Abstract
Thermokarst lakes are important conduits for organic carbon sequestration, soil organic matter (soil-OM) decomposition and release of atmospheric greenhouse gases in the Arctic. They can be classified as either floating-ice lakes, which sustain a zone of unfrozen sediment (talik) at the lakebed year-round, or as bedfast-ice lakes, which freeze all the way to the lakebed in winter. Another key characteristic of thermokarst lakes are their eroding shorelines, depending on the surrounding landscape, they can play a major role in supplying the lakebeds with sediment and OM. These differences in winter ice regime and eroding shorelines are key factors which determine the quantity and quality of OM in thermokarst lake sediments. We used an array of physical, geochemical, and microbiological tools to identify the differences in the environmental conditions, sedimentary characteristics, carbon stocks and microbial community compositions in the sediments of a bedfast-ice and a floating-ice lake in Far East Siberia with different eroding shorelines. Our data show strong differences across most of the measured parameters between the two lakes. For example, the floating-ice lake contains considerably lower amounts of sediment organic matter and dissolved organic carbon, both of which also appear to be more degraded in comparison to the bedfast-ice lake, based on their stable carbon isotope composition (δ13C). We also document clear differences in the microbial community composition, for both archaea and bacteria. We identified the lake water depth (bedfast-ice vs. floating-ice) and shoreline erosion to be the two most likely main drivers of the sedimentary, microbial and biogeochemical diversity in thermokarst lakes. With ongoing climate warming, it is likely that an increasing number of lakes will shift from a bedfast- to a floating-ice state, and that increasing levels of shoreline erosion will supply the lakes with sediments. Yet, still little is known about the physical, biogeochemical and microbial differences in the sediments of these lake types and how different eroding shorelines impact these lake systems.
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Introduction
Arctic permafrost regions store about 50% of the global soil organic carbon (soil-OC) pool (Kuhry et al. 2010), especially near the surface (0–3 m) with an estimated 1307 ± 170 Pg of soil-OC in the northern circumpolar permafrost region alone (Hugelius et al. 2014). A large fraction of this soil-OC is still decoupled from the active carbon cycle and protected from extensive degradation because of freezing temperatures, but strong ongoing climate warming in the Arctic (Jansen et al. 2020) increasingly exposes these soils to thaw (Heslop et al. 2020). The decay of permafrost often occurs in places that are naturally exposed to physical, thermal and environmental forces, such as riverbanks, coastlines, lake shorelines or topographic slopes which allow exposure of the frozen ground (Ballantyne 2018).
Thermokarst lakes are hotspots of rapid permafrost thaw. Here, organic matter (OM) in lakebed sediments, underlying permafrost soils and along eroding shorelines can degrade to greenhouse gases (GHGs) (Walter et al. 2007; van Huissteden 2020). Due to their high abundance and widespread distribution in tundra landscapes, thermokarst lakes play an important role in the Arctic GHG balance (in ’t Zandt et al. 2020). The Northeast Siberian coastal lowlands for example are widely covered by small and large lakes which regionally make up more than 40% of the land surface area (Grosse et al. 2013). Thermokarst lakes impact the Arctic carbon budget since they can act both, as sinks which sequester OC (Schirrmeister et al. 2011) at the lakebed, or as sources through the release of GHGs (Zimov et al. 1997; Matveev et al. 2016) depending on timescales, current climatic, hydrological and local geological conditions (Walter Anthony et al. 2014; Webb et al. 2022). The main sediment (and associated OM) source of thermokarst lakes is allochthonous material that is eroded along their shorelines. Whether the lakes sequester OM or act as catalyst for OM decomposition is highly dependent on their rates of sediment deposition (Walvoord et al. 2019).
Sediment temperatures at the lakebed of thermokarst lakes are strongly controlled by their lake ice regime, which describes two different states of their environmental conditions during winter (Ling and Zhang 2003). Firstly, bedfast-ice lakes that freeze all the way to their lakebed during the winter months, they are shallower than the local maximum winter ice thickness (Arp et al. 2012). Secondly, floating-ice lakes that are deep enough to remain unfrozen at the lakebed also during the peak of winter (Arp et al. 2012). During the summer months, the lakes transfer heat from their water body to the underlying permafrost ground below the lakebed, which gradually thaws the underlying soil over time. This can cause large-scale thermokarst subsidence of the lakebed since the underlying ice-rich permafrost soil can contain 50–90 vol% ice (Nitzbon et al. 2020; Windirsch et al. 2020). During winter, this thawed subsoil naturally refreezes again below bedfast-ice lakes. Over time, ongoing soil subsidence below the lakebed and rising lake water levels can deepen bedfast-ice lakes to such an extent that they exceed the local maximum winter ice thickness. Once this threshold is exceeded, the lake water and the uppermost lake sediment and thawed permafrost soil at the lakebed will remain unfrozen year-round and result in floating-ice lake formation (Arp et al. 2012). Over time, zones of unfrozen ground (taliks) can form below thermokarst lakes and reach vertically 95 m below the lakebed (Schwamborn et al. 2000). The sediment organic carbon (SOC) contained in the lake sediment and thawed permafrost soil of an active talik is no longer subjected to the annual freezing cycle and is exposed to increased year-round microbial activity, resulting in increased degradation of sediment organic matter (SOM) stocks (Walter Anthony et al. 2018; Jongejans et al. 2021).
The conditions for carbon degradation through microbial activity are generally more favorable in floating-ice lakes than in bedfast-ice lakes since its taliks are not frozen throughout the winter. OC degradation through complex microbial networks and CH4 production by methanogenic archaea that occurs under anoxic conditions are both positively affected by increased temperatures (Wik et al. 2014; Thornton et al. 2015). Therefore, it is likely, that GHG fluxes from floating-ice lake systems may increase, since microbial activity responds positively to both, increased temperatures (here during the winter season) and increased availability of SOM and nutrients (here from shoreline erosion) (Walter Anthony et al. 2014; de Jong et al. 2018; in ’t Zandt et al. 2020). Wik et al. (2016) estimated that CH4 emissions from northern lakes will increase 20–54% by 2100 if ice-free conditions on the lakes are extended by only 20 days.
So far, the differences in carbon stocks, sediment properties and microbial community compositions within and between these specific thermokarst lake types remain understudied. Jones et al. (2018) emphasize that most lake systems, which includes thermokarst lakes, are internally heterogeneous, and so far they are not well constrained biochemically (Arsenault et al. 2022). For a better assessment of the OC dynamics and eventually the potential future impact on the Arctic GHG balance, more studies and data are key to better understand the intra- and inter-lake variability of these different lake types. Furthermore, there is a growing need to include biogeochemical and microbiological processes in GHG models for specific environments like wetlands (Chadburn et al. 2020). To model thermokarst lake systems will require field data as presented in this study that can provide input variables.
Here, we investigated sediment cores from four sites located in the Northeast Siberian coastal lowlands; one core from a bedfast-ice lake, within a flat tundra location surrounded by peaty soil, and three cores from a floating-ice lake, which also borders an actively eroding permafrost cliff. The focus was on the role of ice regime and allochthonous sediment input on the lake sediment characteristics and its impact on the carbon dynamics in these lakes. We used sedimentological (grainsize, gamma-ray bulk density (ργ-ray), magnetic susceptibility (MS), porewater content), geochemical (loss-on-ignition (LOI), dissolved organic carbon (DOC) concentration, soil-OC/SOC and DOC stable carbon isotope values (δ13Corg, δ13CDOC), radiocarbon dating (14C), X-ray fluorescence (XRF) elemental composition) and microbiological (16S rRNA gene amplicon sequencing) analyses to create the data base for this study. We aimed to measure a suite of variables to characterize and understand the sedimentological and biogeochemical drivers within two distinct thermokarst lakes. The study of the sediment dynamics in thermokarst lake systems is important considering the likelihood of increasing shifts from bedfast- to floating-ice regimes (Arp et al. 2012) and likely increasing shoreline erosion rates (Jones et al. 2011). These developments might increase the input of eroded OM into thermokarst lake systems and its decomposition rates at the lakebeds. We here document the differences between two thermokarst lake systems which are likely due to a combination of these two main drivers of lake ice regime and shoreline erosion. While in this study we cannot quantify to what extent these drivers impact the lake sediment and its SOC in proportion to each other we still see clear indications that both ice regime and shoreline erosion play important roles.
Methodology
Field site
The study area is in the Kytalyk National Park (Национальный парк Кыталык) in the Russian Republic of Yakutia. It is situated 480 km above the Arctic Circle along the northern bank of the Berelekh (Бёрёлёх) river (Fig. 1) which merges with the larger Indigirka (Индиги́рка) river near the town of Chokurdakh (Чокурда́х). The field site is situated within the largest and most continuous permafrost region of the planet (Strauss et al. 2017) which contains the largest existing yedoma soil deposits. Yedoma is a Pleistocene-aged soil of organic-rich loess with an average soil-OC content of 2–4 wt%, it contains 50–90% of ground ice and is up to 50 m thick and especially common to the tundra of Far East Siberia (Walter et al. 2006; Jones et al. 2011; Schirrmeister et al. 2013; Murton et al. 2017; Windirsch et al. 2020).
The study area mostly contains flat tundra landscapes and lies 11 m above sea level. In the near vicinity of the field camp the highest elevation point is reached by a 25 m high Late Pleistocene-aged yedoma plateau (van Huissteden et al. 2021). Meteorological data from 2005 to 2020 of the Chokurdakh airport weather station (WMO number 21946) show that the daily mean air temperature is − 11.5 °C while the coldest month is January (mean − 32.6 °C) and the warmest month is July (mean 10.4 °C) (https://rp5.ru/Weather_archive_in_Chokurdakh_(airport), accessed 10 Oct 2022). Stationary water bodies like ponds and lakes typically have frozen surfaces from November until April in the study area.
The wider area of the Kytalyk field site is covered by large numbers of ponds and lakes (30%) and drained lake basins (38%) (Siewert et al. 2015). Low-lying areas (e.g. drained lake basins) are mainly covered by characteristic tundra vegetation of Betula nana, mosses and lichens; elevated areas (e.g. yedoma plateaus) are dominated by tussock-sedge (Eriophorum vaginatum); water-locked depressions (e.g. pond areas) are dominated by Sphagnum spp., Eriophorum angustifolium and Carex spp. (Iturrate-Garcia et al. 2020; Magnússon et al. 2021).
The maximum winter ice thickness of water bodies in the study area rarely exceeds 2 m (Duguay et al. 2003; van Huissteden 2019) and maximally reaches 3 m according to local sources. The floating-ice lake of this study has a total surface area of 0.51 km2 and reaches a maximum water depth of 6.9 m (Fig. 1, Supplementary Fig. S1a, b). It is mostly surrounded by peaty tundra shorelines towards the south and west but also borders a Late Pleistocene-aged yedoma plateau along its northwestern slope (Fig. 1) where yedoma is actively eroded (Supplementary Fig. S1b). At the yedoma erosion site massive ground ice and yedoma deposits crop out at the surface. In the summer months blocks of yedoma soil and massive ground ice of several meters in diameter slump and slide into the floating-ice lake. The smaller bedfast-ice lake of this study is located 1.5 km north of the floating-ice lake, has a surface area of 0.14 km2 and a maximum water depth of 2.8 m; thus, most of the lake is shallower than 2 m (Fig. 1, Supplementary Fig. S1c), thereby it classifies as a bedfast-ice lake.
In contrast, the bedfast-ice lake is exclusively surrounded by a low-lying and marshy tundra landscape with peaty soil. Both lakes are located in hydrologically closed depressions and are not connected to rivers or streams. The use of the terminologies bedfast- and floating-ice lake is no interpretive statement towards the sediment or carbon dynamics in the lakes, but simply scientific nomenclature.
Sampling
In the summer of 2015 (14–19 July), lake depth measurements were taken with a Humminbird PiranhaMAX 160 fish finder and a Garmin GPS device (Fig. 1), bathymetry maps were created following Meisel et al. (2021). Along the shoreline of the floating-ice lake three soil samples were collected (Fig. 1; Table 1) from the tundra surface (S1, 0–5 cm depth) and the actively eroding yedoma permafrost cliff (S2 and S3, outcropping cliff face).
In the winter of 2016 (1–6 November), sediment cores were collected from both lakes with a UWITEC gravity corer from the frozen lake surfaces. Three sediment cores (F1–F3) were retrieved at the floating-ice lake. One sediment core (B1) was retrieved at the bedfast-ice lake (Fig. 1,Table 1). At each coring site, a pair of two sediment cores was taken < 1.5 m apart. One core from each site was used for sediment sampling and the other for porewater extractions. After sample recovery, excess lake water was slowly drained from the PVC tubes above the collected sediment to preserve the sediment-water interface. At the sediment-water interface and the bottom the cores were carefully sealed with rubber caps and tape without trapping air pockets. The sediment cores were horizontally stored at 4–7 °C. Sediment porewater samples for DOC analyses were extracted and filtered (0.12–0.18 μm) in the field station within hours after sediment core collection at a 10 cm resolution with 5 cm long, hydrophilic, porous polymer MOM rhizons (Rhizosphere Research Products B.V.) and pre-evacuated vials following Meisel et al. (2021). The porewater samples were additionally treated with potassium iodide (KI) to prevent microbial activity.
The sediment cores and water samples were shipped at 4–7 °C to the laboratories of the Vrije Universiteit Amsterdam where they were stored dark and refrigerated at 4 °C. Due to cargo irregularities and resulting delays, the sediment cores could not be further processed until early 2018. During the transit period, the samples were kept dark and cooled.
Core scanning analysis
At the Royal Netherlands Institute for Sea Research (NIOZ) the sediment cores were split open horizontally and XRF scanning at 10 and 30 kV was carried out with an XRF scanner (Avaatech Analytical X-Ray Technology) on the plain, open sediment surfaces (Hennekam et al. 2019). Amongst other elements, the cores were non-invasively scanned for silicon (Si), aluminum (Al), manganese (Mn) and iron (Fe) at a 1 cm resolution (counts/total counts). Additionally, linescan images were taken along the complete core profiles.
Measurements for MS and ργ-ray were carried out at the sediment laboratory of the VU Amsterdam with a GEOTEK Multi-Sensor Core Logger (MSCL) at a 1 cm resolution. The non-invasive scanning results were calibrated against standardized objects of known magnetic properties and density.
Sediment analysis
Analysis of the relative grainsize composition were carried out with a laser diffraction particle-sizer (Sympatec HELOS KR) at the sediment laboratory of the Vrije Universiteit Amsterdam. Prior to measurement, samples were pre-treated with 5 mL of 30% hydrogen peroxide (H2O2) and brought to boiling point to remove all OM. Subsequently, the samples were soaked in 5 mL of hydrochloric acid (HCl) to dissolve all carbonates and were again brought to boiling point with 300 mg of Na4O2P7 to prevent particle conglomeration (van Buuren et al. 2020).
LOI data were obtained through thermogravimetric analysis (TGA) with a LECO TGA 701 at the sediment laboratory of the VU Amsterdam. The samples were heated in intervals at fixed rates up to 550 °C, while the weight loss through water evaporation and incineration of OM was recorded (van Buuren et al. 2020). The LOI data provided an estimate of the OM amount present in the analyzed sediment.
The porewater content was determined through the difference between wet and dry weights before and after sample drying for at least 48 h at 60 °C (Ackroyd 1957).
OC analyses
The concentrations of DOC and their accompanying δ13CDOC values were measured on the porewater samples. Flocculation of DOC was observed in some samples within days to weeks after collection. In order to quantify the total OC amount that was initially present as porewater DOC (and its δ13C signature) both, the dissolved carbon and the precipitated carbon had to be measured for carbon content and δ13C values following Meisel et al. (2021). The measurement results of the precipitated carbon and the DOC were joined as mass-based averages in order to determine the amount of DOC and its δ13CDOC signature that was present in the porewater prior to flocculation.
The flocculates and the porewater samples were separated by filtering with combusted 0.7 μm GF/F filters. The filters were dried and placed into silver capsules with 25 µL of Milli-Q water and 25 µL of 1 M HCl for 30 min to remove any inorganic carbon compounds. An additional amount of 50 µL of 1 M HCl was added for 30 min; afterwards the samples were dried at 60 °C for 3 h. The filters with the remaining precipitates were combusted and measured for their carbon amounts with a Caro Erba NC 2500 elemental analyzer. The δ13C signatures were measured on a Thermo Finnigan Delta Plus isotope-ratio mass spectrometer (IRMS) coupled to the elemental analyzer. The δ13C measurements were calibrated against internationally recognized standards relative to Vienna Pee Dee Belemnite (VPDB); USGS24 (− 16.05 ± 0.07‰ VPDB), USGS40 (− 26.24 ± 0.04‰ VPDB), USGS41 (+ 37.76 ± 0.05‰ VPDB) and IAEA-CH-7 (− 32.15 ± 0.05‰ VPDB) (Coplen 1996; Qi et al. 2003). Additionally, two in-house standards of glutamic acid (− 24:08‰) and birch leaf (− 27:74‰) were used. The analyses were carried out at the Systems Ecology laboratory at the Vrije Universiteit Amsterdam.
The DOC and δ13CDOC analyses of the sediment porewater were carried out at the laboratory of the KU Leuven in Belgium with an Aurora 1030 W TOC carbon analyzer (OI Analytical) coupled to a Thermo Delta V Advantage IRMS (Meisel et al. 2021; Morana et al. 2015).
Briefly dissolved inorganic carbon was first removed by adding 10% H3PO4 and stripping with He as carrier gas. Afterwards DOC was oxidized by adding 5% sodium persulfate (Na2O2S8) in a reaction at 97 °C for 10 min. The resulting CO2 was transferred to the IRMS after cryofocussing in a liquid N2 trap. The measurements were calibrated against two isotope standards at different carbon concentrations (IAEA-CH-6, − 10.449 ± 0.033‰ VPDB and an in-house sucrose standard − 26.99‰).
The δ13Corg analyses were carried out with a FlashEA 1112 NC series elemental analyzer coupled to a Thermo Finnigan DELTAplusXP IRMS. For the analysis, the sediment samples were weighted into silver capsules and desiccated with 37% HCl for 12 h. Prior to analysis the samples were wrapped into tin capsules. The δ13Corg measurements were calibrated against the internationally recognized standards USGS24 (− 16.05 ± 0.07‰ VPDB), USGS40 (− 26.24 ± 0.04‰ VPDB), and USGS41 (+ 37.76 ± 0.05‰ VPDB) (Coplen 1996; Qi et al. 2003). The analysis was carried out at the Stable Isotope Laboratory of the Vrije Universiteit Amsterdam.
Radiocarbon dating
The sample preparation for the 14C measurement on bulk samples and macrofossil samples was carried out at the Organic Matter laboratory of the Vrije Universiteit Amsterdam. The macrofossil samples (brown moss leaves and stems) were picked under a microscope from sieved (63 μm) bulk sediment samples soaked in 5% sodium hydroxide (NaOH). The macrofossil samples were prepared with an acid-alkali-acid (AAA) treatment. They were successively soaked with 0.5 M HCl (1 h, 60 °C), Milli-Q water (three rinses), 0.1 M NaOH (1 h, 60 °C), Milli-Q water (three rinses), 0.5 M HCl (1 h, 60 °C) and Milli-Q water (three rinses). The bulk lake sediment and shoreline soil samples were desiccated with fuming HCl (37%) and NaOH (5%) in that order at 60 °C over a period of 3 days for each compound. Finally, the macrofossil and bulk samples were dried at 60 °C (24 h).
The 14C measurements were carried out at the Laboratory for Ion Beam Physics of the ETH Zürich, Switzerland. The bulk samples were directly combusted and measured on a gas-ion-source-equipped MICADAS accelerator mass spectrometer (AMS) (Wacker et al. 2013). The macrofossil samples were graphitized prior to a high-precision measurement with a AMS (Wacker et al. 2010). The three measured 14C ages for the macrofossils of core F2 were calibrated to years before present (cal yr BP) using IntCal20 (Reimer et al. 2020) and the program CALIB 8.1.0 which is based on Stuiver and Reimer (1993). The three measured 14C ages for the macrofossils of core B1 were calibrated to negative cal yr BP (post AD 1950) with the software CALIBomb (Reimer and Reimer 2022) using the Northern Hemisphere Zone 1 (NHZ1) data set (Reimer et al. 2004). This was done to make them better comparable to the other 14C ages which are also displayed in cal yr BP. Bulk sample 14C ages were not calibrated due to their extensive mixing of different 14C sources.
DNA extraction and analysis
A total of 72 sediment samples of circa 200 mg each were aseptically taken from the sediment cores at a 5 cm resolution. Before sampling, the top 1 mm of the exposed sediment surface was removed to avoid cross-contamination. After storage of the samples at −20 °C, DNA extraction was performed with the PowerSoil kit (Qiagen, Hilden, Germany) according to the instructions of the manufacturer at the Department of Ecological Sciences of the Vrije Universiteit Amsterdam. The 16S rRNA gene amplicon sequencing was carried out by Macrogen Inc. (Seoul, South Korea). In short, for bacterial diversity the V3–V4 region of the 16S rRNA gene was amplified by a 25 cycle PCR using universal bacterial primers Bac341F (5′-CCTACGGGNGGCWGCAG-3′) and Bac785R (5′-GACTACHVGGGTATCTAATCC-3′). For the amplification of archaeal sequences the same PCR settings were used with the primers Archf349 (5′-GYGCASCAGKCGMGAAW-3′) and Archr789 (5′-GGACTACVSGGGTATCTAAT-3′) (Klindworth et al. 2013). PCR clean ups, index PCR, adapter ligation and library preparation were done following the 16S rRNA gene Metagenomic Sequencing Library Preparation Part #15044223 Rev. B. The amplicon sequences were sequenced on the MiSeq V2-300cycle sequencing platform generating 7,639,276 archaeal reads and 4,235,199 bacterial reads in total. The QIIME2 (version 2019.7) platform was used for bioinformatic analysis. Demultiplexed bacterial sequences were first trimmed 270 bp on the forward read and 250 bp on the reverse reads, while archaeal sequences were trimmed on the forward and reverse reads to 270 and 230 bp, respectively. DADA2 was used for dereplication of the sequences with using default settings and chimera removal using the consensus mode. Amplicon sequence variants (ASV) were then aligned using MAFFT (Katoh and Standley 2013) and phylogenetic distances were calculate with FastTree (Price et al. 2009). Taxonomic classification of the reads based on the SILVA v128 16S SSU NR database (Yilmaz et al. 2014) using QIIME 2’s scikit-learn naive Bayes machine-learning classifier (Bokulich et al. 2018). At last, ASVs were removed that matched to mitochondrial or chloroplast sequences (Katoh and Standley 2013) and phylogenetic distances were calculated with FastTree (Price et al. 2009). Processing of the microbial composition data was done using phyloseq v1.32 (McMurdie and Holmes 2013). We calculated the Shannon index for each sample and used non-metric multidimensional scaling (NMDS) on the Bray–Curtis dissimilarity measures between samples using the R-package ‘vegan’ v2.5 (Oksanen et al. 2022). We used the graphical function ‘envfit’ to describe correlations between microbial community composition and environmental variables. NMDS analysis is a commonly used statistical approach in environmental community analysis (de Jong et al. 2018; Colby et al. 2020). The main reasons to use NMDS analysis were (i) to compare the composition of the sampled microbial communities and (ii) to test which environmental factors correlate with the observed differences in microbial community composition.
Results
Core descriptions
The sediments of the two lakes noticeably differed visually: while the floating-ice lake cores showed layering, the bedfast-ice lake had very homogenous and dark-brown sediment colors reflecting a high abundance of organic material. The floating-ice lake cores F1 and F3 both showed sporadic and indistinct layering due to variations in SOM content and had dark grayish brown, grayish brown and olive brown colors (Fig. 2) based on the Munsell Soil Color Chart (2009). Core F2 was strongly layered and had clear, distinct boundaries with layer thicknesses from a few mm up to 2 cm, the layering was most prominent between 60 and 16 cm depth (Fig. 2). The sediment colors ranged from grayish brown, dark grayish brown, dark brown, very dark brown to black based on the Munsell Soil Color Chart (2009). The top 16 cm of core F2 were especially rich in organic material and visible plant remains. The lower half of the core (111–60 cm) was considerably more homogeneous and lacked the distinct layering of the upper 60 cm.
Core B1 contained two main sediment facies (Fig. 2): (i) a very homogenous, unstratified, organic-rich, dark brown lake sediment at the top (36–0 cm) and bottom (69–59 cm) of the core and (ii) a gray, homogeneous deposit (59–36 cm) with sharp layer boundaries and strong color contrast to the brown lake sediment above and below. The lake sediment of core B1 was considerably more homogenous and of darker brown than the sediments of the cores F1–F3 from the floating-ice lake.
Plant remains (unidentified branches, strongly broken apart plant residues, plant roots, parts of Betula nana, brown mosses, Sphagnum spp.) as well as small shell fragments of bivalves and freshwater ostracods were found throughout all cores in varying abundances.
Physiochemical sediment properties
The sedimentological and physical analysis showed that mineral components in the lake sediments were generally more abundant in the floating-ice lake while a separate pocket of particularly mineral-rich material was also found in the bedfast-ice lake (Fig. 2). Core F2, from the deepest part of the floating-ice lake, recorded with 38% the highest average clay content in the floating-ice lake compared to the cores F1 (26%) and F3 (23%). The clay content within the F2 core profile more than doubled from the bottom (21%, 101 cm) to the top (50%, 0.5 cm) while elevated sand contents were only found in the lower core section. The shoreline samples (S1–S3) had low clay contents around 30%.
Within the floating-ice lake, the average silt content was lowest at core site F2 (59%). With proximity to the shorelines at core sites F1 (68%) and F3 (71%) silt contents increased. Average sand contents were below 7% across the three floating-ice lake cores. This corresponded with the sand content of 7% at the yedoma plateau shoreline samples S2 and S3. The high sand content of 18% (S1) at the peaty western shoreline was not reflected in the nearby sediment core site F1. However, the high sand content at shoreline site S1 was likely due to the general methodology of the grainsize measurement. For all grainsize analyses the organic material was stripped from the sample and only the remaining mineral components were analyzed. If the high abundance of organic material would have been taken into account, too, the relative abundance of the sand component at site S1 would have been considerably lower.
In core B1 of the bedfast-ice lake the lake sediment (36–0 cm and 69–59 cm) had an average clay content of 60% compared to the average floating-ice lake clay content of 30% (F1–F3). The average silt (37%) and sand contents (3%) in the lake sediment of core B1 were lower than the averages of the floating-ice lake with 65% and 5%, respectively. The pocket with the homogenous deposit (59–36 cm depth) in core B1 was dominated by silt (84%) with low contents in sand (6%) and clay (10%).
The average sediment porewater contents of the floating-ice lake cores F1 (36 wt%), F2 (42 wt%) and F3 (30 wt%) were in a similar range. The average porewater content in the lake sediment of core B1 from the bedfast-ice lake was noticeably higher (49 wt%). The sandy silt pocket in core B1 (59–39 cm) contained the least amount of porewater with an average of 22 wt%.
The average sediment density (1.6 g cm−3) and MS (9 cm3 g−1) were higher in the floating-ice lake than in the lake sediment of the bedfast-ice lake core B1 with 1.3 g cm−3 and 8 cm3 g−1, respectively. The sandy silt pocket of core B1 (59–39 cm) was also distinguishable from the surrounding lake sediment by its higher average sediment density of 1.9 g cm−3 (Fig. 3).
The Si/Al and Mn/Fe ratios of all four sediment cores had low, stable downcore values with two main exceptions (Fig. 3). Firstly, the sandy silt pocket in core B1 of the bedfast-ice lake had a considerably higher Si/Al ratio with an average value of 14 in comparison to the surrounding core B1 lake sediment with an average value of 8. Secondly, there was a strong difference in the Mn/Fe ratio within core F2, the lower core half (110–57 cm) had an average value of 0.02 while the top half (57–0 cm) had a significantly higher average value of 0.14.
Sedimentary and dissolved organic matter
SOM content and porewater DOC concentrations were higher in the bedfast-ice lake in comparison to the floating-ice lake. The shoreline samples from the floating-ice lake significantly varied in their LOI values. Sample S1 from the peaty, western shoreline was almost entirely made up of OM with a LOI value of 73.3 wt% while the samples from the eastern shoreline with the eroding yedoma plateau (S2 and S3) were both below 6 wt%. The low OM content at the yedoma permafrost cliff was also reflected in the LOI values of the sediment cores F1–F3 of the floating-ice lake with an average LOI for each core below 8 wt% (Fig. 4).
The lake sediment of core B1 from the bedfast-ice lake had a considerably higher average LOI value with 28 wt% while the sandy silt pocket of core B1 had an average of only 3 wt%. The differing amounts of SOM in the two different lakes were even stronger pronounced in the sediment porewater DOC concentrations. The combined average porewater DOC concentration across all three floating-ice lake cores (F1–F3) was 56 mg L−1 while the lake sediment of core B1 (35–5 cm) had an average of 220 mg L−1 (Fig. 4). No or insufficient amounts of porewater were extracted from the sandy silt pocket of Core B1. In all four cores DOC concentrations increased with sediment depth.
Stable carbon isotope ratios of DOC and SOC in lake sediments
The δ13Corg values across the three cores of the floating-ice lake followed a general pattern from high values at the core bottom towards lower values at the core top (Fig. 4). The shoreline samples also differed strongly in their δ13Corg values from each other. Sample S1 from the peaty, western shoreline had the lowest δ13Corg value with − 27.9‰, while the two shoreline samples S2 and S3 from the yedoma permafrost cliff had higher values of − 26.0 and − 25.8‰, respectively. The difference in δ13Corg signatures between the shoreline samples S1 (peaty, west) and S2–S3 (yedoma, east) near the floating-ice lake was also reflected in the δ13Corg values of the three sediment cores with proximity (lower values) and distance (higher values) to the different shorelines. Within the floating-ice lake core F1 had the lowest average δ13Corg value (− 28.6‰), core F2 had an average value of − 28.2‰ and core F3 had the highest average δ13Corg value with − 27.0‰. The average δ13Corg value in the lake sediment of core B1 from the bedfast-ice lake was considerably lower with − 30.1‰ in comparison to the combined average δ13Corg value of the cores F1–F3 (− 27.9‰). The sandy silt pocket of core B1 had an average δ13Corg value of − 29.1‰ (Fig. 4).
The porewater δ13CDOC profiles of the three cores in the floating-ice lake generally followed the same trend as the δ13Corg profiles with high values at the core bottom and low values at the core top. The highest average porewater δ13CDOC value was detected in core F3 with − 26.3‰, core F1 had an average of − 28.6‰ and core F2 had the lowest average with − 27.7‰. The average porewater δ13CDOC value in the lake sediment of core B1 was − 28.8‰, this was considerably lower than the combined floating-ice lake δ13CDOC average of − 27.1‰. Additionally, δ13CDOC lake water samples were analyzed for coring site F2 with − 28.2‰ and coring site B1 with − 29.3‰ (Fig. 4). Generally, higher SOM abundance appeared to correlate with higher DOC concentrations (Fig. 5a). Similarly, a direct relationship of higher δ13CDOC values with elevated δ13Corg values was also observed (Fig. 5b).
The value ranges of δ13Corg and δ13CDOC in the floating-ice lake developed mostly independent of SOM (LOI) abundances and DOC concentrations (Fig. 6a, b). The opposite trend was observed in the bedfast-ice lake where a larger variability in SOM (LOI) and DOC values did not appear to impact the value range of δ13Corg and δ13CDOC (Fig. 6a, b).
Radiocarbon ages of lake sediments
The most noticeable difference between the two lakes was the presence of young SOC in the bedfast-ice lake sediment, while the floating-ice lake sediment was dominated by considerably older SOC (Fig. 2; Table 2). The youngest bulk 14C age from the lakes was recorded at the top of sediment core B1 in the bedfast-ice lake with 1655 ± 60 yr BP, while the bulk average 14C age from the three core tops of the floating-ice lake cores was much older at 4800 ± 490 yr BP (1σ, n = 3).
Furthermore, two macrofossil 14C age profiles were collected from the cores F2 and B1 for comparison of the lake ages. Core F2 had a chronological macrofossil 14C age profile from the bottom to the top with age ranges of 1611–1516 cal yr BP (111 cm), 1356–1300 cal yr BP (79 cm) and 956–902 cal yr BP (1 cm). The macrofossil 14C age profile of core B1 from the bedfast-ice lake contained contemporary carbon, the yielded 14C ages and age ranges were of modern origin (post AD 1950) with − 5 cal yr BP (67 cm), − 67 to − 69 cal yr BP (32 cm) and − 50 to − 51 cal yr BP (1.5 cm).
The bulk shoreline sample S1 from the peaty western shoreline of the floating-ice lake yielded a 14C age of 3475 ± 70 yr BP. The two bulk samples S2 and S3 from the yedoma permafrost cliff along the eastern shoreline of the same lake resulted in significantly older 14C ages of 17590 ± 130 yr BP and 28170 ± 290 yr BP, respectively.
Microbial diversity of two contrasting lakes
The NMDS of community distance matrices showed that the bacterial and archaeal community compositions clearly differed between the two lakes (Fig. 7).
The bacterial community composition was most influenced by Mg (r2 = 0.58), water depth (r2 = 0.56), Al (r2 = 0.52), and Cr (r2 = 0.42) (Fig. 7, Supplementary Table S1). The environmental parameters with the strongest correlation for the archaeal community composition were Cl (r2 = 0.46), Mg (r2 = 0.45), Rh (r2 = 0.45) and Al (r2 = 0.42) (Fig. 7, Supplementary Table S1). Overall, water depth and elemental composition appeared as the strongest factors for inter-lake microbial community diversity. It is noteworthy, that the sediment depth also appeared to strongly impact the archaeal and bacterial community composition in the floating-ice lake (especially cores F1 and F2) as indicated by the elongated cluster shapes which successively follow the sampling depth (Fig. 7). These observations were also supported by noticeable differences in the Shannon Diversity Index in both, the archaeal and bacterial communities, of the two lakes (Supplementary Fig. S2).
The distribution of the different archaeal taxonomic levels of phylum (Supplementary Fig. S3), class (Supplementary Fig. S4), order (Supplementary Fig. S5), family (Supplementary Fig. S6), and genus (Fig. 8) are also displayed in more detail. In addition, the distribution of the anaerobic methane oxidizing archaeon Candidatus ‘Methanoperedens’ (Supplementary Fig. S7) is shown separately. The distribution of the bacterial taxonomic levels of phylum (Supplementary Fig. S8), class (Supplementary Fig. S9), order (Supplementary Fig. S10), family (Supplementary Fig. S11) are also displayed in detail in the supplementary figures. In addition, the aerobic bacterial methane oxidizers of the Methylomonadaceae family (Supplementary Fig. S12) are shown separately.
We observed 1142 bacterial ASVs across all samples. The bacterial communities were dominated by Proteobacteria (44.0%), Bacteroidota (23.3%), Chloroflexi (5.9%), and Acidobacteriota (3.0%) across all sediment cores (Supplementary Fig. S8). In the three floating-ice lake sediment cores the most abundant bacterial orders were Burkholderiales (36.0%), Bacteroidales (13.0%), Sphingobacteriales (4.1%), Caulobacterales (3.1%), Spirochaetales (3.0%), and Campylobacterales (3.0%) while in the bedfast-ice lake the orders of Burkholderiales (31.5%), Bacteroidales (21.7%), Flavobacteriales (7.4%), Anaerolineales (4.9%), and Pseudomonadales (3.3%) were most dominant (Supplementary Fig. S10). We detected sequences of the aerobic methanotrophic genus Methylobacter of the Methylomonadaceae family in all sampled cores (Supplementary Figs. S11–12).
The archaeal community was dominated by Euryarchaeota (49.0%), Bathyarchaeota (26.7%), Woesearchaeota (DHVEG-6) (14.4%), Thaumarchaeota (3.8%), and Altiarchaeales (1.3%) (Supplementary Fig. S3). However, the bedfast-ice lake samples showed a significant difference in their archaeal community composition compared to the floating-ice lake (envfit; P < 0.05, Figs. 7 and 8). We observed several methanogenic orders, including, Methanomicrobiales and Methanosarcinales (Supplementary Fig. S5). The abundance of these orders varied strongly, for example for Methanosarcinales, with 77.2% in core B1 at 50 cm depth (sandy silt), and 13.4% in sediment core F1 at 55 cm depth (Supplementary Fig. S5).
In both lakes, aceticlastic Methanosaeta, aceticlastic and methylotrophic Methanosarcina and hydrogenotrophic methanogens were observed in the methanogenic communities (Fig. 8). The methanogenic communities of the bedfast-ice lake and floating-ice lake differed in the most abundant methanogenic genera.
In the bedfast-ice lake the methanogenic community was dominated by the hydrogenotrophic Rice Cluster II, Methanosaeta, Methanosarcina and Methanobacterium, while the cores from the floating-ice lake showed a dominance of Methanoregula, Methanosaeta, Rice Cluster II and Methanomicrobiaceae (Fig. 8).
In the bedfast-ice lake core B1, the archaeal community profiling also showed the presence of the anaerobic methanotrophic archaeon Ca. ‘Methanoperedens’ with varying relative abundances of 1.6% (0.5 cm, lake sediment) and 65.8% (50 cm, sandy silt) within the Euryarchaeota (Fig. 8, Supplementary Fig. S7). Ca. ‘Methanoperedens’ was also present in the top 10 cm of core F3, but especially in the top 30 cm of core F2 (Fig. 8 and S7). These archaea oxidize methane at the expense of nitrate, Fe(III) or Mn(IV) (Haroon et al. 2013; Cai et al. 2018; Leu et al. 2020); from the phylotype, however, it was not possible to deduce which substrate they used at this particular site. However, Ca. ‘Methanoperedens’ was mostly absent or present in low abundances (< 1%) in 48 out of 56 floating-ice lake samples (Fig. 8 and S7). No other archaeal methanotrophs were found.
Discussion
Lake sediment dynamics
The visual sediment properties within the floating-ice lake (F1–F3) are variable due to different proximities of the individual coring sites to the shorelines (peaty vs. eroding yedoma permafrost cliff) and differing lake depths (Fig. 1). The biogeochemical properties in the sediments of the bedfast-ice lake (B1) and the floating-ice lake (F1–F3) additionally differ. Partially, this is likely due to the different environmental conditions and temperatures at the lakebeds due to the presence or absence of a talik.
One main difference in sedimentation between the core sites is the high average clay content at site F2 (37.8 ± 9.8%, n = 15) in comparison to the cores F1 (26.4 ± 5.0%, n = 10) and F3 (22.5 ± 4.8%, n = 10) within the floating-ice lake. This difference is likely due to an increased share of suspension-driven particle deposition at the deep core site F2 opposed to the transport of larger sediment particles through wave-induced motion that is naturally more pronounced at the shallower core sites F1 and F3 (Fig. 2). The suspension-driven sedimentation at coring site F2 is also a direct effect of the longer distance to the shorelines (Fig. 1). Over time, the floating-ice lake steadily grew through horizontal shoreline erosion and subsidence through vertical talik growth. At a certain critical water depth suspension-driven clay sedimentation became dominant at the F2 core site which is visible through an increased entry of the clay component and a decrease in sand particles from 60–0 cm depth (Fig. 2).
Ratios of Mn/Fe are widely used in lake studies as semi-quantitative proxies for past changes in redox and hypolimnic conditions (Simola 1983; Bouchard et al. 2011; Biskaborn et al. 2013) since both Mn and Fe are highly redox-sensitive (Davison 1993; Bouchard et al. 2011). Usually, the presence of Mn in lake sediments indicates well-oxygenated conditions of bottom waters and sediment surfaces (Davison 1993) where Mn-bearing minerals authigenically precipitate and accumulate (Bouchard et al. 2011). In contrast, the presence of Mn in core F2 (57–0 cm, 6.5 m water depth) might be an indication for seasonally hypolimnic conditions in winter near the deepest point (6.9 m) of the floating-ice lake (Fig. 3). Mn-bearing minerals at the lakebed would not be stable in stratified and hypolimnic conditions and dissolve in the absence of oxygen. A process called ‘geochemical focusing’ during which cold and heavy bottom water enriches in dissolved Mn at the deepest part of a lake with Mn from the shallower lake sections (Schaller and Wehrli 1996) could provide an explanation. During spring melt, ice breakup and incipient wave motion, oxygen is reintroduced to the bottom water and the dissolved Mn might precipitate as part of various compound minerals (Davison 1993; Scholtysik et al. 2020; Makri et al. 2021). With high sedimentation rates through shoreline erosion, such precipitated Mn-bearing minerals might be quickly buried in the lake sediment. Across all four sediment cores of this study, Mn was only detected in considerable amounts at this deepest part of the floating-ice lake at core site F2 (57–0 cm). This suggests that the Mn/Fe ratio may here be an indicator for at least seasonally anoxic conditions (Fig. 3), however, more data are needed to confirm this hypothesis.
Another interesting feature is the sandy silt pocket that was deposited in the bedfast-ice lake at coring site B1. Since the sandy silt pocket is under- and overlain by lake sediment, a significant physical force had to be present to put the coarse-grained deposit in place. Therefore, it can be assumed that it is of allochthonous origin. Possible explanations for its formation might range from sediment erosion and depositions through ice rafts, sudden lake drainage with erosion and redeposition through strong water currents (Jones and Arp 2015) or cryoturbation processes in the subsoil that pushed the silt deposit into its current position (Ballantyne 2018; French 1996). The origin of this sandy silt deposit is not the focus of this study and is therefore not discussed in further detail.
Si/Al ratios are generally used as indicators for changes in sediment sources over time. A higher value indicates an increase in the relative abundance of silica minerals like quartz (SiO2) which are of terrestrial origin (Aniceto et al. 2014; Ulrich et al. 2021) and usually a by-product of erosion processes. The grainsize distribution, ργ-ray and Si/Al ratio (Fig. 3) all suggest an overall high and steady contribution of mineral, silica-bearing material (likely from the eroding yedoma permafrost cliff) into the floating-ice lake sediment at all three core sites (F1–F3) in comparison to the bedfast-ice lake. The lake sediment of the bedfast-ice lake (B1) contains by comparison much less silica material indicated by a noticeably lower Si/Al ratio, overall lower density (Fig. 3) and lower sand and silt contents (Fig. 2). This observation does not take the sandy silt pocket of core B1 from the bedfast-ice lake into account since it is most likely of allochthonous origin.
Carbon age, origin and degradation in the thermokarst lake sediments
The eroding yedoma permafrost cliff (S2, S3) contains old OC of Late Pleistocene age that slumps into the floating-ice lake (Fig. 1). Similar Late Pleistocene 14C age ranges (20,829 to 31,745 cal yr BP) were measured by Weiss et al. (2015) along the same cliff. Consequently, considerably older SOC is present in the floating-ice lake sediments in comparison to the bedfast-ice lake sediments. This is reflected in both, the bulk and negative macrofossil 14C ages of core B1 (Fig. 2; Table 2). This observation is also supported by Dean et al. (2020) who studied 14C ages of DOC, particulate organic carbon, dissolved CO2 and dissolved CH4 from the same two lakes. The bedfast-ice lake appears to receive the bulk of its SOC from the surrounding peaty soils and tundra vegetation which contains mainly contemporary carbon, which is especially reflected in the negative (post AD 1950) macrofossil 14C ages (Fig. 2; Table 2). The strong differences between the macrofossil and bulk 14C ages from the tops of the cores B1 and F2 are also noteworthy. It shows that younger, contemporary and older, reworked carbon clearly stem from different sources, most likely from the peaty tundra soil and tundra vegetation (contemporary), and the yedoma cliff and other subsoils (old), respectively. Generally, the presence of old OC (to different degrees) at the top of all sediment cores, in both the macrofossil and bulk samples, is a representation of the continuous erosion of old carbon along the lake shorelines and its mixing and deposition in the lake sediments.
The δ13Corg and δ13CDOC values of the bedfast-ice lake are considerably lower than in the floating-ice lake (Fig. 4), and their relationships with the corresponding carbon concentrations and abundances also differ between the two systems (Fig. 6a, b). The concentration of porewater DOC in the sediment across all lakes was found to be strongly related to the amount of available SOM (Fig. 5a), with higher DOC concentrations for the bedfast-ice lake and lower for the floating-ice lake. Similarly, the sediment porewater δ13CDOC values correlated positively to δ13Corg values of the lake sediments (Fig. 5b). The bedfast-ice lake has distinctly different sedimentary carbon characteristics with up to three times higher LOI values as well as DOC concentrations and considerably lower δ13CDOC and δ13Corg values than the cores F1–F3 from the floating-ice lakes (Fig. 6a,b). Interestingly, the measured δ13Corg values of the cores F1 and F2 in the floating-ice lake are rarely lower than − 29‰. A similar observation was also made for lake sediment δ13Corg values from two floating-ice lakes near Utqiaġvik, Alaska (Meisel et al. 2021) (Fig. 5b). These similar δ13Corg values in both the Siberian and Alaskan samples might suggest, that the SOC at these core sites might have undergone a similar degree of degradation under similar floating-ice conditions. This observation is especially noteworthy, since the two Alaskan lakes are not bordering an actively eroding yedoma cliff with Pleistocene-aged OM but have a very similar setting to the Siberian bedfast-ice lake of this study in a flat tundra landscape with characteristic tundra vegetation. This might be an indication that the lake ice regime also plays an important role in how OM in thermokarst lakes is decomposed. Lake sediments in floating-ice lakes remain unfrozen year-round which facilitates OC degradation. Under these conditions the most easily degradable, volatile, and 12C-enriched OC components might be preferentially processed and removed while more 13C-enriched OC might remain in the sediment or porewater (Ågren et al. 1996). Bedfast-ice lakes, on the contrary, have frozen lakebeds in winter. This reduces the overall levels of OC degradation through a more limited time window for microbial activity due to lower soil and sediment temperatures in winter (Thornton et al. 2015; Wik et al. 2016), this might here be reflected in the lower δ13Corg value range of the core B1 lake sediment (− 30.4 to − 30.0‰).
The differences in δ13Corg and δ13CDOC values between both lakes and within the floating-ice lake are certainly also influenced by their SOM origin, which is reflected in the δ13Corg range of the shoreline samples consisting of peat (− 27.9‰) or yedoma (− 26.0‰ and − 25.8‰). The lake sediment of core B1 in the bedfast-ice lake has a low δ13Corg value range (− 30.4 to − 30.0‰, range 0.4‰). This indicates a more homogenous OC source and limited fractionation by OM decomposition. On the contrary, the sediment cores of the floating-ice lake show greater δ13Corg variability (− 29.1 to − 26.5‰, range 2.6‰) which may point towards the input of OC from different and heterogeneous sources. A complicating factor is that these different OC sources may already exhibit different degrees of carbon degradation prior to the secondary deposition as lake sediment. Weiss et al. (2015) found that, at the same Kytalyk field site, the soil-OM of the Late Pleistocene yedoma plateau (S2 and S3) has undergone considerably higher degrees of decomposition than the surrounding younger soil-OM of the peaty tundra landscape (S1) based on lower soil-OM contents, lower C:N ratios and higher δ13Corg values. Especially, deeper layers rich in OC, such as buried peat or cryoturbated layers, were relatively well preserved and undecomposed in comparison to the yedoma soils (Weiss et al. 2015).
In summary, the observed patterns in LOI, DOC, δ13Corg and δ13CDOC in the lake sediments of our study can be explained by a combination of different sediment source inputs and varying intensity of (prior or in situ) degradation processes. These differences between the two lakes are summarized in the schematic overview of Fig. 9 which outlines how the different seasons, lake depths and shorelines impact the OC dynamics. Future studies of lake sediments at this field site would benefit from additional data like C:N ratios and molecular analyses to better differentiate the lake sediment composition with regard to potential aquatic primary production of OM in the lake systems and differences in SOM decomposition. To what extent primary production of OM within the lake contributed to the lake SOC pool was not quantified here. Aquatic production in thermokarst lakes can be significant with increases in nutrient supply (Bouchard et al. 2017) and offset the GHG release from the lake systems over millenial timescales (Walter Anthony et al. 2014). However, primary production of high latitude lakes is known to be low due to the cold temperature conditions and short summer seasons (Shaver and Chapin 1991; Hinkel et al. 2003; Lenz et al. 2016) and is therefore unlikely to be a major contributor of OM to the lakebeds. Manasypov et al. (2022) also pointed out that OM input into thermokarst lakes in Western Siberia appeared to be dominated by allochthonous materials that were drowned below the lakebed and eroded along the shorelines.
Differences in microbial communities between two contrasting thermokarst lakes
The bedfast-ice and floating-ice lake show significant differences in their archaeal and bacterial community compositions. Based on the NMDS analysis both communities were significantly influenced by the differences in mineral sediment components (XRF), SOM content (LOI), OC sources (δ13Corg), the lake type (water depth) and sediment depth (Fig. 7). The overarching factors that are most likely to explain the differences in lake sediment microbial community composition are the lake ice regime (i.e., temperature-driven) and the sediment source (i.e., nutrient-driven). Firstly, the lake ice regime determines the prevailing lake sediment temperature throughout the long winter season which is a main driver for sedimentary microbial activity (Wik et al. 2014; Thornton et al. 2015). In floating-ice lakes this is year-round above freezing temperatures, while in bedfast-ice lakes this is only above freezing temperatures in summer. Secondly, the varying sediment sources from eroding shorelines (peaty tundra soil vs. yedoma soil) act as the main nutrient and OM supplies (Fig. 9) and microbial growth is highly dependent on nutrient availability (de Jong et al. 2018). In this study we could, however, not quantify to which degree each of these factors impacted the microbial community composition.
It is also noticeable, that significant shifts in the composition of both, archaeal and bacterial communities appear to take place with increasing sediment depth within each individual core of the floating-ice lake, as displayed by the elongated core clusters (F1-F3) of the NMDS (Fig. 7). This might be an expression of the talik presence and the clearly stratified and heterogenous sediment layers, especially in cores F1 and F2. The same trend cannot be observed for the lake sediment of core B1 from the bedfast-ice lake. Here, a less pronounced down-core profile in microbial community variability is observed, this might be due to the colder environmental conditions, which are here a more restricting factor for microbial growth in the overall more homogenous lake sediments (B1).
Because microbial activity data are not available for this study, any explanations for the observed differences in microbial community compositions between the two lakes remain to a certain degree speculative. However, as there are clear differences in the methanogenic and methanotrophic communities in the lakes, as well as the SOM content, it is likely that methane dynamics in each of the studied lakes are also different. While both lakes harbor archaea capable of aceticlastic and hydrogenotrophic methanogenesis, the genus of Rice Cluster II is more abundant in the bedfast-ice lake (Fig. 8). In contrast, Methanoregula is more abundant in the floating-ice lake (Fig. 8). Sediment incubations from Alaskan thermokarst lakes have indicated, that the abundance of Rice Cluster II and Methanoregula are often related to hydrogenotrophic and methylotrophic methanogenesis (de Jong et al. 2018). However, the presence of Methanosaeta and Methanosarcina could also indicate potential aceticlastic and methylotrophic methanogenesis (Fig. 8). The large diversity of methanogenic species in the two lakes of this study might support the potential capacity for aerobic methanotrophy by Type I methanotrophs, belonging to the family of Methylomonadaceae, and anaerobic methanotrophy by Ca. Methanoperedens species coupled to either nitrate, Fe(III) or Mn(IV) reduction in both lakes. Particularly, in the bedfast-ice lake sequences of the genus Ca. Methanoperedens were highly abundant. Within this genus, Ca. Methanoperedens nitroreducens is commonly observed in thermokarst lake sediments (Matheus Carnevali et al. 2018; de Jong et al. 2018; Kallistova et al. 2021) and has also been associated with high in situ anaerobic methane oxidation rates in sediments of thermokarst lakes (Winkel et al. 2019). Interestingly, the anaerobic methane oxidizers were less abundant in the floating-ice lake, which could indicate a loss of anaerobic methane oxidation under these warmer conditions (Fig. 8). Further studies (incubations, microbial activity, nutrient availability) comparing the different lake types are needed to fully explain the observed differences in microbial community compositions observed in this study.
Conclusions
Here, we investigated two Siberian thermokarst lakes with distinctly different (i) geographic settings (flat tundra vs. yedoma permafrost cliff) impacting the quantity and quality of sedimentary sources, as well as (ii) maximum lake depths (2.8 m vs. 6.9 m) impacting the prevailing ice regime and subsequently lake sediment temperatures in winter.
The floating-ice lake near the permafrost cliff has high contributions in mineral sediments and receives OC of Late Pleistocene age while the bedfast-ice lake is likely dominated by soil-OM of modern origin. The δ13Corg and δ13CDOC values of the floating-ice lake are higher than in the bedfast-ice lake, which we interpret as an indication for the presence of more degraded SOC in the floating-ice lake sediment likely due to both, higher rates in (microbial) OC degradation, and the input of older, already degraded OC from an eroding yedoma shoreline.
The diversity in geochemical parameters and carbon properties across the two lakes is also well reflected in the microbial community composition. The differences were particularly pronounced in the taxonomic groups responsible for methane cycling, which could potentially influence methane fluxes from thermokarst lakes.
The observed differences across the lakes are likely an expression of two main factors. Firstly, the different lake depths with associated ice regimes (Fig. 9) that likely led to conditions of reduced OM decomposition (bedfast-ice lake) vs. increased OM decomposition (floating-ice lake). Secondly, the source material from the different eroding shorelines (contemporary, organic-rich, peaty soil vs. Late Pleistocene-aged yedoma soil) was reflected in the lake sediment composition and thereby also the supply of nutrients and OM (Fig. 9), which are key drivers for the growth of microbial communities. Even though this study cannot quantify to what degree these two drivers impact the carbon dynamics and microbial communities in thermokarst lake sediments, they are likely the keys to understand how thermokarst lakes process OC.
In the future, a rising number of bedfast-ice lakes is expected to shift their ice regime to floating-ice, if the current trajectory of Arctic warming continues (Arp et al. 2012, 2016), this is highly likely to also increase levels of erosion along thermokarst lake shorelines. Both of these developments would likely increase the level to which sedimentary OM decomposition in lake taliks can take place, which in turn might impact the potential for increasing GHG emissions from Arctic thermokarst lakes (Manasypov et al. 2022).
Data availability
The sedimentological, geochemical and physical data of this study are available on DataverseNL (https://doi.org/10.34894/NPT2CF). The microbial data are available on the Sequence Read Archive (SRA) of the National Center for Biotechnology Information (NCBI) under the Bioproject PRJNA889575 (https://www.ncbi.nlm.nih.gov/bioproject/PRJNA889575).
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Acknowledgements
Special thanks are due for the local field support in Siberia to Roman Petrov and Dr. Alexander Kononov from the Institute for Biological Problems of the Cryolithozone, Siberian Branch Russian Academy of Sciences, Yakutsk, Russian Federation and Tatyana Strioekova and her team from the Fisheries and Nature Inspection in Chokurdakh. We want to express our sincere thanks to Richard van Logtestijn from the Systems Ecology department and Suzanne Verdegaal from the Stable Isotope Laboratory both at the Vrije Universiteit Amsterdam for the δ13C analyses on the solid samples. The XRF-scanning and core splitting were supported by Rineke Gieles, Piet van Gaever and Riek Hennekamp at the NIOZ Institute. The grainsize and TGA analyses were supported by Unze van Buren and Martine Hagen from the Sediment Laboratory of the Vrije Universiteit Amsterdam. The DOC analyses were kindly supported by Cedric Morana from the KU Leuven, Belgium. Special thanks for the cargo shipment support go to Natalia Sidorenko from STS Logistics Benelux. Thanks are also due to Maria Scheel for her support with the microbial interpretations and the NMDS. The authors also thank the two anonymous reviewers and the editor Brian Branfireun for their improvements of the manuscript.
Funding
This work was carried out under the program of the Netherlands Earth Science System Centre (NESSC), which was funded by the Dutch Ministry of Education, Culture and Science (OCW) (Grant No. 024.002.001). The authors also thankfully acknowledge the SIAM Gravitation Grant 024.002.002 and the Netherlands Polar Programme (NWO project id 866.16.042).
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The fieldwork was carried out and supported by OHM, JFD, JvH, SK, LBM and AG. The XRF analyses were carried out and processed by OHM and G-JR. The 14C sample preparation, analyses and processing were carried out by LW and OHM. The DOC analyses were carried out by SB and OHM. The microbial analyses were carried out by MHiZ and RR and interpreted by RR, MHiZ and CUW. The manuscript and figures were written and compiled by OHM and RR with contributions from all co-authors.
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Meisel, O.H., Rijkers, R., Dean, J.F. et al. Geochemical, sedimentological and microbial diversity in two thermokarst lakes of far Eastern Siberia. Biogeochemistry 165, 239–263 (2023). https://doi.org/10.1007/s10533-023-01076-1
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DOI: https://doi.org/10.1007/s10533-023-01076-1