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RECORD NUMBER: 11 OF 23

OLS Field Name OLS Field Data
Main Title Production and Transport of Carbon Dioxide in a Contaminated Vadose Zone: A Stable and Radioactive Carbon Isotope Study.
Author Suchomel, K. H. ; Long, A. ; Kreamer, D. K. ;
CORP Author Arizona Univ., Tucson. Environmental Radioisotope Center. ;Nevada Univ. System, Las Vegas. Water Resources Center.;Robert S. Kerr Environmental Research Lab., Ada, OK.
Publisher c1990
Year Published 1990
Report Number EPA-R-812583; EPA/600/J-90/486;
Stock Number PB91-191478
Additional Subjects Water pollution ; Vadose water ; Path of pollutants ; Isotopic labeling ; Tracer studies ; Aquifers ; Carbon dioxide ; Organic solvent ; Waste disposal ; Biodeterioration ; Aerobic processes ; Volatile organic compounds ; Environmental transport ; Biological indicators ; Reprints ; Soil gases
Holdings
Library Call Number Additional Info Location Last
Modified
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Status
NTIS  PB91-191478 Most EPA libraries have a fiche copy filed under the call number shown. Check with individual libraries about paper copy. NTIS 09/04/1991
Collation 10p
Abstract
Analyses of soil gas compositions and stable and radioactive carbon isotopes in the vadose zone above an alluvial aquifer were conducted at an organic solvent disposal site in southeast Phoenix, AZ. The study investigated the source and movement of carbon dioxide above a plume of organic solvent contamination. Two soil gas monitor wells, each screened and grouted at four discrete depths above the water table, provided sampling access. One well penetrated the uncontaminated vadose zone, the other penetrated a contaminated area now covered with asphalt. Carbon dioxide concentrations in the uncontaminated area range from 1.45% at 8 ft to 3% at 19 ft below land surface. Isotopic evidence suggests root respiration and minor oxidation of organic matter as CO2 sources at this site. Carbon dioxide in soil gas samples from the contaminated area exceeded 15% while O2 levels were as low as 1%. Carbon dioxide concentrations and carbon isotope values are consistent with in situ aerobic biodegradation of the organic pollutants. (Copyright (c) 1990 American Chemical Society.)