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Published online 13 May 2005
Published in Vadose Zone J 4:337-344 (2005)
DOI: 10.2136/vzj2004.0100
© 2005 Soil Science Society of America
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SPECIAL SECTION: ZNS'03 VADOSE ZONE RESEARCH

Volatile Organic Compounds in the Saturated–Unsaturated Interface Region of a Contaminated Phreatic Aquifer

Daniel Ronena,*, Ellen R. Graberb and Yael Laorc

a Research Dep., Israel Hydrological Service, P.O. Box 20365, Tel Aviv 61203, Israel, and Ben-Gurion Univ. of the Negev, The Jacob Blaustein Institute for Desert Research, Dep. of Environmental Hydrology & Microbiology, Sde Boker Campus 84990, Israel
b Institute of Soil, Water and Environmental Sciences, The Volcani Center, Agricultural Research Organization, P.O. Box 6, Bet-Dagan, 50250, Israel
c Institute of Soil, Water and Environmental Sciences, Newe-Ya'ar Research Center, Agricultural Research Organization, P.O. Box 1021, Ramat Yishay, 30095, Israel

* Corresponding author (danronen{at}bgu.ac.il)

Received 24 June 2004.

Three volatile organic compound (VOC) field profiles were obtained during a period of 13 mo with a passive multilayer sampler (MLS) from a monitoring well located in the VOC-contaminated sandy phreatic Coastal Plain aquifer of Israel in the Tel Aviv area. The profiles presented here are unique in that they span both the saturated and unsaturated zones, through the saturated–unsaturated interface region (SUIR), and represent VOC concentrations from a single borehole. In groundwater just below the water table, the major contaminant, trichloroethylene (TCE), was present in concentrations up to 260000 µg/L water, and in the unsaturated zone just above the water table, in concentrations up to 124000 µg/L air. Other contaminants detected in high concentrations (as high as several thousands of µg/L) included tetrachloroethylene (PCE), cis-1,2-dichloroethylene (cis-1,2-DCE) and 1,1-dichloroethylene (1,1-DCE). In the three profiles, TCE and PCE concentrations were greatest at the water table and decreased with increasing distance from the water table both into the saturated and unsaturated zones. Temporal variations in maximal TCE vapor concentrations ranging from 44000 to 124000 µg/L air were also observed between profiles. The passive diffusion sampling characteristic of the MLS makes it possible to obtain unmixed vertical samples such that, for example, differences as great as 24000 µg TCE/L air can be measured in consecutive samples located only 12 cm apart in the unsaturated zone. The vertical detail is unique compared with other field sampling methods. Vertical detail is of utmost importance in interface regions, such as the SUIR, where water content in both the unsaturated and saturated zones varies significantly with depth, time, and space.

Abbreviations: {theta}, vertical water content • DCE, dichloroethylene • DO, dissolved oxygen • EC, electrical conductivity • KH, Henry's constant • MLS, passive multilayer sampler • MQL, minimum quantification level • p, pressure • PCE, tetrachloroethylene • PVC, polyvinyl chloride • SUIR, saturated–unsaturated interface region • TCE, trichloroethylene • VOC, volatile organic compound







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