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R.L. Bassett

Publications and source records attributed to R.L. Bassett.

6 recordsLinked to original sources

Estimation of αL, velocity, Kd and confidence limits from tracer injection test data

Bromide and boron were used as tracers during an injection experiment conducted at an artificial recharge facility near Stanton, Texas. The Ogallala aquifer at the Stanton site represents a heterogeneous alluvial environment and provides the opportunity to report scale dependent dispersivities at observation distances of 2 to 15 m in this setting. Values of longitudinal dispersivities are compared with other published values. Water samples were collected at selected depths both from piezometers and from fully screened observation wells at radii of 2, 5, 10 and 15 m. An exact analytical solution is used to simulate the concentration breakthrough curves and estimate longitudinal dispersivities and velocity parameters. Greater confidence can be placed on these data because the estimated parameters are error bounded using the bootstrap method. The non-conservative behavior of boron transport in clay rich sections of the aquifer were quantified with distribution coefficients by using bromide as a conservative reference tracer.

Texas

Ion exchange separation of chromium from natural water matrix for stable isotope mass spectrometric analysis

A method has been developed for separating the Cr dissolved in natural water from matrix elements and determination of its stable isotope ratios using solid-source thermal-ionization mass spectrometry (TIMS). The separation method takes advantage of the existence of the oxidized form of Cr as an oxyanion to separate it from interfering cations using anion-exchange chromatography, and of the reduced form of Cr as a positively charged ion to separate it from interfering anions such as sulfate. Subsequent processing of the separated sample eliminates residual organic material for application to a solid source filament. Ratios for 53Cr/52Cr for National Institute of Standards and Technology Standard Reference Material 979 can be measured using the silica gel-boric acid technique with a filament-to-filament standard deviation in the mean 53Cr/52Cr ratio for 50 replicates of 0.00005 or less.

Chemical Geology

Reactive transport of metal contaminants in alluvium: Model comparison and column simulation

A comparative assessment of two reactive-transport models, PHREEQC and HYDROGEOCHEM (HGC), was done to determine the suitability of each for simulating the movement of acidic contamination in alluvium. For simulations that accounted for aqueous complexation, precipitation and dissolution, the breakthrough and rinseout curves generated by each model were similar. The differences in simulated equilibrium concentrations between models were minor and were related to (1) different units in model output, (2) different activity coefficients, and (3) ionic-strength calculations. When adsorption processes were added to the models, the rinseout pH simulated by PHREEQC using the diffuse double-layer adsorption model rose to a pH of 6 after pore volume 15, about 1 pore volume later than the pH simulated by HGC using the constant-capacitance model. In PHREEQC simulation of a laboratory column experiment, the inability of the model to match measured outflow concentrations of selected constituents was related to the evident lack of local geochemical equilibrium in the column. The difference in timing and size of measured and simulated breakthrough of selected constituents indicated that the redox and adsorption reactions in the column occurred slowly when compared with the modeled reactions. MINTEQA2 and PHREEQC simulations of the column experiment indicated that the number of surface sites that took part in adsorption reactions was less than that estimated from the measured concentration of Fe hydroxide in the alluvium.

Applied Geochemistry

Preliminary data from a series of artificial recharge experiments at Stanton, Texas

A series of artificial recharge experiments was conducted by the U.S. Geological Survey at an experimental site located in Stanton, Texas. Five tests were performed from March 1977 through December 1978 to: (1) Evaluate the hydraulic properties of the aquifer; (2) test sampling and monitoring equipment; (3) compare tracers for future use in hydrologic investigations; and (4) determine the radial and vertical distribution of hydraulic properties at the site. Suites of inorganic, and both volatile and nonvolatile organic tracers were used in the tests, and comparative data were obtained from sampling points at several radial distances and depths from the injection well. Hydraulic data from aquifer tests and geologic data from core material also were obtained during the investigation.

Texas

Preliminary data describing the distribution of fluoride and silica in the water in the Ogallala aquifer on the High Plains of Texas

The Ogallala aquifer of Texas historically has been known for elevated fluoride concentration, with many areas in excess of 4 milligrams per liter. In addition, on a regional scale, silica concentrations are also somewhat elevated, with concentrations averaging in the 40 to 50 milligrams per liter range. This aquifer provides a unique geochemical and epidemiological study area because it is completely contained within the High Plains physiographic province.

Texas