The future trajectory of greenhouse gas concentrations depends on interactions between climate and the biogeosphere. Thawing of Arctic permafrost could release significant amounts of carbon into the atmosphere in this century. Ancient Ice Complex deposits outcropping along the ~7,000-kilometre-long coastline of the East Siberian Arctic Shelf (ESAS), and associated shallow subsea permafrost, are two large pools of permafrost carbon, yet their vulnerabilities towards thawing and decomposition are largely unknown. Recent Arctic warming is stronger than has been predicted by several degrees, and is particularly pronounced over the coastal ESAS region. There is thus a pressing need to improve our understanding of the links between permafrost carbon and climate in this relatively inaccessible region. Here we show that extensive release of carbon from these Ice Complex deposits dominates (57 ± 2 per cent) the sedimentary carbon budget of the ESAS, the world’s largest continental shelf, overwhelming the marine and topsoil terrestrial components. Inverse modelling of the dual-carbon isotope composition of organic carbon accumulating in ESAS surface sediments, using Monte Carlo simulations to account for uncertainties, suggests that 44 ± 10 teragrams of old carbon is activated annually from Ice Complex permafrost, an order of magnitude more than has been suggested by previous studies. We estimate that about two-thirds (66 ± 16 per cent) of this old carbon escapes to the atmosphere as carbon dioxide, with the remainder being re-buried in shelf sediments. Thermal collapse and erosion of these carbon-rich Pleistocene coastline and seafloor deposits may accelerate with Arctic amplification of climate warming.

In the present study we report hydrological (T and S) and hydrochemical data obtained during a Russian Trans‐Arctic cruise in 2000 onboard the Hydrographic Vessel (HV) Nikolay Kolomeytsev, and describe the top layer of the sediment (a typical sample was taken from the upper 0–5 cm layer of bottom sediment) and the distribution of the organic carbon (δ13Corg) and nitrogen (δ15Norg) isotope ratios. Using both historical water data and data from our cruise, we divide the ESS into two specific areas: the Western area, influenced strongly by Lena River input, and the Eastern area, under direct influence of Pacific‐derived water. We also used the stable δ13Corg and δ15Norg isotopes to detect the sediment geochemical boundary (or “geochemical FZ”) between Pacific “marine‐derived sediments” and “terrestrial derived sediments” which can be considered to reflect the long‐term (on a scale of 102 years) position of the most westward extension of Pacific water. These are among the first reliable hydrological and geochemical data reported for the ESS from the Dmitry Laptev Strait to the Long Strait, and they reveal novel insights about interaction between Pacific water and local shelf water.

Sustained release of methane (CH4) to the atmosphere from thawing Arctic permafrost may be a positive and significant feedback to climate warming. Atmospheric venting of CH4 from the East Siberian Arctic Shelf (ESAS) was recently reported to be on par with flux from the Arctic tundra; however, the future scale of these releases remains unclear. Here, based on results of our latest observations, we show that CH4 emissions from this shelf are likely to be determined by the state of subsea permafrost degradation. We observed CH4 emissions from two previously understudied areas of the ESAS: the outer shelf, where subsea permafrost is predicted to be discontinuous or mostly degraded due to long submergence by seawater, and the near shore area, where deep/open taliks presumably form due to combined heating effects of seawater, river run-off, geothermal flux and pre-existing thermokarst. CH4 emissions from these areas emerge from largely thawed sediments via strong flare-like ebullition, producing fluxes that are orders of magnitude greater than fluxes observed in background areas underlain by largely frozen sediments. We suggest that progression of subsea permafrost thawing and decrease in ice extent could result in a significant increase in CH4 emissions from the ESAS.

Climate warming in northeastern Siberia may induce thaw-mobilization of the organic carbon (OC) now held in permafrost. This study investigated the composition of terrestrial OC exported to Arctic coastal waters to both obtain a natural integration of terrestrial permafrost OC release and to further understand the fate of released carbon in the extensive Siberian Shelf Seas. Application of a variety of elemental, molecular and isotopic (δ¹³C and Δ¹⁴C) analyses of both surface water suspended particulate matter and underlying surface sediments along a 500 km transect from Kolyma River mouth to the mid-shelf of the East Siberian Sea yielded information on the sources, degradation status and transport processes of thaw-mobilized soil OC. A three end-member dual-carbon-isotopic mixing model was applied to deduce the relative contributions from riverine, coastal erosion and marine sources. The mixing model was solved numerically using Monte Carlo simulations to obtain a fair representation of the uncertainties of both end-member composition and the end results. Riverine OC contributions to sediment OC decrease with increasing distance offshore (35±15 to 13±9%), whereas coastal erosion OC exhibits a constantly high contribution (51±11 to 60±12%) and marine OC increases offshore (9±7 to 36±10%). We attribute the remarkably strong imprint of OC from coastal erosion, extending up to ~500 km from the coast, to efficient offshoreward transport in these shallow waters presumably through both the benthic boundary layer and ice-rafting. There are also indications of simultaneous selective preservation of erosion OC compared to riverine OC. Molecular degradation proxies and radiocarbon contents indicated a degraded but young (Δ¹⁴C ca. −60‰ or ca. 500 ¹⁴C years) terrestrial OC pool in surface water particulate matter, underlain by a less degraded but old (Δ¹⁴C ca. −500‰ or ca. 5500 ¹⁴C years) terrestrial OC pool in bottom sediments. We suggest that the terrestrial OC fraction in surface water particulate matter is mainly derived from surface soil and recent vegetation fluvially released as buoyant organic-rich aggregates (e.g., humics), which are subjected to extensive processing during coastal transport. In contrast, terrestrial OC in the underlying sediments is postulated to originate predominantly from erosion of mineral-rich Pleistocene coasts (i.e., yedoma) and inland mineral soils. Sorptive association of this organic matter with mineral particles protects the OC from remineralization and also promotes rapid settling (ballasting) of the OC. Our findings corroborate recent studies by indicating that different Arctic surface soil OC pools exhibit distinguishing susceptibilities to degradation in coastal waters. Consequently, the general postula...

[1] Surface sediments were collected during the 2000 TransArctic Expedition along the Siberian Arctic coastline, including the Ob, Yenisey, Khatanga, Lena, and Indigirka estuaries. Sediments were characterized for elemental composition (total organic carbon, TOC, black carbon, BC, and total N, as well as major and trace elements), isotopic signature (d Sr), and organic molecular composition to better understand river export variations over the large spatial scale of the Siberian Arctic. On average, 79 ± 9% of the total C in sediments was organic while 21 ± 9% was inorganic. BC made up 9 ± 4% of the TOC pool, with a general increasing trend from west to east along the Siberian coast. The combined Nd-and Sr-isotopes (e Nd and 87 Sr/ C values were significantly correlated with the ratio of BC/TOC (R 2 = 0.91, n = 6), consistent with the distribution pattern of increasing permafrost zone from the west to the east along the Siberian coast. Together, our results suggest that older OC was derived from the release of recalcitrant BC during permafrost thawing and riverbank and coastal erosion, likely enhanced by ongoing environmental changes in the northern ecosystem.

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This study seeks an improved understanding of how matrix association affects the redistribution and degradation of terrigenous organic carbon (TerrOC) during cross-shelf transport in the Siberian margin. Sediments were collected at increasing distance from two river outlets (Lena and Kolyma Rivers) and one coastal region affected by erosion. Samples were fractionated according to density, size, and settling velocity. The chemical composition in each fraction was characterized using elemental analyses and terrigenous biomarkers. In addition, a dual-carbon-isotope mixing model (δ 13 C and Δ 14 C) was used to quantify the relative TerrOC contributions from active layer (Topsoil) and Pleistocene Ice Complex Deposits (ICD). Results indicate that physical properties of particles exert first-order control on the redistribution of different TerrOC pools. Because of its coarse nature, plant debris is hydraulically retained in the coastal region. With increasing distance from the coast, the OC is mainly associated with fine/ultrafine mineral particles. Furthermore, biomarkers indicate that the selective transport of fine-grained sediment results in mobilizing high-molecular weight (HMW) lipid-rich, diagenetically altered TerrOC while lignin-rich, less degraded TerrOC is retained near the coast. The loading (μg/m 2 ) of lignin and HMW wax lipids on the fine/ultrafine fraction drastically decreases with increasing distance from the coast (98% and 90%, respectively), which indicates extensive degradation during cross-shelf transport. Topsoil-C degrades more readily (90 ± 3.5%) compared to the ICD-C (60 ± 11%) during transport. Altogether, our results indicate that TerrOC is highly reactive and its accelerated remobilization from thawing permafrost followed by cross-shelf transport will likely represent a positive feedback to climate warming.Previous studies over this margin have exclusively focused on bulk (unfractionated) surface sediments. They have shown contrasting spatial trends for different classes of terrigenous biomarkers, suggesting that the TESI ET AL.SORTING AND DEGRADATION OF TERROC 731 PUBLICATIONS

The world's largest continental shelf, the East Siberian Shelf Sea, receives substantial input of terrestrial organic carbon (terr-OC) from both large rivers and erosion of its coastline. Degradation of organic matter from thawing permafrost in the Arctic is likely to increase, potentially creating a positive feedback mechanism to climate warming. This study focuses on the Buor-Khaya Bay (SE Laptev Sea), an area with strong terr-OC input from both coastal erosion and the Lena river. To better understand the fate of this terr-OC, molecular (acyl lipid biomarkers) and isotopic tools (stable carbon and radiocarbon isotopes) have been applied to both particulate organic carbon (POC) in surface water and sedimentary organic carbon (SOC) collected from the underlying surface sediments. <br><br> Clear gradients in both extent of degradation and differences in source contributions were observed both between surface water POC and surface sediment SOC as well as over the 100 s km investigation scale (about 20 stations). Depleted &delta;¹³C-OC and high HMW/LMW <i>n</i>-alkane ratios signaled that terr-OC was dominating over marine/planktonic sources. <br><br> Despite a shallow water column (10–40 m), the isotopic shift between SOC and POC varied systematically from +2 to +5 per mil for &delta;¹³C and from +300 to +450 for &Delta;¹⁴C from the Lena prodelta to the Buor-Khaya Cape. At the same time, the ratio of HMW <i>n</i>-alkanoic acids to HMW <i>n</i>-alkanes as well as HMW <i>n</i>-alkane CPI, both indicative of degradation, were 5–6 times greater in SOC than in POC. This suggests that terr-OC was substantially older yet less degraded in the surface sediment than in the surface waters. This unusual vertical degradation trend was only recently found also for the central East Siberian Sea. <br><br> Numerical modeling (Monte Carlo simulations) with &delta;¹³C and &Delta;¹⁴C in both POC and SOC was applied to deduce the relative contribution of – plankton OC, surface soil layer OC and yedoma/mineral soil OC. This three end-member dual-carbon-isotopic mixing model suggests quite different scenarios for the POC vs SOC. Surface soil is dominating (63 &plusmn; 10 %) the suspended organic matter in the surface water of SE Laptev Sea. In contrast, the yedoma/mineral soil OC is accounting for 60 ± 9 % of the SOC. We hypothesize that yedoma-OC, associated with mineral-rich matter from coastal erosion is ballasted and thus quickly settles to the bottom. The mineral association may also explain the greater resistance to degradation of this terr-OC component. In contrast, more amorphous humic-like and low-density terr-OC from surface soil and recent vegetation represents a younger but more bioavailable and thus degraded terr-OC component held buoyant in surface water. Hence, these two terr-OC components may represen...