ALBERT

Description: Thawing of permafrost carbon (PF-C) due to climate warming can remobilise considerable amounts of terrestrial carbon from its long-term storage to the marine environment. PF-C can be then be buried in sediments or remineralised to CO2 with implications for the carbon–climate feedback. Studying historical sediment records during past natural climate changes can help us to understand the response of permafrost to current climate warming. In this study, two sediment cores collected from the East Siberian Sea were used to study terrestrial organic carbon sources, composition and degradation during the past  ∼ 9500 cal yrs BP. CuO-derived lignin and cutin products (i.e., compounds solely biosynthesised in terrestrial plants) combined with δ13C suggest that there was a higher input of terrestrial organic carbon to the East Siberian Sea between  ∼ 9500 and 8200 cal yrs BP than in all later periods. This high input was likely caused by marine transgression and permafrost destabilisation in the early Holocene climatic optimum. Based on source apportionment modelling using dual-carbon isotope (Δ14C, δ13C) data, coastal erosion releasing old Pleistocene permafrost carbon was identified as a significant source of organic matter translocated to the East Siberian Sea during the Holocene.

Description: Recent Arctic studies suggest that sea-ice decline and permafrost thawing will affect phytoplankton dynamics and stimulate marine heterotrophic communities. However, in what way the plankton composition will change as the warming proceeds remains elusive. Here we investigate the chemical signature and plankton speciation of the supra-micron (〉 10 μm) particulate organic matter (supra-POM) fraction collected along the Siberian shelf. Supra-POM samples were analysed at bulk (δ13C and Δ14C) and molecular level (CuO oxidation and IP25) while plankton identification established the dominant taxa. In addition, surface water chemical properties were integrated with the plankton dataset to understand the link between plankton composition and environmental conditions. The dual-carbon isotope fingerprint indicates a large variability in the supra-POM distribution while terrestrial biomarkers suggest negligible land-derived input. In the open-waters of the outer Laptev Sea (LS), heterotrophic plankton dominated the assemblages. δ13C and Δ14C suggest that modern terrestrial dissolved organic carbon (DOC) from the Lena river is the primary source of metabolizable carbon which is transferred to the heterotrophic communities via microbial loops. Moving eastwards toward the sea-ice dominated East Siberian Sea (ESS), the system became progressively more autotrophic and dominated by sea-ice and pelagic diatoms which is confirmed. Comparison between δ13C of supra-POM samples and CO2aq concentrations suggests that the carbon isotope fractionation follows the general growth vs CO2aq supply model with the highest δ13C values found in the easternmost, most productive stations. In a warming scenario characterized by enhanced terrestrial release and further sea-ice decline, heterotrophic conditions fuelled by terrestrial DOC will likely persist in the LS while ESS might experience enhanced primary productivity. This will result in a sharp compositional gradient similar to what documented in our semi-synoptic study.

Description: Recent Arctic studies suggest that sea ice decline and permafrost thawing will affect phytoplankton dynamics and stimulate heterotrophic communities. However, in what way the plankton composition will change as the warming proceeds remains elusive. Here we investigate the chemical signature of the plankton-dominated fraction of particulate organic matter (POM) collected along the Siberian Shelf. POM (〉 10 µm) samples were analysed using molecular biomarkers (CuO oxidation and IP25) and dual-carbon isotopes (δ13C and Δ14C). In addition, surface water chemical properties were integrated with the POM (〉 10 µm) dataset to understand the link between plankton composition and environmental conditions. δ13C and Δ14C exhibited a large variability in the POM (〉 10 µm) distribution while the content of terrestrial biomarkers in the POM was negligible. In the Laptev Sea (LS), δ13C and Δ14C of POM (〉 10 µm) suggested a heterotrophic environment in which dissolved organic carbon (DOC) from the Lena River was the primary source of metabolisable carbon. Within the Lena plume, terrestrial DOC probably became part of the food web via bacteria uptake and subsequently transferred to relatively other heterotrophic communities (e.g. dinoflagellates). Moving eastwards toward the sea-ice-dominated East Siberian Sea (ESS), the system became progressively more autotrophic. Comparison between δ13C of POM (〉 10 µm) samples and CO2aq concentrations revealed that the carbon isotope fractionation increased moving towards the easternmost and most productive stations. In a warming scenario characterised by enhanced terrestrial DOC release (thawing permafrost) and progressive sea ice decline, heterotrophic conditions might persist in the LS while the nutrient-rich Pacific inflow will likely stimulate greater primary productivity in the ESS. The contrasting trophic conditions will result in a sharp gradient in δ13C between the LS and ESS, similar to what is documented in our semi-synoptic study.

Description: The Siberian Arctic Sea shelf and slope is a key region for the degradation of terrestrial organic material transported from the organic carbon-rich permafrost regions of Siberia. We report on sediment carbon mineralization rates based on O2 microelectrode profiling, intact sediment core incubations, 35S-sulfate tracer experiments, porewater dissolved inorganic carbon (DIC), δ13CDIC, and iron, manganese, and ammonium concentrations from 20 shelf and slope stations. This data set provides a spatial overview of sediment carbon mineralization rates and pathways over large parts of the outer Laptev and East Siberian Arctic shelf and slope, and allowed us to assess degradation rates and efficiency of carbon burial in these sediments. Rates of oxygen uptake and iron and manganese reduction were comparable to temperate shelf and slope environments, but bacterial sulfate reduction rates were comparatively low. In the topmost 20 to 50 cm of sediment, aerobic carbon mineralization dominated degradation and comprised on average 82 % of the depth-integrated carbon mineralization. Oxygen uptake rates and 35S-sulfate reduction rates were higher in the eastern East Siberian Sea shelf compared to the Laptev Sea shelf. DIC/NH4+ ratios in porewaters and the stable carbon isotope composition of remineralized DIC indicated that the degraded organic matter on the Siberian shelf and slope was a mixture of marine and terrestrial organic matter. Based on dual end member calculations, the terrestrial organic carbon contribution varied between 32 % and 36 %, with a higher contribution in the Laptev Sea than in the East Siberian Sea. Extrapolation of the measured degradation rates using isotope end member apportionment over the outer shelf of the Laptev and East Siberian Sea suggests that about 16 Tg C per year are respired in the outer shelf sea floor sediment. Of the organic matter buried below the oxygen penetration depth, between 0.6 and 1.3 Tg C per year are degraded by anaerobic processes, with a terrestrial organic carbon contribution ranging between 0.3 and 0.5 Tg per year.

Description: Thawing of permafrost carbon (PF-C) due to climate warming can remobilise considerable amounts of terrestrial carbon from its long term storage to the marine environment. PF-C can be then buried in sediments or remineralised to CO2 with implications for the carbon-climate feedback. Studying historical sediment records during past natural climate changes can help to understand the response of permafrost to current climate warming. In this study two sediment cores collected from the East Siberian Sea were used to study terrestrial organic carbon sources, composition and degradation during the past ~ 9500 cal yrs BP. The CuO-derived lignin and cutin products combined with δ13C suggest that there was a higher input of terrestrial organic carbon to the East Siberian Sea between ~ 9500 and 8200 cal yrs BP than in all later periods. This high input was likely caused by marine transgression and permafrost destabilisation in the early Holocene climatic optimum. Based on source apportionment modelling using dual-carbon isotope (∆14C, δ13C) data, coastal erosion releasing old Pleistocene permafrost carbon was identified as a significant source of organic matter translocated to the East Siberian Sea during the Holocene.

Description: Ongoing global warming in high latitudes may cause an increasing supply of permafrost-derived organic carbon through both river discharge and coastal erosion to the Arctic shelves. Here it can be either buried in sediments, transported to the deep sea or degraded to CO2 and outgassed, potentially constituting a positive feedback to climate change. This study aims to assess the fate of terrestrial organic carbon (TerrOC) in the Arctic marine environment by exploring how it changes in concentration, composition and degradation status across the wide Laptev Sea shelf. We analyzed a suite of terrestrial biomarkers as well as source-diagnostic bulk carbon isotopes (δ13C, Δ14C) in surface sediments from a Laptev Sea transect spanning more than 800 km from the Lena River mouth (~ 10 m water depth) across the shelf to the slope and rise (2000–3000 m water depth). These data provide a broad view on different TerrOC pools and their behavior during cross-shelf transport. The concentrations of lignin phenols, cutin acids and high-molecular weight (HMW) wax lipids (tracers of vascular plants) decrease by 89–99 % along the transect. Molecular-based degradation proxies for TerrOC (e.g., the carbon preference index of HMW lipids, the HMW acids/alkanes ratio and the acid/aldehyde ratio of lignin phenols) display a trend to more degraded TerrOC with increasing distance from the coast. We infer that the degree of degradation of permafrost-derived TerrOC is a function of the time spent under oxic conditions during protracted cross-shelf transport. Future work should therefore seek to constrain cross-shelf transport times in order to compute a TerrOC degradation rate and thereby help to quantify potential carbon-climate feedbacks.

Description: Pleistocene ice complex permafrost deposits contain roughly a quarter of the organic carbon (OC) stored in permafrost (PF) terrain. When permafrost thaws, its OC is remobilized into the (aquatic) environment where it is available for degradation, transport or burial. Aquatic or coastal environments contain sedimentary reservoirs that can serve as archives of past climatic change. As permafrost thaw is increasing throughout the Arctic, these reservoirs are important locations to assess the fate of remobilized permafrost OC.We here present compound-specific deuterium (δ2H) analysis on leaf waxes as a tool to distinguish between OC released from thawing Pleistocene permafrost (ice complex deposits; ICD) and from thawing Holocene permafrost (from near-surface soils). Bulk geochemistry (%OC; δ13C; %total nitrogen, TN) was analyzed as well as the concentrations and δ2H signatures of long-chain n-alkanes (C21 to C33) and mid- to long-chain n-alkanoic acids (C16 to C30) extracted from both ICD-PF samples (n =  9) and modern vegetation and O-horizon (topsoil-PF) samples (n =  9) from across the northeast Siberian Arctic. Results show that these topsoil-PF samples have higher %OC, higher OC ∕ TN values and more depleted δ13C-OC values than ICD-PF samples, suggesting that these former samples trace a fresher soil and/or vegetation source. Whereas the two investigated sources differ on the bulk geochemical level, they are, however, virtually indistinguishable when using leaf wax concentrations and ratios. However, on the molecular isotope level, leaf wax biomarker δ2H values are statistically different between topsoil PF and ICD PF. For example, the mean δ2H value of C29 n-alkane was −246 ± 13 ‰ (mean ± SD) for topsoil PF and −280 ± 12 ‰ for ICD PF. With a dynamic isotopic range (difference between two sources) of 34 to 50 ‰; the isotopic fingerprints of individual, abundant, biomarker molecules from leaf waxes can thus serve as endmembers to distinguish between these two sources. We tested this molecular δ2H tracer along with another source-distinguishing approach, dual-carbon (δ13C–Δ14C) isotope composition of bulk OC, for a surface sediment transect in the Laptev Sea. Results show that general offshore patterns along the shelf-slope transect are similar, but the source apportionment between the approaches vary, which may highlight the advantages of either. This study indicates that the application of δ2H leaf wax values has potential to serve as a complementary quantitative measure of the source and differential fate of OC thawed out from different permafrost compartments.

Description: Pleistocene ice complex permafrost deposits contain roughly a quarter of the organic carbon (OC) stored in permafrost terrain. When permafrost thaws, its OC is remobilized into the (aquatic) environment where it is available for degradation, transport or burial. Aquatic or coastal environments contain sedimentary reservoirs that can serve as archives of past climatic change. As permafrost thaw is increasing throughout the Arctic, these reservoirs are important locations to assess the fate of remobilized permafrost OC. We here present compound-specific deuterium (δ2H) analysis on leaf waxes as a tool to distinguish between OC released from thawing Pleistocene permafrost (Ice Complex Deposits; ICD) and from thawing Holocene permafrost (from near-surface soils). Bulk geochemistry (%OC, δ13C, %total nitrogen; TN) was analyzed as well as the concentrations and δ2H signatures of long-chain n-alkanes (C21 to C33) and mid/long-chain n-alkanoic acids (C16 to C30) extracted from both ICD-PF samples (n = 9) and modern vegetation/O-horizon (Topsoil-PF) samples (n = 9) from across the northeast Siberian Arctic. Results show that these Topsoil-PF samples have higher %OC, higher OC/TN values, and more depleted δ13C-OC values than ICD-PF samples, suggesting that these former samples trace a fresher soil and/or vegetation source. Median concentrations of high-molecular weight n-alkanes (sum of C25-C27-C29-C31) were 210 ± 350 µg/gOC (median ± IQR) for Topsoil-PF and 250 ± 81 µg/gOC for ICD-PF samples. Long-chain n-alkanoic acids (sum of C22-C24-C26-C28) were more abundant than long-chain n-alkanes, both in Topsoil-PF samples (4700 ± 3400 µg/gOC) and in ICD samples (6630 ± 3500 µg/gOC). Whereas the two investigated sources differ on the bulk geochemical level, they are, however, virtually indistinguishable when using leaf wax concentrations and ratios. However, on the molecular-isotope level, leaf wax biomarker δ2H values are statistically different between Topsoil-PF and ICD-PF. The mean δ2H value of C29 n-alkane was −246 ± 13 ‰ (mean ± stdev) for Topsoil-PF and −280 ± 12 ‰ for ICD-PF, whereas the C31 n-alkane was −247 ± 23 ‰ for Topsoil-PF and −297 ± 15 ‰ for ICD-PF. The C28 n-alkanoic acid δ2H value was −220 ± 15 ‰ for Topsoil-PF and −267 ± 16 ‰ for ICD-PF. With a dynamic isotopic range (difference between two sources) of 34 to 50 ‰, the isotopic fingerprints of individual, abundant, biomarker molecules from leaf waxes can thus serve as end-members to distinguish between these two sources. We tested this molecular δ2H tracer along with another source-distinguishing approach, dual-carbon (δ13C-δ14C) isotope composition of bulk OC, for a surface sediment transect in the Laptev Sea. Results show that general offshore patterns along the shelf-slope transect are similar, but the source apportionment between the approaches vary, which may highlight the advantages of either. The δ2H molecular approach has the advantage that it circumvents uncertainties related to a marine end-member, yet the δ13C-δ14C approach has the advantage that it represents the bulk OC fraction thereby avoiding issues related to the molecular-bulk upscaling challenge. This study indicates that the application of δ2H leaf wax values has potential to serve as a complementary quantitative measure of the source and differential fate of OC thawed out from different permafrost compartments.

Description: Ongoing global warming in high latitudes may cause an increasing supply of permafrost-derived organic carbon through both river discharge and coastal erosion to the Arctic shelves. Mobilized permafrost carbon can be either buried in sediments, transported to the deep sea or degraded to CO2 and outgassed, potentially constituting a positive feedback to climate change. This study aims to assess the fate of terrigenous organic carbon (TerrOC) in the Arctic marine environment by exploring how it changes in concentration, composition and degradation status across the wide Laptev Sea shelf. We analyzed a suite of terrestrial biomarkers as well as source-diagnostic bulk carbon isotopes (δ13C, Δ14C) in surface sediments from a Laptev Sea transect spanning more than 800 km from the Lena River mouth (

Description: The Siberian Arctic Sea shelf and slope is a key region for the degradation of terrestrial organic material transported from the organic-carbon-rich permafrost regions of Siberia. We report on sediment carbon mineralization rates based on O2 microelectrode profiling; intact sediment core incubations; 35S-sulfate tracer experiments; pore-water dissolved inorganic carbon (DIC); δ13CDIC; and iron, manganese, and ammonium concentrations from 20 shelf and slope stations. This data set provides a spatial overview of sediment carbon mineralization rates and pathways over large parts of the outer Laptev and East Siberian Arctic shelf and slope and allows us to assess degradation rates and efficiency of carbon burial in these sediments. Rates of oxygen uptake and iron and manganese reduction were comparable to temperate shelf and slope environments, but bacterial sulfate reduction rates were comparatively low. In the topmost 50 cm of sediment, aerobic carbon mineralization dominated degradation and comprised on average 84 % of the depth-integrated carbon mineralization. Oxygen uptake rates and anaerobic carbon mineralization rates were higher in the eastern East Siberian Sea shelf compared to the Laptev Sea shelf. DIC ∕ NH4+ ratios in pore waters and the stable carbon isotope composition of remineralized DIC indicated that the degraded organic matter on the Siberian shelf and slope was a mixture of marine and terrestrial organic matter. Based on dual end-member calculations, the terrestrial organic carbon contribution varied between 32 and 36 %, with a higher contribution in the Laptev Sea than in the East Siberian Sea. Extrapolation of the measured degradation rates using isotope end-member apportionment over the outer shelf of the Laptev and East Siberian seas suggests that about 16 Tg C yr−1 is respired in the outer shelf seafloor sediment. Of the organic matter buried below the oxygen penetration depth, between 0.6 and 1.3 Tg C yr−1 is degraded by anaerobic processes, with a terrestrial organic carbon contribution ranging between 0.3 and 0.5 Tg yr−1.