Positron emission tomography to visualise in-situ microbial metabolism in natural sediments.

Positron Emission Tomography simultaneously monitored flow dynamics and in-situ microbial activity in opaque sediment columns. An 18F labelled electron donor, 2-deoxy-2-[18F]-fluoro-D-glucose (18FDG), was added to flowing columns containing sterile sediment, microbially active sediment and quartz sand. 18FDG accumulated in microbially active, glucose primed, sediment (105-106 cells g-1) at 10-16 mol g-1 (~40% of the 100 MBq spike) giving the first example of 18FDG uptake by indigenous microorganisms in a complex sediment system at flow rates representative of the shallow subsurface.

Quantifying Technetium and Strontium Bioremediation Potential in Flowing Sediment Columns.

The high-yield fission products 99Tc and 90Sr are found as problematic radioactive contaminants in groundwater at nuclear sites. Treatment options for radioactively contaminated land include bioreduction approaches, and this paper explores 99mTc and 90Sr behavior and stability under a range of biogeochemical conditions stimulated by electron donor addition methods. Dynamic column experiments with sediment from the Sellafield nuclear facility, completed at site relevant flow conditions, demonstrated that Fe(III)-reducing conditions had developed by 60 days. Sediment reactivity toward 99Tc was then probed using a 99mTc(VII) tracer at <10-10 mol L-1 and γ camera imaging showed full retention of 99mTc in acetate amended systems. Sediment columns were then exposed to selected treatments to examine the effects of different acetate amendment regimes and reoxidation scenarios over 55 days when they were again imaged with 99mTc. Here, partially oxidized sediments with no further electron donor additions remained reactive toward 99mTc under relevant groundwater O2 and NO3- concentrations over 55 days. Immobilization of 99mTc was highest where continuous acetate amendment had resulted in sulfate-reducing conditions. Interestingly, the sulfate reducing system showed enhanced Sr retention when stable Sr2+ was added continuously as a proxy for 90Sr. Overall, sediment reactivity was nondestructively imaged over an extended period to provide new information about dynamic iron and radionuclide biogeochemistry throughout realistic sediment redox cycling regimes.

Alkaline Fe(III) reduction by a novel alkali-tolerant Serratia sp. isolated from surface sediments close to Sellafield nuclear facility, UK.

Extensive denitrification resulted in a dramatic increase in pH (from 6.8 to 9.5) in nitrate-impacted, acetate-amended sediment microcosms containing sediment representative of the Sellafield nuclear facility, UK. Denitrification was followed by Fe(III) reduction, indicating the presence of alkali-tolerant, metal-reducing bacteria. A close relative (99% 16S rRNA gene sequence homology) to Serratia liquefaciens dominated progressive enrichment cultures containing Fe(III)-citrate as the sole electron acceptor at pH 9 and was isolated aerobically using solid media. The optimum growth conditions for this facultatively anaerobic Serratia species were investigated, and it was capable of metabolizing a wide range of electron acceptors including oxygen, nitrate, FeGel, Fe-NTA and Fe-citrate and electron donors including acetate, lactate, formate, ethanol, glucose, glycerol and yeast extract at an optimum pH of c. 6.5 at 20 °C. The alkali tolerance of this strain extends the pH range of highly adaptable Fe(III)-reducing Serratia species from mildly acidic pH values associated with acid mine drainage conditions to alkali conditions representative of subsurface sediments stimulated for extensive denitrification and metal reduction.