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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. 

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. 

Arctic sea-ice loss is emblematic of an amplified Arctic water cycle and has critical feedback implications for global climate. Stable isotopes (δ 18 O, δ 2 H, d-excess ) are valuable tracers for constraining water cycle and climate processes through space and time. Yet, the paucity of well-resolved Arctic isotope data preclude an empirically derived understanding of the hydrologic changes occurring today, in the deep (geologic) past, and in the future. To address this knowledge gap, the Pan-Arctic Precipitation Isotope Network (PAPIN) was established in 2018 to coordinate precipitation sampling at 19 stations across key tundra, subarctic, maritime, and continental climate zones. Here, we present a first assessment of rainfall samples collected in summer 2018 ( n = 281) and combine new isotope and meteorological data with sea ice observations, reanalysis data, and model simulations. Data collectively establish a summer Arctic Meteoric Water Line where δ 2 H = 7.6⋅δ 18 O–1.8 ( r 2 = 0.96, p < 0.01). Mean amount-weighted δ 18 O, δ 2 H, and d-excess values were −12.3, −93.5, and 4.9‰, respectively, with the lowest summer mean δ 18 O value observed in northwest Greenland (−19.9‰) and the highest in Iceland (−7.3‰). Southern Alaska recorded the lowest mean d-excess (−8.2%) and northern Russia the highest (9.9‰). We identify a range of δ 18 O-temperature coefficients from 0.31‰/°C (Alaska) to 0.93‰/°C (Russia). The steepest regression slopes (>0.75‰/°C) were observed at continental sites, while statistically significant temperature relations were generally absent at coastal stations. Model outputs indicate that 68% of the summer precipitating air masses were transported into the Arctic from mid-latitudes and were characterized by relatively high δ 18 O values. Yet 32% of precipitation events, characterized by lower δ 18 O and high d-excess values, derived from northerly air masses transported from the Arctic Ocean and/or its marginal seas, highlighting key emergent oceanic moisture sources as sea ice cover declines. Resolving these processes across broader spatial-temporal scales is an ongoing research priority, and will be key to quantifying the past, present, and future feedbacks of an amplified Arctic water cycle on the global climate system.