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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. 

Arctic rivers transport water, sediment and carbon, playing a central role in coastal stability and biogeochemical cycling. Although freshwater discharge to the Arctic Ocean has increased in recent decades, limited observations have hindered system-wide assessment of long-term, reach-level sediment dynamics. Here we develop a pan-Arctic-specific, satellite- and machine learning-based framework to reconstruct four decades of suspended sediment concentration dynamics for 4,331 river reaches. Our analysis reveals a significant increase in suspended sediment concentration in 40% of river reaches (858 out of 2,158) draining continuous permafrost zone, primarily driven by increasing discharge, intensified thermokarst disturbances and fires. The pan-Arctic land–ocean sediment flux averages 315 ± 33 Mt yr−1, with 198 ± 35 Mt yr−1 (63%) from the six major rivers (Yenisey, Lena, Ob’, Kolyma, Yukon and Mackenzie) and 117 ± 13 Mt yr−1 (37%) from 263 previously overlooked small- and medium-sized coastal rivers. The total land–ocean sediment flux has increased by ~15%, from ~299 ± 28 Mt yr−1 in the 1980s to 344 ± 29 Mt yr−1 in the 2010s. These results provide a baseline for pan-Arctic river sediment dynamics and underscore the essential yet underappreciated contribution of small- and medium-sized coastal rivers to Arctic landscape and carbon cycle changes. 

Far from being frozen and sterile environments, glaciers are biogeochemical reactors and regulators. In this Review, we discuss the hydrology and biogeochemistry of glacierized environments and their impact on downstream ecosystems. Supraglacial meltwaters export labile organic carbon associated with active supraglacial microbial communities, as well as carbon and nutrients delivered via atmospheric deposition. Meltwaters funnelled to the glacier bed and exiting at the glacier snout transport large quantities of rock flour as well as supraglacial and subglacial-derived organic carbon and nutrients to downstream ecosystems. Subglacial water flow paths influence rock–water contact times and vary greatly, affecting weathering reactions. For instance, the hydrology of mountain glaciers and the Greenland Ice Sheet is typically dominated by seasonal melt with short (hours) to medium (weeks) water residence times, although extended biogeochemical isolation can exist in more isolated parts of the Greenland Ice Sheet. Conversely, the Antarctic Ice Sheet is dominated by basal ice melt and residence times that can exceed years and decades. As a result, the latter supports extended biogeochemical isolation and more advanced chemical weathering. Microbial processes and physical-chemical weathering can both sequester or emit greenhouse gases, but the net effect remains unknown. Meltwaters can potentially fuel biological processes in downstream ecosystems by priming glacier-fed streams, fjords, and oceans with rock flour and nutrients. The rapid reduction in glacier area projected for the next century mandates that future research provides a critical assessment of the effects of deglaciation on watershed biogeochemistry, ecology and global biogeochemical cycles. 

Abstract Wetland and permafrost soils contain some of Earth's largest reservoirs of organic carbon, and these stores are threatened by rapid warming across the Arctic. Nearly half of northern wetlands are affected by permafrost. As these ecosystems warm, the cycling of dissolved organic matter (DOM) and the opportunities for microbial degradation are changing. This is particularly evident as the relationship between wetland and permafrost DOM dynamics evolves, especially with the introduction of permafrost‐derived DOM into wetland environments. Thus, understanding the interplay of DOM composition and microbial communities from wetlands and permafrost is critical to predicting the impact of released carbon on global carbon cycling. As little is understood about the interactions between wetland active layer and permafrost‐derived sources as they intermingle, we conducted experimental bioincubations of mixtures of DOM and microbial communities from two fen wetland depths (shallow: 0–15 cm, and deep: 15–30 cm) and two ages of permafrost soil (Holocene and Pleistocene). We found that the source of microbial inoculum was not a significant driver of dissolved organic carbon (DOC) degradation across treatments; rather, DOM source and specifically, DOM molecular composition, controlled the rate of DOC loss over 100 days of bioincubations. DOC loss across all treatments was negatively correlated with modified aromaticity index, O/C, and the relative abundance of condensed aromatic and polyphenolic formula, and positively correlated with H/C and the relative abundance of aliphatic and peptide‐like formula. Pleistocene permafrost‐derived DOC exhibited ∼70% loss during the bioincubation driven by its initial molecular‐level composition, highlighting its high bioavailability irrespective of microbial source. 

Abstract. Glaciers export ancient bioavailable dissolved organic carbon (DOC). Yet, the sources of organic carbon (OC) underpinning bioavailability are poorly constrained. We assessed the isotopic composition of respired OC from bioincubations of glacier DOC. Relative to bulk DOC, respired OC was younger (+4350 to 8940 years) and 13C enriched (+9.2 ‰ to 12.2 ‰), consistent with utilization of an in situ-produced microbial carbon source. These findings provide direct evidence that a hidden pool of young OC may underpin the high bioavailability of ancient glacier DOC. 

Abstract The Amazon River mobilizes organic carbon across one of the world's largest terrestrial carbon reservoirs. Quantifying the sources of particulate organic carbon (POC) to this flux is typically challenging in large systems such as the Amazon River due to hydrodynamic sorting of sediments. Here, we analyze the composition of POC collected from multiple total suspended sediment (TSS) profiles in the mainstem at Óbidos, and surface samples from the Madeira, Solimões and Tapajós Rivers. As hypothesized, TSS and POC concentrations in the mainstem increased with depth and fit well to Rouse models for sediment sorting by grain size. Coupling these profiles with Acoustic Doppler Current Profiler discharge data, we estimate a large decrease in POC flux (from 540 to 370 kg per second) between the rising and falling stages of the Amazon River mainstem. The C/N ratio and stable and radiocarbon signatures of bulk POC are less variable within the cross‐section at Óbidos and suggest that riverine POC in the Amazon River is predominantly soil‐derived. However, smaller shifts in these compositional metrics with depth, including leaf waxn‐alkanes and fatty acids, are consistent with the perspective that deeper and larger particles carry fresher, less degraded organic matter sources (i.e., vegetation debris) through the mainstem. Overall, our cross‐sectional surveys at Óbidos highlight the importance of depth‐specific sampling for estimating riverine export fluxes. At the same time, they imply that this approach to sampling is perhaps less essential with respect to characterizing the composition of POC sources exported by the river. 

Coastal erosion mobilizes large quantities of organic matter (OM) to the Arctic Ocean where it may fuel greenhouse gas emissions and marine production. While the biodegradability of permafrost‐derived dissolved organic carbon (DOC) has been extensively studied in inland soils and freshwaters, few studies have examined dissolved OM (DOM) leached from eroding coastal permafrost in seawater. To address this knowledge gap, we sampled three horizons from bluff exposures near Drew Point, Alaska: seasonally thawed active layer soils, permafrost containing Holocene terrestrial and/or lacustrine OM, and permafrost containing late‐Pleistocene marine‐derived OM. Samples were leached in seawater to compare DOC yields, DOM composition (chromophoric DOM, Fourier transform ion cyclotron resonance mass spectrometry), and biodegradable DOC (BDOC). Holocene terrestrial permafrost leached the most DOC compared to active layer soils and Pleistocene marine permafrost. However, DOC from Pleistocene marine permafrost was the most biodegradable (33 ± 6% over 90 days), followed by DOC from active layer soils (23 ± 5%) and Holocene terrestrial permafrost (14 ± 3%). Permafrost leachates contained relatively more aliphatic and peptide‐like formulae, whereas active layer leachates contained relatively more aromatic formulae. BDOC was positively correlated with nitrogen‐containing and aliphatic formulae, and negatively correlated with polyphenolic and condensed aromatic formulae. Using estimates of eroding OM, we scale our results to estimate DOC and BDOC inputs to the Alaska Beaufort Sea. While DOC inputs from coastal erosion are relatively small compared to rivers, our results suggest that erosion may be an important source of BDOC to the Beaufort Sea when river inputs are low. 

Abstract Biospheric particulate organic carbon (POC_bio) burial and rock petrogenic particulate organic carbon (POC_petro) oxidation are opposing long‐term controls on the global carbon cycle, sequestering and releasing carbon, respectively. Here, we examine how watershed glacierization impacts the POC source by assessing the concentration and isotopic composition (δ¹³C and Δ¹⁴C) of POC exported from four watersheds with 0%–49% glacier coverage across a melt season in Southeast Alaska. We used two mixing models (age‐weight percent and dual carbon isotope) to calculate concentrations of POC_bioand POC_petrowithin the bulk POC pool. The fraction POC_petrocontribution was highest in the heavily glacierized watershed (age‐weight percent: 0.39 ± 0.05; dual isotope: 0.42 (0.37–0.47)), demonstrating a glacial source of POC_petroto fjords. POC_petrowas mobilized via glacier melt and subglacial flow, while POC_biowas largely flushed from the non‐glacierized landscape by rain. Flow normalized POC_bioconcentrations exceeded POC_petroconcentrations for all streams, but surprisingly were highest in the heavily glacierized watershed (mean: 0.70 mgL⁻¹; range 0.16–1.41 mgL⁻¹), suggesting that glacier rivers can contribute substantial POC_bioto coastal waters. Further, the most heavily glacierized watershed had the highest sediment concentration (207 mgL⁻¹; 7–708 mgL⁻¹), and thus may facilitate long‐term POC_bioprotection via sediment burial in glacier‐dominated fjords. Our results suggest that continuing glacial retreat will decrease POC concentrations and increase POC_bio:POC_petroexported from currently glacierized watersheds. Glacier retreat may thus decrease carbon storage in marine sediments and provide a positive feedback mechanism to climate change that is sensitive to future changes in POC_petrooxidation.