Measurements of the stable carbon isotope ratios(
13C)of microbial metabolic end products presents a promisingmethod for monitoring
in situ bioremediation ofpetroleumhydrocarbons. Differences between the
13C valuesofhydrocarbons and indigenous carbon sources (e.g., plantmatter, soil carbonates) can be exploited to trace theorigins of metabolic end products. However, in
zonesofmethanogenesis and/or where the
13C values ofendogenous plant matter overlap those of hydrocarbons,
13Cmeasurements can produce ambiguous results. In suchcases, simultaneous measurement of the radiocarbon(
14C)contents of metabolic end products can be used todetermine their sources. This method was applied at agasoline station spill site where hydrocarbons were theonlysource of
14C-free carbon. Combined
13Cand
14Cmeasurements of soil gas CO
2 and dissolved inorganiccarbonin groundwater enabled quantification of carbon inputs.Furthermore, low
14C contents of high
13C CO
2 were crucialin establishing that the soil gas CO
2 was derivedfrommethanogenesis of hydrocarbons and not shell dissolution.In addition, low
14C content coupled with a 16 dropinthe
13C values of CO
2 across a semipermeablelayer beneaththe gas station building confirmed that microbialoxidationof methane was occurring within this
zone.