Darkening of parts of the Greenland ice sheet surface during the summer months leads to reduced albedo and increased melting. Here we show that heavily pigmented, actively photosynthesising microalgae and cyanobacteria are present on the bare ice. We demonstrate the widespread abundance of green algae in the Zygnematophyceae on the ice sheet surface in Southwest Greenland. Photophysiological measurements (variable chlorophyll fluorescence) indicate that the ice algae likely use screening mechanisms to downregulate photosynthesis when exposed to high intensities of visible and ultraviolet radiation, rather than non-photochemical quenching or cell movement. Using imaging microspectrophotometry, we demonstrate that intact cells and filaments absorb light with characteristic spectral profiles across ultraviolet and visible wavelengths, whereas inorganic dust particles typical for these areas display little absorption. Our results indicate that the phototrophic community growing directly on the bare ice, through their photophysiology, most likely have an important role in changing albedo, and subsequently may impact melt rates on the ice sheet.

The Greenland and Antarctic Ice Sheets cover ~\n10% of global land surface, but are rarely considered as active components of the global iron cycle. The ocean waters around both ice sheets harbour highly productive coastal ecosystems, many of which are iron limited. Measurements of iron concentrations in subglacial runoff from a large Greenland Ice Sheet catchment reveal the potential for globally significant export of labile iron fractions to the near-coastal euphotic zone. We estimate that the flux of bioavailable iron associated with glacial runoff is 0.40–2.54 Tg per year in Greenland and 0.06–0.17 Tg per year in Antarctica. Iron fluxes are dominated by a highly reactive and potentially bioavailable nanoparticulate suspended sediment fraction, similar to that identified in Antarctic icebergs. Estimates of labile iron fluxes in meltwater are comparable with aeolian dust fluxes to the oceans surrounding Greenland and Antarctica, and are similarly expected to increase in a warming climate with enhanced melting.

Peer reviewe

The contribution of ice sheets to the global biogeochemical cycle of phosphorus is largely unknown, due to the lack of field data. Here we present the first comprehensive study of phosphorus export from two Greenland Ice Sheet glaciers. Our results indicate that the ice sheet is a hot spot of phosphorus export in the Arctic. Soluble reactive phosphorus (SRP) concentrations, up to 0.35 μM, are similar to those observed in Arctic rivers. Yields of SRP are among the highest in the literature, with denudation rates of 17-27 kg P km À2 yr À1. Particulate phases, as with nonglaciated catchments, dominate phosphorus export (>97% of total phosphorus flux). The labile particulate fraction differs between the two glaciers studied, with significantly higher yields found at the larger glacier (57.3 versus 8.3 kg P km À2 yr À1). Total phosphorus yields are an order of magnitude higher than riverine values reported in the literature. We estimate that the ice sheet contributes~15% of total bioavailable phosphorus input to the Arctic oceans (~11 Gg yr À1) and dominates total phosphorus input (408 Gg yr À1 ), which is more than 3 times that estimated from Arctic rivers (126 Gg yr À1 ). We predict that these fluxes will rise with increasing ice sheet freshwater discharge in the future.

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 10(15) 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.

Microbes in supraglacial ecosystems have been proposed to be significant contributors to regional and possibly global carbon cycling, and quantifying the biogeochemical cycling of carbon in glacial ecosystems is of great significance for global carbon flow estimations. Here we present data on microbial abundance and productivity, collected along a transect across the ablation zone of the Greenland ice sheet (GrIS) in summer 2010. We analyse the relationships between the physical, chemical and biological variables using multivariate statistical analysis. Concentrations of debris-bound nutrients increased with distance from the ice sheet margin, as did both cell numbers and activity rates before reaching a peak (photosynthesis) or a plateau (respiration, abundance) between 10 and 20 km from the margin. The results of productivity measurements suggest an overall net autotrophy on the GrIS and support the proposed role of ice sheet ecosystems in carbon cycling as regional sinks of CO(2) and places of production of organic matter that can be a potential source of nutrients for downstream ecosystems. Principal component analysis based on chemical and biological data revealed three clusters of sites, corresponding to three 'glacier ecological zones', confirmed by a redundancy analysis (RDA) using physical data as predictors. RDA using data from the largest 'bare ice zone' showed that glacier surface slope, a proxy for melt water flow, accounted for most of the variation in the data. Variation in the chemical data was fully explainable by the determined physical variables. Abundance of phototrophic microbes and their proportion in the community were identified as significant controls of the carbon cycling-related microbial processes.

[1] Glacier surfaces contain a wide diversity of microorganisms and can host a range of microbial activities. However, microbial nutrient cycling on glaciers is poorly understood. This study is the first to document nitrogen fixation (nitrogenase activity) on glaciers and demonstrate its importance in supporting microbial growth. Rates of nitrogen fixation (nitrogenase activity) in cryoconite holes on three valley glaciers in Svalbard ranged from <2.0 to 99.9 mmol ethylene m −2 d −1 with rates inversely correlated to concentrations of available inorganic nitrogen. Annual inputs of nitrogen by nitrogen fixation on a glacier catchment scale are more than 2 orders of magnitude lower than the combined nitrogen inputs from snowmelt and rain. However, nitrogen fixation can be important for supporting microbial growth on the glaciers during the middle to late melt season after the snowline has retreated upslope.

There is very little information about the activity of microbial communities on the surface of glaciers, though there is an increasing body of evidence to show that they strongly influence the biogeochemistry of these habitats. We measured bacterial abundance and production in cryoconite holes on Arctic, Antarctic and Alpine glaciers in order to estimate the role of heterotrophic bacteria within the carbon budget of glacial ecosystems. Our results demonstrate an active bacterial community on the surface of glaciers with doubling times that vary from a few hours to hundreds of days depending on the glacier and position (water or sediments) within the cryoconite hole. However, bacterial production is only ∼2–3% of the published literature values of community respiration from similar habitats, indicating that other types of microbes (e.g. eukaryotic organisms) may also play a role in the C cycle of glaciers. We estimate that only up to 7% of the organic C in cryoconite sediments is utilized by the heterotrophic bacterial community annually, suggesting that the surface of glaciers can accumulate organic carbon, and that this C may be important for biogeochemical activity downstream to adjacent ecosystems.