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J. M. Thomas

Publications and source records attributed to J. M. Thomas.

16 recordsLinked to original sources
USGS2007

Biodegradation of disinfection byproducts as a potential removal process during aquifer storage recovery

The biodegradation potential of two drinking water disinfection byproducts was investigated using aquifer materials obtained from approximately 100 and 200 meters below land surface in an aerobic aquifer system undergoing aquifer storage recovery of treated surface water. No significant biodegradation of a model trihalomethane compound, chloroform, was observed in aquifer microcosms under aerobic or anaerobic conditions. In contrast, between 16 and 27 percent mineralization of a radiolabeled model haloacetic acid compound, chloroacetic acid, was observed. These results indicate that although the potential for biodegradation of chloroacetic acid exists in deep aquifer systems, chloroform entrained within these aquifers or formed in situ will tend to persist. These results have important implications for water managers planning to meet anticipated lowered permissible levels of tri-halomethanes in drinking water.The biodegradation potential of two drinking water disinfection byproducts was investigated using aquifer materials obtained from approximately 100 and 200 meters below land surface in an aerobic aquifer system undergoing aquifer storage recovery of treated surface water. No significant biodegradation of a model trihalomethane compound, chloroform, was observed in aquifer microcosms under aerobic or anaerobic conditions. In contrast, between 16 and 27 percent mineralization of a radiolabeled model haloacetic acid compound, chloroacetic acid, was observed. These results indicate that although the potential for biodegradation of chloroacetic acid exists in deep aquifer systems, chloroform entrained within these aquifers or formed in situ will tend to persist. These results have important implications for water managers planning to meet anticipated lowered permissible levels of trihalomethanes in drinking water.Aquifer-storage-recovery injection water often contains disinfection byproducts. Results are presented from a study in which two model disinfection byproducts, chloroform and chloroacetic acid, were used to examine biodegradation by indigenous microorganisms. The recharge system studied was near Las Vegas, NV, where the aquifers are recharged artificially during the winter months. Microcosms were constructed using aquifer material recovered from two layers. Results showed that no significant biodegradation of chloroform occurred under aerobic or anaerobic conditions, but chloroacetic acid was biodegraded under both aerobic and anaerobic conditions.

Journal of the American Water Resources Associatio↗
USGS2005

Caffeine and pharmaceuticals as indicators of waste water contamination in wells

The presence of caffeine or human Pharmaceuticals in ground water with elevated nitrate concentrations can provide a clear, unambiguous indication that domestic waste water is a source of some of the nitrate. Water from domestic, public supply, and monitoring wells in three communities near Reno, Nevada, was sampled to test if caffeine or Pharmaceuticals are common, persistent, and mobile enough in the environment that they can be detected in nitrate-contaminated ground water and, thus, can be useful indicators of recharge from domestic waste water. Results of this study indicate that these compounds can be used as indicators of recharge from domestic waste water, although their usefulness is limited because caffeine is apparently nonconservative and the presence of prescription Pharmaceuticals is unpredictable. The absence of caffeine or Pharmaceuticals in ground water with elevated nitrate concentrations does not demonstrate that the aquifer is free of waste water contamination. Caffeine was detected in ground water samples at concentrations up to 0.23 μg/L. The human Pharmaceuticals chlorpropamide, phensuximide, and carbamazepine also were detected in some samples.

Groundwater↗
USGS2005

The fate of haloacetic acids and trihalomethanes in an aquifer storage and recovery program, Las Vegas, Nevada

The fate of disinfection byproducts during aquifer storage and recovery (ASR) is evaluated for aquifers in Southern Nevada. Rapid declines of haloacetic acid (HAA) concentrations during ASR, with associated little change in Cl concentration, indicate that HAAs decline primarily by in situ microbial oxidation. Dilution is only a minor contributor to HAA concentration declines during ASR. Trihalomethane (THM) concentrations generally increased during storage of artificial recharge (AR) water and then declined during recovery. The decline of THM concentrations during recovery was primarily from dilution of current season AR water with residual AR water remaining in the aquifer from previous ASR seasons and native ground water. In more recent ASR seasons, for wells with the longest history of ASR, brominated THMs declined during storage and recovery by processes in addition to dilution. These conclusions about THMs are indicated by THM/Cl values and supported by a comparison of measured and model predicted THM concentrations. Geochemical mixing models were constructed using major-ion chemistry of the three end-member waters to calculate predicted THM concentrations. The decline in brominated THM concentrations in addition to that from dilution may result from biotransformation processes.

Nevada↗
USGS2003

Noble gas loss may indicate groundwater flow across flow barriers in southern Nevada

Average calculated noble gas temperatures increase from 10 to 22 o C in groundwater from recharge to discharge areas in carbonate-rock aquifers of southern Nevada. Loss of noble gases from groundwater in these regional flow systems at flow barriers is the likely process that produces an increase in recharge noble gas temperatures. Emplacement of low permeability rock into high permeability aquifer rock and the presence of low permeability shear zones reduce aquifer thickness from thousands to tens of meters. At these flow barriers, which are more than 1,000 m lower than the average recharge altitude, noble gases exsolve from the groundwater by inclusion in gas bubbles formed near the barriers because of greatly reduced hydrostatic pressure. However, re-equilibration of noble gases in the groundwater with atmospheric air at the low altitude spring discharge area, at the terminus of the regional flow system, cannot be ruled out. Molecular diffusion is not an important process for removing noble gases from groundwater in the carbonate-rock aquifers because concentration gradients are small.

Conference Paper↗
USGS1998

Evidence of deep circulation in two perennially ice-covered Antarctic lakes

The perennial ice covers found on many of the lakes in the McMurdo Dry Valley region of the Antarctic have been postulated to severely limit mixing and convective turnover of these unique lakes. In this work, we utilize chlorofluorocarbon (CFC) concentration profiles from Lakes Hoare and Fryxell in the McMurdo Dry Valley to determine the extent of deep vertical mixing occurring over the last 50 years. Near the ice-water interface, CFC concentrations in both lakes were well above saturation, in accordance with atmospheric gas supersaturations resulting from freezing under the perennial ice covers. Evidence of mixing throughout the water column at Lake Hoare was confirmed by the presence of CFCs throughout the water column and suggests vertical mixing times of 20-30 years. In Lake Fryxell, CFC-11, CFC-12, and CFC-113 were found in the upper water column; however, degradation of CFC-11 and CFC-12 in the anoxic bottom waters appears to be occurring with CFC-113 only present in these bottom waters. The presence of CFC-113 in the bottom waters, in conjunction with previous work detecting tritium in these waters, strongly argues for the presence of convective mixing in Lake Fryxell. The evidence for deep mixing in these lakes may be an important, yet overlooked, phenomenon in the limnology of perennially ice-covered lakes.

Limnology and Oceanography↗
USGS1996

Geochemistry and isotope hydrology of representative aquifers in the Great Basin region of Nevada, Utah, and adjacent states

This report briefly describes the general quality and chemical character of the ground water, discusses in detail the geochemical and hydrologic processes that produce the chemical and isotopic compositions of water in the two principal types of aquifers (basin fill and carbonate rock), delineates flow systems in carbonate-rock aquifers of southern Nevada, and discusses ground-water ages and flow velocities within the carbonate-rock systems.

Professional Paper↗
USGS1993

Radionuclides in ground water of the Carson River Basin, western Nevada and eastern California, U.S.A.

Ground water is the main source of domestic and public supply in the Carson River Basin. Ground water originates as precipitation primarily in the Sierra Nevada in the western part of Carson and Eagle Valleys, and flows down gradient in the direction of the Carson River through Dayton and Churchill Valleys to a terminal sink in the Carson Desert. Because radionuclides dissolved in ground water can pose a threat to human health, the distribution and sources of several naturally occurring radionuclides that contribute to gross-alpha and gross-beta activities in the study area were investigated. Generally, alpha and beta activities and U concentration increase from the up-gradient to down-gradient hydrographic areas of the Carson River Basin, whereas 222 Rn concentration decreases. Both 226 Ra and 228 Ra concentrations are similar throughout the study area. Alpha and beta activities and U concentration commonly exceed 100 pCi/l in the Carson Desert at the distal end of the flow system. Radon-222 commonly exceeds 2,000 pCi/l in the western part of Carson and Eagle Valleys adjacent to the Sierra Nevada. Radium-226 and 228 Ra concentrations are <5pCi/l. Four ground water samples were analyzed for 210 Po and one sample contained a high concentration of 21 pCi/l. Seven samples were analyzed for 210 Pb; six contained <3pCi/l and one contained 12 pCi/l. Thorium-230 was detected at concentrations of 0.15 and 0.20 pCi/l in two of four samples. Alpha-emitting radionuclides in the ground water originated from the dissolution of U-rich granitic rocks in the Sierra Nevada by CO 2 , oxygenated water. Dissolution of primary minerals, mainly titanite (sphene) in the granitic rocks, releases U to the water. Dissolved U is probably removed from the water by adsorption on Fe- and Mn-oxide coatings on fracture surfaces and fine-grained sediment, by adsorption on organic matter, and by coprecipitation with Fe and Mn oxides. These coated sediments are transported throughout the basin by fluvial processes. Thus, U is transported as dissolved and adsorbed species. A rise in the water table in the Carson Desert because of irrigation has resulted in the oxidation of U-rich organic matter and dissolution of U-bearing coatings on sediments, producing unusually high U concentration in the ground water. Alpha activity in the ground water is almost entirely from the decay of U dissolved in the water. Beta activity in ground water samples is primarily from the decay of 40 K dissolved in the water and ingrowth of 238 U progeny in the sample before analysis. Approximately one-half of the measured beta activity may not be present in ground water in the aquifer, but instead is produced in the sample after collection and before analysis. Potassium-40 is primarily from the dissolution of K-containing minerals, probably K-feldspar and biotite. Radon-222 is primarily from the decay of 226 Ra in the aquifer materials. Radium in the ground water is thought to be mainly from alpha recoil associated with the decay of Th in the aquifer material. Some Ra may be from dissolution (or desorption) or Ra-rich coatings on sediments.

California, Nevada↗
USGS1991

Emulsification of hydrocarbons by subsurface bacteria

Biosurfactants have potential for use in enhancement of in situ biorestoration by increasing the bioavailability of contaminants. Microorganisms isolated from biostimulated, contaminated and uncontaminated zones at the site of an aviation fuel spill and hydrocarbon-degrading microorganisms isolated from sites contaminated with unleaded gasoline were examined for their abilities to emulsify petroleum hydrocarbons. Emulsifying ability was quantified by a method involving agitation and visual inspection. Biostimulated-zone microbes and hydrocarbon-degrading microorganisms were the best emulsifiers as compared to contaminated and uncontaminated zone microbes. Biostimulation (nutrient and oxygen addition) may have been the dominant factor which selected for and encouraged growth of emulsifiers; exposure to hydrocarbon was also important. Biostimulated microorganisms were better emulsifiers of aviation fuel (the contaminant hydrocarbon) than of heavier hydrocarbon to which they were not previously exposed. By measuring surface tension changes of culture broths, 11 out of 41 emulsifiers tested were identified as possible biosurfactant producers and two isolates produced large surface tension reductions indicating the high probability of biosurfactant production.

Journal of Industrial Microbiology↗
USGS1984

Principal facts for gravity stations in Dixie; Fairview, and Stingaree valleys, Churchill and Pershing counties, Nevada

During March through July 1979, gravity measurements were made at 300 stations in Dixie Valley, Nevada. In December 1981, 45 additional stations were added--7 in Dixie Valley, 23 in Fairview Valley, and 15 in Stingaree Valley. Most altitudes were determined by using altimeters or topographic maps. The gravity observations were made with a Worden temperature-controlled gravimeter with an initial scale factor of 0.0965 milliGal/scale division. Principal facts for each of the 345 stations are tabulated; they consist of latitude, longitude, altitude, observed gravity, free-air anomaly, terrain correction, and Bouguer anomaly values at a bedrock density of 2.67 grams/cu cm. (Lantz-PTT)

Open-File Report↗
USGS1984

Maps showing ground-water units and withdrawal, Basin and Range Province, Nevada

This report on ground-water units and withdrawal in the Basin and Range province of Nevada (see index map) was prepared as part of a program of the U.S. Geological Survey to identify prospective regions for further study relative to isolation of high-level nuclear waste (Bedinger f Sargent, and Reed, 1984), utilizing program guidelines defined in Sargent and Bedinger (1984). Also included in this report are selected references on pertinent geologic and hydrologic studies of the region. Other map reports in this series contain detailed data on ground-water quality, surface distribution of selected rock types, tectonic conditions, areal geophysics, Pleistocene lakes and marshes, and mineral and energy resources.

Nevada↗
USGS1984

Maps showing ground-water levels, springs, and depth to water, Basin and Range Province, Nevada

This report on ground-water levels, springs and depth to ground water in the Basin and Range province of Nevada (see index map) was prepared as part of a program of the U.S. Geological Survey to identify prospective regions for further study relative to isolation of high-level nuclear waste (Bedinger, Sargent, and Reed, 1984), utilizing program guidelines defined in Sargent and Bedinger (1984). Also included in this report are selected references on pertinent geologic and hydrologic studies of the region. Other map reports in this series contain detailed data on ground-water quality, surface distribution of selected rock types, tectonic conditions, areal geophysics, Pleistocene lakes and marshes, and mineral and energy resources.

Nevada↗