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At least 127 records · Page 7Linked to original sources

Physical and chemical characteristics of Terrace Reservoir, Conejos County, Colorado, May 1994 through May 1995

Terrace Reservoir receives drainage of low-pH, metal-enriched water from mineralized areas, including the Summitville Mine, within the Alamosa River Basin. Drainage from the Summitville Mine has contributed a substantial part of the metal load to Terrace Reservoir. From May 1994 through May 1995, a study was done by the U.S. Geological Survey, in cooperation with the U.S. Environmental Protection Agency, to evaluate the physical and chemical characteristics of Terrace Reservoir. Terrace Reservoir was thermally stratified from about mid-May through August 1994. Thermal stratification was absent from September\x111994through March 1995. During periods of stratification, underflow of the Alamosa River was predominant, and residence times of the underflow were shortened by 40 to 75\x11percent of the theoretical residence times for a well-mixed reservoir. Transport and deposition of suspended solids in Terrace Reservoir varied spatially and temporally. Most of the suspended solids were deposited in Terrace Reservoir. The concentration of dissolved oxygen in the reservoir varied little spatially or temporally and generally was within a few tenths of the dissolved-oxygen concentration of the inflow. The pH of water in the reservoir generally ranged from about 4.0 to about 7.0, depending on date, depth, and location. The largest pH values were measured during May. A markeddecrease of about 1.5\x11pH units occurred at site T5 in the reservoir about mid-June. The pH of the reservoir remained at or below 5.5 from mid-June through November. Dissolved-metal concentrations varied spatially and temporally in response to several factors, which included inflow characteristics, reservoir stratification and mixing, inflow-routing and flow-through patterns, residence times, sedimentation, dissolved oxygen, and pH.Inflow chemistry is the dominant controlling factor of metal chemistry within Terrace Reservoir.During periods of stratification, large vertical variations in metal concentrations occurred. The highest metal concentrations in the reservoir generally were measured in the hypolimnion between June and August. During June, epilimnetic water of the reservoir had pH values greater than 6.0, and metal concentrations were lower than hypolimnetic concentrations. In the hypolimnion, pH values were less than 5.5. The difference between the chemistry of the epilimnion and the hypolimnion was due to differences in flow routing and residence times of water in those respective layers. The dissolved-metal concentrations were larger during July and August than during June.During September, small vertical variations in metalconcentrations occurred, and the dissolved-metal concentrations were nearly equivalent to the average August metal concentrations, indicatingthat the metal concentrations measured during September resulted largely from reservoir mixing.During March, the largest metal concentrationsoccurred in the epilimnion, where pH was about 5.5; in the hypolimnion, where the pH was about 6.0, dissolved-metal concentrations were substantially lower and reflected inflow concentrations.

Colorado↗

Physical and chemical characteristics of Terrace Reservoir, Conejos County, Colorado, May 1994 through May 1995; interim report

Terrace Reservoir receives drainage of low-pH, metal-enriched water from mineralized areas, including the Summitville Mine, within the Alamosa River Basin. Drainage from the Summitville Mine has contributed a substantial part of the metal load to Terrace Reservoir. From May 1994 through May 1995, a study was done by the U.S. Geological Survey, in cooperation with the U.S. Environmental Protection Agency, to evaluate the physical and chemical characteristics of Terrace Reservoir. Terrace Reservoir was thermally stratified from about mid-May through August 1994. Thermal stratification was absent from September\x111994through March 1995. During periods of stratification, underflow of the Alamosa River was predominant, and residence times of the underflow were shortened by 40 to 75\x11percent of the theoretical residence times for a well-mixed reservoir. Transport and deposition of suspended solids in Terrace Reservoir varied spatially and temporally. Most of the suspended solids were deposited in Terrace Reservoir. The concentration of dissolved oxygen in the reservoir varied little spatially or temporally and generally was within a few tenths of the dissolved-oxygen concentration of the inflow. The pH of water in the reservoir generally ranged from about 4.0 to about 7.0, depending on date, depth, and location. The largest pH values were measured during May. A markeddecrease of about 1.5\x11pH units occurred at site T5 in the reservoir about mid-June. The pH of the reservoir remained at or below 5.5 from mid-June through November. Dissolved-metal concentrations varied spatially and temporally in response to several factors, which included inflow characteristics, reservoir stratification and mixing, inflow-routing and flow-through patterns, residence times, sedimentation, dissolved oxygen, and pH. Inflow chemistry is the dominant controlling factor of metal chemistry within Terrace Reservoir. During periods of stratification, large vertical variations in metal concentrations occurred. The highest metal concentrations in the reservoir generally were measured in the hypolimnion between June and August. During June, epilimnetic water of the reservoir had pH values greater than 6.0, and metal concentrations were lower than hypolimnetic concentrations. In the hypolimnion, pH values were less than 5.5. The difference between the chemistry of the epilimnion and the hypolimnion was due to differences in flow routing and residence times of water in those respective layers. The dissolved-metal concentrations were larger during July and August than during June. During September, small vertical variations in metal concentrations occurred, and the dissolved-metal concentrations were nearly equivalent to the average August metal concentrations, indicatingthat the metal concentrations measured during September resulted largely from reservoir mixing.During March, the largest metal concentrationsoccurred in the epilimnion, where pH was about 5.5; in the hypolimnion, where the pH was about 6.0, dissolved-metal concentrations were substantially lower and reflected inflow concentrations.

Colorado↗

Great Salt Lake, Utah: Chemical and physical variations of the brine, 1963-1966

Great Salt Lake is a shallow, closed-basin lake in northern Utah. Its surface area and concentration of dissolved solids vary in response to both annual and long-term climatic changes. The lake gains water mainly as streamflow from mountains to the east and loses water through evaporation. In 1965, at a lake-surface altitude of 4,194 feet, the surface area was about 1,000 square miles, and the maximum measured depth was 27 feet. Studies to define the variations in chemical and physical characteristics of the brine began in 1963, and detailed sampling of the lake at 29 sites was made in October 1965 and May 1966. Data resulting from concurrent sampling of the 29 sites indicated that four types of brine coexist in the lake.

Utah↗

Efficiency of a stormwater detention pond in reducing loads of chemical and physical constituents in urban streamflow, Pinellas County, Florida

A multipurpose wet stormwater detention pond in Pinellas Park, Florida was studied to determine its effectiveness in reducing the load of selected water-quality constituents commonly found in urban streamflow. Water-quality samples, and data on streamflow and precipitation were collected at the outflow and principal inflow of detention area 3 on Saint Joe Creek. To compare the constituent loads entering and leaving the detention pond, flows and water quality were monitored simultaneously at the inflow and outflow sites for six storms, and were monitored intermittently during periods of base flow. Lodas od 19 selected chemical and physical constituents were determined. Because all the stormwater entering the detention pond was not measured at the inflow site, computed stormwater inflow loads were adjusted to account for loads from the unmonitored areas. The ratio of storm- water volume measured at the outflow site to stormwater volume measured at the inflow site was used to adjust inflow loads for individual storms. Pond efficiencies for selected water- quality constituents for each of the storms were estimated by dividing the difference in outflow and adjusted inflow loads by the adjusted inflow load. Stormwater loads of the major ions (chloride, calcium and bicarbonate) and dissolved solids at the outflow site exceeded loads at the inflow site, partly as a result of mixing with base flow stored within the pond. However, the detention pond was effective in reducing the stormwater load of such urban-runoff contaminants as metals, nutrients, suspended solids, and biochemical and chemical oxygen demand. Estimated median pond efficiencies for reducing constituent loads ranged from 25 to more than 60 percent for metals, 2 to 52 percent for nutrients, 2 to 52 percent for nutrients, 7 to 11 percent for two measurements of suspended solids, and 16 to 49 percent for the oxygen- consuming substances. The reductions of constituent loads in stormwater are probably a result of dilution with pond water (particularly for smaller storms), adsorption, chemical precipitation, settling, biologic uptake, and oxidation. The establishment of aquatic vegetation midway through the study appears to have increased the efficiency of the pond in reducing loads of urban-runoff contaminants in stormwater. The efficiency of the detention pond in reducing base-flow loads was estimated by comparing base-flow loads at the out- flow site prior to and after construction of the pond. Loads of major ions and dissolved solids in base flow were reduced at median efficiencies ranging from 17 to 35 percent. Urban-runoff con- taminants in base flow were generally reduced at higher efficiencies. Median efficiencies ranged from 38 to 82 percent for metals, 19 to 83 percent for nutrients, 34 to 45 percent for suspended solids, and 43 to 65 for the oxygen-consuming substances. The reductions in loads in base flow are probably a result of adsorption, chemical precipitation, biologic uptake, and settling within the pond. These processes were more effective in reducing base-flow loads after the establishment of aquatic vegetation in the pond.

Water-Resources Investigations Report↗

Physical and Chemical Water-Quality Data from Automatic Profiling Systems, Boulder Basin, Lake Mead, Arizona and Nevada, Water Years 2001-04

Water-quality profile data were collected in Las Vegas Bay and near Sentinel Island in Lake Mead, Arizona and Nevada, from October 2000 to September 2004. The majority of the profiles were completed with automatic variable-buoyancy systems equipped with multiparameter water-quality sondes. Profile data near Sentinel Island were collected in August 2004 with an automatic variable-depth-winch system also equipped with a multiparameter water-quality sonde. Physical and chemical water properties collected and recorded by the profiling systems, including depth, water temperature, specific conductance, pH, dissolved-oxygen concentration, and turbidity are listed in tables and selected water-quality profile data are shown in graphs.

Open-File Report↗

Fish communities and their relation to physical and chemical characteristics of streams from selected environmental settings in the Lower Susquehanna River basin, 1993-95

Studies of fish-community composition were conducted annually in selected reaches (from 100 to 303 meters in length) on seven streams from June 1993 to June 1995 within the Lower Susquehanna River Basin. In 1994, additional reaches were selected on three of the streams, resulting in a total of 28 samples. The study reaches were selected on the basis of type of bedrock and land use/land cover; the major emphasis was on agricultural land use or areas in transition from agricultural to commercial, industrial, and residential land uses. At each reach, environmental characteristics consisting of instream and riparian habitat conditions, hydrology, and water quality were determined. The relation of fish communities at these reaches to physical and chemical characteristics of streams was analyzed to determine if the fish communities differed temporally or spatially. Data were analyzed by parametric and multivariate techniques. During the course of the study, a total of 33,143 fish were collected, consisting of 39 species representing 8 families. Cyprinidae (minnows) were dominant with 17 species, followed by Centrarchidae (sunfishes) with 7 species and Percidae (perches and darters) with 4 species. Three species?blacknose dace ( Rhinichthys atratulus ), white sucker ( Catostomus commersoni ), and the sculpins ( Cottus spp)?accounted for 49 percent of the total fish collected. The environmental variables most closely related to the fish communities present at the reaches were mean channel width, mean water temperature, mean canopy angle, and suspended-sediment concentrations. These variables accounted for about 79 percent of the variation in the environmental-species relation. Channel width and mean water temperature are correlated with stream size variables. The stream size gradient is the most influential variable to the fish communities studied in the Lower Susquehanna River Basin.

Water-Resources Investigations Report↗

Physical and chemical characteristics of water in coal-mine ponds, eastern Oklahoma, June to November 1977-81

Water at 102 sites in 59 coal-mine ponds in eastern Oklahoma was sampled at lease twice during June to November 1977-81 to determine temperature, specific conductance, dissolved oxygen, pH, and dissolved sulfate, chloride, iron, and manganese--as part of a study of the hydrology of the Oklahoma coalfield. These determinations show that during June to October water in ponds deeper than ~10 ft was stratified; ponds which had little or not change of temperature with depth generally were shallow or were sampled in early November. Temperature, dissolved oxygen, and pH usually decreased with depth, whereas specific conductance usually increased with depth. Concentrations of dissolved sulfate, chloride, iron, and manganese varied from site to site. Specific conductance, which is a measure of dissolved solids in the water, ranged from 93 to 4,800 mmho/cm at 25oC. Some physical and chemical characteristics of the mine-pond water are related to the coal bed adjacent to the pond. Mean specific-conductance values and dissolved-sulfate concentrations were greatest in ponds associated with mining of Dawson, Weir-Pittsburg, and Secor coals. Mean dissolved-iron concentrations were greatest in ponds associated with mining of the Dawson, Secor, and Hartshorne coals. Mean dissolved-manganese concentrations were greatest in ponds associated with mining of the Dawson, Weir-Pittsburg, and Secor coals, but greatly exceeded secondary drinking-water limits regardless of coal bed mined.

Oklahoma↗

Use of a single-bowl continuous-flow centrifuge for dewatering suspended sediments: effect on sediment physical and chemical characteristics

The use of a single-bowl continuous-flow centrifuge (CFC, Sharples-Pennwalt Model AS-12) for dewatering suspended sediment from large volumes of river water is evaluated. Sediment-recovery efficiency of 86-91 per cent is comparable to that of other types of CFC units. The recovery efficiency is limited by the particle-size distribution of the feed water and by the limiting particle diameter that is retained in the centrifuge bowl. The limiting particle diameter, using the parameters for this study (bowl radius = 10.5cm; bowl length = 71.1 cm; rotational velocity = 16000 r min −1 ; flow rate = 2 L min −1 , and an assumed hydrated particle density = 1.7 gm cm −3 ), is 370 nm. There seems to be no particle-size fractionation within the centrifuge bowl—the median particle size was the same at the top as at the bottom. Particle electrophoretic mobility plays some role in fractionation of particles within the centrifuge. The mobility ranged from −1.19 to −2.01 × 10 −8 m 2 V −1 s −1 , which is typical of clays coated with organic matter, the charge of which is partially neutralized by divalent cations and iron. Contamination by trace metals and organics is minimized by coating all surfaces that come in contact with the sample with either FEP or PFA Teflon and using a removable FEP Teflon liner in the centrifuge bowl. Because of the physical and chemical factors affecting particle fractionation within the centrifuge, care must be exercised in interpreting the environmental consequences of particles collected by continuous-flow centrifugation.

Hydrological Processes↗

Physical and chemical characteristics of Knowles, Forgotten, and Moqui Canyons, and effects of recreational use on water quality, Lake Powell, Arizona and Utah

Side canyons of Lake Powell are the most popular recreation areas of the Glen Canyon National Recreation Area in Arizona and Utah. There are more than 90 side canyons that are tributaries to the main lake body of Lake Powell. Near Bullfrog and Halls Crossing marinas in Utah, visitors frequent Knowles, Forgotten, and Moqui Canyons to fish, boat, camp, and hike the sandstone formations for which Lake Powell is famous. Areas of recreational activity are greatest near beaches in side canyons. Emissions from houseboats, personal watercraft, speedboats, and from some nonboating recreational activities introduce contaminants to the lake and to beach areas. The U.S. Geological Survey documented concentrations of trace elements, volatile organic compounds, organic wastewater contaminants, and other byproducts of fuel-based contaminants in water and bed material in Knowles, Forgotten, and Moqui Canyons during the summers of 2001 and 2002. Field work was conducted during four trips when recreational use was at a minimum (before Memorial Day in May) and when it was at a maximum (near Labor Day in September). Knowles Canyon was treated as a control; therefore, public access by motorcraft was not permitted during the study. Electric-powered or oar-powered research boats were used to collect samples and measure properties in Knowles Canyon. Record-low reservoir elevations during 2000-2002 limited the availability of camping and day-use beaches in Forgotten and Moqui Canyons. Although more beach areas were exposed during this period, the steep slopes of the beaches made it difficult to use the beaches for camping purposes. Side canyon waters of Knowles, Forgotten, and Moqui Canyons were similarly stratified (physically and chemically) during the study from natural advective and convective reservoir processes. Metalimnetic oxygen minimas were observed in September 2001 and 2002 in the side canyons and the main body of Lake Powell. Chemical concentrations of several organic constituents were elevated in Forgotten and Moqui Canyons during the high-use period in September of 2001 and 2002 compared with concentrations during the low-use period in May of 2001 and 2002. Concentrations of some constituents decreased from the mouth of each canyon to the canyon's headwaters, indicating that there could be a mechanism for constituent removal or that the main body of Lake Powell is not in equilibrium with the headwaters of the side canyons. Concentrations of volatile organic compounds, such as benzene, toluene, ethylbenzene, and xylene (BTEX compounds), were highest in the upper reaches of Forgotten and Moqui Canyons where visitor use was greatest. Trace amounts of some organic wastewater compounds, including cholesterol, N,N-diethyl-meta-toluamide (DEET), and ethylenediaminetetraacetic acid (EDTA), were measured in Forgotten and Moqui Canyons. Except for minor concentrations of some volatile organic compounds and cholesterol, contamination from visitor use in Knowles Canyon was not detected, most likely because the canyon was closed to access. Concentrations of some organic compounds in bed material sampled in the side canyons near popular beach areas, including polyaromatic hydrocarbons, were above the laboratory detection limits. Several other constituents were present in trace amounts. Benzyl n-butylphthalate and bis (2 ethyl)-phthalate were detected at concentrations above laboratory detection limits. Numerous trace elements were detected above laboratory detection limits in Knowles, Forgotten, and Moqui Canyons. All water samples from the side canyon transects had low colony counts of Escherichia coli (E. coli); the highest count was less than one-fourth of the U.S. Environmental Protection Agency recommended limit for recreational water. Four water samples collected near beaches in Moqui Canyon had E. coli colony counts that exceeded the U.S. Environmental Protection Agency recommended limit.

Arizona, Utah↗

Variation in the terrestrial isotopic composition and atomic weight of argon

The isotopic composition and atomic weight of argon (Ar) are variable in terrestrial materials. Those variations are a source of uncertainty in the assignment of standard properties for Ar, but they provide useful information in many areas of science. Variations in the stable isotopic composition and atomic weight of Ar are caused by several different processes, including (1) isotope production from other elements by radioactive decay (radiogenic isotopes) or other nuclear transformations (e.g., nucleogenic isotopes), and (2) isotopic fractionation by physical-chemical processes such as diffusion or phase equilibria. Physical-chemical processes cause correlated mass-dependent variations in the Ar isotope-amount ratios ( 40 Ar/ 36 Ar, 38 Ar/ 36 Ar), whereas nuclear transformation processes cause non-mass-dependent variations. While atmospheric Ar can serve as an abundant and homogeneous isotopic reference, deviations from the atmospheric isotopic ratios in other Ar occurrences limit the precision with which a standard atomic weight can be given for Ar. Published data indicate variation of Ar atomic weights in normal terrestrial materials between about 39.7931 and 39.9624. The upper bound of this interval is given by the atomic mass of 40 Ar, as some samples contain almost pure radiogenic 40 Ar. The lower bound is derived from analyses of pitchblende (uranium mineral) containing large amounts of nucleogenic 36 Ar and 38 Ar. Within this interval, measurements of different isotope ratios ( 40 Ar/ 36 Ar or 38 Ar/ 36 Ar) at various levels of precision are widely used for studies in geochronology, water–rock interaction, atmospheric evolution, and other fields.

Pure and Applied Chemistry↗

Surface-water-quality assessment of the Yakima River basin, Washington: Overview of major findings, 1987-91

Surface-water-quality conditions were assessed in the Yakima River Basin, which drains 6,155 square miles of mostly forested, range, and agricultural land in Washington. The Yakima River Basin is one of the most intensively farmed and irrigated areas in the United States, and is often referred to as the “Nation’s Fruitbowl.” Natural and anthropogenic sources of contaminants and flow regulation control water-quality conditions throughout the basin. This report summarizes the spatial and temporal distribution, sources, and implications of the dissolved oxygen, water temperature, pH, suspended sediment, nutrient, organic compound (pesticide), trace element, fecal indicator bacteria, radionuclide, and aquatic ecology data collected during the 1987–91 water years. The Yakima River descends from a water surface altitude of 2,449 feet at the foot of Keechelus Dam to 340 feet at its mouth downstream from Horn Rapids Dam near Richland. The basin can be divided into three distinct river reaches on the basis of its physical characteristics. The upper reach, which drains the Kittitas Valley, has a high gradient, with an average streambed slope of 14 feet per mile (ft/mi) over the 74 miles from the foot of Keechelus Dam (river mile [RM] 214.5) to just upstream from Umtanum. The middle reach, which drains the Mid Valley, extends a distance of 33 miles from Umtanum (RM 140.4) to just upstream from Union Gap and also has a high gradient, with an average streambed slope of 11 ft/mi. The lower reach of the Yakima River drains the Lower Valley and has an average streambed slope of 7 ft/mi over the 107 miles from Union Gap (RM 107.2) to the mouth of the Yakima River. These reaches exhibited differences in water-quality conditions related to the differences in geologic sources of contaminants and land use. Compared with the rest of the basin, the Kittitas Valley and headwaters of the Naches River Subbasin had relatively low concentrations and loads of suspended sediment, nutrients, organic compounds, and fecal indicator bacteria. There were very few failures to meet the Washington State dissolved oxygen standard or exceedances of the water temperature and pH standards in this reach. In general, these areas are considered to be areas of lessdegraded water quality in the basin. The preTertiary metamorphic and intrusive rocks of the Cle Elum and Teanaway River Subbasins, however, were found to be significant geologic sources of antimony, arsenic, chromium, copper, mercury, nickel, selenium, and zinc. As a result, the arsenic, chromium, and nickel concentrations measured in the streambed sediment of the Kittitas Valley were 13 to 74 times higher than those measured in the Lower Valley. The Mid and Lower Valleys had similar water-quality conditions, governed by the intensive agricultural and irrigation activities, highly erosive landscapes, and flow regulation. Most of the failures to meet the Washington State standards for dissolved oxygen and exceedances of the standards for water temperature and pH occurred in the Mid and Lower Valleys. Agricultural drains in the Mid and Lower Valleys were found to be significant sources of nutrients, suspended sediment, pesticides, and fecal indicator bacteria. Downstream from the irrigation diversions near Union Gap, summertime streamflow in the Yakima River was drastically reduced to only a few hundred cubic feet per second. In the lower Yakima River, agricultural return flow typically accounts for as much as 80 percent of the main stem summertime flow near the downstream terminus of the basin. Therefore, the water-quality characteristics of the lower Yakima River resemble those of the agricultural drains. The highest fecal bacteria concentrations (35,000 colonies of Escherichia coli per 100 milliliters of water) were measured in the Granger/Sunnyside area, the location of most of the livestock in the basin. The east side area of the Lower Valley (area east of the Yakima River) was the predominant source area for suspended sediment and pesticides in the basin. This area had the largest acreage of irrigated land and generally received the largest application of pesticides. Owing to the highly erosive soils of the area, the suspended sediment load from the east side in June 1989 (320 kilograms per day) was five or more times larger than from any other area, and the loads of several of the more hydrophobic organic compounds were four or more times larger. An ecological assessment of the Yakima River Basin ranked physical, chemical, and biological conditions at impaired (degraded) sites against reference sites in an effort to understand how land use changes physical and chemical site characteristics and how biota respond to these changes. For this assessment, the basin was divided into four natural ecological categories: (1) Cascades ecoregion, (2) Eastern Cascades Slopes and Foothills ecoregion, (3) Columbia Basin ecoregion, and (4) large rivers. Each of these categories has a unique combination of climate and landscape features that produces a distinctive terrestrial vegetation assemblage. In the combined Cascades and Eastern Cascades site group, which had the fewest impaired sites, the metals index was the only physical and chemical index that indicated any impairment. The moderate levels of impairment noted in the invertebrate and algal communities were not, however, associated with metals, and may have been related to the effects of logging, although the intensity of logging was not directly quantified in this study. Sites in the Columbia Basin site group were all moderately or severely impaired with the exception of the two reference sites (Umtanum Creek and Satus Creek below Dry Creek), which showed no physical, chemical, or biological impairment. Three sites were heavily affected by agriculture (Granger Drain, Moxee Drain, and Spring Creek) and were listed as severely impaired by most of the physical, chemical, and biological condition indices. Agriculture was the primary cause of the impairment of biological communities in this site group. The primary physical and chemical indicators of agricultural effects were nutrients, pesticides, dissolved solids, and substrate embeddedness, which all tended to increase with agricultural intensity. The biological effects of agriculture were manifested by a decrease in the abundance and number of native species of fish and invertebrates, a shift in algal communities to species indicative of eutrophic conditions, and higher abundances. There was also an increase in the abundance and number of nonnative fish species due to the prevalence of fish that are largely tolerant of nutrient-rich conditions. Main stem (large river) sites downstream from the city of Yakima exhibited severe impairment of fish communities associated with high levels of pesticides in fish tissues and the presence of external anomalies on fish.

Washington↗

Physical and chemical data on sediments deposited in the Missouri and the Mississippi River flood plains during the July through August 1993 flood

In July and August 1993, Missouri and Mississippi River floodwaters overtopped or breached levees and inundated agricultural and urban areas in the flood plains. To assess the regional variability of quality of silt and clay sediments transported and deposited during inundation, sediment samples were collected in September 1993 at 25 sites in the Missouri and the Mississippi River flood plains. The samples were analyzed for physical properties and chemical constituents that included particle-size distribution, water content, volatile solids, nutrients, carbon, selected trace elements, pesticides, and semi volatile organic compounds for post flood sediment samples, and particle-size distribution for preflood soil samples. Pesticides were detected in samples from many of the sites, with alachlor detected in one sample at a concentration of 54 micrograms per kilogram. Many semi volatile organic compounds were detected in samples at several sites, with the concentration of fluoranthene in one sample at 270 milligrams per kilogram. Procedures for selecting sites, techniques developed for sampling, laboratory analytical methods, and quality-assurance sampling methods also are described.

Illinois, Iowa, Missouri↗

Simulating adsorption of U(VI) under transient groundwater flow and hydrochemistry: Physical versus chemical nonequilibrium model

Coupled intragrain diffusional mass transfer and nonlinear surface complexation processes play an important role in the transport behavior of U(VI) in contaminated aquifers. Two alternative model approaches for simulating these coupled processes were analyzed and compared: (1) the physical nonequilibrium approach that explicitly accounts for aqueous speciation and instantaneous surface complexation reactions in the intragrain regions and approximates the diffusive mass exchange between the immobile intragrain pore water and the advective pore water as multirate first-order mass transfer and (2) the chemical nonequilibrium approach that approximates the diffusion-limited intragrain surface complexation reactions by a set of multiple first-order surface complexation reaction kinetics, thereby eliminating the explicit treatment of aqueous speciation in the intragrain pore water. A model comparison has been carried out for column and field scale scenarios, representing the highly transient hydrological and geochemical conditions in the U(VI)-contaminated aquifer at the Hanford 300A site, Washington, USA. It was found that the response of U(VI) mass transfer behavior to hydrogeochemically induced changes in U(VI) adsorption strength was more pronounced in the physical than in the chemical nonequilibrium model. The magnitude of the differences in model behavior depended particularly on the degree of disequilibrium between the advective and immobile phase U(VI) concentrations. While a clear difference in U(VI) transport behavior between the two models was noticeable for the column-scale scenarios, only minor differences were found for the Hanford 300A field scale scenarios, where the model-generated disequilibrium conditions were less pronounced as a result of frequent groundwater flow reversals.

Water Resources Research↗

Bed-Sediment Sampling and Analysis for Physical and Chemical Properties of the Lower Mississippi River near Memphis, Tennessee

In February 2010, the U.S. Geological Survey, in cooperation with the U.S. Army Corps of Engineers, Memphis District, investigated the presence of inorganic elements and organic compounds in bed sediments of the lower Mississippi River. Selected sites were located in the navigation channel near river miles 737, 773, and 790 near Memphis, Tennessee. Bed-sediment samples were collected using a Shipek grab sampler mounted to a boom crane with a motorized winch. Samples then were processed and shipped to the U.S. Geological Survey Sediment Laboratory in Rolla, Missouri, the USGS National Water Quality Laboratory in Denver, Colorado, and to TestAmerica Laboratory, Inc. in West Sacramento, California. Samples were analyzed for grain size, inorganic elements (including mercury), and organic compounds. Chemical results were tabulated and listed with sediment-quality guidelines and presented with the physical property results. All of the bed material samples collected during this investigation yielded concentrations that were less than the Consensus-Based Probable Effect Concentration guidelines. The physical properties were tabulated and listed using a standard U.S. Geological Survey scale of sizes by class for sediment analysis. All of the samples collected during this investigation indicated a percent composition mostly comprised of sand, ranging from less than 0.125 millimeters to less than 2 millimeters.

Open-File Report↗

Thermal state and complex geology of a heterogeneous salty crust of Jupiter's satellite, Europa

The complex geology of Europa is evidenced by many tectonic and cryomagmatic resurfacing structures, some of which are "painted" into a more visible expression by exogenic alteration processes acting on the principal endogenic cryopetrology. The surface materials emplaced and affected by this activity are mainly composed of water ice in some areas, but in other places there are other minerals involved. Non-ice minerals are visually recognized by their low albedo and reddish color either when first emplaced or, more likely, after alteration by Europan weathering processes, especially sublimation and alteration by ionizing radiation. While red chromophoric material could be due to endogenic production of solid sulfur allotropes or other compounds, most likely the red substance is an impurity produced by radiation alteration of hydrated sulfate salts or sulphuric acid of mainly internal origin. If the non-ice red materials or their precursors have a source in the satellite interior, and if they are not merely trace contaminants, then they can play an important role in the evolution of the icy crust, including structural differentiation and the internal dynamics. Here we assume that these substances are major components of Europa's cryo/hydrosphere, as some models have predicted they should be. If this is an accurate assumption, then these substances should not be neglected in physical, chemical, and biological models of Europa, even if major uncertainties remain as to the exact identity, abundance, and distribution of the non-ice materials. The physical chemical properties of the ice-associated materials will contribute to the physical state of the crust today and in the geological past. In order to model the influence of them on the thermal state and the geology, we have determined the thermal properties of the hydrated salts. Our new lab data reveal very low thermal conductivities for hydrated salts compared to water ice. Lower conductivities of salty ice would produce steeper thermal gradients than in pure ice. If there are salt-rich layers inside the crust, forming salt beds over the seafloor or a briny eutectic crust, for instance, the high thermal gradients may promote endogenic geological activity. On the seafloor, bedded salt accumulations may exhibit high thermochemical gradients. Metamorphic and magmatic processes and possible niches for thermophilic life at shallow suboceanic depths result from the calculated thermal profiles, even if the ocean is very cold. ?? 2004 Elsevier Inc. All rights reserved.

Icarus↗

Methods for characterizing stream habitat as part of the National Water-Quality Assessment Program

Stream habitat is characterized in the U.S. Geological Survey's National Water-Quality Assessment Program as part of an integrated physical, chemical, and biological assessment of the Nation's water quality. The goal of stream habitat characterization is to relate habitat to other physical, chemical, and biological factors to describe water-quality conditions. To accomplish this goal, environmental settings are described at sites selected for water-quality assessment. In addition, spatial and temporal patterns in habitat are examined at local, regional, and national levels. Although habitat characterization is an important component of a number of Federal, State, and local water-quality assessment programs, no current set of habitat evaluation procedures meets the objectives of the habitat assessment component of the National Water-Quality Assessment Program. Evaluation of stream habitat is based on a spatially hierarchical framework that incorporates habitat data at basin, segment, reach, and microhabitat scales. This framework provides a basis for national consistency in collection techniques while allowing flexibility in habitat assessment within individual study units. Procedures are described for collecting habitat data at basin and stream segment scales that include use of geographic information system data bases, maps, and aerial photographs. Data collected at the stream reach scale include more than 34 riparian and instream habitat characteristics evaluated during onetime site visits, and surveys of the channel and riparian area during repeated sampling.

Open-File Report↗

Revised Methods for Characterizing Stream Habitat in the National Water-Quality Assessment Program

Stream habitat is characterized in the U.S. Geological Survey's National Water-Quality Assessment (NAWQA) Program as part of an integrated physical, chemical, and biological assessment of the Nation's water quality. The goal of stream habitat characterization is to relate habitat to other physical, chemical, and biological factors that describe water-quality conditions. To accomplish this goal, environmental settings are described at sites selected for water-quality assessment. In addition, spatial and temporal patterns in habitat are examined at local, regional, and national scales. This habitat protocol contains updated methods for evaluating habitat in NAWQA Study Units. Revisions are based on lessons learned after 6 years of applying the original NAWQA habitat protocol to NAWQA Study Unit ecological surveys. Similar to the original protocol, these revised methods for evaluating stream habitat are based on a spatially hierarchical framework that incorporates habitat data at basin, segment, reach, and microhabitat scales. This framework provides a basis for national consistency in collection techniques while allowing flexibility in habitat assessment within individual Study Units. Procedures are described for collecting habitat data at basin and segment scales; these procedures include use of geographic information system data bases, topographic maps, and aerial photographs. Data collected at the reach scale include channel, bank, and riparian characteristics.

Water-Resources Investigations Report↗

Problems of underground storage of wastes

Problems of underground storage of waste involve geology in its broadest sense, including hydrology, geochemistry, and geophysics. Wastes may be solid, liquid, or gaseous, and they may be chemically toxic or noxious, esthetically offensive, or radioactive. Some wastes require only temporary containment, whereas others must be isolated for indefinitely long periods. The means and locale for emplacement underground depend upon many governing geological factors, including the physical, chemical, hydrological, and hydraulic properties of the host formation. These must be studied relative to the physical, chemical, and thermal properties of the waste and of potential interactions between the waste and the host formation. Thorough knowledge is essential because lack of it may lead to undesirable or disastrous environmental consequences. Escape of waste may contaminate the surface or near-surface environment; it may destroy the usefulness or accessibility of resources such as ground water, petroleum, and minerals. Effective management of underground waste requires adaptation of current technology and development of new technology.

Journal of Research of the U.S. Geological Survey↗