Exposure assessment, an essential component of environmental risk analysis, requires quantitative approaches for estimating the distribution and persistence of pollutants at Superfund sites. The most common pollutants are volatile organic compounds (VOCs). In addition to VOCs, perchlorate has recently been discovered as an important groundwater contaminant prevalent at several Superfund sites. This project provides an evaluation of human exposure through the development of innovative stimulation module that considers the geological heterogeneity of field sites. Improving upon existing predictive models requires improved understanding of how physical and chemical heterogeneity impact transport, how mineral and organic matter composition affect reactivity, how variations in oxidation status control both abiotic and biological transformations are coupled, and how each of these changes when chemical mixtures are present. The first goal of this project is to elucidate the physical, chemical, and biological processes that determine the transport, transformation and remediation of perchlorate and VOCs in soil and geologic sediments. The second goal is to integrate this process-level knowledge to predict contaminant movement and potential human exposure under complex field setting such as the Aeroject NPL site in CA. A third goal of the project is to explore techniques for remediation of hazardous waste. We will work on VOCs, perchlorate, and chemical mixtures. A particular focus will be on developing and applying new risk assessment procedures that include state-of-the-art transport and fate modeling approaches, thereby determining probabilistically the extent and duration of past human exposure to perchlorate near Aeroject. This project will investigate the basic physical, chemical, and biological processes affect the fate and transport of perchlorate, VOCs, and mixtures of these chemicals in the vadose zone and groundwater using laboratory batch and column experiments. It will also determine the effect of coupled processes on transport and fate and will investigate the effects of spatially varying processes and properties on field-scale behavior. This understanding of the fundamental processes will be used to explore the potential of in situ subsurface techniques as well as pump-and-treat for remediating perchlorate and TCE contamination at the Aeroject site. Using stochastic transport and fate stimulation models, the effects of multiple transport processes on potential human exposure levels at the field scale as well as human health effects will also be investigated with conjunction with other projects.

Project Start
2001-04-01
Project End
2002-03-31
Budget Start
Budget End
Support Year
15
Fiscal Year
2001
Total Cost
$165,230
Indirect Cost
Name
University of California Davis
Department
Type
DUNS #
094878337
City
Davis
State
CA
Country
United States
Zip Code
95618
Ren, Qian; Ma, Min; Yang, Jun et al. (2018) Soluble epoxide hydrolase plays a key role in the pathogenesis of Parkinson's disease. Proc Natl Acad Sci U S A 115:E5815-E5823
Pecic, Stevan; Zeki, Amir A; Xu, Xiaoming et al. (2018) Novel piperidine-derived amide sEH inhibitors as mediators of lipid metabolism with improved stability. Prostaglandins Other Lipid Mediat 136:90-95
Yamanashi, Haruto; Boeglin, William E; Morisseau, Christophe et al. (2018) Catalytic activities of mammalian epoxide hydrolases with cis and trans fatty acid epoxides relevant to skin barrier function. J Lipid Res 59:684-695
Wang, Fuli; Zhang, Hongyong; Ma, Ai-Hong et al. (2018) COX-2/sEH Dual Inhibitor PTUPB Potentiates the Antitumor Efficacy of Cisplatin. Mol Cancer Ther 17:474-483
Napimoga, M H; Rocha, E P; Trindade-da-Silva, C A et al. (2018) Soluble epoxide hydrolase inhibitor promotes immunomodulation to inhibit bone resorption. J Periodontal Res 53:743-749
Blöcher, René; Wagner, Karen M; Gopireddy, Raghavender R et al. (2018) Orally Available Soluble Epoxide Hydrolase/Phosphodiesterase 4 Dual Inhibitor Treats Inflammatory Pain. J Med Chem 61:3541-3550
Hao, Lei; Kearns, Jamie; Scott, Sheyenne et al. (2018) Indomethacin Enhances Brown Fat Activity. J Pharmacol Exp Ther 365:467-475
Yang, Yang-Ming; Sun, Dong; Kandhi, Sharath et al. (2018) Estrogen-dependent epigenetic regulation of soluble epoxide hydrolase via DNA methylation. Proc Natl Acad Sci U S A 115:613-618
Zheng, Jing; Chen, Juan; Zou, Xiaohan et al. (2018) Saikosaponin d causes apoptotic death of cultured neocortical neurons by increasing membrane permeability and elevating intracellular Ca2+ concentration. Neurotoxicology 70:112-121
Cui, Xiping; Vasylieva, Natalia; Shen, Ding et al. (2018) Biotinylated single-chain variable fragment-based enzyme-linked immunosorbent assay for glycocholic acid. Analyst 143:2057-2065

Showing the most recent 10 out of 1149 publications