Micrometer scale carbon isotopic study of bitumen associated with Athabasca uranium deposits:: Constraints on the genetic relationship with petroleum source-rocks and the abiogenic origin hypothesis

In situ analytical techniques - Fourier transform infrared microspectroscopy (mu FTIR) and ion microprobe - have been used to unravel the origin of solid bitumen associated with the uranium deposits of Athabasca (Saskatchewan, Canada). Both aliphaticity and carbon isotopic compositions within the samples are heterogeneous but spatially organized in concentric zonations at the micrometer scale. Finally, the delta C-13 values are positively correlated to the aliphatic contents over an extremely large isotopic range from similar to-49 parts per thousand to similar to-31 parts per thousand. We infer that this positive correlation may be related to the carbon isotopic fractionations associated with the synthesis of bitumen through the catalytic hydrogenation Of CO2, rather than the result of pre-existing petroleum product precipitation and/or alteration (such as radiolysis). This explanation is consistent with (i) published results of abiogenic synthesis experiments, in which the differences in delta C-13 Values between saturated and unsaturated hydrocarbons range from +2 and +19 parts per thousand, in contrast to the differences systematically observed in conventional bitumen and petroleum ranging from 0 parts per thousand to -4 parts per thousand; (ii) the absence of a similar positive correlation between aliphatic contents and delta C-13 values in the other bitumen analyzed in the present study, for which a biogenic origin has been unequivocally established (samples from Oklo, Gabon, and Lodeve, France, uranium deposits); (iii) the presence Of CO2 and H-2 in the gas-phase of fluid inclusions in the Athabasca uranium deposits, H2 resulting from water radiolysis. The present results suggest that the delta C-13 vs. aliphaticity correlation could be used as a criterion to discriminate between abiogenic vs. biogenic origin of macromolecular organic matter. (c) 2007 Published by Elsevier B.V.