The high abundance with which tricyclic terpenoids have previously been det
ected in Tasmanite oil shales has led to the strong suspicion that the sour
ce of these compounds is the Tasmanites microfossil prevalent in these oil
shales. In this study, the hydrocarbon composition of a Tasmanite oil shale
and isolated Tasmanites were separately investigated by laser micropyrolys
is gas chromatography-mass spectrometry, a recently developed technique tha
t facilitates the analysis of small samples such as microfossils. Major pro
ducts comprised C-19-C-28 tricyclic terpanes, including the ubiquitous 13-m
ethyl, 14-alkylpodocarpanes, as well as a number of additional tricyclic te
rpane isomers, a C-19 monoaromatic hydrocarbon, and several C-19-C-28 tricy
clic terpenes (one and two orders of unsaturation). There have been few pre
vious reports on the tricyclic terpenes and their production is likely attr
ibutable to the pyrolytic cleavage of analogous (probably saturated) tricyc
lic precursors within the macromolecular biopolymer. The only major differe
nce between the tricyclic terpenoid compositions observed from these sample
s was the absence of the less concentrated oil shale products in the Tasman
ites analyses, probably due to the lower organic content of the preextracte
d fossil. The very similar tricyclic content of both samples strongly suppo
rts the proposal of an inherent relationship between the Tasmanites and tri
cyclic terpenoid production. The integrity of the laser data was confirmed
by comparison to a conventional data set obtained by the pyroprobe pyrolysi
s of the Tasmanite oil shale. Copyright (C) 2000 Elsevier Science Ltd.