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  • Other Sources  (5)
  • American Chemical Society
  • Institute of Physics
  • Wiley-Blackwell
  • 2015-2019  (5)
  • 2010-2014
  • 1980-1984
  • 1925-1929
  • 2018  (5)
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  • 2015-2019  (5)
  • 2010-2014
  • 1980-1984
  • 1925-1929
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  • 1
    Publication Date: 2021-02-08
    Description: To enable quality control of measurement procedures for determinations of Mg isotope amount ratios, expressed as δ26Mg and δ25Mg values, in Earth-surface studies, the δ26Mg and δ25Mg values of eight reference materials (RMs) were determined by inter-laboratory comparison between five laboratories and considering published data, if available. These matrix RMs, including river water SLRS-5, spring water NIST SRM 1640a, Dead Sea brine DSW-1, dolomites JDo-1 and CRM 512, limestone CRM 513, soil NIST SRM 2709a and vegetation NIST SRM 1515 apple leaves, are representative for a wide range of Earth-surface materials from low-temperature environments. The inter-laboratory variability, 2s (twice the standard deviation), of all eight RMs ranges from 0.05 to 0.17‰ in δ26Mg. Thus, it is suggested that all these materials are suitable for validation of δ26Mg and δ25Mg determinations of Earth-surface geochemical studies.
    Type: Article , PeerReviewed , info:eu-repo/semantics/article
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  • 2
    Publication Date: 2021-02-08
    Description: Populations of fishes provide valuable services for billions of people, but face diverse and interacting threats that jeopardize their sustainability. Human population growth and intensifying resource use for food, water, energy and goods are compromising fish populations through a variety of mechanisms, including overfishing, habitat degradation and declines in water quality. The important challenges raised by these issues have been recognized and have led to considerable advances over past decades in managing and mitigating threats to fishes worldwide. In this review, we identify the major threats faced by fish populations alongside recent advances that are helping to address these issues. There are very significant efforts worldwide directed towards ensuring a sustainable future for the world's fishes and fisheries and those who rely on them. Although considerable challenges remain, by drawing attention to successful mitigation of threats to fish and fisheries we hope to provide the encouragement and direction that will allow these challenges to be overcome in the future.
    Type: Article , PeerReviewed
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  • 3
    Publication Date: 2021-02-08
    Description: Mass fractions of Sn and In were determined in sixteen geological reference materials including basaltic/mafic (BCR‐2, BE‐N, BHVO‐1, BHVO‐2, BIR‐1, OKUM, W‐2, WS‐E), ultramafic (DTS‐2b, MUH‐1, PCC‐1, UB‐N) and felsic/sedimentary reference materials (AGV‐2, JA‐1, SdAR‐M2, SdAR‐H1). Extensive digestion and ion exchange separation tests were carried out in order to provide high yields (〉 90% for Sn, 〉 85% for In), low total procedural blanks (~ 1 ng for Sn, 〈 3 pg for In) and low analytical uncertainties for the elements of interest in a variety of silicate sample matrices. Replicate analyses (n = 2–13) of Sn‐In mass fractions give a combined measurement uncertainty of 2u that are generally 〈 3% and in agreement with literature data, where available. We present the first high precision In data for reference materials OKUM (32.1 ± 1.5 ng g−1), DTS‐2b (2.03 ± 0.25 ng g−1), MUH‐1 (6.44 ± 0.30 ng g−1), and PCC‐1 (3.55 ± 0.35 ng g−1) as well as the first Sn data for MUH‐1 (0.057 ± 0.010 μg g−1) and DTS‐2b (0.623 ± 0.018 μg g−1).
    Type: Article , PeerReviewed
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  • 4
    Publication Date: 2021-02-08
    Description: Sediment core PS1904 reveals continuous records of planktic and benthic foraminiferal stable isotopes (δ18O/δ13C) from the north-eastern Greenland continental margin. The data show good comparability with other records from the Nordic Seas, allowing the stratigraphic range of PS1904 to be dated to Marine Isotope Stage (MIS) 6. Focusing on MIS 5 reveals light δ18O values during MIS 5a compared to the last interglacial peak (MIS 5e) which indicates that surface and bottom water layers were strongly affected by freshwater during the former event. We present two possible scenarios explaining the origin and routing of the freshwater: (i) drainage of a Eurasian proglacial lake coupled with the collapse of the Kara Sea Ice Sheet at the MIS 5b/a boundary, and (ii) destabilization and melting of the nearby Greenland Ice Sheet. Although both scenarios could have acted simultaneously, sediment records from the Eurasian sector of the Arctic Ocean hint at the proglacial lake system in north-western Siberia as the largest freshwater source. Regardless of the actual source, the freshwater lowered the surface ocean salinity causing water column stratification and sea ice expansion. Increased sea-ice abundance led to a higher albedo and probably contributed to the cooling and global ice sheet growth that occurred subsequently during MIS 4.
    Type: Article , PeerReviewed
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  • 5
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    American Chemical Society
    In:  Energy & Fuels, 32 (8). pp. 8167-8174.
    Publication Date: 2020-07-31
    Description: Methane recovery from artificial hydrate-bearing sandstones by simulated flue gas swapping was tested using a core flooding experimental setup. Seven groups of experiments were conducted to investigate the effect of hydrate saturation as well as the initial porosity and permeability of sandstones on methane production and carbon dioxide capture. The results show that the CH4 recovery efficiency and the amount of CO2 captured increase with the increase of hydrate saturation at the same initial porosity and permeability of sandstone. The highest CH4 recovery obtained is 51.6% and 99.4% of CO2 in simulated flue gas is sequestered in the hydrate phase after swapping at 9.2 MPa and 277.15 K. Hydrate saturation was 82.5% and the initial porosity and permeability of sandstone are 25.1% and 49 mD, respectively. With the increase of initial porosity and permeability of sandstone, the CH4 recovery efficiency and the amount of CO2 captured increase when other conditions (the hydrate saturation and reaction time) are similar. For investigating the CH4-flue gas swapping mechanism, a micro-differential scanning calorimetry was used to test the heat changes in the whole reaction. No noticeable endothermic or exothermic phenomenon was detected in the CH4-flue gas swapping, which indicates that CH4 hydrate would form mixed hydrates directly instead of going through a dissociation and reformation process. Based on the observed experimental results, a CH4-flue gas swapping mechanism is proposed and the reaction process is found to be essentially controlled by mass transfer.
    Type: Article , PeerReviewed
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