An. Bishop et Gd. Abbott, THE INTERRELATIONSHIP OF BIOLOGICAL MARKER MATURITY PARAMETERS AND MOLECULAR YIELDS DURING CONTACT-METAMORPHISM, Geochimica et cosmochimica acta, 57(15), 1993, pp. 3661-3668
Jurassic siltstone samples were collected, on a centimetre scale, as a
function of increasing distance from a dolerite dyke (Isle of Skye, n
orthwest Scotland). The constant origin and type of the organic matter
in this single lithological horizon is indicated by organic petrologi
cal observations as well as organic geochemical analyses. Therefore, c
hanges in biological marker distributions, with distance from the dyke
contact, can be unequivocally correlated with the thermal influence o
f the intrusion. The vitrinite reflectance (R0 Average) values of thes
e samples increase gradually from 0.35% to 3.60% as the dyke contact i
s approached. Four classical biological marker maturity parameters (20
S/(20S + 20R), TA/(TA + MA), C20/(C20 + C28), and 22S/(22S + 22R)), ha
ve been measured from GCMS analyses of the sample extracts. Changes in
these molecular parameters were compared with changes in the concentr
ations of the individual biological marker compounds, expressed relati
ve to mass of rock extracted. This comparison revealed that these mole
cular parameters are not governed by the conventional product-reactant
relationships (chiral isomerisation, aromatisation or side-chain crac
king reactions) operating solely in the free saturated or aromatic hyd
rocarbon structures. Release/formation from macromolecular and/or func
tionalised moieties (hydrocarbon or non-hydrocarbon) followed by compo
und loss provide an alternative paradigm in all four cases in this par
ticular thermal regime. Direct chiral isomerisation in the free steran
e or homohopane cannot, however, be completely ruled out as a contribu
tor to an admixture of processes. Similarly, aromatisation in the free
hydrocarbon fraction may account for a proportion of the triaromatic
steroids.