Abstract
In the anoxic hypolimnion of Lake 227, Experimental Lakes Area, northwestern Ontario [Canada], .SIGMA.H2S exhibits a mid-depth maximum, while Fe2+ increases with depth. At the mid-depth .SIGMA.H2S maximum and below, saturation with respect to amorphous FeS is reached, and the concentration of .SIGMA.H2S is limited by the high Fe2+ concentrations, in accord with the FeS solubility product. Values for pKsp (= aFe2+ .cntdot. aHS-/aH+) for FeS determined from the .SIGMA.H2S maximum and below averaged 3.16 in 1979 and agree well with other in situ and laboratory measurements. In the top 10 cm of sediment, pore water .SIGMA.H2S and Fe2+ are in equilibrium with amorphous FeS. Analyses of cores confirms the existence of an iron sulfide phase. Fe2+, which is produced in the pore water from the decomposition of organic matter, increases to concentrations at which siderite may form, although the presence of siderite has not been verified. Comparison of calculated pore water fluxes of Fe2+ with the observed increase of Fe2+ in the anoxic hypolimnion reveals that about 90% of the observed flux originates at the sediment-water interface, while the remainder is derived from pore water flux.

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