Cm. Graham et al., TIMESCALES AND MECHANISMS OF FLUID INFILTRATION IN A MARBLE - AN ION MICROPROBE STUDY, Contributions to Mineralogy and Petrology, 132(4), 1998, pp. 371-389
Using a recently developed ion microprobe technique, a detailed oxygen
isotope map of calcite grains in a coarse-grained marble has been con
structed, supported by trace element (Mn, Sr, Fe) analysis and cathodo
luminescence (CL) imaging, in order to constrain scales of oxygen isot
ope equilibrium, timescales and mechanisms of metamorphic fluid infilt
ration, and fluid sources and pathways. Results are compared with a pr
evious study of this sample (Wada 1988) carried out using a cryo-micro
tome technique and conventional oxygen isotope analysis. The marble, f
rom the high temperature/low pressure Hida metamorphic belt in north-c
entral Japan, underwent granulite facies followed by amphibolite facie
s metamorphic events, the latter associated with regional granite intr
usion. The CL imaging indicates two types of calcite, a yellow lumines
cing (YLC) and a purple luminescing (PLC) variety. The YLC, which occu
pies grain boundaries, fractures, replacement patches, and most of the
abundant deformation twin lamellae, post-dates the dominant PLC calci
te and maps out fluid pathways. Systematic relationships were establis
hed between oxygen isotope and trace element composition, calcite type
and texture, based on 74 O-18/O-16 and 17 trace element analyses with
20-30 mu m spatial resolution. The YLC is enriched in Mn and Fe, and
depleted in O-18 and Sr compared to PLC, and is much more O-18 deplete
d than is indicated from conventional analyses. Results are interprete
d to indicate infiltration of O-18-depleted (metamorphic or magmatic)
fluid (initial delta(18)O = 9 parts per thousand-10.5 parts per thousa
nd) along grain boundaries, fractures and deformation twin lamellae, d
epleting calcite grains in Sr and enriching them in Mn and Fe. The sam
ple is characterised by gross isotopic and elemental disequilibrium, w
ith important implications for the application of chromatographic theo
ry to constrain fluid fluxes in metacarbonate rocks. Areas of PLC unaf
fected by ''short-circuiting'' fluid pathways contain oxygen diffusion
profiles of similar to 10 parts per thousand/similar to 200 mu m in g
rain boundary regions or adjacent to fractures/patches. When correctio
n is made for estimated grain boundary/fracture and profile orientatio
n in 3D, profiles are indistinguishable within error. Modelling of the
se profiles gives consistent estimates of Dt (where D is the diffusion
coefficient and t is time) of similar to 0.8 x 10(-8) m(2), from whic
h, using experimental data for oxygen diffusion in calcite, timescales
of fluid transport along grain boundaries at amphibolite facies tempe
ratures of similar to 10(3) to similar to 10(4) years are obtained. Th
ese short timescales, which are much shorter than plausible durations
of metamorphism, imply that rock permeabilities may be transiently muc
h higher during fluid flow than those calculated from time integrated
fluid fluxes or predicted from laboratory measurements. The preservati
on of O-18/O-16 profiles requires either rapid cooling rates (similar
to 100-600 degrees C/million years), or, more plausibly, loss of grain
boundary fluid such that a dry cooling history followed the transient
passage of fluid. The delta(18)O/trace element correlations are also
consistent with volume diffusion-controlled transport in the PLC. Flui
d transport and element exchange occurred by two interrelated mechanis
ms on short timescales and on different lengthscales - long-distance f
low along cracks, grain boundaries and twin lamellae coupled to simila
r to 200 mu m-scale volume diffusion of oxygen.