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USGS1998

Comparison of hydrochemical tracers to estimate source contributions to peak flow in a small, forested, headwater catchment

Three-component (throughfall, soil water, groundwater) hydrograph separations at peak flow were performed on 10 storms over a 2-year period in a small forested catchment in north-central Maryland using an iterative and an exact solution. Seven pairs of tracers (deuterium and oxygen 18, deuterium and chloride, deuterium and sodium, deuterium and silica, chloride and silica, chloride and sodium, and sodium and silica) were used for three-component hydrograph separation for each storm at peak flow to determine whether or not the assumptions of hydrograph separation routinely can be met, to assess the adequacy of some commonly used tracers, to identify patterns in hydrograph-separation results, and to develop conceptual models for the patterns observed. Results of the three-component separations were not always physically meaningful, suggesting that assumptions of hydrograph separation had been violated. Uncertainties in solutions to equations for hydrograph separations were large, partly as a result of violations of assumptions used in deriving the separation equations and partly as a result of improper identification of chemical compositions of end-members. Results of three-component separations using commonly used tracers were widely variable. Consistent patterns in the amount of subsurface water contributing to peak flow (45-100%) were observed, no matter which separation method or combination of tracers was used. A general conceptual model for the sequence of contributions from the three end-members could be developed for 9 of the 10 storms. Overall results indicated that hydrochemical and hydrometric measurements need to be coupled in order to perform meaningful hydrograph separations.

Maryland↗

USGS2011

Groundwater quality in the Chemung River Basin, New York, 2008

The second groundwater quality study of the Chemung River Basin in south-central New York was conducted as part of the U.S. Geological Survey 305(b) water-quality-monitoring program. Water samples were collected from five production wells and five private residential wells from October through December 2008. The samples were analyzed to characterize the chemical quality of the groundwater. Five of the wells are screened in sand and gravel aquifers, and five are finished in bedrock aquifers. Two of these wells were also sampled for the first Chemung River Basin study of 2003. Samples were analyzed for 6 physical properties and 217 constituents, including nutrients, major inorganic ions, trace elements, radionuclides, pesticides, volatile organic compounds, phenolic compounds, organic carbon, and four types of bacterial analyses. Results of the water-quality analyses for individual wells are presented in tables, and summary statistics for specific constituents are presented by aquifer type. The results are compared with Federal and New York State drinking-water standards, which typically are identical. Water quality in the study area is generally good, but concentrations of some constituents equaled or exceeded current or proposed Federal or New York State drinking-water standards; these were: sodium (one sample), total dissolved solids (one sample), aluminum (one sample), iron (one sample), manganese (four samples), radon-222 (eight samples), trichloroethene (one sample), and bacteria (four samples). The pH of all samples was typically neutral or slightly basic (median 7.5); the median water temperature was 11.0 degrees Celsius (?C). The ions with the highest median concentrations were bicarbonate (median 202 milligrams per liter [mg/L]) and calcium (median 59.0 mg/L). Groundwater in the study area is moderately hard to very hard, but more samples were hard or very hard (121 mg/L as calcium carbonate (CaCO3) or greater) than were moderately hard (61-120 mg/L as CaCO3); the median hardness was 205 mg/L as CaCO3. The maximum concentration of nitrate plus nitrite was 3.67 mg/L as nitrogen, which did not exceed established drinking-water standards for nitrate plus nitrite (10 mg/L as nitrogen). The trace elements with the highest median concentrations were strontium (median 196.5 micrograms per liter [(u or mu)g/L]), barium (median 186 (u or mu)g/L), and iron (median 72.5 (u or mu)g/L in unfiltered water). Five pesticides and pesticide degradates were detected among four samples at concentrations of 0.11 (u or mu)g/L or less; they included herbicides and herbicide degradates. Six volatile organic compounds (VOCs) were detected among four samples; these included four solvents, methyl tert-butyl ether, and one trihalomethane. Trichloroethene, a solvent, was detected in one production well at 5.5 (u or mu)g/L; the Federal and New York State Maximum Contaminant Level (MCL) (5 (u or mu)g/L) was exceeded. The highest radon-222 activities were in samples from bedrock wells [maximum 1,740 picocuries per liter (pCi/L)]; eight of the wells sampled exceeded a proposed U.S. Environmental Protection Agency (USEPA) drinking-water standard of 300 pCi/L. Any detection of coliform bacteria indicates a potential violation of New York State health regulations; total coliform bacteria were detected in four samples, and fecal coliform bacteria were detected in one sample.μμμ

Open-File Report↗

USGS2005

Water Quality in the Halawa, Haiku, and Kaneohe Drainage Basins Before, During, and After H-3 Highway Construction, Oahu, Hawaii, 1983-1999

Selected water-quality data collected before, during, and after construction of the H-3 Highway at 13 water-quality stations were compared to the State of Hawaii Department of Health water-quality standards to determine the effects of highway construction on the water quality of the affected streams. Highway construction had no effect on the high concentrations of total nitrogen and nitrite plus nitrate nitrogen observed except for increased nitrite plus nitrate nitrogen concentrations at one station on Hooleinaiwa Stream. Exceedences of the 10- and 2-percent-of-the-time concentration standards for total phosphorus, total suspended solids, and turbidity, all constituents associated with sediment, occurred more commonly and at more stations during construction than either before or after. These exceedences may be, in part, due to land disturbance caused by highway construction. Highway construction had no effect on the physical water-quality properties of pH, dissolved oxygen, temperature, and specific conductance except at North Halawa and Kuou Streams, where specific-conductance values increased throughout the study period, most likely due to highway construction. No effects on selected trace metals and organic chemical compounds were observed due to highway construction. No effects due to highway construction were observed in the water quality of Waimaluhia Reservoir. Runoff from areas of urban land use in the Kaneohe drainage basin contributed more to the higher loads of selected water-quality constituents than did runoff from areas affected by highway construction.

Scientific Investigations Report↗

USGS1998

Water-quality assessment of part of the upper Mississippi River Basin, Minnesota and Wisconsin— Ground-water quality in the Prairie du Chien-Jordan aquifer, 1996

The Prairie du Chien-Jordan (PDCJ) aquifer (Prairie du Chien-Trempealeau aquifer in Wisconsin), composed of dolomite and sandstone of Cambrian to Ordovician age, is the principal bedrock aquifer in the Upper Mississippi River study unit of the National Water-Quality Assessment (NAWQA) Program. The aquifer supplies approximately 75 percent of the ground water withdrawn in the area. In certain areas, the aquifer is overlain by bedrock or glacial deposits having low hydraulic conductivity (termed "confined portion" of the aquifer in this report). In other areas the aquifer is overlain by glacial sand and gravel deposits having greater hydraulic conductivity (termed "unconfined portion" of the aquifer in this report). Differences in the hydrogeologic characteristics of these overlying units have potential to affect the downward movement of water and of contaminants into the aquifer from the land surface. Ground-water samples were collected from 50 domestic wells completed in this aquifer in July, August, and September of 1996 as part of the U.S. Geological Survey's National WaterQuality Assessment Program. The purpose of this report is to describe the chemical characteristics of water in the PDCJ aquifer and to summarize the differences in water quality in confined and unconfined portions of the aquifer. Twenty-five wells were sampled in each portion of the aquifer. Water samples from the wells were measured for physical parameters and analyzed for concentrations of major ions, nutrients, dissolved organic carbon, trace metals, radon, tritium, pesticides, and volatile organic compounds. Differences in anthropogenic and naturally occurring materials in water between confined and unconfined portions of the PDCJ aquifer are small and frequently the differences are not statistically significant at the 95 percent confidence level. Dissolved oxygen concentrations were slightly less and specific conductances and alkalinities were slightly greater in water in the confined portion of the aquifer. Only the differences in specific conductance and alkalinity, however, were statistically significant at the 95 percent confidence level (two sample t-test). Concentrations of most major ions were generally greater in water from the confined portion of the aquifer. Nitrate (nitrite plus nitrate as N) and phosphorus were generally greater in the unconfined portion of the PDCJ aquifer although the differences were not statistically significant at the 95 percent confidence level (nonparametric Mann-Whitney test). In the confined portion of the aquifer no samples exceeded the maximum contaminant level of 10 milligrams per liter for nitrate. In the unconfined portion of the aquifer nitrate in two samples exceeded the maximum contaminant level of 10 milligrams per liter. Phosphorus concentrations were generally about an order of magnitude less than nitrate concentrations. Iron and manganese concentrations commonly exceeded the secondary maximum contaminant levels set by the U.S. Environmental Protection Agency and were generally greater in the confined portion of the PDCJ aquifer, although the differences were not statistically significant at the 95 percent confidence level (nonparametric Mann-Whitney test). Radon concentrations were greater in the confined portion of the aquifer than in the unconfined portion, although the difference was not statistically significant at the 95 percent confidence level (two sample t-test), with medians of 500 and 340 picoCuries per liter, respectively. Sixty-six percent of the radon concentrations were greater than the suspended maximum contaminant level of 300 picoCuries per liter. Tritium concentrations indicate that water in the unconfined portion of the PDCJ aquifer may have been recharged more recently than water in the confined portion of the aquifer, although differences in tritium concentrations between confined and unconfined portions of the aquifer were not statistically significant at the 95 percent confidence level (nonparametric MannWhitney test). Atrazine and its metabolite, deethylatrazine, were the most frequently detected pesticide compounds in water samples from the PDCJ aquifer. Volatile organic compounds were detected in 41 of the 50 water samples, but none of the concentrations exceeded 1 microgram per liter. Concentrations of volatile organic compounds were slightly greater in the unconfined portion, although the differences in detection rates were not statistically significant at the 95 percent confidence level (nonparametric Mann-Whitney test). Carbon disulfide and methyl chloride were the most frequently detected volatile organic compounds. Water in the unconfined portion of the PDCJ aquifer in Minnesota and Wisconsin appears to be affected to a greater degree by anthropogenic activities than water in the confined portion of the aquifer. Water in the confined portion has a longer residence time and greater concentrations of dissolution products of minerals. In general, however, differences in anthropogenic and naturally occurring materials among confined and unconfined portions of the aquifer are small and frequently not significantly different.

Minnesota, Wisconsin↗

USGS2008

Ground-Water Quality in Western New York, 2006

Water samples were collected from 7 production wells and 26 private residential wells in western New York from August through December 2006 and analyzed to characterize the chemical quality of ground water. Wells at 15 of the sites were screened in sand and gravel aquifers, and 18 were finished in bedrock aquifers. The wells were selected to represent areas of greatest ground-water use and to provide a geographical sampling from the 5,340-square-mile study area. Samples were analyzed for 5 physical properties and 219 constituents that included nutrients, major inorganic ions, trace elements, radionuclides, pesticides, volatile organic compounds (VOC), phenolic compounds, organic carbon, and bacteria. Results indicate that ground water used for drinking supply is generally of acceptable quality, although concentrations of some constituents or bacteria exceeded at least one drinking-water standard at 27 of the 33 wells. The cations that were detected in the highest concentrations were calcium, magnesium, and sodium; anions that were detected in the highest concentrations were bicarbonate, chloride, and sulfate. The predominant nutrients were nitrate and ammonia; nitrate concentrations were higher in samples from sand and gravel aquifers than in samples from bedrock. The trace elements barium, boron, copper, lithium, nickel, and strontium were detected in every sample; the trace elements with the highest concentrations were barium, boron, iron, lithium, manganese, and strontium. Eighteen pesticides, including 9 pesticide degradates, were detected in water from 14 of the 33 wells, but none of the concentrations exceeded State or Federal Maximum Contaminant Levels (MCLs). Fourteen volatile organic compounds were detected in water from 12 of the 33 wells, but none of the concentrations exceeded MCLs. Eight chemical analytes and three types of bacteria were detected in concentrations that exceeded Federal and State drinking-water standards, which are typically identical. Sulfate concentrations exceeded the U.S. Environmental Protection Agency (USEPA) Secondary Maximum Contaminant Level (SMCL) of 250 milligrams per liter (mg/L) in three samples, and chloride concentrations exceeded the SMCL of 250 mg/L in two samples. Sodium concentrations exceeded the USEPA Drinking Water Health Advisory of 60 mg/L in nine samples. Iron concentrations exceeded the SMCL of 300 ug/L (micrograms per liter) in 14 filtered samples, and manganese exceeded the USEPA SMCL of 50 ug/L in 15 filtered samples, as well as the New York State MCL of 300 ug/L in 1 filtered sample. Arsenic exceeded the USEPA MCL of 10 ug/L in two samples, aluminum exceeded the SMCL for aluminum of 50 ug/L in one sample, and lead exceeded the MCL of 15 ug/L in one sample. Radon-222 exceeded the proposed USEPA MCL of 300 picocuries per liter in 24 samples. Any detection of coliform bacteria indicates a violation of New York State health regulations; total coliform was detected in 12 samples, and Escherichia coli was detected in 2 samples. The plate counts for heterotrophic bacteria exceeded the MCL (500 colony-forming units per milliliter) in four samples.

Open-File Report↗

USGS2018

Dual-phase mass balance modeling of small mineral particle losses from sedimentary rock-derived soils

Losses of small mineral particles can be a significant physical process that affects the elemental composition of soils derived from sedimentary rocks. Shales, in particular, contain abundant clay-sized minerals that can be mobilized by simple disaggregation, and solutional weathering is limited because the parent rock is composed primarily of recalcitrant minerals previously subjected to continental weathering. Here, the dual-phase mass balance model is employed to quantify losses of small mineral particles as water dispersible colloids (WDCs) from three previously studied soil profiles along a hill slope at the Susquehanna Shale Hills Critical Zone Observatory (SSHO). WDCs were isolated from soil in the laboratory to determine their mineralogical and elemental compositions. Clay minerals dominated WDCs, including illite, vermiculite, and chlorite inherited from the parent shale, along with neoformed kaolinite. Quartz present in bulk soil was generally excluded from WDCs. Elements of low solubility and/or bound in recalcitrant forms, like Rb in illite, were employed in tracer ratios in the dual-phase model. Aluminum, Ga, and Rb were enriched in WDCs, and Zr and Hf were partially excluded. Six different combinations of elements into tracer ratios (Al/Zr, Ga/Zr, Rb/Zr, Al/Hf, Ga/Hf, Rb/Hf) each yielded similar model results. Mass losses of WDCs were large, ranging from − 68 ± 7% to − 15 ± 5% relative to soil parent material in different parts of the profiles. Mass losses via solution were smaller, ranging from − 7 ± 2% to a gain of 6 ± 1% in part of one profile. Losses of WDCs account for > 90% of total mass loss, surpassing chemical dissolution, and therefore dominate the weathering portion of denudation at SSHO. Zirconium concentrations were 97–158 ppm in the generally ≤ 1 μm WDCs, suggesting colloidal, Zr-bearing phases. Model-quantified losses of Zr via WDCs were large, with a median loss of 41% relative to parent material. Such losses indicate systematic underestimates of weathering by traditional mass balance that uses Zr as an index element. Losses of Ca, Mg, and K via WDCs exceeded losses via solution, countering assumptions of base cation losses primarily via mineral dissolution. The results illustrate a geochemical fingerprint of physical weathering and the ability of the dual-phase model to quantify that weathering process.

Chemical Geology↗

USGS2002

Physical and stable-isotope evidence for formation of secondary calcite and silica in the unsaturated zone, Yucca Mountain, Nevada

Calcite and silica form coatings on fracture footwalls and cavity floors in the welded tuffs at Yucca Mountain, the potential site of a high-level radioactive waste repository. These secondary mineral deposits are heterogeneously distributed in the unsaturated zone (UZ) with fewer than 10% of possible depositional sites mineralized. The paragenetic sequence, compiled from deposits throughout the UZ, consists of an early-stage assemblage of calcite??fluorite??zeolites that is frequently capped by chalcedony??quartz. Intermediate- and late-stage deposits consist largely of calcite, commonly with opal on buried growth layers or outermost crystal faces of the calcite. Coatings on steep-dipping fractures usually are thin (??? 3 mm) with low-relief outer surfaces whereas shallow-dipping fractures and lithophysal cavities typically contain thicker, more coarsely crystalline deposits characterized by unusual thin, tabular calcite blades up to several cms in length. These blades may be capped with knobby or corniced overgrowths of late-stage calcite intergrown with opal. The observed textures in the fracture and cavity deposits are consistent with deposition from films of water fingering down fracture footwalls or drawn up faces of growing crystals by surface tension and evaporated at the crystal tips. Fluid inclusion studies have shown that most early-stage and some intermediate-stage calcite formed at temperatures of 35 to 85??C. Calcite deposition during the past several million years appears to have been at temperatures < 30??C. The elevated temperatures indicated by the fluid inclusions are consistent with temperatures estimated from calcite ??18O values. Although others have interpreted the elevated temperatures as evidence of hydrothermal activity and flooding of the tuffs of the potential repository, the authors conclude that the temperatures and fluid-inclusion assemblages are consistent with deposition in a UZ environment that experienced prolonged heat input from gradual cooling of nearby plutons. The physical restriction of the deposits (and, therefore, fluid flow) to fracture footwalls and cavity floors and the heterogeneous and limited distribution of the deposits provides compelling evidence that they do not reflect flooding of the thick UZ at Yucca Mountain. The textures and isotopic and chemical compositions of these mineral deposits are consistent with deposition in a UZ setting from meteoric waters percolating downward along fracture flow paths.

Applied Geochemistry↗

USGS2006

A ubiquitous thermoacidophilic archaeon from deep-sea hydrothermal vents

Deep-sea hydrothermal vents are important in global biogeochemical cycles, providing biological oases at the sea floor that are supported by the thermal and chemical flux from the Earth's interior. As hot, acidic and reduced hydrothermal fluids mix with cold, alkaline and oxygenated sea water, minerals precipitate to form porous sulphide-sulphate deposits. These structures provide microhabitats for a diversity of prokaryotes that exploit the geochemical and physical gradients in this dynamic ecosystem. It has been proposed that fluid pH in the actively venting sulphide structures is generally low (pH < 4.5), yet no extreme thermoacidophile has been isolated from vent deposits. Culture-independent surveys based on ribosomal RNA genes from deep-sea hydrothermal deposits have identified a widespread euryarchaeotal lineage, DHVE2 (deep-sea hydrothermal vent euryarchaeotic 2). Despite the ubiquity and apparent deep-sea endemism of DHVE2, cultivation of this group has been unsuccessful and thus its metabolism remains a mystery. Here we report the isolation and cultivation of a member of the DHVE2 group, which is an obligate thermoacidophilic sulphur- or iron-reducing heterotroph capable of growing from pH 3.3 to 5.8 and between 55 and 75??C. In addition, we demonstrate that this isolate constitutes up to 15% of the archaeal population, providing evidence that thermoacidophiles may be key players in the sulphur and iron cycling at deep-sea vents. ?? 2006 Nature Publishing Group.

Nature↗

USGS2008

A Review of Methods Applied by the U.S. Geological Survey in the Assessment of Identified Geothermal Resources

The U. S. Geological Survey (USGS) is conducting an updated assessment of geothermal resources in the United States. The primary method applied in assessments of identified geothermal systems by the USGS and other organizations is the volume method, in which the recoverable heat is estimated from the thermal energy available in a reservoir. An important focus in the assessment project is on the development of geothermal resource models consistent with the production histories and observed characteristics of exploited geothermal fields. The new assessment will incorporate some changes in the models for temperature and depth ranges for electric power production, preferred chemical geothermometers for estimates of reservoir temperatures, estimates of reservoir volumes, and geothermal energy recovery factors. Monte Carlo simulations are used to characterize uncertainties in the estimates of electric power generation. These new models for the recovery of heat from heterogeneous, fractured reservoirs provide a physically realistic basis for evaluating the production potential of natural geothermal reservoirs.

Open-File Report↗

USGS1996

Hydrologic data for the East Poplar oil field, Fort Peck Indian Reservation, Northeastern Montana

This report presents selected hydrologic data for the East Poplar oil field, located in the south-central part of the Fort Peck Indian Reservation in northeastern Montana. Data about the occurrence, quantity, and quality of ground and surface water are presented in tabular form. The tables contain records of privately owned wells (active and abandoned), monitoring wells installed by the U.S. Geological Survey and Montana Bureau of Mines and Geology, oil wells, and brine-injection wells; lithologic descriptions of drill cuttings and well-completion data from monitoring wells; data from two aquifer tests conducted in Quaternary alluvial and glacial deposits; chemical quality of ground water; and information on the quantity and chemical quality of surface water. Records of electromagnetic geophysical measurements collected throughout an area of about 20 square miles of the study area are compiled and included on a floppy disk. Illustrations in this report contain information about study area location, site- numbering system, general physical and cultural features, and construction of monitoring wells installed by the U.S. Geological Survey. plate-sized map presents additional information about privately owned wells, monitoring wells, oil wells, brine-injections wells, surface-water data-collection sites, and area of electromagnetic data collection. The data presented in this report provide a base with which to better define and interpret the occurrence, quantity, and quality of ground and surface water in the vicinity of the Poplar River Valley in the south-central part of the Fort Peck Indian Reservation. The data can be used to help delineate the occurrence of brine and saline water in Quaternary alluvial and glacial deposits in the East Poplar oil field.

Open-File Report↗

USGS2013

Chemical transfers along slowly eroding catenas developed on granitic cratons in southern Africa

A catena is a series of distinct but co-evolving soils arrayed along a slope. On low-slope, slowly eroding catenas the redistribution of mass occurs predominantly as plasma, the dissolved and suspended constituents in soil water. We applied mass balance methods to track how redistribution via plasma contributed to physical and geochemical differentiation of nine slowly eroding (~ 5 mm ky − 1 ) granitic catenas. The catenas were arrayed in a 3 × 3 climate by relief matrix and located in Kruger National Park, South Africa. Most of the catenas contained at least one illuviated soil profile that had undergone more volumetric expansion and less mass loss, and these soils were located in the lower halves of the slopes. By comparison, the majority of slope positions were eluviated. Soils from the wetter climates (550 and 730 mm precipitation yr − 1 ) generally had undergone greater collapse and lost more mass, while soils in the drier climate (470 mm yr − 1 ) had undergone expansion and lost less mass. Effects of differences in catena relief were less clear. Within each climate zone, soil horizon mass loss and strain were correlated, as were losses of most major elements, illustrating the predominant influence of primary mineral weathering. Nevertheless, mass loss and volumetric collapse did not become extreme because of the skeleton of resistant primary mineral grains inherited from the granite. Colloidal clay redistribution, as traced by the ratio of Ti to Zr in soil, suggested clay losses via suspension from catena eluvial zones. Thus illuviation of colloidal clays into downslope soils may be crucial to catena development by restricting subsurface flow there. Our analysis provides quantitative support for the conceptual understanding of catenas in cratonic landscapes and provides an endmember reference point in understanding the development of slowly eroding soil landscapes.

Geoderma↗

USGS2006

Ground-Water Quality in the Upper Susquehanna River Basin, New York, 2004-05

Water samples were collected from 20 production wells and 13 private residential wells throughout the upper Susquehanna River Basin (upstream from the Pennsylvania border) during the fall of 2004 and the spring of 2005 and analyzed to describe the chemical quality of ground water in the upper basin. Wells were selected to represent areas of greatest ground-water use and highest vulnerability to contamination, and to provide a representative sampling from the entire (4,516 square-mile) upper basin. Samples were analyzed for physical properties, nutrients, inorganic constituents, metals, radionuclides, pesticides, volatile organic compounds, and bacteria. The cations that were detected in the highest concentrations were calcium, magnesium, and sodium; the anions that were detected in the greatest concentrations were bicarbonate, chloride, and sulfate. The predominant nutrient was nitrate, the concentrations of which were greater in samples from sand and gravel aquifers than in samples from bedrock. The metals barium, boron, cobalt, copper, and nickel were detected in every sample; the metals with the highest concentrations were barium, boron, iron, manganese, strontium, and lithium. The pesticide compounds detected most frequently were atrazine, deethylatrazine, alachlor ESA, and two degradation products of metolachlor (metolachlor ESA and metolachlor OA); the compounds detected in highest concentration were metolachlor ESA and OA. Volatile organic compounds were detected in 11 samples, and concentrations of 3 of these compounds exceeded 1 microgram per liter (?g/L). Methyl tert-butyl ether (MTBE), a gasollline additive, was not detected in any sample. Several analytes were found in concentrations that exceeded Federal and New York State water-quality standards, which are typically identical. Chloride concentrations exceeded the U.S. Environmental Protection Agency (USEPA) Secondary Maximum Contaminant Level (SMCL) of 250 milligrams per liter (mg/L) in two samples, and sulfate concentrations exceeded the SMCL of 250 mg/L in one sample. Sodium concentrations exceeded the USEPA Drinking Water Advisory of 60 mg/L in six samples. Nitrate concentrations exceeded the USEPA Maximum Contaminant Level (MCL) of 10 mg/L in one sample and approached this limit (at 9.84 mg/L) in another sample. Barium concentrations exceeded the MCL of 2,000 ?g/L in one sample. Iron concentrations exceeded the SMCL of 300 ?g/L in five samples, and manganese concentrations exceeded the SMCL of 50 ?g/L in 14 samples. Arsenic was detected in seven samples, and the MCL for arsenic (10 ?g/L) was exceeded in two samples. Radon-222 exceeded the proposed MCL of 300 picocuries per liter in 24 samples. Any detection of total coliform or fecal coliform bacteria is considered a violation of New York State health regulations; in this study, total coliform was detected in six samples and fecal coliform was detected in one sample, but Escherichia coli (E. coli) was not detected in any sample.

Open-File Report↗

USGS2005

Chemical openness and potential for misinterpretation of the solute environment of coastal sabkhat

Sabkha deposits in the geologic record are commonly used to interpret the environmental conditions of deposition. Implicit in this use is the assumption that the solute system is chemically closed, that is, the authigenic minerals represent the composition of the fluids in their environment of origin. Thermodynamic and mass-balance calculations based on measurements of water and solute flux of contemporary Abu Dhabi coastal sabkha system, however, demonstrate that the system is open for sodium and chloride, where nearly half of the input is lost, but closed for sulfur, where nearly 100% is retained. Sulfur and chloride isotopes were consistent with this observation. If these sabkha deposits were preserved in the geologic record, they would suggest a solute environment rich in sulfate and poor in chloride; yet the reverse is true. In most coastal-sabkha environments, capillary forces bring solutes and water to the surface, where the water evaporates and halite, carnallite, sylvite, and other soluble minerals are precipitated. Retrograde minerals, such as anhydrite, calcite, dolomite, and gypsum, however, precipitate and accumulate in the capillary zone beneath the surface of the coastal sabkha. Because they possess relatively low solubility and are below the surface, these retrograde minerals are protected from dissolution and physical erosion occurring from infrequent but intense rainfall events. Thus, they are more likely to be preserved in the geological record than highly soluble minerals formed on the surface. ?? 2004 Elsevier B.V. All rights reserved.

Chemical Geology↗

USGS2012

The paleohydrology of unsaturated and saturated zones at Yucca Mountain, Nevada, and vicinity

Surface, unsaturated-zone, and saturated-zone hydrologic conditions at Yucca Mountain responded to past climate variations and are at least partly preserved by sediment, fossil, and mineral records. Characterizing past hydrologic conditions in surface and subsurface environments helps to constrain hydrologic responses expected under future climate conditions and improve predictions of repository performance. Furthermore, these records provide a better understanding of hydrologic processes that operate at time scales not readily measured by other means. Pleistocene climates in southern Nevada were predominantly wetter and colder than the current interglacial period. Cyclic episodes of aggradation and incision in Fortymile Wash, which drains the eastern slope of Yucca Mountain, are closely linked to Pleistocene climate cycles. Formation of pedogenic cement is favored under wetter Pleistocene climates, consistent with increased soil moisture and vegetation, higher chemical solubility, and greater evapotranspiration relative to Holocene soil conditions. The distribution and geochemistry of secondary minerals in subsurface fractures and cavities reflect unsaturated-zone hydrologic conditions and the response of the hydrogeologic system to changes in temperature and percolation flux over the last 12.8 m.y. Physical and fluid-inclusion evidence indicates that secondary calcite and opal formed in air-filled cavities from fluids percolating downward through connected fracture pathways in the unsaturated zone. Oxygen, strontium, and carbon isotope data from calcite are consistent with a descending meteoric water source but also indicate that water compositions and temperatures evolved through time. Geochronological data indicate that secondary mineral growth rates are less than 1–5 mm/m.y., and have remained approximately uniform over the last 10 m.y. or longer. These data are interpreted as evidence for hydrological stability despite large differences in surface moisture caused by climate shifts between the Miocene and Pleistocene and between Pleistocene glacial-interglacial cycles. Secondary mineral distribution and δ18O profiles indicate that evaporation in the shallower welded tuffs reduces infiltration fluxes. Several near-surface and subsurface processes likely are responsible for diverting or dampening infiltration and percolation, resulting in buffering of percolation fluxes to the deeper unsaturated zone. Cooler and wetter Pleistocene climates resulted in increased recharge in upland areas and higher water tables at Yucca Mountain and throughout the region. Discharge deposits in the Amargosa Desert were active during glacial periods, but only in areas where the modern water table is within 7–30 m of the surface. Published groundwater models simulate water-table rises beneath Yucca Mountain of as much as 150 m during glacial climates. However, most evidence from Fortymile Canyon up gradient from Yucca Mountain limits water-table rises to 30 m or less, which is consistent with evidence from discharge sites in the Amargosa Desert. The isotopic compositions of uranium in tuffs spanning the water table in two Yucca Mountain boreholes indicate that Pleistocene water-table rises likely were restricted to 25–50 m above modern positions and are in approximate agreement with water-table rises estimated from zeolitic-to-vitric transitions in the Yucca Mountain tuffs (less than 60 m in the last 11.6 m.y.).

Nevada↗

USGS2022

Multidisciplinary constraints on the thermal-chemical boundary between Earth's core and mantle

Heat flux from the core to the mantle provides driving energy for mantle convection thus powering plate tectonics, and contributes a significant fraction of the geothermal heat budget. Indirect estimates of core-mantle boundary heat flow are typically based on petrological evidence of mantle temperature, interpretations of temperatures indicated by seismic travel times, experimental measurements of mineral melting points, physical mantle convection models, or physical core convection models. However, previous estimates have not consistently integrated these lines of evidence. In this work, an interdisciplinary analysis is applied to co-constrain core-mantle boundary heat flow and test the thermal boundary layer (TBL) theory. The concurrence of TBL models, energy balance to support geomagnetism, seismology, and review of petrologic evidence for historic mantle temperatures supports Q CMB ∼15 TW, with all except geomagnetism supporting as high as ∼20 TW. These values provide a tighter constraint on core heat flux relative to previous work. Our work describes the seismic properties consistent with a TBL, and supports a long-lived basal mantle molten layer through much of Earth's history.

Geochemistry, Geophysics, Geosystems↗

USGS2000

Water-quality data for streams in the Boulder River Watershed, Jefferson County, Montana

Chemical data were collected in the Boulder River watershed of southwestern Montana during 1996-99 as part of a detailed interdisciplinary study characterizing the effects of historical inactive mines on streams in the watershed. This report presents water-quality data collected by the U.S. Geological Survey for physical properties, major ions, nutrients, and trace elements for 62 sites in and near the watershed. Supplementary historical water-quality data for 83 sites also are presented.

Montana↗

USGS1997

Quantity and quality of runoff from selected guttered and unguttered roadways in northeastern Ramsey County, Minnesota

Five roadway sections in northeastern Ramsey County, Minnesota were monitored during 1993-95, to evaluate water quality and loading of constituents from roadway runoff. Two snowmelt-runoff and five rainfall-runoff events were monitored per year at each site. Additional samples of rainfall were analyzed to determine if rainfall was a direct source of constituent loading to roadway runoff. Roadway-runoff samples were analyzed for selected physical properties, dissolved solids, nutrients, dissolved ions, selected metals, and semi-volatile compounds. Concentrations of dissolved ions such as sodium, chloride, and metals such as aluminum, chromium, lead, and zinc were detected at much greater levels for snowmelt-runoff samples than rainfall-runoff samples. Analysis of chemical samples from rainfall indicate that rainfall was not a direct source for most constituents. Dissolved nitrate and dissolved ammonia in rainfall, however, can contribute up to one-half the amounts detected in roadway runoff. Concentrations of total phosphorus and fecal Streptococcus bacteria were greater at unguttered sites than at guttered sites. Concentrations of dissolved solids, and some metals were greater at guttered sites than at unguttered sites. This suggests that the vegetated road ditches associated with unguttered sites may filter out heavier particles such as metals and solids, while contributing additional organic matter. Concentrations of aliiminum, copper, lead, and zinc exceeded chronic condition standard limits established by the Minnesota Pollution Control Agency for metropolitan storm water from 96 percent, 52 percent, 9 percent, and 20 percent of the samples collected, respectively. Chemical loadings of specific constituents, such as suspended solids, from an individual rainfall-runoff event accounted for greater than 90 percent of the cumulative loadings of that constituent for all monitored events at site 4, for the entire study period. Length of latent period was statistically compared to constituent concentration levels of total phosphorus, dissolved sulfate, and total zinc and there was a correlation. Constituent loads were not associated with latent period. No correlation was found between traffic volumes which ranged from 1,888 to 7,172 vehicles per day and constituent concentrations or loads for this study.

Minnesota↗

USGS2015

Mechanisms and timescales of generating eruptible rhyolitic magmas at Yellowstone caldera from zircon and sanidine geochronology and geochemistry

We constrain the physical nature of the magma reservoir and the mechanisms of rhyolite generation at Yellowstone caldera via detailed characterization of zircon and sanidine crystals hosted in three rhyolites erupted during the (ca. 170 – 70 ka) Central Plateau Member eruptive episode – the most recent post-caldera magmatism at Yellowstone. We present 238U-230Th crystallization ages and trace-element compositions of the interiors and surfaces (i.e., unpolished rims) of individual zircon crystals from each rhyolite. We compare these zircon data to 238U- 230Th crystallization ages of bulk sanidine separates coupled with chemical and isotopic data from single sanidine crystals. Zircon age and trace-element data demonstrate that the magma reservoir that sourced the Central Plateau Member rhyolites was long-lived (150 – 250 kyr) and genetically related to the preceding episode of magmatism, which occurred ca. 256 ka. The interiors of most zircons in each rhyolite were inherited from unerupted material related to older stages of Central Plateau Member magmatism or the preceding late Upper Basin Member magmatism (i.e., are antecrysts). Conversely, most zircon surfaces crystallized near the time of eruption from their host liquids (i.e., are autocrystic). The repeated recycling of zircon interiors from older stages of magmatism demonstrates that sequentially erupted Central Plateau Member rhyolites are genetically related. Sanidine separates from each rhyolite yield 238U-230Th crystallization ages at or near the eruption age of their host magmas, coeval with the coexisting zircon surfaces, but are younger than the coexisting zircon interiors. Chemical and isotopic data from single sanidine crystals demonstrate that the sanidines in each rhyolite are in equilibrium with their host melts, which considered along with their near-eruption crystallization ages suggests that nearly all CPM sanidines are autocrystic. The paucity of antecrystic sanidine crystals relative to antecrystic zircons require a model where eruptible rhyolites are generated by extracting melt and zircons from a long-lived mush of immobile crystal-rich magma. In this process the larger sanidine crystals remain trapped in the locked crystal network. The extracted melts (plus antecrystic zircon) amalgamate into a liquid dominated (i.e., eruptible) magma body that is maintained as a physically distinct entity relative to the bulk of the long-lived crystal mush. Zircon surfaces and sanidines in each rhyolite crystallize after melt extraction/amalgamation and their ages constrain the residence time of eruptible magmas at Yellowstone. Residence times of the large volume rhyolites (~40 – 70 km3) are ≤ 1 kyr (conservatively < 6 kyr), which suggests that large volumes of rhyolite can be generated rapidly by extracting melt from a crystal mush. Because the lifespan of the crystal mush that sourced the Central Plateau Member rhyolites is two orders of magnitude longer than the residence time of eruptible magma bodies within the reservoir, it is apparent that the Yellowstone magma reservoir spends most of its time in a largely-crystalline (i.e., uneruptible) state, similar to the present-day magma reservoir, and that eruptible magma bodies are ephemeral features.

Idaho, Wyoming↗