Zack, T. & John, T. (accepted): Chemical Geology.
An evaluation of reactive fluid flow and trace element mobility in
subducting slabs
Permeabilities in the subducting slab appear to be too low and
dihedral angles between fluid and relevant minerals too high to allow
for porous flow, hence fluid channelization is critical for the
understanding of subduction zone fluid fluxes. In this review we will
outline how fluid channelization controls reaction rates and element
redistributions during metamorphism of the subducting plate as well as
trace element compositions of subduction-related fluids during
flow.
Channelized fluid flow predicts that from a rock point of
view, most formerly subducted material will show only very limited
evidence for fluid flow, consistent with the rarity of observed high
fluid fluxes in subduction-related rocks. Aqueous fluid produced by
dehydration reactions will not percolate through large rock volumes,
but rather will be carried away from the dehydration sites by a
veining network. Indeed evidence for significant aqueous fluid fluxes
have been found in high-pressure veins with adjacent selvages.. In
such selvages, large lithophile elements (LILE's) generally show the
highest mobilities, followed by light (L) rare earth elements (REE)
and then heavy (H)REE. Compared to high field strength elements
(HFSE), even Th shows higher mobilities.
From a fluid point of
view, equilibrium between aqueous fluid and surrounding rock will only
be approached at sites of fluid production. However, this fluid can be
significantly modified while moving upwards through a veining network
where the wallrocks are out of equilibrium with the fluid. In a
subducting slab, such reactive fluid flow can preferentially dissolve
minerals and release their trace elements (e. g. Ba in phengite, Th
and La in monazite). The degree of change in aqueous-fluid composition
will depend on the amount of fluid-mineral surface interaction. The
chemical exchange reactions will not be possible to model by trace
element partition coefficients alone, instead future models need to
incorporate kinetic parameters such as surface reaction rates.