Beschreibung: Flow of dense shelf water provide an efficient mechanism for pumping CO 2 to the deep ocean along the continental shelf slope, particularly around the Antarctic bottom water (AABW) formation areas where much of the global bottom water is formed. However, the contribution of the formation of AABW to sequestering anthropogenic carbon ( C ant ) and its consequences remain unclear. Here, we show prominent transport of C ant (25.0 ± 4.7 Tg C yr −1 ) into the deep ocean (〉2,000 m) in four AABW formation regions around Antarctica based on an integrated observational data set (1974–2018). This maintains a lower C ant in the upper waters than that of other open oceans to sustain a stronger CO 2 uptake capacity (16.9 ± 3.8 Tg C yr −1 ). Nevertheless, the accumulation of C ant can further trigger acidification of AABW at a rate of −0.0006 ± 0.0001 pH unit yr −1 . Our findings elucidate the prominent role of AABW in controlling the Southern Ocean carbon uptake and storage to mitigate climate change, whereas its side effects (e.g., acidification) could also spread to other ocean basins via the global ocean conveyor belt. Plain Language Summary The Southern Ocean is thought to uptake and store a large amount of anthropogenic CO 2 ( C ant ), but little attention has been paid to the Antarctic coastal regions in the south of 60°S, mainly due to the lack of observations. Based on an integrated data set, we discovered the deep penetration of C ant and a visible pattern of relatively high concentration of C ant along the AABW formation pathway, and the concentration of C ant along the shelf‐slope is higher than that of other marginal seas at low‐mid latitudes, implying a highly effective C ant transport in AABW formation areas. We also found strong upper‐layer CO 2 uptake and a significant acidification rate in the deep waters of the Southern Ocean due to the AABW‐driven CO 2 transport, which is 3 times faster than those in other deep oceans. It is therefore crucial to understand how the Antarctic shelf regions affect the global carbon cycle through the uptake and transport of anthropogenic CO 2 , which also drives acidification in the other ocean basins. Key Points We show evidence for the accumulation of C ant along the Antarctic shelf‐slope into the deep ocean The process of AABW formation drives C ant downward transport at 25.0 ± 4.7 Tg C yr −1 , sustaining the CO 2 uptake in the surface ocean This further triggers acidification of AABW at a rate of −0.0006 ± 0.0001 pH unit yr −1 , which is faster than in other deep oceans

Beschreibung: Accurately predicting future ocean acidification (OA) conditions is crucial for advancing OA research at regional and global scales, and guiding society's mitigation and adaptation efforts. This study presents a new model-data fusion product covering 10 global surface OA indicators based on 14 Earth System Models (ESMs) from the Coupled Model Intercomparison Project Phase 6 (CMIP6), along with three recent observational ocean carbon data products. The indicators include fugacity of carbon dioxide, pH on total scale, total hydrogen ion content, free hydrogen ion content, carbonate ion content, aragonite saturation state, calcite saturation state, Revelle Factor, total dissolved inorganic carbon content, and total alkalinity content. The evolution of these OA indicators is presented on a global surface ocean 1° × 1° grid as decadal averages every 10 years from preindustrial conditions (1750), through historical conditions (1850–2010), and to five future Shared Socioeconomic Pathways (2020–2100): SSP1-1.9, SSP1-2.6, SSP2-4.5, SSP3-7.0, and SSP5-8.5. These OA trajectories represent an improvement over previous OA data products with respect to data quantity, spatial and temporal coverage, diversity of the underlying data and model simulations, and the provided SSPs. The generated data product offers a state-of-the-art research and management tool for the 21st century under the combined stressors of global climate change and ocean acidification. The gridded data product is available in NetCDF at the National Oceanic and Atmospheric Administration (NOAA) National Centers for Environmental Information: https://www.ncei.noaa.gov/data/oceans/ncei/ocads/metadata/0259391.html, and global maps of these indicators are available in jpeg at: https://www.ncei.noaa.gov/access/ocean-carbon-acidification-data-system/synthesis/surface-oa-indicators.html. Key Points: - This study presents the evolution of 10 ocean acidification (OA) indicators in the global surface ocean from 1750 to 2100 - By leveraging 14 Earth System Models (ESMs) and the latest observational data, it represents a significant advancement in OA projections - This inter-model comparison effort showcases the overall agreements among different ESMs in projecting surface ocean carbon variables

Beschreibung: Author Posting. © Oceanography Society, 2009. This article is posted here by permission of Oceanography Society for personal use, not for redistribution. The definitive version was published in Oceanography 22 no. 4 (2009): 16-25.

Beschreibung: Over a period of less than a decade, ocean acidification—the change in seawater chemistry due to rising atmospheric carbon dioxide (CO2) levels and subsequent impacts on marine life—has become one of the most critical and pressing issues facing the ocean research community and marine resource managers alike. The objective of this special issue of Oceanography is to provide an overview of the current scientific understanding of ocean acidification as well as to indicate the substantial gaps in our present knowledge. Papers in the special issue discuss the past, current, and future trends in seawater chemistry; highlight potential vulnerabilities to marine species, ecosystems, and marine resources to elevated CO2; and outline a roadmap toward future research directions. In this introductory article, we present a brief introduction on ocean acidification and some historical context for how it emerged so quickly and recently as a key research topic.

Beschreibung: We thank the National Science Foundation (NSF), National Oceanic and Atmospheric Administration (NOAA), and National Aeronautics and Space Administration (NASA) for research support on ocean acidification. We specifically acknowledge grants supporting the OCB Project Office (NSF OCE-0622984, NSF OCE-0927287, and NASA NNX08AX01G). Richard A. Feely was supported by the NOAA Climate Program under the Office of Climate Observations (Grant No. GC04-314 and the Global Carbon Cycle Program (Grant No. GC05-288).

Beschreibung: Author Posting. © Oceanography Society, 2009. This article is posted here by permission of Oceanography Society for personal use, not for redistribution. The definitive version was published in Oceanography 22 no. 4 (2009): 36-47.

Beschreibung: The uptake of anthropogenic CO2 by the global ocean induces fundamental changes in seawater chemistry that could have dramatic impacts on biological ecosystems in the upper ocean. Estimates based on the Intergovernmental Panel on Climate Change (IPCC) business-as-usual emission scenarios suggest that atmospheric CO2 levels could approach 800 ppm near the end of the century. Corresponding biogeochemical models for the ocean indicate that surface water pH will drop from a pre-industrial value of about 8.2 to about 7.8 in the IPCC A2 scenario by the end of this century, increasing the ocean’s acidity by about 150% relative to the beginning of the industrial era. In contemporary ocean water, elevated CO2 will also cause substantial reductions in surface water carbonate ion concentrations, in terms of either absolute changes or fractional changes relative to pre-industrial levels. For most open-ocean surface waters, aragonite undersaturation occurs when carbonate ion concentrations drop below approximately 66 μmol kg-1. The model projections indicate that aragonite undersaturation will start to occur by about 2020 in the Arctic Ocean and 2050 in the Southern Ocean. By 2050, all of the Arctic will be undersaturated with respect to aragonite, and by 2095, all of the Southern Ocean and parts of the North Pacific will be undersaturated. For calcite, undersaturation occurs when carbonate ion concentration drops below 42 μmol kg-1. By 2095, most of the Arctic and some parts of the Bering and Chukchi seas will be undersaturated with respect to calcite. However, in most of the other ocean basins, the surface waters will still be saturated with respect to calcite, but at a level greatly reduced from the present.

Beschreibung: S. Cooley and S. Doney acknowledge support from NSF ATM-0628582. Richard A. Feely was supported by the NOAA Climate Program under the Office of Climate Observations (Grant No. GC04-314 and the Global Carbon Cycle Program (Grant No. GC05-288).