Further evaluation of the Re-Os geochronometer in organic-rich sedimentary rocks: A test of hydrocarbon maturation effects in the Exshaw Formation, Western Canada Sedimentary Basin

Re-Os isotopic analyses of a single organic-rich sedimentary rock unit (ORS) of known depositional age, and at three levels of regional hydrocarbon maturity, show that hydrocarbon maturation does not affect the ability the (187)Re-(187)Os chronometer to yield a depositional age for such rocks. We present Re-Os isotope analyses from the Late Devonian Exshaw Formation in the subsurface of the Western Canada Sedimentary Basin, Alberta, and obtain a Re-Os isochron age of 358 +/- 10 Ma (2sigma, Model 3, lambda = 1.666 x 10(-11).a(-1)) for samples ranging from hydrocarbon immature to overmature. This age is within uncertainty of the established absolute age for the Exshaw Formation. Hydrocarbon immature, and mature plus overmature samples show no significant age differences if regressed individually, indicating that hydrocarbon maturation did not greatly disturb the Re-Os isotope system in the Exshaw Formation. As such, we propose that the Re-Os geochronometer may be used as a reliable tool for measuring the depositional ages of ORS regardless of their level of hydrocarbon maturity. We find that minimizing natural variation in the initial (187)Os/(188)Os ratio is more important than avoiding hydrocarbon maturation in obtaining precise Re-Os ages. In particular, the Exshaw Formation appears to contain a nonhydrogenous component of unradiogenic Os, in addition to the hydrogenous Os load. A subset of Exshaw Formation samples with >5% total organic carbon (TOC), which should best reflect the hydrogenous Os load alone, yields a very well-fitted isochron having a depositional age of 358 +/- 9 Ma (2sigma, lambda = 1.666 x 10(-11).a(-1)) with an initial (187)Os/(188)Os ratio of 0.59 +/- 0.05 (Model 3, Mean Square of Weighted Deviates (MSWD) = 1.8). The initial (187)Os/(188)Os ratio of this regression may provide an estimate of the Os isotopic composition of local seawater at the time of deposition. Copyright (C) 2002 Elsevier Science Ltd.