G. Blanc et al., NONSTEADY STATE DIFFUSION AND ADVECTION MODEL OF TRANSIENT CONCENTRATION-DEPTH PROFILES FROM THE BARBADOS ACCRETIONARY COMPLEX, Oceanologica acta, 16(4), 1993, pp. 363-372
We present a non-steady-state diffusion and advection model that descr
ibes the distribution of methane, manganese and silica concentrations
versus depth at sites 671, 676, and 672 of ODP Leg 110 through an ocea
nic sedimentary pile undergoing horizontal shortening by means of thru
st-faults and folds. The model suggests that the distribution of these
chemical components above and below fluid flow conduits is controlled
by molecular diffusion. Upward fluid advection from the pathways to t
he surrounding sediments appears to be without significance for this e
nvironment (about 1.10(-11) m.s-1, i.e. almost-equal-to 0.3 mm.yr-1).
Estimates of the time necessary to produce the diffusion profiles indi
cate that average ages of the chemical anomalies increase from Site 67
2 to Site 671, i. e. from the oceanic domain towards the internal part
of the accretionary prism. Using a two-dimensional framework for the
model, fluid-flow velocities along the decollement and protodecollemen
t zones are estimated about 7.10(-9) m.s-1 (i.e. almost-equal-to 0.20
m.yr-1) and 1.10(-7) m.s-1 (i.e. almost-equal-to 3 m.yr-1), respective
ly. Comparisons between ion-activity products of rhodochrosite and amo
rphous silica, and their equilibrium constants suggest the dissolution
of biogenic silica and precipitation of rhodochrosite within the deco
llement zone, which is the major fluid conduit of the Barbados Accreti
onary Complex.