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Research about South Carolina

Source-linked reports with geographic coverage including South Carolina.

At least 325 records · Page 18Linked to original sources
USGS1992

A geochemical investigation of selected areas in Greenville and Laurens Counties, South Carolina: Implications for mineral resources

The purpose of this study is to geochemically evaluate three areas within the Greenville 1&deg; x 2&deg; quadrangle (see index map) that have been shown by previous studies to contain anomalously high amounts of tin. Jackson and Moore (1992) reported the presence of cassiterite (SnO 2 )-bearing heavy-mineral concentrates from stream sediment samples that were collected during a regional geochemical reconnaissance of the Greenville 1&deg; x 2&deg; quadrangle. The data reported here confirm identified in selected heavy-mineral concentrate samples. In addition, anomalously high concentrations of barium, beryllium, lanthanum, and thorium are also reported for parts of the same areas. No significant mineral deposits are known to occur in the study areas. There was, however, minor production of monazite from several nearby localities (Sloan, 1908), and gold was produced from deposits in the northeastern part of Greenville County and nearby Spartanburg County (McCauley and Butler, 1966). The three areas selected for resampling are located in the Inner Piedmont physiographic province of South Carolina (see index map). The generalized tectonic setting of the region and the locations of the study is just north of Greenville, S.C. Much of it is within the moderately to steeply sloped terrane of Paris Mountain State Park where elevations reach approximately 600 m. Simpsonville, S.C., is neat the center of the second study area, and the southernmost study area is near Hickory Tavern, S.C. Both the Simpsonville and Hickory Tavern study areas are in more gently rolling Piedmont terrane. Each of the sampled areas is drained by tributaries of the Enoree and Reedy Rivers. Parts of three different thrust sheets underlie the region covered by this study (fig. 1); in ascending structural position, they are the Six Mile, Paris Mountain, and Laurens thrust sheets (Nelson and others, 1987). Nelson (1988, p. 7) described the contacts between these sheets as being along unnamed faults. The rocks in and around the study areas have undergone sillimanite-muscovite-grade metamorphism (Nelson, 1988, p. 9). Nelson (1988, p. 13) reports that the Six Mile thrust sheet was metamorphosed about 344 Ma. The geology of these sheets as described in this study, including geologic contacts, rock descriptions, and unit names, generally follows that of Nelson and others (1987, 1989). Within the Paris Mountain study area, rocks of the Paris Mountain thrust sheet predominate (fig. 2) and consist of a biotite-muscovite-sillimanite schist (EZsp) that has extensive lenses of fine- to medium- grained biotite granite gneiss (Pzgp). Areas of biotite granite gneiss that occur in the southern part of the Paris Mountain study area contain extensive pegmatitic and leucogranitic phases. These pegmatitic zones consist mostly of coarse-grained microcline feldspar and quartz with minor amounts of muscovite, biotite, and garnet. Smaller pegmatite lenses (<0.5 m thick) that occur within the biotite-muscovite-sillimanite schist of the Paris Mountain study area are generally of similar mineralogy, although some contain tourmaline crystals up to 5 cm in length. The Six Mile thrust sheet underlies the northern edge of the Paris Mountain study area, where it is composed of gneissic biotitic granites of the Caesars Head Granite (figs. 1 and 2). The northwestern part of the Simpsonville study area (figs. 1 and 3), within the Paris Mountain thrust sheet, is underlain by a biotite-muscovite-sillimanite schist (EZsp) that contains lenses of biotite granite gneiss (Pzgp). In the southeastern part of the Simpsonville study area, within the Laurens thrust sheet, biotite gneiss (EZgl), biotite granite gneiss (Pzgf), and minor amphibolite (EZal) are interlayered biotite (EZgl), granite gneiss (Dgg), and amphibolite (EZal) of the Laurens thrust sheet (fig. 4).

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USGS1991

Geochemistry of dissolved inorganic carbon in a Coastal Plain aquifer. 2. Modeling carbon sources, sinks, and δ13C evolution

Stable isotope data for dissolved inorganic carbon (DIC), carbonate shell material and cements, and microbial CO 2 were combined with organic and inorganic chemical data from aquifer and confining-bed pore waters to construct geochemical reaction models along a flowpath in the Black Creek aquifer of South Carolina. Carbon-isotope fractionation between DIC and precipitating cements was treated as a Rayleigh distillation process. Organic matter oxidation was coupled to microbial fermentation and sulfate reduction. All reaction models reproduced the observed chemical and isotopic compositions of final waters. However, model 1, in which all sources of carbon and electron-acceptors were assumed to be internal to the aquifer, was invalidated owing to the large ratio of fermentation CO 2 to respiration CO 2 predicted by the model (5–49) compared with measured ratios (two or less). In model 2, this ratio was reduced by assuming that confining beds adjacent to the aquifer act as sources of dissolved organic carbon and sulfate. This assumption was based on measured high concentrations of dissolved organic acids and sulfate in confining-bed pore waters (60–100 μM and 100–380 μM, respectively) relative to aquifer pore waters (from less than 30 μM and 2–80 μM, respectively). Sodium was chosen as the companion ion to organic-acid and sulfate transport from confining beds because it is the predominant cation in confining-bed pore waters. As a result, excessive amounts of Na-for-Ca ion exchange and calcite precipitation (three to four times more cement than observed in the aquifer) were required by model 2 to achieve mass and isotope balance of final water. For this reason, model 2 was invalidated. Agreement between model-predicted and measured amounts of carbonate cement and ratios of fermentation CO 2 to respiration CO 2 were obtained in a reaction model that assumed confining beds act as sources of DIC, as well as organic acids and sulfate. This assumption was supported by measured high concentrations of DIC in confining beds (2.6–2.7 mM). Results from this study show that geochemical models of confined aquifer systems must incorporate the effects of adjacent confining beds to reproduce observed groundwater chemistry accurately.

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USGS1991

Aerobic biodegradation potential of subsurface microorganisms from a jet fuel-contaminated aquifer

In 1975, a leak of 83,000 gallons (314,189 liters) of jet fuel (JP-4) contaminated a shallow water-table aquifer near North Charleston, S.C. Laboratory experiments were conducted with contaminated sediments to assess the aerobic biodegradation potential of the in situ microbial community. Sediments were incubated with 14 C-labeled organic compounds, and the evolution of 14 CO 2 was measured over time. Gas chromatographic analyses were used to monitor CO 2 production and O 2 consumption under aerobic conditions. Results indicated that the microbes from contaminated sediments remained active despite the potentially toxic effects of JP-4. 14 CO 2 was measured from [ 14 C]glucose respiration in unamended and nitrate-amended samples after 1 day of incubation. Total [ 14 C]glucose metabolism was greater in 1 mM nitrate-amended than in unamended samples because of increased cellular incorporation of 14 C label. [ 14 C]benzene and [ 14 C]toluene were not significantly respired after 3 months of incubation. With the addition of 1 mM NO 3 , CO 2 production measured by gas chromatographic analysis increased linearly during 2 months of incubation at a rate of 0.099 μ mol g -1 (dry weight) day -1 while oxygen concentration decreased at a rate of 0.124 μ mol g -1 (dry weight) day -1 . With no added nitrate, CO 2 production was not different from that in metabolically inhibited control vials. From the examination of selected components of JP-4, the n -alkane hexane appeared to be degraded as opposed to the branched alkanes of similar molecular weight. The results suggest that the in situ microbial community is active despite the JP-4 jet fuel contamination and that biodegradation may be compound specific. Also, the community is strongly nitrogen limited, and nitrogen additions may be required to significantly enhance hydrocarbon biodegradation.

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