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At least 919 records · Page 51Linked to original sources

USGS1979

Selected water resources data, Clarion River and Redbank Creek basins, northwestern Pennsylvania: Part 2

This report presents selected basic data collected during a study of the water resources of the Clarion River and Redbank Creek basins in northwestern Pennsylvania. Hydrologic information including data on aquifers, water levels, and yields is presented for 1,304 wells. Records for 51 springs are also given. The report contains 83 chemical analyses of water samples collected from 30 stream sites and 300 analyses of water from 196 wells and 43 springs. Also included are 103 trace-element analyses. Monthly and annual means of ground-water levels for six observation wells are tabulated. Benthic invertebrate data from 136 stream sites are listed. Locations of data-collection sites are shown on 50 page-size reductions of 7.5-minute topographic quadrangle maps. (Kosco-USGS)

Pennsylvania↗

USGS2005

Questa baseline and premining ground-water quality investigation. 8. Lake-sediment geochemical record from 1960 to 2002, Eagle Rock and Fawn Lakes, Taos County, New Mexico

Geochemical studies of lake sediment from Eagle Rock Lake and upper Fawn Lake were conducted to evaluate the effect of mining at the Molycorp Questa porphyry molybdenum deposit located immediately north of the Red River. Two cores were taken, one from each lake near the outlet where the sediment was thinnest, and they were sampled at 1-cm intervals to provide geochemical data at less than 1-year resolution. Samples from the core intervals were digested and analyzed for 34 elements using ICP–AES (inductively coupled plasma–atomic emission spectrometry). The activity of 137 Cs has been used to establish the beginning of sedimentation in the two lakes. Correlation of the geochemistry of heavy-mineral suites in the cores from both Fawn and Eagle Rock Lakes has been used to develop a sedimentation model to date the intervals sampled. The core from upper Fawn Lake, located upstream of the deposit, provided an annual sedimentary record of the geochemical baseline for material being transported in the Red River, whereas the core from Eagle Rock Lake, located downstream of the deposit, provided an annual record of the effect of mining at the Questa mine on the sediment in the Red River. Abrupt changes in the concentrations of many lithophile and deposit-related metals occur in the middle of the Eagle Rock Lake core, which we correlate with the major flood-of-record recorded at the Questa gage at Eagle Rock Lake in 1979. Sediment from the Red River collected at low flow in 2002 is a poor match for the geochemical data from the sediment core in Eagle Rock Lake. The change in sediment geochemistry in Eagle Rock Lake in the post-1979 interval is dramatic and requires that a new source of sediment be identified that has substantially different geochemistry from that in the pre-1979 core interval. Loss of mill tailings from pipeline breaks are most likely responsible for some of the spikes in trace-element concentrations in the Eagle Rock Lake core. Enrichment of Al 2 O 3 , Cu, and Zn occurred as a result of chemical precipitation of these metals from ground water upstream in the Red River. Comparisons of the geochemistry of the post-1979 sediment core with both mine wastes and with premining sediment from the vicinity of the Questa mine indicate that both are possible sources for this new component of sediment. Existing data have not resolved this enigma.

New Mexico↗

USGS2022

The Shallow Magmatic Plumbing System of the Deccan Traps, Evidence from Plagioclase Megacrysts and Their Host Lavas

We investigate the shallow plumbing system of the Deccan Traps Large Igneous Province using rock and mineral data from Giant Plagioclase Basalt (GPB) lava flows from around the entire province, but with a focus on the Saurashtra Peninsula, the Malwa Plateau, and the base and top of the Western Ghats (WG) lava pile. GPB lavas in the WG typically occur at the transition between chemically distinct basalt formations. Most GPB samples are evolved basalts, with high Fe and Ti contents, and show major and trace elements and Sr-Nd-Pb isotopic compositions generally similar to those of previously studied Deccan basalts. Major element modeling suggests that high-Fe, evolved melts typical of GPB basalts may derive from less evolved Deccan basalts by low-pressure fractional crystallization in a generally dry magmatic plumbing system. The basalts are strongly porphyritic, with 6–25% of mm- to cm-sized plagioclase megacrysts, frequently occurring as crystal clots, plus relatively rare olivine and clinopyroxene. The plagioclase crystals are mostly labradoritic, but some show bytownitic cores (general range of anorthite mol%: 78–55). A common feature is a strong Fe enrichment at the plagioclase rims, indicating interaction with an Fe-rich melt similar to that represented by the matrix compositions (FeOt up to 16–17 wt%). Plagioclase minor and trace elements and Sr isotopic compositions analyzed by laser ablation inductively coupled plasma mass spectrometry show evidence of a hybrid and magma mixing origin. In particular, several plagioclase crystals show variable 87 Sr/ 86 Sr i , which only partially overlaps with the 87 Sr/ 86 Sr i of the surrounding matrix. Diffusion modeling suggests residence times of decades to centuries for most plagioclase megacrysts. Notably, some plagioclase crystal clots show textural evidence of deformation as recorded by electron back-scatter diffraction analyses and chemical maps, which suggest that the plagioclase megacrysts were deformed in a crystal-rich environment in the presence of melt. We interpret the plagioclase megacrysts as remnants of a crystal mush originally formed in the shallow plumbing system of the Deccan basalts. In this environment, plagioclase acquired a zoned composition due to the arrival of chemically distinct basaltic magmas. Prior to eruption, a rapidly rising but dense Fe-rich magma was capable of disrupting the shallow level crystal mush, remobilizing part of it and carrying a cargo of buoyant plagioclase megacrysts. Our findings suggest that basaltic magmas from the Deccan Traps, and possibly from LIPs in general, are produced within complex transcrustal magmatic plumbing systems with widespread crystal mushes developed in the shallow crust.

Journal of Petrology↗

USGS2014

Status and understanding of groundwater quality in the Sierra Nevada Regional study unit, 2008: California GAMA Priority Basin Project

Groundwater quality in the Sierra Nevada Regional (SNR) study unit was investigated as part of the California State Water Resources Control Board’s Groundwater Ambient Monitoring and Assessment Program Priority Basin Project. The study was designed to provide statistically unbiased assessments of the quality of untreated groundwater within the primary aquifer system of the Sierra Nevada. The primary aquifer system for the SNR study unit was delineated by the depth intervals over which wells in the State of California’s database of public drinking-water supply wells are open or screened. Two types of assessments were made: (1) a status assessment that described the current quality of the groundwater resource, and (2) an evaluation of relations between groundwater quality and potential explanatory factors that represent characteristics of the primary aquifer system. The assessments characterize untreated groundwater quality, rather than the quality of treated drinking water delivered to consumers by water distributors. The status assessment was based on water-quality data collected by the U.S. Geological Survey from 83 wells in the SNR study unit in 2008 and from 117 wells in 3 small study units within the SNR study unit in 2006–07 and on water-quality data compiled in the State’s database for 1,066 wells sampled in 2006–08. To provide some context for the results, water-quality data were converted to relative-concentrations (RCs), which are the sample concentrations divided by the concentrations of Federal or California regulatory and non-regulatory benchmarks for drinking-water quality. RCs for inorganic constituents (major ions, trace elements, nutrients, and radioactive constituents) were classified as “high” (RC > 1.0, indicating that concentration is above the benchmark), “moderate” (1.0 ≥ RC > 0.5), or “low” (RC ≤ 0.5). For organic constituents (volatile organic compounds and pesticides) and special-interest constituents (perchlorate and N -nitrosodimethylamine [NDMA]), the boundary between moderate and low RCs was set at 0.1. All benchmarks used for organic constituents were health-based, whereas health-based and aesthetic-based benchmarks were used for inorganic constituents. The primary metric used for quantifying regional-scale groundwater quality was “aquifer-scale proportion.” Aquifer-scale proportions were calculated as the areal percentages of the primary aquifer system having high, moderate, and low RCs for a given constituent or class of constituents. The SNR study unit area was classified into four aquifer lithologic types—granitic rocks, metamorphic rocks, sedimentary deposits, and volcanic rocks—and aquifer-scale proportions were calculated on an area-weighted basis for each of the four aquifer lithologies and for the study unit as a whole (aggregated system). The results of the status assessment indicated that inorganic constituents were present at high and moderate RCs in greater proportions in the SNR study unit aggregated primary aquifer system than were organic constituents and that there were significant differences (p < 0.05) between the four aquifer lithologies. One or more inorganic constituents with health-based benchmarks were present at high RCs in 16 percent of the aggregated primary aquifer system and at moderate RCs in 21 percent. Arsenic (9.7 percent), uranium (2.9 percent), boron (2.0 percent), fluoride (1.8 percent), and nitrate (1.4 percent) were the constituents most commonly present at high RCs. For inorganic constituents with aesthetic-based benchmarks, 18 percent of the aggregated primary aquifer system had high RCs of one or more constituent, and 6.8 percent had moderate RCs. Iron (15.8 percent), manganese (15.1 percent), and total dissolved solids (1.3 percent) were the constituents most commonly present at high RCs. Organic constituents were not detected in 72 percent of the primary aquifer system. One or more organic constituents had high RCs in 0.1 percent of the primary aquifer system, moderate RCs in 3.0 percent, and low RCs in 25 percent. Proportions of the four lithologic primary aquifer systems with high or moderate concentrations of organic constituents were not significantly different. Three organic constituents had area-weighted detection frequencies greater than 10 percent in the primary aquifer system as a whole or at least one of the four lithologic primary aquifer systems: the gasoline oxygenate methyl tert -butyl ether, the trihalomethane chloroform, and the herbicide simazine. The special-interest constituent perchlorate was detected at high RCs in 0.01 percent of the primary aquifer system and at moderate RCs in 1.0 percent, and detection frequencies could be accounted for by the distribution of perchlorate under natural conditions. Statistical tests were used to evaluate relations between constituent concentrations and potential explanatory factors descriptive of land use, geography, depth, geochemical conditions, and groundwater age. Higher concentrations of trace elements, radioactive constituents, and constituents with aesthetic-based benchmarks generally were associated with anoxic conditions, higher pH, and location within a particular compositional band in the Sierra Nevada batholith corresponding to the southwestern part of the study unit. High concentrations of organic constituents generally were associated with greater proportions of urban land use. No significant relations were observed between the concentrations of organic constituents and measures of well depth or groundwater age, perhaps because of the high proportions of springs and modern groundwater in the dataset.

California↗

USGS2006

Sources of polychlorinated biphenyls to Devils Swamp Lake near Baton Rouge, Louisiana

Devils Swamp Lake near Baton Rouge, Louisiana, created in 1973 by dredging in Devils Swamp along the Mississippi River, is contaminated with polychlorinated biphenyls (PCBs) from historical industrial discharges. This study involved the investigation of the occurrence, distribution, and sources of PCBs in the lake, including the possible historical contribution of PCBs from a hazardous-chemical disposal facility by way of a wastewater drainage ditch that was used from 1971 to 1993. Six bed sediment cores from the lake and three bed sediment grab samples from the drainage ditch were collected; 61 subsamples from selected intervals in five of the six cores and the three grab samples from the ditch were analyzed for PCBs using an immunoassay screening method. Sixteen of the core subsamples and one ditch sample were analyzed for organochlorine pesticides, PCBs, polycyclic aromatic hydrocarbons (PAHs) (15 samples), and major and trace elements. PCB congener profiles and a factor analysis of congener composition indicate that PCBs in sediment from the drainage ditch and in lake sediment deposited near the canal since the mid-1980s are similar, which indicates the disposal facility, by way of the wastewater drainage ditch, is the source of the PCBs. Sediment from several hundred meters down the lake to the west, near where Bayou Baton Rouge enters the lake, had a different PCB composition and in a sample deposited in the early 1980s, a much higher concentration, indicating a second source of PCBs in the watershed of Bayou Baton Rouge. Large differences in PAHs and metals between sediment near the ditch and sediment near Bayou Baton Rouge support this conclusion. The identity of the Bayou Baton Rouge source(s) cannot be established using available data. The short duration and relatively high concentrations of PCBs from the bayou source indicate either a spill or a flood-related release-there was a large flood on the Mississippi River in 1983. Older (deeper) samples from cores near the drainage ditch (dated as deposited before the mid-1980s) had PCB compositions that indicate a mixture of sources (Bayou Baton Rouge and the drainage ditch). Elevated PCB concentrations in sediment from the drainage ditch and cores from near the mouth of the ditch in recent (post-2000) samples indicate that some PCB inputs from the ditch might still be occurring.

Scientific Investigations Report↗

USGS2006

Review of Trace Element Blank and Replicate Data Collected in Ground and Surface Water for the National Water-Quality Assessment Program, 1991-2002

The trace elements Sb, Be, and Tl in ground water and Sb, Be, Co, Mo, and U in surface water are unaffected by contamination. Limited quality control data (blanks) for Li and V in ground water and surface water do not allow for a good assessment on the potential contamination associated with these trace elements. Potential contamination was identified for Al, As, Ba, B, Cd, Cr, Cu, Fe, Pb, Mn, Ni, Se, Ag, Sr, and Zn in ground water and surface water. Evidence of potential contamination was shown for Co, Mo, and U in ground water; potential contamination was shown for T1 in surface water. In comparing the potential contamination for these trace elements with the U.S. Environmental Protection Agency's (USEPA) drinking-water standards, the contamination for most of these trace elements is less than 10 percent of the drinking-water standard; therefore, contamination would have little or no effect when comparing trace element concentrations with the USEPA drinking-water standards. The exceptions are Al, Cd, and possibly Pb in ground water, and As and possibly Pb in surface water. Potential contamination identified for these trace elements is greater than 10 percent of the USEPA drinking-water standard, but affects only 5 percent or less of the As, Cd, and Pb samples. For most trace elements, the level of potential contamination is not large enough to significantly affect the measured concentration of the environmental sample. The exceptions may be Fe in ground water and Al in surface water, which have concentrations for at least 10 percent of the environmental samples that exceeded the USEPA drinking-water standards. Sample variability for some of the trace elements could not be determined because there were either no detected concentrations, or there were less than 10 replicate sets with detected concentrations. These trace elements are Be, Ag, and Tl for ground water and Sb, Be, Cr, Co, Pb, Ag, and Tl for surface water. For most trace elements, sample variability was less than 10 percent, which would have little or no affect on the reported concentrations. The exceptions are Al, Cd, Cu, Pb, Rn (at concentrations less than about 700 picocuries per liter), Se, and Zn in ground water and Cu, Se, and Zn in surface water, all of which have sample variability ranging from 10 to 20 percent. Sample variability should be considered when evaluating the potential error associated with a sample measurement. Collection of additional quality control samples for some of these trace elements to determine bias and variability is probably warranted particularly for those trace elements that the NAWQA Program did not begin sampling until 1998. Results obtained from the analysis of the quality control data can be applied to the interpretation of the environmental data collected from 1991 to 2002 and for water-quality data that are currently being collected as part of the NAWQA Program. More...

Scientific Investigations Report↗

USGS2004

Chapter A5. Section 6.4.B. Low-Level Mercury

Collecting and processing water samples for analysis of mercury at a low (subnanogram per liter) level requires use of ultratrace-level techniques for equipment cleaning, sample collection, and sample processing. Established techniques and associated quality-assurance (QA) procedures for the collection and processing of water samples for trace-element analysis at the part-per-billion level (NFM 3-5) are not adequate for low-level mercury samples. Modifications to the part-per-billion procedures are necessary to minimize contamination of samples at a typical ambient mercury concentration, which commonly is at the subnanogram-per-liter level.

Techniques of Water-Resources Investigations↗

USGS1999

Evaluation of water quality and bulk atmospheric deposition in the Guanella Pass area, Clear Creek and Park Counties, Colorado, water year 1995

A study of water quality and bulk atmospheric deposition in the Guanella Pass area during water year 1995 (October 1994 to September 1995) has provided information to characterize conditions in the South Clear Creek and Geneva Creek Basins about 40 miles west of Denver, Colorado, prior to a possible roadreconstruction project. Analytical results of water samples collected from streams, ground water, and lakes and reservoirs indicate that water in the study area generally contained small concentrations of dissolved solids (low-flow stream sample median, 43 milligrams per liter; ground-water median, 104 milligrams per liter) and suspended sediment (high-flow stream sample median, 115 milligrams per liter). Nutrient, trace-element, and organic-carbon concentrations also were small. Acidic pH and large trace-element concentrations were associated with areas affected by natural acid-sulfate weathering or mining. Increases in particulate nutrients, total recoverable trace elements, and suspended sediment were related to seasonal snowmelt and thunderstorms. Benthic macroinvertebrate and periphyton (algae) samples collected from selected sites in August 1995 indicated large variability in characteristics among sites. Macroinvertebrate density ranged from 6.5 to 1,300 organisms per square meter, and periphyton biovolume ranged from 0.023 to 4,700 x 10 6 cubic microns per square centimeter. The discharge of road runoff from any single drainage feature (ditch or culvert) was small compared to streamflows. Analytical results from samples of road runoff indicated a large range in specific conductance, pH in a neutral range, large values of turbidity, and calcium bicarbonate type water. Sodium or magnesium and chloride, however, were predominant in some samples and were probably related to applications of sodium and magnesium chloride to the roads. Although dissolved nutrients and trace elements were detected in samples of road runoff, particulate forms had the largest concentrations. Suspended-sediment concentrations in road runoff were large, and the sediment was primarily fine grained. Large concentrations of dissolved and total recoverable nutrients, total recoverable trace elements, total organic carbon, and suspended sediment in road runoff could cause increased concentrations in streams, lakes, and reservoirs. Ground-water concentrations of chloride, nitrite plus nitrate, and dissolved iron and manganese·could increase if the large concentrations present in road runoff infiltrate shallow aquifers. Bulk atmospheric deposition was collected at three sites with a paved road surface, five sites with a gravel or dirt surface, and five sites with collectors at least 500 feet away from a road. The median bulk -atmospheric-deposition rate for gravel (or dirt) roads was 106 times the median rate at a reference site (located at least 500 feet away from a road) and 39 times the median rate at a typical paved road site. If a stream, lake, or reservoir is located near the road, bulk-atmospheric- deposition products may settle directly onto open water or be washed in by surface runoff. Because the predominant road-runoff trace-element phase is particulate, potential toxic effects on receiving water may be minimal when compared to aquatic-life standards and regulations in the State of Colorado, which are primarily based on dissolved concentrations. U.S. Environmental Protection Agency primary maximum contaminant levels for drinking water were exceeded for dissolved uranium (proposed) in one ground-water sample.

Colorado↗

USGS2015

Impact of wastewater infrastructure upgrades on the urban water cycle: Reduction in halogenated reaction byproducts following conversion from chlorine gas to ultraviolet light disinfection

The municipal wastewater treatment facility (WWTF) infrastructure of the United States is being upgraded to expand capacity and improve treatment, which provides opportunities to assess the impact of full-scale operational changes on water quality. Many WWTFs disinfect their effluent prior to discharge using chlorine gas, which reacts with natural and synthetic organic matter to form halogenated disinfection byproducts (HDBPs). Because HDBPs are ubiquitous in chlorine-disinfected drinking water and have adverse human health implications, their concentrations are regulated in potable water supplies. Less is known about the formation and occurrence of HDBPs in disinfected WWTF effluents that are discharged to surface waters and become part of the de facto wastewater reuse cycle. This study investigated HDBPs in the urban water cycle from the stream source of the chlorinated municipal tap water that comprises the WWTF inflow, to the final WWTF effluent disinfection process before discharge back to the stream. The impact of conversion from chlorine-gas to low-pressure ultraviolet light (UV) disinfection at a full-scale (68,000 m 3 d −1 design flow) WWTF on HDBP concentrations in the final effluent was assessed, as was transport and attenuation in the receiving stream. Nutrients and trace elements (boron, copper, and uranium) were used to characterize the different urban source waters, and indicated that the pre-upgrade and post-upgrade water chemistry was similar and insensitive to the disinfection process. Chlorinated tap water during the pre-upgrade and post-upgrade samplings contained 11 (mean total concentration = 2.7 μg L −1 ; n=5) and 10 HDBPs (mean total concentration = 4.5 μg L −1 ), respectively. Under chlorine-gas disinfection conditions 13 HDBPs (mean total concentration = 1.4 μg L −1 ) were detected in the WWTF effluent, whereas under UV disinfection conditions, only one HDBP was detected. The chlorinated WWTF effluent had greater relative proportions of nitrogenous, brominated, and iodinated HDBPs than the chlorinated tap water. Conversion of the WWTF to UV disinfection reduced the loading of HDBPs to the receiving stream by >90%.

Science of the Total Environment↗

USGS2010

Ferromanganese crusts as archives of deep water Cd isotope compositions

The geochemistry of Cd in seawater has attracted significant attention owing to the nutrient-like properties of this element. Recent culturing studies have demonstrated that Cd is a biologically important trace metal that plays a role in the sequestration of inorganic carbon. This conclusion is supported by recent isotope data for Cd dissolved in seawater and incorporated in cultured phytoplankton. These results show that plankton features isotopically light Cd while Cd-depleted surface waters typically exhibit complimentary heavy Cd isotope compositions. Seawater samples from below 900 m depth display a uniform and intermediate isotope composition of ε 114/110 Cd = +3.3 ± 0.5. This study investigates whether ferromanganese (Fe-Mn) crusts are robust archives of deep water Cd isotope compositions. To this end, Cd isotope data were obtained for the recent growth surfaces of 15 Fe-Mn crusts from the Atlantic, Pacific, Indian, and Southern oceans and two USGS Fe-Mn reference nodules using double spike multiple collector inductively coupled plasma mass spectrometry. The Fe-Mn crusts yield a mean ε 114/110 Cd of +3.2 ± 0.4 (2 SE, n = 14). Data for all but one of the samples are identical, within the analytical uncertainty of ±1.1ε 114/110 Cd (2 SD), to the mean deep water Cd isotope value. This indicates that Fe-Mn crusts record seawater Cd isotope compositions without significant isotope fractionation. A single sample from the Southern Ocean exhibits a light Cd isotope composition of ε 114/110 Cd = 0.2 ± 1.1. The origin of this signature is unclear, but it may reflect variations in deep water Cd isotope compositions related to differences in surface water Cd utilization or long-term changes in seawater ε 114/110 Cd. The results suggest that time series analyses of Fe-Mn crusts may be utilized to study changes in marine Cd utilization.

Geochemistry, Geophysics, Geosystems↗

USGS1987

Effects of land use on ground-water quality in central Florida — Preliminary results: U.S. Geological Survey Toxic Waste — Ground-water Contamination Program

Groundwater is the principal source of drinking water in central Florida. The most important hydrogeologic unit is the Floridan aquifer system, consisting of fractured limestone and dolomite limestone. Activities of man in areas of recharge to the Floridian aquifer system that may be affecting groundwater quality include: (1) the use of drainage wells for stormwater disposal in urban areas, (2) the use of pesticides and fertilizers in citrus groves, and (3) the mining and processing of phosphate ore in mining areas. Preliminary findings about the impacts of these land uses on ground-water quality by comparison with a fourth land use representing the absence of human activity in another area of recharge are presented. Drainage wells convey excess urban stormwater directly to the Upper Floridian aquifer. The volatile organic compounds are the most common contaminants in ground water. Trace elements such as chromium and lead are entering the aquifer but their movement is apparently attenuated by precipitation reactions associated with high pH or by cation-exchange reactions. Among the trace elements and organic chemicals, most ground-water contamination in citrus production areas is caused by pesticides, which include the organic compounds simazine, ametryne, chlordane, DDE , bromacil, aldicarb, EDB, trifluralin, and diazinon, and the trace elements zinc and copper; other contaminants include benzene, toluene, napthalene, and indene compounds. In the phosphate mining area, constituents of concern are arsenic, selenium, and mercury, and secondarily lead, chromium, cadmium, and others. Organic compounds such as fluorene, naphthalene, di-n-butyl phthalate, alkylated benzenes and naphthalenes, and indene compounds also are entering groundwater. (Author 's abstract)

Florida↗

USGS2006

Mineralogical anomalies and their influences on elemental geochemistry of the main workable coal beds from the Dafang Coalfield, Guizhou, China

Mineralogy and geochemistry of the No. 11 Coal bed were investigated by using inductively-coupled plasma mass spectrometry (ICP-MS), X-ray fluorescence (XRF), scanning electron microscopy equipped with energy-dispersive X-ray (SEM-EDX), sequential chemical extraction procedure (SCEP), and optical microscopy. The results show that the No. 11 Coal bed has very high contents of veined quartz (Vol. 11.4%) and veined ankerite (Vol. 10.2 %). The veined ankerite was generally coated by goethite and the veined quartz embraced chalcopyrite, sphalerite, and selenio-galena. In addition, a trace amount of kaolinite was filled in the veins. These seven minerals often occur in the same veins. The formation temperatures of the veined ankerite and quartz are 85??C and 180??C respectively, indicating their origins of iron-rich calcic and siliceous low-temperature hydrothermal fluids in different epigenetic periods. Studies have also found that the veined quartz probably formed earlier than the veined ankerite, and at least three distinct ankerite formation stages were observed by the ration of Ca/Sr and Fe/Mn of ankerite. The mineral formation from the early to late stage is in order of sulfide, quartz, kaolinite, ankerite, and goethite. The veined ankerite is the dominant source of Mn, Cu, Ni, Pb, and Zn, which are as high as 0.09%, 74.0 ??g/g, 33.6 ??g/g, 185 ??g/g, and 289 ??g/g in this coal seam, respectively. However, the veined quartz is the main carrier of Pd, Pt, and Ir, which are 1.57 ??g/g, 0.15 ??g/g, and 0.007 ??g/g in this coal seam, respectively. In addition, chalcopyrite, sphalerite, and selenio-galena of hydrothermal origin were determined in the veined quartz, and these three sulfide minerals are also important carriers of Cu, Zn and Pb in the No. 11 Coal bed.

Acta Geologica Sinica↗

USGS2019

Three-dimensional geologic map of the southern Carson Sink, Nevada, including the Fallon FORGE area

The three-dimensional (3–D) geologic map characterizes the subsurface in the southern Carson Sink region. We created the 3–D map by integrating the results from seismic-reflection, potential-field-geophysical, and lithologic well-logging investigations completed in and around the Fallon FORGE site as part of the U.S. Department of Energy Frontier Observatory for Research in Geothermal Energy (FORGE) initiative from 2015–2018. The FORGE initiative was part of an effort to develop the technologies, techniques, and knowledge needed to make enhanced geothermal systems a commercially viable electricity-generation option for the United States. Geologic units and structures mapped during the Fallon FORGE study, which particularly focused on the Mesozoic basement, were extrapolated to create the 3–D map of the southern Carson Sink area. The 3–D map area is 10 km wide along the east-west and north-south axes and extends 2.5 km below sea level, ~3.7 km below the land surface. Views of the map include horizontal and vertical sections and oblique perspective views from several angles. We describe the geologic units and structures and discuss the methods used to integrate the geologic and geophysical information in a 3–D geologic interpretation. We provide digital data for elements of the map, such as individual 3–D fault and stratigraphic surfaces and surface-fault traces. Input data are available from various data repositories through cited web links. A brief movie displaying the 3–D map is available at https://doi.org/10.3133/sim3437 .

Nevada↗

USGS2004

Background and comparison of water-quality, streambed-sediment, and biological characteristics of streams in the Viburnum Trend and the exploration study areas, southern Missouri, 1995 and 2001

Missouri has a long history of lead mining in the Park Hills and Viburnum Trend areas. Lead ore production has been a significant economic presence since the settlement of Missouri in the 1700?s. As lead sources are depleted in active mining areas, new areas are being explored for economical ore bodies. The exploration area south of Winona, a possible extension of the Viburnum Trend lead-producing area, lies in an area of intense interest because of its scenic beauty and sensitive environment. Water-quality, streambed-sediment, fish tissue, instream and riparian habitat, and invertebrate-community samples were collected from three sites in the Viburnum Trend for the National Water-Quality Assessment (NAWQA) program Black River synoptic study in 1995 and from four sites in the exploration study area in 2001. The samples, which were collected using NAWQA protocols, were analyzed and compared to establish background conditions and similarities between sites. Bacteria, lead, and zinc concentrations were substantially different between the study areas. Habitat characteristics, such as streambed substrate size and embeddedness were similar. The Eleven Point River at Turner?s Mill is substantially larger in size than the other six surveyed sites. Trace element concentrations in fish tissue samples collected in the two study areas are similar. Samples from both areas had elevated mercury levels. Invertebrate community data indicated similarity among the Viburnum Trend study area sites, but these sites had little in common with the exploration study area sites. The invertebrate community structure in the exploration study area were not similar.

Water-Resources Investigations Report↗

USGS1979

Chemical quality of ground water in the eastern Sacramento Valley, California

The study area is about 1,300 square miles in the eastern Sacramento Valley, Calif., extending from the latitude of Roseville on the south to thelatitude of Chico on the north. Considering the increased agricultural development of the area, this report documents the chemical character of the ground water prior to water-level declines that could result from extensive pumping for irrigation or to changes caused by extensive use of imported surface water. Chemical analyses of samples from 222 wells show that most of the area is underlain by ground water of a quality suitable for most agricultural and domestic purposes. Ninety-five percent of the water sampled has dissolved-solids concentrations of less than 700 milligrams per liter. The general water type for the area is a calcium and magnesium bicarbonate water and there are negligible amounts of toxic trace elements. The potential for water-quality problems exists in the area south of Yuba City along the west bank of the Feather River. There, concentrations of chloride, sulfate, and dissolved solids are higher than in other parts of the area, and they could limit future agricultural activities if chloride- and sulfate-sensitive crops are grown. (Woodard-USGS)

California↗

USGS2010

Dissolution-reprecipitation of igneous zircon in mid-ocean ridge gabbro, Atlantis Bank, Southwest Indian Ridge

Zircons recovered from oceanic gabbro exposed on Atlantis Bank, Southwest Indian Ridge, typically display oscillatory and sector zoning consistent with igneous crystallization from mafic magmas. In one rock (of twenty investigated), weak-oscillatory-zonation patterns are overprinted by secondary textural features characterized by mottled, convoluted and wavy internal zonation patterns that are frequently associated with secondary micron- to submicron-scale micro-porosity. These zircons are hosted in a felsic vein that intruded an oxide gabbro, both of which are cross-cut by monomineralic amphibole- and quartz-rich veinlets. Zircons with weak-oscillatory-zonation patterns record a weighted-average 206 Pb/ 238 U age of 12.76 ± 0.20 Ma (mswd = 1.5), and have high trace element concentrations [e.g., ΣREEs (∼ 0.4–2.2 wt.%), Y (∼ 0.6–2.8 wt.%), P (∼ 0.4–0.9 wt.%)], and Th/U (0.1–0.5). These zircons are anomalously old (≥1 Myr) relative to the magnetic age for this portion of oceanic crust (11.75 Ma). In contrast, zircons with non-igneous, secondary textures have a younger weighted-average 206 Pb/ 238 U age of 12.00 ± 0.16 Ma (mswd = 1.7), and have lower trace element concentrations [e.g., ΣREEs (∼ 0.2–0.8 wt.%), Y (∼ 0.3–1.0 wt.%), P (∼ 0.1–0.3 wt.%)], and slightly lower Th/U (0.1–0.3). The weighted-average age of these zircons is similar to the magnetic anomaly age, and other 206 Pb/ 238 U ages of nearby rocks. We do not observe a correlation between crystallographic misorientation, internal texture, or trace element chemistry. We suggest that the decrease in trace element concentrations associated with the development of non-igneous alteration textures is attributed to the purging of non-essential structural constituent cations from the zircon crystal lattice at amphibolite-facies conditions. The mechanism of alteration/re-equilibration was likely an interface-coupled dissolution–reprecipitation processes that affected pre-existing, anomalously old zircons during shallow-level magmatic construction of Atlantis Bank at ∼ 12.0 Ma.

Chemical Geology↗

USGS2022

Plague and trace metals in natural systems

All pathogenic organisms are exposed to abiotic influences such as the microclimates and chemical constituents of their environments. Even those pathogens that exist primarily within their hosts or vectors can be influenced directly or indirectly. Yersinia pestis , the flea-borne bacterium causing plague, is influenced by climate and its survival in soil suggests a potentially strong influence of soil chemistry. We summarize a series of controlled studies conducted over four decades in Russia by Dr. Evgeny Rotshild and his colleagues that investigated correlations between trace metals in soils, plants, and insects, and the detection of plague in free-ranging small mammals. Trace metal concentrations in plots where plague was detected were up to 20-fold higher or lower compared to associated control plots, and these differences were >2-fold in 22 of 38 comparisons. The results were statistically supported in eight studies involving seven host species in three families and two orders of small mammals. Plague tended to be positively associated with manganese and cobalt, and the plague association was negative for copper, zinc, and molybdenum. In additional studies, these investigators detected similar connections between pasturellosis and concentrations of some chemical elements. A One Health narrative should recognize that the chemistry of soil and water may facilitate or impede epidemics in humans and epizootics in non-human animals.

International Journal of Environmental Research an↗

USGS1997

Ambient quality of ground water in the vicinity of Naval Submarine Base Bangor, Kitsap County, Washington, 1995

A study of the ambient ground-water quality in the vicinity of Naval Submarine Base (SUBASE) Bangor was conducted to provide the U.S. Navy with background levels of selected constituents. The Navy needs this information to plan and manage cleanup activities on the base. During March and April 1995, 136 water-supply wells were sampled for common ions, trace elements, and organic compounds; not all wells were sampled for all constituents. Man-made organic compounds were detected in only two of fifty wells, and the sources of these organic compounds were attributed to activities in the immediate vicinities of these off-base wells. Drinking water standards for trichloroethylene, iron, and manganese were exceeded in one of these wells, which was probably contaminated by an old local (off-base) dump. Ground water from wells open to the following hydrogeologic units (in order from shallow to deep) was investigated: the Vashon till confining unit (Qvt, three wells); the Vashon aquifer (Qva, 54 wells); the Upper confining unit (QC1, 16 wells); the Permeable interbeds within QC1 (QC1pi, 34 wells); and the Sea-level aquifer (QA1, 29 wells).The 50th and 90th percentile ambient background levels of 35 inorganic constituents were determined for each hydrogeologic unit. At least ten measurements were required for a constituent in each hydrogeologic unit for determination of ambient background levels, and data for three wells determined to be affected by localized activities were excluded from these analyses. The only drinking water standards exceeded by ambient background levels were secondary maximum contaminant levels for iron (300 micrograms per liter), in QC1 and QC1pi, and manganese (50 micrograms per liter), in all of the units. The 90th percentile values for arsenic in QC1pi, QA1, and for the entire study area are above 5 micrograms per liter, the Model Toxics Control Act Method A value for protecting drinking water, but well below the maximum contaminant level of 50 micrograms per liter for arsenic. The manganese standard was exceeded in 38 wells and the standard for iron was exceeded in 12 wells. Most of these wells were in QC1 or QC1pi and had dissolved oxygen concentrations of less than 1 milligram per liter and dissolved organic carbon concentrations greater than 1 milligram per liter. The dissolved oxygen concentration is generally lower in the deeper units, while pH increases; the recommended pH range of 6.5-8.5 standard units was exceeded in 9 wells. The common-ion chemistry was similar for all of the units.

Washington↗