Geology topics
Publications and source records attributed to C.T. Rightmire.
Explore the source record for details and available documents.
Explore the source record for details and available documents.
Samples of sedimentary material from interbeds between basalt flows and from fractures in the flows, taken from two drill cores at the Radioactive Waste Management Complex at the Idaho National Engineering Laboratory were analyzed for (1) particle-size dribution, (2) bulk mineralogy, (3) clay mineralogy, (4) cation-exchange capacity, and (5) carbonate content. Thin sections of selected sediment material were made for petrographic examination. Preliminary interpretations indicate that (1) it may be possible to distinguish the various sediment interbeds on the basis of their mineralogy, (2) the presence of carbonate horizons in sedimentary interbeds may be utilized to approximate the time of exposure and the climate while the surface was exposed (which affected the hydrogeologic character of the sediment), and the type and orientation of fracture-filling material may be utilized to determine the mechanism by which fractures were filled. (USGS)
Regional dedolomitization is the major process that controls the chemical character of water in the Mississippian Pahasapa Limestone (Madison equivalent) surrounding the Black Hills, South Dakota and Wyoming. The process of dedolomitization consists of dolomite dissolution and concurrent precipitation of calcite; it is driven by dissolution of gypsum. Deuterium and oxygen isotopic data from the ground water, coupled with regional potentiometric maps, show that recharge occurs on the western slope of the Black Hills and that the water flows northward and westward toward the Powder River Basin. A significant part flows around the southern end of the Black Hills to replenish the aquifer to the east of the Hills. Depth of flow was inferred from interpretation of the silica geothermometer based on the temperature-dependent solubilities of quartz and chalcedony in water. Chemical effects of warm water in the Pahasapa Limestone include changes in the solubility products of minerals, conversion of gypsum to anhydrite, solution and precipitation of minerals, and increases in the tendency for outgassing of carbon dioxide. Where sulfate reduction is not important, sulfur isotope data show that (1) in the Mississippian aquifer, most of the sulfate is from dissolution of gypsum and (2) some wells and springs have a hydrologic connection with overlying Permian and Pennsylvanian evaporites. Sulfate ion concentration, a progress variable, shows a strong correlation with pH as a result of the combined effects of the dedolomitization reactions. Mass-balance and mass-transfer calculations were used to adjust 14 C values to determine a range of ground-water flow velocities between 2 and 20 m/yr. These velocities are characteristic of carbonate aquifers. The average rates of dolomite and gypsum dissolution are 1.7 × 10 −4 and 3.4 × 10 −4 mmol/kg of H 2 O/yr, respectively. The precipitation of calcite is occurring at the rate of 3.4 × 10 −4 mmol/kg of H 2 O/yr. The close agreement among the model results demonstrates that dedolomitization is controlling water-rock interactions in this regional carbonate aquifer system.
The δ 34 S values of dissolved sulfide and the sulfur isotope fractionations between dissolved sulfide and sulfate species in Floridan ground water generally correlate with dissolved sulfate concentrations which are related to flow patterns and residence time within the aquifer. The dissolved sulfide derives from the slow in situ biogenic reduction of sulfate dissolved from sedimentary gypsum in the aquifer. In areas where the water is oldest, the dissolved sulfide has apparently attained isotopic equilibrium with the dissolved sulfate ( Δ 34 S = 65 per mil) at the temperature (28°C) of the system. This approach to equilibrium reflects an extremely slow reduction rate of the dissolved sulfate by bacteria; this slow rate probably results from very low concentrations of organic matter in the aquifer. In the reducing part of the Edwards aquifer, Texas, there is a general down-gradient increase in both dissolved sulfide and sulfate concentrations, but neither the δ 34 S values of sulfide nor the sulfide-sulfate isotope fractionation correlates with the ground-water flow pattern. The dissolved sulfide species appear to be derived primarily from biogenic reduction of sulfate ions whose source is gypsum dissolution although upgradient diffusion of H 2 S gas from deeper oil field brines may be important in places. The sulfur isotope fractionation for sulfide-sulfate (about 38 per mil) is similar to that observed for modern oceanic sediments and probably reflects moderate sulfate reduction in the reducing part of the aquifer owing to the higher temperature and significant amount of organic matter present; contributions of isotopically heavy H 2 S from oil field brines are also possible.