HR: 1330h
AN: B12C-0805 [PDF]
TI: Investigations of Fe and Mn Bioreduction in Unconsolidated Clastic Sediments
AU: * McKinley, J P
EM: james.mckinley@pnl.gov
AF: Pacific Northwest National Laboratory, PO Box 999, Richland, WA 99352
AU: Zachara, J M
EM: john.zachara@pnl.gov
AF: Pacific Northwest National Laboratory, PO Box 999, Richland, WA 99352
AU: Fredrickson, J K
EM: jim.fredrickson@pnl.gov
AF: Pacific Northwest National Laboratory, PO Box 999, Richland, WA 99352
AU: Heald, S M
EM: steve.heald@pnl.ov
AF: Pacific Northwest National Laboratory, PO Box 999, Richland, WA 99352
AB:
We studied the microbial reduction of Mn and Fe in sediments from Oak Ridge, TN, and the Hanford Site, WA. Bioreduction was
by incubation of 1 g sediment in 10 ml of 30 mM pH 7 bicarbonate buffer with 7-9 x 107 cells/ml {it S. putrefaciens} CN32 and
10 mM sodium lactate as electron donor. Solution chemistry was monitored during incubation and sediments were pasteurized
before characterization. For the unconsolidated clay-rich saprolite from Oak Ridge, Fe reduction occurred after Mn reduction
was essentially complete. In sediments from the Pliocene Ringold Fm. (Hanford), incubated under the same conditions, Fe
reduction was inhibited, and Mn(III/IV) was incompletely reduced. When Ringold sediments were incubated under conditions
with greater available electron donor, more Fe was reduced after reduction of almost all of the available Mn(IV).
Transmission and scanning electron microscopy and X-ray microprobe and XANES analysis of Ringold sediments were used to
determine the spatial and temporal distribution of Mn. Initially, Mn(III/IV) was present as fragments of phyllomanganate
minerals and as interlammelar precipitates with Fe oxides in micas and on silicate clast surfaces. The precipitates were
botryoidal and chemically heterogeneous at the sub-micron scale. Precipitates within micas had expanded and deformed the
sheet structure of each flake. With the lesser available donor, Mn reduction essentially ceased after 43 days of incubation,
and the bulk Mn XANES spectrum indicated residual Mn(III/IV). X-ray microprobe mapping indicated all of the remaining Mn
was associated with interlamellar and grain-surface iron oxides, and microXANES showed that the Mn valence within a single
mica clast was heterogeneously distributed, and varied from Mn(III/IV) to Mn(II). At longer incubation times, the Mn nearer
to the clast exterior tended to be more uniformly reduced than Mn in the interior. The Mn in clast interiors was apparently
not readily bioavailable, but could act to buffer the sediment's redox capacity and re-oxidize Fe(II) produced during
incubation. Re-oxidation was confirmed by dilute-acid extraction of poorly crystalline Fe(III) oxides.
DE: 0400 Biogeosciences
SC: Biogeosciences [B]
MN: 2003 Fall Meeting