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Abstract Global trends in river nitrogen yields reflect human distortion of the global nitrogen cycle. Climate change and increasing agricultural intensity are projected to enhance river nitrogen yields in temperate watersheds and impair downstream water quality. However, little is known about the environmental drivers of nitrogen yields in major Arctic rivers, which have experienced rapid climatic changes and are important conduits of nutrients and organic matter to the Arctic Ocean. Here we analyze trends in nitrogen yields in the six largest Arctic rivers between 2003 and 2023 and develop generalized additive models to elucidate the watershed characteristics and climatic processes associated with observed spatial and interannual variability. We found significant increases in dissolved organic nitrogen yield and/or declines in dissolved inorganic nitrogen yield in four of the six rivers. While temperature and precipitation, via their relationships to discharge, enhance dissolved nitrogen yields, we attribute the diverging trends to the responses of inorganic and organic nitrogen to temperature via effects on permafrost free extent. Spatially, we attribute differences in nitrogen yields across watersheds to differences in land cover and temperature. Shifts in the amount and composition of river nitrogen yields will impact the balance between primary productivity and heterotrophy in nitrogen limited coastal Arctic Ocean ecosystems. Results from this work highlight the importance of climate‐driven changes in temperature and precipitation on river nitrogen yields in large Arctic rivers and motivate further investigation into how permafrost loss and hydrological shifts interact to drive water quality and biogeochemical cycling in the region. 

Abstract Arctic amplification is leading to increased terrestrial organic carbon (terrOC) mobilization with downstream impacts on riverine and marine biogeochemistry. To improve quantification and characterization of terrOC discharged to the Arctic Ocean, Yukon River delta samples were collected during three stages of the annual hydrograph (ascending limb/peak freshet, descending limb, late summer) and across a land‐to‐ocean salinity gradient (0.08–29.06 ppt). All samples were analyzed for dissolved organic carbon (DOC) concentration and lignin phenols to determine seasonal variability in riverine terrOC and salinity‐induced transformation of highly aromatic terrestrial compounds. Additionally, the relationship between lignin and absorbance at 350 and 412 nm was assessed to determine the feasibility of using optical proxies for accurate quantification, both seasonally and across expansive salinity gradients. Lignin phenols were highest during the ascending limb/peak freshet (0.58–0.97 mg/100 mg OC) when riverine DOC was dominated by young vascular plant sources, whereas lignin phenols were lower (0.15–0.89 mg/100 mg OC) and riverine DOC more variable in terrestrial source and diagenetic state during the descending limb and late summer. Across the sampled salinity gradient, there was disproportionate depletion of lignin (up to 73%) compared to DOC (up to 22%). Finally, while optical proxies can be used to quantify lignin within seasonal or spatial contexts, increased uncertainty is likely when expanding linear correlations across Arctic land‐ocean continuums. Overall, results indicate seasonal, spatial, interannual, and climatic controls that are amplified during high‐flow conditions and important to constrain when investigating Arctic terrOC cycling and land‐ocean DOC flux. 

Abstract Climate change is dramatically altering Arctic ecosystems, leading to shifts in the sources, composition, and eventual fate of riverine dissolved organic matter (DOM) in the Arctic Ocean. Here we examine a 6‐year DOM compositional record from the six major Arctic rivers using Fourier‐transform ion cyclotron resonance mass spectrometry paired with dissolved organic carbon isotope data (Δ¹⁴C, δ¹³C) to investigate how seasonality and permafrost influence DOM, and how DOM export may change with warming. Across the pan‐Arctic, DOM molecular composition demonstrates synchrony and stability. Spring freshet brings recently leached terrestrial DOM with a latent high‐energy and potentially bioavailable subsidy, reconciling the historical paradox between freshet DOM's terrestrial bulk signatures and high biolability. Winter features undiluted baseflow DOM sourced from old, microbially degraded groundwater DOM. A stable core Arctic riverine fingerprint (CARF) is present in all samples and may contribute to the potential carbon sink of persistent, aged DOM in the global ocean. Future warming may lead to shifting sources of DOM and export through: (1) flattening Arctic hydrographs and earlier melt modifying the timing and role of the spring high‐energy subsidy; (2) increasing groundwater discharge resulting in a greater fraction of DOM export to the ocean occurring as stable and aged molecules; and (3) increasing contribution of nitrogen/sulfur‐containing DOM from microbial degradation caused by increased connectivity between groundwater and surface waters due to permafrost thaw. Our findings suggest the ubiquitous CARF (which may contribute to oceanic carbon sequestration) underlies predictable variations in riverine DOM composition caused by seasonality and permafrost extent. 

In contrast to fairly good knowledge of dissolved carbon and major elements in great Arctic rivers, seasonally resolved concentrations of many trace elements remain poorly characterized, hindering assessment of the current status and possible future changes in the hydrochemistry of the Eurasian Arctic. To fill this gap, here we present results for a broad suite of trace elements in the largest rivers of the Russian Arctic (Ob, Yenisey, Lena, and Kolyma). For context, we also present results for major elements that are more routinely measured in these rivers. Water samples for this study were collected during an international campaign called PARTNERS from 2004 through 2006. A comparison of element concentrations obtained for Arctic rivers in this study with average concentrations in the world’s rivers shows that most elements in the Arctic rivers are similar to or significantly lower than the world average. The mineral content of the three greatest rivers (Ob, Yenisey, and Lena) varies within a narrow range (from 107 mg/L for Yenisey to 123 mg/L for Ob). The Kolyma’s mineral content is significantly lower (52.4 mg/L). Fluxes of all major and trace elements were calculated using average concentrations and average water discharge for the 2004–2006 period. Based on these flux estimates, specific export (i.e., t/km2/y) for most of the elements was greatest for the Lena, followed by the Yenisey, Ob, and Kolyma in decreasing order. Element pairwise correlation analysis identified several distinct groups of elements depending on their sources and relative mobility in the river water. There was a negative correlation between Fe and DOC concentration in the Ob River, which could be linked to different sources of these components in this river. The annual yields of major and trace elements calculated for each river were generally consistent with values assessed for other mid-size and small rivers of the Eurasian subarctic. 

Key Points Modeled dissolved organic carbon export was 18.4 Tg C yr ‐1 (median) from 1982‐2019 for the six largest Arctic Rivers Proportional contributions of chromophoric to total dissolved organic carbon (CDOC & DOC) are positively correlated with water discharge Increasing discharge and shifting seasonality, independent of other factors, would have increased CDOC and DOC export from 1982‐2019 

Key Points Mackenzie River biogeochemical discharge decreases the southeastern Beaufort Sea carbon sink Terrestrial dissolved inorganic carbon (DIC) is the primary driver of outgassing events in the SBS, followed by terrestrial DOC Interannual variability in river discharge modulates localized air‐sea CO 2 flux 

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.