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  • 1
    Call number: 9783319256436 (e-book)
    Description / Table of Contents: This book is a useful guide for researchers in ecology and earth science interested in the use of accelerator mass spectrometry technology. The development of research in radiocarbon measurements offers an opportunity to address the human impact on global carbon cycling and climate change. Presenting radiocarbon theory, history, applications, and analytical techniques in one volume builds a broad outline of the field of radiocarbon and its emergent role in defining changes in the global carbon cycle and links to climate change. Each chapter presents both classic and cutting-edge studies from different disciplines involving radiocarbon and carbon cycling. The book also includes a chapter on the history and discovery of radiocarbon, and advances in radiocarbon measurement techniques and radiocarbon theory. Understanding human alteration of the global carbon cycle and the link between atmospheric carbon dioxide levels and climate remains one of the foremost environmental problems at the interface of ecology and earth system science. Many people are familiar with the terms ‘global warming’ and ‘climate change’, but fewer are able to articulate the science that support these hypotheses. This book addresses general questions such as: what is the link between the carbon cycle and climate change; what is the current evidence for the fate of carbon dioxide added by human activities to the atmosphere, and what has caused past changes in atmospheric carbon dioxide? How can the radiocarbon and stable isotopes of carbon combined with other tools be used for quantifying the human impact on the global carbon cycle?
    Type of Medium: 12
    Pages: 1 Online-Ressource (VII, 315 Seiten) , Illustrationen, Diagramme
    ISBN: 9783319256436 , 978-3-319-25643-6
    Language: English
    Note: Contents 1 Radiocarbon and the Global Carbon Cycle / E.A.G. Schuur, S.E. Trumbore, E.R.M. Druffel, J.R. Southon, A. Steinhof, R.E. Taylor and J.C. Turnbull 2 Radiocarbon Dating: Development of a Nobel Method / R.E. Taylor 3 Radiocarbon Nomenclature, Theory, Models, and Interpretation: Measuring Age, Determining Cycling Rates, and Tracing Source Pools / S.E. Trumbore, C.A. Sierra and C.E. Hicks Pries 4 Radiocarbon in the Atmosphere / J.C. Turnbull, H. Graven and N.Y. Krakauer 5 Radiocarbon in the Oceans / E.R.M. Druffel, S.R. Beaupré and L.A. Ziolkowski 6 Radiocarbon in Terrestrial Systems / E.A.G. Schuur, M.S. Carbone, C.E. Hicks Pries, F.M. Hopkins and S.M. Natali 7 Paleoclimatology / J.R. Southon, R. De Pol-Holz and E.R.M. Druffel 8 Accelerator Mass Spectrometry of Radiocarbon / Axel Steinhof 9 Preparation for Radiocarbon Analysis / S.E. Trumbore, X. Xu, G.M. Santos, C.I. Czimczik, S.R. Beaupré, M.A. Pack, F.M. Hopkins, A. Stills, M. Lupascu and L. Ziolkowski
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  • 2
    Electronic Resource
    Electronic Resource
    [s.l.] : Macmillian Magazines Ltd.
    Nature 430 (2004), S. 877-881 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] Seawater dissolved organic matter (DOM) is the largest reservoir of exchangeable organic carbon in the ocean, comparable in quantity to atmospheric carbon dioxide. The composition, turnover times and fate of all but a few planktonic constituents of this material are, however, largely unknown. ...
    Type of Medium: Electronic Resource
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  • 3
    Publication Date: 2018-06-05
    Description: Dissolved organic carbon (DOC) is the largest pool of exchangeable organic carbon in the ocean. However, less than 10% of DOC has been molecularly characterized in the deep ocean to understand DOC's recalcitrance. Here we analyze the radiocarbon ( 14 C) depleted, and presumably refractory, low molecular weight (LMW) DOC from the North Central Pacific using atomic force microscopy to produce the first atomic-resolution images of individual LMW DOC molecules. We evaluate surface and deep LMW DOC chemical structures in the context of their relative persistence and recalcitrance. Atomic force microscopy resolved planar structures with features similar to polycyclic aromatic compounds and carboxylic-rich alicyclic structures with less than five aromatic carbon rings. These compounds comprise 8% and 20% of the measurable molecules investigated in the surface and deep, respectively. Resolving the structures of individual DOC molecules represents a step forward in molecular characterization of DOC and in understanding its long-term stability. ©2018. American Geophysical Union. All Rights Reserved.
    Print ISSN: 0094-8276
    Electronic ISSN: 1944-8007
    Topics: Geosciences , Physics
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  • 4
    Publication Date: 2016-01-26
    Description: Annual radiocarbon from a massive Porites lutea coral collected from Hon Tre Island, Vietnam, South China Sea (SCS) was analyzed over a ~100-yr-long period from AD 1900 to 1986. The pre-bomb results from 1900–1953 show a steady Δ14C value of –54.4±1.8‰ (n=60). These values are similar to coral records located in the central and southern SCS and from Indonesian waters, but are lower than those from Japan. Following the input of anthropogenic bomb 14C, our results show a sharp increase in Δ14C from 1960, reaching a peak value of 155.3‰ in 1973. The Hon Tre Island post-bomb Δ14C values are lower than those of other corals located in the SCS and Japan, but higher compared to those in the Indonesian Seas. This study infers a seasonal input of upwelled water depleted in 14C from the deeper SCS basin that originates from the tropical Pacific via the Luzon Strait. The bifurcation of the North Equatorial Current feeds the surface and intermediate currents in the SCS and Makassar Strait region. However, unlike the Makassar site, this study’s coral Δ14C does not receive lower 14C water from the South Pacific Equatorial Current. The Vietnam record therefore represents a unique oceanographic position, reflecting the seasonal influence of older, deeper SCS waters that upwell periodically in this area and have modified the surface waters locally in this region over the last 100 yr.
    Print ISSN: 0033-8222
    Electronic ISSN: 1945-5755
    Topics: Archaeology , Energy, Environment Protection, Nuclear Power Engineering , Geosciences
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  • 5
    Publication Date: 2004-01-01
    Description: Radiocarbon (Δ14C) measurements of monthly samples from a Galapagos surface coral are among the first data sets from the new Keck Carbon Cycle Accelerator Mass Spectrometry laboratory at the University of California, Irvine. An average Δ14C value of −62 is obtained for 144 measurements of samples from monthly coral bands that lived from about AD 1760–1771 (±6 yr). High Δ14C values were found during January through March, when upwelling was weak or absent at the Galapagos Islands. Low Δ14C values were obtained mid-year during strong upwelling. The average seasonal variability of Δ14C was 15–25, which is greater than that at other tropical and subtropical locations in the Pacific Ocean because of intense seasonal upwelling at this site. Periods of sustained high Δ14C values were found during 1762–1763 and 1766. A spectral analysis revealed that the spectral density for the Δ14C data displays most of its variance at the 5-yr cycle, which is reflective of El Niño periodicity during the 20th century.
    Print ISSN: 0033-8222
    Electronic ISSN: 1945-5755
    Topics: Archaeology , Energy, Environment Protection, Nuclear Power Engineering , Geosciences
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  • 6
    Publication Date: 2016-07-26
    Description: The standard procedure for storing/preserving seawater dissolved organic carbon (DOC) samples after field collection is by freezing (–20°C) until future analysis can be made. However, shipping and receiving large numbers of these samples without thawing presents a significant logistical problem and large monetary expense. Access to freezers can also be limited in remote field locations. We therefore test an alternative method of preserving and storing samples for the measurement of DOC concentrations ([DOC]), stable carbon (δ13C), and radiocarbon (as ∆14C) isotopic values via UV photooxidation (UVox). We report a total analytical reproducibility of frozen DOC samples to be [DOC]±1.3 µM, ∆14C±9.4‰, and δ13C±0.1‰, comparable to previously reported results (Druffel et al. 2013). Open Ocean DOC frozen versus acidified duplicates were on average offset by ∆DOC±1.1 µM, ∆∆14C± –1.3‰, and ∆δ13C± –0.1‰. Coastal Ocean frozen vs. acidified sample replicates, collected as part of a long-term (380-day) storage experiment, had larger, albeit consistent offsets of ∆DOC±2.2 µM, ∆∆14C±1.5‰, and ∆δ13C± –0.2‰. A simple isotopic mass balance of changes in [DOC], ∆14C, and δ13C values reveals loss of semi-labile DOC (2.2±0.6 µM, ∆14C=–94±105‰, δ13C=–27±10‰; n=4) and semi-recalcitrant DOC (2.4±0.7 µM, ∆14C=–478±116‰, δ13C=–23.4±3.0‰; n=3) in Coastal and Open Ocean acidified samples, respectively.
    Print ISSN: 0033-8222
    Electronic ISSN: 1945-5755
    Topics: Archaeology , Energy, Environment Protection, Nuclear Power Engineering , Geosciences
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  • 7
    Publication Date: 2019-04-15
    Description: The first ultraviolet photochemical oxidation (UVox) extraction method for marine dissolved organic carbon (DOC) as CO2 gas was established by Armstrong and co-workers in 1966. Subsequent refinement of the UVox technique has co-evolved with the need for high-precision isotopic (Δ14C, δ13C) analysis and smaller sample size requirements for accelerator mass spectrometry radiocarbon (AMS 14C) measurements. The UVox line at UC Irvine was established in 2004 and the system reaction kinetics and efficiency for isolating seawater DOC rigorously tested for quantitative isolation of ∼1 mg C for AMS 14C measurements. Since then, improvements have been made to sampling, storage, and UVox methods to increase overall efficiency. We discuss our progress, and key UVox system parameters for optimizing precision, accuracy, and efficiency, including (1) ocean to reactor: filtration, storage and preparation of DOC samples, (2) cryogenic trap design, efficiency and quantification of CO2 break through, and (3) use of isotopic standards, blanks and small sample graphitization techniques for the correction of DOC concentrations and Fm values with propagated uncertainties. New DOC UVox systems are in use at many institutions. However, rigorous assessment of quantitative UVox DOC yields and blank contributions, DOC concentrations and carbon isotopic values need to be made. We highlight the need for a community-wide inter-comparison study.
    Print ISSN: 0033-8222
    Electronic ISSN: 1945-5755
    Topics: Archaeology , Energy, Environment Protection, Nuclear Power Engineering , Geosciences
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  • 8
    Publication Date: 2017-11-08
    Description: We report ∆14C measurements of cellulose extracted from near monthly tree ring growth for the 1960s of a white oak that grew in western Oregon, USA. Comparison with ∆14C measurements of atmospheric CO2 reveals that the tree ring ∆14C values were equal to or lower than those in atmospheric CO2 at the time of ring formation. We suggest that the low tree ring ∆14C values during the period 1962–1963 were caused by the presence of an atmospheric front or blocking between subpolar and temperate air masses that delayed the arrival of the bomb signal at the tree’s site.
    Print ISSN: 0033-8222
    Electronic ISSN: 1945-5755
    Topics: Archaeology , Energy, Environment Protection, Nuclear Power Engineering , Geosciences
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  • 9
    Publication Date: 2001-01-01
    Description: We show that high-precision radiocarbon (Δ14C) measurements from annual bands of a Hawaiian surface coral decreased by 7‰ from AD 1893 to 1952. This decrease is coincident with the Suess Effect, which is mostly due to the dilution of natural levels of 14C by 14C-free fossil fuel CO2. This decrease is equal to that expected in surface waters of the subtropical gyres, and indicates that the surface waters of the North Pacific were in steady state with respect to long term mixing of CO2 during the past century. Correlation between Δ14C and North Pacific gyre sea surface temperatures indicates that vertical mixing local to Hawaii and the North Pacific gyre as a whole is the likely physical mechanism to result in variable Δ14C. Prior to 1920, this correlation starts to break down; this may be related to the non-correlation between biennial Δ14C values in corals from the southwest Pacific and El Niño events observed during this period as well.
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    Electronic ISSN: 1945-5755
    Topics: Archaeology , Energy, Environment Protection, Nuclear Power Engineering , Geosciences
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  • 10
    Publication Date: 2018-01-08
    Description: Radiocarbon (14C) in dissolved inorganic carbon (DIC) was measured for water samples collected from six deep stations in the Kuroshio Extension (KE) region in the northwestern North Pacific in April–May 2015. Vertical profiles of Δ14C-DIC indicate that bomb-produced 14C was present from the surface to ~1500 m water depth. Large variations in Δ14C-DIC values (300‰) were observed at 500 m water depth among the stations and the differences were likely controlled by transport and mixing dynamics of different water masses in the region. The major Pacific western boundary currents, such as Kuroshio and Oyashio and regional mesoscale eddies, could play important roles affecting the observed Δ14C-DIC variability. The depth profiles of both Δ14C-DIC and DIC concentrations can be predicted by the solution mixing model and can be used as conservative tracers of water mass movement and water parcel homogenization in the ocean.
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    Electronic ISSN: 1945-5755
    Topics: Archaeology , Energy, Environment Protection, Nuclear Power Engineering , Geosciences
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