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Microbial iron oxyhydroxides are common deposits in natural waters, recent sediments and mine drainage systems and often contain significant accumulations of trace and rare earth elements (TREE). TREE patterns are widely used to characterize minerals and rocks, and to elucidate their evolution and origin. Whether and which characteristic TREE signatures distinguish between a biological and an abiological origin of iron minerals is still not well understood. Long-term flow reactor studies were performed in the Aspo Hard Rock Laboratory to investigate the development of microbial mats dominated by iron-oxidizing bacteria, namely Mariprofundus sp. and Gallionella sp. The experiments investigated the accumulation and fractionation of TREE under controlled conditions and enabled us to assess potential biosignatures evolving within the microbial iron oxyhydroxides. Concentrations of Be, Y, Zn, Zr, Hf, W, Th, Pb, and U in the microbial mats were 1e3- to 1e5-fold higher than in the feeder fluids whereas the rare earth elements and Y (REE+Y) contents were 1e4 and 1e6 fold enriched. Except for a hydrothermally induced Eu anomaly, the normalized REE+Y patterns of the microbial iron oxyhydroxides were very similar to published REE+Y distributions of Archaean Banded Iron Formations. The microbial iron oxyhydroxides from the flow reactors were compared to iron oxyhydroxides that were artificially precipitated from the same feeder fluid. These abiotic and inorganic iron oxyhydroxides show the same REE+Y distribution patterns. Our results indicate that the REE+Y mirror quite exactly the water chemistry, but they do not allow to distinguish microbially mediated from inorganic iron precipitates. All TREE studied showed an overall similar fractionation behavior in biogenic, abiotic and inorganic iron oxyhydroxides. Exceptions are Ni and Tl, which were only accumulated in the microbial iron oxyhydroxides and may point to a potential usage of these elements as microbial biosignatures.

Assessing the utility of trace and rare earth elements as biosignatures in microbial iron oxyhydroxides