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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↗

USGS1982

Preliminary geological investigation of the Bir Hayzan diatomite deposit, Kingdom of Saudi Arabia, with a section on selected physical properties and implications for future geophysical exploration

A 2.2-m-thick lake bed composed entirely of diatomite was found in the southwestern arm of the Nafud sand sea, about 67 km east of Tayma in northwestern Saudi Arabia. Its stratigraphic position above eolian sand and below a large barchanoid dune indicates deposition during an exceptional period of pluvial climate in an otherwise arid sand desert. Radiocarbon-dated carbonate lake beds found in similar stratigraphic settings in other parts of the Nafud suggest that the diatomite was deposited in the late Pleistocene epoch sometime between 32,000 and 20,000 years ago. Diatomite of the same pluvial episode has also been found in the Afar region of Ethiopia. Four samples of the diatomite were analyzed for major chemical components and 32 minor and trace elements. Two of the samples appeared to be representative of the lake bed. These samples contained about 85 percent SiO2, 2.34 percent Fe2O3, 1 4 percent Al2O3, and 8.27 percent ignition loss, with only traces of CaO, P2O5, MgO, Na2O, and TiO2. The high content of silica and low contents of alumina, iron oxide, lime, and other constituents indicate low contamination. Analyses of samples from the two atypical units indicate a small amount of contamination, probably clay or mica, in the basal unit and addition of iron oxide and carbonate by ground water in an isolated green-colored unit. Chemically the Bi'r Hayzan diatomite compares favorably with commercial deposits from other parts of the world. Low bulk densities of 0.64 g/cm3 (30-40 lbs/ft3) and an average porosity of 63 percent for five samples also suggest the deposit is of industrial grade. Further studies are recommended to determine: (1) the size and extent of the deposit and (2) the suitability of the diatomite for commercial applications. As means to these ends, electrical-resistivity surveys following winter rains are suggested to determine both the extent and thickness of the lake bed beneath the overlying sand dunes. A complete species identification of the diatom association and further laboratory testing of physical properties of the diatomite also should be made. Further exploration in the Nafud is recommended to locate other possible diatomite deposits.

Open-File Report↗

USGS1987

Hydrologic and geologic data for the Edwards Aquifer Recharge Zone near Georgetown, Williamson County, Texas, 1986-87

This report presents a compilation and summary of data related to the interchange of water between the Edwards aquifer and streams, and to the hydraulics of vertical movement of water in the Georgetown Limestone in the Georgetown area of Williamson County. It presents hydrologic, geologic, hydraulic, physical, geophysical, and water-quality data collected from selected wells and stream sites in the study area from January 1986 to June 1987. Included are the results from six streamflow gain and loss surveys, two ground-water-level surveys representing low and high water-level conditions, inorganic chemical analyses of water from selected wells and streams, and bulk specific gravity and permeability tests of cores taken at three test-well sites. Water-level altitudes differed by an average of 38 feet between low and high water-level conditions in the confined zone, and by an average of 13 feet in the unconfined zone. Dissolved solids of water from selected wells ranged from 320 to 1,300 milligrams per liter and from 251 to 290 milligrams per liter in water from selected streams.

Open-File Report↗

USGS1965

Variations in chemical character of water in the Englishtown Formation, New Jersey

This investigation describes the variations in the chemical character of the water in the Englishtown Formation of Late Cretaceous age in the Atlantic Coastal Plain of New Jersey, and demonstrates the application of the concept of hydrochemical mapping to the study and evaluation of water-bearing materials. The chemistry of ground water is responsive to the physical environment and lends support to available geologic and hydrologic data. A study of the ground-water chemistry may even suggest concepts for which additional geologic or hydrologic data may not be obtainable by conventional methods of study. Hydrochemical mapping is particularly important in evaluating an aquifer satisfactorily, but it could be equally useful in regional geologic studies concerned with continuity of units or mineralogic differences and similarities.

New Jersey↗

USGS2009

Groundwater Quality in Central New York, 2007

Water samples were collected from 7 production wells and 28 private residential wells in central New York from August through December 2007 and analyzed to characterize the chemical quality of groundwater. Seventeen wells are screened in sand and gravel aquifers, and 18 are finished in bedrock aquifers. The wells were selected to represent areas of greatest groundwater use and to provide a geographical sampling from the 5,799-square-mile study area. Samples were analyzed for 6 physical properties and 216 constituents, including nutrients, major inorganic ions, trace elements, radionuclides, pesticides, volatile organic compounds, phenolic compounds, organic carbon, and 4 types of bacteria. Results indicate that groundwater used for drinking supply is generally of acceptable quality, although concentrations of some constituents or bacteria exceeded at least one drinking-water standard at several wells. The cations detected in the highest concentrations were calcium, magnesium, and sodium; anions detected in the highest concentrations were bicarbonate, chloride, and sulfate. The predominant nutrients were nitrate and ammonia, but no nutrients exceeded Maximum Contaminant Levels (MCLs). The trace elements barium, boron, lithium, and strontium were detected in every sample; the trace elements present in the highest concentrations were barium, boron, iron, lithium, manganese, and strontium. Fifteen pesticides, including seven pesticide degradates, were detected in water from 17 of the 35 wells, but none of the concentrations exceeded State or Federal MCLs. Sixteen volatile organic compounds were detected in water from 15 of the 35 wells. Nine analytes and three types of bacteria were detected in concentrations that exceeded Federal and State drinking-water standards, which typically are identical. One sample had a water color that exceeded the U.S. Environmental Protection Agency (USEPA) Secondary Maximum Contaminant Level (SMCL) and the New York State MCL of 10 color units. Sulfate concentrations exceeded the USEPA SMCL and the New York State MCL of 250 milligrams per liter (mg/L) in two samples, and chloride concentrations exceeded the USEPA SMCL and the New York State MCL of 250 mg/L in two samples. Sodium concentrations exceeded the USEPA Drinking Water Health Advisory of 60 mg/L in eight samples. Iron concentrations exceeded the USEPA SMCL and the New York State MCL of 300 micrograms per liter (ug/L) in 10 filtered samples. Manganese exceeded the USEPA SMCL of 50 ug/L in 10 filtered samples and the New York State MCL of 300 ug/L in 1 filtered sample. Barium exceeded the MCL of 2,000 ug/L in one sample, and aluminum exceeded the SMCL of 50 ug/L in three samples. Radon-222 exceeded the proposed USEPA MCL of 300 picocuries per liter in 12 samples. One sample from a private residential well had a trichloroethene concentration of 50.8 ug/L, which exceeded the MCL of 5 ug/L. Any detection of coliform bacteria indicates a potential violation of New York State health regulations; total coliform bacteria were detected in 19 samples, and fecal coliform bacteria were detected in one sample. The plate counts for heterotrophic bacteria exceeded the MCL (500 colony-forming units per milliliter) in three samples.

Open-File Report↗

USGS2007

Occurrence of Agricultural Chemicals in Shallow Ground Water and the Unsaturated Zone, Northeast Nebraska Glacial Till, 2002-04

Agricultural chemicals applied at the land surface in northeast Nebraska can move downward, past the crop root zone, to ground water. Because agricultural chemicals applied at the land surface are more likely to be observed in the shallowest part of an aquifer, an assessment of shallow ground-water and unsaturated zone quality in the northeast Nebraska glacial till was completed between 2002 and 2004. Ground-water samples were collected at the first occurrence of ground water or just below the water table at 32 sites located in areas likely affected by agriculture. Four of the 32 sites were situated along a ground-water flow path with its downgradient end next to Maple Creek. Twenty-eight sites were installed immediately adjacent to agricultural fields throughout the glacial-till area. In addition to those 32 sites, two sites were installed in pastures to represent ground-water conditions in a non-cropland setting. Ground-water samples were analyzed for physical properties and concentrations of nitrogen and phosphorus compounds, selected pesticides and pesticide degradates, dissolved solids, major ions, trace elements, and dissolved organic carbon. Chlorofluorocarbons (CFCs) or sulfur hexafluoride (SF6) concentrations were analyzed at about 70 percent of the monitoring wells to estimate the residence time of ground water. Borehole-core samples were collected from 28 of the well boreholes. Sediment in the unsaturated zone was analyzed for nitrate, chloride, and ammonia concentrations. Analytical results indicated that the agricultural chemicals most often detected during this study were nitrates and herbicides. Nitrate as nitrogen (nitrate-N) concentrations (2003 median 9.53 milligrams per liter) indicated that human activity has affected the water quality of recently recharged ground water in approximately two-thirds of the wells near corn and soybean fields. The principal pesticide compounds that were detected reflect the most-used pesticides in the area and included parent or degradate compounds of acetochlor, alachlor, atrazine, and metolachlor. Overall, pesticide concentrations in ground-water samples collected in 2003 and 2004 were small and did not exceed public drinking-water standards where established. On average, more pesticides were detected in the flow-path wells than in the glacial-till network wells. The presence of a perennial stream within 1,640 feet of a well was correlated to smaller nitrate-N concentrations in the well water, and the presence of a road ditch within 164 feet of the well was correlated to the presence of detectable pesticides in the well water. All other variables tested showed no significant correlations to nitrate-N concentrations or pesticide detections. Unsaturated zone soil cores collected in 2002 from well boreholes indicated that nitrogen in the forms of nitrate-N and ammonia as nitrogen (ammonia-N) was available in the unsaturated zone for transport to ground water. Concentrations of nitrate-N and ammonia-N in these soil cores were inversely correlated to depth, and nitrate-N concentrations were correlated to chloride concentrations.

Scientific Investigations Report↗

USGS2004

Approaches to surface complexation modeling of Uranium(VI) adsorption on aquifer sediments

Uranium(VI) adsorption onto aquifer sediments was studied in batch experiments as a function of pH and U(VI) and dissolved carbonate concentrations in artificial groundwater solutions. The sediments were collected from an alluvial aquifer at a location upgradient of contamination from a former uranium mill operation at Naturita, Colorado (USA). The ranges of aqueous chemical conditions used in the U(VI) adsorption experiments (pH 6.9 to 7.9; U(VI) concentration 2.5 · 10 −8 to 1 · 10 −5 M; partial pressure of carbon dioxide gas 0.05 to 6.8%) were based on the spatial variation in chemical conditions observed in 1999–2000 in the Naturita alluvial aquifer. The major minerals in the sediments were quartz, feldspars, and calcite, with minor amounts of magnetite and clay minerals. Quartz grains commonly exhibited coatings that were greater than 10 nm in thickness and composed of an illite-smectite clay with occluded ferrihydrite and goethite nanoparticles. Chemical extractions of quartz grains removed from the sediments were used to estimate the masses of iron and aluminum present in the coatings. Various surface complexation modeling approaches were compared in terms of the ability to describe the U(VI) experimental data and the data requirements for model application to the sediments. Published models for U(VI) adsorption on reference minerals were applied to predict U(VI) adsorption based on assumptions about the sediment surface composition and physical properties (e.g., surface area and electrical double layer). Predictions from these models were highly variable, with results overpredicting or underpredicting the experimental data, depending on the assumptions used to apply the model. Although the models for reference minerals are supported by detailed experimental studies (and in ideal cases, surface spectroscopy), the results suggest that errors are caused in applying the models directly to the sediments by uncertain knowledge of: 1) the proportion and types of surface functional groups available for adsorption in the surface coatings; 2) the electric field at the mineral-water interface; and 3) surface reactions of major ions in the aqueous phase, such as Ca 2+ , Mg 2+ , HCO 3 − , SO 4 2− , H 4 SiO 4 , and organic acids. In contrast, a semi-empirical surface complexation modeling approach can be used to describe the U(VI) experimental data more precisely as a function of aqueous chemical conditions. This approach is useful as a tool to describe the variation in U(VI) retardation as a function of chemical conditions in field-scale reactive transport simulations, and the approach can be used at other field sites. However, the semi-empirical approach is limited by the site-specific nature of the model parameters.

Geochimica et Cosmochimica Acta↗