USGS Science⌕ Search

SEARCH · USGS Science

Results for “Chemical Geology”

Search indexed USGS publications on groundwater, aquifers, geologic maps, mineral resources and earthquakes. Explore source records by subject and place.

Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.

At least 1,027 records · Page 57Linked to original sources
USGS1957

Geology and ground-water resources of Outagamie County, Wisconsin

Outagamie County is in east-central Wisconsin. It has no serious groundwater problem at present, but the county is important as a recharge area for the principal aquifers supplying water to Brown County and industrial Green Bay to the east. The county is covered by glacial drift and lake deposits of the Wisconsin stage of glaciation. In the northwestern quarter of the county these deposits rest upon Precambrian crystalline rocks; throughout the remainder of the county they are underlain by sandstone, limestone, dolomite, and shale of Cambrian and Ordovician age. ·where they are sufficiently thick, and where more productive formations are absent, glacial sand and gravel are an important source of ground water. The major sources, however, are the St. Peter sandstone, of Ordovician age, and the sandstones of the Upper Cambrian series. The Precambrian crystalline rocks, which underlie all the county, yield little or no water to wells. The regional dip of the Paleozoic bedrocks is 25 to 30 feet per mile eastward and southeastward. There are no major folds, but the thickness of each geologic unit may change from place to place because of predepositional or postdepositional erosion. There is no conclusive evidence of major faulting in the area. Ground water in Outagamie County occurs under both water-table (unconfined) and artesian (confined) conditions. The source of the ground water is precipitation which falls on the surface and percolates downward into the underlying permeable materials. Regional movement of ground water in the eastern third of the county is controlled by the bedrock structure, and the discharge is toward the east and south. Throughout the rest of the county the movement of water is controlled mainly by bedrock and surface topography, and the water moves toward the streams and bedrock valleys. Water-level :fluctuations follow definite patterns. Where the effects of pumping are at a minimum, water levels reach a high in April or May, decline through the summer months owing to natural discharge, and lack of recharge, and do not begin to recover until after the ground thaws in the spring. In areas of heavy pumping where this pattern is distorted, the lowest water levels occur in the early fall and recoveries begin in October or November after the period of heaviest pumping. Pumpage in the county was estimated to be about 9.0 million gallons per day (mgd) in 1951 and 1952. Nearly half of this was for industrial, commercial, and public-supply use along the Fox River. Wells, most of which are drilled by the cable-tool method, range in diameter from 3 to 16 inches and in depth from 10 or 20 feet to 804 feet. In the alluvium and glacial drift 1~- to 2¥2-inch driven wells are common. Pumping tests were made to determine the hydraulic characteristics of the aquifers at Seymour, Appleton, and Hortonville. The average coefficient of transmissibility at Seymour is about 18,000 gpd per foot; at Appleton it is about 19,000 gpd per foot. The coefficients of storage are 0.00022 and 0.00015 at Seymour and Appleton, respectively. Movement of ground water out of the county, assuming an average transmissibility of 18,000 gpd per foot, was calculated to be more than 10 mgd toward the southeast. The ground water differs greatly in chemical quality from well to well, but it is generally a very hard calcium magnesium bicarbonate water, some of it high in iron. To aid in determining the source of well waters, 22 chemical analyses were plotted on a logarithmic diagram to obtain characteristic patterns for waters from several geologic sources.

Wisconsin↗
USGS1958

The relation of phosphorites to ground water in Beaufort County, North Carolina

Recent ground-water studies undertaken by the U.S. Geological Survey in cooperation with the North Carolina Division of Mineral Resources have delineated phosphorite deposits, tentatively regarded as being of middle Miocene age, in Beaufort County. These deposits lie unconforma-bly on limestone of Eocene age and are unconformably overlain by late Miocene marl. The phosphorites, buried beneath strata ranging in thickness from 45 to 250 feet, underlie an area approximating 450 square miles. The total thickness of the phosphorite column throughout the area ranges from several feet to nearly 90 feet. The phosphorite column consists of phosphatic sands and intercalated shell limestones. The sands, composed of pellets of brown sand-size collophane (probably carbonate-fluorapatite) and sand-size, flat-sided angular quartz with some silt, clay, and organic material, have a median diameter between 0.50 and 0.25 mm. Chemical analyses of representative samples of the raw sand show a variation in PaOs content from 8 to 31 percent. The P2O5 content is apparently proportionate to the collophane content throughout the area. Reconstruction of the geologic history suggests that the phosphorites were deposited as chemical precipitates and as in situ replacements in a restricted marine basin where the pH of the water acted as the primary depositional control. Reconstruction of the hydrologic history of the phosphorites indicates that the deposits were preserved under artesian conditions; they were never subjected to alteration under water-table conditions. The absence of postpositional alteration makes this area a potentially classic one for studies of phosphorite genesis. Chemical analyses of artesian waters from the phosphorites and from limestones overlain by phosphorites reveal significantly greater concentrations of iodide and bromide in solution than are present in water from overlying sediments or from underlying limestones not overlain by phosphorites. Such anomalies, if present in other similar terranes, may indicate the presence of buried phosphorites. The depth and size distribution of the material suggest a recovery method utilizing wells constructed to "pump sand."

North Carolina↗
USGS2004

Effects of highway deicing chemicals on shallow unconsolidated aquifers in Ohio — Final report

As a result of concerns about salt intrusion into drinking water aquifers, the effects of highway deicing chemicals on shallow aquifers were studied at eight locations in Ohio from 1988 through 2002. The study was done by the U.S. Geological Survey, in cooperation with the Ohio Department of Transportation and the Federal Highway Administration. Sites were selected along major undivided highways where drainage is by open ditches and ground-water flow is approximately perpendicular to the highway. Records of deicer application rates were kept, and apparent movement of deicing chemicals through shallow, unconsolidated aquifers was monitored by means of periodic measurements of specific conductance and concentrations of dissolved sodium, calcium, and chloride. The State routes monitored were the following: State Route (SR) 3 in Ashland County, SR 84 in Ashtabula County, SR 29 in Champaign County, SR 4 in Clark County, SR 2 in Lucas County, SR 104 in Pickaway County, SR 14 in Portage County, and SR 97 in Richland County. The study began in 1988 with background data collection, extensive literature review, and site selection. This process, including drilling of wells at numerous test sites and the eight selected sites, lasted 3 years. Routine groundwater sampling at 4- to 6-week intervals began in January 1991 and continued through September 1999. A multilevel, passive flow ground-water sampling device was constructed and used. Other conditions monitored on a regular basis included ground-water level (monitored continuously), specific conductance, air and soil temperature, precipitation,chloride concentration in soil samples, and deicing-chemical application times and rates. Evidence from water analysis, specific-conductance measurements, and surface-geophysical measurements indicates that three of the eight sites (Ashtabula County, Lucas County, and Portage County sites) were affected by direct application of deicing chemicals. Climatic data collected during the study show that cold weather, and therefore deicing-chemical application rates, varied from south to north across the State. As a consequence, only minor traces of dissolved chloride (mean, 24–43 mg/L (milligrams per liter)) above background concentrations (mean, 13–23 mg/L) were determined in ground-water samples from the southernmost sites (approximately 3930' to 40 N latitude—Champaign County, Clark County, and Pickaway County). At the Ashland and Richland County sites (approximately 4030' N latitude), dissolved-chloride concentrations increased above background concentrations only intermittently (mean background concentrations 4–41 mg/L, rising to a mean of 40–56 mg/L in downgradient wells). At the northernmost sites (41 30' to 42 N latitude—Lucas County, Portage County, and Ashtabula County), deicing-chemical application was consistent throughout the winter, and downgradient dissolved-chloride concentrations (mean, 124–345 mg/L) rarely returned to background concentrations (mean, 7–37 mg/L) throughout the study period. Other factors than application rate that may affect the movement of deicing chemicals through an aquifer were precipitation amounts, the types of subsurface materials, ground-water velocity and gradient, hydraulic conductivity, soil type, land use, and Ohio Department of Transportation deicing priority.

Ohio↗
USGS1980

Chemical, physical, and radiological quality of selected public water supplies in Florida : January-May 1979

Verde Valley--an area of complex geology where the crust of the North American plate changes from unstable to stable--is in central Arizona in the transition zone between the Basin and Range and the Colorado Plateaus tectonic provinces. Volcanism and tectonism have been progressing northeastward along the transition zone for about 20 million years. The Verde Hot Springs area is the focal point of the intersection of three major lineaments. More than 100 water samples were collected from wells and springs in the valley, and temperatures of the potential geothermal resources were calculated using two geochemical methods or geothermometers--silica and Na-K-Ca geothermometers. Because of the high concentration of dissolved magnesium in the ground water, the silica geotemperatures are considered to be more reliable than the Na-K-Ca geotemperatures. The Camp Verde and Verde Hot Springs areas contain ground water that has quartz-silica geotemperatures of between 99 and 135C and chalcedony-silica geotemperatures of between 73 and 111C. The geochemical evidence to substantiate a geothermal resource in Verde Valley is not conclusive, and further work including test drilling, should be done to verify the silica geotemperatures given in the map. (Kosco-USGS)

Water-Resources Investigations Report↗
USGS1993

Properties and chemical constituents in ground water from the middle Claiborne Aquifer, Gulf Coast regional aquifer systems, south-central United States

The U.S. Geological Survey used four programs in 1990 to provide external data quality assurance for the National Atmospheric Deposition Program/National Trends Network (NADP/NTN). Results of the intersite- comparison program indicate that 80 and 74 percent of the site operators met the NADP/NTN goals for pH determination and 98 and 95 percent of the site operators met the NADP/NTN goals for specific- conductance determination during the two studies in 1990. The effects of routine sample handling, processing, and shipping determined in the blind-audit program indicated significant positive bias for calcium, magnesium, sodium, potassium, chloride, nitrate, and sulfate. Significant negative bias was determined for hydrogen ion and specific conductance. A Kruskal-Wallis test indicated that there were no significant (a=0.01) differences in analytical results from the three laboratories participating in the interlaboratory-comparison program. Results from the collocated-sampler study indicate the median relative error for potassium and ammonium concentration and deposition exceeded 15 percent at most sites while the median relative error for sulfate and nitrate at all sites was less than 6 percent for concentration and was less than 15 percent for deposition.

Water-Resources Investigations Report↗
USGS1998

Evaluation of chemical data from selected sites in the Surface-Water Ambient Monitoring Program (SWAMP) in Florida

A cooperative study between the Florida Department of Environmental Protection (FDEP) and the U.S. Geological Survey was conducted to assess the integrity of selected water-quality data collected at 150 sites in the FDEP Surface-Water Ambient Monitoring Program (SWAMP) in Florida. The assessment included determining the consistency of the water-quality data collected statewide, including commonality of monitoring procedures and analytes, screening of the gross validity of a chemical analysis, and quality assurance and quality control (QA/QC) procedures. Four tests were used to screen data at selected SWAMP sites to estimate the gross validity of selected chemical data: (1) the ratio of dissolved solids (in milligrams per liter) to specific conductance (in microsiemens per centimeter); (2) the ratio of total cations (in milliequivalents per liter) multiplied by 100 to specific conductance (in microsiemens per centimeter); (3) the ratio of total anions (in milliequivalents per liter) multiplied by 100 to specific conductance (in microsiemens per centimeter); and (4) the ionic charge-balance error. Although the results of the four screening tests indicate that the chemical data generally are quite reliable, the extremely small number of samples (less than 5 percent of the total number of samples) with sufficient chemical information to run the tests may not provide a representative indication of the analytical accuracy of all laboratories in the program. In addition to the four screening tests, unusually low or high values were flagged for field and laboratory pH (less than 4.0 and greater than 9.0) and specific conductance (less than 10 and greater than 10,000 microsiemens per centimeter). The numbers of flagged data were less than 1 percent of the 19,937 water samples with pH values and less than 0.6 percent of the 16,553 water samples with specific conductance values. Thirty-four agencies responded to a detailed questionnaire that was sent to more than 60 agencies involved in the collection and analysis of surface-water-quality data for SWAMP. The purpose of the survey was to evaluate quality assurance methods and consistency of methods statewide. Information was compiled and summarized on monitoring network design, data review and upload procedures, laboratory and field sampling methods, and data practices. Currently, most agencies that responded to the survey follow FDEP-approved QA/QC protocol for sampling and have quality assurance practices for recording and reporting data. Also, most agencies responded that calibration procedures were followed in the laboratory for analysis of data, but no responses were given about the specific procedures. Approximately 50 percent of the respondents indicated that laboratory analysis methods have changed over time. With so many laboratories involved in analyzing samples for SWAMP, it is difficult to compare water quality from one site to another due to different reporting conventions for chemical constituents and different analytical methods over time. Most agencies responded that calibration methods are followed in the field, but no specific details were provided. Grab samples are the most common method of collection. Other data screening procedures are necessary to further evaluate the validity of chemical data collected at SWAMP sites. High variability in the concentration of targeted constituents may signal analytical problems, but more likely changes in concentration are related to hydrologic conditions. This underscores the need for accurate measurements of discharge, lake stage, tidal stage at the time of sampling so that changes in constituent concentrations can be properly evaluated and fluxes (loads) of nutrients or metals, for example, can be calculated and compared over time.

Florida↗
USGS2012

Chemical mixtures in untreated water from public-supply wells in the U.S. — Occurrence, composition, and potential toxicity

Chemical mixtures are prevalent in groundwater used for public water supply, but little is known about their potential health effects. As part of a large-scale ambient groundwater study, we evaluated chemical mixtures across multiple chemical classes, and included more chemical contaminants than in previous studies of mixtures in public-supply wells. We (1) assessed the occurrence of chemical mixtures in untreated source-water samples from public-supply wells, (2) determined the composition of the most frequently occurring mixtures, and (3) characterized the potential toxicity of mixtures using a new screening approach. The U.S. Geological Survey collected one untreated water sample from each of 383 public wells distributed across 35 states, and analyzed the samples for as many as 91 chemical contaminants. Concentrations of mixture components were compared to individual human-health benchmarks; the potential toxicity of mixtures was characterized by addition of benchmark-normalized component concentrations. Most samples (84%) contained mixtures of two or more contaminants, each at concentrations greater than one-tenth of individual benchmarks. The chemical mixtures that most frequently occurred and had the greatest potential toxicity primarily were composed of trace elements (including arsenic, strontium, or uranium), radon, or nitrate. Herbicides, disinfection by-products, and solvents were the most common organic contaminants in mixtures. The sum of benchmark-normalized concentrations was greater than 1 for 58% of samples, suggesting that there could be potential for mixtures toxicity in more than half of the public-well samples. Our findings can be used to help set priorities for groundwater monitoring and suggest future research directions for drinking-water treatment studies and for toxicity assessments of chemical mixtures in water resources.

Science of the Total Environment↗
USGS2002

Environmental impacts of petroleum production: Fate of inorganic and organic chemicals in produced water from the Osage-Skiatook Petroleum Environmental Research sites, Osage County, Oklahoma

About 15 scientists from the U. S. Geological Survey, other Federal agencies and academia are involved in a multidisciplinary investigation to study the transport, fate, and natural attenuation of inorganic salts, trace metals, radionuclides and organic compounds present in produced water, and their impacts on soil, surface and ground water and the local ecosystem at the Osage-Skiatook Petroleum Environmental Research (OSPER) A and B sites, located in Osage County, OK. The Branstetter lease, OSPER B site, is typical of many aging petroleum fields in Osage County, which ranks among the top oil and gas producing counties in Oklahoma with close to 40,000 wells. Current production in Osage County is mainly from stripper wells (averaging ~2.8 bbls/d oil and >30 bbls/d brine) that are shallow, mostly 300-700 m in depth, and produce from several sandstones of Pennsylvanian age. About one hectare of land at the OSPER B site is affected by salt scarring, soil salinization and brine and petroleum contamination due to the leakage of produced water and associated hydrocarbons from two brine pits and due to accidental releases from active tank batteries. Eventually, the bulk of inorganic salts and some dissolved organic species in the released brine reach, directly or via the two local streams, the adjacent Skiatook Lake, a 4250-hectare reservoir that provides drinking water to the local communities and is a major recreational fishery. About 40 water samples were obtained from several oil wells at the B site and adjoining areas, the two brine pits, several brine pools and seeps in the impacted area, local streams, Skiatook Lake, and from about 20 boreholes (1-71 m deep), recently drilled and completed with slotted PVC tubing. Water level monitoring and additional sampling is continuing. Results to date show that the produced water is a high-salinity (~150,000 mg/L total dissolved solids) Na-Ca-Cl brine, with relatively high concentrations of Sr, Mg and NH4, but low amounts of SO4 and H2S. With the exception of Fe and Mn, the concentrations of trace metals are low, and the values of dissolved organics are relatively low. As the brine flows from the brine pits through the shallow eolian sand, colluvial and alluvial deposits to the streams and Skiatook Lake, it is diluted by infiltrating water from precipitation. Its chemical composition is modified by sorption, mineral precipitation/dissolution, transpiration, volatilization and oxidation/reduction reactions. Bacteria likely play an important role in many of these reactions.

Oklahoma↗
USGS1979

Reconnaissance evaluation of surface-water quality in Eagle, Grand, Jackson, Pitkin, Routt, and Summit Counties, Colorado

Water-quality data were collected from streams in a six-county area to determine if the streams were polluted and, if so, to determine the sources of the pollution. Eighty-three stream sites were selected for sampling in Eagle, Grand, Jackson, Pitkin, Routt, and Summit Counties. Also included are data from 28 sites in Routt County collected for a U.S. Geological Survey cooperative study on the Yampa River basin. A summary of data collected prior to this study, results of current chemical and biological sampling, and needs for future water-quality monitoring are reported for each county. The kinds of data collected were site specific depending upon land-use activities. Data collected at selected sites included temperature, pH, specific conductance, dissolved oxygen, and stream discharge. Chemical data collected included nutrients, inorganics, organics, and trace elements. Biological data collected included counts and species composition of total and fecal-coliform bacteria, fecal-streptococcus bacteria, benthic invertebrates, and phytoplankton. Most of the sites were sampled three times: in April-June 1976, August 1976, and January 1977. The major water-quality problems at the 17 sites sampled in Eagle County are related to mining, recreation, and geology. The Eagle River and Cross Creek in the vicinity of Minturn have concentrations of trace elements that exceed water-quality standards. Gore Creek is influenced by winter recreational use and the water during the winter has total bacteria counts as great as 72,000 per 100 milliliters and concentrations of un-ionized ammonia greater than 0.02 milligrams per liter downstream from the sewage-treatment plant. Mineralized water in the downstream reaches of the Eagle River results from natural chemical processes. The water-quality problems in Grand County, especially on the Fraser River, are related to recreation and urban activities. Chemical and biological indications of water-quality degradation exist for the Fraser River downstream from Winter Park.

Colorado↗
USGS2012

Weathering, landscape equilibrium, and carbon in four watersheds in eastern Puerto Rico: Chapter H in Water quality and landscape processes of four watersheds in eastern Puerto Rico

The U.S. Geological Survey's Water, Energy, and Biogeochemical Budgets (WEBB) program research in eastern Puerto Rico involves a double pair-wise comparison of four montane river basins, two on granitic bedrock and two on fine-grained volcaniclastic bedrock; for each rock type, one is forested and the other is developed. A confounding factor in this comparison is that the developed watersheds are substantially drier than the forested (runoff of 900–1,600 millimeters per year compared with 2,800–3,700 millimeters per year). To reduce the effects of contrasting runoff, the relation between annual runoff and annual constituent yield were used to estimate mean-annual yields at a common, intermediate mean-annual runoff of 1,860 millimeters per year. Upon projection to this intermediate runoff, the ranges of mean-annual yields among all watersheds became more compact or did not substantially change for dissolved bedrock, sodium, silica, chloride, dissolved organic carbon, and calcium. These constituents are the primary indicators of chemical weathering, biological activity on the landscape, and atmospheric inputs; the narrow ranges indicate little preferential influence by either geology or land cover. The projected yields of biologically active constituents (potassium, nitrate, ammonium ion, phosphate), and particulate constituents (suspended bedrock and particulate organic carbon) were considerably greater for developed landscapes compared with forested watersheds, consistent with the known effects of land clearing and human waste inputs. Equilibrium rates of combined chemical and physical weathering were estimated by using a method based on concentrations of silicon and sodium in bedrock, river-borne solids, and river-borne solutes. The observed rates of landscape denudation greatly exceed rates expected for a dynamic equilibrium, except possibly for the forested watershed on volcaniclastic rock. Deforestation and agriculture can explain the accelerated physical erosion in the two developed watersheds. Because there has been no appreciable deforestation, something else, possibly climate or forest-quality change, must explain the accelerated erosion in the forested watersheds on granitic rocks. Particulate organic carbon yields are closely linked to sediment yields. This relation implies that much of the particulate organic carbon transport in the four rivers is being caused by this enhanced erosion aided by landslides and fast carbon recovery. The increase in particulate organic carbon yields over equilibrium is estimated to range from 300 kilomoles per square kilometer per year (6 metric tons carbon per square kilometer per year) to 1,700 kilomoles per square kilometer per year (22 metric tons carbon per square kilometer per year) and is consistent with human-accelerated particulate-organic-carbon erosion and burial observed globally. There is no strong evidence of human perturbation of silicate weathering in the four study watersheds, and differences in dissolved inorganic carbon are consistent with watershed geology. Although dissolved organic carbon is slightly elevated in the developed watersheds, that elevation is not enough to unambiguously demonstrate human causes; more work is needed. Accordingly, the dissolved organic carbon and dissolved inorganic carbon yields of tropical rivers, although large, are of secondary importance in the study of the anthropgenically perturbed carbon cycle.

Professional Paper↗
USGS2015

Chemical and biotic characteristics of prairie lakes and large wetlands in south-central North Dakota—Effects of a changing climate

The climate of the prairie pothole region of North America is known for variability that results in significant interannual changes in water depths and volumes of prairie lakes and wetlands; however, beginning in July 1993, the climate of the region shifted to an extended period of increased precipitation that has likely been unequaled in the preceding 500 years. Associated changing water volumes also affect water chemical characteristics, with potential effects on fish and wildlife populations. To explore the effect of changing climate patterns, in 2012 and 2013, the U.S. Geological Survey revisited 167 of 178 prairie lakes and large wetlands of south-central North Dakota that were originally sampled in the mid-1960s to mid-1970s. During the earlier sampling period, these lakes and wetlands displayed a great range of chemical characteristics (for example, specific conductance ranged from 365 microsiemens per centimeter at 25 degrees Celsius to 70,300 microsiemens per centimeter at 25 degrees Celsius); however, increased water volumes have resulted in greatly reduced variation among lakes and wetlands and a more homogeneous set of chemical conditions defined by pH, specific conductance, and concentrations of major cations and anions. High concentrations of dissolved solids previously limited fish occurrence in many of the lakes and wetlands sampled; however, freshening of these lakes and large wetlands has allowed fish to populate and flourish where they were previously absent. Conversely, the freshening of previously saline lakes and wetlands has resulted in concurrent shifts away from invertebrate species adapted to live in these highly saline environments. A shift in the regional climate has changed a highly diverse landscape of wetlands (fresh to highly saline) to a markedly more homogeneous landscape that has reshaped the fish and wildlife communities of this ecologically and economically important region.

North Dakota↗
USGS1968

Water Resources Data for California, 1967; Part 2: Water Quality Records

Water-resources investigations of the U.S. Geollogical Survey include the collection of water-quality data on the chemical and physical characteristics of surface-and ground-water supplies of the Nation. These data for the 1967 water year for the quality of surface waters in California are presented in this report. Data for a few water quality stations in bordering States are also included. The data were collected by the Water Resources Division of the U.S. Geological Survey under the direction of R. Stanley Lord, district chief, Menlo Park, Calif. Water-quality information is presented for chemical quality, fluvial sediment, and water temperatures. The chemical quality includes concentrations of individual dissolved constituents and certain properties or characteristics such as hardness, sodium adsorption ratio, specific conductance, and pH. Fluvial-sediment information is given for suspended-sediment discharges and concentrations and for particle size distribution of suspended sediment and bed material. Water-temperature data represent once-daily observations except for stations where a continuous temperature recorder furnishes information from which daily minimums and maximums are obtained.

California↗
USGS2009

A Collection of Chemical, Mineralogical, and Stable Isotopic Compositional Data for Green River Oil Shale from Depositional Center Cores in Colorado, Utah, and Wyoming

For over half a century, the U.S. Geological Survey and collaborators have conducted stratigraphic and geochemical studies on the Eocene Green River Formation, which is known to contain large oil shale resources. Many of the studies were undertaken in the 1970s during the last oil shale boom. One such study analyzed the chemistry, mineralogy, and stable isotopy of the Green River Formation in the three major depositional basins: Piceance basin, Colo.; Uinta basin, Utah; and the Green River basin, Wyo. One depositional-center core from each basin was sampled and analyzed for major, minor, and trace chemistry; mineral composition and sulfide-mineral morphology; sulfur, nitrogen, and carbon forms; and stable isotopic composition (delta34S, delta15N, delta13C, and delta18O). Many of these data were published and used to support interpretative papers (see references herein). Some bulk-chemical and carbonate-isotopic data were never published and may be useful to studies that are currently exploring topics such as future oil shale development and the climate, geography, and weathering in the Eocene Epoch. These unpublished data, together with most of the U.S. Geological Survey data already published on these samples, are tabulated in this report.

Open-File Report↗
USGS2007

Organic Chemical Concentrations and Reproductive Biomarkers in Common Carp (Cyprinus carpio) Collected from Two Areas in Lake Mead, Nevada, May 1999-May 2000

The U.S. Geological Survey, in cooperation with the U.S. Fish and Wildlife Service, National Park Service, Bureau of Reclamation, and Nevada Department of Wildlife, collected and assessed data to determine the general health and reproductive status of common carp (Cyprinus carpio) at two study areas in Lake Mead, Nevada, during May 1999-May 2000. These data will form the basis of interpretations and provide a comparison for continuing studies on the health of the ecosystem in Lake Mead. One study area, Las Vegas Bay, is in the western part of Lake Mead. Las Vegas Bay receives inflows from Las Vegas Wash, which is predominantly tertiary-treated wastewater effluent, and to a lesser extent stormwater runoff from Las Vegas, Henderson, and other nearby communities, and from ground water underlying Las Vegas Valley. The other study area, Overton Arm, is in the northern extent of Lake Mead. Overton Arm receives inflow from the Virgin and Muddy Rivers, which historically are not influenced by wastewater effluent. Both sexes of common carp were collected bimonthly for 12 months using boat-mounted electrofishing gear (a direct electric current is used to temporarily immobilize fish for capture) to determine their health and reproductive status and any relation between these factors and environmental contaminants. This report presents fish tissue chemistry, organic chemical compound concentrations, and biomarker data for 83 male common carp collected from Las Vegas Bay, similar organic chemistry results for 15 male common carp, and similar biomarker measures for 80 male common carp collected from Overton Arm. Tissue chemistry results also are presented for 16 female common carp and biomarker measures for 79 female common carp collected from Las Vegas Bay, and tissue chemistry results for 15 female common carp and biomarker measures for 81 female common carp collected from Overton Arm. Thirty-three organic chemical compounds plus total concentrations for four groups of compounds (chlordanes, polychlorinated biphenyls [PCBs], brominated diphenyl ethers [BDEs], and triclosans) were analyzed from extracts of whole-body tissue using gas chromatography/mass spectrometry in male common carp from Las Vegas Bay during May 1999 through May 2000. All 33 compounds were detected in at least one sample of whole-body tissue from male common carp collected in Las Vegas Bay. In Overton Arm, 37 organic compounds plus total concentrations of three groups of compounds (PCBs, BDEs, and triclosans) were analyzed in male common carp where 20 (54 percent) of the compounds were detected. Sixteen of the 33 compounds detected in male common carp from Las Vegas Bay and 10 compounds detected in males from Overton Arm have the potential to disrupt the endocrine system in fish in Lake Mead. During May and June 1999, the mean concentration of all organic compounds detected in male common carp was 670 micrograms per kilogram from Las Vegas Bay and 109 micrograms per kilogram from Overton Arm. Twenty-seven organic compounds plus total PCBs were analyzed from extracts of whole-body tissue in female common carp collected in Las Vegas Bay and Overton Arm during May 1999. Twenty-four (86 percent) of these compounds were detected in at least one sample of whole-body tissue from female common carp collected from Las Vegas Bay while 10 (36 percent) chemical compounds were detected in female common carp from Overton Arm during that same period. Median concentrations of all chemical compounds were higher in female common carp from Las Vegas Bay compared to those collected from Overton Arm except Dacthal (DCPA), which was similar between sites. Biomarker measures obtained for male and female common carp include gonadosomatic index (percentage of gonad weight to total body weight), plasma vitellogenin (a phospholipid protein normally produced by female common carp and other oviparous fish), and condition factor [body weight/(fork length)3]. Biomarker measures for male c

Data Series↗
USGS1998

Radiochemical and chemical constituents in water from selected wells and springs from the southern boundary of the Idaho National Engineering and Environmental Laboratory to the Hagerman Area, Idaho, 1997

The U.S. Geological Survey and the Idaho Department of Water Resources, in cooperation with the U.S. Department of Energy, sampled 18 sites as part of the fourth round of a long-term project to monitor water quality of the Snake River Plain aquifer from the southern boundary of the Idaho National Engineering and Environmental Laboratory to the Hagerman area. Water samples were collected and analyzed for selected radiochemical and chemical constituents. The samples were collected from seven domestic wells, six irrigation wells, two springs, one dairy well, one observation well, and one stock well. Two quality-assurance samples also were collected and analyzed. None of the radiochemical or chemical constituents exceeded the established maximum contaminant levels for drinking water. Many of the radionuclide- and inorganic-constituent concentrations were greater than their respective reporting levels.

Idaho↗
USGS2015

Geological processes and orchid biogeography with applications to southeast central America

This contribution owes its origins to a paper presentation by Dr. Calloway H. Dodson at the Second International Conference on Neotropical Orchidology held in San José, Costa Rica in May of2003 (Dodson 2003). Dr. Dodson outlined some ofthe reasons to suspect that regional geological fac-tors may play important roles in orchid speciation and biogeography and gave examples from the northwestern South America. He also suggested that evolutionary change in orchid might occur over fairly short time periods, perhaps even as short as decades, centuries or millennia (Dodson 2003, SHK lecture notes). These ideas stimulated the author, a professional earth scientist, to begin thinking about how these exciting ideas could begin to be tested in Costa Rica neighboring and Central American countries, an area that has drawn him to return frequently over the last decade. The present contribution is a proposal for integrating geological observations, such as the chronology of arc volcanic activity in Nicaragua,Costa Rica, and Panama, in hypothesis forming and testing of the geographic distribution of orchids (and possibly other biota). I initially focus on comparisons between orchid inventories on the windward slopes of mountainous regions (elevation > 1000 m)with high rainfall (> 1-2 m) in tropical regions, the so-called tropical cloud forests. These regions represent the tropical pre-montane rain forestto lower montane tropical rain forest life zones of Holdridge(1967) and the montane vegetation zone applied to Costa Rica and Panama by Dressler (1993). An important message of this paper is that such tropical mountainous regions are not necessarily static, but may change in elevation over geologic time due to active tectonic deformation and uplift and that the presence of active volcanism in a mountain range may also introduce additional chemical factors, such as volcanic gases, acid rain, and volcanic soils, and also physical factors, such as interruption of gene flow by explosive eruptions and coverage by their air fall products such as ash (tephra), lava flows, and lahars (volcanic mudflows). Thus over a given geological time interval, forests may be slowly increasing in elevation by tectonic uplift or by the accumulation of volcanic products such as steep-sided strato volcanoes (built from both lavas and tephra), or by down-slope accumulations of lava flows or lahars. Mountains may also lose elevation by erosion or by tectonic subsidence. As we shall see, tropical Central America shows an extraordinarily high level of tectonic and volcanic history that has changed its geography and, by implication, climate, life zones,and likely orchid distribution. My working hypo thesis put forward for testing is that orchid adaptations to these changes may have led to the development of new species and endemism in this region.

Lankesteriana↗