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- Routh, Joyanto, 1968-, et al.
(författare)
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Sedimentary organic matter sources and depositional environment in the Yegua formation (Brazos County, Texas)
- 1999
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Ingår i: Organic Geochemistry. - : Elsevier. - 0146-6380 .- 1873-5290. ; 30:11, s. 1437-1453
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Tidskriftsartikel (refereegranskat)abstract
- The complex depositional environment of the Eocene Yegua formation (Brazos County, Texas) can be better understood by integrating organic matter (OM) geochemistry with stratigraphy. Yegua sediments represent parasequences separated by exposure surfaces. Organic petrography and geochemistry (biomarkers, C/N ratios, and carbon isotopes) indicate the presence of both terrestrial and marine OM in transgressive sediments. In contrast, regressive sediments contain only terrestrial OM. These differences relate to contrasting OM sources and depositional styles on the shelf. OM in the sediments is immature and the potential for generating hydrocarbons is poor. The study suggests that organic geochemical data can help in distinguishing transgressive and regressive environments in sedimentary formations.
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| 2. |
- Routh, Joyanto, 1968-, et al.
(författare)
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Trace-element geochemistry of Onion Creek near Van Stone lead-zinc mine (Washington, USA) — Chemical analysis and geochemical modeling
- 1996
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Ingår i: Chemical Geology. - : Elsevier. - 0009-2541 .- 1872-6836. ; 133:1, s. 211-224
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Tidskriftsartikel (refereegranskat)abstract
- Van Stone lead-zinc mine in Washington is a possible contamination source of Columbia River water. Breaching of an old tailings pond, seepage of contaminated water, and surficial transport of mine tailings have increased trace-element (TE) concentrations in the Onion Creek water and sediments. Chemical analyses of water and sediment samples indicate high TE levels near the breached tailings pond. TE contamination indices for sediments indicate high values of Pb, Zn, and other TE’s which decrease downstream. High Kd values (> 104) for several TE’s (e.g., Al, Cd, Fe, Mn, Pb, V, and Zn) suggest their enrichment in the solid phase. TE concentrations in Onion Creek water and sediment sharply attenuate downstream due to: (1) enhanced carbonate dissolution, thereby increasing pH and immobilizing TE’s; (2) sorption to oxides; and (3) change in lithology from carbonate to granite. Speciation model MINTEQA2 was used to study the effect on TE dispersion due to dissolution-precipitation reactions and adsorption to ferrihydrite. In addition to the field and chemical data, the model also supports the hypothesis that Onion Creek sediments are the major sink for TE’s at VSM. Model runs indicate precipitation of Al, Ba, Ca, Fe, Mg, and Mn minerals from oversaturation, whereas TE’s with low concentrations (Cr, Cu, Ni, Se) or geochemically more mobile (As, Mo, Sb) remain dissolved in water. Near the tailings ponds, high pH and abundance of sorption sites in sediments contribute to the complete adsorption of Pb and Zn species. Because ambient conditions result in the sorption of most Pb and Zn ions, Onion Creek water quality meets EPA regulatory standards. These species will persist in Onion Creek sediments as sorbed or insoluble complexes, and without drastic pH changes (< 4.0) they will remain immobilized. However, continued TE enrichment in sediments will prove hazardous to filter feeding and aquatic organisms.
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| 3. |
- Ulrich, G. A., et al.
(författare)
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Sulfur Cycling in the Terrestrial Subsurface : Commensal Interactions, Spatial Scales, and Microbial Heterogeneity
- 1998
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Ingår i: Microbial Ecology. - : Springer. - 0095-3628 .- 1432-184X. ; 36:2, s. 141-151
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Tidskriftsartikel (refereegranskat)abstract
- Microbiological, geochemical, and isotopic analyses of sediment and water samples from the unconsolidated Yegua formation in east-central Texas were used to assess microbial processes in the terrestrial subsurface. Previous geochemical studies suggested that sulfide oxidation at shallow depths may provide sulfate for sulfate-reducing bacteria (SRB) in deeper aquifer formations. The present study further examines this possibility, and provides a more detailed evaluation of the relationship between microbial activity, lithology, and the geochemical environment on meter-to-millimeter scales. Sediment of varied lithology (sands, silts, clays, lignite) was collected from two boreholes, to depths of 30 m. Our findings suggest that pyrite oxidation strongly influences the geochemical environment in shallow sediments ( 5 m), and produces acidic waters (pH 3.8) that are rich in sulfate (28 mM) and ferrous iron (0.3 mM). Sulfur and iron-oxidizing bacteria are readily detected in shallow sediments; they likely play an indirect role in pyrite oxidation. In consistent fashion, there is a relative paucity of pyrite in shallow sediments and a low 34S/32S-sulfate ratio (0.2ￜ) (reflecting contributions from 34S-depleted sulfides) in shallow regions. Pyrite oxidation likely provides a sulfate source for both oxic and anoxic aquifers in the region. A variety of assays and direct-imaging techniques of 35S-sulfide production in sediment cores indicates that sulfate reduction occurs in both the oxidizing and reducing portions of the sediment profile, with a high degree of spatial variability. Narrow zones of activity were detected in sands that were juxtaposed to clay or lignite-rich sediments. The fermentation of organic matter in the lignite-rich laminae provides small molecular weight organic acids to support sulfate reduction in neighboring sands. Consequently, sulfur cycling in shallow sediments, and sulfate transport represent important mechanisms for commensal interaction among subsurface microorganisms by providing electron donors for chemoautotrophic bacteria and electron acceptors for SRB. The activity of SRB is linked to the availability of suitable electron donors from spatially distinct zones.
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