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

The study area of this report includes about 1,200 square miles in the central Sacramento Valley adjacent to the Sacramento River from Knights Landing to Los Molinos. With recent agricultural development in the area, additional land has been brought under irrigation from land which had been used primarily for dry farming and grazing. This report documents the chemical character of the ground water prior to water-level declines resulting from extensive pumping for irrigation or to changes caused by extensive use of imported surface water. Chemical analyses of samples from 209 wells show that most of the area is underlain by ground water of a quality suitable for most agricultural and domestic purposes. Most of the water sampled in the area has dissolved-solids concentrations ranging from 100 to 700 milligrams per liter. The general water types for the area are a calcium magnesium bicarbonate or magnesium calcium bicarbonate and there are negligible amounts of toxic trace elements.

California↗

Organic compounds and trace elements in fish tissue and bed sediment from streams in the Yellowstone River basin, Montana and Wyoming, 1998

A comprehensive water-quality investigation of the Yellowstone River Basin began in 1997, under the National Water-Quality Assessment (NAWQA) Program. Twenty-four sampling sites were selected for sampling of fish tissue and bed sediment during 1998. Organic compounds analyzed included organochlorine insecticides and their metabolites and total polychlorinated biphenyls (PCBs) from fish-tissue and bed-sediment samples, and semivolatile organic compounds from bed-sediment samples. A broad suite of trace elements was analyzed from both fish-tissue and bed-sediment samples, and a special study related to mercury also was conducted. Of the 12 organochlorine insecticides and metabolites detected in the fish-tissue samples, the most compounds per site were detected in samples from integrator sites which represent a mixture of land uses. The presence of DDT, and its metabolites DDD and DDE, in fish collected in the Yellowstone Park area likely reflects long-term residual effects from historical DDT-spraying programs for spruce budworm. Dieldrin, chlordane, and other organic compounds also were detected in the fish-tissue samples. The compound p, p'-DDE was detected at 71 percent of the sampling sites, more than any other compound. The concentrations of total DDT in fish samples were low, however, compared to concentrations from historical data from the study area, other NAWQA studies in the Rocky Mountains, and national baseline concentrations. Only 2 of the 27 organochlorine insecticides and metabolites and total PCBs analyzed in bed sediment were detected. Given that 12 of the compounds were detected in fish-tissue samples, fish appeared to be more sensitive indicators of contamination than bed sediment.Concentrations of some trace elements in fish and bed sediment were higher at sites in mineralized areas than at other sites. Concentrations of selenium in fish tissue from some sites were above background levels. Concentrations of arsenic, chromium, copper, and lead in some of the bed-sediment samples potentially exceeded criteria for the protection of aquatic life.

Water-Resources Investigations Report↗

Borehole Geophysical, Water-Level, and Water-Quality Investigation of a Monitoring Well Completed in the St. Francois Aquifer in Oregon County, Missouri, 2005-08

A deep (more than 2,000 feet) monitoring well was installed in an area being explored for lead and zinc deposits within the Mark Twain National Forest in southern Missouri. The area is a mature karst terrain where rocks of the Ozark aquifer, a primary source of water for private and public supplies and major springs in the nearby Eleven Point National Wild and Scenic River and the Ozark National Scenic Riverways, are exposed at the surface. The potential lead deposits lie about 2,000 feet below the surface within a deeper aquifer, called the St. Francois aquifer. The two aquifers are separated by the St. Francois confining unit. The monitoring well was installed as part of a series of investigations to examine potentiometric head relations and water-quality differences between the two aquifers. Results of borehole flowmeter measurements in the open borehole and water-level measurements from the completed monitoring well USGS-D1 indicate that a seasonal upward gradient exists between the St. Francois aquifer and the overlying Ozark aquifer from about September through February. The upward potentiometric heads across the St. Francois confining unit that separates the two aquifers averaged 13.40 feet. Large reversals in this upward gradient occurred during the late winter through summer (about February through August) when water levels in the Ozark aquifer were as much as 138.47 feet higher (average of 53.84 feet) than water levels in the St. Francois aquifer. Most of the fluctuation of potentiometric gradient is caused by precipitation and rapid recharge that cause large and rapid increases in water levels in the Ozark aquifer. Analysis of water-quality samples collected from the St. Francois aquifer interval of the monitoring well indicated a sodium-chloride type water containing dissolved-solids concentrations as large as 1,300 milligrams per liter and large concentrations of sodium, chloride, sulfate, boron, and lithium. In contrast, water in the overlying Ozark aquifer interval of the monitoring well was a calcium-magnesium-bicarbonate type water containing less than 250 milligrams per liter dissolved solids and substantially smaller concentrations of major and trace elements.

Scientific Investigations Report↗

Cadmium isotope fractionation during coal combustion: Insights from two U.S. coal-fired power plants

Coal combustion, one of the principal energy sources of electricity in the United States, produces over 100 million tons of coal combustion products (CCPs) per year in the U.S. The reuse and disposal of CCPs has the potential to release toxic trace elements, including cadmium (Cd), into the environment. In this study, we investigated CCPs, including bottom ash (BA), economizer fly ash (EFA), and fly ash (FA), as well as feed coal (FC) and pulverized coal (PC) collected from two U.S. coal-fired power plants in New Mexico and Ohio with different coal supplies. The New Mexico plant uses high volatile C bituminous, low-sulfur coals mined from the San Juan Basin (Cretaceous Fruitland Formation) and the Ohio plant uses high volatile A bituminous, high-sulfur central Appalachian Basin coals (Upper Pennsylvanian Monongahela Formation). Mineralogical and elemental analysis showed that these CCP samples consist of ∼70% amorphous Al-Si-rich glasses and ∼30% mineral phases of quartz (SiO 2 ) and mullite (Ai 6 Si 2 O 13 ). The Cd isotope compositions (δ 114 Cd, normalized to NIST Cd standard 3108) of FA and EFA samples (ranging from −0.51 to +0.47‰) are distinctively heavier than those of BA samples (−0.75 to −0.52‰) in both power plants. We interpret this Cd isotope difference as a result of Cd condensation from the gas phase during flue gas cooling, instead of evaporation of Cd phase during coal combustion. Cd condensation is the main process to generate the isotopically heavy Cd signatures that preferentially partition on the fine FA particles. We also investigated Cd isotope compositions in different leachate products from a series of batch-leaching experiments with these CCPs, using diluted acetic acid, hydroxyl ammonium chloride, hydrogen peroxide followed by ammonium acetate, and 5% nitric acid, as a possible means to identify CCP-released Cd in the environment. Unusually and significantly heavier Cd isotope compositions were observed in each leachate of FA samples (+1.10 to +7.09‰), which fall far outside from the range of Cd isotope ratios observed in natural soils and rocks, but less so for the EFA samples (−0.43 to +1.18‰). Such an observation is consistent with the interpretation that isotopically heavy Cd preferentially partitions on the fine FA particles after coal combustion and is readily to be released during these leaching experiments. This study demonstrates that high-temperature coal combustion can lead to a very large degree of fractionation of Cd isotopes that can be used as a unique tracer for identifying anthropogenic metal inputs in the environment. The major Cd isotope fractionation process occurs as the Cd gas phase condenses on fine FA particles during the flue gas cooling stage after coal combustion.

New Mexico, Ohio↗

Petrology, mineralogy and geochemistry of mined coals, western Venezuela

Upper Paleocene to middle Miocene coal samples collected from active mines in the western Venezuelan States of Táchira, Mérida and Zulia have been characterized through an integrated geochemical, mineralogical and petrographic investigation. Proximate, ultimate, calorific and forms of sulfur values, major and trace element, vitrinite reflectance, maceral concentrations and mineral matter content have been determined for 16 channel samples from 14 mines. Ash yield generally is low, ranging from < 1 to 17 wt.% (mean = 5 wt.%) on a dry basis (db). Total sulfur content is low to moderate, ranging from 1 to 6 wt.%, db (average = 1.7 wt.%). Calorific value ranges from 25.21 to 37.21 MJ/kg (10,840–16,000 Btu/lb) on a moist, mineral-matter-free basis (average = 33.25 MJ/kg, 14,300 Btu/lb), placing most of the coal samples in the apparent rank classification of high-volatile bituminous. Most of the coal samples exhibit favorable characteristics on the various indices developed to predict combustion and coking behavior and concentrations of possible environmentally sensitive elements (As, Be, Cd, Cr, Co, Hg, Mn, Ni, Pb, Sb, Se, Th and U) generally are similar to the concentrations of these elements in most coals of the world, with one or two exceptions. Concentrations of the liptinite maceral group range from < 1% to 70 vol.%. Five samples contain > 20 vol.% liptinite, dominated by the macerals bituminite and sporinite. Collotelinite dominates the vitrinite group; telinite was observed in quantities of ≤ 1 vol.% despite efforts to better quantify this maceral by etching the sample pellets in potassium permanganate and also by exposure in an oxygen plasma chamber. Inertinite group macerals typically represent < 10 vol.% of the coal samples and the highest concentrations of inertinite macerals are found in distantly spaced (> 400 km) upper Paleocene coal samples from opposite sides of Lago de Maracaibo, possibly indicating tectonic controls on subsidence related to construction of the Andean orogen. Values of maximum reflectance of vitrinite in oil ( R o max ) range between 0.42% and 0.85% and generally are consistent with the high-volatile bituminous rank classification obtained through ASTM methods. X-ray diffraction analyses of low-temperature ash residues indicate that kaolinite, quartz, illite and pyrite dominate the inorganic fraction of most samples; plagioclase, potassium feldspar, calcite, siderite, ankerite, marcasite, rutile, anatase and apatite are present in minor or trace concentrations. Semiquantitative values of volume percent pyrite content show a strong correlation with pyritic sulfur and some sulfide-hosted trace element concentrations (As and Hg). This work provides a modern quality dataset for the western Venezuela coal deposits currently being exploited and will serve as the foundation for an ongoing coal quality research program in Venezuela.

International Journal of Coal Geology↗

Complete Analytical Data for Samples of Jurassic Igneous Rocks in the Bald Mountain Mining District, Nevada

This report presents all petrographic, major oxide, and trace element data for a set of 109 samples collected during an investigation of Jurassic igneous rocks in the Bald Mountain mining district, Nevada. Igneous rocks in the district include the Bald Mountain stock, quartz-feldspar porphyry dikes, basaltic andesite dikes, aplite sills, and rare lamprophyre dikes. These rocks, although variably altered near intrusion-related mineral deposits, are fresh in many parts of the district. Igneous rocks in the district are hosted by Paleozoic sedimentary rocks.

Open-File Report↗

Sediment deposition and trends and transport of phosphorus and other chemical constituents, Cheney Reservoir watershed, south-central Kansas

Sediment deposition, water-quality trends, and mass transport of phosphorus, nitrogen, selected trace elements, and selected pesticides within the Cheney Reservoir watershed in south-central Kansas were investigated using bathymetric survey data and reservoir bottom-sediment cores. Sediment loads in the reservoir were investigated by comparing 1964 topographic data to 1998 bathymetric survey data. Approximately 7,100 acre-feet of sediment deposition occurred in Cheney Reservoir from 1965 through 1998. As of 1998, sediment had filled 27 percent of the reservoir's inactive conservation storage pool, which is less than the design estimate of 34 percent. Mean annual sediment deposition was 209 acre-feet per year, or 0.22 acre-feet per year per square mile, and the mean annual sediment load was 453 million pounds per year. During the 3-year period from 1997 through 1999, 23 sediment cores were collected from the reservoir, and subsamples were analyzed for nutrients (phosphorus and nitrogen species), selected trace elements, and selected organic pesticides. Mean concentrations of total phosphorus in reservoir bottom sediment ranged from 94 milligrams per kilogram at the upstream end of the reservoir to 710 milligrams per kilogram farther downstream near the reservoir dam. The mean concentration for all sites was 480 milligrams per kilogram. Total phosphorus concentrations were greatest when more silt- and clay-sized particles were present. The implications are that if anoxic conditions (inadequate oxygen) occur near the dam, phosphorus could be released from the sediment and affect the drinking-water supply. Analysis of selected cores also indicates that total phosphorus concentrations in the reservoir sediment increased over time and were probably the result of nonpoint-source activities in the watershed, such as increased fertilizer use and livestock production. Mean annual phosphorus loading to Cheney Reservoir was estimated to be 226,000 pounds per year on the basis of calculations from deposited sediment in the reservoir. Mean total phosphorus concentration in the surface-water inflow to Cheney Reservoir was 0.76 milligram per liter, mean annual phosphorus yield of the watershed was estimated to be 0.38 pound per year per acre, and both are based on sediment deposition in the reservoir. A comparison of the Cheney Reservoir watershed to the Webster Reservoir, Tuttle Creek Lake, and Hillsdale Lake watersheds showed that phosphorus yields were smallest in the Webster Reservoir watershed where precipitation was less than in the other watersheds. Mean concentrations of total ammonia plus organic nitrogen in bottom sediment from Cheney Reservoir ranged from 1,200 to 2,400 milligrams per kilogram as nitrogen. A regression analysis between total ammonia plus organic nitrogen as nitrogen and sediment particle size showed a strong relation between the two variables and suggests, as with phosphorus, that total ammonia plus organic nitrogen as nitrogen adsorbs to the silt- and clay-sized particles that are transported to the deeper parts of the reservoir. An analysis of trends with depth of total ammonia plus organic nitrogen as nitrogen did not indicate a strong relation between the two variables despite the increase in fertilizer use in the watershed during the past 40 years. Selected cores were analyzed for trace elements. Concentrations of arsenic, chromium, copper, and nickel at many sites exceeded levels where adverse effects on aquatic organisms sometimes occur. Larger concentrations of these elements also occurred in sediment closer to the reservoir dam where there is a larger percentage of silt and clay in the bottom sediment than farther upstream. However, the lack of industrial or commercial land use in the watershed suggests that these concentrations may be the result of natural conditions. Organochlorine insecticides were detected in the reservoir-bottom sediment in Cheney Reservoir. DDT and its degradation products DDD and DD

Water-Resources Investigations Report↗

An update of hydrologic conditions and distribution of selected constituents in water, eastern Snake River aquifer and perched groundwater zones, Idaho National Laboratory, Idaho, emphasis 2019–21

Since 1952, wastewater discharged to infiltration ponds (also called “percolation ponds”) and disposal wells at the Idaho National Laboratory (INL) has affected water quality in the eastern Snake River Plain (ESRP) aquifer and perched groundwater zones underlying the INL. The U.S. Geological Survey (USGS), in cooperation with the U.S. Department of Energy (DOE), maintains groundwater-monitoring networks at the INL to determine hydrologic trends and to delineate the movement of radiochemical and chemical wastes in both the aquifer and perched groundwater zones. This report presents an analysis of water-level and water-quality data collected from the ESRP aquifer and perched groundwater wells from the USGS groundwater monitoring networks during 2019–21. From March–May 2018 to March–May 2021, water levels in wells completed in the ESRP aquifer increased in the northern part of the INL and decreased in the southwestern part. Water-level increases ranged from 0.02 to 1.04 feet in the northern part and decreases ranged from 0.03 to 2.94 feet in the southwestern part of the INL. Detectable concentrations of radiochemical constituents in water samples from wells in the ESRP aquifer at the INL generally decreased or remained constant during 2019–21. Decreases in concentrations were attributed to radioactive decay, changes in waste-disposal methods, and dilution from recharge and underflow. In 2021, tritium was detected above reporting levels in water samples collected from 46 of 105 aquifer wells and ranged from 150±50 to 4,280±150 picocuries per liter (pCi/L). Tritium concentrations from eight wells completed in deep perched groundwater near the Advanced Test Reactor Complex (ATRC) generally were greater than or equal to the reporting level during at least one sampling event during 2019–21, and concentrations ranged from 160±50 to 2,097±107 pCi/L. Concentrations of strontium-90 in water from 12 of 45 aquifer wells sampled in 2021 exceeded the reporting level, and concentrations ranged from 2.5±0.7 to 299±6 pCi/L. During 2021, concentrations of strontium-90 from five wells completed in deep perched groundwater at the ATRC equaled or exceeded the reporting levels, and concentrations ranged from 3±0.9 pCi/L to 27.8±1.3 pCi/L. Concentrations of cesium-137 were less than the reporting level in all but one aquifer well, and concentrations of plutonium-238, plutonium-239, -240 (undivided), and americium-241 were less than the reporting level in water samples from all aquifer wells sampled during this study period. Dissolved chromium concentrations in water samples from 64 ESRP aquifer wells ranged from less than (<) 0.5 to 76.4 micrograms per liter (μg/L). During 2019–21, dissolved chromium was detected in water from wells completed in deep perched groundwater above the ESRP aquifer at the ATRC, and concentrations ranged from <1 to 82.1 μg/L. In 2021, concentrations of dissolved sodium in water from most ESRP aquifer wells in the southern part of the INL were greater than the western tributary groundwater background concentration of 8.3 milligrams per liter (mg/L). During 2021, dissolved sodium concentrations in water from 15 wells completed in deep perched groundwater ranged from 11.7 to 122.5 mg/L. Variations in sodium concentrations in aquifer wells and perched groundwater zones are attributed to either migration of remnant water from the former chemical-waste ponds or disposal volume and composition variability in percolation ponds installed in 2008. In 2021, concentrations of chloride in most water samples from ESRP aquifer wells south of the Idaho Nuclear Technology and Engineering Center (INTEC) and at the Central Facilities Area (CFA) exceeded background concentrations. Chloride concentrations in water from wells south of the INTEC have generally decreased because of discontinued chloride disposal to the legacy percolation ponds since 2002 when the discharge of wastewater was discontinued. During 2019–21, dissolved chloride concentrations in deep perched groundwater above the ESRP aquifer from 18 wells at the ATRC ranged from 8.15 to 231 mg/L. In 2021, sulfate concentrations in water samples from ESRP aquifer wells in the south-central part of the INL that exceeded the background concentration of sulfate, ranged from 21 to 141 mg/L. The greater-than-background concentrations in water from these wells are attributed to sulfate disposal at the ATRC infiltration ponds or the legacy INTEC percolation ponds. In 2021, sulfate concentrations in water samples from aquifer wells near the Radioactive Waste Management Complex (RWMC) were mostly greater than background concentrations. The maximum dissolved sulfate concentration in shallow perched groundwater near the ATRC was 575 mg/L in 2021. During 2021, dissolved sulfate concentrations in water from wells completed in deep perched groundwater near the cold waste ponds at the ATRC ranged from 22.3 to 519 mg/L. In 2021, concentrations of nitrate in water from most ESRP aquifer wells at and near the INTEC exceeded the western tributary groundwater background concentration of 0.655 mg/L. Concentrations of nitrate in aquifer wells southwest of INTEC and farther away from the influence of disposal areas and the Big Lost River, in intermittent source of surface water recharge to the aquifer, show a general decrease in nitrate concentration over time. Two aquifer wells south of INTEC show increasing trends that could result from wastewater beneath the INTEC tank farm being mobilized to the aquifer. During 2019–21, water samples from several ESRP aquifer wells were collected and analyzed for volatile organic compounds (VOCs). Twelve VOCs were detected, and 1–4 VOCs were detected in water samples from 10 wells. The most frequently detected VOCs include carbon tetrachloride (tetrachloromethane), trichloromethane, tetrachloroethene, 1,1,1-trichloroethane, and trichloroethene. In 2019–21, concentrations for all VOCs were less than their respective maximum contaminant levels (MCLs) for drinking water, except carbon tetrachloride in one well, trichloroethene in two wells, and vinyl chloride in one well. During 2019–21, variability and bias were evaluated from 34 replicate and 14 blank quality-assurance samples. Results from replicate analyses were investigated to evaluate sample variability. Constituents with acceptable reproducibility were major ions, trace elements, nutrients, and VOCs. All radiochemical constituents including gross alpha- and beta- radioactivity, strontium-90, cesium-137, and tritium, had acceptable reproducibility. Bias from sample contamination was evaluated from equipment, field, and source-solution blanks. Chloride and sulfate were detected slightly above their respective method detection limits in equipment and field blanks, but at concentrations well below the co-collected sample for that well. These chloride and sulfate detections in the field and equipment blanks were inconsequential because they weren’t detected above the analysis-specific variability for those constituents as determined by replicate sample result evaluation. None of the detections of nutrients and trace inorganic constituents were high enough to indicate environmental sample or analytical procedure bias.

Idaho↗

An update of hydrologic conditions and distribution of selected constituents in water, Eastern Snake River Plain aquifer and perched groundwater zones, Idaho National Laboratory, Idaho, emphasis 2016–18

Since 1952, wastewater discharged to infiltration ponds (also called percolation ponds) and disposal wells at the Idaho National Laboratory (INL) has affected water quality in the eastern Snake River Plain (ESRP) aquifer and perched groundwater zones underlying the INL. The U.S. Geological Survey (USGS), in cooperation with the U.S. Department of Energy, maintains groundwater-monitoring networks at the INL to determine hydrologic trends and to delineate the movement of radiochemical and chemical wastes in the aquifer and in perched groundwater zones. This report presents an analysis of water-level and water-quality data collected from the ESRP aquifer and perched groundwater wells in the USGS groundwater monitoring networks during 2016–18. From March–May 2015 to March–May 2018, water levels in wells completed in the ESRP aquifer declined in the northern part of the INL and increased in the southwestern part. Water-level decreases ranged from 0.5 to 3.0 feet (ft) in the northern part of the INL and increases ranged from 0.5 to 3.0 ft in the southwestern part. Detectable concentrations of radiochemical constituents in water samples from wells in the ESRP aquifer at the INL generally decreased or remained constant during 2016–18. Decreases in concentrations were attributed to radioactive decay, changes in waste-disposal methods, and dilution from recharge and underflow. In 2018, concentrations of tritium in water samples collected from 46 of 111 aquifer wells were greater than the reporting level of three times the sample standard deviation and ranged from 260±50 to 5,100±190 picocuries per liter (pCi/L). Tritium concentrations in water from 10 wells completed in deep perched groundwater above the ESRP aquifer near the Advanced Test Reactor (ATR) Complex generally were greater than or equal to the reporting level during at least one sampling event during 2016–18, and concentrations ranged from 150 ±50 to 12,900 ±200 pCi/L. Concentrations of strontium-90 in water from 17 of 60 ESRP aquifer wells sampled during April or October 2018 exceeded the reporting level, ranging from 2.2±0.7 to 363±19 pCi/L. Strontium-90 was not detected in the ESRP aquifer beneath the ATR Complex. During at least one sampling event during 2016–18, concentrations of strontium-90 in water from eight wells completed in deep perched groundwater above the ESRP aquifer at the ATR Complex equaled or exceeded the reporting levels, and concentrations ranged from 0.57±0.17 to 34.3±1.2 pCi/L. During 2016–18, concentrations of cesium-137 were less than the reporting level in all but one ESRP aquifer well, and concentrations of plutonium-238, -239, and -240 (undivided), and americium-241 were less than the reporting level in water samples from all ESRP aquifer wells. In April 2009, the dissolved chromium concentration in water from one ESRP aquifer well, USGS 65, south of the ATR Complex equaled the maximum contaminant level (MCL) of 100 micrograms per liter (μg/L). In April 2018, the concentration of chromium in water from that well had decreased to 76.0 μg/L, less than the MCL. Concentrations in water samples from 62 other ESRP aquifer wells sampled ranged from less than 0.6 to 21.6 μg/L. During 2016–18, dissolved chromium was detected in water from all wells completed in deep perched groundwater above the ESRP aquifer at the ATR Complex, and concentrations ranged from 4.2 to 98.8 μg/L. In 2018, concentrations of sodium in water from most ESRP aquifer wells in the southern part of the INL were greater than the western tributary background concentration of 8.3 milligrams per liter (mg/L). After the new percolation ponds were put into service in 2002 southwest of the Idaho Nuclear Technology and Engineering Center (INTEC), concentrations of sodium in water samples from the Rifle Range well increased steadily until 2008, when concentrations generally began decreasing. The increases and decreases were attributed to disposal variability in the new percolation ponds. During 2016–18, dissolved sodium concentrations in water from 18 wells completed in deep perched groundwater above the ESRP aquifer at the ATR Complex ranged from 6.37 to 143 mg/L. In 2018, concentrations of chloride in most water samples from ESRP aquifer wells south of the INTEC and at the Central Facilities Area exceeded the background concentrations. Chloride concentrations in water from wells south of the INTEC generally have decreased since 2002 when chloride disposal to the old percolation ponds was discontinued. After the new percolation ponds southwest of the INTEC were put into service in 2002, concentrations of chloride in water samples from one well rose steadily until 2008 then began decreasing. During 2016–18, dissolved chloride concentrations in deep perched groundwater above the ESRP aquifer from 18 wells at the ATR Complex ranged from 3.89 to 176 mg/L. In 2018, sulfate concentrations in water samples from ESRP aquifer wells in the south-central part of the INL exceeded the background concentration of sulfate and ranged from 22 to 151 mg/L. The greater-than-background concentrations in water from these wells probably resulted from sulfate disposal at the ATR Complex infiltration ponds or the old INTEC percolation ponds. In 2018, sulfate concentrations in water samples from wells near the Radioactive Waste Management Complex (RWMC) mostly were greater than background concentrations and could have resulted from well construction techniques and (or) waste disposal at the RWMC or the ATR complex. The maximum dissolved sulfate concentration in shallow perched groundwater above the ESRP aquifer near the ATR Complex was 215 mg/L in well CWP 3 in April 2016. During 2018, dissolved sulfate concentrations in water from wells completed in deep perched groundwater above the ESRP aquifer near the cold-waste ponds at the ATR Complex ranged from 65.8 to 171 mg/L. In 2018, concentrations of nitrate in water from most ESRP aquifer wells at and near the INTEC exceeded the western tributary background concentration of 0.655 mg/L. Concentrations of nitrate in wells southwest of the INTEC and farther away from the influence of disposal areas and the Big Lost River show a general decrease in nitrate concentration through time. Two wells south of the INTEC show increasing trends that could be the result of wastewater beneath the INTEC tank farm being mobilized to the aquifer. During 2016–18, water samples from several ESRP aquifer wells were collected and analyzed for volatile organic compounds (VOCs). Sixteen VOCs were detected. At least 1 and as many as 7 VOCs were detected in water samples from 15 wells. The primary VOCs detected include carbon tetrachloride, trichloromethane, tetrachloroethene, 1,1,1-trichloroethane, and trichloroethene. In 2016–18, concentrations for all VOCs were less than their respective MCLs for drinking water, except carbon tetrachloride in water from two wells and trichloroethene in one well. During 2016–18, variability and bias were evaluated from 37 replicate and 15 blank quality-assurance samples. Results from replicate analyses were investigated to evaluate sample variability. Constituents with acceptable reproducibility were major ions, trace elements, nutrients, and VOCs. All radiochemical constituents had acceptable reproducibility except for gross alpha- and beta-particle radioactivity. The gross alpha- and beta-particle radioactivity samples that did not meet reproducibility criteria had low concentrations. Bias from sample contamination was evaluated from equipment, field, and source-solution blanks. Cadmium had a concentration slightly greater than its reporting level in a source-solution blank, and chloride and ammonia had concentrations that were slightly greater than their respective reporting levels in field and equipment blanks. Subtracting concentrations of chloride and ammonia in field blanks from the concurrently collected equipment blank indicates that adjusted concentrations for chloride and ammonia in the equipment blanks were less than their respective reporting levels. Therefore, no sample bias was observed for any of the sample periods.

Idaho↗

Leaching of trace elements from Pittsburgh coal mill rejects compared with coal combustion products from a coal-fired power plant in Ohio, USA

We investigated the leachability of elements from mill rejects from the high-sulfur, bituminous Upper Pennsylvanian Pittsburgh coal, using the synthetic groundwater leaching procedure (SGLP), long-term leaching (LTL), and the U.S. Environmental Protection Agency's (EPA's) toxicity characteristic leaching procedure (TCLP), and compared their leaching behavior with that of three coal combustion products (CCPs)—bottom ash, economizer fly ash , and fly ash—from the same coal. None of the environmentally hazardous Resource Conservation and Recovery Act of 1976 (RCRA) metals analyzed in the leachates from the mill rejects or the CCPs exceeded U.S. EPA toxicity characteristics (As, Ba, Cd, Cr, Hg, Pb, and Se). Most trace elements leached the least from mill rejects and bottom ash and leached the most from fly ash. The elements Ca, Co, Mg, Mn, and Sr, however, were more concentrated in mill reject leachates than CCP leachates. Most trace elements increased in concentration with increasing SGLP and LTL leaching duration, but As and V decreased in concentration with time in mill reject leachates, suggesting sorption or precipitation of these elements was occurring.

Ohio↗

Trace and minor element variations and sulfur isotopes in crystalline and colloform ZnS: Incorporation mechanisms and implications for their genesis

Various models have been proposed to explain the formation mechanism of colloform sphalerite, but the origin is still under debate. In order to decipher influences on trace element incorporation and sulfur isotope composition, crystalline and colloform sphalerite from the carbonate-hosted Mississippi-Valley Type (MVT) deposit near Wiesloch, SW Germany, were investigated and compared to sphalerite samples from 52 hydrothermal vein-type deposits in the Schwarzwald ore district, SW Germany to study the influence of different host rocks, formation mechanisms and fluid origin on trace element incorporation. Trace and minor element incorporation in sphalerite shows some correlation to their host rock and/or origin of fluid, gangue, paragenetic minerals and precipitation mechanisms (e.g., diagenetic processes, fluid cooling or fluid mixing). Furthermore, crystalline sphalerite is generally enriched in elements like Cd, Cu, Sb and Ag compared to colloform sphalerite that mainly incorporates elements like As, Pb and Tl. In addition, sulfur isotopes are characterized by positive values for crystalline and strongly negative values for colloform sphalerite. The combination of trace element contents, typical minerals associated with colloform sphalerite from Wiesloch, sulfur isotopes and thermodynamic considerations helped to evaluate the involvement of sulfate-reducing bacteria in water-filled karst cavities. Sulfate-reducing bacteria cause a sulfide-rich environment that leads in case of a metal-rich fluid supply to a sudden oversaturation of the fluid with respect to galena, sphalerite and pyrite. This, however, exactly coincides with the observed crystallization sequence of samples involving colloform sphalerite from the Wiesloch MVT deposit.

Wiesloch↗

Assessment of diel cycling in nutrients and trace elements in the Eagle River Basin, 2017–18

Diel cycles are known to occur in all types of waters, and increasing studies indicate routine water samples may not provide an accurate snapshot in concentrations of trace elements and nutrients. Diel behavior in neutral to alkaline pH ranges is independent of streamflow variability and concentration. Extensive historical U.S. Geological Survey (USGS) water-quality data have been collected in the Eagle River Basin during daylight hours, which is defined as the period of time between one-half hour prior to sunrise and one-half hour after sunset. However, no USGS data have been collected throughout the nighttime, defined as the time between one-half hour after sunset and one-half hour prior to sunrise, making the evaluation of diel cycles impossible. To assess the importance of diel cycling within the Eagle River Basin, the USGS, in cooperation with Eagle River Watershed Council, developed a study to assess the mechanisms, patterns, and magnitude of change during the diel cycle for selected constituents. Water-quality monitors at five USGS streamgage sites (09065500, Gore Creek at Upper Station, near Minturn, Colorado, 09063000, Eagle River at Red Cliff, Colorado, 09064600, Eagle River near Minturn, Colorado, 09066325, Gore Creek above Red Sandstone Creek at Vail, Colorado, and 394220106431500, Eagle River below Milk Creek near Wolcott, Colorado) were deployed in 2017 to evaluate the water-quality field parameters and to determine if water conditions were favorable for the diel cycling of nutrients and trace elements. Based on the evaluation of water-quality parameters, three of the five sites were sampled for nutrient and trace-element concentrations in 2018 to confirm the presence and magnitude of diel cycling. Historical data were also analyzed to assess the effect of time of day on measured nutrient and trace-element concentrations. An assessment of the effect of land use on diel cycling was also investigated. Measurable nutrients displayed a diel cycle at all three sites with the largest percentage change at the most downstream site (394220106431500), located on the Eagle River. More notable diel cycles at this site include filtered nitrate plus nitrite, which varied 179 percent, with concentrations from 0.24 to 0.67 milligrams per liter (mg/L) and filtered orthophosphate, which varied 71 percent, with concentrations from 0.07 to 0.12 mg/L. Filtered nitrate plus nitrite at site 09066325 varied 57 percent, ranging from 0.14 to 0.22 mg/L. Maximum concentrations occurred prior to noon, decreased through the afternoon (between noon and sunset), and increased during the night (between sunset and sunrise). That pattern is consistent with nutrient uptake in response to daytime (between sunrise and sunset) photosynthesis along with biologically driven denitrification and nitrification cycles. Nutrient concentrations at sites 09064600 and 09066325 were generally low and below laboratory reporting limits, which is the smallest measured concentration that nutrients could be measured by a given analytical method. Trace-element concentrations were detectable at all sites with the largest percentage change at the most downstream site (394220106431500) and exhibited diel concentration variation from 11.6 to 284 percent. Appreciable diel cycles included filtered copper (0.98–1.40 micrograms per liter [µg/L], 42.9 percent), filtered zinc (less than [<] 4.00–5.50 µg/L, greater than [>] 37.5 percent), total manganese (9.70–19.5 µg/L, 101 percent), and total arsenic (0.30–0.40 µg/L, 33.3 percent). The largest percentage change in concentration was filtered manganese (2.84–10.9 µg/L, 284 percent). Diel cycles at site 09064600 ranged from 9.1 to 64.5 percent across the trace elements measured. Dissolved trace elements with appreciable diel cycles during the sampling period include filtered cadmium (0.09–0.12 µg/L, 33.3 percent), filtered copper (0.99–1.40 µg/L, 41.4 percent), and total arsenic (0.20–0.30 µg/L, 50 percent). The largest percentage change was filtered zinc (38.3–63.0 µg/L, 65 percent). Trace-element concentrations at site 09066325 were below laboratory reporting limits for many parameters, and no diel cycle could be assessed for these parameters. However, total recoverable iron, filtered barium, filtered manganese, and filtered selenium exhibited changes in concentrations of <10.0–19.4 µg/L (>94 percent), 115–121 µg/L (5 percent), 1.44–1.72 µg/L (19.4 percent), and 0.25–0.28 µg/L (12 percent), respectively. At sites 09064600 and 394220106431500, maximum trace-element concentrations occurred during nighttime with some variation regarding the timing of the peak. The exceptions to this were filtered copper, total arsenic, and filtered selenium, which had maximum concentrations around noon or as the sun disappeared below the horizon. The timing of minimum concentrations occurred in the afternoon for many trace elements, with filtered copper, total arsenic, and filtered selenium having minimum concentrations in the morning or just prior to the appearance of the sun. Analysis of historical data also showed evidence of diel cycling. Historical samples collected from July through October were used to identify diel cycling in base-flow conditions. The resulting diel pattern in the median concentration for filtered manganese, filtered zinc at water-quality site 09064600, and filtered manganese and filtered nitrate plus nitrite at water-quality site 39422016431500 were consistent with the diel pattern in the September 2018 samples, and indicate time of day can bias sampling results even during daylight hours. Diel cycling in the Eagle River Basin appears to be driven primarily by instream, biological processes. However, land use, particularly human effects downstream from urban areas, mining, and agriculture, may affect these processes. At some locations, diel variations in nutrient and trace-element concentrations are small enough to be of low concern. At other locations, however, variations in concentrations up to 284 percent in the data collected for this study and 214 percent in base-flow historical data, indicate daytime-only sampling, particularly in late afternoon, can underestimate daily average nutrient and trace-element concentrations. When feasible, the potential of diel cycling warrants consideration in sample design to account for the potential of diel cycles, or at a minimum, be recognized as a component of the river dynamic and the potential consequences that diel cycles may have in data interpretation and river management decisions.

Colorado↗

Review of Trace-Element Field-Blank Data Collected for the California Groundwater Ambient Monitoring and Assessment (GAMA) Program, May 2004-January 2008

Trace-element quality-control samples (for example, source-solution blanks, field blanks, and field replicates) were collected as part of a statewide investigation of groundwater quality in California, known as the Priority Basins Project of the Groundwater Ambient Monitoring and Assessment (GAMA) Program. The GAMA Priority Basins Project is being conducted by the U.S. Geological Survey (USGS) in cooperation with the California State Water Resources Control Board (SWRCB) to assess and monitor the quality of groundwater resources used for drinking-water supply and to improve public knowledge of groundwater quality in California. Trace-element field blanks were collected to evaluate potential bias in the corresponding environmental data. Bias in the environmental data could result from contamination in the field during sample collection, from the groundwater coming into contact with contaminants on equipment surfaces or from other sources, or from processing, shipping, or analyzing the samples. Bias affects the interpretation of environmental data, particularly if any constituents are present solely as a result of extrinsic contamination that would have otherwise been absent from the groundwater that was sampled. Field blanks were collected, analyzed, and reviewed to identify and quantify extrinsic contamination bias. Data derived from source-solution blanks and laboratory quality-control samples also were considered in evaluating potential contamination bias. Eighty-six field-blank samples collected from May 2004 to January 2008 were analyzed for the concentrations of 25 trace elements. Results from these field blanks were used to interpret the data for the 816 samples of untreated groundwater collected over the same period. Constituents analyzed were aluminum (Al), antimony (Sb), arsenic (As), barium (Ba), beryllium (Be), boron (B), cadmium (Cd), chromium (Cr), cobalt (Co), copper (Cu), iron (Fe), lead (Pb), lithium (Li), manganese (Mn), mercury (Hg), molybdenum (Mo), nickel (Ni), selenium (Se), silver (Ag), strontium (Sr), thallium (Tl), tungsten (W), uranium (U), vanadium (V), and zinc (Zn). The detection frequency and the 90th percentile concentration at greater than 90 percent confidence were determined from the field-blank data for each trace element, and these results were compared to each constituent's long-term method detection level (LT-MDL) to determine whether a study reporting level (SRL) was necessary to ensure that no more than 10 percent of the detections in groundwater samples could be attributed solely to contamination bias. Only two of the trace elements analyzed, Li and Se, had zero detections in the 86 field blanks. Ten other trace elements (Sb, As, Be, B, Cd, Co, Mo, Ag, Tl, and U) were detected in fewer than 5 percent of the field blanks. The field-blank results for these constituents did not necessitate establishing SRLs. Of the 13 constituents that were detected in more than 5 percent of the field blanks, six (Al, Ba, Cr, Mn, Hg, and V) had field-blank results that indicated a need for SRLs that were at or below the highest laboratory reporting levels (LRL) used during the sampling period; these SRLs were needed for concentrations between the LT-MDLs and LRLs. The other seven constituents with detection frequencies above 5 percent (Cu, Fe, Pb, Ni, Sr, W, and Zn) had field-blank results that necessitated SRLs greater than the highest LRLs used during the study period. SRLs for these seven constituents, each set at the 90th percentile of their concentrations in the field blanks, were at least an order of magnitude below the regulatory thresholds established for drinking water for health or aesthetic purposes; therefore, reporting values below the SRLs as less than or equal to (=) the measured value would not prevent the identification of values greater than the drinking-water thresholds. The SRLs and drinking-water thresholds, respectively, for these 7 trace elements are Cu (1.7 ?g/L and 1,300

Scientific Investigations Report↗

Transient effects on groundwater chemical compositions from pumping of supply wells at the Nevada National Security Site, 1951-2008

Nuclear testing and support activities at the Nevada National Security Site have required large amounts of water for construction, public consumption, drilling, fire protection, hydraulic and nuclear testing, and dust control. To supply this demand, approximately 20,000 million gallons of water have been pumped from 23 wells completed in 19 boreholes located across the Nevada National Security Site starting as early as the 1950s. As a consequence of more or less continuous pumping from many of these wells for periods as long as 58 years, transient groundwater flow conditions have been created in the aquifers that supplied the water. To evaluate whether long-term pumping caused changes in water compositions over time, available chemical analyses of water samples from these 19 boreholes were compiled, screened, and evaluated for variability including statistically significant temporal trends that can be compared to records of groundwater pumping. Data used in this report have been extracted from a large database (Geochem08, revision 3.0, released in September 2008) containing geochemical and isotopic information created and maintained by primary contractors to the U.S. Department of Energy, National Nuclear Security Administration, Nevada Site Office. Data extracted from this source were compiled for the entire period of record, converted to uniform reporting units, and screened to eliminate analyses of poor or unknown quality, as well as clearly spurious values. The resulting data are included in accompanying spreadsheets that give values for (1) pH and specific conductance, (2) major ion concentrations, (3) trace element concentrations and environmental isotope ratios, and (4) mean, median, and variance estimates for major ion concentrations. The resulting data vary widely in quality and time-series density. An effort has been made to establish reasonable ranges of analytical uncertainty expected for each analyte and eliminate analyses that are obvious outliers. Analysis of chemical trends in this report primarily rely on specific conductance measurements and major ion concentrations, data considered to be the most accurate and reliable over the entire time span of investigation. The analysis uses parametric and non-parametric evaluations to provide a statistical basis for trend identification. Trace element and isotope data are examined for consistency, but typically are too inaccurate or infrequent to provide a reliable long term basis for trend evaluation. Groundwater withdrawal records compiled in a companion report are included graphically in this report to allow qualitative comparisons between water quality and pumping history. Data for each supply well include (1) a borehole description and summary of pumping history, (2) a description of water-quality parameters, (3) an evaluation of temporal variations of specific conductance and major ion concentrations, and (4) an examination of supporting information from trace element and isotope data. A range of responses are observed for individual supply wells that likely include the effects of both aquifer dynamics and changing borehole conditions. Data from most wells show little or no evidence for temporal variation in water-quality parameters indicating that aquifers at the Nevada National Security Site are capable of producing large volumes of compositionally uniform water over many years of pumping. A smaller number of wells show evidence of transient changes. Wells that have ceased pumping commonly show compositions that shift toward lower concentrations in subsequent bailed samples, which indicates that more dilute water entered the well over time due to either leakage of meteoric water into the well casing or more wide-spread recharge into the shallow phreatic zone. Wells that show systematic changes in water compositions during episodes of pumping commonly have multiple open intervals whose contributions to water in the well may change over time due to hydraulic conditions or well dynamics.

Nevada↗

Trace elements and synthetic organic compounds in streambed sediment and fish tissue in the Great and Little Miami River basins, Ohio and Indiana, 1990-98

Streambed-sediment and fish-tissue samples were collected at eight sites in the Great and Little Miami Basins as part of the U.S. Geological Survey's National Water Quality Assessment Program. The samples were analyzed for trace elements and synthetic organic compounds, including organochlorine insecticides, polychlorinated biphenyls (PCBs), and semivolatile compounds (SVOCs). Data from state-agency investigations within the study unit (more than 200 sites) were incorporated to gain a broader perspective of the occurrence and distribution of contaminants in the study unit. All data were compared to streambed-sediment-quality guidelines and fish-tissue guidelines to identify elevated contaminant concentrations. Guideline exceedances were plotted on distribution maps to identify areas in the study unit that may be of potential concern for wildlife health. Several trace elements were detected in both sediment and fish-tissue samples. In sediment, lead and zinc were most frequently detected at levels that may have adverse effects on aquatic organisms. Generally, only one of the trace elements analyzed for per site exceeded concentrations above which adverse biological effects are frequently anticipated. Organochlorine insecticides were infrequently detected in sediment or fish tissue throughout the study unit. More organochlorine insecticides were detected in fish tissues than in sediment; however, more guidelines were exceeded in sediment. No distinct geographic overlap between sediment and fish-tissue sites was evident with respect to elevated organochlorine insecticide concentrations. Sediment-quality guideline exceedances were generally widespread throughout the study unit, whereas fish-tissue guidelines were exceeded only on the Mad River. PCBs were detected more often in fish tissue than in sediment throughout the study unit. Elevated PCB concentrations in fish tissue were common and widespread. No distinct geographic overlap of PCB exceedances was evident between sediment and fish-tissue sites. In sediments, elevated concentrations were detected most often for SVOCs, particularly for polycyclic aromatic hydrocarbons (PAHs). Areas where SVOC guidelines were frequently exceeded include the Great Miami River main stem from Dayton to south of Hamilton, and the Upper Little Miami River Basin in Greene County. Overall, a higher frequency of trace-element detections in fish tissue and sediment trace-element guideline exceedances was found in the Great Miami River Basin than in the Little Miami River Basin. Organochlorine insecticide guidelines for fish tissue and sediment, as well as PCB and SVOC guidelines for sediment also were exceeded more frequently in the Great Miami River Basin. PCB guideline exceedances for fish tissue were found more often in the Little Miami River Basin.

Water-Resources Investigations Report↗

Updated study reporting levels (SRLs) for trace-element data collected for the California Groundwater Ambient Monitoring and Assessment (GAMA) Priority Basin Project, October 2009-March 2013

Groundwater samples have been collected in California as part of statewide investigations of groundwater quality conducted by the U.S. Geological Survey for the Groundwater Ambient Monitoring and Assessment (GAMA) Priority Basin Project (PBP). The GAMA-PBP is being conducted in cooperation with the California State Water Resources Control Board to assess and monitor the quality of groundwater resources used for drinking-water supply and to improve public knowledge of groundwater quality in California. Quality-control samples (source-solution blanks, equipment blanks, and field blanks) were collected in order to ensure the quality of the groundwater sample results. Olsen and others (2010) previously determined study reporting levels (SRLs) for trace-element results based primarily on field blanks collected in California from May 2004 through January 2008. SRLs are raised reporting levels used to reduce the likelihood of reporting false detections attributable to contamination bias. The purpose of this report is to identify any changes in the frequency and concentrations of detections in field blanks since the last evaluation and update the SRLs for more recent data accordingly. Constituents analyzed were aluminum (Al), antimony (Sb), arsenic (As), barium (Ba), beryllium (Be), boron (B), cadmium (Cd), chromium (Cr), cobalt (Co), copper (Cu), iron (Fe), lead (Pb), lithium (Li), manganese (Mn), molybdenum (Mo), nickel (Ni), selenium (Se), silver (Ag), strontium (Sr), thallium (Tl), tungsten (W), uranium (U), vanadium (V), and zinc (Zn). Data from 179 field blanks and equipment blanks collected from March 2006 through March 2013 by the GAMA-PBP indicated that for trace elements that had a change in detection frequency and concentration since the previous review, the shift occurred near October 2009, in conjunction with a change in the capsule filters used by the study. Results for 89 field blanks and equipment blanks collected from October 2009 through March 2013 were evaluated for potential contamination bias by using the same approach developed by Olsen and others (2010). Some data collected by the National Water-Quality Assessment (NAWQA) Program for the Southern California Coastal Drainages study unit were included to supplement the GAMA-PBP data. The detection frequency and upper threshold of potential contamination bias (BD-90/90) were determined from field-blank and equipment-blank data for each trace element. The BD-90/90 is the 90th percentile concentration of potential extrinsic contamination calculated by using the binomial probability distribution for greater than 90 percent confidence. Additionally, data from laboratory blanks and blind blanks analyzed by the National Water Quality Laboratory (NWQL) during water years 2010 through 2013, and compiled by the USGS Branch of Quality Systems (BQS), were considered for each trace element. These results were compared to each constituent’s reporting level to determine whether an SRL was necessary to minimize the potential for detections in the groundwater samples, attributed principally to contamination bias. Results of the evaluation were used to set SRLs for trace-element data for about 1,135 samples of groundwater collected by the GAMA-PBP between October 2009 and March 2013. Ten trace elements analyzed (Sb, As, Be, B, Cd, Li, Se, Ag, Tl, and U) had blank results that did not necessitate establishing SRLs during this review or the review by Olsen and others (2010). Five trace elements analyzed (Al, Ba, Cr, Sr, and V) had blank results that necessitated establishing an SRL during the previous review but did not need an SRL starting October 2009. One trace element (Fe) had field and laboratory-blank results that necessitated keeping the previous SRL (6 micrograms per liter [μg/L]). Two trace elements (Ni and W) had quality-control results that warranted decreasing the previous SRL, and five trace elements (Cu, Pb, Mn, Mo, and Zn) had field, laboratory, or blind blank results that warranted establishing an SRL for the first time or increasing the previous SRL. SRLs for Cu (2.1 μg/L), Pb (0.82 μg/L), Mn (0.66 μg/L), Mo (0.023 μg/L), Ni (0.21 μg/L), W (0.023 μg/L), and Zn (6.2 μg/L) were changed to these levels starting October 2009, based on the BD-90/90 concentration for field blanks or the 99th percentile concentration for laboratory or blind blanks. The SRL for Fe was maintained at 6 μg/L, based on the minimum laboratory reporting level for iron. SRLs for these eight constituents were at least an order of magnitude below the regulatory benchmarks established for drinking water for health and aesthetic purposes; therefore, the practice of reporting concentrations below the SRLs as less than or equal to (≤) the measured value would not prevent the identification of values greater than the drinking-water benchmarks. Co was detected in 99 percent of field blanks, and with a BD-90/90 concentration of 0.38 μg/L, all groundwater results starting October 2009 were coded as “reviewed and rejected.” Co does not currently have a regulatory benchmark for drinking water. The primary sources of contamination for trace elements inferred from this review are the equipment or processes used in the field to collect the samples or in the laboratory. In particular, contamination in field blanks of Co and Mn was attributed to the high-capacity 0.45-micrometer pore-size capsule filters that were in regular use beginning in October 2009 by several USGS programs, including the GAMA-PBP and NAWQA Program, for filtering samples for analysis of trace elements. The SRLs determined in this report are intended to be used for GAMA groundwater-quality data for samples collected October 2009 through March 2013, or for as long as quality-control data indicate contamination similar to what was observed in this report; quality-control data should be continuously reviewed and SRLs re-assessed on at least a study-unit basis.

California↗

Petrogenesis of the Apollo 14 high-alumina basalts: Implications from ion microprobe analyses

In this study, ion microprobe analyses of individual minerals are used to investigate the petrogenesis of the Apollo 14 high-Al basalts. We use trace element concentrations from individual minerals in the Apollo 14 high-Al basalts to evaluate both endogenic and exogenic models. The data show that if the Apollo 14 high-Al basalts were produced by melting within the lunar mantle, these basalts cannot be related to one another by closed-system fractional crystallization of a single basaltic melt. Rather, the trace element data show that variable amounts of a KREEP component were added to the basalts by either assimilation, mixing into mantle sources, or impact melting. Single-stage assimilation–fractional crystallization models can only explain the data from this study if an excessively large mass of urKREEP is assimilated into the parent magma before olivine crystallization. Alternatively, the trace element data can be explained if the Apollo 14 high-Al basalts were produced by melting multiple Al-rich mantle sources that contain different amounts of urKREEP. Finally, for impact melting to be a relevant process, the data require that multiple large impact melts be formed from mixed KREEP-rich target lithologies. The resulting impact melts must then crystallize to produce basalts with igneous textures, high Al 2 O 3 concentrations, uniform major element compositions, and a wide range of incompatible trace element concentrations.

Geochimica et Cosmochimica Acta↗

SUBMICROSCOPIC ( less than 1 mu m) MINERAL CONTENTS OF VITRINITES IN SELECTED BITUMINOUS COAL BEDS.

An important aspect of the petrographic description of coal is the characterization of coal quality, including chemical attributes. For geologic investigations, data on the concentrations, distribution, and modes of occurrence of minor and trace elements provide a basis for reconstructing the probable geochemical environment of the swamp material that was converted into peat, and the geochemical conditions that prevailed during and subsequent to coalification. We have been using electron (EPMA) and proton (PIXE) microprobe analytical methods to obtain data on the chemical characteristics of specific coal constituents in their original associations within coal samples. The present study is aimed at evaluation of the nature of mineral occurrences and heterogeneous elemental concentrations within vitrinites. Vitrinites are usually the most abundant, and therefore most important, maceral group in bituminous coal. 8 refs.

Conference Paper↗