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Magnesium and zinc isotopic evidence for the involvement of recycled carbonates in the petrogenesis of Gaussberg lamproites, Antarctica

Identifikátory výsledku

  • Kód výsledku v IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F67985831%3A_____%2F22%3A00561358" target="_blank" >RIV/67985831:_____/22:00561358 - isvavai.cz</a>

  • Nalezeny alternativní kódy

    RIV/00216305:26110/22:PU147110

  • Výsledek na webu

    <a href="https://www.sciencedirect.com/science/article/pii/S0009254122003618?via%3Dihub" target="_blank" >https://www.sciencedirect.com/science/article/pii/S0009254122003618?via%3Dihub</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.chemgeo.2022.121067" target="_blank" >10.1016/j.chemgeo.2022.121067</a>

Alternativní jazyky

  • Jazyk výsledku

    angličtina

  • Název v původním jazyce

    Magnesium and zinc isotopic evidence for the involvement of recycled carbonates in the petrogenesis of Gaussberg lamproites, Antarctica

  • Popis výsledku v původním jazyce

    Lamproites are rare mantle-derived peralkaline ultrapotassic rocks, and they are commonly geographically associated with the ultramafic lamprophyres and kimberlites. Their unique geochemistry and mineralogy make determining their mantle source and origin important because of the significance for inferring specific geodynamic processes. In this study, we further examine lamproite petrogenesis using new Mg and Zn isotopic data for the typical Gaussberg lamproites, Antarctica, the source of which were thought to be contributed by recycled crustal materials. Results show that these lamproites have lower δ26Mg (−0.44‰ to −0.39‰) and higher δ66Zn (0.36‰ to 0.39‰) values than terrestrial mantle (δ26Mg = −0.25 ± 0.04‰, δ66Zn = 0.18 ± 0.05‰). The post-magmatic alteration and crustal contamination as well as fractional crystallization and partial melting cannot account for these anomalous Mg and Zn isotopic values. By contrast, the involvement of sedimentary carbonates which are characterized by light δ26Mg (average approximately −2.0‰) and heavy δ66Zn (average ~ +0.91‰) values in their mantle source can explain these Mg and Zn isotopic anomalies. Quantitative modelling suggests that addition of 10–15% subducted dolomite into the source of Gaussberg lamproites can well reproduce their Mg and Zn isotopic values. The source component with light Mg and heavy Zn isotopic compositions can either be sub-continental lithospheric mantle metasomatized by carbonate melts or residue of subducted carbonate-bearing sediments after deep melting in the mantle transition zone. A lithospheric mantle contribution is indeed required to explain their strongly enriched radiogenic isotopic compositions. However, in terms of carbonate component, their positive Zrsingle bondHf anomalies (Hf/Hf* = 1.28–2.19), and extremely high K/U (~40, 000) and Ba/Th (~400) ratios lead us to favor the latter deep recycling model in which the recycled carbonate-bearing sediments subducted as K-hollandite and majorite underwent partial melting within the mantle transition zone.

  • Název v anglickém jazyce

    Magnesium and zinc isotopic evidence for the involvement of recycled carbonates in the petrogenesis of Gaussberg lamproites, Antarctica

  • Popis výsledku anglicky

    Lamproites are rare mantle-derived peralkaline ultrapotassic rocks, and they are commonly geographically associated with the ultramafic lamprophyres and kimberlites. Their unique geochemistry and mineralogy make determining their mantle source and origin important because of the significance for inferring specific geodynamic processes. In this study, we further examine lamproite petrogenesis using new Mg and Zn isotopic data for the typical Gaussberg lamproites, Antarctica, the source of which were thought to be contributed by recycled crustal materials. Results show that these lamproites have lower δ26Mg (−0.44‰ to −0.39‰) and higher δ66Zn (0.36‰ to 0.39‰) values than terrestrial mantle (δ26Mg = −0.25 ± 0.04‰, δ66Zn = 0.18 ± 0.05‰). The post-magmatic alteration and crustal contamination as well as fractional crystallization and partial melting cannot account for these anomalous Mg and Zn isotopic values. By contrast, the involvement of sedimentary carbonates which are characterized by light δ26Mg (average approximately −2.0‰) and heavy δ66Zn (average ~ +0.91‰) values in their mantle source can explain these Mg and Zn isotopic anomalies. Quantitative modelling suggests that addition of 10–15% subducted dolomite into the source of Gaussberg lamproites can well reproduce their Mg and Zn isotopic values. The source component with light Mg and heavy Zn isotopic compositions can either be sub-continental lithospheric mantle metasomatized by carbonate melts or residue of subducted carbonate-bearing sediments after deep melting in the mantle transition zone. A lithospheric mantle contribution is indeed required to explain their strongly enriched radiogenic isotopic compositions. However, in terms of carbonate component, their positive Zrsingle bondHf anomalies (Hf/Hf* = 1.28–2.19), and extremely high K/U (~40, 000) and Ba/Th (~400) ratios lead us to favor the latter deep recycling model in which the recycled carbonate-bearing sediments subducted as K-hollandite and majorite underwent partial melting within the mantle transition zone.

Klasifikace

  • Druh

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

  • CEP obor

  • OECD FORD obor

    10507 - Volcanology

Návaznosti výsledku

  • Projekt

  • Návaznosti

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Ostatní

  • Rok uplatnění

    2022

  • Kód důvěrnosti údajů

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

Údaje specifické pro druh výsledku

  • Název periodika

    Chemical Geology

  • ISSN

    0009-2541

  • e-ISSN

    1872-6836

  • Svazek periodika

    609

  • Číslo periodika v rámci svazku

    October

  • Stát vydavatele periodika

    NL - Nizozemsko

  • Počet stran výsledku

    12

  • Strana od-do

    121067

  • Kód UT WoS článku

    000851373400004

  • EID výsledku v databázi Scopus

    2-s2.0-85136454362