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At least 1,207 records · Page 67Linked to original sources
USGS2011

Bathymetric survey of Carroll Creek Tributary to Lake Tuscaloosa, Tuscaloosa County, Alabama, 2010

The U.S. Geological Survey, in cooperation with the City of Tuscaloosa, conducted a bathymetric survey of Carroll Creek, on May 12-13, 2010. Carroll Creek is one of the major tributaries to Lake Tuscaloosa and contributes about 6 percent of the surface drainage area. A 3.5-mile reach of Carroll Creek was surveyed to prepare a current bathymetric map, determine storage capacities at specified water-surface elevations, and compare current conditions to historical cross sections. Bathymetric data were collected using a high-resolution interferometric mapping system consisting of a phase-differencing bathymetric sonar, navigation and motion-sensing system, and a data acquisition computer. To assess the accuracy of the interferometric mapping system and document depths in shallow areas of the study reach, an electronic total station was used to survey 22 cross sections spaced 50 feet apart. The data were combined and processed and a Triangulated Irregular Network (TIN) and contour map were generated. Cross sections were extracted from the TIN and compared with historical cross sections. Between 2004 and 2010, the area (cross section 1) at the confluence of Carroll Creek and the main run of LakeTuscaloosa showed little to no change in capacity area. Another area (cross section 2) showed a maximum change in elevation of 4 feet and an average change of 3 feet. At the water-surface elevation of 224 feet (National Geodetic Vertical Datum of 1929), the cross-sectional area has changed by 260 square feet for a total loss of 28 percent of cross-sectional storage area. The loss of area may be attributed to sedimentation in Carroll Creek and (or) the difference in accuracy between the two surveys.

Tuscaloosa, Alabama↗
USGS2004

Method of Analysis by the U.S. Geological Survey California District Sacramento Laboratory?Determination of Trihalomethane Formation Potential, Method Validation, and Quality-Control Practices

An analytical method for the determination of the trihalomethane formation potential of water samples has been developed. The trihalomethane formation potential is measured by dosing samples with chlorine under specified conditions of pH, temperature, incubation time, darkness, and residual-free chlorine, and then analyzing the resulting trihalomethanes by purge and trap/gas chromatography equipped with an electron capture detector. Detailed explanations of the method and quality-control practices are provided. Method validation experiments showed that the trihalomethane formation potential varies as a function of time between sample collection and analysis, residual-free chlorine concentration, method of sample dilution, and the concentration of bromide in the sample.

Scientific Investigations Report↗
USGS2005

Recharge processes in an alluvial aquifer riparian zone, Norman Landfill, Norman, Oklahoma, 1998-2000

Analyses of stable isotope profiles (d2H and d18O) in the saturated zone, combined with water-table fluctuations, gave a comprehensive picture of recharge processes in an alluvial aquifer riparian zone. At the Norman Landfill U.S. Geological Survey Toxic Substances Hydrology research site in Norman, Oklahoma, recharge to the aquifer appears to drive biodegradation, contributing fresh supplies of electron acceptors for the attenuation of leachate compounds from the landfill. Quantifying recharge is a first step in studying this process in detail. Both chemical and physical methods were used to estimate recharge. Chemical methods included measuring the increase in recharge water in the saturated zone, as defined by isotopic signature, specific conductance or chloride measurements; and infiltration rate estimates using storm event isotopic signatures. Physical methods included measurement of water-table rise after individual rain events and on an approximately monthly time scale. Evapotranspiration rates were estimated using diurnal watertable fluctuations; outflux of water from the alluvial aquifer during the growing season had a large effect on net recharge at the site. Evaporation and methanogenesis gave unique isotopic signatures to different sources of water at the site, allowing the distinction of recharge using the offset of the isotopic signature from the local meteoric water line. The downward movement of water from large, isotopically depleted rain events in the saturated zone yielded recharge rate estimates (2.2 - 3.3 mm/day), and rates also were determined by observing changes in thickness of the layer of infiltrated recharge water at the top of the saturated zone (1.5 - 1.6 mm/day). Recharge measured over 2 years (1998-2000) in two locations at the site averaged 37 percent of rainfall, however, part of this water had only a short residence time in the aquifer. Isotopes showed recharge water entering the ground-water system in winter and spring, then being removed during the growing season by phreatophyte transpiration. Recharge timing was variable over the course of the study; July and August were the only months that had no recharge in both years. Recharge to the aquifer from the slough (wetland pond) was estimated at one location using the isotopic signature of water affected by evaporation. Recharge was correlated with the rainfall amount over the period of estimation, suggesting that recharge from the slough to the downgradient aquifer was an episodic process, corresponding to elevated water levels in the slough after large rain events.

Oklahoma↗
USGS2005

Stream-sediment geochemistry in mining-impacted streams: Sediment mobilized by floods in the Coeur D'Alene-Spokane River system, Idaho and Washington

Environmental problems associated with the dispersion of metal-enriched sediment into the Coeur d'Alene-Spokane River system downstream from the Coeur d'Alene Mining District in northern Idaho have been a cause of litigation since 1903, 18 years after the initiation of mining for lead, zinc, and silver. Although direct dumping of waste materials into the river by active mining operations stopped in 1968, metal-enriched sediment continues to be mobilized during times of high runoff and deposited on valley flood plains and in Coeur d'Alene Lake (Horowitz and others, 1993). To gauge the geographic and temporal variations in the metal contents of flood sediment and to provide constraints on the sources and processes responsible for those variations, we collected samples of suspended sediment and overbank deposits during and after four high-flow events in 1995, 1996, and 1997 in the Coeur d'Alene-Spokane River system with estimated recurrence intervals ranging from 2 to 100 years. Suspended sediment enriched in lead, zinc, silver, antimony, arsenic, cadmium, and copper was detected over a distance of more than 130 mi (the downstream extent of sampling) downstream of the mining district. Strong correlations of all these elements in suspended sediment with each other and with iron and manganese are apparent when samples are grouped by reach (tributaries to the South Fork of the Coeur d'Alene River, the South Fork of the Coeur d'Alene River, the main stem of the Coeur d'Alene River, and the Spokane River). Elemental correlations with iron and manganese, along with observations by scanning electron microscopy, indicate that most of the trace metals are associated with Fe and Mn oxyhydroxide compounds. Changes in elemental correlations by reach suggest that the sources of metal-enriched sediment change along the length of the drainage. Metal contents of suspended sediment generally increase through the mining district along the South Fork of the Coeur d'Alene River, decrease below the confluence of the North and South Forks, and then increase again downstream of the gradient flattening below Cataldo. Metal contents of suspended sediment in the Spokane River below Coeur d'Alene Lake were comparable to those of suspended sediment in the main stem of the Coeur d'Alene River above the lake during the 1997 spring runoff, but with somewhat higher Zn contents. Daily suspended-sediment loads were about 100 times larger in the 1996 flood (50-100-year recurrence interval) than in the smaller 1997 floods (2-5-year recurrence intervals). Significant differences in metal ratios and contents are also apparent between the two flood types. The predominant source of suspended sediment in the larger 1996 flood was previously deposited, metal-enriched flood-plain sediment, identified by its Zn/Pb ratio less than 1. Suspended sediment in the smaller 1997 floods had metal ratios distinct from those of the flood-plain deposits and was primarily derived from metal-enriched sediment stored within the stream channel, identified by a Zn/Pb ratio greater than 1. Sediment deposited during overbank flooding on the immediate streambank or natural levee of the river typically consists of sandy material with metal ratios and contents similar to those of the sandy streambed sediment in the adjacent river reach. Samples of overbank deposits in backlevee marshes collected after the 1996 flood have metal ratios similar to those of peak-flow suspended sediment in the same river reach, but generally lower metal contents.

Idaho, Washington↗
USGS2005

Mercury accumulation by lower trophic-level organisms in lentic systems within the Guadalupe River watershed, California

The water columns of four reservoirs (Almaden, Calero, Guadalupe and Lexington Reservoirs) and an abandoned quarry pit filled by Alamitos Creek drainage for recreational purposes (Lake Almaden) were sampled on September 14 and 15, 2004 to provide the first measurements of mercury accumulation by phytoplankton and zooplankton in lentic systems (bodies of standing water, as in lakes and reservoirs) within the Guadalupe River watershed, California. Because of widespread interest in ecosystem effects associated with historic mercury mining within and downgradient of the Guadalupe Riverwatershed, transfer of mercury to lower trophic-level organisms was examined. The propensity of mercury to bioaccumulate, particularly in phytoplankton and zooplankton at the base of the food web, motivated this attempt to provide information in support of developing trophic-transfer and solute-transport models for the watershed, and hence in support of subsequent evaluation of load-allocation strategies. Both total mercury and methylmercury were examined in these organisms. During a single sampling event, replicate samples from the reservoir water column were collected and processed for dissolved-total mercury, dissolved-methylmercury, phytoplankton mercury speciation, phytoplankton taxonomy and biomass, zooplankton mercury speciation, and zooplankton taxonomy and biomass. The timing of this sampling event was coordinated with sampling and analysis of fish from these five water bodies, during a period of the year when vertical stratification in the reservoirs generates a primary source of methylmercury to the watershed. Ancillary data, including dissolved organic carbon and trace-metal concentrations as well as vertical profiles of temperature, dissolved oxygen, specific conductance and pH, were gathered to provide a water-quality framework from which to compare the results for mercury. This work, in support of the Guadalupe River Mercury Total Maximum Daily Load (TMDL) Study, provides the first measurements of mercury trophic transfer through planktonic communities in this watershed. It is worth reemphasizing that this data set represents a single ?snap shot? of conditions in water bodies within the Guadalupe River watershed to: (1) fill gaps in trophic transfer information, and (2) provide a scientific basis for future process-based studies with enhanced temporal and spatial coverage. This electronic document was unconventionally formatted to enhance the accessibility of information to a wide range of interest groups.

California↗
USGS2005

Method of analysis at the U.S. Geological Survey California Water Science Center, Sacramento Laboratory - determination of haloacetic acid formation potential, method validation, and quality-control practices

An analytical method for the determination of haloacetic acid formation potential of water samples has been developed by the U.S. Geological Survey California Water Science Center Sacramento Laboratory. The haloacetic acid formation potential is measured by dosing water samples with chlorine under specified conditions of pH, temperature, incubation time, darkness, and residual-free chlorine. The haloacetic acids formed are bromochloroacetic acid, bromodichloroacetic acid, dibromochloroacetic acid, dibromoacetic acid, dichloroacetic acid, monobromoacetic acid, monochloroacetic acid, tribromoacetic acid, and trichloroacetic acid. They are extracted, methylated, and then analyzed using a gas chromatograph equipped with an electron capture detector. Method validation experiments were performed to determine the method accuracy, precision, and detection limit for each of the compounds. Method detection limits for these nine haloacetic acids ranged from 0.11 to 0.45 microgram per liter. Quality-control practices include the use of blanks, quality-control samples, calibration verification standards, surrogate recovery, internal standard, matrix spikes, and duplicates.

Scientific Investigations Report↗
USGS2007

Effects of Regulation and Technology on End Uses of Nonfuel Mineral Commodities in the United States

The regulatory system and advancement of technologies have shaped the end-use patterns of nonfuel minerals used in the United States. These factors affected the quantities and types of materials used by society. Environmental concerns and awareness of possible negative effects on public health prompted numerous regulations that have dramatically altered the use of commodities like arsenic, asbestos, lead, and mercury. While the selected commodities represent only a small portion of overall U.S. materials use, they have the potential for harmful effects on human health or the environment, which other commodities, like construction aggregates, do not normally have. The advancement of technology allowed for new uses of mineral materials in products like high-performance computers, telecommunications equipment, plasma and liquid-crystal display televisions and computer monitors, mobile telephones, and electronic devices, which have become mainstream products. These technologies altered the end-use pattern of mineral commodities like gallium, germanium, indium, and strontium. Human ingenuity and people?s demand for different and creative services increase the demand for new materials and industries while shifting the pattern of use of mineral commodities. The mineral commodities? end-use data are critical for the understanding of the magnitude and character of these flows, assessing their impact on the environment, and providing an early warning of potential problems in waste management of products containing these commodities. The knowledge of final disposition of the mineral commodity allows better decisions as to how regulation should be tailored.

Scientific Investigations Report↗
USGS2007

Vertical gradients in water chemistry and age in the Northern High Plains Aquifer, Nebraska, 2003

The northern High Plains aquifer is the primary source of water used for domestic, industrial, and irrigation purposes in parts of Colorado, Kansas, Nebraska, South Dakota, and Wyoming. Despite the aquifer’s importance to the regional economy, fundamental ground-water characteristics, such as vertical gradients in water chemistry and age, remain poorly defined. As part of the U.S. Geological Survey’s National Water-Quality Assessment Program, water samples from nested, short-screen monitoring wells installed in the northern High Plains aquifer were analyzed for major ions, nutrients, trace elements, dissolved organic carbon, pesticides, stable and radioactive isotopes, dissolved gases, and other parameters to evaluate vertical gradients in water chemistry and age in the aquifer. Chemical data and tritium and radiocarbon ages show that water in the aquifer was chemically and temporally stratified in the study area, with a relatively thin zone of recently recharged water (less than 50 years) near the water table overlying a thicker zone of older water (1,800 to 15,600 radiocarbon years). In areas where irrigated agriculture was an important land use, the recently recharged ground water was characterized by elevated concentrations of major ions and nitrate and the detection of pesticide compounds. Below the zone of agricultural influence, major-ion concentrations exhibited small increases with depth and distance along flow paths because of rock/water interactions. The concentration increases were accounted for primarily by dissolved calcium, sodium, bicarbonate, sulfate, and silica. In general, the chemistry of ground water throughout the aquifer was of high quality. None of the approximately 90 chemical constituents analyzed in each sample exceeded primary drinking-water standards. Mass-balance models indicate that changes in groundwater chemistry along flow paths in the aquifer can be accounted for by small amounts of feldspar and calcite dissolution; goethite and clay-mineral precipitation; organic-carbon and pyrite oxidation; oxygen reduction and denitrification; and cation exchange. Mixing with surface water affected the chemistry of ground water in alluvial sediments of the Platte River Valley. Radiocarbon ages in the aquifer, adjusted for carbon mass transfers, ranged from 1,800 to 15,600 14C years before present. These results have important implications with respect to development of ground-water resources in the Sand Hills. Most of the water in the aquifer predates modern anthropogenic activity so excessive removal of water by pumping is not likely to be replenished by natural recharge in a meaningful timeframe. Vertical gradients in ground-water age were used to estimate long-term average recharge rates in the aquifer. In most areas, the recharge rates ranged from 0.02 to 0.05 foot per year. The recharge rate was 0.2 foot per year in one part of the aquifer characterized by large downward hydraulic gradients. Nitrite plus nitrate concentrations at the water table were 0.13 to 3.13 milligrams per liter as nitrogen, and concentrations substantially decreased with depth in the aquifer. Dissolved-gas and nitrogen-isotope data indicate that denitrification in the aquifer removed 0 to 97 percent (average = 50 percent) of the nitrate originally present in recharge. The average amount of nitrate removed by denitrification in the aquifer north of the Platte River (Sand Hills) was substantially greater than the amount removed south of the river (66 as opposed to 0 percent), and the extent of nitrate removal appears to be related to the presence of thick deposits of sediment on top of the Ogallala Group in the Sand Hills that contained electron donors, such as organic carbon and pyrite, to support denitrification. Apparent rates of dissolved-oxygen reduction and denitrification were estimated on the basis of decreases in dissolved-oxygen concentrations and increases in concentrations of excess nitrogen gas and ground-water ages along flow paths from the water table to deeper wells. Median rates of dissolved-oxygen reduction and denitrification south of the Platte River were at least 10 times smaller than the median rates north of the river in the Sand Hills. The relatively large denitrification rates in the Sand Hills indicate that the aquifer in that area may have a greater capacity to attenuate nitrate contamination than the aquifer south of the river, depending on rates of ground-water movement in the two areas. Small denitrification rates south of the river indicate that nitrate contamination in that part of the aquifer would likely persist for a longer period of time.

Nebraska↗
USGS2007

Survey of chemical contaminants in the Hanalei River, Kaua'i, Hawai'i, 2001

The Hanalei River on the island of Kaua'i in Hawai'i was designated an American Heritage River in 1998, providing special attention to natural resource protection, economic revitalization, and historic and cultural preservation. Agricultural, urban, and tourism-related activities are potential sources of contamination within the Hanalei River watershed. The objective of this study was to measure certain persistent organic chemicals and elements in the Hanalei River. During a relatively low-flow period in December of 2001, samples of native Akupa sleeper fish ( Eleotris sandwicensis ), freshwater Asian clam ( Corbicula fluminea ), giant mud crab ( Scylla serrata ), surface water, and stream bed sediment were collected from a lower estuarine reach of the river near its mouth at Hanalei Bay and from an upper reach at the Hanalei National Wildlife Refuge. Samples were analyzed for residues of urban and agricultural chemicals including organochlorine pesticides, polychlorinated biphenyls, polycyclic aromatic hydrocarbons, and elements (including mercury, lead, cadmium, arsenic, and selenium). Organic contaminants were extracted from the samples with solvent, enriched, and then analyzed by gas chromatographic analysis with electron capture or mass spectrometric detection. Samples were acid-digested for semi-quantitative analysis for elements by inductively-coupled plasma-mass spectrometry and for quantitative analysis by atomic absorption spectrophotometry. Concentrations of organochlorine pesticides, polycyclic aromatic hydrocarbons, and polychlorinated biphenyls in biota, surface water, and bed sediment sampled from the Hanalei River ranged from nondetectable to very low levels. Polychlorinated biphenyls were below detection in all samples. Dieldrin, the only compound detected in the water samples, was present at very low concentrations of 1-2 nanograms per liter. Akupa sleeper fish and giant mud crabs from the lower reach ranged from 1 to 5 nanograms per gram (wet weight) dieldrin and from less than 0.3 to 2.1 nanograms per gram total chlordane. Concentrations of individual polycyclic aromatic hydrocarbons in the lower reach bed sediments ranged from less than 1 to 190 nanograms per gram (dry weight). Relative concentrations (patterns) of the polycyclic aromatic hydrocarbons in one portion of a sediment sample indicated combustion sources. Concentrations of elements in the surface water, biota, and sediment samples were below toxicity thresholds of ecological concern. In summary, concentrations of the organic contaminants and elements targeted by this study of the Hanalei River in 2001 were below U.S. Environmental Protection Agency probable adverse effects levels for aquatic organisms.

Scientific Investigations Report↗
USGS2009

Hypothetical modeling of redox conditions within a complex ground-water flow field in a glacial setting

This report describes a modeling approach for studying how redox conditions evolve under the influence of a complex ground-water flow field. The distribution of redox conditions within a flow system is of interest because of the intrinsic susceptibility of an aquifer to redox-sensitive, naturally occurring contaminants - such as arsenic - as well as anthropogenic contaminants - such as chlorinated solvents. The MODFLOW-MT3D-RT3D suite of code was applied to a glacial valley-fill aquifer to demonstrate a method for testing the interaction of flow patterns, sources of reactive organic carbon, and availability of electron acceptors in controlling redox conditions. Modeling results show how three hypothetical distributions of organic carbon influence the development of redox conditions in a water-supply aquifer. The distribution of strongly reduced water depends on the balance between the rate of redox reactions and the capability of different parts of the flow system to transmit oxygenated water. The method can take account of changes in the flow system induced by pumping that result in a new distribution of reduced water.

Scientific Investigations Report↗
USGS2008

Material Use in the United States - Selected Case Studies for Cadmium, Cobalt, Lithium, and Nickel in Rechargeable Batteries

This report examines the changes that have taken place in the consumer electronic product sector as they relate to (1) the use of cadmium, cobalt, lithium, and nickel contained in batteries that power camcorders, cameras, cell phones, and portable (laptop) computers and (2) the use of nickel in vehicle batteries for the period 1996 through 2005 and discusses forecasted changes in their use patterns through 2010. Market penetration, material substitution, and technological improvements among nickel-cadmium (NiCd), nickel-metal-hydride (NiMH), and lithium-ion (Li-ion) rechargeable batteries are assessed. Consequences of these changes in light of material consumption factors related to disposal, environmental effects, retail price, and serviceability are analyzed in a series of short case studies.

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↗
USGS2009

Processing, Analysis, and General Evaluation of Well-Driller Logs for Estimating Hydrogeologic Parameters of the Glacial Sediments in a Ground-Water Flow Model of the Lake Michigan Basin

In 2005, the U.S. Geological Survey began a pilot study for the National Assessment of Water Availability and Use Program to assess the availability of water and water use in the Great Lakes Basin. Part of the study involves constructing a ground-water flow model for the Lake Michigan part of the Basin. Most ground-water flow occurs in the glacial sediments above the bedrock formations; therefore, adequate representation by the model of the horizontal and vertical hydraulic conductivity of the glacial sediments is important to the accuracy of model simulations. This work processed and analyzed well records to provide the hydrogeologic parameters of horizontal and vertical hydraulic conductivity and ground-water levels for the model layers used to simulated ground-water flow in the glacial sediments. The methods used to convert (1) lithology descriptions into assumed values of horizontal and vertical hydraulic conductivity for entire model layers, (2) aquifer-test data into point values of horizontal hydraulic conductivity, and (3) static water levels into water-level calibration data are presented. A large data set of about 458,000 well driller well logs for monitoring, observation, and water wells was available from three statewide electronic data bases to characterize hydrogeologic parameters. More than 1.8 million records of lithology from the well logs were used to create a lithologic-based representation of horizontal and vertical hydraulic conductivity of the glacial sediments. Specific-capacity data from about 292,000 well logs were converted into horizontal hydraulic conductivity values to determine specific values of horizontal hydraulic conductivity and its aerial variation. About 396,000 well logs contained data on ground-water levels that were assembled into a water-level calibration data set. A lithology-based distribution of hydraulic conductivity was created by use of a computer program to convert well-log lithology descriptions into aquifer or nonaquifer categories and to calculate equivalent horizontal and vertical hydraulic conductivities (K and KZ, respectively) for each of the glacial layers of the model. The K was based on an assumed value of 100 ft/d (feet per day) for aquifer materials and 1 ft/d for nonaquifer materials, whereas the equivalent KZ was based on an assumed value of 10 ft/d for aquifer materials and 0.001 ft/d for nonaquifer materials. These values were assumed for convenience to determine a relative contrast between aquifer and nonaquifer materials. The point values of K and KZ from wells that penetrate at least 50 percent of a model layer were interpolated into a grid of values. The K distribution was based on an inverse distance weighting equation that used an exponent of 2. The KZ distribution used inverse distance weighting with an exponent of 4 to represent the abrupt change in KZ that commonly occurs between aquifer and nonaquifer materials. The values of equivalent hydraulic conductivity for aquifer sediments needed to be adjusted to actual values in the study area for the ground-water flow modeling. The specific-capacity data (discharge, drawdown, and time data) from the well logs were input to a modified version of the Theis equation to calculate specific capacity based horizontal hydraulic conductivity values (KSC). The KSC values were used as a guide for adjusting the assumed value of 100 ft/d for aquifer deposits to actual values used in the model. Water levels from well logs were processed to improve reliability of water levels for comparison to simulated water levels in a model layer during model calibration. Water levels were interpolated by kriging to determine a composite water-level surface. The difference between the kriged surface and individual water levels was used to identify outlier water levels. Examination of the well-log lithology data in map form revealed that the data were not only useful for model input, but also were useful for understanding th

Scientific Investigations Report↗
USGS2009

Design and Performance of an Enhanced Bioremediation Pilot Test in a Tidal Wetland Seep, West Branch Canal Creek, Aberdeen Proving Ground, Maryland

Because of a lack of available in situ remediation methods for sensitive wetland environments where contaminated groundwater discharges, the U.S. Geological Survey, in cooperation with the U.S. Army Garrison, Aberdeen Proving Ground, Maryland, conceived, designed, and pilot tested a permeable reactive mat that can be placed horizontally at the groundwater/surface-water interface. Development of the reactive mat was part of an enhanced bioremediation study in a tidal wetland area along West Branch Canal Creek at Aberdeen Proving Ground, where localized areas of preferential discharge (seeps) transport groundwater contaminated with carbon tetrachloride, chloroform, tetrachloroethene, trichloroethene, and 1,1,2,2-tetrachloroethane from the Canal Creek aquifer to land surface. The reactive mat consisted of a mixture of commercially available organic- and nutrient-rich peat and compost that was bioaugmented with a dechlorinating microbial consortium, WBC-2, developed for this study. Due to elevated chlorinated methane concentrations in the pilot test site, a layer of zero-valent iron mixed with the peat and compost was added at the base of the reactive mat to promote simultaneous abiotic and biotic degradation. The reactive mat for the pilot test area was designed to optimize chlorinated volatile organic compound degradation efficiency without altering the geotechnical and hydraulic characteristics, or creating undesirable water quality in the surrounding wetland area, which is referred to in this report as achieving geotechnical, hydraulic, and water-quality compatibility. Optimization of degradation efficiency was achieved through the selection of a sustainable organic reactive matrix, electron donor, and bioaugmentation method. Consideration of geotechnical compatibility through design calculations of bearing capacity, settlement, and geotextile selection showed that a 2- to 3-feet tolerable thickness of the mat was possible, with 0.17 feet settlement predicted for unconsolidated sediments between 1.5 and 6 years following installation of the reactive mat. To ensure hydraulic compatibility in the mat design, mat materials that had a hydraulic conductivity greater than the surrounding wetland sediments were selected, and the mixture was optimized to consist of 1.5 parts compost, 1.5 parts peat and 1 part sand as a safeguard against fluidization. Sediment and matrix properties also indicated that a nonwoven geotextile with a cross-plane flow greater than that of the native sediments was suitable as the base of the reactive mat. Another nonwoven geotextile was selected for installation between the iron mix and organic zones of the mat to create more laminar flow conditions within the mat. Total metals and sequential extraction procedure analyses of mat materials, which were conducted to evaluate water-quality compatibility of the mat materials, showed that concentrations of metals in the compost ranged from one-half to one order of magnitude below consensus-based probable effect concentrations in sediment. A 22-inch-thick reactive mat, containing 0.5 percent WBC-2 by volume, was constructed at seep area 3-4W and monitored from October 2004 through October 2005 for the pilot test. No local, immediate failure of the mat or of wetland sediments was observed during mat installation, indicating that design estimates of bearing capacity and geotextile textile selection ensured the integrity of the mat and wetland sediments during and following installation. Measurements of surface elevation of the mat showed an average settlement of the mat surface of approximately 0.25 feet after 10 months, which was near the predicted settlement for unconsolidated sediment. Monitoring showed rapid establishment and sustainment throughout the year of methanogenic conditions conducive to anaerobic biodegradation and efficient dechlorination activity by WBC-2. The median mass removal of chloromethanes and total chloroethenes and ethane during the

Scientific Investigations Report↗
USGS2009

Community exposure to lahar hazards from Mount Rainier, Washington

Geologic evidence of past events and inundation modeling of potential events suggest that lahars associated with Mount Rainier, Washington, are significant threats to downstream development. To mitigate potential impacts of future lahars and educate at-risk populations, officials need to understand how communities are vulnerable to these fast-moving debris flows and which individuals and communities may need assistance in preparing for and responding to an event. To support local risk-reduction planning for future Mount Rainier lahars, this study documents the variations among communities in King, Lewis, Pierce, and Thurston Counties in the amount and types of developed land, human populations, economic assets, and critical facilities in a lahar-hazard zone. The lahar-hazard zone in this study is based on the behavior of the Electron Mudflow, a lahar that traveled along the Puyallup River approximately 500 years ago and was due to a slope failure on the west flank of Mount Rainier. This lahar-hazard zone contains 78,049 residents, of which 11 percent are more than 65 years in age, 21 percent do not live in cities or unincorporated towns, and 39 percent of the households are renter occupied. The lahar-hazard zone contains 59,678 employees (4 percent of the four-county labor force) at 3,890 businesses that generate $16 billion in annual sales (4 and 7 percent, respectively, of totals in the four-county area) and tax parcels with a combined total value of $8.8 billion (2 percent of the study-area total). Employees in the lahar-hazard zone are primarily in businesses related to manufacturing, retail trade, transportation and warehousing, wholesale trade, and construction. Key road and rail corridors for the region are in the lahar-hazard zone, which could result in significant indirect economic losses for businesses that rely on these networks, such as the Port of Tacoma. Although occupancy values are not known for each site, the lahar-hazard zone contains numerous dependent-population facilities (for example, schools and child day-care centers), public venues (for example, religious organizations and hotels), and critical facilities (for example, police and fire stations). The lahar-hazard zone also includes high-volume tourist sites, such as Mount Rainier National Park and the Puyallup Fairgrounds. Community exposure to lahars associated with Mount Rainier varies considerably among 27 communities and four counties—some may experience great losses that reflect only a small portion of their community and others may experience relatively small losses that devastate them. Among 27 communities, the City of Puyallup has the highest number of people and assets in the lahar-hazard zone, whereas the communities of Carbonado, Fife, Orting, and Sumner have the highest percentages of people and assets in this zone. Based on a composite index, the cities of Puyallup, Sumner, and Fife have the highest combinations of the number and percentage of people and assets in lahar-prone areas.

Washington↗
USGS2011

Development of flood-inundation maps for the West Branch Susquehanna River near the Borough of Jersey Shore, Lycoming County, Pennsylvania

Streamflow data, water-surface-elevation profiles derived from a Hydrologic Engineering Center River Analysis System hydraulic model, and geographical information system digital elevation models were used to develop a set of 18 flood-inundation maps for an approximately 5-mile reach of the West Branch Susquehanna River near the Borough of Jersey Shore, Pa. The inundation maps were created by the U.S. Geological Survey in cooperation with the Susquehanna River Basin Commission and Lycoming County as part of an ongoing effort by the National Oceanic and Atmospheric Administration's National Weather Service to focus on continued improvements to the flood forecasting and warning abilities in the Susquehanna River Basin and to modernize flood-forecasting methodologies. The maps, ranging from 23.0 to 40.0 feet in 1-foot increments, correspond to river stage at the U.S. Geological Survey streamgage 01549760 at Jersey Shore. The electronic files used to develop the maps were provided to the National Weather Service for incorporation into their Advanced Hydrologic Prediction Service website. The maps are displayed on this website, which serves as a web-based floodwarning system, and can be used to identify areas of predicted flood inundation associated with forecasted flood-peak stages. During times of flooding or predicted flooding, these maps can be used by emergency managers and the public to take proactive steps to protect life and reduce property damage caused by floods.

Pennsylvania↗
USGS2012

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

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

Scientific Investigations Report↗
USGS2012

Estimating basin lagtime and hydrograph-timing indexes used to characterize stormflows for runoff-quality analysis

A nationwide study to better define triangular-hydrograph statistics for use with runoff-quality and flood-flow studies was done by the U.S. Geological Survey (USGS) in cooperation with the Federal Highway Administration. Although the triangular hydrograph is a simple linear approximation, the cumulative distribution of stormflow with a triangular hydrograph is a curvilinear S-curve that closely approximates the cumulative distribution of stormflows from measured data. The temporal distribution of flow within a runoff event can be estimated using the basin lagtime, (which is the time from the centroid of rainfall excess to the centroid of the corresponding runoff hydrograph) and the hydrograph recession ratio (which is the ratio of the duration of the falling limb to the rising limb of the hydrograph). This report documents results of the study, methods used to estimate the variables, and electronic files that facilitate calculation of variables. Ten viable multiple-linear regression equations were developed to estimate basin lagtimes from readily determined drainage basin properties using data published in 37 stormflow studies. Regression equations using the basin lag factor (BLF, which is a variable calculated as the main-channel length, in miles, divided by the square root of the main-channel slope in feet per mile) and two variables describing development in the drainage basin were selected as the best candidates, because each equation explains about 70 percent of the variability in the data. The variables describing development are the USGS basin development factor (BDF, which is a function of the amount of channel modifications, storm sewers, and curb-and-gutter streets in a basin) and the total impervious area variable (IMPERV) in the basin. Two datasets were used to develop regression equations. The primary dataset included data from 493 sites that have values for the BLF, BDF, and IMPERV variables. This dataset was used to develop the best-fit regression equation using the BLF and BDF variables. The secondary dataset included data from 896 sites that have values for the BLF and IMPERV variables. This dataset was used to develop the best-fit regression equation using the BLF and IMPERV variables. Analysis of hydrograph recession ratios and basin characteristics for 41 sites indicated that recession ratios are random variables. Thus, recession ratios cannot be estimated quantitatively using multiple linear regression equations developed using the data available for these sites. The minimums of recession ratios for different streamgages are well characterized by a value of one. The most probable values and maximum values of recession ratios for different streamgages are, however, more variable than the minimums. The most probable values of recession ratios for the 41 streamgages analyzed ranged from 1.0 to 3.52 and had a median of 1.85. The maximum values ranged from 2.66 to 11.3 and had a median of 4.36.

Scientific Investigations Report↗