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Controls on chemical evolution and rare element enrichment in crystallising albite-spodumene pegmatite and wallrocks: Constraints from mineral chemistry

Identifikátory výsledku

  • Kód výsledku v IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216224%3A14310%2F20%3A00114506" target="_blank" >RIV/00216224:14310/20:00114506 - isvavai.cz</a>

  • Výsledek na webu

    <a href="https://doi.org/10.1016/j.lithos.2019.105289" target="_blank" >https://doi.org/10.1016/j.lithos.2019.105289</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.lithos.2019.105289" target="_blank" >10.1016/j.lithos.2019.105289</a>

Alternativní jazyky

  • Jazyk výsledku

    angličtina

  • Název v původním jazyce

    Controls on chemical evolution and rare element enrichment in crystallising albite-spodumene pegmatite and wallrocks: Constraints from mineral chemistry

  • Popis výsledku v původním jazyce

    Internal differentiation and consequent geochemical evolution in pegmatites are significant processes in the development of economically viable deposits of metal-bearing minerals. Albite-spodumene pegmatites, which represent important resources of Li and Ta worldwide, challenge the general rules of pegmatite petrogenesis as these are nearly homogeneous bodies with little or no intrusion-scale pegmatite zonation. Bulk intrusion concentrations of Li are in the uppermost range obtained by magmatic enrichment experiments, around 2 wt% Li2O, and extensive volumes of saccharoidal or platy albite are present. In Leinster, southeast Ireland, weakly zoned to homogeneous albitised spodumene pegmatites and their wallrocks were studied to compare mineral chemistry variations and understand the internal evolution of pegmatites, characteristics linked to the poor development of zonation, and links between internal evolution and pegmatite-wallrock interactions. Leinster pegmatites present mineralogical, textural and geochemical characteristics coherent with Li-saturation, and possibly supersaturation, prior to crystallisation. Weak border to centre zonation in the thickest bodies can be attributed to geochemically evolved initial melt, likely leading to nearly contemporaneous crystallisation throughout the intrusion and resulting in limited internal geochemical fractionation. Increased abundance of minerals bearing highly incompatible elements (e.g. columbite-group minerals and cassiterite) and network modifiers (e.g. phosphates) in albitite indicates it is a fractionation product from pegmatite crystallisation. Enrichment in incompatible elements B, Li, Rb, Cs and F in spodumene pegmatite exocontacts in different country rock types suggests unmixing of a hydrous fluid from the residual melt after the crystallisation of main pegmatitic assemblages, and that the H2O-rich component was mobilised into country rocks. (C) 2019 Elsevier B.V. All rights reserved.

  • Název v anglickém jazyce

    Controls on chemical evolution and rare element enrichment in crystallising albite-spodumene pegmatite and wallrocks: Constraints from mineral chemistry

  • Popis výsledku anglicky

    Internal differentiation and consequent geochemical evolution in pegmatites are significant processes in the development of economically viable deposits of metal-bearing minerals. Albite-spodumene pegmatites, which represent important resources of Li and Ta worldwide, challenge the general rules of pegmatite petrogenesis as these are nearly homogeneous bodies with little or no intrusion-scale pegmatite zonation. Bulk intrusion concentrations of Li are in the uppermost range obtained by magmatic enrichment experiments, around 2 wt% Li2O, and extensive volumes of saccharoidal or platy albite are present. In Leinster, southeast Ireland, weakly zoned to homogeneous albitised spodumene pegmatites and their wallrocks were studied to compare mineral chemistry variations and understand the internal evolution of pegmatites, characteristics linked to the poor development of zonation, and links between internal evolution and pegmatite-wallrock interactions. Leinster pegmatites present mineralogical, textural and geochemical characteristics coherent with Li-saturation, and possibly supersaturation, prior to crystallisation. Weak border to centre zonation in the thickest bodies can be attributed to geochemically evolved initial melt, likely leading to nearly contemporaneous crystallisation throughout the intrusion and resulting in limited internal geochemical fractionation. Increased abundance of minerals bearing highly incompatible elements (e.g. columbite-group minerals and cassiterite) and network modifiers (e.g. phosphates) in albitite indicates it is a fractionation product from pegmatite crystallisation. Enrichment in incompatible elements B, Li, Rb, Cs and F in spodumene pegmatite exocontacts in different country rock types suggests unmixing of a hydrous fluid from the residual melt after the crystallisation of main pegmatitic assemblages, and that the H2O-rich component was mobilised into country rocks. (C) 2019 Elsevier B.V. All rights reserved.

Klasifikace

  • Druh

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

  • CEP obor

  • OECD FORD obor

    10504 - Mineralogy

Návaznosti výsledku

  • Projekt

    <a href="/cs/project/GA19-05198S" target="_blank" >GA19-05198S: Greisenizace a albitizace - geologické procesy s potenciálem koncentrovat některé kritické suroviny pro moderní technologie</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

    Lithos

  • ISSN

    0024-4937

  • e-ISSN

    1872-6143

  • Svazek periodika

    352

  • Číslo periodika v rámci svazku

    JAN 2020

  • Stát vydavatele periodika

    NL - Nizozemsko

  • Počet stran výsledku

    19

  • Strana od-do

    1-19

  • Kód UT WoS článku

    000515201500023

  • EID výsledku v databázi Scopus

    2-s2.0-85075884610