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USGS1967

Water resources data for Indiana, 1966

The surface-water records for the 1966 water year for gaging stations, partial-record stations, and miscellaneous sites within the State of Indiana are given in this report. For convenience there are also included records for a few pertinent gaging stations in bordering states. The quality-of-water investigations of the U.S. Geological Survey are concerned with the chemical and physical characteristics of surface- and ground-water supplies of the Nation. The basic records for the 1966 water year for quality of surface waters within the State of Indiana are given in this report. For convenience and interest, there are also records for a few water quality stations in bordering states.

Indiana↗

USGS1968

Water resources data for Indiana, 1967

The surface-water records for the 1967 water year for gaging stations, partial-record stations, and miscellaneous sites within the State of Indiana are given in this report. For convenience there are also included records for a few pertinent gaging stations in bordering States. The quality-of-water investigations of the U.S. Geological Survey are concerned with the chemical and physical characteristics of surface- and ground-water supplies of the Nation. The basic records for the 1967 water year for quality of surface waters within the State of Indiana are given in this report. For convenience and interest, there are also records for a few water quality stations in bordering states.

Indiana↗

USGS1974

Rates of salt solution in the Permian basin

For safe, long-term storage of radioactive materials in salt beds, rates of solution of salt which might imperil such storage must be known. For solution to continue, fluid must move through the system. Major fluid discharge from the system is by surface streams. Using U.S. Geological Survey records of streamflow and chemical quality of water, computations of sodium chloride discharges of numerous subbasins have been made. A map has been constructed showing tons of sodium chloride discharged per day and tons of sodium chloride discharged per square mile per year. Also shown are locations of major saline springs and their rate of discharge of sodium chloride in tons per day.

Colorado, Kansas, New Mexico, Oklahoma, Texas↗

USGS1985

Physical characteristics and chemical quality of selected springs in parts of Juab, Millard, Tooele, and Utah counties, Utah

Hydrologic, geologic, and partial water quality data were collected at 90 selected springs in west-central Utah, and chemical analyses performed on water samples from 62 of the springs. Descriptions of the physiographic and geologic conditions, climate, and vegetation patterns for the study area are included. Allowable limits of certain chemical constituents in water for human and livestock consumption are included with the water quality data. Three classifications of springs were established based on physical characteristics of the springs, and chemical composition of the springflow: (1) mountain springs; (2) non-thermal valley springs, and (3) thermal valley springs. Mountain springs are in and near recharge areas, have seasonal variations of discharge and temperature, typically discharge from extrusive and metamorphic geohydrologic units, and generally discharge freshwater. Non-thermal valley springs are peripheral to recharge areas, have seasonal variations of discharge and temperature, typically discharge from a variety of geohydrologic units, and have variable water composition. Thermal valley springs are near topographic low areas of valleys , and have little seasonal variation of discharge or temperature. They typically discharge from unconsolidated deposits (but the discharge probably has flowed through buried carbonate geohydrologic units). They also have a considerable range of water composition that reflects the relative complexity of the groundwater system. (Author 's abstract)

Utah↗

USGS1977

Map showing general chemical quality of ground water in the Kaiparowits coal-basin area, Utah

This is one of a series of maps that describe the geology and related natural resources in the Kaiparowits coal-basin area. Chemical analyses of water from about 40 widely scattered springs, 20 coal-exploration holes in the Kaiparowits Plateau, and 7 water wells in the vicinity of the communities of Escalante and Glen Canyon were used to compile this map. All the water samples were from depths of less than 1,000 feet (305 m). Water-quality data were also available from a number of petroleum wells and exploration holes more than 5,000 feet (1,524 m) deep; however, those data were used with considerable discretion because water produced by deep petroleum wells and exploration holes usually is more saline than water found at shallower depths at the drilling sites. Most of the chemical analyses used were collected by the U.S. Geological Survey in cooperation with State, local, and other Federal agencies. Published sources of data included Phoenix (1963), Iorns, Hembree, and Phoenix (1964), Cooley (1965), Feltis (1966), and Goode (1966, 1969), and the Environmental Impact Statement of the proposed Kaiparowits power project (U.S. Bureau of Land Management, 1976). Little or no ground-water-quality data were available for large areas in the Kaiparowits coal basin. In those areas, the indicated ranged of dissolved-solids concentrations in water from springs and wells are inferred largely from the geology as compiled by Stokes (1964) and Hackman and Wyant (1973). This is especially true for those areas where the designated ranges of dissolved-solids concentrations are 100-1,000 and 500-3,000 mg/l (milligrams per liter). El Paso Natural Gas Co., Resources Co., Kaiser Engineers, and Southern California Edison Co. provided ground-water samples and specific water-quality data collected from their exploratory drill holes on the Kaiparowits Plateau. The cooperation of those firms is gratefully acknowledged.

Utah↗

USGS1964

Geology and ground-water resources of Washington, D.C., and vicinity, with a section on chemical quality of the water

The area of this report includes 436 square miles centered about the District of Columbia. The area contains parts of two distinctly different physiographic provinces-the Piedmont and the Coastal Plain. The Fall Line, which separates the Piedmont province on the west from the Coastal Plain Province on the east, bisects the area diagonally from northeast to southwest. Northwest of the Fall Line, deeply weathered igneous and metamorphic rocks are exposed ; to the southeast, these rocks are covered by Coastal Plain sediments; the nonconformity between crystalline rock and sediments dips southeast at an average rate of about 125 feet per mile. The rocks of the Piedmont include: (1) schist, phyllite, and quartzite of the Wissahickon Formation; (2) altered mafic rocks such as greenstone and serpentine; (3) the Laurel Gneiss of Chapman, 1942, and the Sykesville Formation of Jonas, 1928--both probably derived from the Wissahickon ; and (4) later granitic intrusive rocks. Lying upon this basement of hard rocks east of the Fall Line are the generally unconsolidated sediments of the Coastal Plain, which include gravel, sand, and clay, ranging in age from Cretaceous to Recent. These sediments measure only a few inches at their western extremity but thicken to 1,800 feet at the southeast corner of the mapped area. Owing to the great diversity in the geology of the two provinces, the waterbearing characteristics of the rocks also vary greatly. In the Piedmont, ground water occurs under unconfined or water-table conditions in openings and fissures in the hard rocks or in the residual weathered blanket that overlies them. In the Coastal Plain, the shallow wells tap unconfined water, but beneath the upper clay layers the water is contained in the sand and gravel under artesian pressure and must be recovered by deep drilled wells. Wells are of three types--drilled, bored, and dug. Drilled wells furnish a permanent water supply and are the least subject to pollution when properly constructed. Bored or dug wells allow greater storage capacity and are satisfactory for domestic supplies in some locations, but they are polluted easily. If not properly constructed or of sufficient depth, they may fail in dry weather. Ground-water supplies for domestic use, 5 to 10 gpm (gallons per minute), are obtainable in most places. In the Piedmont, recorded yields in drilled wells range from 0.2 to 212 gpm. In the Coastal Plain, wells yield from 1 to 800 gpm. The quality of the ground water in the report area is generally satisfactory for domestic, industrial, and irrigation use. High iron content and corrosiveness are troublesome in places. The water is soft to moderately hard--2 to 175 ppm (parts per million). Water in the Piedmont province is. dominantly the calcium and bicarbonate type; in the Coastal Plain most water is of calcium-magnesium bicarbonate type. In the Piedmont, careful location of wells with respect to the geology (rock type and structure) and to topography usually results in higher yields and may mean the difference between success and failure. In the Coastal Plain, drilled artesian wells are not affected by topography, but the yield obtained depends upon the penetration of a water-bearing sand or gravel bed at sufficient depth. The early settlers obtained water from the springs and streams, and later from dug wells. After Washington was established as the Capital in 1800, water was obtained from public and privately owned wells. Water was piped from some of the springs to government buildings and to private homes and business houses. In 1863 a diversion dam was completed in the Potomac above Great Falls and a conduit was built into the city to furnish a public water supply. This system with modifications has been in use ever since. A new diversion dam and pumping station at Little Falls was put into service in the summer of 1959.

District of Columbia↗

USGS2018

Chemical and isotopic characteristics of methane in groundwater of Ohio, 2016

In 2016, the U.S. Geological Survey, in cooperation with the Ohio Water Development Authority, investigated the hydrogeologic setting, chemical and isotopic characteristics, and origin of methane in groundwater of Ohio. Understanding the occurrence and distribution of methane in groundwater is important in terms of public safety because methane in water wells can pose a risk of explosion. In addition, documenting the chemical and isotopic characteristics of methane in groundwater can make an important contribution to future stray gas investigations. Water samples were collected from 15 domestic water wells known to produce methane, which were in 12 counties in diverse parts of Ohio. The wells were 75–345 feet deep and tapped a range of aquifer types, including glacial deposits and bedrock of Upper Ordovician, Upper Devonian, Lower Mississippian, and Pennsylvanian ages. Although the hydrogeologic settings were varied, there was a broad similarity among the well sites in that the bedrock was predominantly shale and the glacial deposits were predominantly clay. The wells were sampled for dissolved inorganic constituents; dissolved organic carbon; methane and other dissolved gases; stable isotopes (carbon, hydrogen, and oxygen) of methane, water, and dissolved inorganic carbon; and carbon-14 of methane. Gas composition and stable isotopes of methane were used to differentiate thermogenic and microbial methane. The degree of fractionation of hydrogen and carbon isotopes was used to evaluate the pathway of microbial methanogenesis (carbon dioxide [CO 2 ] reduction or acetate fermentation) and the effects of secondary processes such as oxidation, mixing, and migration. The concentration of carbon-14 of methane was used to evaluate the relative age of the carbon source. The quality of water from the 15 wells differed greatly; water types ranged from CaMgHCO 3 to NaCl, and total dissolved solids concentrations ranged from 318 to 2,940 milligrams per liter (mg/L). Methane concentrations ranged from 1.2 to 120 mg/L. Of the 15 samples, 12 had methane concentrations greater than 28 mg/L, the level that can pose a risk of explosion. Of the 15 samples, 12 had chemical and isotopic characteristics or "signatures" consistent with microbial methane formed by CO 2 reduction. CO 2 reduction is commonly associated with microbial degradation of organic matter in anaerobic aquifers and with the formation of microbial shale gas and coalbed methane along margins of sedimentary basins. Two of 15 samples were interpreted as having a component of thermogenic methane based on the δ 13 C of methane (−50.96 and −47.74 parts per thousand [per mil]) and gas dryness (28 and 5). One of 15 samples (from the shallowest well) had chemical and isotopic characteristics consistent with methane oxidation by sulfate reduction based on light δ 13 C of dissolved inorganic carbon (−31.6 per mil) and evidence of sulfate reduction in terms of the odor and appearance of the water. For the 12 samples interpreted as microbial methane formed by CO 2 reduction, the δ 13 C of methane varied from −75 to −56 per mil. Multiple samples from the same aquifer demonstrated a general trend of increasing δ 13 C of methane with depth. Samples with lighter δ 13 C of methane (−75 to −62 per mil) were from shallower wells (or wells with shallow open intervals), and the isotopic signature of the water was consistent with modern or postglacial groundwater recharge. Three samples with heavier δ 13 C of methane (−61 to −56 per mil) were from deeper wells or more confined aquifers where the isotopic signature of water was consistent with older (glacial) recharge. In addition, δ 13 C of dissolved inorganic carbon was enriched (+12 to +18.9 per mil), and carbon-14 of methane was consistent with carbon associated with Paleozoic bedrock or older glacial deposits. These observations are generally consistent with increased Rayleigh-type fractionation at greater depths; however, other interpretations are possible. Isotopic signatures can be ambiguous, especially in areas with complex geologic histories that include multiple episodes of migration, mixing, and (or) oxidation. Many of the wells were in proximity to multiple potential natural and anthropogenic pathways of methane migration; however, it is not possible to determine if the methane in any of the wells is related to human activities based on the chemical and isotopic data collected for this study.

Ohio↗

USGS2014

Placing prairie pothole wetlands along spatial and temporal continua to improve integration of wetland function in ecological investigations

We evaluated the efficacy of using chemical characteristics to rank wetland relation to surface and groundwater along a hydrologic continuum ranging from groundwater recharge to groundwater discharge. We used 27 years (1974–2002) of water chemistry data from 15 prairie pothole wetlands and known hydrologic connections of these wetlands to groundwater to evaluate spatial and temporal patterns in chemical characteristics that correspond to the unique ecosystem functions each wetland performed. Due to the mineral content and the low permeability rate of glacial till and soils, salinity of wetland waters increased along a continuum of wetland relation to groundwater recharge, flow-through or discharge. Mean inter-annual specific conductance (a proxy for salinity) increased along this continuum from wetlands that recharge groundwater being fresh to wetlands that receive groundwater discharge being the most saline, and wetlands that both recharge and discharge to groundwater (i.e., groundwater flow-through wetlands) being of intermediate salinity. The primary axis from a principal component analysis revealed that specific conductance (and major ions affecting conductance) explained 71% of the variation in wetland chemistry over the 27 years of this investigation. We found that long-term averages from this axis were useful to identify a wetland’s long-term relation to surface and groundwater. Yearly or seasonal measurements of specific conductance can be less definitive because of highly dynamic inter- and intra-annual climate cycles that affect water volumes and the interaction of groundwater and geologic materials, and thereby influence the chemical composition of wetland waters. The influence of wetland relation to surface and groundwater on water chemistry has application in many scientific disciplines and is especially needed to improve ecological understanding in wetland investigations. We suggest ways that monitoring in situ wetland conditions could be linked with evolving remote sensing technology to improve our ability to better inform decisions affecting wetland sustainability and provide periodic inventories of wetland ecosystem services to document temporal trends in wetland function and how they respond to contemporary land-use change.

North Dakota↗

USGS2024

Editorial: From cold seeps to hydrothermal vents: Geology, chemistry, microbiology, and ecology in marine and coastal environments

This Research Topic compiles contemporary studies on cold seeps, hydrothermal vents, mud volcanoes, and related seafloor features that are associated with focused fluid emissions and the transfer of carbon, other chemical species, and sometimes heat from the geosphere to the ocean. Because these features sometimes tap fluids and gas originating kilometers below the seafloor, they provide an important window into deep processes that are otherwise inaccessible to scientists. At the shallow portion of their journey, migrating fluids nearing the seafloor contribute to a range of unique biological, physical, and chemical processes within the sediments themselves and at the sediment-water interface. Seafloor fluid emissions play a critical role in global biogeochemical cycles, ocean chemistry, and possibly even climate change. Seafloor leakage points often emit hydrocarbon gases (especially methane and CO 2 ) and are sometimes the loci for deposition of seafloor minerals that have economic value. A burgeoning area of research focuses on natural products generated at these features, seeking compounds with potential pharmaceutical or other applications. Multidisciplinary studies have become routine for characterization of seafloor fluid emission sites, attesting to the inseparability of geologic, physical, chemical, and biological processes in these settings. It is increasingly common for researchers to combine in a single research cruise: subbottom imaging and seafloor mapping; porewater and water column geochemistry and gas sampling; sediment retrieval for lithologic, biostratigraphic, and solid phase analyses; and studies of benthic and subseafloor communities at the microbial to macrofaunal scales. This multidisciplinary approach has the advantage of ensuring the spatial and temporal coincidence of surveys and samples, an important factor at highly dynamic seafloor fluid emission sites. In addition, researchers often use remotely operated vehicles (ROVs), autonomous underwater vehicles (AUVs), or human-occupied vehicles (HOVs) to record video of the seafloor, compile photomosaics, collect targeted samples, and survey with high-resolution geophysical near-seafloor systems, providing a degree of detail about seafloor fluid emission sites that is unprecedented compared to most areas of the deep ocean. While rarer, long-term cabled observatories or shorter-term deployments of portable observatories are also used at some loci for seafloor fluid flux and are particularly helpful for capturing temporal variations at these dynamic features. Here we summarize the Research Topic’s contribution to multidisciplinary seafloor emission studies in the categories of cold seeps, mud volcanoes, and hydrothermal vents. Figure 1 shows the geographic distribution of the studies in this Research Topic and key features referred to in this Introduction.

Frontiers in Earth Science↗

USGS2008

Pathogen and chemical transport in the karst limestone of the Biscayne aquifer: 1. Revised conceptualization of groundwater flow

The Biscayne aquifer is a highly transmissive karst limestone that serves as the sole source of drinking water to over two million residents in south Florida. The aquifer is characterized by eogenetic karst, where the most transmissive void space can be an interconnected, touching‐vug, biogenically influenced porosity of biogenic origin. Public supply wells in the aquifer are in close proximity to lakes established by surface mining. The mining of the limestone has occurred to the same depths as the production wells, which has raised concerns about pathogen and chemical transport from these surface water bodies. Hydraulic and forced gradient tracer tests were conducted to augment geologic and geophysical studies and to develop a hydrogeologic conceptual model of groundwater flow and chemical transport in the Biscayne aquifer. Geologic and geophysical data indicate multiple, areally extensive subhorizontal preferential flow zones of vuggy limestone separated by rock with a matrix pore system. The hydraulic response from an aquifer test suggests that the Biscayne aquifer behaves as a dual‐porosity medium; however, the results of the tracer test showed rapid transport similar to other types of karst. The tracer test and concurrent temperature logging revealed that only one of the touching‐vug flow zones dominates transport near the production wells. On the basis of the rising limb of the breakthrough curve, the dispersivity is estimated to be less than 3% of the tracer travel distance, which suggests that the fastest flow paths in the formation are likely to yield limited dilution of chemical constituents.

Water Resources Research↗

USGS1989

Physical and chemical properties of San Francisco Bay, California, 1980

The U.S. Geological Survey conducted hydrologic investigations in both the deep water channels and the shallow-water regions of the San Francisco Bay estuarine system during 1980. Cruises were conducted regularly, usually at two-week intervals. Physical and chemical properties presented in this report include temperature , salinity, suspended particulate matter, turbidity, extinction coefficient, partial pressure of CO2, partial pressure of oxygen , dissolved organic carbon, particulate organic carbon, discrete chlorophyll a, fluorescence of photosynthetic pigments, dissolved silica, dissolved phosphate, nitrate plus nitrite, nitrite, ammonium, dissolved inorganic nitrogen, dissolved nitrogen, dissolved phosphorus, total nitrogen, and total phosphorus. Analytical methods are described. The body of data contained in this report characterizes hydrologic conditions in San Francisco Bay during a year with an average rate of freshwater inflow to the estuary. Concentrations of dissolved silica (discrete-sample) ranged from 3.8 to 310 micro-M in the northern reach of the bay, whereas the range in the southern reach was limited to 63 to 150 micro-M. Concentrations of phosphate (discrete-sample) ranged from 1.3 to 4.4 micro-M in the northern reach, which was narrow in comparison with that of 2.2 to 19.0 micro-M in the southern reach. Concentrations of nitrate plus nitrite (discrete-sample) ranged from near zero to 53 micro-M in the northern reach, and from 2.3 to 64 micro-M in the southern reach. Concentrations of nitrite (discrete-sample) were low in both reaches, exhibiting a range from nearly zero to approximately 2.3 micro-M. Concentrations of ammonium (discrete-sample) ranged from near zero to 14.2 micro-M in the northern reach, and from near zero to 8.3 micro-M in the southern reach. (USGS)

Open-File Report↗

USGS2006

Some aspects of chemical equilibrium in ground water

The influence of individual factors such as geologic and hydrologic characteristics of environment, biologic activity in soil, and pollutants on ground ‐ water composition is discussed. Aspects of chemical equilibria in ground water , sorption reactions, carbonate equilibria, chemistry of iron, and factors altering equilibria are presented.

Groundwater↗

USGS2006

Integration of coral reef ecosystem process studies and remote sensing

Worldwide, local-scale anthropogenic stress combined with global climate change is driving shifts in the state of reef benthic communities from coral-rich to micro- or macroalgal-dominated (Knowlton, 1992; Done, 1999). Such phase shifts in reef benthic communities may be either abrupt or gradual, and case studies from diverse ocean basins demonstrate that recovery, while uncertain (Hughes, 1994), typically involves progression through successional stages (Done, 1992). These transitions in benthic community structure involve changes in community metabolism, and accordingly, the holistic evaluation of associated biogeochemical variables is of great intrinsic value (Done, 1992). Effective reef management requires advance prediction of coral reef alteration in the face of anthropogenic stress and change in the global environment (Hatcher, 1997a). In practice, this goal requires techniques that can rapidly discern, at an early stage, sublethal effects that may cause long-term increases in mortality (brown, 1988; Grigg and Dollar, 1990). Such methods would improve our understanding of the differences in the population, community, and ecosystem structure, as well as function, between pristine and degraded reefs. This knowledge base could then support scientifically based management strategies (Done, 1992). Brown (1988) noted the general lack of rigor in the assessment of stress on coral reefs and suggested that more quantitative approaches than currently exist are needed to allow objective understanding of coral reef dynamics. Sensitive techniques for the timely appraisal of pollution effects or generalized endemic stress in coral reefs are sorely lacking (Grigg and Dollar, 1990; Wilkinsin, 1992). Moreover, monitoring methods based on population inventories, sclerochronology, or reproductive biology tend to myopic and may give inconsistent results. Ideally, an improved means of evaluating reef stress would discriminate mortality due to natural causes from morality to anthropogenic causes (Brown, 1988). Models of coral reef ecosystems, parameterized by process measurements and scaled in time-space using remote sensing, have the potential to address pressing research questions that are central to devising valid management strategies (Grigg el al., 1984; Hatcher, 1997b). To attain this goal, ecosystem-level models that integrate studies of physical and chemical forcing with observed biological and geological responses are required. This interdisciplinary approach to understanding reef biogeochemical dynamics can allow investigations that integrate the scales of time and space (Hatcher, 1997a), thereby enabling prediction of coral reef change (Andréfouët and Payri, 2001). In turn, prediction of holistic ecosystem function within various environmental focusing scenarios has substantial promise in mitigating future disturbance. Indeed, management of coral reefs at the ecosystem level has been suggested as the only meaningful approach to preserving coral reefs (Bohnsack and Ault, 1996; Christensen et al., 1996).

Florida↗

USGS2009

Pilot studies for the North American Soil Geochemical Landscapes Project - Site selection, sampling protocols, analytical methods, and quality control protocols

In 2004, the US Geological Survey (USGS) and the Geological Survey of Canada sampled and chemically analyzed soils along two transects across Canada and the USA in preparation for a planned soil geochemical survey of North America. This effort was a pilot study to test and refine sampling protocols, analytical methods, quality control protocols, and field logistics for the continental survey. A total of 220 sample sites were selected at approximately 40-km intervals along the two transects. The ideal sampling protocol at each site called for a sample from a depth of 0-5 cm and a composite of each of the O, A, and C horizons. The <2-mm fraction of each sample was analyzed for Al, Ca, Fe, K, Mg, Na, S, Ti, Ag, As, Ba, Be, Bi, Cd, Ce, Co, Cr, Cs, Cu, Ga, In, La, Li, Mn, Mo, Nb, Ni, P, Pb, Rb, Sb, Sc, Sn, Sr, Te, Th, Tl, U, V, W, Y, and Zn by inductively coupled plasma-mass spectrometry and inductively coupled plasma-atomic emission spectrometry following a near-total digestion in a mixture of HCl, HNO 3 , HClO 4 , and HF. Separate methods were used for Hg, Se, total C, and carbonate-C on this same size fraction. Only Ag, In, and Te had a large percentage of concentrations below the detection limit. Quality control (QC) of the analyses was monitored at three levels: the laboratory performing the analysis, the USGS QC officer, and the principal investigator for the study. This level of review resulted in an average of one QC sample for every 20 field samples, which proved to be minimally adequate for such a large-scale survey. Additional QC samples should be added to monitor within-batch quality to the extent that no more than 10 samples are analyzed between a QC sample. Only Cr (77%), Y (82%), and Sb (80%) fell outside the acceptable limits of accuracy (% recovery between 85 and 115%) because of likely residence in mineral phases resistant to the acid digestion. A separate sample of 0-5-cm material was collected at each site for determination of organic compounds. A subset of 73 of these samples was analyzed for a suite of 19 organochlorine pesticides by gas chromatography. Only three of these samples had detectable pesticide concentrations. A separate sample of A-horizon soil was collected for microbial characterization by phospholipid fatty acid analysis (PLFA), soil enzyme assays, and determination of selected human and agricultural pathogens. Collection, preservation and analysis of samples for both organic compounds and microbial characterization add a great degree of complication to the sampling and preservation protocols and a significant increase to the cost for a continental-scale survey. Both these issues must be considered carefully prior to adopting these parameters as part of the soil geochemical survey of North America.

Applied Geochemistry↗

USGS2006

Composition of aeolian dust in natural traps on isolated surfaces of the central Mojave Desert - Insights to mixing, sources, and nutrient inputs

The recognition and characterization of aeolian dust in soil contribute to a better understanding of landscape and ecosystem dynamics of drylands. Results of this study show that recently deposited dust, sampled in isolated, mostly high-ground settings, is chemically and mineralogically similar on varied geologic substrates over a large area (15 000 km2) in the Mojave Desert. The silt-plus-clay fraction (fines) on these isolated surfaces is closely alike in magnetic-mineral composition, in contrast to greatly dissimilar magnetic compositions of rock surfaces of vastly different lithologies, on which the fines have accumulated. The fines, thus, are predominantly deposited dust. The amounts of potential nutrients in the sampled dust are much more uniform than might be provided by direct, local weathering of bedrock or by dust locally derived from nearby weathered products. The compositional similarity of the dust on these surfaces is interpreted to result from mixing of fines in the atmosphere as well as in fluvial, alluvial, and lacustrine depositional settings prior to dust emission.

Journal of Arid Environments↗

USGS2004

Evaluation of multidimensional transport through a field-scale compacted soil liner

A field-scale compacted soil liner was constructed at the University of Illinois at Urbana-Champaign by the U.S. Environmental Protection Agency (USEPA) and Illinois State Geological Survey in 1988 to investigate chemical transport rates through low permeability compacted clay liners (CCLs). Four tracers (bromide and three benzoic acid tracers) were each added to one of four large ring infiltrometers (LRIs) while tritium was added to the pond water (excluding the infiltrometers). Results from the long-term transport of Br - "> Br - from the localized source zone of LRI are presented in this paper. Core samples were taken radially outward from the center of the Br - "> Br - LRI and concentration depth profiles were obtained. Transport properties were evaluated using an axially symmetric transport model. Results indicate that (1) transport was diffusion controlled; (2) transport due to advection was negligible and well within the regulatory limits of k sat ⩽ 1 × 10 - 7 cm / s ; "> k sat ⩽ 1 × 10 − 7 cm / s; (3) diffusion rates in the horizontal and vertical directions were the same; and (4) small positioning errors due to compression during soil sampling did not affect the best fit advection and diffusion values. The best-fit diffusion coefficient for bromide was equal to the molecular diffusion coefficient multiplied by a tortuosity factor of 0.27, which is within 8% of the tortuosity factor (0.25) found in a related study where tritium transport through the same liner was evaluated. This suggests that the governing mechanisms for the transport of tritium and bromide through the CCL were similar. These results are significant because they address transport through a composite liner from a localized source zone which occurs when defects or punctures in the geomembrane of a composite system are present.

Journal of Geotechnical and Geoenvironmental Engin↗

USGS1886

Report of work done in the division of chemistry and physics mainly during the fiscal year 1884-85

The present bulletin contains some of the more important results obtained in the chemical laboratory of the United States Geological Survey during the fiscal year 1884—'85. It also contains two physical papers representing work which was mainly done during previous fiscal years, but completed during the one for which this bulletin is issued. These papers are practically continuations of or supplements to Bulletin 14.

Bulletin↗

USGS1973

Selected hydrologic data in the upper Colorado River basin

Most of the information in this atlas pertains to the ground-water resources of the basin. The surface-water resources, climate, and geohydrologic framework have been described in considerable detail by Iorns and others (1964, 1965). The maps in this atlas are highly generalized, and are intended to provide the reader with only a general understanding of the geology, ground-water conditions, and chemical quality of the water in the basin as a whole. In most instances, the availability, depth to, and chemical quality of ground water at a given well site can be determined only by special investigations. Only previously collected data were used to compile the maps in this atlas. More detailed information for specific parts of the basin can be found in the reports and maps in the list of references.

Arizona, Colorado, New Mexico, Utah, Wyoming↗