Grzegorz P. Lis

Potential methane reservoirs beneath Antarctica

Once thought to be devoid of life, the ice-covered parts of Antarctica are now known to be a reservoir of metabolically active microbial cells and organic carbon. The potential for methanogenic archaea to support the degradation of organic carbon to methane beneath the ice, however, has not yet been evaluated. Large sedimentary basins containing marine sequences up to 14 kilometres thick and an estimated 21,000 petagrams (1 Pg equals 1015 g) of organic carbon are buried beneath the Antarctic Ice Sheet. No data exist for rates of methanogenesis in sub-Antarctic marine sediments. Here we present experimental data from other subglacial environments that demonstrate the potential for overridden organic matter beneath glacial systems to produce methane. We also numerically simulate the accumulation of methane in Antarctic sedimentary basins using an established one-dimensional hydrate model and show that pressure/temperature conditions favour methane hydrate formation down to sediment depths of about 300 metres in West Antarctica and 700 metres in East Antarctica. Our results demonstrate the potential for methane hydrate accumulation in Antarctic sedimentary basins, where the total inventory depends on rates of organic carbon degradation and conditions at the ice-sheet bed. We calculate that the sub-Antarctic hydrate inventory could be of the same order of magnitude as that of recent estimates made for Arctic permafrost. Our findings suggest that the Antarctic Ice Sheet may be a neglected but important component of the global methane budget, with the potential to act as a positive feedback on climate warming during ice-sheet wastage.

Organic matter content and quality in supraglacial debris across the ablation zone of the Greenland ice sheet

Abstract Quantifying the biogeochemical cycling of carbon in glacial ecosystems is of great significance for regional, and potentially global, carbon flow estimations. The concentration and quality of organic carbon (OC) is an important indicator of biogeochemical and physical processes that prevail in an ice-sheet ecosystem. Here we determine the content and quality of OC in debris from the surface of the Greenland ice sheet (GrIS) using microscopic, chromatographic, spectrophotometric and high-temperature combustion techniques. The total OC content in the debris increased with distance from the edge of the ice sheet, from virtually zero to >6% dry weight at 50 km inland, and there was a peak in the carbohydrate proportion and the microbial abundance at ∼6km inland. The highest (galactose + mannose)/(arabinose + xylose) ratios, indicating maximum autochthonous microbial production, were found at >10km inland. We propose that three key processes influence the carbon cycling on the GrIS: aeolian input of microbial inoculum and nutrients, in situ biological C transformation and the wash-away of supraglacial debris by meltwaters. We show that all these processes have significant spatial variability. While the total OC content of the debris on the ice sheet is probably controlled by the physical processes of wind transport and wash-away by meltwater, the microbial abundance and the quantity of the labile cell-contained OC within the debris is likely to be driven by the balance between the wash-away and the microbial productivity.

Characterization of dissolved organic matter (DOM) from glacial environments using total fluorescence spectroscopy and parallel factor analysis.

Abstract Aquatic dissolved organic matter (DOM) is a major reservoir of reduced organic carbon and has a significant influence on heterotrophic biological productivity and water quality in marine and freshwater environments. Although the forms and transformations of DOM in temperate aquatic and soil environments have been studied extensively, this is not the case for glacial environments. In this study, fluorescent excitation–emission matrices (EEMs), parallel factor analysis (PARAFAC) and cluster analysis were used to characterize the fluorescing components of DOM in ice and water samples from supraglacial, englacial, subglacial and proglacial environments of seven glaciers in the Canadian Arctic, Norway and Antarctica. At least five significant fluorescent DOM fractions were identified, which accounted for 98.2% of the variance in the dataset. These included four protein-like components and one humic-like component. The predominantly proteinaceous character of DOM from these glaciers is very different from the more humic character of DOM described previously from lacustrine, fluvial, estuarine and marine environments. DOM from the sampled glaciers is broadly similar in character despite their geographically distinct locations, different thermal regimes and inter- and intra-site differences in potential organic matter sources. Glacier ice samples had a relatively low ratio of humic-like :protein-like fluorescence while meltwater samples had a higher ratio.