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  • 1
    Monograph available for loan
    Monograph available for loan
    Searbrook, NJ : The Johns Hopkins Univ., Laboratory of Climatology
    Call number: MOP 19622
    Type of Medium: Monograph available for loan
    Pages: 11 S. , Ill.
    Series Statement: Publications in Climatology 5,2
    Location: MOP - must be ordered
    Branch Library: GFZ Library
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  • 2
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    PANGAEA
    In:  Supplement to: Higgins, J A; Schrag, Daniel P (2010): Constraining magnesium cycling in marine sediments using magnesium isotopes. Geochimica et Cosmochimica Acta, 74(17), 5039-5053, https://doi.org/10.1016/j.gca.2010.05.019
    Publication Date: 2024-01-09
    Description: Magnesium concentrations in deep-sea sediment pore-fluids typically decrease down core due to net precipitation of dolomite or clay minerals in the sediments or underlying crust. To better characterize and differentiate these processes, we have measured magnesium isotopes in pore-fluids and sediment samples from Ocean Drilling Program sites (1082, 1086, 1012, 984, 1219, and 925) that span a range of oceanographic settings. At all sites, magnesium concentrations decrease with depth. At sites where diagenetic reactions are dominated by the respiration of organic carbon, pore-fluid d26Mg values increase with depth by as much as 2 per mil. Because carbonates preferentially incorporate 24Mg (low d26Mg), the increase in pore-fluid d26Mg values at these sites is consistent with the removal of magnesium in Mg-carbonate (dolomite). In contrast, at sites where the respiration of organic carbon is not important and/or weatherable minerals are abundant, pore-fluid d26Mg values decrease with depth by up to 2 per mil. The decline in pore-fluid d26Mg at these sites is consistent with a magnesium sink that is isotopically enriched relative to the pore-fluid. The identity of this enriched magnesium sink is likely clay minerals. Using a simple 1D diffusion-advection-reaction model of pore-fluid magnesium, we estimate rates of net magnesium uptake/removal and associated net magnesium isotope fractionation factors for sources and sinks at all sites. Independent estimates of magnesium isotope fractionation during dolomite precipitation from measured d26Mg values of dolomite samples from sites 1082 and 1012 are very similar to modeled net fractionation factors at these sites, suggesting that local exchange of magnesium between sediment and pore-fluid at these sites can be neglected. Our results indicate that the magnesium incorporated in dolomite is 2.0-2.7 per mil depleted in d26Mg relative to the precipitating fluid. Assuming local exchange of magnesium is minor at the rest of the studied sites, our results suggest that magnesium incorporated into clay minerals is enriched in d26Mg by 0 per mil to +1.25 per mil relative to the precipitating fluid. This work demonstrates the utility of magnesium isotopes as a tracer for magnesium sources/sinks in low-temperature aqueous systems.
    Keywords: 154-925A; 167-1012; 175-1082; 175-1086; 199-1219; Benguela Current, South Atlantic Ocean; COMPCORE; Composite Core; DRILL; Drilling/drill rig; Joides Resolution; Leg154; Leg167; Leg175; Leg199; North Pacific Ocean; Ocean Drilling Program; ODP; South Atlantic Ocean
    Type: Dataset
    Format: application/zip, 2 datasets
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  • 3
    Publication Date: 2024-01-09
    Keywords: 154-925A; 167-1012; 175-1082; 175-1086; 199-1219; Benguela Current, South Atlantic Ocean; COMPCORE; Composite Core; DEPTH, sediment/rock; DRILL; Drilling/drill rig; Event label; Joides Resolution; Leg154; Leg167; Leg175; Leg199; Magnesium; Multi-collector inductively coupled plasma mass spectrometer (MC-ICP-MS); North Pacific Ocean; Number; Ocean Drilling Program; ODP; Sample amount; South Atlantic Ocean; δ26Mg; δ26Mg, dolomite; δ26Mg, standard deviation
    Type: Dataset
    Format: text/tab-separated-values, 269 data points
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  • 4
    Publication Date: 2024-01-09
    Keywords: 167-1012; 175-1082; Benguela Current, South Atlantic Ocean; COMPCORE; Composite Core; DEPTH, sediment/rock; Event label; Joides Resolution; Leg167; Leg175; Magnesium/Calcium ratio; North Pacific Ocean; Ocean Drilling Program; ODP; δ13C, dolomite; δ18O, dolomite
    Type: Dataset
    Format: text/tab-separated-values, 18 data points
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  • 5
    Publication Date: 2024-01-09
    Keywords: 130-807; Aluminium/Calcium ratio; COMPCORE; Composite Core; DEPTH, sediment/rock; DSDP/ODP/IODP sample designation; Joides Resolution; Leg130; Magnesium/Calcium ratio; Manganese/Calcium ratio; North Pacific Ocean; Ocean Drilling Program; ODP; Sample code/label; Size fraction; Strontium/Calcium ratio
    Type: Dataset
    Format: text/tab-separated-values, 162 data points
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  • 6
    Publication Date: 2024-01-09
    Keywords: 130-807; COMPCORE; Composite Core; DEPTH, sediment/rock; DSDP/ODP/IODP sample designation; Joides Resolution; Leg130; Method comment; North Pacific Ocean; Ocean Drilling Program; ODP; Sample code/label; Sample comment; δ25Mg; δ25Mg, standard deviation; δ26Mg; δ26Mg, standard deviation
    Type: Dataset
    Format: text/tab-separated-values, 259 data points
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  • 7
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    PANGAEA
    In:  Supplement to: Higgins, J A; Schrag, Daniel P (2012): Records of Neogene seawater chemistry and diagenesis in deep-sea carbonate sediments and pore fluids. Earth and Planetary Science Letters, 357-358, 386-396, https://doi.org/10.1016/j.epsl.2012.08.030
    Publication Date: 2024-01-09
    Description: Deep-sea pore fluids are potential archives of ancient seawater chemistry. However, the primary signal recorded in pore fluids is often overprinted by diagenetic processes. Recent studies have suggested that depth profiles of Mg concentration in deep-sea carbonate pore fluids are best explained by a rapid rise in seawater Mg over the last 10-20 Myr. To explore this possibility we measured the Mg isotopic composition of pore fluids and carbonate sediments from Ocean Drilling Program (ODP) site 807. Whereas the concentration of Mg in the pore fluid declines with depth, the isotopic composition of Mg in the pore fluid increases from -0.78 per mil near the sediment–water interface to -0.15 per mil at 778 mbsf. The Mg isotopic composition of the sediment, with few important exceptions, does not change with depth and has an average d26Mg value of -4.72 per mil. We reproduce the observed changes in sediment and pore-fluid Mg isotope values using a numerical model that incorporates Mg, Ca and Sr cycling and satisfies existing pore-fluid Ca isotope and Sr data. Our model shows that the observed trends in magnesium concentrations and isotopes are best explained as a combination of two processes: a secular rise in the seawater Mg over the Neogene and the recrystallization of low-Mg biogenic carbonate to a higher-Mg diagenetic calcite. These results indicate that burial recrystallization will add Mg to pelagic carbonate sediments, leading to an overestimation of paleo-temperatures from measured Mg/Ca ratios. The Mg isotopic composition of foraminiferal calcite appears to be only slightly altered by recrystallization making it possible to reconstruct the Mg isotopic composition of seawater through time.
    Keywords: 130-807; COMPCORE; Composite Core; Joides Resolution; Leg130; North Pacific Ocean; Ocean Drilling Program; ODP
    Type: Dataset
    Format: application/zip, 2 datasets
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  • 8
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    Cambridge University Press
    In:  EPIC3https://www.ipcc.ch/report/ar6/wg2/, Cambridge University Press, pp. 197-377
    Publication Date: 2023-04-17
    Repository Name: EPIC Alfred Wegener Institut
    Type: Inbook , peerRev
    Format: application/pdf
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  • 9
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 90 (1989), S. 6691-6700 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The late stages of phase separation by spinodal decomposition have been studied by light scattering in an oligomeric blend of polystyrene (PS) with polybutadiene (PB) as a function of both quench depth and composition. The scattering function I(q,t) follows a dynamical scaling law of the form S(q,t)=qm(t)−3S˜[q/qm(t)] where the wave vector qm corresponds to the maximum in I(q,t). The profiles of the normalized scaled structure functions are compared with that predicted by Furukawa for critical mixtures (percolation regime) which is given by S˜(x)=4x2/(3+x8)[S˜(1)=1]. Apart from one exception, Furukawa's function adequately describes the form of the normalized structure functions for a 60% PS mixture. However there are problems with some of the comparisons with the 50% and 70% PS blends. These disparities may in part be attributable to the fact that some of the data may lie outside the "true'' late stages.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 96 (1992), S. 7672-7682 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Dynamic light scattering (depolarized Rayleigh and polarized Rayleigh–Brillouin) and quasielastic neutron scattering are employed to study the dynamics of the glass-forming liquid di-2-ethylhexyl phthalate (DOP) (Tg=184 K). The depolarized Rayleigh scattering measurements were made in the temperature range from 303 to 433 K, the polarized Rayleigh–Brillouin measurements in the range from 263 to 433 K, and the quasielastic neutron-scattering measurements in the range from 37 to 312 K and in the Q range from 0.33 to 1.84 A(ring)−1. The orientation times for DOP, obtained from a single Lorentzian fit to the experimental depolarized spectra at high T, are in good agreement with recent dielectric data for the primary (α) relaxation. However, at lower T, the viscosity increases more strongly than the orientation times and the Stokes–Einstein–Debye equation which can adequately describe the dynamics in the high-T range is insufficient at temperatures close to Tg. The relaxation time obtained from the Rayleigh–Brillouin experiment is about 1 order of magnitude faster than the orientation times. In the neutron-scattering experiment we find a strong decrease of the elastic intensity and a corresponding increase of the quasielastic intensity around Tg.The data analysis with respect to the dynamics (from a two Lorentzian fit) revealed the existence of three processes affecting the high-frequency range: (i) a "fast'' (τ2∼10 ps) Q-independent motion with weak T dependence (E2=1.54 kcal/mol), (ii) a "slow'' Q-dependent motion, and (iii) a flat background increasing with T and Q. The fast process is discussed in terms of a very localized motion of the phenyl group (β relaxation) and, as such, as a precursor of the the primary (α) relaxation. The relaxation time of this process (τ2) was found to compare nicely with the time τmax from the Rayleigh–Brillouin (RB) experiment suggesting that the latter is caused by fast localized motions. The slow process is discussed in terms of the jump-diffusion model. The activation energy associated with the jump-diffusion times is 6.1 kcal/mol and it is associated with large-scale diffusional motion of the DOP molecule. The relaxation times obtained from this process are compared with the relaxation times obtained from the depolarized and dielectric techniques for the primary relaxation. Finally, the background can be identified with fast local motions and/or low-frequency excitations relaxing outside the energy window of our experiment.
    Type of Medium: Electronic Resource
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