FLUID-FLUX AND REACTION-RATE FROM ADVECTIVE-DIFFUSIVE CARBONATION OF MAFIC SILL MARGINS IN THE DALRADIAN, SOUTHWEST SCOTTISH HIGHLANDS

Citation
Adl. Skelton et al., FLUID-FLUX AND REACTION-RATE FROM ADVECTIVE-DIFFUSIVE CARBONATION OF MAFIC SILL MARGINS IN THE DALRADIAN, SOUTHWEST SCOTTISH HIGHLANDS, Earth and planetary science letters, 146(3-4), 1997, pp. 527-539
Citations number
30
Categorie Soggetti
Geochemitry & Geophysics
ISSN journal
0012821X
Volume
146
Issue
3-4
Year of publication
1997
Pages
527 - 539
Database
ISI
SICI code
0012-821X(1997)146:3-4<527:FARFAC>2.0.ZU;2-V
Abstract
Greenschist facies mafic sills in the Dalradian of the southwest Highl ands, Scotland, have been carbonated by infiltration of a CO2-bearing hydrous fluid from adjacent calc-phyllites. The primary amphibole-epid ote bearing assemblage is preserved in the cores of many sills in whic h the margins were altered to calcite, chlorite and quartz. The asymme tric widths of the carbonated margins allow determination of flow dire ction and magnitude, and indicate that sill margins were buffered to n early constant fluid composition by copious flow in the more permeable phyllites. Partially carbonated amphibole-epi dote assemblages within the reaction fronts preserve evidence for sluggish reaction kinetics. Downstream margins developed by diffusion against the flow direction and this allows calculation of reaction front broadening due to both d iffusion and reaction kinetics. An advective-diffusive transport model with linear reaction kinetics has been fitted to the reaction progres s profile for a sill at Port Gill Maluaig, Knapdale, This implies a cr oss-layer time-integrated fluid flux of 62.1 +/- 1.3 m(3)/m(2), a Damk ohler Number of 22.4 +/- 4.2 and a Peclet Number of 66.2 +/- 20.3 (1 s igma errors). The Peclet Number and time-integrated fluid flux imply t hat the flow event lasted between 0.02 and 20 Ma for plausible porosit ies in the range 10(-3) to 10(-6). The inferred rate constant for the reaction kinetics is two or more orders of magnitude slower than that calculated by extrapolation of experimentally determined surface react ion rates. Either the kinetic dispersion arose from factors additional to reaction kinetics or fluid-solid reaction was controlled by a slow er mechanism such as diffusion away from flow channels. The latter con clusion implicates deformation as an important control on the rates of fluid infiltration and fluid-rock reaction.