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At least 937 records · Page 52Linked to original sources
USGS2012

Geochemical modeling of changes in shallow groundwater chemistry observed during the MSU-ZERT CO2 injection experiment

A field experiment involving the release of carbon dioxide (CO 2 ) into a shallow aquifer was conducted near Bozeman, Montana, during the summer of 2008, to investigate the potential groundwater quality impacts in the case of leakage of CO 2 from deep geological storage. As an essential part of the Montana State University Zero Emission Research and Technology (MSU-ZERT) field program, food-grade CO 2 was injected over a 30 day period into a horizontal perforated pipe a few feet below the water table of a shallow aquifer. The impact of elevated CO 2 concentrations on groundwater quality was investigated by analyzing water samples taken before, during, and following CO 2 injection, from observation wells located in the vicinity of the injection pipe, and from two distant monitoring wells. Field measurements and laboratory analyses showed rapid and systematic changes in pH, alkalinity, and conductance, as well as increases in the aqueous concentrations of naturally occurring major and trace element species. The geochemical data were evaluated using principal component analysis (PCA) to (1) understand potential correlations between aqueous species, and (2) to identify minerals controlling the chemical composition of the groundwater prior to CO 2 injection. These evaluations were used to assess possible geochemical processes responsible for the observed increases in the concentrations of dissolved constituents, and to simulate these processes using a multicomponent reaction path model. Reasonable agreement between observed and modeled data suggests that (1) calcite dissolution was the primary pH buffer, yielding increased Ca +2 concentrations in the groundwater, (2) increases in the concentrations of most major and trace metal cations except Fe could be a result of Ca +2 -driven exchange reactions, (3) the release of anions from adsorption sites due to competitive adsorption of carbonate could explain the observed trends of most anions, and (4) the dissolution of reactive Fe minerals (presumed ferrihydrite and fougerite, from thermodynamic analyses) could explain increases in total Fe concentration. Highlights ► Because the possibility of CO 2 leakage cannot be completely ruled out, the potential impact of CO 2 intrusion on the quality of fresh water aquifers overlying CO 2 storage sites needs to be investigated. ► Geochemical data from a field experiment involving the release of carbon dioxide (CO 2 ) into a shallow aquifer were evaluated. ► Geochemical model used to assess possible geochemical processes responsible for the observed increases in the concentrations of dissolved constituents. ► Reasonable agreement between observed and modeled data suggests that increases in the concentrations of most major and trace metal cations except Fe could be a result of Ca +2 -driven exchange reactions and the release of anions from adsorption sites due to competitive adsorption of carbonate could explain the observed trends of most anions.

Montana↗
USGS2003

Chemistry and age of ground water in the southwestern Hueco Bolson, New Mexico and Texas

This report, prepared in cooperation with El Paso Water Utilities, presents the results of an investigation to determine the chemistry and age of ground water on the southwestern side of the Hueco Bolson. The radioactive isotope carbon-14 was used to estimate the length of time that water from wells has been isolated from the atmosphere, which is the modern carbon-14 reservoir. Nine wells on the southwestern side of the Hueco Bolson were sampled for analysis of common constituents, nutrients, total organic carbon, trace elements, stable isotopes, and radioactive isotopes. Dissolved-solids concentrations in water from the wells sampled ranged from 269 to 2,630 milligrams per liter. Sodium concentrations generally increased linearly with chloride concentrations, possibly indicating mixing of dilute recharge water with sodium chloride brine. Concentrations of nutrients and trace elements generally were small. The deuterium and oxygen-18 composition in all samples except those from wells adjacent to the Rio Grande indicates that infiltration of precipitation is the main source of water to these wells and that evaporation has not affected the isotopic composition of the water. The source of water from wells adjacent to the Rio Grande is probably not the same source as the water from wells adjacent to the Franklin Mountains. The calculated apparent carbon-14 ages ranged from 12,100 to 25,500 years.

Water-Resources Investigations Report↗
USGS2008

Environmental chemical data for perishable sediments and soils collected in New Orleans, Louisiana, and along the Louisiana Delta following Hurricanes Katrina and Rita, 2005

In October 2005, nearly one month after Hurricanes Katrina and Rita, a team of scientists from the U.S. Geological Survey and the Missouri University of Science and Technology deployed to southern Louisiana to collect perishable environmental data resulting from the impacts of these storms. Perishable samples collected for this investigation are subject to destruction or ruin by removal, mixing, or natural decay; therefore, collection is time-critical following the depositional event. A total of 238 samples of sediment, soil, and vegetation were collected to characterize chemical quality. For this analysis, 157 of the 238 samples were used to characterize trace element, iron, total organic carbon, pesticide, and polychlorinated biphenyl concentrations of deposited sediment and associated shallow soils. In decreasing order, the largest variability in trace element concentration was detected for lead, vanadium, chromium, copper, arsenic, cadmium, and mercury. Lead was determined to be the trace element of most concern because of the large concentrations present in the samples ranging from 4.50 to 551 milligrams per kilogram (mg/kg). Sequential extraction analysis of lead indicate that 39.1 percent of the total lead concentration in post-hurricane sediment is associated with the iron-manganese oxide fraction. This fraction is considered extremely mobile under reducing environmental conditions, thereby making lead a potential health hazard. The presence of lead in post-hurricane sediments likely is from redistribution of pre-hurricane contaminated soils and sediments from Lake Pontchartrain and the flood control canals of New Orleans. Arsenic concentrations ranged from 0.84 to 49.1 mg/kg. Although Arsenic concentrations generally were small and consistent with other research results, all samples exceeded the U.S. Environmental Protection Agency’s Human Health Medium-Specific Screening Level of 0.39 mg/kg. Mercury concentrations ranged from 0.02 to 1.30 mg/kg. Comparing the mean mercury concentration present in post-hurricane samples with regional background data from the U.S. Geological Survey National Geochemical Dataset, indicates that mercury concentrations in post-hurricane sediment generally are larger. Sequential extraction analysis of 51 samples for arsenic indicate that 54.5 percent of the total arsenic concentration is contained in the extremely mobile iron-manganese oxide fraction. Pesticide and polychlorinated biphenyl Arochlor concentrations in post-hurricane samples were small. Prometon was the most frequently detected pesticide with concentrations ranging from 2.4 to 193 micrograms per kilogram (µg/kg). Methoxychlor was present in 22 samples with a concentration ranging from 3.5 to 3,510 µg/kg. Although methoxychlor had the largest detected pesticide concentration, it was well below the U.S. Environmental Protection Agency’s High-Priority Screening Level for residential soils. Arochlor congeners were not detected for any sample above the minimum detection level of 7.9 µg/kg.

Louisiana↗
USGS2006

Ground-water quality data in the north San Francisco Bay hydrologic provinces, California, 2004: Results from the California Ground-water Ambient Monitoring and Assessment (GAMA) program

Ground-water quality in the ~1,000 square-mile (mi2) North San Francisco Bay study unit was investigated from August to November, 2004, as part of the California Groundwater Ambient Monitoring and Assessment (GAMA) program. Samples were collected from 89 public-supply wells, 7 hydrothermal wells, and 1 hydrothermal spring in Napa, Sonoma and Marin Counties. Eighty-four of the public-supply wells sampled were selected to provide a spatially distributed, randomized monitoring network for statistical calculations and constituent detection frequency. The study was designed to provide a spatially-unbiased assessment of raw ground-water quality within the study unit, as well as a statistically-consistent basis for comparing the water quality of different study units. Ground-water samples were analyzed for major and minor ions, trace elements, nutrients, volatile organic compounds, pesticides and pesticide degradates, waste-water indicators, dissolved methane, nitrogen, carbon dioxide and noble gases (in collaboration with Lawrence Livermore National Laboratory). Naturally occurring isotopes (tritium, carbon-14, oxygen-18, deuterium and helium-4) also were measured in the samples to help identify the source and age of the ground water. Results show that no anthropogenic constituents were detected at concentrations higher than those levels set for regulatory purposes, and relatively few naturally-occurring constituents were detected at concentrations greater than regulatory levels. In this study, 21 of the 88 volatile organic compounds (VOCs) and gasoline additives and (or) oxygenates investigated were detected in ground-water samples, however, detected concentrations were one-half to one-forty-thousandth the maximum contaminant levels (MCL). Thirty-two percent of the randomized wells sampled had at least a single detection of a VOC or gasoline additive and (or) oxygenate. The most frequently detected compounds were chloroform, found in 12 of the 84 randomized wells; carbon disulfide, found in 8 of the 84 randomized wells; and toluene, found in 4 of the 84 randomized wells. Trihalomethanes were the most frequently detected class of VOCs. Nine of the 122 pesticides and (or) pesticide degradates investigated were detected in ground-water samples, however, concentrations were one-seventieth to one-eight-hundredth the MCLs. Seventeen percent of the randomized wells sampled had at least a single detection of pesticide and pesticide degradate. Herbicides were the most frequently detected class of pesticides. The most frequently detected compound was simazine, found in 8 of the 84 of the randomized wells. Chlordiamino-s-triazine and deisopropyl atrazine were both found in 2 of the 84 randomized wells sampled. Thirteen out of 63 compounds that may be indicative of the prescence of waste-water were detected in ground-water samples. Twenty-six percent of the randomized wells sampled for waste-water indicators had at least one detection. Isophorone was the most frequently detected in 6 of the 84 randomized wells. Bisphenol-A, caffeine, and indole each were detected in 3 of the 84 randomized wells. Major and minor ions and dissolved solids (DS) samples were collected at 33 public-supply wells; 3 samples had DS concentrations above the secondary maximum contaminant level (SMCL) of 500 mg/L. Ground-water samples from 32 public-supply wells were analyzed for trace elements. Arsenic concentrations above the MCL of 10 μg/L were measured at 4 public-supply wells, boron concentrations above the detection level for the purpose of reporting (DLR) of 100 μg/L were measured at 19 wells. Iron concentrations above the SMCL of 300 μg/L were measured at 7 wells, a lead concentration above the California notification level (NL) of 15 μg/L at one well, and manganese concentrations above the SMCL of 50 μg/L were measured at 17 wells. Vanadium concentrations above the DLR of 3 μg/L were measured at 9 public-supply wells; and chromium(VI) concentrations above the DLR of 1 μg/L were measured at 48 public-supply wells. Major and minor ions and dissolved solids (DS) samples were collected at 33 public-supply wells; 3 samples had DS concentrations above the secondary maximum contaminant level (SMCL) of 500 mg/L. Ground-water samples from 32 public-supply wells were analyzed for trace elements. Arsenic concentrations above the MCL of 10 μg/L were measured at 4 public-supply wells, boron concentrations above the detection level for the purpose of reporting (DLR) of 100 μg/L were measured at 19 wells. Iron concentrations above the SMCL of 300 μg/L were measured at 7 wells, a lead concentration above the California notification level (NL) of 15 μg/L at one well, and manganese concentrations above the SMCL of 50 μg/L were measured at 17 wells. Vanadium concentrations above the DLR of 3 μg/L were measured at 9 public-supply wells; and chromium(VI) concentrations above the DLR of 1 μg/L were measured at 48 public-supply wells. Microbial constituents were analyzed in 22 ground-water samples. Total coliform was detected in three wells. Counts ranged from 2 colonies per 100 mL to 20 colonies per 100 mL. MCLs for microbial constituents are based on reoccurring detection, and will be monitored during future sampling.

California↗
USGS2009

Groundwater quality data in the Mojave study unit, 2008: Results from the California GAMA Program

Groundwater quality in the approximately 1,500 square-mile Mojave (MOJO) study unit was investigated from February to April 2008, as part of the Priority Basin Project of the Groundwater Ambient Monitoring and Assessment (GAMA) Program. The GAMA Priority Basin Project was developed in response to the Groundwater Quality Monitoring Act of 2001 and is being conducted by the U.S. Geological Survey (USGS) in cooperation with the California State Water Resources Control Board (SWRCB). MOJO was the 23rd of 37 study units to be sampled as part of the GAMA Priority Basin Project. The MOJO study was designed to provide a spatially unbiased assessment of the quality of untreated ground water used for public water supplies within MOJO, and to facilitate statistically consistent comparisons of groundwater quality throughout California. Samples were collected from 59 wells in San Bernardino and Los Angeles Counties. Fifty-two of the wells were selected using a spatially distributed, randomized grid-based method to provide statistical representation of the study area (grid wells), and seven were selected to aid in evaluation of specific water-quality issues (understanding wells). The groundwater samples were analyzed for a large number of organic constituents [volatile organic compounds (VOCs), pesticides and pesticide degradates, and pharmaceutical compounds], constituents of special interest (perchlorate and N-nitrosodimethylamine [NDMA]) naturally occurring inorganic constituents (nutrients, dissolved organic carbon [DOC], major and minor ions, silica, total dissolved solids [TDS], and trace elements), and radioactive constituents (gross alpha and gross beta radioactivity, radium isotopes, and radon-222). Naturally occurring isotopes (stable isotopes of hydrogen, oxygen, and carbon, stable isotopes of nitrogen and oxygen in nitrate, and activities of tritium and carbon-14), and dissolved noble gases also were measured to help identify the sources and ages of the sampled ground water. In total, over 230 constituents and water-quality indicators (field parameters) were investigated. Three types of quality-control samples (blanks, replicates, and matrix spikes) each were collected at approximately 5–8 percent of the wells, and the results for these samples were used to evaluate the quality of the data for the groundwater samples. Field blanks rarely contained detectable concentrations of any constituent, suggesting that contamination was not a significant source of bias in the data for the groundwater samples. Differences between replicate samples generally were within acceptable ranges, indicating acceptable analytical reproducibility. Matrix spike recoveries were within acceptable ranges for most compounds. This study did not attempt to evaluate the quality of water delivered to consumers; after withdrawal from the ground, untreated groundwater typically is treated, disinfected, or blended with other waters to maintain water quality. Regulatory thresholds apply to water that is served to the consumer, not to untreated ground water. However, to provide some context for the results, concentrations of constituents measured in the untreated ground water were compared with regulatory and non-regulatory health-based thresholds established by the U.S. Environmental Protection Agency (USEPA) and California Department of Public Health (CDPH) and thresholds established for aesthetic and technical concerns by CDPH. Comparisons between data collected for this study and thresholds for drinking-water are for illustrative purposes only, and are not indicative of compliance or non-compliance with those thresholds. Most constituents that were detected in groundwater samples in the 59 wells in MOJO were found at concentrations below drinking-water thresholds. In MOJO’s 52 grid wells, volatile organic compounds (VOCs) were detected in 40 percent of the wells, and pesticides and pesticide degradates were detected in 23 percent of the grid wells. Results for health-based thresholds in MOJO grid wells showed that all of the detections of organic compounds in samples from MOJO grid wells were below health-based thresholds, with the exception of a single detection of NDMA above the California Department of Public Health notification level (NL-CA). Trace elements and radioactive constituents were sampled for at 19 MOJO grid wells and most detections were below health-based thresholds. Exceptions include: six detections of arsenic above the USEPA maximum contaminant level (MCL-US), two detections of boron and one detection of vanadium above the NL-CA, one detection each of molybdenum and strontium that were above the USEPA lifetime health advisory level (HAL-US), and one detection of fluoride just above the MCL-CA of 2 µg/L. Most detections of radioactive constituents in the MOJO grid wells were below health-based thresholds, with the exception of one detection of gross alpha radioactivity (72-hour count and 30-day count) above the MCL-CA, and 17 grid wells (of 19 sampled) that had activities of radon-222 above the proposed MCL-US of 300 pCi/L, but all were below the proposed alternative MCL-US of 4,000 pCi/L. All of the samples collected from the 19 MOJO grid wells for trace elements, and most of the samples for major ions and total dissolved solids (TDS), had measured concentrations below the non-enforceable thresholds set for aesthetic concerns. Four grid wells had TDS concentrations above the California Department of Public Health secondary maximum contaminant level (SMCL-CA) recommended threshold of 500 mg/L, and three of these wells were also above the SMCL-CA upper threshold of 1,000 mg/L. Four grid wells (of 19 sampled) had sulfate measured at concentrations above the recommended SMCL-CA threshold of 250 mg/L, and one of these detections was also above the upper SMCL-CA threshold of 500 mg/L. One grid well had chloride levels at a concentration above the upper SMCL-CA threshold of 500 mg/L. Eleven grid wells (of 52 sampled) had pH values outside of the SMCL-US range for pH.

California↗
USGS2015

Geospatial compilation of results from field sample collection in support of mineral resource investigations, Western Alaska Range, Alaska, July 2013

This Data Series summarizes results from July 2013 sampling in the western Alaska Range near Mount Estelle, Alaska. The fieldwork combined in situ and camp-based spectral measurements of talus/soil and rock samples. Five rock and 48 soil samples were submitted for quantitative geochemi­cal analysis (for 55 major and trace elements), and the 48 soils samples were also analyzed by x-ray diffraction to establish mineralogy and geochemistry. The results and sample photo­graphs are presented in a geodatabase that accompanies this report. The spectral, mineralogical, and geochemical charac­terization of these samples and the sites that they represent can be used to validate existing remote-sensing datasets (for example, ASTER) and future hyperspectral studies. Empiri­cal evidence of jarosite (as identified by x-ray diffraction and spectral analysis) corresponding with gold concentrations in excess of 50 parts per billion in soil samples suggests that surficial mapping of jarosite in regional surveys may be use­ful for targeting areas of prospective gold occurrences in this sampling area.

Alaska↗
USGS2011

Occurrence and distribution of pesticides in surface waters of the Hood River basin, Oregon, 1999-2009

The U.S. Geological Survey analyzed pesticide and trace-element concentration data from the Hood River basin collected by the Oregon Department of Environmental Quality (ODEQ) from 1999 through 2009 to determine the distribution and concentrations of pesticides in the basin's surface waters. Instream concentrations were compared to (1) national and State water-quality standards established to protect aquatic organisms and (2) concentrations that cause sublethal or lethal effects in order to assess their potential to adversely affect the health of salmonids and their prey organisms. Three salmonid species native to the basin are listed as "threatened" under the U.S. Endangered Species Act: bull trout, steelhead, and Chinook salmon. A subset of 16 sites was sampled every year by the ODEQ for pesticides, with sample collection targeted to months of peak pesticide use in orchards (March-June and September). Ten pesticides and four pesticide degradation products were analyzed from 1999 through 2008; 100 were analyzed in 2009. Nineteen pesticides were detected: 11 insecticides, 6 herbicides, and 2 fungicides. Two of four insecticide degradation products were detected. All five detected organophosphate insecticides and the one detected organochlorine insecticide were present at concentrations exceeding water-quality standards, sublethal effects thresholds, or acute toxicity values in one or more samples. The frequency of organophosphate detection in the basin decreased during the period of record; however, changes in sampling schedule and laboratory reporting limits hindered clear analysis of detection frequency trends. Detected herbicide and fungicide concentrations were less than water-quality standards, sublethal effects thresholds, or acute toxicity values. Simazine, the most frequently detected pesticide, was the only herbicide detected at concentrations within an order of magnitude (factor of 10) of concentrations that impact salmonid olfaction. Some detected pesticides are of concern, not for their toxicity alone, but for their ability to potentiate the harmful impacts of other pesticides, particularly organophosphates, on salmonids or their prey. Many samples contained mixtures of pesticides, but the effects to salmonids of relevant mixtures at environmentally realistic concentrations for the basin are unknown. Trace-element concentration data, although limited, indicate that eight trace elements are also of concern for their potential to harm salmonid health. The dataset is limited with regard to the spatial and seasonal distribution of pesticides and trace elements in all salmonid-bearing streams, the presence of particle-bound pesticides, and the presence of several unmonitored pesticides known to be used in the basin.

Oregon↗
USGS1993

Reconnaissance investigation of water quality, bottom sediment, and biota associated with irrigation drainage in and near Humboldt Wildlife Management Area, Churchill and Pershing Counties, Nevada, 1990-91

A reconnaissance investigation was begun in 1990 to determine whether the quality of irrigation drainage in and near the Humboldt Wildlife Management Area, Nevada, has caused or has the potential to cause harmful effects on human health, fish, and wildlife or to impair beneficial uses of water. Samples of surface and ground water, bottom sediment, and biota collected from sites upstream and downstream from the Lovelock agricultural area were analyzed for potentially toxic trace elements. Also analyzed were radioactive substances, major dissolved constitu- ents, and nutrients in water, as well as pesticide residues in bottom sediment and biota. In samples from areas affected by irrigation drainage, the following constituents equaled or exceeded baseline concentrations or recommended standards for protection of aquatic life or propagation of wildlife--in water: arsenic, boron, dissolved solids, mercury, molybdenum, selenium, sodium, and un-ionized ammonia; in bottom sediment; arsenic and uranium; and in biota; arsenic, boron, and selenium. Selenium appears to be biomagnified in the Humboldt Sink wetlands. Biological effects observed during the reconnaissance included reduced insect diversity in sites receiving irrigation drainage and acute toxicity of drain water and sediment to test organisms. The current drought and upstream consumption of water for irrigation have reduced water deliveries to the wetlands and caused habitat degradation at Humboldt Wildlife Management Area. During this investigation. Humboldt and Toulon Lakes evaporated to dryness because of the reduced water deliveries.

Water-Resources Investigations Report↗
USGS1993

Streamflow, dissolved solids, suspended sediment, and trace elements, San Joaquin River, California, June 1985-September 1988

The 1985-88 study period included hydrologic extremes throughout most of central California. Except for an 11-month period during and after the 1986 flood, San Joaquin River streamflows during 1985-88 were generally less than median for 1975-88. The Merced Tuolumne, and Stanislaus Rivers together comprised 56 to 69 percent of the annual San Joaquin River flow, Salt and Mud Sloughs together comprised 6 to 19 percent, the upper San Joaquin River comprised 2 to 25 percent, and unmeasured sources from agricultural discharges and ground water accounted for 13 to 20 percent. Salt and Mud Sloughs and the unmeasured sources contribute most of the dissolved-solids load. The Merced, Tuolumne, and Stanislaus Rivers greatly dilute dissolved-solids concentrations. Suspended-sediment concentration peaked sharply at more than 600 milligrams per liter during the flood of February 1986. Concentrations and loads varied seasonally during low-flow conditions, with concentrations highest during the early summer irrigation season. Trace elements present primarily in dissolved phases are arsenic, boron, lithium, molybdenum, and selenium. Boron concentrations exceeded the irrigation water-quality criterion of 750 micrograms per liter more than 75 percent of the time in Salt and Mud Sloughs and more than 50 percent of the time at three sites on the San Joaquin River. Selenium concentrations exceeded the aquatic-life criterion of 5 micrograms per liter more than 75 percent of the time in Salt Slough and more than 50 percent of the time in Mud Slough and in the San Joaquin River from Salt Slough to the Merced River confluence. Concentrations of dissolved solids, boron, and selenium usually are highest during late winter to early spring, lower in early summer, higher again in mid-to-late summer, and the lowest in autumn, and generally correspond to seasonal inflows of subsurface tile-drain water to Salt and Mud Sloughs. Trace elements present primarily in particulate phases are aluminum, chromium, copper, iron, manganese, nickel, and zinc, none of which cause significant water-quality problems in the river.

California↗
USGS2025

Combining scanning electron microscopy, X-ray diffraction, and X-ray fluorescence to characterize shear zones at the Pogo gold deposit, Alaska

This study employs a multi-method analytical approach to characterize the mineralogical, geochemical, and textural properties of fault rocks from the Pogo gold mine in the Yukon-Tanana Upland, central Alaska. Specifically, we examine cataclasites, to document the structural and geochemical evolution of shear zones and their associations with gold mineralization. To investigate the shear zone, we integrate portable X-ray fluorescence (pXRF), scanning electron microscopy-based automated mineralogy (SEM-AM), X-ray diffraction (XRD), and high-resolution micro-X-ray fluorescence (micro-XRF) mapping. These methods collectively provide insights into bulk and trace element chemistry, mineralogical composition, and deformation-related textures across multiple scales. Handheld pXRF enables rapid geochemical screening, guiding SEM-AM and XRD analyses to ensure consistent mineralogical interpretation. X-ray diffraction identifies and quantifies crystalline phases, while SEM-AM produces high-resolution mineral maps, revealing mineral abundances, grain-scale textures, and gold associations. Micro-XRF mapping further refines our understanding by showing visual trace element distributions at sub-millimetre resolution. By integrating these techniques, we improve our understanding of the nature and geochemistry of Pogo shear zones, their role in gold mineralization, and support metallurgical processing strategies. This approach enhances exploration models and resource characterization for structurally complex gold deposits.

Alaska↗
USGS1978

Tin and related elements in sediments and beach sands from Afghanistan, Iran, and Turkey

Sixty samples of sediments from stream beds, outwash plains, and beaches were collected in Afghanistan, Iran, and Turkey by Fred L. Klinger, U.S. Bureau of Mines, as part of the field work undertaken by the National Geographic-Smithsonian Pyrotechnological Expedition of 1968. Facilities for the analysis of the samples for tin and other metals were not immediately available, but in 1973 arrangements were made for analyses to be made on a time-permitting basis in the U.S. Geological Survey. The original purpose in collecting the samples was to determine whether tin was present in amounts indicative of sources for tin ores used in antiquity for the manufacture of bronze. The results of the analyses not only permitted an evaluation of the potential for tin in the localities sampled, but also afforded chemical and mineralogical data that were interpretable in the context of regional potential for other elements of current industrial use. These include gold, base metals, ferro-alloy metals, beryllium, rare earths, and barium. The original 60 samples of sand were sieved to make three size fraction (>0.707 mm, <O.707->O.177 mm, and <0.177 mm) for spectrographic and chemical analysis. Splits of these fractions were used for replicate analyses to permit evaluation of the precision of the analytical procedures. Further splitting of the <0.707->0.177 mm sand gave fractions from each sample that were separated in bromoform. Concentrates from the heavy-liquid separations were divided magnetically into six parts from most magnetic to least magnetic. These concentrates were analyzed spectrographically. The precision of the spectrographic analyses is well within the limits of precision expected from semiquantitative procedures. Such precision allows semiquantitative spectrographic procedures to be used with confidence as a valuable tool for reconnaissance investigations in which multi-element analyses are necessary. The analyses of the various fractions of sediments and sediment concentrates indicate the sample media in which an element was most likely to occur. Tin exhibited no preferential concentration into any particular medium. However, many elements with which tin is associated, and other elements of industrial use, do concentrate into one or more of the sample media. This indication of a preferred medium permits interpretation of the analyses as to the best sample medium for a particular element in the environment of western Asia. Cassiterite and/or tin were detected in many samples from Afghanistan, Iran, and Turkey, but in most of the samples the tin was present in normal crustal abundance. Sixteen samples, including seven from Afghanistan, eight from Iran, and one from Turkey contain unusually large amounts of tin. The most notable areas of anomalous tin are near Mirzaka, Qala-i-Asad, and Shah Agha in Afghanistan; near Meshed, Shir Kuh, Natanz, Nodus, and Talmesi in Iran; and on the shore of the Balck Sea just west of Trabzon in Turkey. Even in these localities the tin appears to be a minor element associated with other ores. The most common association of tin is with copper at known mineralized areas. This relation may have historical significance in the context of the development of bronze. The results of the analyses provided geochemical data on the distribution of other elements of industrial use and clearly identified nine of the ten known mineral deposits represented by the samples. The known metallization at the reported deposits may be only a part of more complex groups of metals. In Afghanistan an array of anomalous elements at the known gold placers around Mirzaka and along the Anguri River signals the presence of complex ore deposits. These elements are silver, arsenic, gold, bismuth, cadmium, copper, mercury, indium, molybdenum, lead, antimony, tin, thallium, tungsten, and zinc. They may indicate a Carlin-type gold deposit in which the wall-rocks are enriched in micron-sized particles of gold. Other localities in Afghanistan signalled by the results of the analyses to be anomalous and to merit further geochemical exploration are: (1) a reach of the Panjshir River for beryllium, lead, zinc, chromium and nickel; (2) the area near Bamian for beryllium; (3) the Siakhak village area for gold and copper; (4) around Qala-i-Asad and Shah Agha for lead, zinc, gold, and tungsten. Some attention to the distribution of monazite around Siakhak, Shahjui, Qala-i-Asad, and Shah Agha is justified to determine if this ore mineral for the rare earths and thorium is enriched over its normally expectable trace as an accessory mineral in granitic rocks, pelitic schists, and gneisses. In Iran, the pluton of granodiorite porphyry near Sar Cheshmeh, an area where a huge porphyry copper deposit was being investigated by the Geological Survey of Iran when the present samples were collected in 1968, shows as a strong geochemical anomaly for copper and molybdenum. The granitic area near Meshed is geochemically enriched persistently in beryllium, tin, and barium, and locally in gold, lanthanum, niobium, yttrium, and other elements. This area deserves a thorough regional geochemical survey for beryl and nonberyl sources of beryllium, for fluorite, and for the ores of niobium, tin, barium, the rare earths, and thorium. Other localities in Iran that merit geochemical exploration on the basis of these data are: ;1) the areas between Tabas and Deyhuk, east of Naiband, and south of Naiband for barium and zinc; (2) a locality about midway between Kerman and Sirdjan for barium, lanthanum, strontium, and zinc; (4) the Meskani copper mine area for mercury, lead, and nickel as well as copper; (5) the Talmesi copper mine area for such other elements as barium, cobalt, mercury, strontium, and zinc; (6) a small pluton of granodiorite north of Natanz for tungsten and base metals; (7) the vicinity of Zendjan for auriferous polymetallic sufide deposits; (8) gold in the gorge 15 km east of Miyaneh; and (9) the area near Nodus for gold, base metals, molybdenum, and niobium, and possibly uranium. The Harsit River basin in Turkey appears to be a suitable target for geochemical exploration for gold and low-temperature hydrothermal deposits of base metals, barium, and mercury.

Open-File Report↗
USGS2024

Constraining magma storage conditions of the Toba magmatic system: A plagioclase and amphibole perspective

Silicic magma reservoirs are responsible for producing the largest explosive eruptions in the geologic record. Petrologic and geochronological data provide evidence for these systems spending substantial periods of time (10 4 –10 5 yrs) within the upper crust prior to eruption; however, the long-term thermochemical evolution of these systems is not fully understood, as existing petrologic data make it challenging to quantify the time interval a magmatic system has spent at certain temperatures, or its “thermal history”. Here, we investigate the 74 ka Youngest Toba Tuff (YTT), one of the largest explosive eruptions in the geologic record, to better constrain the long-term thermal evolution of its magmatic system. We combine forward models of Sr diffusion in plagioclase and hornblende, mineral thermometry, and pre-existing trace-element evolution models to quantify the thermochemical evolution of the YTT magmatic system. We find that plagioclase crystals record decades to centuries of storage at temperatures 750 C, while hornblende records up to 6200 years at the same temperatures. Hornblende crystallizes at temperatures around 820 C and adjusting our diffusion modeling to this temperature results in no more than 900 years at initial crystallization conditions. Combined with previous trace-element modeling work, these results indicate that although there was chemical diversity for long durations in the YTT magma system sufficient to produce unique composition eruptive products, the entire system was experiencing a relatively similar thermal history that did not allow for large bodies of eruptible magma to be present for long periods ( 10 2 –10 3 years). Rather, we suggest that magmas within the YTT magmatic system were stored for long durations at thermal conditions where they were uneruptible and only remobilized within a few centuries prior to eruption.

Sumatra↗
USGS1971

Problems on the origin of ore deposits in the lower Ordovician formations of east Tennessee

Most recent workers in the East Tennessee zinc and barite districts are in general agreement that the host breccias were formed by solution-collapse processes in early Middle Ordovician time, probably in an ancient carbonate aquifer system of regional extent. There is little agreement, however, on the source and nature of the ore fluids from which the epigenetic minerals were formed. In this symposium Hanshaw and his colleagues have presented evidence in support of the concept that much secondary dolomite may have been formed by ground water. On the other hand, Roedder has shown that fluid inclusion studies indicate hot saline brines (75 degrees -150 degrees C) as the source fluids for the ore minerals, and he suggests that they may have been deeply circulating connate brines. Other investigators in the past have proposed a variety of source fluids, including juvenile waters, meteoric waters that have become enriched by the leaching of particular elements from the surrounding rock, and sea water. In the zinc deposits, sphalerite is accompanied locally by minor amounts of galena and pyrite, and occasionally, traces of chalcopyrite. Dolomite is the chief gangue mineral and is associated with lesser amounts of quartz, calcite, barite, fluorite, anhydrite, gypsum, and bitumen. Some deposits containing barite as the dominant ore mineral have various amounts of fluorite and pyrite; sphalerite and galena may be present locally along with the other gangue minerals typical of the zinc deposits. The paragenetic sequences of the minerals have been determined for most of the mines and many of the prospects, and, except for minor refinements, will be little changed by additional studies. The real problem, though, is the correlation of these depositional sequences from mine to mine and from district to district. Perhaps the major difficulty in the correlation is the seemingly uncomplicated mineralogy that disguises a rather complex regional paragenesis. Questions regarding the routes the ore fluids travelled to reach the sites of deposition, the reasons why the ores are concentrated in some areas more than others, and the reasons why the mineralogy varies from area to area are questions that are unanswered or at best only partly answered. Studies to date have produced convincing evidence concerning the nature of the structures and the physical conditions responsible for the localization of ore in the Kingsport Formation (Lower Ordovician). On the other hand, the relation of the Kingsport ores to the smaller deposits in the underlying Lower Ordovician and Cambrian rocks is but little understood, and no final answer to the origin of these deposits can be reached until this relationship has been satisfactorily explained. Fluid inclusion studies, trace element analysis, and isotopic studies of all sorts are needed to further our understanding of these seemingly simple ores. Continued detailed studies of field relations, both regional and local, are of major importance, not only for what they will reveal in themselves, but also to perfect the frames of reference in which to place the growing mass of laboratory data.

Tennessee↗
USGS2001

Water-quality characteristics in the Black Hills area, South Dakota

This report summarizes the water-quality characteristics of ground-water and surface-water in the Black Hills area. Differences in groundwater quality by aquifer and differences in surfacewater quality by water source are presented. Ground-water characteristics are discussed individually for each of the major aquifers in the Black Hills area, referred to herein as the Precambrian, Deadwood, Madison, Minnelusa, Minnekahta, and Inyan Kara aquifers. Characteristics for minor aquifers also are discussed briefly. Surface-water characteristics are discussed for hydrogeologic settings including headwater springs, crystalline core sites, artesian springs, and exterior sites. To characterize the water quality of aquifers and streams in the Black Hills area, data from the U.S. Geological Survey National Water Information System water-quality database were examined. This included samples collected as part of the Black Hills Hydrology Study as well as for other studies within the time frame of October 1, 1930, to September 30, 1998. Tables of individual results are not presented in this report, only summaries. Constituents summarized and discussed include physical properties, common ions, nutrients, trace elements, and radionuclides. Comparisons of concentration levels are made to drinking-water standards as well as beneficial-use and aquatic-life criteria. Ground water within the Black Hills and surrounding area generally is fresh and hard to very hard. Concentrations exceeding various Secondary and Maximum Contaminant Levels may affect the use of the water in some areas for many aquifers within the study area. Concentrations that exceed Secondary Maximum Contaminant Levels (SMCL's) generally affect the water only aesthetically. Radionuclide concentrations may be especially high in some of the major aquifers used within the study area and preclude the use of water in some areas. The sodiumadsorption ratio and specific conductance may affect irrigation use for some wells. High concentrations of iron and manganese are the only concentrations that may hamper the use of water from Precambrian aquifers. The principal deterrents to use of water from the Deadwood aquifer are the high concentrations of radionuclides as well as iron and manganese. Iron, manganese, and hardness may deter use of water from the Madison aquifer as well as dissolved solids and sulfate in downgradient wells (generally deeper than 2,000 feet). Iron, manganese, and hardness may also deter use of the Minnelusa aquifer. Water from the Minnekahta aquifer generally is suitable for all water uses although it is hard to very hard. High concentrations of dissolved solids, iron, sulfate, and manganese may hamper the use of water from the Inyan Kara aquifer. In the southern Black Hills, radium-226 and uranium concentrations also may preclude use of water from the Inyan Kara aquifer. Suitability for irrigation may be affected by high specific conductance and sodium-adsorption ratio for the Inyan Kara. Surface-water quality within the Black Hills and surrounding area generally is very good but the water is hard to very hard. Concentrations of some constituents in the study area tend to be higher exterior to the Black Hills, primarily due to influences from the Cretaceous-age marine shales, including dissolved solids, sodium, sulfate, selenium, and uranium. Headwater springs have relatively constant discharge, specific conductance, dissolved solids, and concentrations of most other constituents. Concentrations at crystalline core sites are very similar to those found in samples from Precambrian aquifers. Some high nitrate concentrations greater than the Maximum Contaminant Level (MCL) of 10 mg/L (milligrams per liter) have occurred at Annie Creek near Lead, which have been attributed to mining impacts. Trace elements generally are low with the exception of arsenic, for which 60 percent of samples exceed the proposed MCL of 10 ug/L (micrograms per liter) and one sample

Water-Resources Investigations Report↗
USGS2008

Major- and trace-element concentrations in soils from northern California: Results from the Geochemical Landscapes Project pilot study

In 2004, the U.S. Geological Survey (USGS), the Geological Survey of Canada (GSC), and the Mexican Geological Survey (Servicio Geologico Mexicano, or SGM) initiated pilot studies in preparation for a soil geochemical survey of North America called the Geochemical Landscapes Project. The purpose of this project is to provide a better understanding of the variability in chemical composition of soils in North America. The data produced by this survey will be used to construct baseline geochemical maps for regions within the continent. Two initial pilot studies were conducted: (1) a continental-scale study involving a north-south and east-west transect across North America and (2) a regional-scale study. The pilot studies were intended to test and refine sample design, sampling protocols, and field logistics for the full continental soils geochemical survey. Smith and others (2005) reported the results from the continental-scale pilot study. The regional-scale California study was designed to represent more detailed, higher resolution geochemical investigations in a region of particular interest that was identified from the low-sample-density continental-scale survey. A 20,000-km2 area of northern California (fig. 1), representing a wide variety of topography, climate, and ecoregions, was chosen for the regional-scale pilot study. This study area also contains diverse geology and soil types and supports a wide range of land uses including agriculture in the Sacramento Valley, forested areas in portions of the Sierra Nevada, and urban/suburban centers such as Sacramento, Davis, and Stockton. Also of interest are potential effects on soil geochemistry from historical hard rock and placer gold mining in the foothills of the Sierra Nevada, historical mercury mining in the Coast Range, and mining of base-metal sulfide deposits in the Klamath Mountains to the north. This report presents the major- and trace-element concentrations from the regional-scale soil geochemical survey in northern California.

California↗
USGS2020

Trends in thermal maturity indicators for the organic sulfur-rich Eagle Ford Shale

Thermal maturity is critical to evaluate petroleum systems and to interpret biomarker results for paleoenvironmental and geobiology studies. Many thermal maturity indices were developed for marine source rocks containing type II kerogen, but their behavior in organic sulfur-rich source rocks requires more investigation. Here, we present geochemical analyses of whole and extracted rock, isolated kerogens, and extractable organic matter across a natural thermal maturity transect of the Upper Cretaceous Eagle Ford Shale to evaluate the behavior of maturity parameters in organic sulfur-rich source rocks. The samples contain similar mineralogy and trace element composition, minimizing potential facies effects on thermal maturity parameters. Atomic H/C ratios of isolated kerogens, extractable organic matter yield, and programmed pyrolysis results show that the samples range from the pre-oil through dry gas generation windows. Programmed pyrolysis data and kerogen elemental ratios show that the immature samples host both type IIS (atomic Sorg/C > 0.04) and sulfur-rich type II kerogen (kerogen Sorg/C: 0.032 to 0.045) while the samples with lower kerogen Sorg/C ratios (kerogen Sorg/C < 0.03) are more mature. The vitrinite reflectance values corresponding to the onset of oil generation in the Eagle Ford are comparable to other type II petroleum systems. Likewise, the organic sulfur-rich Eagle Ford follows a similar hydrogen index and kerogen H/C trend as other marine type II source rocks. Hopane and sterane stereoisomer maturity ratios are anomalously elevated at low thermal maturities, so they should not be applied in organic sulfur-rich petroleum systems to infer thermal maturity. However, some biomarker ratios, including those that are more commonly used as source parameters, strongly track thermal maturity in this case study with limited facies variability.

Texas↗
USGS2007

Assessment of hydrology, water quality, and trace elements in selected placer-mined creeks in the birch creek watershed near central, Alaska, 2001-05

Executive Summary The U.S. Geological Survey, in cooperation with the Bureau of Land Management, completed an assessment of hydrology, water quality, and trace-element concentrations in streambed sediment of the upper Birch Creek watershed near Central, Alaska. The assessment covered one site on upper Birch Creek and paired sites, upstream and downstream from mined areas, on Frying Pan Creek and Harrison Creek. Stream-discharge and suspended-sediment concentration data collected at other selected mined and unmined sites helped characterize conditions in the upper Birch Creek watershed. The purpose of the project was to provide the Bureau of Land Management with baseline information to evaluate watershed water quality and plan reclamation efforts. Data collection began in September 2001 and ended in September 2005. There were substantial geomorphic disturbances in the stream channel and flood plain along several miles of Harrison Creek. Placer mining has physically altered the natural stream channel morphology and removed streamside vegetation. There has been little or no effort to re-contour waste rock piles. During high-flow events, the abandoned placer-mine areas on Harrison Creek will likely contribute large quantities of sediment downstream unless the mined areas are reclaimed. During 2004 and 2005, no substantial changes in nutrient or major-ion concentrations were detected in water samples collected upstream from mined areas compared with water samples collected downstream from mined areas on Frying Pan Creek and Harrison Creek that could not be attributed to natural variation. This also was true for dissolved oxygen, pH, and specific conductance-a measure of total dissolved solids. Sample sites downstream from mined areas on Harrison Creek and Frying Pan Creek had higher median suspended-sediment concentrations, by a few milligrams per liter, than respective upstream sites. However, it is difficult to attach much importance to the small downstream increase, less than 10 milligrams per liter, in median suspended-sediment concentration for either basin. During low-flow conditions in 2004 and 2005, previously mined areas investigated on Harrison Creek and on Frying Pan Creek did not contribute substantial suspended sediments to sample sites downstream from the mined areas. No substantial mining-related water- or sediment-quality problems were detected at any of the sites investigated in the upper Birch Creek watershed during low-flow conditions. Average annual streamflow and precipitation were near normal in 2002 and 2003. Drought conditions, extreme forest fire impact, and low annual streamflow set apart the 2004 and 2005 summer seasons. Daily mean streamflow for upper Birch Creek varied throughout the period of record-from maximums of about 1,000 cubic feet per second to minimums of about 20 cubic feet per second. Streamflow increased and decreased rapidly in response to rainfall and rapid snowmelt events because the steep slopes, thin soil cover, and permafrost areas in the watershed have little capacity to retain runoff. Median suspended-sediment concentrations for the 115 paired samples from Frying Pan Creek and 101 paired samples from Harrison Creek were less than the 20 milligrams per liter total maximum daily load. The total maximum daily load was set by the U.S. Environmental Protection Agency for the upper Birch Creek basin in 1996. Suspended-sediment paired-sample data were collected using automated samplers in 2004 and 2005, primarily during low-flow conditions. Suspended-sediment concentrations in grab samples from miscellaneous sites ranged from less than 1 milligram per liter during low-flow conditions to 1,386 milligrams per liter during a high-flow event on upper Birch Creek. Streambed-sediment samples were collected at six sites on Harrison Creek, two sites on Frying Pan Creek, and one site on upper Birch Creek. Trace-element concentrations of mercury, lead, and zinc in streambed sedimen

Scientific Investigations Report↗