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ORIGINAL RESEARCH article

Front. Earth Sci., 18 June 2021 | https://doi.org/10.3389/feart.2021.681511

Paleo-Ecology of the Yedoma Ice Complex on Sobo-Sise Island (EasternLena Delta, Siberian Arctic)

  • 1Alfred Wegener Institute Helmholtz Centre for Polar and Marine Research, Potsdam, Germany
  • 2PaleoData Lab, Institute of Archaeology and Ethnography SB RAS, Novosibirsk, Russia
  • 3Biological Institute, Tomsk State University, Tomsk, Russia
  • 4Institute of Geosciences, University of Potsdam, Potsdam, Germany
  • 5Research Laboratory of Palaeoclimatology, Palaeoecology, Palaeomagnetism, Kazan (Volga Region) Federal University, Kazan, Russia
  • 6Faculty of Geography, Herzen State Pedagogical University of Russia, St. Petersburg, Russia
  • 7Melnikov Permafrost Institute Siberian Branch of the Russian Academy of Science, Yakutsk, Russia
  • 8Department of Cryolithology and Glaciology, Faculty of Geography, Lomonosov Moscow State University, Moscow, Russia
  • 9Institute of Biochemistry and Biology, University of Potsdam, Potsdam, Germany
  • 10Department of Paleontology, Faculty of Geology, Lomonosov Moscow State University, Moscow, Russia
  • 11Department of Polar Geography, Arctic and Antarctic Research Institute, St. Petersburg, Russia
  • 12Institute of Earth Sciences, Petersburg State University, St. Petersburg, Russia

Late Pleistocene permafrost of the Yedoma type constitutes a valuable paleo-environmental archive due to the presence of numerous and well-preserved floral and faunal fossils. The study of the fossil Yedoma inventory allows for qualitative and quantitative reconstructions of past ecosystem and climate conditions and variations over time. Here, we present the results of combined paleo-proxy studies including pollen, chironomid, diatom and mammal fossil analyses from a prominent Yedoma cliff on Sobo-Sise Island in the eastern Lena Delta, NE Siberia to complement previous and ongoing paleo-ecological research in western Beringia. The Yedoma Ice Complex (IC) cliff on Sobo-Sise Island (up to 28 m high, 1.7 km long) was continuously sampled at 0.5 m resolution. The entire sequence covers the last about 52 cal kyr BP, but is not continuous as it shows substantial hiatuses at 36–29 cal kyr BP, at 20–17 cal kyr BP and at 15–7 cal kyr BP. The Marine Isotope Stage (MIS) 3 Yedoma IC (52–28 cal kyr BP) pollen spectra show typical features of tundra–steppe vegetation. Green algae remains indicate freshwater conditions. The chironomid assemblages vary considerably in abundance and diversity. Chironomid-based TJuly reconstructions during MIS 3 reveal warmer-than-today TJuly at about 51 cal kyr BP, 46-44 and 41 cal kyr BP. The MIS 2 Yedoma IC (28–15 cal kyr BP) pollen spectra represent tundra-steppe vegetation as during MIS 3, but higher abundance of Artemisia and lower abundances of algae remains indicate drier summer conditions. The chironomid records are poor. The MIS 1 (7–0 cal kyr BP) pollen spectra indicate shrub-tundra vegetation. The chironomid fauna is sparse and not diverse. The chironomid-based TJuly reconstruction supports similar-as-today temperatures at 6.4–4.4 cal kyr BP. Diatoms were recorded only after about 6.4 cal kyr BP. The Sobo-Sise Yedoma record preserves traces of the West Beringian tundra-steppe that maintained the Mammoth fauna including rare evidence for woolly rhinoceros’ presence. Chironomid-based TJuly reconstructions complement previous plant-macrofossil based TJuly of regional MIS 3 records. Our study from the eastern Lena Delta fits into and extends previous paleo-ecological Yedoma studies to characterize Beringian paleo-environments in the Laptev Sea coastal region.

Introduction

Late Pleistocene permafrost of the Yedoma type is a prominent and widespread permafrost feature that formed during sea-level lowstands on vast areas of the unglaciated Beringian lowlands and on the nowadays flooded East Siberian shelf between the Laurentide to the east and the Scandinavian ice sheets to the west during marine isotope stages (MIS) 4 to 2 (Hopkins, 1959). Ice Complex (IC) permafrost aggradation took place by evolving ice-wedge polygons forming the so-called Yedoma IC (Katasonov, 1954/2009) of up to 50 m thick sequences. In West Beringia, the main area of potential Yedoma IC distribution includes the now submerged East Siberian shelf and Arctic coastal lowlands from Taymyr Peninsula to Chukotka (Grosse et al., 2013), although it is also described from interior regions of Central Yakutia (Soloviev, 1959) and the Yana Upland (Kunitsky et al., 2013; Opel et al., 2019). In East Beringia, muck deposits comparable in genesis to those of Siberian Yedoma IC occur at the Arctic Foothills, on Seward Peninsula, in interior Alaska and in the Yukon Territory (Péwé, 1955; Kanevskiy et al., 2011; Schirrmeister et al., 2016).

Large syngenetic ice wedges, ice-oversaturated fine-grained deposits and a considerable organic content characterize Yedoma IC deposits (Schirrmeister et al., 2013). The organic component of Yedoma IC preserves floral and faunal fossils, and thus evidence of late Pleistocene environmental and climatic conditions of Beringia and their variations over time (e.g., Sher et al., 2005). The Yedoma permafrost archive has been widely used to infer rather qualitative than quantitative paleo-environmental reconstructions by applying numerous fossil records such as those from Mammoth fauna bones (e.g., Kuznetsova et al., 2019), insect remains (e.g., Sher et al., 2005), plant macro-remains (e.g., Kienast et al., 2005), pollen (e.g., Andreev et al., 2011), testate amoebae (e.g., Bobrov et al., 2004) or ostracods (Wetterich et al., 2005). Generally, the combination of several fossil proxy records from a certain permafrost sequence largely enhances its significance for paleo-ecological interpretations (e.g., Kienast et al., 2011; Wetterich et al., 2018). In this context, the present study combines a pollen-based paleo-vegetation reconstruction with lacustrine chironomid and diatom analyses. While pollen analysis provides detailed insights into vegetation dynamics over time with high comparability to other regional pollen records (Andreev et al., 2011), lacustrine fossil proxies highlight on-site freshwater conditions by habitat preferences of certain species, and species diversity (Palagushkina et al., 2012; Hoff et al., 2015; Palagushkina et al., 2017; Biskaborn et al., 2019). If specimen counts per sample are sufficiently high, numerical reconstructions of certain ecological parameters are deducible such as mean air temperature of the warmest month (TJuly), water depth, ion content and pH (Nazarova et al., 2013; Nazarova et al., 2017a; Pestryakova et al., 2018).

The study area on Sobo-Sise Island in the eastern Lena Delta fits into and extends previous paleo-ecological Yedoma studies in the Laptev Sea coastal region including the Lena Delta and Bykovsky Peninsula (Schirrmeister et al., 2002a; Schirrmeister et al., 2003; Bobrov et al., 2004; Kienast et al., 2005; Sher et al., 2005; Wetterich et al., 2005; Wetterich et al., 2008a; Wetterich et al., 2011; Schirrmeister et al., 2011a; Schirrmeister et al., 2011b; Wetterich et al., 2014; Schirrmeister et al., 2017; Khazin et al., 2019; Kuznetsova et al., 2019; Wetterich et al., 2019a), which examined floral and faunal fossils. These studies characterized the West Beringian environments generally as tundra-steppe covering a considerable patchiness of different habitats that created a landscape mosaic of dry uplands and slopes, wetlands, floodplains and shallow waters of low-center polygon tundra as especially well seen in insect and plant macrofossil data (Kienast et al., 2005; Sher et al., 2005; Wetterich et al., 2008a). However, aquatic conditions in West Beringia during MIS 3-2 are rather poorly constrained yet and are mainly based on findings of: 1) green algae Botryococcus and Pediastrum remains in palynological samples, 2) submerged and water plant macro-fossils, and 3) ostracod valves in Yedoma IC deposits. Other aquatic fossils such as from branchiopods, cladocerans and chironomids have only little been studied yet in Yedoma IC deposits (Neretina et al., 2020; Rogers et al., 2021). Numerical reconstructions of paleo-climate parameters such as summer air temperature and annual precipitation in West Beringia are scarce (Andreev et al., 2011) or poorly developed in case of ice-wedge stable water isotopic composition reflecting winter climate (Opel et al., 2018; Wetterich et al., 2021). Pitulko et al. (2017) present TJuly and precipitation reconstructions from 34 to 10 kyr BP for the western part of the Yana-Indigirka Lowland (east of our study region), while from the Bykovsky Yedoma archive only two points in time, at around 48 and 35 kyr BP, provide estimated TJuly values based on plant macrofossils (Kienast et al., 2005). Further quantitative paleo-proxy reconstruction data are lacking for the Laptev Sea coastal region. Thus, additional information is mandatory to better constrain the West Beringian climate and environment through stadial-interstadial as well as glacial-interglacial transitions.

In addition to a recent study of the cryostratigraphic inventory of the Sobo-Sise Yedoma cliff (Wetterich et al., 2020) and to previous paleo-environmental Yedoma research in the Laptev Sea coastal region, the present study aims

1) To provide detailed pollen-based reconstructions of paleo-vegetation in combination with occasional bone findings of the Mammoth fauna;

2) To reconstruct past freshwater lacustrine conditions such as water depth, salinity, pH, and TJuly air temperatures based on chironomid and diatom fossils;

3) To disentangle regional paleo-environmental dynamics in West Beringia by combining the present record with previous research results and interpretations.

Study Site and Previous Research

Sobo-Sise Island in the Eastern Lena Delta

The Lena Delta is the largest delta in the Arctic and occupies about 32,000 km2 (Are and Reimnitz, 2000). It is divided by six major channels (Fedorova et al., 2015) of which the Sardakhskaya Channel drains the eastern part of the delta (Figure 1). Here, on Sobo-Sise Island at the Sardakhskaya Channel Yedoma uplands occupy about 19% of the land surface while most of the island is characterized by permafrost degradation features such thermokarst basins and thermo-erosional valleys of Holocene age (Fuchs et al., 2018). A prominent Yedoma IC remnant at the north-eastern shore of Sobo-Sise Island builds an up to about 28 m high almost vertical cliff (72°32′ N, 128°17′ E) stretching about 1,700 m along the shore (Figure 1).

FIGURE 1
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FIGURE 1. Study area in north-eastern Siberia showing (A) the Lena Delta with key locations, (B) Sobo-Sise Island (image based on Sentinel-2A scene, June 27, 2018) and (C) the Sobo-Sise Yedoma cliff facing the Sardakhskaya Channel (image based on GeoEye-1 scene, July 08, 2014) with positions of the sampled sediment profiles SOB18-01, SOB18-03 and SOB18-06. Panel (A) is based on the semitransparent layer of the ESRI ArcGIS Living Atlas of the World (World Topo Base, 2021) with underlying bathymetry of (IBCAO grid, 2021).

The modern meteorological conditions in the Lena Delta are monitored on Samoylov Island where a mean annual air temperature of −12.3°C, mean July air temperature of 9.5°C and mean February air temperature of −32.7°C are recorded for the last two decades (1998–2017; Boike et al., 2019), while the mean annual rainfall amounts to 169 mm and the mean annual winter snow cover to 0.3 m (2002–2017; Boike et al., 2019).

On Sobo-Sise Island, dwarf shrub-moss-tussock tundra plant communities inhabit the structured land surface of Yedoma uplands, pingos, floodplains, and thermokarst basins. Species of the Salix, Dryas, Saxifraga, Polygonum, Carex, Poa, Trisetum, Equisetum, and Luzula genera, and unspecified mosses and lichens are common (Raschke and Savelieva, 2017).

Evolution of the Sobo-Sise Yedoma Sequence

The Sobo-Sise Yedoma cliff attracts scientific attention due to both, the exceptionally high and vertically exposed permafrost archive spanning MIS 3-1 (Wetterich et al., 2020) and the ongoing rapid thermo-erosion releasing substantial amounts of organic matter into the Lena River (Fuchs et al., 2020).

The geochronological record of the Sobo-Sise Yedoma spans the last 52 cal kyr BP based on radiocarbon dating and age-height modeling (Figure 2; Wetterich et al., 2020). The permafrost sequence differentiates into three cryostratigraphic units that are MIS 3 Yedoma IC (unit A; 52–28 cal kyr BP), MIS 2 Yedoma IC (unit B; 28–15 cal kyr BP) and MIS 1 Holocene cover (unit C; 7–0 cal kyr BP). The cryostratigraphic sequence of the Sobo-Sise Yedoma cliff is not continuous, but has chronological gaps (hiatuses) at 36–29 cal kyr BP, at 20–17 cal kyr BP and at 15–7 cal kyr BP (Figure 2).

FIGURE 2
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FIGURE 2. Overview of the sampled profiles at Sobo-Sise showing (A) the Yedoma cliff, (B) profiles SOB18-01 and SOB18-03, (C) profile SOB18-06, (D) sampling scheme across the Yedoma cliff and (E) age-height relation of the exposure in meter above river level (m arl) and calibrated radiocarbon ages (redrawn from Wetterich et al., 2020). Note the sampling overlap of the profiles SOB18-01 (circles), SOB18-03 (diamonds) and SOB18-06 (stars) and their alignment to cryostratigraphic units A, B and C. The hollow symbols indicate ages of re-deposited material or infinite radiocarbon ages.

The chronological gaps provide evidence of past changes in climatic conditions as well as in sediment deposition and erosion regimes. Similar observations have been made on adjacent Yedoma IC sites on Bykovsky Peninsula and Kurungnakh-Sise Island (Wetterich et al., 2020). The two older gaps during MIS 3 and MIS 2 are likely related to repeated changes in the regional hydrological systems due to outburst floods of glacial Lake Vitim along the Lena Valley into the Arctic Ocean as proposed by Margold et al. (2018), while the MIS 2-1 gap corresponds to deglacial permafrost thaw (thermokarst) that took place Arctic-wide at the late Pleistocene-Holocene transition.

The Sobo-Sise Yedoma cliff rapidly erodes with a mean annual shoreline retreat rate of up to 9.1 m yr−1 over the last decades (1965–2018; Fuchs et al., 2020). Surface elevation changes due to thaw subsidence on Yedoma uplands range between −2 cm yr−1 (based on Sentinel-1 InSAR, 2017, for the entire Sobo-Sise Island; Chen et al., 2018) and −3.4 cm yr−1 (based on on-site rLiDAR at the studied Yedoma cliff, Günther et al., 2018). Thus, the Sobo-Sise Yedoma IC remnant of today is characterized by substantial and rapid permafrost degradation (Fuchs et al., 2020).

Methods

Fieldwork and Dating

Three vertical sediment profiles were sampled on rope at accessible positions of the Yedoma cliff to cover the entire exposed permafrost inventory (Wetterich et al., 2019b; Figure 2). The frozen samples were obtained using a hammer and axe at 0.5-m resolution. Vertical overlaps of the three profiles guaranteed complete coverage of the exposure (Figure 2D).

The sampling resulted in a total of 61 sediment samples. Upon return to the labs, samples were freeze-dried (Zirbus Subliminator 3–4–5) and split into subsamples for several analyses. Accelerator mass spectrometry (AMS) radiocarbon dating was applied to identified organic macro-remains in 31 sediment samples totaling in 32 radiocarbon dates (Wetterich et al., 2020), which were calibrated using the IntCal13 calibration dataset (Reimer et al., 2013). Ages are given as calibrated years before present (cal yr BP) or calibrated thousand years before present (cal kyr BP). Paleo-ecological analyses were conducted on a sample set of 33 samples from the profiles SOB18-01 (n = 14), SOB18-03 (n = 7) and SOB18-06 (n = 12) covering the entire sequences at resolution of less than 1 m.

Pollen Analysis

The pollen samples (2–6 g of dry sediment) were prepared using standard procedures including treatment with 10% HCl and 10% KOH, sieving (250 mm), treatment with 45% HF, acetolysis, and mounting in glycerin (cf. Fægri and Iversen, 1989). One Lycopodium spore tablet was added to each sample to calculate total pollen and spore concentrations (cf. Stockmarr, 1971). Pollen and spore residues mounted in water-free glycerin were analyzed under a Zeiss AxioImager D2 light microscope at 400 magnification. The identification of pollen and spores was performed using a reference pollen collection and pollen atlases (e.g., Beug, 2004). Non-pollen palynomorphs (NPPs) were identified using descriptions, sketches, and photographs published by van Geel (2001). The percentages of all taxa were calculated based on setting the total of all pollen and spore taxa equal to 100%. The results of pollen analysis are displayed in the pollen diagram produced with the Tilia/TiliaGraph software. The visual definition of the pollen record is supported by cluster analysis in CONISS (Grimm, 2004).

Mammal Bone Analysis

Mammal bone findings in fresh slump debris at the cliff foot were collected in 2018 during fieldwork (Table 1), later on identified, and are currently stored at the Lena Delta Reserve (LDR), Tiksi, Russia. Archive data of late Pleistocene mammal bones from Sobo-Sise Island (Table 1) are available from sampling in 1927 (Zoological Institute Russian Academy of Science - ZIN RAS, Sankt-Petersburg, Russia), in 1990 and 2000 (LDR, Tiksi, Russia) and in 1998 (Collection of the Russian-German “Lena Delta” Expedition, Moscow, Russia), Radiocarbon dates are available for five specimens of these archive collections (Table 2).

TABLE 1
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TABLE 1. List of bone findings of the late Pleistocene Mammoth fauna on Sobo-Sise Island in the eastern Lena Delta.

TABLE 2
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TABLE 2. Radiocarbon ages of Mammuthus primigenius bone fragments from Sobo-Sise Island (Eastern Lena Delta) calibrated using CALIB REV8.2 (Reimer et al., 2020). Results are rounded to the nearest 10 yr for samples with standard deviation in the radiocarbon age greater than 50 yr.

Chironomid Analysis

The treatment of sediment samples for chironomid analysis followed standard techniques described in Brooks et al. (2007). Subsamples of wet sediments were deflocculated in 10% KOH, heated to 70°C for 10 min by adding boiling water and left for another 20 min. The sediment was then passed through stacked 225 and 90 µm sieves. Chironomid larval head capsules (HC) were picked out of a grooved Bogorov sorting tray under a stereomicroscope at 25–40x magnification and were mounted in Hydromatrix two at a time, ventral side up, under a 6 mm diameter cover slip. Chironomids were identified to the highest possible taxonomic resolution following Wiederholm (1983) and Brooks et al. (2007). Information on ecological preferences of identified chironomid taxa was taken from Brooks et al. (2007), Moller Pillot (2009), Moller Pillot (2013) and Nazarova et al. (2008); Nazarova et al. (2011); Nazarova et al. (2015); Nazarova et al. (2017b).

Mean July air temperatures (TJuly) were inferred by using a North Russian (NR) chironomid-based temperature inference model (WA-PLS, 2 component; r2 boot = 0.81; RMSEP boot = 1.43°C) (Nazarova et al., 2015) based on a modern calibration data set of 193 lakes and 162 taxa from East and West Siberia (61–75°N, 50–140°E, TJuly range 1.8–18.8°C) (Nazarova et al., 2008; Nazarova et al., 2011; Nazarova et al., 2015). TJuly for the lakes from the calibration data set was derived from New et al. (2002). The TJuly model previously applied for paleo-climatic inferences in East Siberia and Russian and European Arctic demonstrates high reliability of the reconstructed parameters (Syrykh et al., 2017; Nazarova et al., 2017c; Plikk et al., 2019; Nazarova et al., 2020). Chironomid-based reconstruction was performed in C2 version 1.7.7 (Juggins, 2007). The data were square-rooted to stabilize species variance.

In order to capture the diversity of the chironomid communities that is necessary for a reliable temperature reconstruction we aimed at extracting at least 50 chironomid larval head capsules (HC) from each sample (Heiri and Lotter, 2001; Larocque, 2001), though as low as 30 head capsules can be enough for assessing dominant environmental trends (Quinlan and Smol, 2001). The profiles SOB18-06 and SOB18-01 contained mostly sufficient numbers of HC, apart from the samples SOB18-06-18, SOB18-01-02 and SOB18-01-01, where chironomids were not found. The profile SOB18-03 contained very low concentration of chironomid samples (2–14 HC). Therefore, chironomids from this profile were used for qualitative ecological reconstruction while quantitative air temperature reconstruction should be considered with caution. The reliability of the chironomid-inferred temperature reconstruction was assessed by two methods. First, the percentages of the fossil chironomid taxa that are absent or rare in the modern calibration dataset were calculated. A taxon is considered to be rare in the dataset when it has a Hill’s N2 below 5 (Hill, 1973). The environmental optima of taxa that are rare in the modern dataset are likely to be poorly estimated (Brooks and Birks, 2000). Second, to determine whether the modern calibration models had adequate analogues for the fossil assemblages, the modern analogue technique (MAT) was performed using C2 version 1.7.7 (Juggins, 2007), with squared chord distance as the dissimilarity coefficient (DC) (Overpeck et al., 1985). Confidence intervals were based on minimum DC distance within the calibration sets (Laing et al., 1999). Fossil assemblages above the 95% confidence interval were considered to have no analogues in the calibration set; while assemblages with the confidence interval between 75 and 95% were considered to have fair analogues (Francis et al., 2006; Solovieva et al., 2015; Palagushkina et al., 2017).

Diatom Analysis

Diatom samples were prepared in a water bath following Battarbee (1986). High-refractive Naphrax resin was used for the production of permanent slides. The diatom species identification followed international and Russian literature (Zabelina et al., 1951; Krammer and Lange-Bertalot, 1986; Krammer and Lange-Bertalot, 1988; Krammer and Lange-Bertalot, 1991a; Krammer and Lange-Bertalot, 1991b). Specimen counts followed parallel transects across the slide under light microscope Zeiss Axioplan and immersion oil. However, specimen counts remained generally low and far below 300 individuals per sample that are commonly used for quantitative interpretations and the potential application of transfer functions. Instead, the ecological characteristics of single species findings are described in relation to habitat preference, salinity, pH of the host water, geographical distribution, and water velocity (Barinova et al., 2006) and TJuly (Pestryakova et al., 2018), but should not be overinterpreted due to the limited dataset.

Results

Paleo-Vegetation

The cluster analysis of the Sobo-Sise Yedoma pollen record results in three units, which correspond to the cryolithological units A-C that were previously defined by Wetterich et al. (2020) of MIS 3, MIS 2 and MIS 1 age, respectively (Figure 3).

FIGURE 3
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FIGURE 3. Pollen diagram of the Sobo-Sise Yedoma record. For several taxa the concentrations (Conc.) are given (grain/g x1,000). AP - arboreal pollen, NAP - non-arboreal pollen, NPP - non-pollen palynomorphs.

Pollen spectra of MIS 3 (Unit A, 52-28 cal kyr BP) are characterized by high percentages of herbaceous pollen with the prevalence of sedge (up to 70%) and grass (up to 53%). Deciduous trees and shrubs were represented by Salix whose abundance increased after 39.3 cal kyr BP. Betula sect. Apterocaryon (dwarf birches) and Alnus subg. Alnobetula (shrubby alder species), however, remain in low abundance. Rubus chamaemorus appeared at 44.1 cal kyr BP and became an abundant taxon after 39.3 cal kyr BP and until the Holocene. To estimate the presence of conifers in the past vegetation we have used not only percentages but also estimated the pollen concentrations. These are independent of the total percentage indicator. Only for conifers, the concentration numbers showed a different picture compared to percentages throughout the entire record. While the percentages of Pinus sylvestris in Unit A are similar to its respective concentrations, suggesting its real low abundance in the vegetation, the concentrations of Larix are more representative than the Larix pollen percentages because Larix pollen tends to accumulate directly on the site. The entire record of Unit A reveals both relatively high percentages and concentrations of Picea. Another characteristic feature of Unit A is the constant presence of green algae Botryococcus and Pediastrum remnants; an indicator of freshwater ponds close to the site.

The MIS 2 (Unit B, 28–15 cal kyr BP) pollen spectra are similar to those of Unit A, but differ by lower pollen concentrations, lower abundances of sedge and grass and increased Artemisia pollen. The concentration of Larix decreased. All these features are characteristic for more arid conditions than in Unit A. MIS 2 landscapes in the eastern Lena Delta were dominated by steppe-like communities.

The MIS 1 (Unit C, 7–0 cal kyr BP) pollen composition differs sharply from those of units A and B by increased total pollen concentrations, and high percentages and concentrations of arboreal pollen. The main feature is the dominance of dwarf birch (Betula sect. Apterocaryon) as well as the significant amount of alder (Alnus subg. Alnobetula), and Ericaceae pollen. The percentages of Poaceae, Cyperaceae and Artemisia significantly decreased, while the concentrations of all conifers sharply increased. Green algae are absent in Unit C.

Mammoth Fauna

Bone findings of the Mammoth fauna are commonly rare on Sobo-Sise Island and mostly found below the Yedoma cliff. Only Grigoriev (1988) mentions a “bone horizon” at about 13–15 m arl. In 2018, during fieldwork bones of Mammoth fauna species were found in fresh slump debris well above the beach level are thought to originate from the cliff. According to Kuznetsova et al. (2019) such bones findings are classified as group C bone fossils whose original position can be related to the outcrop above. The preservation of vivianite (bluish crystals and accretions of hydrated iron phosphate that might form under anoxic conditions on bone material; Guthrie, 1990; Rothe et al., 2016) on some bones supports our assumption that the bones originated from the Sobo-Sise Yedoma cliff. In total, 11 bone fragments were obtained (Table 1; Supplementary Table S1) and are currently stored at the Lena Delta Reserve Tiksi (Russia). Six bones belong to Mammuthus primigenius (BLUMENBACH, 1799), three to Rangifer tarandus L., 1758 and one to Bison priscus (BOJANUS, 1827) and Coelodonta antiquitatis (BLUMENBACH, 1799) each. One tusk fragment (SOB18-bone-02; M. primigenius) was radiocarbon dated to 13,668 ± 57 yr BP (16,520 cal yr BP; Table 2; Wetterich et al., 2020).

It should be noted that bones of R. tarandus might belong to modern representatives of this species. Despite the low number of bone findings from the present study, main features of such bone collections of the West Beringian Mammoth fauna (Sher et al., 2005; Kuznetsova et al., 2019) are represented. Those are the prevalence of mammoth bones and the presence of other large grazers such as horse and bison. The finding of woolly rhinoceros remains is somewhat remarkable as it has not been found in the Lena Delta records so far (Wetterich et al., 2008a; Kuznetsova et al., 2019). In addition to the recent bone collection we consider further unpublished data of mammal bones from Sobo-Sise Island stored in several collections in Russia. First bone findings on extinct Mammoth fauna species on Sobo-Sise Island were obtained in July 19–20, 1927 by the Hunting and Fishing Team of the Yakut Expedition (A. Romanov). In total 18 bone samples from Sobo-Sise were transferred in 1928 to the Zoological Institute of the Russian Academy of Sciences (ZIN RAS) in St. Petersburg (Russia). This collection comprises three species that are M. primigenius, B. priscus and Equus ex eg. caballus. Mammoth is represented by 11 bones of which most probably eight belong to the same skeleton (cervical vertebrae, left heel bone and fragments of the lower jaw, tusk, left branch of pelvis, left femur, left humerus) because those were collected at one location - the thawing slope of a conical thermokarst mound (baidzherakh) at a lake shore. Six bison bones (two cervical vertebrae and four skull fragments) and one horse bone (third phalanx) complement this collection (Table 1).

In 1988, the first radiocarbon date on bone material from Sobo-Sise was published where a tusk fragment found in situ at about 13–15 m arl revealed an age of 14,340 ± 120 yr BP (17,490 cal yr BP; GIN-4115) (Grigoriev, 1988). Another mammoth bone found on Sobo-Sise was dated to 24,400 ± 650 yr BP (28,620 cal yr BP; IM-835) although no further information is available (Table 2). Six bones were found on Sobo-Sise in 1998 in course of the Russian-German Expedition “Lena Delta,” of which five belong to mammoth (one skull fragment, two rib fragments and two vertebral fragments) and one to horse (humerus fragment). One mammoth rib fragment (MKh-O621) was radiocarbon-dated to 19,200 ± 220 yr BP (23,180 cal yr BP; GIN-10235) and one mammoth vertebral fragment (MKh-O624) to >45,000 yr BP (GIN-13929, GrA 46013) (Table 2).

The bone collection of the Lena Delta Reserve Tiksi (Russia) contains eight mammoth bones collected on Sobo-Sise in 1990 and identified in 2005 by T.V. Kuznetsova (MSU, Russia) as forearm bones (radius and ulna), two fragments of tibia and fragments of cervical vertebra, vertebra, right branch of pelvis, heel bone. Two more horse bones were found in 2000 and identified as the damaged shoulder blade and the right branch of pelvis. A sample of a mammoth forearm (LDR-O299) from this collection was radiocarbon-dated to 17,070 ± 70 yr BP (20,630 cal yr BP; KIA-32839). The overall collection of Mammoth fauna bones from Sobo-Sise in various years comprises 45 specimens (Figure 4): M. primigenius – 66.7% (30 specimens), B. priscus – 15.6% (7 specimens), E. ex gr. caballus – 8.9% (4 specimens), R. tarandus – 6.6% (3 specimens) and C. antiquitatis – 2.2% (1 specimen) (Figure 4). The sparse available radiocarbon dates of M. primigenius comprise five finite and one infinite ages. Two ages fall into the MIS 3 interstadial period and four into the MIS 2 stadial (Table 2).

FIGURE 4
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FIGURE 4. Percentage of bone findings on Sobo-Sise Island comprising archive and new data. Percentages are given above species names.

Paleo-Limnology

The chironomid record of the Sobo-Sise Yedoma record exhibits three zones, which delineate the cryolithological stratification into three units A-C covering MIS 3 to MIS 1 (Figure 5). The chironomid fauna of the record comprises 39 taxa. The number of chironomid HC per sample varies considerably with highest concentration found in Unit A, while units B and C show relatively low concentrations. All fossil chironomid taxa were represented in the modern training sets. Only three taxa that had only single occurrence in the investigated profiles have Hill’s N2 <5 in the training set and therefore were defined as not well-represented in the NR training sets and model: Orthocladius/Cricotopus (N2 = 1.9 in the SOB samples and 0 in the NR training set), Pseudorthocladius (N2 = 1.8 in the SOB samples and 4.0 in the NR training set), Tanytarsus lactescens-type (N2 = 1 in the SOB samples and 1 in the NR training set). The low representation of these taxa in the SOB profiles does not hamper the quality of the reconstruction. MAT for TJuly reconstruction revealed that the samples from the interval 43.3–42.5 cal kyr BP had no analogues in the calibration set (MAT above 95%; Figure 5). The remaining profile samples have good or fair analogue in the NR training set. The high representation of the taxa in the training set, together with the predominantly good MAT statistics results, indicated that the temperature reconstruction from the investigated profiles is mainly reliable. Samples with poor MAT tests should be interpreted with caution.

FIGURE 5
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FIGURE 5. Chironomid diagram of the Sobo-Sise Yedoma record. HC - head capsule, MAT - Modern Analogue Technique, PCA 1 - first axis of the principal component analysis. The dotted line in the reconstruction TJuly reconstruction indicates the modern value of 11°C. The dotted lines in the MAT indicate the 75% (30.40) and 95% (34.97) confidence intervals. Note that hollow symbols of the reconstructed TJuly are based on low HC concentrations and should therefore be considered with caution.

The MIS 3 chironomid fauna of Unit A (52-28 cal kyr BP) is composed of 36 taxa, while their diversity (N2) varies considerably. Several periods within Unit A exhibit rich chironomid fauna: 52 to 49 cal kyr BP, 48 to 46 cal kyr BP and 43 to 40 cal kyr BP (median N2 = 8.9; Figure 5). The representation of typical aquatic taxa vs. semiterrestrial taxa varies within unit A. Between 52 and 49 cal kyr BP the communities are dominated by taxa characteristic for moderate climatic conditions: Endochironomus albipennis-type, Micropsectra insignilobus-type, Chironomus anthracinus-type, Tanytarsus pallidicornis-type and Cricotopus interectus-type. The reconstructed TJuly varies around modern level (11°C) with one excursion of about 1.5°C above modern TJuly at 50.8 cal kyr BP. The decline of semiterrestrial taxa at the same time might indicate higher water level under relatively warm conditions. Later on, until about 49 cal kyr BP the share of semiterrestrial taxa reaches up to 57% and the reconstructed TJuly declines to about 1°C below modern. Such cooling might have induced shallowing of the water level by reducing the seasonally thawed uppermost ground below the ponds. Between 48 and 38 cal kyr BP, the chironomid fauna is dominated by typical aquatic taxa although chironomid counts and diversity decrease considerably between 46 and 44 cal kyr BP when the reconstructed TJuly rises up to 1.5°C above modern. The period between 44 and 41.5 cal kyr BP is characterized by the highest diversity and concentration of chironomids. The communities are dominated by the Heterotrissocladius grimschawi-type that occurs in oligotrophic lakes and is indicative of moderate conditions with temperature optima of 11–12°C. Reconstructed TJuly slightly varies around modern with warmer-than-today TJuly around 41 cal kyr BP. After 41.5 cal kyr BP, a strong decline of chironomid communities is observed and also reflected in the PCA 1 sample scores. Between 40.4 and 38 cal kyr BP only few chironomid remains have been found. Semiterrestrial taxa disappear around 39 cal kyr BP probably indicating another episode of a higher water level. At 36.7 cal kyr BP no chironomids have been found in the sediments, which probably suggest another dry out. Above the hiatus, the uppermost sample from Unit A (SOB18-03-03) is dated to 28.4 cal kyr BP. Here, the chironomid fauna is poor and is represented mainly by semiterrestrial (Limnophies-Paralimnophies, Metriocnemus eurinotus-type) or phytophilic taxa (Tanytarsini). The reconstructed TJuly is of about 8°C, which is about 3°C below modern TJuly.

The abundance and diversity of chironomids are generally low during MIS 2 (Unit B, 28 – 15 cal kyr BP). Between 27.7 and 23.3 cal kyr BP, the chironomid fauna is dominated by aquatic taxa (Tanytarus mendax-type, Heterotrissocladius grimschawi-type). After 21.8 cal kyr BP the proportion of semiterrestrial taxa rise and taxa characteristic for littoral zone of lakes (Eukiefferiella claripennis-type) and for cold environments (Orthocladius type S, Sergentia coracina-type) appear. In the sediment layer dated to 20.4 cal kyr BP no chironomid remains have been found. The samples between 16.7 and 15.4 cal kyr BP are represented either by littoral phytophilic and acidophilic Psectrocladius sordidellus-type or by the typical semiterrestrial Smittia-Parasmittia, Limnophies-Paralimnophies-types that are both indicative for unstable water levels and erosion processes.

In MIS 1 (Unit C, 7 – 0 cal kyr BP) chironomid remains were found only between 6.4 and 4.4 cal kyr BP. The chironomid fauna is poor (median N2 = 2.9) and dominated by semiterrestrial taxa such as Smittia-Parasmittia, and Limnophies-Paralimnophies in presence of the phytophilic Tanytarsini taxa. The reconstructed TJuly at 6.4 cal kyt BP is at modern level (11.1°C) with a slight increase toward 4.4 cal kyr BP (11.7°C). After 4.4 cal kyr BP chironomids are absent from the record. Diatom fossil valves were only found in three samples of the uppermost unit C after 6.4 cal kyr BP. Highest counts were found in the uppermost sample SOB18-01 with 185 specimens, while sample SOB18-01-02 contained only five specimens. The diatom flora of the Sobo-Sise Yedoma record is represented by 25 taxa, belonging to 17 genera (Supplementary Table S2) and dominated by benthic species (Supplementary Table S3) while benthic–planktonic species occur much less and planktonic species are absent from the record. Most of the diatom species are indifferent to salinity. Alkaliphilic and alkalibiontic species dominate the record and most of the diatom species are cosmopolitans while boreal species are present with Hannaea arcus and Pinnularia alpina, and arctic-alpine species with Pinnularia gibba and Navicula vulpina. Flow-velocity preferences are known for 19 species of the 25 species identified in the Sobo-Sise record. Nine of them are indifferent, six species indicate flowing water and three standing water. Overall, the diatom flora of Unit C indicates the presence of shallow water with low salinity and neutral pH. The low representation of diatoms in the record might point to low silica availability in the host water or generally aquatic conditions not suitable to maintain stable diatom communities. For the normal development of diatoms, a rather significant concentration of silica is required, which is used for building of their frustules (Wasser et al., 1989). In the absence or lack of silica, the diatom frustules become thinner, and when the concentration of silicon in water falls below 0.3 mg L−1, the growth of diatoms completely stops (Proshkina-Lavrenko, 1974; Martin-Jézéquell, Lopez, 2003).

Discussion

Paleo-Ecology of the Sobo-Sise Yedoma Cliff in Regional Context

Detailed paleo-ecological information has been obtained from Yedoma IC deposits and its Holocene cover from two nearby locations on Bykovsky Peninsula (outcrop Mamontova Khayata) and Kurungnakh-Sise Island in the central Lena Delta (Figure 1). The Bykovsky Yedoma archive has been intensively studied for pollen, plant macrofossils, testate amoebae, freshwater ostracods, fossil insect remains and mammal bones of the late Pleistocene Mammoth fauna (Schirrmeister et al., 2002a; Bobrov et al., 2004; Kienast et al., 2005; Sher et al., 2005; Wetterich et al., 2005; Andreev et al., 2011; Kuznetsova et al., 2019) based on well-described cryolithological properties of the frozen deposits with well-established radiocarbon-based chronology (Schirrmeister et al., 2002b). The Yedoma IC and its stratigraphic context of fluvial sands underneath and Holocene cover on top exposed at the shore of Kurungnakh-Sise Island has been studied in terms of paleo-ecology of pollen, plant macrofossils, testate amoebae, ostracods, insect fossil remains and fossil mammal bones in detail by Schirrmeister et al. (2003) and Wetterich et al. (2008a). Main paleo-ecological results from both locations are discussed in comparison to those from the present study on Sobo-Sise Island below for the MIS 3 interstadial, the MIS 2 stadial and the MIS 1 interglacial periods.

Interstadial MIS 3 Environments

The new pollen record from Sobo-Sise Island matches those from Bykovsky Peninsula (Andreev et al., 2002; Schirrmeister et al., 2002a) and Kurungnakh-Sise Island (Schirrmeister et al., 2003; Wetterich et al., 2008a) and is further supported and enhanced by plant macrofossil studies from Bykovsky Peninsula (Kienast et al., 2005) and Kurungnakh-Sise Island (Wetterich et al., 2008a). The regional vegetation during MIS 3 as reconstructed from pollen and plant macrofossils of Yedoma IC deposits is characterized tundra-steppe vegetation with dominance of Cyperaceae and Poaceae pollen and some amounts of Artemisia and Salix between 53 and 43 cal kyr BP. High abundance of these taxa and presence of Caryophyllaceae as well as generally higher pollen concentrations are noted between 40 and 36 cal kyr BP. The permanent presence of Salix pollen points to the occurrence of willow shrubs in more protected and wet places. Low percentages and low concentrations of Pinus sylvestris point to low abundance in the past vegetation. In contrast, Larix shows a distinct difference with low percentages but high concentrations. Assuming that Larix tends to accumulate directly on the site, we deduce that Larix pollen concentrations are more representative than the Larix pollen percentages. We therefore suggest that Larix was a member of plant communities associated with Unit A and Pinus sylvestris pollen were rather derived from long-distance transport. The entire record of Unit A reveals relatively high percentages and concentrations of Picea. Since it is difficult to assume suitable conditions for spruce in the late Pleistocene of the Lena Delta region, we have to conclude that this is redeposition driven by wind or river transport. The redeposition in situ is also possible, however, age-height modeling did not reveal any inversions within Unit A (Wetterich et al., 2020). Stagnant water is indicated by the presence of green algae Botryococcus and Pediastrum remains. The Bykovsky and Kurungnakh-Sise records both show that remains of typical steppe and meadow plants of the Festuca, Kobresia, Linum, Silene, and Potentilla genera (Kienast et al., 2005) as well as wetland plants such as Carex sect. Phacocystis, Saxifraga hirculus, and Eriophorum angustifolium are common in the fossil record. At about 51 cal kyr BP and 40 cal kyr BP in the Bykovsky record, the occurrence of the temperate aquatic plant Callitriche hermaphroditica provides evidence of mean TJuly of 12°C or more, while the finding of the steppe taxon Thesium dated to 51 cal kyr suggests TJuly of 15°C or more. The chironomid-based TJuly reconstruction for MIS 3 from the Sobo-Sise Yedoma record shows some variation (Figure 5) and points to warmer-than-today (>11°C) temperatures at about 51 cal kyr BP, 46-44 and 41 cal kyr BP showing a general agreement with the plant macrofossil-based TJuly estimates from the Bykovsky Yedoma record (Kienast et al., 2005). Interstadial climate variability during MIS 3 has been previously deduced from proxy records across West Beringia (Anderson and Lozhkin, 2001) although with regional differences in the onset and duration of climatic optimum conditions (Wetterich et al., 2014). Those were recorded on Kurungnakh-Sise Island between 43 and 36 cal kyr BP and on Bykovsky Peninsula 45-38 cal kyr BP (Wetterich et al., 2014 and references therein). Thus, the Sobo-Sise chironomid record supports warmer-than-today summers as recorded in the Bykovsky and Kurungnakh-Sise Yedoma archives given dating uncertainties and different proxies. TJuly reconstructions from the western part of the Yana-Indigirka lowland (east of the study area) reveal similar-to or warmer-than-today temperatures (by up to 4–4.5°C) and higher-than-today annual precipitation (by up to 50–100 mm) between about 39 and 31 cal kyr BP (Pitulko et al., 2017), although older deposits are not captured in this record starting at 39.2 cal kyr BP. The early MIS 3 warmer-than-today conditions are represented by the Bykovsky and Sobo-Sise data, while late MIS 3 deposits are missing in these records and the Yana-Indigirka Lowland data misses the early MIS 3 deposits but represent the late MIS 3 phase of warmer (and moister)-than-today summer conditions in western Beringia.

The regional MIS 3 interstadial environments and vegetation as reconstructed from pollen data provided favorable conditions to maintain the Mammoth fauna as seen in the Bykovsky records (Schirrmeister et al., 2002a; Sher et al., 2005; Kuznetsova et al., 2019), but also supported by Sobo-Sise record with one radiocarbon-dated mammoth bone of 28,620 cal yr BP (Table 2).

The aquatic conditions during MIS 3 are reflected by the chironomid data from the Sobo-Sise Yedoma. Varying dominance of aquatic and semiterrestrial taxa over time represent the transition from higher to shallower water levels (Nazarova et al., 2017a). However, the supposed main freshwater type of the Beringian tundra-steppe environments are ice-wedge low-center polygon ponds which rarely exceed 1 m water depth in modern tundra landscapes (Wetterich et al., 2008b). The onset of ice-wedge polygon development with shallow ponds is represented by prevailing semiterrestrial chironomid taxa between 52 and 48 cal kyr BP. Evolving low-center polygons during MIS 3 climatic optimum with warmer-than-today TJuly likely induced deeper thaw and thus higher water level in the ponds that explains the higher share of aquatic chironomid taxa from 48 to 36 cal kyr BP. Freshwater ostracod fossil findings with highest abundance and diversity recorded at about 44 cal kyr BP on Kurungnakh-Sise Island (Wetterich et al., 2008a) support the existence of permanent water bodies. The Bykovsky ostracod record is more diverse and its best representation spans from about 48 to 41 cal kyr BP (Wetterich et al., 2005). Later on the ostracod fauna in the Bykovsky Yedoma record vanishes toward the MIS 3-2 transition, and in the Sobo-Sise chironomid record the uppermost sample at 28 cal kyr BP after the hiatus at 36–29 cal kyr BP exhibits a poor representation of only semiterrestrial taxa. Both dynamics reflect deterioration of the aquatic habitats in polygon ponds, probably induced by cooling at the MIS 3-2 transition leading to shallowing or dry-out of the water bodies.

Stadial MIS 2 Environments

The pollen-based paleo-vegetation records from Sobo-Sise Island and from Bykovsky Peninsula both highlight open tundra-steppe with prevailing Poaceae with present Cyperaceae, Artemisia, Brassicaceae and Caryophyllaceae pollen (Schirrmeister et al., 2002a; Andreev et al., 2002; Andreev et al., 2011) while MIS 2 deposits are largely missing in the Kurungnakh-Sise sequence (Schirrmeister et al., 2003; Wetterich et al., 2008a). MIS 2 pollen concentrations are generally lower than during MIS 3. Selaginella rupestris spores indicate very dry habitats, while larger amounts of reworked Pinaceae pollen and Glomus spores indicate disturbed soils due to the presence of large grazers of the Mammoth fauna. Such pollen composition reflects rather cold and dry summer climate conditions if compared to MIS 3. The Larix concentrations are low suggesting colder summers than during MIS 3. Still present green algae Botryococcus and Pediastrum remains point to the occasional presence of low-centred polygons while the absence of aquatic plant macro-fossils in deposits dated to 26.3 cal kyr BP (Kienast et al., 2005) suggests unstable aquatic environments during MIS 2. Dominating arctic pioneer species and decreased floristic diversity of the plant macro-fossil record point to harsh summer climate.

Evidence for subsistence of the Mammoth fauna during the MIS 2 stadial is found in four mammoth radiocarbon dates from Sobo-Sise Island ranging from 23,180 to 16,520 cal yr BP (Table 2) and corresponding to comparable data from Bykovky Peninsula in regional context (Schirrmeister et al., 2002a; Sher et al., 2005; Kuznetsova et al., 2019). Interestingly, one age of 17,490 cal yr BP falls into the MIS 2 sedimentary hiatus (20 - 17 cal yr BP) as estimated in the Sobo-Sise record sampled in 2018 (Wetterich et al., 2020) although a lack of deposits in a sequence due to hampered deposition or post-depositional erosion does not necessarily indicate a lack of past wildlife.

Cold and dry summer climate with unstable aquatic conditions is further seen in the chironomid record of Sobo-Sise with very low concentrations and diversity during the entire MIS 2 unit. Aquatic taxa are found from 28 to 23 cal kyr BP, afterward semiterrestrial taxa prevail. The period from 17 to 15 cal kyr BP is characterized by littoral phytophilic and acidophilic taxa as well as by typical semiterrestrial taxa. The ostracod record from the Bykovsky Yedoma lacks findings in the MIS 3-2 transition period from 32 to 25 cal kyr BP (zone III in Wetterich et al., 2005) and was interpreted as extremely unfavorable conditions for aquatic life due to dry-out of polygon ponds. Starting from about 25 cal kyr BP until about 21 cal kyr BP the ostracod record from Bykovsky is poor in abundance and diversity and no ostracods were found after 21 cal kyr BP. Improved aquatic conditions and present ostracod fossils are seen in a sample dated to 16.9 cal kyr BP. MIS 2 aquatic conditions as seen in chironomids from Sobo-Sise and ostracods from Bykovsky point to shallow polygon ponds or just wet polygon centers due to low summer precipitation feeding the water bodies and cold summer temperatures causing shallow thaw depth and inhibited ground ice melt. Due to the unfavorable aquatic conditions and the resulting poor chironomid record, the chironomid-based TJuly reconstruction for MIS 2 relies on very low concentration of chironomids in sediments (Figure 5) and its reliability is therefore limited. Therefore, warmer-than-today TJuly as seen in the chironomid record between 27 and 23 cal kyr BP seems unlikely to represent MIS 2 conditions. However, the coldest TJuly up to about 4°C below modern is found at about 20 cal kyr BP (Figure 5). This reconstructed low TJuly is caused by a high representation of indicative for colder conditions chironomid taxa like Orthocladius type S (T optimum in the NR model 9.5°C) and Metriocnemus eurinotus-type (T optimum in the NR model 9.2°C) (Nazarova et al., 2015).

Interglacial MIS 1 Holocene

In the Sobo-Sise record, the Holocene pollen spectra of Unit C differ noticeably from those of the late Pleistocene Yedoma IC units A and B, and are characterized by dominating Betula sect. Apterocaryon and the significant amounts of Alnus subg. Alnobetula and Ericaceae pollen, all together indicating humid shrub-tundra vegetation after about 7 cal kyr BP with isolated Larix stands. The increased concentration of Pinus sylvestris and Picea can be a result of long-distance transport of Holocene coniferous forests located south of the Lena Delta (Müller et al., 2009). The pollen records of the Holocene cover deposits of the Bykovsky Yedoma and the Kurungnakh-Sise Yedoma span from about 9.2 cal kyr BP to modern and from about 9.1 to 2.9 cal kyr BP, respectively. These records differentiate into early to middle Holocene and late Holocene pollen zones (Schirrmeister et al., 2002b; Wetterich et al., 2008a). The early Holocene pollen spectra indicate shrub-tundra (or forest tundra) vegetation dominated by Alnus subg. Alnobetula, Betula sect. Apterocaryon and Salix as well as by Ericales with some Cyperaceae and Poaceae until about 8.4 cal kyr BP (Andreev et al., 2011). After 8.4 cal kyr BP the shrub-tundra gradually disappears and is replaced by modern high Arctic and Arctic tundra vegetation. The plant macrofossil record from Bykovsky comprises two records dated to about 8.6 and 3 cal kyr BP. Warmer summers are reflected by the early Holocene plant species composition while the late Holocene record points to increased humidity and decreased summer temperatures by a smaller share of cryoxerophilous pioneer vegetation and tundra-steppe vegetation and a larger share of tundra bog species. Such Holocene climatic deterioration is seen in prevalence of tundra bog plants, while the occurrence of nival meadow plants such as Saxifraga nivalis and Ranunculus nivalis suggests a short growing season due to a thick snow cover and predominating cool and moist conditions (Schirrmeister et al., 2002b). The absence of true water plant species in the late Holocene and the reduced share of plants inhabiting marshy sites at shallow water lake shores point to impoverishment of aquatic conditions. The plant macrofossil record from Kurungnakh-Sise differentiates into data from the early Holocene dated to about 9.1 cal kyr BP and the mid to late Holocene dated to about 6.7 to 2.9 cal kyr BP (Wetterich et al., 2008a). The early Holocene plant composition comprises tundra-steppe species such as Kobresia myosuroides and Potentilla cf. stipularis while the number of wetland and tundra bog plants is low. Thus, the temperature increase toward the early Holocene is not reflected in these data although a single Betulaceae fruit was found. The pollen data from Kurungnakh-Sise, however, show a clear increase in Betula sect. Apterocaryon, Alnus subg. Alnobetula, Betula sect. Betula, and Ericales pollen as mentioned above. The mid to late Holocene plant species composition from Kurungnakh-Sise reflects wet tundra with wetland sedges such as Carex sect. Phacocystis and dominating willow shrubs. The presence of Betula cf. fruticosa and Ledum palustre suggests subarctic temperature conditions (Wetterich et al., 2008a).

The Holocene chironomid from Unit C of the Sobo-Sise Yedoma record is sparse. Semiterrestrial and phytophilic taxa dominated till ca 4.4 cal kyr BP and disappeared thereafter. The composition of chironomid communities indicates the presence of a very shallow overgrown waterbody that dried out after 4.4 cal kyr BP. Rare diatom fossils were only found within the uppermost samples of the Holocene cover after about 6.4 cal kyr BP. The dominating ecological preferences of the diatom species are characterized as cosmopolitan, benthic, alkaliphilic, indifferent to salinity. If compared to modern Yakutian diatom reference data with statistically quantified optimum ecological rages of certain conditions (Pestryakova et al., 2018) three species are found in the Holocene Sobo-Sise diatom record. Those are Diploneis elliptica (optimum TJuly of 11.9°C) and Stauroneis anceps (optimum TJuly of 11.2°C) from Unit C deposits dated from 6.4 to 2.5 cal kyr BP. Compared to the Holocene chironomid-based TJuly reconstruction of ca 11.5°C at 6.4 to 4.4 cal kyr BP it seems obvious that the chironomid-based and diatom-based TJuly reconstructions do not contradict each other. The finding of the diatom species Epithemia adnata (TJuly >15°C) in the uppermost sample of Unit C points to warmer conditions than today, while the indication of optimum ion content (expressed as electrical conductivity of 586 μs cm-1) of E. adnata would support such warm summer temperatures with increased evaporation. Modern electrical conductivity values in polygon ponds in the Lena Delta are more than two-fold lower and range from 27 to 254 μs cm-1 (Wetterich et al., 2008b). However, the Sobo-Sise fossil diatom record is very limited and its environmental indication should be interpreted with caution. Ostracod fossils have not been found in the Holocene cover deposits on the Yedoma IC on Bykovsky Peninsula (Wetterich et al., 2005) and Kurungnakh-Sise Island (Wetterich et al., 2008a), but are found on Bykovsky in late Holocene deposits dated to about 3 cal kyr BP that accumulated in thermokarst basins here and elsewhere in the region (Wetterich et al., 2009; Morgenstern et al., 2013). Such observation might be explained by landscape reorganization due to massive permafrost thaw starting in the lateglacial period when climate warming toward the Holocene increased thermokarst processes and thus the rates of northern lake formation starting ∼14 cal kyr BP and peaking around 10.4 cal kyr BP (Brosius et al., 2021). Although lake formation slowed down around 10–8 cal kyr BP, the major occurrence of Holocene aquatic habitats in West Beringian Yedoma landscapes is found in thermokarst basins evolving since the deglacial rather than on degrading Yedoma uplands.

Conclusion

The regional Yedoma records in the Lena Delta and on Bykovsky Peninsula confirm the existence of late Pleistocene tundra-steppe environments in West Beringia during MIS 3 with partly warmer-than-today summers and wetter conditions allowing for stagnant water (i.e., polygon ponds). During MIS 2, summers were probably colder than during MIS 3 and drier with unstable aquatic conditions in the polygonal landscape. However, the aquatic conditions in shallow ponds of low-center polygons during MIS 3 and MIS 2 were suitable for maintaining chironomid faunae although highly dynamic and prone to episodically dry-out or drainage causing low abundance and diversity of chironomids in the records. Diatom frustules occurred in the sediment record only after 6.4 cal kyr BP, probably due to post-depositional dissolution processes or to the lack of silica in the earlier period of pond development.

In addition to previous plant macrofossil-based TJuly reconstructions from the Bykovsky Yedoma record available for only two periods around 51 and 40 cal kyr BP, the present chironomid-based TJuly estimates fills the period in between with data from about 52 to 41 cal kyr BP. The record reveals warmer-than-today TJuly at about 51 cal kyr BP, 46-44 and 41 cal kyr BP highlighting early MIS 3 climate optimum conditions.

The Sobo-Sise pollen record suggests that Larix was a member of the regional MIS 3 tundra-steppe communities. The Holocene vegetation differentiates into early Holocene shrub-tundra replaced by mid- and late Holocene modern wet tundra.

The finding of a bone from woolly rhinoceros (Coelodonta antiquitatis) most likely originating from the Sobo-Sise Yedoma cliff is somewhat remarkable since the species has not been reported yet from the Lena Delta region or Bykovsky Peninsula, and is generally rare in collections of fossil bones of the late Pleistocene Mammoth fauna in northern part of West Beringia.

Data Availability Statement

The original contributions presented in the study are included in the article/Supplementary Material, further inquiries can be directed to the corresponding author.

Author Contributions

SW, NR and LN designed the study and wrote the original draft of the manuscript. SW, AK, LN and NR acquired funding. AK, AA, SW, LSc and MF participated in the field investigation and collected sample material. KS supervised pollen preparation. NR and MP performed pollen analysis and interpretation. LN and LSy performed chironomid analysis and interpretation. OP performed diatom analysis and interpretation. TK performed mammal bone analysis and interpretation. JW and MF supported overall proxy data interpretation. All authors contributed in writing and editing the manuscript.

Funding

This work has been supported by the by the Russian Foundation of Basic Research (RFBR grant No. 18-05-60221 to AK) and the Deutsche Forschungsgemeinschaft (DFG grants No. WE4390/7-1 to SW and NA760/8-1 to LN). NR worked in the frame of project NIR IAET SB RAS No. 0264-2019-0010. MF was supported by the NUNATARYUK project that has received funding from the European Union’s Horizon 2020 research and innovation program under grant agreement No. 773421.

Conflict of Interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

The reviewer NS declared a past co-authorship with several of the authors LN, NR, LSy, and OP.

Acknowledgments

We thank our colleagues from the Hydrobaza Tiksi for help with fieldwork in 2018 that was conducted in the framework of the joint Russian-German expeditions LENA 2018 supported by the Samoylov Research Station. Sarah Olischläger (AWI Potsdam) is acknowledged for pollen preparation.

Supplementary Material

The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/feart.2021.681511/full#supplementary-material

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Keywords: permafrost, Yedoma, paleo-ecology, pollen, chironomids, Mammoth fauna, late Pleistocene, Beringia

Citation: Wetterich S, Rudaya N, Nazarova L, Syrykh L, Pavlova M, Palagushkina O, Kizyakov A, Wolter J, Kuznetsova T, Aksenov A, Stoof-Leichsenring KR, Schirrmeister L and Fritz M (2021) Paleo-Ecology of the Yedoma Ice Complex on Sobo-Sise Island (EasternLena Delta, Siberian Arctic). Front. Earth Sci. 9:681511. doi: 10.3389/feart.2021.681511

Received: 16 March 2021; Accepted: 03 June 2021;
Published: 18 June 2021.

Edited by:

Davide Tiranti, Agenzia Regionale per la Protezione Ambientale (ARPA), Italy

Reviewed by:

Nadia Solovieva, University College London, United Kingdom
Xiaozhong Huang, Lanzhou University, China

Copyright © 2021 Wetterich, Rudaya, Nazarova, Syrykh, Pavlova, Palagushkina, Kizyakov, Wolter, Kuznetsova, Aksenov, Stoof-Leichsenring, Schirrmeister and Fritz. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: S. Wetterich, sebastian.wetterich@awi.de