Variable aging and storage of dissolved black carbon in the ocean

Author:

Coppola Alysha I.1ORCID,Druffel Ellen R. M.2,Broek Taylor A.3ORCID,Haghipour Negar14,Eglinton Timothy I.1ORCID,McCarthy Matthew5,Walker Brett D.26

Affiliation:

1. Department of Earth Sciences, Geological Institute, ETH Zürich, Zürich 8092, Switzerland

2. Department of Earth System Science, University of California, Irvine, CA 92697

3. Geology and Geophysics Department, Woods Hole Oceanographic Institution, Woods Hole, MA 02543

4. Laboratory of Ion Beam Physics, ETH Zürich, Zürich 8093, Switzerland

5. Department of Ocean Science, University of California, Santa Cruz, CA 95064

6. Department of Earth and Environmental Sciences, University of Ottawa, Ottawa, ON K1N 6N5, Canada

Abstract

During wildfires and fossil fuel combustion, biomass is converted to black carbon (BC) via incomplete combustion. BC enters the ocean by rivers and atmospheric deposition contributing to the marine dissolved organic carbon (DOC) pool. The fate of BC is considered to reside in the marine DOC pool, where the oldest BC 14 C ages have been measured (>20,000 14 C y), implying long-term storage. DOC is the largest exchangeable pool of organic carbon in the oceans, yet most DOC (>80%) remains molecularly uncharacterized. Here, we report 14 C measurements on size-fractionated dissolved BC (DBC) obtained using benzene polycarboxylic acids as molecular tracers to constrain the sources and cycling of DBC and its contributions to refractory DOC (RDOC) in a site in the North Pacific Ocean. Our results reveal that the cycling of DBC is more dynamic and heterogeneous than previously believed though it does not comprise a single, uniformly “old” 14 C age. Instead, both semilabile and refractory DBC components are distributed among size fractions of DOC. We report that DBC cycles within DOC as a component of RDOC, exhibiting turnover in the ocean on millennia timescales. DBC within the low-molecular-weight DOC pool is large, environmentally persistent and constitutes the size fraction that is responsible for long-term DBC storage. We speculate that sea surface processes, including bacterial remineralization (via the coupling of photooxidation of surface DBC and bacterial co-metabolism), sorption onto sinking particles and surface photochemical oxidation, modify DBC composition and turnover, ultimately controlling the fate of DBC and RDOC in the ocean.

Funder

SNSF Ambizione Research Grant

Canada Research Chairs

US NSF Chemical Oceanography Program

Publisher

Proceedings of the National Academy of Sciences

Reference79 articles.

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