Potential Activity of Subglacial Microbiota Transported to Anoxic River Delta Sediments
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- Cameron, K.A., Stibal, M., Olsen, N.S. et al. Microb Ecol (2017). doi:10.1007/s00248-016-0926-2
The Watson River drains a portion of the SW Greenland ice sheet, transporting microbial communities from subglacial environments to a delta at the head of Søndre Strømfjord. This study investigates the potential activity and community shifts of glacial microbiota deposited and buried under layers of sediments within the river delta. A long-term (12-month) incubation experiment was established using Watson River delta sediment under anaerobic conditions, with and without CO2/H2 enrichment. Within CO2/H2-amended incubations, sulphate depletion and a shift in the microbial community to a 52% predominance of Desulfosporosinus meridiei by day 371 provides evidence for sulphate reduction. We found evidence of methanogenesis in CO2/H2-amended incubations within the first 5 months, with production rates of ~4 pmol g−1 d−1, which was likely performed by methanogenic Methanomicrobiales- and Methanosarcinales-related organisms. Later, a reduction in methane was observed to be paired with the depletion of sulphate, and we hypothesise that sulphate reduction out competed hydrogenotrophic methanogenesis. The structure and diversity of the original CO2/H2-amended incubation communities changed dramatically with a major shift in predominant community members and a decline in diversity and cell abundance. These results highlight the need for further investigations into the fate of subglacial microbiota within downstream environments.
KeywordsSubglacial environment River delta Sulphate reduction Methanogenesis Meltwater export Methane oxidation
Greenland has been estimated to contribute towards ~7% of the world’s suspended sediment flux . At Leverett Glacier, in the southwest of the Greenland Ice Sheet (GrIS), approximately 1011 microbial cells per cubic meter of meltwater are exported alongside these sediments . These cells and sediments are mostly sourced from the subglacial environment [1, 2], and the Watson River channels them to the downstream fjord with minimal changes to their community composition . Under the assumption that cells are deposited alongside glacial sediments in the river delta at the fjord head, which likely amass at rates of 9–16 mm yr−1 , and assuming that once buried under subsequent depositions the environment becomes waterlogged and anoxic, this study sought to consider the potential activity of transported subglacial communities, especially methanogens, whose potential activity and greenhouse gas production has been reported previously [3, 4, 5, 6, 7, 8]. We hypothesised that subglacial methanogens resume their activity after deposition within anoxic sediments.
To test our hypothesis, we established long-term (12-month) anaerobic incubations using sediment core material sampled from the Watson River delta at the head of Søndre Strømfjord, where the meltwaters of four southwest GrIS outlet glaciers drain (Leverett, Russell, Ørkendalen and Isorlersuup glaciers). Incubations were set up at 2 °C in the dark, with and without CO2/H2 enrichment. We measured changes in methane and sulphate concentrations and assessed the temporal variability of bacterial and archaeal abundance and community structure in order to gain insight into anaerobic microbial activity. Details of the sample site, experimental set-up, gas and water sample analyses, qPCR set-up, sequencing protocol and sequence analysis are provided within Online Resource 1.
Bacterial and archaeal cell abundance decreased threefold during the CO2/H2-amended incubations from 2.61 × 105 ± 0.96 × 105 cells per gram at day 0 to 7.67 × 104 ± 1.20 × 104 cells per gram at day 371. Catchall-calculated alpha diversity of 16S rRNA gene amplicons was notably and significantly reduced during the CO2/H2-amended experiment, from 1307 ± 65 at the start of the experiment to 268 ± 77 at the end (LRR2 = 0.78; p < 0.01). No significant change in diversity was observed within the control incubations (LRR2 = 0.27; p = 0.09). The CO2/H2-amended communities were found to be highly dissimilar to the control incubation communities when a two-way analysis of similarity (ANOSIM) was performed, accounting for differences in sampling time (R = 0.83; p < 0.01). Due to the reduction in cell abundance and diversity, and their ANOSIM-calculated uniqueness, we focus on the CO2/H2-amended communities herein.
The relative abundance of methane cycling organisms sequenced was low (0.10 ± 0.17%; Online Resource 2), contrary to previous studies of subglacial discharge samples [2, 5]. Methanogen-related amplicons that were closely related to Methanomicrobiales (two OTU) and Methanosarcinales (five OTU), including three OTU that were most closely related to anaerobic methanotrophic archaea (ANME) organisms, known also to be involved in sulphate-driven anaerobic oxidation of methane (AOM) , were identified in the day 0 and day 60 communities, which were consistent with previous studies of subglacial environments [5, 7, 11, 12] (Online Resource 2). Aerobic methylotrophs belonging to Methylobacteriaceae (four OTU) and Methylocystaceae (one OTU) were additionally identified (Online Resource 2). No methane cycling-related amplicons were detected within the final day 371 incubation.
The results of our methane cycling analysis are inconclusive; however, they inspire several hypotheses that warrant further investigation. First, we suggest that viable sulphate reducers and hydrogenotrophic methanogens are exported to the river delta from subglacial environments. Under the CO2/H2-amended experimental conditions, sulphate reducers thrive, while the concurrent loss of diversity and cell abundance suggests that a sizable portion of the original community is rendered unviable. Second, methane production is likely substrate limited, as it was only notably detected in incubations where hydrogenotrophic methanogenesis substrates were added. Based on the concurrent decrease in methane and sulphate concentrations, and the increasing relative abundance of D. meridiei, a sulphate-reducing bacterium, we propose that methanogens are out competed by sulphate-reducing bacteria, possibly as a result of the latter having a higher affinity to hydrogen . Third, AOM by ANME species, which were identified within the incubations, although not on day 252, coupled with sulphate-reducing bacteria  such as Desulfobulbaceae and Desulfobacteraceae , may explain the methane sink that was observed between days 147 and 252, and this process may similarly occur in subglacial environments. Decreased partial pressures of hydrogen and elevated partial pressures of methane during the first months of incubation may have stimulated reverse methanogenesis, which likely mediates AOM . We hypothesise that once sulphate is depleted, net methanogenesis may resume. Freshwater flux from the GrIS is predicted to increase over the coming decades , which will likely increase biomass transport from the subglacial environment . This study finds that subglacial microbiota are a dynamic community that have the potential to contribute to the biogeochemical cycling of delta ecosystems, and we therefore suggest that any ecological significance will increase as climate warming continues.
This research was funded by Danish Research Council grants FNU 10-085274 to CSJ and CENPERM DNRF100. It has additionally been supported by a Czech Science Foundation grant GACR 15-17346Y to MS. We thank Pernille Stockmarr and Michael Petersen for the technical assistance.
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Conflict of Interest
The authors declare that they have no conflict of interest.
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