Jennifer Pett-Ridge1, Pamela Templer2, Eric Dubinsky3, Whendee L. Silver3, and Mary K. Firestone3. (1) Lawrence Livermore National Lab, (2) Boston University, (3) University of California, Berkeley
Microbial inhabitants of wet tropical and temperate rainforest soils actively produce and consume atmospheric trace gases, yet little is known about in situ dynamics of trace gases and microbial populations in such systems. This is particularly true in soils where redox fluctuates rapidly, creating a mosaic of spatial and temporal gradients. Of particular interest are the mechanisms regulating soil fluxes of molecular hydrogen (H2), as there is significant uncertainty in the global atmospheric H2 budget. Using soils from a wet tropical forest, we assayed microbial community composition and soil O2 along with other redox-active chemical species (H2, N2O, CH4, CO2, CO) in both field and laboratory settings. Under controlled conditions, increasing the labile organic carbon pool by 5% increased the rate of O2 consumption tenfold, dramatically accelerated the timescale of redox depletion, and enhanced CO2, H2, and CH4 production. Under oxic conditions, we saw significant production of N2O. Immediately after O2 disappeared, a pulse of H2 production occurred, but was quickly consumed by methanogens. Under highly reduced conditions, we measured high concentrations of CH4, followed by anaerobic consumption. In situ field measurements of the same gases were highly variable, yet also showed sequential redox processing in both space and time. With daily sampling, we show that belowground O2 depletion and N2O, CH4, and H2 production are correlated with rainfall from the previous two days. These gases are also correlated with variations in microbial community composition that occur along a spatial redox gradient. Using universal 16S rRNA microarrays, we identified over 2000 distinct operational taxonomic groups (OTUs) in these soils and analyzed spatial patterns for several phylogenetic/functional groups. While diversity (richness) does not vary along our redox gradient, the DNA copy number (a proxy for abundance) of methanogenic archaea and clostridia is significantly higher in the low-redox end of our gradient.