Abstract:
Black 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.