A dolerite sample from the Middle Proterozoic McArthur Basin in northe
rn Australia has solid bitumen on fracture surfaces and liquid hydroca
rbon fluid inclusions in secondary calcite mineralization. The extract
of this sample is rich in polar compounds and contains an unusual and
novel series of saturated ketone isomers, including homologous series
of n-alkan-2-ones and n-alkan-3-ones, together with a complicated ser
ies of branched mid-chain ketones. These ketone isomers were identifie
d by the monitoring of diagnostic mass chromatograms, including those
due to rearrangement ions. n-Alkanes are only three to four times more
abundant than the ketones. The n-alkan-2-ones have a similar distribu
tion to the n-alkanes and may have been formed by the pyrolysis and be
ta-oxidation of carboxylic acids, followed by decarboxylation of the r
esultant beta-keto acids. The n-alkan-3-ones and the mid-chain isomers
have a distribution which is biased towards the low molecular weight
isomers, probably due to the pyrolysis of a different kerogen moiety,
perhaps alkyl chains cross-linked by ether groups. Ketones are known t
o occur when oil shales are pyrolysed and in hydrothermal oil, so by a
nalogy the natural pyrolysis of kerogen in the fine-grained sediments
by the dolerite sill resulted in the generation of liquid products (pr
edominantly n-alkanes and ketones) which were preserved as hydrocarbon
-bearing fluid inclusions and as solid bitumen in a fracture.