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  • 1
    Electronic Resource
    Electronic Resource
    [s.l.] : Macmillan Magazines Ltd.
    Nature 398 (1999), S. 597-601 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] The equatorial oceans are the dominant oceanic source of CO2 to the atmosphere, annually amounting to a net flux of 0.7–1.5 Pg (10 15 g) of carbon, up to 72% of which emanates from the equatorial Pacific Ocean. Limited observations indicate that the size of ...
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  • 2
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] About half of the ‘anthropogenic’ CO2 emitted to the atmosphere is taken up by the oceans and terrestrial biosphere, and the amount sequestered by the ocean is generally estimated using numerical ocean carbon-cycle models. But these models often differ markedly, resulting ...
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  • 3
    Electronic Resource
    Electronic Resource
    [s.l.] : Macmillan Magazines Ltd.
    Nature 396 (1998), S. 155-159 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] An improved understanding of the partitioning of carbon between the atmosphere, terrestrial biosphere, and ocean allows for more accurate predictions of future atmospheric CO2 concentrations under various fossil-fuel CO2-emission scenarios. One of the more poorly ...
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  • 4
    Publication Date: 2022-05-25
    Description: 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.
    Description: 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.
    Description: 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).
    Repository Name: Woods Hole Open Access Server
    Type: Article
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  • 5
    Publication Date: 2022-05-25
    Description: 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.
    Description: 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.
    Description: 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).
    Repository Name: Woods Hole Open Access Server
    Type: Article
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