B. Hales et S. Emerson, CALCITE DISSOLUTION IN SEDIMENTS OF THE CEARA RISE - IN-SITU MEASUREMENTS OF POREWATER O-2, PH, AND CO2(AQ), Geochimica et cosmochimica acta, 61(3), 1997, pp. 501-514
In situ electrode measurements of porewater oxygen and pH from four si
tes on the Ceara Rise in the western Tropical Atlantic unequivocally d
emonstrate that calcite dissolution driven by metabolic CO2 produced w
ithin the sediments is a significant part of the diagenesis of sedimen
tary calcite, dissolving at least 20% of the calcite rain to the seafl
oor. The first ever in situ absorbance-based measurements of porewater
CO2(aq) support the dissolution estimates based on models of the obse
rved pH distributions and are incompatible with scenarios excluding me
tabolic CO2-driven dissolution. Our dissolution estimates are consiste
nt with those estimated by an independent study of porewater calcium a
nd alkalinity profiles (Martin and Sayles, 1996) at this location. The
consistency of these disparate porewater measurements and our ability
to interpret them with simple models of respiration and dissolution i
mplies that no special mechanism is required to describe this process.
The calcite dissolution rate constant in the sediments of the deepest
station in this study is significantly higher than determined by in s
itu studies at other locations; values approach those determined by ea
rly laboratory measurements. The dissolution rate constant here must b
e at least two orders of magnitude higher than for calcite in sediment
s on the Ontong-Java Plateau, based on in situ electrode-measurements
there (Hales and Emerson, 1996). The calcite solubility consistent wit
h these data is not compatible with that consistent with the Ontong-Ja
va data. The reason for this difference is currently unresolved, but m
ay be due to the high order of the empirical dissolution rate law assu
med in this study. Copyright (C) 1997 Elsevier Science Ltd.