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At least 1,585 records · Page 88Linked to original sources
USGS1982

Diatremes of the Hopi Buttes, Arizona; chemical and statistical analyses

Lacustrine sediments deposited in maar lakes of the Hopi Buttes diatremes are hosts for uranium mineralization of as much as 1500 ppm. The monchiquites and limburgite turfs erupted from the diatremes are distinguished from normal alkalic basalts of the Colorado Plateau by their extreme silica undersaturation and high water, TiO2, and P2O5 contents. Many trace elements are also unusually abundant, including Ag, As, Ba, Be, Ce, Dy, Eu, F, Gd, Hf, La, Nd, Pb, Rb, Se, Sm, Sn, Sr, Ta, Tb, Th, U, V, Zn, and Zr. The lacustrine sediments, which consist predominantly of travertine and clastic rocks, are the hosts for syngenetic and epigenetic uranium mineralization of as much as 1500 ppm uranium. Fission track maps show the uranium to be disseminated within the travertine and clastic rocks, and although microprobe analyses have not, as yet, revealed discrete uranium-bearing phases, the clastic rocks show a correlation of high Fe, Ti, and P with areas of high U. Correlation coefficients show that for the travertines, clastics, and limburgite ruffs, Mo, As, Sr, Co, and V appear to have the most consistent and strongest correlations with uranium. Many elements, including many of the rare-earth elements, that are high in these three rocks are also high in the monchiquites, as compared to the average crustal abundance for the respective rock type. This similar suite of anomalous elements, which includes such immobile elements as the rare earths, suggests that Fluids which deposited the travertines were related to the monchiquitic magma. The similar age of about 5 m.y. for both the lake beds and the monchiquites also appears to support this source for the mineralizing fluids.

Open-File Report↗
USGS1987

Rock geochemistry in the Mahd adh Dhahab district, Kingdom of Saudi Arabia

Ten sets of geochemical samples from country rock, altered country rock, and quartz veins were collected to determine metal abundances and distributions in the Mahd adh Dhahab district. Gold, silver, copper, lead, and zinc are present throughout the district in veins and altered country rock. Although four generations of quartz veins are defined, there is complete gradation between types. The metals present are the same in all four, only the abundances vary. The concentrations of gold, silver, copper, lead, and zinc in altered country rock are zoned around known or projected mineralized-vein zones. Similarities in metal populations of all quartz veins, altered rock, and mineralized zones, plus the distribution of metals and some major elements, suggest that all formed as part of a single hydrothermal system. Gold in abundances greater than 1 ppm does not correlate with any other element and its distribution is very erratic. The variance in gold values between replicate samples collected in 0.5 m square panels is very high. Radio-element analyses (radium-equivalent uranium, thorium, and potassium) for 40 widely distributed sample localities indicate little variation in these elements throughout the district. If the hydrothermal system had an effect on the distribution of these elements, the system must have extended beyond the limits of the sampled area. Anomalous values of gold, silver, lead, and to a lesser extent copper and zinc in surface rock samples clearly delineated the northern mineralized zone in the upper agglomerate, and an east-vein area and west-vein area of the southern mineralized zone in the lower agglomerate. A third geochemically anomalous area occurs farther to the west in the lower agglomerate, suggesting that mineralization may have extended at least to this area along the lower agglomerate-lower tuff contact, and possibly even further to the west.

Open-File Report↗
USGS1994

Sediment-quality assessment of Franklin D. Roosevelt Lake and the upstream reach of the Columbia River, Washington, 1992

The occurrence and distribution of trace elements and of wood-pulp-related compounds in the sediments of Lake Roosevelt and the upstream reach sampler of the Columbia River were studied in 1992. In addition, an analysis of benthic invertebrate community structure and tests of sediment toxicity were conducted. Concentrations of trace elements were elevated, relative to background reference sites, in samples of bed sediment. Copper, lead, and zinc most often exceeded the sediment-quality guidelines for benthic organisms. In whole-water samples, trace-element concentrations did not exceed criteria for freshwater organisms. These concentrations were relatively small, reflecting the small suspended-sediment concentrations and the large water-diluting capacity of the Columbia River. Elevated concentrations of trace elements in sediments are attributable to the transport of metallurgical waste from a smelter discharging to the Columbia River in Canada. Dioxins and furans were found in Columbia River water, but only a few isomers were detected. A furan isomer common in effluent from pulp and paper mills was found in suspended sediment. Dioxins and furans in the water phase were isolated using solid-phase extraction to concentrate these compounds from large volumes of water. Few of the many other organic compounds associated with wood-pulp waste were detected in the bed sediments of Lake Roosevelt. Benthic invertebrate communities in the Columbia River showed effects from trace elements in bed sediments or from loss of physical habitat. Lethal and sublethal effects were observed in toxicity tests of selected aquatic organisms exposed to bed sediments from the Columbia River near the international boundary.

Washington↗
USGS1998

Analytical results for forty-two fluvial tailings cores and seven stream sediment samples from High Ore Creek, northern Jefferson County, Montana

Metal-mining related wastes in the Boulder River basin study area in northern Jefferson County, Montana have been implicated in their detrimental effects on water quality with regard to acid-generation and toxic-metal solubility. Sediments, fluvial tailings and water from High Ore Creek have been identified as significant contributors to water quality degradation of the Boulder River below Basin, Montana. A study of 42 fluvial tailings cores and 7 stream sediments from High Ore Creek was undertaken to determine the concentrations of environmentally sensitive elements (i.e. Ag, As, Cd, Cu, Pb, Zn) present in these materials, and the mineral phases containing those elements. Two sites of fluvial deposition of mine-waste contaminated sediment on upper High Ore Creek were sampled using a one-inch soil probe. Forty-two core samples were taken producing 247 subsamples. The samples were analyzed by ICP-AES (inductively coupled-plasma atomic emission spectroscopy) using a total mixed-acid digestion. Results of the core analyses show that the elements described above are present at very high concentrations (to 22,000 ppm As, to 460 ppm Ag, to 900 ppm Cd, 4,300 ppm Cu, 46,000ppm Pb, and 50,000 ppm Zn). Seven stream-sediment samples were also analyzed by ICP-AES for total element content and for leachable element content. Results show that the sediment of High Ore Creek has elevated levels of ore-related metals throughout its length, down to the confluence with the Boulder River, and that the metals are, to a significant degree, contained in the leachable phase, namely the hydrous amorphous iron- and manganese-hydroxide coatings on detrital sediment particles.

Montana↗
USGS1999

SutraPlot, a graphical post-processor for SUTRA, a model for ground-water flow with solute or energy transport

This report documents a graphical display post-processor (SutraPlot) for the U.S. Geological Survey Saturated-Unsaturated flow and solute or energy TRAnsport simulation model SUTRA, Version 2D3D.1. This version of SutraPlot is an upgrade to SutraPlot for the 2D-only SUTRA model (Souza, 1987). It has been modified to add 3D functionality, a graphical user interface (GUI), and enhanced graphic output options. Graphical options for 2D SUTRA (2-dimension) simulations include: drawing the 2D finite-element mesh, mesh boundary, and velocity vectors; plots of contours for pressure, saturation, concentration, and temperature within the model region; 2D finite-element based gridding and interpolation; and 2D gridded data export files. Graphical options for 3D SUTRA (3-dimension) simulations include: drawing the 3D finite-element mesh; plots of contours for pressure, saturation, concentration, and temperature in 2D sections of the 3D model region; 3D finite-element based gridding and interpolation; drawing selected regions of velocity vectors (projected on principal coordinate planes); and 3D gridded data export files. Installation instructions and a description of all graphic options are presented. A sample SUTRA problem is described and three step-by-step SutraPlot applications are provided. In addition, the methodology and numerical algorithms for the 2D and 3D finite-element based gridding and interpolation, developed for SutraPlot, are described. 1

Open-File Report↗
USGS1925

The evolution and disintegration of matter

In any attempt to study the evolution of matter it is necessary to begin with its simplest known forms, the so-called chemical elements. During a great part of the nineteenth century many philosophical chemists held a vague belief that these elements were not distinct entities but manifestations of one primal substance-the protyle, as it is sometimes called. Other chemists, more conservative, looked askance at all such speculations and held fast to what they regarded as established facts. To them an element was something distinct from other kinds of matter, a substance which could neither be decomposed nor transmuted into anything else. This belief, however, was based entirely upon negative evidence-the inadequacy of our existing resources to produce such sweeping changes. Many important facts were ignored, and especially the fact that the elements are connected by very intimate relations, such as are best shown in the periodic law of Mendeleef, who, from gaps in his table of atomic weights, predicted the existence of three unknown metals, which have since been discovered. For these metals, scandium, gallium, and germanium, he foretold not only their atomic weights but also their most characteristic physical properties and the sort of compounds that each one would form. His prophecies have been verified in every essential particular. One obvious conclusion was soon drawn from Mendeleef's "law," although he was too cautious to admit it, namely, that the chemical elements must have had some community of origin. The philosophical speculations as to their nature were fully justified.

Professional Paper↗
USGS2023

Groundwater chemistry and hexavalent chromium

Water samples collected by the U.S. Geological Survey from more than 100 wells between March 2015 and November 2017 in Hinkley and Water Valleys, in the Mojave Desert 80 miles northeast of Los Angeles, California, were analyzed for field parameters, major ions, nutrients, and selected trace elements, including hexavalent chromium, Cr(VI). Water from most wells was alkaline and oxic. The pH ranged from 6.9 in water-table wells near recharge areas along the Mojave River to 9.4 in deeper wells farther downgradient in the northern subarea. Hexavalent chromium concentrations measured by ion chromatography using U.S. Environmental Protection Agency Method 218.6 and a version of that method used for detection of Cr(VI) concentrations as low as 0.06 micrograms per liter (μg/L), produced results comparable to field speciation with subsequent analyses by graphite furnace atomic absorption spectroscopy (coefficient of determination, R 2 , of 0.97). Hexavalent chromium concentrations ranged from less than the study reporting level of 0.10 to 2,500 μg/L. The highest concentrations were within the October–December 2015 (Q4 2015) regulatory Cr(VI) plume downgradient from the Hinkley compressor station. Hexavalent chromium concentrations outside the Q4 2015 regulatory Cr(VI) plume were as high as 11 μg/L. Hexavalent chromium concentrations in water from most wells were distributed in a narrow redox potential and pH band within the overlapping chromate ion, CrO 4 2− (aqueous) , and manganese-3, Mn(III) (solid) , stability fields. The redox potential of water from some wells completed in carbonate-rich mudflat/playa deposits approached the more oxic manganese-4, Mn(IV) (solid) , stability field. However, Cr(VI) concentrations in porewater pressure-extracted from Mn(IV)-containing deposits in the eastern subarea did not exceed 3.3 μg/L, and porewater does not appear to be a source of Cr(VI) concentrations greater than this concentration in water from wells in the eastern subarea. On the basis of comparison with California-wide data, Cr(VI) concentrations at the measured pH were higher than expected for uncontaminated water from wells (1) within the Q4 2015 regulatory Cr(VI) plume, (2) within the eastern subarea nominally crossgradient from the Hinkley compressor station and upgradient from the Q4 2015 regulatory Cr(VI) plume, and (3) from shallow wells in the northern subarea downgradient from the leading edge of the Q4 2015 regulatory Cr(VI) plume. Hexavalent chromium concentrations in alkaline water from wells in the northern subarea of Hinkley Valley and in Water Valley were within ranges expected for uncontaminated water elsewhere in California given their pH and trace-element composition. Hexavalent chromium concentrations were higher than expected on the basis of selected trace-element concentrations that co-occur with Cr(VI) in water from wells within the Q4 2015 regulatory Cr(VI) plume and from wells in the eastern and northern subareas near the plume margins. Hexavalent chromium concentrations did not exceed 4 μg/L in water from domestic wells sampled in Hinkley and Water Valleys and were generally within ranges expected for uncontaminated groundwater given their pH and trace-element composition. Interpretations derived from Cr(VI) and pH, and from Cr(VI) and selected trace-element concentrations collected between March 2015 and November 2017 were used within a summative-scale analysis to determine the Cr(VI) plume extent (chapter G). However, Cr(VI) background concentrations (chapter G) were calculated from regulatory data collected from selected wells between April 2017 and January 2018.

California↗
USGS2004

Chemical Data for Detailed Studies of Irrigation Drainage in the Salton Sea Area, California, 1995?2001

The primary purpose of this report is to present all chemical data from the Salton Sea area collected by the U.S. Geological Survey between 1995 and 2001. The data were collected primarily for the Department of the Interior's National Irrigation Water Quality Program (NIWQP). The report also contains a brief summary and citation to investigations done for the NIWQP between 1992 and 1995. The NIWQP began studies in the Salton Sea area in 1986 to evaluate effects on the environment from potential toxins, especially selenium, in irrigation-induced drainage. This data report is a companion to several reports published from the earlier studies and to interpretive publications that make use of historical and recent data from this area. Data reported herein are from five collection studies. Water, bottom material, and suspended sediment collected in 1995-96 from the New River, the lower Colorado River, and the All-American Canal were analyzed for elements, semi-volatile (extractable) organic compounds, and organochlorine compounds. Sufficient suspended sediment for chemical analyses was obtained by tangential-flow filtration. A grab sample of surficial bottom sediment collected from near the deepest part of the Salton Sea in 1996 was analyzed for 44 elements and organic and inorganic carbon. High selenium concentration confirmed the effective transfer (sequestration) of selenium into the bottom sediment. Similar grab samples were collected 2 years later (1998) from 11 locations in the Salton Sea and analyzed for elements, as before, and also for nutrients, organochlorine compounds, and polycyclic aromatic hydrocarbons. Nutrients were measured in bottom water, and water-column profiles were obtained for pH, conductance, temperature, and dissolved oxygen. Element and nutrient concentrations were obtained in 1999 from cores at 2 of the above 11 sites, in the north subbasin of the Salton Sea. The most-recent study reported herein was done in 2001 and contains element data on suspended material isolated by continuous-flow centrifugation on samples collected in transects extending out from the Whitewater, the Alamo, and the New Rivers into the Salton Sea. Chemical data on suspended sediment and bottom material from tributory rivers and the Salton Sea itself show that many insoluble constituents, including selenium and DDE, are concentrated in the fine-grained, organic- and carbonate-rich bottom sediment from deep areas near the center of the Salton Sea. Data also show that selenium and arsenic are markedly enriched in seston (plankton, partially-degraded algal detritus, and mineral matter that compose suspended particulates in the lake) collected just below the water surface in the Salton Sea. This result indicates that bio-concentration in primary producers in the water column provides an important pathway whereby high selenium residues accumulate in fish and fish-eating birds at the Salton Sea.

Scientific Investigations Report↗
USGS2006

Hydrologic requirements of and consumptive ground-water use by riparian vegetation along the San Pedro River, Arizona

This study is a coordinated effort by the U.S. Geological Survey (USGS), the U.S. Department of Agriculture, Agricultural Research Service (USDA ARS), and Arizona State University, with assistance from the U.S. Army Corps of Engineers, the University of Wyoming, and the University of Arizona. The specific objectives of the study were: to determine the water needs of riparian vegetation through the riparian growing season and throughout the SPRNCA to ensure its long-term ecological integrity; to quantify the total water use of riparian vegetation within the SPRNCA; and to determine the source of water used by key riparian plant species within the SPRNCA. To meet these objectives, the study was divided into three elements: (1) a characterization of the status and variability of hydrologic factors within the riparian system (USGS), (2) a riparian biohydrology study to relate spatial and temporal aspects of riparian changes and condition to the hydrologic variables (Arizona State University), and (3) a water-use evapotranspiration (ET) study to quantify annual consumptive ground-water use by riparian transpiration and direct evaporation from the stream channel (USDA ARS) in cooperation with the U.S. Army Corps of Engineers, the University of Wyoming, and the University of Arizona. Twenty-six sites within the SPRNCA were selected for collection of vegetation data from three primary streamflow regimes (perennial, intermittent-wet, intermittent-dry), which include the principal vegetation communities. Detailed hydrologic-condition data were collected at a subset of 16 of these sites, called the SPRNCA biohydrology sites. Water-use and water-source data were collected at a subset of 5 of the 16 biohydrology sites. Vegetation data also were collected at supplemental sites within the SPRNCA boundary in the Upper San Pedro Basin and in the Lower San Pedro Basin. In addition to information about vegetation and geomorphic conditions, hydrologic data collected at the 16 biohydrology sites were used to delineate 14 reaches that were internally homogenous in terms of streamflow hydrology (spatial intermittence of streamflow) and geomorphology (channel sinuosity and flood-plain width). Although this overall study consisted of three elements, the elements were closely coordinated to derive integrated results. Specifically, the connection between water demand, water availability, and riparian functioning represents a synthesis of the study elements. The effects of intra- and inter-annual as well as spatial variability of hydrologic and riparian factors were observed in each of the three study elements.

Arizona↗
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↗
USGS2007

Tectonic setting and metallogenesis of volcanogenic massive sulfide deposits in the Bonnifield Mining District, Northern Alaska Range: Chapter B in Recent U.S. Geological Survey studies in the Tintina Gold Province, Alaska, United States, and Yukon, Canada--results of a 5-year project

This paper summarizes the results of field and laboratory investigations, including whole-rock geochemistry and radiogenic isotopes, of outcrop and drill core samples from volcanogenic massive sulfide (VMS) deposits and associated metaigneous rocks in the Wood River area of the Bonnifield mining district, northern Alaska Range (see fig. 1 of Editors’ Preface and Overview). U-Pb zircon igneous crystallization ages from felsic rocks indicate a prolonged period of Late Devonian to Early Mississippian (373±3 to 357±4 million years before present, or Ma) magmatism. This magmatism occurred in a basinal setting along the ancient Pacific margin of North America. The siliceous and carbonaceous compositions of metasedimentary rocks, Precambrian model ages based on U-Pb dating of zircon and neodymium ages, and for some units, radiogenic neodymium isotopic compositions and whole-rock trace-element ratios similar to those of continental crust are evidence for this setting. Red Mountain (also known as Dry Creek) and WTF, two of the largest VMS deposits, are hosted in peralkaline metarhyolite of the Mystic Creek Member of the Totatlanika Schist. The Mystic Creek Member is distinctive in having high concentrations of high-field-strength elements (HFSE) and rare-earth elements (REE), indicative of formation in a within-plate (extensional) setting. Mystic Creek metarhyolite is associated with alkalic, within-plate basalt of the Chute Creek Member; neodymium isotopic data indicate an enriched mantle component for both members of this bimodal (rhyolite-basalt) suite. Anderson Mountain, the other significant VMS deposit, is hosted by the Wood River assemblage. Metaigneous rocks in the Wood River assemblage span a wide compositional range, including andesitic rocks, which are characteristic of arc volcanism. Our data suggest that the Mystic Creek Member likely formed in an extensional, back-arc basin that was associated with an outboard continental-margin volcanic arc that included rocks of the Wood River assemblage. We suggest that elevated HFSE and REE trace-element contents of metavolcanic rocks, whose major-element composition may have been altered, are an important prospecting tool for rocks of VMS deposit potential in east-central Alaska.

Alaska;Yukon↗
USGS2008

Net Acid Production, Acid Neutralizing Capacity, and Associated Mineralogical and Geochemical Characteristics of Animas River Watershed Igneous Rocks Near Silverton, Colorado

This report presents results from laboratory and field studies involving the net acid production (NAP), acid neutralizing capacity (ANC), and magnetic mineralogy of 27 samples collected in altered volcanic terrain in the upper Animas River watershed near Silverton, Colo., during the summer of 2005. Sampling focused mainly on the volumetrically important, Tertiary-age volcanic and plutonic rocks that host base- and precious-metal mineralization in the study area. These rocks were analyzed to determine their potential for neutralization of acid-rock drainage. Rocks in the study area have been subjected to a regional propylitic alteration event, which introduced calcite, chlorite (clinochlore), and epidote that have varying amounts and rates of acid neutralizing capacity (ANC). Locally, hydrothermal alteration has consumed any ANC and introduced minerals, mainly pyrite, that have a high net acid production (NAP). Laboratory studies included hydrogen pyroxide (H2O2) acid digestion and subsequent sodium hydroxide (NaOH) titration to determine NAP, and sulfuric acid (H2SO4) acid titration experiments to determine ANC. In addition to these environmental rock-property determinations, mineralogical, chemical, and petrographic characteristics of each sample were determined through semiquantitative X-ray diffractometry (Rietveld method), optical mineralogy, wavelength dispersive X-ray fluorescence, total carbon-carbonate, and inductively coupled plasma?mass spectrometric analysis. An ANC ranking was assigned to rock samples based on calculated ANC quantity in kilograms/ton (kg/t) calcium carbonate equivalent and ratios of ANC to NAP. Results show that talus near the southeast Silverton caldera margin, composed of andesite clasts of the Burns Member of the Silverton Volcanics, has the highest ANC (>100 kg/t calcium carbonate equivalent) with little to no NAP. The other units found to have moderate to high ANC include (a) andesite lavas and volcaniclastic rocks of the San Juan Formation, west and northwest of the Silverton caldera, and (b) the Picayune Megabreccia Member of Sapinero Mesa Tuff along the western San Juan caldera margin. Sultan Mountain stock, composed of granitoid intrusive rocks, was shown to have low ANC and moderate NAP. Sequential leachate analyses on a suite of whole-rock samples from the current and a previous study indicate that host rock composition and mineralogy control leachate compositions. The most mafic volcanic samples had high leachate concentrations for Mg, Fe, and Ca, whereas silicic volcanic samples had lower ferromagnesiun compositions. Samples with high chlorite abundance also had high leachable Mg concentrations. Trace-element substitution, such as Sr for Ca in plagioclase, controls high Sr concentrations in those samples with high plagioclase abundance. High Ti abundance in leachate was observed in those samples with high magnetite concentrations. This is likely due to samples containing intergrown magnetite-ilmenite. Whole rocks having high trace-element concentrations have relatively high leachate trace-element abundances. Some lavas of the San Juan Formation and Burns Member of the Silverton Volcanics had elevated Zn-, Cd-, and Pb-leachate concentrations. Manganese was also elevated in one San Juan Formation sample. Other San Juan Formation and Burns Member lavas had low to moderate trace-element abundances. One sample of the pyroxene andesite member of the Silverton Volcanics had elevated concentrations for As and Mo. Most other pyroxene andesite member samples had low leachate trace-element abundances. Mine-waste-leachate analyses indicated that one mine-waste sample had elevated concentrations of Cu (1.5 orders of magnitude), Zn (1 order of magnitude), As (1 order of magnitude), Mo (1.5 to 2 orders of magnitude), Cd (1 to 2 orders of magnitude), and Pb (2 to 3 orders of magnitude) compared to whole rocks. These data indicate the importance of whole-rock geochemistry or leachate analys

Scientific Investigations Report↗
USGS2008

Assessment of nonpoint source chemical loading potential to watersheds containing uranium waste dumps associated with uranium exploration and mining, San Rafael Swell, Utah

During July and August of 2006, 117 solid-phase samples were collected from abandoned uranium waste dumps, geologic background sites, and adjacent streambeds in the San Rafael Swell, in southeastern Utah. The objective of this sampling program was to assess the nonpoint source chemical loading potential to ephemeral and perennial watersheds from uranium waste dumps on Bureau of Land Management property. Uranium waste dump samples were collected using solid-phase sampling protocols. After collection, solid-phase samples were homogenized and extracted in the laboratory using a field leaching procedure. Filtered (0.45 micron) water samples were obtained from the field leaching procedure and were analyzed for Ag, As, Ba, Be, Cd, Cr, Cu, Fe, Mn, Mo, Ni, Pb, Sb, Se, U, V, and Zn at the Inductively Coupled Plasma-Mass Spectrometry Metals Analysis Laboratory at the University of Utah, Salt Lake City, Utah and for Hg at the U.S. Geological Survey National Water Quality Laboratory, Denver, Colorado. For the initial ranking of chemical loading potential of suspect uranium waste dumps, leachate analyses were compared with existing aquatic life and drinking-water-quality standards and the ratio of samples that exceeded standards to the total number of samples was determined for each element having a water-quality standard for aquatic life and drinking-water. Approximately 56 percent (48/85) of the leachate samples extracted from uranium waste dumps had one or more chemical constituents that exceeded aquatic life and drinking-water-quality standards. Most of the uranium waste dump sites with elevated trace-element concentrations in leachates were along Reds Canyon Road between Tomsich Butte and Family Butte. Twelve of the uranium waste dump sites with elevated trace-element concentrations in leachates contained three or more constituents that exceeded drinking-water-quality standards. Eighteen of the uranium waste dump sites had three or more constituents that exceeded trace-element concentrations for aquatic life water-quality standards. The proximity of the uranium waste dumps in the Tomsich Butte area near Muddy Creek, coupled with the elevated concentration of trace elements, increases the offsite impact potential to water resources. Future assessment and remediation priority of these areas may be done by using GIS-based risk-mapping techniques, such as Sensitive Catchment Integrated Mapping and Analysis Project.

Utah↗
USGS2018

Status and understanding of groundwater quality in the Monterey-Salinas Shallow Aquifer Study Unit, 2012–13: California GAMA Priority Basin Project

Groundwater quality in the approximately 7,820-square-kilometer (km 2 ) Monterey-Salinas Shallow Aquifer (MS-SA) study unit was investigated from October 2012 to May 2013 as part of the second phase of the Priority Basin Project of the Groundwater Ambient Monitoring and Assessment (GAMA) Program. The study unit is in the central coast region of California in the counties of Santa Cruz, Monterey, and San Luis Obispo. The GAMA Priority Basin Project is being conducted by the California State Water Resources Control Board in cooperation with the U.S. Geological Survey and the Lawrence Livermore National Laboratory. The MS-SA study was designed to provide a statistically robust assessment of untreated-groundwater quality in the shallow aquifer systems. The assessment was based on water-quality samples collected by the U.S. Geological Survey from 100 groundwater sites and 70 household tap sites, along with ancillary data such as land use and well-construction information. The shallow aquifer systems were defined by the depth interval of wells associated with domestic supply. The MS-SA study unit consisted of four study areas—Santa Cruz (210 km 2 ), Pajaro Valley (360 km 2 ), Salinas Valley (2,000 km 2 ), and Highlands (5,250 km 2 ). This study had two primary components: the status assessment and the understanding assessment . The first primary component of this study—the status assessment —assessed the quality of the groundwater resource indicated by data from samples analyzed for volatile organic compounds (VOCs), pesticides, and naturally present inorganic constituents, such as major ions and trace elements. The status assessment is intended to characterize the quality of groundwater resources in the shallow aquifer system of the MS-SA study unit, not the treated drinking water delivered to consumers by water purveyors. As opposed to the public wells, however, water from private wells, which often tap the shallow aquifer, is usually consumed without any treatment. The second component of this study—the understanding assessment —identified the natural and human factors that potentially affect groundwater quality by evaluating land-use characteristics, measures of location, geologic factors, groundwater age, and geochemical conditions of the shallow aquifer. An additional component of this study was a comparison of MS-SA water-quality results to those of the GAMA Monterey Bay and Salinas Valley Groundwater Basins study unit. This study unit covered much of the same areal extent as the MS-SA, but assessed the deeper, public drinking-water aquifer system. Relative concentrations (sample concentration divided by the benchmark concentration) were used to evaluate concentrations of constituents in groundwater samples relative to water-quality benchmarks for those constituents that have Federal or California benchmarks, such as maximum contaminant levels. For organic and special-interest constituents, relative concentrations were classified as high, greater than 1.0; moderate, greater than 0.1 and less than or equal to 1.0; or low, less than or equal to 0.1. For inorganic constituents, relative concentrations were classified as high, greater than 1.0; moderate, greater than 0.5 and less than or equal to 1.0; or low, less than or equal to 0.5. A relative concentration greater than 1.0 indicates that the concentration was greater than a benchmark. Aquifer-scale proportions were used to quantify regional-scale groundwater quality. The aquifer-scale proportions are the areal percentages of the shallow aquifer system where relative concentrations for a given constituent or class of constituents were high, moderate, or low. Inorganic constituents were measured at high and moderate relative concentrations more frequently than organic constituents. In the MS-SA study unit, inorganic constituents with benchmarks were detected at high relative concentrations in 51 percent of the study unit. The greatest proportions of high relative concentrations of trace elements and radioactive constituents were in the Highlands and Santa Cruz study areas, whereas high relative concentrations of nutrients were most often detected in the Salinas Valley and Pajaro Valley study areas and salinity indicators were most often detected in the Highlands and Salinas Valley study areas. The trace elements detected at high relative concentrations were arsenic, boron, iron, manganese, molybdenum, selenium, and strontium. The radioactive constituents detected at high relative concentrations were adjusted gross alpha radioactivity and uranium. The nutrient detected at high relative concentrations was nitrate plus nitrite. The salinity indicators detected at high relative concentrations were chloride, sulfate, and total dissolved solids. Organic constituents (VOCs and pesticides) were not detected at high relative concentrations in any of the study areas. The fumigant 1,2-dichloropropane was detected at moderate relative concentrations. The VOC chloroform and the pesticide simazine were the only organic constituents detected in more than 10 percent of samples. The constituents of special interest NDMA ( N -nitrosodimethylamine) and perchlorate were detected at high relative concentrations in the MS-SA study unit. Selected constituents were evaluated with explanatory factors to identify potential sources or processes that could explain their presence and distribution. Trace elements and radioactive constituents came from natural sources and were not elevated by anthropogenic sources or processes, except for selenium and the radioactive constituent uranium. Arsenic, manganese, iron, selenium, and uranium concentrations were all influenced by oxidation-reduction conditions. Unlike other trace elements and radioactive constituents, uranium and selenium can be affected by agricultural practices. Uranium and selenium can be released from aquifer sediments as a result of irrigation recharge water interacting with bicarbonate systems. Nitrate can be strongly affected by anthropogenic sources. Nitrate concentrations were significantly higher in modern groundwater, indicating recent inputs of nitrate to the shallow aquifer system. Nitrate was positively correlated with agricultural land use, indicating that irrigation-return water could be leaching nitrogen fertilizer and naturally present nitrate to elevate nitrate concentrations in shallow groundwater. The salinity indicators total dissolved solids, chloride, and sulfate all had natural sources in the MS-SA study unit, primarily marine sediments. Concentrations of the constituents were elevated as a result of evaporative concentration of irrigation water or precipitation. Sulfate concentrations were significantly correlated to agricultural land use, indicating that agricultural land-use practices are a contributing source of sulfate to groundwater. The samples with most of the detections of VOCs were from sites in the Pajaro Valley and northern part of the Salinas Valley. Most of the samples with pesticide detections were from sites in the Salinas Valley study area. The herbicide simazine was positively correlated to the percentage of agricultural land use, and its concentrations were higher in modern groundwater than in pre-modern groundwater. Perchlorate, similar to nitrate, has natural and anthropogenic sources. Correlations of perchlorate to dissolved oxygen, nitrate, and percentage of agricultural land use indicated that the irrigation-return water could be leaching naturally present perchlorate, as well as perchlorate from historical applications of Chilean nitrate fertilizer, to increase perchlorate concentrations in groundwater. The quality of the water in the shallow aquifer system from this study was compared with the quality of water in the public drinking-water aquifer in a previous GAMA (MS-PA) study in the same area. The shallow system was more oxic and had more sites with modern groundwater than the public drinking-water aquifer, which was more anoxic and had sites with more pre-modern groundwater. Arsenic and selenium were found at high relative concentrations in a greater proportion of the shallow system. Manganese and iron were found at high relative concentrations in a greater proportion of the public drinking-water aquifer. Uranium was found at higher relative concentrations in a greater proportion of the shallow system. Concentrations of arsenic, iron, manganese, and molybdenum are not likely to change much as groundwater percolates from the shallow system to the public drinking-water aquifer because there are no anthropogenic sources affecting these constituents. Uranium and selenium concentrations in the public drinking-water aquifer could be affected by the higher concentrations in the shallow system because of irrigation-return water, however. Nitrate and salinity indicators had concentrations that were much higher in the shallow system than the deeper public drinking-water aquifer. High concentrations of these constituents in the shallow system could lead to increased concentrations in the public drinking-water aquifer in parts of the study units because of land-use practices, such as irrigated agriculture. Organic constituents were detected more frequently in the public drinking-water aquifer than in the shallow system, possibly because more of the sites sampled in the public drinking-water aquifer were in urban areas compared to the sites sampled for the shallow system or because sources of contamination have decreased as a result of changes in use at the land surface.

California↗
USGS2022

Depth to water and water quality in groundwater wells in the Ogallala aquifer within the North Plains Groundwater Conservation District, Texas Panhandle, 2019–20, and comparison to 2012–13 conditions

The Ogallala aquifer is the primary source of water for agricultural and municipal purposes in the Texas Panhandle. Because most of the groundwater in the Texas Panhandle is withdrawn from the Ogallala aquifer, information on the quality of groundwater in the Ogallala aquifer in this part of Texas is useful for resource characterization. During 2012–13, the U.S. Geological Survey in cooperation with the North Plains Groundwater Conservation District (NPGCD), collected and analyzed water-quality samples from 30 groundwater monitoring wells in the Texas Panhandle. The results of the initial 2012–13 synoptic sampling were published in 2014 to help provide an initial characterization of the spatial and temporal variability of water quality in the NPGCD management area. This report documents the results of a followup synoptic sampling completed between March 2019 and July 2020 by the U.S. Geological Survey, in cooperation with the NPGCD, to further characterize the spatial and temporal characteristics of groundwater in the NPGCD management area; measurements of the depth to water, in feet below land surface, and water-quality samples were obtained from the same 30 monitoring wells that were sampled during 2012–13. The water-quality samples were analyzed for major ions, nutrients, trace elements, and selected organic compounds. Results from the 2019–20 synoptic sampling were compared to drinking-water standards and to the results from the 2012–13 synoptic sampling. Between the 2012–13 and 2019–20 sampling periods, the depth to water increased in 28 of the 30 wells, with a median difference of 18.17 feet. Results from major ion analyses indicate that most of the groundwater samples collected during 2019–20 were classified as magnesium-bicarbonate type, the same water type indicated for most samples during 2012–13. Dissolved-solids concentrations for the wells sampled during 2019–20 ranged from 260 to 774 milligrams per liter (mg/L) with a median dissolved-solids concentration of 316 mg/L, which was slightly higher than the median dissolved-solids concentration of 311 mg/L for the 2012–13 sampling period. Of the four nutrients analyzed, nitrate was the dominant nitrogen species, with a median nitrate concentration of 2.25 mg/L for the 2019–20 sampling period, which was a slight increase relative to the median nitrate concentration of 2.05 mg/L for the 2012–13 sampling period. Accounting for variability in analyses, median major ion concentrations and median concentrations for nutrient species were similar during the 2012–13 and 2019–20 sampling periods. None of the trace element concentrations exceeded any maximum contaminant level or secondary drinking-water standards. Median concentrations of trace elements from the 2012–13 sampling period were compared to those from the 2019–20 sampling period for constituents in cases where at least 50 percent of concentrations measured in the samples were detected at concentrations greater than the highest applicable laboratory reporting level, and variability in analyses was accounted for. Comparison results indicated that that median concentrations of two trace elements (lithium and uranium) increased, whereas median concentrations for two of the other trace elements measured (barium and molybdenum) decreased. Atrazine and deethylatrazine were the only organic compounds detected; both were detected in four of the six samples collected from different wells and analyzed for organic compounds. Concentrations of atrazine and deethylatrazine detections were all less than 0.05 micrograms per liter.

Texas↗
USGS2014

Two graphical user interfaces for managing and analyzing MODFLOW groundwater-model scenarios

Scenario Manager and Scenario Analyzer are graphical user interfaces that facilitate the use of calibrated, MODFLOW-based groundwater models for investigating possible responses to proposed stresses on a groundwater system. Scenario Manager allows a user, starting with a calibrated model, to design and run model scenarios by adding or modifying stresses simulated by the model. Scenario Analyzer facilitates the process of extracting data from model output and preparing such display elements as maps, charts, and tables. Both programs are designed for users who are familiar with the science on which groundwater modeling is based but who may not have a groundwater modeler’s expertise in building and calibrating a groundwater model from start to finish. With Scenario Manager, the user can manipulate model input to simulate withdrawal or injection wells, time-variant specified hydraulic heads, recharge, and such surface-water features as rivers and canals. Input for stresses to be simulated comes from user-provided geographic information system files and time-series data files. A Scenario Manager project can contain multiple scenarios and is self-documenting. Scenario Analyzer can be used to analyze output from any MODFLOW-based model; it is not limited to use with scenarios generated by Scenario Manager. Model-simulated values of hydraulic head, drawdown, solute concentration, and cell-by-cell flow rates can be presented in display elements. Map data can be represented as lines of equal value (contours) or as a gradated color fill. Charts and tables display time-series data obtained from output generated by a transient-state model run or from user-provided text files of time-series data. A display element can be based entirely on output of a single model run, or, to facilitate comparison of results of multiple scenarios, an element can be based on output from multiple model runs. Scenario Analyzer can export display elements and supporting metadata as a Portable Document Format file.

Techniques and Methods↗
USGS2002

Investigation of water quality and aquatic-community structure in Village and Valley Creeks, City of Birmingham, Jefferson County, Alabama, 2000-01

The U.S. Geological Survey conducted a 16-month investigation of water quality, aquatic-community structure, bed sediment, and fish tissue in Village and Valley Creeks, two urban streams that drain areas of highly intensive residential, commercial, and industrial land use in Birmingham, Alabama. Water-quality data were collected between February 2000 and March 2001 at four sites on Village Creek, three sites on Valley Creek, and at two reference sites near Birmingham?Fivemile Creek and Little Cahaba River, both of which drain less-urbanized areas. Stream samples were analyzed for major ions, nutrients, fecal bacteria, trace and major elements, pesticides, and selected organic constituents. Bed-sediment and fish-tissue samples were analyzed for trace and major elements, pesticides, polychlorinated biphenyls, and additional organic compounds. Aquatic-community structure was evaluated by conducting one survey of the fish community and in-stream habitat and two surveys of the benthic-invertebrate community. Bed-sediment and fish-tissue samples, benthic-invertebrates, and habitat data were collected between June 2000 and October 2000 at six of the nine water-quality sites; fish communities were evaluated in April and May 2001 at the six sites where habitat and benthic-invertebrate data were collected. The occurrence and distribution of chemical constituents in the water column and bed sediment provided an initial assessment of water quality in the streams. The structure of the aquatic communities, the physical condition of the fish, and the chemical analyses of fish tissue provided an indication of the cumulative effects of water quality on the aquatic biota. Water chemistry was similar at all sites, characterized by strong calcium-bicarbonate component and magnesium components. Median concentrations of total nitrogen and total phosphorus were highest at the headwaters of Valley Creek and lowest at the reference site on Fivemile Creek. In Village Creek, median concentrations of nitrite and ammonia increased in a downstream direction. In Valley Creek, median concentrations of nitrate, nitrite, ammonia, organic nitrogen, suspended phosphorus, and orthophosphate decreased in a downstream direction. Median concentrations of Escherichia coli and fecal coliform bacteria were highest at the most upstream site of Valley Creek and lowest at the reference site on Fivemile Creek. Concentrations of enterococci exceeded the U.S. Environmental Protection Agency criterion in 80 percent of the samples; concentrations of Escherichia coli exceeded the criterion in 56 percent of the samples. Concentrations of bacteria at the downstream sites on Village and Valley Creeks were elevated during high flow rather than low flow, indicating the presence of nonpoint sources. Surface-water samples were analyzed for chemical compounds that are commonly found in wastewater and urban runoff. The median number of wastewater indicators was highest at the most upstream site on Valley Creek and lowest at the reference site on Fivemile Creek. Concentrations of total recoverable cadmium, copper, lead, and zinc in surface water exceeded acute and chronic aquatic life criteria in up to 24 percent of the samples that were analyzed for trace and major elements. High concentrations of trace and major elements in the water column were detected most frequently during high flow, indicating the presence of nonpoint sources. Of the 24 pesticides detected in surface water, 17 were herbicides and 7 were insecticides. Atrazine, simazine, and prometon were the most commonly detected herbicides; diazinon, chlorpyrifos, and carbaryl were the most commonly detected insecticides. Concentrations of atrazine, carbaryl, chlorpyrifos, diazinon, and malathion periodically exceeded criteria for the protection of aquatic life. Trace-element priority pollutants, pesticides, and other organic compounds were detected in higher concentrations in bed sediment at the Village and Valley Creek sites t

Water-Resources Investigations Report↗
USGS2003

Resurvey of quality of surface water and bottom material of the Barataria Preserve of Jean Lafitte National Historical Park and Preserve, Louisiana, 1999-2000

The quality of water and bottom material in the Barataria Preserve of Jean Lafitte National Historical Park and Preserve, Louisiana, was surveyed from March 1999 to May 2000. Organochlorine, chlorophenoxy acid, and organophosphorus pesticides; polychlorinated biphenyls (PCB's); and trace elements were analyzed in surface water and bottom material from three sites previously sampled in a 1981-82 survey. Surface water at six sites was sampled and analyzed for selected nutrients and major inorganic ions based on their importance to human health, the health of the marshes of the Barataria Preserve, or their usefulness in tracking the circulation of Mississippi River water in the Barataria Preserve. Southern Louisiana was in a moderate to severe drought during most of the sampling period, which elevated salinity in the Barataria Preserve for at least 8 months. Specific conductance values were less than 3,000 µS/cm (microsiemens per centimeter at 25 degrees Celsius) in surface water throughout the Barataria Preserve from March through September 1999. Specific conductance values increased over the next 2 months and then remained between 5,000 and 6,000 µS/cm. The herbicide 2,4-D was detected in water at the two sites sampled in August 1999 but not at any site during the two other sampling times. Iron, manganese, and the trace elements copper, nickel, and zinc were detected in dissolved and whole-water samples at all three sites. Nitrite+ nitrate, as nitrogen, concentrations ranged from less than 0.002 to 0.19 mg/L (milligrams per liter). Ammonia, as nitrogen, concentrations ranged from less than 0.01 to 0.16 mg/L. Orthophosphate, as phosphorus, concentrations ranged from less than 0.002 to 0.14 mg/L. Calcium, magnesium, potassium, sulfate, and chloride concentrations in surface water were elevated due to the marine influence on the composition of surface water in the Barataria Preserve during the sampling period. Sulfate and chloride concentrations reached 379 and 2,830 mg/L, respectively. Polychlorinated biphenyls, chlordane, and DDT were detected in bottom material. Trace elements were detected in bottom material at all three of the sampled sites. Arsenic concentrations ranged from 4 to 9 µg/g (micrograms per gram) and lead concentrations from 20 to 31 µg/g. Mercury concentrations also were above laboratory reporting levels (LRL's) for bottom material at all three sites. The herbicide 2,4-D was detected in surface water during both surveys. Other organic compounds were not detected in surface water. Mercury and chromium were detected in surface water at all three sites during the 1981-82 survey but were below LRL?s during the 1999-2000 survey. Changes in chemical characteristics of bottom material occurred during the years between the 1981-82 and 1999-2000 surveys. DDT decreased in the bottom material at Bayou Segnette near Barataria. DDE, a degradation product, increased at this site, indicating that over time, DDT concentrations are decreasing in bottom material. PCB's were present in similar concentrations (Bayou Segnette near Barataria) or increased (Bayou Segnette 4.6 miles below Westwego) from 1981-82 to 1999-2000. Cadmium concentrations consistently decreased by half or more at all three sites from 1981-82 to 1999-2000. Mercury concentrations were consistently lower at all three sites in the 1999-2000 survey, but the differences from the 1981-82 survey were small. Chromium concentrations increased at two of the three sites from 1981-82 to the present survey. At the third site, no chromium value was available for the earlier survey. Concentrations of copper and nickel increased in bottom material at the two sites on Bayou Segnette, but decreased at Kenta Canal northwest of Westwego. Probable Effects Levels (PEL's) and Interim Sediment Quality Guidelines (ISQG's) concentrations, as tabulated by the Canadian Council of Ministers of the of the Environment, were used to assess the probability of biological impairment in the Barataria Preserve. PEL’s are concentrations of a chemical at or above which some biological impairment is likely. ISQG concentrations are those at or below which biological impairment is unlikely. Concentrations of 2,4-D and trace elements, when detected in surface water, were substantially lower than levels at which biological impairment could be expected. Concentrations of organic compounds in bottom material were at most less than 25 percent of PEL’s, and usually much lower. Arsenic, cadmium, copper, and lead concentrations in bottom material were generally slightly above or lower than ISQG concentrations in both surveys, although arsenic was as high as 53 percent of PEL’s at one site in the 1999-2000 survey. All other trace elements in bottom material were present in concentrations lower than ISQG concentrations.

Louisiana↗