to a specific source. Phosphorus concentrations generally were highest where samples indicated anoxic and reducing conditions in the aquifers. Elevated dissolved phosphorus concentrations in base-flow samples from two streams in the study area suggest that transport of phosphorus with groundwater is a potential source contributing to high yields of phosphorus in the lower Mississippi River basin. Water from 55 deep wells (greater than 200 feet deep) completed in regional aquifers of Tertiary age represent a sample of the principal aquifers used for drinking-water supply in the study area. The wells were screened in both confined and

Scientific Investigations Report↗

USGS2008

Geochemical trends and natural attenuation of RDX, nitrate, and perchlorate in the hazardous test area Fractured-Granite aquifer, White Sands Missile Range, New Mexico, 1996-2006

A fractured-granite aquifer at White Sands Missile Range is contaminated with the explosive compound RDX, nitrate, and perchlorate (oxidizer associated with rocket propellant) from the previous use of the Open Burn/Open Detonation site at the Hazardous Test Area. RDX, nitrate, and perchlorate ground-water concentrations were analyzed to examine source characteristics, spatial and temporal variability, and the influence of the natural attenuation processes of dilution and degradation in the Hazardous Test Area fractured-granite aquifer. Two transects of ground-water wells from the existing monitoring-site network - one perpendicular to ground-water flow (transect A-A') and another parallel to ground-water flow (transect B-B') - were selected to examine source characteristics and the spatial and temporal variability of the contaminant concentrations. Ground-water samples collected in 2005 from a larger sampling of monitoring sites than the two transects were analyzed for various tracers including major ions, trace elements, RDX degradates, dissolved gases, water isotopes, nitrate isotopes, and sulfate isotopes to examine the natural attenuation processes of dilution and degradation. Recharge entrains contaminants at the site and transports them downgradient towards the Tularosa Basin floor through a poorly connected fracture system(s). From 1996 to 2006, RDX, nitrate, and perchlorate concentrations in ground water downgradient from the Open Burn/Open Detonation site have been relatively stable. RDX, nitrate, and perchlorate in ground water from wells near the site indicate dispersed contaminant sources in and near the Open Burn/Open Detonation pits. The sources of RDX and nitrate in the pit area have shifted with time, and the shift correlates with the regrading of the south and east berms of each pit in 2002 and 2003 following closure of the site. The largest RDX concentrations were in ground water about 0.1 mile downgradient from the pits, the largest perchlorate concentrations were in ground water about 0.15 mile downgradient from the pits, and the largest nitrate concentrations were in ground water about 0.25 mile down-gradient from the pits. Strong and moderate correlation of water level and the contaminant concentrations near the source areas and low correlation outside and downgradient from the source areas indicates a diminishing of the water level/contaminant relation with downgradient flow. Ground water was not progressively older at all locations downgradient from the Open Burn/Open Detonation site indicating multiple recharge areas. Major ion and strontium concentrations and d2H and d18O values identified similar sources of recharge waters comprising the aquifer except along the basin periphery where recharge water may be influenced by dissolution of mineral assemblages associated with ore deposits that are present along the basin margins. Ground-water ages, dissolved-solids concentrations, and calcium-strontium concentrations indicate limited or partial connectivity between fractures and contributions of uncontaminated recharge water downgradient from the site that dilutes contaminant concentrations. Changes in RDX and nitrate concentration patterns, the presence of methane, changes in carbon dioxide concentrations and d15N and d34S values, and variable reduction-oxidation conditions suggest degradation of contaminants in the downgradient direction. Estimated values of electron potential were assigned to ground water collected in October 2005 from all monitoring sites at the Hazardous Test Area. Moderate to strong reducing conditions were present upgradient from the Open Burn/Open Detonation site, at the site, and at various locations downgradient from the site, but the aquifer contained well-oxygenated water between many of the reducing areas. The spatial variability of reduction-oxidation conditions in the aquifer exemplifies the partial connectivity of the fracture system(s). Dilution of the contaminants i

New Mexico↗

USGS2016

Occurrence and concentrations of selected trace elements, halogenated organic compounds, and polycyclic aromatic hydrocarbons in streambed sediments and results of water-toxicity testing in Westside Creeks and the San Antonio River, San Antonio, Texas, 2014

Sediment samples and samples for water-toxicity testing were collected during 2014 from several streams in San Antonio, Texas, known locally as the Westside Creeks (Alazán, Apache, Martínez, and San Pedro Creeks) and from the San Antonio River. Samples were collected during base flow and after periods of stormwater runoff (poststorm conditions) to determine baseline sediment- and water-quality conditions. Streambed-sediment samples were analyzed for selected constituents, including trace elements and organic contaminants such as pesticides, polychlorinated biphenyls (PCBs), brominated flame retardants, and polycyclic aromatic hydrocarbons (PAHs). Potential risks of contaminants in sediment were evaluated by comparing concentrations of contaminants in sediment to two effects-based sediment-quality guidelines: (1) a lower level, called the threshold effect concentration, below which, harmful effects to benthic biota are not expected, and (2) a higher level, the probable effect concentration (PEC), above which harmful effects are expected to occur frequently. Samples for water-toxicity testing were collected from each stream to provide information about fish toxicity in the study area. The trace metal lead was detected at potentially toxic concentrations greater than the PEC in both the base-flow and poststorm samples collected at two sites sampled on San Pedro Creek. The PECs for the pesticides dichlorodiphenyldichloroethane, dichlorodiphenyldichloroethylene, dichlorodiphenyltrichloroethane, and chlordane were exceeded in some of the samples at the same two sites on San Pedro Creek. Brominated flame retardants and polybrominated diphenyl ether (PBDE) 85, 153, and 154 were found in all streambed-sediment samples. Federal Environmental Quality Guidelines established by Environment Canada for PBDE 99 and PBDE 100 were exceeded in all samples in which PBDE 99 was detected and in a majority of the samples in which PBDE 100 was detected; the greatest concentrations occurred in samples collected at the same two sites on San Pedro Creek where the samples containing elevated lead and pesticide concentrations were collected. All concentrations of total PCBs (computed as the sum of the 18 reported PCB congeners) in the individual streambed-sediment samples were less than the threshold effect concentration, but the concentrations were elevated in the two sites on San Pedro Creek compared to concentrations at other sites. At one site on Apache Creek, 6 of the individual PAHs measured in the sample collected during base-flow conditions exceeded the PECs and 8 of the 9 PECs were exceeded in the sample collected during poststorm conditions. The total PAH concentration in the sample collected at the site during poststorm conditions was 3.3 times greater than the PEC developed for total PAHs. Average PAH profiles computed for base-flow samples and poststorm samples most closely resemble the parking lot coal-tar sealcoat dust PAH source profile, defined as the average PAH concentrations in dust swept from parking lots in six cities in the United States that were sealed with a black, viscous liquid containing coal-tar pitch. Six of ten water samples collected during base-flow conditions caused reductions in Pimephales promelas (fathead minnow) survival and were considered to be toxic.

Texas↗

USGS2014

Groundwater-quality characteristics for the Wyoming Groundwater-Quality Monitoring Network, November 2009 through September 2012

Groundwater samples were collected from 146 shallow (less than or equal to 500 feet deep) wells for the Wyoming Groundwater-Quality Monitoring Network, from November 2009 through September 2012. Groundwater samples were analyzed for physical characteristics, major ions and dissolved solids, trace elements, nutrients and dissolved organic carbon, uranium, stable isotopes of hydrogen and oxygen, volatile organic compounds, and coliform bacteria. Selected samples also were analyzed for gross alpha radioactivity, gross beta radioactivity, radon, tritium, gasoline range organics, diesel range organics, dissolved hydrocarbon gases (methane, ethene, and ethane), and wastewater compounds. Water-quality measurements and concentrations in some samples exceeded numerous U.S. Environmental Protection Agency (EPA) drinking water standards. Physical characteristics and constituents that exceeded EPA Maximum Contaminant Levels (MCLs) in some samples were arsenic, selenium, nitrite, nitrate, gross alpha activity, and uranium. Total coliforms and Escherichia coli in some samples exceeded EPA Maximum Contaminant Level Goals. Measurements of pH and turbidity and concentrations of chloride, sulfate, fluoride, dissolved solids, aluminum, iron, and manganese exceeded EPA Secondary Maximum Contaminant Levels in some samples. Radon concentrations in some samples exceeded the alternative MCL proposed by the EPA. Molybdenum and boron concentrations in some samples exceeded EPA Health Advisory Levels. Water-quality measurements and concentrations also exceeded numerous Wyoming Department of Environmental Quality (WDEQ) groundwater standards. Physical characteristics and constituents that exceeded WDEQ Class I domestic groundwater standards in some samples were measurements of pH and concentrations of chloride, sulfate, dissolved solids, iron, manganese, boron, selenium, nitrite, and nitrate. Measurements of pH and concentrations of chloride, sulfate, dissolved solids, aluminum, iron, manganese, boron, and selenium exceeded WDEQ Class II agriculture groundwater standards in some samples. Measurements of pH and concentrations of sulfate, dissolved solids, aluminum, boron, and selenium exceeded WDEQ Class III livestock groundwater standards in some samples. The concentrations of dissolved solids in two samples exceeded the WDEQ Class IV industry groundwater standard. Measurements of pH and concentrations of dissolved solids, aluminum, iron, manganese, and selenium exceeded WDEQ Class special (A) fish and aquatic life groundwater standards in some samples. Stable isotopes of hydrogen and oxygen measured in water samples were compared to the Global Meteoric Water Line and Local Meteoric Water Lines. Results indicated that recharge to all of the wells was derived from precipitation and that the water has undergone some fractionation, possibly because of evaporation. Concentrations of organic compounds did not exceed any State or Federal water-quality standards. Few volatile organic compounds were detected in samples, whereas gasoline range organics, diesel range organics, and methane were detected most frequently. Concentrations of wastewater compounds did not exceed any State or Federal water-quality standards. The compounds N,N-diethyl-meta-toluamide (DEET), benzophenone, and phenanthrene were detected most frequently. Bacteria samples were collected, processed, incubated, and enumerated in the field or at the U.S. Geological Survey Wyoming-Montana Water Science Center. Total coliforms and Escherichia coli were detected in some samples.

Wyoming↗

USGS2015

Water quality of groundwater and stream base flow in the Marcellus Shale Gas Field of the Monongahela River Basin, West Virginia, 2011-12

The Marcellus Shale gas field underlies portions of New York, Pennsylvania, Ohio, Virginia, Maryland, Tennessee, and West Virginia. Development of hydraulic fracturing and horizontal drilling technology led to extensive development of gas from the Marcellus Shale beginning about 2007. The need to identify and monitor changes in water-quality conditions related to development of the Marcellus Shale gas field prompted the U.S. Geological Survey, in cooperation with the West Virginia Department of Environmental Protection, Division of Water and Waste Management, to document water quality for comparison with water quality in samples collected at a future date. The identification of change in water-quality conditions over time is more difficult if baseline water-quality conditions have not been documented. U.S. Geological Survey personnel sampled groundwater and surface water in West Virginia’s Monongahela River Basin during 2011–12. A groundwater survey, in which 39 wells and 2 springs were sampled, was conducted during June through September 2011. A base-flow survey was conducted during July through October 2012; 50 stream sites were sampled under base-flow conditions in this survey. Because additives to hydraulic fracturing fluids are variable and decrease in flowback water over a relatively short time, water-quality analyses for this study focused on documenting the water-quality characteristics typical of water from shallow aquifers; water derived from contact with the Marcellus Shale (flowback from hydraulic fracturing or formation water); and water with constituents from conventional oil and gas development, sewage effluent, and coal-mine drainage. All samples were analyzed for field properties (water temperature, pH, specific conductance, dissolved oxygen, and turbidity), major ions, trace elements, naturally occurring radioactive materials, and stable isotopes. In addition to documenting baseline water-quality conditions for an area of shale-gas development, these data were examined for patterns in water quality. Groundwater and base-flow survey data were compared to historical data from the Monongahela River Basin in West Virginia. Additionally, groundwater- and base-flow survey samples were grouped by Marcellus Shale gas production in the subbasin in which that sampling site was located. The comparisons of data collected as part of this study with historical data identified few differences. No significant difference was found in a comparison of groundwater survey data and historical data. Base-flow survey samples differed significantly from historical data for pH, chloride, and strontium, all of which had higher concentrations in the base-flow survey samples. Differences in pH are likely related to changes in mining regulation beginning in 1977. Concentrations of chloride and strontium elevated above background concentrations may be related to saline groundwater; saline water is within 300 feet of the land surface in parts of the study area. In the comparison of base-flow survey samples grouped by shale-gas-production setting, significant differences were found for fluoride and barium. Concentrations of fluoride and barium were higher in stream subbasins with active Marcellus Shale production than in subbasins not near active Marcellus Shale production. Elevated fluoride and barium are associated with deep brines. Generally, naturally occurring radioactive materials were not found in elevated concentrations in either groundwater or base-flow samples. Only 3 samples, 2 from the groundwater survey and one from the base-flow survey, exceeded the U.S. Environmental Protection Agency maximum contaminant level for radium isotopes of 5.0 picocurie per liter for either a single isotope or a combined value of radium-226 and radium-228. Stable isotope composition indicates broad similarity among surface water, shallow groundwater, and precipitation in the region. Neither shallow groundwater nor surface water showed a marked similarity with the deep brines associated with shale gas. In most of the groundwater survey samples, 38 of 41 samples, dissolved gas profiles were similar to those previously found in samples from shallow, domestic wells in the region. This study provides a baseline of water-quality conditions in the Monongahela River Basin in West Virginia during the early phases of development of the Marcellus Shale gas field. Although not all inclusive, the results of this study provide a set of reliable water-quality data against which future data sets can be compared and the effects of shale-gas development may be determined.

West Virginia↗

USGS2004

Effects of surface applications of biosolids on soil, crops, ground water, and streambed sediment near Deer Trail, Colorado, 1999-2003

The U.S. Geological Survey, in cooperation with Metro Wastewater Reclamation District and North Kiowa Bijou Groundwater Management District, studied natural geochemical effects and the effects of biosolids applications to the Metro Wastewater Reclamation District properties near Deer Trail, Colorado, during 1999 through 2003 because of public concern about potential contamination of soil, crops, ground water, and surface water from biosolids applications. Parameters analyzed for each monitoring component included arsenic, cadmium, copper, lead, mercury, molybdenum, nickel, selenium, and zinc (the nine trace elements regulated by Colorado for biosolids), gross alpha and gross beta radioactivity, and plutonium, as well as other parameters. Concentrations of the nine regulated trace elements in biosolids were relatively uniform and did not exceed applicable regulatory standards. All plutonium concentrations in biosolids were below the minimum detectable level and were near zero. The most soluble elements in biosolids were arsenic, molybdenum, nickel, phosphorus, and selenium. Elevated concentrations of bismuth, mercury, phosphorus, and silver would be the most likely inorganic biosolids signature to indicate that soil or streambed sediment has been affected by biosolids. Molybdenum and tungsten, and to a lesser degree antimony, cadmium, cobalt, copper, mercury, nickel, phosphorus, and selenium, would be the most likely inorganic 'biosolids signature' to indicate ground water or surface water has been affected by biosolids. Soil data indicate that biosolids have had no measurable effect on the concentration of the constituents monitored. Arsenic concentrations in soil of both Arapahoe and Elbert County monitoring sites (like soil from all parts of Colorado) exceed the Colorado soil remediation objectives and soil cleanup standards, which were determined by back-calculating a soil concentration equivalent to a one-in-a-million cumulative cancer risk. Lead concentrations in soil slightly exceed the U.S. Environmental Protection Agency toxicity-derived ecological soil-screening levels for avian wildlife. Plutonium concentration in the soil was near zero. Wheat-grain data were insufficient to determine any measurable effects from biosolids. Comparison with similar data from other parts of North America where biosolids were not applied indicates similar concentrations. However, the Deer Trail study area had higher nickel concentrations in wheat from both the biosolids-applied fields and the control fields. Plutonium content of the wheat was near zero. Ground-water levels generally declined at most wells during 1999 through 2003. Ground-water quality did not correlate with ground-water levels. Vertical ground-water gradients during 1999 through 2003 indicate that bedrock ground-water resources downgradient from the biosolids-applied areas are not likely to be contaminated by biosolids applications unless the gradients change as a result of pumping. Ground-water quality throughout the study area varied over time at each site and from site to site at the same time, but plutonium concentrations in the ground water always were near zero. Inorganic concentrations at well D6 were relatively high compared to other ground-water sites studied. Ground-water pH and concentrations of fluoride, nitrite, aluminum, arsenic, barium, chromium, cobalt, copper, lead, mercury, nickel, silver, zinc, and plutonium in the ground water of the study area met Colorado standards. Concentrations of chloride, sulfate, nitrate, boron, iron, manganese, and selenium exceeded Colorado ground-water standards at one or more wells. Nitrate concentrations at well D6 significantly (alpha = 0.05) exceeded the Colorado regulatory standard. Concentrations of arsenic, cadmium, chromium, lead, mercury, nickel, and zinc in ground water had no significant (alpha = 0.05) upward trends. During 1999-2003, concentrations of nitrate, copper, molybdenum, and selenium

Scientific Investigations Report↗

USGS1997

Effects of urbanization on water quality in the Kansas River, Shunganunga Creek Basin, and Soldier Creek, Topeka, Kansas, October 1993 through September 1995

A study of urban-related water-qulity effects in the Kansas River, Shunganunga Creek Basin, and Soldier Creek in Topeka, Kansas, was conducted from October 1993 through September 1995. The purpose of this report is to assess the effects of urbanization on instream concentrations of selected physical and chemical constituents within the city of Topeka. A network of seven sampling sites was established in the study area. Samples principally were collected at monthly intervals from the Kansas River and from the Shunganunga Creek Basin, and at quarterly intervals from Soldier Creek. The effects of urbanization werestatistically evaluated from differences in constituent concentrations between sites on the same stream. No significant differences in median concentrations of dissolved solids, nutrients, or metals and trace elements, or median densities offecal bacteria were documented between sampling sites upstream and downstream from the major urbanized length of the Kansas River in Topeka.Discharge from the city's primary wastewater- treatment plant is the largest potential source of contamination to the Kansas River. This discharge increased concentrations of dissolved ammonia, totalphosphorus, and densities of fecal bacteria.Calculated dissolved ammonia as nitrogen concentrations in water from the Kansas River ranged from 0.03 to 1.1 milligrams per liter after receiving treatment-plant discharge. However, most of the calculated concentrations wereconsiderably less than 50 percent of Kansas Department of Health and Environment water- quality criteria, with a median value of 20 percent.Generally, treatment-plant discharge increased calculated total phosphorus concentrations in water from the Kansas River by 0.01 to 0.04 milligrams per liter, with a median percentage increase of 7.6 percent. The calculated median densities of fecal coliform and fecal Streptococci bacteria in water from the Kansas River increased from 120 and 150colonies per 100 milliliters of water, respectively, before treatment-plant discharge to a calculated 4,900 and 4,700 colonies per 100 milliliters of water, respectively, after discharge. Median concentrations of dissolved solids were not significantly different between three sampling sites in the Shunganunga Creek Basin. Median concentrations of dissolved nitrate as nitrogen, total phosphorus, and dissolved orthophosphate were significantly larger in water from the upstream- most Shunganunga Creek sampling site than in water from either of the other sampling sites in the Shunganunga Creek Basin probably because of the site's proximity to a wastewater-treatment plant.Median concentrations of dissolved nitrate as nitrogen and total phosphorus during 1993-95 at upstream sampling sites were either significantlylarger than during 1979-81 in response to increase of wastewater-treatment plant discharge or smaller because of the elimination of wastewater-treatment plant discharge. Median concentrations of dissolved ammonia as nitrogen were significantly less during 1993-95 than during 1979-81. Median concentrations of total aluminum, iron, maganese, and molybdenum were significantly larger in water from the downstream-mostShunganunga Creek sampling site than in water from the upstream-most sampling site. This probably reflects their widespread use in the urbanenvironment between the upstream and downstream Shunganunga Creek sampling sites. Little water-quality effect from the urbanization was indicated by results from the Soldier Creek sampling site. Median concentrations of most water-quality constituents in water from this sampling site were the smallest in water from any sampling site in the study area. Herbicides were detected in water from all sampling sites. Some of the more frequently detected herbicides included acetochlor, alachlor,atrazine, cyanazine, EPTC, metolachlor, prometon, simazine, and tebuthiuron. Detected insecticides including chlordane,

Water-Resources Investigations Report↗

USGS2004

Geochemistry of Mercury and other trace elements in fluvial tailings upstream of Daguerre Point Dam, Yuba River, California, August 2001

This study was designed to characterize the particle-size distribution and the concentrations of total mercury (HgT), methylmercury (MeHg), and other constituents in sediments trapped behind Daguerre Point Dam, a 28-foot-high structure on the lower Yuba River in California. The results of the study will assist other agencies in evaluating potential environmental impacts from mobilization of sediments if Daguerre Point Dam is modified or removed to improve the passage of anadromous fish. Methylmercury is of particular concern owing to its toxicity and propensity to bioaccumulate. A limited amount of recent work on hydraulic and dredge tailings in other watersheds has indicated that mercury and MeHg concentrations may be elevated in the fine-grained fractions of placer mining debris, particularly clay and silt. Mercury associated with tailings from placer gold mines is a source of continued contamination in Sierra Nevada watersheds and downstream water bodies, including the Sacramento?San Joaquin Delta and the San Francisco Bay of northern California. Churn drilling was used to recover sediments and heavy minerals at 5-foot intervals from six locations upstream of Daguerre Point Dam. Maximum depth of penetration ranged from 17.5 to 35 feet below land surface, resulting in 31 discreet drilled intervals. Drilling in permeable, unconsolidated sediments below the streambed of the Yuba River released a significant volume of water along with the sediment, which complicated the sampling and characterization effort. Overflow of a silty fraction sampled at the drill site contained suspended sediment consisting predominantly of silt and clay, with HgT concentration ranging from 33 to 1,100 ng/g (nanogram per gram) dry weight. A sandy fraction, collected after sieving sediment through a 2-millimeter vibratory screen, contained from 14 to 82 percent sand and 1 to 29 percent silt plus clay, and had HgT concentrations ranging from 6.8 to 81 ng/g dry weight. A clay-silt fraction, sampled from material remaining in suspension after the sandy fraction settled for 15-20 minutes, contained mercury concentrations from 23 to 370 ng/g dry weight. Concentrations of MeHg were less than the detection limit (<0.001 ng/g dry weight) in 30 of 31 samples of the sandy fraction. In the suspended clay-silt fraction, MeHg was detected in 16 of 31 samples, in which it ranged in concentration from 0.04 (estimated) to 0.61 ng/g wet weight. Potential rates of mercury methylation and demethylation were evaluated in seven samples using radiotracer methods. Mercury methylation (MeHg production) potentials were generally low, ranging from less than 0.15 to about 1.6 ng/g/d (nanogram per gram of dry sediment per day). Mercury demethylation (MeHg degradation) potentials were moderately high, ranging from 1.0 to 2.2 ng/g/d. The ratio of methylation potential (MP) to demethylation potential (DP) ranged from less than 0.14 to about 1.4 (median = 0.24, mean = 0.44, number of samples = 7), suggesting that the potential for net production of MeHg in deep sediments is generally low. The MeHg production rates and MP/DP ratios were higher in the shallower interval in two of the three holes where two depth intervals were assessed, whereas the MeHg concentrations were higher in the shallower interval for all three holes. A similar spatial distribution was found for concentrations of solid-phase sulfide (measured as total reduced sulfur and likely representing iron-sulfide and iron-disulfide compounds), which were much higher in shallower samples (about 700 to about 2,100 nanomoles per gram, dry sediment) than in deeper samples (32 to 55 nanomoles per gram, dry sediment) in these three holes. If reduced sulfur compounds are oxidized to sulfate as a consequence of sediment disturbance, the activity of sulfate-reducing bacteria might be stimulated, causing a short-term increase in methylation of inorganic Hg(II) (divalent mercury).

California↗

USGS2005

Ground-water quality in the carbonate-rock aquifer of the Great Basin, Nevada and Utah, 2003

The carbonate-rock aquifer of the Great Basin is named for the thick sequence of Paleozoic limestone and dolomite with lesser amounts of shale, sandstone, and quartzite. It lies primarily in the eastern half of the Great Basin and includes areas of eastern Nevada and western Utah as well as the Death Valley area of California and small parts of Arizona and Idaho. The carbonate-rock aquifer is contained within the Basin and Range Principal Aquifer, one of 16 principal aquifers selected for study by the U.S. Geological Survey’s National Water- Quality Assessment Program. Water samples from 30 ground-water sites (20 in Nevada and 10 in Utah) were collected in the summer of 2003 and analyzed for major anions and cations, nutrients, trace elements, dissolved organic carbon, volatile organic compounds (VOCs), pesticides, radon, and microbiology. Water samples from selected sites also were analyzed for the isotopes oxygen-18, deuterium, and tritium to determine recharge sources and the occurrence of water recharged since the early 1950s. Primary drinking-water standards were exceeded for several inorganic constituents in 30 water samples from the carbonate-rock aquifer. The maximum contaminant level was exceeded for concentrations of dissolved antimony (6 μg/L) in one sample, arsenic (10 μg/L) in eleven samples, and thallium (2 μg/L) in one sample. Secondary drinking-water regulations were exceeded for several inorganic constituents in water samples: chloride (250 mg/L) in five samples, fluoride (2 mg/L) in two samples, iron (0.3 mg/L) in four samples, manganese (0.05 mg/L) in one sample, sulfate (250 mg/L) in three samples, and total dissolved solids (500 mg/L) in seven samples. Six different pesticides or metabolites were detected at very low concentrations in the 30 water samples. The lack of VOC detections in water sampled from most of the sites is evidence thatVOCs are not common in the carbonate-rock aquifer. Arsenic values for water range from 0.7 to 45.7 μg/L, with a median value of 9.6 μg/L. Factors affecting arsenic concentration in the carbonate-rock aquifer in addition to geothermal heating are its natural occurrence in the aquifer material and time of travel along the flow path. Most of the chemical analyses, especially for VOCs and nutrients, indicate little, if any, effect of overlying land-use patterns on ground-water quality. The water quality in recharge areas for the aquifer where human activities are more intense may be affected by urban and/or agricultural land uses as evidenced by pesticide detections. The proximity of the carbonate-rock aquifer at these sites to the land surface and the potential for local recharge to occur through the fractured rock likely results in the occurrence of these and other land-surface related contaminants in the ground water. Water from sites sampled near outcrops of carbonate-rock aquifer likely has a much shorter residence time resulting in a potential for detection of anthropogenic or land-surface related compounds. Sites located in discharge areas of the flow systems or wells that are completed at a great depth below the land surface generally show no effects of land-use activities on water quality. Flow times within the carbonate-rock aquifer, away from recharge areas, are on the order of thousands of years, so any contaminants introduced at the land surface that will not degrade along the flow path have not reached the sampled sites in these areas.

Nevada, Utah↗

USGS1997

Water-quality assessment of the Rio Grande Valley, Colorado, New Mexico, and Texas: Summary and analysis of water-quality data for the basic-fixed-site network, 1993-95

The Rio Grande Valley study unit of the U.S. Geological Survey National Water-Quality Assessment Program collected monthly water- quality samples at a network of surface-water sites from April 1993 through September 1995. This basic-fixed-site network consisted of nine main-stem sites on the Rio Grande, five sites on tributaries of the Rio Grande, two sites on streams in the Rio Grande Valley study unit that are not directly tributary to the Rio Grande, and one site on a conveyance channel. During each monthly sampling, field properties were measured and samples were collected for the analysis of dissolved solids, major constituents, nutrients, selected trace elements, and suspended-sediment concentrations. During selected samplings, supplemental samples were collected for the analysis of additional trace elements, organic carbon, and/or pesticides. Spatial variations of dissolved-solids, major-constituent, and nutrient data were analyzed. The report presents summary statistics for the monthly water-quality data by sampling site and background information on the drainage basin upstream from each site. Regression equations are presented that relate dissolved-solids, major-constituent, and nutrient concentrations to streamflow, selected field properties, and time. Median instantaneous streamflow at each basic-fixed site ranged from 1.4 to 1,380 cubic feet per second. Median specific conductance at each basic-fixed site ranged from 84 to 1,680 microsiemens per centimeter at 25 degrees Celsius, and median pH values ranged from 7.8 to 8.5. The water sampled at the basic-fixed sites generally was well oxygenated and had a median dissolved-oxygen percent of saturation range from 89 to 108. With the exception of Rio Grande above mouth of Trinchera Creek, near Lasauses, Colorado, dissolved-solids concentrations in the main stem of the Rio Grande generally increased in a downstream direction. This increase is from natural sources such as ground-water inflow and evapotranspiration and from anthropogenic sources such as irrigation- return flows, urban runoff, and wastewater-treatment plant discharges. The smallest median dissolved-solids concentration detected at a basic- fixed site was 58 milligrams per liter and the largest was 1,240 milligrams per liter. The spatial distribution of calcium, magnesium, sodium, sulfate, chloride, and fluoride was similar to the spatial distribution of dissolved solids. The spatial distribution of potassium and bicarbonate varied slightly from that of dissolved solids. Median silica concentrations generally decreased in a downstream direction. Of all cations, calcium and sodium had the largest concentrations at most basic-fixed sites. Bicarbonate and sulfate were the anions having the largest concentrations at most sites. The largest median silica concentration was at Rito de los Frijoles in Bandelier National Monument, New Mexico, where silica composed approximately 50 percent of the dissolved solids. The largest concentrations and largest median concentrations of dissolved-nutrient analytes were detected at Santa Fe River above Cochiti Lake, New Mexico, and Rio Grande at Isleta, New Mexico. The relatively large dissolved-nutrient concentrations at these sites probably were due to discharges from wastewater-treatment plants and urban runoff. The largest concentrations and largest median concentrations of total ammonia plus organic nitrogen and total phosphorus were detected at Rio Puerco near Bernardo, New Mexico. The largest concentrations of these nutrients at this site were associated with runoff from summer thunderstorms. Dissolved-iron concentrations ranged from censored concentrations to 914 micrograms per liter. Median dissolved-iron concentrations ranged from 3 to 160 micrograms per liter.

Colorado, New Mexico, Texas↗

USGS2000

Water quality in alluvial aquifers of the southern Rocky Mountains Physiographic Province, upper Colorado River basin, Colorado, 1997

Water-quality samples were collected in the summer of 1997 from 45 sites (43 wells and 2 springs) in selected alluvial aquifers throughout the Southern Rocky Mountains physiographic province of the Upper Colorado River Basin study unit as part of the U.S. Geological Survey National Water-Quality Assessment Program. The objective of this study was to assess the water-quality conditions in selected alluvial aquifers in the Southern Rocky Mountains physiographic province. Alluvial aquifers are productive aquifers in the Southern Rocky Mountains physiographic province and provide for easily developed wells. Water-quality samples were collected from areas where ground water is used predominantly for domestic or public water supply. Twenty-three of the 45 sites sampled were located in or near mining districts. No statistical differences were observed between the mining sites and sites not associated with mining activities for the majority of the constituents analyzed. Water samples were analyzed for major ions, nutrients, dissolved organic carbon, trace elements, radon-222, pesticides, volatile organic compounds, bacteria, and methylene blue active substances. In addition, field parameters consisting of water temperature, specific conductance, dissolved oxygen, pH, turbidity, and alkalinity were measured at all sites. Specific conductance for the ground-water sites ranged from 57 to 6,650 microsiemens per centimeter and had higher concentrations measured in areas such as the northwestern part of the study unit. Dissolved oxygen ranged from 0.1 to 6.0 mg/L (milligrams per liter) and had a median concentration of 2.9 mg/L. The pH field values ranged from 6.1 to 8.1; about 4 percent of the sites (2 of 45) had pH values outside the range of 6.5 to 8.5 and so did not meet the U.S. Environmental Protection Agency secondary maximum contaminant level standard for drinking water. About 5 percent (2 of 43) of the samples exceeded the U.S. Environmental Protection Agency recommended turbidity value of 5 nephelometric turbidity units; one of these samples was from a monitoring well. The U.S. Environmental Protection Agency secondary maximum contaminant levels for dissolved solids, sulfate, iron, and manganese were exceeded at some of the sites. Higher dissolved-solids concentrations were detected where sedimentary rocks are exposed, such as in the northwestern part of the Southern Rocky Mountains physiographic province. The dominant water compositions for the sites sampled are calcium, magnesium, and bicarbonate. However, sites in areas where sedimentary rocks are exposed and sites located in or near mining areas show more sulfate-dominated waters. Nutrient concentrations were less than the U.S. Environmental Protection Agency drinking-water standards. Only one site had a nitrate concentration greater than 3.0 mg/L, a level indicating possible influence from human activities. No significant differences among land-use/land-cover classifications (forest, rangeland, and urban) for drinking-water wells (42 sites) were identified for dissolved-solids, sulfate, nitrate, iron or manganese concentrations. Radon concentrations were higher in parts of the study unit where Precambrian rocks are exposed. All radon concentrations in ground water exceeded the previous U.S. Environmental Protection Agency proposed maximum contaminant level for drinking water, which has been withdrawn pending further review. Pesticide detections were at concentrations below the reporting limits and were too few to allow for comparison of the data. Eight volatile organic compounds were detected at six sites; all concentrations complied with U.S. Environmental Protection Agency drinking-water standards. Total coliform bacteria were detected at six sites, but no Escherichia coli ( E. coli ) was detected. Methylene blue active substances were detected at three sites at concentrations just above the reporting limit. Overall, the water quality in the Southern Rocky Mountains physiographic province is suitable for most uses, but natural and human factors affect the water quality.

Colorado↗

USGS2007

Ground-Water Quality and Potential Effects of Individual Sewage Disposal System Effluent on Ground-Water Quality in Park County, Colorado, 2001-2004

In 2000, the U.S. Geological Survey, in cooperation with Park County, Colorado, began a study to evaluate ground-water quality in the various aquifers in Park County that supply water to domestic wells. The focus of this study was to identify and describe the principal natural and human factors that affect ground-water quality. In addition, the potential effects of individual sewage disposal system (ISDS) effluent on ground-water quality were evaluated. Ground-water samples were collected from domestic water-supply wells from July 2001 through October 2004 in the alluvial, crystalline-rock, sedimentary-rock, and volcanic-rock aquifers to assess general ground-water quality and effects of ISDS's on ground-water quality throughout Park County. Samples were analyzed for physical properties, major ions, nutrients, bacteria, and boron; and selected samples also were analyzed for dissolved organic carbon, human-related (wastewater) compounds, trace elements, radionuclides, and age-dating constituents (tritium and chlorofluorocarbons). Drinking-water quality is adequate for domestic use throughout Park County with a few exceptions. Only about 3 percent of wells had concentrations of fluoride, nitrate, and (or) uranium that exceeded U.S. Environmental Protection Agency national, primary drinking-water standards. These primary drinking-water standards were exceeded only in wells completed in the crystalline-rock aquifers in eastern Park County. Escherichia coli bacteria were detected in one well near Guffey, and total coliform bacteria were detected in about 11 percent of wells sampled throughout the county. The highest total coliform concentrations were measured southeast of the city of Jefferson and west of Tarryall Reservoir. Secondary drinking-water standards were exceeded more frequently. About 19 percent of wells had concentrations of one or more constituents (pH, chloride, fluoride, sulfate, and dissolved solids) that exceeded secondary drinking-water standards. Currently (2004), there is no federally enforced drinking-water standard for radon in public water-supply systems, but proposed regulations suggest a maximum contaminant level of 300 picocuries per liter (pCi/L) and an alternative maximum contaminant level of 4,000 pCi/L contingent on other mitigating remedial activities to reduce radon levels in indoor air. Radon concentrations in about 91 percent of ground-water samples were greater than or equal to 300 pCi/L, and about 25 percent had radon concentrations greater than or equal to 4,000 pCi/L. Generally, the highest radon concentrations were measured in samples collected from wells completed in the crystalline-rock aquifers. Analyses of ground-water-quality data indicate that recharge from ISDS effluent has affected some local ground-water systems in Park County. Because roughly 90 percent of domestic water used is assumed to be recharged by ISDS's, detections of human-related (wastewater) compounds in ground water in Park County are not surprising; however, concentrations of constituents associated with ISDS effluent generally are low (concentrations near the laboratory reporting levels). Thirty-eight different organic wastewater compounds were detected in 46 percent of ground-water samples, and the number of compounds detected per sample ranged from 1 to 17 compounds. Samples collected from wells with detections of wastewater compounds also had significantly higher (p-value < 0.05) chloride and boron concentrations than samples from wells with no detections of wastewater compounds. ISDS density (average subdivision lot size used to estimate ISDS density) was related to ground-water quality in Park County. Chloride and boron concentrations were significantly higher in ground-water samples collected from wells located in areas that had average subdivision lot sizes of less than 1 acre than in areas that had average subdivision lot sizes greater than or equal to 1 acre. For wells completed in the crystalline-

Scientific Investigations Report↗

USGS1996

Occurrence of selected trace elements and organic compounds and their relation to land use in the Willamette River basin, Oregon, 1992-94

Between 1992 and 1994, the U.S.Geological Survey conducted a study of trace elements and organic compounds in the Willamette River Basin, Oregon, as part of the Willamette River Basin Water Quality Study. Low-level analyses were performed for trace elements, volatile organic compounds, organochlorine compounds, and pesticides. Overall, 94 water samples were collected from 40 sites, during predominantly high-flow conditions, representing urban, agricultural, mixed, and forested land uses. Although most observed concentrations were relatively low, some exceedances of water-quality criteria for acute and chronic toxicity and for the protection of human health were observed. Concentrations of chromium, copper, lead, and zinc in unfiltered water were well correlated with concentrations of suspended sediment. The highest trace-element concentrations generally were found at urban sites that receive a large portion of their runoff from industrial areas, particularly at high suspended- sediment concentrations. In contrast, concentrations of trace elements in some urban streams draining primarily residential areas appeared to approach a maximum as sediment concentrations increased. Whether this difference was due to a difference in the nature of the suspended sediments or to different concentrations in the aqueous phases from the two site types was not addressed. Eight organochlorine compounds were detected at 14 sites. Lindane, dieldrin, and DDT or its metabolites were each detected in about 30 percent of the samples, predominantly in samples collected from agricultural and urban areas. Polychlorinated biphenyl (PCB) compounds were detected in samples from two urban sites. For samples in which DDT and its metabolites were examined for partitioning, the largest proportion of the mass of DDT and its metabolites was associated with suspended sediment. In contrast, dieldrin and lindane were almost completely (greater than 99 percent) associated with the dissolved phase. Sixty-one of the 94 pesticides analyzed in filtered water were documented to have been used in the basin in 1987; 43 of these were detected at least once during 1992–94. An additional five were detected that were not documented in the 1987 estimates. Although a comparison between the frequency of detected pesticides and 1987 estimates of pesticide usage in the basin showed generally little correlation, some patterns of detections did appear to reflect land use in the basin. Of the 25 most frequently detected pesticides, 3 were found primarily at urban sites, 6 were found primarily at agricultural sites, and 7 were found at all types of sites except forested. The four most commonly detected pesticides in the basin, observed at all except forested site 2 types, were atrazine, metolachlor, simazine, and diuron. A greater variety of compounds was detected at sites in the northern portion of the basin than in the southern portion of the basin probably because the northern portion has more diverse agricultural practices and a larger urban component. Possible reasons for the lack of agreement between pesticide detections and pesticide usage estimates include (1) uncertainty in the usage estimates due to spatial and temporal variability or due to changes in agricultural practices since the 1987 estimates were compiled, (2) chemical or biological transformations in the compounds after application, (3) variable hydrologic conditions among sites at the time of sampling, or (4) the ability of laboratory analytical procedures to detect low concentrations of some analytes. Results from repeated samplings at two sites during sequential storms in the fall of 1994 indicated that concentrations and loads of several constituents, including suspended sediment, suspended organic carbon, DDT, metolachlor, and atrazine were highest during peak flows of the first or second significant storms of the fall. Samplings during subsequent storms indicated that instantaneous concentrations and loads were generally reduced; however, data were not sufficient to compare overall transport during sequential storms.

Oregon↗

USGS1996

Water quality of the lower Columbia River Basin: Analysis of current and historical water-quality data through 1994

The lower Columbia River Basin includes the river basins draining into the Columbia River below Bonneville Dam—the largest of which is the Willamette River. This report presents the results of a study by the U.S. Geological Survey, done in cooperation with the Lower Columbia River Bi-State Water- Quality Program, to describe the water-quality conditions in the lower Columbia River Basin by interpreting historical data collected and data collected in 1994. Historical water-quality data spanning more than 50 years and comprising more than 200 parameters were collated for interpretation in this report. The U.S. Geological Survey, the Oregon Department of Environmental Quality, and the Washington Department of Ecology collected water-quality data at 10 sites in the lower Columbia River Basin from January to December of 1994. Water-quality constituents measured in 1994 were screened against U.S. Environmental Protection Agency (EPA) and State guidelines. Arsenic, a human carcinogen, was detected in 15 of 16 samples in the lower Columbia River, but was not detected in any of the sampled tributaries. All 15 arsenic detections had concentrations that exceeded both the EPA ambient water-quality criteria for the protection of human health and the EPA human-health advisories for drinking water. Chromium was detected at all four Columbia River sites—most frequently in the Columbia River at Hayden Island. None of the chromium concentrations detected, however, exceeded water-quality criteria or guidelines. Measurements of suspended trace-element concentrations (trace-element concentrations associated with the suspended-sediment fraction) showed that the suspended form is the dominant transport phase for aluminum, iron, and manganese, whereas the dissolved form is the dominant transport phase for arsenic, barium, chromium, and copper. On the basis of tributary loads during summer low-flow months, sources of suspended silver, nickel, aluminum, and antimony exist in the lower Columbia River Basin, whereas the sources of suspended zinc and arsenic exist outside of the lower basin. Twenty organic compounds were detected of the 47 compounds analyzed for this study. None of the organic compounds measured exceeded EPA’s ambient water-quality criteria or drinking-water guidelines. The Willamette River at Portland had the largest number of detections, and all 20 compounds were detected at one time or another at that site. The largest concentrations of the agricultural pesticides, atrazine, metolachlor, and simazine were detected in the Willamette River, where they were detected in 93, 86, 93 percent, respectively, of the samples collected. The highest concentrations of atrazine in the Willamette River were associated with the spring application and fall runoff periods. Both historical and current data showed that the highest water temperatures in the lower Columbia River Basin are present during August. For water years 1977–81 in the Columbia River at Bradwood (river mile 38.9), 75 percent of the daily mean water temperatures during August exceeded 20 degrees Celsius, a “special condition” criterion for the State of Washington. The special condition criterion was exceeded at four sites on the lower Columbia River during July and August, 1994—a period coinciding with season-high air temperatures and low streamflow. Trend tests using data from 1974 to 1994 showed significant (r < 0.05) upward trends for water temperature at the Columbia River at Warrendale and the Willamette River at Portland. Concentrations of dissolved oxygen and total dissolved gas were above saturation levels during high stormflows in the lower Columbia River and the Willamette River during 1994. The high concentrations of total dissolved gas in the Columbia River exceeded Oregon and Washington State standards of 110 percent of saturation and were caused by spilling water at the Columbia River dams. Aquatic life in the lower Columbia River Basin was not subjected to low dissolved-oxygen concentrations. Comparison of dissolved-oxygen concentrations in the Willamette River from 1949–58 to 1972–94 showed a significant increase in dissolved-oxygen concentrations during the low-streamflow months of summer. Trend tests showed significant (r < 0.05) downward trends from 1973 to 1994 for three constituents at the Columbia River at Warrendale: phosphorus in unfiltered water, total dissolved solids, and specific conductance. These trends may be a consequence of more conservative agricultural practices in the area upstream from Warrendale.

Oregon↗

USGS2009

Quality characteristics of ground water in the Ozark aquifer of northwestern Arkansas, southeastern Kansas, southwestern Missouri and northeastern Oklahoma, 2006-07

Because of water quantity and quality concerns within the Ozark aquifer, the State of Kansas in 2004 issued a moratorium on most new appropriations from the aquifer until results were made available from a cooperative study between the U.S. Geological Survey and the Kansas Water Office. The purposes of the study were to develop a regional ground-water flow model and a water-quality assessment of the Ozark aquifer in northwestern Arkansas, southeastern Kansas, southwestern Missouri, and northeastern Oklahoma (study area). In 2006 and 2007, water-quality samples were collected from 40 water-supply wells completed in the Ozark aquifer and spatially distributed throughout the study area. Samples were analyzed for physical properties, dissolved solids and major ions, nutrients, trace elements, and selected isotopes. This report presents the results of the water-quality assessment part of the cooperative study. Water-quality characteristics were evaluated relative to U.S. Environmental Protection Agency drinking-water standards. Secondary Drinking-Water Regulations were exceeded for dissolved solids (11 wells), sulfate and chloride (2 wells each), fluoride (3 wells), iron (4 wells), and manganese (2 wells). Maximum Contaminant Levels were exceeded for turbidity (3 wells) and fluoride (1 well). The Maximum Contaminant Level Goal for lead (0 milligrams per liter) was exceeded in water from 12 wells. Analyses of isotopes in water from wells along two 60-mile long ground-water flow paths indicated that water in the Ozark aquifer was at least 60 years old but the upper age limit is uncertain. The source of recharge water for the wells along the flow paths appeared to be of meteoric origin because of isotopic similarity to the established Global Meteoric Water Line and a global precipitation relation. Additionally, analysis of hydrogen-3 (3H) and carbon-14 (14C) indicated that there was possible leakage of younger ground water into the lower part of the Ozark aquifer. This may be caused by cracks or fissures in the confining unit that separates the upper and lower parts of the aquifer, poorly constructed or abandoned wells, or historic mining activities. Analyses of major ions in water from wells along the flow paths indicated a transition from freshwater in the east to saline water in the west. Generally, ground water along flow paths evolved from a calcium magnesium bicarbonate type to a sodium calcium bicarbonate or a sodium calcium chloride bicarbonate type as water moved from recharge areas in Missouri into Kansas. Much of this evolution occurred within the last 20 to 25 miles of the flow paths along a water-quality transition zone near the Kansas-Missouri State line and west. The water quality of the Kansas part of the Ozark aquifer is degraded compared to the Missouri part. Geophysical and well-bore flow information and depth-dependent water-quality samples were collected from a large-capacity (1,900-2,300 gallons per minute) municipal-supply well to evaluate vertical ground-water flow accretion and variability in water-quality characteristics at different levels. Although the 1,050-foot deep supply well had 500 feet of borehole open to the Ozark aquifer, 77 percent of ground-water flow entering the borehole came from two 20-foot thick rock layers above the 1,000-foot level. For the most part, water-quality characteristics changed little from the deepest sample to the well-head sample, and upwelling of saline water from deeper geologic formations below the well was not evident. However, more saline water may be present below the bottom of the well.

Arkansas, Kansas, Missouri, Oklahoma↗

USGS2012

Hydrogeology of the Mammoth Spring groundwater basin and vicinity, Markagunt Plateau, Garfield, Iron, and Kane Counties, Utah

The Markagunt Plateau, in southwestern Utah, lies at an altitude of about 9,500 feet, largely within Dixie National Forest. The plateau is capped primarily by Tertiary- and Quaternary-age volcanic rocks that overlie Paleocene- to Eocene-age limestone of the Claron Formation, which forms escarpments on the west and south sides of the plateau. In the southwestern part of the plateau, an extensive area of sinkholes has formed that resulted primarily from dissolution of the underlying limestone and subsequent subsidence and (or) collapse of the basalt, producing sinkholes as large as 1,000 feet across and 100 feet deep. Karst development in the Claron Formation likely has been enhanced by high infiltration rates through the basalt. Numerous large springs discharge from the volcanic rocks and underlying limestone on the Markagunt Plateau, including Mammoth Spring, one of the largest in Utah, with discharge that ranges from less than 5 to more than 300 cubic feet per second (ft 3 /s). In 2007, daily mean peak discharge of Mammoth Spring was bimodal, reaching 54 and 56 ft 3 /s, while daily mean peak discharge of the spring in 2008 and in 2009 was 199 ft 3 /s and 224 ft 3 /s, respectively. In both years, the rise from baseflow, about 6 ft 3 /s, to peak flow occurred over a 4- to 5-week period. Discharge from Mammoth Spring accounted for about 54 percent of the total peak streamflow in Mammoth Creek in 2007 and 2008, and about 46 percent in 2009, and accounted for most of the total streamflow during the remainder of the year. Results of major-ion analyses for water samples collected from Mammoth and other springs on the plateau during 2006 to 2009 indicated calcium-bicarbonate type water, which contained dissolved-solids concentrations that ranged from 91 to 229 milligrams per liter. Concentrations of major ions, trace elements, and nutrients did not exceed primary or secondary drinking-water standards; however, total and fecal coliform bacteria were present in water from Mammoth and other springs. Temperature and specific conductance of water from Mammoth and other springs showed substantial variance and generally were inversely related to changes in discharge during snowmelt runoff and rainfall events. Over the 3-year study period, daily mean temperature and specific conductance of water from Mammoth Spring ranged from 3.4 degrees Celsius (°C) and 112 microsiemens per centimeter (μS/cm) during peak flow from snowmelt runoff to 5.3°C and 203 μS/cm during baseflow conditions. Increases in specific conductance of the spring water prior to an increase in discharge in 2008–09 were likely the result of drainage of increasingly older water from storage. Variations in these parameters in water from two rise pools upstream from Mammoth Spring were the largest observed in relation to discharge and indicate a likely hydraulic connection to Mammoth Creek. Variations in water quality, discharge, and turbidity indicate a high potential for transport of contaminants from surface sources to Mammoth and other large springs in a matter of days. Results of dye-tracer tests indicated that recharge to Mammoth Spring largely originates from southwest of the spring and outside of the watershed for Mammoth Creek, particularly along the drainages of Midway and Long Valley Creeks, and in the Red Desert, Horse Pasture, and Hancock Peak areas, where karst development is greatest. A significant component of recharge to the spring takes place by both focused and diffuse infiltration through the basalt and into the underlying Claron limestone. Losing reaches along Mammoth Creek are also a source of rapid recharge to the spring. Maximum groundwater travel time to the spring during the snowmelt runoff period was about 7 days from sinking streams as far as 9 miles away and 1,900 feet higher, indicating a velocity of more than a mile per day. Response of the spring to rainfall events in the recharge area, however, indicated potential lag times of only about 1 to 2 days. Samples collected from Mammoth Spring during baseflow conditions and analyzed for tritium and sulfur-35 showed that groundwater in storage is relatively young, with apparent ages ranging from less than 1 year to possibly a few tens of years. Ratios of oxygen-18 and deuterium also showed that water from the spring represents a mixture of waters from different sources and altitudes. On the basis of evaluating results of dye-tracer tests and relations to adjacent basins, the recharge area for Mammoth Spring probably includes about 40 square miles within the Mammoth Creek watershed as well as at least 25 square miles outside and to the south of the watershed. Additional dye-tracer tests are needed to better define boundaries between the groundwater basins for Mammoth Spring and Duck Creek, Cascade, and Asay Springs.

Utah↗

USGS2022

Characterization of water quality, biology, and habitat of the Pearl River and selected tributaries contiguous to and within Tribal lands of the Pearl River Community of the Mississippi Band of Choctaw Indians, 2017–18

The U.S. Geological Survey, in cooperation with the Mississippi Band of Choctaw Indians (MBCI), conducted a baseline assessment of the physical, chemical, and biological quality of selected streams and rivers within and contiguous to the Pearl River Community (PRC) in 2017 and 2018. The MBCI is a federally recognized tribe with territories in Mississippi and Tennessee. MBCI Tribal government and communities have sovereign authority over their natural resources and are responsible for protecting the quality of waters within the Tribal lands from sources of pollution and restoring impaired waters. The quality of these surface waters has a profound effect upon the health and welfare of MBCI Tribal members. Data generated from this study may be used with other relevant water-quality data for comparison and development of Tribal water-quality standards. The PRC territory is drained by the Pearl River and associated tributaries. Water-quality and biological samples were collected and habitat surveys were conducted at sites on the mainstem of the Pearl River and major tributaries of the Pearl River—Wolf Creek, Beasha Creek, Jones Creek, and Kentawka Creek. The selected stream sites represent a range of land use/land cover and potential sources of alteration and contamination from within their respective drainage areas. In particular, Wolf Creek watershed has the highest relative percentage of developed land. Ambient physicochemical properties, major ions, nutrients, and organic wastewater compounds (OWCs) were analyzed quarterly from surface-water samples from October 2017 through August 2018. Physicochemical properties were also measured in June 2018 over a continuous 48-hour period. Trace elements and polycyclic aromatic hydrocarbons were analyzed from streambed sediments in August 2018. Biological samples included the collection of periphyton algae (August 2018), benthic macroinvertebrate (March 2017 and March 2018), and fish communities (April 2018). Physical stream habitat characteristics were assessed using qualitative (March 2017 and March 2018) and quantitative surveys (August 2018). While not directly applicable, the State of Mississippi Water Quality Standards were used as reference to evaluate Tribal water quality. Physicochemical water-quality constituents—water temperature, specific conductance (SC), pH, and dissolved oxygen (DO)—were generally within natural ranges among sites and samples, with a few exceptions that exceeded existing Mississippi water-quality standards. pH and DO periodically were below the minimum State standards at some sampled sites. Specific conductance was also relatively high at both Wolf Creek sites but did not exceed the existing maximum standard for recreational waters. The surface water among stream sites was predominantly calcium bicarbonate type, with a shift toward sodium-bicarbonate water type at the downstream Wolf Creek (Wolf DS) site. Major ion concentrations were generally highest at the Wolf Creek sites. Nutrient concentrations were also often highest at Wolf DS, but total nitrogen and total phosphorus periodically exceeded recommended State and Federal nutrient criteria thresholds among most sampled sites. Twenty-nine OWCs, including 10 known or suspected endocrine disruptors, were detected among sites. Concentrations of OWCs were relatively low, and only 19 percent of all detections were above the reporting level. Concentrations of copper and nickel in streambed sediments were detected above consensus-based threshold-effect concentrations (TECs) at one site each, and arsenic and chromium exceeded TECs at most sites. Concentrations of all polycyclic aromatic hydrocarbons in streambed sediments were low and well below TECs at all sites. The periphyton, macroinvertebrate, and fish communities at most sampled sites appear typical of central Mississippi streams; however, the diversity, composition, and abundance of taxa sampled from Wolf DS were particularly distinctive compared to other sampled stream sites. Periphyton taxa richness was low at both Wolf Creek sites, and both sites had greater abundances of diatom taxa, which are indicative of high nutrient concentrations, than of soft-algae taxa. Similarly, Wolf DS had relatively low macroinvertebrate diversity, the fewest Ephemeroptera, Plecoptera, and Trichoptera taxa, a high abundance of Tubificid taxa, and the lowest overall Mississippi-Benthic Index of Stream Quality score. Fish species richness was also relatively low at Wolf DS compared to some other sampled sites. Habitat characteristics also appeared to be generally typical of most central Mississippi streams. Qualitative habitat assessment scores were at or above the regional least disturbed streams for Wolf DS, the upstream Wolf Creek (Wolf US) site, and Jones Creek. Habitat scores among the remaining sites indicate fair conditions. Quantitative and qualitative habitat characteristics indicate relatively lower habitat quality at the two Beasha Creek sites.

Mississippi↗