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Theresa S. Presser

Publications and source records attributed to Theresa S. Presser.

21 records · Page 2Linked to original sources

Mass balance approach to selenium cycling through the San Joaquin Valley, sources to river to bay

Surface and ground waters of the Central Valley of California (e.g., rivers, dams, off-stream storage reservoirs, pumping facilities, irrigation and drinking water supply canals, agricultural drainage canals) are part of a hydrologic system that makes up a complex ecosystem extending from the riparian wetlands of the Sacramento and San Joaquin Rivers through the San Francisco Bay/Delta Estuary to the Pacific Ocean (Fig. 1). Water quality concerns center on elevated selenium (Se) and salt concentrations in irrigation drainage water discharged into the waterways of the relatively arid San Joaquin Valley (SJV), including the San Joaquin River (SJR). These waters are made unique by dissolved Se, weathered from marine sedimentary rocks of the Coast Ranges to the west, being ultimately concentrated to toxic levels in aquatic wildlife in the wetlands of the SJV/SJR trough (Figs. 1 and 2) (Presser and Ohlendorf, 1987; Presser, 1994). Scientific and environmental concerns focus on the bioreactive properties of Se and its partitioning among biota, water, and sediment, and on whether simple dilution models can be applied to an element that bioaccumulates. Because of state and federal commitments to provide water for irrigation, as well as drainage of irriga­ tion wastewater by the year 2000 drainage from over 180,000 ha of seleniferous, salinized farmland within the western SJV will create approximately 387 million cubic meters of potentially toxic drainage water annually (i.e., “problem water,” as defined by the San Joaquin Valley Drainage Program, 1990), thus lending urgency to an understanding of the biogeochemistry of Se in this environment.

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Selenate reduction to elemental selenium by anaerobic bacteria in sediments and culture: Biogeochemical significance of a novel, sulfate-independent respiration

Interstitial water profiles of SeO 4 2− , SeO 3 2− , SO 4 2− , and Cl − in anoxic sediments indicated removal of the seleno-oxyanions by a near-surface process unrelated to sulfate reduction. In sediment slurry experiments, a complete reductive removal of SeO 4 2− occurred under anaerobic conditions, was more rapid with H 2 or acetate, and was inhibited by O 2 , NO 3 − , MnO 2 , or autoclaving but not by SO 4 2− or FeOOH. Oxidation of acetate in sediments could be coupled to selenate but not to molybdate. Reduction of selenate to elemental selenium was determined to be the mechanism for loss from solution. Selenate reduction was inhibited by tungstate and chromate but not by molybdate. A small quantity of the elemental selenium precipitated into sediments from solution could be resolublized by oxidation with either nitrate or FeOOH, but not with MnO 2 . A bacterium isolated from estuarine sediments demonstrated selenate-dependent growth on acetate, forming elemental selenium and carbon dioxide as respiratory end products. These results indicate that dissimilatory selenate reduction to elemental selenium is the major sink for selenium oxyanions in anoxic sediments. In addition, they suggest application as a treatment process for removing selenium oxyanions from wastewaters and also offer an explanation for the presence of selenite in oxic waters.

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