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Robert G. Striegl

Publications and source records attributed to Robert G. Striegl.

122 records · Page 7Linked to original sources
USGS1997

Tritium, deuterium, and oxygen-18 in water collected from unsaturated sediments near a low-level radioactive-waste burial site south of Beatty, Nevada

Pore water was extracted in March 1996 from cores collected from test holes UZB-1 and UZB-2 drilled November 1992 and September 1993, respectively, in the Amargosa Desert south of Beatty, Nevada. The test holes are part of a study to determine factors affecting water and gas movement through unsaturated sediments. The holes are about 100 meters south of the southwest corner of the fence enclosing a commercial burial area for low-level radioactive waste. Water vapor collected from test hole UZB-2 in April 1994 and July 1995 had tritium concentrations greater than would be expected from atmospheric deposition. An apparatus was built in which pore water was extracted by cryodistillation from the previously obtained core samples. The extracted core water was analyzed for the radioactive isotope tritium and for the stable isotopes deuterium (D) and oxygen-18 ( 18 O). The isotopic composition of core water was compared with that of water vapor previously collected from air ports in test hole UZB-2 and to additional samples collected during May 1996. Core water becomes increasingly depleted in D and 18 O from the land surface to a depth of 30 meters, indicating that net evaporation of water is occurring near the land surface. Below a depth of 30 meters the stable-isotopic composition of core water becomes nearly constant and roughly equal to that of ground water. The stable isotopes plot on an evaporation trend. The source of the partly evaporated water could be either ground water or past precipitation having the same average isotopic composition as ground water but not modern precipitation, based on 18 months of record. Profiles of D and 18 O in water vapor roughly parallel those in core water. The stable isotopes of core water appear to be in isotopic equilibrium with water vapor from UZB-2 when temperature-dependent fractionation is considered. The data are consistent with the hypothesis of evaporative discharge of ground water at the land surface. The concentration of tritium in core water from depths less than 50 meters was higher than that of present-day atmospheric air, indicating that elevated tritium concentrations preceded the drilling. The concentrations of tritium in core water from the deepest sample (85 meters) and in UZB-2 groundwater (110 meters) were below detection. Thus, tritium in the unsaturated zone is not being introduced through ground water. The shape of the tritium profile for core water was similar to the shape of the tritium profile for water vapor collected April 1994, except that concentrations were consistently lower in core water than in water vapor. Tritium concentrations in water vapor increased from April 1994 to May 1996. Similar to the stable isotopes, the highest tritium concentrations were measured at shallow depths. Concentrations of tritium in water vapor during core collection were estimated assuming isotopic equilibrium with core water. The computed concentrations for November 1992 and September 1993 form consistent temporal trends with subsequent tritium concentrations in water vapor collected April 1994, July 1995, and May 1996. Observations of a bimodal distribution of tritium, in which the highest concentrations are in a gravel layer at a depth of 1-2 meters, indicate lateral migration of tritium through the vicinity of UZB-2.

Nevada↗
USGS1996

Factors affecting tritium and 14carbon distributions in the unsaturated zone near the low-level radioactive-waste burial site south of Beatty, Nevada

Interpretations of the distributions of tritiated water vapor (HTO V ) and 14 carbon dioxide gas ( 14 CO 2 ) concentrations in the unsaturated zone adjacent to the low-level radioactive-waste burial site south of Beatty, Nevada, suggest that observed concentrations of 14 CO 2 could be explained by either diffusive or advective transport of the radioactive gas from the site. The distribution of HTO V cannot be explained by vapor transport, either by diffusive or advective mechanisms. Thus, liquid transport appears to have played a role in moving HTO V to well UZB-2. Although the process by which this occurred cannot be determined from available data (and indeed may never be known), it is likely that liquid wastes disposed directly into the trenches during the period from 1962 to 1975 contributed to the offsite contamination. Liquid transport may have been enhanced by precipitation and runoff into open trenches that resulted in the occasional accumulation of ponded water in the trenches and flow along preferential pathways in the underlying unsaturated zone

Nevada↗
USGS1996

Potential methane emission from north-temperate lakes following ice melt

Methane, a radiatively active 'greenhouse' gas, is emitted from lakes to the atmosphere throughout the open-water season. However, annual lake CH4 emissions calculated solely from open-water measurements that exclude the time of spring ice melt may substantially underestimate the lake CH4 source strength. We estimated potential spring CH4 emission at the time of ice melt for 19 lakes in northern Minnesota and Wisconsin. Lakes ranged in area from 2.7 to 57,300 ha and varied in littoral zone sediment type. Regression analyses indicated that lake area explained 38% of the variance in potential CH4 emission for relatively undisturbed lakes; as lake area increases potential CH4 emission per unit area decreases. Inclusion of a second term accounting for the presence or absence of soft organic-rich littoral-zone sediments explained 83% of the variance in potential spring CH4 emission. Total estimated spring CH4 emission for 1993 for all Minnesota lakes north of 45?? with areas ???4 ha was 1.5 x 108 mol CH4 assuming a 1 : 1 ratio of soft littoral sediment to hard littoral sediment lakes. Emission estimates ranged from 5.3 x 107 tool assuming no lakes have soft organic-rich littoral sediments to 4.5 x 108 mol assuming all lakes have soft organic-rich littoral sediments. This spring CH4 pulse may make up as much as 40% of the CH4 annually emitted to the atmosphere by small lakes.

Limnology and Oceanography↗
USGS1995

Tritium and radioactive carbon (14C) analyses of gas collected from unsaturated sediments next to a low-level radioactive-waste burial site south of Beatty, Nevada, April 1994 and July 1995

Tritium activities in water vapor and radioactive carbon ( 14 C) activities in carbon dioxide were determined in gas samples pumped from small-diameter air ports installed in a test hole within the unsaturated sediments next to a commercial burial site for low-level radioactive waste south of Beatty, Nevada. In April 1994, gas samples were collected from test hole UZB-2, which was drilled about 350 feet south of the southwest corner of the fence enclosing the burial site. The test hole is part of a study to determine the depth to which atmospheric air circulates through the unsaturated sediments at the desert site. Laboratory results completed in May 1995 show activities of tritium and 14 C were greater than expected, with measured tritium in the water vapor as high as 762 tritium units at a depth of 79 feet and measured 14 C in carbon dioxide as high as 1,700 percent modern carbon at a depth of 18 feet. In July 1995, the uppermost five air ports in test hole UZB-2 were resampled. In addition, water vapor was collected for tritium analyses at a distant test hole, and water vapor for tritium analyses and carbon dioxide for 14 C analyses were collected from three depths at the research shaft about 200 feet north of test hole UZB-2, and at two shallow probes (depth of 5.5 feet) next to the fence enclosing the burial site. Analyses of samples collected in the upper 112 feet from test hole UZB-2 in July 1995 show the same distribution of tritium and 14 C as analyses of samples collected in April 1994, except that activities were somewhat greater in July. The greatest activities of tritium and 14 C were measured from a shallow probe next to the fence with activities of 29,400 tritium units and 517,000 percent modern carbon, respectively.

Nevada↗
USGS1993

Diffusional limits to the consumption of atmospheric methane by soils

Net transport of atmospheric gases into and out of soil systems is primarily controlled by diffusion along gas partial pressure gradients. Gas fluxes between soil and the atmosphere can therefore be estimated by a generalization of the equation for ordinary gaseous diffusion in porous unsaturated media. Consumption of CH4 by methylotrophic bacteria in the top several centimeters of soil causes the uptake of atmospheric CH4 by aerated soils. The capacity of the methylotrophs to consume CH4 commonly exceeds the potential of CH4 to diffuse from the atmosphere to the consumers. The maximum rate of uptake of atmospheric CH4 by soil is, therefore, limited by diffusion and can be calculated from soil physical properties and the CH4 concentration gradient. The CH4 concentration versus depth profile is theoretically described by the equation for gaseous diffusion with homogeneous chemical reaction in porous unsaturated media. This allows for calculation of the in situ rate of CH4 consumption within specified depth intervals.

Conference Paper↗
USGS1992

Consumption of atmospheric methane by desert soils

Atmospheric concentrations of methane, a greenhouse gas, are increasing at a rate of about 1% yr -1 (refs 1–4). Oxidation by methylotrophic bacteria in soil is the largest terrestrial sink for atmospheric CH 4 , and is estimated to consume about 30 x 10 12 g CH 4 yr -1 (refs 4–6). Spatial and temporal variability in the rate of soil CH 4 consumption are incompletely understood 6–19 , as are the apparent inhibitory 12,13,18 or enhancing 20 effects of changes in land use. Dry deserts, which constitute 20% of total land surface, are not currently included in global soil uptake estimates. Here we describe measurements of the rate of uptake of atmospheric CH 4 by undisturbed desert soils. We observed rates as great as 4.38 mg CH 4 m -2 day -1 ; 50% of the measured rates were between 0.24 and 0.92 mg CH 4 m -2 d -1 . Uptake of CH 4 by desert soil is enhanced by rainfall after an initial soil-drainage period—opposite to the response of temperate forest soils 12 . Methane is consumed to a depth of about 2 m, allowing for deep removal of atmospheric CH 4 if near-surface conditions are unfavourable for consumption. On the basis of an annual average CH 4 consumption rate of 0.66 mg CH 4 m -2 d -1 , we estimate that the global CH 4 sink term needs to be increased by about 7 x 10 12 g yr -1 to account for the contribution of desert soils.

Nevada↗
USGS1990

Carbon dioxide retention and carbon exchange on unsaturated Quaternary sediments

Retention of CO 2 on three air-dried and partly water-saturated glacial and eolian sediments was measured at 20°C for a range in, P CO 2 that commonly occurs in unsaturated zones. Ratios of the relative losses of CO 2 and 14 CO 2 from a surrogate atmosphere overlying the sediments were 1:1 for the dry condition. For the wet condition, those relative losses were generally ⪯ 1:2, indicating bicarbonateion formation and C-isotope exchange. Mass losses of CO 2 per surface area of sediment were similar for dry and wet conditions; however, CO 2 losses for the wet condition were 8 to 17 times greater than losses predicted by calcite equilibria. Occurrence of this comparatively large reservoir of immobile, exchangeable C in unsaturated zones can cause alteration of the C-isotope composition of soil CO 2 and of dissolved inorganic C in interstitial water, and needs to be considered when modeling 14 CO 2 movement in the unsaturated zone or when interpreting radiocarbon ages of infiltrating water.

Geochimica et Cosmochimica Acta↗
USGS1989

Diffusion and consumption of methane in an unsaturated zone in north-central Illinois, U.S.A.

The distribution of CH 4 in unsaturated glacial and eolian deposits adjacent to buried low-level radioactive waste was measured, and movement of the gas from the waste source was simulated using a two-dimensional finite-difference model for gas diffusion in the unsaturated zone. Mean P CH 4 was greatest (1.56 Pa) in a pebbly-sand deposit 11.6 m below the land surface and 12 m from the waste, and generally decreased with increased horizontal distance from the waste. Mean P CH 4 was least (0.07 Pa) at depth of 1.8 m below land surface, regardless of distance from the waste. P CH 4 at the land surface averaged 0.17 Pa. Depth versus P CH 4 profiles suggest consumption of both waste-produced and atmospheric CH 4 in the upper unsaturated zone, presumably by methanotrophic microorganisms. Numerical simulations of methane movement support the consumption observation; inclusion of a term in the model for consumption of CH 4 in the upper 2 m of the unsaturated zone resulted in simulated P CH 4 within 30% of mean P CH 4 at eleven of thirteen sampling locations. A similar fit of the data was obtained for only four locations when consumption was not considered.

Illinois↗
USGS1989

A numerical solution for the diffusion equation in hydrogeologic systems

The documentation of a computer code for the numerical solution of the linear diffusion equation in one or two dimensions in Cartesian or cylindrical coordinates is presented. Applications of the program include molecular diffusion, heat conduction, and fluid flow in confined systems. The flow media may be anisotropic and heterogeneous. The model is formulated by replacing the continuous linear diffusion equation by discrete finite-difference approximations at each node in a block-centered grid. The resulting matrix equation is solved by the method of preconditioned conjugate gradients. The conjugate gradient method does not require the estimation of iteration parameters and is guaranteed convergent in the absence of rounding error. The matrixes are preconditioned to decrease the steps to convergence. The model allows the specification of any number of boundary conditions for any number of stress periods, and the output of a summary table for selected nodes showing flux and the concentration of the flux quantity for each time step. The model is written in a modular format for ease of modification. The model was verified by comparison of numerical and analytical solutions for cases of molecular diffusion, two-dimensional heat transfer, and axisymmetric radial saturated fluid flow. Application of the model to a hypothetical two-dimensional field situation of gas diffusion in the unsaturated zone is demonstrated. The input and output files are included as a check on program installation. The definition of variables, input requirements, flow chart, and program listing are included in the attachments. (USGS)

Water-Resources Investigations Report↗
USGS1989

An inventory and evaluation of biological investigations that relate to stream-water quality in the upper Illinois River basin of Illinois, Indiana, and Wisconsin

Results of studies of the aquatic biology of the upper Illinois River basin provide a historical data source from which inferences can be made about changes in the quality of water in the main stem river and its tributaries. The results of biological investigations that have been conducted throughout the basin since 1900 are summarized and their relevance to stream-water-quality assessment is described, particularly their relevance to the upper Illinois River basin pilot project for the National Water Quality Assessment program. Four general categories of biological investigations were identified: Populations and community structure, chemical concentrations in tissue, organism health, and toxicity measurements. Biological investigations were identified by their location in the basin and by their relevance to each general investigation category. The most abundant literature was in the populations and community structure category. Tissue data were limited to polychlorinated biphenyls, organochlorine pesticides, dioxin, and several metals. The most cited measure of organism health was a condition factor for fish that associates body length with weight or body depth. Toxicity measurements included bioassays and the Ames Tests. The bioassays included several testing methods and test organism. (USGS)

Water-Resources Investigations Report↗
USGS1988

Distribution of gases in the unsaturated zone at a low-level radioactive-waste disposal site near Sheffield, Illinois

The unsaturated zone is a medium that provides pneumatic communication for the movement of gases from wastes buried in landfills to the atmosphere, biota, and groundwater. Gases in unsaturated glacial and eolian deposits near a waste-disposal trench at the low-level radioactive-waste disposal site near Sheffield, Bureau County, Illinois, were identified, and the spatial and temporal distributions of the partial pressures of those gases were determined for the period January 1984 through January 1986. Methods for the collection and analyses of the gases are described, as are geologic and hydrologic characteristics of the unsaturated zone that affect gas transport. The identified gases, which are of natural and of waste origin, include nitrogen, oxygen, and argon, carbon dioxide, methane, propane, butane, tritiated water vapor, 14carbon dioxide, and 222 radon. Concentrations of methane and 14carbon dioxide originated at the waste, as shown by partial-pressure gradients of the gases; 14carbon dioxide partial pressures exceeded natural background partial pressures by factors greater than 1 million at some locations. Variations in partial pressures of oxygen and carbon dioxide were seasonal among piezometers because of increased root and soil-microbe respiration during summer. Variations in methane and 14carbon dioxide partial pressures were apparently related to discrete releases from waste sources at unpredictable intervals of time. No greater than background partial pressures for tritiated water vapor or 222 radon were measured. (USGS)

Water-Resources Investigations Report↗
USGS1987

Relations between quality of urban runoff and quality of Lake Ellyn at Glen Ellyn, Illinois

Comparison of flow and chemical data collected at the principal inlet and at the outlets of Lake Ellynman urban lake in the Chicago metropolitan are--shows that detention storage alters the discharge and the quality of urban runoff. Peak water discharge and variation in the concentration of constituents transported by the runoff are usually reduced. Mass-balance relations based on comparison of measured constituent loads at the inlet and the outlets show that the lake is very efficient in trapping suspended solids, suspended sediment, and sediment-associated metals. Calculated trap efficiencies for many dissolved constituents were negative. However, negative efficiencies appear to be influenced mostly by insufficient sampling in winter. Trap efficiencies for nitrogen and phosphorus are intermediate to those determined for other constituents. Solids accumulate on the lake bottom as organic-rich muds that reduce lake storage and cover potential habitat for aquatic organisms. Lake sediments, particularly fine-grained sediments, have elevated concentrations of metals associated with them. Several organic compounds, not detected in inlet- or outlet-water samples, were detected in a lake-sediment sample collected near the inlet. Concentrations of many constituents dissolved in lake water are seasonally cyclic, with annual concentration peaks occurring during the winter. Establishment and maintenance of desirable benthic invertebrate and fish populations appear to be inhibited by sediment deposition.

Water Supply Paper↗
USGS1986

Concepts and data-collection techniques used in a study of the unsaturated zone at a low-level radioactive-waste disposal site near Sheffield, Illinois

A study of water and radionuclide movement through the unsaturated zone is being conducted at the low level radioactive waste disposal site near Sheffield, Illinois. Included in the study are detailed investigations of evapotranspiration, movement of water through waste trench covers, and movement of water and radionuclides (dissolved and gaseous) from the trenches. An energy balance/Bowen ratio approach is used to determine evapotranspiration. Precipitation, net radiation, soil-heat flux, air temperature and water vapor content gradients, wind speed, and wind direction are measured. Soil water tension is measured with tensiometers which are connected to pressure transducers. Meteorological sensors and tensiometers which are connected to pressure transducers. Meteorological sensors and tensiometers are monitored with automatic data loggers. Soil moisture contents are measured through small-diameter access tubes with neutron and gamma-ray attenuation gages. Data beneath the trenches are obtained through a 130-meter-long tunnel which extends under four of the trenches. Water samples are obtained with suction lysimeters, and samples of the geologic material are obtained with core tubes. These samples are analyzed for radiometric and inorganic chemistry. Gas samples are obtained from gas piezometers and analyzed for partial pressures of major constituents, Radon-222, tritiated water vapor, and carbon-14 dioxide. (USGS)

Water-Resources Investigations Report↗