Arctic climate warming is causing permafrost thaw and erosion, which may lead to enhanced inputs of terrestrial organic matter into Arctic Ocean shelf sediments. Degradation of terrestrial organic matter in sediments might contribute to carbon dioxide production and bottom water acidification. Yet, the degradability of organic matter in shallow Arctic Ocean sediments, as well as the contribution of terrestrial input, is poorly quantified. Here, potential organic matter degradation rates were investigated for 16 surface sediments from the Kara Sea, Laptev Sea, and the western East Siberian Sea and compared with physicochemical sediment properties including molecular biomarkers, stable and radioactive carbon isotopes, and grain size. Aerobic oxygen and carbon dioxide fluxes, measured in laboratory incubations of sediment slurry, showed high spatial variability and correlated significantly with organic carbon content as well as with the amount and degradation state of terrestrial organic matter. The dependency on terrestrial organic matter declined with increasing distance from land, indicating that the presence of terrestrial organic matter is likely a constraining factor for organic matter degradation in shallow shelf seas. However, sediment oxygen consumption rates, measured in incubations of intact sediment cores, also exhibited substantial spatial variability but were not related to organic carbon content or terrestrial influence. Oxygen consumption of intact sediments may be more strongly influenced by in situ redox conditions. Together with previous observations, our findings support that terrestrial organic matter is easily degradable in shelf sea sediments and might substantially contribute to aerobic carbon dioxide production and oxygen consumption.

Arctic climate warming is causing permafrost thaw and erosion, which may lead to enhanced inputs of terrestrial organic matter into Arctic Ocean shelf sediments. Degradation of terrestrial organic matter in sediments might contribute to carbon dioxide production and bottom water acidification. Yet, the degradability of organic matter in shallow Arctic Ocean sediments, as well as the contribution of terrestrial input, is poorly quantified. Here, potential organic matter degradation rates were investigated for 16 surface sediments from the Kara Sea, Laptev Sea, and the western East Siberian Sea and compared with physicochemical sediment properties including molecular biomarkers, stable and radioactive carbon isotopes, and grain size. Aerobic oxygen and carbon dioxide fluxes, measured in laboratory incubations of sediment slurry, showed high spatial variability and correlated significantly with organic carbon content as well as with the amount and degradation state of terrestrial organic matter. The dependency on terrestrial organic matter declined with increasing distance from land, indicating that the presence of terrestrial organic matter is likely a constraining factor for organic matter degradation in shallow shelf seas. However, sediment oxygen consumption rates, measured in incubations of intact sediment cores, also exhibited substantial spatial variability but were not related to organic carbon content or terrestrial influence. Oxygen consumption of intact sediments may be more strongly influenced by in situ redox conditions. Together with previous observations, our findings support that terrestrial organic matter is easily degradable in shelf sea sediments and might substantially contribute to aerobic carbon dioxide production and oxygen consumption.

Continental margins receive, process and sequester most of the terrestrial organic carbon (terrOC) released into the ocean. In the Arctic, increasing fluvial discharge and collapsing permafrost are expected to enhance terrOC release and degradation, leading to ocean acidification and translocated CO2 release to the atmosphere. However, the processes controlling terrOC transport beyond the continental shelf, and the amount of terrOC that reaches the slope and the rise are poorly described. Here we study terrOC transport to the Laptev Sea continental slope and rise by probing surface sediments with dual-isotope (δ13C/Δ14C) source apportionment, degradation-diagnostic terrestrial biomarkers (n-alkanes, n-alkanoic acids, lignin phenols) and 210Pbxs-based mass accumulation rates (MAR). The MAR-terrOC (g m−2 yr−1) decrease from 14.7 ± 12.2 on the shelf, to 7.0 ± 5.8 over the slope, to 2.3 ± 0.3 for the rise. Scaling this to the respective regimes yields that 80% of the terrOC accumulates on the shelf, while 11% and 9% of the accumulation occurs in slope and rise sediments, respectively. TerrOC remineralization is evidenced by biomarker degradation proxies (CPI of n-alkanes and 3,5Bd/V) indicating 40% and 60% more terrOC degradation from slope to rise, consistent with a decline in terrOC concentrations by 57%. TerrOC degradation only partially explains this decline. An updated Laptev Sea terrOC budget suggests that sediment transport dynamics such as turbidity currents may drive terrOC shelf-basin export, contributing to the observed accumulation pattern. This study quantitatively demonstrates that Arctic shelf seas are key receptor systems for remobilized terrOC, emphasizing their importance in the carbon cycle of the rapidly changing Arctic.

The availability of silicon (Si) in the ocean plays an important role in regulating biogeochemical and ecological processes. The Si budget of the Arctic Ocean appears balanced, with inputs equivalent to outputs, though it is unclear how a changing climate might aggravate this balance. In this study, we focus on Si cycling in Arctic coastal areas and continental shelf sediments to better constrain the Arctic Ocean Si budget. We provide the first estimate of amorphous Si (ASi) loading from erosion of coastal Yedoma deposits (30-90 Gmol yr-1), demonstrating comparable rates to particulate Si loading from rivers (10-90 Gmol yr-1). We found a positive relationship between surface sediment ASi and organic matter content on continental shelves. Combining these values with published Arctic shelf sediment properties and burial rates we estimate 70 Gmol Si yr-1 is buried on Arctic continental shelves, equivalent to 4.5% of all Si inputs to the Arctic Ocean. Sediment dissolved Si fluxes increased with distance from river mouths along cruise transects of shelf regions influenced by major rivers in the Laptev and East Siberian seas. On an annual basis, we estimate that Arctic shelf sediments recycle approximately up to twice as much DSi (680 Gmol Si) as is loaded from rivers (340-500 Gmol Si). Coastal erosion loads 30-90 Gmol Si yr-1 to the Arctic Ocean in the form of amorphous siliconContinental shelf sediments in the Arctic Ocean recycle more silicon than is loaded from riversApproximately 4.5% of silicon loaded on the Arctic Ocean is buried in continental shelf sediments

The environmental fate of hazardous hydrophobic pollutants in the marine environment is strongly influenced by organic carbon (OC) cycling. As an example, the seasonality in primary production impacts both water column OC quantity and quality, which may influence pollutant mass transport from the water column to the sediment. This study aims to better understand the role of water column OC variability for the fate of pollutants in a near-coastal area. We conducted an in situ sampling campaign in the coastal Baltic Proper during two seasons, summer and autumn. We used polycyclic aromatic hydrocarbons (PAHs) and polychlorinated biphenyls (PCBs) as model compounds, as they represent a wide range in physicochemical properties and are ubiquitous in the environment. Freely dissolved, and OC-bound concentrations were studied in the water column and surface sediment. We found stronger sorption of pollutants to suspended particulate matter (SPM) during the summer compared to the autumn (average 0.6 and 0.9 log unit higher particle-water partition coefficients during summer for PAHs and PCBs). Our data suggest that stronger sorption mirrors a compositional change of the OC towards higher contribution of labile OC during the summer, characterized by two times higher fatty acid and 24% higher dicarboxylic acids in SPM during summer. High concentrations of OC in the water column during the autumn resulted in increased SPM-mediated sinking fluxes of pollutants. Our results suggest that future changes in primary production are prone to influence the bioavailability and mobility of pollutants in costal zones, potentially affecting the residence time of these hazardous substances in the circulating marine environment.

Arctic change is expected to destabilize terrestrial carbon (terrOC) in soils and permafrost, leading to fluvial release, greenhouse gas emission and climate feedback. However, landscape heterogeneity and location-specific observations complicate large-scale assessments of terrOC mobilization. Here we reveal differences in terrOC release, deduced from the Circum-Arctic Sediment Carbon Database (CASCADE) using source-diagnostic (δ¹³C-Δ¹⁴C) and carbon accumulation data. The results show five-times larger terrOC release from the Eurasian than from the American Arctic. Most of the circum-Arctic terrOC originates from near-surface soils (61%); 30% stems from Pleistocene-age permafrost. TerrOC translocation, relative to land-based terrOC stocks, varies by a factor of five between circum-Arctic regions. Shelf seas with higher relative terrOC translocation follow the spatial pattern of recent Arctic warming, while such with lower translocation reflect long-distance lateral transport with efficient remineralization of terrOC. This study provides a receptor-based perspective for how terrOC release varies across the circum-Arctic.

Significant reserves of methane (CH₄) are held in the Arctic shelf, but the release of CH₄ to the overlying ocean and, subsequently, to the atmosphere has been believed to be restricted by impermeable subsea permafrost, which has sealed the upper sediment layers for thousands of years. Our studies demonstrate progressive degradation of subsea permafrost which controls the scales of CH₄ release from the sediment into the water-atmospheric system. Thus, new knowledge about the thermal state of subsea permafrost is crucial for better understanding of the permafrost -hydrate system and associated CH₄ release from the East Siberian Arctic Shelf (ESAS) – the broadest and shallowest shelf in the World Ocean, which contains about 80% of subsea permafrost and giant pools of hydrates. Meanwhile, the ESAS, still presents large knowledge gaps in many aspects, especially with respect to subsea permafrost distribution and physical properties of bottom sediments. New field data show that the ESAS has an unfrozen (ice-free) upper sediment layer, which in-situ temperature is −1.0 to −1.8 °C and 0.6оС above the freezing point. On one hand, these cold temperature patterns may be related to the presence of subsea permafrost, which currently primarily occurs in the part of the ESAS that is shallower than 100 m, while ice-bearing sediments may also exist locally under deeper water in the Laptev Sea. On the other hand, the negative bottom sediment temperatures of −1.8 °C measured on the Laptev Sea continental slope sediments underlying water columns as deep as down to 330 m may result from dissociation of gas hydrates or possibly from dense water cascading down from the shelf. In contrast, data collected on recent expeditions in the northern Laptev shelf, zones of warmer bottom temperatures are coinciding with methane seeps, likely induced by seismic and tectonic activity in the area. These warm temperatures are not seen in the East Siberian Sea area, not even in areas of methane seeps, yet with little seismic activity.

The thermal conductivity and heat capacity of bottom sediments recorded in the database of thermal parameters for the ESAS areas mainly depend on their lithification degree (density or porosity), moisture content, and particle size distribution. The thermal conductivity and heat capacity average about 1.0 W/(m·K) and 2900 kJ/(m³·K), with ±20% and ±10% variance, respectively, in all sampled Arctic sediments to a sub-bottom interval of 0–0.5 m.

Global warming triggers permafrost thaw, which increases the release of terrigenous organic matter (terr-OM) to the Arctic Ocean by coastal erosion and rivers. Terrigenous OM degradation in the Arctic Ocean contributes to greenhouse gas emissions and severe ocean acidification, yet the vulnerability of different terr-OM components is poorly resolved. Here, terr-OM degradation dynamics are studied with unprecedented spatial coverage over the World's largest shelf sea system—the East Siberian Arctic Shelf (ESAS), using a multi-proxy molecular biomarker approach. Mineral-surface-area-normalized concentrations of terr-OM compounds in surface sediments decreases offshore. Differences between terr-OM compound classes (lignin phenols, high-molecular weight [HMW] n-alkanes, n-alkanoic acids and n-alkanols, sterols, 3,5-dihydroxybenzoic acids, cutin acids) reflect contrasting influence of sources, propensity to microbial degradation and association with sedimenting particles, with lignin phenols disappearing 3-times faster than total terr-OM, and twice faster than other biomarkers. Molecular degradation proxies support substantial terr-OM degradation across the ESAS, with clearest trends shown by: 3,5-dihydroxybenzoic acid/vanillyl phenol ratios, acid-to-aldehyde ratios of syringyl and vanillyl phenols, Carbon Preference Indices of HMW n-alkyl compounds and sitostanol/β-sitosterol. The combination of terr-OM biomarker data with δ¹³C/Δ¹⁴C-based source apportionment indicates that the more degraded state of lignin is influenced by the relative contribution of river-transported terr-OM from surface soils, while HMW n-alkanoic acids and stigmasterol are influenced by erosion-derived terr-OM from Ice Complex deposits. Our findings demonstrate differences in vulnerability to degradation between contrasting terr-OM pools, and underscore the need to consider molecular properties for understanding and modeling of large-scale biogeochemical processes of the permafrost carbon-climate feedback.

Biogeochemical cycling in the semi-enclosed Arctic Ocean is strongly influenced by land-ocean transport of carbon and other elements and is vulnerable to environmental and climate changes. Sediments of the Arctic Ocean are an important part of biogeochemical cycling in the Arctic and provide the opportunity to study present and historical input and the fate of organic matter (e.g., through permafrost thawing). Comprehensive sedimentary records are required to compare differences between the Arctic regions and to study Arctic biogeochemical budgets. To this end, the Circum-Arctic Sediment CArbon DatabasE (CASCADE) was established to curate data primarily on concentrations of organic carbon (OC) and OC isotopes (delta C-13, Delta C-14) yet also on total N (TN) as well as terrigenous biomarkers and other sediment geochemical and physical properties. This new database builds on the published literature and earlier unpublished records through an extensive international community collaboration. This paper describes the establishment, structure and current status of CASCADE. The first public version includes OC concentrations in surface sediments at 4244 oceanographic stations including 2317 with TN concentrations, 1555 with delta C-13-OC values and 268 with Delta C-14-OC values and 653 records with quantified terrigenous biomarkers (high-molecular-weight n-alkanes, n-alkanoic acids and lignin phenols). CASCADE also includes data from 326 sediment cores, retrieved by shallow box or multi-coring, deep gravity/piston coring, or sea-bottom drilling. The comprehensive dataset reveals large-scale features of both OC content and OC sources between the shelf sea recipients. This offers insight into release of pre-aged terrigenous OC to the East Siberian Arctic shelf and younger terrigenous OC to the Kara Sea. Circum-Arctic sediments thereby reveal patterns of terrestrial OC remobilization and provide clues about thawing of permafrost. CASCADE enables synoptic analysis of OC in Arctic Ocean sediments and facilitates a wide array of future empirical and modeling studies of the Arctic carbon cycle. The database is openly and freely available online (https://doi.org/10.17043/cascade; Martens et al., 2021), is provided in various machine-readable data formats (data tables, GIS shapefile, GIS raster), and also provides ways for contributing data for future CASCADE versions. We will continuously update CASCADE with newly published and contributed data over the foreseeable future as part of the database management of the Bolin Centre for Climate Research at Stockholm University.

The transport and fate of hydrophobic organic contaminants (HOCs) in the marine environment are closely linked to organic carbon (OC) cycling processes. We investigated the influence of marine versus terrestrial OC origin on HOC fluxes at two Baltic Sea coastal sites with different relative contributions of terrestrial and marine OC. Stronger sorption of the more than four-ring polycyclic aromatic hydrocarbons and penta-heptachlorinated polychlorinated biphenyls (PCBs) was observed at the marine OC-dominated site. The site-specific partition coefficients between sediment OC and water were 0.2–1.0 log units higher at the marine OC site, with the freely dissolved concentrations in the sediment pore-water 2–10 times lower, when compared with the terrestrial OC site. The stronger sorption at the site characterized with marine OC was most evident for the most hydrophobic PCBs, leading to reduced fluxes of these compounds from sediment to water. According to these results, future changes in OC cycling because of climate change, leading to increased input of terrestrial OC to the marine system, can have consequences for the availability and mobility of HOCs in aquatic systems and thereby also for the capacity of sediments to store HOCs.