OXYGEN-ISOTOPE COMPOSITIONS OF MIXED-LAYER SERPENTINE-CHLORITE AND ILLITE-SMECTITE IN THE TUSCALOOSA FORMATION (US GULF-COAST) - IMPLICATIONS FOR PORE FLUIDS AND MINERALOGIC REACTIONS
Pc. Ryan et al., OXYGEN-ISOTOPE COMPOSITIONS OF MIXED-LAYER SERPENTINE-CHLORITE AND ILLITE-SMECTITE IN THE TUSCALOOSA FORMATION (US GULF-COAST) - IMPLICATIONS FOR PORE FLUIDS AND MINERALOGIC REACTIONS, Clays and clay minerals, 46(4), 1998, pp. 357-368
Oxygen isotopic compositions were determined for coexisting mixed-laye
r serpentine-chlorite (Sp-Ch) and illite-smectite (I-S) from 5 Tuscalo
osa Formation sandstone cores sampled between 1937 and 5470 m burial d
epth. High gradient magnetic separation (HGMS) was used to concentrate
Sp-Ch and I-S from the <0.5 mu m fraction of each core sample into fr
actions with a range in the Sp-Ch:I-S ratio, and end-member delta(18)O
compositions were determined by extrapolation. The Sp-Ch delta(18)O v
alues range from +10.4 to 13.7 parts per thousand and increase with bu
rial between 3509 and 5470 m. The only exception is Sp-Ch from 1937 m,
which has an anomalously high delta(18)O value of +12.6 parts per tho
usand. The I-S delta(18)O values range from +16.1 to 17.3 parts per th
ousand and do not change significantly between 3509 and 5470 m burial
depth. Pore water delta(18)O compositions calculated from Sp-Ch and I-
S values and measured borehole temperatures range from -2.6 to +10.3 p
arts per thousand. The isotopically light values indicate that Sp-Ch f
ormed at shallow burial depths in the presence of brackish to marine w
ater and/or meteoric water. The depth-related increase in delta(18)O o
f Sp-Ch is attributed to oxygen exchange between mineral and pore wate
r during diagenetic mineral reactions. Increasing delta(18)O values, i
n conjunction with XRD and SEM data, indicate that transformation of s
erpentine layers to chlorite layers and Ibb polytype layers to Iaa pol
ytype layers occurred on a layer-by-layer basis when individual layers
dissolved and recrystallized within the confines of coherent crystals
. Possible explanations for the variation in I-S delta(18)O values inc
lude depth-related differences in pore water delta(18)O values present
at the time of I-S crystallization, contamination by detrital 2M(1) m
ica and 1M polytype rotations that facilitated oxygen exchange.