生物地球化学循环
溶解有机碳
环境科学
碳循环
北极的
总有机碳
有机质
海洋学
环境化学
陆地生态系统
碳纤维
生物地球化学
生物圈
二氧化碳
焊剂(冶金)
有色溶解有机物
海洋酸化
碳通量
气候变化
水团
海水
生态系统
化学海洋学
铅(地质)
地球科学
地表水
深海
作者
Xianyu Kong,Oliver J. Lechtenfeld,Jan Kaesler,Mats A. Granskog,Colin A. Stedmon,Martin Graeve,Boris Koch
标识
DOI:10.1038/s41561-025-01847-5
摘要
Abstract Arctic warming is expected to increase the terrestrial dissolved organic carbon flux into the central Arctic Ocean, altering biogeochemical cycling by modulating light attenuation, microbial respiration and carbon dioxide release. Quantifying terrestrial inputs remains challenging due to biases in common proxies and uncertainties in endmember characteristics, which complicate traditional mixing models, introducing uncertainties in predicting climate change impacts. Here we present a high-resolution mass spectrometric approach allowing direct analysis of original seawater, tracing and quantifying terrestrial contributions to dissolved organic carbon. Terrestrial dissolved organic carbon in the central Arctic Ocean contributed at least 0.97 ± 0.05 PgC (16.4%) to the dissolved organic carbon inventory of 5.93 ± 0.09 PgC, including 15.0% in deep water (7.9 ± 0.4 µmol l −1 ). In surface water within the Transpolar Drift, the average terrestrial dissolved organic carbon concentrations were 117% higher (31.5 ± 4.8 µmol l −1 ) than outside the Transpolar Drift (14.5 ± 1.0 µmol l −1 ). The terrestrial dissolved organic matter is compositionally distinct, being more aromatic, hydrophobic and nitrogen-poor than marine sources. This approach provides chemical information that reflects changes in organic matter sources and bioavailability, both of which are central to understanding future climatic impacts on Arctic biogeochemical cycles.
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