2004 Denver Annual Meeting (November 7–10, 2004)
Paper No. 202-9
Presentation Time: 10:30 AM-10:45 AM

DISSOLVED NOBLE GASES AND EXCESS AIR IN CALIFORNIA GROUNDWATERS

CEY, Bradley D., Jackson School of Geosciences, Univ of Texas at Austin, 1 University Station C1100, Austin, TX 78712-0254, bdc@mail.utexas.edu, HUDSON, G. Bryant, Lawrence Livermore National Lab, Livermore, CA 94550, MORAN, Jean E., Lawrence Livermore National Lab, L-231, P.O. Box 808, Livermore, CA 94550, and SCANLON, Bridget R., Bureau of Economic Geology, Univ. of Texas at Austin, 10100 Burnet Rd, Bldg. 130, Austin, TX 78758

The composition and concentration of dissolved gases in groundwater are useful for understanding both groundwater flow (e.g. age dating, recharge temperature) and geochemical reactions (e.g. denitrification).  Lawrence Livermore National Laboratory, in collaboration with the US Geological Survey, has analyzed dissolved gases in more than 1200 water supply wells across California as part of the Groundwater Ambient Monitoring and Assessment (GAMA) program of the California State Water Resources Control Board.  Samples were analyzed for noble gases (He, Ne, Ar, Kr, Xe) as well as tritium and delta 18O.  A noteworthy aspect of the data set is the large range in excess air concentrations.  The majority of high excess air samples are from wells in coastal basins, while wells in Central Valley basins show much lower values.  For example, significant fractions of wells within Orange County and Santa Clara County have excess air concentrations of >15 cm3/kg (some as high as 40 cm3/kg) while both Sacramento and San Joaquin County have mean excess air <5 cm3/kg.  Many high excess air values in the heavily urbanized coastal basins are attributed to artificial recharge; however high values are also found in areas of Santa Clara County without major artificial recharge facilities.  Groundwater recharged prior to the 1950s (i.e. tritium <1 pCi/L) generally contains lower amounts of excess air relative to more recently recharged water.  The presence of 15 cm3/kg of excess air introduces ~50% more dissolved oxygen to groundwater than equilibrium solubility alone.  Increased dissolved oxygen can greatly impact geochemical reactions such as denitrification and oxidation of organic carbon during groundwater recharge and transport.  

    This work was performed under the auspices of the U.S. Department of Energy by University of California, Lawrence Livermore National Laboratory under Contract W-7405-Eng-48.

2004 Denver Annual Meeting (November 7–10, 2004)
General Information for this Meeting
Session No. 202
Dissolved Gases as Indicators of Geochemical and Hydrogeologic Processes
Colorado Convention Center: 201
8:00 AM-12:00 PM, Wednesday, November 10, 2004

Geological Society of America Abstracts with Programs, Vol. 36, No. 5, p. 470

© Copyright 2004 The Geological Society of America (GSA), all rights reserved. Permission is hereby granted to the author(s) of this abstract to reproduce and distribute it freely, for noncommercial purposes. Permission is hereby granted to any individual scientist to download a single copy of this electronic file and reproduce up to 20 paper copies for noncommercial purposes advancing science and education, including classroom use, providing all reproductions include the complete content shown here, including the author information. All other forms of reproduction and/or transmittal are prohibited without written permission from GSA Copyright Permissions.