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Large Zn isotope variations in the Ni-Mo polymetallic sulfide layer in the lower Cambrian, South China

Identifikátory výsledku

  • Kód výsledku v IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00025798%3A_____%2F20%3A00000012" target="_blank" >RIV/00025798:_____/20:00000012 - isvavai.cz</a>

  • Výsledek na webu

    <a href="https://www.sciencedirect.com/science/article/abs/pii/S1342937X2030157X?via%3Dihub" target="_blank" >https://www.sciencedirect.com/science/article/abs/pii/S1342937X2030157X?via%3Dihub</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.gr.2020.04.009" target="_blank" >10.1016/j.gr.2020.04.009</a>

Alternativní jazyky

  • Jazyk výsledku

    angličtina

  • Název v původním jazyce

    Large Zn isotope variations in the Ni-Mo polymetallic sulfide layer in the lower Cambrian, South China

  • Popis výsledku v původním jazyce

    In South China, black organic-rich shales in the lower Cambrian Niutitang Formation host a Ni-Mo polymetallic sulfide layer that discontinuously extends over ~1600 km. Seawater and hydrothermal origins are among the many suggested hypotheses and are still under debate. In order to discriminate Zn sources, we report Zn isotopes in Ni-Mo polymetallic sulfide layers and their host shales from the Nayong and Zunyi locations in Guizhou province and the Zhangjiajie section in Hunan province. In each section, host organic-rich shales show homogeneous Zn isotope compositions which likely resulted from quantitative scavenging of dissolved Zn from seawater under euxinic conditions. The difference in the average delta66Zn values of organic-rich shales between the two sections in Guizhou (0.76 ± 0.09per mille) and one section in Hunan (0.59 ± 0.10per mille)might reflect variations of Zn isotope gradient with the depth of seawater. Therefore, the organic-rich sediments need not always represent an isotopically light Zn sink, which is dependent on Zn isotope fractionation in the local basin. However, the delta66Zn values in the Ni-Mo polymetallic sulfide layers are different from those of their host shales, indicating that these sulfide layers did not inherit the Zn isotope signal of seawater. Based on the regular increasing trend in delta66Zn values from Nayong (0.54 ± 0.06per mille) to Zhangjiajie (1.34 ± 0.09per mille) and the presence of Pb-Zn mineralization in the Dengying/Doushantuo Formations, we argue that hydrothermal fluids associated with Pb-Zn mineralization could be a major source of Zn in Ni-Mo sulfide layers, especially in the Nayong location. A possible model is that the hydrothermal fluids related to MVT-type mineralization got overprinted on a multiple-sourced synsedimentary sulfide-rich layer. We provide additional evidence that Zn isotopes have great potential as a tracer of metal source and can be applied to similar types of mineralization as e.g., the late Devonian Ni-Zn-PGE Nick deposit (Selwyn Basin, Canada) or elsewhere.

  • Název v anglickém jazyce

    Large Zn isotope variations in the Ni-Mo polymetallic sulfide layer in the lower Cambrian, South China

  • Popis výsledku anglicky

    In South China, black organic-rich shales in the lower Cambrian Niutitang Formation host a Ni-Mo polymetallic sulfide layer that discontinuously extends over ~1600 km. Seawater and hydrothermal origins are among the many suggested hypotheses and are still under debate. In order to discriminate Zn sources, we report Zn isotopes in Ni-Mo polymetallic sulfide layers and their host shales from the Nayong and Zunyi locations in Guizhou province and the Zhangjiajie section in Hunan province. In each section, host organic-rich shales show homogeneous Zn isotope compositions which likely resulted from quantitative scavenging of dissolved Zn from seawater under euxinic conditions. The difference in the average delta66Zn values of organic-rich shales between the two sections in Guizhou (0.76 ± 0.09per mille) and one section in Hunan (0.59 ± 0.10per mille)might reflect variations of Zn isotope gradient with the depth of seawater. Therefore, the organic-rich sediments need not always represent an isotopically light Zn sink, which is dependent on Zn isotope fractionation in the local basin. However, the delta66Zn values in the Ni-Mo polymetallic sulfide layers are different from those of their host shales, indicating that these sulfide layers did not inherit the Zn isotope signal of seawater. Based on the regular increasing trend in delta66Zn values from Nayong (0.54 ± 0.06per mille) to Zhangjiajie (1.34 ± 0.09per mille) and the presence of Pb-Zn mineralization in the Dengying/Doushantuo Formations, we argue that hydrothermal fluids associated with Pb-Zn mineralization could be a major source of Zn in Ni-Mo sulfide layers, especially in the Nayong location. A possible model is that the hydrothermal fluids related to MVT-type mineralization got overprinted on a multiple-sourced synsedimentary sulfide-rich layer. We provide additional evidence that Zn isotopes have great potential as a tracer of metal source and can be applied to similar types of mineralization as e.g., the late Devonian Ni-Zn-PGE Nick deposit (Selwyn Basin, Canada) or elsewhere.

Klasifikace

  • Druh

    J<sub>imp</sub> - Článek v periodiku v databázi Web of Science

  • CEP obor

  • OECD FORD obor

    10505 - Geology

Návaznosti výsledku

  • Projekt

    <a href="/cs/project/GA17-15700S" target="_blank" >GA17-15700S: Formace černých břidlic jako geochemický indikátor paleoenvironmentálních změn a tektonických podmínek podél aktivních kontinentálních okrajů</a><br>

  • Návaznosti

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Ostatní

  • Rok uplatnění

    2020

  • Kód důvěrnosti údajů

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Údaje specifické pro druh výsledku

  • Název periodika

    Gondwana research

  • ISSN

    1342-937X

  • e-ISSN

  • Svazek periodika

    85

  • Číslo periodika v rámci svazku

    September

  • Stát vydavatele periodika

    NL - Nizozemsko

  • Počet stran výsledku

    13

  • Strana od-do

    224-236

  • Kód UT WoS článku

    000546704800012

  • EID výsledku v databázi Scopus

    2-s2.0-85086726243