USGS ScienceSearch

Geology topics

Brian J. Andraski

Publications and source records attributed to Brian J. Andraski.

At least 19 recordsLinked to original sources

Emerging and historical contaminants detected in desert rodents collected near a low‐level radioactive waste site

In an effort to determine contaminant presence, concentrations, and movement from a low‐level radioactive waste (LLRW) burial disposal site to ecosystems in the surrounding area, a study was developed to assess concentrations of per‐ and polyfluoroalkyl substances (PFAS), polychlorinated biphenyls (PCBs), and tritium. To complete this assessment small mammals, vegetation, soil, and insect samples were collected from areas within and adjacent to the Beatty, Nevada, LLRW site and from a reference area located approximately 3 km south of the LLRW site. Samples underwent analysis via liquid chromatography tandem mass spectrometry, gas chromatography mass spectrometry, or scintillation spectroscopy depending on the analyte of interest. Small mammal tissues showed maximum concentrations of over 1700 ng/g for PFAS, 1600 ng/g for PCBs, and 10 000 Bq/kg for tritium. The primary contaminants found in soil samples were PCBs, with maximum concentrations exceeding 25 ng/g. Trace amounts of PFAS were also detected in soils and insects. Only qualitative data were obtained from vegetation samples because of the complex matrix of the dominant plant species (creosote bush; Larrea tridentata [Sessé & Moc. ex DC.] Coville). Overall, these data indicate the presence of various anthropogenic contaminants in the ecosystem surrounding the LLRW area, but additional analyses are necessary to confirm the sources and migration pathways of PFAS and PCBs in this hyperarid environment. Environ Toxicol Chem 2020;00:1–8. © 2020 SETAC

Nevada

Spatial fingerprinting of biogenic and anthropogenic volatile organic compounds in an arid unsaturated zone

Subsurface volatile organic compounds (VOCs) can pose risks to human and environmental health and mediate biological processes. VOCs have both anthropogenic and biogenic origins, but the relative importance of these sources has not been explored in subsurface environments. This study synthesizes 17 years of VOC data from the Amargosa Desert Research Site (ADRS) with the goal of improving understanding of spatial and temporal variations that distinguish sources of VOCs from a landfill and surrounding ambient sources including biogenic VOCs (bVOCs). Gas samples were collected from 1999 to 2016 from an array of shallow sample points (0.5 m and 1.5 m depth) and from vertical profiles at three deep boreholes, two (109 m deep) near the border of a waste facility (33 and 100 m distant), and one (29 m deep) in a remote area 3 km to the south. Samples were analyzed for target VOCs and a subset was analyzed for non-target VOCs to enumerate a greater variety of potential bVOCs. Principal components analysis of the target and non-target VOCs provided an assessment of spatial variability of VOCs originating from the landfill site and from ambient sources. Ambient VOCs occurred at all sample sites over a range of depths and most were consistent with biogenic origins, indicating, for the first time, presence of bVOCs in the deep unsaturated zone. Because some VOCs have both anthropogenic and biogenic sources, discrimination of sources can be important for estimating the extent and migration of anthropogenic plumes in arid unsaturated zones.

Nevada

Thermocouple psychrometry

Thermocouple psychrometry is a technique that infers the water potential of the liquid phase of a sample from measurements within the vapor phase that is in equilibrium with the sample. The theoretical relation between water potential of the liquid phase and relative humidity of the vapor phase is given by the Kelvin equation Ψ = energy/volume = (RT/Vw) ln(p/po) [3.2.3–1] where ψ is water potential (sum of matric and osmotic potential, MPa), R is the universal gas constant (8.314 × 10 -6 MJ mol -1 K -1 ), T is temperature (K), Vw is molar volume of water (1.8 × 10 -5 m 3 mol -1 ), and p/p o is relative humidity expressed as a fraction where p is actual vapor pressure of air in equilibrium with the liquid phase (MPa) and p o is saturation vapor pressure (MPa) at T.

Soil Science Society of America Book Series

Miscellaneous methods for measuring matric or water potential

A variety of techniques to measure matric potential or water potential in the laboratory and in the field are described in this section. The techniques described herein require equilibration of some medium whose matric or water potential can be determined from previous calibration or can be measured directly. Under equilibrium conditions the matric or water potential of the medium is equal to that of the soil. The techniques can be divided into: (i) those that measure matric potential and (ii) those that measure water potential (sum of matric and osmotic potentials). Matric potential is determined when the sensor matrix is in direct contact with the soil, so salts are free to diffuse in or out of the sensor matrix, and the equilibrium measurement therefore reflects matric forces acting on the water. Water potential is determined when the sensor is separated from the soil by a vapor gap, so salts are not free to move in or out of the sensor, and the equilibrium measurement reflects the sum of the matric and osmotic forces acting on the water. Seven different techniques are described in this section. Those that measure matric potential include (i) heat dissipation sensors, (ii) electrical resistance sensors, (iii) frequency domain and time domain sensors, and (iv) electro-optical switches. A method that can be used to measure matric potential or water potential is the (v) filter paper method. Techniques that measure water potential include (vi) the Dew Point Potentiameter (Decagon Devices, Inc., Pullman, WA1) (water activity meter) and (vii) vapor equilibration. The first four techniques are electronically based methods for measuring matric potential. Heat dissipation sensors and electrical resistance sensors infer matric potential from previously determined calibration relations between sensor heat dissipation or electrical resistance and matric potential. Frequency-domain and timedomain matric potential sensors measure water content, which is related to matric potential of the sensor through calibration. Electro-optical switches measure changes in light transmission through thin, nylon filters as they absorb or desorb water in response to changes in matric potential. Heat dissipation sensors and electrical resistance sensors are used primarily in the field to provide information on matric potential. Frequency domain matric potential sensors are new and have not been widely used. Time domain matric potential sensors and electro-optical switches are new and have not been commercialized. For the fifth technique, filter paper is used as the standard matrix. The filter paper technique measures matric potential when the filter paper is in direct contact with soil or water potential when separated from soil by a vapor gap. The Dew Point Potentiameter calculates water potential from the measured dew point and sample temperature. The vapor equilibration technique involves equilibration of soil samples with salt solutions of known osmotic potential. The filter paper, Dew Point Potentiameter, and vapor equilibration techniques are generally used in the laboratory to measure water potential of disturbed field samples or to measure water potential for water retention functions.

Soil Science Society of America Book Series

Unsaturated zone CO2, CH4, and δ13C-CO2 at an arid region low-level radioactive waste disposal site

Elevated tritium, radiocarbon, Hg, and volatile organic compounds associated with low-level radioactive waste (LLRW) at the USGS Amargosa Desert Research Site (ADRS) have stimulated research on factors and processes that affect contaminant gas distribution and transport. Consequently, we examined the sources, mixing, and biogeochemistry of CO 2 and CH 4 , two additional important species in the unsaturated zone at ADRS. In spring 2015 and 2016, shallow unsaturated zone gas samples were collected from the 1.5-m depth both inside and outside the LLRW disposal area. Samples also were collected from two 110-m-deep multilevel gas-sampling boreholes and a distant background site. These samples were analyzed for CO 2 mole fraction ( x CO 2 ) and C isotopic composition (δ 13 C-CO 2 ) and CH 4 mole fraction ( x CH 4 ). Graphical analysis of the results indicates mixing of CO 2 characteristic of the root zone (δ 13 C −18 to −19‰), deep soil gas of the capillary fringe (−13 to −15‰), and CO 2 produced by microbial respiration of organic matter disposed in the LLRW trenches (−22 to −25‰). Distribution of CH 4 overall reflects atmospheric sources and production in anaerobic microzones in the LLRW area and methanotrophy in the undisturbed shallow subsurface outside the LLRW area. Although x CH 4 reflecting lateral transport from the LLRW area is decreasing with time in the deep profiles, deep unsaturated zone x CO 2 has changed little in recent decades. The results imply that CH 4 and δ 13 C-CO 2 may serve as good tracers of anthropogenic effects in the unsaturated zone even when CO 2 primarily reflects natural processes.

Nevada

Groundwater discharge by evapotranspiration, flow of water in unsaturated soil, and stable isotope water sourcing in areas of sparse vegetation, Amargosa Desert, Nye County, Nevada

This report documents methodology and results of a study to evaluate groundwater discharge by evapotranspiration (GWET) in sparsely vegetated areas of Amargosa Desert and improve understanding of hydrologic-continuum processes controlling groundwater discharge. Evapotranspiration and GWET rates were computed and characterized at three sites over 2 years using a combination of micrometeorological, unsaturated zone, and stable-isotope measurements. One site (Amargosa Flat Shallow [AFS]) was in a sparse and isolated area of saltgrass ( Distichlis spicata ) where the depth to groundwater was 3.8 meters (m). The second site (Amargosa Flat Deep [AFD]) was in a sparse cover of predominantly shadscale ( Atriplex confertifolia ) where the depth to groundwater was 5.3 m. The third site (Amargosa Desert Research Site [ADRS]), selected as a control site where GWET is assumed to be zero, was located in sparse vegetation dominated by creosote bush ( Larrea tridentata ) where the depth to groundwater was 110 m. Results indicated that capillary rise brought groundwater to within 0.9 m (at AFS) and 3 m (at AFD) of land surface, and that GWET rates were largely controlled by the slow but relatively persistent upward flow of water through the unsaturated zone in response to atmospheric-evaporative demands. Greater GWET at AFS (50 ± 20 millimeters per year [mm/yr]) than at AFD (16 ± 15 mm/yr) corresponded with its shallower depth to the capillary fringe and constantly higher soil-water content. The stable-isotope dataset for hydrogen (δ 2 H) and oxygen (δ 18 O) illustrated a broad range of plant-water-uptake scenarios. The AFS saltgrass and AFD shadscale responded to changing environmental conditions and their opportunistic water use included the time- and depth-variable uptake of unsaturated-zone water derived from a combination of groundwater and precipitation. These results can be used to estimate GWET in other areas of Amargosa Desert where hydrologic conditions are similar.

Nevada

Steady state fractionation of heavy noble gas isotopes in a deep unsaturated zone

To explore steady state fractionation processes in the unsaturated zone (UZ), we measured argon, krypton, and xenon isotope ratios throughout a ∼110 m deep UZ at the United States Geological Survey (USGS) Amargosa Desert Research Site (ADRS) in Nevada, USA. Prior work has suggested that gravitational settling should create a nearly linear increase in heavy-to-light isotope ratios toward the bottom of stagnant air columns in porous media. Our high-precision measurements revealed a binary mixture between (1) expected steady state isotopic compositions and (2) unfractionated atmospheric air. We hypothesize that the presence of an unsealed pipe connecting the surface to the water table allowed for direct inflow of surface air in response to extensive UZ gas sampling prior to our first (2015) measurements. Observed isotopic resettling in deep UZ samples collected a year later, after sealing the pipe, supports this interpretation. Data and modeling each suggest that the strong influence of gravitational settling and weaker influences of thermal diffusion and fluxes of CO 2 and water vapor accurately describe steady state isotopic fractionation of argon, krypton, and xenon within the UZ. The data confirm that heavy noble gas isotopes are sensitive indicators of UZ depth. Based on this finding, we outline a potential inverse approach to quantify past water table depths from noble gas isotope measurements in paleogroundwater, after accounting for fractionation during dissolution of UZ air and bubbles.

Nevada

Multimodel analysis of anisotropic diffusive tracer-gas transport in a deep arid unsaturated zone

Gas transport in the unsaturated zone affects contaminant flux and remediation, interpretation of groundwater travel times from atmospheric tracers, and mass budgets of environmentally important gases. Although unsaturated zone transport of gases is commonly treated as dominated by diffusion, the characteristics of transport in deep layered sediments remain uncertain. In this study, we use a multimodel approach to analyze results of a gas-tracer (SF 6 ) test to clarify characteristics of gas transport in deep unsaturated alluvium. Thirty-five separate models with distinct diffusivity structures were calibrated to the tracer-test data and were compared on the basis of Akaike Information Criteria estimates of posterior model probability. Models included analytical and numerical solutions. Analytical models provided estimates of bulk-scale apparent diffusivities at the scale of tens of meters. Numerical models provided information on local-scale diffusivities and feasible lithological features producing the observed tracer breakthrough curves. The combined approaches indicate significant anisotropy of bulk-scale diffusivity, likely associated with high-diffusivity layers. Both approaches indicated that diffusivities in some intervals were greater than expected from standard models relating porosity to diffusivity. High apparent diffusivities and anisotropic diffusivity structures were consistent with previous observations at the study site of rapid lateral transport and limited vertical spreading of gas-phase contaminants. Additional processes such as advective oscillations may be involved. These results indicate that gases in deep, layered unsaturated zone sediments can spread laterally more quickly, and produce higher peak concentrations, than predicted by homogeneous, isotropic diffusion models.

California, Nevada

Global patterns and environmental controls of perchlorate and nitrate co-occurrence in arid and semi-arid environments

Natural perchlorate (ClO 4 − ) is of increasing interest due to its wide-spread occurrence on Earth and Mars, yet little information exists on the relative abundance of ClO 4 − compared to other major anions, its stability, or long-term variations in production that may impact the observed distributions. Our objectives were to evaluate the occurrence and fate of ClO 4 − in groundwater and soils/caliche in arid and semi-arid environments (southwestern United States, southern Africa, United Arab Emirates, China, Antarctica, and Chile) and the relationship of ClO 4 − to the more well-studied atmospherically deposited anions NO 3 − and Cl − as a means to understand the prevalent processes that affect the accumulation of these species over various time scales. ClO 4 − is globally distributed in soil and groundwater in arid and semi-arid regions on Earth at concentrations ranging from 10 −1 to 10 6 μg/kg. Generally, the ClO 4 − concentration in these regions increases with aridity index, but also depends on the duration of arid conditions. In many arid and semi-arid areas, NO 3 − and ClO 4 − co-occur at molar ratios (NO 3 − /ClO 4 − ) that vary between ∼10 4 and 10 5 . We hypothesize that atmospheric deposition ratios are largely preserved in hyper-arid areas that support little or no biological activity (e.g. plants or bacteria), but can be altered in areas with more active biological processes including N 2 fixation, N mineralization, nitrification, denitrification, and microbial ClO 4 − reduction, as indicated in part by NO 3 − isotope data. In contrast, much larger ranges of Cl − /ClO 4 − and Cl − /NO 3 − ratios indicate Cl − varies independently from both ClO 4 − and NO 3 − . The general lack of correlation between Cl − and ClO 4 − or NO 3 − implies that Cl − is not a good indicator of co-deposition and should be used with care when interpreting oxyanion cycling in arid systems. The Atacama Desert appears to be unique compared to all other terrestrial locations having a NO 3 − /ClO 4 − molar ratio ∼10 3 . The relative enrichment in ClO 4 − compared to Cl − or NO 3 − and unique isotopic composition of Atacama ClO 4 − may reflect either additional in-situ production mechanism(s) or higher relative atmospheric production rates in that specific region or in the geological past. Elevated concentrations of ClO 4 − reported on the surface of Mars, and its enrichment with respect to Cl − and NO 3 − , could reveal important clues regarding the climatic, hydrologic, and potentially biologic evolution of that planet. Given the highly conserved ratio of NO 3 − /ClO 4 − in non-biologically active areas on Earth, it may be possible to use alterations of this ratio as a biomarker on Mars and for interpreting major anion cycles and processes on both Mars and Earth, particularly with respect to the less-conserved NO 3 − pool terrestrially.

Geochimica et Cosmochimica Acta

Groundwater discharge by evapotranspiration, Dixie Valley, west-central Nevada, March 2009-September 2011

With increasing population growth and land-use change, urban communities in the desert Southwest are progressively looking toward remote basins to supplement existing water supplies. Pending applications by Churchill County for groundwater appropriations from Dixie Valley, Nevada, a primarily undeveloped basin east of the Carson Desert, have prompted a reevaluation of the quantity of naturally discharging groundwater. The objective of this study was to develop a revised, independent estimate of groundwater discharge by evapotranspiration (ET g ) from Dixie Valley using a combination of eddy-covariance evapotranspiration (ET) measurements and multispectral satellite imagery. Mean annual ET g was estimated during water years 2010 and 2011 at four eddy-covariance sites. Two sites were in phreatophytic shrubland dominated by greasewood, and two sites were on a playa. Estimates of total ET and ET g were supported with vegetation cover mapping, soil physics considerations, water‑level measurements from wells, and isotopic water sourcing analyses to allow partitioning of ET g into evaporation and transpiration components. Site-based ET g estimates were scaled to the basin level by combining remotely sensed imagery with field reconnaissance. Enhanced vegetation index and brightness temperature data were compared with mapped vegetation cover to partition Dixie Valley into five discharging ET units and compute basin-scale ET g . Evapotranspiration units were defined within a delineated groundwater discharge area and were partitioned as (1) playa lake, (2) playa, (3) sparse shrubland, (4) moderate-to-dense shrubland, and (5) grassland. Groundwater ET is influenced primarily by phreatophytic vegetative cover, salinity of soil and groundwater within the playa, depth to groundwater, solar radiation, and air temperature. The annual groundwater contribution to site‑scale ET ranged from 24 to 61 percent of total ET at vegetated sites and 4 to 15 percent of total ET at playa sites. Mean annual ET g from vegetated sites ranged from 53 millimeters (mm) (0.17 foot [ft], 7.3 percent vegetative cover) to 225 mm (0.74 ft, 24.8 percent vegetative cover). Cumulative liquid‑water fluxes in the unsaturated zone indicate that ET g at vegetated sites was influenced primarily by plant transpiration. Binary mixing analyses of oxygen-18 isotopes in groundwater and shallow soil water indicate that plants predominantly use groundwater throughout the year. Groundwater fractions in greasewood stem water varied seasonally and ranged from 0.63 to 1.0. Mean annual playa ET g ranged from about 11 mm (0.04 ft) at the inner playa site (near-surface volumetric water content of 37–53 percent) to about 20 mm (0.07 ft) at the outer playa site located within 2 kilometers of the playa edge (near-surface volumetric water content of 25–38 percent), but playa ET g estimates were within the probable error (plus or minus [±] 20–23 mm; 0.06–0.08 ft). Varying playa ET g was influenced predominantly by salinity rather than depth to groundwater. Osmotic resistance and physical impediments to ET (such as surface salt crusts and salt precipitate in the soil pore space) increased with increasing salinity toward the playa center, whereas vapor pressure decreased. Mean annual basin-scale ET g totaled about 28 million cubic meters (Mm 3 ) (23,000 acre-feet [acre-ft]), and represents the sum of ET g from all ET units. Annual groundwater ET from vegetated areas totaled about 26 Mm 3 (21,000 acre-ft), and was dominated by the moderate-to-dense shrubland ET unit (54 percent), followed by sparse shrubland (37 percent) and grassland (9 percent) ET units. Senesced grasses observed in the northern most areas of the moderate-to-dense ET unit likely confounded the vegetation index and led to an overestimate of ET g for this ET unit. Therefore, mean annual ET g for moderate-to-dense shrubland presented here is likely an upper bound. Annual groundwater ET from the playa ET unit was 2.2 Mm 3 (1,800 acre-ft), whereas groundwater ET from the playa lake ET unit was 0–0.1 Mm 3 (0–100 acre-ft). Oxygen-18 and deuterium data indicate discharge from the playa center predominantly represents removal of local precipitation-derived recharge. The playa lake estimate, therefore, is considered an upper bound. Mean annual ET g estimates for Dixie Valley are assumed to represent the pre‑development, long-term ET g rates within the study area.

Nevada

Field-scale sulfur hexafluoride tracer experiment to understand long distance gas transport in the deep unsaturated zone

A gas-tracer test in a deep arid unsaturated zone demonstrates that standard estimates of effective diffusivity from sediment properties allow a reasonable first-cut assessment of gas contaminant transport. Apparent anomalies in historic transport behavior at this and other waste disposal sites may result from factors other than nonreactive gas transport properties. A natural gradient SF 6 tracer experiment provided an unprecedented evaluation of long distance gas transport in the deep unsaturated zone (UZ) under controlled (known) conditions. The field-scale gas tracer test in the 110-m-thick UZ was conducted at the U.S. Geological Survey’s Amargosa Desert Research Site (ADRS) in southwestern Nevada. A history of anomalous (theoretically unexpected) contaminant gas transport observed at the ADRS, next to the first commercial low-level radioactive waste disposal facility in the United States, provided motivation for the SF 6 tracer study. Tracer was injected into a deep UZ borehole at depths of 15 and 48 m, and plume migration was observed in a monitoring borehole 9 m away at various depths (0.5–109 m) over the course of 1 yr. Tracer results yielded useful information about gas transport as applicable to the spatial scales of interest for off-site contaminant transport in arid unsaturated zones. Modeling gas diffusion with standard empirical expressions reasonably explained SF 6 plume migration, but tended to underpredict peak concentrations for the field-scale experiment given previously determined porosity information. Despite some discrepancies between observations and model results, rapid SF 6 gas transport commensurate with previous contaminant migration was not observed. The results provide ancillary support for the concept that apparent anomalies in historic transport behavior at the ADRS are the result of factors other than nonreactive gas transport properties or processes currently in effect in the undisturbed UZ.

California, Nevada

Soil, plant, and terrain effects on natural perchlorate distribution in a desert landscape

Perchlorate (ClO 4 − ) is a contaminant that occurs naturally throughout the world, but little is known about its distribution and interactions in terrestrial ecosystems. The objectives of this Amargosa Desert, Nevada study were to determine (i) the local-scale distribution of shallow-soil (0–30 cm) ClO 4 − with respect to shrub proximity (far and near) in three geomorphic settings (shoulder slope, footslope, and valley floor); (ii) the importance of soil, plant, and terrain variables on the hillslope-distribution of shallow-soil and creosote bush [ Larrea tridentata (Sessé & Moc. ex DC.) Coville] ClO 4 − ; and (iii) atmospheric (wet plus dry, including dust) deposition of ClO 4 − in relation to soil and plant reservoirs and cycling. Soil ClO 4 − ranged from 0.3 to 5.0 μg kg −1 . Within settings, valley floor ClO 4 − was 17× less near shrubs due in part to enhanced leaching, whereas shoulder and footslope values were ∼2× greater near shrubs. Hillslope regression models (soil, R 2 = 0.42; leaf, R 2 = 0.74) identified topographic and soil effects on ClO 4 − deposition, transport, and cycling. Selective plant uptake, bioaccumulation, and soil enrichment were evidenced by leaf ClO 4 − concentrations and Cl − /ClO 4 − molar ratios that were ∼8000× greater and 40× less, respectively, than soil values. Atmospheric deposition ClO 4 − flux was 343 mg ha −1 yr −1 , ∼10× that for published southwestern wet-deposition fluxes. Creosote bush canopy ClO 4 − (1310 mg ha−1) was identified as a previously unrecognized but important and active reservoir. Nitrate δ 18 O analyses of atmospheric deposition and soil supported the leaf-cycled–ClO 4 − input hypothesis. This study provides basic data on ClO 4 − distribution and cycling that are pertinent to the assessment of environmental impacts in desert ecosystems and broadly transferable to anthropogenically contaminated systems.

Nevada

Tritium plume dynamics in the shallow unsaturated zone in an arid environment

The spatiotemporal variability of a tritium plume in the shallow unsaturated zone and the mechanisms controlling its transport were evaluated during a 10-yr study. Plume movement was minimal and its mass declined by 68%. Upward-directed diffusive-vapor tritium fluxes and radioactive decay accounted for most of the observed plume-mass declines. Effective isolation of tritium ( 3 H) and other contaminants at waste-burial facilities requires improved understanding of transport processes and pathways. Previous studies documented an anomalously widespread (i.e., theoretically unexpected) distribution of 3 H (>400 m from burial trenches) in a dry, sub-root-zone gravelly layer (1–2-m depth) adjacent to a low-level radioactive waste (LLRW) burial facility in the Amargosa Desert, Nevada, that closed in 1992. The objectives of this study were to: (i) characterize long-term, spatiotemporal variability of 3 H plumes; and (ii) quantify the processes controlling 3 H behavior in the sub-root-zone gravelly layer beneath native vegetation adjacent to the facility. Geostatistical methods, spatial moment analyses, and mass flux calculations were applied to a spatiotemporally comprehensive, 10-yr data set (2001–2011). Results showed minimal bulk-plume advancement during the study period and limited Fickian spreading of mass. Observed spreading rates were generally consistent with theoretical vapor-phase dispersion. The plume mass diminished more rapidly than would be expected from radioactive decay alone, indicating net efflux from the plume. Estimates of upward 3 H efflux via diffusive-vapor movement were >10× greater than by dispersive-vapor or total-liquid movement. Total vertical fluxes were >20× greater than lateral diffusive-vapor fluxes, highlighting the importance of upward migration toward the land surface. Mass-balance calculations showed that radioactive decay and upward diffusive-vapor fluxes contributed the majority of plume loss. Results indicate that plume losses substantially exceeded any continuing 3 H contribution to the plume from the LLRW facility during 2001 to 2011 and suggest that the widespread 3 H distribution resulted from transport before 2001.

Nevada

On the conversion of tritium units to mass fractions for hydrologic applications

We develop a general equation for converting laboratory-reported tritium levels, expressed either as concentrations (tritium isotope number fractions) or mass-based specific activities, to mass fractions in aqueous systems. Assuming that all tritium is in the form of monotritiated water simplifies the derivation and is shown to be reasonable for most environmental settings encountered in practice. The general equation is nonlinear. For tritium concentrations c less than 4.5×10 12 tritium units (TU) - i.e. specific tritium activities<5.3×10 11 Bq kg -1 - the mass fraction w of tritiated water is approximated to within 1 part per million by w ≈ c×2.22293×10 -18 , i.e. the conversion is linear for all practical purposes. Terrestrial abundances serve as a proxy for non-tritium isotopes in the absence of sample-specific data. Variation in the relative abundances of non-tritium isotopes in the terrestrial hydrosphere produces a minimum range for the mantissa of the conversion factor of [2.22287; 2.22300].

Isotopes in Environmental and Health Studies

Micrometeorological, evapotranspiration, and soil-moisture data at the Amargosa Desert Research site in Nye County near Beatty, Nevada, 2006-11

This report describes micrometeorological, evapotranspiration, and soil-moisture data collected since 2006 at the Amargosa Desert Research Site adjacent to a low-level radio-active waste and hazardous chemical waste facility near Beatty, Nevada. Micrometeorological data include precipitation, solar radiation, net radiation, air temperature, relative humidity, saturated and ambient vapor pressure, wind speed and direction, barometric pressure, near-surface soil temperature, soil-heat flux, and soil-water content. Evapotranspiration (ET) data include latent-heat flux, sensible-heat flux, net radiation, soil-heat flux, soil temperature, air temperature, vapor pressure, and other principal energy-budget data. Soil-moisture data include periodic measurements of volumetric water-content at experimental sites that represent vegetated native soil, devegetated native soil, and simulated waste disposal trenches - maximum measurement depths range from 5.25 to 29.25 meters. All data are compiled in electronic spreadsheets that are included with this report.

Nevada

Volatile organic compounds in the unsaturated zone from radioactive wastes

Volatile organic compounds (VOCs) are often comingled with low-level radioactive wastes (LLRW), but little is known about subsurface VOC emanations from LLRW landfills. The current study systematically quantified VOCs associated with LLRW over an 11-yr period at the USGS Amargosa Desert Research Site (ADRS) in southwestern Nevada. Unsaturated-zone gas samples of VOCs were collected by adsorption on resin cartridges and analyzed by thermal desorption and GC/MS. Sixty of 87 VOC method analytes were detected in the 110-m-thick unsaturated zone surrounding a LLRW disposal facility. Chlorofluorocarbons (CFCs) were detected in 100% of samples collected. Chlorofluorocarbons are powerful greenhouse gases, deplete stratospheric ozone, and are likely released from LLRW facilities worldwide. Soil-gas samples collected from a depth of 24 m and a horizontal distance 100 m south of the nearest waste-disposal trench contained >60,000 ppbv total VOCs, including >37,000 ppbv CFCs. Extensive sampling in the shallow unsaturated zone (0&ndash;2 m deep) identified areas where total VOC concentrations exceeded 5000 ppbv at the 1.5-m depth. Volatile organic compound concentrations exceeded background levels up to 300 m from the facility. Maximum vertical diffusive fluxes of total VOCs were estimated to be 1 g m -2 yr -1 . Volatile organic compound distributions were similar but not identical to those previously determined for tritium and elemental mercury. To our knowledge, this study is the first to characterize the unsaturated zone distribution of VOCs emanating from a LLRW landfill. Our results may help explain anomalous transport of radionuclides at the ADRS and elsewhere.

Nevada

Interacting vegetative and thermal contributions to water movement in desert soil

Thermally driven water-vapor flow can be an important component of total water movement in bare soil and in deep unsaturated zones, but this process is often neglected when considering the effects of soil–plant–atmosphere interactions on shallow water movement. The objectives of this study were to evaluate the coupled and separate effects of vegetative and thermal-gradient contributions to soil water movement in desert environments. The evaluation was done by comparing a series of simulations with and without vegetation and thermal forcing during a 4.7-yr period (May 2001–December 2005). For vegetated soil, evapotranspiration alone reduced root-zone (upper 1 m) moisture to a minimum value (25 mm) each year under both isothermal and nonisothermal conditions. Variations in the leaf area index altered the minimum storage values by up to 10 mm. For unvegetated isothermal and nonisothermal simulations, root-zone water storage nearly doubled during the simulation period and created a persistent driving force for downward liquid fluxes below the root zone (total net flux ~1 mm). Total soil water movement during the study period was dominated by thermally driven vapor fluxes. Thermally driven vapor flow and condensation supplemented moisture supplies to plant roots during the driest times of each year. The results show how nonisothermal flow is coupled with plant water uptake, potentially influencing ecohydrologic relations in desert environments.

Vadose Zone Journal

Waste isolation and contaminant migration - Tools and techniques for monitoring the saturated zone-unsaturated zone-plant-atmosphere continuum

In 1976 the U.S. Geological Survey (USGS) began studies of unsaturated zone hydrology next to the Nation’s first commercial disposal facility for low-level radioactive waste (LLRW) near Beatty, NV. Recognizing the need for long-term data collection, the USGS in 1983 established research management areas in the vicinity of the waste-burial facility through agreements with the Bureau of Land Management and the State of Nevada. Within this framework, the Amargosa Desert Research Site (ADRS; http://nevada.usgs.gov/adrs/) is serving as a field laboratory for the sustained study of water-, gas-, and contaminant-transport processes, and the development of models and methods to characterize flow and transport. The research is built on multiple lines of data that include: micrometeorology; evapotranspiration; plant metrics; soil and sediment properties; unsaturated-zone moisture, temperature, and gas composition; geology and geophysics; and groundwater. Contaminant data include tritium, radiocarbon, volatile-organic compounds (VOCs), and elemental mercury. Presented here is a summary of monitoring tools and techniques that are being applied in studies of waste isolation and contaminant migration.

Conference Paper