An. Roychoudhury et al., A PLUG FLOW-THROUGH REACTOR FOR STUDYING BIOGEOCHEMICAL REACTIONS IN UNDISTURBED AQUATIC SEDIMENTS, Applied geochemistry, 13(2), 1998, pp. 269-280
A slow flow, plug-through reactor was developed for measuring equilibr
ium and kinetic parameters of biogeochemical reactions on intact secti
ons of sediment cores. The experimental approach was designed to prese
rve the structural, geochemical and microbiological integrity of the s
ediment sections and, hence, retrieve reaction parameters that apply t
o in-situ conditions. Inert tracer breakthrough experiments were perfo
rmed on a variety of unconsolidated surface sediments from lacustrine,
estuarine and marine depositional environments. The sediments studied
cover wide ranges of composition, porosity (46-83%) and mean grain si
ze (10(-4)-10(-2) cm). Longitudinal dispersion coefficients were deter
mined from the breakthrough curves of Br-. The curves were also used t
o check for early breakthrough or trailing, that is, features indicati
ve of non-ideal flow conditions. Sediment plugs that exhibited these f
eatures were eliminated from further experiments. Dimensionless equili
brium adsorption coefficients (K) of NH4+, were calculated from measur
ed retardation times between the breakthrough of NH4+ and Br-. The val
ues of K at 5 degrees C vary between 0.3 and 2.3, with the highest val
ue obtained in a fine-grained marine sediment, the lowest in a coarse-
grained lake sediment. The values for the marine and estuarine sedimen
ts agree with values reported in the literature. The dependencies of K
on ionic strength (range 0.2-0.7 m) and temperature (range 5-25 degre
es C) in an estuarine sediment confirm that the main sorption mechanis
m for NH4+ is ion exchange. The reactor was used in recirculation mode
to measure steady-state rates of dissimilatory SO42- reduction in a s
alt-marsh sediment. Recirculation homogenizes solute concentrations wi
thin the reactor, hence facilitating the derivation of reaction rate e
xpressions that depend on solution composition. The rate of microbial
SO(4)(2-)reduction was found to be nearly independent of the dissolved
SO42- concentration in the range of 2.2-1 mM. Fitting of the experime
ntal rates to a Monod relationship resulted in a maximum estimate of t
he half-saturation concentration, K-s, of 240 mu M. This value is comp
arable to those reported for a pure culture of SO42--reducing bacteria
, but is significantly smaller than the only other K-s value reported
in the literature for SO42- utilization in a natural marine sediment.
(C) 1998 Elsevier Science Ltd. All rights reserved.