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  • 1995-1999  (300)
  • 1935-1939  (31)
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  • 1
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    PANGAEA
    In:  Supplement to: Emeis, Kay-Christian; Doose, Heidi; Mix, Alan C; Schulz-Bull, Detlef (1995): Alkenone sea-surface temperatures and carbon burial at Site 846 (eastern equatorial Pacific Ocean): the last 1.3 m.y. In: Pisias, NG; Mayer, LA; Janecek, TR; Palmer-Julson, A; van Andel, TH (eds.), Proceedings of the Ocean Drilling Program, Scientific Results, College Station, TX (Ocean Drilling Program), 138, 605-613, https://doi.org/10.2973/odp.proc.sr.138.131.1995
    Publication Date: 2024-01-09
    Description: We analyzed the unsaturation ratio (Uk37) of long-chain ketones - a molecular sea-surface temperature (SST) indicator û concentrations of carbonate and organic carbon in sediments from Site 846 in the eastern equatorial Pacific Ocean. Based on an isotopic age model for the composite depth section of 0-46 m below seafloor and on estimates of sediment density, accumulation rates of these biogenic compounds were calculated. Our combined temperature and biogenic flux record traces conditions at the origin of the South Equatorial Current over the last 1.3 m.y. SSTs have fluctuated considerably over the interval studied. A long trend of gradual decrease from 24°C at 1.3 Ma ends between 500 and 400 Ka, when lowest values of 19°C were reached. Since this time, the temperature data indicate a warming trend to the Holocene modulated by high-amplitude variation (19° to 27°C). The inversion of the trend between 400 and 500 Ka coincides with maximal accumulation rates of carbonate, which since then have decreased. In contrast, organic carbon accumulation since then has increased in variability and in absolute values. On shorter time scales, the records show a strong link to the global climatic background. Since 1.3 Ma, carbonate (0.2-3 g/cm**2/k.y.) and organic carbon accumulation rates (2-30 mg/cm**2/k.y.) were consistently high (more than twice their modern values and those of interglacials) during glacial maxima in the benthic isotope record, when temperatures were low. However, cross-spectral analyses with the d18O record suggest that variation in organic carbon flux is not linked directly to variations in SST. Temperature maxima in our record led interglacial events by 7 k.y. in the 100-k.y. eccentricity cycle and by 5 k.y. in the 41-k.y. obliquity cycle. In contrast, maxima in organic carbon accumulation lag behind glacial maxima and low temperatures by 14 k.y. in the eccentricity cycle. On glacial/interglacial time scales, a prominent influence on SST - but not on organic carbon burial - at Site 846 appears to be the advection of cold water into the South Equatorial Current.
    Keywords: 138-846; Accumulation rate, calcium carbonate; Accumulation rate, mass; Accumulation rate, total organic carbon; AGE; Alkenone, unsaturation index UK37; Calcium carbonate; Calculated; Calculated from UK37 (Prahl et al., 1988); Carbon, organic, total; Carbon, organic, total, standard deviation; Carbon, total; COMPCORE; Composite Core; Density, dry bulk; Density, wet bulk; Depth, composite revised; DEPTH, sediment/rock; DSDP/ODP/IODP sample designation; Element analyser CHNS-O, Carlo Erba EA1108; Gamma-ray attenuation porosity evaluator (GRAPE); Intercore correlation; Joides Resolution; Leg138; Ocean Drilling Program; ODP; Sample code/label; Sea surface temperature, annual mean; Sea surface temperature, annual mean, standard deviation; Sedimentation rate; South Pacific Ocean
    Type: Dataset
    Format: text/tab-separated-values, 3062 data points
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  • 2
    Publication Date: 2019-07-16
    Repository Name: EPIC Alfred Wegener Institut
    Type: Conference , notRev
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  • 3
    Publication Date: 2020-02-12
    Keywords: 550 - Earth sciences
    Type: info:eu-repo/semantics/article
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  • 4
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 39 (1935), S. 577-584 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 40 (1936), S. 9-20 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 40 (1936), S. 125-131 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 41 (1937), S. 463-468 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 41 (1937), S. 985-986 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Review of Scientific Instruments 67 (1996), S. 4360-4363 
    ISSN: 1089-7623
    Source: AIP Digital Archive
    Topics: Physics , Electrical Engineering, Measurement and Control Technology
    Notes: The new sediment trap has a 0.5 m2 aperture, a funnel slope of 34° and is capable of collecting 21 samples at programmed intervals (1 min–1 year) during deployment in the deep ocean. The trap has been designed to allow reliable data on trace inorganic and organic components (such as trace elements, n-alkanes, PCBs, PAHs, amino/fatty acids) in addition to the standard biogeochemical variables in the collected particles. Due to the exclusive use of synthetic (such as fiberglass, PVC, PTFE, or POM-Delrin®) and highly resistant metallic materials contamination problems have been eliminated for these species. Blank values determined in several tests in the open ocean were as low as 1% or even less of the amounts present in trap material, even at low particulate loadings. Another major aim was the elimination of loss of dissolved components from the sample cups into seawater. Microbial and chemical processes modify the collected particles, thereby mobilizing originally particulate species into solution. It is thus essential to avoid greater losses of dissolved species through diffusion into the surrounding seawater after collection. This was achieved by means of an especially designed sealing mechanism. Tests with tracer substances during field studies proved that losses of dissolved components from supernatants during one year of deployment are as low as 10%. Additionally, the relationship between flow characteristics around the traps and their excursions from the vertical position in a bottom-tethered array was studied during a one-year deployment in the North Atlantic. © 1996 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 10
    ISSN: 1539-6924
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Energy, Environment Protection, Nuclear Power Engineering
    Notes: Trichloroacetic acid (TCA) is major metabolite of trichloroethylene (TRI) thought to contribute to its hepatocarcinogenic effects in mice. Recent studies have shown that peak blood concentrations of TCA in rats do not occur until approximately 12 hours following an oral dose of TRI. However, blood concentrations of TRI reach maximum within an hour and are nondetectable after 2 hours.(1) The results of study which examined the enterohepatic recirculation (EHC) of the principle TRI metabolited(2) was used to develop physiologically-based pharmacokinetic model for TRI, which includes enterohepatic recirculation of its metabolites. The model quantitatively predicts the uptake, distribution and elimination of TRI, trichloroethanol, trichloroethanol-glucuronide, and TCA and includes production of metabolites through the enterohepatic recirculation pathway. Physiologic parameters used in the model were obtained from the literature.(3.4) Parameters for TRI metabolism were taken from Fisher et al.(5) Other kinetic parameters were found in the literature or estimated from experimental data.(2) The model was calibrated to data from experiments of an earlier study where TRI was orally administered(2) Verification of the model was conducted using data on the enterohepatic recirculation of TCEOH and TCA(2) chloral hydrate data (infusion doses) from Merdink,(1) and TRI data from Templin(l) and Larson and Bull.(1)
    Type of Medium: Electronic Resource
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