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Abstract The West Siberian Lowland (WSL) contains some of the largest wetlands and most extensive peatlands on Earth, storing vast amounts of vulnerable carbon across permafrost‐free to continuous permafrost zones. As temperature and precipitation changes continue to alter the Siberian landscape, carbon transfer to the atmosphere and export to the Arctic Ocean will be impacted. However, the drivers of organic carbon transfer are largely unknown across this region. We characterized seasonal dissolved organic carbon (DOC) concentration and dissolved organic matter (DOM) composition of WSL rivers from the middle reaches of the Ob’ River in the permafrost‐free zone, as well as tributaries of the Taz River in the northern continuous permafrost zone. DOC and aromatic DOM properties increased from spring to autumn in the Ob’ tributaries, reflecting the seasonal transition from groundwater‐sourced to terrestrial DOM. Differences in molecular‐level signatures via ultra‐high resolution mass spectrometry revealed the influence of redox processes on DOM composition in the winter while terrestrial DOM sourcing shifted from surface litter aliphatics and highly unsaturated and phenolic high‐O/C (HUP_{High O/C}) compounds in the spring to subsurface soils and HUP_{Low O/C}compounds by autumn. Furthermore, aromaticity and organic N were related to landscape properties including peatlands, forest cover, and the ratio of needleleaf:broadleaf forests. Finally, the Taz River tributaries were similar to summer and autumn Ob’ tributaries, but more enriched in N and S‐containing compounds. These signatures were likely derived from thawing permafrost, which we expect to increase in northern rivers due to active layer expansion in a warming Arctic. 

Key Points Total organic carbon export out of the delta to the ocean from April to September 2019 was 1.5 Tg C, 65% of which was dissolved organic carbon 50% and 25% of the total delta export of dissolved and particulate organic carbon crossed the 10 m isobath into the coastal ocean The breakdown of riverine organic matter increases light for phytoplankton growth in the surface ocean 100 s of kilometers into the ocean 

Abstract. Across the Arctic, vast areas of permafrost are being degraded by climatechange, which has the potential to release substantial quantities ofnutrients, including nitrogen into large Arctic rivers. These rivers heavilyinfluence the biogeochemistry of the Arctic Ocean, so it is important tounderstand the potential changes to rivers from permafrost degradation. Thisstudy utilized dissolved nitrogen species (nitrate and dissolved organicnitrogen (DON)) along with nitrogen isotope values (δ15N-NO3- and δ15N-DON) of samples collectedfrom permafrost sites in the Kolyma River and the six largest Arctic rivers.Large inputs of DON and nitrate with a unique isotopically heavy δ15N signature were documented in the Kolyma, suggesting the occurrenceof denitrification and highly invigorated nitrogen cycling in the Yedomapermafrost thaw zones along the Kolyma. We show evidence for permafrost-derived DON being recycled to nitrate as it passes through the river,transferring the high 15N signature to nitrate. However, the potentialto observe these thaw signals at the mouths of rivers depends on the spatialscale of thaw sites, permafrost degradation, and recycling mechanisms. Incontrast with the Kolyma, with near 100 % continuous permafrost extent,the Ob River, draining large areas of discontinuous and sporadicpermafrost, shows large seasonal changes in both nitrate and DON isotopicsignatures. During winter months, water percolating through peat soilsrecords isotopically heavy denitrification signals in contrast with thelighter summer values when surface flow dominates. This early yeardenitrification signal was present to a degree in the Kolyma, but the abilityto relate seasonal nitrogen signals across Arctic Rivers to permafrostdegradation could not be shown with this study. Other large rivers in theArctic show different seasonal nitrogen trends. Based on nitrogen isotopevalues, the vast majority of nitrogen fluxes in the Arctic rivers is fromfresh DON sourced from surface runoff through organic-rich topsoil and notfrom permafrost degradation. However, with future permafrost thaw, otherArctic rivers may begin to show nitrogen trends similar to the Ob. Ourstudy demonstrates that nitrogen inputs from permafrost thaw can beidentified through nitrogen isotopes, but only on small spatial scales.Overall, nitrogen isotopes show potential for revealing integrated catchmentwide nitrogen cycling processes. 

Arctic landscapes are warming and becoming wetter due to changes in precipitation and the timing of snowmelt which consequently alters seasonal runoff and river discharge patterns. These changes in hydrology lead to increased mobilization and transport of terrestrial dissolved organic matter (DOM) to Arctic coastal seas where significant impacts on biogeochemical cycling can occur. Here, we present measurements of dissolved organic carbon (DOC) and chromophoric DOM (CDOM) in the Yukon River-to-Bering Sea system and two river plumes on the Alaska North Slope which flow into the Beaufort Sea. Our sampling characterized optical and biogeochemical properties of DOM during high and low river discharge periods for the Yukon River-Bering Sea system. The average DOC concentration at the multiple Yukon River mouths ranged from a high of 10.36 mg C L -1 during the ascending limb of the 2019 freshet (late May), 6.4 mg C L -1 during the descending limb of the 2019 freshet (late June), and a low of 3.86 mg C L -1 during low river discharge in August 2018. CDOM absorption coefficient at 412 nm ( a CDOM (412)) averaged 8.23 m -1 , 5.07 m -1 , and 1.9 m -1 , respectively. Several approaches to model DOC concentration based on its relationship with CDOM properties demonstrated cross-system seasonal and spatial robustness for these Arctic coastal systems despite spanning an order of magnitude decrease in DOC concentration from the lower Yukon River to the Northern Bering Sea as well as the North Slope systems. “Snapshot” fluxes of DOC and CDOM across the Yukon River Delta to Norton Sound were calculated from our measurements and modeled water fluxes forced with upstream USGS river gauge data. Our findings suggest that during high river flow, DOM reaches the delta largely unaltered by inputs or physical and biogeochemical processing and that the transformations of Yukon River DOM largely occur in the plume. However, during low summer discharge, multiple processes including local precipitation events, microbial decomposition, photochemistry, and likely others can alter the DOM properties within the lower Yukon River and Delta prior to flowing into Norton Sound. 

Arctic rivers provide an integrated signature of the changing landscape and transmit signals of change to the ocean. Here, we use a decade of particulate organic matter (POM) compositional data to deconvolute multiple allochthonous and autochthonous pan-Arctic and watershed-specific sources. Constraints from carbon-to-nitrogen ratios (C:N), δ 13 C, and Δ 14 C signatures reveal a large, hitherto overlooked contribution from aquatic biomass. Separation in Δ 14 C age is enhanced by splitting soil sources into shallow and deep pools (mean ± SD: −228 ± 211 vs. −492 ± 173‰) rather than traditional active layer and permafrost pools (−300 ± 236 vs. −441 ± 215‰) that do not represent permafrost-free Arctic regions. We estimate that 39 to 60% (5 to 95% credible interval) of the annual pan-Arctic POM flux (averaging 4,391 Gg/y particulate organic carbon from 2012 to 2019) comes from aquatic biomass. The remainder is sourced from yedoma, deep soils, shallow soils, petrogenic inputs, and fresh terrestrial production. Climate change-induced warming and increasing CO 2 concentrations may enhance both soil destabilization and Arctic river aquatic biomass production, increasing fluxes of POM to the ocean. Younger, autochthonous, and older soil-derived POM likely have different destinies (preferential microbial uptake and processing vs. significant sediment burial, respectively). A small (~7%) increase in aquatic biomass POM flux with warming would be equivalent to a ~30% increase in deep soil POM flux. There is a clear need to better quantify how the balance of endmember fluxes may shift with different ramifications for different endmembers and how this will impact the Arctic system. 

The mechanisms controlling the extraordinarily slow carbon (C) mineralization rates characteristic of Sphagnum -rich peatlands (“bogs”) are not fully understood, despite decades of research on this topic. Soluble phenolic compounds have been invoked as potentially significant contributors to bog peat recalcitrance due to their affinity to slow microbial metabolism and cell growth. Despite this potentially significant role, the effects of soluble phenolic compounds on bog peat C mineralization remain unclear. We analyzed this effect by manipulating the concentration of free soluble phenolics in anaerobic bog and fen peat incubations using water-soluble polyvinylpyrrolidone (“PVP”), a compound that binds with and inactivates phenolics, preventing phenolic-enzyme interactions. CO 2 and CH 4 production rates (end-products of anaerobic C mineralization) generally correlated positively with PVP concentration following Michaelis-Menten (M.M.) saturation functions. Using M.M. parameters, we estimated that the extent to which phenolics inhibit anaerobic CO 2 production was significantly higher in the bog—62 ± 16%—than the fen—14 ± 4%. This difference was found to be more substantial with regards to methane production—wherein phenolic inhibition for the bog was estimated at 54 ± 19%, while the fen demonstrated no apparent inhibition. Consistent with this habitat difference, we observed significantly higher soluble phenolic content in bog vs. fen pore-water. Together, these findings suggest that soluble phenolics could contribute to bogs’ extraordinary recalcitrance and high (relative to other peatland habitats) CO 2 :CH 4 production ratios. 

Abstract Climate change is thawing and potentially mobilizing vast quantities of organic carbon (OC) previously stored for millennia in permafrost soils of northern circumpolar landscapes. Climate‐driven increases in fire and thermokarst may play a key role in OC mobilization by thawing permafrost and promoting transport of OC. Yet, the extent of OC mobilization and mechanisms controlling terrestrial‐aquatic transfer are unclear. We demonstrate that hydrologic transport of soil dissolved OC (DOC) from the active layer and thawing permafrost to headwater streams is extremely heterogeneous and regulated by the interactions of soils, seasonal thaw, fire, and thermokarst. Repeated sampling of streams in eight headwater catchments of interior Alaska showed that the mean age of DOC for each stream ranges widely from modern to ∼2,000 years B.P. Together, an endmember mixing model and nonlinear, generalized additive models demonstrated that Δ¹⁴C‐DOC signature (and mean age) increased from spring to fall, and was proportional to hydrologic contributions from a solute‐rich water source, related to presumed deeper flow paths found predominantly in silty catchments. This relationship was correlated with and mediated by catchment properties. Mean DOC ages were older in catchments with >50% burned area, indicating that fire is also an important explanatory variable. These observations underscore the high heterogeneity in aged C export and difficulty of extrapolating estimates of permafrost‐derived DOC export from watersheds to larger scales. Our results provide the foundation for developing a conceptual model of permafrost DOC export necessary for advancing understanding and prediction of land‐water C exchange in changing boreal landscapes.