Zd. Sharp et al., STABLE-ISOTOPE VARIATIONS (H, C, O) IN A PROGRADE METAMORPHIC TRIASSIC RED-BED FORMATION, CENTRAL SWISS ALPS, Schweizerische Mineralogische und Petrographische Mitteilungen, 75(2), 1995, pp. 147-161
In the Swiss Central Alps, the Upper Triassic red beds range from unme
tamorphosed Keuper sediments in the northern foreland to staurolite-gr
ade pelites (Quartenschiefer) farther to the south. Individual stratig
raphic sequences can be followed intermittently throughout the prograd
e metamorphic sequence, allowing for isotopic variations in hydrogen,
carbon and oxygen to be traced in a single protolith that has undergon
e essentially a single Alpine metamorphic event. Samples were analyzed
from each of four metamorphic grades: 1) unmetamorphosed sediments fr
om the Lindau borehole in the Molasse Basin (MB), T approximate to 100
degrees C; 2) anchimetamorphosed sediments from the northern Glarus A
lps (GA), T approximate to 200-250 degrees C; 3) epimetamorphic-grade
(lower greenschist facies) sediments from the Urseren Zone (UZ), T app
roximate to 400 degrees C; 4) epi- and mesometamorphic pelites from th
e Lukmanier Pass are (LP), T similar or equal to 500-550 degrees C The
delta(18)O (parts per thousand vs SMOW) and the delta(13)C (parts per
thousand vs PDB) values of the carbonate fraction, the delta(18)O and
delta D values of the silicate residue (parts per thousand vs SMOW) a
nd the total wt% H2O and wt% carbonate were measured for each sample.
Averages and variability for each zone are given as follows: [GRAPHICS
] The silicates are the dominant oxygen reservoir at all but the lowes
t grades; hence the delta(18)O(silicate), values are essentially const
ant throughout the sequence. The delta(18)O(carbonate), values systema
tically decrease with increasing grade, approaching equilibrium with t
he silicates. The scattered delta(13)C carbonate values may be due to
varying degrees of decarbonation or interaction with organic matter (f
rom adjacent black shales?). The delta D values of the hydrous silicat
es initially increase, indicating interaction with deuterium-enriched
pore waters, and then decrease at higher metamorphic grades due to the
removal of water associated with dehydration reactions. The overall i
sotopic variations can be interpreted in terms of minor C-O-H fluid lo
ss, with no external fluid input.