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  • Articles  (3)
  • OceanRep
  • Canada Basin  (2)
  • Analytical Chemistry and Spectroscopy  (1)
  • 1
    ISSN: 0935-6304
    Keywords: Isotope ratio monitoring-Gas Chromatography-Mass Spectrometry (irm-GC-MS) ; Compound specific isotope analysis (CSIA) ; Pyrolysis ; Stable carbon isotopes ; Kerogen ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: This study describes the application of isotope ratio monitoring gas chromatography- mass spectrometry (irm-GC-MS) for compound-specific stable carbon isotopic analysis of aliphatic hydrocarbon and phenolic products from flash pyrolysis (800 °C, 20s) of natural biopolymers and sedimentary kerogens. As part of this work, we provide a detailed description of the analysis of complex samples, including approaches for peak integration, data handling and correction for derivative carbons. Several aliphatic and aromatic biopolymers are analyzed by irm-GC-MS in order to establish relationships between the isotopic signatures of pyrolysis products and those of their parent macromolecules. We also analyze a select group of kerogens and kerogen precursors of different ages and biopolymer compositions to evaluate the applicability of combined pyrolysis/irm-GC-MS to complex geochemical mixtures. Our findings suggest that, in spite of the wide degree of heterogeneity, the isotopic values of individual aliphatic and phenolic pyrolysis products determined by irm-GC-MS can be related to the isotopic composition of the total organic carbon in kerogens and used to trace its biological sources. This study also highlights the need for optimum chromatographic separation in order to fully realize the potential of compound specific isotope analyses.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Publication Date: 2022-05-25
    Description: Author Posting. © American Geophysical Union, 2008. This article is posted here by permission of American Geophysical Union for personal use, not for redistribution. The definitive version was published in Geophysical Research Letters 35 (2008): L11607, doi:10.1029/2008GL034271.
    Description: Understanding the processes driving the carbon cycle in the Arctic Ocean is important for assessing the impacts of the predicted rapid and amplified climate change in this region. We analyzed settling particle samples intercepted by a time-series sediment trap deployed in the abyssal Canada Basin (at 3067 m) in order to examine carbon export to the deep Arctic Ocean. Strikingly old radiocarbon ages (apparent mean 14C age = ∼1900 years) of the organic carbon, abundant lithogenic material (∼80%), and mass flux variations temporally decoupled from the cycle of primary productivity in overlying surface waters together suggest that, unlike other ocean basins, the majority of the particulate organic carbon entering the deep Canada Basin is supplied from the surrounding margins.
    Description: This research was funded by the NSF Ocean Sciences Division (Chemical Oceanography program) and NSF Office of Polar Programs, Office of Naval Research, as well as the Ocean and Climate Change Institute and Arctic Research Initiative at the Woods Hole Oceanographic Institution.
    Keywords: POC ; Lateral transport ; Canada Basin
    Repository Name: Woods Hole Open Access Server
    Type: Article
    Format: application/pdf
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  • 3
    Publication Date: 2022-05-25
    Description: © The Author(s), 2015. This article is distributed under the terms of the Creative Commons Attribution License. The definitive version was published in Journal of Geophysical Research: Oceans 120 (2015): 2784–2799, doi:10.1002/2014JC010643.
    Description: To better understand the current carbon cycle and potentially detect its change in the rapidly changing Arctic Ocean, we examined sinking particles collected quasi-continuously over a period of 7 years (2004–2011) by bottom-tethered sediment trap moorings in the central Canada Basin. Total mass flux was very low (〈100 mg m−2 d−1) at all sites and was temporally decoupled from the cycle of primary production in surface waters. Extremely low radiocarbon contents of particulate organic carbon and high aluminum contents in sinking particles reveal high contributions of resuspended sediment to total sinking particle flux in the deep Canada Basin. Station A (75°N, 150°W) in the southwest quadrant of the Canada Basin is most strongly influenced while Station C (77°N, 140°W) in the northeast quadrant is least influenced by lateral particle supply based on radiocarbon content and Al concentration. The results at Station A, where three sediment traps were deployed at different depths, imply that the most likely mode of lateral particle transport was as thick clouds of enhanced particle concentration extending well above the seafloor. At present, only 1%–2% of the low levels of new production in Canada Basin surface waters reaches the interior basin. Lateral POC supply therefore appears to be the major source of organic matter to the interior basin. However, ongoing changes to surface ocean boundary conditions may influence both lateral and vertical supply of particulate material to the deep Canada Basin.
    Description: This research was funded by the NSF Division of Polar Programs (ARC-0909377), the Ocean and Climate Change Institute of Woods Hole Oceanographic Institution, and ETH Zürich. J.H. and M.K. were partly supported by the National Research Foundation of Korea grant funded by the Korean Government (2011–0013629).
    Keywords: Canada Basin ; Particulate organic carbon ; Lateral supply ; Radiocarbon ; Carbon cycle
    Repository Name: Woods Hole Open Access Server
    Type: Article
    Format: application/pdf
    Format: application/vnd.ms-excel
    Format: application/msword
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