Description: Estuaries are recognized as one of the habitats most vulnerable to coastal ocean acidification due to seasonal extremes and prolonged duration of acidified conditions. This is combined with co-occurring environmental stressors such as increased temperature and low dissolved oxygen. Despite this, evidence of biological impacts of ocean acidification in estuarine habitats is largely lacking. By combining physical, biogeochemical, and biological time-series observations over relevant seasonal-to-interannual time scales, this study is the first to describe both the spatial and temporal variation of biological response in the pteropod Limacina helicina to estuarine acidification in association with other stressors. Using clustering and principal component analyses, sampling sites were grouped according to their distribution of physical and biogeochemical variables over space and time. This identified the most exposed habitats and time intervals corresponding to the most severe negative biological impacts across three seasons and three years. We developed a cumulative stress index as a means of integrating spatial-temporal OA variation over the organismal life history. Our findings show that over the 2014–2016 study period, the severity of low aragonite saturation state combined with the duration of exposure contributed to overall cumulative stress and resulted in severe shell dissolution. Seasonally-variable estuaries such as the Salish Sea (Washington, U.S.A.) predispose sensitive organisms to more severe acidified conditions than those of coastal and open-ocean habitats, yet the sensitive organisms persist. We suggest potential environmental factors and compensatory mechanisms that allow pelagic calcifiers to inhabit less favorable habitats and partially offset associated stressors, for instance through food supply, increased temperature, and adaptation of their life history. The novel metric of cumulative stress developed here can be applied to other estuarine environments with similar physical and chemical dynamics, providing a new tool for monitoring biological response in estuaries under pressure from accelerating global change.

Description: © The Author(s), 2019. This article is distributed under the terms of the Creative Commons Attribution License. The definitive version was published in WHOI Fennel, K., Alin, S., Barbero, L., Evans, W., Bourgeois, T., Cooley, S., Dunne, J., Feely, R. A., Martin Hernandez-Ayon, J., Hu, X., Lohrenz, S., Muller-Karger, F., Najjar, R., Robbins, L., Shadwick, E., Siedlecki, S., Steiner, N., Sutton, A., Turk, D., Vlahos, P., & Wang, Z. A. Carbon cycling in the north american coastal ocean: A synthesis. Biogeosciences, 16(6), (2019):1281-1304, doi:10.5194/bg-16-1281-2019.

Description: 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.

Description: This paper builds on synthesis activities carried out for the second State of the Carbon Cycle Report (SOCCR2). We would like to thank Gyami Shrestha, Nancy Cavallero, Melanie Mayes, Holly Haun, Marjy Friedrichs, Laura Lorenzoni, and Erica Ombres for the guidance and input. We are grateful to Nicolas Gruber and Christophe Rabouille for their constructive and helpful reviews of the paper. It is a contribution to the Marine Biodiversity Observation Network (MBON), the Integrated Marine Biosphere Research (IMBeR) project, the International Ocean Carbon Coordination Project (IOCCP), and the Cooperative Institute of the University of Miami and the National Oceanic and Atmospheric Administration (CIMAS) under cooperative agreement NA10OAR4320143. Katja Fennel was funded by the NSERC Discovery program. Steven Lohrenz was funded by NASA grant NNX14AO73G. Ray Najjar was funded by NASA grant NNX14AM37G. Frank Muller-Karger was funded through NASA grant NNX14AP62A. This is Pacific Marine Environmental Laboratory contribution number 4837 and Lamont-Doherty Earth Observatory contribution number 8284. Simone Alin and Richard A. Feely also thank Libby Jewett and Dwight Gledhill of the NOAA Ocean Acidification Program for their support.