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At least 289 records · Page 16Linked to original sources
USGS2026

Sediment transport, terrace incision, and sediment chemistry in subbasins of differing land use, Stinking Water Creek Basin near Rangely, Colorado

In many areas of western Colorado, Late Cretaceous Mancos Shale is a source of sediment, salinity, and selenium to surface water. Natural weathering processes and human activity can expose and move sediments from the Mancos Shale, leading to increased salinity and selenium concentrations in surface water. The U.S. Geological Survey, in cooperation with the Bureau of Land Management, studied four subbasins of Stinking Water Creek near Rangely, Colorado, to provide information regarding landscapes on Mancos Shale that have undergone land-use change. Rangeland grazing is present in all four subbasins. Subbasins A1 and A2 have land use related to energy development and subbasins B1 and B2 do not. Aerial photographs, sediment chemistry, optically stimulated luminescence (OSL) ages, cross-section surveys, and Watershed Erosion Prediction Project (WEPP) modeling were used to characterize the history of land-use change by estimating stream channel incision rates and sediment, salinity, and selenium loads. All subbasins had upper and lower terraces and a modern streambed channel, and these surfaces were dated using OSL. In subbasins A1, A2, and B1, the streambed age was older than the terraces, indicating the channels are incising and widening into the older alluvium. In subbasin B2, however, the streambed age was much younger than the terraces, indicating aggradation is the main process. Differences in channel morphology were not always related to land use but to the subbasin position (upstream compared to downstream). Channels in subbasins A1 and A2 were generally wider and shallower than channels in subbasins B1 and B2. Landscape disturbances related to energy development in subbasins A1 and A2 could have caused channel evolution to progress from incision to widening processes.

Colorado↗
USGS2003

Methods of analysis by the U.S. Geological Survey Organic Geochemistry Research Group: Determination of acetamide herbicides and their degradation products in water using online solid-phase extraction and liquid chromatography/mass spectrometry

An analytical method for the determination of 6 acetamide herbicides (acetochlor, alachlor, dimethenamid, flufenacet, metolachlor, and propachlor) and 16 of their degradation products in natural water samples using solid-phase extraction and liquid chromatography/mass spectrometry is described in this report. Special consideration was given during the development of the method to prevent the formation of degradation products during the analysis. Filtered water samples were analyzed using octadecylsilane as the solid-phase extraction media on online automated equipment followed by liquid chromatography/mass spectrometry. The method uses only 10 milliliters of sample per injection. Three different water-sample matrices, a reagent-water, a ground-water, and a surface-water sample spiked at 0.10 and 1.0 microgram per liter, were analyzed to determine method performance. Method detection limits ranged from 0.004 to 0.051 microgram per liter for the parent acetamide herbicides and their degradation products. Mean recoveries for the acetamide compounds in the ground- and surface-water samples ranged from 62.3 to 117.4 percent. The secondary amide of acetochlor/metolachlor ethanesulfonic acid (ESA) was recovered at an average rate of 43.5 percent. The mean recoveries for propachlor and propachlor oxanilic acid (OXA) were next lowest, ranging from 62.3 to 95.5 percent. Mean recoveries from reagent-water samples ranged from 90.3 to 118.3 percent for all compounds. Overall the mean of the mean recoveries of all compounds in the three matrices spiked at 0.10 and 1.0 microgram per liter ranged from 89.9 to 100.7 percent, including the secondary amide of acetochlor/metolachlor ESA and the propachlor compounds. The acetamide herbicides and their degradation products are reported in concentrations ranging from 0.05 to 2.0 micrograms per liter. The upper concentration limit is 2.0 micrograms per liter for all compounds without dilution. With the exception of the secondary amide of acetochlor/metolachlor ESA, good precision and accuracy for the chloroacetanalide herbicides and their degradation compounds were demonstrated for the method in buffered reagent water, ground water, and surface water. The extraction method as used did not optimize the recovery of the secondary amide of acetochlor/metolachlor ESA.

Open-File Report↗
USGS1984

Development of a model to predict the adsorption of lead from solution on a natural streambed sediment

Adsorption of solutes by solid mineral surfaces commonly influences the dissolved ionic composition of natural waters. A model based on electrical double-layer theory has been developed which appears to be capable of characterizing the surface chemical behavior of a natural fine-grained sediment containing mostly quartz and feldspar. This variable surface charge-variable surface potential (VSC-VSP) model differs from others in being capable of evaluating more closely the effect of total metal ion activity on the pH-dependent change in electrical potential at the solid surface. The model was tested using 10-4 molar solutions of lead and a silt-size fraction of sediment from the bed of Colma Creek, a small stream in urban northern San Mateo County, California. The average deviation of measured percent adsorption and values calculated from the model was 6.6 adsorption percent from pH 2.0 to pH 7.0.

Water Supply Paper↗
USGS2018

Seeking excellence: An evaluation of 235 international laboratories conducting water isotope analyses by isotope-ratio and laser-absorption spectrometry

Rationale Water stable isotope ratios ( δ 2 H and δ 18 O values) are widely used tracers in environmental studies; hence, accurate and precise assays are required for providing sound scientific information. We tested the analytical performance of 235 international laboratories conducting water isotope analyses using dual-inlet and continuous-flow isotope ratio mass spectrometers and laser spectrometers through a water isotope inter-comparison test. Methods Eight test water samples were distributed by the IAEA to international stable isotope laboratories. These consisted of a core set of five samples spanning the common δ -range of natural waters, and three optional samples (highly depleted, enriched, and saline). The fifth core sample contained unrevealed trace methanol to assess analyst vigilance to the impact of organic contamination on water isotopic measurements made by all instrument technologies. Results For the core and optional samples ~73 % of laboratories gave acceptable results within 0.2 ‰ and 1.5 ‰ of the reference values for δ 18 O and δ 2 H, respectively; ~27 % produced unacceptable results. Top performance for δ 18 O values was dominated by dual-inlet IRMS laboratories; top performance for δ 2 H values was led by laser spectrometer laboratories. Continuous-flow instruments yielded comparatively intermediate results. Trace methanol contamination of water resulted in extreme outlier δ -values for laser instruments, but also affected reactor-based continuous-flow IRMS systems; however, dual-inlet IRMS δ -values were unaffected. Conclusions Analysis of the laboratory results and their metadata suggested inaccurate or imprecise performance stemmed mainly from skill- and knowledge-based errors including: calculation mistakes, inappropriate or compromised laboratory calibration standards, poorly performing instrumentation, lack of vigilance to contamination, or inattention to unreasonable isotopic outcomes. To counteract common errors, we recommend that laboratories include 1–2 'known' control standards in all autoruns; laser laboratories should screen each autorun for spectral contamination; and all laboratories should evaluate whether derived d- excess values are realistic when both isotope ratios are measured. Combined, these data evaluation strategies should immediately inform the laboratory about fundamental mistakes or compromised samples.

Rapid Communications in Mass Spectrometry↗
USGS1967

Standards for water quality

The quality which is necessary depends on the use to which the water will be put. Because uses vary, so also must quality standards. Maintaining any level of quality presents a problem of cost and depends on variations in natural water characteristics, in time and space, and variations in volume and types of wastes. For quality standards appropriate to a given water body, hydrologic network data can provide duration curves of flow, concentrations of dissolved oxygen, dissolved solids, including nutrients (nitrates and phosphates), turbidity, temperature, and other significant chemical, physical, and biological parameters. Standards can then be expressed as occurrences in percentage of time or with respect to flow.

Conference Paper↗
USGS1985

Statistical evaluation of an inductively coupled plasma atomic emission spectrometric method for routine water quality testing

In an interlaboratory test, inductively coupled plasma atomic emission spectrometry (ICP-AES) was compared with flame atomic absorption spectrometry and molecular absorption spectrophotometry for the determination of 17 major and trace elements in 100 filtered natural water samples. No unacceptable biases were detected. The analysis precision of ICP-AES was found to be equal to or better than alternative methods. Known-addition recovery experiments demonstrated that the ICP-AES determinations are accurate to between plus or minus 2 and plus or minus 10 percent; four-fifths of the tests yielded average recoveries of 95-105 percent, with an average relative standard deviation of about 5 percent.

Applied Spectroscopy↗
USGS1989

Solubility of jarosite solid solutions precipitated from acid mine waters, Iron Mountain, California

Because of the common occurrence of 15 to 25 mole percent hydronium substitution on the alkali site in jarosites, it is necessary to consider the hydronium content of jarosites in any attempt at rigorous evaluation of jarosite solubility or of the saturation state of natural waters with respect to jarosite. A Gibbs free energy of 3293.5±2.1 kJ mol-1 is recommended for a jarosite solid solution of composition K.77Na.03(H3O).20Fe3(SO4)2(OH)6. Solubility determinations for a wider range of natural and synthetic jarosite solid solutions will be necessary to quantify the binary and ternary mixing parameters in the (K-Na-H3O) system. In the absence of such studies, molar volume data for endmember minerals indicate that the K-H3O substitution in jarosite is probably closer to ideal mixing than either the Na-K or Na-H3O substitution.

California↗
USGS2014

The chronic toxicity of sodium bicarbonate, a major component of coal bed natural gas produced waters

Sodium bicarbonate (NaHCO 3 ) is the principal salt in coal bed natural gas produced water from the Powder River Structural Basin, Wyoming, USA, and concentrations of up to 3000 mg NaHCO 3 /L have been documented at some locations. No adequate studies have been performed to assess the chronic effects of NaHCO 3 exposure. The present study was initiated to investigate the chronic toxicity and define sublethal effects at the individual organism level to explain the mechanisms of NaHCO 3 toxicity. Three chronic experiments were completed with fathead minnows (Pimephales promelas), 1 with white suckers (Catostomus commersoni), 1 with Ceriodaphnia dubia, and 1 with a freshwater mussel, (Lampsilis siliquoidea). The data demonstrated that approximately 500 mg NaHCO 3 /L to 1000 mg NaHCO 3 /L affected all species of experimental aquatic animals in chronic exposure conditions. Freshwater mussels were the least sensitive to NaHCO 3 exposure, with a 10-d inhibition concentration that affects 20% of the sample population (IC20) of 952 mg NaHCO 3 /L. The IC20 for C. dubia was the smallest, at 359 mg NaHCO 3 /L. A significant decrease in sodium–potassium adenosine triphosphatase (Na + /K + ATPase) together with the lack of growth effects suggests that Na + /K + ATPase activity was shut down before the onset of death. Several histological anomalies, including increased incidence of necrotic cells, suggested that fish were adversely affected as a result of exposure to >450 mg NaHCO 3 /L.

Environmental Toxicology and Chemistry↗
USGS2002

Determination of small quantities of fluoride in water: A modified zirconium-alizarin method

The zirconium-alizarin method has been modified to facilitate the convenient and accurate determination of small amounts of fluoride in a large number of water samples. Sulfuric acid is used to acidify the samples to reduce the interference of sulfate. The pH is accurately controlled to give the most sensitive comparisons. Most natural waters can be analyzed by the modified procedure without resorting to correction curves. The fluoride content of waters containing less than 500 parts per million of sulfate, 500 parts per million of bicarbonate, and 1000 parts per million of chloride may be determined within a limit of about 0.1 part per million when a 100-ml. sample is used.

Industrial And Engineering Chemistry Analytical Ed↗
USGS1972

Water in St. John, U.S. Virgin Islands

Water for domestic and municipal supply on St. John, in the past, has been obtained from rain catchments, dug wells, and barge shipments from St. Thomas and Puerto Rico. As a result of this study, small ground-water supplies have been developed for the Virgin Islands National Park. Ground water occurs in significant but limited quantities in the fractured volcanic rock throughout most of the Island. Yield of wells in this aquifer ranges from less than 100 to about 2,000 gpd (gallons per day). The average long-term yield of the three drilled wells in use by the National Park Service in 1967 was about 1,000 gpd. Yield ofl,000 to 5,000 gpd may be expected in the Coral Bay and the Reef Bay areas. Estimated total recharge of the fractured volcanic rock on St. John, based on a recharge of 1 to 3 inches per year, is 1,000,000 to 3,000,000 gpd. Perhaps as much as a quarter to a third of this water could be developed practically, depending on the rainfall in a given year. The chemical quality of the ground water in the fractured-rock aquifer in areas uncontaminated by sea water ranges from 600 to 2,000 mg/l (milligrams per liter) or more dissolved solids. Water from-formations in the higher altitudes is of better quality than that in the lower formations. Small quantities of ground water are available from beach sand, alluvium, and fractured rock near the sea. However, these sources tend to be brackish and are subject to salt-water encroachment. There are no perennial streams on St. John. There are a few spring-fed pools in stream channels, however, that are sustained, except in severe drought. Storm runoff is estimated to average 1 inch over the island annually, and evaporation from open water surfaces is about 70 inches per year. Ponds can be developed, but because of the high .evaporation they may be unreliable during droughts. Rain water collected in cisterns from roofs and catchments yield about 50 gpd per 1,000 square feet of catch area during an average year of rainfall. This is the main method of Water supply for domestic use on the Island; it will probably be continued even if a public distribution system is made available, because of the limited quantity of other natural water.

Open-File Report↗
USGS1978

Phosphorus in hydrothermal waters of Yellowstone National Park, Wyoming

Ninety-seven hot-spring and geyser samples (field acidified to pH<1.4 with HCl or HNO 3 ) from Yellowstone National Park, Wyo., were analyzed for PO 4 -P using reduced molybdenum-blue and the selective arsenate reducing agent, metabisulfite-thiosulfate. The PO 4 -P concentrations ranged from below detection limit (~1-73 micrograms per liter). Twenty-five springs had PO 4 -P concentrations exceeding 6.8 &mu; g/L; seven spring samples exceeded 20 &mu;g/L. Elevated PO 4 -P contents were invariably associated with mixed springs, as evidenced by diluted chloride concentrations and, commonly, subboiling temperatures, low pH's, and elevated calcium concentrations. Alkaline high-chloride (>400 milligrams per liter) hydrothermal waters from Upper and Norris Geyser Basins had PO 4 -P concentrations below 2 &mu;g/L and represent the low end of the range of PO 4 -P contents in natural waters.

Wyoming↗
USGS2014

Acute toxicity of sodium bicarbonate, a major component of coal bed natural gas produced waters, to 13 aquatic species as defined in the laboratory

Water produced during coal bed natural gas (CBNG) extraction in the Powder River Structural Basin of Wyoming and Montana (USA) may contain concentrations of sodium bicarbonate (NaHCO 3 ) of more than 3000 mg/L. The authors evaluated the acute toxicity of NaHCO 3 , also expressed as bicarbonate (HCO 3 − ), to 13 aquatic organisms. Of the 13 species tested, 7 had a median lethal concentration (LC50) less than 2000 mg/L NaHCO 3 , or 1300 mg/L HCO 3 − . The most sensitive species were Ceriodaphnia dubia, freshwater mussels (Lampsilis siliquoidea), pallid sturgeon (Scaphirhynchus albus), and shovelnose sturgeon (Scaphirhynchus platorynchus). The respective LC50s were 989 mg/L, 1120 mg/L, 1249 mg/L, and 1430 mg/L NaHCO 3 , or 699 mg/L, 844 mg/L, 831 mg/L, and 1038 mg/L HCO 3 − . Age affected the sensitivity of fathead minnows, even within life stage. Two days posthatch, fathead minnows were more sensitive to NaHCO 3 and HCO 3 − compared with 4-d-old fish, even though fish up to 14 d old are commonly used for toxicity evaluations. The authors recommend that ion toxicity exposures be conducted with organisms less than 24 h posthatch to ensure that experiments document the most sensitive stage of development. The results of the present study, along with historical and current research regarding the toxicity of bicarbonate, may be useful to establish regulatory standards for HCO 3 − .

Environmental Toxicology and Chemistry↗
USGS1992

Brine history indicated by argon, krypton, chlorine, bromine, and iodine analyses of fluid inclusions from the Mississippi Valley type lead-fluorite-barite deposits at Hansonburg, New Mexico

Argon, krypton, chlorine, bromine, and iodine were measured in a homogeneous population of high-salinity hydrothermal fluid inclusions from the Tertiary-age Mississippi Valley-type (MVT) lead-fluorite-barite deposits at Hansonburg, New Mexico to establish new types of evidence for the history of both the fluid and the major dissolved salts. Noble gases and halogens in fluid inclusions containing 10 −10 –10 −9 L of brine ( Cl= 3 molal) were analyzed by laser microprobe noble-gas mass spectrometry ( lmngms ) on neutron-irradiated samples. The concentrations of 36 Ar ( 4.7 × 10 −8 molal) and 84 Kr 1.8 × 10 −9 molal) in the fluid inclusions are equal to those of fresh surface waters in equilibrium with air at approximately 20 ± 5 °. The mole ratios of Br/Cl ( 1.2 × 10 −4 ) and I/Cl ( 1–2 × 10 −6 ) are among the lowest measured in any natural waters, similar to those of modern brines formed by dissolution of Permian NaCl-bearing evaporites in southeast New Mexico. 40 Ar/ 36 Ar ratios (600) are twice that of air, and indicate that the fluid inclusions had excess radiogenic 40 Ar ( 1.4 × 10 −5 molal) when trapped. The amount of excess 40 Ar appears to be too large to have been acquired with Cl by congruent dissolution of halite-bearing evaporites, and possibly too small to have been acquired with Pb by congruent dissolution of granitic basement rocks with Proterozoic K Ar ages. From the lmngms data, combined with published Pb and S isotope data, we infer the following sequence of events in the history of the Hansonburg MVT hydrothermal brine: (1) the brine originated as relatively dilute meteoric water, and it did not gain or lose atmospheric Ar or Kr after recharge; (2) the originally dilute fluid acquired the bulk of its Cl and sulfate in the subsurface after recharge by dissolving halite-bearing Permian? marine evaporites; (3) the high salinity brine then acquired most of its Pb and excess radiogenic 40 Ar from interactions with aquifer rocks other than evaporites, possibly clastic sedimentary rocks or basement rocks with Phanerozoic K Ar “ages”; and (4) the brine deposited fluorite without having boiled or degassed.

Earth and Planetary Science Letters↗
USGS1996

Theoretical considerations and a simple method for measuring alkalinity and acidity in low-pH waters by gran titration

Titrations for alkalinity and acidity using the technique described by Gran (1952, Determination of the equivalence point in potentiometric titrations, Part II: The Analyst, v. 77, p. 661-671) have been employed in the analysis of low-pH natural waters. This report includes a synopsis of the theory and calculations associated with Gran's technique and presents a simple and inexpensive method for performing alkalinity and acidity determinations. However, potential sources of error introduced by the chemical character of some waters may limit the utility of Gran's technique. Therefore, the cost- and time-efficient method for performing alkalinity and acidity determinations described in this report is useful for exploring the suitability of Gran's technique in studies of water chemistry.

Water-Resources Investigations Report↗
USGS2013

Raman spectroscopy of efflorescent sulfate salts from Iron Mountain Mine Superfund Site, California

The Iron Mountain Mine Superfund Site near Redding, California, is a massive sulfide ore deposit that was mined for iron, silver, gold, copper, zinc, and pyrite intermittently for nearly 100 years. As a result, both water and air reached the sulfide deposits deep within the mountain, producing acid mine drainage consisting of sulfuric acid and heavy metals from the ore. Particularly, the drainage water from the Richmond Mine at Iron Mountain is among the most acidic waters naturally found on Earth. The mineralogy at Iron Mountain can serve as a proxy for understanding sulfate formation on Mars. Selected sulfate efflorescent salts from Iron Mountain, formed from extremely acidic waters via drainage from sulfide mining, have been characterized by means of Raman spectroscopy. Gypsum, ferricopiapite, copiapite, melanterite, coquimbite, and voltaite are found within the samples. This work has implications for Mars mineralogical and geochemical investigations as well as for terrestrial environmental investigations related to acid mine drainage contamination.

California↗
USGS1981

High-performance, liquid-chromatographic method for the analysis of polynuclear aromatic hydrocarbons in water

High-performance liquid chromatography provides a rapid and sensitive means for determining polynuclear aromatic hydrocarbons in water samples. A high-performance liquid chromatograph, coupled with ultraviolet or fluorescence detectors has greater selectivity for analysis than methods using gas-chromatographic and flame-ionization systems. Several natural water samples were fortified with mixtures of polynuclear aromatic hydrocarbons containing naphthalene, acenaphthene, fluorene, phenanthrene, anthracene, fluoranthrene, pyrene, chrysene, 1,2-benzanthracene, benzo(a)pyrene, 1,2:5,6-dibenzanthracene, and benzo(g,h,i)perylene. Resulting solutions, with concentrations of individual polynuclear aromatic hydrocarbons ranging from 0.05 to 11.0 micrograms per liter, were analyzed by high-performance liquid chromatography to investigate limits of method applicability and to acquire necessary precision data. The polynuclear aromatic hydrocarbons considered in this study were detected in the micrograms per liter range and were found to have a total chromatographic elution time of approximately 35 minutes. Successive determinations of standard mixtures, followed by statistical analysis of the data, showed an average mean recovery of 83.1 percent, an average standard deviation of ± 0.130 microgram per liter, and an average relative standard deviation of 7.45 percent.

Water-Resources Investigations Report↗
USGS2013

Evaluation of internal loading and water level changes: implications for phosphorus, algal production, and nuisance blooms in Kabetogama Lake, Voyageurs National Park, Minnesota

Hydrologic manipulations have the potential to exacerbate or remediate eutrophication in productive reservoirs. Dam operations at Kabetogama Lake, Minnesota, were modified in 2000 to restore a more natural water regime and improve water quality. The US Geological Survey and National Park Service evaluated nutrient, algae, and nuisance bloom data in relation to changes in Kabetogama Lake water levels. Comparison of the results of this study to previous studies indicates that chlorophyll a concentrations have decreased, whereas total phosphorus (TP) concentrations have not changed significantly since 2000. Water and sediment quality data were collected at Voyageurs National Park during 2008–2009 to assess internal phosphorus loading and determine whether loading is a factor affecting TP concentrations and algal productivity. Kabetogama Lake often was mixed vertically, except for occasional stratification measured in certain areas, including Lost Bay in the northeastern part of Kabetogama Lake. Stratification, higher bottom water and sediment nutrient concentrations than in other parts of the lake, and phosphorus release rates estimated from sediment core incubations indicated that Lost Bay is one of several areas that may be contributing to internal loading. Internal loading of TP is a concern because increased TP may cause excessive algal growth including potentially toxic cyanobacteria.

Minnesota↗
USGS2007

Ultraviolet radiation and bio-optics in Crater Lake, Oregon

Crater Lake, Oregon, is a mid-latitude caldera lake famous for its depth (594 m) and blue color. Recent underwater spectral measurements of solar radiation (300-800 nm) support earlier observations of unusual transparency and extend these to UV-B wavelengths. New data suggest that penetration of solar UVR into Crater Lake has a significant ecological impact. Evidence includes a correlation between water column chlorophyll-a and stratospheric ozone since 1984, the scarcity of organisms in the upper water column, and apparent UV screening pigments in phytoplankton that vary with depth. The lowest UV-B diffuse attenuation coefficients (K d,320) were similar to those reported for the clearest natural waters elsewhere, and were lower than estimates for pure water published in 1981. Optical proxies for UVR attenuation were correlated with chlorophyll-a concentration (0-30 m) during typical dry summer months from 1984 to 2002. Using all proxies and measurements of UV transparency, decadal and longer cycles were apparent but no long-term trend since the first optical measurement in 1896. ?? 2007 Springer Science+Business Media B.V.

Hydrobiologia↗