Ice sheets are currently ignored in global methane budgets1,2. Although ice sheets have been proposed to contain large reserves of methane that may contribute to a rise in atmospheric methane concentration if released during periods of rapid ice retreat3,4, no data exist on the current methane footprint of ice sheets. Here we find that subglacially produced methane is rapidly driven to the ice margin by the efficient drainage system of a subglacial catchment of the Greenland ice sheet. We report the continuous export of methane-supersaturated waters (CH4(aq)) from the ice-sheet bed during the melt season. Pulses of high CH4(aq) concentration coincide with supraglacially forced subglacial flushing events, confirming a subglacial source and highlighting the influence of melt on methane export. Sustained methane fluxes over the melt season are indicative of subglacial methane reserves that exceed methane export, with an estimated 6.3 tonnes (discharge-weighted mean; range from 2.4 to 11 tonnes) of CH4(aq) transported laterally from the ice-sheet bed. Stable-isotope analyses reveal a microbial origin for methane, probably from a mixture of inorganic and ancient organic carbon buried beneath the ice. We show that subglacial hydrology is crucial for controlling methane fluxes from the ice sheet, with efficient drainage limiting the extent of methane oxidation5 to about 17 per cent of methane exported. Atmospheric evasion is the main methane sink once runoff reaches the ice margin, with estimated diffusive fluxes (4.4 to 28 millimoles of CH4 per square metre per day) rivalling that of major world rivers6. Overall, our results indicate that ice sheets overlie extensive, biologically active methanogenic wetlands and that high rates of methane export to the atmosphere can occur via efficient subglacial drainage pathways. Our findings suggest that such environments have been previously underappreciated and should be considered in Earth’s methane budget.

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Data availability

The data used in this article are available from the corresponding author on request. The 16S rRNA gene sequence data are available from the NCBI Sequence Read Archive (https://www.ncbi.nlm.nih.gov/sra) under BioProject PRJNA495593 (BioSamples SAMN10228172-SAMN10228185; SAMN10228190- SAMN10228206).

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We thank all of those who assisted with fieldwork at LG, especially J. Hatton, as well as F. Sgouridis and J. Williams at the LOWTEX laboratory of the University of Bristol. This research is part of the UK NERC-funded DELVE programme (NERC grant NE/I008845/1 to J.L.W.). G.L.-G. was funded by the University of Bristol Scholarship Programme and a FRQNT Scholarship (number 185136). The work was also supported by a Leverhulme research fellowship to J.L.W., a UK NERC grant (NE/J02399X/1) to A.M.A. for DNA analyses, as well as Czech Science Foundation grants (GACR; 15-17346Y and 18-12630S) to M.S. Isotopic analyses were conducted by G. Lacrampe-Couloume at the University of Toronto with support provided by the Natural Sciences and Engineering Research Council of Canada (NSERC) to B.S.L. We also thank the Kangerlussuaq International Science Station, especially R. Møller, for support with field logistics, as well as M. A. Cooper, M. Macdonald and S. Hoffer for comments.

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Nature thanks J. Crawford and the other anonymous reviewer(s) for their contribution to the peer review of this work.

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  1. School of Geographical Sciences, University of Bristol, Bristol, UK

    • Guillaume Lamarche-Gagnon
    • , Jemma L. Wadham
    • , Andrew J. Tedstone
    •  & Jon R. Hawkings
  2. Department of Earth Sciences, University of Toronto, Toronto, Ontario, Canada

    • Barbara Sherwood Lollar
  3. Department of Geoscience, Environment and Society, Université Libre de Bruxelles, Brussels, Belgium

    • Sandra Arndt
  4. Kongsberg Maritime Contros GmbH, Kiel, Germany

    • Peer Fietzek
  5. National Oceanography Centre, Southampton, UK

    • Alexander D. Beaton
    •  & Matthew C. Mowlem
  6. School of Natural and Environmental Sciences, Newcastle University, Newcastle, UK

    • Jon Telling
  7. School of Earth and Ocean Sciences, Cardiff University, Cardiff, UK

    • Elizabeth A. Bagshaw
  8. National High Magnetic Field Lab and Earth, Ocean and Atmospheric Sciences, Florida State University, Tallahassee, FL, USA

    • Jon R. Hawkings
  9. German Research Centre for Geosciences GFZ, Potsdam, Germany

    • Jon R. Hawkings
  10. Department of Ecology, Faculty of Science, Charles University, Prague, Czechia

    • Tyler J. Kohler
    • , Jakub D. Zarsky
    •  & Marek Stibal
  11. Department of Environmental Sciences, Aarhus University, Roskilde, Denmark

    • Alexandre M. Anesio


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J.L.W. and G.L.-G. designed the study. B.S.L. supervised the stable-isotope analyses. S.A. performed the reaction-transport hydrate model calculations. P.F. assisted in the interpretation and analysis of the CONTROS HydroC CH4 raw results. G.L.-G., J.T., E.A.B., A.D.B., M.C.M. and J.R.H. conducted field logistical preparations. J.L.W., J.T. and M.S. led the 2015 Greenland field campaign. G.L.-G., A.D.B., A.J.T., J.T., E.A.B., J.R.H., T.J.K., J.D.Z. and M.S. collected the sensor field data. G.L.-G. and J.D.Z. collected manual water samples in the field. G.L.-G. and A.M.A. analysed molecular data. G.L.-G. performed the data analysis and wrote the manuscript with significant contribution from all co-authors.

Competing interests

P.F. works for the sensor manufacturer Kongsberg Maritime Contros, but the sensor data discussed here were validated by independent measurements. The other authors declare no competing interests.

Corresponding author

Correspondence to Guillaume Lamarche-Gagnon.

Extended data figures and tables

  1. Extended Data Fig. 1 Leverett Glacier and proglacial stream.

    a, Leverett Glacier (LG), with catchment boundaries38 outlined in grey; ‘SFJ’ denotes the Kangerlussuaq airport. b, Zoomed image of the LG, with the sampling site and portal marked by dots. c, Sensor deployment site during the early melt season, with the LG visible in the background; the image faces upstream. d, Sensor deployment site in late June; the image faces downstream. Also visible is the HydroC sensor inside a steel cage, during inspection and before redeployment. e, LG portal in late May, while still covered with both glacial and river ice. The photograph was taken one hour before the appearance of the glacial upwelling (see Supplementary Information 2b). The arrow marks the location of the chainsawed hole, shown in the inset (photograph taken on 10 May 2015). f, LG portal in mid-July 2015. Map images from USGS/NASA Landsat.

  2. Extended Data Fig. 2 Comparison of CH4(aq) concentrations measured with the HydroC sensor and from manual samples.

    a, CH4(aq) time series. Red points correspond to the HydroC pump power during operation. The continuous line depicts HydroC measurements, with the dashed section corresponding to times when the sensor experienced low pump power and thus a reduced water flow induced by the pump (19 June to 1 July). Open circles correspond to manual samples. The thin grey-shaded area around the CH4(aq) time series corresponds to the uncertainty of the HydroC measurements (about 3%). The uncertainty on manual measurements, indicated by the error bars, reflects the error on vial internal pressures and volumes (119 ± 0.76 ml, where the uncertainty represents standard deviation; internal pressures are derived from volumes—see Methods for details). b, Regression plot between the HydroC and manual sample measurements. Only manual samples taken during times when the HydroC pump power was above about 7 W were considered for the regression (black circles, black line); grey circles correspond to samples taken during times of lower pump power. Horizontal error bars reflect errors on manual measurements; vertical error bars are smaller than the size of the markers. The orange dashed line depicts a hypothetical 1:1 relationship between the sensor and manual measurements. Source data

  3. Extended Data Fig. 3 Combination plot of δ13C-CO2 and δ13C-CH4 of LG runoff.

    Points denote δ13C CO2-CH4 values for LG manual samples. Methanogenesis and microbial oxidation classification zones are derived and adapted from ref. 25. Source data

  4. Extended Data Fig. 4 LG 16S rRNA gene sequences related to methanotrophic and methanogenic clades.

    a, Relative abundance of the dominant operational taxonomical units related to bacterial methanotrophs (OTU00009) and archaeal methanogens. The box mid-lines represent medians; the IQR is represented by the lower and upper box boundaries and denote the 25th and 75th percentiles, respectively; whiskers indicate confidence intervals of 1.5 times the IQR, and points are outliers. b, c, Maximum-likelihood trees of 16S rRNA sequences related to methanotrophs rooted with the sequences of Clostridium frigoriphilum (b) and methanogens rooted with the sequences of Acidibilus sulfurireducens and Caldisphaera draconis (c).

  5. Extended Data Fig. 5 Relationship between rates of subglacial methanogenesis, sediment thickness and observed annual CH4 flux at LG.

    Each panel corresponds to the different yearly lateral CH4(aq) flux estimates measured in 2015 (see Fig. 2). Each line type corresponds to the sediment thickness required under different catchment area conditions: 100% (solid line), 50% (long-dashed line) or 10% (short-dashed line) of the subglacial catchment to contribute to the observed CH4 flux. Any point on a line corresponds to the methanogenesis rate and subglacial sediment thickness required to generate the observed lateral CH4 flux. The four points on each line correspond to known methanogenic rates recorded from different subglacial habitats17. Source data

  6. Extended Data Fig. 6 Summary of model conditions required for subglacial methane hydrate formation.

    ad, Model results for a fixed methanogenic depth (100 m) but varying methanogenic rates (R2 to R10; that is, 2 × 10−15 to 10 × 10−15 grams CH4 per gram of sediment per second). eh, Outputs of model runs under a fixed methanogenic rate (5 × 10−15 grams CH4 per gram of sediment per second) but varying methanogenic depths (20–100 m). a, b, e, f, Vertical profiles of methane solubility, dissolved methane and methane hydrates; methane concentrations are normalized to equilibrium concentration. c, g, Time required for methane hydrate formation under the modelled conditions. d, h, Diffusive CH4 flux at the sediment–ice interface under methane hydrate conditions assuming three different catchment cover areas for methane hydrates (that is, 10%, 50% and 100% of the LG catchment), compared to the three lateral flux scenarios (a, b, d; Fig. 2); see Supplementary Information 2f.

  7. Extended Data Fig. 7 Extended time series of geochemical measurements from the LG proglacial river.

    ad, The EC, pH and SSC time series include those depicted in Fig. 1 but extend to measurements before and after the methane record. It should be noted that the CH4(aq) data in c are the HydroC partial pressure (in microatmospheres) measurements. Left and right vertical axes correspond to black and orange datasets, respectively. Source data

  8. Extended Data Table 1 CH4(aq) concentration, fluxes and areal yield from LG, the GrIS and other world rivers
  9. Extended Data Table 2 Stable-isotope details for CH4 and CO2
  10. Extended Data Table 3 Site-specific parameters applied in the one-dimensional hydrate model

Supplementary information

  1. Supplementary Information

    This file contains Supplementary Methods, a Supplementary Discussion and Supplementary References.

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