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Climate warming is expected to mobilize northern permafrost and peat organic carbon (PP-C), yet magnitudes and system specifics of even current releases are poorly constrained. While part of the PP-C will degrade at point of thaw to CO 2 and CH 4 to directly amplify global warming, another part will enter the fluvial network, potentially providing a window to observe large-scale PP-C remobilization patterns. Here, we employ a decade-long, high-temporal resolution record of 14 C in dissolved and particulate organic carbon (DOC and POC, respectively) to deconvolute PP-C release in the large drainage basins of rivers across Siberia: Ob, Yenisey, Lena, and Kolyma. The 14 C-constrained estimate of export specifically from PP-C corresponds to only 17 ± 8% of total fluvial organic carbon and serves as a benchmark for monitoring changes to fluvial PP-C remobilization in a warming Arctic. Whereas DOC was dominated by recent organic carbon and poorly traced PP-C (12 ± 8%), POC carried a much stronger signature of PP-C (63 ± 10%) and represents the best window to detect spatial and temporal dynamics of PP-C release. Distinct seasonal patterns suggest that while DOC primarily stems from gradual leaching of surface soils, POC reflects abrupt collapse of deeper deposits. Higher dissolved PP-C export by Ob and Yenisey aligns with discontinuous permafrost that facilitates leaching, whereas higher particulate PP-C export by Lena and Kolyma likely echoes the thermokarst-induced collapse of Pleistocene deposits. Quantitative 14 C-based fingerprinting of fluvial organic carbon thus provides an opportunity to elucidate large-scale dynamics of PP-C remobilization in response to Arctic warming. 

Abstract. Biogeochemical cycling in the semi-enclosed Arctic Ocean is stronglyinfluenced by land–ocean transport of carbon and other elements and isvulnerable to environmental and climate changes. Sediments of the ArcticOcean are an important part of biogeochemical cycling in the Arctic andprovide the opportunity to study present and historical input and the fate oforganic matter (e.g., through permafrost thawing). Comprehensive sedimentary records are required to compare differencesbetween the Arctic regions and to study Arctic biogeochemical budgets. Tothis end, the Circum-Arctic Sediment CArbon DatabasE (CASCADE) wasestablished to curate data primarily on concentrations of organic carbon(OC) and OC isotopes (δ13C, Δ14C) yet also ontotal N (TN) as well as terrigenous biomarkers and other sedimentgeochemical and physical properties. This new database builds on thepublished literature and earlier unpublished records through an extensiveinternational community collaboration. This paper describes the establishment, structure and current status ofCASCADE. The first public version includes OC concentrations in surfacesediments at 4244 oceanographic stations including 2317 with TNconcentrations, 1555 with δ13C-OC values and 268 with Δ14C-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 shallowbox or multi-coring, deep gravity/piston coring, or sea-bottom drilling.The comprehensive dataset reveals large-scale features of both OC contentand OC sources between the shelf sea recipients. This offers insight intorelease of pre-aged terrigenous OC to the East Siberian Arctic shelf andyounger terrigenous OC to the Kara Sea. Circum-Arctic sediments therebyreveal patterns of terrestrial OC remobilization and provide clues about thawing of permafrost. CASCADE enables synoptic analysis of OC in Arctic Ocean sediments andfacilitates a wide array of future empirical and modeling studies of theArctic carbon cycle. The database is openly and freely available online(https://doi.org/10.17043/cascade; Martens et al., 2021), is provided in variousmachine-readable data formats (data tables, GIS shapefile, GIS raster), andalso provides ways for contributing data for future CASCADE versions. Wewill continuously update CASCADE with newly published and contributed dataover the foreseeable future as part of the database management of the BolinCentre for Climate Research at Stockholm University. 

Abstract Radium isotopes have been used to trace nutrient, carbon, and trace metal fluxes inputs from ocean margins. However, these approaches require a full accounting of radium sources to the coastal ocean including rivers. Here, we aim to quantify river radium inputs into the Arctic Ocean for the first time for²²⁶Ra and to refine the estimates for²²⁸Ra. Using new and existing data, we find that the estimated combined (dissolved plus desorbed) annual²²⁶Ra and²²⁸Ra fluxes to the Arctic Ocean are [7.0–9.4] × 10¹⁴dpm y⁻¹and [15–18] × 10¹⁴dpm y⁻¹, respectively. Of these totals, 44% and 60% of the river²²⁶Ra and²²⁸Ra, respectively are from suspended sediment desorption, which were estimated from laboratory incubation experiments. Using Ra isotope data from 20 major rivers around the world, we derived global annual²²⁶Ra and²²⁸Ra fluxes of [7.4–17] × 10¹⁵and [15–27] × 10¹⁵dpm y⁻¹, respectively. As climate change spurs rapid Arctic warming, hydrological cycles are intensifying and coastal ice cover and permafrost are diminishing. These river radium inputs to the Arctic Ocean will serve as a valuable baseline as we attempt to understand the changes that warming temperatures are having on fluxes of biogeochemically important elements to the Arctic coastal zone. 

Abstract Permafrost degradation is delivering bioavailable dissolved organic matter (DOM) and inorganic nutrients to surface water networks. While these permafrost subsidies represent a small portion of total fluvial DOM and nutrient fluxes, they could influence food webs and net ecosystem carbon balance via priming or nutrient effects that destabilize background DOM. We investigated how addition of biolabile carbon (acetate) and inorganic nutrients (nitrogen and phosphorus) affected DOM decomposition with 28‐day incubations. We incubated late‐summer stream water from 23 locations nested in seven northern or high‐altitude regions in Asia, Europe, and North America. DOM loss ranged from 3% to 52%, showing a variety of longitudinal patterns within stream networks. DOM optical properties varied widely, but DOM showed compositional similarity based on Fourier transform ion cyclotron resonance mass spectrometry (FT‐ICR MS) analysis. Addition of acetate and nutrients decreased bulk DOM mineralization (i.e., negative priming), with more negative effects on biodegradable DOM but neutral or positive effects on stable DOM. Unexpectedly, acetate and nutrients triggered breakdown of colored DOM (CDOM), with median decreases of 1.6% in the control and 22% in the amended treatment. Additionally, the uptake of added acetate was strongly limited by nutrient availability across sites. These findings suggest that biolabile DOM and nutrients released from degrading permafrost may decrease background DOM mineralization but alter stoichiometry and light conditions in receiving waterbodies. We conclude that priming and nutrient effects are coupled in northern aquatic ecosystems and that quantifying two‐way interactions between DOM properties and environmental conditions could resolve conflicting observations about the drivers of DOM in permafrost zone waterways.