Abstract
AbstractBlack carbon (BC) has emerged as an integral part of the global carbon (C) cycle, constituting 12% ± 5% of the organic C pool in rivers and soils, with the potential to generate negative climate feedback. However, its ability to sequester C depends on the recalcitrant nature of BC in the environment, which is under debate. Using CTO‐375 method and by measuring concentrations and isotopic compositions of particulate BC (δ13CPBC), we explore the transformation of particulate black carbon (PBC) along the atmosphere‐river‐ocean continuum. Significantly high δ13CPBC in the ocean compared to rivers and atmospheric particulate matter indicates (a) degradation of PBC, potentially through photodegradation and leaching, and/or (b) availability of an enriched source other than fluvial or aeolian inputs. This evidence for degradation of PBC in aquatic systems warrants rethinking on its C sequestration potential and role in aquatic C biogeochemistry and further raises concerns regarding the use of sedimentary BC as a paleoenvironmental proxy.
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