Precipitation of exceptionally 13C-depleted authigenic carbonate is a result of, and thus a tracer for, sulphate-dependent anaerobic methane oxidation, particularly in marine sediments. Although these carbonates typically are less depleted in 13C than in the source methane, because of incorporation of C also from other sources, they are far more depleted in 13C (δ13C as light as −69‰ V-PDB) than in carbonates formed where no methane is involved. Here we show that oxidation of biogenic methane in carbon-poor deep groundwater in fractured granitoid rocks has resulted in fracture-wall precipitation of the most extremely 13C-depleted carbonates ever reported, δ13C down to −125‰ V-PDB. A microbial consortium of sulphate reducers and methane oxidizers has been involved, as revealed by biomarker signatures in the carbonates and S-isotope compositions of co-genetic sulphide. Methane formed at shallow depths has been oxidized at several hundred metres depth at the transition to a deep-seated sulphate-rich saline water. This process is so far an unrecognized terrestrial sink of methane.
Although there are observations supporting anaerobic oxidation of methane (AOM) in deep groundwater in fractured granitic rock1,2,3,4, the vast majority of observations of this phenomenon are from marine seabed systems including fossil methane seeps5,6,7,8,9 and active methane seeps10,11,12,13. At marine methane seeps microbial AOM has been shown to occur with sulphate as an electron acceptor14, involving a defined, syntrophic two-membered bacterial consortium: anaerobic methane oxidizing (ANME) archaea and sulphate-reducing bacteria (SRB)12,13,15, although AOM solely by ANME has also been suggested16. The AOM occurs at the sulphate-methane transition zone (SMTZ), where sulphate-rich descending water mix with deeper-seated methane and SRB outcompete methanogens12,13,15. Here methane is oxidized by ANME via a proposed reversal CO2 reduction and, as a consequence, authigenic carbonates precipitate from the produced bicarbonate9. Because the methane generally has light carbon isotope values (13C/12C expressed as δ13C) of down to −50‰ when it is thermogenic and typically −60 to −110‰ when it is biogenic17, the authigenic carbonates are 13C-depleted with values as low as −69‰ (refs 5, 6, 7, 8, 10, 11, 12, 18).
In contrast to shallow marine sediments where sulphate is generally depleted with depth, numerous granitic shield areas worldwide host sulphate-rich water at great depth, in brines derived from a proposed marine source such as basinal brines from overlying sedimentary rock successions19,20,21. When the basement rock eventually has been re-exposed after erosion of the sedimentary successions, repeated infiltrations of surface water, including glacial melt water, marine water and meteoric water, are possible and controlled by factors such as location and topography. Fresh water (meteoric) therefore typically occupies the upper bedrock fracture volume, a mixture of brackish and glacial water is found at intermediate depth, and saline sulphate-rich water is generally restricted to great depth, such as described for the crystalline bedrock of southeastern Sweden in the Baltic Shield22,23. Owing to changing hydrochemical conditions during infiltration of occasionally carbon-rich water from the terrestrial environment above and increased alkalinity in response to microbial breakdown of organic matter and methane, carbonates (as a rule calcite) can become oversaturated and precipitate on the fracture walls. The stable carbon isotope composition of these calcites can thus be used to identify biological processes in the fractured upper crust, especially across depth-related hydrochemical boundaries, at which microbial communities thrive14. However, low-temperature calcite has only been sparsely used to reveal microbial processes in deep bedrock fractures because of its’ rare, fine-grained and finely zoned nature, as well as because of challenges and costs of sampling representative calcite crystals deep in the Earth’s crust3,24,25,26,27,28.
In the present study we have examined more than 40 cored boreholes drilled in one of the most extensively studied granitic bedrock sites in the world, the Laxemar area, Sweden, and sampled fine-grained-zoned calcite crystals throughout the upper 1,000 m of the bedrock. These calcites postdate fluid-inclusion-rich calcite formed at >50 °C (refs 25, 29) and have single-phased fluid inclusions suggesting, although few in numbers, formation at <50 °C (ref. 30). The stable isotopic composition of carbon and oxygen was determined in transects across the numerous growth zones present within the calcite crystals, in a total of more than 430 analyses by secondary ion mass spectrometry (SIMS; 10 μm wide, 1–2 μm deep spots). The sulphur isotope inventory, 34S/32S presented as δ34S, of co-genetic pyrite crystals were explored by similar SIMS analyses (n=101), which can reveal coeval SRB activity31. The organic inventory of the calcites and the groundwater chemistry are also explored. Thereby, the hydrochemical and biological evolution in situ in the fractures could be revealed in detail.
Here we report extremely 13C-depleted carbonates precipitated in fractures deep within granitoid rocks. The δ13C values are by far the lowest ever reported for carbonates (δ13C:−125‰) and are suggested to be related to microbial sulphate-dependent anaerobic oxidation of biogenic methane. Methane oxidation occurring in the energy-limited and carbon-poor groundwater systems deep within Earth’s terrestrial landscape evidently results in a unique carbon isotope variability compared with other environments, such as the well-characterized sedimentary AOM settings.
Extreme carbon isotope variation of calcite in rock fractures
Within the individual calcite crystals (Fig. 1) there is large δ13C variation, of up to almost 110‰ between different growth zones, thus revealing large temporal variation of the processes in the fractures (Figs 2b and 3, Supplementary Table 1, location in Supplementary Fig. 1). The range of the δ13C values depends on the depth at which the calcites were precipitated and reside and, therefore, mark different biological processes at different depths within the fracture network (Fig. 2b). In the upper 200 m several calcites have zones with positive δ13C values (for example, in Fig. 3a). Such 13C-enriched carbonate pools develop where methanogenesis occurs32,33, leading to a 12C-rich methane and 13C-rich residual CO2 from which calcite formed. Although measurements of methane are relatively scarce in this area and the concentrations are generally low (<0.2 ml l−1), anomalies with elevated concentrations (>0.6 ml l−1, related to waters with abundant cultivatable methanogens and high concentrations of dissolved organic carbon, DOC34), are indeed restricted to shallower depths than the sulphate-rich saline waters (Fig. 2a, Supplementary Table 2). The organic input to the system in the form of descending DOC, which fuels the methanogenesis, evidently has a surficial origin.
Extreme 13C depletion of −125 to −50‰ was observed in calcites between 200 and 730 m. This 13C depletion is so strong that it cannot originate from any other source compound than methane. For methane to be incorporated in calcite, it first has to be oxidized, in this particular setting by anaerobic mechanisms because of consistently reducing conditions (absence of O2; Eh ranges from −210 to −380 mV (ref. 22)), far below the redox transition at 20 m depth35. In addition, aerobic methane oxidation would have resulted in calcite dissolution rather than precipitation36. The oxidation of methane causes a decrease in 13C in the produced CO2, with fractionation (αCH4–CO2) commonly in the order of 1.009–1.024 (refs 17, 37, 38). The calcites with the lightest δ13C must therefore have been produced from a source methane with δ13C lighter than −100‰. Consequently, the C-isotope data suggest a dominantly biological origin of the source methane because thermogenic methane rarely exceed values lighter than −50‰ (ref. 17). Thirteen fractures from boreholes spread out over a 3 × 3 km area featured AOM-related calcite, which in seven fractures had lighter δ13C than −90‰ (four lighter than −100‰), marking that extraordinary 13C depletions are widespread in this environment and not single occurrences. All of these 13 fractures carried calcite with minimum δ13C values that were similar to or lighter than reported for AOM-related authigenic marine carbonate (−69‰ (ref. 5)). Minimum sulphur isotope values of pyrite (δ34Spyrite, full results in Supplementary Table 3) co-genetic with AOM calcite are mainly 22–33‰ lighter, and in the rare case 46.8‰ lighter, than the anticipated source sulphate (+25‰ (ref. 31)). This is evidence of activity of SRB, which preferentially use the lighter S isotope in their metabolism, with large related fractionation between sulphate and produced sulphide as a consequence39. Large fractionation of the sulphur isotopes characterizes AOM-related microbial sulphate reduction, particularly when methane concentrations are low, such as at SMTZ40. These findings are in accordance with previous observations of SRB-related pyrite in the deep fracture system at Laxemar31 (Fig. 2d) and at nearby Äspö3. In the latter case, pyrite was accompanied by 13C-depleted calcite (at lightest −46.5‰ V-PDB; Vienna Pee Dee Belemnite), although not specifically interpreted to be AOM-related3.
Other δ13C values than those related to methanogenesis (heavy) or AOM (light) within the crystals reflect a dominance of inorganic C (−10 to −3‰) observed at all depth, and dominance of C from microbial degradation of organic matter (down to −30±5, potentially reflecting mixing of different C sources, including a minor AOM part). The latter δ13C signatures appear down to −730 m, which thus represent a depth limit for the descent of DOC from the terrestrial ecosystem above.
Organic inventory of the calcite crystals
In addition to the diagnostic 13C-depleted carbonate, the presence of typically 13C-depleted specific lipid biomarker signatures of ANME and its SRB partner frequently serve as diagnostic tracers for active or fossil AOM in marine settings14,18,41. In the tiny calcite crystals from bedrock fractures studied here, it is impossible to determine δ13C of specific organic compounds. Nevertheless, our coupled gas chromatograph mass spectrometer (GC/MS) and Time-of-Flight (ToF)-SIMS analyses revealed signatures of methylated anteiso- (ai) and iso- (i) fatty acids (ai-C15:0, 10Me-C16:0, i- and ai-C17:0, Fig. 4), hopanes (norhopane and hopene) and several non-isoprenoidal dialkyl glycerol diethers with branched alkyl, cyclohexyl or cyclopropyl units (DAGE, Fig. 4, Supplementary Table 4), in the AOM-related calcites. These organic molecules clearly originate from in situ microbial activity because they are mostly SRB-specific, and in the case of DAGEs, and ai-C15:0 highly AOM-specific8,9,18. This suggests that a similar two-membered ANME-SRB microbial consortium as described at other AOM sites13,18 operated here as well. The organic material within the calcites generally clusters along intracrystal grain boundaries (the borders between different growth zones), as shown by ToF-SIMS analyses of crystal interiors. Raman spectroscopy and ToF-SIMS revealed that there is no abundant organic material in the calcite matrix apart from along these grain boundaries. The GC/MS and ToF-SIMS analyses of calcite leachates (from up to 220 mg large calcite samples), which represent accumulated organic material from grain boundaries of several crystals showed more pronounced signatures of organic compounds compared with spot analyses of the crystals. Raman spectroscopy and scanning electron microscopy (SEM) investigations showed, however, that fine-grained clay minerals and pyrite dominate along the grain boundaries (Supplementary Fig. 2, Supplementary Note 1 and Supplementary Table 5). Numerous observations from crystalline rock fractures and vesicles elsewhere report complete mineralization of microbial structures to, for example, clay minerals, embedded in calcite42,43,44. Significant, but not complete, fossilization of the microorganisms in biofilms at the grain boundaries is therefore proposed on the basis of the observations of the interiors of the AOM crystals.
General mechanisms of methane formation and oxidation
Taken together, the δ13C data of the calcites suggest a mechanism whereby methane is formed in shallow fractures (Fig. 2a,b), transported downwards and oxidized and precipitated as calcite at the border to the sulphate-rich, methane-poor saline water deep in the crust at 200–730 m. The oxygen isotope composition (18O/16O expressed as δ18O) of the calcites can be used to link the calcites to different climatic/hydrological events through comparison with the δ18O of the infiltrating waters, which in the studied setting is approximately −21‰ V-SMOW for glacial water, −6 to 0‰ for the variety of transgressed marine and/or brackish waters (ocean-type water at c. 0‰, Holocene brackish Baltic Sea waters at −5.9 to −4.7‰), −10‰ for meteoric and c. −9‰ for the deep sulphate-rich brine at >500 m depth45. Although mixing of these waters have resulted in mixing of the δ18O values, generally one of the water types dominates45. Because the δ18O values of the AOM- and methanogenesis-related calcites are generally similar and constant at −6±2‰ PDB with depth (Fig. 2b), these two types of calcites can be causally and temporally linked to the infiltration of a similar type of groundwater. On the basis of the δ18O values and consideration of the fractionation occurring when calcite precipitates, this water was dominantly brackish-marine (δ18O values in line with brackish/marine waters during Holocene and the Eemian interstadial, cf.22,46, and heavier than all other potential source water types). The AOM- and methanogenesis-related calcite generally do not make up the whole crystals but can be both preceded and succeeded by calcite with distinctly different δ13C- and δ18O-signatures (Fig. 3b–e). This reflects that methanogenesis and AOM have been initiated but also terminated in response to changing hydrochemical conditions in the fracture system. The AOM-related calcite growth is frequently accompanied by relative enrichment in 18O in the calcites, indicative of increased proportion of marine water relative to fresh waters (Fig. 3b,c), further supported by brackish-marine salinities (2.4 wt.% NaCl) estimated in the only AOM sample with measurable fluid inclusions (at −642 m, Supplementary Table 6, Supplementary Note 2, Supplementary Figs 3 and 4). This is in line with the sequence of infiltration of surficial water during the repeated Pleistocene deglaciation cycles in this area, involving high hydraulic heads that pressed glacial melt water several hundred metres into the fracture network and subsequent marine transgressions over the depressed land masses22. During the marine transgression, dense marine (brackish) water was brought on top of light fresh water in the fractures. In such a system advection can occur, under ideal conditions, with a velocity of up to the order of 1 cm s−1 (see Supplementary Note 3), corresponding to a travel time of about a single day for a vertical downward distance of 500 m. In contrast to methane diffusion, which is too slow (Supplementary Note 3), advective transport, particularly favourable after a glaciation but certainly possible also in other situations, is thus fully capable of carrying dissolved methane deep into the crust, down to the deep sulphate-rich brines, within a short period of time.
Marine waters descending through organic-rich sediments will have delivered to the superficial fractures dissolved organic matter that favour methanogenesis but also dissolved sulphate that will lead to methane oxidation. In near-surface fractures, however, pyrite crystals with extremely heavy δ34S values of up to more than +90‰ V-CDT (Vienna Canyon Diablo Troilite) exist31. This is evidence for extensive sulphate consumption by SRB because values as heavy as these can have been formed only where the dissolved sulphate pool was nearly exhausted in the fracture. Consequently, because sulphate was exhausted, methane concentrations were allowed to build up and descend downwards.
Dominantly pre-Holocene methane oxidation
The Holocene post-glacial marine transgression generally did not reach as far inland as the investigated boreholes. Hence, the groundwater captured by these is still made up of a significant portion of glacial meltwater on top of the deep saline water. This C-poor Holocene glacial meltwater mixed with and/or replaced an older marine water, to which AOM is possibly related. Therefore, ongoing AOM is not believed to be significant at this site. This scenario is supported by (1) AOM-related and methanogenesis-related calcite being succeeded by calcite without AOM δ13C signature of fresh water type (dominantly glacial or meteoric water replacing the marine/saline water, Fig. 3d,e), (2) the overall heavier δ18O of the AOM- and methanogenesis-related calcites (dominantly marine) than those expected for calcite precipitated from the current groundwater with a large glacial component at great depth and a large meteoric component at shallow depth (Fig. 2c) and (3) limited variation in δ13CDIC values in the current groundwater compared with the calcites. This supports dominant formation of the AOM calcites in a groundwater system predating the latest (Weichselian) glaciation but within the last 10 Ma when the Paleozoic cover had been eroded away47, allowing the border to the deep sulphate-rich water to be depressed to depths of several hundred meteres where AOM calcites formed. A minor number of overlapping calculated δ18O values of shallow groundwater and calcite (Fig. 2c) indicate potential but limited methanogenesis-related (and minor deeper AOM-related) calcite formation from the current DOC-rich meteoric waters at these depths, in accordance with the observed scattered enhanced methane concentrations (Fig. 2a) and presence of methanogens and SRB34.
Our study shows that AOM-related calcite precipitation was established at the border between a descending sulphate-exhausted water, carrying dissolved methane, and a deeper sulphate-rich old saline water. The processes are outlined in Fig. 5 and include reduction of sulphate to 34S-depleted sulphide and oxidation of 13C-depleted biogenic methane to 13C-depleted bicarbonate by a syntrophic consortium of ANME and SRB. These reactions cause an increased alkalinity invoking precipitation of 13C-depleted calcite on the fracture wall. This calcite formed from reaction of the produced bicarbonate with the abundant dissolved Ca2+ in the deep saline water (up to 740 mg l−1 (ref. 24)). The most likely explanation why the calcites are considerably more 13C-depleted than the numerous marine AOM calcites observed worldwide is that the latter form in DOC- and DIC-rich sediment porewaters and thus more readily incorporate carbonate from other carbon sources than oxidized methane9,48. In strong contrast, the deep groundwater in crystalline rocks carries low concentrations of DIC and DOC (in Laxemar, each less than 2 mg l−1 compared with maximum values of 330 and 21 mg l−1, respectively, in the upper 200 m), indicating that methane has been an almost exclusive carbon source for the 13C-depleted calcites. The low concentrations of DOC in the deep groundwater were likely also partly refractory to microbial degradation in similarity with the limited availability and poor reactivity of organic substrates in deep-sea sediments49. Pyrite (depleted in 34S compared with sulphate) is formed by reaction of the SRB-produced dissolved sulphide and Fe2+ (present at 0.1–0.8 mg l−1 (ref. 24)). The large range in δ34Spyrite of 68.9‰ (−22.1 to +46.8‰, for example, in Fig. 3f) and frequent progressively heavier δ34S with growth clearly reflect bacterial sulphate reduction in a system where the reduction rate has exceeded the supply of sulphate by advection and diffusion50. Increase in δ34S values by up to almost 40‰ over a crystal growth distance of 50 μm (Fig. 3f) strongly suggests very local microscale isotope systematics at the fracture wall, in spatial relation to microbial communities31. Similarly, the contrasting δ13C values in the calcites compared with those in the bulk fracture water (Fig. 3b) support local incorporation of 13C-depleted bicarbonate formed by AOM at the fracture wall. However, the generally irregular δ13C evolution within these calcites rules out similar closed system evolution of the carbon system as for the sulphur system. The irregular δ13C variation of up to 45‰ in the AOM-related zone within the calcite crystals instead reflects either (1) local variability of incorporation of carbonate into calcite from other carbon sources than methane and/or (2) substantial variation of the δ13C values of the oxidized biogenic methane as a result of methanogenesis during substrate-limited conditions51 occurring in the deep biosphere, or because of other factors that influence the kinetic carbon isotope effect during methanogenesis, including sulphate availability (cf. ref. 52), substrate utilized and temperature17,51. As the δ13C value of the oxidized methane is unknown, we cannot exclude that the source methane of the <−100‰ calcites has been extremely depleted in 13C. It has recently been demonstrated that low sulphate concentrations (<50 mg l−1) can lead to microbially mediated carbon isotope equilibration between methane and carbon dioxide resulting in some degree of reversibility of the methane oxidation (that is, back-flux)53,54. This causes progressively decreased δ13C values of the residual methane. An extraordinary 13C-depleted methane, affected by partial and reversible oxidation in a sulphate-limited system, such as in most of the current shallow and intermediate waters (Fig. 2a), can therefore indeed have been the source of the extremely 13C-depleted calcites.
The setting described here is not unique for the Baltic Shield, but is found on all continents in a variety of regions. Therefore, the identified methane-consumption mechanism in bedrock fractures and similar 13C-depleted carbonates can occur worldwide. Our finding of AOM at a transition between biogenic methane formed at shallow depth and a deeper sulphate-rich saline water is, however, completely reverse to the SMTZ observed in typical well-characterized sedimentary AOM settings and at another well-characterized crystalline rock site (Olkiluoto, Finland)1,2, where deep-seated methane instead intersects with sulphate from superficial layers. Deep sulphate-bearing brine incursions that fuel AOM below the SMTZ have, however, been reported from a few marine sediments as well55. Although hydrochemical data are scarce from great depth in crystalline rocks, deep sulphate-rich waters, capable of ultimately producing the reversed SMTZ as described here, have been reported elsewhere19,20,56,57, offering opportunities for similar biogeochemical processes on a global scale. Although SRB- and methanogenesis-related isotopic signatures have been reported from groundwater and minerals in fractured crystalline rock in for example Sweden, Finland and USA3,26,31,33,58,59,60, and a few scattered possible AOM indications of calcite (bulk samples) from Sweden exist3,59,61, more detailed and comprehensive in situ studies of low-temperature calcite are needed to better constrain the extent of past and present AOM deep in crystalline rocks globally. The episodic nature of the processes indicates dependency of certain conditions for initiation of AOM that may vary from site to site.
In conclusion, our study reveals a previously unknown methane–sulphate transition zone with consumption of biogenic methane at the border to sulphate-rich deep saline water at great depth in crystalline rocks. The relatively energy-limited and C-poor environment at great depth within these granite fractures has resulted in utilization and almost exclusive incorporation of C from biogenic methane into the extremely 13C-depleted calcites precipitated on the fracture walls during AOM by ANME-SRB consortia. These findings greatly expand the observed range of carbon isotope variation in carbonates in natural environments, even when compared with sediment-hosted AOM occurrences, which previously were considered to host the most 13C-depleted carbonates globally. The conditions associated with methane oxidation deep within Earth’s terrestrial landscape is evidently substantially different compared to methane oxidation in other environments.
Calcite and pyrite crystals sampled from 18 drill cores were mounted in epoxy, polished to expose crystal cross-sections and examined using SEM (to trace zonations). Intracrystalline SIMS analysis (10 μm lateral beam dimension, 1–2 μm depth dimension) of carbon, oxygen and sulphur isotopes were performed on a Cameca IMS1280 ion microprobe. Analytical transects were made within several crystals from each sample. Settings follow those described in ref. 31, with some differences; O was measured on two Faraday cages (FC) at mass resolution 2,500, whereas C used a FC/EM combination, with mass resolution 2,500 on the 12C peak and 4,000 on the 13C peak to resolve it from 12C1H. Data were normalized using Brown Yule Marble (δ18O: 24.11±0.13‰ V-SMOW, converts to 6.55±0.13‰ V-PDB, δ13C: −2.28±0.08‰V-PDB, derived from three replicate bulk analyses, J. Craven, University of Edinburgh, personal communication) and Balmat pyrite (+16.515±0.005‰ V-CDT62). Precision was δ18O: ±0.3–0.4‰, δ13C: ±0.4–0.5‰ and δ34S: ±0.13‰. Potential matrix effects for SIMS analysis due to Mg and Fe substitutions in the calcites (cf. ref. 63) are negligible because of very low molar fractions of Mg and Fe (XMg and XFe) in these and other low-temperature calcites in the area (up to only 0.002 and 0.004, respectively24,64). Significant influence of organic carbon was avoided in the SIMS analyses by careful spot placement to areas in the crystals without microfractures or inclusions, at a sufficient distance from grain boundaries where fine-grained clusters of other minerals and remnants of organic material may appear. The uncertainty associated with potential organic inclusions and matrix composition is therefore considered to be insignificant compared with the isotopic variations.
ToF-SIMS and GC/MS
Extraction of calcites for analyses of organic compounds was carried out accordingly. Calcite powder was extracted with 2 ml of predistilled dichloromethane in a Teflon-capped glass vial (ultrasonication, 35 min, 50 °C). The supernatant was decanted after centrifuging. Extraction was repeated three times. After evaporation of the combined extracts and re-dissolution in pure dichloromethane, the solvents were dried with N2. Extracts were re-dissolved with 20 μl of n-Hexane and derivatized by adding 20 μl BSTFA (N,O-bis(trimethylsilyl)trifluoroacetamide)/pyridine and heated (40 °C, 1.5 h). Remnant calcite powder was decarbonized with BSTFA, TMCS (trimethylchlorosilane)/methanol and derivatized by heating (80 °C, 1.5 h). The lipid fraction was separated by mixing with hexane and decanting the supernate. Extraction was repeated three times. The samples were dried with N2, redissolved with 50 μl of n-Hexane and analysed with GC/MS and ToF-SIMS. One microlitre of each sample extract was analysed with a Varian CP-3,800 GC/1,200-quadrupole MS (settings in ref. 64). ToF-SIMS analyses of single calcite grains and organic extracts were conducted using a ToF-SIMS IV (ION-TOF GmbH, with liquid bismuth cluster ion source; settings in ref. 65). Compounds and corresponding characteristic fragments detected with ToF-SIMS and GC/MS within the AOM calcites are listed in Supplementary Table 4.
The Raman spectrometry analyses were performed on seven samples with a confocal laser Raman spectrometer (Horiba instrument LabRAM HR 800), equipped with a multichannel air-cooled (−70 °C) 1,024 × 256 pixel CCD (charge-coupled device) array detector. Acquisitions were obtained with a 1,800-line per mm grating. The excitation source was provided by a 514-nm Argon laser (Melles Griot 543) with a laser power at the sample surface of 8 mW. An Olympus BX41 microscope was coupled to the instrument. The laser beam was focused through a × 100 objective to obtain a spot size of ∼1 μm. The spectral resolution was ∼0.3 cm−1 per pixel. The accuracy of the instrument was controlled by repeated use of a silicon wafer calibration standard with a characteristic Raman line at 520.7 cm−1. The Raman spectra were achieved with the LabSpec 5 software. Results are briefly presented in Supplementary Note 1.
Fluid inclusion microthermometry
Fluid inclusions were analysed in handpicked calcite crystals (0.5–1.5 mm in size) and in the epoxy-mounted crystals used for SIMS analysis following polishing of the mount to a 150-μm double-polished section. Microthermometric analyses of fluid inclusions were made with a Linkam THM 600 stage mounted on a Nikon microscope utilizing a × 40 long working-distance objective. The working range of the stage is from −196 to +600 °C (for details see ref. 66). The thermocouple readings were calibrated by means of SynFlinc synthetic fluid inclusions and well-defined natural inclusions in Alpine quartz. The reproducibility was ±0.1 °C for temperatures below 40 and ±0.5 °C for temperatures above 40 °C.
Scanning electron microscopy
The zonation and inclusions of other minerals within polished hand-picked calcite crystals mounted in epoxy were examined using a Hitachi S-3,400 N SEM equipped with an integrated energy-dispersive spectroscopy system. The acceleration voltage was 20 kV, and the working distance 9.2 mm. During semiquantitative energy-dispersive spectroscopy analyses of other minerals within the calcites, oxide and element calibration standards (Smithsonian mineral standards) were used, linked to a cobalt drift standard (calibrated twice every hour) and a stable specimen current. Spot size was ∼5 μm.
Groundwater from water-conducting fractures were sampled in 3- to 10-m packed-off boreholes by SKB, and results were extracted from their database (SICADA). Only sections with <1% drilling water are used. Quality control of the analyses and details of methods are described in ref. 67.
How to cite this article: Drake, H. et al. Extreme 13C depletion of carbonates formed during oxidation of biogenic methane in fractured granite. Nat. Commun. 6:7020 doi: 10.1038/ncomms8020 (2015).
We are grateful to the Swedish Nuclear Fuel and Waste Management Co. (SKB) and Nova Centre for University Studies Research & Development for giving access to the hydrochemical database and the drill cores. We thank the University of Gothenburg for providing access to their SEM laboratory. We also thank Lev Ilyinksy and Kerstin Lindén at NordSIM, for assistance during SIMS analyses. This is NordSIM contribution 397.
Supplementary Figures 1-4, Supplementary Tables 1-6, Supplementary Notes 1-3 and Supplementary References