Abstract
Organic biomarker distribution and stable isotope composition was used to investigate biogeochemical carbon cycling in the anoxic basin of Lake Untersee, Antarctica. Phospholipid fatty acid (PLFA) concentrations indicative of microbial abundances were low in the oxic water column overlying the basin but rose in the suboxic transition zone and further increased within the underlying anoxic water, with the highest abundances near the sediment water interface. Archaeol (up to 24.8 mg/kg) and glycerol dialkyl glycerol tetraethers were only detected within the deepest water sample and sediment. High methane (CH4) concentrations (ca. 172 mg/L or 11 mmol/L) were observed in the deepest water samples and produced via hydrogenotrophy (CO2-reduction) based on methane isotopes and highly 13C-enriched dissolved inorganic carbon. Methane concentration slowly decreased away from the sediment, across the anoxic water column and then decreased rapidly at the oxic/anoxic interface (78–68 m). Here a ca. 10‰ increase in δ13CCH4 values combined with δ13CPLFA values that decreased as CH4 concentrations rapidly declined indicated an aerobic methanotrophy fueled microbial community. Findings suggest that upward methane diffusion drives microbial productivity within the suboxic/anoxic zones resulting in the observed high PLFA biomass. Subsequent sinking of detrital material from these communities supports heterotrophic microbes throughout the anoxic water column and potentially supplied nutrients to support phototrophy in the upper suboxic transition zone, itself contributing to sinking detrital material and accumulation of sedimentary organic material. Notably, while a clear biosignature of methane oxidation is present in suboxic zone PLFA, this signature is not recognizable within the sediments.
Similar content being viewed by others
Data availability
All data generated or analysed during this study are included in this published article and its supplementary information files.
References
Alvarez HM, Steinbüchel A (2002) Triacylglycerols in prokaryotic microorganisms. Appl Microbiol Biotechnol 60:367–376
Abraham W-R, Hesse C, Pelz O (1998) Ratios of carbon isotopes in microbial lipids as an indicator of substrate usage. Appl Environ Microbiol 64:4202–4209
Andersen DT, McKay CP, Wharton RA Jr (1998) Dissolved gases in perennially ice-covered lakes of the McMurdo Dry Valleys, Antarctica. Antarct Sci 10:124–133
Andersen DT, Sumner DY, Hawes I, Webster-Brown J, McKay CP (2011) Discovery of large conical stromatolites in Lake Untersee, Antarctica. Geobiology 9:280–293
Bligh EG, Dyer WJ (1959) A rapid method of total lipid extraction and purification. Can J Biochem Physiol 37:911–917
Boschker HTS, Middelburg JJ (2002) Stable isotopes and biomarkers in microbial ecology. FEMS Microbiol Ecol 40:85–95
Bauersachs T, Speelman EN, Hopmans EC, Reichart G-J, Schouten S, Sinninghe Damsté JS (2010) Fossilized glycolipids reveal past oceanic N2 fixation by heterocystous cyanobacteria. Proc Natl Acad Sci 107:19190–19194
Bevington J, McKay CP, Davila A, Hawes I, Tanabe Y, Andersen DT (2018) The thermal structure of the anoxic trough in Lake Untersee, Antarctica. Antarct Sci. https://doi.org/10.1017/S095410201800035
Biddle JF, Lipp JS, Lever MA, Lloyd KG, Sørensen KB, Anderson R, Fredricks HF, Elvert M, Kelly TJ, Schrag DP, Sogin ML, Brenchley JE, Teske A, House CH, Hinrichs K-U (2006) Heterotrophic Archaea dominate sedimentary subsurface ecosystems off Peru. Proc Natl Acad Sci 103:3846–3851
Blair N, Leu A, Munoz E, Olsen J, Kwong E, Des Marais D (1985) Carbon isotopic fractionation in heterotrophic microbial metabolism. Appl Environ Microbiol 50:996–1001
Bodelier PLE, Bär Gillisen MJ, Hordijk K, Sinninghe Damsté JS, Rijpstra WIC, Geenevasen JAJ, Dunfield PF (2009) A reanalysis of phospholipid fatty acids ecological biomarkers for methanotrophic bacteria. ISME J 3:606–617
Boon JJ, de Leeuw JW, van de Hoek GJ, Vosjan JH (1977) Significance and taxonomic value of iso and anteiso monoenoic fatty acids and branded beta-hydroxy acids in Desulfovibrio desulfuricans. J Bacteriol 129:1183–1191
Boudière L, Michaud M, Petroutsos D, Rébeillé F, Falconet D, Bastien O, Roy S, Finazzi G, Rolland N, Jouhet J, Block MA, Maréchal E (2014) Glycerolipids in photosynthesis: composition, synthesis and trafficking. Biochim Biophys Acta 1837:470–480
Bowman JP, Skerrat JH, Nichols PD, Sly LI (1991) Phospholipid fatty acid and lipopolysaccharide fatty acid signature lipids in methane-utilizing bacteria. FEMS Microbiol Lett 85:15–21
Brady AL, Druschel G, Leoni L, Lim DSS, Slater GF (2013) Isotopic biosignatures in carbonate-rich, cyanobacteria-dominated microbial mats of the Cariboo Plateau, B.C. Geobiology 11:437–456
Brady AL, Laval B, Lim DSS, Slater GF (2014) Autotrophic and heterotrophic associated biosignatures in modern freshwater microbialites over seasonal and spatial gradients. Org Geochem 67:8–18
Brady AL, Goordial J, Sun HJ, Whyte LG, Slater GF (2018) Variability in carbon uptake and (re)cycling in Antarctic cryptoendolithic microbial ecosystems demonstrated through radiocarbon analysis of organic biomarkers. Geobiology 16:62–79
Conrad R (1999) Contribution of hydrogen to methane production and control of hydrogen concentrations in methanogenic soils and sediments. FEMS Microbiol Ecol 28:193–202
Cronan JE Jr, Gelmann EP (1979) Physical properties of membrane lipids: biological relevance and regulation. Bacteriol Rev 39:232–256
Collier J, Herbert S, Fork D, Grossman A (1994) Changes in the cyanobacterial photosynthetic apparatus during acclimation to macronutrient deprivation. Photosynth Res 42:173–183
Dias RF, Freeman KH (1997) Carbon isotope analyses of semivolatile organic compounds in aqueous media using solid-phase microextraction and isotope ration monitoring GC/MS. Anal Chem 69:944–950
Dijkman NA, Kromkamp JC (2006) Phospholipid-derived fatty acids as chemotaxic markers for phytoplankton: application for interring phytoplankton composition. Mar Ecol Prog Ser 324:113–125
Duan Z, Mao S (2006) A thermodynamic model for calculating methane solubility, density and gas phase composition of methane-bearing aqueous fluids from 273 to 523 K and from 1 to 2000 bar. Geochim Cosmochim Acta 70:3369–3386
Dijkman NA, Boschker HTS, Stal LJ, Kromkamp JC (2010) Composition and heterogeneity of the microbial community in a coastal microbial mat as revealed by the analysis of pigments and phospholipid-derived fatty acids. J Sea Res 63:62–70
Dowling NJE, Widdel F, White DC (1986) Phospholipid ester-linked fatty acid biomarkers of acetate-oxidizing sulfate-reducers and other sulfide-forming bacteria. J Gen Microbiol 132:1815–1825
Dubois N, Barthomeuf C, Bergé J-P (2006) Convenient preparation of picolinyl derivatives from fatty acid esters. Eur J Lipid Sci Technol 108:28–32
Elvert M, Boetius A, Knittel K, Jørgensen BB (2003) Characterization of specific membrane fatty acids as chemotaxonomic markers for sulfate-reducing bacteria involved in anaerobic oxidation of methane. Geomicrobiol J 20:403–419
Faucher B, Lacelle D, Fisher DA, Andersen DT, McKay CP (2019) Energy and water mass balance of Lake Untersee and its perennial ice cover, East Antarctica. Antarct Sci 31(05):271–285. https://doi.org/10.1017/s0954102019000270
Faucher B, Lacelle D, Marsh NB, Jasperse L, Clark ID, Andersen DT (2021) Glacial lake outburst floods enhance benthic microbial productivity in perennially ice-covered Lake Untersee (East Antarctica). Nat Commun. https://doi.org/10.1038/s43247-021-00280-x
Galchenko VF (1994) Sulfate reduction, methane production, and methane oxidation in various water bodies of Bunger Hills Oasis of Antarctica. Microbiology 63:388–396
Green CT, Scow KM (2000) Analysis of phospholipid fatty acids (PLFA) to characterize microbial communities in aquifers. Hydrogeol J 8:126–141
Greco C, Andersen DT, Hawes I, Bowles AMC, Yallop ML, Barker G, Jungblut AD (2020) Microbial diversity of pinnacle and conical microbial mats in the perennially ice-covered Lake Untersee, East Antarctica. Front Microbiol. https://doi.org/10.3389/fmicb.2020.607251
Guckert JB, Antworth CP, Nichols PD, White DC (1985) Phospholipid, ester-linked fatty acid profiles as reproducible assays for changes in prokaryotic community structure of estuarine sediments. FEMS Microb Ecol 31:147–158
Hayes JM (2001) Fractionation of the isotopes of carbon and hydrogen in biosynthetic processes. Rev Mineral Geochem 43:225–277
Hanson RS, Hanson TE (1996) Methanotrophic bacteria. Microbiol Rev 60:439–471
Harwood JL, Guschina IA (2009) The versatility of algae and their lipid metabolism. Biochimie 91:679–684
Hawes I, Schwartz AM (1999) Photosynthesis in an extreme shade environment: benthic microbial mats from Lake Hoare, a permanently ice-covered Antarctic lake. J Phycol 35:448–459
Hölzl G, Dörmann P (2007) Structure and function of glycoglycerolipids in plants and bacteria. Prog Lipid Res 46:225–243
Harvey HR, Fallon RD, Patton JS (1986) The effect of organic matter and oxygen on the degradation of bacterial membrane lipids in marine sediments. Geochim Cosmochim Acta 50:795–804
Hedrick DB, Peacock AD, Long P, White DC (2008) Multiply methyl-branched fatty acids and diacids in the polar lipids of a microaerophilic subsurface microbial community. Lipids 43:843–851
Hermichen W-D, Kowski P, Wand U (1985) Lake Untersee, a first isotope study of the largest freshwater lake in the interior of East Antarctica. Nature 315:131–133
Jahnke LL, Summons RE, Hope JM, Des Marais DJ (1999) Carbon isotopic fractionation in lipids from methanotrophic bacteria II: the effects of physiology and environmental parameters on the biosynthesis and isotopic signatures of biomarkers. Geochim Cosmochim Acta 63:79–93
Kenyon CN (1972) Fatty acid composition of unicellular strains of blue-green algae. J Bacteriol 109:827–834
Kellermann MY, Wegener G, Elvert M, Yoshinaga MY, Lin Y-S, Holler T, Mollar XP, Knittel K, Hinrichs K-U (2012) Autotrophy as a predominant mode of carbon fixation in anaerobic methane-oxidizing microbial communities. Proc Natl Acad Sci 109:19321–19326
Kieft TL, Ringelberg DB, White DC (1994) Changes in ester-linked phospholipid fatty acid profiles of subsurface bacteria during starvation and desiccation in a porous medium. Appl Environ Microbiol 60:3292–3299
Koo H, Mojib N, Hakim JA, Hawes I, Tanabe Y, Andersen DT, Bej AK (2017) Microbial communities and their predicted metabolic functions in growth laminae of a unique large conical mat from Lake Untersee East Antarctica. Front Microbiol 8:1347. https://doi.org/10.3389/fmicb.2017.01347
Kool DM, Zhu B, Rijpstra IC, Jetten MSM, Ettwig KF, Sinninghe Damsté JS (2012) Rare branched fatty acids characterize the lipid composition of the intra-aerobic methane oxidizer “Candidatus Methylomirabilis oxyfera.” Appl Environ Microbiol 78:8650–8656
Lipp JS, Hinrichs K-U (2009) Structural diversity and fate of intact polar lipids in marine sediments. Geochim Cosmochim Acta 73:6816–6833
Lengger SK, Hopmans EC, Sinninghe Damsté JS, Schouten S (2014) Fossilization and degradation of archaeal intact polar tetraether lipids in deeply buried marine sediments (Peru Margin). Geobiology 12:212–220
Lipp JS, Morono Y, Inagaki F, Hinrichs K-U (2008) Significant contribution of Archaea to extant biomass in marine subsurface sediments. Nature 454:991–994
Logemann J, Graue J, Köster J, Engelen B, Rullkötter J, Cypionka H (2011) A laboratory experiment of intact polar lipid degradation in sandy sediments. Biogeosciences 8:2547–2560
Londry KL, Jahnke LL, Des Marais DJ (2004) Stable carbon isotope ratios of lipid biomarkers of sulfate-reducing bacteria. Appl Environ Microbiol 70:745–751
Marsh NB, Lacelle D, Faucher B, Cotroneo S, Jasperse L, Clark ID, Andersen DT (2020) Sources of solutes and carbon cycling in perennially ice-covered Lake Untersee Antarctica. Sci Rep 10:12290. https://doi.org/10.1038/s41598-020-69116-6
Mulyukin AL, Demkina EV, Manucharova NA, Akimov VN, Andersen D, McKay C, Gal’chenko VF (2014) The prokaryotic community of subglacial bottom sediments of Antarctic Lake Untersee: detection by cultural and direct microscopic techniques. Microbiology 83:77–84
Niemann H, Elvert M (2008) Diagnostic lipid biomarker and stable carbon isotope signatures of microbial communities mediating the anaerobic oxidation of methane with sulphate. Org Geochem 39:1668–1677
O’Leary MH (1988) Carbon isotopes in photosynthesis. Bioscience 38:328–336
Pancost RD, Sinninghe Damsté JS (2003) Carbon isotopic compositions of prokaryotic lipids as tracers of carbon cycling in diverse settings. Chem Geol 195:29–58
Pancost RD, Sinninghe Damsté JS, de Lint S, van der Maarel MJEC, Gottschal JC, The Medinaut Shipboard Scientific Party (2000) Biomarker evidence for widespread anaerobic methane oxidation in Mediterranean sediments by a consortium of methanogenic archaea and bacteria. Appl Environ Microbiol 66:1126–1132
Pancost RD, McClymont EL, Bingham EM, Roberts Z, Charman DJ, Hornibrook ERC, Blundell A, Chambers FM, Lim KLH, Evershed RP (2011) Archaeol as a methanogen biomarker in ombrotrophic bogs. Org Geochem 42:1279–1287
Parenteau MN, Jahnke LL, Farmer JD, Cady SL (2014) Production and early preservation of lipid biomarkers in iron hot springs. Astrobiology 14:502–521
Parkes RJ, Dowling NJE, White DC, Herbert RA, Gibson GR (1993) Characterization of sulphate-reducing bacterial populations within marine and estuarine sediments with different rates of sulphate reduction. FEMS Microbiol Ecol 102:235–250
Pikuta EV, Lyu Z, Hoover RB, Liu Y, Patel NB, Busse HJ, Lawson PA (2017) Williamwhitmania taraxaci gen. nov., sp. nov., a proteolytic anaerobe with a novel type of cytology from Lake Untersee in Antarctica, description of Williamwhitmaniaceae fam. nov., and emendation of the order Bacteroidales Krieg 2012. Int J Syst Evol MicroBiol 67:4132–4145
Pinkart H, Ringelberg D, Piceno Y, Macnaughton S, White DC (2002) Biochemical approaches to biomass measurements and community structure. Man Environ Microbiol 2:101–113
Piorreck M, Baasch K-H, Pohl P (1984) Biomass production, total protein, chlorophylls, lipids and fatty acids of freshwater green and blue-green algae under different nitrogen regimes. Phytochemistry 23:207–216
Popp BN, Laws EA, Bidigare RR, Dore JE, Hanson KL, Wakeham SG (1998) Effect of phytoplankton cell geometry on carbon isotopic fractionation. Geochim Cosmochim Acta 62:69–77
Preuß A, Schauder R, Fuchs G (1989) Carbon isotope fractionation by autotrophic bacteria with three different CO2 fixation pathways. Z für Naturforschung 44c:397–402
Pushparaj B, Buccioni A, Paperi R, Piccardi R, Ena A, Carlozzi P, Sili C (2008) Fatty acid composition of Antarctic cyanobacteria. Phycologia 47:430–434
Russell NJ (1990) Cold adaptation of microorganisms. Philos Trans Royal Soc Lond B 326:595–611
St. Jean G, (2003) Automated quantitative and isotopic (13C) analysis of dissolved inorganic carbon and dissolved organic carbon in continuous-flow using a total organic carbon analyser. Rapid Commun Mass Spectrom 17:419–428
Sakamoto T, Los DA, Higashi S, Wada H, Nishida I, Ohmori M, Murata N (1994) Cloning of ω3 desaturase from cyanobacteria and its use in altering the degree of membrane-lipid unsaturation. Plant Mol Biol 26:249–263
Sakata S, Hayes JM, McTaggart AR, Evans RA, Leckrone KJ, Togasaki RK (1997) Carbon isotopic fractionation associated with lipid biosynthesis by a cyanobacterium: relevance for interpretation of biomarker records. Geochim Cosmochim Acta 61:5379–5389
Schouten S, Huguet C, Hopmans EC, Kienhuis MVM, Sinninghe Damsté JS (2007) Analytical methodology for the TEX86 paleothermometry by high-performance liquid chromatography/atmospheric pressure chemical ionization-mass spectrometry. Anal Chem 79:2940–2944
Schouten S, Middelburg JJ, Hopmans EC, Sinninghe Damsté JS (2010) Fossilization and degradation of intact polar lipids in deep subsurface sediments: a theoretical approach. Geochim Cosmochim Acta 74:3806–3814
Schouten S, Hopmans E, Sinninghe Damsté JS (2013) The organic geochemistry of glycerol dialkyl glycerol tetraether lipids: a review. Org Geochem 54:19–61
Schubotz F, Wakeham SG, Lipp JS, Fredricks HF, Hinrichs K-U (2009) Detection of microbial biomass by intact polar membrane lipid analysis in the water column and surface sediments of the Black Sea. Environ Microbiol 11:2720–2734
Simkus DN, Slater GF, Sherwood Lollar B, Wilkie K, Kieft TL, Magnabosco C, Lau MCY, Pullin MJ, Hendrickson SB, Wommack KE, Sakowski EG, van Heerden E, Kuloyo O, Linage B, Borgonie G, Onstott TC (2016) Variations in microbial carbon sources and cycling in the deep continental subsurface. Geochim Cosmochim Acta 173:264–283
Sinninghe Damsté JS, van Dongen BE, Rijpstra IC, Schouten S, Volkman JK, Greenevasen JAJ (2001) Novel intact glycolipids in sediments from an Antarctic lake (Ace Lake). Org Geochem 32:321–332
Slater GF, Goad CA, Lindsay MB, Mumford KG, Colenbrander Nelson TE, Brady AL, Jessen GL, Warren LA (2021) Isotopic and chemical assessment of the dynamics of methane sources and microbial cycling during early development of an oil sands pit lake. Microorganisms 9:2509. https://doi.org/10.3390/microorganisms9122509
Smith RL, Miller LG, Howes BL (1993) The geochemistry of methane in Lake Fryxell, an amictic, permanently ice-covered, Antarctic lake. Biogeochemistry 21:95–115
Steel HCB, McKay CP, Andersen DT (2015) Modeling circulation and seasonal fluctuations in perennially ice-covered and ice-walled Lake Untersee, Antarctica. Limnol Oceanogr 60:1139–1155
Sturt HF, Summons RE, Smith K, Elvert M, Hinrichs K-U (2004) Intact polar membrane lipids in prokaryotes and sediments deciphered by high-performance liquid chromatography/electrospray ionization multistage mass spectrometry—new biomarkers for biogeochemistry and microbial ecology. Rapid Commun Mass Spectrom 18:617–628
Sültemeyer D, Schmidt C, Fock HP (1993) Carbonic anhydrases in higher plants and aquatic microorganisms. Physiol Plant 88:179–190
Summons RE, Jahnke LL, Roksandic Z (1994) Carbon isotopic fractionation in lipids from methanotrophic bacteria: relevance for interpretation of the geochemical record of biomarkers. Geochim Cosmochim Acta 58:2853–2863
Taylor J, Parkes RJ (1983) The cellular fatty acids of the sulphate-reducing bacteria, Desulfobacter sp., Desulfobulbus sp. and Desulfovibrio desulfuricans. J Gen Microbiol 129:3303–3309
Templeton AS, Kung-Hui C, Alvarez-Cohen L, Conrad ME (2006) Variable carbon isotope fractionation expressed by aerobic CH4-oxidizing bacteria. Geochim Cosmochim Acta 70:1739–1752
Vestal JR (1988) Carbon metabolism of the cryptoendolithic microbiota from the Antarctic desert. Appl Environ Microbiol 54:960–965
Vestal JR, White DC (1989) Lipid analysis in microbial ecology. Bioscience 39:535–541
Vincent WF, Vincent CL (1982) Factors controlling phytoplankton production in Lake Vanda (77 °S). Can J Fisheries Aquat Sci 39:1602–1609
Whiticar MJ (1999) Carbon and hydrogen isotope systematics of bacterial formation and oxidation of methane. Chem Geol 161:291–314
White DC, Ringelberg DB (1996) Monitoring deep subsurface microbiota for assessment of safe long-term nuclear waste disposal. Can J Microbiol 42:375–381
Wagner NY, Andersen DT, Hahn AS, Johnson SS (2022) Survival strategies of an anoxic microbial ecosystem in Lake Untersee, a potential analog for Enceladus. Nat Sci Rep. https://doi.org/10.1038/s41598-022-10876-8
Wand U, Schwarz G, Brüggeman E, Bräuer K (1997) Evidence for physical and chemical stratification in Lake Untersee (central Dronning Maud Land, East Antarctica). Antarct Sci 9:43–45
Wand U, Samarkin VA, Nitzsche H-M, Hubberten H-W (2006) Biogeochemistry of methane in the permanently ice-covered Lake Untersee, central Dronning Maud Land, East Antarctica. Limnol Oceanogr 51:1180–1194
Ward DM, Panke S, Kloeppel KD, Christ R, Fredrickson H (1994) Complex polar lipids of a hot spring cyanobacterial mat and its cultivated inhabitants. Appl Environ Microbiol 60:3358–3367
Weijers JWH, Panoto E, van Bleijswijk J, Schouten S, Rijpstra WIC, Balk M, Stams AJM, Sinninghe Damsté JS (2009) Constraints on the biological source(s) of the orphan branched tetraether membrane lipids. Geomicrobiol J 26:402–414
Weisleitner K, Perras A, Moissl-Eichinger C, Andersen DT, Sattler B (2019) Source environments of the microbiome in perennially ice-covered Lake Untersee, Antarctica. Front Microbiol 10:1019. https://doi.org/10.3389/fmicb.2019.01019
White DC, Davis WM, Nickels JS, King JD, Bobbie RJ (1979) Determination of the sedimentary microbial biomass by extractible lipid phosphate. Oecologia 40:51–62
Xie S, Lipp JS, Wegener G, Ferdelman TG, Hinrichs K-U (2013) Turnover of microbial lipids in the deep biosphere and growth of benthic archaeal populations. Proc Natl Acad Sci 110:6010–6014
Yao Y, Gerde JA, Lee S-L, Wang T, Harrata KA (2015) Microalgae lipid characterization. J Agric Food Chem 63:1773–1787
Zelles L (1999) Fatty acid patterns of phospholipids and lipopolysaccharides in the characterisation of microbial communities in soil: a review. Biol Fertil Soils 29:111–129
Ziolkowski LA, Wierzchos J, Davila AF, Slater GF (2013) Radiocarbon evidence of active endolithic microbial communities in the hyperarid core of the Atacama Desert. Astrobiology 13:607–616
Acknowledgements
Primary support for this research was provided by the TAWANI Foundation of Chicago, the Trottier Family Foundation, NASA’s Exobiology Program (80NSSC18K1094, Andersen), the Arctic and Antarctic Research Institute/Russian Antarctic Expedition’s Subprogram ‘‘Study and Research of the Antarctic’’ of the Federal Target Program ‘‘World Ocean”, and the Natural Sciences and Engineering Research Council of Canada (NSERC). Logistics support was provided by Antarctic Logistics Centre International (ALCI), Cape Town, South Africa. We are grateful to Colonel (IL) J. N. Pritzker, IL ARNG (retired), of the TAWANI Foundation, Lorne Trottier of the Trottier Family Foundation, and fellow field team members for their support during the expedition. Special thanks to V. Akimov for help with water collection.
Funding
This work was supported by TAWANI Foundation of Chicago, the Trottier Family Foundation, NASA’s Exobiology Program (Grant #80NSSC18K1094 to DTA), the Arctic and Antarctic Research Institute/Russian Antarctic Expedition’s Subprogram ‘‘Study and Research of the Antarctic’’ of the Federal Target Program ‘‘World Ocean”, and the Natural Sciences and Engineering Research Council of Canada (NSERC, Grant #10535810 to GFS).
Author information
Authors and Affiliations
Contributions
All authors contributed to the study conception and design. Sample collection was carried out by ALB and DTA. ALB performed the analyses and result interpretation. ALB wrote the manuscript with input from other authors. All authors reviewed, edited, and approved the final manuscript.
Corresponding author
Ethics declarations
Competing interests
The authors have no relevant financial or non-financial interests to disclose.
Additional information
Responsible Editor: Scott Neubauer.
Publisher’s Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Supplementary Information
Below is the link to the electronic supplementary material.
Rights and permissions
Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.
About this article
Cite this article
Brady, A.L., Andersen, D.T. & Slater, G.F. Biosignatures of in situ carbon cycling driven by physical isolation and sedimentary methanogenesis within the anoxic basin of perennially ice-covered Lake Untersee, Antarctica. Biogeochemistry 164, 555–575 (2023). https://doi.org/10.1007/s10533-023-01053-8
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s10533-023-01053-8