Fluvial discharge and coastal erosion of the permafrost-dominated East Siberian Arctic delivers large quantities of terrigenous organic carbon (Terr-OC) to marine waters. The composition and fate of the remobilized Terr-OC needs to be better constrained as it impacts the potential for a climate–carbon feedback. In the present study, the bulk isotope (δ¹³C and Δ¹⁴C) and macromolecular (lignin-derived phenols) composition of the cross-shelf exported organic carbon (OC) in different marine pools is evaluated. For this purpose, as part of the SWERUS-C3 expedition (July–September 2014), sediment organic carbon (SOC) as well as water column (from surface and near-bottom seawater) dissolved organic carbon (DOC) and particulate organic carbon (POC) samples were collected along the outer shelves of the Kara Sea, Laptev Sea and East Siberian Sea. The results show that the Lena River and the DOC may have a preferential role in the transport of Terr-OC to the outer shelf. DOC concentrations (740–3600 µg L⁻¹) were 1 order of magnitude higher than POC (20–360 µg L⁻¹), with higher concentrations towards the Lena River plume. The δ¹³C signatures in the three carbon pools varied from −23.9 ± 1.9 ‰ in the SOC, −26.1 ± 1.2 ‰ in the DOC and −27.1 ± 1.9 ‰ in the POC. The Δ¹⁴C values ranged between −395 ± 83 (SOC), −226 ± 92 (DOC) and −113 ± 122 ‰ (POC). These stable and radiocarbon isotopes were also different between the Laptev Sea and the East Siberian Sea. Both DOC and POC showed a depleted and younger trend off the Lena River plume. Further, the Pacific inflow and the sea-ice coverage, which works as a barrier preventing the input of “young” DOC and POC, seem to have a strong influence in these carbon pools, presenting older and more enriched δ¹³C signatures under the sea-ice extent. Lignin phenols exhibited higher OC-normalized concentrations in the SOC (0.10–2.34 mg g⁻¹ OC) and DOC (0.08–2.40 mg g⁻¹ OC) than in the POC (0.03–1.14 mg g⁻¹ OC). The good relationship between lignin and Δ¹⁴C signatures in the DOC suggests that a significant fraction of the outer-shelf DOC comes from “young” Terr-OC. By contrast, the slightly negative correlation between lignin phenols and Δ¹⁴C signatures in POC, with higher lignin concentrations in older POC from near-bottom waters, may reflect the off-shelf transport of OC from remobilized permafrost in the nepheloid layer. Syringyl ∕ vanillyl and cinnamyl ∕ vannillyl phenol ratios presented distinct clustering between DOC, POC and SOC, implying that those pools may be carrying different Terr-OC of partially different origin. Moreover, 3,5-dihydroxybenzoic acid to vanillyl phenol ratios and p-coumaric acid to ferulic acid ratios, used as a diagenetic indicators, enhanced in POC and SOC, suggesting more degradation within these pools. Overall, the key contrast between enhanced lignin yields both in the youngest DOC and the oldest POC samples reflects a significant decoupling of terrestrial OC sources and pathways.

The Arctic is undergoing dramatic changes which cover the entire range of natural processes, from extreme increases in the temperatures of air, soil, and water, to changes in the cryosphere, the biodiversity of Arctic waters, and land vegetation. Small changes in the largest marine carbon pool, the dissolved inorganic carbon pool, can have a profound impact on the carbon dioxide (CO₂) flux between the ocean and the atmosphere, and the feedback of this flux to climate. Knowledge of relevant processes in the Arctic seas improves the evaluation and projection of carbon cycle dynamics under current conditions of rapid climate change. Investigation of the CO₂ system in the outer shelf and continental slope waters of the Eurasian Arctic seas (the Barents, Kara, Laptev, and East Siberian seas) during 2006, 2007, and 2009 revealed a general trend in the surface water partial pressure of CO₂ (pCO₂) distribution, which manifested as an increase in pCO₂ values eastward. The existence of this trend was defined by different oceanographic and biogeochemical regimes in the western and eastern parts of the study area; the trend is likely increasing due to a combination of factors determined by contemporary change in the Arctic climate, each change in turn evoking a series of synergistic effects. A high-resolution in situ investigation of the carbonate system parameters of the four Arctic seas was carried out in the warm season of 2007; this year was characterized by the next-to-lowest historic sea-ice extent in the Arctic Ocean, on satellite record, to that date. The study showed the different responses of the seawater carbonate system to the environment changes in the western vs. the eastern Eurasian Arctic seas. The large, open, highly productive water area in the northern Barents Sea enhances atmospheric CO₂ uptake. In contrast, the uptake of CO₂ was strongly weakened in the outer shelf and slope waters of the East Siberian Arctic seas under the 2007 environmental conditions. The surface seawater appears in equilibrium or slightly supersaturated by CO₂ relative to atmosphere because of the increasing influence of river runoff and its input of terrestrial organic matter that mineralizes, in combination with the high surface water temperature during sea-ice-free conditions. This investigation shows the importance of processes that vary on small scales, both in time and space, for estimating the air–sea exchange of CO₂. It stresses the need for high-resolution coverage of ocean observations as well as time series. Furthermore, time series must include multi-year studies in the dynamic regions of the Arctic Ocean during these times of environmental change.

Seeps found offshore in the East Siberian Arctic Shelf may mark zones of degrading subsea permafrost and related destabilization of gas hydrates. Sonar surveys provide an effective tool for mapping seabed methane fluxes and monitoring subsea Arctic permafrost seepage. The paper presents an overview of existing approaches to sonar estimation of methane bubble flux from the sea floor to the water column and a new method for quantifying CH₄ ebullition. In the suggested method, the flux of methane bubbles is estimated from its response to insonification using the backscattering cross section. The method has demonstrated its efficiency in the case study of single- and multi-beam acoustic surveys of a large seep field on the Laptev Sea shelf.

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.

Global warming in high latitudes causes destabilization of vulnerable permafrost deposits followed by massive thaw-release of organic carbon. Permafrost-derived carbon may be buried in the nearshore sediments, transported towards the deeper basins or degraded into the greenhouse gases, potentially initiating a positive feedback to climate change. In the present study, we aim to identify the sources, distribution and degradation state of organic matter (OM) stored in the surface sediments of the Laptev Sea (LS), which receives a large input of terrestrial carbon from both Lena River discharge and intense coastal erosion. We applied a suite of geochemical indicators including the Rock Eval parameters, traditionally used for the matured OM characterization, and terrestrial lipid biomarkers. In addition, we analyzed a comprehensive grain size data in order to assess hydrodynamic sedimentation regime across the LS shelf. Rock-Eval (RE) data characterize LS sedimentary OM with generally low hydrogen index (100–200 mg HC/g TOC) and oxygen index (200 and 300 CO₂/g TOC) both increasing off to the continental slope. According to T_peak values, there is a clear regional distinction between two groups (369–401 °C for the inner and mid shelf; 451–464 °C for the outer shelf). We suggest that permafrost-derived OM is traced across the shallow and mid depths with high T_peak and slightly elevated HI values if compared to other Arctic continental margins. Molecular-based degradation indicators show a trend to more degraded terrestrial OC with increasing distance from the coast corroborating with RE results. However, we observed much less variation of the degradation markers down to the deeper sampling horizons, which supports the notion that the most active OM degradation in LS land-shelf system takes part during the cross-shelf transport, not while getting buried deeper.

This paper presents the results of an acoustic survey carried out from the fast ice in the shallow waters of the East Siberian Arctic Shelf (ESAS) using a single beam echosounder. The aim of this paper is to demonstrate an improved approach to study seafloor seepages in the Arctic coastal zone with an echosounder calibrated on site. During wintertime field observations of natural rising gas bubbles, we recorded three periods of their increased activity with a total of 63 short-term ejections of bubbles from the seabed. This study presents quantitative estimates of the methane (CH₄) flux obtained in wintertime at two levels of the water column: (1) at the bottom/water interface and (2) at the water/sea ice interface. In winter, the flux of CH₄ transported by rising bubbles to the bottom water in the shallow part of the ESAS was estimated at ~19 g·m⁻² per day, while the flux reaching the water/sea ice interface was calculated as ~15 g·m⁻² per day taking into account the diffusion of CH₄ in the surrounding water and the enrichment of rising bubbles with nitrogen and oxygen. We suggest that this bubble-transported CH₄ flux reaching the water /sea ice interface can be emitted into the atmosphere through numerous ice trenches, leads, and polynyas. This CH₄ ebullition value detected at the water/sea ice interface is in the mid high range of CH₄ ebullition value estimated for the entire ESAS, and two orders higher than the upper range of CH₄ ebullition from the northern thermocarst lakes, which are considered as a significant source to the atmospheric methane budget.