B21C-0460
Nitrogen cycling within an alluvial aquifer during groundwater fluctuations

Tuesday, 15 December 2015
Poster Hall (Moscone South)
Nicholas Bouskill1, Mark E Conrad1, Markus Bill1, Eoin Brodie1, Matthew Sean Forbes2, Karen L Casciotti3 and Kenneth Hurst Williams1, (1)Lawrence Berkeley National Laboratory, Berkeley, CA, United States, (2)Stanford Earth Sciences, Stanford, CA, United States, (3)Stanford University, Earth System Science, Stanford, CA, United States
Abstract:
Subsurface terrestrial-aquatic interfaces are hotspots of biogeochemical cycling of terrestrially derived organic matter and nutrients. However, pathways of nitrogen (N) loss within subsurface aquifers are poorly understood. Here we take an experimental and mechanistic modeling approach to gauge the contribution of different microbial functional groups to the transformation and loss of N in an unconfined aquifer at Rifle, Colorado. During 2014 we measured nitrate (NO3), ammonia, gaseous nitrous oxide (N2O) and the corresponding isotopic composition of NO3 and N2O. Coincident with an annual Spring/ Summer excursion in groundwater elevation, we observed a rapid decline in NO3 concentrations at three discrete depths (2, 2.5 and 3 m) within the aquifer. Isotopic measurements (i.e., δ18O and δ15N) of NO3 suggest an immediate onset of biological N loss at 2 m, but not at 3 m where the isotopic composition demonstrated dilution of NO3 concentration prior to the onset of biological N loss. This implies that the groundwater becomes increasingly anoxic as it rises within the capillary fringe. We observed the highest rates of N2O production concomitant with the largest enrichment of the δ18ONO3 and δ15NNO3 isotopes. A mechanistic microbial model representing the diverse physiology of nitrifiers, aerobic and anaerobic (denitrifying) heterotrophs and anammox bacteria indicates that the bulk of N2O production and N loss is attributable to denitrifying heterotrophs. However, this relationship is dependent on the coupling between aerobic and anaerobic microbial guilds at the oxic-anoxic interface. Modeling results suggest anammox plays a more prominent role in N loss under conditions where the organic matter input is low and rapidly drawn down by aerobic heterotrophs prior to the rise of the water table. We discuss our modeling results in light of recent molecular microbiology work at this site, but also with respect to implications for N loss across terrestrial-aquatic interfaces.