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  • 1
    Publication Date: 2022-10-26
    Description: © The Author(s), 2019. This article is distributed under the terms of the Creative Commons Attribution License. The definitive version was published in Terlouw, G. J., Knor, L. A. C. M., De Carlo, E. H., Drupp, P. S., Mackenzie, F. T., Li, Y. H., Sutton, A. J., Plueddemann, A. J., & Sabine, C. L. Hawaii coastal seawater CO2 network: A statistical evaluation of a decade of observations on tropical coral reefs. Frontiers in Marine Science, 6, (2019):226, doi:10.3389/fmars.2019.00226.
    Description: A statistical evaluation of nearly 10 years of high-resolution surface seawater carbon dioxide partial pressure (pCO2) time-series data collected from coastal moorings around O’ahu, Hawai’i suggest that these coral reef ecosystems were largely a net source of CO2 to the atmosphere between 2008 and 2016. The largest air-sea flux (1.24 ± 0.33 mol m−2 yr−1) and the largest variability in seawater pCO2 (950 μatm overall range or 8x the open ocean range) were observed at the CRIMP-2 site, near a shallow barrier coral reef system in Kaneohe Bay O’ahu. Two south shore sites, Kilo Nalu and Ala Wai, also exhibited about twice the surface water pCO2 variability of the open ocean, but had net fluxes that were much closer to the open ocean than the strongly calcifying system at CRIMP-2. All mooring sites showed the opposite seasonal cycle from the atmosphere, with the highest values in the summer and lower values in the winter. Average coastal diurnal variabilities ranged from a high of 192 μatm/day to a low of 32 μatm/day at the CRIMP-2 and Kilo Nalu sites, respectively, which is one to two orders of magnitude greater than observed at the open ocean site. Here we examine the modes and drivers of variability at the different coastal sites. Although daily to seasonal variations in pCO2 and air-sea CO2 fluxes are strongly affected by localized processes, basin-scale climate oscillations also affect the variability on interannual time scales.
    Description: We acknowledge with gratitude the financial support of our research provided in part by a grant/cooperative agreement from the National Oceanic and Atmospheric Administration, Project R/IR-27, which is sponsored by the University of Hawaii Sea Grant College Program, SOEST, under Institutional Grant No. NA14OAR4170071 from NOAA Office of Sea Grant, Department of Commerce. Additional support was granted by the NOAA/Ocean Acidification Program (to EDC and AS) and the NOAA/Climate Program Office (AP), and the NOAA Ocean Observing and Monitoring Division, Climate Program Office (FundRef number 100007298) through agreement NA14OAR4320158 of the NOAA Cooperative Institute for the North Atlantic Region (AP). The views expressed herein are those of the author(s) and do not necessarily reflect the views of NOAA or any of its subagencies. This is SOEST contribution number 10684, PMEL contribution number 4845, and Hawai’i Sea Grant contribution UNIHI-SEAGRANT-JC-15-30.
    Keywords: Time series ; CO2 ; Reef ; Coastal ; Ocean acidification ; Variability ; Fluxes
    Repository Name: Woods Hole Open Access Server
    Type: Article
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  • 2
    Publication Date: 2022-10-26
    Description: © The Author(s), 2019. This article is distributed under the terms of the Creative Commons Attribution License. The definitive version was published in Turk, D., Wang, H., Hu, X., Gledhill, D. K., Wang, Z. A., Jiang, L., & Cai, W. Time of Emergence of surface ocean carbon dioxide trends in the North American coastal margins in support of ocean acidification observing system design. Frontiers in Marine Science, 6, (2019):91, doi:10.3389/fmars.2019.00091.
    Description: Time of Emergence (ToE) is the time when a signal emerges from the noise of natural variability. Commonly used in climate science for the detection of anthropogenic forcing, this concept has recently been applied to geochemical variables, to assess the emerging times of anthropogenic ocean acidification (OA), mostly in the open ocean using global climate and Earth System Models. Yet studies of OA variables are scarce within costal margins, due to limited multidecadal time-series observations of carbon parameters. ToE provides important information for decision making regarding the strategic configuration of observing assets, to ensure they are optimally positioned either for signal detection and/or process elicitation and to identify the most suitable variables in discerning OA-related changes. Herein, we present a short overview of ToE estimates on an OA variable, CO2 fugacity f(CO2,sw), in the North American ocean margins, using coastal data from the Surface Ocean CO2 Atlas (SOCAT) V5. ToE suggests an average theoretical timeframe for an OA signal to emerge, of 23(±13) years, but with considerable spatial variability. Most coastal areas are experiencing additional secular and/or multi-decadal forcing(s) that modifies the OA signal, and such forcing may not be sufficiently resolved by current observations. We provide recommendations, which will help scientists and decision makers design and implement OA monitoring systems in the next decade, to address the objectives of OceanObs19 (http://www.oceanobs19.net) in support of the United Nations Decade of Ocean Science for Sustainable Development (2021–2030) (https://en.unesco.org/ocean-decade) and the Sustainable Development Goal (SDG) 14.3 (https://sustainabledevelopment.un.org/sdg14) target to “Minimize and address the impacts of OA.”
    Description: HW was partially supported by an NSF grant (OCE#1654232) while being a research associate at TAMUCC.
    Keywords: Ocean acidification ; CO2 fugacity ; Time of emergence ; Climate change ; Novel statistical approaches ; Observing system optimization ; Decision making tool
    Repository Name: Woods Hole Open Access Server
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  • 3
    Publication Date: 2022-10-26
    Description: © The Author(s), 2018. This article is distributed under the terms of the Creative Commons Attribution License. The definitive version was published in Farfan, G. A., Cordes, E. E., Waller, R. G., DeCarlo, T. M., & Hansel, C. M. (2018). Mineralogy of deep-sea coral aragonites as a function of aragonite saturation state. Frontiers in Marine Science, 5, (2018): 473. doi:10.3389/fmars.2018.00473.
    Description: In an ocean with rapidly changing chemistry, studies have assessed coral skeletal health under projected ocean acidification (OA) scenarios by characterizing morphological distortions in skeletal architecture and measuring bulk properties, such as net calcification and dissolution. Few studies offer more detailed information on skeletal mineralogy. Since aragonite crystallography will at least partially govern the material properties of coral skeletons, such as solubility and strength, it is important to understand how it is influenced by environmental stressors. Here, we take a mineralogical approach using micro X-ray diffraction (XRD) and whole pattern Rietveld refinement analysis to track crystallographic shifts in deep-sea coral Lophelia pertusa samples collected along a natural seawater aragonite saturation state gradient (Ωsw = 1.15–1.44) in the Gulf of Mexico. Our results reveal statistically significant linear relationships between rising Ωsw and increasing unit cell volume driven by an anisotropic lengthening along the b-axis. These structural changes are similarly observed in synthetic aragonites precipitated under various saturation states, indicating that these changes are inherent to the crystallography of aragonite. Increased crystallographic disorder via widening of the full width at half maximum of the main (111) XRD peaks trend with increased Ba substitutions for Ca, however, trace substitutions by Ba, Sr, and Mg do not trend with crystal lattice parameters in our samples. Instead, we observe a significant trend of increasing calcite content as a function of both decreasing unit cell parameters as well as decreasing Ωsw. This may make calcite incorporation an important factor to consider in coral crystallography, especially under varying aragonite saturation states (ΩAr). Finally, by defining crystallography-based linear relationships between ΩAr of synthetic aragonite analogs and lattice parameters, we predict internal calcifying fluid saturation state (Ωcf = 11.1–17.3 calculated from b-axis lengths; 15.2–25.2 calculated from unit cell volumes) for L. pertusa, which may allow this species to calcify despite the local seawater conditions. This study will ideally pave the way for future studies to utilize quantitative XRD in exploring the impact of physical and chemical stressors on biominerals.
    Description: Funding for this project was made possible by Mineralogical Society of America Edward H. Kraus Crystallographic Research Fund and the WHOI Ocean Ventures Fund. GF was supported by a National Science Foundation Graduate Research Fellowship grant no. 1122374 and a Ford Foundation Dissertation Fellowship. Sample collections from RW were funded under NSF grant nos. 1245766 and 1127582 and NOAA Ocean Exploration Deep Atlantic Stepping Stones. Collections from the Gulf of Mexico were supported by NSF BIO-OCE grant #1220478 to EC.
    Keywords: Deep-sea corals ; Lophelia pertusa ; Crystallography ; Mineralogy ; X-ray diffraction ; Ocean acidification ; Aragonite saturation state ; Aragonite
    Repository Name: Woods Hole Open Access Server
    Type: Article
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