GRAIN-SCALE STABLE-ISOTOPE DISEQUILIBRIUM DURING FLUID-ROCK INTERACTION .1. SERIES APPROXIMATIONS FOR ADVECTIVE-DISPERSIVE TRANSPORT AND FIRST-ORDER KINETIC MINERAL-FLUID EXCHANGE

Authors
Citation
R. Abart et R. Sperb, GRAIN-SCALE STABLE-ISOTOPE DISEQUILIBRIUM DURING FLUID-ROCK INTERACTION .1. SERIES APPROXIMATIONS FOR ADVECTIVE-DISPERSIVE TRANSPORT AND FIRST-ORDER KINETIC MINERAL-FLUID EXCHANGE, American journal of science, 297(7), 1997, pp. 679-706
Citations number
36
Categorie Soggetti
Geosciences, Interdisciplinary
Journal title
ISSN journal
00029599
Volume
297
Issue
7
Year of publication
1997
Pages
679 - 706
Database
ISI
SICI code
0002-9599(1997)297:7<679:GSDDFI>2.0.ZU;2-T
Abstract
Stable isotope fronts provide lasting evidence of fluid-rock interacti on. The processes involved in material transport and mineral-fluid exc hange may be identified from an analysis of front geometries based on transport theory. For the interpretation of stable isotope fronts the distinction between equilibrium and disequilibrium scenarios is crucia l. For fossil systems this distinction can be made only if two or more minerals are considered as stable isotope monitors simultaneously. We derive approximations that describe one-dimensional advective-dispers ive transport and coupled first-order kinetic mineral-fluid exchange, where the various constituent minerals of the rock are allowed to have different exchange rates. The new formalism is an extension of transp ort theory that accounts for the polyphase nature of rocks and allows integration of isotopic information from several monitoring phases. Co mparison of the geometries of stable isotope fronts monitored by diffe rent phases permits identification of departures from local equilibriu m that occurred during fluid-rock interaction. Furthermore it permits distinction of the contributions of diffusion-dispersion and of kineti cally controlled mineral-fluid exchange to the distension of an initia lly sharp front. If mineral-fluid exchange is kinetically controlled, this has an interesting implication for stable isotope thermometry in that the inter-mineral fractionations may vary as a function of space and time irrespective of the system temperature. The series approximat ions presented here provide a formal basis for the interpretation of s uch disequilibrium phenomena, In particular they facilitate extraction of quantitative relations among transport velocities, exchange rates, and the duration of fluid-rock interaction from front geometries.