ISSN:
1572-9729
Keywords:
estuarine
;
oligohaline
;
sediment
;
sulfate reduction
;
sulfur
;
sulfide oxidation
Source:
Springer Online Journal Archives 1860-2000
Topics:
Biology
,
Energy, Environment Protection, Nuclear Power Engineering
,
Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
Notes:
Abstract Inorganic sulfur turnover was examined in oligohaline (salinity 〈 2 g kg-1) Chesapeake Bay sediments during the summer. Cores incubated for 〈 3 hr exhibited higher sulfate reduction (SR) rates (13–58 mmol m-2 d-1) than those incubated for 3–8 hr (3–8 mmol m-2 d-1). SR rates (determined with35SO 4 2- ) increased with depth over the top few cm to a maximum at 5 cm, just beneath the boundary between brown and black sediment. SR rates decreased below 5 cm, probably due to sulfate limitation (sulfate 〈 25 μM). Kinetic experiments yielded an apparent half-saturating sulfate concentration (Ks) of 34 μM, ≈ 20-fold lower than that determined for sediments from the mesohaline region of the estuary. Sulfate loss from water overlying intact cores, predicted on the basis of measured SR rates, was not observed over a 28-hr incubation period. Reduction of35SO 4 2- during diffusion experiments with intact core segments from 0–4 and 5–9 cm horizons was less than predicted by non-steady state diagenetic models based on35SO 4 2- reduction in whole core injection experiments. The results indicate that net sulfate flux into sediments was an order of magnitude lower than the gross sulfur turnover rate. Solid phase reduced inorganic sulfur concentrations were only 2–3 times less than those in sediments from the mesohaline region of the Bay, despite the fact that oligohaline bottom water sulfate concentrations were 10-fold lower. Our results demonstrate the potential for rapid SR in low salinity estuarine sediments, which are inhabited by sulfate-reducing bacteria with a high affinity for sulfate, and in which sulfide oxidation processes replenish the pore water sulfate pool on a time scale of hours.
Type of Medium:
Electronic Resource
URL:
http://dx.doi.org/10.1007/BF00002706
