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    Carbon cycling in the North American coastal ocean: a synthesis

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    Date Issued
    2019-03-27
    Author
    Fennel, Katja
    Alin, Simone
    Barbero, Leticia
    Evans, Wiley
    Bourgeois, Timothée
    Cooley, Sarah
    Dunne, John
    Feely, Richard A.
    Hernandez-Ayon, Jose Martin
    Hu, Xinping
    Lohrenz, Steven
    Muller-Karger, Frank
    Najjar, Raymond
    Robbins, Lisa
    Shadwick, Elizabeth
    Siedlecki, Samantha
    Steiner, Nadja
    Sutton, Adrienne
    Turk, Daniela
    Vlahos, Penny
    Wang, Zhaohui Aleck
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    DOI
    https://doi.org/10.5194/bg-16-1281-2019
    URI
    https://hdl.handle.net/1969.6/89413
    Abstract
    A quantification of carbon fluxes in the coastal ocean and across its boundaries with the atmosphere, land, and the open ocean is important for assessing the current state and projecting future trends in ocean carbon uptake and coastal ocean acidification, but this is currently a missing component of global carbon budgeting. This synthesis reviews recent progress in characterizing these carbon fluxes for the North American coastal ocean. Several observing networks and high-resolution regional models are now available. Recent efforts have focused primarily on quantifying the net air–sea exchange of carbon dioxide (CO2). Some studies have estimated other key fluxes, such as the exchange of organic and inorganic carbon between shelves and the open ocean. Available estimates of air–sea CO2 flux, informed by more than a decade of observations, indicate that the North American Exclusive Economic Zone (EEZ) acts as a sink of 160±80 Tg C yr−1, although this flux is not well constrained. The Arctic and sub-Arctic, mid-latitude Atlantic, and mid-latitude Pacific portions of the EEZ account for 104, 62, and −3.7 Tg C yr−1, respectively, while making up 51 %, 25 %, and 24 % of the total area, respectively. Combining the net uptake of 160±80 Tg C yr−1 with an estimated carbon input from land of 106±30 Tg C yr−1 minus an estimated burial of 65±55 Tg C yr−1 and an estimated accumulation of dissolved carbon in EEZ waters of 50±25 Tg C yr−1 implies a carbon export of 151±105 Tg C yr−1 to the open ocean. The increasing concentration of inorganic carbon in coastal and open-ocean waters leads to ocean acidification. As a result, conditions favoring the dissolution of calcium carbonate occur regularly in subsurface coastal waters in the Arctic, which are naturally prone to low pH, and the North Pacific, where upwelling of deep, carbon-rich waters has intensified. Expanded monitoring and extension of existing model capabilities are required to provide more reliable coastal carbon budgets, projections of future states of the coastal ocean, and quantification of anthropogenic carbon contributions.
    Citation
    Fennel, K., Alin, S., Barbero, L., Evans, W., Bourgeois, T., Cooley, S., Dunne, J., Feely, R. A., Hernandez-Ayon, J. M., Hu, X., Lohrenz, S., Muller-Karger, F., Najjar, R., Robbins, L., Shadwick, E., Siedlecki, S., Steiner, N., Sutton, A., Turk, D., Vlahos, P., and Wang, Z. A.: Carbon cycling in the North American coastal ocean: a synthesis, Biogeosciences, 16, 1281–1304, https://doi.org/10.5194/bg-16-1281-2019, 2019.
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