M. Holmer et al., BIOGEOCHEMICAL CYCLING OF SULFUR AND IRON IN SEDIMENTS OF A SOUTH-EAST ASIAN MANGROVE, PHUKET ISLAND, THAILAND, Biogeochemistry, 26(3), 1994, pp. 145-161
Benthic sulfate reduction and sediment pools of sulfur and iron were e
xamined during January 1992 at 3 stations in the Ao Nam Bor mangrove,
Phuket, Thailand. Patterns of sulfate reduction rates (0-53 cm) reflec
ted differences in physical and biological conditions at the 3 station
s, and highest rates were found at the vegetated site within the mangr
ove (Rhizophora apiculata) forest. Due to extended oxidation of mangro
ve sediments, a large portion of the added S-35-label was recovered in
the chromium reducible pools (FeS2 and S0) (41-91% of the reduced sul
fur). Pyrite was the most important inorganic sulfur component, attain
ing pool sizes 50-100 times higher than acid volatile pools (FeS). HCl
-extractable (0.5 M HCl) iron pools, including Fe(II)HCl and Fe(III)HC
l, were generally low and Fe(III)HCl was only present in the upper sur
face layers (0-5 cm). Maximum concentrations of dissolved Fe2+ 35-285
muM) occurred just about the depth where dissolved SIGMAH2S accumulate
d. Furthermore Fe2+ and SIGMAH2S coexisted only where concentrations o
f both were low. There was an accumulation of organic sulfur in the de
ep sediment at 2 stations in the inner part of the mangrove. The reoxi
dation of reduced sulfides was rapid, and storage of sulfur was minor
in the upper sediment layers, where factors like bioturbation, the pre
sence of roots, or tidal mixing enhance oxidation processes.