S. Salvi et Ae. Williamsjones, FISCHER-TROPSCH SYNTHESIS OF HYDROCARBONS DURING SUB-SOLIDUS ALTERATION OF THE STRANGE LAKE PERALKALINE GRANITE, QUEBEC LABRADOR, CANADA/, Geochimica et cosmochimica acta, 61(1), 1997, pp. 83-99
The composition of the carbonic phase(s) of fluid inclusions in pegmat
ite quartz from the Strange Lake peralkaline complex has been analysed
by gas chromatography using online extraction of inclusion contents a
nd a PoraPLOT(R) Q capillary column. The measured gas species are, in
order of abundance, CH4, H-2, C2H6, CO2, N-2, C3H8, n-C4H10, n-C5H12,
C2H2, i-C4H10, and C2H4. Minor amounts of i-C5H12, n-C6H14, i-C6H14, a
nd neo-C6H14 were also detected (but not quantified) in some samples.
A suite of quartz samples from Ca-metasomatised pegmatites contains fl
uid inclusions with a similar distribution of hydrocarbons but much hi
gher proportions of CO2. The carbonic fluid coexisted immiscibly with
a brine (Salvi and Williams-Jones, 1992), which on the basis of field
and petrographic evidence, was interpreted to have originated from the
magma. However, thermodynamic calculations indicate that the above ga
s species, specifically the hydrocarbons, could not have coexisted at
equilibrium in the proportions measured, at any geologically reasonabl
e conditions either prior to or post entrapment. We propose, instead,
that the gas compositions measured in the Strange Lake inclusions, and
in inclusions from other alkalic complexes, resulted from the product
ion of H-2 during the alteration of arfvedsonite to aegirine, and the
subsequent reaction of this H-2 With orthomagmatic CO2 and CO to form
hydrocarbons in a magnetite-catalysed Fischer-Tropsch synthesis. Local
ly, influx of an oxidised calcic brine, derived externally from the pl
uton, altered the original composition of the fluid by converting hydr
ocarbons to CO2. Copyright (C) 1997 Elsevier Science Ltd